SE447826B - Salt av ett polyamidderivat av en polyoxialkylendiamin, vattenhaltig funktionell fluidkompositon derav samt metallbearbetningsforfarande - Google Patents

Salt av ett polyamidderivat av en polyoxialkylendiamin, vattenhaltig funktionell fluidkompositon derav samt metallbearbetningsforfarande

Info

Publication number: SE447826B
Authority: SE; Sweden
Prior art keywords: radical; salt; polyamide; water; functional fluid
Prior art date: 1981-07-21

Application number

SE8202946A

Other languages

English (en)

Swedish (sv)

Other versions

SE8202946D0 (sv

SE8202946L (sv

Inventor

W E Rieder

Original Assignee

Cincinnati Milacron Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-07-21

Filing date

1982-05-11

Publication date

1986-12-15

1982-05-11 Application filed by Cincinnati Milacron Inc filed Critical Cincinnati Milacron Inc

1982-05-11 Publication of SE8202946D0 publication Critical patent/SE8202946D0/xx

1983-01-22 Publication of SE8202946L publication Critical patent/SE8202946L/

1986-12-15 Publication of SE447826B publication Critical patent/SE447826B/sv

Links

239000004952 Polyamide Substances 0.000 title claims description 109
229920002647 polyamide Polymers 0.000 title claims description 109
150000003839 salts Chemical class 0.000 title claims description 77
239000012530 fluid Substances 0.000 title claims description 58
239000000203 mixture Substances 0.000 title claims description 50
238000000034 method Methods 0.000 title claims description 16
229910052751 metal Inorganic materials 0.000 title claims description 4
239000002184 metal Substances 0.000 title claims description 4
-1 aliphatic radical Chemical class 0.000 claims description 109
239000002253 acid Substances 0.000 claims description 53
125000002843 carboxylic acid group Chemical group 0.000 claims description 35
125000003277 amino group Chemical group 0.000 claims description 29
229910052757 nitrogen Inorganic materials 0.000 claims description 29
150000004985 diamines Chemical class 0.000 claims description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 20
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 19
229910052760 oxygen Inorganic materials 0.000 claims description 19
239000001301 oxygen Substances 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 18
150000001412 amines Chemical class 0.000 claims description 17
229910052717 sulfur Inorganic materials 0.000 claims description 15
239000011593 sulfur Substances 0.000 claims description 15
229920001577 copolymer Polymers 0.000 claims description 13
239000000314 lubricant Substances 0.000 claims description 13
229920001519 homopolymer Polymers 0.000 claims description 12
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 10
125000004429 atom Chemical group 0.000 claims description 9
229910052783 alkali metal Inorganic materials 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 8
238000005555 metalworking Methods 0.000 claims description 7
235000014113 dietary fatty acids Nutrition 0.000 claims description 6
229930195729 fatty acid Natural products 0.000 claims description 6
239000000194 fatty acid Substances 0.000 claims description 6
150000004665 fatty acids Chemical class 0.000 claims description 6
125000006413 ring segment Chemical group 0.000 claims description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
150000001340 alkali metals Chemical class 0.000 claims description 5
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 5
238000006116 polymerization reaction Methods 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 2
150000001735 carboxylic acids Chemical class 0.000 claims 2
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
238000003754 machining Methods 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
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 15
239000000126 substance Substances 0.000 description 14
229920003171 Poly (ethylene oxide) Polymers 0.000 description 11
239000000539 dimer Substances 0.000 description 11
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 10
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 10
229920001451 polypropylene glycol Polymers 0.000 description 9
150000001732 carboxylic acid derivatives Chemical class 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
150000003141 primary amines Chemical group 0.000 description 8
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 7
150000004820 halides Chemical class 0.000 description 7
239000000047 product Substances 0.000 description 7
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
239000001530 fumaric acid Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
239000012736 aqueous medium Substances 0.000 description 4
238000005520 cutting process Methods 0.000 description 4
239000002609 medium Substances 0.000 description 4
239000000178 monomer Substances 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000008064 anhydrides Chemical class 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
229920001400 block copolymer Polymers 0.000 description 3
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
230000015556 catabolic process Effects 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000006731 degradation reaction Methods 0.000 description 3
230000001050 lubricating effect Effects 0.000 description 3
238000005461 lubrication Methods 0.000 description 3
229920005604 random copolymer Polymers 0.000 description 3
239000013638 trimer Substances 0.000 description 3
150000004670 unsaturated fatty acids Chemical class 0.000 description 3
235000021122 unsaturated fatty acids Nutrition 0.000 description 3
238000005698 Diels-Alder reaction Methods 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
125000002837 carbocyclic group Chemical group 0.000 description 2
239000007795 chemical reaction product Substances 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
TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 2
229910001651 emery Inorganic materials 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
JJOJFIHJIRWASH-UHFFFAOYSA-N icosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCC(O)=O JJOJFIHJIRWASH-UHFFFAOYSA-N 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
BNJOQKFENDDGSC-UHFFFAOYSA-N octadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCC(O)=O BNJOQKFENDDGSC-UHFFFAOYSA-N 0.000 description 2
125000005702 oxyalkylene group Chemical group 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
GJAWHXHKYYXBSV-UHFFFAOYSA-N quinolinic acid Chemical compound OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
