CA1299164C - Compositions lubrifiantes pour les fibres tisses - Google Patents

Compositions lubrifiantes pour les fibres tisses

Info

Publication number: CA1299164C
Authority: CA; Canada
Prior art keywords: carbon atoms; groups; alkyl; composition; process according
Prior art date: 1987-08-06
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 - Fee Related

Application number

CA000573637A

Other languages

English (en)

Inventor

Gregory A. Lentz

Richard Yodice

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Lubrizol Corp

Original Assignee

Lubrizol Corp

Priority date (The priority date 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 date listed.)

1987-08-06

Filing date

1988-08-02

Publication date

1992-04-21

1988-08-02 Application filed by Lubrizol Corp filed Critical Lubrizol Corp

1992-04-21 Application granted granted Critical

1992-04-21 Publication of CA1299164C publication Critical patent/CA1299164C/fr

2009-04-21 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 89
239000000835 fiber Substances 0.000 title claims abstract description 40
239000000314 lubricant Substances 0.000 title claims abstract description 28
150000002148 esters Chemical class 0.000 claims abstract description 42
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 39
125000000217 alkyl group Chemical group 0.000 claims abstract description 28
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 22
239000007788 liquid Substances 0.000 claims abstract description 18
239000000463 material Substances 0.000 claims abstract description 11
238000000034 method Methods 0.000 claims description 28
-1 alpha-naphthyl Chemical group 0.000 claims description 22
125000003342 alkenyl group Chemical group 0.000 claims description 16
125000003118 aryl group Chemical group 0.000 claims description 12
238000006243 chemical reaction Methods 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
125000002877 alkyl aryl group Chemical group 0.000 claims description 5
125000003710 aryl alkyl group Chemical group 0.000 claims description 5
239000012141 concentrate Substances 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 3
230000000996 additive effect Effects 0.000 claims description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
239000003377 acid catalyst Substances 0.000 claims description 2
239000002657 fibrous material Substances 0.000 claims 8
239000003995 emulsifying agent Substances 0.000 abstract description 21
238000009987 spinning Methods 0.000 abstract description 8
230000001050 lubricating effect Effects 0.000 abstract description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 14
238000006386 neutralization reaction Methods 0.000 description 10
238000012545 processing Methods 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 7
239000000047 product Substances 0.000 description 7
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
229940014800 succinic anhydride Drugs 0.000 description 6
239000004215 Carbon black (E152) Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195733 hydrocarbon Natural products 0.000 description 5
150000002430 hydrocarbons Chemical class 0.000 description 5
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 5
229920000742 Cotton Polymers 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
150000008064 anhydrides Chemical class 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
239000003240 coconut oil Substances 0.000 description 4
235000019864 coconut oil Nutrition 0.000 description 4
150000002009 diols Chemical class 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
230000003068 static effect Effects 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
239000004753 textile Substances 0.000 description 4
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
CWPPDTVYIJETDF-UHFFFAOYSA-N 2,2,4-trimethylpentan-1-ol Chemical compound CC(C)CC(C)(C)CO CWPPDTVYIJETDF-UHFFFAOYSA-N 0.000 description 3
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
239000005639 Lauric acid Substances 0.000 description 3
239000005642 Oleic acid Substances 0.000 description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
125000002723 alicyclic group Chemical group 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
150000001336 alkenes Chemical class 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
125000005842 heteroatom Chemical group 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
229920005862 polyol Polymers 0.000 description 3
150000003077 polyols Chemical class 0.000 description 3
229920001155 polypropylene Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000000600 sorbitol Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
229920002994 synthetic fiber Polymers 0.000 description 3
239000012209 synthetic fiber Substances 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
229920002292 Nylon 6 Polymers 0.000 description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 2
PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 2
238000009825 accumulation Methods 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
239000010696 ester oil Substances 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
GPSDUZXPYCFOSQ-UHFFFAOYSA-N m-toluic acid Chemical compound CC1=CC=CC(C(O)=O)=C1 GPSDUZXPYCFOSQ-UHFFFAOYSA-N 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
239000011976 maleic acid Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
238000012544 monitoring process Methods 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 2
KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 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
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
238000005292 vacuum distillation Methods 0.000 description 2
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
