US2289222A - Yarn preparation - Google Patents
Yarn preparation Download PDFInfo
- Publication number
- US2289222A US2289222A US378943A US37894341A US2289222A US 2289222 A US2289222 A US 2289222A US 378943 A US378943 A US 378943A US 37894341 A US37894341 A US 37894341A US 2289222 A US2289222 A US 2289222A
- Authority
- US
- United States
- Prior art keywords
- yarn
- snag
- tacky
- film
- knitting
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000002360 preparation method Methods 0.000 title description 8
- 239000000203 mixture Substances 0.000 description 87
- 239000000463 material Substances 0.000 description 58
- 239000004744 fabric Substances 0.000 description 42
- 238000009940 knitting Methods 0.000 description 42
- 239000004952 Polyamide Substances 0.000 description 38
- 229920002647 polyamide Polymers 0.000 description 38
- 238000000034 method Methods 0.000 description 33
- 239000000243 solution Substances 0.000 description 28
- 239000007788 liquid Substances 0.000 description 20
- 229920000642 polymer Polymers 0.000 description 20
- 239000002253 acid Substances 0.000 description 17
- 229920000180 alkyd Polymers 0.000 description 16
- -1 polyhexamethylene Polymers 0.000 description 16
- 238000004519 manufacturing process Methods 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 11
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 230000008569 process Effects 0.000 description 9
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- 238000001035 drying Methods 0.000 description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 7
- 229930195725 Mannitol Natural products 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000000594 mannitol Substances 0.000 description 6
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- 229920002554 vinyl polymer Polymers 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 150000003505 terpenes Chemical class 0.000 description 5
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
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- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
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- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 239000004342 Benzoyl peroxide Substances 0.000 description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
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- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
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- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- 239000000908 ammonium hydroxide Substances 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000025 natural resin Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- YUQFYQHUZOPVPH-UHFFFAOYSA-N 12-amino-octadecanoic acid Chemical compound CCCCCCC(N)CCCCCCCCCCC(O)=O YUQFYQHUZOPVPH-UHFFFAOYSA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
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- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 235000012907 honey Nutrition 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 229940063557 methacrylate Drugs 0.000 description 2
- 229940063559 methacrylic acid Drugs 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 239000012260 resinous material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
- GTQHJCOHNAFHRE-UHFFFAOYSA-N 1,10-dibromodecane Chemical compound BrCCCCCCCCCCBr GTQHJCOHNAFHRE-UHFFFAOYSA-N 0.000 description 1
- DGXAGETVRDOQFP-UHFFFAOYSA-N 2,6-dihydroxybenzaldehyde Chemical compound OC1=CC=CC(O)=C1C=O DGXAGETVRDOQFP-UHFFFAOYSA-N 0.000 description 1
- YXYJVFYWCLAXHO-UHFFFAOYSA-N 2-methoxyethyl 2-methylprop-2-enoate Chemical compound COCCOC(=O)C(C)=C YXYJVFYWCLAXHO-UHFFFAOYSA-N 0.000 description 1
- JNRLEMMIVRBKJE-UHFFFAOYSA-N 4,4'-Methylenebis(N,N-dimethylaniline) Chemical compound C1=CC(N(C)C)=CC=C1CC1=CC=C(N(C)C)C=C1 JNRLEMMIVRBKJE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004801 Chlorinated PVC Substances 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004348 Glyceryl diacetate Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001417534 Lutjanidae Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Chemical group 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001617 Vinyon Polymers 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- QLNXEIHDVAGZKV-UHFFFAOYSA-N acetic acid;piperazine Chemical compound CC([O-])=O.CC([O-])=O.C1C[NH2+]CC[NH2+]1 QLNXEIHDVAGZKV-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- GVRNUDCCYWKHMV-UHFFFAOYSA-N bis(2-methoxyethyl) hexanedioate Chemical compound COCCOC(=O)CCCCC(=O)OCCOC GVRNUDCCYWKHMV-UHFFFAOYSA-N 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
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
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- 238000010924 continuous production Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- DFJYZCUIKPGCSG-UHFFFAOYSA-N decanedinitrile Chemical compound N#CCCCCCCCCC#N DFJYZCUIKPGCSG-UHFFFAOYSA-N 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- XPKFJIVNCKUXOI-UHFFFAOYSA-N formaldehyde;2-hydroxybenzoic acid Chemical compound O=C.OC(=O)C1=CC=CC=C1O XPKFJIVNCKUXOI-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 235000019443 glyceryl diacetate Nutrition 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- ZDCHZHDOCCIZIY-UHFFFAOYSA-N phthalic acid;propane-1,2,3-triol Chemical class OCC(O)CO.OC(=O)C1=CC=CC=C1C(O)=O ZDCHZHDOCCIZIY-UHFFFAOYSA-N 0.000 description 1
- 229920000052 poly(p-xylylene) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920006123 polyhexamethylene isophthalamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
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- 239000002195 soluble material Substances 0.000 description 1
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- 125000002298 terpene group Chemical group 0.000 description 1
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- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/17—Natural resins, resinous alcohols, resinous acids, or derivatives 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
- D06M15/21—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
- D06M15/41—Phenol-aldehyde or phenol-ketone resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—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
- D06M15/507—Polyesters
Definitions
- the present invention relates to the treatment of water-insensitive synthetic linear polymer yarns, of which synthetic linear polyamide yarns are an outstanding example, with a snag-proofing composition so that the said yarns may be fiat-knit into a sheer, full-fashioned hosiery fab- For a long time silk has dominated the sheer, full-fashioned hosiery field.
- a class of synthetic yarns prepared from a class of materials known as synthetic linear polyamides, has come to be used for sheer, fullfashioned hosiery. The preparation of this type of material and the production of yarn from the material are described in United States Patents Nos. 2,071,250, 2,130,523, and 2,130,948.
- compositions have been, heretofore, applied to textile yarns for a wide variety of purposes, especially to stiffen and to strengthen yarns for the purpose of weaving. Such stiffening action is undesirable inthe case. of knitting yarn, which must be bent over very sharp angles to form the knit fabric, since resistance to bending would result in uneven stitch formation. For this reason both natural silk yarns and yarns of synthetic linear polyamides are thoroughly wetted before knitting to render them more flexible. Moreover, most of these compositions do not adhere well to synthetic linear polyamides and other synthetic linear polymer yarns in spite of their very good adhesion to other textile fibers.
- an object of the present invention to furnish an improved type of snag-proofing composition particularly suitable for water-. insensitive, continuous filament, synthetic linear polymer knitting yarns to be used in the production of sheer, full-fashioned hosiery.
- a still further object of the invention is to provide a snag-proof, water-insensitive, continuous filament, synthetic linear polyamide yarn capable of being successfully knitted into fullfashioned hosiery.
- a specific object of the invention is to obtain snag-resistant, fiat-knit fabrics, in the gray, composed of water-insensitive, continuous filament, synthetic linear polymer textile yarns, particularly synthetic linear polyamide yarns, suitable for the production of sheer, full-fashioned hosiery.
- fabrics in the gray possessing resistance to snagging and suitable for the preparation of sheer, full-fashioned hosiery may be obtained by fiat-knitting waterinsensitive, continuous filament, synthetic linear polymer yarns, in particular linear polyamide yarns, which have been treated by depositing thereon, as a snag-proofing composition, a filmforming material which is tacky in the air-dried state and which is dispersible in an aqueous liquid.
- Yarns so treated have good running properties on full-fashioned knitting machines, have excellent protection from snags and runs, and the composition deposited on the yarn prevents serious edge-rolling of the full-fashioned stocking fabric.
- the snag-proofing composition may be readily removed from the fabric after the completion of the stocking, for example by means of an aqueous boil-off bath.
- ffilm-forming is meant the ability to form a substantially coherent film or coating upon evaporation of a thin layer of a dispersion, or solution, of the material in question.
- dispersible as used in the present specification. is meant to include solubility; that is, a material which is soluble in an aqueous liquid is considered to be dispersible in said liquid.
