WO2003052206A1 - A paper product comprising a polyvinylamine polymer - Google Patents
A paper product comprising a polyvinylamine polymer Download PDFInfo
- Publication number
- WO2003052206A1 WO2003052206A1 PCT/US2002/029937 US0229937W WO03052206A1 WO 2003052206 A1 WO2003052206 A1 WO 2003052206A1 US 0229937 W US0229937 W US 0229937W WO 03052206 A1 WO03052206 A1 WO 03052206A1
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- WO
- WIPO (PCT)
- Prior art keywords
- polyvinylamine
- web
- paper product
- complexing agent
- fibers
- Prior art date
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Classifications
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H5/00—Special paper or cardboard not otherwise provided for
- D21H5/26—Special paper or cardboard manufactured by dry method; Apparatus or processes for forming webs by dry method from mainly short-fibre or particle material, e.g. paper pulp
- D21H5/265—Treatment of the formed web
- D21H5/2657—Consolidation
- D21H5/2664—Addition of a binder, e.g. synthetic resins or water
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/18—Reinforcing agents
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/76—Processes or apparatus for adding material to the pulp or to the paper characterised by choice of auxiliary compounds which are added separately from at least one other compound, e.g. to improve the incorporation of the latter or to obtain an enhanced combined effect
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/36—Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
- D21H17/56—Polyamines; Polyimines; Polyester-imides
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/71—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
- D21H17/72—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic material
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/002—Tissue paper; Absorbent paper
Definitions
- wet strength agents have been added to paper products in order to increase the strength or otherwise control the properties of the product when contacted with water and/or when used in a wet environment.
- wet strength agents are added to paper towels so that the paper towel can be used to wipe and scrub surfaces after being wetted without the towel disintegrating.
- Wet strength agents are also added to facial tissues to prevent the tissues from tearing when contacting fluids.
- wet strength agents are also added to bath tissues to provide strength to the tissues during use.
- wet strength agents When added to bath tissues, however, the wet strength agents should not prevent the bath tissue from disintegrating when dropped in a commode and flushed into a sewer line. Wet strength agents added to bath tissues are sometimes referred to as temporary wet strength agents since they only maintain wet strength in the tissue for a specific length of time.
- the present invention is generally directed to the use of polyvinylamines in fibrous and textile products, such as paper products, in order to control and improve various properties of the product.
- a polyvinylamine can be combined with a complexing agent to increase the wet strength of a paper product.
- the combination of a polyvinylamine and a complexing agent can also be used to render a web more hydrophobic, to facilitate the application of dyes to a cellulosic material, or to otherwise apply other additives to a cellulosic material.
- the present invention is directed to a paper product having improved wet strength properties.
- the paper product includes a fibrous web containing cellulosic fibers.
- the fibrous web further includes a combination of a polyvinylamine polymer and a polymeric anionic reactive compound.
- the polyvinylamine polymer and the polymeric anionic reactive compound can form a polyelectrolyte complex within the fibrous web.
- the paper product can be a paper towel, a facial tissue, a bath tissue, a wiper, or any other suitable product.
- the polyvinylamine polymer can be incorporated into the web by being added to an aqueous suspension of fibers that is used to form the web. Alternatively, the polyvinylamine polymer can be applied to after the web has been formed. When applied to the surface, the polyvinylamine polymer can be printed or sprayed onto to the surface in a pattern in one application. The polyvinylamine polymer can be added prior to the polymeric anionic reactive compound, can be added after the polymeric anionic reactive compound, or can be applied simultaneously with the polymeric anionic reactive compound. The polyvinylamine polymer can be combined with the fibrous web as a homopolymer or a copolymer.
- the polyvinylamine polymer is combined with the fibrous web as a partially hydrolyzed polyvinylformamide.
- the polyvinylformamide can be hydrolyzed from about 50% to about 90%, and particularly, from about 75% to about 95%.
- any suitable, polymeric anionic reactive compound can be used in the present invention.
- the polymeric anionic reactive compound can be an anionic polymer containing carboxylic acid groups, anhydride groups, or salts thereof.
- the polymeric anionic reactive compound can be, for instance, a copolymer of a maleic anhydride or a maleic acid or, alternatively, poly-1 ,2-diacid.
- the polyvinylamine polymer and polymeric anionic reactive compound can each be added to the fibrous web in an amount of at least about 0.1 % by weight, particularly at least 0.2% by weight, based upon the dry weight of the web.
- each polymer can be added to the fibrous web in an amount from about 0.1% to about 10% by weight, and particularly from about 0.1% to about 6% by weight.
- greater quantities of the components can be added to the fibrous web depending upon the particular application. For instance, in some applications it may be desirable to add one of the polymers in a quantity of greater than 50% by weight.
- the polyvinylamine polymer in combination with the polymeric anionic reactive compound increases the wet strength of the web.
- the polymers are added to the fibrous web in an amount such that the web has a 25 microliter Pipette Intake Time of greater than 30 seconds, and particularly greater than 60 seconds.
- the fibrous web can have a Water Drop Intake Time of greater than 30 seconds, and particularly greater than 60 seconds.
- the present invention is directed to products and processes using the combination of a polyvinylamine polymer and a polymeric aldehyde functional compound, a glyoxylated polyacrylamide, or an anionic surfactant.
- polymeric aldehyde functional compounds include aldehyde celluloses and aldehyde functional polysaccharides.
- a polymeric aldehyde functional compound, a glyoxylated polyacrylamide, or anionic surfactant can be used similar to a polymeric anionic reactive compound as discussed above.
- the present invention is directed to a method for improving the wet strength properties of a paper product. The method includes the steps of providing a fibrous web containing pulp fibers. The fibrous web is combined with a polyvinylamine and a complexing agent.
- the complexing agent can be a polymeric anionic reactive compound, a polymeric aldehyde functional compound, a glyoxylated polyacrylamide, an anionic surfactant, or mixtures thereof.
- the fibrous web is formed from an aqueous suspension of fibers.
- the polyvinylamine and the complexing agent are added to the aqueous suspension in order to be incorporated into the fibrous web.
- the complexing agent is added to the aqueous suspension while the polyvinylamine is added after the web is formed.
- the polyvinylamine is added to the aqueous suspension, while the complexing agent is added after the web is formed.
- the polyvinylamine polymer and the complexing agent are both added after the web is formed.
- the process of the present invention can also be used to facilitate dyeing of a fibrous material.
- the present invention is further directed to a process for dyeing fibrous materials such as a textile with an acid dye.
- the process includes the steps of contacting a cellulosic fibrous material with a polyvinylamine and a complexing agent, such as a polymeric anionic reactive compound. Thereafter, the cellulosic fibrous material is contacted with an acid dye. It is believed that the complexing agent holds the polyvinylamine to the cellulosic material while the acid dye binds to the polyvinylamine.
- the fibrous material can be a fiber, a yarn, or a fabric.
- the cellulosic material can be paper fibers, cotton fibers, or rayon fibers.
- a polyvinylamine can be used in accordance with the present invention to bind other additives to the material.
- the process of the present invention is directed to applying polysiloxanes to fibrous materials that have been previously treated with a polyvinylamine in accordance with the present invention.
- Figures 1 through 11 are graphical representations of some of the results obtained in the examples described below.
- the present invention is directed to adding polyvinylamine in combination with another agent, such as a complexing agent, to a fibrous material in order to improve the properties of the material.
- a complexing agent such as a complexing agent
- the polyvinylamine and the complexing agent can be added to a paper web in order to improve the strength properties of the web.
- the polyvinylamine in combination with the complexing agent can also be used to render a web hydrophobic.
- the combination of the above components can produce a sizing effect on a web to the point that applied water will bead up on the web and not penetrate the web.
- the combination of a polyvinylamine and a complexing agent can be added to a textile material in order to increase the affinity of the textile material to acid dyes.
- the textile material can be made from, for instance, pulp fibers, cotton fibers, rayon fibers, or any other suitable cellulosic material.
- polyvinylamine in combination with a complexing agent can also receive and bond to other treating agents.
- the polyvinylamine and complexing agent can also increase the affinity of the web for softening agents, such as polysiloxanes.
- treating webs in accordance with the present invention can also increase the wet to dry strength ratio, provide improved sizing behavior such as increased contact angle or decreased wettability, and can improve the tactile properties of the web, such as lubricity.
- Various different polymers and chemical compounds can be combined with a polyvinylamine in accordance with the present invention.
- Suitable complexing agents include polymeric anionic reactive compounds, polymeric aldehyde functional compounds, anionic surfactants, mixtures thereof, and the like.
- Cellulosic webs prepared in accordance with the present invention can be used for a wide variety of applications.
- products made according to the present invention include tissue products such as facial tissues or bath tissues, paper towels, wipers, and the like.
- Webs made according to the present invention can also be used in diapers, sanitary napkins, wet wipes, composite materials, molded paper products, paper cups, paper plates, and the like.
- Materials treated with an acid dye according to the present invention can be used in various textile applications, particularly in textile webs comprising a blend of cellulosic materials and wool, nylon, silk or other polyamide or protein-based fibers.
- any suitable polyvinylamine may be used in the present invention.
- the polyvinylamine polymer can be a homopolymer or can be a copolymer.
- Useful copolymers of polyvinylamine include those prepared by hydrolyzing polyvinylformamide to various degrees to yield copolymers of polyvinylformamide and polyvinylamine.
- Exemplary materials include the Catiofast® series sold commercially by BASF (Ludwigshafen, Germany). Such materials are also described in U.S. Patent No. 4,880,497 to Phohl, et al. and U.S. Patent No. 4,978,427 also to Phohl, et al., which are incorporated herein by reference.
- polyvinylamine polymers can have a molecular weight range of from about 5,000 to 5,000,000, more specifically from about 50,000 to 3,000,0000, and most specifically from about 80,000 to 500,000.
- the degree of hydrolysis, for polyvinylamines formed by hydrolysis of polyvinylformamide or a copolymer of polyvinylformamide or derivatives thereof can be about any of the following or greater: 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, and 95%, with exemplary ranges of from about 30% to 100%, or from about 50% to about 95%. In general, better results are obtained when a majority of the polyvinylformamide is hydrolyzed.
- Polyvinylamine compounds that may be used in the present invention include copolymers of N-vinylformamide and other groups such as vinyl acetate or vinyl propionate, where at least a portion of the vinylformamide groups have been hydrolyzed. Exemplary compounds and methods are disclosed in U.S. Pat. Nos. 4,978,427; No. 4,880,497; 4,255,548; 4,421 ,602; and 2,721 ,140, all of which are herein incorporated by reference. Copolymers of polyvinylamine and polyvinyl alcohol are disclosed in US Patent No. 5,961 ,782, "Crosslinkable Creping Adhesive Formulations," issued Oct. 5, 1999 to Luu et al., herein incorporated by reference. Polymeric Anionic Reactive Compounds
- a polyvinylamine polymer is combined with a second component to arrive at the benefits and advantages of the present invention.
- the polyvinylamine polymer is combined with a polymeric anionic reactive compound.
- the combined polyvinylamine and the polymeric anionic reactive compound When combined and added to a fibrous material such as a web made from cellulosic fibers, the combined polyvinylamine and the polymeric anionic reactive compound not only improve strength such as wet strength, but can also produce a sizing effect as well, offering increased control over the surface chemistry and wettability of the treated web.
- polymeric anionic reactive compounds have been used in wet strength applications.
- the combination of a polymeric anionic reactive compound with a polyvinylamine has produced unexpected benefits and advantages. For instance, web treated with a polymeric anionic reactive compound alone will have an increase in wet strength but will generally remain hydrophilic. Likewise, webs treated with a polyvinylamine will also show an increase in wet strength and remain hydrophilic.
- addition of both ingredients, a polymeric anionic reactive compound and polyvinylamine polymer can result not only in enhanced wet and dry strength, but can also, in one embodiment, provide a sizing effect wherein the treated web becomes hydrophobic.
- wet and dry tensile properties can be controlled as well as the wettability or surface contact angle of the treated web by adjusting the amount of polyvinylamine in combination with the polymeric anionic reactive compound.
- Polymeric anionic reactive compounds are polymers having repeating units containing two or more anionic functional groups that will covalently bond to hydroxyl groups of cellulosic fibers. Such compounds will cause inter-fiber crosslinking between individual cellulose fibers.
- the functional groups are carboxylic acids, anhydride groups, or the salts thereof.
- the repeating units include two carboxylic acid groups on adjacent atoms, particularly adjacent carbon atoms, wherein the carboxylic acid groups are capable of forming cyclic anhydrides and specifically 5- member ring anhydrides. This cyclic anhydride, in the presence of a cellulosic hydroxyl group at elevated temperature, forms ester bonds with the hydroxyl groups of the cellulose.
- Polymers, including copolymers, terpolymers, block copolymers, and homopolymers, of maleic acid represent one embodiment, including copolymers of acrylic acid and maleic acid.
