US3152919A - Stabilized acrylic fabrics and method for treatment of acrylic fabrics - Google Patents

Stabilized acrylic fabrics and method for treatment of acrylic fabrics Download PDF

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US3152919A
US3152919A US143536A US14353661A US3152919A US 3152919 A US3152919 A US 3152919A US 143536 A US143536 A US 143536A US 14353661 A US14353661 A US 14353661A US 3152919 A US3152919 A US 3152919A
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fabrics
acrylonitrile
copolymer
fibers
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James R Biles
Doyle C Nicely
Sellers G W Franklin
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Monsanto Co
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Monsanto Co
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Priority to BE623358D priority Critical patent/BE623358A/xx
Priority to NL284131D priority patent/NL284131A/xx
Priority to NL129478D priority patent/NL129478C/xx
Priority to US143536A priority patent/US3152919A/en
Application filed by Monsanto Co filed Critical Monsanto Co
Priority to GB36750/62A priority patent/GB967318A/en
Priority to CH1167462A priority patent/CH386385A/en
Priority to FR911536A priority patent/FR1335773A/en
Priority to DK433962AA priority patent/DK105979C/en
Priority to SE10771/62A priority patent/SE311337B/xx
Priority to DE19621444095 priority patent/DE1444095A1/en
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • D06M13/232Organic carbonates
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/587Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06CFINISHING, DRESSING, TENTERING OR STRETCHING TEXTILE FABRICS
    • D06C29/00Finishing or dressing, of textile fabrics, not provided for in the preceding groups
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/267Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/2395Nap type surface
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23986With coating, impregnation, or bond
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23993Composition of pile or adhesive
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31935Ester, halide or nitrile of addition polymer

