US2853453A - Textile lubricants - Google Patents
Textile lubricants Download PDFInfo
- Publication number
- US2853453A US2853453A US494256A US49425655A US2853453A US 2853453 A US2853453 A US 2853453A US 494256 A US494256 A US 494256A US 49425655 A US49425655 A US 49425655A US 2853453 A US2853453 A US 2853453A
- Authority
- US
- United States
- Prior art keywords
- oil
- parts
- soluble
- water
- textile
- 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
- 239000004753 textile Substances 0.000 title claims description 25
- 239000000314 lubricant Substances 0.000 title claims description 16
- 239000000203 mixture Substances 0.000 claims description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 18
- 239000003208 petroleum Substances 0.000 claims description 16
- 229910052708 sodium Inorganic materials 0.000 claims description 11
- 239000011734 sodium Substances 0.000 claims description 11
- 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 claims description 10
- 239000012141 concentrate Substances 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- 239000010688 mineral lubricating oil Substances 0.000 claims description 7
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 239000003921 oil Substances 0.000 description 21
- 235000019198 oils Nutrition 0.000 description 21
- 239000000839 emulsion Substances 0.000 description 18
- -1 aromatic sulfonates Chemical class 0.000 description 16
- 239000000835 fiber Substances 0.000 description 16
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 14
- 239000003995 emulsifying agent Substances 0.000 description 13
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 10
- 230000003068 static effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- AFSHUZFNMVJNKX-UHFFFAOYSA-N 1,2-di-(9Z-octadecenoyl)glycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCC=CCCCCCCCC AFSHUZFNMVJNKX-UHFFFAOYSA-N 0.000 description 6
- AFSHUZFNMVJNKX-LLWMBOQKSA-N 1,2-dioleoyl-sn-glycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-LLWMBOQKSA-N 0.000 description 6
- WGIMXKDCVCTHGW-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCCO WGIMXKDCVCTHGW-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 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
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Chemical class C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-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
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Chemical class 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 5
- 239000002253 acid Substances 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Chemical class OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 4
- 239000012875 nonionic emulsifier Substances 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 150000003460 sulfonic acids Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 229940049964 oleate Drugs 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- AFSHUZFNMVJNKX-CLFAGFIQSA-N 1,2-dioleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCC\C=C/CCCCCCCC AFSHUZFNMVJNKX-CLFAGFIQSA-N 0.000 description 2
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- WGKYSFRFMQHMOF-UHFFFAOYSA-N 3-bromo-5-methylpyridine-2-carbonitrile Chemical compound CC1=CN=C(C#N)C(Br)=C1 WGKYSFRFMQHMOF-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 150000002918 oxazolines Chemical class 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- YGCMLNDQGHTAPC-UHFFFAOYSA-N 2-(octadecylamino)ethanol Chemical compound CCCCCCCCCCCCCCCCCCNCCO YGCMLNDQGHTAPC-UHFFFAOYSA-N 0.000 description 1
- FQHUDZKKDCTQET-UHFFFAOYSA-N 2-undecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCC1=NCCN1 FQHUDZKKDCTQET-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
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 1
- SIINAHBZNVOMMM-UHFFFAOYSA-N 6-tert-butyl-2,3-dimethylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1C SIINAHBZNVOMMM-UHFFFAOYSA-N 0.000 description 1
- COKWFBRXJFYIOJ-UHFFFAOYSA-N CCCCCCCCCCCC[S+]=C(N)N Chemical compound CCCCCCCCCCCC[S+]=C(N)N COKWFBRXJFYIOJ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000158728 Meliaceae Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000002877 alkyl aryl group Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical class OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002028 dodecanols Chemical class 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical class OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- NQYKSVOHDVVDOR-UHFFFAOYSA-N n-hexadecylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCC NQYKSVOHDVVDOR-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical class CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FFQLQBKXOPDGSG-UHFFFAOYSA-N octadecyl benzenesulfonate Chemical compound CCCCCCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 FFQLQBKXOPDGSG-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 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
- D06M13/322—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
- D06M13/432—Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/063—Peroxides
-
- 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
- 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
- C10M2203/102—Aliphatic fractions
-
- 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
- C10M2203/104—Aromatic fractions
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- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/064—Thiourea type compounds
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- C10N2040/46—Textile oils
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- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/15—Antistatic agents not otherwise provided for
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
Definitions
- the present invention relates to lubricants for textiles and to a method of lubricating textile fibers. More particularly, it relates to emulsifiable and water emulsion textile lubricants and to the lubrication of textile fibers therewith during spinning and the like.
