JPS61143492A - 燃料油組成物 - Google Patents

燃料油組成物

Info

Publication number: JPS61143492A
Authority: JP; Japan
Prior art keywords: oil; fuel oil; acid; alkaline earth; earth metal
Prior art date: 1984-12-14
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.): Granted

Application number

JP26494984A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0417238B2 (fr

Inventor

Shigeru Okada

茂岡田

Keiichi Akimoto

秋本　啓一

Toshiro Suzuki

敏朗鈴木

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Sanyo Chemical Industries Ltd

Original Assignee

Sanyo Chemical Industries Ltd

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.)

1984-12-14

Filing date

1984-12-14

Publication date

1986-07-01

1984-12-14 Application filed by Sanyo Chemical Industries Ltd filed Critical Sanyo Chemical Industries Ltd

1984-12-14 Priority to JP26494984A priority Critical patent/JPS61143492A/ja

1986-07-01 Publication of JPS61143492A publication Critical patent/JPS61143492A/ja

1992-03-25 Publication of JPH0417238B2 publication Critical patent/JPH0417238B2/ja

Status Granted legal-status Critical Current

Links

239000000295 fuel oil Substances 0.000 title claims abstract description 48
239000000203 mixture Substances 0.000 title claims abstract description 38
150000001341 alkaline earth metal compounds Chemical class 0.000 claims abstract description 15
238000005336 cracking Methods 0.000 claims abstract description 12
239000010802 sludge Substances 0.000 claims abstract description 9
239000003208 petroleum Substances 0.000 claims abstract description 8
239000003112 inhibitor Substances 0.000 claims abstract description 5
-1 carboxylate salt Chemical class 0.000 claims description 27
239000003352 sequestering agent Substances 0.000 claims description 20
238000009835 boiling Methods 0.000 claims description 10
238000004523 catalytic cracking Methods 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 5
238000004040 coloring Methods 0.000 claims description 4
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims description 4
RURPJGZXBHYNEM-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]propyliminomethyl]phenol Chemical group C=1C=CC=C(O)C=1C=NC(C)CN=CC1=CC=CC=C1O RURPJGZXBHYNEM-UHFFFAOYSA-N 0.000 claims description 3
229910052788 barium Inorganic materials 0.000 claims description 3
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 3
229910052712 strontium Inorganic materials 0.000 claims description 3
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 3
238000004227 thermal cracking Methods 0.000 claims 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 abstract description 5
230000000694 effects Effects 0.000 abstract description 5
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 abstract description 5
238000004140 cleaning Methods 0.000 abstract description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 2
239000000779 smoke Substances 0.000 abstract description 2
159000000009 barium salts Chemical class 0.000 abstract 1
239000002981 blocking agent Substances 0.000 abstract 1
230000007797 corrosion Effects 0.000 abstract 1
238000005260 corrosion Methods 0.000 abstract 1
238000002845 discoloration Methods 0.000 abstract 1
230000002401 inhibitory effect Effects 0.000 abstract 1
FRKHZXHEZFADLA-UHFFFAOYSA-L strontium;octadecanoate Chemical compound [Sr+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O FRKHZXHEZFADLA-UHFFFAOYSA-L 0.000 abstract 1
239000003921 oil Substances 0.000 description 26
235000019198 oils Nutrition 0.000 description 26
125000004432 carbon atom Chemical group C* 0.000 description 20
239000002253 acid Substances 0.000 description 19
125000003118 aryl group Chemical group 0.000 description 13
238000000034 method Methods 0.000 description 12
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
150000002989 phenols Chemical class 0.000 description 11
229920006395 saturated elastomer Polymers 0.000 description 9
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 8
150000001298 alcohols Chemical class 0.000 description 7
235000014113 dietary fatty acids Nutrition 0.000 description 7
239000000194 fatty acid Substances 0.000 description 7
229930195729 fatty acid Natural products 0.000 description 7
150000002430 hydrocarbons Chemical group 0.000 description 7
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
150000001735 carboxylic acids Chemical class 0.000 description 6
238000004821 distillation Methods 0.000 description 6
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 6
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
229910052784 alkaline earth metal Inorganic materials 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
