DK167285B1 - Vandig smoerende vaeskeblanding og metalbearbejdningsfremgangsmaade - Google Patents
Vandig smoerende vaeskeblanding og metalbearbejdningsfremgangsmaade Download PDFInfo
- Publication number
- DK167285B1 DK167285B1 DK324882A DK324882A DK167285B1 DK 167285 B1 DK167285 B1 DK 167285B1 DK 324882 A DK324882 A DK 324882A DK 324882 A DK324882 A DK 324882A DK 167285 B1 DK167285 B1 DK 167285B1
- Authority
- DK
- Denmark
- Prior art keywords
- group
- salt
- polyamide
- water
- liquid mixture
- Prior art date
Links
- 239000007788 liquid Substances 0.000 title claims description 45
- 230000001050 lubricating effect Effects 0.000 title claims description 43
- 238000000034 method Methods 0.000 title claims description 18
- 238000005555 metalworking Methods 0.000 title claims description 17
- 239000004952 Polyamide Substances 0.000 claims description 93
- 229920002647 polyamide Polymers 0.000 claims description 93
- -1 amine salt Chemical class 0.000 claims description 71
- 150000003839 salts Chemical class 0.000 claims description 57
- 239000000203 mixture Substances 0.000 claims description 53
- 239000002253 acid Substances 0.000 claims description 45
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 35
- 150000004985 diamines Chemical class 0.000 claims description 22
- 125000003277 amino group Chemical group 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 15
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- 229910052717 sulfur Inorganic materials 0.000 claims description 15
- 239000011593 sulfur Substances 0.000 claims description 15
- 150000001412 amines Chemical group 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 229920001519 homopolymer Polymers 0.000 claims description 12
- 125000004429 atom Chemical group 0.000 claims description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 150000004665 fatty acids Chemical class 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 3
- 125000002619 bicyclic group Chemical group 0.000 claims description 3
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 238000003754 machining Methods 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 150000001340 alkali metals Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000012530 fluid Substances 0.000 description 27
- 239000000539 dimer Substances 0.000 description 21
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 16
- 239000000314 lubricant Substances 0.000 description 12
- KYXHKHDZJSDWEF-LHLOQNFPSA-N CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 Chemical compound CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 KYXHKHDZJSDWEF-LHLOQNFPSA-N 0.000 description 11
- 239000009261 D 400 Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 229920001451 polypropylene glycol Polymers 0.000 description 9
- 229910000831 Steel Inorganic materials 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- 150000004820 halides Chemical class 0.000 description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 6
- 125000005702 oxyalkylene group Chemical group 0.000 description 6
- 238000005698 Diels-Alder reaction Methods 0.000 description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 229910003460 diamond Inorganic materials 0.000 description 5
- 239000010432 diamond Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 150000003973 alkyl amines Chemical class 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 4
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 235000011087 fumaric acid Nutrition 0.000 description 3
