US3425856A - Process for producing permanent creases and other desirable properties in textile fabrics - Google Patents
Process for producing permanent creases and other desirable properties in textile fabrics Download PDFInfo
- Publication number
- US3425856A US3425856A US396714A US3425856DA US3425856A US 3425856 A US3425856 A US 3425856A US 396714 A US396714 A US 396714A US 3425856D A US3425856D A US 3425856DA US 3425856 A US3425856 A US 3425856A
- Authority
- US
- United States
- Prior art keywords
- fabric
- resin
- garment
- permanent
- curing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004744 fabric Substances 0.000 title description 66
- 238000000034 method Methods 0.000 title description 17
- 239000004753 textile Substances 0.000 title description 7
- 229920005989 resin Polymers 0.000 description 34
- 239000011347 resin Substances 0.000 description 34
- 229920001169 thermoplastic Polymers 0.000 description 22
- 239000000203 mixture Substances 0.000 description 15
- 229920001187 thermosetting polymer Polymers 0.000 description 15
- 230000037303 wrinkles Effects 0.000 description 15
- 239000000376 reactant Substances 0.000 description 12
- 238000003825 pressing Methods 0.000 description 11
- 239000004416 thermosoftening plastic Substances 0.000 description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- -1 carboxy, amino Chemical group 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 7
- 238000009958 sewing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical group COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 2
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
- 125000005157 alkyl carboxy group Chemical group 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- PMZIUAOBHNJYQT-UHFFFAOYSA-N (1-hydroxy-2-methylpropan-2-yl)azanium;chloride Chemical compound Cl.CC(C)(N)CO PMZIUAOBHNJYQT-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical group NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002821 Modacrylic Polymers 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- PPBYBJMAAYETEG-UHFFFAOYSA-N ethene;formaldehyde;urea Chemical compound C=C.O=C.NC(N)=O PPBYBJMAAYETEG-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- SAESCDGAKWEZRD-UHFFFAOYSA-N formaldehyde;triazin-4-amine Chemical compound O=C.NC1=CC=NN=N1 SAESCDGAKWEZRD-UHFFFAOYSA-N 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/693—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural or synthetic rubber, or derivatives thereof
Definitions
- This invention relates to a process for producing a permanent crease in garments made from resin impregnated wrinkle resistant fabrics, after cutting and sewing of the garment, and without the necessity of any heating of the garment to cure the resin after pressing of the crease therein, or any pretreatment of the garment to permit creasing. No one heretofore has been able to obtain this commercially important result despite numerous efforts.
- Warnock Patent No. 2,974,432 issued Mar. 14, 1961. It provides ultimate wrinkle resistant properties by first resin irnpregnation of the fabric, next drying of the fabric at a low temperature to avoid curing of the resin, followed by cutting and sewing of the fabric to produce garments such as mens slacks, pressing creases in the slacks with the usual heated press or iron, then suspending the creased slacks in an oven and heating the slacks in the oven for a period of time and at sufiiciently high temperature to cause the resin to cure or set and to render the crease permanent.
- This prior process has the disadvantage of not being able to complete the finishing of the fabric at the finishing plant by persons especially skilled in finishing processes and techniques, and requires the garment manufacturer to complete the finishing of the fabric, i.e., the curing of the resin.
- This prior patented process also has the objection of requiring careful control of the drying process at the finishing mill to prevent over drying or preliminary curing of the resin, which in turn would prevent permanent 3,425,856 Patented Feb. 4, 1969 creasing by the garment manufacturer; or premature curing of the resin during storage of the fabric, which likewise would prevent subsequent creasing of the garment by the garment manufacturer.
- Another prior process involves curing of the resin in the fabric at the finishing plant to give the wrinkle resistant property, followed by making of the garment and imparting the crease by a special procedure.
- the latter comprises applying an acid or other suitable chemical to the restricted area of the garment where the crease is to be made and then pressing the garment along the line of the treatment.
- This process has the objection of requiring special treatment by the garment manufacturer beyond his usual field of experience, and renders the creasing operation tedious.
- the acid treatment creates the problem of spotting or discoloration of the goods.
- thermoplastic resin component which contain reactive side groups that. effect cross-linking of the themoplastic component with the thermosetting component.
