JP2016525623A5 - - Google Patents

Info

Publication number

JP2016525623A5

JP2016525623A5 JP2016530544A JP2016530544A JP2016525623A5 JP 2016525623 A5 JP2016525623 A5 JP 2016525623A5 JP 2016530544 A JP2016530544 A JP 2016530544A JP 2016530544 A JP2016530544 A JP 2016530544A JP 2016525623 A5 JP2016525623 A5 JP 2016525623A5

Authority

JP

Japan

Prior art keywords

compound

lubricant composition

moiety

formula

dithiocarbamate

Prior art date

2014-08-01

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

Pending

Links

• Espacenet
• Global Dossier
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• 239000000203 mixture Substances 0.000 description 40
• 239000000314 lubricant Substances 0.000 description 34
• 150000001875 compounds Chemical class 0.000 description 23
• DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 14
• 125000004432 carbon atom Chemical group C* 0.000 description 13
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 10
• 239000004215 Carbon black (E152) Substances 0.000 description 9
• 229930195733 hydrocarbon Natural products 0.000 description 9
• 239000002184 metal Substances 0.000 description 9
• 150000002430 hydrocarbons Chemical class 0.000 description 8
• DCYNAHFAQKMWDW-UHFFFAOYSA-N azane;carbamodithioic acid Chemical compound N.NC(S)=S DCYNAHFAQKMWDW-UHFFFAOYSA-N 0.000 description 7
• 229940126062 Compound A Drugs 0.000 description 6
• OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 6
• UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical group C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 5
• 125000000217 alkyl group Chemical group 0.000 description 5
• 239000012990 dithiocarbamate Substances 0.000 description 5
• LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 5
• NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 4
• 150000001768 cations Chemical class 0.000 description 4
• 229920006395 saturated elastomer Polymers 0.000 description 4
• -1 alkyl hydrocarbon Chemical class 0.000 description 3
• VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 3
• 239000002199 base oil Substances 0.000 description 2
• 0 **(*)[N+]([N-])[N+]([O-])=O Chemical compound **(*)[N+]([N-])[N+]([O-])=O 0.000 description 1
• 229920002367 Polyisobutene Polymers 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 239000003963 antioxidant agent Substances 0.000 description 1
• 230000003078 antioxidant effect Effects 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 230000005540 biological transmission Effects 0.000 description 1
• 239000002270 dispersing agent Substances 0.000 description 1
• 150000002148 esters Chemical class 0.000 description 1
• 239000000446 fuel Substances 0.000 description 1
• 230000001050 lubricating effect Effects 0.000 description 1
• 150000002989 phenols Chemical class 0.000 description 1
• CJSZLPWCFGHOPN-UHFFFAOYSA-N triazanium dioxido-sulfanylidene-sulfido-lambda5-phosphane Chemical compound P([O-])([O-])(=S)[S-].[NH4+].[NH4+].[NH4+] CJSZLPWCFGHOPN-UHFFFAOYSA-N 0.000 description 1