- the lubricated fibers possess little or no resistance to slipping with the result that they shift and slip constantly during processing and are therefore difiicult if not impossible to process satisfactorily.
- an improved textile lubricant whose static coefficient of friction exceeds its dynamic coeflicieut of friction, is provided by an emulsifiable concentrate comprising a major proportion of a mineral lubricating oil and minor proportions each, of an oil-soluble organic sulfonate, an oil-soluble non-ionic emulsifier and a nitrogenous emulsifier which is soluble in oil but substantially insoluble in water.
- sulfonates from about 2% to about non-ionic emulsifier, from about0.5% to about 10% and the nitrogenous emulsifier from about 1% to about 13% by weight.
- the amount of nitrogenous emulsifier used is governed by the amount of sulfonate present in the blend. By properly adjusting their proportions the static coefiicient of friction can be maintained greater than the dynamic coefiicient of friction. Generally, the nitrogenous emulsifier is used in amounts equal to about one-half of the amount of sulfonate used in the blend.
- the concentrates of the invention preferably contain a minor proportion of water, for example, up to 10% and preferably about 1 to 5% by weight of the composition.
- concentrates may be used as such or they may be used in the form of aqueous emulsions obtained on diluting them with from about 19 to 99 volumes of water.
- aqueous emulsions containing about 2% by volume of the concentrate are used.
- Emulsification usually occurs spontaneously on diluting with water and the aqueous emulsions have very high stability.
- the aqueous emulsions are included within the scope of the invention.
- the emulsifiable compositions of the invention are preferably so constituted as by the incorporation of a water-soluble inorganic base, that an emulsion containing 2 parts by volume thereof in 98 parts by volume'of distilled water has a pH value greater than 7, preferably greater than 9.
- the mineral lubricating oil used in the compositions of the invention may be of any type. It may be a lightly refined oil, such as has been refined by distillation, solvent extraction, clay treatment or treatment with dilute acid or other chemical, or a highly refined oil, such as has been treated with fuming sulfuric acid, withor without prior solvent extraction.
- the oils may be, highly parafiinic oils containing at least 65% by weight of material remaining unsulfonated when treated with concentrated sulfuric acid, or may contain naphthenic and aromatic constituents.
- highly refined oils are preferred because of their greater stability and resistance to the development of odor and col-or on exposure to light and air; they should have a flash point sufiiciently high to satisfy the requirements of any particular section of the industry. Thus, in the worstedand woolen trades, a minimum flash point of 340 F. is required.
- oil-soluble sulfonates used in the compositions of this invention can be of various types such as neutral and/ or basic and can be derived from any suitable material and prepared by any of the well-known suitable methods.
- Preferred materials for making oil-soluble sulfonates include mineral lubricating oil fractions, alkyl-substituted aromatic compounds and alkyl-substituted polar containing aromatic compounds.
- Petroleum sulf-onates suitable for use in compositions of this invention are described in United States Patents 2,280,419, 2,344,988, 2,361,804, 2,375,222, 2,480,638, 2,485,861, 2,509,863, 2,501,731, 2,523,582 and 2,585,520.
- the sulfonates can'be purified by the methods described in United States Patents 2,441,258 and 2,488,721.
- Suitable aromatic sulfonates include those described in United States Patents 2,411,583, 2,418,894, 2,442,915, 2,483,501, 2,531,324, 2,556,108 and 2,556,848.
- various metal sulfonates are contemplated in the practice of the invention, including alkali metal sulfonates, alkaline earth metal sulfonates (including magnesium) and other polyvalent metal sulfonates
- the nitrogen base sulfonates obtained by treating sulfonic acids with ammonia orv an amine such as aliphatic amines or alkylolamines such as triethanolamine also can be used.