- tacky is defined by the following test: A No. 9 lead shot is dropped from a height of 1 centimeter onto a freshly prepared film of the composition having a thickness of approximately 0.2 millimeter and which has been dried in the atmosphere for 24 hours at a temperature of 25 C. and a relative humidity of 50%. If, upon inverting the film, the lead shot does not fall free within a period of seconds, the composition is considered to be tacky in the air-dried state. If, on the other hand, the shot does not remain in contact with the film for at least 5 seconds, the composition is not tacky and is not suitable for the purposes of this invention. In the cases of the preferred compositions of this invention, the shot will remain in contact with the film for a period as great as seconds or more.
- tackiness is an essential feature of the snagproofing compositions of this invention. It is known, of course, that tackiness is extremely undesirable in warp sizes or in dressings for finished fabrics, including finished knitted fabrics.
- finished fabrics is used here in the sense of contrast with the terms "unfinished fabrics or "fabrics in the gray. It was, therefore, contrary to all expectations that materials possessing that characteristic would be adapted to the treatment of knitting yarns and furthermore would be outstanding in the impartation of snag-proof properties to fabrics knit from said yarns. Neither could it have been expected that tacky, film-forming materials would not stick to or deposit excessively on the needles, sinkers and other parts of the knitting machines.
- the tacky snag-proofing compositions operable in the process of this invention are in general not adapted to the problem of dressing finished fabrics, including finished knitted fabrics, since they tend to leave the fabric in a tacky condition.
- agents known to be useful for the treatment of finished fabrics are not in general satisfactory for the treatment of the yarn previous to knitting, in that they do not impart snag resistance to fabrics knitted from the yarn.
- alkyd resins vinyl interpolymers, natural resins, and carbohydrates are particularly suitable, provided, of course, that they are dispersible in an aqueous liquid, that they are film-forming in character and that they are tacky in their air-dried state.
- Those materials falling within these classes which are not tacky in the air-dried state may often be rendered tacky by the addition of a plasticizer, and thus made suitable for use in accordance with the invention.
- Example I The following example illustrates the preparation of snag-resistant, fiat-knit hosiery fabrics prepared from synthetic linear polyamides, utilizing as the snag-proofing composition an alkyd resin which is insoluble in water, but soluble in dilute aqueous alkalies.
- a 30-denier, 10-filament 30-turn, Z twist, oriented, continuous polyhexamethylene adipamide yarn is treated by passing through a solution comprising 3.3 parts of ethanol, 86.7 parts of water, and 10 parts of the neutral ammonium salt of the alkyd resin of acid number 35, prepared by heating substantially equimolecular quantities of diethylene glycol and the maleic anhydride adduct of a. terpene fraction boiling within the range 172 C.-180 C., consisting es-,
- the newly formed fabric tend to stick tojthe needles.
- the resulting fabric is highly resistant to snagging, and consequently receives little damage, due to pulled threads, in the subsequent operations of stocking manufacture.
- Example II phthalate, 3 parts of a polymerized ethylene oxide with an average molecular weight of approximately 1500, 74 parts of water; and parts of the neutral ammonium salt of the alkyd resin of acid number 35, prepared by heating in substantially "equimolecular quantities a mixture comprising 15% glycerol and 85% ethylene glycol and the maleic anhydride adduct of a terpene fraction boiling within the range 172' C.- 180 C., consisting essentially of alpha-terpinene, obtained by the rearrangement of alphapinene.
- Alkyd resins of the above-mentioned general type are marketed by the Hercules Powder Company under the trade-name, Petrex Resins.”
- the yarn is passed over the roll at a speed of 1000 feet per minute, while the roll rotates with a circumferential speed of 12.2 feet per minute. In this manner, 3 .2% of th snagsubstantially the same amount of snag-proofing composition as the treated yarn.
- Example IV The. following example typifies the production of snag-resistant synthetic linear polyamide fabrics from yarns treated with an oil-modified, water-insoluble, alkali-soluble alkyd resin.
- a bath is prepared from the oil-modified alkyd resin, with an acid number of 100, prepared by heating 228.2 parts of glycerol, 539.4 parts of phthalic anhydride, and 232.4 parts of castor oil, by dissolving it in 5000 parts of water and 441 parts of commercial concentrated a nmonium hydroxide solution.
- a skein of 45-denier, -turn, "z" twist, oriented, continuous polyhexamethylene adipamide yarn is immersed in this bath at C. for 5 minutes. The excess solution is removed from'the yarn by whirling in a centrifuge for 2 minutes, and the yarn is finally dried at room temperature. The amount of dry material j deposited on the yarn is 8.5% of the weight of proofing composition is applied to the yarn.
- Eagample III The following example illustrates the use of a. snag-proofing composition based on an acidic, water-soluble alkyd resin derived from a polyhydric alcohol and a dibasie acid, and which is neutralized before application to the yarn.
- An oriented, continuous, 10-filament, SO-denier polyhexamethylene adipamide yarn with 30 turns of Z twist per inch is treated with a solution comprising 15 parts of a mannitol maleate resin, prepared by heating mannitol and maleic anhydride in the molecular ratio of 10:8 at 150 C., until the acid number of the resulting resin drops to 70, 10.2 parts of 29% ammonium hydroxide solution, and 74.8 parts of water, and dried.
- This is-accomplished using the bobbin-to-bobbin type machine of Example II, utilizing a yarn speed of 1000 feet per minute and a circumferentialroll speed of 7.2 feet per minute.
- the treated yarn is found to contain 6.5% mannitol maleate, based on the original weight of the yarn.
- the yarn is knit as in the preceding examples to form a highly snag-resistant flat fabric containing the dry yarn.
- the .yarn is flat knit to a fabric whic s good resistance to snagging.
- Example V The following example is representative of the production of snag-resistant. flat-knit hosiery fabrics prepared from synthetic linear polyamides treated with a tacky vinyl interpolymer composition.
- the yarn is processed at a speed of 1000 feet per minute with a circumferential roll speed of 4.5 feet per minute.
- the treated yarn is found
- the following example further illustrates the production of snag-resistant flat-knit fabrics prepared from water-insensitive, synthetic, continuous yarns by the use of a typical tacky vinyl 'interpolymer composition as the snag-proofing composition.
- polyhexamethylene a'dipamide yarn having 30 turns of Z twist per inch is treated on the bobbin-to-bobbin type machine of Example H with a solution of a sodium'salt of a hydrolyzed propylene-maleic anhydride copolymer.
- the copolymer is prepared in an autoclave from 30 parts of maleic anhydride dissolved in 200 parts of toluene and 35 parts of propylene, using 1.5 parts of benzoyl peroxide as catalyst.
- the initial pressure, at room temperature, is 280 pounds per square inch. Upon heating the mixture to 100 C. an exothermic reaction occurs.
- the snag-proofing composition is prepared by heating 10 parts of the interpolymer and 5 parts of sodium hydroxide in 85 parts of water at 90 C.
- the yarn is treated at a speed of 1000 feet per minute and a circumferential roll speed of 4.5 feet per minute. After coning in the usual manner, the yarn is knit as in the preceding examples to form a snag-resistant flat fabric suitable for further processing in the preparation of sheer, full-fashioned hosiery.
- Example VII The following example illustrates the treatment of a polyamide yarn with a composition of a methacrylate polymer which is not tacky of itself, but is rendered tacky by the addition of suitable plasticizing agents.
- An oriented, continuous, lo-filament polyhexamethylene adipamide yarn is impregnated on the bobbin-to-bobbin type machine of Example II with a solution comprising 325 parts of di-beta-methoxyethyl adipate, 325 parts of a polymerized ethylene oxide of an average molecular weight of approximately 1500, 8500 parts of water, and an interpolymer prepared by emulsion type polymerization from 640 parts of beta-methoxyethyl methacrylate and 110 parts of methacrylic acid, using 7.5 parts of benzoyl peroxide as the catalyst and 7.5 parts of methylated starch as the emulsifying agent.
- a circumferential roll speed of 9.4 feet per minute and a yarn speed of 1000 feet per minute is used.
- a highly snag-resistant fabric results upon flat knitting the yarn according to the procedure of the previous examples.
