WO2002061018A1 - Additif pour mazout et produit de mazout comprenant l'additif pour mazout - Google Patents
Additif pour mazout et produit de mazout comprenant l'additif pour mazout Download PDFInfo
- Publication number
- WO2002061018A1 WO2002061018A1 PCT/CN2002/000047 CN0200047W WO02061018A1 WO 2002061018 A1 WO2002061018 A1 WO 2002061018A1 CN 0200047 W CN0200047 W CN 0200047W WO 02061018 A1 WO02061018 A1 WO 02061018A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- acid
- metal
- gasoline
- fuel
- additive
- Prior art date
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- 239000000295 fuel oil Substances 0.000 title claims abstract description 30
- 239000003747 fuel oil additive Substances 0.000 title abstract 4
- 239000003502 gasoline Substances 0.000 claims abstract description 103
- 229910052751 metal Inorganic materials 0.000 claims abstract description 67
- 239000002184 metal Substances 0.000 claims abstract description 67
- 150000007524 organic acids Chemical class 0.000 claims abstract description 50
- 150000003839 salts Chemical class 0.000 claims abstract description 36
- 239000006079 antiknock agent Substances 0.000 claims abstract description 34
- 239000003921 oil Substances 0.000 claims abstract description 32
- 150000001768 cations Chemical class 0.000 claims abstract description 23
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 16
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 15
- 239000003350 kerosene Substances 0.000 claims abstract description 15
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 15
- 150000004671 saturated fatty acids Chemical class 0.000 claims abstract description 14
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims abstract description 14
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims abstract description 14
- 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 claims abstract description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 13
- 150000002910 rare earth metals Chemical class 0.000 claims abstract description 12
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 11
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 11
- 239000002283 diesel fuel Substances 0.000 claims abstract description 11
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 11
- 150000003624 transition metals Chemical class 0.000 claims abstract description 11
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000654 additive Substances 0.000 claims description 92
- 230000000996 additive effect Effects 0.000 claims description 59
- 239000000446 fuel Substances 0.000 claims description 54
- -1 trim Chemical compound 0.000 claims description 38
- 229910052777 Praseodymium Inorganic materials 0.000 claims description 35
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 claims description 35
- 239000002816 fuel additive Substances 0.000 claims description 28
- 150000002500 ions Chemical class 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 13
- 229910017052 cobalt Inorganic materials 0.000 claims description 11
- 239000010941 cobalt Substances 0.000 claims description 11
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229910052684 Cerium Inorganic materials 0.000 claims description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 10
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- 229910052718 tin Inorganic materials 0.000 claims description 9
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 8
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 8
- 229910052787 antimony Inorganic materials 0.000 claims description 8
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 8
- 229910052733 gallium Inorganic materials 0.000 claims description 8
- 229910052732 germanium Inorganic materials 0.000 claims description 8
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 8
- 229910052738 indium Inorganic materials 0.000 claims description 8
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 8
- 229910052744 lithium Inorganic materials 0.000 claims description 8
- 150000002739 metals Chemical class 0.000 claims description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 229910052746 lanthanum Inorganic materials 0.000 claims description 7
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 7
- 239000011777 magnesium Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052719 titanium Inorganic materials 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- 239000011701 zinc Substances 0.000 claims description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 229910052735 hafnium Inorganic materials 0.000 claims description 6
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052727 yttrium Inorganic materials 0.000 claims description 6
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 229910021645 metal ion Inorganic materials 0.000 claims description 5
- 229910052697 platinum Inorganic materials 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- 239000011591 potassium Substances 0.000 claims description 5
- 229910052701 rubidium Inorganic materials 0.000 claims description 5
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 229910052779 Neodymium Inorganic materials 0.000 claims description 4
- 150000001299 aldehydes Chemical class 0.000 claims description 4
- 229910052788 barium Inorganic materials 0.000 claims description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052790 beryllium Inorganic materials 0.000 claims description 4
- 229910052792 caesium Inorganic materials 0.000 claims description 4
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000003254 gasoline additive Substances 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 229910052712 strontium Inorganic materials 0.000 claims description 4
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 239000010931 gold Substances 0.000 claims description 3
- 229910052741 iridium Inorganic materials 0.000 claims description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052758 niobium Inorganic materials 0.000 claims description 3
