NO861856L - Preaktivert geleringsmiddel for smoerefett i form av organofil leire og fremgangsmaate for fremstilling derav. - Google Patents
Preaktivert geleringsmiddel for smoerefett i form av organofil leire og fremgangsmaate for fremstilling derav.Info
- Publication number
- NO861856L NO861856L NO861856A NO861856A NO861856L NO 861856 L NO861856 L NO 861856L NO 861856 A NO861856 A NO 861856A NO 861856 A NO861856 A NO 861856A NO 861856 L NO861856 L NO 861856L
- Authority
- NO
- Norway
- Prior art keywords
- gelling agent
- approx
- organophilic clay
- preactivated
- clay
- Prior art date
Links
- 239000003795 chemical substances by application Substances 0.000 title claims description 61
- 238000000034 method Methods 0.000 title claims description 59
- 239000000314 lubricant Substances 0.000 title 1
- 239000004927 clay Substances 0.000 claims description 322
- 239000003349 gelling agent Substances 0.000 claims description 167
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 80
- 239000004519 grease Substances 0.000 claims description 59
- -1 p-nitrophenyl alcohol Chemical compound 0.000 claims description 55
- 239000000203 mixture Substances 0.000 claims description 54
- 150000002892 organic cations Chemical class 0.000 claims description 52
- 230000001050 lubricating effect Effects 0.000 claims description 48
- 239000002002 slurry Substances 0.000 claims description 42
- 125000004432 carbon atom Chemical group C* 0.000 claims description 39
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 28
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 28
- 239000000440 bentonite Substances 0.000 claims description 27
- 229910000278 bentonite Inorganic materials 0.000 claims description 27
- 239000003921 oil Substances 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims description 18
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 18
- 239000006185 dispersion Substances 0.000 claims description 18
- 229920006395 saturated elastomer Polymers 0.000 claims description 18
- 238000005341 cation exchange Methods 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 17
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 16
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 239000000454 talc Substances 0.000 claims description 15
- 229910052623 talc Inorganic materials 0.000 claims description 15
- 230000035515 penetration Effects 0.000 claims description 14
- 239000012530 fluid Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 13
- 239000003760 tallow Substances 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 229960000907 methylthioninium chloride Drugs 0.000 claims description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
- JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 claims description 10
- 238000012360 testing method Methods 0.000 claims description 10
- JKTYGPATCNUWKN-UHFFFAOYSA-N 4-nitrobenzyl alcohol Chemical compound OCC1=CC=C([N+]([O-])=O)C=C1 JKTYGPATCNUWKN-UHFFFAOYSA-N 0.000 claims description 9
- BWRBVBFLFQKBPT-UHFFFAOYSA-N (2-nitrophenyl)methanol Chemical compound OCC1=CC=CC=C1[N+]([O-])=O BWRBVBFLFQKBPT-UHFFFAOYSA-N 0.000 claims description 8
- CWNPOQFCIIFQDM-UHFFFAOYSA-N 3-nitrobenzyl alcohol Chemical compound OCC1=CC=CC([N+]([O-])=O)=C1 CWNPOQFCIIFQDM-UHFFFAOYSA-N 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 229910021647 smectite Inorganic materials 0.000 claims description 8
- 239000004359 castor oil Substances 0.000 claims description 7
- 235000019438 castor oil Nutrition 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 claims description 6
- IKFGSOJYHVTNDV-UHFFFAOYSA-N 1-(4-phenylmethoxyphenyl)propan-1-one Chemical compound C1=CC(C(=O)CC)=CC=C1OCC1=CC=CC=C1 IKFGSOJYHVTNDV-UHFFFAOYSA-N 0.000 claims description 5