- 239000002655 kraft paper Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000005263 alkylenediamine group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 229910001651 emery Inorganic materials 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 125000004957 naphthylene group Chemical group 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229920006301 statistical copolymer Polymers 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 125000005838 1,3-cyclopentylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:2])C([H])([H])C1([H])[*:1] 0.000 description 1
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 1
- 125000004958 1,4-naphthylene group Chemical group 0.000 description 1
- BFIAIMMAHAIVFT-UHFFFAOYSA-N 1-[bis(2-hydroxybutyl)amino]butan-2-ol Chemical compound CCC(O)CN(CC(O)CC)CC(O)CC BFIAIMMAHAIVFT-UHFFFAOYSA-N 0.000 description 1
- KODLUXHSIZOKTG-UHFFFAOYSA-N 1-aminobutan-2-ol Chemical compound CCC(O)CN KODLUXHSIZOKTG-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
- 125000004959 2,6-naphthylene group Chemical group [H]C1=C([H])C2=C([H])C([*:1])=C([H])C([H])=C2C([H])=C1[*:2] 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- SLWIPPZWFZGHEU-UHFFFAOYSA-N 2-[4-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=C(CC(O)=O)C=C1 SLWIPPZWFZGHEU-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
- MNEXQJIOTUAEPH-UHFFFAOYSA-N 3-(2-ethoxyethoxy)propan-1-amine Chemical compound CCOCCOCCCN MNEXQJIOTUAEPH-UHFFFAOYSA-N 0.000 description 1
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
- QVIAMKXOQGCYCV-UHFFFAOYSA-N 4-methylpentan-1-amine Chemical compound CC(C)CCCN QVIAMKXOQGCYCV-UHFFFAOYSA-N 0.000 description 1
- PIUSRRUXGNYCSS-UHFFFAOYSA-N 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7,8-tetramethoxy-4H-chromen-4-one Chemical compound COC1=C(OC)C(OC)=C(O)C(C(C=2OC)=O)=C1OC=2C1=CC=C(O)C=C1 PIUSRRUXGNYCSS-UHFFFAOYSA-N 0.000 description 1
- 241000173529 Aconitum napellus Species 0.000 description 1
- SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- 241000566113 Branta sandvicensis Species 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 229910000997 High-speed steel Inorganic materials 0.000 description 1
- 108010093488 His-His-His-His-His-His Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- 229930183415 Suberin Natural products 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229940023019 aconite Drugs 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 159000000006 cesium salts Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002238 fumaric acids Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- LVPMIMZXDYBCDF-UHFFFAOYSA-N isocinchomeronic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)N=C1 LVPMIMZXDYBCDF-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229940109615 oxy 10 Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 235000019303 thiodipropionic acid Nutrition 0.000 description 1
- HIHKYDVSWLFRAY-UHFFFAOYSA-N thiophene-2,3-dicarboxylic acid Chemical compound OC(=O)C=1C=CSC=1C(O)=O HIHKYDVSWLFRAY-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G07—CHECKING-DEVICES
- G07D—HANDLING OF COINS OR VALUABLE PAPERS, e.g. TESTING, SORTING BY DENOMINATIONS, COUNTING, DISPENSING, CHANGING OR DEPOSITING
- G07D3/00—Sorting a mixed bulk of coins into denominations
- G07D3/14—Apparatus driven under control of coin-sensing elements
-
- 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
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/044—Polyamides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Polyamides (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28557581 | 1981-07-21 | ||