- the thermoplastic polymer component is a medium soft to medium hard, film forming, linear, water insoluble (in latex form) copolymer (or mixture of copolymers) formed from a preponder'ant amount, e.g., about %99%, of one or more monomers of the type in which R is selected from the group consisting of hydrogen, alkyl, and a-ryl and R is selected from the group consisting of cyano, chloro, alkylcarboxy, and acetoxy, and a minor amount, e.g., about 1%20%, of one or more monomers of the type Ra CHFO/ R4 in which R is selected from the group consisting of hydrogen, chloro, alkyl, aryl, alkylcarboxy, alkoxy, and acetoxy, and R is selected from the group consisting of carboxy,
- Illustrative but non-limiting examples of the above mentioned preponderant amount of monomers are butadiene, acrylonitrile, styrene, acrylic esters, vinyl acetate, and vinyl chloride.
- Illustrative but non-limiting examples of the minor amount of monomers are acrylic acid, methacrylic acid, acrylamide, and methacrylamide.
- the soluble reactive component i.e., the thermosetting resin of the resin composition
- the resin accelerator may be selected from the group consisting of acid, ammonium salt, amine salt or metal salt. Suitable examples are magnesium chloride, zinc nitrate and 2-amino-2-methyl-l-propanol hydrochloride.
- thermoplastic component with reactive side groups e.g., polystyrene resin
- thermosetting component e.g., polystyrene resin
- suitable resinous compositions which contain predominant proportions of the thermoplastic component with reactive side groups, and minor proportions of the thermosetting component, for impregnating the fabric so as to obtain good wrinkle resistant effects yet render it susceptible for imparting a permanent crease in garments produced from this fabric, are as follows:
- Example I A solution is prepared by mixing the following ingredients:
- Non-ionic wetting agent trimethyl nonyl ether of polyethylene glycol
- Magnesium chloride (30% solution) (on basis of anhydrous salt)
- Thermosetting reactant (50% solution) (mixture of water soluble, essentially monomeric condensation products of melamine, formaldehyde, and methanol, having the empirical composition of the dimethyl ether of trimethylol melamine)
- Water dispersion (45%) of a medium hard thermoplastic copolymer formed from ethyl acrylate, methyl methacrylate, and methacrylate acid Total 100.0
- the solution described above is applied on a three roll padder at 55% wet pick up (14% of the combined dry weight of the thermosetting reactant and thermoplastic copolyrner on the basis of the dry weight of the fabric) to a twill fabric (7 ounces per square yard) containing 50% cotton and 50% polyester fibers.
- the fabric is dried at 250-300 F. on a steam heated tenter frame and cured 2 minutes at 325350 F. in a gas heated curing oven.
- the fabric weighs approximately 8 ounces per square yard and contains a resinous composition in the amount of approximately 12 percent of the finished fabric. It has durable wrinkle resistance and durable shrink stabilization.
- Example 11 polyethylene glycol) 4 Hydrochloride (30%) of 2 amino 2 methyl-1- propanol T hermosetting reactant solution) (mixture of water soluble, essentially monomeric condensation products of melamine, formaldehyde, and methanol, having the empirical composition of the dimethyl ether of trimethylol melamine) Water dispersion (45%) of a reactive thermoplastic (formed from 92.5% ethyl acrylate, 5% methyl methacrylate, and 2.5% acrylic acid Total 100.0
- the solution described above is applied on a three roll padder at 55% wet pick-up (12% combined dry weight of the thermosetting reactant and the reactive thermoplastic polymer on the basis of the dry weight of the untreated fabric) to vat dyed cotton twill weighing 7 ounces per square yard.
- the fabric is dried at 250- 300 F. in a steam heated housed tenter frame and cured 2 minutes at 325350 F. in a gas heated curing oven.
- the finished fabrio weighs approximately 8 ounces per square yard. It contains approximately 10.5% resinous composition on the basis of the weight of finished fabric.
- the fabric has durable wrinkle resistance and durable shrink resistance.
- Example III Same as Example II except that the reactive thermoplastic polymer is formed from 43% butadiene, 52% styrene, and 5% acrylic acid.
- Example 1V Same as Example II except the reactive thermoplastic polymer is formed from 64% butadiene, 31% acrylonitrile, and 5% methacrylic acid.
- Example V A solution is prepared by mixing the following ingredients:
- the solution described above is applied on a three roll padder at 55% wet pick up (12% of the combined dry weight of the thermosetting reactant and the reactive thermoplastic polymer on the basis of the dry weight of the untreated fabric) to a shirting fabric weighing 5 ounces per square yard.
- the fabric is dried and cured in a heated tenter frame for 2 minutes at 325 F.
- the finished fabric weighs approximately 5.6 ounces per square yard. It has durable wrinkle resistance and durable shrink resistance.