- SLRIOXRBAPBGEI-UHFFFAOYSA-N 2-(2-nitrophenyl)ethanol Chemical compound OCCC1=CC=CC=C1[N+]([O-])=O SLRIOXRBAPBGEI-UHFFFAOYSA-N 0.000 claims description 5
- PWZWTSYUZQZFKE-UHFFFAOYSA-N 2-(3-nitrophenyl)ethanol Chemical compound OCCC1=CC=CC([N+]([O-])=O)=C1 PWZWTSYUZQZFKE-UHFFFAOYSA-N 0.000 claims description 5
- IKMXRUOZUUKSON-UHFFFAOYSA-N 2-(4-nitrophenyl)ethanol Chemical compound OCCC1=CC=C([N+]([O-])=O)C=C1 IKMXRUOZUUKSON-UHFFFAOYSA-N 0.000 claims description 5
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 5
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 claims description 5
- 125000006182 dimethyl benzyl group Chemical group 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 claims description 5
- 229910000271 hectorite Inorganic materials 0.000 claims description 5
- 229960005323 phenoxyethanol Drugs 0.000 claims description 5
- 239000001069 triethyl citrate Substances 0.000 claims description 5
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 claims description 5
- 235000013769 triethyl citrate Nutrition 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 238000001879 gelation Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- 229910052698 phosphorus Chemical group 0.000 claims description 3
- 239000011574 phosphorus Chemical group 0.000 claims description 3
- 230000009467 reduction Effects 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 238000007580 dry-mixing Methods 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 150000003141 primary amines Chemical class 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 claims 2
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 238000005342 ion exchange Methods 0.000 claims 1
- 125000005506 phthalide group Chemical group 0.000 claims 1
- 238000002360 preparation method Methods 0.000 description 30
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 28
- 239000007787 solid Substances 0.000 description 28
- 230000000052 comparative effect Effects 0.000 description 24
- 235000019198 oils Nutrition 0.000 description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 235000019197 fats Nutrition 0.000 description 17
- 238000003756 stirring Methods 0.000 description 15
- 239000000976 ink Substances 0.000 description 14
- 239000012190 activator Substances 0.000 description 13
- 239000012065 filter cake Substances 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 11
- 235000019270 ammonium chloride Nutrition 0.000 description 10
- 150000002430 hydrocarbons Chemical group 0.000 description 9
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 238000005119 centrifugation Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000012066 reaction slurry Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 150000001768 cations Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000356 contaminant Substances 0.000 description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000013065 commercial product Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical class O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000006254 rheological additive Substances 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 2
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 2
- 239000005695 Ammonium acetate Substances 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229910002483 Cu Ka Inorganic materials 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 241000276498 Pollachius virens Species 0.000 description 2
- 244000305267 Quercus macrolepis Species 0.000 description 2
- 235000016976 Quercus macrolepis Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 2
- 229940043376 ammonium acetate Drugs 0.000 description 2
