US3606993A - Durable press cotton textile products produced conducting graft copolymerization process followed by cross-linking with dmdheu - Google Patents
Durable press cotton textile products produced conducting graft copolymerization process followed by cross-linking with dmdheu Download PDFInfo
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- US3606993A US3606993A US843237A US3606993DA US3606993A US 3606993 A US3606993 A US 3606993A US 843237 A US843237 A US 843237A US 3606993D A US3606993D A US 3606993DA US 3606993 A US3606993 A US 3606993A
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Links
- 238000000034 method Methods 0.000 title claims abstract description 29
- 230000008569 process Effects 0.000 title claims abstract description 16
- 238000007334 copolymerization reaction Methods 0.000 title abstract description 8
- 238000004132 cross linking Methods 0.000 title abstract description 7
- 229920000742 Cotton Polymers 0.000 title description 32
- 239000004753 textile Substances 0.000 title description 12
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 title description 10
- 150000003254 radicals Chemical class 0.000 abstract description 9
- 238000011084 recovery Methods 0.000 abstract description 9
- 230000037303 wrinkles Effects 0.000 abstract description 9
- 238000002360 preparation method Methods 0.000 abstract description 5
- 239000004744 fabric Substances 0.000 description 36
- -1 poly(acrylonitrile) Polymers 0.000 description 20
- 229920002678 cellulose Polymers 0.000 description 15
- 239000001913 cellulose Substances 0.000 description 15
- 239000003431 cross linking reagent Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 238000005299 abrasion Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 230000005865 ionizing radiation Effects 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229920000578 graft copolymer Polymers 0.000 description 4
- 230000000877 morphologic effect Effects 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 230000001143 conditioned effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 229920002239 polyacrylonitrile Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 238000003795 desorption Methods 0.000 description 2
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229920000196 poly(lauryl methacrylate) Polymers 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/18—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation
- D06M14/20—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin
- D06M14/22—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin of vegetal origin, e.g. cellulose or derivatives thereof
Definitions
- This invention relates to a process for the preparation of durable-press cellulosic products. More particularly, this invention relates to a multistep process for the preparation of durable-press cellulosic products by a free radical initiated graft copolymerization process followed by a normal cross-linking process to yield products with high washwear ratings and high wrinkle recovery angles.
- This invention relates to a multistep process for the preparation of durable press cotton textile products, wherein (l) the macromolecular properties of the cotton cellulose and the morphological structure of cotton are selectively and permanently changed by a free radical initiated graft copolymerization process and then (2) the modified cotton is cross-linked to yield all cotton textile products with higher wash-wear ratings and wrinkle recovery angles than unmodified cotton products which have only been cross-linked.
- the method of this invention has as its objective the modification of both the chemical and physical structures of cotton fibers, mechanically organized into both fabrics suitable for trouser and/or shirting garments, so that the natural properties of cotton are conserved to a maximum extent while imparting durable press properties to the resulting all cotton textile products.
- the instant invention defines a distinct improvement in selectively and permanently changing the morphological structure of the cotton fibers in the fabrics.
- solvents for the vinyl monomer can be selected which do not cause dimensional changes in the cotton fibers, maintaining the natural shape of the fibers.
- the grafted copolymer can be formed primarily in the outer layers of the fibers.
- solvents for the vinyl monomers can be selected which cause dimensional changes in the fibers, that is, swelling and rounding of the cross section of the fibers.
- the grafted copolymer can be formed in the outer layers of the fibers, uniformly within the fibers, or within the fibers while causing a layering effect.
- the molecular relationships between the cellulose molecule and grafted copolymer are such that the chemical reactivity of cellulose toward crosslinking reagents remains high.
- the moisture sorption and desorption properties of the resulting cotton product, based on the content of cellulose, is about the same as untreated cotton.
- Cotton twill fabric was dried to less than 2 percent moisture in a vacuum oven at 50 C., sealed in a nitrogen atmosphere in a thin metal container, and irradiated to a dosage of l megarad by cobalt-6O gamma-radiation.