- 239000010955 niobium Substances 0.000 claims description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 4
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 claims 4
- 229910052716 thallium Inorganic materials 0.000 claims 3
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 claims 3
- 229910052742 iron Inorganic materials 0.000 claims 2
- 229910052706 scandium Inorganic materials 0.000 claims 2
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims 2
- 239000000945 filler Substances 0.000 claims 1
- 150000007519 polyprotic acids Polymers 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 abstract description 12
- 231100000989 no adverse effect Toxicity 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 81
- 230000000694 effects Effects 0.000 description 24
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- 238000004140 cleaning Methods 0.000 description 14
- 238000002485 combustion reaction Methods 0.000 description 10
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 7
- 230000003247 decreasing effect Effects 0.000 description 7
- 239000003344 environmental pollutant Substances 0.000 description 7
- 231100000719 pollutant Toxicity 0.000 description 7
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 6
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 235000011054 acetic acid Nutrition 0.000 description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000003208 petroleum Substances 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 6
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 238000007689 inspection Methods 0.000 description 5
- 239000010705 motor oil Substances 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical group OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 5
- 235000019260 propionic acid Nutrition 0.000 description 5
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- LJOODBDWMQKMFB-UHFFFAOYSA-N cyclohexylacetic acid Chemical compound OC(=O)CC1CCCCC1 LJOODBDWMQKMFB-UHFFFAOYSA-N 0.000 description 4
- JBDSSBMEKXHSJF-UHFFFAOYSA-N cyclopentanecarboxylic acid Chemical compound OC(=O)C1CCCC1 JBDSSBMEKXHSJF-UHFFFAOYSA-N 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
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- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 4
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- 150000002170 ethers Chemical class 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
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- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
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- 238000012423 maintenance Methods 0.000 description 4
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 4
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- 239000000779 smoke Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 4
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 3
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 3
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- INJDRHAMLGVMHB-UHFFFAOYSA-N C1C2=CC=CC=C2C3=C1C(=CC=C3)C4=C(C=CC(=C4C5=CC=CC6=C5CC7=CC=CC=C76)O)O Chemical compound C1C2=CC=CC=C2C3=C1C(=CC=C3)C4=C(C=CC(=C4C5=CC=CC6=C5CC7=CC=CC=C76)O)O INJDRHAMLGVMHB-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 1
- 244000256297 Euphorbia tirucalli Species 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- UWIULCYKVGIOPW-UHFFFAOYSA-N Glycolone Natural products CCOC1=C(CC=CC)C(=O)N(C)c2c(O)cccc12 UWIULCYKVGIOPW-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CNVZJPUDSLNTQU-UHFFFAOYSA-N Petroselaidic acid Natural products CCCCCCCCCCCC=CCCCCC(O)=O CNVZJPUDSLNTQU-UHFFFAOYSA-N 0.000 description 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 229910001422 barium ion Inorganic materials 0.000 description 1
- AESMDVCWMVZFRQ-UHFFFAOYSA-L barium(2+);butanoate Chemical compound [Ba+2].CCCC([O-])=O.CCCC([O-])=O AESMDVCWMVZFRQ-UHFFFAOYSA-L 0.000 description 1
- CKKNDGDDQKFVQM-UHFFFAOYSA-N barium;butanedioic acid Chemical compound [Ba].OC(=O)CCC(O)=O CKKNDGDDQKFVQM-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229910001423 beryllium ion Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- OVYQSRKFHNKIBM-UHFFFAOYSA-N butanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)CCC(O)=O OVYQSRKFHNKIBM-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000003442 catalytic alkylation reaction Methods 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- HZMBANJECWHRGE-GNOQXXQHSA-K cerium(3+);(z)-octadec-9-enoate Chemical compound [Ce+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O HZMBANJECWHRGE-GNOQXXQHSA-K 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- TXWOGHSRPAYOML-UHFFFAOYSA-N cyclobutanecarboxylic acid Chemical compound OC(=O)C1CCC1 TXWOGHSRPAYOML-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- VLDDESWWZPLNJD-UHFFFAOYSA-J cyclooctanecarboxylate titanium(4+) Chemical compound [Ti+4].[O-]C(=O)C1CCCCCCC1.[O-]C(=O)C1CCCCCCC1.[O-]C(=O)C1CCCCCCC1.[O-]C(=O)C1CCCCCCC1 VLDDESWWZPLNJD-UHFFFAOYSA-J 0.000 description 1
- URAXDCBRCGSGAT-UHFFFAOYSA-N cyclooctanecarboxylic acid Chemical compound OC(=O)C1CCCCCCC1 URAXDCBRCGSGAT-UHFFFAOYSA-N 0.000 description 1
- YZFOGXKZTWZVFN-UHFFFAOYSA-N cyclopentane-1,1-dicarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1 YZFOGXKZTWZVFN-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- PLYZFCVUMQOYCR-UHFFFAOYSA-L dilithium;pentanedioate Chemical compound [Li+].[Li+].[O-]C(=O)CCCC([O-])=O PLYZFCVUMQOYCR-UHFFFAOYSA-L 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000539 dimer Chemical class 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- FPIQZBQZKBKLEI-UHFFFAOYSA-N ethyl 1-[[2-chloroethyl(nitroso)carbamoyl]amino]cyclohexane-1-carboxylate Chemical compound ClCCN(N=O)C(=O)NC1(C(=O)OCC)CCCCC1 FPIQZBQZKBKLEI-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- XEOSBIMHSUFHQH-UHFFFAOYSA-N fulvalene Chemical compound C1=CC=CC1=C1C=CC=C1 XEOSBIMHSUFHQH-UHFFFAOYSA-N 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- ROBFUDYVXSDBQM-UHFFFAOYSA-N hydroxymalonic acid Chemical compound OC(=O)C(O)C(O)=O ROBFUDYVXSDBQM-UHFFFAOYSA-N 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- YAQXGBBDJYBXKL-UHFFFAOYSA-N iron(2+);1,10-phenanthroline;dicyanide Chemical compound [Fe+2].N#[C-].N#[C-].C1=CN=C2C3=NC=CC=C3C=CC2=C1.C1=CN=C2C3=NC=CC=C3C=CC2=C1 YAQXGBBDJYBXKL-UHFFFAOYSA-N 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- MAZKNBXUMANNDL-UHFFFAOYSA-M lithium;2-ethylhexanoate Chemical compound [Li+].CCCCC(CC)C([O-])=O MAZKNBXUMANNDL-UHFFFAOYSA-M 0.000 description 1
