WO2010077161A2 - Synergistic octane booster additives containing aromatics amines and manganese and gasoline resulted from their usage - Google Patents
Synergistic octane booster additives containing aromatics amines and manganese and gasoline resulted from their usage Download PDFInfo
- Publication number
- WO2010077161A2 WO2010077161A2 PCT/RO2009/000015 RO2009000015W WO2010077161A2 WO 2010077161 A2 WO2010077161 A2 WO 2010077161A2 RO 2009000015 W RO2009000015 W RO 2009000015W WO 2010077161 A2 WO2010077161 A2 WO 2010077161A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gasoline
- octane
- manganese
- additives
- synergistic
- Prior art date
Links
- 239000000654 additive Substances 0.000 title claims abstract description 62
- 239000011572 manganese Substances 0.000 title claims description 48
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 title claims description 32
- 230000002195 synergetic effect Effects 0.000 title claims description 23
- 229910052748 manganese Inorganic materials 0.000 title claims description 14
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title claims description 10
- 150000001412 amines Chemical class 0.000 title claims description 4
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims abstract description 98
- 230000000996 additive effect Effects 0.000 claims abstract description 19
- 150000004982 aromatic amines Chemical class 0.000 claims abstract description 15
- 150000002902 organometallic compounds Chemical class 0.000 claims abstract description 9
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims abstract description 3
- KDZSOJJFEINEDS-UHFFFAOYSA-N C[Mn]C1C=CC=C1 Chemical compound C[Mn]C1C=CC=C1 KDZSOJJFEINEDS-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 8
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 6
- 150000001298 alcohols Chemical class 0.000 claims description 5
- 150000002170 ethers Chemical class 0.000 claims description 5
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000006078 metal deactivator Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 abstract description 4
- 239000001301 oxygen Substances 0.000 abstract description 4
- 150000002148 esters Chemical class 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 16
- 230000000694 effects Effects 0.000 description 14
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 8
- 150000003254 radicals Chemical class 0.000 description 7
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 230000003993 interaction Effects 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 4
- -1 hydrocarbon radicals Chemical class 0.000 description 4
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 4
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 4
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 230000003042 antagnostic effect Effects 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000009044 synergistic interaction Effects 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000001473 noxious effect Effects 0.000 description 2
- 125000002524 organometallic group Chemical group 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical group CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- VIIZJXNVVJKISZ-UHFFFAOYSA-N 2-(n-methylanilino)ethanol Chemical compound OCCN(C)C1=CC=CC=C1 VIIZJXNVVJKISZ-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- LGCHWMXWPGNCLH-UHFFFAOYSA-N 5-methylidenecyclopenta-1,3-dien-1-amine Chemical class NC1=CC=CC1=C LGCHWMXWPGNCLH-UHFFFAOYSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- ITZXULOAYIAYNU-UHFFFAOYSA-N cerium(4+) Chemical compound [Ce+4] ITZXULOAYIAYNU-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- RKEZHXGBECEYGM-UHFFFAOYSA-N cyclopenta-1,3-diene iron(2+) 5-propylcyclopenta-1,3-diene Chemical compound [Fe++].c1cc[cH-]c1.CCC[c-]1cccc1 RKEZHXGBECEYGM-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- QFEOTYVTTQCYAZ-UHFFFAOYSA-N dimanganese decacarbonyl Chemical group [Mn].[Mn].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-] QFEOTYVTTQCYAZ-UHFFFAOYSA-N 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003254 gasoline additive Substances 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- AMWRITDGCCNYAT-UHFFFAOYSA-L manganese oxide Inorganic materials [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 1
- PPNAOCWZXJOHFK-UHFFFAOYSA-N manganese(2+);oxygen(2-) Chemical class [O-2].[Mn+2] PPNAOCWZXJOHFK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000004776 molecular orbital Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- VXHFNALHLRWIIU-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)OC(=O)C(C)(C)C VXHFNALHLRWIIU-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000012855 volatile organic compound 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
- 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
-
- 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
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
-
- 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
- C10L1/183—Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom
- C10L1/1832—Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom mono-hydroxy
-
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/223—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/228—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles
- C10L1/2283—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles containing one or more carbon to nitrogen double bonds, e.g. guanidine, hydrazone, semi-carbazone, azomethine
-
- 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
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
Definitions
- the present invention refers to a process for obtaining octane-booster additives whose compositions comprise at least an aromatic amine, such as N-methylaniline; a manganese compound such as bis-(dicypentadienyl)manganese, methylcyclopentadienyl manganese tricarbonyl or manganese carbonyl, and optionally an oxygenated compound belonging to the class of ethers or alcohols and also to the automotive gasoline obtained from basic gasoline and the above mentioned additives.