- the radiation-activated fabric was immersed in a solution comprising acrylonitrile (15 parts by volume), dimethylsulfoxide (25 parts), and water 15 parts) at 25 C. in the absence of oxygen for 7 minutes to give 8 percent add-on of poly(acrylonitrile).
- the graft copolymerized fabric was washed and dried in air and then treated with cross-linking agent, dimethylol dihydroxyethylene urea (DMDHEU) in the usual manner to give an add-on of 7-9 percent, dried in an air oven followed by pressing on a hot head steam press, and then cured in a forced draft oven at C. for 12 minutes.
- the breaking strength of the grafted and cross-linked fabric was 65 pounds (raveled strip method), tearing strength 1300 grams (Elmendorf method), fiex abrasion resistance (American Society for Testing Materials method) 420 cycles, and flat abrasion 520 cycles. Values for cross-linked fabric was, respectively, 46 pounds, 1070 grams, 220 cycles, and 290 cycles.
- EXAMPLE 2 The method of example 1, except that the radiation-activated fabric was immersed in the monomer solution for 25 minutes to give 19 percent add-on of poly(acrylonitrile).
- the properties of the grafted and cross-linked fabric and of the cross-linked fabric were, respectively: breaking strength, 73 pounds and 46 pounds; tearing strength, l270 grams and l070 grams; flex abrasion resistance, 370 cycles and 220 cycles; fiat abrasion resistance, 590 cycles and 290 cycles.
- EXAMPLE 3 The method of example 1, except that after grafting, crosslinking drying, and pressing, simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C. for 12 minutes. After thirty washing and drying cycles in commercially available washers and dryers, the trouser cuffs were rated for appearance (American Association of Textile Chemists and Colorists Test Method No. 124) on a scale from 1 to 5, Cuffs, cross-linked only, had an appearance rating of 4.0; cuffs, grafted and cross-linked had an appearance rating of 4.5.
- EXAMPLE 4 The method of example 1, except that 7 days after radiation activation of the twill fabric, it was immersed in a solution comprising methyl methacrylate (15 parts by volume), methanol (45 parts), and water (40 parts) at 25 C. in the absence of oxygen for 2.5 minutes to give l4 percent add-on of poly(methyl methacrylate).
- the graft copolymerized fabric was washed and dried in air, treated with crosslinking agent DMDHEU in the usual manner to give an add-on of 7-9 percent, and then dried in an air oven, followed by pressing on a hot head steam press. Simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C.
- trouser cuffs cross-linked only had an appearance rating of 4.0; cuffs, grafted and cross-linked, had an appearance rating of 4.5.
- add-ons of poly(methyl methacrylate) were 17 and 30 percent, respectively; after 30 washing and drying cycles trouser cuffs, grafted for these times and later cross-linked had appearance ratings of 4.5 and 4.6, respectively.
- Example 5 absence of oxygen for 6 minutes to give 6 percent add-on of poly(butyl methacrylate).
- the graft copolymerized fabric was washed and dried in air, treated with cross-linking agent DMDHEU in the usual manner to give an add-on of 7-9 percent, and then dried in an air oven, followed by pressing on a hot head steam press.
- Simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C. for 12 minutes. After 30 washing and drying cycles, trouser cuffs cross-linked only had an appearance rating of 4.0; cuffs, grafted and cross-linked had an appearance rating of 4.6.
- EXAMPLE 6 The method of example I except that 7 days after radiation activation of the twill fabric, it was immersed in a solution comprising lauryl methacrylate (20 parts by volume) and methanol (80 parts) at C. in the absence of oxygen for minutes to give 4 percent add-on of poly(lauryl methacrylate).
- the graft copolymerized fabric was washed and dried in air, treated with cross-linking agent DMDHEU in the usual EXAMPLE 7
- the method of example 1 was followed, except that cotton printcloth fabric was used.
- Conditioned wrinkle recovery angle, warp plus fill for printcloth fabric cross-linked only was 274 (360 being complete recovery); printcloth fabric grafted with poly(acrylonitrile) and then cross-linked gave at 9 percent grafted polymer add-on, 293; at l 1 percent, 296; at 18 percent, 304.