- 235000019257 ammonium acetate Nutrition 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- XSIFPSYPOVKYCO-UHFFFAOYSA-N butyl benzoate Chemical compound CCCCOC(=O)C1=CC=CC=C1 XSIFPSYPOVKYCO-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- 239000002385 cottonseed oil Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000001027 hydrothermal synthesis Methods 0.000 description 2
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical group 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 125000001421 myristyl 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])[H] 0.000 description 2
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 150000002895 organic esters Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000010690 paraffinic oil Substances 0.000 description 2
- 238000003921 particle size analysis Methods 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
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- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
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- 239000005643 Pelargonic acid Substances 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
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- 244000044822 Simmondsia californica Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
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- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
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- 230000015572 biosynthetic process Effects 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
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- 239000003729 cation exchange resin Substances 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
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- 239000002537 cosmetic Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical group CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 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
- 238000009837 dry grinding Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000002356 laser light scattering Methods 0.000 description 1
- 125000005644 linolenyl group Chemical group 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- ZHCAAFJSYLFLPX-UHFFFAOYSA-N nitrocyclohexatriene Chemical group [O-][N+](=O)C1=CC=C=C[CH]1 ZHCAAFJSYLFLPX-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 125000001117 oleyl 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])=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])[H] 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 125000002958 pentadecyl 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])[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000379 polypropylene carbonate Polymers 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000005932 reductive alkylation reaction Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 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
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 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
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- LZTRCELOJRDYMQ-UHFFFAOYSA-N triphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1=CC=CC=C1 LZTRCELOJRDYMQ-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/20—Silicates
- C01B33/36—Silicates having base-exchange properties but not having molecular sieve properties
- C01B33/38—Layered base-exchange silicates, e.g. clays, micas or alkali metal silicates of kenyaite or magadiite type
- C01B33/44—Products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds, e.g. organoclay material
-
- 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
- C10M113/00—Lubricating compositions characterised by the thickening agent being an inorganic material
- C10M113/16—Inorganic material treated with organic compounds, e.g. coated
-
- 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
- C10M2201/14—Inorganic compounds or elements as ingredients in lubricant compositions inorganic compounds surface treated with organic compounds