- Example VIII The following example is illustrative of the use of a natural resinous material of the terpene type to produce highly snag-resistant, fiat-knit, synthetic linear polyamide hosiery fabrics.
- Oriented, continuous polyhexamethylene adip amide yarn is impregnatedin a continuous manner by passing it through a aqueous solution of the sodium salt of rosin at a rate of 100 feet per minute.
- the length of the path of the yarn through the bath is 4 inches, and the 'distance between the bath and the wind-up bobbin is 30 feet.
- the yarn is flat knit as in the previous examples to give a hosiery fabric with a very high degree of resistance to snagging.
- Example IX The following example illustrates the production of snag-resistant synthetic linear polyamide hosiery fabric by the use, as a snag-proofing composition for the yarn, of a typical tacky carbohydrate composition.
- Oriented, continuous multifilament polyhexamethylene adipamide yarn is passed through a 20% solution of honey, using a circumferential roll speed of 7.2 feet per minute and a yarn speed of 1000 feet per minute on the bobbinto-bobbin type machine of Example II.
- the process of this invention is particularly applicable to any synthetic linear polymer,
- water-insensitive continuous yarn since the snag-proofing compositions employed in this invention adhere well to these yarns, in contrast to the more well-known compositions.
- water-insensitive it is meant that the individual filaments of the yarn absorb less than 10% of their weight of water at 25 C. and 100% relative humidity.
- yarns are the synthetic material made of a vinyl chloridevinyl acetate interpolymer marketed by the Carbide and Carbon Corporation under the name Vinyon; yarns composed of .polymerized methyl methacrylate or polymerized ethyl methacrylate; polyvinyl chloride yarns; chlorinated polyvinyl chloride yarns; and yarns composed of high molecular weight ethylene polymers.
- nylon Of particular interest in this invention are the synthetic linear polyamide materials generically known as nylon.
- polyamides derived from diamines and dibasic acids or their amideforming derivatives examples of the various classes of synthetic linear polyamides from which fibers suitable for the purposes of this invention may be prepared may be cited the polyamides derived from diamines and dibasic acids or their amideforming derivatives; those derived from polyamide-forming amino acids; and interpolyamides prepared from diamines, dibasic acids, and polyamide-forming amino acids.
- polyamides of the diamine dibasic acid type may be mentioned polytetramethylene subacamide, polypentamethylene adipamide, polypentamethylene sebacamide, polyhexamethylene sebacamide, polyoctamethylene adipamide, polydecamethylene adipamide, poly-p-xylylene sebacamide, polyhexamethylene hexahydroterephthalamide, polyhexamethylene isophthalamide, poly-3-methyl hexamethylene-2-methyl adipamide, polyhexamethylene- 4-ketopimelamide, the polyamide prepared from hexamethylenediamine and sulfonedibutyric acid, the polyamide derived from hexamethylenediamine and piperazine diacetic acid, and the interpolamide prepared from equimolecular quantities of hexamethylenediamine, decamethylenediamine, adipic acid, and sebacic acid.
- Polyamides of the amino acid type include polymerized-G-aminocaproic acid, polymerized-9- aminononanoic acid, polymerized 12-aminostearic acid, and the interpolyamide derived from equimolecular quantities of G-aminocaproic acid and IO-aminodecanoic acid.
- interpolyamides prepared from diamines, dibasic acids, and amide-forming amino acids include the polymers derived from equimolecular quantities of hexamethylenediamine, adipic acid, and 12-aminostearic acid, and the polyamide derived from hexamethylenediamine, sebacic acid, and G-aminocaproic acid in which the molecular quantities are in the ratio of 3:3:1.
- the process is of particular utility with yarns of denier of or less since it is with fabrics knit from these yarns that snag resistance is most needed. Higher denier yarns tend to give more snag-resistant fabrics without a snag-proofing treatment. Likewise the process is also of greatest advantage with yarns of smoother contour which are especially prone to give easily snagged fabrics. Such a contour is typical of the synthetic polymer yarns.
- compositions are suitable for use as snag-proofing compositions in accordance with the present invention. Chemically, these compositions are quite unrelated and they comprise a variety of divers materials. It is through their physical characteristics that they form a unitary, generic group, within which any composition is applicable to this process. As already indicated, these physical characteristic are (a) film-forming ability, (b) tackiness in the airdried state, (c) dispersibility in an aqueous liquid.
- tacky compositions comprising alkyd resins, vinyl interpolymers, methacrylate polymers, natural resins, and carbohydrates have been found to be particularly suitable.
- a preferred embodiment of this invention comprises the use of tacky compositions based on alkyd resins as a class.
- alkyd resins are those of relatively high acid number derived from polyhydric alcohols and diand polybasic acids, such as the mannitol maleates, sorbitol phthalates, mannitol phthalates and sorbitol citrates with acid numbers of 30 to 150.
- alkyd resins which have been found suitable for use in the process of this invention, those based on compounds of the terpene group are unusually effective.
- alkyd type resins based on terpene acids such as the adduct between rosin and maleic anhydride, or the terpene-maleic anhydride adduct known as Petrex acid, marketed by the Hercules Powder Company, are especially efiective snag-proofing compositions.
- Another preferred embodiment of this invention comprises the use of tacky compositions based on vinyl polymers.
- tacky compositions based on vinyl polymers Completely or partially hydrolyzed copolymer of olefin hydrocarbons and maleic anhydride such as an ethylene-maleic anhydride interpolymer, are examples of tacky vinyl polymers which are especially preferred for the purposes of this invention.
- a typical natural resin is represented by pine rosin, preferably in the form of it emulsion or water-soluble salts.
- Non-crystallizing sugar syrups such as honey or corn syrup are typical tacky carbyhydrates.
- tacky compositions of the classes mentioned in the examples above include highly plasticized glycerol phthalates with acid numbers of 6D or above, plasticized oil-modified alkyd resins obtained from terpene-maleic anhydride condensates and dior polyhydric alcohols, and plasticized composition containing the resin prepared from 75% methyl methacrylate and 25% of methacrylicacid under the influence of peroxide catalysts.
- tacky, film-formin materials suitable for use in snag-proofing compositions according to this invention are urea-formaldehyde resins, phenol-formaldehyde type resins, resinous terpene derivatives, synthetic linear polyamides, synthetic linear polyamidines, and synthetic linear polyquaternary ammonium salts.
- An example of a urea-formaldehyde resin suitable for use in snag-proofing compositions, according to this invention is a reaction product of urea and formaldehyde which has been condensed only to the water-soluble syrupy state.
- Compositions containing resorcinol-formaldehyde, or salicylic acid-formaldehyde resins and a plasticizing agent are suitable snag-proofing compositions for the purposes of this invention.
- a plasticized sodium salt of a sulfonated resin obtained by the condensation of pinene and phenol in the presence of dihydroxy-fluoboric acid is representative of suitable compositions based Polytriglycol adipamide, and polyamidine prepared from sebaconitrile and decamethylenediamine, and the polyquatemary ammonium salts prepared from 4,4'-tetramethyl diaminodiphenylmethane and decamethylene dibromide are typical examples of synthetic.
- suitable water-soluble plasticizing agents include glycerol, triethylene glycol, polymerized' ethylene oxide, sorbitol, diacetin, triethanolamine oleate, and N-(beta-hydroxyethyDfOrmamide.
- Suitable water-insoluble plasticizers include di(betamethoxyethyl) adipate, dibutyl phthalate, and tributyl phosphate. It has been found that most satisfactory results are usually obtained by use of a water-soluble material.
- plasticizers are compatible with the treating solutions and in many cases reduce the tackiness of the treated yarn upon wetting, which in turn improves the knitting characteris-' tics of the yarn under wet conditions.
- the snag-proofing compositions are preferably applied in the 'form of their solutions in water or in aqueous liquids.
- dilute alkalies such as sodium hydroxide, ammonium hydroxide or triethanolamine, may be used to effect solution.
- suitable means for example,
- an ethylene-maleic anhydride interpolymer may be solubilized in water by refluxing with 50%- 70% of its weight of sodium hydroxide in dilute aqueous solution.
- the aqueous solution may be' neutralized with dilute ammonium hydroxide before use.