- Specific sulfonates which are suitable for use in compositions of this' invention include: Na, K, Li, Ca, Ba, Mg, ammonia, triethanolamine petroleum sulfonate, tetra-tertiary-butylnaphthalene sulfonate, diwaxbenzenesulfonate, stearylbenzenesulfonate, diwaxnaphthalenesulfonate, diisobutylencphenolsulfonatc, tertiaryctylphenol sulfonate, ditertiary-amylphcno-l sulfonate, alkylated-dibcnzothiophene sulfonate and mixtures thereof.
- Preferred are thes a'lts of these acids in which the cationicportion is a water, soluble base of a monovalent cation.
- Preferred sulfonates for use in compositions of thisinvention are obtained as a by-product during the menu:
- petroleum sulfonic acids whose salts are used in the compositions of the invention preferably have an average molecular weight of from 420 to 450, although they can be as much as 350 to as high as 600, the sodium petroleum sulfonates which are available commercially being preferred.
- oilsoluble non-ionic emulsifier A wide variety of compounds may be used as the oilsoluble non-ionic emulsifier. These compounds are preferentially oilsoluble but may also be soluble in water to a minor extent. Suitable compounds are those containing an alcoholic hydroxyl group and the following classes of compounds have proved effective:
- Oil-soluble monohydric alcohols e. g., the octanols, nonanols, decanols, undecanols, dodecanols and the higher aliphatic alcohols.
- These may be synthetic alcohols, e. g., alcohols produced by the so-called Oxo process, or they may be of natural origin, e. g., fatty alcohols from sperm oil.
- oil-soluble aromatic and cycle aliphatic alcohols such as benzyl alcohol and methylcyclohexanol may be used.
- Oil-soluble dihydric alcohols such as the hexylene glycols, octylene glycols, decylene glycols and the higher glycols.
- Oil-soluble alcohols containing substituents such as ether and/or ester groups are particularly effective members of this class. Particularly effective members of this class are the partial esters of polyhydric al cohols and fatty acids such as glycerol monoor di-oleate or stearate, ethylene glycol mono-oleate or stearate and the mono-esters of ethers of polyethylene glycols such as the mono-oleate or stearate of nonaethylene glycol. Compounds such as glycerol di-oleate have the valuable property of lowering the friction values of the compositions.
- a single oil-soluble non-ionic emulsifier may be employed but it is often useful to use a mixture of two or more such compounds in order to obtain optimum scourability and spontaneity of emulsion formation.
- a mixture of glycerol dioleate and a minor proportion of diglycol laurate, and a mixture of glycerol dioleate with minor proportions of diglycol laurate and nonaethylene glycol mono-oleate have been found particularly effective.
- the nitrogenous emulsifier which is used in the compositions of the invention is soluble in mineral oil but substantially insoluble in water.
- Suitable nitrogenous emulsifiers of this type are the primary, secondary and tertiary amines containing at least one hydrophobic group attached to the nitrogen atom, for example, dodecylamine, octadecylamine, dicetylamine, N- octadecyl-N-hydroxyethylamine, N-alkyl-N-hydroxypropylpiperidines in which the alkyl radicals are derived from coconut oil and the mono-acyl or as-diacyl derivatives of aliphatic polyamines such as oleyl ethylenediamine and as-distearylethylene diamine.
- nitrogenous emulsifiers for use in the compositions of the invention are the organic compounds free from sulfonic acid groups which contain the atomic grouping
- the 4 iminazoles, imidazolines and pyrimidines are the organic compounds free from sulfonic acid groups which contain the atomic grouping
- the 4 iminazoles, imidazolines and pyrimidines are the organic compounds free from sulfonic acid groups which contain the atomic grouping
- the 4 iminazoles, imidazolines and pyrimidines are O-ethylurea, S-dodecylthiourea, 1-guanidino-palmitic acid, lhydroxyethylguanidine, 2-undecylimidazoline, 1-/3-hydroxyethyl-2-heptadecyleneimidazoline, Z-naphthenyl-imidazoline, 2-heptadecylbenziminazole, Z-undecylpyrimidine and
- compositions of the invention are intended for use as textile fiber lubricants, the proportion of nitrogenous emulsifier present is dependent to a large extent on the content of petroleum sulfonate.
