US3652419A - Antistatic fiber lubricant - Google Patents
Antistatic fiber lubricant Download PDFInfo
- Publication number
- US3652419A US3652419A US710761A US3652419DA US3652419A US 3652419 A US3652419 A US 3652419A US 710761 A US710761 A US 710761A US 3652419D A US3652419D A US 3652419DA US 3652419 A US3652419 A US 3652419A
- Authority
- US
- United States
- Prior art keywords
- parts
- alcohol
- fiber
- weight
- emulsion
- 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
- 239000000835 fiber Substances 0.000 title abstract description 36
- 239000000314 lubricant Substances 0.000 title abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 36
- 239000000839 emulsion Substances 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- -1 ethoxylated alkyl phenol Chemical compound 0.000 abstract description 16
- 150000003014 phosphoric acid esters Chemical class 0.000 abstract description 11
- 239000002480 mineral oil Substances 0.000 abstract description 9
- 235000010446 mineral oil Nutrition 0.000 abstract description 9
- 125000005233 alkylalcohol group Chemical group 0.000 abstract description 8
- 150000004702 methyl esters Chemical class 0.000 abstract description 6
- 239000001816 polyoxyethylene sorbitan tristearate Substances 0.000 abstract description 6
- 235000010988 polyoxyethylene sorbitan tristearate Nutrition 0.000 abstract description 6
- 150000004668 long chain fatty acids Chemical class 0.000 abstract description 2
- 230000007774 longterm Effects 0.000 abstract description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- 239000004753 textile Substances 0.000 description 8
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- 239000005642 Oleic acid Substances 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
- 229940043276 diisopropanolamine Drugs 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229940070765 laurate Drugs 0.000 description 2
- 229940049918 linoleate Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- 239000007764 o/w emulsion Substances 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- REIUXOLGHVXAEO-UHFFFAOYSA-N pentadecan-1-ol Chemical compound CCCCCCCCCCCCCCCO REIUXOLGHVXAEO-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- XEFJFCAXFQMSSY-UHFFFAOYSA-N 13-hydroxytridecanal Chemical compound OCCCCCCCCCCCCC=O XEFJFCAXFQMSSY-UHFFFAOYSA-N 0.000 description 1
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
- ILJOIOLSOMYKNF-UHFFFAOYSA-N 2,3-didodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCCCCC ILJOIOLSOMYKNF-UHFFFAOYSA-N 0.000 description 1
- PTMRDOLOEDPHLB-UHFFFAOYSA-N 2,3-dipentylphenol Chemical compound CCCCCC1=CC=CC(O)=C1CCCCC PTMRDOLOEDPHLB-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- HTRVTKUOKQWGMO-UHFFFAOYSA-N 2-ethyloctan-1-ol Chemical compound CCCCCCC(CC)CO HTRVTKUOKQWGMO-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920004934 Dacron® Polymers 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-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
- 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
- 239000005639 Lauric acid Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004165 Methyl ester of fatty acids Substances 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940058344 antitrematodals organophosphorous compound Drugs 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 150000002028 dodecanols Chemical class 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- ZAZKJZBWRNNLDS-UHFFFAOYSA-N methyl tetradecanoate Chemical class CCCCCCCCCCCCCC(=O)OC ZAZKJZBWRNNLDS-UHFFFAOYSA-N 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- 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
- D06M15/53—Polyethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
-
- 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
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
Definitions
- ABSTRACT An emulsifiable antistatic fiber lubricant composition, which exhibits excellent long term emulsion stability, comprising a mixture of a mineral oil, a methyl ester of a long chain fatty acid, a neutralized phosphoric acid ester of an ethoxylated alkyl phenol or alkyl alcohol, a polyoxyethylene sorbitan tristearate and fatty alkanolamide.
- compositions applied to textile fibers must also have antistatic properties.
- the problem of preventing the accumulation of static changes on textiles has troubled the industry for a number of years. This property of retaining static electrical charges is most often encountered in the processing of synthetic fibers such as are manufactured from polyesters and polyamides, polyvinyl chloride, polyvinyl acetate and other vinyl polymerization products as well as polymers of acrylic acid derivatives.
- a novel emulsifiable antistatic fiber lubricant which comprises in combination one or more of each of the following materials in the stated parts by weight:
- a polyoxyethylene sorbitan tristearate from about eight to 10 parts;
- An alkanolamide of a C to C normally liquid fatty acid from about 3 to 4 parts.