- spark-ignition engines require gasoline having high octane numbers, Research Octane Number (RON) > 95 and Motor Octane Number (MON) > 85.
- the terms RON and MON are specific to the measurement procedure. Further, in USA and Canada the octane number AKI (average knocking index) representing the mean (RON + M0N)/2 is used.
- compositions of the gasoline approved for the use in the automotive engines imply drastic restrictions: S ⁇ 10 mg/kg; aromatic hydrocarbons ⁇ 35% vol/vol. (content of benzene: ⁇ 1% vol/vol; olefin ⁇ 18% vol/vol, final boiling point 210 0 C, % vol/vol distillation residue ⁇ 2%, density at 15 0 C: 720-775 kg / m 3 etc., and in the future, in order to reduce noxious emissions, new restrictions on the content of aromatic materials will be imposed. Because of all these restrictions, the oil processing becomes more complicated and new technical problems arise.
- gasoline having high octane number there are used processing fractions containing isoparaffins, cycloparaffins, and aromatic materials, these classes of hydrocarbons being characterized by high octane numbers.
- the octane number of gasoline represents its knocking resistance. Due to the influence of the temperature of the flame front, the vapour of the hydrocarbon molecules having long straight chain produce high quantities of reactive hydrocarbon radicals. They react with the oxygen of the ignition air and keep the formation of the OH * and O * radicals. These radicals propagate the knock by generating radical branched chains. The branched molecules and those bond to the aromatic or saturated cycles are more resistant to the effect of the temperature this explaining the high octane numbers.
- the increase of the octane number of the basic gasoline to a value required by the optimal operation of the spark-ignition engines is carried out by using the octane- booster additives.
- the oxygenated additives produce a local decrease of the temperature, deactivating the radical branched chains.
- the additives containing metals react with the OH * and O * radicals splitting the propagation branched chains.
- the first octane-booster additives used on a large scale were lead tertalkyls which, due to their toxicity, are now prohibited, the lead content in the current gasoline being limited to 5 mg/l.
- organometallic compounds containing cerium (IV), especially salts with 2,2,6,6-tetramethyl-3,5- heptadione US3794473; US 4036605 or containing alkaline metals: RU2203927; RU2152981 ; US3770397.
- Octane-booster additives containing organometallics have as a main advantage that, at very low concentrations 10-100 mg metal/L, they increase the octane number of the basic gasoline, thus being the cheapest technical solution.
- the main drawbacks of using organometallic compounds are correlated to the effect of the formation of the metallic oxides onto the equipments of the engine.
- the iron oxides have an abrasive effect on the valves of the engine and on the sparking plugs, where, by depositing, they alter the dielectric characteristics.
- MMT When MMT is used at a concentration of 9-12 mg/L Mn it protects the valves of the engine.
- Both the iron and manganese oxides alter the operation of the exhaust gas catalytic converter. For this reason the use of manganese with a concentration of maximum 18 mg/L is preferred. For its use at reasonable concentrations, it does not cause negative effects on the noxious gases emissions.
- ethers of tert-butanol with low aliphatic alcohols are used in large amount as octane-booster additives, the most known being tert-butyl methyl ether (MTBE) and low aliphatic alcohols: Mohammad Ashraf SIi, Halim Hamid, Mohammad Ashraf AIi in "Handbook of MTBE and Other Gasoline Oxygenates" Printed in USA, Marcel Dekker Inc, New York. Basel; 1979; US4468233; US5752992. These additives are generically called oxygenated additives. It is also cited the use of the ethers of the phenols with low alcohols RU2005138060.
- octane-booster additives industrially used are aromatic amines, especially
- N-methylaniline GB252019; GB334181A; GB530597; FR1255840; RU2184767; US2819953; US5470358; EP0235280; WO2008076759.
- the aromatic amines are 4-15 times more efficient than the oxygenated additives, however their drawback is their price and sometimes the high toxicity (aniline and o-toluidine).
- aminofulvenes US5118325; aminophenols: WO2007105982; WO2007117176; colouring agents and other structures having extended molecular orbitals: WO2006076020; ortho- azidophenol; ortho-azidoaniline: US4280458.
- aminofulvenes US5118325; aminophenols: WO2007105982; WO2007117176; colouring agents and other structures having extended molecular orbitals: WO2006076020; ortho- azidophenol; ortho-azidoaniline: US4280458.