- the nitrogenous emulsifier promotes emulsion stability and produces compositions which lower the coefiicients of inter fiber friction. If present in too high concentration relative to the quantity of sulfonate in the blend, however, the nitrogenous emulsifier will cause the dynamic coefficient of inter fiber friction to become greater than the static coefficient of friction with consequent unsatisfactory processing of the lubricated fibers.
- the amount of nitrogenous emulsifier present should be just sufiicient to produce a composition of suitable frictional properties, i. e., with a static coefficient of friction greater than the dynamic coefficient of friction.
- compositions of the invention In addition to the aforementioned essential ingredients, other substances having particular properties may be incorporated in minor amounts in the compositions of the invention.
- a coupling agent or mutual solvent to aid in solubilizing the ingredients, in promoting spontaneous emulsion formation, and in stabilizing the emulsion.
- Such substances include mon-ohydric alcohols containing less than 8 carbon atoms in the molecule, for example, isopropyl alcohol, butyl and amyl alcohols, cyclohexanol, diacetone alcohol, phenols, the glycols, such as hexylene glycol, and polyethylene lycol and glycol mono-ethers such as the ethyl or butyl ether of ethylene glycol.
- compositions of the invention can be incorporated in minor amounts in the compositions of the invention, as for example, the alkali metal soaps of higher fatty acids and rosin acids, alkali metal salts of sulfuric acid esters of higher primary and secondary alcohols and alkali metal salts of alkyl aryl sulfouates.
- alkali metal soaps of higher fatty acids and rosin acids alkali metal salts of sulfuric acid esters of higher primary and secondary alcohols
- alkali metal salts of alkyl aryl sulfouates alkali metal salts of alkyl aryl sulfouates.
- Anti oxidants are also desirable additional ingredients in the compositions of the invention, for example, 2,4-
- anti-foaming agents such as silicones and fine dispersions of N,N-distearyl ethylene diamine or N,N- distearyl hexamethylene diamine in mineral oil may also advantageously be incorporated.
- compositions of the invention are to be used as textile oils, it may also be desirable to incorporate small proportions of compounds which will inhibit the growth of mildew on the wetted fibers.
- Salicylanilide is a suitable fungicide for this purpose.
- Corrosion inhibitors may also be incorporated in the invention.
- Compounds which are particularly suitable are the primary amines containing from 6 to 15; carbon atoms in the molecule, such as octylamine and octadecylamine and the heterocyclic nitrogen containing organic compounds such as the alkyl substituted oxazolines and the oxazoline salts of fatty acids.
- Example I A blend was prepared from 63 parts of spindle oil, 4.9 parts of 1-fi-hydroxyethyl-2-heptadecylene imidazoline, 4.9 parts of glycerol dioleate, 1.2 parts of diglycol laurate, 9.8 parts of oil-soluble sodium petroleum sulfonates (molecular weight 420-450), 6.5 parts of colophony rosin, 3.3 parts of oleic acid, 1.2 parts of potassium hydroxide, 2.6 parts of isopropyl alcohol and 2.6 parts of water.
- Example 11 This blend was prepared from 54.6 parts of spindle oil, 4.8 parts of 1-fi-hydroxyethyl-2-heptadecylene imidazoline, 4.8 parts of glycerol dioleate, 0.6 part of diglycol laurate, 13.0 parts of oil-soluble sodium petroleum sulfonates (molecular weight 420-450), 8.7 parts of colophony rosin, 4.4 parts of oleic acid, 2.1 parts of potassium hydroxide, 3.5 parts of isopropyl alcohol and 3.5 parts of water.
- This blend readily emulsified with water to give a clear oil-in-water emulsion, which was unchanged after 2 weeks storage.
- a 2% vol./vol. emulsion in distilled water had a pH of 10.9.
- the static coefficient of friction was 0.185 and the dynamic coefficient of friction was 0.175, when measured by the Roder method referred to above.