- Polyacrylic acid can be useful for the present invention if a significant portion of the polymer (e.g., 15% of the monomeric units or greater, more specifically 40% or greater, more specifically still 70% or greater) comprises monomers that are joined head to head, rather than head to tail, to ensure that carboxylic acid groups are present on adjacent carbons.
- the polymeric anionic reactive compound is a poly- 1 ,2-diacid.
- Exemplary polymeric anionic reactive compounds include the ethylene/maleic anhydride copolymers described in U.S. Patent No. 4,210,489 to Markofsky, herein incorporated by reference. Vinyl/maleic anhydride copolymers and copolymers of epichlorohydrin and maleic anhydride or phthalic anhydride are other examples. Copolymers of maleic anhydride with olefins can also be considered, including poly(styrene/maleic anhydride), as disclosed in German Patent No. 2,936,239. Copolymers and terpolymers of maleic anhydride that can be used are disclosed in U.S. Patent No. 4,242,408 to Evani et al., herein incorporated by reference.
- polymeric anionic reactive compounds examples include terpolymers of maleic acid, vinyl acetate, and ethyl acetate known as BELCLENE® DP80 (Durable Press 80) and BELCLENE® DP60 (Durable Press 60), from FMC Corporation (Philadelphia, PA).
- maleic anhydride polymers are disclosed in WO 99/67216, "Derivatized Polymers of Alpha Olefin Maleic Anhydride Alkyl Half Ester or Full Acid," published Dec. 29, 1999.
- Other polymers of value can include maleic anhydride-vinyl acetate polymers, polyvinyl methyl ether-maleic anhydride copolymers, such as the commercially available Gantrez-AN119 from International Specialty Products (Calvert City, Kentucky), isopropenyl acetate-maleic anhydride , copolymers, itaconic acid-vinyl acetate copolymers, methyl styrene-maleic anhydride copolymers, styrene-maleic anhydride copolymers, methylmethacrylate- maleic anhydride copolymers, and the like.
- the polymeric anionic reactive compound can have any viscosity provided that the compound can be applied to the web.
- the polymeric anionic reactive compound has a relatively low molecular weight and thus a low viscosity to permit effective spraying or printing onto a web.
- Useful polymeric anionic reactive compounds according to the present invention can have a molecular weight less than about 5,000, with an exemplary range of from about 500 to 5,000, more specifically less than about 3,000, more specifically still from about 600 to about 2,500, and most specifically from about 800 to 2,000 or from about 500 to 1 ,400.
- the polymeric anionic reactive compound BELCLENE@ DP80 for instance, is believed to have a molecular weight of from about 800 to about 1000.
- molecular weight refers to number averaged molecular weight determined by gel permeation chromatography (GPC) or an equivalent method.
- the polymeric anionic reactive compound can be a copolymer or terpolymer to improve flexibility of the molecule relative to the homopolymer alone. Improved flexibility of the molecule can be manifest by a reduced glass transition temperature as measured by differential scanning calorimetry.
- a low molecular weight compound such as BELCLENE® DP80 will generally have a low viscosity, simplifying the processing and application of the compound.
- low viscosity is useful for spray application, whether the spray is to be applied uniformly or nonuniformly (e.g., through a template or mask) to the product.
- a saturated (50% by weight) solution of BELCLENE ⁇ DP80 for example, has a room temperature viscosity of about 9 centipoise, while the viscosity of a solution diluted to 2%, with 1% SHP catalyst, is approximately 1 centipoise (only marginally greater than that of pure water).
- the polymeric anionic reactive compound to be applied to the paper web can have a viscosity at 25°C of about 50 centipoise or less, specifically about 10 centipoise or less, more specifically about 5 centipoise or less, and most specifically from about 1 centipoise to about 2 centipoise.
- the solution at the application temperature can exhibit a viscosity less than 10 centipoise and more specifically less than 4 centipoise.
- the liquid viscosity can be less than 100 centipoise, more specifically about 50 centipoise or less; more specifically still about 15 centipoise or less, and most specifically from about 4 to about 10 centipoise.
- viscosity is measured with a Sofrasser SA Viscometer (Villemandeur, France) connected to a type MIVI-6001 measurement panel.
- the viscometer employs a vibrating rod which responds to the viscosity of the surrounding fluid.
- a 30 ml glass tube (Corex H No. 8445) supplied with the viscometer is filled with 10.7 ml of fluid and the tube is placed over the vibrating rod to immerse the rod in fluid.
- a steel guide around the rod receives the glass tube and allows the tube to be completely inserted into the device to allow the liquid depth over the vibrating rod to be reproducible.
- polymeric anionic reactive compounds of the present invention is that relatively high pH values can be used when the catalyst is present, making the compound more suitable for neutral and alkaline papermaking processes and more suitable for a variety of processes, machines, and fiber types.
- polymeric anionic reactive compound solutions with added catalyst can have a pH above 3, more specifically above 3.5, more specifically still above 3.9, and most specifically of about 4 or greater, with an exemplary range of from 3.5 to 7 or from 4.0 to 6.5. These same pH values can be maintained in combination with the polyvinylamine polymer solution.
- the polymeric anionic reactive compounds of the present invention can yield we dry tensile ratios much higher than traditional wet strength agents, with values reaching ranges as high as from 30% to 85%, for example.
- the PARC need not be neutralized prior to treatment of the fibers.
- the PARC need not be neutralized with a fixed base.
- a fixed base is a monovalent base that is substantially nonvolatile under the conditions of treatment, such as sodium hydroxide, potassium hydroxide, or sodium carbonate, and t-butylammonium hydroxide.
- co-catalysts including volatile basic compounds such as imidazole or triethyl amine, with sodium hypophosphite or other catalysts.
- a polyvinylamine polymer containing amino groups can react in solution with the polymeric anionic reactive compound, particularly with the carboxyl groups to yield a polyelectrolyte complex (sometimes termed a coacervate) that upon heating, reacts to form amide bonds that crosslink the two molecules, leaving a hydrophobic backbone.
- a polyelectrolyte complex sometimes termed a coacervate
- carboxyl groups on the polymeric anionic reactive compound can form ester cross links with hydroxyl groups on the cellulose
- amino groups on the polyvinylamine polymer can form hydrogen bonds with hydroxyl groups on the cellulose or covalent bonds with functional groups on the cellulose, such as aldehyde groups that may have been added by enzymatic or chemical treatment, or with carboxyl groups on the cellulose that may have been provided by chemical treatment such as certain forms of bleaching or ozonation.
- the polymeric anionic reactive compound can be used in conjunction with a catalyst.
- Suitable catalysts for use with PARC include any catalyst that increases the rate of bond formation between the PARC and cellulose fibers.
- Useful catalysts include alkali metal salts of phosphorous containing acids such as alkali metal hypophosphites, alkali metal phosphites, alkali metal polyphosphonates, alkali metal phosphates, and alkali metal suifonates.
- Particularly desired catalysts include alkali metal polyphosphonates such as sodium hexametaphosphate, and alkali metal hypophosphites such as sodium hypophosphite.
- IMDZ imidazole
- TAA triethyl amine
- Inorganic compounds such as aluminum chloride and organic compounds such as hydroxyethane diphosphoric acid can also promote crosslinking.
- catalysts are disodium acid pyrophosphate, tetrasodium pyrophosphate, pentasodium tripolyphosphate, sodium trimetaphosphate, sodium tetrametaphosphate, lithium dihydrogen phosphate, sodium dihydrogen phosphate and potassium dihydrogen phosphate.
- the catalyst is typically present in an amount in the range from about 5 to about 100 weight percent of the PARC.
- the catalyst is present in an amount of about 25 to 75% by weight of the polycarboxylic acid, most desirably about 50% by weight of the PARC.
- the polymeric anionic reactive compound can be added with a polyvinylamine polymer using various methods and techniques depending upon the particular application.
- one or both of the components can be added during formation of the cellulosic material or can be applied to a surface of the material.
- the two components can be added simultaneously or can be added one after the other.
- the PARC can be applied independently of the polyvinylamine polymers on the web, meaning that it can be applied in a distinct step or steps and/or applied to a different portion of the web or the fibers than the polyvinylamine polymers.
- the PARC can be applied in an aqueous solution to an existing papermaking web.
- the solution can be applied either as an online step in a continuous papermaking process along a section of a papermaking machine or as an offline or converting step following formation, drying, and reeling of a paper web.
- the PARC solution is can be added at about 10 to 200% add-on, more specifically from about 20% to 100% add-on, most specifically from about 30% to 75% add-on, where add-on is the percent by weight of PARC solution to the dry weight of the web. In other words, 100% add-on is a 1 :1 weight ratio of PARC solution to dry web.
- the final percent by weight PARC to the web can be from about 0.1 to 6%, more specifically from about 0.2% to 1.5%.
- the concentration of the PARC solution can be adjusted to ensure that the desired amount of PARC is added to the web.
- the PARC is applied heterogeneously to the web, with heterogeneity due to the z-direction distribution of PARC or due to the distribution of the PARC in the plane of the web.
- the PARC may be selectively applied to one or both surfaces of the web, with a relatively lower concentration of the PARC in the middle of the web or on an untreated surface.
- the PARC may be applied to the web in a pattern such that some portions of the treated surface or surfaces of the web have little or no PARC, while other portions have an effective quantity capable of significantly increasing wet performance in those portions.
- any ratio of polyvinylamine compound mass to PARC mass can be used.
- the ratio of polyvinylamine compound mass to PARC mass can be from 0.01 to 100, more specifically from 0.1 to 10, more specifically still from 2 to 5, and most specifically from 0.5 to 1.5.
- polymeric anionic reactive compounds another class of compounds that can be used with a polyvinylamine in accordance with the present invention are polymeric aldehyde-functional compounds.
- polyvinylamines can be combined with polymeric aldehyde- functional compounds and papermaking fibers or other cellulosic fibers to create improved physical and chemical properties in the resulting web.
- the polymeric aldehyde-functional compounds can comprise gloxylated polyacrylamides, aldehyde-rich cellulose, aldehyde-functional polysaccharides, and aldehyde functional cationic, anionic or non-ionic starches.
- Exemplary materials include those disclosed by lovine, et.al., in US Patent No.
- the polymeric aldehyde-functional compounds can have a molecular weight of about 10,000 or greater, more specifically about 100,000 or greater, and more specifically about 500,000 or greater. Alternatively, the polymeric aldehyde-functional compounds can have a molecular weight below about 200,000, such as below about 60,000.
- aldehyde-functional polymers of use in the present invention include dialdehyde guar, aldehyde-functional wet strength additives further comprising carboxylic groups as disclosed in WO 01/83887, published November 8, 2001 by Thornton, et al.. dialdehyde inulin; and the dialdehyde- modified anionic and amphoteric polyacrylamides of WO 00/11046, published March 2, 2000, the U.S. equivalent of which is application Serial No. 99/18706, filed August 19, 1998 by Geer and Staib of Hercules, Inc., herein incorporated by reference.
- Aldehyde-containing surfactants as disclosed in U.S. Patent No. 6,306,249 issued October 23, 2001 to Galante, et al.. can also be used.
- the aldehyde-functional compound can have at least 5 milliequivalents (meq) of aldehyde per 100 grams of polymer, more specifically at least 10 meq, more specifically still about 20 meq or greater, and most specifically about 25 meq per 100 grams of polymer or greater.
- polyvinylamine when combined with aldehyde-rich cellulose such as dialdehyde cellulose or a sulfonated dialdehyde cellulose, can significantly increase wet and dry strength beyond what is possible with curing of dialdehyde cellulose alone, and that these gains can be achieved without the need for temperatures above the normal drying temperatures of paper webs (e.g., about 100°C).
- aldehyde-rich cellulose can include cellulose oxidized with periodate solutions, as disclosed in US Patent No. 5,703,225, issued Dec.
- cellulose treated with enzymes such as the cellulase-treated cellulose of WO 97/27363, "Production of Sanitary Paper,” published July 31, 1997, and the aldehyde-modified cellulose products of National Starch, including that disclosed in EP 1 ,077,286-A1 , published Feb. 21 , 2001.
- the polymeric aldehyde-functional compound can be a glyoxylated polyacrylamide, such as a cationic glyoxylated polyacrylamide.
- a glyoxylated polyacrylamide such as a cationic glyoxylated polyacrylamide.
- Such compounds include PAREZ 631 NC wet strength resin available from Cytec Industries of West Patterson, New Jersey, chloroxylated polyacrylamides described in U.S. Patent No. 3,556,932 to Coscia, et al. and U.S. Patent No. 3,556,933 to Williams, et al. which are incorporated herein by reference, and HERCOBOND 1366, manufactured by Hercules, Inc. of Wilmington, Delaware.
- PAREZ 745 is a glyoxylated poly(acrylamide-co-diallyl dymethyl ammonium chloride). At times it may be advantageous to utilize a mixture of high and low molecular weight glyoxylated polyacrylamides to obtain a desire effect.
- a temporary wet strength agent as opposed to a permanent wet strength agent, is defined as those resins which, when incorporated into paper or tissue products, will provide a product which retains less than 50% of its original wet strength after exposure to water for a period of at least 5 minutes.
