JP2022512603A - 低速早期着火事象を低減する添加剤としてのヒドリド供与体 - Google Patents
低速早期着火事象を低減する添加剤としてのヒドリド供与体 Download PDFInfo
- Publication number
- JP2022512603A JP2022512603A JP2021518609A JP2021518609A JP2022512603A JP 2022512603 A JP2022512603 A JP 2022512603A JP 2021518609 A JP2021518609 A JP 2021518609A JP 2021518609 A JP2021518609 A JP 2021518609A JP 2022512603 A JP2022512603 A JP 2022512603A
- Authority
- JP
- Japan
- Prior art keywords
- reducing agent
- organic hydride
- based reducing
- agents
- fuel
- Prior art date
- 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
- 150000004678 hydrides Chemical class 0.000 title claims abstract description 41
- 239000000654 additive Substances 0.000 title claims description 37
- 230000002028 premature Effects 0.000 title abstract description 5
- 230000000996 additive effect Effects 0.000 title description 9
- 239000000203 mixture Substances 0.000 claims abstract description 64
- 239000000446 fuel Substances 0.000 claims abstract description 46
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 40
- 238000002485 combustion reaction Methods 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 21
- 239000010687 lubricating oil Substances 0.000 claims description 25
- 229930195733 hydrocarbon Natural products 0.000 claims description 23
- 150000002430 hydrocarbons Chemical class 0.000 claims description 21
- 239000004215 Carbon black (E152) Substances 0.000 claims description 18
- 239000003502 gasoline Substances 0.000 claims description 16
- 239000002199 base oil Substances 0.000 claims description 14
- 238000009835 boiling Methods 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 7
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 6
- SBBRCICYNAOFFG-UHFFFAOYSA-O 2-amino-6-(aminomethyl)-5-methylidene-4-oxo-1,4,5,6,7,8-hexahydropteridin-5-ium Chemical compound NCC1CNc2[nH]c(N)nc(=O)c2[N+]1=C SBBRCICYNAOFFG-UHFFFAOYSA-O 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- CHVJITGCYZJHLR-UHFFFAOYSA-N cyclohepta-1,3,5-triene Chemical compound C1C=CC=CC=C1 CHVJITGCYZJHLR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 230000001050 lubricating effect Effects 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- KORRUKUGQCKJCU-UHFFFAOYSA-N 2,3,4-triazatricyclo[7.3.1.05,13]trideca-1(12),9(13),10-triene Chemical compound N1NNC2CCCC3=CC=CC1=C23 KORRUKUGQCKJCU-UHFFFAOYSA-N 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 239000012459 cleaning agent Substances 0.000 claims description 3
- 239000003599 detergent Substances 0.000 claims description 3
- VWWQXMAJTJZDQX-UYBVJOGSSA-N flavin adenine dinucleotide Chemical compound C1=NC2=C(N)N=CN=C2N1[C@@H]([C@H](O)[C@@H]1O)O[C@@H]1CO[P@](O)(=O)O[P@@](O)(=O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C2=NC(=O)NC(=O)C2=NC2=C1C=C(C)C(C)=C2 VWWQXMAJTJZDQX-UYBVJOGSSA-N 0.000 claims description 3
- 235000019162 flavin adenine dinucleotide Nutrition 0.000 claims description 3
- 239000011714 flavin adenine dinucleotide Substances 0.000 claims description 3
- 229940093632 flavin-adenine dinucleotide Drugs 0.000 claims description 3
- 239000003112 inhibitor Substances 0.000 claims description 3