- the phosphoric acid esters which, as prepared, are generally mixtures of monoand di-esters, are preferably made by reacting 1 mol of P with from 2 to 4.5 mols of the ethylene oxide adducts of the linear alkyl alcohol or the alkyl phenol, as the case may be, at a temperature in the range up about 100 C, in the presence or in the absence of an inert organic liquid diluent, most advantageously in the range of about 50 to 65 C.
- Such phosphating procedures are disclosed, for instance, in US. Pat. Nos. 2,441,295; 2,676,975; 2,701,258 and 3,004,056; Chemical Industries, Oct. 1942, pp. 516-521 and 557; and Organo Phosphorous Compounds, John Wiley & Sons, New York, 1950, pp. 220-223.
- Illustrative alcohols and alkyl phenols from which the aforesaid ethylene oxide-adducts are made and which are reacted, for example, with P 0 to produce said phosphoric acid esters are n-octyl alcohol, n-nonyl alcohol, n-decyl alcohol, n-dodecyl alcohol, n-tridecyl alcohol, n-tetradecyl alcohol, n-pentadecyl alcohol, n-hexadecyl alcohol, oleyl alcohol, n-stearyl alcohol; Oxo alcohols containing from to 20 carbon exemplified by Oxo tridecyl alcohol, 0x0 hexadecyl alcohol, and Oxopentadecyl alcohol (and others as shown in U.S.
- dodecyl phenol and didodecyl phenol are the phosphoric acid esters of the 2 to 8 mol ethylene oxide adducts of C to C linear alkyl alcohols (decyl undecyl, dodecyl, tridecyl and tetradecyl alcohols) and mixtures of two or more of said alcohols.
- the phosphoric acid ester may be neutralized with an alkali (e.g. hydroxide of an alkali metal such as sodium, potassium, lithium or ammonium) in situ during the preparation of the lubricant composition or it may be added in the neutralized form.
- an alkali e.g. hydroxide of an alkali metal such as sodium, potassium, lithium or ammonium
- potassium hydroxide is used as the neutralizing agent because of its better solubility, and it is conveniently added as a 45 percent solution.
- the exact quantity of base added is dependent upon stoichiometric considerations. Generally, a slight excess over the stoichiometric amount is used since the desired pH range of the ultimate emulsion composition is in the range of 7.5-8.5. This final pH has been found particularly suitable because of emulsion stability demands and, also, to prevent or inhibit corrosion when the composition is contacted with textile fibers and machincry.
- the methyl esters of fatty acids useful in the compositions of the present invention comprise the methyl esters of C to C saturated and unsaturated fatty acids, illustrative examples of said acids being lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, palmitoleic acid, tall oil fatty acids, and commercial and other mixtures of said acids such as coconut oil mixed fatty acids and various narrower fractions of mixed fatty acids.
- a particularly desirable commercial mixture of fatty acid methyl esters is that sold under the designation CE-l8 by The Procter & Gamble Company and consisting of about percent oleate, linoleate and stearate, 25 percent palmitate and the remainder varying amounts of laurate and myristate methyl esters.
- the polyoxyethylene sorbitan tristearate is generally produced by condensing sorbitan tristearate with ethylene oxide.
- this compound should have an HLB value of from about 8 to 15, or 40 to weight percent ethylene oxide.
- a polyoxyethylene sorbitan tristearate containing about 52 weight percent ethylene oxide is particularly suitable.
- alkanolamides of the C to C normally liquid fatty acids which constitute one of the ingredients of the compositions of the present invention include, by way of illustration, oleic diethanolamide, tall oil fatty acid diethanolamide, linole ic acid diethanolamide and the corresponding fatty acid amides of glycerol monoand di-amines, dipropanolamine, diisopropanolamine, aminoethyl ethanolamine, dibutanolamine and diisobutanolamine.
- Oleic diethanolamide is especially satisfactory and it may be made, for instance, by condensing equal mols of diethanolamine and oleic acid, or by condensing about 1.5 to 2 mols of diethanolamine with 1 mol of oleic acid, at temperatures of 150 to 165 C. for several hours, or by condensing the oleic acid, in the form of an ester thereof, such as the triglyceride ester, with diethanolamine, or by condensing methyl oleate with diethanolamine in the presence of sodium methylate as a catalyst, or by oxyethylating the amide of oleic acid.
- the order of mixing the ingredients in preparing the emulsifiable lubricant compositions of the present invention is not critical but it is usually more convenient to add the several ingredients, with mixing, to the mineral oil.
- emulsification occurs readily at temperatures above as well as below room temperatures in water, including tap water, by simply mixing the lubricant composition with the water.
- an emulsion containing 10 percent by weight of the lubricant composition may be prepared quite readily at 10 C. with no separation observable over a 24 hour period.