- Permanent wet strength agents provide a product that will retain more than 50% of its original wet strength after exposure to water for a period of at least 5 minutes.
- the wet strength characteristics of a paper product can be carefully controlled by adjusting the relative amounts of the glyoxylated polyacrylamide and the polyvinylamine polymer.
- Other Compositions That Can Be Used With A Polyvinlamine Polymer can also be combined with the polyvinylamine polymer. For instance, in one application, other wet strength agents not identified above can be used.
- wet strength agents are materials used to immobilize the bonds between fibers in the wet state.
- the means by which fibers are held together in paper and tissue products involve hydrogen bonds and sometimes combinations of hydrogen bonds and covalent and/or ionic bonds.
- the wet state usually will mean when the product is largely saturated with water or other aqueous solutions, but could also mean significant saturation with body fluids such as urine, blood, mucus, menses, runny bowel movement, lymph and other body exudates.
- wet strength agent any material that when added to a paper web or sheet results in providing the sheet with a mean wet geometric tensile strength: dry geometric tensile strength ratio in excess of 0.1 will, for purposes of this invention, be termed a wet strength agent. As described above, typically these materials are termed either as permanent wet strength agents or as temporary wet strength agents.
- various permanent wet strength agents and temporary wet strength agents can be used in combination with a polyvinylamine polymer.
- temporary wet strength agents combined with a polyvinylamine polymer can result in a composition having permanent wet strength characteristics.
- the wet strength agents that can be used in accordance with the present invention can be cationic, nonionic or anionic.
- the additives are not strongly cationic to decrease repulsive forces in the presence of cationic polyvinylamine.
- Permanent wet strength agents comprising cationic oligomeric or polymeric resins can be used in the present invention, but do not generally yield the synergy observed with less cationic additives.
- Polyamide-polyamine-epichlorohydrin type resins such as KYMENE 557H sold by Hercules, Inc. (Wilmington, Delaware) are the most widely used permanent wet-strength agents, but have come under increasing environmental scrutiny due to the reactive halogen group in these molecules.
- cationic resins include polyethylenimine resins and aminoplast resins obtained by reaction of formaldehyde with melamine or urea.
- surfactants can include, for instance, linear and branched-chain sodium alkylbenzenesulfonat.es, linear and branched-chain alkyl sulfates, and linear and branched chain alkyl ethoxy sulfates.
- Noncationic and zwitterionic surfactants are further described in U.S. Patent No. 4,959,125, "Soft Tissue Paper Containing Noncationic Surfactant," issued September 25, 1990 to Spendel, herein incorporated by reference.
- the surfactant can be applied by any conventional means, such as spraying, printing, brush coating, and the like. Two or more surfactants may be combined in any manner, if desired.
- a polyvinylamine polymer is added to a paper web in conjunction with a complexing agent, such as a polymeric anionic reactive compound or a polymeric aldehyde functional compound in order to provide various benefits to the web, including improved wet strength.
- a complexing agent such as a polymeric anionic reactive compound or a polymeric aldehyde functional compound
- the polyvinylamine polymer and the complexing agent in one embodiment, can be applied as aqueous solutions to a cellulosic web, fibrous slurry or individual fibers.
- the complexing agent can also be applied in the form of a suspension, a slurry or as a dry reagent depending upon the particular application. When used as a dry reagent, sufficient water should be available to permit interaction of the complexing agent with the molecules of the polyvinylamine polymer.
- the polyvinylamine polymer and the complexing agent may be combined first and then applied to a web or fibers, or the two components may be applied sequentially in either order. After the two components have been applied to the web, the web or fibers are dried and heatedly sufficiently to achieve the desired interaction between the two compounds.
- Slurry consistency can be from 0.2% to about 50%, specifically from about 0.2% to 10%, more specifically from about 0.3% to about 5%, and most specifically from about 1% to 4%.
- a spray applied to a fibrous web may be mounted over a moving paper web to apply a desired dose of a solution to a web that can be moist or substantially dry.
- Printing onto a web such as by offset printing, gravure printing, flexographic printing, ink jet printing, digital printing of any kind, and the like.
- Coating onto one or both surfaces of a web such as blade coating, air knife coating, short dwell coating, cast coating, and the like.
- comminuted or flash dried fibers may be entrained in an air stream combined with an aerosol or spray of the compound to treat individual fibers prior to incorporation into a web or other fibrous product.
- Impregnation of a wet or dry web with a solution or slurry wherein the compound penetrates a significant distance into the thickness of the web, such as more than 20% of the thickness of the web, more specifically at least about 30% and most specifically at least about 70% of the thickness of the web, including completely penetrating the web throughout the full extent of its thickness.
- One useful method for impregnation of a moist web is the Hydra-Sizer® system, produced by Black Clawson Corp., Watertown, NY, as described in "New Technology to Apply Starch and Other Additives," Pulp and Paper Canada, 100(2):
- T42-T44 (Feb. 1999).
- This system includes a die, an adjustable support structure, a catch pan, and an additive supply system.
- a thin curtain of descending liquid or slurry is created which contacts the moving web beneath it. Wide ranges of applied doses of the coating material are said to be achievable with good runnability.
- the system can also be applied to curtain coat a relatively dry web, such as a web just before or after creping.
- Foam application of the additive to a fibrous web e.g., foam finishing
- a pressure differential e.g., vacuum-assisted impregnation of the foam.
- Principles of foam application of additives such as binder agents are described in the following publications: F. Clifford, "Foam Finishing Technology: The Controlled Application of Chemicals to a Moving Substrate,” Textile Chemist and Colorist, Vol. 10, No. 12, 1978, pages 37-40; C.W. Aurich, "Uniqueness in Foam
- the application level can be from about 0.1 % to about 10% by weight relative to the dry mass of the web for of any of the polyvinylamine polymer and the complexing agent. More specifically, the application level can be from about 0.1% to about 4%, or from about 0.2% to about 2%. Higher and lower application levels are also within the scope of the present invention. In some embodiments, for example, application levels of from 5% to 50% or higher can be considered.
- the polyvinylamine polymer when combined with the web or with cellulosic fibers can have any pH, though in many embodiments it is desired that the polyvinylamine solution in contact with the web or with fibers have a pH below any of 10, 9, 8 and 7, such as from 2 to about 8, specifically from about 2 to about 7, more specifically from about 3 to about 6, and most specifically from about 3 to 5.5. Alternatively, the pH range may be from about 5 to about 9, specifically from about 5.5 to about 8.5, and most specifically from about 6 to about 8. These pH values can apply to the polyvinylamine polymer prior to contacting the web or fibers, or to a mixture of polyvinylamine polymer and a second compound in contact with the web or the fibers prior to drying.
- the solids level of the web may be about 10% or higher (i.e., the web comprises about 10 grams of dry solids and 90 grams of water, such as about any of the following solids levels or higher: 12%, 15%, 18%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 60%, 75%, 80%, 90%, 95%, 98%, and 99%, with exemplary ranges of from about 30% to about 100% and more specifically from about 65% to about 90%.
- polyvinylamine polymers can be distributed in a wide variety of ways.
- polyvinylamine polymers may be uniformly distributed, or present in a pattern in the web, or selectively present on one surface or in one layer of a multilayered web.
- the entire thickness of the paper web may be subjected to application of polyvinylamine polymers and other chemical treatments described herein, or each individual layer may be independently treated or untreated with the polyvinylamine polymers and other chemical treatments of the present invention.
- the polyvinylamine polymers of the present invention are predominantly applied to one layer in a multilayer web.
- at least one layer is treated with significantly less polyvinylamine than other layers.
- an inner layer can serve as a treated layer with increased wet strength or other properties.
- the polyvinylamine polymers may also be selectively associated with one of a plurality of fiber types, and may be adsorbed or chemisorbed onto the surface of one or more fiber types.
- bleached kraft fibers can have a higher affinity for polyvinylamine polymers than synthetic fibers that may be present.
- the polyvinylamine or other chemicals can be selectively concentrated in the densified regions of the web (e.g., a densified network corresponding to regions of the web compressed by an imprinting fabric pressing the web against a Yankee dryer, wherein the densified network can provide good tensile strength to the three-dimensional web).
- a densified network corresponding to regions of the web compressed by an imprinting fabric pressing the web against a Yankee dryer, wherein the densified network can provide good tensile strength to the three-dimensional web.
- the densified regions have been imprinted against a hot dryer surface while the web is still wet enough to permit migration of liquid between the fibers to occur by means of capillary forces when a portion of the web is dried.
- migration of the aqueous solution of polyvinylamine can move the polymer toward the densified regions experiencing the most rapid drying or highest levels of heat transfer.
- regions of the web disposed above the deflection conduits may have a higher concentration of polyvinylamine or other water-soluble chemicals than the densified regions, for drying will tend to occur first in the regions of the web through which air can readily pass, and capillary wicking can bring fluid from adjacent portions of the web to the regions where drying is occurring most rapidly.
- water-soluble reagents may be present at a relatively higher concentration (compared to other portions of the web) in the densified regions or the less densified regions ("domes").
- the reagents may also be present substantially uniformly in the web, or at least without a selective concentration in either the densified or undensified regions.
- the fibrous web to be treated in accordance with the present invention can be made by any method known in the art. Airiaid webs can be used, such as those made with DanWeb or Kroyer equipment.
- the web can be wetlaid, such as webs formed with known papermaking techniques wherein a dilute aqueous fiber slurry is disposed on a moving wire to filter out the fibers and form an embryonic web which is subsequently dewatered by combinations of units including suction boxes, wet presses, dryer units, and the like. Examples of known dewatering and other operations are given in U.S. Patent No. 5,656,132 to Farrington et al. Capillary dewatering can also be applied to remove water from the web, as disclosed in US Patents 5,598,643 issued February 4, 1997 and 4,556,450 issued December 3, 1985, both to S. C. Chuang et al.
- Drying operations can include drum drying, through drying, steam drying such as superheated steam drying, displacement dewatering, Yankee drying, infrared drying, microwave drying, radio frequency drying in general, and impulse drying, as disclosed in US Patent No. 5,353,521 , issued Oct. 11 , 1994 to Orloff; and US Patent No. 5,598,642, issued Feb. 4, 1997 to Orloff et al.
- Other drying technologies can be used, such as those described by R. James in “Squeezing More out of Pressing and Drying," Pulp and Paper International, Vol. 41 , No. 12 (Dec. 1999), pp. 13-17.
- Displacement dewatering is described by J.D. Lindsay, “Displacement Dewatering To Maintain Bulk,” Paperi Ja Puu, vol.
- the dryer drum can also be a Hot Roll Press (HRP), as described by M. Foulger and J. Parisian in "New Developments in Hot Pressing," Pulp and Paper Canada, Vol. 101 , No. 2, Feb., 2000, pp. 47-49.
- HRP Hot Roll Press
- Other methods employing differential gas pressure include the use of air presses as disclosed US Patent No. 6,096,169, “Method for Making Low-Density Tissue with Reduced Energy Input,” issued Aug. 1 , 2000 to Hemans et al.; and US Patent No. 6,143,135, "Air Press For Dewatering A Wet Web,” issued Nov. 7, 2000 to Hada et al. Also relevant are the paper machines disclosed in US Patent No. 5,230,776 issued July 27, 1993 to I A Andersson et al.
- a moist fibrous web can also be formed by foam forming processes, wherein the fibers are entrained or suspended in a foam prior to dewatering, or wherein foam is applied to an embryonic web prior to dewatering or drying.
- foam forming processes include those of US Patent 5,178,729, issued Jan. 12, 1993 to Janda; and US Patent No. 6,103,060, issued Aug. 15, 2000 to Munerelle et al., both of which are herein incorporated by reference.
- embryonic tissue webs may be imprinted against a deflection member prior to complete drying.
- Deflection members have deflection conduits between raised elements, and the web is deflected into the deflection member by an air pressure differential to create bulky domes, while the portions of the web residing on the surface of the raised elements can be pressed against the dryer surface to create a network of pattern densified areas offering strength.
- Deflection members and fabrics of use in imprinting a tissue, as well as related methods of tissue manufacture are disclosed in the following: in US Patent No. 5,855,739, issued to Ampulski et al. Jan. 5, 1999; US Patent No. 5,897,745, issued to Ampulski et al.
- the fibrous web is generally a random plurality of papermaking fibers that can, optionally, be joined together with a binder. Any papermaking fibers, as previously defined, or mixtures thereof may be used, such as bleached fibers from a kraft or sulfite chemical pulping process. Recycled fibers can also be used, as can cotton linters or papermaking fibers comprising cotton. Both high-yield and low-yield fibers can be used.
- the fibers may be predominantly hardwood, such as at least 50% hardwood or about 60% hardwood or greater or about 80% hardwood or greater or substantially 100% hardwood.
- the web is predominantly softwood, such as at least about 50% softwood or at least about 80% softwood, or about 100% softwood.