229920006395 saturated elastomer Polymers 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
239000003784 tall oil Substances 0.000 description 2
229920001897 terpolymer Polymers 0.000 description 2
238000010998 test method Methods 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
MHVJRKBZMUDEEV-APQLOABGSA-N (+)-Pimaric acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CC[C@](C=C)(C)C=C2CC1 MHVJRKBZMUDEEV-APQLOABGSA-N 0.000 description 1
MHVJRKBZMUDEEV-UHFFFAOYSA-N (-)-ent-pimara-8(14),15-dien-19-oic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(C=C)(C)C=C1CC2 MHVJRKBZMUDEEV-UHFFFAOYSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
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
PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 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
KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 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
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-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
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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
GFIWSSUBVYLTRF-UHFFFAOYSA-N 2-[2-(2-hydroxyethylamino)ethylamino]ethanol Chemical compound OCCNCCNCCO GFIWSSUBVYLTRF-UHFFFAOYSA-N 0.000 description 1
CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
JAEJSNFTJMYIEF-UHFFFAOYSA-N 2-benzylpropanedioic acid Chemical compound OC(=O)C(C(O)=O)CC1=CC=CC=C1 JAEJSNFTJMYIEF-UHFFFAOYSA-N 0.000 description 1
ULDVOPUXMRCBDH-UHFFFAOYSA-N 2-butyl-3-methylidenebutanedioic acid Chemical compound CCCCC(C(O)=O)C(=C)C(O)=O ULDVOPUXMRCBDH-UHFFFAOYSA-N 0.000 description 1
ROAMHGQDEBUBQV-UHFFFAOYSA-N 2-chlorohexanedioic acid Chemical compound OC(=O)CCCC(Cl)C(O)=O ROAMHGQDEBUBQV-UHFFFAOYSA-N 0.000 description 1
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ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
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150000001243 acetic acids Chemical class 0.000 description 1
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LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
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239000007864 aqueous solution Substances 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
125000002619 bicyclic group Chemical group 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
150000003940 butylamines Chemical group 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 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
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical class ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
MUYSADWCWFFZKR-UHFFFAOYSA-N cinchomeronic acid Chemical compound OC(=O)C1=CC=NC=C1C(O)=O MUYSADWCWFFZKR-UHFFFAOYSA-N 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
238000010549 co-Evaporation Methods 0.000 description 1
XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Substances CC(C)NC(C)C UAOMVDZJSHZZME-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
MPFLRYZEEAQMLQ-UHFFFAOYSA-N dinicotinic acid Chemical compound OC(=O)C1=CN=CC(C(O)=O)=C1 MPFLRYZEEAQMLQ-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
238000005553 drilling Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
JOTDFEIYNHTJHZ-UHFFFAOYSA-N furan-2,4-dicarboxylic acid Chemical compound OC(=O)C1=COC(C(O)=O)=C1 JOTDFEIYNHTJHZ-UHFFFAOYSA-N 0.000 description 1
SYLAFCZSYRXBJF-UHFFFAOYSA-N furan-3,4-dicarboxylic acid Chemical compound OC(=O)C1=COC=C1C(O)=O SYLAFCZSYRXBJF-UHFFFAOYSA-N 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
150000002500 ions Chemical class 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
MJIVRKPEXXHNJT-UHFFFAOYSA-N lutidinic acid Chemical compound OC(=O)C1=CC=NC(C(O)=O)=C1 MJIVRKPEXXHNJT-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
230000008018 melting Effects 0.000 description 1
238000002844 melting Methods 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
HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
SRLHDBRENZFCIN-UHFFFAOYSA-N n,n-di(butan-2-yl)butan-2-amine Chemical compound CCC(C)N(C(C)CC)C(C)CC SRLHDBRENZFCIN-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
WSTNFGAKGUERTC-UHFFFAOYSA-N n-ethylhexan-1-amine Chemical compound CCCCCCNCC WSTNFGAKGUERTC-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
239000012430 organic reaction media Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
238000006213 oxygenation reaction 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
RIXVESSVKLKKFV-UHFFFAOYSA-N piperazine-1,4-dicarboxylic acid Chemical compound OC(=O)N1CCN(C(O)=O)CC1 RIXVESSVKLKKFV-UHFFFAOYSA-N 0.000 description 1
230000000379 polymerizing effect Effects 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
238000001556 precipitation Methods 0.000 description 1
230000008569 process Effects 0.000 description 1
238000004080 punching Methods 0.000 description 1
ZUCRGHABDDWQPY-UHFFFAOYSA-N pyrazine-2,3-dicarboxylic acid Chemical compound OC(=O)C1=NC=CN=C1C(O)=O ZUCRGHABDDWQPY-UHFFFAOYSA-N 0.000 description 1
GMIOYJQLNFNGPR-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CN=C(C(O)=O)C=N1 GMIOYJQLNFNGPR-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
238000005096 rolling process Methods 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
238000007127 saponification reaction Methods 0.000 description 1
235000015067 sauces Nutrition 0.000 description 1
BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
ZIKJCAPMXXTMDD-UHFFFAOYSA-M sodium;2-(1-hydroxycyclohexyl)butanoate Chemical compound [Na+].CCC(C([O-])=O)C1(O)CCCCC1 ZIKJCAPMXXTMDD-UHFFFAOYSA-M 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
GFKSKVCFBACPGK-UHFFFAOYSA-N terephthalic acid;hydrochloride Chemical compound Cl.OC(=O)C1=CC=C(C(O)=O)C=C1 GFKSKVCFBACPGK-UHFFFAOYSA-N 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
UVZICZIVKIMRNE-UHFFFAOYSA-N thiodiacetic acid Chemical compound OC(=O)CSCC(O)=O UVZICZIVKIMRNE-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
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
FNZBSNUICNVAAM-UHFFFAOYSA-N trimethyl-[methyl-[methyl-(methyl-phenyl-trimethylsilyloxysilyl)oxy-phenylsilyl]oxy-phenylsilyl]oxysilane Chemical compound C=1C=CC=CC=1[Si](C)(O[Si](C)(C)C)O[Si](C)(C=1C=CC=CC=1)O[Si](C)(O[Si](C)(C)C)C1=CC=CC=C1 FNZBSNUICNVAAM-UHFFFAOYSA-N 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000003466 welding Methods 0.000 description 1
239000008096 xylene 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)
Lubricants (AREA)
Polyamides (AREA)
Compositions Of Macromolecular Compounds (AREA)