- PNDUWCHQCLZPAH-UHFFFAOYSA-M lithium;hexanoate Chemical compound [Li+].CCCCCC([O-])=O PNDUWCHQCLZPAH-UHFFFAOYSA-M 0.000 description 1
- BTAUEIDLAAYHSL-UHFFFAOYSA-M lithium;octanoate Chemical compound [Li+].CCCCCCCC([O-])=O BTAUEIDLAAYHSL-UHFFFAOYSA-M 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- CBUZSVKDOHZQRF-UHFFFAOYSA-L magnesium;2,2-dimethylpropanoate Chemical compound [Mg+2].CC(C)(C)C([O-])=O.CC(C)(C)C([O-])=O CBUZSVKDOHZQRF-UHFFFAOYSA-L 0.000 description 1
- ABSWXCXMXIZDSN-UHFFFAOYSA-L magnesium;hexadecanoate Chemical compound [Mg+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O ABSWXCXMXIZDSN-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- MHJIJZIBANOIDE-UHFFFAOYSA-K neodymium(3+);prop-2-enoate Chemical compound [Nd+3].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C MHJIJZIBANOIDE-UHFFFAOYSA-K 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical group 0.000 description 1
- 150000002978 peroxides Chemical group 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- CNVZJPUDSLNTQU-SEYXRHQNSA-N petroselinic acid Chemical compound CCCCCCCCCCC\C=C/CCCCC(O)=O CNVZJPUDSLNTQU-SEYXRHQNSA-N 0.000 description 1
- YKQNYRADBBHWOK-UHFFFAOYSA-N phenylarsonamidic acid Chemical compound N[As](O)(=O)C1=CC=CC=C1 YKQNYRADBBHWOK-UHFFFAOYSA-N 0.000 description 1
- LVKZSFMYNWRPJX-UHFFFAOYSA-N phenylarsonic acid Chemical group O[As](O)(=O)C1=CC=CC=C1 LVKZSFMYNWRPJX-UHFFFAOYSA-N 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- RWMKSKOZLCXHOK-UHFFFAOYSA-M potassium;butanoate Chemical compound [K+].CCCC([O-])=O RWMKSKOZLCXHOK-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- MFBOGIVSZKQAPD-UHFFFAOYSA-M sodium butyrate Chemical compound [Na+].CCCC([O-])=O MFBOGIVSZKQAPD-UHFFFAOYSA-M 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003442 suberic acids Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- FKLSONDBCYHMOQ-ONEGZZNKSA-N trans-dodec-9-enoic acid Chemical compound CC\C=C\CCCCCCCC(O)=O FKLSONDBCYHMOQ-ONEGZZNKSA-N 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- SSWMLKYBHOTWFA-UHFFFAOYSA-J tris[(2-hydroxybenzoyl)oxy]stannyl 2-hydroxybenzoate Chemical compound [Sn+4].Oc1ccccc1C([O-])=O.Oc1ccccc1C([O-])=O.Oc1ccccc1C([O-])=O.Oc1ccccc1C([O-])=O SSWMLKYBHOTWFA-UHFFFAOYSA-J 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- WDHVIZKSFZNHJB-UHFFFAOYSA-L zinc;butanoate Chemical compound [Zn+2].CCCC([O-])=O.CCCC([O-])=O WDHVIZKSFZNHJB-UHFFFAOYSA-L 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
- 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1828—Salts thereof
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1886—Carboxylic acids; metal salts thereof naphthenic acid
-
- 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
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/189—Carboxylic acids; metal salts thereof having at least one carboxyl group bound to an aromatic carbon atom
-
- 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
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
-
- 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
- C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
Definitions
- the invention relates to the improvement of fuel performance, and in particular to a fuel additive.
- the use of the additive can effectively improve the combustion performance of fuel in the combustion chamber of a motor vehicle and an oil-fired boiler, and has the effects of energy saving, pollution reduction, and friction reduction. It also relates to fuel products with such additives.
- the invention particularly relates to a gasoline anti-knock additive and a gasoline product containing the anti-knock agent. Background of the invention
- the combustion performance in the combustion chamber of a motor vehicle and in an oil-fired boiler is one of the important performance indicators of the fuel. It determines whether a fuel has the properties of energy saving and environmental protection.
- an important performance indicator is anti-knock performance.
- the anti-knock index is generally expressed by the average of the octane number (RON) determined by the research method and the octane number (M0N) determined by the motor method.
- RON octane number
- M0N octane number
- U.S. Patent No. 4,871,375 discloses the use of a mixture of tribasic acid amide or tetracarboxylic acid amide and an inorganic salt of an alkali metal or alkaline earth metal (rather than a compound) to add fuel to the engine. Anti-wear and anti-corrosion effect. However, the use of amine compounds will increase due to the addition of nitrogen atoms. Nitrogen content in motor vehicle exhaust. In addition, this document does not describe such an additive in terms of improving the explosion resistance of gasoline, providing energy-saving effects of gasoline, diesel, kerosene, heavy oil, residue oil, and the like, and reducing exhaust pollution.
- U.S. Patent No. 5,593,464 discloses a diesel fuel additive, which is a synthetic product of steamed residual oil and alkali metal, alkaline earth metal or rare earth metal, which can inhibit the carbon accumulation and It is not documented whether soot has energy-saving effect and has anti-friction effect on the engine, and whether it is also applicable to fuel oils other than diesel is not described.
- Gasoline anti-knock additives can also be divided into two categories.
- One is pure organic compounds, such as alcohols, ethers, aldehydes, ketones, esters, and nitrogen-containing compounds.