- the papermaking fibers or the resulting paper of the present invention can have an ISO brightness of about 60 percent or greater, more specifically about 80 percent or greater, more specifically about 85 percent or greater, more specifically from about 75 percent to about 90 percent, more specifically from about 80 percent to about 90 percent, and more specifically still from about 83 percent to about 88 percent.
- the fibrous web of the present invention may be formed from a single layer or multiple layers. Both strength and softness are often achieved through layered tissues, such as stratified webs wherein at least one layer comprises softwood fibers while another layer comprises hardwood or other fiber types. Layered structures produced by any means known in the art are within the scope of the present invention, including those disclosed by Edwards et al. in U.S. Patent No.
- the layers are generally positioned in a juxtaposed or surface-to-surface relationship and all or a portion of the layers may be bound to adjacent layers.
- the paper web may also be formed from a plurality of separate paper webs wherein the separate paper webs may be formed from single or multiple layers.
- the webs can be made by employing a single headbox with two or more strata, or by employing two or more headboxes depositing different furnishes in series on a single forming fabric, or by employing two or more headboxes each depositing a furnish on a separate forming fabric to form an embryonic web followed by joining ("couching") the embryonic webs together to form a multi-layered web.
- the distinct furnishes may be differentiated by at least one of consistency, fiber species (e.g., eucalyptus vs. softwood, or southern pine versus northern pine), fiber length, bleaching method (e.g., peroxide bleaching vs. chlorine dioxide bleaching), pulping method (e.g., kraft versus sulfite pulping, or BCTMP vs.
- fiber species e.g., eucalyptus vs. softwood, or southern pine versus northern pine
- bleaching method e.g., peroxide bleaching vs. chlorine dioxide bleaching
- pulping method e.g., kraft versus sulfite pulping, or BCTMP vs.
- additives such as fillers (e.g., CaCO 3 , talc, zeolites, mica, kaolin, plastic particles such as ground polyethylene, and the like) wet strength agents, starch, dry strength additives, antimicrobial additives, odor control agents, chelating agents, chemical debonders, quaternary ammonia compounds, viscosity modifiers (e.g., CMC, polyethylene oxide, guar gum, xanthan gum, mucilage, okra extract, and the like), silicone compounds, fluorinated polymers, optical brighteners, and the like.
- fillers e.g., CaCO 3 , talc, zeolites, mica, kaolin, plastic particles such as ground polyethylene, and the like
- wet strength agents e.g., starch, dry strength additives, antimicrobial additives, odor control agents, chelating agents, chemical debonders, quaternary ammonia compounds, viscosity modifiers (e.g., C
- useful headboxes can include a four-layer Beloit (Beloit, Wise.) Concept III headbox or a Voith Sulzer (Ravensburg, Germany) ModuleJet® headbox in multilayer mode.
- Principles for stratifying the web are taught by Kearney and Wells in U.S. Patent No. 4,225,382, issued Sept. 30, 1980, which discloses the use of two or more layers to form ply-separable tissue.
- a first and second layer are provided from slurry streams differing in consistency.
- two well-bonded layers are separated by an interior barrier layer such as a film of hydrophobic fibers to enhance ply separability. Dunning in U.S. Patent No.
- the papermaking web itself comprises multiple layers having different fibers or chemical additives.
- Tissue in layered form can be produced with a stratified headbox or by combining two or more moist webs from separate headboxes.
- an initial pulp suspension is fractionated into two or more fractions differing in fiber properties, such as mean fiber length, percentage of fines, percentage of vessel elements, and the like. Fractionation can be achieved by any means known in the art, including screens, filters, centrifuges, hydrocyclones, application of ultrasonic fields, electrophoresis, passage of a suspension through spiral tubing or rotating disks, and the like. Fractionation of a pulp stream by acoustic or ultrasonic forces is described in P.H.
- the fractionated pulp streams can be treated separately by known processes, such as by combination with additives or other fibers, or adjustment of the consistency to a level suitable for paper formation, and then the streams comprising the fractionated fibers can be directed to separate portions of a stratified headbox to produce a layered tissue product.
- the layered sheet may have two, three, four, or more layers.
- a two- layered sheet may have splits based on layer basis weights such that the lighter layer has a mass of about 5% or more of the basis weight of the overall web, or about 10% or more, 20% or more, 30% or more, 40% or more, or about 50%.
- Exemplary weight percent splits for a three-layer web include 20%/20%/60%; 20%/60%/20%; 37.5%/25%/37.5%.; 10%/50%/40%; 40%/20%/40%; and approximately equal splits for each layer.
- the ratio of the basis weight of an outer layer to an inner layer can be from about 0.1 to about 5; more specifically from about 0.2 to 3, and more specifically still from about 0.5 to about 1.5.
- a layered paper web according to the present invention can serve as a basesheet for a double print creping operation, as described in US Patent No. 3,879,257, issued Apr. 22, 1975 to Gentile et al., previously incorporated by reference.
- tissue webs of the present invention comprise multilayered structures with one or more layers having over 20% high yield fibers such as CTMP or BCTMP.
- the tissue web comprises a first strength layer having cellulosic fibers and polyvinylamine, optionally further comprising a second compound which interacts with the polyvinylamine to modify strength properties or wetting properties of the web.
- the web further comprises a second high yield layer having at least 20% by weight high yield fibers and optional binder material such as synthetic fibers, including thermally bondable bicomponent binder fibers, resulting in a bulky multilayered structure having good strength properties.
- Related structures are disclosed in EP 1 ,039,027 and EP 851- 950B.
- the high yield layer has at least 0.3% by weight of a wet strength agent such as Kymene.
- Airlaid webs can also be treated with polyvinylamine polymers.
- Airlaid webs can be formed by any method known in the art, and generally comprise entraining fiberized or comminuted cellulosic fibers in an air stream and depositing the fibers to form a mat. The mat may then be calendered or compressed, before or after chemical treatment using known techniques, including those of U.S. Patent No. 5,948,507 to Chen et al., herein incorporated by reference.
- the web can be substantially free of latex and substantially free of film-forming compounds.
- the applied solution or slurry comprising polyvinylamine polymers and/or the complexing agent can also be free of formaldehyde or cross-linking agents that evolve formaldehyde.
- the polyvinylamine polymer and complexing agent combination can be used in conjunction with any known materials and chemicals that are not antagonistic to its intended use.
- odor control agents may be present, such as odor absorbents, activated carbon fibers and particles, baby powder, baking soda, chelating agents, zeolites, perfumes or other odor-masking agents, cyclodextrin compounds, oxidizers, and the like.
- the absorbent article may further comprise metalphthalocyanine material for odor control, antimicrobial properties, or other purposes, including the materials disclosed in WO 01/41689, published June 14, 2001 by Kawakami et al. Superabsorbent particles, fibers, or films may be employed.
- an absorbent fibrous mat of comminuted fibers or an airlaid web treated with a polyvinylamine polymer may be combined with superabsorbent particles to serve as an absorbent core or intake layer in a disposable absorbent article such as a diaper.
- a wide variety of other compounds known in the art of papermaking and tissue production can be included in the webs of the present invention.
- Debonders such as quaternary ammonium compounds with alkyl or lipid side chains, can be used to provide high we dry tensile strength ratios by lowering the dry strength without a correspondingly large decrease in the wet strength.
- Softening compounds, emollients, silicones, lotions, waxes, and oils can also have similar benefits in reducing dry strength, while providing improved tactile properties such as a soft, lubricious feel.
- Fillers, fluorescent whitening agents, antimicrobials, ion-exchange compounds, odor-absorbers, dyes, and the like can also be added.
- Hydrophobic matter added to selected regions of the web, especially the uppermost portions of a textured web, can be valuable in providing improved dry feel in articles intended for absorbency and removal of liquids next to the skin.
- the above additives can be added before, during, or after the application of the complexing agent (e.g., a polymeric reactive anionic compound) and /or a drying or curing step.
- Webs treated with polyvinylamine polymers may be further treated with waxes and emollients, typically by a topical application.
- Hydrophobic material can also be applied over portions of the web. For example, it can be applied topically in a pattern to a surface of the web, as described in Patent No. 5,990,377, "Dual-Zoned Absorbent Webs," issued on November 23, 1999, herein incorporated by reference.
- any debonding agent or softener known in the art may be utilized.
- the debonders may include silicone compounds, mineral oil and other oils or lubricants, quaternary ammonium compounds with alkyl side chains, or the like known in the art.
- Exemplary debonding agents for use herein are cationic materials such as quaternary ammonium compounds, imidazolinium compounds, and other such compounds with aliphatic, saturated or unsaturated carbon chains.
- the carbon chains may be unsubstituted or one or more of the chains may be substituted, e.g. with hydroxyl groups.
- Non-limiting examples of quaternary ammonium debonding agents useful herein include hexamethonium bromide, tetraethylammonium bromide, lauryl trimethylammonium chloride, and dihydrogenated tallow dimethylammoniurn methyl sulfate.
- the suitable debonders may include any number of quaternary ammonium compounds and other softeners known in the art, including but not limited to, oleylimidazolinium debonders such as C-6001 manufactured by Goldschmidt or Prosoft TQ-1003 from Hercules (Wilmington, Delaware); Berocell 596 and 584 (quaternary ammonium compounds) manufactured by Eka Nobel Inc., which are believed to be made in accordance with U.S. Patent Nos.
- Adogen 442 (dimethyl dihydrogenated tallow ammonium chloride) manufactured by Cromtpon; Quasoft 203 (quaternary ammonium salt) manufactured by Quaker Chemical Company; Arquad 2HT75 (di(hydrogenated tallow) dimethyl ammonium chloride) manufactured by Akzo Chemical Company; mixtures thereof; and the like.
- debonders can be tertiary amines and derivatives thereof; amine oxides; saturated and unsaturated fatty acids and fatty acid salts; alkenyl succinic anhydrides; alkenyl succinic acids and corresponding alkenyl succinate salts; sorbitan mono-, di- and tri-esters, including but not limited to stearate, palmitate, oleate, myristate, and behenate sorbitan esters; and particulate debonders such as clay and silicate fillers.
- Useful debonding agents are described in, for example, U.S. Patent Nos. 3,395,708, 3,554,862, and 3,554,863 to Hervey et al., U.S. Patent No.
- the debonding agent can be added at a level of at least about 0.1 %, specifically at least about 0.2%, more specifically at least about 0.3%, on a dry fiber basis. Typically, the debonding agent will be added at a level of from about 0.1 to about 6%, more typically from about 0.2 to about 3%, active matter on dry fiber basis. The percentages given for the amount of debonding agent are given as an amount added to the fibers, not as an amount actually retained by the fibers.
- Softening agents known in the art of tissue making may also serve as debonders or hydrophobic matter suitable for the present invention and may include but not limited to: fatty acids; waxes; quaternary ammonium salts; dimethyl dihydrogenated tallow ammonium chloride; quaternary ammonium methyl sulfate; carboxylated polyethylene; cocamide diethanol amine; coco betaine; sodium lauroyl sarcosinate; partly ethoxylated quaternary ammonium salt; distearyl dimethyl ammonium chloride; methyl-1 -oleyl amidoethyl-2-oleyl imidazolinium methylsulfate (Varisoft 3690 from Witco Corporation, now Crompton in Middlebury, CT); mixtures thereof; and, the like known in the art.
- Debonder and a PARC, or other complexing agent can be used together with polyvinylamine polymers.
- the debonder can be added to the web in the furnish or otherwise prior to application of the PARC and subsequent crosslinking. However, debonder may also be added to the web after application of PARC solution and even after crosslinking of the PARC.
- the debonder is present in the PARC solution and thus is applied to the web as the same time as the PARC, provided that adverse reactions between the PARC and the debonder are avoided by suitable selection of temperatures, pH values, contact time, and the like.
- PARC or any other additives can be applied heterogeneously using either a single pattern or a single means of application, or using separate patterns or means of application. Heterogeneous application of the chemical additive can be by gravure printing, spraying, or any method previously discussed.
- Surfactants may also be used, being mixed with either the polyvinylamine polymer, the second compound (or complexing agent), or added separately to the web or fibers.
- the surfactants may be anionic, cationic, or non-ionic, including but not limited to: tallow trimethylammonium chloride; silicone amides; silicone amido quaternary amines; silicone imidazoline quaternary amines; alkyl polyethoxylates; polyethoxylated alkylphenols; fatty acid ethanol amides; dimethicone copolyol esters; dimethiconol esters; dimethicone copolyols; mixtures thereof; and, the like known in the art.
- Charge-modifying agents can also be used.
- Commercially available charge-modifying agents include Cypro 514, produced by Cytec, Inc. of Stamford, Conn; Bufloc 5031 and Bufloc 534, both products of Buckman Laboratories, Inc. of Memphis, Tenn.
- the charge-modifying agent can comprise low-molecular-weight, high charge density polymers such as polydiallyldimethylammonium chloride (DADMAC) having molecular weights of about 90,000 to about 300,000, polyamines having molecular weights of about 50,000 to about 300,000 (including polyvinylamine polymers) and polyethyleneimine having molecular weights of about 40,000 to about 750,000.