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

Oct. 13, 1964 J. R. BILES ETAL 3,152,919
T STABILIZED ACRYLIC FABRICS AND METHOD FOR TREATMENT OF ACRYLIC FABRICS Filed 001;. 9. 1961 ETHYLENE CARBONATE BONDS ACRYLIC INVENTORS JAMES R. BILES DOYLE C. NICELY BYG.W. FRANKLIN SELLERS ATTORNE United States Patent STABILHZED ACRYLHC FABRICS AND METHOD FOR TREATMENT OF ACRYLIC FAliRlCS James R. Biles, Doyle C. Nicely, and G. W. Franklin Sellers, Decatur, Ala., assignors, by mesne assignments,
to Monsanto Company, a corporation of Deiaware Filed Oct. 9, 1961, Ser. No. 143,536 16 Claims. (Cl. 1l7138.8)
This invention is concerned with the treatment of the raised surface of woven, non-woven and knitted synthetic fabrics to prevent distortion of the raised surface due to normal wearing and laundering conditions. More specifically, this invention is concerned with preventing the matting, shedding and pilling of the nap of acrylic fabrics, as well as preserving a soft hand, after subjecting these fabrics to normal laundering and wearing conditions.
In the past the raised surfaces of fabrics composed of synthetic fibers have been stabilized by the use of salts which were toxic and corrosive; therefore, special and expensive production equipment was necessary to apply these salts, usually as a solution, to the raised surface of the fabrics. Some of the salts were the pure metal halides such as zinc chloride, lithium bromide and water soluble thiocyanates. These salts were very corrosive to the standard finishing mill equipment. In addition, these salts gave the fabrics a harsh; brittle or gritty hand which was very undesirable and afiected the color to such an extent that the fabrics were unacceptable. The use of ethylene carbonate has been disclosed in a pending application,
S.N. 133,299, dated August 23, 1961.
An object of this invention is to provide a method by which the nap of synthetic fabrics are stabilized against ing composition for the nap of acrylonitrile fabrics which renders the fabricsfree of excessive matting, pilling and shedding under normal laundering conditions and normal wearing conditions as well as preserving a soft hand.
Another object of ttu's invention is to provide permanent stability of high pile fabrics against matting, pilling, shedding.
Other objects and advantages of this invention will .become apparent from the hereinafter detailed description.
The objects of this invention are generally accomplished by applying an aqueous solution of ethylene carbonate and a coplymer of ethyl acrylate and methyl methacrylate to the nap or raised surface of synthetic fabrics, either woven, non-woven or knitted. This composition may be applied by spraying, fogging or padding. Other agents may be added on the fabrics during this operation such as an anti-static agent of Aston 108 which is a polyamine resin such as diethylene-triamine crossed linked with polyethylene glycol diiodide or an epoxy resin and a water repellent agent such as Phobotex F.T.C., a melamine derivative. These agents will not affect the hand or color of the fabrics but do give additional useful properties.
More specifically, the synthetic fabrics, either woven, non woven or knitted, were napped and then treated with an aqueous solution of ethylene carbonate and a copolymer of ethyl acrylate and methyl methacrylate. In this stabilizing composition the, ethylene carbonate and the 3,152,919 Fatented Get. 13, 1964 copolymer vary in a ratio of 1 to 1, 2 to 1 and 1 to 2 based on the weight of the aqueous solution with the preferred ratio being 1 part of ethylene carbonate to 1 par-t of the copolymer. The napped and treated fabrics were then heated in a conventional drying apparatus, such as a chain dryer or an oven, to evaporate any water and to cure the copolymer; in addition, during this heating step, ethylene carbonate is concentrated at the points of inter section of the fibers in the nap to form a durable bond between and among themselves as depicted in the drawing.
The period of time the fabrics were heated ranged from 2 minutes to 15 minutes, with the preferred being 4 to 5 minutes, at a temperature of from 250 F. to 350 F. with the preferred temperature being 280 F. The napped fabrics were then withdrawn from the drying apparatus, and it was found that the hand was of acceptable softness and the color was unaffected. The stabilizing composition was added onto the nap by conventional spraying or fogging methods well known in the textile field. Other agents such as water repellents and anti-static agents may be added to the original stabilizing composition solution which would have resulted in giving the mapped fabrics not only stability to laundering, wearing, and a soft hand, but a permanent anti-static and water repellent property. The dyed fabrics were then washed and their shedding, pilling and matting properties were observed along with the hand. There was no excessive shedding, pilling and matting and the hand remained soft.