- fluorenyl tert-butyl ether (MTBE) is widely used, and ethanol, methanol, benzene, tert-butylfluorene, methyl acetate, acetone are also disclosed in Chinese patents 95111841, 96102483, 97108562, and 94112533. , Isopentane, etc.
- MTBE fluorenyl tert-butyl ether
- the purpose of the present invention is to provide a novel fuel additive, which has the effects of improving oil quality, reducing fuel consumption, reducing carbon deposits, reducing harmful substances in motor vehicle exhaust gas and fuel boiler smoke, and reducing engine component wear and corrosion.
- the invention also provides a novel fuel oil with the above additives added.
- the fuel additive provided by the present invention contains an oil-soluble organic acid metal salt of the general formula MR, where R is an organic acid radical, and the corresponding organic acid is a saturated or unsaturated fatty acid containing 1-40 carbon atoms, 4-40 A carbon atom of naphthenic acid, aromatic acid or alkyl phenol; where M is a metal cation or a metal ion and an inclusion complex ion, and the corresponding metal is an alkali metal, an alkaline earth metal, a rare earth metal, a transition metal or an optional metal Main metals from the metals aluminum, gallium, germanium, indium, tin, antimony.
- MR oil-soluble organic acid metal salt of the general formula MR, where R is an organic acid radical, and the corresponding organic acid is a saturated or unsaturated fatty acid containing 1-40 carbon atoms, 4-40 A carbon atom of naphthenic acid, aromatic acid or alkyl phenol; where M is a metal cation or a metal ion and an
- Fuel additives provided by the present invention include gasoline additives, diesel fuel additives, kerosene additives, heavy oil additives and residue additives. Different from similar additive products used in the prior art, the present invention selects a suitable organic acid metal salt as an additive or as an effective component of the additive, and integrates good cleanability, energy saving, and antifriction properties into one body, and its oil solubility Good, low addition and high efficiency.
- the invention particularly provides the use of the additive as a gasoline anti-knock additive.
- it integrates good anti-explosiveness, cleanliness, energy saving and friction reduction, which can greatly increase the octane number of gasoline.
- the use effect proves that it can be used as a replacement product of tetraethyl lead because of its excellent anti-knock performance.
- the organic acid metal salt used in the present invention can be obtained commercially or synthesized according to a known method.
- the present invention also provides a fuel oil to which the additive is added, including gasoline, diesel oil, kerosene, and heavy oil (containing residual oil), and the added amount is 0.1 to 15 grams of the organic acid metal salt per liter of fuel oil, and ordinary fuel oil
- the fuel of the present invention has better combustion performance, and the oil quality is significantly improved, which is beneficial to maintaining the normal working state of the engine combustion system and reducing fuel consumption and pollutant emissions.
- the present invention provides a fuel additive containing an oil-soluble organic acid metal salt of the general formula MR, where R is an organic acid radical, and the corresponding organic acid is a saturated acid containing 1-40 carbon atoms. Or unsaturated fatty acids, naphthenic acids of 4-40 carbon atoms, aromatic acids or alkylphenols of 6-40 carbon atoms; where M is a metal cation, or a metal ion and an inclusion complex ion,
- the corresponding metal is an alkali metal, an alkaline earth metal, a rare earth metal, a transition metal, or a main group metal selected from the metals aluminum, gallium, germanium, indium, tin, and antimony.
- the fuel oil according to the present invention includes fuels such as gasoline, diesel, kerosene, heavy oil, and residual oil.
- the invention particularly provides the use of the additive as a gasoline anti-knock additive.
- the organic acid radical is derived from a saturated or unsaturated fatty acid containing 1 to 25 carbon atoms, a naphthenic acid or an alkyl phenol having 4 to 25 carbon atoms, Especially the compounds of 10 carbons or less.
- a metal salt of a monocarboxylic acid is used.
- the organic acid radical has a carbon atom of 1-25, preferably 1-20, and more preferably 1-10, it can impart excellent anti-knock performance to gasoline.
- the saturated fatty acids (organic carboxylic acids represented by C n ii 2n + 1 C00H) and polycarboxylic acids according to the present invention, such as: formic acid, acetic acid, trimethylacetic acid, propionic acid, isopropyl acid, butyric acid, isopropyl Butyric acid, valeric acid, isovaleric acid, pivalic acid, 2-ethylbutanoic acid, hexanoic acid, 2-ethylhexanoic acid, heptanoic acid, caprylic acid, isooctanoic acid, nonanoic acid, capric acid, undecanoic acid, Lauric acid, myristic acid, hexadecanoic acid, octadecanoic acid, eicosanoic acid, dodecanoic acid, pentacosanoic acid, tricosanoic acid, glycolic acid, hydroxypropionic acid, hydroxybutyric acid
- the naphthenic acid according to the present invention includes an organic acid having a cycloalkyl group in a molecular structure and having a carbon number within the above range, such as a monocarboxylic acid or a dicarboxylic acid of a cycloalkyl group of C3-C10.
- Examples are: Cyclohexanecarboxylic acid, cyclopentanecarboxylic acid, cyclopentanedicarboxylic acid, cyclopropanecarboxylic acid, cyclobutanecarboxylic acid, cyclopentanecarboxylic acid, cycloheptanecarboxylic acid, cyclooctanecarboxylic acid, these carboxylic acids
- the acid may be acetic acid, acetic acid, propionic acid, and the like, such as cyclohexane acetic acid, cyclohexane acetic acid, cyclopentane diacetic acid, cyclopentane acetic acid, and the like, and the cyclic basic body may further have a substituent.