239000002904 solvent Substances 0.000 description 5
235000010205 Cola acuminata Nutrition 0.000 description 4
244000228088 Cola acuminata Species 0.000 description 4
235000015438 Cola nitida Nutrition 0.000 description 4
229910019142 PO4 Inorganic materials 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
235000008331 Pinus X rigitaeda Nutrition 0.000 description 4
235000011613 Pinus brutia Nutrition 0.000 description 4
241000018646 Pinus brutia Species 0.000 description 4
150000001342 alkaline earth metals Chemical class 0.000 description 4
239000002199 base oil Substances 0.000 description 4
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
150000007524 organic acids Chemical class 0.000 description 4
239000010452 phosphate Substances 0.000 description 4
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 3
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000005711 Benzoic acid Substances 0.000 description 3
WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000005642 Oleic acid Substances 0.000 description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
235000021355 Stearic acid Nutrition 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000000654 additive Substances 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
229910000147 aluminium phosphate Inorganic materials 0.000 description 3
235000010233 benzoic acid Nutrition 0.000 description 3
150000001558 benzoic acid derivatives Chemical class 0.000 description 3
238000007865 diluting Methods 0.000 description 3
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
229940049964 oleate Drugs 0.000 description 3
229940055577 oleyl alcohol Drugs 0.000 description 3
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 3
239000008117 stearic acid Substances 0.000 description 3
238000005292 vacuum distillation Methods 0.000 description 3
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
NSENZNPLAVRFMJ-UHFFFAOYSA-N 2,3-dibutylphenol Chemical compound CCCCC1=CC=CC(O)=C1CCCC NSENZNPLAVRFMJ-UHFFFAOYSA-N 0.000 description 2
IXKVYSRDIVLASR-UHFFFAOYSA-N 2,3-dioctylphenol Chemical compound CCCCCCCCC1=CC=CC(O)=C1CCCCCCCC IXKVYSRDIVLASR-UHFFFAOYSA-N 0.000 description 2
CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
239000005639 Lauric acid Substances 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
235000021314 Palmitic acid Nutrition 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
239000010775 animal oil Substances 0.000 description 2
239000003849 aromatic solvent Substances 0.000 description 2
229950011260 betanaphthol Drugs 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
235000019864 coconut oil Nutrition 0.000 description 2
239000003240 coconut oil Substances 0.000 description 2
238000004939 coking Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000002828 fuel tank Substances 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
APIYXLWHDLHUBS-UHFFFAOYSA-N icos-2-ene-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCCCCC=CCS(O)(=O)=O APIYXLWHDLHUBS-UHFFFAOYSA-N 0.000 description 2
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
235000021313 oleic acid Nutrition 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
GJYCVCVHRSWLNY-UHFFFAOYSA-N ortho-butylphenol Natural products CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
238000003860 storage Methods 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
239000003784 tall oil Substances 0.000 description 2
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 2
GROJOWHVXQYQGN-UHFFFAOYSA-N tetradecyl sulfonic acid Chemical compound CCCCC(CC)CCC(CC(C)C)OS(O)(=O)=O GROJOWHVXQYQGN-UHFFFAOYSA-N 0.000 description 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 1
CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
ILJOIOLSOMYKNF-UHFFFAOYSA-N 2,3-didodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCCCCC ILJOIOLSOMYKNF-UHFFFAOYSA-N 0.000 description 1
ONBMZSARMOMISG-UHFFFAOYSA-N 2,3-dioctylbenzenesulfonic acid Chemical compound CCCCCCCCC1=CC=CC(S(O)(=O)=O)=C1CCCCCCCC ONBMZSARMOMISG-UHFFFAOYSA-N 0.000 description 1
BYLSIPUARIZAHZ-UHFFFAOYSA-N 2,4,6-tris(1-phenylethyl)phenol Chemical compound C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C(C)C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 BYLSIPUARIZAHZ-UHFFFAOYSA-N 0.000 description 1
RRKBRXPIJHVKIC-UHFFFAOYSA-N 2-(2-ethylhexyl)phenol Chemical compound CCCCC(CC)CC1=CC=CC=C1O RRKBRXPIJHVKIC-UHFFFAOYSA-N 0.000 description 1
OEHNVKBOQOXOJN-UHFFFAOYSA-N 2-(4-nitrophenyl)phenol Chemical compound OC1=CC=CC=C1C1=CC=C([N+]([O-])=O)C=C1 OEHNVKBOQOXOJN-UHFFFAOYSA-N 0.000 description 1