- Suitable concentrations of the film-forming materials in the snag-proofing compositions lie in the range of about 2% to about 35%, based on the total solids concentration of the solution.
- the viscosity of the snag-proofing composition may vary within wide limits, but a 4% aqueous dispersion of the film-forming material should solution of the composition.
- the speed at which the roll rotates will vary with the speed of the yarn and will depend upon t. e amount of composition which it is desired to apply to the yarn. Thus, for example, at a yarn speed of 1000 feet per minute and with a roll 3 inches in diameter, a suitable range of roll speeds lies between 2 and 16 revolutions per minute.
- the composition it is also suitable to apply the composition by passing the yarn in a continuous fashion through a solution or dispersion thereof, or by dipping loosely wound skeins into,the solution, followed by wringing to remove excess liquor. Any other suitable method may be employed.
- the snag-proofing composition may be sprayed on a moving strand of yarn.
- the amount of residual, air-dried film-forming material applied to the yarn may vary within wide limits but the preferred amount-will lie within the range of 1% to 20% of film-forming material, based on the weight of the dry yarn.
- the amount of the material on the yarn may in most cases be simply determined by boiling a weighed sample of the treated yarn in a dilute alkaline solution and re-weighing the yarn after drying.
- the quantity of snag-proofing composition to be applied to the yarn will depend upon the degree of snag protection required and the method to be employed in handling the yarn during knitting. In general, snag protection is increased as the quantity of composition is increased, but with excessive quantities the yarn may stick in the supply package, or undesirable friction may be set up between the yarn and the knitting machine parts.
- the quantity of snag-proofing composition which can be applied will also vary, depending upon the denier of the yarn, the firmness of the yarn package, and the speed of knitting.
- the snag-proofing composition may be applied to the unseamed and unlooped fabric in the gray as obtained from the knitting machine.
- this process results in a high degree of resistance to snagging, it is inconvenient and expensive and, in addition, offers the danger of excessive snag production before treatment can be effected.
- the residual film-forming material is subsequently removed before or during the final finishing treatment.
- the temperature of application of the snagproofing composition may vary between just above the freezing point and just below the boiling point of the solution.
- Drying of the treated yarn may be effected at normal temperature or under the influence of heat, as by means of a radiant heater or by a current of heated air.
- drying may be effected before collecting on the bobbin, as by increasing the length of yarn travel from the point of treatment to the bobbin, or it may be allowed to dry on the bobbin during winding, or by any suitable combination of these two methods.
- the concentration of the snag-proofing composition, the temperature of application, and the drying temperature are so chosen in cases of continuous application that appreciable migration of the solution on the wind-up bobbin, and consequent uneven distribution of the filmforming material does not occur. Since the comprising a film-forming material migrat on will be toward the edges of the package, analyses for the amount of the material on yarn cut from the center and edge portions of he bobbin will show whether excessive migration has occurred.
- the knitting of the yarn to form a hosiery fabric may be effected on any suitable hosiery knitting machine designed for fiat knitting.
- a Wildman, 54-gauge, single-unit, fullfashioned hosiery knitting machine is satis actory for the purposes of this invention.
- the yarn is knit preferably in the wet condition and may suitably be moistened in a wetting trough just before entering the needles.
- the products prepared according to the process of this invention may be described as snagresistant, fiat-knit fabrics in the gray, suitable for the preparation of sheer, full-fashioned hosiery comprising synthetic polymer yarns in combination with at least 1% of a dry filmforming composition, basedon the dry fabric, which is tacky in the air-dried state and which is dispersible in an aqueous liquid.
- the amount of snag-proofing composition in combination with the knit fabric may be determined by the boil-off procedure outlined above for the estimation of the tacky film-forming material on the treated yarn, and will be substantially the same as for the yarn from which the fabric was knit.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a, snag-proofing composition, an aqueous solution which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a snag-proofing composition,' an aqueous solution comprising between 2% and 35% of a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a snag-proofing composition, a solution comprisyarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a resinous film-forming material which is tacky in the airdried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising a film-forming matrial whichis tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a film-forming material which is tacky in the air-dried state, andwhich is dispersible in an aqueous liquid,
- an' aqueous solution comprising a resinous film-forming material whereby to produce a yarn having a tacky coating of said film-forming materiakand knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
- the method of producing sheer knit goods, substantially free fron snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueousliquid, whereby to produce a yarn having a tacky coating of'said film-forming material, and knitting said yarn to form sheer knit goods.
- a snag-proofing composition a sufficient quantity of a film-forming material to render the yarn snag resistantin the production of sheer knit goods, said film-forming material being tacky in the air-dried state, and being dispersible in an aqueous liquid.
- a synthetic linear polymer yarn containing, as a snag-proofing composition, 1% to 20% (based on the weight of the dry yarn) of a filmforming material to render the yarn snag resistant in the .production of sheer knit goods, said film-forming material being tacky in the airdried state, and being dispersible in an aqueous liquid.
- a synthetic linear polyamide yarn containing, as a snag-proofing composition, a sufficient quantity of a film-forming material to render the yarn snag resistant in the production of sheer knit goods, said film-forming material being tacky in the air-dried state, and being dispersible in an aqueous liquid.
- a synthetic linear polyamide yarn containing, as a snag-proofing composition.'1% to 20% (based on the weight of the dry yarn) of a film-forming material to render the yarn snag resistant in the production of sheer knit goods,
- said film-forming material being tacky in the
Description
Patented July 7, 1942 YARN PREPARATION Edgar W. Spanagel, Wilmington, DeL, assignor to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware No Drawing. Application February 14, 1941, Serial No. 378,943
21 Claims.
The present invention relates to the treatment of water-insensitive synthetic linear polymer yarns, of which synthetic linear polyamide yarns are an outstanding example, with a snag-proofing composition so that the said yarns may be fiat-knit into a sheer, full-fashioned hosiery fab- For a long time silk has dominated the sheer, full-fashioned hosiery field. Relatively recently, a class of synthetic yarns, prepared from a class of materials known as synthetic linear polyamides, has come to be used for sheer, fullfashioned hosiery. The preparation of this type of material and the production of yarn from the material are described in United States Patents Nos. 2,071,250, 2,130,523, and 2,130,948.
It will be observed, with respect to the structure of the above said synthetic linear polyamides, that they contain amide groups XR III where X is oxygen or sulphur and where R is hydrogen or a monovalent hydrocarbon radical) as an integral part of the main chain of atoms in the polymer. It will also be observed that in these polyamides the average number of carbon atoms in'the segments of the chain separating the amide groups is at least two. Accordingly, throughout the present specification and claims, the expression synthetic linear polyamide is tobe understood as applying to the polyamides described in the aforesaid patents and coming within the limitations set forth in this paragraph.
The preparation of sheer, knit ladies fullfashioned stockings from this type of yarn is described in United States PatentsNos. 2,157,116 and 2,157,119. The knitting of ladies sheer stockings from yarns of synthetic linear polyamides created new and serious problems in the satisfactory treatment of such yarns. Without any treatment these yarns, when knitted into sheer, full-fashioned stockings and subsequently handled, developed an undesirably large proportion of pulled threads. For years, the art has been confronted with a similar problem in the knitting of sheer stockings from ingrain silk.
The knitting of sheer stockings from ingrain silk operations very slow and ditficult. For this readuring knitting.
10 tion leads to an irregular stitch formation and in extreme cases holes are formed in the fabric. The treated yarn also must not stick to the guides and snappers following a shut-down of the knitting machine, otherwise press-ofis will occur when the machine is started again.
Numerous compositions have been, heretofore, applied to textile yarns for a wide variety of purposes, especially to stiffen and to strengthen yarns for the purpose of weaving. Such stiffening action is undesirable inthe case. of knitting yarn, which must be bent over very sharp angles to form the knit fabric, since resistance to bending would result in uneven stitch formation. For this reason both natural silk yarns and yarns of synthetic linear polyamides are thoroughly wetted before knitting to render them more flexible. Moreover, most of these compositions do not adhere well to synthetic linear polyamides and other synthetic linear polymer yarns in spite of their very good adhesion to other textile fibers.