- methylcyclohexanecarboxylic acid, ethylcyclopentaneacetic acid and the like are examples of the cyclic basic body.
- Aromatic acids or alkyl phenols include: phenylarsinic acid, phenylacetic acid, m / p / o-phthalic acid, hydroxyphenylarsinic acid, hydrocarbyl substituted phenylarsinic acid, phenylacetic acid, etc., aminophenylarsinic acid, p-hydroxyl Phenyl acrylic acid, abietic acid (C 19 H 29 COOH) coumaric acid, phenol, o-methylphenol, 2, 4, 6-trimethylphenol, 2, 3 -difluorene hydroquinone, 3-ethyl Catechol, etc.
- organic acids described in the present invention also include their various isomers.
- the fuel additive of the present invention improves the octane number of gasoline, improves the burning state of the fuel, and reduces the abrasion of related parts of the engine.
- the above-mentioned oil-soluble organic acid metal salt is used, which has the properties of catalysis, cracking, dilution, excitation and hybridization. Characteristics, so it can effectively increase the octane number of gasoline, and can improve engine friction, reduce engine working resistance, and also allow the fuel to fully burn. The ultimate effect is to improve the anti-knock performance of gasoline, fast start-up and fuel consumption of motor vehicles. Low, reduce carbon deposits, clean exhaust emissions, and extend the service life of the engine system.
- the organic acid metal salt used in the present invention also has the effects of cleaning, saving energy and reducing engine wear on motor vehicle fuels such as diesel and kerosene, and cleaning and energy saving on boiler fuels such as heavy oil, residue, diesel, and kerosene. effect.
- the alkali metal may be lithium, sodium, potassium, rubidium, cesium, and the like, and the corresponding cation is a monovalent ion, preferably 4 mil, sodium, and potassium ion.
- Alkaline earth metals include beryllium, magnesium, calcium, strontium, barium, etc.
- the corresponding cations are divalent ions, especially beryllium, magnesium, calcium and barium ions.
- Rare earth metals include praseodymium, yttrium, lanthanum, cerium, praseodymium, neodymium, praseodymium, praseodymium, praseodymium, praseodymium, dysprosium, praseodymium, praseodymium, praseodymium, praseodymium, praseodymium, praseodymium, praseodymium, etc., preferably praseodymium, palladium, lanthanum, cerium, praseodymium, and the like, which The corresponding cations are trivalent or tetravalent ions, especially they are trivalent ions.
- Transition metals are titanium, zirconium, hafnium, niobium, tantalum, molybdenum, tungsten, ruthenium, hafnium, cobalt, rhodium, iridium, nickel, palladium, platinum, silver, gold,
- the corresponding cations of zinc and the like are monovalent, divalent, trivalent, or tetravalent ions, and divalent and trivalent ions are preferred, and titanium, cobalt, nickel, and zinc are particularly preferred.
- the corresponding cations of the main group metals such as aluminum, gallium, germanium, indium, tin, and antimony are trivalent, tetravalent, or pentavalent ions, preferably aluminum and tin, and trivalent and tetravalent ions are preferred.
- the preparation method of the organic acid metal salt is usually a direct reaction method or a metathesis reaction method.
- the additive according to the present invention may contain one or more of said oil-soluble organic acid metal salts. That is, a single organic acid metal salt compound may be used, or two or more of the oil-soluble organic acid metal salts described above may be mixed to form the fuel additive of the present invention.
- the ratio is not particularly limited as long as it is suitable for the fuel oil used.
- the additive according to the present invention may further include organic solvents such as alcohols, ethers, ketones, phenols, hydrocarbons, esters, aldehydes, or nitrogen-containing solvents, preferably alcohols, ethers, phenols, esters, hydrocarbon solvents, and nitrogen-containing solvents.
- organic solvents such as alcohols, ethers, ketones, phenols, hydrocarbons, esters, aldehydes, or nitrogen-containing solvents, preferably alcohols, ethers, phenols, esters, hydrocarbon solvents, and nitrogen-containing solvents.
- Compounds, especially alcohols, ethers, phenols, and hydrocarbon solvents are preferred, and their combined use can achieve better results. It can reduce the viscosity of the additives, increase the compatibility between the additives and the fuel, and be more convenient to use.
- the organic solvent may be used alone or in combination with an organic acid metal salt.
- Organic solvents suitable for the present invention include: methanol, ethanol, propanol, isopropanol, butanol, isobutanol, tert-butanol, octanol, isooctanol, 2-ethylhexanol, propyl ether, isopropyl ether , Butyl ether, o / m / p-fluorenyl phenol, difluorenyl phenol, di-tert-butyl p-phenol, benzamine, diphenylamine, triethylamine, p-aniline, 120 # solvent oil, 200 # solvent oil, Kerosene, ethylene glycol monoethyl ether, diethylene glycol-methyl ether / ether / butyl ether, triethylene glycol monomethyl ether / ether / butyl ether, diethylene glycol-dimethyl ether / ether / butyl ether, triethylene
- the amount of the organic solvent is not particularly limited, but it is preferably 0-90 g per 100 g of the organic solvent.
- the fuel additive includes a gasoline additive, a diesel fuel additive, a heavy oil additive, and a residual oil additive.
- the organic acid metal salt is preferably derived from a fatty acid, especially Saturated fatty acids, and compounds synthesized from organic acid radicals of naphthenic acids and alkali metal cations or earth-reducing metal cations, more preferably 1-10 carbon saturated fatty acid alkali metal salts, alkaline earth metal salts, or naphthenic alkali metal Salt, alkaline earth metal salt.