- 239000006078 metal deactivator Substances 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 2
- 238000005299 abrasion Methods 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 230000007797 corrosion Effects 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 2
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 2
- BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 claims 2
- 229950006238 nadide Drugs 0.000 claims 2
- 239000006184 cosolvent Substances 0.000 claims 1
- 239000004088 foaming agent Substances 0.000 claims 1
- 230000003449 preventive effect Effects 0.000 claims 1
- 239000000314 lubricant Substances 0.000 abstract description 16
- 239000003921 oil Substances 0.000 description 26
- 235000019198 oils Nutrition 0.000 description 26
- 125000000217 alkyl group Chemical group 0.000 description 18
- 125000003118 aryl group Chemical group 0.000 description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- -1 hydrogen anion Chemical class 0.000 description 9
- YNGDWRXWKFWCJY-UHFFFAOYSA-N 1,4-Dihydropyridine Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 description 8
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000002480 mineral oil Substances 0.000 description 6
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 6
- 229920013639 polyalphaolefin Polymers 0.000 description 6
- 150000001336 alkenes Chemical group 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- 239000002612 dispersion medium Substances 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002816 fuel additive Substances 0.000 description 4
- 238000007871 hydride transfer reaction Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001408 amides Chemical group 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- 239000013626 chemical specie Substances 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 150000002148 esters Chemical group 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000010705 motor oil Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 238000006479 redox reaction Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- GYUDLEOKVQWEHB-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21.C1=CC=CC2=CC3=CC=CC=C3N=C21 GYUDLEOKVQWEHB-UHFFFAOYSA-N 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003879 lubricant additive Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- CZVDNUJJDUXGGT-UHFFFAOYSA-N C1=CC=CC=CC1.C1=CC=CC=CC1 Chemical compound C1=CC=CC=CC1.C1=CC=CC=CC1 CZVDNUJJDUXGGT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- YPZRHBJKEMOYQH-UYBVJOGSSA-N FADH2 Chemical compound C1=NC2=C(N)N=CN=C2N1[C@@H]([C@H](O)[C@@H]1O)O[C@@H]1COP(O)(=O)OP(O)(=O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C(NC(=O)NC2=O)=C2NC2=C1C=C(C)C(C)=C2 YPZRHBJKEMOYQH-UYBVJOGSSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000006683 Mannich reaction Methods 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001345 alkine derivatives Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000006079 antiknock agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-N benzoquinolinylidene Natural products