- the fabric is usually dried in a housed tenter frame and cured in an oven operating in tandem.
- a fast curing reactant-accelerator composition such as disclosed in Example V above, the fabric may be dried and cured in a housed tenter frame alone.
- the amount of resin composition, containing both the thermoplastic and thermosetting components, used for treating the fabric in accordance with our invention may
- the dry weight of resin will vary from approximately 6% to 27% based on the total Weight of the treated fabric.
- the fabrics treated with any of the resins described in the foregoing examples and in accordance with the process steps discussed above may be used.
- the garments made with these fabrics may be fashioned by conventional cutting and sewing operations, commonly employed in the production of mens trousers and womens skirts, and without requiring any skill on the part of the garment manufacturer with respect to finishing of the fabric.
- the fabric as shipped from the finishing mill is ready for immediate fabrication into the desired garments and pressing of a permanent crease or creases in the garments so produced.
- the permanent creases may be imparted by conventional means, such as for example steam emitting hot head presses adjusted to give a minimum pressure on the garment of about 10* pounds per square inch and a minimum temperature of about 350 F. After pressing of the permanent creases in the garments, they require no further processing.
- Fabrics suitable for use in the above described process or product consist of fibers made from cellulose or hydrophilic cellulose derivatives, blends of these fibers with each other, or blends of these fibers with other fibers.
- Suitable but non-limiting examples are cotton, linen, rayon, cellulose acetate, cotton-polynosic rayon, cottonpolyamide, cotton-polyester, cotton-acrylic, rayon-modacrylic, cotton-polypropylene, cotton-cellulose triacetate, and rayon-wool.
- the wrinkle resistant and permanent crease properties of the garments made from the above described resin impregnated fabrics are obtained because a portion of the reactant and accelerator penetrates the cellulose fibers and on curing crosslinks the cellulose molecules to give a wrinkle resistant and shrink stabilized fabric; and another portion of the reactant and accelerator and substantially all of the thermoplastic polymer remains on the surface of the fibers and on curing forms a coating of a crosslinked thermoplastic composition.
- This coating of crosslinked thermoplastic composition imparts to the fabric that property which results in a permanent crease when the garment made from the fabric is pressed at an elevated temperature in the and amido groups, and a minor amount of 20%-40% of a soluble reactive thermosetting resin component, drying the resin impregnated fabric and heating the fabric sufficiently to cure the resin and effect crosslin'king between the reactive thermoplastic polymer and the thermosettirrg resin component to form a crosslinked thermoplastic coating which renders the impregnated textile fabric receptive to permanent creasing by pressing at elevated temperatures, cutting and sewing of the fabric to produce the desired garment, and pressing a permanent crease in the garment without further curing of the resin.
- thermoplastic polymer is formed from a major proportion of monomers selected from the group consisting of butadiene, alcrylonitrile, styrene, acrylic esters, vinyl acetate, and vinyl chloride, and a minor proportion of monomers selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, and methacrylamide.
- thermosetting reactant is selected from the group consisting of urea formaldehyde, ethylene urea formaldehyde, amino triazine formaldehyde and alkyl 'carbamate form'- aldehyde.