- suitable organic acid metal salts of the present invention may be: lithium, sodium, potassium, rubidium, cesium, beryllium, magnesium, calcium, strontium, barium, rubidium, yttrium, lanthanum, cerium, neodymium, titanium, cobalt, nickel, zinc Isometallic ions of the following organic acids: formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, 2-ethylbutyric acid, valeric acid, isovaleric acid, pivalic acid, trimethylacetic acid, hexanoic acid , 2-ethylhexanoic acid, heptanoic acid, octanoic acid, isooctanoic acid, nonanoic acid, capric acid, undecanoic acid, dodecanoic acid, myristic acid, hexadecanoic acid, octadecanoic acid, eicosane Acid, pen
- organic acid metal salt suitable for the present invention for example: lithium butyrate, sodium butyrate, potassium butyrate, barium butyrate, zinc butyrate, tin butyrate , Lithium valerate, magnesium pivalate, isooctanoate (such as zinc 2-ethylhexanoate, lithium 2-ethylhexanoate, magnesium 2-ethylhexanoate), lithium trimethylacetate, succinic acid Barium, neodymium acrylate, titanium cyclohexylacetate, tin o-hydroxybenzoate, magnesium hexadecanoate, undecylenic acid, cerium cycloheptane acetate, sodium nonanoate, calcium acrylate, titanium cyclopentanesulfonate , Cerium oleate, nickel cyclopentanesulfonate, potassium eicosanoate, 4 methyl oleate
- the existence ratio thereof can be determined according to the actual situation, but the preferred solution is that one of the salts occupies 40-80%,
- the determination of this salt depends on the metal ions used, and the order of selection is based on alkali metals, alkaline earth metals, rare earth metals, transition metals and other main group metals.
- the metals used belong to the same group, the metal with the smallest atomic number is preferred
- the proportion of organic acid salts is 40-80%.
- the fuel additive is a gasoline anti-knock additive. Adding 0.1 to 15 grams of the additive (based on the contained organic acid metal salt) per liter of gasoline will significantly increase the octane number of the gasoline and enhance Anti-knock performance of gasoline. It is preferable to use an organic acid metal salt having 1 to 10 carbon atoms, examples of which are as mentioned above.
- the organic acid described in the present invention may also be a dicarboxylic acid, a tricarboxylic acid, or a polymeric carboxylic acid, such as: substituted phthalic acid, dimer acid, trimer acid, and the like.
- the metal cation according to the present invention may also be an oil-soluble metal complex formed by the alkali metal ion, alkaline earth metal ion, rare earth metal ion, and transition metal ion or metal aluminum, gallium, germanium, indium, tin, and antimony.
- the role of ions or clathrate ions, ligands in complexes and acceptors in clathrates corresponds to organic acids.
- the present invention also provides a fuel oil to which the fuel additive is added, including gasoline, diesel, kerosene, heavy oil, and residual oil, and the added amount is 0.1-15 g (based on organic acid metal salt) per liter of fuel. Especially gasoline with good anti-knock performance and diesel with good cleaning performance.
- the fuel additives of the present invention especially the gasoline anti-knock additive, while providing anti-knock performance, also have very good cleaning and energy saving, anti-corrosion and anti-wear effects.
- the additive of the present invention can also be used as an additive for gasoline cleaning, energy saving, anticorrosion and friction reduction. That is, the present invention also provides the use of the additive as an additive for oil cleaning, energy saving, antifriction and anticorrosion.
- the organic acid metal salt of the present invention can be used for diesel and kerosene motor vehicles to achieve very significant cleaning, energy saving, reduce the wear of engine-related parts, and prevent corrosion of engine-related parts.
- Function and effect that is, the present invention also provides the use of the additive as a diesel fuel, kerosene and other motor vehicle fuel cleaning, energy saving, antifriction and anticorrosive additives.
- the organic acid metal salt of the present invention is used in heavy oil, residue oil, diesel, and kerosene burners, and can play a very significant cleaning, energy saving, and anticorrosive effect. Therefore, the present invention
- the use of the additive as a fuel cleaning and energy saving additive such as heavy oil and residual oil is also provided.
- the oil-soluble organic acid metal salt used in the additive of the present invention does not contain harmful substances, has no odor, has no toxicity, does not pollute the environment, does not endanger health, has no adverse effects on automobile engine parts, and requires only a small amount to be added. It can greatly improve the combustion performance of fuel oil, especially increase the octane number of gasoline, and give the gasoline good anti-knock performance. Therefore, it has the advantages of convenient use, high efficiency, low cost, and simple production process. All technical, economic, and environmental indicators meet or exceed national and international standards, and will not affect automotive exhaust gas purifiers. They can be completely replaced by tetraethyl lead. Implementation and beneficial effects
- Table 2 shows the increase of octane number when the above two compounds are added to gasoline.
- Lead content R / L is not more than 0. 013 0. 0013 1 0. 00029 0. 00030 0. 00022 0. 00024 Distillation range
- 10% evaporation temperature is not higher than CC) 70 61. 5 51. 5 52. 0 52. 5 56. 5 59. 5
- 503 ⁇ 4 Evaporation temperature is not higher than ('C) 120 99. 0 93. 0 94. 0 96. 5 94. 5 94. 5 94. 5
- composition of gasoline anti-knock additive is Composition of gasoline anti-knock additive:
- Lithium isooctanoate 90 g; Ethanol: 1 g; Propyl ether: 1 g; Isoamyl acetate: 3 g; Diethylene glycol-methyl ether: 3 g; After mixing the five compounds, they are added to gasoline as an additive in a certain proportion.