ONHMWXJSVBNXOB-KTKRTIGZSA-N 2-[(z)-octadec-9-enyl]phenol Chemical compound CCCCCCCC\C=C/CCCCCCCCC1=CC=CC=C1O ONHMWXJSVBNXOB-KTKRTIGZSA-N 0.000 description 1
CILHYLRKAGMYJB-UHFFFAOYSA-N 2-chloro-4-hexylphenol Chemical compound CCCCCCC1=CC=C(O)C(Cl)=C1 CILHYLRKAGMYJB-UHFFFAOYSA-N 0.000 description 1
MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 1
FDIPWBUDOCPIMH-UHFFFAOYSA-N 2-decylphenol Chemical compound CCCCCCCCCCC1=CC=CC=C1O FDIPWBUDOCPIMH-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
HMWIHOZPGQRZLR-UHFFFAOYSA-N 2-hexadecylphenol Chemical compound CCCCCCCCCCCCCCCCC1=CC=CC=C1O HMWIHOZPGQRZLR-UHFFFAOYSA-N 0.000 description 1
GRTYOAWYBTYJTH-UHFFFAOYSA-N 2-hexyl-4-methoxyphenol Chemical compound CCCCCCC1=CC(OC)=CC=C1O GRTYOAWYBTYJTH-UHFFFAOYSA-N 0.000 description 1
LNNXFUZKZLXPOF-UHFFFAOYSA-N 2-methylpropyl nitrate Chemical compound CC(C)CO[N+]([O-])=O LNNXFUZKZLXPOF-UHFFFAOYSA-N 0.000 description 1
ZZXILYOBAFPJNS-UHFFFAOYSA-N 2-octylbenzene-1,4-diol Chemical compound CCCCCCCCC1=CC(O)=CC=C1O ZZXILYOBAFPJNS-UHFFFAOYSA-N 0.000 description 1
WWPLDSOFBMZGIJ-UHFFFAOYSA-N 2-propan-2-yloxybenzoic acid Chemical compound CC(C)OC1=CC=CC=C1C(O)=O WWPLDSOFBMZGIJ-UHFFFAOYSA-N 0.000 description 1
WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
BAKOSPCCAAZZSP-UHFFFAOYSA-N 2-tert-butylbenzene-1,3-diol Chemical compound CC(C)(C)C1=C(O)C=CC=C1O BAKOSPCCAAZZSP-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
PQWYDYCCMSDGMR-UHFFFAOYSA-N 3-nonyl-2-phenylphenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1C1=CC=CC=C1 PQWYDYCCMSDGMR-UHFFFAOYSA-N 0.000 description 1
HAPOFQBCBUWOEQ-UHFFFAOYSA-N 3-nonylbenzene-1,2-diol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1O HAPOFQBCBUWOEQ-UHFFFAOYSA-N 0.000 description 1
ITTJZRWYPYUKIJ-UHFFFAOYSA-N 6-hydroxy-3-nonyl-2-phenylcyclohexa-2,4-diene-1-thione Chemical compound C(CCCCCCCC)C1=C(C(C(C=C1)O)=S)C1=CC=CC=C1 ITTJZRWYPYUKIJ-UHFFFAOYSA-N 0.000 description 1
235000021357 Behenic acid Nutrition 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
DCFGGGCMICWSJX-SNAWJCMRSA-N Butyl oleate sulfate Chemical compound CCCCOC(=O)CCCCCCC\C=C\CCCCCCCCOS(O)(=O)=O DCFGGGCMICWSJX-SNAWJCMRSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
SZWRCOPXGZPKIB-UHFFFAOYSA-N CCCCCCCCCC1=CC=CC([S+]=P([O-])(O)S)=C1CCCCCCCCC Chemical group CCCCCCCCCC1=CC=CC([S+]=P([O-])(O)S)=C1CCCCCCCCC SZWRCOPXGZPKIB-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical group COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 1
235000019484 Rapeseed oil Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
DISXVWCBTJHKBC-UHFFFAOYSA-N [Na].OCCOCCO Chemical compound [Na].OCCOCCO DISXVWCBTJHKBC-UHFFFAOYSA-N 0.000 description 1
MTRXGAJLJMXRKV-UHFFFAOYSA-N [ethyl(hexyl)-lambda4-sulfanylidene]-dihydroxy-sulfanyl-lambda5-phosphane Chemical group CCCCCCS(CC)=P(O)(O)S MTRXGAJLJMXRKV-UHFFFAOYSA-N 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 description 1
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
125000001204 arachidyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
150000008107 benzenesulfonic acids Chemical group 0.000 description 1
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000005536 corrosion prevention Methods 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
239000000539 dimer Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
PZLGBVIKYPHZTH-UHFFFAOYSA-N ethene;2-nonylphenol Chemical group C=C.CCCCCCCCCC1=CC=CC=C1O PZLGBVIKYPHZTH-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
IDNUEBSJWINEMI-UHFFFAOYSA-N ethyl nitrate Chemical compound CCO[N+]([O-])=O IDNUEBSJWINEMI-UHFFFAOYSA-N 0.000 description 1
239000012530 fluid Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
ZSSIYIZVIFNDRJ-UHFFFAOYSA-N hydroxy-phenoxy-phenylsulfanyl-sulfanylidene-lambda5-phosphane Chemical group C=1C=CC=CC=1SP(=S)(O)OC1=CC=CC=C1 ZSSIYIZVIFNDRJ-UHFFFAOYSA-N 0.000 description 1
SZNYYWIUQFZLLT-UHFFFAOYSA-N isopropylmethyl ether Natural products CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
230000002265 prevention Effects 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
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 1
238000000197 pyrolysis Methods 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
229910052705 radium Inorganic materials 0.000 description 1
HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
229960003656 ricinoleic acid Drugs 0.000 description 1
FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
230000009291 secondary effect Effects 0.000 description 1
229940012831 stearyl alcohol Drugs 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000003760 tallow Substances 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1