C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000002272 engine oil additive Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229920006213 ethylene-alphaolefin copolymer Polymers 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- RZTAMFZIAATZDJ-UHFFFAOYSA-N felodipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1C1=CC=CC(Cl)=C1Cl RZTAMFZIAATZDJ-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 238000006053 organic reaction Methods 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
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/40—Six-membered ring containing nitrogen and carbon only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/08—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for compression ignition
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/12—Use of additives to fuels or fires for particular purposes for improving the cetane number
-
- 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
- C10M127/00—Lubricating compositions characterised by the additive being a non- macromolecular hydrocarbon
- C10M127/04—Lubricating compositions characterised by the additive being a non- macromolecular hydrocarbon well-defined aromatic
-
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/16—Ethers
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
- C10M133/46—Imidazoles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
- C10L1/1855—Cyclic ethers, e.g. epoxides, lactides, lactones
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
- C10L1/233—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring containing nitrogen and oxygen in the ring, e.g. oxazoles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2200/00—Components of fuel compositions
- C10L2200/04—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2200/00—Components of fuel compositions
- C10L2200/04—Organic compounds
- C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
- C10L2200/0415—Light distillates, e.g. LPG, naphtha
- C10L2200/0423—Gasoline
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2200/00—Components of fuel compositions
- C10L2200/04—Organic compounds
- C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
- C10L2200/0438—Middle or heavy distillates, heating oil, gasoil, marine fuels, residua
- C10L2200/0446—Diesel
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2270/00—Specifically adapted fuels
- C10L2270/02—Specifically adapted fuels for internal combustion engines
- C10L2270/023—Specifically adapted fuels for internal combustion engines for gasoline engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2270/00—Specifically adapted fuels
- C10L2270/02—Specifically adapted fuels for internal combustion engines
- C10L2270/026—Specifically adapted fuels for internal combustion engines for diesel engines, e.g. automobiles, stationary, marine
-
- 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
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
- C10M2215/224—Imidazoles
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/76—Reduction of noise, shudder, or vibrations
-
- 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