- aminofulvenes US5118325
- aminophenols WO2007105982
- WO2007117176 colouring agents and other structures having extended molecular orbitals
- ortho- azidophenol ortho-azidoaniline
- the present invention provides several multi-compound compositions which combine the characteristics of several octane-booster additives so that by synergistic interactions the maximum effects can be realized.
- the synergistic effect ⁇ Sx occurs when, in the same gasoline, a series of components A 1 ; A 2 ;... A n , each one with an individual concentration C 1 ; C 2 ;... C n individually induces an increase of the octane number A[X] 1 ; A[X] 2 ;...
- the patent RU2235117 shows the ferrocene - alcohols (esters) - aromatic amines interactions.
- the level of Fe is very high (40-62mg/kg), but comparing with the individual activity of the components, it can be estimated that the presence of iron results in an antagonism.
- the patent RU2110561 reports a detailed study referring to the aromatic amines (NMA, xilidine) - MTBE - additives containing iron ( ⁇ - hidroxy propyl ferrocene; ferrocene) interactions, but the interpretation of the shown data does not allow to establish the nature of the interactions between the components.
- the patent RU2117691 claims the binary additives Mn (MMT) - xilidine, the manganese concentrations being much above the admitted limits; 45 - 136 mg/kg, and the interactions effects certainly are antagonistic.
- the patent RU2129141 shows different compositions of an tri-component additive N-methyl aniline - ethanol - additives containing iron (ferrocene and ⁇ - hidroxy-isopropyl ferrocene).
- the composition of the additive 5-10% wt N-methyl aniline, Fe 150 - 145,5 mg/kg; ethanol about up to 100%, was dosed 5% wt. into a synthetic gasoline 70% isooctane and 30% n-heptane rendering obvious certain synergetic effects which can be deduced by the results extrapolating.
- organometallic octane - booster additives especially those having high concentrations, alter the different parts of the engine; valves, ignition plugs, catalytic converter and can poluate the environment.
- the octane - booster additives belonging to the oxygenated compounds class requires high concentrations into the gasoline, usually 5 -16% and, while increasing their concentrations, the the emission of volatile organic compounds and nitric oxides in the exhaust gases increase.
- the octane - booster additives belonging to the aromatic amines class have the drawback of a high cost, and at high concentrations, they can cause the stylificant increase of the nitric oxides emission in the exhaust gases.
- the technical problem solved by the present invention is the preparation of the multi-component octane - booster additives having high effiency, based on the synergistic interaction of the organometallic compounds containing manganese, preferably as MMT with aromatic amines or mixtures of aromatic amines and oxygenated compounds, the ratio manganese / amines being in a well defined concentration range.
- the additive dosing is ground on the author's find that for weight ratios of >0-25 mg Mn/g aromatic amine, significant synergistic and demonstrable effects occur, their maximum intensity occurring in the composition range 0,5 - 1 ,0 mg Mn /g aromatic amine.
- the gasoline used for experiments was refinery blending type whose characteristics are shown in Table 2
- the gasoline can be further added with deactivating metals, preferably N,N-disalicylidene-1 ,2-diaminopropane [CAS 94-91-7] and antioxidants belonging to the class of sterically hindered phenols, preferably 2,6-di-tert-butyl-p-cresol [CAS 128-37-0] in order to prevent the gums formation phenomena and the oxidation, processes catalyzed by the metals.
- deactivating metals preferably N,N-disalicylidene-1 ,2-diaminopropane [CAS 94-91-7] and antioxidants belonging to the class of sterically hindered phenols, preferably 2,6-di-tert-butyl-p-cresol [CAS 128-37-0] in order to prevent the gums formation phenomena and the oxidation, processes catalyzed by the metals.
- the concentration of the manganese in the gasoline is between 4 and 9 mg/L, thus eliminating the negative effects of the metals presence. Further, 5 examples are shown.
- Example 1 Into the gasoline having the composition of table 2 with MMT is then added, at different concentrations, N-methyl aniline and finally mixtures of N-methyl aniline and MMT, followed by the measuring of the octane number according to the Standards SR EN ISO 5164:06; SR EN ISO 5183:06. The results of the individually adding of N-methyl aniline and MMT are shown in the tables 3 and 4 ( ⁇ RON; ⁇ MON shows the increase of the octane number after adding the additives).
- NMA N-methyl aniline
- MMT MMT
- the data interpretation renders obvious the existence of the synergistic interactions.