SE8202946A 1981-07-21 1982-05-11 Salt av ett polyamidderivat av en polyoxialkylendiamin, vattenhaltig funktionell fluidkompositon derav samt metallbearbetningsforfarande SE447826B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/285,575 US4374741A (en)	1981-07-21	1981-07-21	Polyamide and functional fluid containing same

Publications (3)

Publication Number	Publication Date
SE8202946D0 SE8202946D0 (sv)	1982-05-11
SE8202946L SE8202946L (sv)	1983-01-22
SE447826B true SE447826B (sv)	1986-12-15

Family

ID=23094845

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8202946A SE447826B (sv)	1981-07-21	1982-05-11	Salt av ett polyamidderivat av en polyoxialkylendiamin, vattenhaltig funktionell fluidkompositon derav samt metallbearbetningsforfarande

Country Status (18)

Country	Link
US (1)	US4374741A (da)
JP (1)	JPS5815530A (da)
KR (1)	KR850001885B1 (da)
AU (1)	AU530507B2 (da)
BE (1)	BE892969A (da)
BR (1)	BR8204222A (da)
CA (1)	CA1220484A (da)
CH (1)	CH654582A5 (da)
DE (2)	DE3207842A1 (da)
DK (1)	DK167285B1 (da)
FR (1)	FR2510126B1 (da)
GB (1)	GB2101998B (da)
IT (1)	IT1156481B (da)
MX (1)	MX159541A (da)
NL (1)	NL185569C (da)
NZ (1)	NZ199954A (da)
SE (1)	SE447826B (da)
ZA (1)	ZA821165B (da)