-
- 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
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/901—Organically modified inorganic solid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Lubricants (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/792,146 US4664820A (en) | 1985-10-28 | 1985-10-28 | Preactivated organophilic clay gellant lubricating grease thickened with preactivated organophilic clay gellant and process for preparing preactivated organophilic clay gellants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO861856L true NO861856L (no) | 1987-04-29 |
Family
ID=25155941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO861856A NO861856L (no) | 1985-10-28 | 1986-05-09 | Preaktivert geleringsmiddel for smoerefett i form av organofil leire og fremgangsmaate for fremstilling derav. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4664820A (sv) |
| JP (1) | JPH07108990B2 (sv) |
| AR (1) | AR242823A1 (sv) |
| AU (1) | AU578405B2 (sv) |
| BE (1) | BE905668A (sv) |
| BR (1) | BR8604431A (sv) |
| CA (1) | CA1258670A (sv) |
| CH (1) | CH672497A5 (sv) |
| DE (1) | DE3636473B4 (sv) |
| DK (1) | DK512786A (sv) |
| FI (1) | FI864292A (sv) |
| FR (1) | FR2589162B1 (sv) |
| GB (1) | GB2185246B (sv) |
| GR (1) | GR862613B (sv) |
| IT (1) | IT1197824B (sv) |
| LU (1) | LU86639A1 (sv) |
| MX (1) | MX163724B (sv) |
| NL (1) | NL194756C (sv) |
| NO (1) | NO861856L (sv) |
| SE (1) | SE463562B (sv) |
| ZA (1) | ZA863560B (sv) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8615478D0 (en) * | 1986-06-25 | 1986-07-30 | Bp Chem Int Ltd | Low toxity oil composition |
| US4929644A (en) * | 1986-10-24 | 1990-05-29 | Rheox, Inc. | Thickened organic composition having biocidal activity and an additive for thickening and imparting biocidal activity to an organic composition |
| US4753974A (en) * | 1986-12-12 | 1988-06-28 | E C.C. International Limited | Dispersible organoclay for unsaturated polyester resins |
| US4915857A (en) * | 1987-05-11 | 1990-04-10 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
| JPS6474294A (en) * | 1987-09-17 | 1989-03-20 | Nippon Steel Corp | Production of lubricating grease |
| US5075033A (en) * | 1987-10-19 | 1991-12-24 | Rheox, Inc. | Processes for preparing organophilic clay gellants |
| US4876030A (en) * | 1987-11-12 | 1989-10-24 | Phillips Petroleum Company | Organophilic clay suspension medium |
| JP2605373B2 (ja) * | 1988-08-23 | 1997-04-30 | エヌオーケー株式会社 | 機能性流体の製造法 |
| US4919934A (en) * | 1989-03-02 | 1990-04-24 | Richardson-Vicks Inc. | Cosmetic sticks |
| WO1992015098A1 (en) * | 1991-02-21 | 1992-09-03 | Noakes John E | Solidification of organic waste materials in cement |
| US5186747A (en) * | 1991-03-28 | 1993-02-16 | United Catalysts Inc. | Organophilic clays preactivated with propylene carbonate |
| US5376604A (en) * | 1991-07-11 | 1994-12-27 | Co-Op Chemical Co., Ltd. | Organophilic clay |
| IT1255519B (it) * | 1992-09-24 | 1995-11-09 | Agip Spa | Argille pretrattate, loro preparazione ed impiego nella formulazione di fanghi di perforazione non aggressivi verso le argille di strato |
| US6130256A (en) * | 1993-05-07 | 2000-10-10 | Rheox, Inc. | Organoclay thickener compatible with system to be thickened |
| DE4418613A1 (de) * | 1994-05-27 | 1995-11-30 | Sued Chemie Ag | Dichtmaterial gegen organische Flüssigkeiten |
| JP2001505174A (ja) * | 1995-05-09 | 2001-04-17 | サザン クレイ プロダクツ インク | 分枝を有するアルキル第四アンモニウムイオンを含んだオルガノクレー |
| US5616286A (en) * | 1995-09-12 | 1997-04-01 | T.O.W. Inc. | Process for the manufacture of organophilic clay |
| US6187719B1 (en) * | 1998-04-28 | 2001-02-13 | Rheox, Inc. | Less temperature dependent drilling fluids for use in deep water and directional drilling and processes for providing less temperature dependent rheological properties to such drilling fluids |