- DADMAC polydiallyldimethylammonium chloride
- the debonder includes an ammonium surfactant component and a nonionic surfactant component as noted above.
- the paper webs of the present invention are laminated with additional plies of tissue or layers of nonwoven materials such as spunbond or meltblown webs, or other synthetic or natural materials.
- the web may also be calendered, embossed, slit, rewet, moistened for use as a wet wipe, impregnated with thermoplastic material or resins, treated with hydrophobic matter, printed, apertured, perforated, converted to multiply assemblies, or converted to bath tissue, facial tissue, paper towels, wipers, absorbent articles, and the like.
- tissue products of the present invention can be converted in any known tissue product suitable for consumer use.
- Converting can comprise calendering, embossing, slitting, printing, addition of perfume, addition of lotion or emollients or health care additives such as menthol, stacking preferably cut sheets for placement in a carton or production of rolls of finished product, and final packaging of the product, including wrapping with a poly film with suitable graphics printed thereon, or incorporation into other product forms.
- Acid Dyeing can comprise calendering, embossing, slitting, printing, addition of perfume, addition of lotion or emollients or health care additives such as menthol, stacking preferably cut sheets for placement in a carton or production of rolls of finished product, and final packaging of the product, including wrapping with a poly film with suitable graphics printed thereon, or incorporation into other product forms.
- the textile material can be any textile material containing cellulosic fibers.
- Such fibers include not only pulp fibers, but also cotton fibers, rayon fibers, hemp, jute, ramie, and other synthetic natural or regenerated cellulosic fibers, including lyocell materials.
- the textile materials being dyed can be in the form of fibers, yarns, or fabrics.
- cellulosic fibers were not receptive to acid dyes, the cellulosic fibers did not dye evenly when mixed with other fibers, such as polyester fibers, nylon fibers, wool fibers, and the like.
- cellulosic fibers can be mixed with other types of fibers and dyed in one process to produce fibers that all have about the same color and shade.
- This embodiment of the present invention can also be used in connection with paper webs. For instance, once a paper web is treated with a complexing agent and a polyvinylamine polymer, the web can then be dyed to produce paper products having a particular color. Alternatively, a decorative pattern can be applied to the product using a suitable acid dye.
- a complexing agent once contacting a cellulosic fiber will bind to the fiber.
- the complexing agent can be, for instance, a polymeric anionic reactive compound.
- the complexing agent can facilitate the formation of a covalent bond between a polyvinylamine and the fiber.
- the polyvinylamine polymer provides dye sites for the acid dye.
- the complexing agent such as a polymeric anionic reactive compound
- each component can be applied to the cellulosic material in an amount from about 0.1% to about 10% by weight, and particularly from about 0.2% to about 6% by weight, and more particularly at about 4% by weight, based upon the weight of the cellulosic material.
- the complexing agent such as the polymeric anionic reactive compound
- the amount of complexing agent added in relation to the polyvinylamine polymer can be determined for a particular application using routine experimentation.
- cellulosic fibers or webs are treated with a complexing agent and a polyvinylamine polymer and then optionally cured at temperatures of at least about 120°C and more particularly at temperatures of at least about 130°C.
- the cellulosic material being dyed can be combined with non-cellulosic fibers and dyed or can be dyed first and then optionally combined with non-cellulosic fibers.
- the non-cellulosic fibers can be any suitable fiber for acid dyeing, such as wool, nylon, silk, other protein-based fibers, polyester fibers, synthetic polyamides, other nitrogen containing fibers, and the like.
- the cellulosic material can be contacted with any suitable acid dye.
- acid dyes include pre- metallized acid dyes, pre-metallized acid nonionic solubilized dyes, pre-metallized acid asymmetrical monosulphonated dyes, and pre-metallized acid symmetrical dye-sulphonated/dicarboxylated dyes. It should be understood, however, that other acid dyes besides the dyes identified above can also be used.
- the dye used in the process of the present invention can be an acid mordant dye.
- Such dyes include metallic mordant dyes, such as a chrome mordant dye.
- the cellulosic material can be placed in a dye bath at a particular temperature and for a particular amount of time until the proper shade is obtained. For instance, in one embodiment, after pretreatment, the cellulosic material can be immersed in a dye bath containing an acid dye.
- auxiliary agents can also be contained in the bath, such as a chelated metal, which can be for instance, a multivalent transition metal such as chromium, cobalt, copper, zinc and iron.
- the conditions of dyeing would depend upon the specific nature of the acid dye used. For most applications, dyeing will take place at temperatures of from about 50°C to about 100°C and at a pH that is in the range of from about 5 to about 7.
- the concentration of the acid dye can be from about 0.1 % to about 5% based upon the weight of the dry fiber.
- a blend of cellulosic fibers treated with a complexing agent and a polyvinylamine compound can blended with synthetic fibers such as nylon, or with wool fibers, silk fibers, and the like, and then treated with an acid dye and a quaternary ammonium compound such as a quaternary ammonium salt having antimicrobial properties.
- synthetic fibers such as nylon, or with wool fibers, silk fibers, and the like
- an acid dye and a quaternary ammonium compound such as a quaternary ammonium salt having antimicrobial properties.
- the blend treated with the softening agent can have improved tactile properties that persist after washing.
- Kim and Sun in the above referenced article disclose treating fibers with acid dyes at levels of from 0.125 to 2% based on fabric weight. Acid dyes used in their study include Red 18, Blue 113, and Violet 7. Acid Red 88 was also used. They used N-(3-chloro-2hydroxylpropyl)-N,N-dimethyl- dodecylammoniumchloride as the ammonium salt.
- the concentration of the acid dye in solution when applied to the fibers can be less than 3 wt. %, specifically less than 2 wt %, more specifically less than 1 wt. %, and most specifically less than about 0.5 wt. %, with exemplary ranges of from about 0.01 wt. % to about 1.5 wt. %, or from about 0.1 wt. % to about 1 wt. %.
- Beside acid dyes and/or antimicrobial agents, cellulosic materials treated with a polyvinylamine and a complexing agent in accordance with the present invention can be more receptive to other finishing treatments.
- cellulosic materials treated in accordance with the present invention can have a greater affinity for silicone compounds, such as amino-functional polysiloxanes, including those disclosed in U.S. Patent No. 6,201 ,093, which is incorporated herein by reference.
- Such polysiloxanes soften fabrics and cellulosic webs.
- Such finishing treatments can be especially desirable when treated cellulosic fibers are combined with other fibers to provide a woven or nonwoven textile web, before or after dyeing or without dyeing, that has uniform properties.
- Applying polysiloxanes in accordance with the present invention can also be done to paper webs, especially tissues for increasing the softness of the product.
- silicone compounds that can be used include organofunctional, hydrophilic, and/or anionic polysiloxanes for improved immobilization and fastness of the polysiloxane or other silicone compound.
- organofunctional or anionic polysiloxanes are disclosed in US Patent No. 4,137,360, issued Jan. 30, 1979 to Reischl; US Patent No. 5,614,598, issued march 25, 1997 to Barringer and Ledford; and other compounds known in the art.
- silicone-based debonders include silicone-based debonders, anti- static agents, softness agents, surface active agents, and the like, many of which can be obtained from Lambent Technologies, Inc., as described by A.J. O'Lenick, Jr., and J.K. Parkinson, in "Silicone Compounds: Not Just Oil Phases Anymore,” Soap/Cosmetics/Chemical Specialties, Vol. 74, No. 6, June 1998, pp. 55-57.
- Exemplary silicone compounds include silicone quats such as silicone alkylamido quaternary compounds based on dimethicone copolyol chemistry, which can be useful as softeners, antistatic agents, and debonders; silicone esters, including phosphate esters which can provide lubricity or other functions, such as the esters disclosed in US Pat. No.
- Hydrophilic debonders may be applied at the same doses and in a similar manner as hydrophobic debonders.
- silicone compounds can be applied to webs that also comprise polyvinylamine compounds, whether the compounds interact directly with the polyvinylamine or not.
- methods of producing tissue containing cationic silicone are disclosed in US Patent No. 6,030,675, issued Feb. 29, 2000 to Schroeder et al., herein incorporated by reference.
- a material is said to be "absorbent" if it can retain an amount of water equal to at least 100% of its dry weight as measured by the test for Intrinsic Absorbent Capacity given below (i.e., the material has an Intrinsic Absorbent Capacity of at about 1 or greater).
- the absorbent materials used in the absorbent members of the present invention can have an Intrinsic Absorbent Capacity of about 2 or greater, more specifically about 4 or greater, more specifically still about 7 or greater, and more specifically still about 10 or greater, with exemplary ranges of from about 3 to about 30 or from about 4 to about 25 or from about 12 to about 40.
- high yield pulp fibers are those papermaking fibers of pulps produced by pulping processes providing a yield of about 65 percent or greater, more specifically about 75 percent or greater, and still more specifically from about 75 to about 95 percent. Yield is the resulting amount of processed fiber expressed as a percentage of the initial wood mass.
- High yield pulps include bleached chemithermomechanical pulp (BCTMP), chemithermomechanical pulp (CTMP), pressure/pressure thermomechanical pulp (PTMP), thermomechanical pulp (TMP), thermomechanical chemical pulp (TMCP), high yield sulfite pulps, and high yield Kraft pulps, all of which contain fibers having high levels of lignin.
- Characteristic high-yield fibers can have lignin content by mass of about 1% or greater, more specifically about 3% or greater, and still more specifically from about 2% to about 25%. Likewise, high yield fibers can have a kappa number greater than 20, for example. In one embodiment, the high-yield fibers are predominately softwood, such as northern softwood or, more specifically, northern softwood BCTMP.
- the term "cellulosic” is meant to include any material having cellulose as a major constituent, and specifically comprising about 50 percent or more by weight of cellulose or cellulose derivatives.
- the term includes cotton, typical wood pulps, nonwoody cellulosic fibers, cellulose acetate, cellulose triacetate, rayon, viscose fibers, thermomechanical wood pulp, chemical wood pulp, debonded chemical wood pulp, lyocell and other fibers formed from solutions of cellulose in NMMO, milkweed, or bacterial cellulose. Fibers that have not been spun or regenerated from solution can be used exclusively, if desired, or at least about 80% of the web can be free of spun fibers or fibers generated from a cellulose solution.
- the "wet:dry ratio” is the ratio of the geometric mean wet tensile strength divided by the geometric mean dry tensile strength.
- Geometric mean tensile strength (GMT) is the square root of the product of the machine direction tensile strength and the cross-machine direction tensile strength of the web. Unless otherwise indicated, the term “tensile strength” means “geometric mean tensile strength.”
- the absorbent webs used in the present invention can have a wefcdry ratio of about 0.1 or greater and more specifically about 0.2 or greater.
- Tensile strength can be measured using an Instron tensile tester using a 3-inch jaw width (sample width), a jaw span of 2 inches (gauge length), and a crosshead speed of 25.4 centimeters per minute after maintaining the sample under TAPPI conditions for 4 hours before testing.
- the absorbent webs of the present invention can have a minimum absolute ratio of dry tensile strength to basis weight of about 0.01 gram/gsm, specifically about 0.05 grams/gsm, more specifically about 0.2 grams/gsm, more specifically still about 1 gram/gsm and most specifically from about 2 grams/gsm to about 50 grams/gsm.
- “bulk” and “density,” unless otherwise specified, are based on an oven-dry mass of a sample and a thickness measurement made at a load of 0.34 kPa (0.05 psi) with a 7.62-cm (three-inch) diameter circular platen. Details for thickness measurements and other forms of bulk are described hereafter.
- “Debonded Void Thickness” is a measure of the void volume at a microscopic level along a section of the web, which can be used to discern the differences between densified and undensified portions of the tissue or between portions that have been highly sheared and those that have been less sheared. The test method for measuring "Debonded Void Thickness" is described in US Patent No.
- Debonded Void Thickness is the void area or space not occupied by fibers in a cross-section of the web per unit length. It is a measure of internal web bulk (as distinguished from external bulk created by simply molding the web to the contour of the fabric).
- the "Normalized Debonded Void Thickness” is the Debonded Void Thickness divided by the weight of a circular, four inch diameter sample of the web. The determination of these parameters is described in connection with FIGS. 8-13 of US Patent No. 5,411 ,636. Debonded Void
- Thickness reveal some aspects of asymmetrically imprinted or molded tissue.
- Debonded Void Thickness when adapted for measurement of a short section of a protrusion of a molded web by using a suitably short length of a cross- directional cross-section, can reveal that the leading side of a protrusion has a different degree of bonding than the trailing side, with average differences of about 10% or more or of about 30% or more being contemplated.
- elastic modulus is a measure of slope of stress-strain of a web taken during tensile testing thereof and is expressed in units of kilograms of force.
- Tappi conditioned samples with a width of 3 inches are placed in tensile tester jaws with a gauge length (span between jaws) of 2 inches.