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JPS58122993A (ja) *	1982-01-19	1983-07-21	Nippon Oil & Fats Co Ltd	水系潤滑油組成物
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
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
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
GB2172891A (en) *	1985-03-27	1986-10-01	Hoechst Gosei Kk	Process for preparing aqueous gel and use thereof
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
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
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
MXPA02009493A (es) *	2000-03-29	2003-09-22	Huntsman Spec Chem Corp	Amidas primarias de punto de fluidez bajo.
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
DE602005023768D1 (de) *	2004-11-22	2010-11-04	Novartis Ag	Vernetzbare, Polyoxyalkylen-enthaltende Polyamidprepolymere
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
CN104582480B (zh) *	2013-05-23	2018-12-11	亨斯迈石油化学有限责任公司	聚酰胺和聚酰亚胺粘着剂助剂
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
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WO2017167692A1 (en)	2016-04-01	2017-10-05	Solvay Specialty Polymers Usa, Llc	(co)polyamides obtainable from 1,4-cyclohexanedicarboxylic acid and a diamine of formula h2n-(ch2)2-o-(ch2)2-o-(ch2)2-nh2
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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 DE19823207842 patent/DE3207842A1/de active Granted
- 1982-03-04 DE DE3249701A patent/DE3249701C2/de not_active Expired - Lifetime
- 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 IP Right Cessation
- 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
DE3207842C2 (da)	1990-01-11
DE3207842A1 (de)	1983-02-10
FR2510126B1 (da)	1986-01-10
DE3249701A1 (da)	1985-04-18
GB2101998B (en)	1985-11-13
NL185569C (nl)	1990-05-16
SE8202946D0 (sv)	1982-05-11
BE892969A (fr)	1982-08-16
MX159541A (es)	1989-06-29
CH654582A5 (de)	1986-02-28
SE8202946L (sv)	1983-01-22
FR2510126A1 (da)	1983-01-28
IT8267933A0 (it)	1982-07-20
DK324882A (da)	1983-01-22
NZ199954A (en)	1985-01-31
US4374741A (en)	1983-02-22
KR850001885B1 (ko)	1985-12-28
JPS5815530A (ja)	1983-01-28
NL8201014A (nl)	1983-02-16
BR8204222A (pt)	1983-07-12
NL185569B (nl)	1989-12-18
AU8094882A (en)	1983-01-27
JPH0152418B2 (da)	1989-11-08
AU530507B2 (en)	1983-07-21
KR830010187A (ko)	1983-12-26
ZA821165B (en)	1983-01-26
DE3249701C2 (de)	1993-12-09
IT1156481B (it)	1987-02-04
DK167285B1 (da)	1993-10-04
CA1220484A (en)	1987-04-14
GB2101998A (en)	1983-01-26

Publication	Publication Date	Title
SE447826B (sv)	1986-12-15	Salt av ett polyamidderivat av en polyoxialkylendiamin, vattenhaltig funktionell fluidkompositon derav samt metallbearbetningsforfarande
SE449365B (sv)	1987-04-27	Karboxylsyragrupp-avslutad polyoxialkylendiamid och metallbearbetningkomposition innehallande densamma
KR850001965B1 (ko)	1985-12-31	수성 작용유체 조성물
CN110452766B (zh)	2021-12-21	一种铝合金加工用全合成环保切削液及其制备方法
USRE31522E (en)	1984-02-14	Salt of a polyamide and functional fluid containing same
USRE30885E (en)	1982-03-23	Novel diamide and lubricants containing same
US4419251A (en)	1983-12-06	Aqueous lubricant
US4172802A (en)	1979-10-30	Aqueous metal working fluid containing carboxylic acid group terminated diesters of polyoxyalkylene diols
JPS63500459A (ja)	1988-02-18	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
KR850001966B1 (ko)	1985-12-31	수성 작용유체 조성물
US3787458A (en)	1974-01-22	Oil-soluble aliphatic acid modified high molecular weight mannich condensation products
US20120088705A1 (en)	2012-04-12	Polyalkylene glycol-based ether pyrrolidone carboxylic acids, and concentrates for the production of synthetic cooling lubricants containing the same
WO1994028093A1 (en)	1994-12-08	Base fluid
EP0055488B1 (en)	1984-07-04	Water-based energy transmitting fluid composition
US11685876B2 (en)	2023-06-27	Maleated soybean oil derivatives as additives in metalworking fluids
CA1191835A (en)	1985-08-13	Water-soluble lubricant
EP0591771A1 (en)	1994-04-13	A synthetic, mineral oil free, forming oil composition dispersed in a hydroalcoholic medium
JP7407591B2 (ja)	2024-01-04	無機材料の加工に用いる油剤組成物及び加工液
CN116622434B (zh)	2024-11-15	一种具有抗杂油性能的水基全合成切削液及其制备方法
JPS63168493A (ja)	1988-07-12	難燃性切削油剤

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