US2524022A - Water repellent fabrics and composition and process for making same - Google Patents
Water repellent fabrics and composition and process for making same Download PDFInfo
- Publication number
- US2524022A US2524022A US13077A US1307748A US2524022A US 2524022 A US2524022 A US 2524022A US 13077 A US13077 A US 13077A US 1307748 A US1307748 A US 1307748A US 2524022 A US2524022 A US 2524022A
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- United States
- Prior art keywords
- parts
- water
- wax
- styrene
- amine
- 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
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- 239000004744 fabric Substances 0.000 title claims description 51
- 239000000203 mixture Substances 0.000 title claims description 20
- 239000005871 repellent Substances 0.000 title claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 33
- 238000000034 method Methods 0.000 title description 6
- 230000002940 repellent Effects 0.000 title description 3
- 239000002253 acid Substances 0.000 claims description 17
- 239000007864 aqueous solution Substances 0.000 claims description 16
- 239000000839 emulsion Substances 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- -1 ALIPHATIC HYDROCARBON PRIMARY AMINE Chemical class 0.000 claims description 9
- 238000009877 rendering Methods 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 50
- 239000001993 wax Substances 0.000 description 32
- 239000004753 textile Substances 0.000 description 26
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 23
- 150000001412 amines Chemical class 0.000 description 20
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- 229920001577 copolymer Polymers 0.000 description 17
- 239000007921 spray Substances 0.000 description 16
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 15
- 150000003863 ammonium salts Chemical class 0.000 description 15
- 238000005108 dry cleaning Methods 0.000 description 15
- 239000004204 candelilla wax Substances 0.000 description 14
- 235000013868 candelilla wax Nutrition 0.000 description 14
- 229940073532 candelilla wax Drugs 0.000 description 14
- 239000006185 dispersion Substances 0.000 description 14
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 14
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 12
- 238000013019 agitation Methods 0.000 description 11
- 238000010438 heat treatment Methods 0.000 description 10
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 10
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 9
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 9
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 9
- 235000011114 ammonium hydroxide Nutrition 0.000 description 9
- 235000019837 monoammonium phosphate Nutrition 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 7
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 150000003141 primary amines Chemical class 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 239000007970 homogeneous dispersion Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 230000002706 hydrostatic effect Effects 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical class CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical class CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- CXJAFLQWMOMYOW-UHFFFAOYSA-N 3-chlorofuran-2,5-dione Chemical compound ClC1=CC(=O)OC1=O CXJAFLQWMOMYOW-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- BIGPRXCJEDHCLP-UHFFFAOYSA-N ammonium bisulfate Chemical compound [NH4+].OS([O-])(=O)=O BIGPRXCJEDHCLP-UHFFFAOYSA-N 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical compound [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- BUHXFUSLEBPCEB-UHFFFAOYSA-N icosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN BUHXFUSLEBPCEB-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- FYFFGSSZFBZTAH-UHFFFAOYSA-N methylaminomethanetriol Chemical compound CNC(O)(O)O FYFFGSSZFBZTAH-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229940045860 white wax Drugs 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
-
- 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/325—Amines
-
- 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
Definitions
- the present invention relates to new materials which produce water-repellent textiles when deposited thereon and to the process for the preparation of such textiles. More particularly, this invention relates to compositions which, when deposited on textiles and heated thereon at an elevated temperature form a permanent waterrepellent finish of soft feel.
- linear polymeric polycarboxylic acids such as a copolymer of styrene and maleic anhydride
- a relatively non-volatile aliphatic primary amine such as stearylamine
- these reaction products are compatible with waxes, which further increases the water repellency of coated textiles and in addition imparts a soft feel to the treated textile.
- water-soluble salts of the heretofore mentioned polycarboxylic acids act as dispersing agents in the formulation of stable dispersions or emulsions of longchain amines and natural or synthetic waxes.
- the primary object of the present invention is to provide a water-dispersible composition containing an alkaline salt of an acidic polymer such as a styrenemaleic copolymer, a long-chain aliphatic amine such as stearylamine, and an added wax (natural or synthetic) which, when applied to cloth, the impregnated cloth dried, and heated at elevated temperatures, imparts a suitable water-repellency to the cloth.
- an acidic polymer such as a styrenemaleic copolymer
- a long-chain aliphatic amine such as stearylamine
- an added wax naturally or synthetic
- the materials of the present invention impart to textiles a water-repellent finish having extraordinary durability. This effect is not predictable from the nature of the components of the composition and it is therefore thought that additional complex reactions occur during heating to give this surprising durability to the finish.
- a solution of a long-chain amine such as stearlyamine and a wax such as candelilla wax in a solvent such as xylol is heated to about 60-100 C.
- a neutral salt of styrene-maleic (either anhydrous or in the form of an aqueous solution) is then added while agitating and cooling to room temperature.
- a uniform, soft paste containing, preferably, 40% to 60% active material is thus secured, which readily emulsifles in hot water (70-90 C.) to form a homogenous dispersion of emulsion which is stable.
- Dispersions containing from 1% to 10% active material when applied to cloth, dried, and baked, impart excellent water-repellency and soft feel even after subjecting the treated cloth to repeated washings and dry cleanings. While it has been found that baking temperatures of 160 C. are preferred, baking conditions covering a temperature range of 100200 C. over a period of 1 to minutes are suitable.