- C10N2040/25—Internal-combustion engines
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Lubricants (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
Abstract
Description
近年、エンジン製造業者は、摩擦損失およびポンプ損失を低減しながらより高い出力密度および優れた性能を提供する、より小型のエンジンを開発してきた。この性能向上は、ターボチャージャーまたは機械式スーパーチャージャーを使用してブースト圧力を増加させること、およびより低いエンジン速度でのトルク発生の増加で可能となる、より高い変速比を使用してエンジンを減速することによって達成される。欠点は、これらのエンジンは低速かつ高負荷駆動条件で動作することが多く、確率論的な早期着火または低速早期着火(LSPI)として知られる早期着火現象の影響をより受けやすくなることである。最悪のケースのシナリオでは、気筒のピーク圧力が極端に上昇し、壊滅的なエンジン故障につながる。この故障発生度によって、エンジン製造業者は、このようなより小型の高出力エンジンにおいて、より低いエンジン速度でエンジントルクを完全に最適化することができない。
本明細書において使用される場合、以下の単語および表現は、以下に記載される意味を有する。
低速早期着火(LSPI)の、可能性がある1つの原因は、エンジンが低速で動作しており、かつ圧縮行程時間が最長である期間中に、高圧下でピストン隙間からエンジン燃焼室に入るエンジンオイル滴の自動着火である。ターボチャージャー使用、エンジン設計、エンジンコーティング、ピストン形状、燃料選択、またはエンジンオイル添加剤などの要因が、LSPI事象の増加に寄与し得る。エンジンノッキングおよび早期着火の問題のいくつかは、新しいエンジン技術の使用またはエンジン動作条件の最適化によって解決することができるが、新たな燃料および/または潤滑油組成物によってLSPIを低減することは、最も費用効果の高いアプローチであり得る。
燃焼機関においてLSPI事象を防止するか、またはLSPI活動を低減する有機ヒドリド系還元剤を本明細書で提供する。これらの有機ヒドリド系還元剤は、ヒドリド移動工程中にヒドリドを供与しやすい有機分子である。これらの還元剤は無灰添加剤であり、通常、炭素、水素、窒素および/または酸素原子を含有する。用途に応じて、有機ヒドリド系還元剤は、油溶性または燃料可溶性である。
DHPDまたはDHPD型還元剤は、一般化構造(式1)によって例示される。式1に言及すると、R1およびR2は、以下の群、すなわち、H、エステル部分、アミド部分、シアニド部分、それらの任意の誘導体などから各々独立して選択される成分である。R3およびR4は、以下の群、すなわち、H、アルキル部分、それらの任意の誘導体などから各々独立して選択される成分である。R5は、以下の群、すなわち、H、アルキル部分、アリル部分、アリール部分、ベンジル部分、アルカノール部分、およびそれらの任意の誘導体などから選択される成分である。
NADHまたはNADH型還元剤は、一般化構造(式2)によって例示される。式2に言及すると、R1およびR2は、以下の群、すなわち、H、エステル部分、アミド部分、シアニド部分、それらの任意の誘導体などから各々独立して選択される成分である。R3およびR4は、以下の群、すなわち、H、アルキル部分、それらの任意の誘導体などから各々独立して選択される成分である。R5は、以下の群、すなわち、H、アルキル部分、アリル部分、アリール部分、ベンジル部分、アルカノール部分、およびそれらの任意の誘導体などから選択される成分である。R6は、以下の群、すなわちH、アルキル部分、それらの任意の誘導体などから選択される。いくつかの実施形態では、R1およびR4またはR2およびR3は、環式または複素環式構造(例えば、式2Cおよび式2E)を形成し得る。
メチレンテトラヒドロメタノプテリンまたはメチレンテトラヒドロメタノプテリン型還元体を一般化構造(式3)で示す。式3に言及すると、R1、R2、R3、およびR4は、以下の群、すなわちH、アルキル部分、アリル部分、アルカノール部分、それらの任意の誘導体などから各々独立して選択される成分である。R5は、以下の群、すなわちH、アルキル部分、それらの任意の誘導体などから選択される。
アクリジンまたはアクリジン型還元剤を一般化構造(式4)で示す。式4に言及すると、Xは、NまたはOである(式4H)。XがNである場合、R1は、以下の群、すなわちH、アルキル部分、アリル部分、アリール部分、ベンジル部分、それらの任意の誘導体などから選択される。R2は、以下の群、すなわち、H、アルキル部分、アリル部分、アリール部分、ベンジル部分、アルカノール部分、およびそれらの任意の誘導体などから選択される。R3およびR4は、以下の群、すなわち、H、アルキル部分、アリール部分、ベンジル部分、アミン部分、アルコキシ部分、ヘテロ原子、それらの任意の誘導体などから各々独立して選択される成分である。さらに、R3およびR4は、独立して、それぞれの環内で2つ以上の置換位置を占有してもよい。いくつかの実施形態では、R1およびR3またはR1およびR4は、環式構造(例えば、式4Eおよび式4F)を形成し得る。
トリアリールメタンまたはトリアリールメタン型還元剤を一般化構造(式5)で示す。式5に言及すると、R1、R2およびR3は、以下の群、すなわちH、アルキル部分、アリール部分、ベンジル部分、アリル部分、アミド部分、エステル部分、エーテル部分、ヒドロキシル部分、アミン部分、それらの任意の誘導体などから独立して選択される。いくつかの実施形態では、R1、R2およびR3は、独立して、それらのそれぞれの環内で2つ以上の置換位置を占有してもよい(例えば、式5Aおよび式5B)。
アリールベンゾイミダリンまたはアリールベンゾイミダリン型還元剤を、一般化構造(式7)によって示す。式7を参照すると、XはN、O、またはSである。XがNである場合、R1およびR2は、以下の群、すなわちH、アルキル部分、それらの任意の誘導体などから各々独立して選択される成分である。R3は、以下の群、すなわちH、アルキル部分、アルケン部分、アルキン部分、アリール部分、ベンジル部分、それらの任意の誘導体などから選択される。R4は、以下の群、すなわちH、アルキル部分、アリール部分、ベンジル部分、アリル部分、それらの任意の誘導体などから選択される。いくつかの実施形態では、R4は、独立して2つ以上の置換位置を占有してもよい。
ジオキソランまたはジオキソラン型還元剤を一般化構造(式8)で示す。式8に言及すると、Rは、以下の群、すなわち、H、アルキル部分、アリル部分、ベンジル部分、アルカノール部分、それらの任意の誘導体などから選択される成分である。
ジエーテルシクロヘキサジエンまたはジエーテルシクロヘキサジエン型還元剤を、一般化構造(式9)によって示す。式9に言及すると、Rは、以下の群、すなわち、H、アルキル部分、アリル部分、ベンジル部分、アルカノール部分、それらの任意の誘導体などから選択される成分である。