- EXAMPLE 8 The method of example 4 was followed, except that cotton printcloth fabric was used. Conditioned wrinkle recovery angle for printcloth fabric crosslmked only was 274; printcloth fabric grafted with poly(methyl methacrylate) and then cross-linked gave at 13 percent grafted polymer add-on; at 20 percent, 31 1; at 27 percent, 307.
- EXAMPLE 9 The method of example 5 was followed, except that cotton printcloth fabric was used. Conditioned wrinkle recovery angle for printcloth fabric cross-linked only was 274; printcloth fabric grafted with poly(butyl methacrylate) and then cross-linked at 4 percent grafted polymer add-on, 311; at 8 percent, 292; at 15 percent, 293.
- a process for preparing durable press cellulosic products which process comprises:
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- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
This invention relates to a process for the preparation of durable-press cellulosic products. More particularly, this invention relates to a multistep process for the preparation of durable-press cellulosic products by a free radical initiated graft copolymerization process followed by a normal cross-linking process to yield products with high wash-wear ratings and high wrinkle recovery angles.
Description
United States Patent Inventors Jett C. Arthur, Jr.;
James A. Harris; Trinidad Mares, all of Metairie, LI.
July 18, 1969 Sept. 21, 1971 The United States of America as represented by the Secretary of Agriculture Appl. No. Filed Patented Assignee DURABLE PRESS CO'I'ION TEXTILE PRODUCTS PRODUCED CONDUCTING GRAF'I' COPOLYMERI ZATION PROCESS FOLLOWED BY CROSS-LINKING WITH DMDHEU [56] References Cited UNlTED STATES PATENTS 3,254,939 6/1966 Munzel 8/ 1 16 OTHER REFERENCES Arthur et al., Textile Industries, Vol. 132, No. 9, pp. 77- 79, 81 (1968) Primary Examiner-George F. Lesmes Assistant Examiner-4. Cannon Attorneys-R. Hoffman and W. Bier ABSTRACT: This invention relates to a process for the preparation of durable-press cellulosic products. More particularly, this invention relates to a multistep process for the preparation of durable-press cellulosic products by a free radical initiated graft copolymerization process followed by a normal cross-linking process to yield products with high washwear ratings and high wrinkle recovery angles.
DURABLE PRESS COTTON TEXTILE PRODUCTS PRODUCED CONDUCTING GRAFT COPOLYMERIZATION PROCESS FOLLOWED BY CROSS-LINKING WITH DMDHEU A nonexclusive, irrevocable, royalty-free license in the inventicn herein described, throughout the world for all purposes of the United Ftates Government, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.
This invention relates to a multistep process for the preparation of durable press cotton textile products, wherein (l) the macromolecular properties of the cotton cellulose and the morphological structure of cotton are selectively and permanently changed by a free radical initiated graft copolymerization process and then (2) the modified cotton is cross-linked to yield all cotton textile products with higher wash-wear ratings and wrinkle recovery angles than unmodified cotton products which have only been cross-linked. The method of this invention has as its objective the modification of both the chemical and physical structures of cotton fibers, mechanically organized into both fabrics suitable for trouser and/or shirting garments, so that the natural properties of cotton are conserved to a maximum extent while imparting durable press properties to the resulting all cotton textile products.
The manufacture of durable press all cotton textile products has been severely limited due to the fact that when cotton is reacted with finishes which impart high wrinkle recovery angles to cotton products prohibitive decreases in natural properties of cotton textile products, such as decreases in abrasion resistance, tearing strength, and wash-wear performance ratings, are obtained. Generally, manufacturers have blended manmade fibers with cotton fibers prior to finishing to give textile products with good wrinkle recovery angles, abrasion resistance, tearing strength, and wash-wear performance ratings. Cotton is included in the blends, usually comprising less than 35 percent of the finished fabric because of its desirable natural properties, such as its moisture sorption and desorption properties, which add to the comfort of textile garments, and its chemical reactivity toward finishing agents, generally cross-linking agents, which impart increased wrinkle resistance to the products. The presence of manmade fibers probably assists in the retention of tearing strength and abrasion resistance by the products.