- the range of synergism is maximum in the ratios range Mn/NMA 0,6 - 1 mg/kg N-methyl aniline. This range is suggestively shown in figure 1 , where the percentage increase of the synergistic additive efficiency % ⁇ E is shown comparing with the individual contribution of NMA and MMT, depending on the ratio Mn/ NMA expressed as mg/kg:
- the synergistic effect decreases while increasing the concentration of N-methyl aniline.
- concentration of N-methyl aniline is 1% wt.
- the synergism area is comprised between >0 and >2,2 mg Mn/g N-methyl aniline, while for a concentration of 2% wt. N-methyl aniline, the synergism area is diminished to the range 0,4 - 1 ,8 mg Mn/g N-methyl aniline, and its intensity is reduced to a half.
- the preferred range of the synergistic additives compositions is 0,5 - 1 ,0 mg Mn/g N-methyl aniline, range in which the synergistic effect intensity is maximum.
- Example 2 97g of N-methyl aniline was admixed to homogenization with 3g of N,N- dimethyl aniline, resulting 100g solution containing 97% wt. N-methyl aniline (NMA) and 3% wt. N,N-dimethyl aniline (NNDMA).
- NMA N-methyl aniline
- NMDMA N,N-dimethyl aniline
- 0,52 g MMT was admixed with 9,48g solution 97% wt. aniline and 3% wt. N,N-dimethyl aniline previously prepared, resulting a 13,16 mg/g Mn solution.
- Example 3 Following the procedure of example 2 the admixtures I - IX having octane - booster properties and representing the comparison standard and the multi-component synergistic additives I-Mn - IX-Mn having the content of Mn within the synergism range of 0,6 - 1 mgMn/g were prepared. For the additives VII-Mn si IX-Mn, the Mn concentrations were calculated so they be within the range 0,6 - 1 mg Mn/g N-methyl aniline. All these compositions are shown in table 7. The additives prepared in this way were dosed up into the basic gasoline having the composition of table 2 and the octane numbers were measured according to the Standards mentioned in example 1 ; the test results are shown in table 8.
- Example 4 1kg of multi-component synergistic additive was prepared by admixing and homogenizing 929g N-methyl aniline; 29,7g N,N-dimethyl aniline; 29,7g anisole; 3,6 g MMT; 4g N,N-disalicylidene-1 ,2-diaminopropane [CAS 94-91-7]; 4g 2,6-di-tert-butyl-p- cresol [CAS 128-37-0].
- Example 5 6,5kg of multi-component synergistic additive were prepared by admixing and homogenizing 1891g N-methyl aniline; 58,5g N,N-dimethyl aniline; 450Og anhydrous denaturated ethanol; 3,8 g MMT; 4g N,N-disalicylidene-1 ,2-diaminopropane 4g 2,6-di-tert- butyl-p-cresol.
- the resulted amount of multi-component synergistic additive was admixed and homogenized with 99kg gasoline having the composition of table 2, resulting 100 kg of gasoline RON 95, whose octane numbers were measured according to the Standards mentioned in example 1 ; the results are shown in table 10.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
The invention refers to an additive for the gasoline. The additive according to the invention is an admixture of aromatic amines, preferably N-methylaniline and organometallic compounds containing manganese, preferably methylcyclopentadienyl manganese (II) tricarbonyl and optionally an organic compound containing oxygen, such as an ether, an ester or an alcohol.
Description
SYNERGISTIC OCTANE BOOSTER ADDITIVES CONTAINING AROMATICS AMINES AND MANGANESE AND GASOLINE RESULTED FROM THEIR USAGE
The present invention refers to a process for obtaining octane-booster additives whose compositions comprise at least an aromatic amine, such as N-methylaniline; a manganese compound such as bis-(dicypentadienyl)manganese, methylcyclopentadienyl manganese tricarbonyl or manganese carbonyl, and optionally an oxygenated compound belonging to the class of ethers or alcohols and also to the automotive gasoline obtained from basic gasoline and the above mentioned additives.