US06/285,575 US4374741A (en) | 1981-07-21 | 1981-07-21 | Polyamide and functional fluid containing same |
Publications (2)
Publication Number | Publication Date |
---|---|
DK324882A DK324882A (da) | 1983-01-22 |
DK167285B1 true DK167285B1 (da) | 1993-10-04 |
Family
ID=23094845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK324882A DK167285B1 (da) | 1981-07-21 | 1982-07-20 | Vandig smoerende vaeskeblanding og metalbearbejdningsfremgangsmaade |
Country Status (18)
Country | Link |
---|---|
US (1) | US4374741A (en, 2012) |
JP (1) | JPS5815530A (en, 2012) |
KR (1) | KR850001885B1 (en, 2012) |
AU (1) | AU530507B2 (en, 2012) |
BE (1) | BE892969A (en, 2012) |
BR (1) | BR8204222A (en, 2012) |
CA (1) | CA1220484A (en, 2012) |
CH (1) | CH654582A5 (en, 2012) |
DE (2) | DE3249701C2 (en, 2012) |
DK (1) | DK167285B1 (en, 2012) |
FR (1) | FR2510126B1 (en, 2012) |
GB (1) | GB2101998B (en, 2012) |
IT (1) | IT1156481B (en, 2012) |
MX (1) | MX159541A (en, 2012) |
NL (1) | NL185569C (en, 2012) |
NZ (1) | NZ199954A (en, 2012) |
SE (1) | SE447826B (en, 2012) |
ZA (1) | ZA821165B (en, 2012) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58122993A (ja) * | 1982-01-19 | 1983-07-21 | Nippon Oil & Fats Co Ltd | 水系潤滑油組成物 |
IT1191045B (it) * | 1982-10-25 | 1988-02-24 | Aic Approvvigio Ind Chim | Additivi anti-corrosione per liquidi acquosi per la lavorazione di metalli e procedimento per la loro preparazione |
IT1191046B (it) * | 1982-10-25 | 1988-02-24 | Aic Approvvigio Ind Chim | Additivi anti-corrosione per liquidi acquosi per la lavorazione di metalli e procedimento per la loro preparazione |
US4743387A (en) * | 1983-02-17 | 1988-05-10 | Mobil Oil Corporation | Polyoxyalkylene diamides as lubricant additives |
US4537694A (en) * | 1983-09-23 | 1985-08-27 | Mobil Oil Corporation | Diamine carboxylates and lubricant compositions containing same |
US4581039A (en) * | 1983-09-23 | 1986-04-08 | Mobil Oil Corporation | Diamine carboxylates and lubricant and fuel compositions containing same |
DE3425318A1 (de) * | 1984-07-10 | 1986-01-16 | Bayer Ag, 5090 Leverkusen | Verzweigte, thermoplastisch verarbeitbare, schlagzaehe polyamide |
DE3609928A1 (de) * | 1985-03-27 | 1986-10-09 | Hoechst Gosei K.K., Tokio/Tokyo | Waessrige gelzusammensetzung, verfahren zu ihrer herstellung und ihre verwendung in der metallbearbeitung |
US4664834A (en) * | 1985-07-29 | 1987-05-12 | The Lubrizol Corporation | Hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products, and aqueous systems containing same |
US4661275A (en) * | 1985-07-29 | 1987-04-28 | The Lubrizol Corporation | Water-based functional fluid thickening combinations of surfactants and hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products |
US4676917A (en) * | 1986-02-27 | 1987-06-30 | Texaco Inc. | Railway diesel crankcase lubricant |
US5239048A (en) * | 1987-07-27 | 1993-08-24 | Texaco Chemical Company | Aromatic polyoxyalkylene amidoamines |
US5128441A (en) * | 1987-07-27 | 1992-07-07 | Texaco Chemical Company | Block polyamido condensation products |
US5179175A (en) * | 1990-12-14 | 1993-01-12 | Texaco Chemical Company | Polyamides from polyetheramines, hexamethylene diamine and adipic acid |
US5260268A (en) * | 1991-07-18 | 1993-11-09 | The Lubrizol Corporation | Methods of drilling well boreholes and compositions used therein |
US5378798A (en) * | 1992-07-10 | 1995-01-03 | Shell Oil Company | Composition and process for coating metallic substrates |
US5599777A (en) * | 1993-10-06 | 1997-02-04 | The Lubrizol Corporation | Methods of using acidizing fluids in wells, and compositions used therein |