Developments in using free radical initiators for copolymerizing vinyl monomers with cellulose have offered the possibility of modifying the macromolecular properties of cellulose with minimum decrease in the chemical reactivity of the modified cellulose toward cross-linking reagents. One of the promising methods for free radical initiation of the copolymerization reaction ionizing vinyl monomers is the interaction of ionizing radiation with cotton to produce longlived free radical sites on the cellulose molecule. The number of free radical sites on the cellulose molecule can be controlled by the radiation dosage, that is, time of exposure of the cotton fabric to a given source of ionizing radiation. So that after macromolecular properties of the cellulose molecule and morphological properties of the cotton fibers are selectively altered, the chemical reactivity of the cellulose molecule is not greatly reduced toward cross-linking reagents. Therefore, (I) in one step, the cotton fabrics are exposed to ionizing radiation to give a desired number of free radical sites on the cellulose molecule; (2) in a second step, which may be immediately after or several days after exposure of the fabric to ionizing radiation, the activated cotton fabrics are immersed in a solution of vinyl monomer for a predetermined time to give the desired degree of copolymerization of the activated cellulose with the vinyl monomer to alter the macromolecular properties of the cellulose and to change selectively the morphological properties of the cotton fibers; and (3) in a third step, treatment of the cellulose-graft copolymer fabric with crosslinking reagents to give all-cotton durable press products, with improved wash-wear performance ratings and related properties.
The instant invention defines a distinct improvement in selectively and permanently changing the morphological structure of the cotton fibers in the fabrics. Using ionizing radiation to produce long-lived free radicals on the cellulose molecule, solvents for the vinyl monomer can be selected which do not cause dimensional changes in the cotton fibers, maintaining the natural shape of the fibers. In this case, the grafted copolymer can be formed primarily in the outer layers of the fibers. On the other hand, solvents for the vinyl monomers can be selected which cause dimensional changes in the fibers, that is, swelling and rounding of the cross section of the fibers. ln this case, depending on the vinyl monomer selected, the grafted copolymer can be formed in the outer layers of the fibers, uniformly within the fibers, or within the fibers while causing a layering effect. The molecular relationships between the cellulose molecule and grafted copolymer are such that the chemical reactivity of cellulose toward crosslinking reagents remains high. The moisture sorption and desorption properties of the resulting cotton product, based on the content of cellulose, is about the same as untreated cotton.
The following examples set forth the invention in more detail.
EXAMPLE 1 Cotton twill fabric was dried to less than 2 percent moisture in a vacuum oven at 50 C., sealed in a nitrogen atmosphere in a thin metal container, and irradiated to a dosage of l megarad by cobalt-6O gamma-radiation. Four days later the radiation-activated fabric was immersed in a solution comprising acrylonitrile (15 parts by volume), dimethylsulfoxide (25 parts), and water 15 parts) at 25 C. in the absence of oxygen for 7 minutes to give 8 percent add-on of poly(acrylonitrile). The graft copolymerized fabric was washed and dried in air and then treated with cross-linking agent, dimethylol dihydroxyethylene urea (DMDHEU) in the usual manner to give an add-on of 7-9 percent, dried in an air oven followed by pressing on a hot head steam press, and then cured in a forced draft oven at C. for 12 minutes. The breaking strength of the grafted and cross-linked fabric was 65 pounds (raveled strip method), tearing strength 1300 grams (Elmendorf method), fiex abrasion resistance (American Society for Testing Materials method) 420 cycles, and flat abrasion 520 cycles. Values for cross-linked fabric was, respectively, 46 pounds, 1070 grams, 220 cycles, and 290 cycles.