BTANRVKWQNVYAZ-SCSAIBSYSA-N (2R)-butan-2-ol Chemical compound CC[C@@H](C)O BTANRVKWQNVYAZ-SCSAIBSYSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical class CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
FAMOAJMEFGYSNY-UHFFFAOYSA-N 2,2,3-trimethylbutan-1-ol Chemical compound CC(C)C(C)(C)CO FAMOAJMEFGYSNY-UHFFFAOYSA-N 0.000 description 1
DPQMSIBAADLGOH-UHFFFAOYSA-N 2,2,3-trimethylheptan-1-ol Chemical compound CCCCC(C)C(C)(C)CO DPQMSIBAADLGOH-UHFFFAOYSA-N 0.000 description 1
JOIXNHFTNRBQKV-UHFFFAOYSA-N 2,2,3-trimethylhexan-1-ol Chemical compound CCCC(C)C(C)(C)CO JOIXNHFTNRBQKV-UHFFFAOYSA-N 0.000 description 1
UZLMLMBSIFQWNQ-UHFFFAOYSA-N 2,2,3-trimethyloctan-1-ol Chemical compound CCCCCC(C)C(C)(C)CO UZLMLMBSIFQWNQ-UHFFFAOYSA-N 0.000 description 1
GBONVOIRPAJSLA-UHFFFAOYSA-N 2,2,3-trimethylpentan-1-ol Chemical compound CCC(C)C(C)(C)CO GBONVOIRPAJSLA-UHFFFAOYSA-N 0.000 description 1
RUCVXMGJYFHUNW-UHFFFAOYSA-N 2,2,4-trimethylheptan-1-ol Chemical compound CCCC(C)CC(C)(C)CO RUCVXMGJYFHUNW-UHFFFAOYSA-N 0.000 description 1
JNWGRGISOITMRT-UHFFFAOYSA-N 2,2,4-trimethylhexan-1-ol Chemical compound CCC(C)CC(C)(C)CO JNWGRGISOITMRT-UHFFFAOYSA-N 0.000 description 1
MLLTYLFVMSOCDE-UHFFFAOYSA-N 2,2,4-trimethyloctan-1-ol Chemical compound CCCCC(C)CC(C)(C)CO MLLTYLFVMSOCDE-UHFFFAOYSA-N 0.000 description 1
CBHXDVOSUKFRBE-UHFFFAOYSA-N 2,2-diethylbutan-1-ol Chemical compound CCC(CC)(CC)CO CBHXDVOSUKFRBE-UHFFFAOYSA-N 0.000 description 1
MTSKTUBCXKHUNW-UHFFFAOYSA-N 2,2-diethylheptan-1-ol Chemical compound CCCCCC(CC)(CC)CO MTSKTUBCXKHUNW-UHFFFAOYSA-N 0.000 description 1
ZJWBZTYQOAZXFH-UHFFFAOYSA-N 2,2-diethylhexan-1-ol Chemical compound CCCCC(CC)(CC)CO ZJWBZTYQOAZXFH-UHFFFAOYSA-N 0.000 description 1
MJKPLVMBVACMFD-UHFFFAOYSA-N 2,2-diethyloctan-1-ol Chemical compound CCCCCCC(CC)(CC)CO MJKPLVMBVACMFD-UHFFFAOYSA-N 0.000 description 1
PHSORZZLPKIHMG-UHFFFAOYSA-N 2,2-diethylpentan-1-ol Chemical compound CCCC(CC)(CC)CO PHSORZZLPKIHMG-UHFFFAOYSA-N 0.000 description 1
KEXGXAGJHHCTKD-UHFFFAOYSA-N 2,2-dimethyl-1-Octanol Chemical compound CCCCCCC(C)(C)CO KEXGXAGJHHCTKD-UHFFFAOYSA-N 0.000 description 1
XRMVWAKMXZNZIL-UHFFFAOYSA-N 2,2-dimethyl-1-butanol Chemical compound CCC(C)(C)CO XRMVWAKMXZNZIL-UHFFFAOYSA-N 0.000 description 1
WENIXZFPXMQPQQ-UHFFFAOYSA-N 2,2-dimethylheptan-1-ol Chemical compound CCCCCC(C)(C)CO WENIXZFPXMQPQQ-UHFFFAOYSA-N 0.000 description 1
GSSDZVRLQDXOPL-UHFFFAOYSA-N 2,2-dimethylhexan-1-ol Chemical compound CCCCC(C)(C)CO GSSDZVRLQDXOPL-UHFFFAOYSA-N 0.000 description 1
QTOMCRXZFDHJOL-UHFFFAOYSA-N 2,2-dimethylpentan-1-ol Chemical compound CCCC(C)(C)CO QTOMCRXZFDHJOL-UHFFFAOYSA-N 0.000 description 1
FGHRPUDKGNHDRL-UHFFFAOYSA-N 2,3,3-trimethyloctan-1-ol Chemical compound CCCCCC(C)(C)C(C)CO FGHRPUDKGNHDRL-UHFFFAOYSA-N 0.000 description 1
YPIJDMPDVZUWJO-UHFFFAOYSA-N 2-ethyl-2,3-dimethylbutan-1-ol Chemical compound CCC(C)(CO)C(C)C YPIJDMPDVZUWJO-UHFFFAOYSA-N 0.000 description 1
KMWHQWJVSALJAW-UHFFFAOYSA-N 2-ethyl-2-methylbutan-1-ol Chemical compound CCC(C)(CC)CO KMWHQWJVSALJAW-UHFFFAOYSA-N 0.000 description 1
JILNFHMXFBDGGA-UHFFFAOYSA-N 2-ethyl-2-methylheptan-1-ol Chemical compound CCCCCC(C)(CC)CO JILNFHMXFBDGGA-UHFFFAOYSA-N 0.000 description 1
DKYDBQBEFXCOJY-UHFFFAOYSA-N 2-ethyl-2-methylhexan-1-ol Chemical compound CCCCC(C)(CC)CO DKYDBQBEFXCOJY-UHFFFAOYSA-N 0.000 description 1
WYXFVKVSSZIDSO-UHFFFAOYSA-N 2-ethyl-2-methyloctan-1-ol Chemical compound CCCCCCC(C)(CC)CO WYXFVKVSSZIDSO-UHFFFAOYSA-N 0.000 description 1
VZCOFGHOKLEMPL-UHFFFAOYSA-N 2-ethyl-2-methylpentan-1-ol Chemical compound CCCC(C)(CC)CO VZCOFGHOKLEMPL-UHFFFAOYSA-N 0.000 description 1
WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
QYFVEEMPFRRFNN-UHFFFAOYSA-N 5,5-dimethylhexan-1-ol Chemical compound CC(C)(C)CCCCO QYFVEEMPFRRFNN-UHFFFAOYSA-N 0.000 description 1
235000021357 Behenic acid Nutrition 0.000 description 1
DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
206010019233 Headaches Diseases 0.000 description 1
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
235000020661 alpha-linolenic acid Nutrition 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
VWUKKHOWCKZNLN-UHFFFAOYSA-N benzoic acid 2-methylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1.CC1=CC=CC=C1C(O)=O VWUKKHOWCKZNLN-UHFFFAOYSA-N 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
238000010622 cold drawing Methods 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
239000013058 crude material Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004122 cyclic group Chemical class 0.000 description 1
125000000392 cycloalkenyl group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000002704 decyl 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])* 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
239000004744 fabric Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000012530 fluid Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
231100000869 headache Toxicity 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229940070765 laurate Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
150000002646 long chain fatty acid esters Chemical class 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
229960002446 octanoic acid Drugs 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000035939 shock Effects 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
PGAANEHXBMZPPR-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O.OC(=O)CCCCCCCCCCCC(O)=O PGAANEHXBMZPPR-UHFFFAOYSA-N 0.000 description 1
229940005605 valeric acid Drugs 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
238000004804 winding Methods 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—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
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/188—Monocarboxylic acids; Anhydrides, halides or salts 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
- 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
- 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