BR0109899A (pt) * | 2000-03-29 | 2006-08-29 | Huntsman Spec Chem Corp | amidas primárias com baixo grau de umidade |
KR100480970B1 (ko) * | 2000-11-06 | 2005-05-17 | (주)내츄럴엔도텍 | 당귀 추출물을 유효성분으로 하는 다이옥신 유사물질에대한 길항성 조성물 |
US6956099B2 (en) * | 2003-03-20 | 2005-10-18 | Arizona Chemical Company | Polyamide-polyether block copolymer |
TW200514826A (en) | 2003-09-19 | 2005-05-01 | Kyung In Synthetic Corp | Alpha-hydroxy-benzeneacetic acid derivatives, and compounds having two 5-membered lactone rings fused to central cyclohexa-1, 4-diene nucleus using the same, and uses of the compounds |
KR100555624B1 (ko) * | 2004-08-26 | 2006-03-03 | (주)경인양행 | 알파-히드록시 벤젠아세틱 엑시드 유도체, 그것에 기반한시클로 헥사-1,4-디엔 모체에 2 개의 5환 락톤링을 가진화합물, 및 그것의 용도 |
WO2006053777A1 (en) * | 2004-11-22 | 2006-05-26 | Novartis Ag | Crosslinkable poly(oxyalkylene)-containing polyamide prepolymers |
US8413745B2 (en) * | 2009-08-11 | 2013-04-09 | Baker Hughes Incorporated | Water-based mud lubricant using fatty acid polyamine salts and fatty acid esters |
AR093299A1 (es) | 2012-11-01 | 2015-05-27 | Huntsman Petrochemical Llc | Adyuvantes adherentes de poliamida y poliimida |
JP6275732B2 (ja) * | 2013-05-23 | 2018-02-07 | ハンツマン ペトロケミカル エルエルシーHuntsman Petrochemical LLC | ポリアミド系およびポリイミド系ステッカーアジュバント |
JP6435689B2 (ja) * | 2014-07-25 | 2018-12-12 | Agc株式会社 | 研磨剤と研磨方法、および研磨用添加液 |
US10526447B2 (en) * | 2015-04-15 | 2020-01-07 | Houghton Technical Corp. | Materials that provide bioresistance and/or defoaming and slower cooling properties for aqueous quenchants |
JP6895989B2 (ja) | 2016-04-01 | 2021-06-30 | ソルベイ スペシャルティ ポリマーズ ユーエスエー, エルエルシー | 1,4−シクロヘキサンジカルボン酸と式h2n−(ch2)2−o−(ch2)2−o−(ch2)2−nh2のジアミンから得られる(コ)ポリアミド |
EP3969498B1 (en) * | 2019-05-16 | 2024-03-13 | Evonik Operations GmbH | Curing composition |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB574713A (en) * | 1942-11-24 | 1946-01-17 | Wingfoot Corp | Polyamides |
DE1595758A1 (de) * | 1966-08-02 | 1970-02-12 | Glanzstoff Ag | Verfahren zur Herstellung von Polyamiden mit AEtherbindungen |
US3729449A (en) * | 1969-08-27 | 1973-04-24 | Kanegafuchi Spinning Co Ltd | Polyamide fibers composed of the polyamide and methods for producing thereof |
US3804763A (en) * | 1971-07-01 | 1974-04-16 | Lubrizol Corp | Dispersant compositions |
US3882090A (en) * | 1973-06-04 | 1975-05-06 | Eastman Kodak Co | Water-soluble polyamides from alkyleneoxy bis(propyl-amine) |
JPS5119280A (en) * | 1974-08-06 | 1976-02-16 | Sanyo Chemical Ind Ltd | Shinkinamizu gurikoorugatafunenseisadoyu |
DE2552518A1 (de) * | 1974-11-29 | 1976-08-12 | Texaco Development Corp | Thermoplastische klebstoffmasse und verfahren zu ihrer herstellung |
US4107061A (en) * | 1977-11-07 | 1978-08-15 | Emery Industries, Inc. | Amino-amide lubricants derived from polymeric fatty acids and poly(oxyethylene) diamines |
IT1098305B (it) * | 1978-06-02 | 1985-09-07 | Snam Progetti | Antiruggine per sistemi acquosi e composizione lubrificante antiruggine |
US4239635A (en) * | 1979-06-11 | 1980-12-16 | Cincinnati Milacron Inc. | Novel diamide and lubricants containing same |
-
1981
- 1981-07-21 US US06/285,575 patent/US4374741A/en not_active Expired - Lifetime
-
1982
- 1982-02-23 ZA ZA821165A patent/ZA821165B/xx unknown
- 1982-02-26 AU AU80948/82A patent/AU530507B2/en not_active Ceased
- 1982-03-04 DE DE3249701A patent/DE3249701C2/de not_active Expired - Lifetime
- 1982-03-04 DE DE19823207842 patent/DE3207842A1/de active Granted
- 1982-03-09 NZ NZ199954A patent/NZ199954A/en unknown
- 1982-03-11 NL NLAANVRAGE8201014,A patent/NL185569C/xx not_active IP Right Cessation
- 1982-03-17 CA CA000398669A patent/CA1220484A/en not_active Expired