One reason for this lies-in the very low moisture absorption and the surface smoothness of the synthetic linear polymer yarns. In addition, the conventional compositions which do adhere to 55 synthetic linear polyamide yarns, in general, give a low degree of snag resistance to the knit fabric and tend to accumulate excessively on the needles and sinkers during the knitting operation.
The number of snag-proofing compositions which may be applied to the yarn before knitting is very limited, and in addition, most of the known compositions tend to dertsit excessively on the needles and sinkers and U0 stick to the needles Moreover, the way in which snag-proofing compositions for knitting yarns act is obscure and the necessary characteristics of compositions of this type are not completely understood. In fact, up to the time of the dis- 0 covery of the present invention no prediction could be made as to the eifectiveness of a given composition for the snag-proofing of knitting yarns.
It is, therefore, an object of the present invention to furnish an improved type of snag-proofing composition particularly suitable for water-. insensitive, continuous filament, synthetic linear polymer knitting yarns to be used in the production of sheer, full-fashioned hosiery.
It is a further object of the present invention to furnish an improved method of snag proofing water-insensitive, continuous filament, synthetic linear polymer textile yarns, particularly synthetic linear polyamide knitting yarns, to be used in the production of sheer, full-fashioned hosiery.
A still further object of the invention is to provide a snag-proof, water-insensitive, continuous filament, synthetic linear polyamide yarn capable of being successfully knitted into fullfashioned hosiery.
A specific object of the invention is to obtain snag-resistant, fiat-knit fabrics, in the gray, composed of water-insensitive, continuous filament, synthetic linear polymer textile yarns, particularly synthetic linear polyamide yarns, suitable for the production of sheer, full-fashioned hosiery.
Other objects of the invention will become apparent hereinafter.
It has now been found that fabrics in the gray possessing resistance to snagging and suitable for the preparation of sheer, full-fashioned hosiery may be obtained by fiat-knitting waterinsensitive, continuous filament, synthetic linear polymer yarns, in particular linear polyamide yarns, which have been treated by depositing thereon, as a snag-proofing composition, a filmforming material which is tacky in the air-dried state and which is dispersible in an aqueous liquid. Yarns so treated have good running properties on full-fashioned knitting machines, have excellent protection from snags and runs, and the composition deposited on the yarn prevents serious edge-rolling of the full-fashioned stocking fabric. The snag-proofing composition may be readily removed from the fabric after the completion of the stocking, for example by means of an aqueous boil-off bath.
By the term ffilm-forming" is meant the ability to form a substantially coherent film or coating upon evaporation of a thin layer of a dispersion, or solution, of the material in question.
The term dispersible, as used in the present specification. is meant to include solubility; that is, a material which is soluble in an aqueous liquid is considered to be dispersible in said liquid.
The term tacky," as used in the present specification, is defined by the following test: A No. 9 lead shot is dropped from a height of 1 centimeter onto a freshly prepared film of the composition having a thickness of approximately 0.2 millimeter and which has been dried in the atmosphere for 24 hours at a temperature of 25 C. and a relative humidity of 50%. If, upon inverting the film, the lead shot does not fall free within a period of seconds, the composition is considered to be tacky in the air-dried state. If, on the other hand, the shot does not remain in contact with the film for at least 5 seconds, the composition is not tacky and is not suitable for the purposes of this invention. In the cases of the preferred compositions of this invention, the shot will remain in contact with the film for a period as great as seconds or more.
That the physical characteristic described as tackiness is an essential feature of the snagproofing compositions of this invention will no doubt be quite surprising to those skilled in the art. It is known, of course, that tackiness is extremely undesirable in warp sizes or in dressings for finished fabrics, including finished knitted fabrics. The term finished fabrics" is used here in the sense of contrast with the terms "unfinished fabrics or "fabrics in the gray. It was, therefore, contrary to all expectations that materials possessing that characteristic would be adapted to the treatment of knitting yarns and furthermore would be outstanding in the impartation of snag-proof properties to fabrics knit from said yarns. Neither could it have been expected that tacky, film-forming materials would not stick to or deposit excessively on the needles, sinkers and other parts of the knitting machines.
It should be emphasized, in connection with the above, that the tacky snag-proofing compositions operable in the process of this invention are in general not adapted to the problem of dressing finished fabrics, including finished knitted fabrics, since they tend to leave the fabric in a tacky condition.- Conversely, agents known to be useful for the treatment of finished fabrics are not in general satisfactory for the treatment of the yarn previous to knitting, in that they do not impart snag resistance to fabrics knitted from the yarn.
Among the various classes of materials which may be used in snag-proofing compositions in accordance with the present invention, alkyd resins, vinyl interpolymers, natural resins, and carbohydrates are particularly suitable, provided, of course, that they are dispersible in an aqueous liquid, that they are film-forming in character and that they are tacky in their air-dried state. Those materials falling within these classes which are not tacky in the air-dried state may often be rendered tacky by the addition of a plasticizer, and thus made suitable for use in accordance with the invention.
The following examples are given to illustrate preferred snag-proofing compositions and preferred methods of applying the same. The details set forth in the examples are not, however, to be considered as limitative of the invention. The percentages set forth in the examples designate percentages by weight.
Example I The following example illustrates the preparation of snag-resistant, fiat-knit hosiery fabrics prepared from synthetic linear polyamides, utilizing as the snag-proofing composition an alkyd resin which is insoluble in water, but soluble in dilute aqueous alkalies.
A 30-denier, 10-filament 30-turn, Z twist, oriented, continuous polyhexamethylene adipamide yarn is treated by passing through a solution comprising 3.3 parts of ethanol, 86.7 parts of water, and 10 parts of the neutral ammonium salt of the alkyd resin of acid number 35, prepared by heating substantially equimolecular quantities of diethylene glycol and the maleic anhydride adduct of a. terpene fraction boiling within the range 172 C.-180 C., consisting es-,
sentially of alpha-terpinene, and obtained by the rearrangement of alpha-pinene using sulfuric acid as catalyst. Alkyd resins of the above-mentioned general type are marketed by the Hercules Powder Company under the trade-name, Petrex Resins." The yarn is passed through the bath at a speed of feet a minute and the length of the travel in the bath is 4 inches. The distance from the bath to the wind-up bobbin is 30 feet. After drying and coning, the treated yarn is knit in a wet condition in a Wildman 45-gauge, single-unit, full fashioned hosiery knitting machine. None of the snag-proofing composition is deposited on either the needles or the sinkers, nor
does the newly formed fabric tend to stick tojthe needles. The resulting fabric is highly resistant to snagging, and consequently receives little damage, due to pulled threads, in the subsequent operations of stocking manufacture.
Example II phthalate, 3 parts of a polymerized ethylene oxide with an average molecular weight of approximately 1500, 74 parts of water; and parts of the neutral ammonium salt of the alkyd resin of acid number 35, prepared by heating in substantially "equimolecular quantities a mixture comprising 15% glycerol and 85% ethylene glycol and the maleic anhydride adduct of a terpene fraction boiling within the range 172' C.- 180 C., consisting essentially of alpha-terpinene, obtained by the rearrangement of alphapinene. Alkyd resins of the above-mentioned general type are marketed by the Hercules Powder Company under the trade-name, Petrex Resins." The yarn is passed over the roll at a speed of 1000 feet per minute, while the roll rotates with a circumferential speed of 12.2 feet per minute. In this manner, 3 .2% of th snagsubstantially the same amount of snag-proofing composition as the treated yarn.
Example IV The. following example typifies the production of snag-resistant synthetic linear polyamide fabrics from yarns treated with an oil-modified, water-insoluble, alkali-soluble alkyd resin.
A bath is prepared from the oil-modified alkyd resin, with an acid number of 100, prepared by heating 228.2 parts of glycerol, 539.4 parts of phthalic anhydride, and 232.4 parts of castor oil, by dissolving it in 5000 parts of water and 441 parts of commercial concentrated a nmonium hydroxide solution. A skein of 45-denier, -turn, "z" twist, oriented, continuous polyhexamethylene adipamide yarn is immersed in this bath at C. for 5 minutes. The excess solution is removed from'the yarn by whirling in a centrifuge for 2 minutes, and the yarn is finally dried at room temperature. The amount of dry material j deposited on the yarn is 8.5% of the weight of proofing composition is applied to the yarn.