- the cloth is preferably a cellulosic fabric.
- the present invention is concerned with the use of a linear polymeric polycarboxylic acid as a primary constitutent of the herein-described water-repellent materials, since on baking it combines with the long-chain amine and the fabric to form water-resistant products and, furthermore, in the form of the ammonium salt it serves as a dispersing medium for the long-chain amines and waxes, thus giving water-dispersible products which are readily and cheaply applied to the cloth.
- the linear polymeric polycarboxylic acids used herein consists of a linear carbon atom chain having carboxyl groups along the length thereof. They are characterized by the formation of water-soluble salts which act as emulsifying agents in aqueous solution for waxes and long-chain primary amines.
- acids suitable for use herein are polyacrylic acid, polymethacrylic acid, copolymers of alpha-beta ethylenically unsaturated monocarboxylic or dicarboxylic acids with polymerizable compounds containing a single unsubstituted 'methylene group joined directly to a carbon atom through a double bond, and the like. More'particularly, the present invention is concerned with the copolymers of styrene and maleic anhydride as the linear polymeric polycarboxylic acid.
- water-soluble salt of the copolymer is employed in the process of the present invention. While a readily volatile base such as ammonia has been specifically mentioned and is to be preferred since it is most readily removed under the baking conditions employed, it is also apparent that the neutral salts of less volatile bases such as ethylene diamine, picoline, pyridine, vinyl pyridine, diethylamine, dimethylamine and the like may be also employed.
- a readily volatile base such as ammonia
- the neutral salts of less volatile bases such as ethylene diamine, picoline, pyridine, vinyl pyridine, diethylamine, dimethylamine and the like may be also employed.
- long-chain aliphatic amine component of the products of the present invention stearylamine has been found to be admirably suitable.
- laurylamine, myristylamine, palmitylamine, arachidylamine, tallow amine, and the like may be employed.
- reaction products of long-chain aliphatic saturated monocarboxylic acids and mono or polyalkylene polyamines such as the reaction product of equal moles of ethylene diamine and stearic acid which contains a long-chain hydrocarbon radical and a primary amine group may also be employed as the long-chain amine.
- the long-chain hydrocarbon radical preferably contains from to 22 carbon atoms.
- the amount of long-chain amine varies from less than 1 to not more than 2 moles (say, from .3 to 1.9 moles) per mole of dicarboxylic acid in a copolymer such as styrene-maleic or, in general, from .15 to about .95 mole per carboxyl group of the linear polymeric polycarboxylic acid.
- waxes such as candelilla wax, carnauba wax, beeswax, paraflin microcrystalline wax, and the like may be employed.
- synthetic waxes as glyceryl tristearate, or glyceryl stearate modified with polycarboxylic acids may be employed.
- Amino alcohols, such as trihydroxy-methyl aminomethane, may also be used to form the above-mentioned synthetic waxes.
- the proportion of wax employed in the preparation of the products of the present invention is not limiting, but it is preferred to employ at least 1 part and as much as 4 parts of wax for 1 partof styrene-maleic and long-chain aliphatic amine combined, since in addition to good water repellency, a soft feel is also imparted to the treated textiles.
- compositions of the present invention for producing water-repellent finishes on textiles by impregnating the textiles therewith, removing water by drying and finally heating an elevated temperature of from 100 to 200 C., consist of emulsions which contain, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxylic acid (such as the ammonium salt of a styrene-maleic copolymer) and, as the disperse phase, a mixture of a wax and a relatively non-volatile long-chain aliphatic primary amine.
- emulsions which contain, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxylic acid (such as the ammonium salt of a styrene-maleic copolymer) and, as the disperse phase, a mixture of a wax and a relatively non-volatile long-chain aliphatic primary
- Example 1 30 parts of a styrene-maleic copolymer (formed from 2 moles of styrene and 1 mole of maleic anhydride), parts of 28% aqueous ammonia solution, and 180 parts of water are warmed together to form a clear solution.
- Example 2 30.6 parts of stearylamine, 51.8 parts of candelilla wax, and 103 parts of microcrystalline white paraifin "'ax (M. P. 190 F.-l F.) are warmed with 154.8 parts of xylene. At 60 C.-'70 C. 46.8 parts of dried ammonium salt of a styrene-maleic copolymer (formed from 2 moles of styrene to 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 60% active ingredients.
- a styrene-maleic copolymer formed from 2 moles of styrene to 1 mole of maleic anhydride
- Example 3 2.5 parts of stearylamine and 6 parts of xylene are warmed together to form a clear solution. 3.5 parts of the dried ammonia salt of a styrenemaleic anhydride copolymer (formed from 2 moles of styrene to 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 50% solids. While rapidly agitating, a solution having 2 parts of ammonium dihydrogen phosphate in 112 parts of hot water (80 C.) is added to form a homogeneous, stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at 160 C. The treated textile possessed an initial spray rating of 90, and 60 after dry cleaning.
- a styrenemaleic anhydride copolymer formed from 2 moles of styrene to 1 mole of maleic anhydride
- Example 5 2.1 parts of stearylamine, 3.4 parts of candelilla wax, and 6.7 parts of microcrystalline yellow paraffln wax (M. P. 190 F.-195 F.) are warmed to 60 C. in 9.4 parts of xylene to form a clear solution. While cooling, 2.95 parts of the a-picoline salt of styrene-maleic anhydride copolymer (formed from 2 moles of styrene and 1 mole of maleic anhydride) are added with stirring to form a homogeneous paste.