While this application has been generally directed to synthetic fabrics, it is especially useful in stabilizing the nap of fabrics made from fibersof acrylic polymers. The polymeric materials, which may be employed in the practice of the present invention, are polyacrylonitrile, copolymers, including binary and ternary polymers containing at least percent by weight of acrylonitrile in the polymer molecule, or a blend comprising polyacrylonitrile or copolymers comprising acrylonitrile with from 2 to 50 percent of another polymeric material, the blend having an overall polymerized acrylonitrile content of at least 80 percent by weight. While the preferred polymers employed in the instant invention are those containing at least 80 percent of acrylonitrile, generally recognized as the fiber-forming acryloni-trile polymers, it will be understood that the invention'is likewise applicable to polymers containing less than 80 percent acrylonitrile. The acrylonitrile polymers containing less than 80 percent acrylonitrile are useful in forming films, coating compositions, molding operations, lacquers, etc.
For example, the polymer may be a copolymer of from 80 to 98 percent acrylonitrile and from 2 to 20 percent of another monomer containing the C=C linkage and copolymerizable with acrylonitrile. Suitable monoolefinic monomers include acrylic, alpha-chloroacrylic and methacrylic acids; the acrylates, such as methylmethacrylate, ethylmethacrylate, butylmethacrylate, methoxymethyl methacrylate, beta-chloroethyl methacrylate, and
the corresponding esers of acrylic and alpha-chloroacrylic acids; vinyl chloride, vinyl fluoride, vinyl bromide, vinylidene chloride, l-chloro-l-bromo-ethylene; methacrylonitrile; acrylamide and methacrylamide; alpha-chloroacrylamide; or monoalkyl substitution products thereof; methylvinyl ketone; vinyl carboxylates, such as vinyl acetate,} vinyl chloroacetate, vinyl propionate, and vinyl stearate; N-vinylimides, such as N-vinylphthalimide and N-vinylsuccinimide; methylene malonic esters; itaconic acid and itaconic esters; N-vinylcarbazole; vinyl furane; alkyl vinyl esters; vinyl sulfonic acid; ethylene alpha,
betadicarboxylic acids or their anhydrides or derivatives,
such as diethyicitraconate, diethylmesaconate, styrene,
vinyl naphthalene; vinyl-substituted tertiary heterocyclic I amines, such as the vinylpyridines and alkyl-substituted 'vinylpyridines, for example, 2-vinylpyridine, 4-vinylpyridine, Z-methyl-S-vinylpyridine, etc.; l-vinylimidazole and alkyl-substituted l-vinylimidazoles, such as 2-, 4-, or 5- methyl-l-vinylimidazole, and other C=C containing polyrnerizable materials.
. The polymer may be a ternary or'higher .interpolymer, for example, products obtained by the interpolymerization of acrylonitrile and two or more of any of the monomers, other than acrylonitrile, enumerated above. More specifically, and preferably, the ternary polymer comprises acrylonitrile, methacrylonitrile, and 2-vinylpyridine. The
ternary polymers-preferably contain from 80 to 98 per- 'cent by acrylonitrile, from 1 tov 10 percent of a vinyl- ..pyridine or a l-vinylimidazole, and from 1 to 18 percent of another substance such 'as methacrylonitr'ile or vinyl chloride.
. The polymer may'also be a blend of a polyacrylonitrile 'or. of a binary interpolymer of from 80 to 99 percent acrylonitrileand from 1 to.20 percent of at least one other. C='C containing substance with from 2'to 50 percent of the weight of theblend of a copolymer of from 10,, to 70 percent ofacrylonitrile and from 30 to 90" percent of at least one other C=C containing polymerizable monomer. Preferably, when the polymeric material comprises a blend, it will be a blend of a copolymer of 90 to 98 percent acrylonit'rile and from 2 to 10 percent of another monomer-olefinic monomer, such as vinyl acetate, which is not receptive to dyestuff, with a suflicientamount of a copolymer of from 10 to 70 percent of acrylonitrile and from 30 to 90 percent of a vinyl-substituted tertiary 'heterocyclic. amine, such as vinylpyridine or l-vinylimid- Exam le 1 In the following chart the 'fabric samp s were comijpiosed of fibers 'of i94 percent acrylonitrile and 5 percent vinyl acetate. Also, the samples were all treatedby spraying withan aqueous solution of lto 1 ratio byweight I of ethylene carbc inateandthe copolymer of ethyl acrylate and methyljmethacrylate; all samples were dryed for 4 minutes at 290 F.; in addition the solution contained 10 percent solids of the copolymer.
-. Solution Handand Rating Sample Dry- Wetwt. Percent cone. of appearafter No. wt., in Difi. addon ethylene --ance washgrams grams carbonate before ing 5 W washing times .QThuslwitli a stabilizing composition solution of 1.25 percent concentratiom and addons in'the r ange of 5 percentto ,zpercem; after five consecutive launderings of the .Qtraited fabric there is good. resistance to pilling, matting, 13 's edding'and aisoft hand is still. present, in fact generally .f improved. ,Thecolor of the sample wasnot affected after j the,tr'ea ting and Washing process of this invention. This 1132515 561551; with a 2.5 percent concentration of the ,iistabilizing composition with addons in the range of V 3 i per centt Y percent aswell as 3.5 percent addonsand i a 10 percent, concentration and a 3,5 jpercent addons and la 5 percent concent1 ation.' The rating was done according to al tor5 rating with 3 being commercially acceptable, with all ratings above 3 being of superioriquality as to shedding, pilling, matting and soft hand.
lcent concentration of "the stabilizing composition and a rangefof 3percent to SKpercent JaddOns'and with a 1.25
and ethy jinehac ylae h i ly. solidsfallsaniples weredri'ed' for 4"m1iii1tes' at 300 F and t an. satisfied t9 .aah i st mer.