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Lubricants (AREA)

CA000573637A 1987-08-06 1988-08-02 Compositions lubrifiantes pour les fibres tisses Expired - Fee Related CA1299164C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US8276987A	1987-08-06	1987-08-06
US82,769		1987-08-06

Publications (1)

Publication Number	Publication Date
CA1299164C true CA1299164C (fr)	1992-04-21

Family

ID=22173352

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000573637A Expired - Fee Related CA1299164C (fr)	1987-08-06	1988-08-02	Compositions lubrifiantes pour les fibres tisses

Country Status (10)

Country	Link
EP (1)	EP0340250B1 (fr)
JP (1)	JPH02500292A (fr)
AT (1)	ATE112594T1 (fr)
BR (1)	BR8807291A (fr)
CA (1)	CA1299164C (fr)
DE (1)	DE3851748T2 (fr)
HK (1)	HK31695A (fr)
MX (1)	MX164866B (fr)
WO (1)	WO1989001071A1 (fr)
ZA (1)	ZA885775B (fr)

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3177143A (en) *	1959-05-25	1965-04-06	Exxon Research Engineering Co	Emulsion for the conditioning of raw cotton fibers
FR1336631A (fr) *	1961-10-27	1963-08-30	British Nylon Spinners Ltd	Apparêts pour filaments synthétiques
FR1442882A (fr) *	1964-08-05	1966-06-17	Hoechst Ag	Produits anti-mousse
US3464922A (en) *	1965-12-10	1969-09-02	Drew Chem Corp	Trimethylolalkane esters and method of treating textile filaments therewith
US3575856A (en) *	1967-07-06	1971-04-20	Du Pont	Fiber lubricating composition and method
GB1492052A (en) *	1974-10-28	1977-11-16	Pvo International Inc	Filament finishing
US4103068A (en) *	1976-01-30	1978-07-25	Allied Chemical Corporation	Polyester filamentary yarns