- styrene-maleic anhydride copolymer formed from 2 moles of styrene and 1 mole of maleic anhydride
- Example 6 3.06 parts of stearyiamine, 5.18 parts of candelilla wax, and 10.3 parts of microcrystalline white parailln wax (M. P. 190-195 F.) are warmed with 15.48 parts of xylene. At 60-70 C. 4.68 parts of dried ammonium salt of a methyl methacrylate-maleic anhydride copolymer (formed from 1.5 moles of methyl methacrylate and 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 60% active material.
- a methyl methacrylate-maleic anhydride copolymer formed from 1.5 moles of methyl methacrylate and 1 mole of maleic anhydride
- Example 7 2.68 parts of an amine (prepared by heating 20.6 parts of diethylene triamine (1 mole) and 56.4parts of stearic acid (1 mole) together to 220 C.-250 C. for 6 hours while removing 3.6 parts of water) of formula NI-IaCI-IaCI-IzNI-ICI-IzCI-IeNHCOCmHzs 4.1! parts of candelilla wax, 8.35 parts of microcrystalline white parafiin wax (M. P. 190-195 R), and 12.52 parts of xylene are warmed to 60 C. to form a clear solution.
- amine prepared by heating 20.6 parts of diethylene triamine (1 mole) and 56.4parts of stearic acid (1 mole) together to 220 C.-250 C. for 6 hours while removing 3.6 parts of water
- Example 8 The preparation of Example 7 is repeated using 3.85 parts 01' the amine.
- the textile treated in the same manner has an initial spray rating of 80 and after dry cleaning 70.
- Example 9 phosphate in 378 parts 01' hot water (80 C.) is" added to form a homogeneous, stable dispersion.
- a piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at C.
- the treated textile possesses an initial spray rating of 90 and 60 after dry cleaning.
- Example 10 2.1 parts of tallow amine, 3.4 parts of candelilla wax, 6.7 parts of micro-crystalline white paraflin wax (M. P. -175 C.), and 9.4 parts of xylol are warmed together to 60 C. to form a clear solution. While cooling, 2.95 parts of the ammonia salt of styrene-maleic copolymer (2 moles of styrene and 1 mole of maleic anhydride) are added with agitation to form a homogeneous paste.
- Example 11 2.1 parts of stearylamine, 10.1 parts of candelilla wax, and 9.4 parts of xylol are warmed together to 60 C. to form a clear solution. 5 parts of the ammonium salt of polyacrylic acid (prepared by the hydrolysis of an emulsion of polyethyl acrylate which is acidified, dissolved in aqueous ammonia, and the aqueous solution evaporated to dryness to secure the ammonium Example 12 4 parts of a copolymer of styrene and maleic anhydride (containing 2 moles of styrene and 1 mole of maleic anhydride), 6 parts of 28% aqueous ammonia, and 20 parts 01 water are warmed together to 01m a clear syrupy solution.
- the ammonium salt of polyacrylic acid prepared by the hydrolysis of an emulsion of polyethyl acrylate which is acidified, dissolved in aqueous ammonia, and the aqueous solution evaporated to dry
- Example 13 18 parts of a synthetic wax (prepared by the distillation of 26.8 parts of a 50% solution of a methylolmelamine resin in methanol, 84.9 parts of stearamide and 100 parts of xylol together until the resulting wax solution contained 55.1% wax solids) are mixed together with 2 parts of stearylamine, 6 parts of xylol, and 4 parts of the ammonium salt of a styrene-maleic anhydride copolymer (having 2 moles of styrene to 1 mole of maleic anhydride) to form a homogeneous paste. 290 parts of water at 90 C. are now added and agitation continued until a homogeneous dispersion results. A piece of O. D. poplin cloth is impregnated. dried, and baked at 150-160 C. for 15 minutes. The treated textile has an initial spray rating of 90 and after dry cleaning 80.
- a synthetic wax prepared by the distillation of 26.8 parts of a 50% solution
- Example 14 4.5 parts of a styrene-maleic copolymer (containing 3 moles of styrene and one mole of maleic anhydride), 5.0 parts of 28% aqueous ammonia solution, and 20 parts of water are warmed together to form a solution.
- Example 1 parts of the above paste is agitated in 190 parts of water at 80 C. to form a stable dispersion.
- a piece of 0. D. poplin is impregnated, dried, and baked for 10 minutes at 145-150 C.
- the treated textile has a slightly harsher feel than that from Example 1. It has an initial spray rating of 90 and alter dry cleaning '70.
- Example 16 8.4 parts of stearylamine, 12.2 parts of candelilla wax, 18.2 parts of microcrystalline white wax (M. P. 190-195 F.), and 16.? parts 0! xylene are warmed to 60 C. to form a clear solution.
- the water repellent products of the present invention in addition to giving high spray ratings, also possess the unique property of imparting a very. igh hydrostatic resistance to the treated textiles.
- a composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxyllc acid and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the.
- amount of wax being from 1 to 4 parts per 1 part of the polymeric acid and the amine combined.