4 Example 2 In the following chart the: fabric samples were composed of fibers of 94 percent acrylonitrile and 6 percent vinyl acetate. Also, the samples were all treated by spray- 7 ing with an aqueous solutionofja2 to 1 ratio by weight of ethylene carbonate to the copo'lyn er of ethyl acrylate and methyl methacrylate, with5 percent solids of the copoly- All samples were dried for'4 minutes at a temperature of 300 F. and fthenl subjected to 5 consecutive washings under normal laundering conditions.
. Hand. Gone; and Rating Sample ,Dry ,Wet Dirt. Percentof appearafter 5 No. Wt. Wt. addon ethylene ance -wash carbonate before ings washing Thus I with a stabilizing eornposition solution of 10 present,infact generally improved. "The' color of the 's'antmawasnet affected. This was also the result 'with a 5"peficent'concentration bf the: stabilizing composition and a rangeofZpe'rcent to 5 percent addon, a 2.5 perpercent concentration and SLS-pe'rce ntaddOn.
' In the" following chart, the "fabric samples were composed of fibe rs'of 94 percent anywmnueanae percent vinyl tease; jAlso, thesanipleswer'ej all treated by spraying'with'an 'aqueoussolutionof a2 to 1 ratioby weight of ethylene carbo fnate and the copolyiner of ethyl acrylate "iig 2.5:per'cent Cone. 1 Perethyl: H n .Wt. .Wt. cent Sample tDry ,Wet .Per-. .ene .before before after .lost No. Wt. Wt. Difi. ,eent -earshed-shed-sheddue addon bonding ding ding to 3 ate shedding Thusrwith a stabilizingcompositionsolution of 5 percent .-'and addons from 4 percent'to 5' percent, there was only t0 1, t .2 an t jlb ts nt e Ws ary sfro M1 25 percent'to lfipercent and addons varying from 1 per- "centitol, percent, depending upon theconcentration of the'jsp'lntion, the inventors ave been very successful in stabilizing the nappedl surfaces of synthetic linear acrylic fabrics to pilling, matting, "shedding as well as nraintainliing a soft and acceptable'handafter numerous launderings under normal laundering conditions.
It'is understood'that changes and variationsrnay be made in the present invention by one skilled in the art without departing from the spirit and scope thereof as defined in the appended claims.
We claim:
1. An article composed of the napped fabric of fibers of linear polymers of acrylonitrile stabilized with a composition comprising ethylene carbonate and a copolymer of ethyl acrylate and methyl methacrylate, wherein the amount of ethylene carbonate varies from 0.1 to 10 percent based on the weight of the fibers.
2. The article of claim 1 wherein the mapped fabric is composed of fibers of a copolymer of acrylonitrile and up to 20% of a copolymerizable olefinic monomer.
3. The article of claim 2 in which the napped fabric is composed of fibers of a copolymer of 94 percent acrylonitrile and 6 percent vinyl acetate.
4. The article of claim 2 wherein the napped fabric is composed of a blend of fibers composed of 88 percent of one copolymer of 94 percent acrylonitrile and 6 percent vinyl acetate and 12 percent of another copolymer of 50 percent acrylonitrile and 50 percent methyl vinyl pyridine.
5. A method of stabilizing the napped fabric of fibers of linear polymers of acrylonitrile which comprises impregnating the napped fabric with an aqueous solution comprising ethylenecarbonate and a copolymer of ethyl acrylate and methyl methacrylate, wherein the amount of ethylene carbonate varies from 0.1 to 10 percent based on the Weight of the fibers, and heating the impregnated napped fabric. 7
6. The method of claim 5 wherein the mapped fabric is composed of fibers of a copolymer of acrylonitrile and up to 20 percent of a copolymerizable olefinic monomer.
7. The method of claim 6 in which the fibers are composed of a copolymer of 94 percent acrylonitrile and 6 percent vinyl acetate. 7
8. The method of claim 6 in which the fibers are composed of a blend of 88 percent of one copolymer of 94 percent acrylonitrile and 6 percent vinyl acetate and 12 percent of another copolymer composed of 50 percent acrylonitrile and 50 percent methyl vinyl pyridine.
9. A method of stabilizing the napped fabrics of fibers of a copolymer of acrylonitrile and up to 20 percent of a copolymerizable olefinic monomer which comprises impregnating the mapped fabric with an aqueous solution 10. The method of claim 9 in which the ratio is 1 to 1 V and the impregnated napped fabric is heated to 280 F. for 4 minutes.
11. The method of claim 9 in which the ratio is 2 to 1 and the impregnated napped fabric is heated to 300 F. for 2 minutes.
12. The method of claim 9 in which the ratio is 1 to 2 and the impregnated napped fabric is heated to 300 F. for 2 minutes.
13. A method of stabilizing the napped fabric of fibers of a copolymer of 94 percent acrylonitrile and 6 percent vinyl acetate which comprises spraying onto the nap of the fabric an aqueous solution comprising ethylene carbonate and a copolymer of ethyl acrylate and methyl methacrylate, wherein the ratio of ethylene carbonate to copolymer in said solution is from 2 to 1 to 1 to 2 with the amount of ethylene carbonate varying from 0.1 to 10 percent based on the weight of the fibers, heating the sprayed napped fabric in a drying oven to a temperature of 280 F. for 4 minutes, removing said sprayed napped fabric from the drying oven and allowing the same to 8 References Cited in the file of this patent UNITED STATES PATENTS 2,136,423 Fields et a1 Nov. 15, 1938 2,354,210 Jacobson July 25, 1944 2,734,041 Jones et al Feb. 7, 1956