After drying. coning and oiling, theyarn is knit as in Example I to form a fabric with excellent resistance to snagging. e
' In the manufacture of full-fashioned hosiery using yarn treated with the composition of this example only about nine snags were produced per hundred stockings, whereas substantially all the stockings knit from untreated yarn were snagged.
Eagample III The following example illustrates the use of a. snag-proofing composition based on an acidic, water-soluble alkyd resin derived from a polyhydric alcohol and a dibasie acid, and which is neutralized before application to the yarn.
An oriented, continuous, 10-filament, SO-denier polyhexamethylene adipamide yarn with 30 turns of Z twist per inch is treated with a solution comprising 15 parts of a mannitol maleate resin, prepared by heating mannitol and maleic anhydride in the molecular ratio of 10:8 at 150 C., until the acid number of the resulting resin drops to 70, 10.2 parts of 29% ammonium hydroxide solution, and 74.8 parts of water, and dried. This is-accomplished using the bobbin-to-bobbin type machine of Example II, utilizing a yarn speed of 1000 feet per minute and a circumferentialroll speed of 7.2 feet per minute. The treated yarn is found to contain 6.5% mannitol maleate, based on the original weight of the yarn. After coning in the usual manner, the yarn is knit as in the preceding examples to form a highly snag-resistant flat fabric containing the dry yarn. After spooling and coning in the known manner, the .yarn is flat knit to a fabric whic s good resistance to snagging.
Example V The following example is representative of the production of snag-resistant. flat-knit hosiery fabrics prepared from synthetic linear polyamides treated with a tacky vinyl interpolymer composition. A
A ill-filament, 30-denier, oriented, continuous,
polyhexamethylene adipamide yarn with 30 turns of Z twist per inchis treated on the bobbinto-bobbin" machine mentioned in Example 11 with a solution 'of the neutral sodium salt of a hydrolyzed ethylene-maleic anhydride interpolymer. This copolymer is prepared in an 'autoclave from a solution of 24 parts .of maleic anhydride in 140 parts of xylene and 27 parts of' ethylene at an initial pressure, at room temperature, of 320 pounds per square inch. One part of benzoyl peroxide is used as catalyst. Exothermic reaction is effected upon heating the mixture to 75 C. The solution is prepared by heating 10 parts of the interpolymer and 5 parts of sodium hydroxide in parts of water at C. for 18 hours.
The yarn is processed at a speed of 1000 feet per minute with a circumferential roll speed of 4.5 feet per minute. The treated yarn is found The following example further illustrates the production of snag-resistant flat-knit fabrics prepared from water-insensitive, synthetic, continuous yarns by the use of a typical tacky vinyl 'interpolymer composition as the snag-proofing composition.
An oriented 10-fi1ament, 30-denier, continuous,
polyhexamethylene a'dipamide yarn having 30 turns of Z twist per inch is treated on the bobbin-to-bobbin type machine of Example H with a solution of a sodium'salt of a hydrolyzed propylene-maleic anhydride copolymer.
The copolymer is prepared in an autoclave from 30 parts of maleic anhydride dissolved in 200 parts of toluene and 35 parts of propylene, using 1.5 parts of benzoyl peroxide as catalyst. The initial pressure, at room temperature, is 280 pounds per square inch. Upon heating the mixture to 100 C. an exothermic reaction occurs.
The snag-proofing composition is prepared by heating 10 parts of the interpolymer and 5 parts of sodium hydroxide in 85 parts of water at 90 C. The yarn is treated at a speed of 1000 feet per minute and a circumferential roll speed of 4.5 feet per minute. After coning in the usual manner, the yarn is knit as in the preceding examples to form a snag-resistant flat fabric suitable for further processing in the preparation of sheer, full-fashioned hosiery.
Example VII The following example illustrates the treatment of a polyamide yarn with a composition of a methacrylate polymer which is not tacky of itself, but is rendered tacky by the addition of suitable plasticizing agents.
An oriented, continuous, lo-filament polyhexamethylene adipamide yarn is impregnated on the bobbin-to-bobbin type machine of Example II with a solution comprising 325 parts of di-beta-methoxyethyl adipate, 325 parts of a polymerized ethylene oxide of an average molecular weight of approximately 1500, 8500 parts of water, and an interpolymer prepared by emulsion type polymerization from 640 parts of beta-methoxyethyl methacrylate and 110 parts of methacrylic acid, using 7.5 parts of benzoyl peroxide as the catalyst and 7.5 parts of methylated starch as the emulsifying agent. A circumferential roll speed of 9.4 feet per minute and a yarn speed of 1000 feet per minute is used. A highly snag-resistant fabric results upon flat knitting the yarn according to the procedure of the previous examples.
Example VIII The following example is illustrative of the use of a natural resinous material of the terpene type to produce highly snag-resistant, fiat-knit, synthetic linear polyamide hosiery fabrics.
Oriented, continuous polyhexamethylene adip amide yarn is impregnatedin a continuous manner by passing it through a aqueous solution of the sodium salt of rosin at a rate of 100 feet per minute. The length of the path of the yarn through the bath is 4 inches, and the 'distance between the bath and the wind-up bobbin is 30 feet. After coming in the usual manner, the yarn is flat knit as in the previous examples to give a hosiery fabric with a very high degree of resistance to snagging.
Example IX The following example illustrates the production of snag-resistant synthetic linear polyamide hosiery fabric by the use, as a snag-proofing composition for the yarn, of a typical tacky carbohydrate composition.
Oriented, continuous multifilament polyhexamethylene adipamide yarn is passed through a 20% solution of honey, using a circumferential roll speed of 7.2 feet per minute and a yarn speed of 1000 feet per minute on the bobbinto-bobbin type machine of Example II. Coning and fiat knitting, according to the procedure of the preceding examples, results in a hosiery fabric showing resistance to snagging.
The process of this invention is particularly applicable to any synthetic linear polymer,
water-insensitive, continuous yarn since the snag-proofing compositions employed in this invention adhere well to these yarns, in contrast to the more well-known compositions. By the term water-insensitive it is meant that the individual filaments of the yarn absorb less than 10% of their weight of water at 25 C. and 100% relative humidity. Examples of such yarns are the synthetic material made of a vinyl chloridevinyl acetate interpolymer marketed by the Carbide and Carbon Corporation under the name Vinyon; yarns composed of .polymerized methyl methacrylate or polymerized ethyl methacrylate; polyvinyl chloride yarns; chlorinated polyvinyl chloride yarns; and yarns composed of high molecular weight ethylene polymers.
Of particular interest in this invention are the synthetic linear polyamide materials generically known as nylon.
While the process has been described as applied to yarn, i. e., multiple filaments, it is obviously equally applicable to single filaments (monofils) of any desired denier.
As examples of the various classes of synthetic linear polyamides from which fibers suitable for the purposes of this invention may be prepared may be cited the polyamides derived from diamines and dibasic acids or their amideforming derivatives; those derived from polyamide-forming amino acids; and interpolyamides prepared from diamines, dibasic acids, and polyamide-forming amino acids. As further examples of polyamides of the diamine dibasic acid type may be mentioned polytetramethylene subacamide, polypentamethylene adipamide, polypentamethylene sebacamide, polyhexamethylene sebacamide, polyoctamethylene adipamide, polydecamethylene adipamide, poly-p-xylylene sebacamide, polyhexamethylene hexahydroterephthalamide, polyhexamethylene isophthalamide, poly-3-methyl hexamethylene-2-methyl adipamide, polyhexamethylene- 4-ketopimelamide, the polyamide prepared from hexamethylenediamine and sulfonedibutyric acid, the polyamide derived from hexamethylenediamine and piperazine diacetic acid, and the interpolamide prepared from equimolecular quantities of hexamethylenediamine, decamethylenediamine, adipic acid, and sebacic acid.