シクロヘプタトリエンまたはシクロヘプタトリエン型還元体を、一般化構造(式10)によって示す。式10に言及すると、Rは、以下の群、すなわち、H、アルキル部分、アリル部分、ベンジル部分、アルカノール部分、それらの任意の誘導体などから選択される成分である。いくつかの実施形態では、Rは、2つ以上の置換位置を占有してもよい(例えば、式10B)。
本開示の有機ヒドリド系供与体は、燃焼機関における望ましくない着火事象を防止または低減するための、炭化水素燃料の添加剤として有用であり得る。燃料に使用される場合、所望のLSPI低減または有効性を達成するために必要な添加剤の適切な濃度は、使用される燃料の種類、他の清浄剤または分散剤または他の添加剤の存在などを含む様々な要因に依存する。一般に、本開示の添加剤の炭化水素燃料中の濃度の範囲は、25~5000重量百万分率(ppmw)の範囲(50~4000ppm、100~3500、150~3000、200~2500、250~2000、300~1500、350~1000などを含むが限定されない)であり得る。他のヒドリド供与体が燃料組成物中に存在する場合、添加剤の使用量を減らしてもよい。
本開示の有機ヒドリド供与体は、燃焼機関における望ましくない着火事象を防止または低減するための、潤滑油の添加剤として有用であり得る。このようにして使用される場合、添加剤は通常、潤滑油組成物の総重量に対して0.001~10wt.%(限定されないが、0.01~5wt.%、0.2~4wt.%、0.5~3wt.%、1~2wt.%など)の濃度で潤滑油組成物中に存在する。他のヒドリド供与体が潤滑油組成物中に存在する場合、添加剤の使用量を減らしてもよい。
以下の説明的な例は、非限定的であることを意図している。
試験化合物をガソリンまたは潤滑油に混合し、LSPI事象を低減するそれらの能力を以下に記載される試験方法を用いて決定した。
LSPI頻度=[(端を切り取った6つの区分におけるLSPI影響燃焼サイクルの総数)/(端を切り取った6つの区分における燃焼サイクルの総数)]×1,000,000
Claims (20)
- (1)50wt.%超の、ガソリンまたはディーゼルの沸点範囲で沸騰する炭化水素燃料、および(2)1種以上の少量の有機ヒドリド系還元剤、を含む、燃料組成物。
- 前記有機ヒドリド系還元剤が、ハロゲン、ホウ素またはケイ素を実質的に含まない、請求項1に記載の燃料組成物。
- 前記有機ヒドリド系還元剤が、ジヒドロピリジン、ニコチンアミドアデニンジヌクレオチド、メチレンテトラヒドロメタノプテリン、アクリジン、トリアリールメタン、ヘキサヒドロトリアザフェナレン、トリアミン、アリールベンゾイミダゾリン、ジオキソラン、ジエーテルシクロヘキサジエン、シクロヘプタトリエン、フラビンアデニンジヌクレオチド、またはそれらの類似体である、請求項1に記載の燃料組成物。
- 前記有機ヒドリド系還元剤が、25~5000重量ppmで存在する、請求項1に記載の燃料組成物。
- 前記有機ヒドリド系還元剤が、250~2000重量ppmで存在する、請求項1に記載の燃料組成物。
- 酸素化物、アンチノック剤、清浄剤、分散剤、摩擦調整剤、酸化防止剤、金属不活性化剤、解乳化剤、流動点降下剤、流動性向上剤、セタン価向上剤、または潤滑性添加剤を含む、請求項1に記載の燃料組成物。
- 内燃機関の望ましくない着火事象を防止または低減する方法であって、
(1)50wt.%超の、ガソリンまたはディーゼルの沸点範囲で沸騰する炭化水素燃料、および(2)1種以上の少量の有機ヒドリド系還元剤、を含む燃料組成物をエンジンに供給することを含む、方法。 - 前記内燃機関が火花点火式である、請求項7に記載の方法。
- 前記内燃機関が3000rpm未満で動作する、請求項7に記載の方法。
- 前記火花点火式内燃機関が、少なくとも1MPa(10バール)の正味平均有効圧力を含む負荷の下で動作する、請求項7に記載の方法。
- (1)50wt.%超のベースオイル、および(2)1種以上の少量の有機ヒドリド系還元剤を含む潤滑油組成物。
- 前記有機ヒドリド系還元剤が、ハロゲン、ホウ素、またはケイ素を実質的に含まない、請求項11に記載の潤滑油組成物。
- 前記有機ヒドリド系還元剤が、ジヒドロピリジン、ニコチンアミドアデニンジヌクレオチド、メチレンテトラヒドロメタノプテリン、アクリジン、トリアリールメタン、ヘキサヒドロトリアザフェナレン、トリアミン、アリールベンゾイミダゾリン、ジオキソラン、ジエーテルシクロヘキサジエン、シクロヘプタトリエン、フラビンアデニンジヌクレオチド、またはそれらの類似体である、請求項11に記載の潤滑油組成物。
- 前記有機ヒドリド系還元剤が、0.001~10重量%で存在する、請求項11に記載の潤滑油組成物。
- 前記有機ヒドリド系還元剤が、0.5~5重量%で存在する、請求項11に記載の潤滑油組成物。
- 酸化防止剤、無灰分散剤、耐摩耗剤、清浄剤、防錆剤、かすみ除去剤(dehazing agent)、解乳化剤、摩擦調整剤、金属不活性化剤、流動点降下剤、粘度調整剤、消泡剤、共溶媒、パッケージ相溶化剤、腐食防止剤、染料、または極圧剤をさらに含む、請求項11に記載の潤滑油組成物。
- 内燃機関の望ましくない着火事象を防止または低減する方法であって、
(1)50wt.%超のベースオイル、および(2)1種以上の少量の有機ヒドリド系還元剤を含む潤滑油組成物をエンジンに供給することを含む、方法。 - 前記内燃機関が火花点火式である、請求項17に記載の方法。
- 前記内燃機関が3000rpm未満で作動する、請求項17に記載の方法。
- 前記内燃機関が、少なくとも1MPa(10バール)の正味平均有効圧力を含む負荷の下で動作する、請求項17に記載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862741229P | 2018-10-04 | 2018-10-04 | |
US62/741,229 | 2018-10-04 | ||
PCT/IB2019/058397 WO2020070672A1 (en) | 2018-10-04 | 2019-10-02 | Hydride donors as an additive for reducing low speed pre-ignition events |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2022512603A true JP2022512603A (ja) | 2022-02-07 |
Family
ID=68165675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2021518609A Pending JP2022512603A (ja) | 2018-10-04 | 2019-10-02 | 低速早期着火事象を低減する添加剤としてのヒドリド供与体 |
Country Status (12)
Country | Link |
---|---|
US (1) | US20200109343A1 (ja) |