- the base oil is 90 # unleaded gasoline, and the above additives are added at a ratio of 1% ow / w, and the two tests are compared with no additives.
- Coolant (ethylene glycol) temperature 135 ⁇ 1 ° C
- test results (1) Adding additives (2) Inadequate p-additive piston ring weight loss (mg) 26. 2 101. 7
- the average fuel consumption of the test without additives is 172.41 seconds / 100ml
- the average fuel consumption of the dosing test is 197.55 seconds and 800ml
- Fuel consumption without additive test is 149kg
- Fuel consumption test for dosing is 132kg
- the gasoline anti-knock agent has a significant anti-wear effect.
- the gasoline antiknock agent of the present invention has a very obvious effect of reducing the concentration of CO and HC, which are exhaust pollutants from automobiles.
- the anti-knock agent is lithium pivalate.
- the test conditions and results are as follows:
- SYZZ-1 speed fuel consumption automatic measuring instrument.
- Test oil 90 # unleaded oil gasoline, engine oil, lubricating oil.
- Gasoline anti-knock agent composition lithium valerate: 80 g, tert-butanol: 5 g, ethylene glycol ether: 5 g, octane: 5 g, dibutyl propionate: 5 g.
- Gasoline anti-knock agent formula 95 grams of lithium isovalerate, 5 grams of ethanol. 1% (g / l) in gasoline.
- the additive was lithium octoate, which was adjusted to 1%.
- the weight ratio is added to diesel, and the test results are as follows:
- test vehicle was a Beijing-made Fuyue diesel truck, which had traveled 20,000 kilometers.
- the car has no effect when it is just started, as usual, because when the diesel car is cold started, some black smoke will be emitted from the exhaust pipe.
- the black smoke will gradually disappear. This is normal for all diesel vehicles during cold starts.
- the car's engine was running for ten minutes, it became apparent that the additive's idling speed was higher than before, while the engine noise was lower than before.
- the car's water temperature gauge was checked, and no temperature rise was found, indicating that the engine temperature was normal.
- the additive uses lithium hexanoate, added to -10 # diesel, and the added amount is 1.5%. (G / l), using the -10 # diesel oil as the base oil for comparison.
- the additive has the functions of energy saving, cleaning, and reducing engine wear. It is a good comprehensive additive. When added to the engine fuel, it can reduce the number of engine maintenance, extend the service life of the engine, and has significant energy savings. effect.
- Example 15 When added to the engine fuel, it can reduce the number of engine maintenance, extend the service life of the engine, and has significant energy savings. effect.
- Lithium butyrate 75 g, ethanedioic acid: 16 g, lithium cyclohexanesulfonate: 9 g, after mixing, add it to -10 # diesel oil at a ratio of 1% »(g / l), and test each item
- the physical and chemical indicators are as follows:
- Lithium glutarate was added to 200 # heavy oil at a ratio of 0.1% (g / l) and mixed uniformly.
- a comparative test was performed using heavy oil without additives as a control. The results are shown in the table below:
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CNB028039556A CN100460487C (zh) | 2001-02-01 | 2002-02-01 | 燃油添加剂及含有该燃油添加剂的燃油产品 |
US10/631,965 US20040065002A1 (en) | 2001-02-01 | 2003-08-01 | Fuel oil additive and fuel oil products containing the fuel oil additive |
US11/798,493 US20070266622A1 (en) | 2001-02-01 | 2007-05-14 | Fuel oil additive and fuel oil products containing said fuel oil additive |
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CN01106124A CN1368540A (zh) | 2001-02-01 | 2001-02-01 | 一种汽油抗爆添加剂及其配制的汽油 |
CN01106124.3 | 2001-02-01 |
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JP2022509195A (ja) | 2018-11-26 | 2022-01-20 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ | 燃料組成物 |
CN110041975A (zh) * | 2019-05-17 | 2019-07-23 | 王慕容 | 一种燃油添加剂及其制备方法 |
EP3933014A1 (de) * | 2020-06-30 | 2022-01-05 | Basf Se | Additivierung von kraftstoffen zur verringerung unkontrollierter zündungen in verbrennungsmotoren |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1228802A (zh) * | 1996-07-29 | 1999-09-15 | 多塔乐精制销售有限公司 | 含有至少三种金属的混合有机金属组合物及其作为燃料添加剂的应用 |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2097773A (en) * | 1929-05-27 | 1937-11-02 | Patent Fuels & Color Corp | Stabilized colored gasoline |
US2851417A (en) * | 1953-04-10 | 1958-09-09 | Socony Mobil Oil Co Inc | Complex alkoxy metal salts of organic acids and lubricating and fuel compositions thereof |
US2798797A (en) * | 1953-05-28 | 1957-07-09 | Ethyl Corp | Gasoline fuel additives |