Claims (1)

  1. 5. A METHOD OF STABILIZING THE NAPPED FABRIC OF FIBERS OF LINEAR POLYMERS OF ACRYLONITRILE WHICH COMPRISES IMPREGNATING THE NAPPED FABRIC WITH AN AQUEOUS SOLUTION COMPRISING ETHYLENE CARBONATE AND A COPOLYMER OF ETHYL ACRYLATE AND METHYL METHACRYLATE, WHEREIN THE AMOUNT OF ETHYLENE CARBONATE VARIES FRO 0.1 TO 10 PERCENT BASED ON THE WEIGHT OF THE FIBERS, AND HEATING THE IMPREGNATED NAPPED FABRIC.
US143536A 1961-10-09 1961-10-09 Stabilized acrylic fabrics and method for treatment of acrylic fabrics Expired - Lifetime US3152919A (en)

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Application Number Priority Date Filing Date Title
BE623358D BE623358A (en) 1961-10-09
NL284131D NL284131A (en) 1961-10-09
NL129478D NL129478C (en) 1961-10-09
US143536A US3152919A (en) 1961-10-09 1961-10-09 Stabilized acrylic fabrics and method for treatment of acrylic fabrics
GB36750/62A GB967318A (en) 1961-10-09 1962-09-27 Improvements in the treatment of acrylonitrile polymer fabrics
CH1167462A CH386385A (en) 1961-10-09 1962-10-04 Method of stabilizing the woolen surface of fabrics and fabrics treated by this process
FR911536A FR1335773A (en) 1961-10-09 1962-10-08 Improvements in the treatment of synthetic fabrics, in particular acrylic fabrics
DK433962AA DK105979C (en) 1961-10-09 1962-10-08 Method for stabilizing the pile on a textile material of acrylonitrile polymer fibers with pile surface against entanglement, abrasion and peeling and for maintaining a soft grip of the stabilized material.
SE10771/62A SE311337B (en) 1961-10-09 1962-10-08
DE19621444095 DE1444095A1 (en) 1961-10-09 1962-10-09 Process for stabilizing the roughening or the pile of textile goods

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BE (1) BE623358A (en)
CH (1) CH386385A (en)
DE (1) DE1444095A1 (en)
DK (1) DK105979C (en)
GB (1) GB967318A (en)
NL (2) NL129478C (en)
SE (1) SE311337B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3431159A (en) * 1964-06-17 1969-03-04 David Gordon Manufacture of mouldings from acrylonitrile copolymers
US3496054A (en) * 1967-01-13 1970-02-17 Kem Wove Ind Inc Flocked nonwoven textile material having a relief pattern therein
US3501366A (en) * 1964-05-29 1970-03-17 Anthony Bramley Production of netting
US3634163A (en) * 1970-05-28 1972-01-11 Allied Chem Method of imparting wrinkle resistance to fabrics
US3900618A (en) * 1973-12-13 1975-08-19 American Cyanamid Co Process for reducing pilling tendencies of acrylic fibers and fiber products thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2136423A (en) * 1937-06-02 1938-11-15 Du Pont Polymerization process
US2354210A (en) * 1942-10-20 1944-07-25 Du Pont Polymerization of acrylic compounds
US2734041A (en) * 1953-03-13 1956-02-07 Compositions of matter comprising

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2136423A (en) * 1937-06-02 1938-11-15 Du Pont Polymerization process
US2354210A (en) * 1942-10-20 1944-07-25 Du Pont Polymerization of acrylic compounds
US2734041A (en) * 1953-03-13 1956-02-07 Compositions of matter comprising

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3501366A (en) * 1964-05-29 1970-03-17 Anthony Bramley Production of netting
US3431159A (en) * 1964-06-17 1969-03-04 David Gordon Manufacture of mouldings from acrylonitrile copolymers
US3496054A (en) * 1967-01-13 1970-02-17 Kem Wove Ind Inc Flocked nonwoven textile material having a relief pattern therein
US3634163A (en) * 1970-05-28 1972-01-11 Allied Chem Method of imparting wrinkle resistance to fabrics
US3900618A (en) * 1973-12-13 1975-08-19 American Cyanamid Co Process for reducing pilling tendencies of acrylic fibers and fiber products thereof

Also Published As

Publication number Publication date
SE311337B (en) 1969-06-09
DE1444095A1 (en) 1969-01-23
NL284131A (en) 1900-01-01
BE623358A (en) 1900-01-01
NL129478C (en) 1900-01-01
DK105979C (en) 1966-12-05
GB967318A (en) 1964-08-19
CH386385A (en) 1964-09-30

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