- the jaws move apart at a crosshead speed of 25.4 cm/min and the slope is taken as the least squares fit of the data between stress values of 50 grams of force and 100 grams of force, or the least squares fit of the data between stress values of 100 grams of force and 200 grams of force, whichever is greater. If the sample is too weak to sustain a stress of at least 200 grams of force without failure, an additional ply is repeatedly added until the multi-ply sample can withstand at least 200 grams of force without failure.
- the term “hydrophobic” refers to a material having a contact angle of water in air of at least 90 degrees.
- hydrophilic refers to a material having a contact angle of water in air of less than 90 degrees.
- surfactant includes a single surfactant or a mixture of two or more surfactants. If a mixture of two or more surfactants is employed, the surfactants may be selected from the same or different classes, provided only that the surfactants present in the mixture are compatible with each other. In general, the surfactant can be any surfactant known to those having ordinary skill in the art, including anionic, cationic, nonionic and amphoteric surfactants.
- anionic surfactants include, among others, linear and branched-chain sodium alkylbenzenesulfonat.es; linear and branched-chain alkyl sulfates; linear and branched-chain alkyl ethoxy sulfates; and silicone phosphate esters, silicone sulfates, and silicone carboxylates such as those manufactured by Lambent Technologies, located in Norcross, Georgia.
- Cationic surfactants include, by way of illustration, tallow trimethylammonium chloride and, more generally, silicone amides, silicone amido quaternary amines, and silicone imidazoline quaternary amines.
- nonionic surfactants include, again by way of illustration only, alkyl polyethoxylates; polyethoxylated alkylphenols; fatty acid ethanol amides; dimethicone copolyol esters, dimethiconol esters, and dimethicone copolyols such as those manufactured by Lambent Technologies ; and complex polymers of ethylene oxide, propylene oxide, and alcohols.
- alkyl polyethoxylates include, again by way of illustration only, alkyl polyethoxylates; polyethoxylated alkylphenols; fatty acid ethanol amides; dimethicone copolyol esters, dimethiconol esters, and dimethicone copolyols such as those manufactured by Lambent Technologies ; and complex polymers of ethylene oxide, propylene oxide, and alcohols.
- One exemplary class of amphoteric surfactants are the silicone amphoterics manufactured by Lambent Technologies (Norcross, Georgia
- softening agents can be used to enhance the softness of the tissue product and such softening agents can be incorporated with the fibers before, during or after disperging. Such agents can also be sprayed, printed, or coated onto the web after formation, while wet, or added to the wet end of the tissue machine prior to formation.
- Suitable agents include, without limitation, fatty acids, waxes, quaternary ammonium salts, dimethyl dihydrogenated tallow ammonium chloride, quaternary ammonium methyl sulfate, carboxylated polyethylene, cocamide diethanol amine, coco betaine, sodium lauryl sarcosinate, partly ethoxylated quaternary ammonium salt, distearyl dimethyl ammonium chloride, polysiloxanes and the like.
- Suitable commercially available chemical softening agents include, without limitation, Berocell 596 and 584 (quaternary ammonium compounds) manufactured by Eka Nobel Inc., Adogen 442 (dimethyl dihydrogenated tallow ammonium chloride) manufactured by Sherex Chemical Company, Quasoft 203 (quaternary ammonium salt) manufactured by Quaker Chemical Company, and Arquad 2HT-75 ( dihydrogenated tallow) dimethyl ammonium chloride) manufactured by Akzo Chemical Company.
- Suitable amounts of softening agents will vary greatly with the species selected and the desired results. Such amounts can be, without limitation, from about 0.05 to about 1 weight percent based on the weight of fiber, more specifically from about 0.25 to about 0.75 weight percent, and still more specifically about 0.5 weight percent.
- the slurry is then agitated gently with a standard perforated mixing plate that is inserted into the slurry and moved up and down seven times, then removed.
- the water is then drained from the mold through a wire assembly at the bottom of the mold which retains the fibers to form an embryonic web.
- the forming wire is a 90x9O mesh, stainless-steel wire cloth.
- the web is couched from the mold wire with two blotter papers placed on top of the web with the smooth side of the blotter contacting the web. The blotters are removed and the embryonic web is lifted with the lower blotter paper, to which it is attached. The lower blotter is separated from the other blotter, keeping the embryonic web attached to the lower blotter.
- the blotter is positioned with the embryonic web face up, and the blotter is placed on top of two other dry blotters. Two more dry blotters are also placed on top of the embryonic web.
- the stack of blotters with the embryonic web is placed in a Valley hydraulic press and pressed for one minute with 75 psi applied to the web.
- the pressed web is removed from the blotters and placed on a Valley steam dryer containing steam at 2.5 psig pressure and heated for 2 minutes, with the wire-side surface of the web next to the metal drying surface and a felt under tension on the opposite side of the web.
- Felt tension is provided by a 17.5 lbs of weight pulling downward on an end of the felt that extends beyond the edge of the curved metal dryer surface.
- the dried handsheet is trimmed to 7.5 inches square with a paper cutter and then weighed in a heated balance with the temperature maintained at 105°C to obtain the oven dry weight of the web.
- the percent consistency of the diluted pulp slurry from which the sheet is made is calculated by dividing the dry weight of the sheet by the initial volume (in terms of milliliters, ranging from 900 to 1000) and multiplying the quotient by 100. Based on the resulting percent consistency value, the volume of pulp slurry necessary to give a target sheet basis weight of 60 gsm (or other target value) is calculated. The calculated volume of diluted pulp is used to make additional handsheets.
- the above procedure is the default handsheet procedure that was used unless otherwise specified.
- Several trials, hereafter specified, employed handsheets made with an alternate but similar procedure (hereafter the "alternate handsheet procedure") in which 50 grams of fibers are soaked for 5 minutes in 2 liters of deionized water prior to disintegration in the British disintegrator as specified above.
- the slurry was then diluted with deionized water to a volume of 8 liters.
- a first chemical (if used) was then added to the low consistency slurry as a dilute (1.0%) solution.
- the slurry was mixed with a standard mechanical mixer at moderate shear for 10 minutes after addition of the first chemical.
- a second chemical (if used) was then added and mixing continued for an additional 2-5 minutes.
- Handsheets were made with a target basis weight of about 60 gsm, unless otherwise specified.
- the appropriate amount of fiber slurry (0.625% consistency) required to make a 60 gsm sheet was measure into a graduated cylinder.
- the slurry was then poured from the graduated cylinder into an 8.5-inch by 8.5-inch Valley handsheet mold (Valley Laboratory Equipment, Voith, Inc.) that had been preOfilled to the appropriate level with water.
- Web formation and drying is done as described in the default handsheet method described above, with the exception that the wet web in the Valley hydraulic press was pressed for one minute at 100 psi instead of 75 psi.
- Handsheet testing is done under laboratory conditions of 23.0 +/- 1.0 °C, 50.0 +/- 2.0 % relative humidity, after the sheet has equilibrated to the testing conditions for four hours.
- the testing is done on a tensile testing machine maintaining a constant rate of elongation, and the width of each specimen tested is 1 inch.
- the specimen are cut into strips having a 1 ⁇ 0.04 inch width using a precision cutter.
- the "jaw span" or the distance between the jaws, sometimes referred to as gauge length, is 5.0 inches.
- the crosshead speed is 0.5 inches per minute (12.5 mm/min.)
- a load cell is chosen so that peak load results generally fall between about 20 and about 80 percent of the full scale load (e.g., a 100N load cell).
- Suitable tensile testing machines include those such as the Sintech QAD IMAP integrated testing system or an MTS Alliance RT/1 universal test machine with TestWorks 4 software. This data system records at least 20 load and elongation points
- distilled water is poured into a container to a depth of approximately % of an inch.
- An open loop is formed by holding each end of a test specimen and carefully lowering the specimen until the lowermost curve of the loop touches the surface of the water without allowing the inner side of the loop to come together.
- the lowermost point of the curve on the handsheet is contacted with the surface of the distilled water in such a way that the wetted area on the inside of the loop extends at least 1 inch and not more than 1.5 inches lengthwise on the specimen and is uniform across the width of the specimen. Care is taken to not wet each specimen more than once or allow the opposite sides of the loop to touch each other or the sides of the container.
- test specimen Excess water is removed from the test specimen by lightly touching the wetted area to a blotter. Each specimen is blotted only once. Each specimen is then immediately inserted into the tensile tester so that the jaws are clamped to the dry area of the test specimen with the wet area approximately midway between the span. The test specimen are tested under the same instrument conditions and using same calculations as for Dry Tensile Strength measurements.
- Soluble charge testing is done with an ECA 2100 Electrokinetic Charge Analyzer from ChemTrac (Norcross, GA). Titration is done with a Mettler DL21 Titrator using 0.001 N DADMAC (diallyl dimethyl ammonium chloride) when the sample is anionic, or 0.001 N PVSK (potassium polyvinyl sulphate) when the sample is cationic. 500 ml of the pulp slurry prepared for use in handsheet making (slurry having about 1.5 g of fibers) is dewatered on a Whatman No.4 filter on a Buechner funnel. Approximately 150 ml of filtrate (the exact weight to 0.01 grams is recorded for soluble charge calculations) is withdrawn and used to complete the titration.
- DADMAC diallyl dimethyl ammonium chloride
- PVSK potential polyvinyl sulphate
- the streaming potential (streaming current) of the filtrate is then measured after 5 to 10 minutes, once the reading has stabilized.
- the sign of the streaming potential is then used to determine which reagent to apply in titration.
- the titration is complete when the current reaches zero. Soluble charge is calculated using the titrant normality (0.001 N), titrant volume consumed, and filtrate weight; soluble charge is reported in units of milliequivalents per liter (meq/L).
- the strength benefits of polyvinylamine were explored with application to an uncreped through-dried tissue having a basis weight of 43 gsm, generally made according to the uncreped through-air dried method as disclosed in U.S. Patent No. 5,048,589 to Cook et al.
- the tissue was made from a 50/50 blend of Fox River RF recycled fibers and Kimberly-Clark Mobile wet lap bleached kraft softwood fibers (Mobile, Alabama). The fibers were converted to a dilute slurry of about 0.5% consistency and formed into a web onto a pilot paper machine operating at 40 feet per minute.
- the embryonic web was dewatered by foils and vacuum boxes to about 18%) consistency, whereupon the web was transferred to a through drying fabric with 15% rush transfer, meaning that the through drying fabric traveled at a velocity 15% less than the forming wire and that the differential velocity transfer occurred over a vacuum pickup shoe, as described in U.S. Patent No. 5,667,636 to Engel et al.
- Through drying was done on a 44 GST through-drying fabric from AstenJohnson Company (Charleston, SC). No wet strength agents were added, resulting in a sheet with minimal wet strength.
- the tissue was cut to either 5-inch by 8-inch rectangles each having a weight of about 1.2 grams (room conditions of 30% RH and 73° F) or to 8-inch by 8-inch rectangles with a dry mass of about 1.85 grams.
- the cut tissues were treated in six different trials, labeled A through F and described below.
- the polymeric anionic reactive compound used was BELCLENE® DP80 (Durable Press 80), a terpolymer of maleic anhydride, vinyl acetate, and ethyl acetate from FMC Corporation. This was prepared as a 1 % by weight aqueous solution in deionized water.
- the PARC solution also included sodium hypophosphite (SHP) as a catalyst, with one part of SHP for each two parts by weight of polymeric reactive compound (i.e., 0.5% SHP).
- the polyvinylamine compound used was either Catiofast® PR 8106 or Catiofast® PR 8104, both by BASF (Ludwigshafen, Germany), each diluted with deionized water to form an 0.5 wt% solution. These compounds include forms of polyvinylformamide which have been hydrolyzed to various extents to convert the formamide groups to amine groups on a polyvinyl backbone. CatioFast® 8106 is about 90% hydrolyzed and Catiofast 8104 is about 10% hydrolyzed. In the following trials, application of solutions to the web was done by spraying both sides of the web with a spray of the solution generated by a handheld spray bottle.
- Trial B 1.25 g of PARC solution were added to a 5-inch by 8-inch tissue web for a PARC add-on level of 1.1 % on a dry solids basis. The moist web was then sprayed with 2.7 g of Catiofast® 8106 solution for a polyvinylamine add-on of 1.2% on a dry solids basis (polyvinylamine solids mass/dry fiber mass x 100%). The moist web was dried and cured in a convection oven at 160°C for 18 minutes.
- Trial C 2.85 g of Catiofast® 8106 solution were added to a 5-inch by 8- inch tissue web for a polyvinylamine add-on level of 2.5% on a dry solids basis. The moist web was then sprayed with 0.6 g of PARC solution for a PARC add-on of 0.26% on a dry solids basis (polyvinylamine solids mass/dry fiber mass * 100%). The moist web was dried and cured in a convection oven at 160°C for 16 minutes.
- Trial D 4.54 g of Catiofast® 8106 solution were added to a 5-inch by 8- inch tissue web for a polyvinylamine add-on level of 4.0% on a dry solids basis. No PARC solution was added. The moist web was dried and cured in a convection oven at 160°C for about 20 minutes.