US2935974A (en) * | 1957-02-18 | 1960-05-10 | Du Pont | Hydrocarbon fuels having improved antiknock properties |
US3009879A (en) * | 1957-10-01 | 1961-11-21 | Texaco Inc | Lubricating grease thickened with indigo and soap mixture |
US3013869A (en) * | 1959-02-16 | 1961-12-19 | Du Pont | Hydrocarbon-soluble alkali metal compositions |
US2999065A (en) * | 1960-11-07 | 1961-09-05 | Socony Mobil Oil Co Inc | Lubricant containing a calcium saltcalcium soaps mixture and process for forming same |
DE1300105C2 (de) * | 1966-03-29 | 1982-01-28 | Akzo Chemie GmbH, 5160 Düren | Verfahren zur herstellung von neutralen metallseifengemischen |
FR2244745B1 (ko) * | 1973-09-26 | 1977-05-27 | Ugine Kuhlmann | |
US4139349A (en) * | 1977-09-21 | 1979-02-13 | E. I. Du Pont De Nemours & Co. | Fuel compositions containing synergistic mixtures of iron and manganese antiknock compounds |
US4211535A (en) * | 1978-08-07 | 1980-07-08 | Gulf Research And Development Company | Gasoline fuel compositions containing antiknock additive |
US4264336A (en) * | 1979-09-28 | 1981-04-28 | Phillips Petroleum Company | Halogenated substituted fulvenes useful as fuel antiknock additives |
US4280458A (en) * | 1980-09-02 | 1981-07-28 | Shell Oil Company | Antiknock component |
US4417904A (en) * | 1981-12-16 | 1983-11-29 | Phillips Petroleum Company | N,N'-Dialkyl-N,N'-diphenyl alkylene diamine derivatives as antiknock agents |
US4444567A (en) * | 1982-07-01 | 1984-04-24 | Phillips Petroleum Company | Motor fuel composition containing an ashless antiknock agent |
US4437436A (en) * | 1982-10-04 | 1984-03-20 | Shell Oil Company | Antiknock additive compositions and unleaded gasoline containing same |
FR2537593B1 (fr) * | 1982-12-10 | 1986-04-11 | Raffinage Cie Francaise | Compositions organometalliques mixtes comprenant des elements des groupes du fer et des lanthanides, procede de preparation et application desdites compositions comme additifs pour combustibles ou carburants |
US4507214A (en) * | 1983-11-02 | 1985-03-26 | Union Oil Company Of California | Rare earth halide grease compositions |
US4568357A (en) * | 1984-12-24 | 1986-02-04 | General Motors Corporation | Diesel fuel comprising cerium and manganese additives for improved trap regenerability |
US4586357A (en) * | 1985-02-14 | 1986-05-06 | The U. S. Baird Corporation | Digital control spring forming machine |
US4649065A (en) * | 1985-07-08 | 1987-03-10 | Mooney Chemicals, Inc. | Process for preserving wood |
US4871375A (en) * | 1987-07-30 | 1989-10-03 | Basf Aktiensellschaft | Fuels for Otto engines |
USH935H (en) * | 1989-11-13 | 1991-07-02 | M-I Drilling Fluids Company | Compositions for oil-base drilling fluids |
US5118325A (en) * | 1990-12-31 | 1992-06-02 | Exxon Research And Engineering Company | Aminofulvene derivatives as antiknock compounds |
TW230781B (ko) * | 1991-05-13 | 1994-09-21 | Lubysu Co | |
US5449387A (en) * | 1992-06-17 | 1995-09-12 | Rhone-Poulenc Chemicals Limited | Cerium (IV) catalyst compounds and promoting combustion of hydrocarbon fuels therewith |
GB9315974D0 (en) * | 1993-08-02 | 1993-09-15 | Ass Octel | Fuel additives |
JP3453469B2 (ja) * | 1996-01-31 | 2003-10-06 | 花王株式会社 | 炭酸ガス硬化用粘結剤組成物 |
-
2001
- 2001-02-01 CN CN01106124A patent/CN1368540A/zh active Pending
-
2002
- 2002-02-01 WO PCT/CN2002/000047 patent/WO2002061018A1/zh not_active Application Discontinuation
- 2002-02-01 CN CNB028039556A patent/CN100460487C/zh not_active Expired - Fee Related
-
2003
- 2003-08-01 US US10/631,965 patent/US20040065002A1/en not_active Abandoned
-
2007
- 2007-05-14 US US11/798,493 patent/US20070266622A1/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1228802A (zh) * | 1996-07-29 | 1999-09-15 | 多塔乐精制销售有限公司 | 含有至少三种金属的混合有机金属组合物及其作为燃料添加剂的应用 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2505589C2 (ru) * | 2010-03-30 | 2014-01-27 | Федеральное государственное автономное образовательное учреждение высшего профессионального образования "Уральский федеральный университет им. Первого Президента России Б.Н. Ельцина" | Способ снижения требований автомобильных бензиновых двигателей к величине октанового числа |
CN102690690A (zh) * | 2012-06-13 | 2012-09-26 | 洛阳华燃石化科技有限公司 | 一种复合燃料油 |
CN106867601A (zh) * | 2017-03-13 | 2017-06-20 | 宜兴市星光宝亿化工有限公司 | 一种柴油抗磨剂及其制备方法 |
CN108690667A (zh) * | 2018-05-24 | 2018-10-23 | 宁波蒙曼生物科技有限公司 | 一种环保汽油添加剂及其制备方法及该添加剂的制备设备 |
Also Published As
Publication number | Publication date |
---|---|
CN100460487C (zh) | 2009-02-11 |
US20040065002A1 (en) | 2004-04-08 |
CN1368540A (zh) | 2002-09-11 |
WO2002061018A8 (fr) | 2002-11-14 |
CN1531584A (zh) | 2004-09-22 |
US20070266622A1 (en) | 2007-11-22 |
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