- Example III This blend was prepared from 57.7 parts of spindle oil, 4.6 parts of 1- 3-hydroxyethyl-2-heptadecylene imidazoline, 4.6 parts of glycerol di-oleate, 1.1 parts of diglycol laurate, 5.4 parts of glycol monooleate, 10.0 parts of oilsoluble sodium naphthasulfonates (molecular weight 420-450), 6.5 parts of colophony rosin, 3.3 parts of oleic acid, 1.6 parts of potassium hydroxide, 2.6 parts of isopropyl alcohol and 2.6 parts of water.
- This blend was a satisfactory knitting medium for sized nylon fibers when used as a 2% vol./vol. aqueous emul- SlOIl.
- compositions of the invention may be applied to textile fibers by any of the well-known methods, for example, by spraying running textile yarns or by running textile yarns through baths or over wicks or other similar devices from which they pick up the composition in emulsion form as described above.
- the textile yarns may be dipped in baths containing the composition.
- An anti-static emulsifiable textile lubricant concentrate composition comprising a major amount of mineral lubricating oiland containing from about 2% to about 20% by weight of an oil-soluble sodium petroleum sulfonate, from about 0.5% to about 10% by weight of an oil-soluble partial ester of a polyhydric alcohol with a fatty acid, from about 1% to about 13% of l-fl-hydroxyethyI-Z-heptadecylene-imidazoline and from about 1% to about 10% of water.
- An anti-static emulsifiable textile lubricant concentrate composition comprising a major amount of mineral lubricating oil and containing from about 2% to about 20%by weight of an oil-soluble sodium petroleum sulfonate, from about 0.5% to about 10% by weight of an oil-soluble partial ester of a polyhydric alcohol with a fatty acid, from about 1% to about 13%v of 2- naphthenylimidazoline and from about 1% to about 10% of water.
- An anti-static emulsifiable textile lubricant c centrate composition comprising a major amount of mineral lubricating oil and containing from about 2% to about 20% by weight of an oil-soluble sodium petroleum sulfo-nate, from about 0.5 to about 10% by weight of glycerol dioleate, from about 1% to about 10% iby weight of water and from about 1% to about 13% of l-,B- hydroxyethyl-Z-heptadecyleneimidazoline.
- An anti-static emulsifiable textile lubricant concentrate composition comprising about 4.8 parts of 1-[3- hydroxyethyl-Z-heptadecyleneimidazoline, about 4.8 parts of glycerol dioleate, about 0.6 parts of diglycol laurate, about 13 parts of oil-soluble sodium petroleum sulfonate, about 8.7 parts of colophony rosin, about 4.4 parts of oleic acid, about 2.1 parts of potassium hydroxide, about 3.5 parts of isopropyl alcohol, about 3.5 parts of water and about 54.6 parts of spindle oil.
- composition of claim 4 diluted with from 19 to 99 volumes of water.
- An anti-static emulsifiable textileizibricant concentrate composition comprising a major amount of mineral lubricating oil and containing from about 2% to about 20% by weight o-f an oil-soluble alkali metal petroleum sulfonate, from about 0.5 to about 10% by weight of an oil-soluble partial ester of a polyhydric alcohol with a higher fatty acid, from about 1% to about 13% of an oil-soluble hydrocarbon-substituted.imidazoline and from about 1% to about 10% of water.