- Trial E 3.78 g of Catiofast® 8104 solution were added to a 5-inch by 8-inch tissue web for a polyvinylamine add-on level of 3.3% on a dry solids basis. No PARC solution was added. The moist web was dried and cured in a convection oven at 160°C for 20 minutes.
- Trial F 2.65 g of PARC solution were added to a 8-inch by 8-inch tissue web for a PARC add-on level of 1.5% on a dry solids basis. The moist web was then sprayed with 3.96 g of Catiofast® 8104 solution for a polyvinylamine add-on of 1.1% on a dry solids basis. The moist web was then dried and cured in a convection oven at 160°C for about 20 minutes. Samples were tested in a conditioned Tappi laboratory (50% RH, 73°F) for
- Example 1 The untreated tissue and the solutions of Example 1 were employed again to explore the generation of hydrophobic properties associated with Trial C. In this example, however, the tissue was treated with a uniform application of both compounds simultaneously.
- the polyvinylamine solution was directly mixed with the PARC solution prior to application to the tissue.
- 5 ml of 0.5% Catiofast® PR 8106 were mixed at 73°F with 5 ml of the PARC solution.
- the solution rapidly became cloudy, as if a colloidal suspension had formed.
- a similar mixture was also prepared using 5 ml of 0.5% Catiofast® PR 8104 which were mixed with 5 ml of the PARC solution. This second mixture remained clear. It is believed that the more highly hydrolyzed Catiofast® PR 8106 solution formed polyelectrolyte complexes with the anionic polymer that created a colloidal suspension.
- the two mixtures were then applied to separate regions of another 8-inch by 8-inch tissue sample.
- the cloudy mixture of Catiofast® PR 8106 with PARC solution was applied dropwise to a portion of the sheet until 2.78 ml had been applied to a region about 7-cm in diameter.
- the clear mixture of Catiofast® PR 8104 with PARC solution was also applied dropwise to a remote portion of the tissue until 1 ml had been added.
- the tissue web with two distinct wetted areas was then placed in a convection oven at 160°C for 5 minutes, where it was dried and cured. The dried tissue was then wetted by pouring tap water onto the web. The region that had been treated with the clear mixture of Catiofast® PR 8104 with PARC solution wetted easily.
- Sections of the tissue used in Example 1 were treated with aqueous solutions of 0.5% Catiofast® PR 8106 (a polyvinylamine) and/or PARC (0.5% of DP80 with 0.25% of sodium hypophosphite) or mixtures thereof.
- Three mixtures of the polyvinylamine and PARC were prepared with ratios of 30:70, 50:50, and 70:30.
- 5 tissue samples were cut into 5-inch by 8-inch rectangles, with the 8-inch dimension being in the cross direction of the web.
- Most of the trials comprised spraying a total mass of treatment solution(s) having 350% of the dry mass of the web (relative to the web at room conditions, with about 5% moisture already in the "dry" web in a room with a relative humidity of about 30% and a temperature of about 72°F).
- a mixture of the PARC and polyvinylamine was applied to the web.
- both compounds were applied separately.
- trials were conducted in which either the PARC or the polyvinylamine were applied first. At that point, the web was dried in some cases and not dried in others before applying the other solution, followed by drying and, in most cases, curing. Some cases were run with only one of the two compounds applied, no applied compound, or deionized water only applied to the web.
- the pH of the various solutions were checked with an Orion ResearchTM Model 611 digital pH/millivolt meter.
- the PARC solution had a pH of 3.28.
- the polyvinylamine solution (0.5% Catiofast® PR 8106) had a pH of 7.30.
- the 30:70 mixture of PARC and polyvinylamine (30 parts PARC solution and 70 parts polyvinylamine solution) had a pH of 4.32.
- the 50:50 mixture of PARC and polyvinylamine had a pH of 3.90
- the 70:30 mixture of PARC and polyvinylamine had a pH of 3.50.
- Spraying was performed with a Paasche® Model VL Airbrush Set (Paasche Airbrush Company, Harwood Heights, IL). Solutions were sprayed with the airbrush on both sides of the sample until the required mass was applied, seeking to apply each solution uniformly and equally divided between the two sides of the web. When spraying, a back and forth sweeping motion was used, with spray extended past the edges of the sheet to avoid over-saturation on the return strokes. The sheet was turned after one side was sprayed, and the second side sprayed. The spray and turn sequence was repeated a number of times, until desired amount of wet pick-up was measured. The sample was manually transferred to a balance to determine % weight gain.
- a disposable plastic pipette was used to apply drops having a volume of about 0.03 to 0.04 ml onto the surface of the sample.
- a pendant drop was formed by gently squeezing the pipette until the drop was near the point of falling. The drop was then gently released onto the surface of the web, such that the drop contacted the web at about the same time as contact with the pipette was broken. (Downward momentum from falling was minimized.)
- the time in seconds required for the drop to be completely absorbed into the web was then recorded, with complete absorption being defined as the time when there was no longer a glossy body of water visible on the surface of the web where the drop had been placed.
- trial L2 showed low intake times characteristic of a hydrophilic web, but trial L1 required over 30 seconds in the 25- ⁇ l Pipette Intake test and over 100 seconds for the Water Drop Intake test.
- the curing step increases hydrophobicity by driving reactions between the carboxyl groups of the PARC and the amine groups of the polyvinylamine to yield a reaction product having a hydrophobic backbone and a reduced number of hydrophilic functional groups.
- trials L3 and L4 the two solutions were sprayed on without an intermediate drying step (polyvinylamine first, then PARC). The samples of trial L3 were then cured, but those of trial L4 were not. Both exhibited high hydrophobicity.
- polyelectrolyte complexes between the PARC and the polyvinylamine form better when both are available to migrate and interact with each other in solution.
- the polyvinylamine probably had already formed hydrogen bonds with the cellulose and was not as free to recombine into polyelectrolyte complexes with the PARC as it is when present in solution form with PARC also present, as is the case then the two compounds are applied to the web without intermediate drying or as a mixture.
- webs treated with polyvinylamine and anionic compounds can have 25- ⁇ l Pipette Intake Times or Water Drop Intake Times greater than any of the following, in seconds: 5, 10, 15, 20, 30, 45, 60, 120, and 360.
- Webs can also be prepared by application of the polyvinylamine and another compound, such as an anionic polymer or surfactant, without an intermediate drying step, such that the polyvinylamine is in solution form when the second compound is added, or such that both the polyvinylamine and the second compound are simultaneously present in solution form in the presence of the web.
- Tensile testing was conducted for a number of the trials listed in Table 2 above. Testing was done with a 3-inch gauge length and a 3-inch sample width, with a crosshead speed of 10 inches per minute. Raw data for the tested trials are reported in Table 3, with means and standard deviations.
- the airbrush technique may still have resulted in regions with uneven mixtures of the two compounds, such that some portions of the web were relatively less hydrophobic than others, allowing tensile failure to occur in regions of relatively lower wet strength during testing.
- the samples in each trial were treated on two different days with the same mixed solutions. The first of the three samples in each of these trials was treated with the mixture on the same day the mixture was created (within 2 hours of preparation). The other two samples reported for each of these trials was treated with the mixtures 13 days later or with a new mixture comprising roughly 50% of the old mixture and a newly prepared mixture.
- the we dry ratios for the samples made with freshly prepared mixture were consistently higher (25%, 20%, and 25% for trials O1, P1, and Q1, respectively) than for the six samples prepared with "aged" mixtures, none of which exceeded 20%.
- it may be desirable to apply a mixture of polyvinylamine with a second compound shortly after the mixture is prepared e.g., within 24 hours, specifically within 2 hours, more specifically within 20 minutes, and most specifically substantially immediately after preparation).
- the tissue for this Example is the untreated towel basesheet of Example 1.
- Three aqueous reaction solutions were prepared, with concentrations reported on a mass basis (mass of solids/total solution mass x 100%): Solution A: 4% Catiofast® PR 8106 solution.
- Solution B1 0.5% DP80 with 0.25% sodium hypophosphite catalyst (a PARC solution).
- Solution B2 1% DP80 with 0.5% sodium hypophosphite catalyst (a PARC solution).
- Solution A was applied to untreated tissue at a wet pick-up level of 100% (1 gram of solution added per dry gram of tissue) by spray, and then dried at 80°C.
- the dried sheets were then treated either with Solution B1 or Solution B2 by spray with a wet pick-up of 100% and then dried at 80°C, followed by curing at 175°C for 3 minutes in a convection oven.
- These treated sheets were then dyed by immersion for 5 minutes in a 1 wt% solution of OI.
- Acid Blue 9 (a triphenylmethane acid dyestuff with a OI. Constitution # of 42,090) at a pH of about 3.5, adjusted with sulfuric acid, and at a temperature of about 90°C (85°C to 95°C is suitable).
- Sample D without polyvinylamine, showed a barely noticeable blue tinge, but generally appeared white. Samples A and C appeared equally dark, while Sample B was also strongly dyed but somewhat less intensely than Samples A or C.
- Handsheets were prepared using dialdehyde cellulose (DAC) pulp and a control pulp, Kimberly-Clark LL19 bleached kraft northern softwood. DAC pulp was also prepared from Kimberly-Clark LL19 northern softwood. 500 grams of LL-19 pulp with enough deionized water to make a 3% consistency slurry were soaked for 10 minutes then dispersed for 5 minutes in a Cowles Dissolver (Morehouse- COWLES, Fullerton, CA), Type 1VT. The slurry was dewatered using a Bock centrifuge, Model 24BC (Toledo, Ohio), operating for 2 minutes to yield a pulp consistency of about 60%.
- DAC dialdehyde cellulose
- One half of the dewatered sample (about 250 grams of fiber, oven-dry basis) was used as a control, and the other half was used for chemical treatment.
- Sodium metaperiodate (NalO solution was prepared by dissolving 13.7 of NalO 4 in 1.5 liters of deionized water. The pulp was then placed in a Quantum Mark IV High Intensity Mixer/Reactor (Akron, Ohio) and the sodium metaperiodate solution was poured over the pulp. The mixer was turned on every 30 seconds for a 5-second interval at 150 rpm to mix the pulp to allow the pulp to react with the sodium metaperiodate at 20°C for one hour. The reacted pulp was then dewatered and washed with 8 liters of water two times.
- Fibers were kept moist and not allowed to dry. This treatment increased the aldehyde content of the cellulose from 0.5 meq/100g to 30 meq/100g, as measured by TAPPI Procedure T430 om-94, "Copper Number of Pulp, Paper, and Paperboard.” The control pulp was also exposed to the same treatment but without the sodium metaperiodate.
- Handsheets with a basis weight of 60 grams per square meter (gsm) made from the DAC pulp and the untreated pulp were treated with polyvinylamine polymers, either Catiofast® PR 8106 from BASF, which is a 90%-hydrolyzed polyvinylformamide, or Catiofast PR 8104, which is a 10%-hydrolyzed polyvinylformamide.
- Some of the handsheets were not treated with the polyvinylamine polymers. Treatment with polyvinylamine polymers was done to the pulp slurry before handsheet formation by adding 0.05% polyvinylamine polymer solution to the British disintegrator prior to the normal 5-minute disintegration period.
- Soluble charge testing was performed individually for the two handsheets treated with polyvinylamine polymers. Testing was done in the range of 5 to 8 pH to insure that the chemicals would have a cationic charge. The pH did not appear to have a significant effect on the charge. For soluble charge testing two samples per code were tested and the standard deviation was less than 5%. Results are shown in Table 5. The soluble charge of fibers treated with Catiofast® PR 8106 was two to three times higher than Catiofast® PR 8104. For a 0.002% solution of Catiofast® PR 8106 the soluble charge was about 150 meq/L and for Catiofast® PR 8104 it was about 60 meq/L; substantially independent of pH in the range tested.
- Typical soluble charge values for the control pulp range from -10 to -2 meq/L. At 1% addition of Catiofast® PR 8104, both the soluble charge for the control pulp and DAC pulp were slightly cationic; therefore, it is believed that the chemical was retained on the pulp instead of remaining in the water. Table 5. Soluble Charges for polyvinylamine Treated DAC and Control
- the handsheets were also tested for tensile strength, with results shown in Figure 1.
- the DAC pulp had reduced tensile strength relative to the LL19 pulp, apparently due to the known degradation of cellulose that occurs when it is oxidized to its dialdehyde form.
- the control pulp without added polyvinylamine polymer had a tensile index of about 28 Nm/g, whereas a typical unprocessed LL19 sample normally yields a tensile index about 20 Nm/g; the increased strength of the control pulp is believed to be attributable to the mechanical processing in the Quantum mixer, adding a degree of refining to the fibers.
- Catiofast® PR 8106 For both the DAC pulp and the control pulp, application of Catiofast® PR 8106 led to higher strength gains than application of Catiofast® PR 8104.
- the higher number of amino groups on the Catiofast® PR 8106 is believed to allow increased hydrogen bonding with cellulose for increased strength. Much higher gains in strength were seen with the DAC pulp.