- the preferred oil-in-water emulsions consist of 10 weight parts of the lubricating composition and weight parts of water. However, this range may be varied considerably as, for example, 5 to 20 parts of the lubricating composition and to 80 parts of water. Generally, it is not desirable to exceed about 30 percent by weight of the lubricating composition since the emulsion tends to thicken at these higher levels and stability tends to become marginal. Hence, generally speaking, said emulsions will comprise 70 to 99 parts of water and 30 to l parts of the lubricant composition.
- compositions of the present invention achieve highly satisfactory fiber to fiber and fiber to metal frictional properties. An accumulation of electrostatic charges on treated fibers is largely or substantially eliminated.
- Application to the fibers may be by any conventional means such as by immersion, spraying or roll application.
- a liquid emulsifiable antistatic fiber lubricant was prepared by combining the following components:
- a 10 percent emulsion was prepared using each of the compositions of examples ll-V and stored at room temperature for visual observations of the stability of the emulsion. After 24 hours, little or no evidence of creaming, oiling or ring formation was perceived.
- EXAMPLE VII The following results demonstrate the friction characteristics of fibers which were treated with emulsions prepared using compositions of the present invention. The tests were conducted using a Rothschild tension analyzer, which furnishes a continuous recording of tension in grams as the fibers are tested.
- An oil-in-water fiber lubricant emulsion consisting essentially of 70-99 parts by weight of water and 30-1 parts by weight of a mineral oil composition consisting essentially of, by weight,
- An aqueous emulsion comprising, by weight, about parts of water and about 10 parts of the composition of claim 1.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71076168A | 1968-03-06 | 1968-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3652419A true US3652419A (en) | 1972-03-28 |
Family
ID=24855415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US710761A Expired - Lifetime US3652419A (en) | 1968-03-06 | 1968-03-06 | Antistatic fiber lubricant |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3652419A (fr) |
| BE (1) | BE749964A (fr) |
| DE (1) | DE2022888A1 (fr) |
| FR (1) | FR2088014B1 (fr) |
| GB (1) | GB1285391A (fr) |
| NL (1) | NL7006309A (fr) |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3888775A (en) * | 1972-01-29 | 1975-06-10 | Teijin Ltd | Oil composition for synthetic staple fibers |
| US3898166A (en) * | 1973-01-16 | 1975-08-05 | Gaf Corp | Organic antistatic composition |
| FR2292068A1 (fr) * | 1973-11-22 | 1976-06-18 | Ici Ltd | Ensimage pour textiles et applications |
| US3977979A (en) * | 1973-09-14 | 1976-08-31 | George A. Goulston Company, Inc. | Yarn finish formulations |
| US3997450A (en) * | 1972-04-10 | 1976-12-14 | Fiber Industries, Inc. | Synthetic fibers of enhanced processability |
| US4051299A (en) * | 1974-03-15 | 1977-09-27 | Fiber Industries Inc. | Synthetic fibers of enhanced processability |
| US4052321A (en) * | 1976-03-17 | 1977-10-04 | Dixie Yarns, Inc. | Flame-retardant yarn or thread containing brominated ester of oleic or linoleic acid |
| US4080301A (en) * | 1975-06-27 | 1978-03-21 | Hoechst Aktiengesellschaft | Conditioning agents for the texturizing of polyester fibers |
| US4085052A (en) * | 1974-04-16 | 1978-04-18 | The Procter & Gamble Company | Fabric treatment compositions |
| US4446034A (en) * | 1981-09-25 | 1984-05-01 | Bayer Aktiengesellschaft | Textile-treatment agents, and their use for finishing textile materials |
| US5190676A (en) * | 1989-11-30 | 1993-03-02 | Kao Corporation | High-speed spinning oil composition containing an organophosphoric ester salt and an oxyalkylene polymer |
| US5288416A (en) * | 1992-01-27 | 1994-02-22 | Milliken Research Corporation | Finish for textile fibers containing silahydrocarbon lubricants and nonionic emulsifiers having a plurality of hydrocarbon chains |