- a process for producing permanent creases and other desirable properties in textile fabrics comprising impregnating the fabric with an aqueous resinous composition comprising about 60%-80% of an insoluble reactive thermoplastic polymer having a reactive group and formed from an acrylic ester and an acrylic acid, and about 20%- 40% of a soluble reactive thermosetting resin component, drying the resin impregnated fabric and heating the fabric sufficiently to cure the resin and effect crosslinking between the reactive thermoplastic polymer and the thermosetting resin component to form' a crosslinked thermoplastic coating which renders the impregnated textile fabric receptive to permanent creasing by pressing at elevated temperatures, and pressing a permanent crease in the fabric without further curing of the resin.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Treatment Of Fiber Materials (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39671464A | 1964-09-15 | 1964-09-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3425856A true US3425856A (en) | 1969-02-04 |
Family
ID=23568365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US396714A Expired - Lifetime US3425856A (en) | 1964-09-15 | 1964-09-15 | Process for producing permanent creases and other desirable properties in textile fabrics |
Country Status (6)
Country | Link |
---|---|
US (1) | US3425856A (enrdf_load_stackoverflow) |
BE (1) | BE723171A (enrdf_load_stackoverflow) |
CH (1) | CH1615668D (enrdf_load_stackoverflow) |
DE (1) | DE1804968A1 (enrdf_load_stackoverflow) |
FR (1) | FR1590359A (enrdf_load_stackoverflow) |
NL (1) | NL6814551A (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1226301A1 (en) * | 1999-09-10 | 2002-07-31 | Nano-Tex LLC | Abrasion- and wrinkle-resistant finish for textiles |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2536050A (en) * | 1947-11-10 | 1951-01-02 | American Cyanamid Co | Treatment of cellulosic textile materials and products thereof |
US2864093A (en) * | 1954-10-20 | 1958-12-16 | Chicopec Mfg Corp | Washable garment part |
US2929743A (en) * | 1956-11-08 | 1960-03-22 | American Cyanamid Co | Process for treating cellulose material with thermoplastic material and product thereof |
US2950553A (en) * | 1957-01-16 | 1960-08-30 | Rohm & Haas | Method of producing wrinkle resistant garments and other manufactured articles of cotton-containing fabrics |
US2974432A (en) * | 1956-02-20 | 1961-03-14 | Koret Of California | Press-free crease retained garments and method of manufacture thereof |
US2987421A (en) * | 1955-09-19 | 1961-06-06 | Goodrich Co B F | Composition for treating textile materials, method, and article produced thereby |
US3017293A (en) * | 1959-04-28 | 1962-01-16 | Interchem Corp | Coated cured synthetic rubber substrate |
US3094371A (en) * | 1957-06-13 | 1963-06-18 | American Cyanamid Co | Textile treatment with aminoplast and polyacrylamides and the textile so treated |
US3096524A (en) * | 1961-04-11 | 1963-07-09 | Williamson Dickie Mfg Company | Process for improving crease-retention properties of cotton garments |
US3249457A (en) * | 1962-09-28 | 1966-05-03 | Interchem Corp | Flocked article and method of manufacture |
US3341955A (en) * | 1964-07-21 | 1967-09-19 | Everprest Inc | Producing wrinkle-free, permanently creased garments |
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0
- CH CH1615668D patent/CH1615668D/xx unknown
-
1964
- 1964-09-15 US US396714A patent/US3425856A/en not_active Expired - Lifetime
-
1968
- 1968-10-11 NL NL6814551A patent/NL6814551A/xx unknown
- 1968-10-24 DE DE19681804968 patent/DE1804968A1/de active Pending
- 1968-10-30 BE BE723171A patent/BE723171A/xx unknown
- 1968-10-30 FR FR171980A patent/FR1590359A/fr not_active Expired
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2536050A (en) * | 1947-11-10 | 1951-01-02 | American Cyanamid Co | Treatment of cellulosic textile materials and products thereof |
US2864093A (en) * | 1954-10-20 | 1958-12-16 | Chicopec Mfg Corp | Washable garment part |
US2987421A (en) * | 1955-09-19 | 1961-06-06 | Goodrich Co B F | Composition for treating textile materials, method, and article produced thereby |
US2974432A (en) * | 1956-02-20 | 1961-03-14 | Koret Of California | Press-free crease retained garments and method of manufacture thereof |
US2929743A (en) * | 1956-11-08 | 1960-03-22 | American Cyanamid Co | Process for treating cellulose material with thermoplastic material and product thereof |
US2950553A (en) * | 1957-01-16 | 1960-08-30 | Rohm & Haas | Method of producing wrinkle resistant garments and other manufactured articles of cotton-containing fabrics |
US3094371A (en) * | 1957-06-13 | 1963-06-18 | American Cyanamid Co | Textile treatment with aminoplast and polyacrylamides and the textile so treated |
US3017293A (en) * | 1959-04-28 | 1962-01-16 | Interchem Corp | Coated cured synthetic rubber substrate |
US3096524A (en) * | 1961-04-11 | 1963-07-09 | Williamson Dickie Mfg Company | Process for improving crease-retention properties of cotton garments |
US3249457A (en) * | 1962-09-28 | 1966-05-03 | Interchem Corp | Flocked article and method of manufacture |
US3341955A (en) * | 1964-07-21 | 1967-09-19 | Everprest Inc | Producing wrinkle-free, permanently creased garments |
Also Published As
Publication number | Publication date |
---|---|
NL6814551A (enrdf_load_stackoverflow) | 1970-04-14 |
CH1615668D (enrdf_load_stackoverflow) | |
BE723171A (enrdf_load_stackoverflow) | 1969-04-01 |
DE1804968A1 (de) | 1970-06-11 |
FR1590359A (enrdf_load_stackoverflow) | 1970-04-13 |
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