EXAMPLE 2 The method of example 1, except that the radiation-activated fabric was immersed in the monomer solution for 25 minutes to give 19 percent add-on of poly(acrylonitrile). The properties of the grafted and cross-linked fabric and of the cross-linked fabric were, respectively: breaking strength, 73 pounds and 46 pounds; tearing strength, l270 grams and l070 grams; flex abrasion resistance, 370 cycles and 220 cycles; fiat abrasion resistance, 590 cycles and 290 cycles.
EXAMPLE 3 The method of example 1, except that after grafting, crosslinking drying, and pressing, simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C. for 12 minutes. After thirty washing and drying cycles in commercially available washers and dryers, the trouser cuffs were rated for appearance (American Association of Textile Chemists and Colorists Test Method No. 124) on a scale from 1 to 5, Cuffs, cross-linked only, had an appearance rating of 4.0; cuffs, grafted and cross-linked had an appearance rating of 4.5.
EXAMPLE 4 The method of example 1, except that 7 days after radiation activation of the twill fabric, it was immersed in a solution comprising methyl methacrylate (15 parts by volume), methanol (45 parts), and water (40 parts) at 25 C. in the absence of oxygen for 2.5 minutes to give l4 percent add-on of poly(methyl methacrylate). The graft copolymerized fabric was washed and dried in air, treated with crosslinking agent DMDHEU in the usual manner to give an add-on of 7-9 percent, and then dried in an air oven, followed by pressing on a hot head steam press. Simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C. for 12 minutes. After thirty washing and drying cycles, trouser cuffs cross-linked only had an appearance rating of 4.0; cuffs, grafted and cross-linked, had an appearance rating of 4.5. When the grafting reaction times were 5 minutes and 9 minutes, add-ons of poly(methyl methacrylate) were 17 and 30 percent, respectively; after 30 washing and drying cycles trouser cuffs, grafted for these times and later cross-linked had appearance ratings of 4.5 and 4.6, respectively.
Example 5 absence of oxygen for 6 minutes to give 6 percent add-on of poly(butyl methacrylate). The graft copolymerized fabric was washed and dried in air, treated with cross-linking agent DMDHEU in the usual manner to give an add-on of 7-9 percent, and then dried in an air oven, followed by pressing on a hot head steam press. Simulated trouser cuffs were made, pressed on a hot head steam press, and then cured in a forced draft oven at 160 C. for 12 minutes. After 30 washing and drying cycles, trouser cuffs cross-linked only had an appearance rating of 4.0; cuffs, grafted and cross-linked had an appearance rating of 4.6. When the grafting reaction times were I 1 minutes and 16 minutes, add-ons of poly(butyl methacrylate) were l0 and percent, respectively; after thirty washing and drying cycles trouser cuffs, grafted for these times and later cross-linked had appearance ratings of 4.6 and 4.2, respectively.
EXAMPLE 6 The method of example I except that 7 days after radiation activation of the twill fabric, it was immersed in a solution comprising lauryl methacrylate (20 parts by volume) and methanol (80 parts) at C. in the absence of oxygen for minutes to give 4 percent add-on of poly(lauryl methacrylate). The graft copolymerized fabric was washed and dried in air, treated with cross-linking agent DMDHEU in the usual EXAMPLE 7 The method of example 1 was followed, except that cotton printcloth fabric was used. Conditioned wrinkle recovery angle, warp plus fill (Monsanto method) for printcloth fabric cross-linked only was 274 (360 being complete recovery); printcloth fabric grafted with poly(acrylonitrile) and then cross-linked gave at 9 percent grafted polymer add-on, 293; at l 1 percent, 296; at 18 percent, 304.
EXAMPLE 8 The method of example 4 was followed, except that cotton printcloth fabric was used. Conditioned wrinkle recovery angle for printcloth fabric crosslmked only was 274; printcloth fabric grafted with poly(methyl methacrylate) and then cross-linked gave at 13 percent grafted polymer add-on; at 20 percent, 31 1; at 27 percent, 307.
EXAMPLE 9 The method of example 5 was followed, except that cotton printcloth fabric was used. Conditioned wrinkle recovery angle for printcloth fabric cross-linked only was 274; printcloth fabric grafted with poly(butyl methacrylate) and then cross-linked at 4 percent grafted polymer add-on, 311; at 8 percent, 292; at 15 percent, 293.