- composition of claim 6 diluted with from 19 to 99 volumes of water.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9079/54A GB753749A (en) | 1954-03-29 | 1954-03-29 | Improvements in or relating to textile oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US2853453A true US2853453A (en) | 1958-09-23 |
Family
ID=9864957
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US494256A Expired - Lifetime US2853453A (en) | 1954-03-29 | 1955-03-14 | Textile lubricants |
Country Status (6)
Country | Link |
---|---|
US (1) | US2853453A (en:Method) |
BE (1) | BE536867A (en:Method) |
DE (1) | DE1129255B (en:Method) |
FR (1) | FR1127014A (en:Method) |
GB (1) | GB753749A (en:Method) |
NL (2) | NL103782C (en:Method) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3056705A (en) * | 1958-06-19 | 1962-10-02 | Owens Corning Fiberglass Corp | Surface treated glass and similar fibers |
US3485913A (en) * | 1965-10-20 | 1969-12-23 | Toho Beslon Co | New method of manufacturing acrylic fibers and the related products |
US3522175A (en) * | 1965-02-13 | 1970-07-28 | Kao Corp | Lubricant composition for synthetic fibers |
US3850819A (en) * | 1972-08-25 | 1974-11-26 | Ici America Inc | Low fuming spin finish for nylon weaving yarns |
US4014800A (en) * | 1973-05-26 | 1977-03-29 | Hoechst Aktiengesellschaft | Fiber-lubricating compositions |
US4186126A (en) * | 1978-04-11 | 1980-01-29 | Messick John J | Sulfonate antioxidants for synthetic and natural rubber |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE591186A (en:Method) * | 1959-05-25 | 1900-01-01 | ||
US4082679A (en) * | 1977-03-10 | 1978-04-04 | Witco Chemical Corporation | Light stabilized textile mineral oil |
GB2285630A (en) * | 1994-01-12 | 1995-07-19 | Diversey Corp | Aqueous lubricant compositions for conveyor tracks |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2025434A (en) * | 1933-07-01 | 1935-12-24 | American Enka Corp | Lubricating natural and artificial fibers |
US2036470A (en) * | 1931-10-24 | 1936-04-07 | Standard Oil Co California | Emulsifiable oil product and process of making the same |
US2122593A (en) * | 1935-03-05 | 1938-07-05 | Henry A Stafford | Treatment of textile fibers |
US2730464A (en) * | 1951-05-17 | 1956-01-10 | Shell Dev | Antistatic treatment of textile yarns |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE445755A (en:Method) * | 1941-06-07 | |||
US2684311A (en) * | 1950-02-18 | 1954-07-20 | Celanese Corp | Process for lubricating regenerated cellulose yarns |
-
0
- NL NL195998D patent/NL195998A/xx unknown
-
1954
- 1954-03-29 GB GB9079/54A patent/GB753749A/en not_active Expired
-
1955
- 1955-03-14 US US494256A patent/US2853453A/en not_active Expired - Lifetime
- 1955-03-28 BE BE536867A patent/BE536867A/nl unknown
- 1955-03-28 DE DES43220A patent/DE1129255B/de active Pending
- 1955-03-28 NL NL195998A patent/NL103782C/nl active
- 1955-03-28 FR FR1127014D patent/FR1127014A/fr not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2036470A (en) * | 1931-10-24 | 1936-04-07 | Standard Oil Co California | Emulsifiable oil product and process of making the same |
US2025434A (en) * | 1933-07-01 | 1935-12-24 | American Enka Corp | Lubricating natural and artificial fibers |
US2122593A (en) * | 1935-03-05 | 1938-07-05 | Henry A Stafford | Treatment of textile fibers |
US2730464A (en) * | 1951-05-17 | 1956-01-10 | Shell Dev | Antistatic treatment of textile yarns |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3056705A (en) * | 1958-06-19 | 1962-10-02 | Owens Corning Fiberglass Corp | Surface treated glass and similar fibers |
US3522175A (en) * | 1965-02-13 | 1970-07-28 | Kao Corp | Lubricant composition for synthetic fibers |
US3485913A (en) * | 1965-10-20 | 1969-12-23 | Toho Beslon Co | New method of manufacturing acrylic fibers and the related products |
US3850819A (en) * | 1972-08-25 | 1974-11-26 | Ici America Inc | Low fuming spin finish for nylon weaving yarns |
US4014800A (en) * | 1973-05-26 | 1977-03-29 | Hoechst Aktiengesellschaft | Fiber-lubricating compositions |
US4186126A (en) * | 1978-04-11 | 1980-01-29 | Messick John J | Sulfonate antioxidants for synthetic and natural rubber |
Also Published As
Publication number | Publication date |
---|---|
GB753749A (en) | 1956-08-01 |
NL103782C (en:Method) | 1962-09-17 |
DE1129255B (de) | 1962-05-10 |
BE536867A (en:Method) | 1955-09-28 |
FR1127014A (fr) | 1956-12-06 |
NL195998A (en:Method) | 1900-01-01 |
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