- strength For a 3% add-on level of Catiofast® PR 8106, strength increased by 67% with the DAC pulp as compared to an 18% increase with the control pulp.
- Example 6 Handsheets of LL19 pulp (pulp which was not processed in a Quantum mixer, as was the case for the control pulp of Example 5) were prepared and treated with combinations of polyvinylamine, a commercial wet strength additive (Kymene 55LX from Hercules Inc., Wilmington, Delaware), and ProSoft debonder (ProSoft TQ1003 softener, manufactured by Hercules Inc., Wilmington, Delaware).
- ProSoft is an imidazoline debonder (more specifically, an oleylimidazolinium debonder) which inhibits hydrogen bonding, resulting in a weaker sheet. Unless otherwise specified, chemicals were added to the slurry prior to disintegration.
- Handsheets were treated with polyvinylamines and Kymene at lower levels than in the previous Examples. Two Kymene-polyvinylamine systems were evaluated to determine if crosslinking between the two polymers readily occurred.
- the dry tensile strength of LL19 handsheets is shown as a function of add-on levels for Catiofast® PR 8106 and Kymene. Error bars show the range of the results, which 5 samples being tested per reported mean.
- Kymene and polyvinylamine develop dry strength similarly at the add-on level of 0.5 kg per metric tonne (kg/t), but Kymene gives higher wet strength at 1 kg/t than the polyvinylamine.
- Figure 5 presents the wet/dry for the two chemicals.
- Figure 5 shows the wetdry tensile strength ratios as a function of chemical add-on. Again, Kymene leads to greater levels of wet strength increase than Catiofast® PR 8106.
- the curve with the positive slope (1 kg/t polyvinylamine added first and held constant) shows an increase in strength with increasing amounts of Kymene added to fibers already treated with Catiofast® PR 8106, though the end-point strength with 1 kg/t each of Kymene and polyvinylamine was surprisingly low, being slightly less than the strength obtained with 1 kg/t of Kymene alone, indicating that the polyvinylamine may interfere with strength development from Kymene.
- the curve with the negative slope was constructed by first treating the pulp with 1 kg/t Kymene followed by varying addition (0, 0.5, and 1.0 kg/t) of polyvinylamine (Catiofast® PR 8106). Surprisingly, the dry strength decreased as the polyvinylamine addition increased, showing an interference between the two compounds in terms of strength development.
- the data points at the far right side of Figure 6 have the same quantities of added chemicals, 1 kg/t each of polyvinylamine and Kymene, yet show significantly different tensile strengths, apparently due to the order of addition. Addition of polyvinylamine to fibers first, followed by addition of Kymene, results in significantly lower strength than a similar composition prepared with the reverse order of addition of the two additives. Thus, the order of addition of two or more compounds, including polyvinylamine, can be adjusted to obtain different mechanical and chemical properties of the web for a given quantity of added chemicals.
- Figure 7 shows the wet strength data for the samples of Figure 6.
- the effect of order of addition on wet strength again can be determined from the results shown therein.
- 1 kg/t polyvinylamine addition yielded a wet strength index of 1.24 Nm/g, not significantly different from that of the untreated LL19, 0.93 Nm/g.
- the addition of Kymene to the polyvinylamine treated pulp increased the wet strength to 3.16 Nm/g, generating a wetdry ratio of 16%.
- 1 kg/t of Kymene alone yielded a wet strength index of 1.71 Nm/g and wetdry ratio of about 19%.
- ProSoft an imidazoline debonder (ProSoft TQ1003 softener, manufactured by Hercules Inc., Wilmington, Delaware), was tested in combination with polyvinylamine to determine if further control over dry and wet strength development could be obtained.
- Pulp samples were treated with either 0.5 kg/t or 1.0 kg/t ProSoft, followed by various addition levels of polyvinylamine. The intent was to debond the sheet by reducing the hydrogen bonding between fibers, then rebuild strength with either polyvinylamine or Kymene. The effect of addition order was examined. Results are shown in Figures 8 and 9, which show dry strength results and wet strength results, respectively. The three labeled points on the upper portions of Figures 8 and 9 show additional experiments not on the labeled curves. For these points, the compound listed first was added first, followed by addition of the second-listed compound.
- Handsheets were prepared from LL19 pulp and treated with Catiofast® PR
- Handsheets with a target basis weight of 63.3 gsm were prepared according to the alternate handsheet procedure given above from 65% bleached kraft eucalyptus and 35% Kimberly-Clark LL-19 northern softwood pulp. Pulp was soaked 5 minutes then disintegrated for 5 minutes. After disintegration the 50 grams of pulp was diluted to 8 liters (0.625% consistency) before chemicals were added. Chemicals added included a 1% aqueous solution of Parez 631 NC (a glyoxylated polyacrylamide) manufactured by Cytec Industries and a 1% aqueous solution of Catiofast® PR 8106 polyvinylamine. Polyvinylamine add-on levels relative to dry fiber content expressed in weight percents were 0, 0.25, 0.5 and 1.
- Parez levels expressed in weight percents were 0, 0.25, 0.5 and 1.
- the polyvinylamine was added first and stirred for 10 minutes.
- the Parez solution was added next and stirred for 2 minutes before starting handsheet preparation.
- a standard mechanical mixer was used at moderate shear.
- the furnish was stirred 10 minutes after Parez addition then Catiofast added and solution stirred for 2 minutes prior to handsheet preparation.
- Handsheets were prepared as in Example 11 , but with addition of Parez first followed by polyvinylamine for codes 17 through 26.
- Code 27 polyvinylamine was added first. Results are shown in Table 8.
- Code 27 is a repeat of Code 11 in Example 11
- Code 22 is a repeat of Code 13 in Example 11.
- the good reproducibility in the results confirms the observation that treatment of the fibers with Parez first followed by addition of polyvinylamine gives significantly better results than treatment in the reverse order.
- An unusually high level of dry strength gain is shown for some of the codes, such as Codes 25 and 26, where the dry strength of the treated samples is nearly triple that of the control Code 17 (i.e., nearly a 200% increase in dry tensile index).
- Dry Tensile Synergy Factor can any of the following: about 20% or greater, 40% or greater, 50% or greater, 60% or greater, or 80% or greater. Similar results are obtained in the analysis of the wet tensile index in Tables
- a Wet Tensile Synergy Factor can also be calculated based on wet tensile index values.
- the Wet Tensile Synergy Factor can any of the following: about 20% or greater, 40% or greater, 50% or greater, 60% or greater, 80% or greater, or 100% or greater. The same set of values can also apply to a Dry TEA Synergy Factor, calculated based on dry TEA values.
- Figure 11 compares several codes from Tables 7 and 8.
- Diamonds, circles, and squares represent polyvinylamine (polyvinylamine) add-on levels of 0.25%, 0.50%, and 1%, respectively.
- Filled (black) symbols indicate that polyvinylamine was added before the Parez, while hollow symbols indicate polyvinylamine was added after the Parez.
- Significant effects of the order of addition are evident.
- the effect of order of addition is especially great at the highest Parez level of 1% for the two higher polyvinylamine levels.
- the SSB-6 polymer is a copolymer with a molecular weight of about 1 million and is formed from the following monomers: 60% acrylic acid, 24.5% butacrylic acid, 10.5% 2-ethylhexyl-acrylic acid, and 5% AMPS. After polymerization the AMPS is converted to its sodium salt. The SSB-6 / polyvinylamine precipitate could be redissolved in copious amounts of water. On the other hand, a cationic water soluble copolymer of n-butyl acrylate and [2-(methacryloyloxy)ethyl]trimethylammonium chloride, was completely miscible with Catiofast® PR 8106.
- the amine in the polyvinylamine is acting as a proton acceptor resulting in an insoluble or poorly soluble polyelectrolyte complex with SSB-6 or the poly(methylvinylether-a/.-maleic acid).
- Other anionic polymers such as anionic surfactants and other polymeric anionic reactive compounds are expected to form such complexes with polyvinylamines that are sufficiently hydrolyzed.
- the complexes can result in increased wet strength and dry strength, and can show significant synergy factors.
- the polyvinylamine may be present in the furnish, with the anionic compound added before or after addition of the polyvinylamine, such as topical application of an anionic compound to a web comprising polyvinylamine to increase dry and/or wet strength of the web.
- Parez 631 NC and Catiofast 8106 formed an insoluble precipitate fairly rapidly. This precipitate did not disappear after 20 minutes indicating that the reaction is irreversible in the presence of water.
Abstract
Description
Claims
Priority Applications (7)
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EP02761763A EP1456472B2 (en) | 2001-12-18 | 2002-09-20 | A method of making a paper product comprising a polyvinylamine polymer |
AU2002327002A AU2002327002A1 (en) | 2001-12-18 | 2002-09-20 | A paper product comprising a polyvinylamine polymer |
BR0214713-0A BR0214713A (en) | 2001-12-18 | 2002-09-20 | Paper product comprising a polyvinylamine polymer |
CA002469039A CA2469039A1 (en) | 2001-12-18 | 2002-09-20 | A paper product comprising a polyvinylamine polymer |
DE60230060T DE60230060D1 (en) | 2001-12-18 | 2002-09-20 | A paper product containing a polyvinylamine |
KR1020047008549A KR100917519B1 (en) | 2001-12-18 | 2002-09-20 | A paper product comprising a polyvinylamine polymer |
MXPA04005291A MXPA04005291A (en) | 2001-12-18 | 2002-09-20 | A paper product comprising a polyvinylamine polymer. |
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US10/023,489 US6824650B2 (en) | 2001-12-18 | 2001-12-18 | Fibrous materials treated with a polyvinylamine polymer |
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KR (1) | KR100917519B1 (en) |
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CA (1) | CA2469039A1 (en) |
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- 2002-09-20 WO PCT/US2002/029937 patent/WO2003052206A1/en not_active Application Discontinuation
- 2002-09-20 DE DE60230060T patent/DE60230060D1/en not_active Expired - Lifetime
- 2002-09-20 EP EP08006500A patent/EP1942226A1/en not_active Withdrawn
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- 2002-09-20 KR KR1020047008549A patent/KR100917519B1/en not_active IP Right Cessation
- 2002-09-20 EP EP02761763A patent/EP1456472B2/en not_active Expired - Fee Related
- 2002-09-20 MX MXPA04005291A patent/MXPA04005291A/en active IP Right Grant
- 2002-12-05 TW TW091135246A patent/TW593835B/en not_active IP Right Cessation
- 2002-12-11 AR ARP020104812A patent/AR037802A1/en unknown
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Cited By (10)
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WO2005016393A1 (en) * | 2003-07-31 | 2005-02-24 | Kimberly-Clark Worldwide, Inc. | Absorbent materials and articles |
US7696401B2 (en) | 2003-07-31 | 2010-04-13 | Evonik Stockhausen, Inc. | Absorbent materials and absorbent articles incorporating such absorbent materials |
US8269060B2 (en) | 2003-07-31 | 2012-09-18 | Evonik Stockhausen, Llc | Absorbent materials and absorbent articles incorporating such absorbent materials |
US8349134B2 (en) | 2004-11-23 | 2013-01-08 | Basf Se | Method for producing high dry strength paper, paperboard or cardboard |
US7922867B2 (en) | 2006-03-16 | 2011-04-12 | Basf Se | Method for producing paper, paperboard and cardboard having high dry strength |
US8404083B2 (en) | 2008-08-18 | 2013-03-26 | Basf Se | Process for increasing the dry strength of paper, board and cardboard |
WO2010122224A1 (en) * | 2009-04-20 | 2010-10-28 | Upm-Kymmene Oyj | Composite intermediate, method for forming same, and use of the composite intermediate |
US8795471B2 (en) | 2009-04-20 | 2014-08-05 | Elastopoli Oy | Composite intermediate, method for forming same, and use of the composite intermediate |
US9873983B2 (en) | 2013-09-12 | 2018-01-23 | Ecolab Usa Inc. | Process and compositions for paper-making |
US9873986B2 (en) | 2013-09-12 | 2018-01-23 | Ecolab Usa Inc. | Paper-making aid composition and process for increasing ash retention of finished paper |
Also Published As
Publication number | Publication date |
---|---|
EP1456472A1 (en) | 2004-09-15 |
TW593835B (en) | 2004-06-21 |
AR037802A1 (en) | 2004-12-01 |
US6824650B2 (en) | 2004-11-30 |
EP1456472B1 (en) | 2008-11-26 |
BR0214713A (en) | 2005-05-03 |
KR20040066868A (en) | 2004-07-27 |
EP1456472B2 (en) | 2012-05-02 |
US20040256066A1 (en) | 2004-12-23 |
TW200303387A (en) | 2003-09-01 |
EP1942226A1 (en) | 2008-07-09 |
AU2002327002A1 (en) | 2003-06-30 |
CA2469039A1 (en) | 2003-06-26 |
DE60230060D1 (en) | 2009-01-08 |
KR100917519B1 (en) | 2009-09-16 |
MXPA04005291A (en) | 2004-09-13 |
US20030131962A1 (en) | 2003-07-17 |
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