Polyamides of the amino acid type, suitable for the purposes of this invention, include polymerized-G-aminocaproic acid, polymerized-9- aminononanoic acid, polymerized 12-aminostearic acid, and the interpolyamide derived from equimolecular quantities of G-aminocaproic acid and IO-aminodecanoic acid.
Examples of interpolyamides prepared from diamines, dibasic acids, and amide-forming amino acids, include the polymers derived from equimolecular quantities of hexamethylenediamine, adipic acid, and 12-aminostearic acid, and the polyamide derived from hexamethylenediamine, sebacic acid, and G-aminocaproic acid in which the molecular quantities are in the ratio of 3:3:1.
The process is of particular utility with yarns of denier of or less since it is with fabrics knit from these yarns that snag resistance is most needed. Higher denier yarns tend to give more snag-resistant fabrics without a snag-proofing treatment. Likewise the process is also of greatest advantage with yarns of smoother contour which are especially prone to give easily snagged fabrics. Such a contour is typical of the synthetic polymer yarns.
A wide variety of compositions is suitable for use as snag-proofing compositions in accordance with the present invention. Chemically, these compositions are quite unrelated and they comprise a variety of divers materials. It is through their physical characteristics that they form a unitary, generic group, within which any composition is applicable to this process. As already indicated, these physical characteristic are (a) film-forming ability, (b) tackiness in the airdried state, (c) dispersibility in an aqueous liquid.
As above indicated, tacky compositions comprising alkyd resins, vinyl interpolymers, methacrylate polymers, natural resins, and carbohydrates have been found to be particularly suitable. A preferred embodiment of this invention comprises the use of tacky compositions based on alkyd resins as a class. Especially suitable examples of alkyd resins are those of relatively high acid number derived from polyhydric alcohols and diand polybasic acids, such as the mannitol maleates, sorbitol phthalates, mannitol phthalates and sorbitol citrates with acid numbers of 30 to 150. Among other alkyd resins which have been found suitable for use in the process of this invention, those based on compounds of the terpene group are unusually effective. Thus, alkyd type resins based on terpene acids, such as the adduct between rosin and maleic anhydride, or the terpene-maleic anhydride adduct known as Petrex acid, marketed by the Hercules Powder Company, are especially efiective snag-proofing compositions.
Another preferred embodiment of this invention comprises the use of tacky compositions based on vinyl polymers. Completely or partially hydrolyzed copolymer of olefin hydrocarbons and maleic anhydride such as an ethylene-maleic anhydride interpolymer, are examples of tacky vinyl polymers which are especially preferred for the purposes of this invention.
A typical natural resin is represented by pine rosin, preferably in the form of it emulsion or water-soluble salts. Non-crystallizing sugar syrups such as honey or corn syrup are typical tacky carbyhydrates.
Further species of tacky compositions of the classes mentioned in the examples above include highly plasticized glycerol phthalates with acid numbers of 6D or above, plasticized oil-modified alkyd resins obtained from terpene-maleic anhydride condensates and dior polyhydric alcohols, and plasticized composition containing the resin prepared from 75% methyl methacrylate and 25% of methacrylicacid under the influence of peroxide catalysts. Y
Other classes of tacky, film-formin materials suitable for use in snag-proofing compositions according to this invention are urea-formaldehyde resins, phenol-formaldehyde type resins, resinous terpene derivatives, synthetic linear polyamides, synthetic linear polyamidines, and synthetic linear polyquaternary ammonium salts. An example of a urea-formaldehyde resin suitable for use in snag-proofing compositions, according to this invention, is a reaction product of urea and formaldehyde which has been condensed only to the water-soluble syrupy state. Compositions containing resorcinol-formaldehyde, or salicylic acid-formaldehyde resins and a plasticizing agent are suitable snag-proofing compositions for the purposes of this invention.
a on resinous terpene derivatives.
A plasticized sodium salt of a sulfonated resin obtained by the condensation of pinene and phenol in the presence of dihydroxy-fluoboric acid is representative of suitable compositions based Polytriglycol adipamide, and polyamidine prepared from sebaconitrile and decamethylenediamine, and the polyquatemary ammonium salts prepared from 4,4'-tetramethyl diaminodiphenylmethane and decamethylene dibromide are typical examples of synthetic. linear polyamides, p lyamidines, and
cizing agents may be used for this purpose. Ex-
amples of suitable water-soluble plasticizing agents include glycerol, triethylene glycol, polymerized' ethylene oxide, sorbitol, diacetin, triethanolamine oleate, and N-(beta-hydroxyethyDfOrmamide. Suitable water-insoluble plasticizers include di(betamethoxyethyl) adipate, dibutyl phthalate, and tributyl phosphate. It has been found that most satisfactory results are usually obtained by use of a water-soluble material. Such plasticizers are compatible with the treating solutions and in many cases reduce the tackiness of the treated yarn upon wetting, which in turn improves the knitting characteris-' tics of the yarn under wet conditions.
The snag-proofing compositions are preferably applied in the 'form of their solutions in water or in aqueous liquids. In the case of acidic resinous materials which are insoluble in water, dilute alkalies, such as sodium hydroxide, ammonium hydroxide or triethanolamine, may be used to effect solution. In some cases it may be desirable to add a certain proportion of a water-miscible ,organic solvent to aid solubility and accelerate drying. Quantities up to 50% have been found useful. It is often desirable to neutralize either acidic or basic water-soluble snag-proofing compositions by suitable means. Thus, for example,
an ethylene-maleic anhydride interpolymer may be solubilized in water by refluxing with 50%- 70% of its weight of sodium hydroxide in dilute aqueous solution. In the case of water-soluble alkyd resins of strongly acid reaction, such as mannitol maleates, the aqueous solution may be' neutralized with dilute ammonium hydroxide before use.
Suitable concentrations of the film-forming materials in the snag-proofing compositions lie in the range of about 2% to about 35%, based on the total solids concentration of the solution.
Concentrations of 4% to 25% have been found most useful.
The viscosity of the snag-proofing composition may vary within wide limits, but a 4% aqueous dispersion of the film-forming material should solution of the composition. The speed at which the roll rotates will vary with the speed of the yarn and will depend upon t. e amount of composition which it is desired to apply to the yarn. Thus, for example, at a yarn speed of 1000 feet per minute and with a roll 3 inches in diameter, a suitable range of roll speeds lies between 2 and 16 revolutions per minute.
It is also suitable to apply the composition by passing the yarn in a continuous fashion through a solution or dispersion thereof, or by dipping loosely wound skeins into,the solution, followed by wringing to remove excess liquor. Any other suitable method may be employed. For example, the snag-proofing composition may be sprayed on a moving strand of yarn.
The amount of residual, air-dried film-forming material applied to the yarn may vary within wide limits but the preferred amount-will lie within the range of 1% to 20% of film-forming material, based on the weight of the dry yarn. The amount of the material on the yarn may in most cases be simply determined by boiling a weighed sample of the treated yarn in a dilute alkaline solution and re-weighing the yarn after drying. The quantity of snag-proofing composition to be applied to the yarn will depend upon the degree of snag protection required and the method to be employed in handling the yarn during knitting. In general, snag protection is increased as the quantity of composition is increased, but with excessive quantities the yarn may stick in the supply package, or undesirable friction may be set up between the yarn and the knitting machine parts. Some experiment is usually necessary to determine the quantity of snag-proofing composition which can be applied to give good protection without excessive sticking or friction. The quantity of composition to be applied will also vary, depending upon the denier of the yarn, the firmness of the yarn package, and the speed of knitting.
As an alternative method, the snag-proofing composition may be applied to the unseamed and unlooped fabric in the gray as obtained from the knitting machine. Although this process results in a high degree of resistance to snagging, it is inconvenient and expensive and, in addition, offers the danger of excessive snag production before treatment can be effected. The residual film-forming material is subsequently removed before or during the final finishing treatment.
The temperature of application of the snagproofing composition may vary between just above the freezing point and just below the boiling point of the solution.
Drying of the treated yarn may be effected at normal temperature or under the influence of heat, as by means of a radiant heater or by a current of heated air. When the yarn is impregnated by a continuous process involving passing the yarn from the original package to a wind-up bobbin, drying may be effected before collecting on the bobbin, as by increasing the length of yarn travel from the point of treatment to the bobbin, or it may be allowed to dry on the bobbin during winding, or by any suitable combination of these two methods.