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Liquid Carbonaceous Fuels (AREA)

JP26494984A 1984-12-14 1984-12-14 燃料油組成物 Granted JPS61143492A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP26494984A JPS61143492A (ja)	1984-12-14	1984-12-14	燃料油組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP26494984A JPS61143492A (ja)	1984-12-14	1984-12-14	燃料油組成物

Publications (2)

Publication Number	Publication Date
JPS61143492A true JPS61143492A (ja)	1986-07-01
JPH0417238B2 JPH0417238B2 (fr)	1992-03-25

Family

ID=17410428

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP26494984A Granted JPS61143492A (ja)	1984-12-14	1984-12-14	燃料油組成物

Country Status (1)

Country	Link
JP (1)	JPS61143492A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1999003953A1 (fr) *	1997-07-15	1999-01-28	Infineum Usa L.P.	Compositions de fuel-oil ameliorees

Citations (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4884814A (fr) *	1972-02-18	1973-11-10
JPS4961137A (fr) *	1972-06-14	1974-06-13
US3829381A (en) *	1970-02-02	1974-08-13	Lubrizol Corp	Boron-and calcium-containing compositions and process
JPS5029604A (fr) *	1973-03-15	1975-03-25
JPS5048002A (fr) *	1973-07-02	1975-04-28
JPS5343965A (en) *	1976-09-30	1978-04-20	Matsushita Electric Works Ltd	Washstand pan
JPS5420204A (en) *	1977-07-18	1979-02-15	Hino Motors Ltd	Piston of precombustion chamber type diersel engine
JPS6272786A (ja) *	1985-09-25	1987-04-03	フュージョン　エイデッド　カンバッション　テクノロジー　インターナショナル　コーポレーション	水素エネルギ−解放触媒