We claim:
1. A process for preparing durable press cellulosic products which process comprises:
a. drying a cellulosic fabric to about a 2 percent moisture content,
b. irradiating the fabric to a dosage of about 1 megarad,
c. copolymerizing the radiation-activated fabric in the absence of oxygen with a vinyl monomer selected from a group consisting of acrylonitrile, methyl methacrylate, butyl methacrylate, and lauryl methacrylate,
d. washing the copolymerized fabric from (c) free of excess reagents and drying the washed fabric, and
e. cross-linking the dried fabric from (d) with dimethylol dihydroxy ethylene urea.
2. The product produced by the process of claim 1.
Claims (1)
- 2. The product produced by the process of claim 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US84323769A | 1969-07-18 | 1969-07-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3606993A true US3606993A (en) | 1971-09-21 |
Family
ID=25289415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US843237A Expired - Lifetime US3606993A (en) | 1969-07-18 | 1969-07-18 | Durable press cotton textile products produced conducting graft copolymerization process followed by cross-linking with dmdheu |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3606993A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912449A (en) * | 1973-01-31 | 1975-10-14 | Trinidad Mares | Process for preparing water repellent cotton textiles and the product |
| US3926549A (en) * | 1973-10-10 | 1975-12-16 | Us Agriculture | Cellulose terpolymer textiles |
| US4401688A (en) * | 1978-09-11 | 1983-08-30 | Unisearch Limited (N.S.W.)Australia | Imparting permanent press characteristics |
| US5614591A (en) * | 1994-12-15 | 1997-03-25 | The Virkler Company | Process and composition for imparting durable press properties to textile fabrics |
| US5852066A (en) * | 1994-09-26 | 1998-12-22 | Financiere Elysees Balzac | Regenerated cellulose based materials with improved resistance to bleach, and a process for their preparation |
| US6872424B2 (en) | 1999-09-10 | 2005-03-29 | Nano-Tex, Llc | Durable finishes for textiles |
| US20130122215A1 (en) * | 2009-06-23 | 2013-05-16 | 3M Innovative Properties Company | Functionalized nonwoven article |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3254939A (en) * | 1965-02-01 | 1966-06-07 | Herberlein & Co Ag | Process of modifying cellulosic materials with ionizing radiation |
-
1969
- 1969-07-18 US US843237A patent/US3606993A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3254939A (en) * | 1965-02-01 | 1966-06-07 | Herberlein & Co Ag | Process of modifying cellulosic materials with ionizing radiation |
Non-Patent Citations (1)
| Title |
|---|
| Arthur et al., Textile Industries, Vol. 132, No. 9, pp. 77 79, 81 (1968) * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912449A (en) * | 1973-01-31 | 1975-10-14 | Trinidad Mares | Process for preparing water repellent cotton textiles and the product |
| US3926549A (en) * | 1973-10-10 | 1975-12-16 | Us Agriculture | Cellulose terpolymer textiles |
| US4401688A (en) * | 1978-09-11 | 1983-08-30 | Unisearch Limited (N.S.W.)Australia | Imparting permanent press characteristics |
| US5852066A (en) * | 1994-09-26 | 1998-12-22 | Financiere Elysees Balzac | Regenerated cellulose based materials with improved resistance to bleach, and a process for their preparation |
| US5614591A (en) * | 1994-12-15 | 1997-03-25 | The Virkler Company | Process and composition for imparting durable press properties to textile fabrics |
| US6872424B2 (en) | 1999-09-10 | 2005-03-29 | Nano-Tex, Llc | Durable finishes for textiles |
| US20130122215A1 (en) * | 2009-06-23 | 2013-05-16 | 3M Innovative Properties Company | Functionalized nonwoven article |
| US9259689B2 (en) * | 2009-06-23 | 2016-02-16 | 3M Innovative Properties Company | Functionalized nonwoven article |
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