The concentration of the snag-proofing composition, the temperature of application, and the drying temperature are so chosen in cases of continuous application that appreciable migration of the solution on the wind-up bobbin, and consequent uneven distribution of the filmforming material does not occur. Since the comprising a film-forming material migrat on will be toward the edges of the package, analyses for the amount of the material on yarn cut from the center and edge portions of he bobbin will show whether excessive migration has occurred.
The knitting of the yarn to form a hosiery fabric may be effected on any suitable hosiery knitting machine designed for fiat knitting. For example, a Wildman, 54-gauge, single-unit, fullfashioned hosiery knitting machine is satis actory for the purposes of this invention. The yarn is knit preferably in the wet condition and may suitably be moistened in a wetting trough just before entering the needles.
The products prepared according to the process of this invention may be described as snagresistant, fiat-knit fabrics in the gray, suitable for the preparation of sheer, full-fashioned hosiery comprising synthetic polymer yarns in combination with at least 1% of a dry filmforming composition, basedon the dry fabric, which is tacky in the air-dried state and which is dispersible in an aqueous liquid.
The amount of snag-proofing composition in combination with the knit fabric may be determined by the boil-off procedure outlined above for the estimation of the tacky film-forming material on the treated yarn, and will be substantially the same as for the yarn from which the fabric was knit.
Since it is obvious that many changes and modifications can be made in the above-described details without departing from the nature and spirit of the invention, it is not to be limited to the details described herein except as set forth in the appended claims.
I claim:
1. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
2. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a, snag-proofing composition, an aqueous solution which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
3. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a snag-proofing composition,' an aqueous solution comprising between 2% and 35% of a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
4. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a snag-proofing composition, a solution comprisyarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
5. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
6. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polymer yarn, which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a resinous film-forming material which is tacky in the airdried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
'7. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn, which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
8. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn, which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising a film-forming matrial whichis tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
9. The method of producing sheer knit goods,
substantially free from snags and pulled threads,
from water-insensitive synthetic linear polyamide yarn, which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a film-forming material which is tacky in the air-dried state, andwhich is dispersible in an aqueous liquid,
as a snag-proofing composition, an' aqueous solution comprising a resinous film-forming material whereby to produce a yarn having a tacky coating of said film-forming materiakand knitting said yarn to form sheer knit goods.
10. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn, which comprises applying to said yarn, as a snag-proofing composition, a solution comprising a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
11. The method of producing sheer knit goods, substantially free from snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn,
which is tacky inthe air-dried state, and which is dispersible in an aqueous liquid, whereby to produce a yarn having a tacky coating of said film-forming material, and knitting said yarn to form sheer knit goods.
12. The method of producing sheer knit goods, substantially free fron snags and pulled threads, from water-insensitive synthetic linear polyamide yarn which comprises applying to said yarn, as a snag-proofing composition, an aqueous solution comprising between 2% and 35% of a resinous film-forming material which is tacky in the air-dried state, and which is dispersible in an aqueousliquid, whereby to produce a yarn having a tacky coating of'said film-forming material, and knitting said yarn to form sheer knit goods.
13. The method of producing sheer knit goods, as defined in claim 1, in which the viscosity of the solution of film-forming material is such that a 4% aqueous dispersion of said material has a viscosity of less than 12 poises at the temperature of application. 7
14. The method of producing sheer knit goods, as defined in claim 2, in which the viscosity of the solution of film-forming material is such that a 4% aqueous dispersion of said material has a viscosity of less than 12 poises at the temperature of application,
15. The method of producing sheer knit goods, as defined in claim 3, in which the viscosity of the solution of film-forming material is such that a 4% aqueous dispersion of said material has a viscosity of less than 12 poises at the temperature of application.
16. A synthetic linear polymer yarn containing,
as a snag-proofing composition, a sufficient quantity of a film-forming material to render the yarn snag resistantin the production of sheer knit goods, said film-forming material being tacky in the air-dried state, and being dispersible in an aqueous liquid.
17. A synthetic linear polymer yarn containing, as a snag-proofing composition, 1% to 20% (based on the weight of the dry yarn) of a filmforming material to render the yarn snag resistant in the .production of sheer knit goods, said film-forming material being tacky in the airdried state, and being dispersible in an aqueous liquid. I
18. A synthetic linear polyamide yarn containing, as a snag-proofing composition, a sufficient quantity of a film-forming material to render the yarn snag resistant in the production of sheer knit goods, said film-forming material being tacky in the air-dried state, and being dispersible in an aqueous liquid.
19. A synthetic linear polyamide yarn containing, as a snag-proofing composition.'1% to 20% (based on the weight of the dry yarn) of a film-forming material to render the yarn snag resistant in the production of sheer knit goods,
said film-forming material being tacky in the
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US378943A US2289222A (en) | 1941-02-14 | 1941-02-14 | Yarn preparation |
GB7099/42A GB560084A (en) | 1941-02-14 | 1942-05-26 | Improvements in or relating to the production of knitted fabrics from synthetic linear polyamide yarns |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US378943A US2289222A (en) | 1941-02-14 | 1941-02-14 | Yarn preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
US2289222A true US2289222A (en) | 1942-07-07 |
Family
ID=23495168
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US378943A Expired - Lifetime US2289222A (en) | 1941-02-14 | 1941-02-14 | Yarn preparation |
Country Status (2)
Country | Link |
---|---|
US (1) | US2289222A (en) |
GB (1) | GB560084A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2571251A (en) * | 1946-07-20 | 1951-10-16 | Celanese Corp | Polymeric carboxy amide compounds and processes for their production |
US2676164A (en) * | 1950-03-09 | 1954-04-20 | Ici Ltd | Coated nylon fabrics |
US2686137A (en) * | 1951-11-26 | 1954-08-10 | Monsanto Chemicals | Sized yarn and process of sizing |
US3066383A (en) * | 1957-02-14 | 1962-12-04 | Owens Corning Fiberglass Corp | Finish for staple glass fibers and yarns manufactured thereof |
US3214252A (en) * | 1962-04-02 | 1965-10-26 | Colgate Palmolive Co | Fuel gel compositions |
WO2008049251A1 (en) * | 2006-10-23 | 2008-05-02 | Schoeller Textil Ag | Microbicidal nano- and meso-polymer fibers produced from polymers and honey, for textile applications |
CN108120625A (en) * | 2017-09-30 | 2018-06-05 | 广东华科检测技术服务有限公司 | Total lead and total cadmium standard sample and preparation method thereof in textile |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB815830A (en) * | 1955-09-06 | 1959-07-01 | Monsanto Chemicals | Sizing nylon yarns |
-
1941
- 1941-02-14 US US378943A patent/US2289222A/en not_active Expired - Lifetime
-
1942
- 1942-05-26 GB GB7099/42A patent/GB560084A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2571251A (en) * | 1946-07-20 | 1951-10-16 | Celanese Corp | Polymeric carboxy amide compounds and processes for their production |
US2676164A (en) * | 1950-03-09 | 1954-04-20 | Ici Ltd | Coated nylon fabrics |
US2686137A (en) * | 1951-11-26 | 1954-08-10 | Monsanto Chemicals | Sized yarn and process of sizing |
US3066383A (en) * | 1957-02-14 | 1962-12-04 | Owens Corning Fiberglass Corp | Finish for staple glass fibers and yarns manufactured thereof |
US3214252A (en) * | 1962-04-02 | 1965-10-26 | Colgate Palmolive Co | Fuel gel compositions |
WO2008049251A1 (en) * | 2006-10-23 | 2008-05-02 | Schoeller Textil Ag | Microbicidal nano- and meso-polymer fibers produced from polymers and honey, for textile applications |
CN108120625A (en) * | 2017-09-30 | 2018-06-05 | 广东华科检测技术服务有限公司 | Total lead and total cadmium standard sample and preparation method thereof in textile |
Also Published As
Publication number | Publication date |
---|---|
GB560084A (en) | 1944-03-20 |
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