| USRE35621E (en) * | 1989-05-30 | 1997-10-07 | Hercules Incorporated | Cardable hydrophobic polypropylene fiber, material and method for preparation thereof |
| US5721048A (en) * | 1990-11-15 | 1998-02-24 | Fiberco, Inc. | Cardable hydrophobic polyolefin fiber, material and method for preparation thereof |
| US5733863A (en) * | 1997-01-17 | 1998-03-31 | The Procter & Gamble Company | Process for making a free-flowing particule detergent admix containing nonionic surfactant |
| US5739094A (en) * | 1997-01-17 | 1998-04-14 | The Procter & Gamble Company | Free-flowing particulate detergent admix composition containing nonionic surfactant |
| US5830240A (en) * | 1996-10-23 | 1998-11-03 | Solutia Inc. | Fibers and textile materials having enhanced dyeability and finish compositions used thereon |
| US5944852A (en) * | 1996-10-23 | 1999-08-31 | Solutia Inc. | Dyeing process |
| US5980772A (en) * | 1997-02-25 | 1999-11-09 | Takemoto Yushi Kabushiki Kaisha | Lubricants for and methods of processing synthetic fibers |
| US6139764A (en) * | 1998-02-09 | 2000-10-31 | Bayer Aktiengesellschaft | Biodegradable coating compositions |
| US20040007687A1 (en) * | 2002-07-11 | 2004-01-15 | Hubert Dobbelstein | Formulation of a highly viscous mineral oil for the production of filters for tobacco products |
| US20040131790A1 (en) * | 2003-01-07 | 2004-07-08 | Voegtli Leo Paul | Method for using an ethoxylated alkyl phosphate ester additive as plugmaker processing aid |
| US20050202993A1 (en) * | 2003-01-07 | 2005-09-15 | Voegtli Leo P. | Method for using an ethoxylated alkyl phosphate ester additive as a plugmaker processing aid |
| BE1023475B1 (nl) * | 2016-06-09 | 2017-04-03 | Vertexco Nv | Werkwijze voor het vervaardigen van een spinolie |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6269881A (ja) * | 1985-09-17 | 1987-03-31 | 花王株式会社 | 合成繊維処理用油剤 |
| JP4097266B2 (ja) * | 2003-08-07 | 2008-06-11 | 竹本油脂株式会社 | 合成繊維処理剤の低濃度水性液の調製方法、合成繊維処理剤の低濃度水性液及び合成繊維の処理方法 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2496631A (en) * | 1946-07-08 | 1950-02-07 | Nopco Chem Co | Wool treatment |
| US2690426A (en) * | 1950-03-07 | 1954-09-28 | Atlas Powder Co | Lubricating compositions |
| US2730498A (en) * | 1952-01-09 | 1956-01-10 | Celanese Corp | Textile lubricants |
| US3056744A (en) * | 1957-09-18 | 1962-10-02 | Gen Aniline & Film Corp | Textile assistant |
| US3170877A (en) * | 1961-12-21 | 1965-02-23 | Gen Aniline & Film Corp | Antistatic treating solution for polyacrylonitrile fibers and method |
| US3336222A (en) * | 1965-01-19 | 1967-08-15 | Nopco Chem Co | Cotton treating compositions |
| US3428560A (en) * | 1967-02-27 | 1969-02-18 | Du Pont | Yarn-lubricating composition |
-
1968
- 1968-03-06 US US710761A patent/US3652419A/en not_active Expired - Lifetime
-
1970
- 1970-04-22 GB GB09181/70A patent/GB1285391A/en not_active Expired
- 1970-04-29 NL NL7006309A patent/NL7006309A/xx unknown
- 1970-05-05 BE BE749964A patent/BE749964A/fr unknown
- 1970-05-08 FR FR7016769A patent/FR2088014B1/fr not_active Expired
- 1970-05-11 DE DE19702022888 patent/DE2022888A1/de active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2496631A (en) * | 1946-07-08 | 1950-02-07 | Nopco Chem Co | Wool treatment |
| US2690426A (en) * | 1950-03-07 | 1954-09-28 | Atlas Powder Co | Lubricating compositions |
| US2730498A (en) * | 1952-01-09 | 1956-01-10 | Celanese Corp | Textile lubricants |
| US3056744A (en) * | 1957-09-18 | 1962-10-02 | Gen Aniline & Film Corp | Textile assistant |
| US3170877A (en) * | 1961-12-21 | 1965-02-23 | Gen Aniline & Film Corp | Antistatic treating solution for polyacrylonitrile fibers and method |
| US3336222A (en) * | 1965-01-19 | 1967-08-15 | Nopco Chem Co | Cotton treating compositions |
| US3428560A (en) * | 1967-02-27 | 1969-02-18 | Du Pont | Yarn-lubricating composition |
Cited By (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3888775A (en) * | 1972-01-29 | 1975-06-10 | Teijin Ltd | Oil composition for synthetic staple fibers |