1988
- 1988-07-22 DE DE3851748T patent/DE3851748T2/de not_active Expired - Fee Related
- 1988-07-22 JP JP63506730A patent/JPH02500292A/ja active Pending
- 1988-07-22 EP EP88906685A patent/EP0340250B1/fr not_active Expired - Lifetime
- 1988-07-22 WO PCT/US1988/002498 patent/WO1989001071A1/fr not_active Ceased
- 1988-07-22 BR BR888807291A patent/BR8807291A/pt not_active IP Right Cessation
- 1988-07-22 AT AT88906685T patent/ATE112594T1/de active
- 1988-08-02 CA CA000573637A patent/CA1299164C/fr not_active Expired - Fee Related
- 1988-08-03 MX MX12529A patent/MX164866B/es unknown
- 1988-08-05 ZA ZA885775A patent/ZA885775B/xx unknown
1995
- 1995-03-09 HK HK31695A patent/HK31695A/en not_active IP Right Cessation

Also Published As

Publication number	Publication date
BR8807291A (pt)	1990-04-10
ZA885775B (en)	1989-04-26
WO1989001071A1 (fr)	1989-02-09
HK31695A (en)	1995-03-17
ATE112594T1 (de)	1994-10-15
EP0340250A1 (fr)	1989-11-08
JPH02500292A (ja)	1990-02-01
MX164866B (es)	1992-09-29
DE3851748T2 (de)	1995-04-27
DE3851748D1 (de)	1994-11-10
EP0340250B1 (fr)	1994-10-05

Legal Events

Date	Code	Title	Description
2005-04-21	MKLA	Lapsed

Publication	Publication Date	Title
CN112778527B (zh)	2022-05-27	一种多元醇脂肪酸酯/苯基/聚醚共改性硅油、制备方法及碳纤维专用低硅油剂
US4343616A (en)	1982-08-10	Lubricant compositions for finishing synthetic fibers
US4957648A (en)	1990-09-18	Spin fiber lubricant compositions
US4252528A (en)	1981-02-24	Lubricant compositions for finishing synthetic fibers
US5569408A (en)	1996-10-29	New water-soluble, biologically decomposable carbonic acid polyesters and their use as preparing and slip additives of synthetic fibres
EP0778822B1 (fr)	2001-06-20	Nouveaux esters de polyol d'acides ether carboxyliques et procedes d'appretage de fibres
US4169062A (en)	1979-09-25	Random copolymers of polyoxyethylene polyoxypropylene glycol monoester, process of making the same and textile fiber containing the same
EP0628101B1 (fr)	1997-01-15	Procedes de finissage de fibres
US5240743A (en)	1993-08-31	Fiber finishing methods
US5478485A (en)	1995-12-26	Thermally stable textile lubricants
US4297407A (en)	1981-10-27	Finish composition for the spinning of highly crimped cellulose fibers using a composition cont. fatty acid ester, organic phosphoric acid ester, fatty acid ethylene oxide cond. prod. and fatty acid salt
US4294990A (en)	1981-10-13	Alkyl-polyglycol mixed formals as fiber preparation agents
US4014800A (en)	1977-03-29	Fiber-lubricating compositions
US5464546A (en)	1995-11-07	Thermally stable textile lubricants
EP0340250B1 (fr)	1994-10-05	Compositions lubrifiantes pour filage de fibres
US3464922A (en)	1969-09-02	Trimethylolalkane esters and method of treating textile filaments therewith
AU2256688A (en)	1989-03-01	Spin fiber lubricant compositions
US4261839A (en)	1981-04-14	Tertiary butyl ethers as fiber preparation agents
EP0127293A2 (fr)	1984-12-05	Compositions lubrifiantes pour le bobinage à base d'huiles
US4883495A (en)	1989-11-28	Amino-containing alkenylsuccinic esters
KR910000525B1 (ko)	1991-01-26	섬유 또는 섬유제품 처리제
CN111635806A (zh)	2020-09-08	可自然降解针织机油组合物、制备方法及其用途
JP2664372B2 (ja)	1997-10-15	ポリアミド系合成繊維用油剤
CN113980723A (zh)	2022-01-28	一种加弹机热箱除静电试剂及其制备方法
US3594200A (en)	1971-07-20	Textile yarn finish