- a composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxylic acid consisting of a copolymer of an alpha-beta ethylenic dicarboxylic acid and a polymerizable compound containing a single unsubstituted methylene group joined directly to a carbon atom through a double bond, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per '1 part of the polymeric acid and the amine combined.
- a composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a copolymer of maleic anhydride and styrene, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
- a composition particularly adapted for tendering fabrics water-repellent when said fabrics are impregnated therewith and heated comprising an emulsion containing, as the dispersing phase an aqueous solution of the ammonium salt of a copolymer of maleic anhydride and styrene, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
- a composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated comprising an emulsion containing, as the dispersing phase an aqueous solution of the ammonium salt of a copolymer of maleic anhydride and styrene and, as the disperse phase, candelilla wax and stearyl amine, the amount of amine being from 0.15 to 0.95 mole per carboxyl group. and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
- a fabric rendered water-repellent by impregnating the fabric with the composition of claim 1, removing water from the impregnated fabric. and heating same at an elevated temperature of from 100 to 200 C.
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Description
Patented Sept. 26, 1950 WATER REPELLENT FABRICS AND COMPO- SITION AND PROCESS FOR MAKING SAME John B. Rust, East Hanover, and William B. Canfield, Montclair, N. J., assignors, by direct and mesne assignments, of one-half to Montclair Research Corporation, a corporation of New Jersey, and one-half to Ellis-Foster Company, a corporation of New Jersey No Drawing. Application March Serial No. 13,077
Claims.
The present invention relates to new materials which produce water-repellent textiles when deposited thereon and to the process for the preparation of such textiles. More particularly, this invention relates to compositions which, when deposited on textiles and heated thereon at an elevated temperature form a permanent waterrepellent finish of soft feel.
It has been found that linear polymeric polycarboxylic acids (such as a copolymer of styrene and maleic anhydride) and a relatively non-volatile aliphatic primary amine such as stearylamine may be converted into coatings which show a. remarkable resistance to water, aqueous soap solution, and dry-cleaning naphthas. Also, these reaction products are compatible with waxes, which further increases the water repellency of coated textiles and in addition imparts a soft feel to the treated textile.
In addition, it has been found that water-soluble salts of the heretofore mentioned polycarboxylic acids (for example, such salts as from ammonia, picoline, pyridine, vinyl pyridine and the like), act as dispersing agents in the formulation of stable dispersions or emulsions of longchain amines and natural or synthetic waxes.
It is therefore apparent that the primary object of the present invention is to provide a water-dispersible composition containing an alkaline salt of an acidic polymer such as a styrenemaleic copolymer, a long-chain aliphatic amine such as stearylamine, and an added wax (natural or synthetic) which, when applied to cloth, the impregnated cloth dried, and heated at elevated temperatures, imparts a suitable water-repellency to the cloth.
Surprisingly, it has been found that the materials of the present invention impart to textiles a water-repellent finish having extraordinary durability. This effect is not predictable from the nature of the components of the composition and it is therefore thought that additional complex reactions occur during heating to give this surprising durability to the finish.
According to a preferred process of the present invention, a solution of a long-chain amine such as stearlyamine and a wax such as candelilla wax in a solvent such as xylol is heated to about 60-100 C. A neutral salt of styrene-maleic (either anhydrous or in the form of an aqueous solution) is then added while agitating and cooling to room temperature. A uniform, soft paste containing, preferably, 40% to 60% active material is thus secured, which readily emulsifles in hot water (70-90 C.) to form a homogenous dispersion of emulsion which is stable. Dispersions containing from 1% to 10% active material, when applied to cloth, dried, and baked, impart excellent water-repellency and soft feel even after subjecting the treated cloth to repeated washings and dry cleanings. While it has been found that baking temperatures of 160 C. are preferred, baking conditions covering a temperature range of 100200 C. over a period of 1 to minutes are suitable. The cloth is preferably a cellulosic fabric.
The present invention is concerned with the use of a linear polymeric polycarboxylic acid as a primary constitutent of the herein-described water-repellent materials, since on baking it combines with the long-chain amine and the fabric to form water-resistant products and, furthermore, in the form of the ammonium salt it serves as a dispersing medium for the long-chain amines and waxes, thus giving water-dispersible products which are readily and cheaply applied to the cloth. The linear polymeric polycarboxylic acids used herein consists of a linear carbon atom chain having carboxyl groups along the length thereof. They are characterized by the formation of water-soluble salts which act as emulsifying agents in aqueous solution for waxes and long-chain primary amines. Illustrations of such acids suitable for use herein are polyacrylic acid, polymethacrylic acid, copolymers of alpha-beta ethylenically unsaturated monocarboxylic or dicarboxylic acids with polymerizable compounds containing a single unsubstituted 'methylene group joined directly to a carbon atom through a double bond, and the like. More'particularly, the present invention is concerned with the copolymers of styrene and maleic anhydride as the linear polymeric polycarboxylic acid. Methods described in the literature teach the practice of heating styrene and maleic anhydride in the presence of small percentages of benzoyl peroxide to form a copolymer soluble in dioxan, acetone and the like. Proportions of 1 mole ofmaleic anhydride to 2 moles of styrene are preferably employed although as high as 4 moles of styrene to 1 mole of maleic anhydride and as little as 1 mole of styrene to 1 mole of maleic anhydride have been found to be applicable. While copolymers of styrene and maleic anhydride are emphasized, it is apparent that fumaric acid. itaconic anhydride, citraconic anhydride, chloromaleic anhydride, acrylonitrile, acrylic acid and its esters, methacrylic acid and its esters, and the like may be also employed. Hydrolyzed polymers of acrylonitrile, acrylic acid esters, methacrylic acid esters, and the like have been employed in place of the styrene-maleic copolymers.