1984
- 1984-12-14 JP JP26494984A patent/JPS61143492A/ja active Granted

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3829381A (en) *	1970-02-02	1974-08-13	Lubrizol Corp	Boron-and calcium-containing compositions and process
JPS4884814A (fr) *	1972-02-18	1973-11-10
JPS4961137A (fr) *	1972-06-14	1974-06-13
JPS5029604A (fr) *	1973-03-15	1975-03-25
JPS5048002A (fr) *	1973-07-02	1975-04-28
JPS5343965A (en) *	1976-09-30	1978-04-20	Matsushita Electric Works Ltd	Washstand pan
JPS5420204A (en) *	1977-07-18	1979-02-15	Hino Motors Ltd	Piston of precombustion chamber type diersel engine
JPS6272786A (ja) *	1985-09-25	1987-04-03	フュージョン　エイデッド　カンバッション　テクノロジー　インターナショナル　コーポレーション	水素エネルギ−解放触媒

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1999003953A1 (fr) *	1997-07-15	1999-01-28	Infineum Usa L.P.	Compositions de fuel-oil ameliorees

Also Published As

Publication number	Publication date
JPH0417238B2 (fr)	1992-03-25

Publication	Publication Date	Title
US6402797B1 (en)	2002-06-11	Fuel oil compositions
DE3685877T2 (de)	1992-12-17	Heizoelprodukte.
US4505718A (en)	1985-03-19	Organo transition metal salt/ashless detergent-dispersant combinations
DE69006029T2 (de)	1994-05-05	Kohlenwasserkraftstoffzusammensetzungen und Zusätze dazu.
RU2449005C2 (ru)	2012-04-27	Смазывающие композиции для углеводородной смеси и полученные продукты
CA2265439A1 (fr)	1998-03-19	Concentre d'additifs destine a des compositions de carburant
JP2000511172A (ja)	2000-08-29	燃料添加剤
US2908711A (en)	1959-10-13	Itaconic acid-amine reaction product
EP1230330B1 (fr)	2004-04-07	Utilisation de sels d'acide gras d'oligoamines alcoxylees comme agents ameliorants du pouvoir lubrifiant de produits petroliers
EP0290534B1 (fr)	1990-12-19	Additif pour carburant, constitue d'un sel metallique et stabilise avec un thiadiazole
FI93652B (fi)	1995-01-31	Polttoainekoostumus, joka sisältää venttiilin istukan kulumista alentavaa lisäainetta
US5630852A (en)	1997-05-20	Organophosphorus additives for improved fuel lubricity
US3525599A (en)	1970-08-25	Barium-containing dispersion
JP2020164826A (ja)	2020-10-08	燃料油組成物
US6488724B1 (en)	2002-12-03	Heavy oils having improved properties and an additive therefor
US6652609B1 (en)	2003-11-25	Fuel oil compositions
WO2020196386A1 (fr)	2020-10-01	Composition d'huile combustible
DE69805225T2 (de)	2002-12-05	Schmierzusatzverwendung zur Schaumverminderung in Brennstoffen
US3092475A (en)	1963-06-04	Fuel composition
FI96222B (fi)	1996-02-15	Polttoainekoostumus
JPH01502990A (ja)	1989-10-12	改良燃料油組成物
US4040797A (en)	1977-08-09	Arsenic containing fuels
JPH0417238B2 (fr)	1992-03-25
US3718444A (en)	1973-02-27	Jet fuel additive
US3481716A (en)	1969-12-02	Diesel fuel composition

JPS61143492A - 燃料油組成物 - Google Patents

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Links

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Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=17410428

Family Applications (1)

Country Status (1)

Cited By (1)

Citations (8)

Patent Citations (8)

Cited By (1)

Also Published As

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