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 PDF

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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
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fabric
resin
garment
permanent
curing
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Linton C Reynolds
Alfred T Clifford
Wesley K Fooshe Jr
Stewart M Thomson
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Riegel Textile Corp
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Riegel Textile Corp
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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
    • 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
    • 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
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • 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
    • D06M15/693Treating 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.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatment Of Fiber Materials (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

United States Patent 3,425,856 PROCESS FOR PRODUCING PERMANENT CREASES AND OTHER DESIRABLE PROP- ERTIES IN TEXTILE FABRICS Linton C. Reynolds and Alfred T. Clifford, Ware Shoals, Wesley K. Fooshe, Jr., Greenwood, and Stewart M. Thomson, Ware Shoals, S.C., assignors to Riegel Textile Corporation, a corporation of Delaware No Drawing. Filed Sept. 15, 1964, Ser. No. 396,714 U.S. Cl. 117-11 4 Claims Int. Cl. D06m /36, 15/46 ABSTRACT OF THE DISCLOSURE Process for producing a permanent crease in garments made from wrinkle-resistant fabric and the product thereof comprising impregnating the fabric, prior to cutting and sewing of the garment, Wit-h a composition comprising a predominant amount of a reactive thermoplastic polymer having a reactive group and a minor amount of a thermosetting reactant, drying the resin-impregnated fabric and heating the fabric sufiiciently to cure the resin and effect cross-linking between the reactive thermoplastic polymer and the thermosetting reactant, thereby rendering the impregnated textile fabric receptive to permanent creasing by pressing at elevated temperatures, cutting and sewing the fabric to produce the desired garment, and pressing a permanent crease in the garment without further curing of the resin.
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.
There is at present wide commercial interest in wrinkle resistant fabrics that are adapted to be creased permanently when cut and sewn to produce certain garments, such as mens trousers and womens pleated skirts. But the major problem has been that of obtaining adequate permanent wrinkle resistant efiects, by treatment of the fabric with resins or other chemicals before the fabric is converted into garments, and still leave the fabric receptive to permanent creasing of the garment without heating of the garment, after creasing, to cure the resin.
One of the current processes that has attracted substantial attention in this field is disclosed in 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.
Also, it requires the garment manufacturer to make substantial capital investment in curing ovens which are already available at the finishing plant but cannot be used for the reason that final curing of the conventional resin impregnated fabric, before garment manufacture, would prevent subsequent permanent creasing of the fabric in the garment.
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. Further, the acid treatment creates the problem of spotting or discoloration of the goods.
With the single exception mentioned above, which created other problems, all of the prior attempts of which we are aware in the field of permanent creases, have contemplated curing of the resin after the crease has been imparted to the finished garment, for the reason that it was not considered possible or practical to provide a permanent crease in a garment made from fabric in which the resin impregnant had already been cured prior to cutting and sewing of the garment.
In accordance with the present invention, we have accomplished the long desired objective of being able to complete the resin finishing of the fabric at the finishing plant, by using a special form of resin composition which gives good wrinkle resistance and at the same time perrnits imparting of a permanent crease in garments formed from fabrics treated with this special resin composition, after the garment is produced. One of the important and unique features of our invention which has made this possible for the first time, is the use of a resin composition that comprises a soluble reactive thermosetting resin component in minor amount, e.g., 20%- 40%, and an insoluble reactive thermoplastic resin component in unusually large porportion, e.g., 60%80%.
Another important feature of our invention is the use of special forms of the 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, amino, amido, hydroxyalkyl, aminoalkyl, and amidoalkyl.
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, may be any of the reactants or reactant resins used to crosslink cellulose and give wrinkle resistant properties to cellulose fabrics. It may be selected from the group consisting of the condensation products of urea and formaldehyde, ethylene urea and formaldehyde, amino triazine and formaldehyde, and alkyl car-bamate and formaldehyde.
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.
Illustrative but non-limiting examples of 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:
Parts by wt. Water 33.0 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 soft thermoplastic copolymer formed from ethyl acrylate, lauryl methacrylate, acrylamide, and methacrylic acid 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.
In the above described processes for preparing the wrinkle resistant, shrink stabilized fabric which can be permanently creased by hot pressing in the presence of moisture, the fabric is usually dried in a housed tenter frame and cured in an oven operating in tandem. However, when a fast curing reactant-accelerator composition is used, 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
vary widely with different types of fabrics and in general, the dry weight of resin will vary from approximately 6% to 27% based on the total Weight of the treated fabric.
For the final step of producing garments with permanent creases in accordance with our invention, 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. In other words, 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.
It is believed that 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.
2. A process as defined in claim 1 and in which the 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.
3. A process as defined in claim 1 and in which the thermosetting reactant is selected from the group consisting of urea formaldehyde, ethylene urea formaldehyde, amino triazine formaldehyde and alkyl 'carbamate form'- aldehyde.
4. 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.
References Cited UNITED STATES PATENTS 3,341,955 9/1967 Pyke et al. 1l7134.4 X 2,536,050 1/1951 Pluck 117--1'39.4 2,929,743 3/1960 Mino et al. 117-139.5 2,950,553 8/1960 Hurwitz '117139.4 X 2,974,432 3/ 1961 Warnock et al.. 117139.4 X 2,987,421 6/1961 Sherwood 1 17--16 l 3,017,293 1/1962 Kutik 117-16 1 3,094,371 6/1963 Van Loo et al. 260851 X 3,096,524 7/1963 Mizell 117'139.4 X 3,249,457 5/1966 Lynch l17-161 2,864,093 12/1958 Sumner et a1. 117-139.4 X 3,341,955 9/1967 Pyke et al 117139.4 X
WILLIAM D. MARTIN, Primary Examiner. THEODORE G. DAVIS, Assistant Examiner.
US. Cl. X.R.
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BE723171A (en) 1969-04-01
NL6814551A (en) 1970-04-14
DE1804968A1 (en) 1970-06-11
CH1615668D (en)
FR1590359A (en) 1970-04-13

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