As has been previously stated, water-soluble salt of the copolymer is employed in the process of the present invention. While a readily volatile base such as ammonia has been specifically mentioned and is to be preferred since it is most readily removed under the baking conditions employed, it is also apparent that the neutral salts of less volatile bases such as ethylene diamine, picoline, pyridine, vinyl pyridine, diethylamine, dimethylamine and the like may be also employed.
As the long-chain aliphatic amine component of the products of the present invention, stearylamine has been found to be admirably suitable. However, laurylamine, myristylamine, palmitylamine, arachidylamine, tallow amine, and the like may be employed. It is also apparent that reaction products of long-chain aliphatic saturated monocarboxylic acids and mono or polyalkylene polyamines, such as the reaction product of equal moles of ethylene diamine and stearic acid which contains a long-chain hydrocarbon radical and a primary amine group may also be employed as the long-chain amine. It will be apparent that numerous modifications are possible and should be considered within the scope of the present invention. The long-chain hydrocarbon radical preferably contains from to 22 carbon atoms.
The amount of long-chain amine varies from less than 1 to not more than 2 moles (say, from .3 to 1.9 moles) per mole of dicarboxylic acid in a copolymer such as styrene-maleic or, in general, from .15 to about .95 mole per carboxyl group of the linear polymeric polycarboxylic acid. Apparently during heating of the fabric (which carries a dry deposit from the treating emulsion), the volatile base of the polycarboxylate salt is eliminated and a reaction occurs in which both the primary amine and the cellulose of the fabric react with the polymeric polycarboxylic acid, the primary amine by amide or imide formation and the cellulose by superficial esteriflcation. The wax, which is uniformly distributed in the applied composition, acts as a plasticizer for the finish and imparts a soft feel to the cloth.
Numerous natural waxes such as candelilla wax, carnauba wax, beeswax, paraflin microcrystalline wax, and the like may be employed. Also such synthetic waxes as glyceryl tristearate, or glyceryl stearate modified with polycarboxylic acids may be employed. Amino alcohols, such as trihydroxy-methyl aminomethane, may also be used to form the above-mentioned synthetic waxes. The proportion of wax employed in the preparation of the products of the present invention is not limiting, but it is preferred to employ at least 1 part and as much as 4 parts of wax for 1 partof styrene-maleic and long-chain aliphatic amine combined, since in addition to good water repellency, a soft feel is also imparted to the treated textiles.
It has been heretofore mentioned that from 1% to 10% of the reaction products of the present invention are sufficient to impart a durable water-repellent finish to textiles. In the preparation of aqueous dispersions, it has been found that the use of approximately 1% aqueous 28% ammonia and up to 1% (based upon the dispersion) of an ammonium salt of an inorganic acid assists in the formation of stable dispersions. Among the ammonium salts of inorganic acids most applicable are ammonium dihydrogen phosphate, di-ammonium hydrogen phosphate,
triammonium phosphate, ammonium hydrogen sulphate, diam-monium sulphate and the like.
Therefore, the compositions of the present invention for producing water-repellent finishes on textiles, by impregnating the textiles therewith, removing water by drying and finally heating an elevated temperature of from 100 to 200 C., consist of emulsions which contain, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxylic acid (such as the ammonium salt of a styrene-maleic copolymer) and, as the disperse phase, a mixture of a wax and a relatively non-volatile long-chain aliphatic primary amine.
The following examples are given by way of illustration only and should not be considered to be limiting. All proportions are in parts by weight.
Example 1 30 parts of a styrene-maleic copolymer (formed from 2 moles of styrene and 1 mole of maleic anhydride), parts of 28% aqueous ammonia solution, and 180 parts of water are warmed together to form a clear solution.
150 parts of candelilla wax and 50 parts of stearylamine are melted together at C. The aqueous solution of the ammonium salt of the styrene-maleic copolymer is added with rapid agitation. A smooth dispersible paste is secured which contains 50% active ingredients.
10 parts of the above paste is agitated in 190 parts of water at 80 C. to form a stable emulsion. A piece of O. D. poplin is impregnated, dried, and baked for 10 minutes at l45-l50 C. The treated textile possesses a spray rating of 100, after dry cleaning 70, and after washing 80.
Example 2 30.6 parts of stearylamine, 51.8 parts of candelilla wax, and 103 parts of microcrystalline white paraifin "'ax (M. P. 190 F.-l F.) are warmed with 154.8 parts of xylene. At 60 C.-'70 C. 46.8 parts of dried ammonium salt of a styrene-maleic copolymer (formed from 2 moles of styrene to 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 60% active ingredients.
24 parts of the above paste are added to a solution at 90 C. of 1.2 parts of ammonium dihydrogen phosphate, 4 parts of 28% aqueous ammonia, and 370.8 parts of water to form a stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at C. The treated textile possessed an initial spray rating of 100, after dry cleaning 90, and after washing 80.
