DEST008831MA - - Google Patents

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Publication number

DEST008831MA

DEST008831MA DEST008831MA DE ST008831M A DEST008831M A DE ST008831MA DE ST008831M A DEST008831M A DE ST008831MA

Authority

DE

Germany

Prior art keywords

diol

gasoline

carbon atoms

engine

methyl

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.)

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• 239000000446 fuel Substances 0.000 claims description 28
• 125000004432 carbon atom Chemical group C* 0.000 claims description 24
• 150000002009 diols Chemical class 0.000 claims description 13
• 150000001875 compounds Chemical class 0.000 claims description 12
• 125000001931 aliphatic group Chemical group 0.000 claims description 9
• 239000000203 mixture Substances 0.000 claims description 8
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
• 229910052760 oxygen Inorganic materials 0.000 claims description 5
• 239000001301 oxygen Substances 0.000 claims description 5
• 229920006395 saturated elastomer Polymers 0.000 claims description 4
• 125000000524 functional group Chemical group 0.000 claims description 3
• 230000015572 biosynthetic process Effects 0.000 description 16
• 238000004821 distillation Methods 0.000 description 10
• -1 2-methyl-3-pentene-diol Chemical compound 0.000 description 8
• 239000000243 solution Substances 0.000 description 7
• 239000000654 additive Substances 0.000 description 6
• 238000009835 boiling Methods 0.000 description 6
• 238000000034 method Methods 0.000 description 6
• 238000012360 testing method Methods 0.000 description 5
• 230000001588 bifunctional effect Effects 0.000 description 4
• MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 4
• 229910052799 carbon Inorganic materials 0.000 description 3
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
• 238000010792 warming Methods 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• KQWPPKFUTRANJS-UHFFFAOYSA-N 2-(methoxymethyl)-2,4-dimethylpentane-1,5-diol Chemical compound COCC(C)(CO)CC(C)CO KQWPPKFUTRANJS-UHFFFAOYSA-N 0.000 description 2
• JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 2
• 238000007792 addition Methods 0.000 description 2
• 230000005540 biological transmission Effects 0.000 description 2
• 230000000694 effects Effects 0.000 description 2
• 238000001704 evaporation Methods 0.000 description 2
• 238000007710 freezing Methods 0.000 description 2
• 230000008014 freezing Effects 0.000 description 2
• 239000003112 inhibitor Substances 0.000 description 2
• TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
• 239000012047 saturated solution Substances 0.000 description 2
• 239000000126 substance Substances 0.000 description 2
• 238000003419 tautomerization reaction Methods 0.000 description 2
• 238000010998 test method Methods 0.000 description 2
• PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
• AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
• 206010000369 Accident Diseases 0.000 description 1
• 108010053481 Antifreeze Proteins Proteins 0.000 description 1
• 229940126657 Compound 17 Drugs 0.000 description 1
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
• GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
• 230000001133 acceleration Effects 0.000 description 1
• 238000009825 accumulation Methods 0.000 description 1
• 230000002730 additional effect Effects 0.000 description 1
• 125000000217 alkyl group Chemical group 0.000 description 1
• 230000002528 anti-freeze Effects 0.000 description 1
• 239000006079 antiknock agent Substances 0.000 description 1
• 239000003963 antioxidant agent Substances 0.000 description 1
• 125000004429 atom Chemical group 0.000 description 1
• CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
• 239000003795 chemical substances by application Substances 0.000 description 1
• 238000002485 combustion reaction Methods 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 230000002542 deteriorative effect Effects 0.000 description 1
• 239000002283 diesel fuel Substances 0.000 description 1
• 238000010790 dilution Methods 0.000 description 1
• 239000012895 dilution Substances 0.000 description 1
• 239000000975 dye Substances 0.000 description 1
• GWNFQAKCJYEJEW-UHFFFAOYSA-N ethyl 3-[8-[[4-methyl-5-[(3-methyl-4-oxophthalazin-1-yl)methyl]-1,2,4-triazol-3-yl]sulfanyl]octanoylamino]benzoate Chemical compound CCOC(=O)C1=CC(NC(=O)CCCCCCCSC2=NN=C(CC3=NN(C)C(=O)C4=CC=CC=C34)N2C)=CC=C1 GWNFQAKCJYEJEW-UHFFFAOYSA-N 0.000 description 1
• 230000008020 evaporation Effects 0.000 description 1
• 238000002474 experimental method Methods 0.000 description 1
• 230000002349 favourable effect Effects 0.000 description 1
• 239000003254 gasoline additive Substances 0.000 description 1
• 150000004820 halides Chemical class 0.000 description 1
• 229930195733 hydrocarbon Natural products 0.000 description 1
• 150000002430 hydrocarbons Chemical class 0.000 description 1
• 230000003301 hydrolyzing effect Effects 0.000 description 1
• 238000011835 investigation Methods 0.000 description 1
• JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
• 239000011133 lead Substances 0.000 description 1
• 239000002184 metal Substances 0.000 description 1
• 239000006078 metal deactivator Substances 0.000 description 1
• 238000012986 modification Methods 0.000 description 1
• 230000004048 modification Effects 0.000 description 1
• OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
• 230000002265 prevention Effects 0.000 description 1
• 230000003252 repetitive effect Effects 0.000 description 1
• 239000011347 resin Substances 0.000 description 1
• 229920005989 resin Polymers 0.000 description 1
• 239000007965 rubber solvent Substances 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1