- 1982-04-26 BE BE0/207925A patent/BE892969A/fr not_active IP Right Cessation
- 1982-04-30 FR FR8207513A patent/FR2510126B1/fr not_active Expired
- 1982-05-08 JP JP57077389A patent/JPS5815530A/ja active Granted
- 1982-05-11 SE SE8202946A patent/SE447826B/sv not_active IP Right Cessation
- 1982-05-29 KR KR8202410A patent/KR850001885B1/ko not_active Expired
- 1982-06-09 MX MX193074A patent/MX159541A/es unknown
- 1982-06-11 CH CH3647/82A patent/CH654582A5/de not_active IP Right Cessation
- 1982-07-06 GB GB08219533A patent/GB2101998B/en not_active Expired
- 1982-07-20 DK DK324882A patent/DK167285B1/da active
- 1982-07-20 IT IT67933/82A patent/IT1156481B/it active
- 1982-07-20 BR BR8204222A patent/BR8204222A/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
GB2101998A (en) | 1983-01-26 |
DE3207842A1 (de) | 1983-02-10 |
KR830010187A (ko) | 1983-12-26 |
ZA821165B (en) | 1983-01-26 |
DE3249701C2 (de) | 1993-12-09 |
SE8202946D0 (sv) | 1982-05-11 |
KR850001885B1 (ko) | 1985-12-28 |
AU530507B2 (en) | 1983-07-21 |
US4374741A (en) | 1983-02-22 |
DE3249701A1 (en, 2012) | 1985-04-18 |
FR2510126B1 (en, 2012) | 1986-01-10 |
BR8204222A (pt) | 1983-07-12 |
MX159541A (es) | 1989-06-29 |
IT8267933A0 (it) | 1982-07-20 |
FR2510126A1 (en, 2012) | 1983-01-28 |
IT1156481B (it) | 1987-02-04 |
JPS5815530A (ja) | 1983-01-28 |
SE8202946L (sv) | 1983-01-22 |
AU8094882A (en) | 1983-01-27 |
NL185569B (nl) | 1989-12-18 |
CH654582A5 (de) | 1986-02-28 |
DE3207842C2 (en, 2012) | 1990-01-11 |
DK324882A (da) | 1983-01-22 |
SE447826B (sv) | 1986-12-15 |
NL185569C (nl) | 1990-05-16 |
NZ199954A (en) | 1985-01-31 |
GB2101998B (en) | 1985-11-13 |
JPH0152418B2 (en, 2012) | 1989-11-08 |
BE892969A (fr) | 1982-08-16 |
CA1220484A (en) | 1987-04-14 |
NL8201014A (nl) | 1983-02-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DK167285B1 (da) | Vandig smoerende vaeskeblanding og metalbearbejdningsfremgangsmaade | |
CA1198548A (en) | High molecular weight water-soluble copolymers, their preparation and use | |
US4491526A (en) | Thickened, water-based hydraulic fluid with reduced dependence of viscosity on temperature | |
KR101335890B1 (ko) | 수용성 폴리히드록시아미노에테르 및 그의 제조 방법 | |
USRE31522E (en) | Salt of a polyamide and functional fluid containing same | |
SE449365B (sv) | Karboxylsyragrupp-avslutad polyoxialkylendiamid och metallbearbetningkomposition innehallande densamma | |
EP0131657A1 (en) | Aqueous lubricant composition | |
US4702854A (en) | Water-based hydraulic fluids comprising poly-oxazines or poly-oxazolines | |
CA1203527A (en) | Functional fluid | |
EP0062890B1 (en) | Water-based low foam hydraulic fluid concentrates | |
USRE30885E (en) | Novel diamide and lubricants containing same | |
NO179076B (no) | Vannbasert, hydraulisk væske | |
CN114805770A (zh) | 一种聚醚酯润滑剂及其制备方法 | |
JPS63500459A (ja) | ヒドロカルビル置換こはく酸及び/又は無水物とアミン末端付ポリ(オキシアルキレン)との反応生成物並びに同上を含む水性システム | |
US3462492A (en) | Condensation products of phenylene diamines and alkylene oxides | |
US4855070A (en) | Energy transmitting fluid | |
JP5706405B2 (ja) | ポリアルキレングリコールに基づくエーテルピロリドンカルボン酸及びそれを含む合成冷却潤滑剤の製造のための濃厚物 | |
JP5429983B2 (ja) | 抗乳化剤、その製造法及びそれを含有する水溶性加工油剤組成物 | |
US3544637A (en) | Polyoxyalkylated hydraulic fluids | |
EP0273460B1 (en) | Energy transmitting fluid | |
JPH0227393B2 (ja) | Mizukeijunkatsuyusoseibutsu | |
JPH07233391A (ja) | 水溶性潤滑油 | |
JP2608537B2 (ja) | 増粘型高含水作動液 | |
CN111040825A (zh) | 一种羧酸胺盐改性聚环氧乙烷水基液压液抗磨添加剂 | |
NO871307L (no) | Hydrokarbylsubstituerte ravsyre- og/eller anhydrid/amin-terminerte poly(oksyalkylen)-reaksjonsprodukter og vandige systemer inneholdende slike. |