Example 3 2.5 parts of stearylamine and 6 parts of xylene are warmed together to form a clear solution. 3.5 parts of the dried ammonia salt of a styrenemaleic anhydride copolymer (formed from 2 moles of styrene to 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 50% solids. While rapidly agitating, a solution having 2 parts of ammonium dihydrogen phosphate in 112 parts of hot water (80 C.) is added to form a homogeneous, stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at 160 C. The treated textile possessed an initial spray rating of 90, and 60 after dry cleaning.
2.1 parts of stearylamine, 3.4 parts of candelilla wax, 6.7 parts of microerystalline yellow paramn wax (M. P. 190 F.-195 F.) and 9.4 parts of xylol are warmed to 60 C. to form a clear solution. While cooling, 2.95 parts of the pyridine salt of styrene-maleic anhydride copolymer (formed from 2 moles of styrene and 1 mole of maleic anhydride) are added with agitation to form a homogeneous paste.
15 parts of the above paste, 0.54 part of ammonium dihydrogen phosphate and 185 parts of water at 90 C. are agitated to form a stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked at 160 C. for 15 minutes. spray rating of 90 and after dry cleaning '70.
Example 5 2.1 parts of stearylamine, 3.4 parts of candelilla wax, and 6.7 parts of microcrystalline yellow paraffln wax (M. P. 190 F.-195 F.) are warmed to 60 C. in 9.4 parts of xylene to form a clear solution. While cooling, 2.95 parts of the a-picoline salt of styrene-maleic anhydride copolymer (formed from 2 moles of styrene and 1 mole of maleic anhydride) are added with stirring to form a homogeneous paste.
parts of the above paste, 0.54 part of ammonium dihydrogen phosphate and 185 parts of water at 90 C. are agitated together to form a homogeneous dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked at 160 C. for 15 minutes. The treated textile possesses an initial spray rating of 80, and after dry cleani g 70.
Example 6 3.06 parts of stearyiamine, 5.18 parts of candelilla wax, and 10.3 parts of microcrystalline white parailln wax (M. P. 190-195 F.) are warmed with 15.48 parts of xylene. At 60-70 C. 4.68 parts of dried ammonium salt of a methyl methacrylate-maleic anhydride copolymer (formed from 1.5 moles of methyl methacrylate and 1 mole of maleic anhydride) are added with agitation to form a smooth, homogeneous paste having 60% active material.
24 parts of the above paste are added to a solution at 90 C. of 1.2 parts of ammonium dihydrogen phosphate, 4 parts of 28% aqueous ammonia, and 370.8 parts of water to form a stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at 160 C. The treated textile possesses an initial spray rating of 100, after dry cleaning 70, and after washing 80.
Example 7 2.68 parts of an amine (prepared by heating 20.6 parts of diethylene triamine (1 mole) and 56.4parts of stearic acid (1 mole) together to 220 C.-250 C. for 6 hours while removing 3.6 parts of water) of formula NI-IaCI-IaCI-IzNI-ICI-IzCI-IeNHCOCmHzs 4.1! parts of candelilla wax, 8.35 parts of microcrystalline white parafiin wax (M. P. 190-195 R), and 12.52 parts of xylene are warmed to 60 C. to form a clear solution. 3.58 parts of the ammonium salt of a styrene-maleic anhydride copolymer (from 2 moles of styrene and 1 mole oi maleic anhydride) are added while agitating The treated textile possesses an initial and cooling to form a homogeneous, water-dispersible paste having 60% active ingredients.
18 parts of the above paste is dispersed in an aqueous solution at C. having 1.2 parts 01' ammonium dihydrogen phosphate, 6 parts of concentrated ammonia and 274.8 parts of water. A piece of O. D. poplin is impregnated, dried, and baked at C. for 10 minutes. The treated textile possesses an initial spray rating of 90 and after dry cleaning '70.
Example 8 The preparation of Example 7 is repeated using 3.85 parts 01' the amine. The textile treated in the same manner has an initial spray rating of 80 and after dry cleaning 70.
Example 9 phosphate in 378 parts 01' hot water (80 C.) is" added to form a homogeneous, stable dispersion. A piece of O. D. poplin cloth is impregnated, dried, and baked for 15 minutes at C. The treated textile possesses an initial spray rating of 90 and 60 after dry cleaning.
Example 10 2.1 parts of tallow amine, 3.4 parts of candelilla wax, 6.7 parts of micro-crystalline white paraflin wax (M. P. -175 C.), and 9.4 parts of xylol are warmed together to 60 C. to form a clear solution. While cooling, 2.95 parts of the ammonia salt of styrene-maleic copolymer (2 moles of styrene and 1 mole of maleic anhydride) are added with agitation to form a homogeneous paste.
15 parts of the above paste are agitated in a solution of 0.6 part of ammonium dihydrogen phosphate, 2.4 parts of 28% aqueous ammonia solution, and parts of water at 90 C. to form a stable dispersion. A piece of O. D. poplin cloth is impregnated. dried, and baked at 160 C. for 15 minutes. The treated textile possesses an initial spray rating of 90 and after dry cleaning 60.