| US6024170A (en) * | 1998-06-03 | 2000-02-15 | Halliburton Energy Services, Inc. | Methods of treating subterranean formation using borate cross-linking compositions |
| WO2000055277A1 (en) * | 1999-03-16 | 2000-09-21 | Technology Partners International Llc | High solids bentonite slurries and method for preparing same |
| AU4422400A (en) | 1999-04-30 | 2000-11-17 | Alcan International Limited | Fire retardant compositions |
| US6462096B1 (en) * | 2000-03-27 | 2002-10-08 | Elementis Specialties, Inc. | Organophilic clay additives and oil well drilling fluids with less temperature dependent rheological properties containing said additives |
| JP2003533619A (ja) * | 2000-05-15 | 2003-11-11 | インペリアル・ケミカル・インダストリーズ・ピーエルシー | 石油／ガス井刺激方法 |
| US7122507B2 (en) * | 2000-05-15 | 2006-10-17 | Imperial Chemical Industries Plc | Drilling fluids and method of drilling |
| US6911488B2 (en) | 2000-09-27 | 2005-06-28 | Shamrock Technologies, Inc. | Physical methods of dispersing characteristic use particles and compositions thereof |
| WO2004009019A2 (en) * | 2002-07-18 | 2004-01-29 | Shamrock Technologies, Inc. | Method for incorporating cationic molecules into a substrate for increasing dispersibility of cationic molecules |
| US20040058168A1 (en) * | 2002-07-18 | 2004-03-25 | Cody Charles A. | Method for incorporating anionic molecules into a substrate for increasing dispersibility of anionic molecules |
| EP1581587B1 (de) * | 2003-01-08 | 2007-04-11 | Süd-Chemie Ag | Masterbatche auf der basis pre-exfolierter nanoclays und ihre verwendung |
| PL1560879T3 (pl) | 2003-06-12 | 2006-08-31 | Sued Chemie Ag | Sposób wytwarzania dodatku nanokompozytowego o polepszonym rozwarstwieniu w polimerach |
| US20070166262A1 (en) * | 2003-09-15 | 2007-07-19 | Pratley Stuart K | Leave-on hair care composition |
| US7829512B2 (en) * | 2003-10-17 | 2010-11-09 | Exxonmobil Research And Engineering Company | Method and equipment for making a complex lithium grease |
| DE102004039451A1 (de) * | 2004-08-13 | 2006-03-02 | Süd-Chemie AG | Polymerblend aus nicht verträglichen Polymeren |
| DE602005018070D1 (de) * | 2004-08-17 | 2010-01-14 | Unilever Nv | Haarpflegezusammensetzung |
| FR2882997B1 (fr) * | 2005-03-10 | 2008-04-18 | Olmix Sarl | Procede d'exfoliation d'argiles intercalees |
| JP5405729B2 (ja) | 2007-03-12 | 2014-02-05 | パナソニック株式会社 | 便座装置 |
| JP4780025B2 (ja) * | 2007-04-20 | 2011-09-28 | パナソニック株式会社 | 便座装置 |
| JP4910901B2 (ja) * | 2007-06-21 | 2012-04-04 | パナソニック株式会社 | 便座用ヒータおよびそれを使用した便座装置 |
| CN101903489A (zh) * | 2007-10-22 | 2010-12-01 | 伊莱门蒂斯专业有限公司 | 热稳定的组合物及其在钻井液中的应用 |
| RU2503712C2 (ru) * | 2011-10-31 | 2014-01-10 | Общество с ограниченной ответственностью Научно-технический центр "Вамива" | Смазка для лубрикации зоны контакта колес и рельсов |
| US10662365B2 (en) | 2018-06-06 | 2020-05-26 | Elementis Specialties, Inc. | Oil based drilling fluids useful having reduced change in high shear viscosity over a wide temperature range |
| JP2020083956A (ja) * | 2018-11-19 | 2020-06-04 | 株式会社ジェイテクト | グリース組成物および転がり軸受 |
| JP2024012214A (ja) * | 2021-03-30 | 2024-01-26 | シェルルブリカンツジャパン株式会社 | グリース組成物 |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2033856A (en) * | 1934-07-05 | 1936-03-10 | Claude R Smith | Compounds of bentonite with organic bases and process of producing same |
| US2531427A (en) * | 1946-05-03 | 1950-11-28 | Ernst A Hauser | Modified gel-forming clay and process of producing same |
| BE504196A (sv) * | 1950-06-24 | |||
| US2885360A (en) * | 1951-09-08 | 1959-05-05 | Minerals & Chemicals Corp Of A | Clay bodied organic liquids and a process for the preparation thereof |
| US2750296A (en) * | 1952-02-13 | 1956-06-12 | Sun Chemical Corp | Printing ink |