| US3997450A (en) * | 1972-04-10 | 1976-12-14 | Fiber Industries, Inc. | Synthetic fibers of enhanced processability |
| US3898166A (en) * | 1973-01-16 | 1975-08-05 | Gaf Corp | Organic antistatic composition |
| US3977979A (en) * | 1973-09-14 | 1976-08-31 | George A. Goulston Company, Inc. | Yarn finish formulations |
| US4098703A (en) * | 1973-09-14 | 1978-07-04 | George A. Goulston Company, Inc. | Yarn finish formulations |
| FR2292068A1 (fr) * | 1973-11-22 | 1976-06-18 | Ici Ltd | Ensimage pour textiles et applications |
| US4051299A (en) * | 1974-03-15 | 1977-09-27 | Fiber Industries Inc. | Synthetic fibers of enhanced processability |
| US4085052A (en) * | 1974-04-16 | 1978-04-18 | The Procter & Gamble Company | Fabric treatment compositions |
| US4080301A (en) * | 1975-06-27 | 1978-03-21 | Hoechst Aktiengesellschaft | Conditioning agents for the texturizing of polyester fibers |
| US4052321A (en) * | 1976-03-17 | 1977-10-04 | Dixie Yarns, Inc. | Flame-retardant yarn or thread containing brominated ester of oleic or linoleic acid |
| US4446034A (en) * | 1981-09-25 | 1984-05-01 | Bayer Aktiengesellschaft | Textile-treatment agents, and their use for finishing textile materials |
| EP0075770A3 (en) * | 1981-09-25 | 1985-01-16 | Bayer Ag | Textile treating composition and its use in finishing textile materials |
| USRE35621E (en) * | 1989-05-30 | 1997-10-07 | Hercules Incorporated | Cardable hydrophobic polypropylene fiber, material and method for preparation thereof |
| US5190676A (en) * | 1989-11-30 | 1993-03-02 | Kao Corporation | High-speed spinning oil composition containing an organophosphoric ester salt and an oxyalkylene polymer |
| US5721048A (en) * | 1990-11-15 | 1998-02-24 | Fiberco, Inc. | Cardable hydrophobic polyolefin fiber, material and method for preparation thereof |
| US5288416A (en) * | 1992-01-27 | 1994-02-22 | Milliken Research Corporation | Finish for textile fibers containing silahydrocarbon lubricants and nonionic emulsifiers having a plurality of hydrocarbon chains |
| US5830240A (en) * | 1996-10-23 | 1998-11-03 | Solutia Inc. | Fibers and textile materials having enhanced dyeability and finish compositions used thereon |
| US5944852A (en) * | 1996-10-23 | 1999-08-31 | Solutia Inc. | Dyeing process |
| US5733863A (en) * | 1997-01-17 | 1998-03-31 | The Procter & Gamble Company | Process for making a free-flowing particule detergent admix containing nonionic surfactant |
| US5739094A (en) * | 1997-01-17 | 1998-04-14 | The Procter & Gamble Company | Free-flowing particulate detergent admix composition containing nonionic surfactant |
| US5980772A (en) * | 1997-02-25 | 1999-11-09 | Takemoto Yushi Kabushiki Kaisha | Lubricants for and methods of processing synthetic fibers |
| US6139764A (en) * | 1998-02-09 | 2000-10-31 | Bayer Aktiengesellschaft | Biodegradable coating compositions |
| US20040007687A1 (en) * | 2002-07-11 | 2004-01-15 | Hubert Dobbelstein | Formulation of a highly viscous mineral oil for the production of filters for tobacco products |
| US7153447B2 (en) * | 2002-07-11 | 2006-12-26 | Emini Shefqet | Formulation of a highly viscous mineral oil for the production of filters for tobacco products |
| US20040131790A1 (en) * | 2003-01-07 | 2004-07-08 | Voegtli Leo Paul | Method for using an ethoxylated alkyl phosphate ester additive as plugmaker processing aid |
| US20050202179A1 (en) * | 2003-01-07 | 2005-09-15 | Voegtli Leo P. | Method for using an ethoxylated alkyl phosphate ester additive as a plugmaker processing aid |
| US20050202993A1 (en) * | 2003-01-07 | 2005-09-15 | Voegtli Leo P. | Method for using an ethoxylated alkyl phosphate ester additive as a plugmaker processing aid |
| BE1023475B1 (nl) * | 2016-06-09 | 2017-04-03 | Vertexco Nv | Werkwijze voor het vervaardigen van een spinolie |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7006309A (fr) | 1971-11-02 |
| BE749964A (fr) | 1970-10-16 |
| DE2022888A1 (de) | 1971-11-25 |
| FR2088014B1 (fr) | 1974-09-20 |
| GB1285391A (en) | 1972-08-16 |
| FR2088014A1 (fr) | 1972-01-07 |
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