Example 11 2.1 parts of stearylamine, 10.1 parts of candelilla wax, and 9.4 parts of xylol are warmed together to 60 C. to form a clear solution. 5 parts of the ammonium salt of polyacrylic acid (prepared by the hydrolysis of an emulsion of polyethyl acrylate which is acidified, dissolved in aqueous ammonia, and the aqueous solution evaporated to dryness to secure the ammonium Example 12 4 parts of a copolymer of styrene and maleic anhydride (containing 2 moles of styrene and 1 mole of maleic anhydride), 6 parts of 28% aqueous ammonia, and 20 parts 01 water are warmed together to 01m a clear syrupy solution.
6 parts of stearylamine, and 15 parts of a wax consisting of a modified alkyd resin (having an acid number of 19.3 and prepared from 32 parts of pentaerythritol, 169.2 parts 01' stearic acid, and 14.8 parts of phthalic anhydride) are warmed together to form a clear wax melt. The above aqueous solution of the ammonium salt of styrene maleic anhydride copolymer is added with rapid agitation to form a homogeneous paste. 193 parts of water at 80 C. are now added and agitation continued to form a homogeneous dispersion. A piece of 0. D. poplin cloth is impregnated, dried, and baked at 150 C. for 15 minutes. The treated textile possesses an initial spray rating of 90 and after dry cleaning 60.
Example 13 18 parts of a synthetic wax (prepared by the distillation of 26.8 parts of a 50% solution of a methylolmelamine resin in methanol, 84.9 parts of stearamide and 100 parts of xylol together until the resulting wax solution contained 55.1% wax solids) are mixed together with 2 parts of stearylamine, 6 parts of xylol, and 4 parts of the ammonium salt of a styrene-maleic anhydride copolymer (having 2 moles of styrene to 1 mole of maleic anhydride) to form a homogeneous paste. 290 parts of water at 90 C. are now added and agitation continued until a homogeneous dispersion results. A piece of O. D. poplin cloth is impregnated. dried, and baked at 150-160 C. for 15 minutes. The treated textile has an initial spray rating of 90 and after dry cleaning 80.
Example 14 4.5 parts of a styrene-maleic copolymer (containing 3 moles of styrene and one mole of maleic anhydride), 5.0 parts of 28% aqueous ammonia solution, and 20 parts of water are warmed together to form a solution.
15 parts of candelilla wax and 5 parts of stearylamine are melted together to 90 C. The aqueous solution of the ammonium salt of the styrene maleic copolymer is added with rapid agitation. A smooth, dispersible paste is secured having 50% active ingredients.
parts of the above paste is agitated in 190 parts of water at 80 C. to form a stable dispersion. A piece of 0. D. poplin is impregnated, dried, and baked for 10 minutes at 145-150 C. The treated textile has a slightly harsher feel than that from Example 1. It has an initial spray rating of 90 and alter dry cleaning '70.
Example 5.0 parts of a styrene-maleic copolymer (formed from 1 mole of styrene and 1 mole of maleic anhydride), 5 parts of 28% aqueous ammonia solution, and 15 parts oi water are warmed together to form a clear solution.
15 parts of candelilla wax and 5 parts of stearylamine are melted together to 90 C. The aqueous solution of the ammonium saltof the styrene maleic copolymer is added with rapid agitation. A smooth paste is obtained having 55% active ingredients.
10 parts of the above paste is agitated in 190 parts of water at 80 C. to forma stable dispersion. A piece of O. D. poplin is impregnated, dried, and baked for 10 minutes at 150 C. The treated textile possesses a soft hand. It has an 8 initial spray rating of so and after dry cleaning 60.
Example 16 8.4 parts of stearylamine, 12.2 parts of candelilla wax, 18.2 parts of microcrystalline white wax (M. P. 190-195 F.), and 16.? parts 0! xylene are warmed to 60 C. to form a clear solution.
11.3 parts of the ammonium salt of a styrenemaleic anhydride copolymer (containing 2 moles of styrene and 1 mole of maleic anhydride) are mixed together to form a thin slurry.
The above wax-xylene solution is then added while stirring and cooling to form a homogeneous, water-dispersible paste having 60% active in gredients.
40 parts of the above paste are dispersed in an aqueous solution at C. of 2 parts or ammonium dihydrogen phosphate, 4 parts of 28% aqueous ammonia solution and 354 parts of water. A piece of O. D. poplin cloth is impregnated, dried, and baked at- 160 C. for 3 minutes. The treated textile possesses an initial spray rating of and a hydrostatic resistance of 52 cm.
Thus it may be seen that the water repellent products of the present invention in addition to giving high spray ratings, also possess the unique property of imparting a very. igh hydrostatic resistance to the treated textiles.
We claim:
1. A composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated, comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxyllc acid and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the.
amount of wax being from 1 to 4 parts per 1 part of the polymeric acid and the amine combined.
2. A composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated, comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a linear polymeric polycarboxylic acid consisting of a copolymer of an alpha-beta ethylenic dicarboxylic acid and a polymerizable compound containing a single unsubstituted methylene group joined directly to a carbon atom through a double bond, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per '1 part of the polymeric acid and the amine combined.