EP (1) | EP3861089A1 (ja) |
JP (1) | JP2022512603A (ja) |
KR (1) | KR20210069064A (ja) |
CN (1) | CN112789346A (ja) |
AU (1) | AU2019353900A1 (ja) |
CA (1) | CA3115036A1 (ja) |
CO (1) | CO2021005685A2 (ja) |
MX (1) | MX2021003690A (ja) |
SG (1) | SG11202103198WA (ja) |
WO (1) | WO2020070672A1 (ja) |
ZA (1) | ZA202102156B (ja) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2754216A (en) * | 1953-03-11 | 1956-07-10 | Universal Oil Prod Co | Metal deactivator |
JPS61500318A (ja) * | 1983-11-07 | 1986-02-27 | エシル コ−ポレ−シヨン | ジ−ゼル燃料セタン向上剤 |
JPH05230475A (ja) * | 1992-02-20 | 1993-09-07 | Nippon Oil Co Ltd | ガソリン組成物 |
JP2000080092A (ja) * | 1986-12-29 | 2000-03-21 | Lubrizol Corp:The | ジオキソランおよびチオ類似物、それらの誘導体、およびそれらを含有する潤滑剤および燃料 |
US6156081A (en) * | 1997-04-11 | 2000-12-05 | Combustion Technologies, Inc. | Combustion catalyst |
US20070204505A1 (en) * | 2006-03-02 | 2007-09-06 | Novus International Inc. | Gasoline fuel compositions having increased oxidative stability |
JP2017514983A (ja) * | 2014-05-09 | 2017-06-08 | エクソンモービル リサーチ アンド エンジニアリング カンパニーExxon Research And Engineering Company | 低速プレイグニッションを防止または低減する方法 |
WO2018172911A2 (en) * | 2017-03-22 | 2018-09-27 | Sabic Global Technologies B.V. | Octane-boosting fuel additives, method of manufacture, and uses thereof |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1346765A (en) | 1970-06-16 | 1974-02-13 | Shell Int Research | Fuel compositions |
US4191537A (en) | 1976-06-21 | 1980-03-04 | Chevron Research Company | Fuel compositions of poly(oxyalkylene) aminocarbamate |
DE3826797A1 (de) | 1988-08-06 | 1990-02-08 | Basf Ag | Kraftstoffzusammensetzungen, die polycarbonsaeureester langkettiger alkohole enthalten |
DE3838918A1 (de) | 1988-11-17 | 1990-05-23 | Basf Ag | Kraftstoffe fuer verbrennungsmaschinen |
EP0382159A1 (en) | 1989-02-06 | 1990-08-16 | E.I. Du Pont De Nemours And Company | Defouling of fuel systems |
WO2011091203A2 (en) * | 2010-01-21 | 2011-07-28 | Shell Oil Company | Hydrocarbon composition |
US8349777B2 (en) * | 2010-11-22 | 2013-01-08 | Chevron Oronite Company Llc | Lubricating composition containing 1,3-dioxolane-4-methanol compounds as antiwear additives |
JP5545684B2 (ja) * | 2012-05-23 | 2014-07-09 | 株式会社大丸テクノ | 洗浄剤 |
JP6404934B2 (ja) * | 2013-09-19 | 2018-10-17 | ザ ルブリゾル コーポレイションThe Lubrizol Corporation | 直噴エンジン用潤滑剤組成物 |
EP3345952A4 (en) * | 2015-08-31 | 2019-01-09 | Mitsui Chemicals, Inc. | COPOLYMER AND LUBRICATING OIL COMPOSITION |
FR3043691A1 (fr) * | 2015-11-12 | 2017-05-19 | Total Marketing Services | Compositions lubrifiantes pour prevenir ou diminuer la combustion anormale dans un moteur de vehicule automobile |
DE102016116348A1 (de) * | 2016-09-01 | 2018-03-01 | Tunap Gmbh & Co. Kg | Kraftstoffadditiv zur reinigung eines verbrennungsmotors |
-
2019
- 2019-10-02 KR KR1020217012248A patent/KR20210069064A/ko active Search and Examination
- 2019-10-02 CN CN201980065359.8A patent/CN112789346A/zh active Pending
- 2019-10-02 SG SG11202103198WA patent/SG11202103198WA/en unknown
- 2019-10-02 JP JP2021518609A patent/JP2022512603A/ja active Pending
- 2019-10-02 EP EP19783721.4A patent/EP3861089A1/en active Pending