| US2739067A (en) * | 1952-11-12 | 1956-03-20 | Nat Lead Co | Printing inks |
| US2754219A (en) * | 1953-03-09 | 1956-07-10 | Huber Corp J M | Anti-misting printing inks |
| BE554481A (sv) * | 1956-01-27 | |||
| US2859234A (en) * | 1956-12-07 | 1958-11-04 | American Colloid Co | Chemical compounds and the production thereof |
| BE582883A (sv) * | 1958-10-28 | |||
| US3213037A (en) * | 1961-12-29 | 1965-10-19 | Gen Aniline & Film Corp | Clay catalyst and method of preparation thereof |
| GB980143A (en) * | 1962-09-14 | 1965-01-13 | Rolls Royce | Improvements in or relating to the forming of metal articles |
| GB1009458A (en) * | 1963-02-07 | 1965-11-10 | Shell Int Research | Improvements in or relating to greases |
| GB1106281A (en) * | 1963-09-24 | 1968-03-13 | Ici Ltd | Gelled compositions |
| US3537994A (en) * | 1967-07-25 | 1970-11-03 | Nat Lead Co | Organophilic clay greases |
| US3620789A (en) * | 1969-04-10 | 1971-11-16 | Georgia Kaolin Co | Surface modified clays and methods of making the same |
| GB1439828A (en) * | 1973-04-17 | 1976-06-16 | Laporte Industries Ltd | Organophilic clay mineral derivatives |
| US3929849A (en) * | 1973-10-01 | 1975-12-30 | Exxon Research Engineering Co | Tetraalkyl phosphonium aluminosilicates |
| US3974125A (en) * | 1974-09-27 | 1976-08-10 | Exxon Research And Engineering Company | Higher dialkyl dimethyl ammonium clay gelling agents for unsaturated polyester compositions |
| US4287086A (en) * | 1975-05-02 | 1981-09-01 | Nl Industries, Inc. | Viscous organic systems containing an organophilic clay gellant without an organic dispersant therefor |
| US4054537A (en) * | 1976-04-26 | 1977-10-18 | N L Industries, Inc. | Process for synthesizing compositions containing smectite-type clays and gellants produced thereby |
| US4105578A (en) * | 1976-12-10 | 1978-08-08 | N L Industries, Inc. | Organophilic clay having enhanced dispersibility |
| GB1592271A (en) * | 1977-03-23 | 1981-07-01 | Exxon Research Engineering Co | Overtreated higher dialkyl dimethyl ammonium clay gellants and their use in greases |
| US4317737A (en) * | 1977-03-23 | 1982-03-02 | Exxon Research & Engineering Co. | Polyolefin based greases gelled by clays overtreated by higher dialkyl dimethyl ammonium salts |
| US4097437A (en) * | 1977-05-27 | 1978-06-27 | M & T Chemicals Inc. | Thixotropic aqueous coating composition of solubilized polymer with dispersion of quaternary ammonium clay in aliphatic hydrocarbon |
| DE2727053C2 (de) * | 1977-06-15 | 1982-11-25 | Süd-Chemie AG, 8000 München | Adsorptiv wirkendes silikatisches Mittel zur Bindung von Erdalkali-Ionen |
| US4193806A (en) * | 1977-06-27 | 1980-03-18 | N L Industries, Inc. | Viscosity increasing additive for printing inks |
| US4116866A (en) * | 1977-07-01 | 1978-09-26 | N L Industries, Inc. | Organophilic clay gellant |
| US4216135A (en) * | 1978-03-27 | 1980-08-05 | Nl Industries, Inc. | Organophilic clays and thixotropic polyester compositions containing the same |
| US4434075A (en) * | 1981-10-19 | 1984-02-28 | Nl Industries, Inc. | Anionically modified organophilic clays and their preparation |
| US4434076A (en) * | 1981-10-19 | 1984-02-28 | Nl Industries, Inc. | Clay cation complexes and their use to increase viscosity of liquid organic systems |
| US4450095A (en) * | 1980-11-17 | 1984-05-22 | Nl Industries, Inc. | Organophilic clay gellant having enhanced dispersibility |
| DE3145457A1 (de) * | 1980-11-17 | 1982-09-09 | NL Industries, Inc., 10020 New York, N.Y. | Fluid auf oelbasis enthaltend kationische organophile tone |
| US4412018A (en) * | 1980-11-17 | 1983-10-25 | Nl Industries, Inc. | Organophilic clay complexes, their preparation and compositions comprising said complexes |
| US4464274A (en) * | 1981-08-13 | 1984-08-07 | Venture Innovations, Inc. | Organophilic clay suspending agents |