3. A composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated, comprising an emulsion containing, as the dispersing phase, an aqueous solution of a salt of a volatile base and a copolymer of maleic anhydride and styrene, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from 10 to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
4. A composition particularly adapted for tendering fabrics water-repellent when said fabrics are impregnated therewith and heated, comprising an emulsion containing, as the dispersing phase an aqueous solution of the ammonium salt of a copolymer of maleic anhydride and styrene, and, as the disperse phase, a wax and an aliphatic hydrocarbon primary amine containing from to 22 carbon atoms, the amount of amine being from 0.15 to 0.95 mole per carboxyl group and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
5. A composition particularly adapted for rendering fabrics water-repellent when said fabrics are impregnated therewith and heated, comprising an emulsion containing, as the dispersing phase an aqueous solution of the ammonium salt of a copolymer of maleic anhydride and styrene and, as the disperse phase, candelilla wax and stearyl amine, the amount of amine being from 0.15 to 0.95 mole per carboxyl group. and the amount of wax being from 1 to 4 parts per 1 part of the maleic anhydride-styrene copolymer and amine combined.
6. A fabric rendered water-repellent by impregnating the fabric with the composition of claim 1, removing water from the impregnated fabric. and heating same at an elevated temperature of from 100 to 200 C.
7. A fabric rendered water-repellent by impregnating the fabric with the composition of claim 2, removing water from the impregnated fabric, and heating same at an elevated temperature of from to 200 C.
8. A fabric rendered water-repellent by impregnating the fabric with the composition of claim 3, removing water from the impregnated fabric, and heating same at an elevated temperature of from 100 to 200 C.
9. A fabric rendered water-repellent by impregnating the fabric with the composition of claim 4, removing water from the impregnated fabric, and heating same at an elevated temperature of from 100 to 200 C.
10. A fabric rendered water-repellent by impregnatin the fabric with the composition of claim 5, removing water from the impregnated fabric, and heating same at an elevated temperature of from 100 to 200 C.
JOHN B. RUST. WILLIAM B. CANFIELD.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,976,679 Flkentscher et al. Oct. 9, 1934 2,160,375 Voss et al May 30, 1939 2,169,366 Melgs Aug. 29, 1939 2,356,879 Pense et a1. Aug. 29, 1944
Claims (1)
1. A COMPOSITION PARTICULARLY ADAPTED FOR RENDERING FABRICS WATER-REPELLENT WHEN SAID FABRICS ARE IMPREGNATED THEREWITH AND HEATED, COMPRISING AN EMULSION CONTAINING, AS THE DISPERSING PHASE, AN AQUEOUS SOLUTION OF A SALT OF A VOLATILE BASE AND A LINEAR POLYMERIC POLYCARBOXYLIC ACID AND, AS THE DISPERSE PHASE, A WAX AND AN ALIPHATIC HYDROCARBON PRIMARY AMINE CONTAINING FROM 10 TO 22 CARBON ATOMS, THE AMOUNT OF AMINE BEING FROM 0.15 TO 0.95 MOLE PER CARBOXYL GROUP AND THE AMOUNT OF WAX BEING FROM 1 TO 4 PARTS PER 1 PART OF THE POLYMERIC ACID AND THE AMINE COMBINED.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13077A US2524022A (en) | 1948-03-04 | 1948-03-04 | Water repellent fabrics and composition and process for making same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13077A US2524022A (en) | 1948-03-04 | 1948-03-04 | Water repellent fabrics and composition and process for making same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2524022A true US2524022A (en) | 1950-09-26 |
Family
ID=21758188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13077A Expired - Lifetime US2524022A (en) | 1948-03-04 | 1948-03-04 | Water repellent fabrics and composition and process for making same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2524022A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2702796A (en) * | 1950-05-31 | 1955-02-22 | Atlas Powder Co | Textile size comprising a partially neutralized polymethacrylic acid |
| US2975067A (en) * | 1957-02-01 | 1961-03-14 | Winterberg Alexander | Method of preserving comestibles |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1976679A (en) * | 1930-05-26 | 1934-10-09 | Ig Farbenindustrie Ag | Production of dispersions |
| US2160375A (en) * | 1936-01-04 | 1939-05-30 | Ig Farbenindustrie Ag | Water-repellent textile material and process of manufacturing it |
| US2169366A (en) * | 1937-05-27 | 1939-08-15 | Du Pont | Moistureproof material and method of making the same |
| US2356879A (en) * | 1939-12-12 | 1944-08-29 | Pense Walter | Process of preparing lustrous coatings |
-
1948
- 1948-03-04 US US13077A patent/US2524022A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1976679A (en) * | 1930-05-26 | 1934-10-09 | Ig Farbenindustrie Ag | Production of dispersions |
| US2160375A (en) * | 1936-01-04 | 1939-05-30 | Ig Farbenindustrie Ag | Water-repellent textile material and process of manufacturing it |
| US2169366A (en) * | 1937-05-27 | 1939-08-15 | Du Pont | Moistureproof material and method of making the same |
| US2356879A (en) * | 1939-12-12 | 1944-08-29 | Pense Walter | Process of preparing lustrous coatings |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2702796A (en) * | 1950-05-31 | 1955-02-22 | Atlas Powder Co | Textile size comprising a partially neutralized polymethacrylic acid |
| US2975067A (en) * | 1957-02-01 | 1961-03-14 | Winterberg Alexander | Method of preserving comestibles |
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