- 2019-10-02 MX MX2021003690A patent/MX2021003690A/es unknown
- 2019-10-02 WO PCT/IB2019/058397 patent/WO2020070672A1/en active Application Filing
- 2019-10-02 US US16/590,983 patent/US20200109343A1/en active Pending
- 2019-10-02 AU AU2019353900A patent/AU2019353900A1/en active Pending
- 2019-10-02 CA CA3115036A patent/CA3115036A1/en active Pending
-
2021
- 2021-03-30 ZA ZA2021/02156A patent/ZA202102156B/en unknown
- 2021-04-29 CO CONC2021/0005685A patent/CO2021005685A2/es unknown
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2754216A (en) * | 1953-03-11 | 1956-07-10 | Universal Oil Prod Co | Metal deactivator |
JPS61500318A (ja) * | 1983-11-07 | 1986-02-27 | エシル コ−ポレ−シヨン | ジ−ゼル燃料セタン向上剤 |
JP2000080092A (ja) * | 1986-12-29 | 2000-03-21 | Lubrizol Corp:The | ジオキソランおよびチオ類似物、それらの誘導体、およびそれらを含有する潤滑剤および燃料 |
JPH05230475A (ja) * | 1992-02-20 | 1993-09-07 | Nippon Oil Co Ltd | ガソリン組成物 |
US6156081A (en) * | 1997-04-11 | 2000-12-05 | Combustion Technologies, Inc. | Combustion catalyst |
US20070204505A1 (en) * | 2006-03-02 | 2007-09-06 | Novus International Inc. | Gasoline fuel compositions having increased oxidative stability |
JP2017514983A (ja) * | 2014-05-09 | 2017-06-08 | エクソンモービル リサーチ アンド エンジニアリング カンパニーExxon Research And Engineering Company | 低速プレイグニッションを防止または低減する方法 |
WO2018172911A2 (en) * | 2017-03-22 | 2018-09-27 | Sabic Global Technologies B.V. | Octane-boosting fuel additives, method of manufacture, and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
US20200109343A1 (en) | 2020-04-09 |
SG11202103198WA (en) | 2021-04-29 |
EP3861089A1 (en) | 2021-08-11 |
CN112789346A (zh) | 2021-05-11 |
KR20210069064A (ko) | 2021-06-10 |
CO2021005685A2 (es) | 2021-05-20 |
ZA202102156B (en) | 2022-09-28 |
CA3115036A1 (en) | 2020-04-09 |
WO2020070672A1 (en) | 2020-04-09 |
AU2019353900A1 (en) | 2021-05-06 |
MX2021003690A (es) | 2021-06-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1357170B9 (en) | Friction modifier additives for fuel compositions and methods of use thereof | |
US11142715B2 (en) | Amino alkanediols and carboxylate salts as additives for improving fuel efficiency | |
JP2022512603A (ja) | 低速早期着火事象を低減する添加剤としてのヒドリド供与体 | |
JP2021518470A (ja) | 火花点火内燃機関の低速予備点火を防止または低減するための組成物および方法 | |
JP5511784B2 (ja) | 重質燃料によって駆動される2ストロークエンジンを潤滑するのに適切な潤滑添加組成物 | |
CN113227332B (zh) | 用于防止或降低火花点燃式内燃机的低速早燃的组合物和方法 | |
US20200017789A1 (en) | Composition and method for preventing or reducing low speed pre-ignition in spark-ignited internal combustion engines | |
JP2024512707A (ja) | 低速早期着火事象を低減するための燃料添加剤 | |
JP2022507597A (ja) | 火花点火内燃機関の低速予備点火を防止または低減するための組成物および方法 | |
EP4314207A1 (en) | Compositions for mitigating low speed pre-ignition events | |
RU2326156C1 (ru) | Топливная композиция |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20220921 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20230628 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20230630 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20230926 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240104 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20240221 |