| US4425244A (en) * | 1981-08-13 | 1984-01-10 | Venture Innovations, Inc. | Organophilic clay gellants |
| US4382868A (en) * | 1981-08-13 | 1983-05-10 | Venture Innovations, Inc. | Organophilic clay gellants |
| BR8107427A (pt) * | 1981-10-19 | 1983-05-24 | Nl Industries Inc | Fluido a base de oleo em particular fluido de recheio a base de oleo processo para isolar um tubo para revestimento em uma perfuracao de poco e gelificante |
| US4517112A (en) * | 1982-02-18 | 1985-05-14 | Nl Industries, Inc. | Modified organophilic clay complexes, their preparation and non-aqueous systems containing them |
| US4435218A (en) * | 1982-11-15 | 1984-03-06 | Jubanowsky Louis J | Viscosity increasing additive for non-aqueous fluid systems |
| FR2547826B1 (fr) * | 1983-06-27 | 1986-12-26 | Ceca Sa | Argiles organophiles modifiees |
| EP0141668B1 (en) * | 1983-11-05 | 1989-03-15 | Akzo N.V. | Organoclay materials |
| TR22515A (tr) * | 1984-04-27 | 1987-09-17 | English Clays Lovering Pochin | Bir organik vasat icinde kolayca dispersiyon hale getirilebilir bir organo-kilin hazirlanmasi |
-
1985
- 1985-10-28 US US06/792,146 patent/US4664820A/en not_active Expired - Lifetime
-
1986
- 1986-05-09 NO NO861856A patent/NO861856L/no unknown
- 1986-05-14 ZA ZA863560A patent/ZA863560B/xx unknown
- 1986-05-30 CA CA000510489A patent/CA1258670A/en not_active Expired
- 1986-06-05 AR AR86304244A patent/AR242823A1/es active
- 1986-06-19 GB GB8614900A patent/GB2185246B/en not_active Expired
- 1986-06-19 MX MX2857A patent/MX163724B/es unknown
- 1986-09-09 CH CH3642/86A patent/CH672497A5/de not_active IP Right Cessation
- 1986-09-16 BR BR8604431A patent/BR8604431A/pt unknown
- 1986-09-22 IT IT21781/86A patent/IT1197824B/it active
- 1986-09-26 NL NL8602444A patent/NL194756C/nl not_active IP Right Cessation
- 1986-10-23 FI FI864292A patent/FI864292A/fi not_active Application Discontinuation
- 1986-10-24 FR FR8614828A patent/FR2589162B1/fr not_active Expired - Lifetime
- 1986-10-24 JP JP61252112A patent/JPH07108990B2/ja not_active Expired - Fee Related
- 1986-10-24 GR GR862613A patent/GR862613B/el unknown
- 1986-10-27 AU AU64418/86A patent/AU578405B2/en not_active Expired
- 1986-10-27 DE DE3636473A patent/DE3636473B4/de not_active Expired - Lifetime
- 1986-10-27 DK DK512786A patent/DK512786A/da not_active Application Discontinuation
- 1986-10-27 SE SE8604583A patent/SE463562B/sv not_active IP Right Cessation
- 1986-10-28 BE BE0/217339A patent/BE905668A/fr not_active IP Right Cessation
- 1986-10-28 LU LU86639A patent/LU86639A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1258670A (en) | 1989-08-22 |
| MX163724B (es) | 1992-06-17 |
| DE3636473B4 (de) | 2004-07-29 |
| AR242823A1 (es) | 1993-05-31 |
| BR8604431A (pt) | 1987-11-17 |
| GB8614900D0 (en) | 1986-07-23 |
| FR2589162B1 (fr) | 1993-06-25 |
| SE8604583L (sv) | 1987-06-25 |
| ZA863560B (en) | 1987-01-28 |
| FI864292A (fi) | 1987-04-29 |
| DK512786A (da) | 1987-04-29 |
| FI864292A0 (fi) | 1986-10-23 |
| US4664820A (en) | 1987-05-12 |
| NL194756B (nl) | 2002-10-01 |
| FR2589162A1 (fr) | 1987-04-30 |
| AU6441886A (en) | 1987-04-30 |
| SE8604583D0 (sv) | 1986-10-27 |
| IT1197824B (it) | 1988-12-06 |
| BE905668A (fr) | 1987-02-16 |
| CH672497A5 (sv) | 1989-11-30 |
| GR862613B (en) | 1987-03-03 |
| NL194756C (nl) | 2003-02-04 |
| DE3636473A1 (de) | 1987-04-30 |
| SE463562B (sv) | 1990-12-10 |
| JPH07108990B2 (ja) | 1995-11-22 |
| GB2185246A (en) | 1987-07-15 |
| GB2185246B (en) | 1989-10-18 |
| JPS62161897A (ja) | 1987-07-17 |
| DK512786D0 (da) | 1986-10-27 |
| LU86639A1 (fr) | 1987-04-02 |
| IT8621781A1 (it) | 1988-03-22 |
| IT8621781A0 (it) | 1986-09-22 |
| AU578405B2 (en) | 1988-10-20 |
| NL8602444A (nl) | 1987-05-18 |
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