For a correct operation, spark-ignition engines require gasoline having high octane numbers, Research Octane Number (RON) > 95 and Motor Octane Number (MON) > 85. The terms RON and MON are specific to the measurement procedure. Further, in USA and Canada the octane number AKI (average knocking index) representing the mean (RON + M0N)/2 is used. The gasoline is manufactured by processing the crude oil by distillation, cracking, isomerization and alkylation. Since in most cases the manufacture of gasoline having RON =95 implies increased costs and simultaneously decreased efficiency, by admixing gasoline manufactured by different technological processes, the so-called basic gasoline having generally RON<95 is obtained. Furthermore, according to the Standard EN 228:2004 applied in EU, when referring to the compositions and physical characteristics, the compositions of the gasoline approved for the use in the automotive engines imply drastic restrictions: S< 10 mg/kg; aromatic hydrocarbons < 35% vol/vol. (content of benzene: < 1% vol/vol; olefin < 18% vol/vol, final boiling point 2100C, % vol/vol distillation residue < 2%, density at 150C: 720-775 kg / m3 etc., and in the future, in order to reduce noxious emissions, new restrictions on the content of aromatic materials will be imposed. Because of all these restrictions, the oil processing becomes more complicated and new technical problems arise.
For obtaining gasoline having high octane number, there are used processing fractions containing isoparaffins, cycloparaffins, and aromatic materials, these classes of hydrocarbons being characterized by high octane numbers. The octane number of gasoline represents its knocking resistance. Due to the influence of the temperature of the flame front, the vapour of the hydrocarbon molecules having long straight chain produce high quantities of reactive hydrocarbon radicals. They react with the oxygen of the ignition air and keep the formation of the OH* and O* radicals. These radicals propagate the knock by generating radical branched chains. The branched molecules and those bond to the aromatic or saturated cycles are more resistant to the effect of the temperature this explaining the high octane numbers. The increase of the octane number of the basic
gasoline to a value required by the optimal operation of the spark-ignition engines is carried out by using the octane- booster additives. The radicals resulted from the octane- booster additives or even the additives themselves interfere with the radicals generating the knock. Generally, the oxygenated additives produce a local decrease of the temperature, deactivating the radical branched chains. The additives containing metals react with the OH* and O* radicals splitting the propagation branched chains.
The first octane-booster additives used on a large scale were lead tertalkyls which, due to their toxicity, are now prohibited, the lead content in the current gasoline being limited to 5 mg/l. Currently, organometallic compounds containing iron, especially in form of ferrocene, GB226731 ; US4139349; WO 0116257, containing manganese especially in form of methylpentadienyl manganese(ll) tricarbonyl (MMT): US4139349; EP0466511 ; EP0476197. It was also reported the possibility to use organometallic compounds containing cerium (IV), especially salts with 2,2,6,6-tetramethyl-3,5- heptadione: US3794473; US 4036605 or containing alkaline metals: RU2203927; RU2152981 ; US3770397. Octane-booster additives containing organometallics have as a main advantage that, at very low concentrations 10-100 mg metal/L, they increase the octane number of the basic gasoline, thus being the cheapest technical solution. The main drawbacks of using organometallic compounds are correlated to the effect of the formation of the metallic oxides onto the equipments of the engine. Thus, the iron oxides have an abrasive effect on the valves of the engine and on the sparking plugs, where, by depositing, they alter the dielectric characteristics. When MMT is used at a concentration of 9-12 mg/L Mn it protects the valves of the engine. Both the iron and manganese oxides alter the operation of the exhaust gas catalytic converter. For this reason the use of manganese with a concentration of maximum 18 mg/L is preferred. For its use at reasonable concentrations, it does not cause negative effects on the noxious gases emissions.
Currently, the ethers of tert-butanol with low aliphatic alcohols are used in large amount as octane-booster additives, the most known being tert-butyl methyl ether (MTBE) and low aliphatic alcohols: Mohammad Ashraf SIi, Halim Hamid, Mohammad Ashraf AIi in "Handbook of MTBE and Other Gasoline Oxygenates" Printed in USA, Marcel Dekker Inc, New York. Basel; 1979; US4468233; US5752992. These additives are generically called oxygenated additives. It is also cited the use of the ethers of the phenols with low alcohols RU2005138060. The main drawback resulted from the use of these additives is the necessity of using high levels. For example, a concentration of 1 % wt. MTBE in gasoline increases RON with 0,2-0,3 units, depending on the type of gasoline. The presence of the oxygenated additives results also in the increase of the volatile carbonyl compounds emission in the exhaust gases. In the case of the alcohols, another drawback is the
increase of the corrosion. Therefore, according to the Standard EN 228:2004 applicable in EU, the presence of oxygenated additives in gasoline is restricted to 2,8% wt. oxygen.
Other octane-booster additives industrially used are aromatic amines, especially
N-methylaniline: GB252019; GB334181A; GB530597; FR1255840; RU2184767; US2819953; US5470358; EP0235280; WO2008076759. The aromatic amines are 4-15 times more efficient than the oxygenated additives, however their drawback is their price and sometimes the high toxicity (aniline and o-toluidine).
Among the octane-booster additives having high efficiency it can be listed: aminofulvenes: US5118325; aminophenols: WO2007105982; WO2007117176; colouring agents and other structures having extended molecular orbitals: WO2006076020; ortho- azidophenol; ortho-azidoaniline: US4280458. Generally, it is difficult to prepare these compounds which further have prohibitive prices.
The present invention provides several multi-compound compositions which combine the characteristics of several octane-booster additives so that by synergistic interactions the maximum effects can be realized. There are several patents referring to multi-compounds systems of octane-booster additives which claim the synergistic effects, but only in few cases the shown data resist to an objective analysis of the results, considering the definition of the synergism phenomena. The synergistic effect ΔSx occurs when, in the same gasoline, a series of components A1; A2;... An, each one with an individual concentration C1; C2;... Cn individually induces an increase of the octane number A[X]1; A[X]2;... Δ[X]i....Δ[X]n , where [X] can be RON; MON; AKI, and the mixture of the compounds A1; A2;... An, each one with the same concentration C1JC2...Cn, in the same gasoline as in the case of their individual participation, has as result a joint increase of the octane number Δ[X] so that:
ΔSX = Δ [X] - Σ Δ[X], respectively
With respect to the multi-component octane-booster additives there are several references in the prior art.
Thus, although the patent US4139349 claims the synergetic effects of the mixtures MMT - ferrocene, in all shown cases ΔSRON ≤0; being in the range from 0 to -1 ,5.
The patent application WO2005087901 claims several multi-compound systems containing Fe, Mn, K, Ca, Mn organometallic compounds and aromatic amines (aniline,
N-methylaniline, ortho-toluidine §i para-toluidine). When the shown data allow a calculation of the interactions Fe-K-N-methyl aniline, the effects are antagonistic. In the
case of a gasoline initially having RON=95,0 and MON=83,9, for the additive compositions: Fe 12g/L; K 4,5ppm, it was obtained ΔSRON= -0,7; ΔSMON= -1 >6; for Fe 12g/L; N-methyl aniline 0,3% vol/vol. it was obtained ΔSRON= - 0,3; ΔSMON = 1 ,0; for Fe 12g/L; K 4,5ppm; N-methyl aniline 0,3% vol/vol. it was obtained ΔSRON= - 0,2; ΔSMON = - 0,8. In the case of the compositions 12 -18 g/L Mn; 0 - 4,5 ppm K si 0 - 0,3% vol/vol N- methyl aniline, although the data are not sufficient for an accurate calculation, it can however be estimated that the effects are antagonistic.
The patent RU2235117 shows the ferrocene - alcohols (esters) - aromatic amines interactions. The level of Fe is very high (40-62mg/kg), but comparing with the individual activity of the components, it can be estimated that the presence of iron results in an antagonism.
The patent RU2110561 reports a detailed study referring to the aromatic amines (NMA, xilidine) - MTBE - additives containing iron (α - hidroxy propyl ferrocene; ferrocene) interactions, but the interpretation of the shown data does not allow to establish the nature of the interactions between the components.
The patent RU2117691 claims the binary additives Mn (MMT) - xilidine, the manganese concentrations being much above the admitted limits; 45 - 136 mg/kg, and the interactions effects certainly are antagonistic.
The patent RU2129141 shows different compositions of an tri-component additive N-methyl aniline - ethanol - additives containing iron (ferrocene and α - hidroxy-isopropyl ferrocene). The composition of the additive 5-10% wt N-methyl aniline, Fe 150 - 145,5 mg/kg; ethanol about up to 100%, was dosed 5% wt. into a synthetic gasoline 70% isooctane and 30% n-heptane rendering obvious certain synergetic effects which can be deduced by the results extrapolating. The patent FR1255840 claims a very strong synergistic effect of the N-methyl aniline (NMA) and MMT added into a gasoline containing 0,18% Pb (as lead tetraethyl). Thus, [RON]=I 09,5 is obtained by adding NMA 0,036 % wt. This means an exceptional contribution of NMA1 corresponding to an individual octane number in admixture of [RON]A0=9828. Further adding 0,36 % Mn as MMT a further exceptional increase of Δ[RON]=4,5 occurs. In the absence of NMA the contribution of MMT at the same concentration is only Δ[RON]=2,7.
Other obvious synergism examples between lead tetraethyl and tert-butyl pivalate or Ce(IV) β-diketonate and free β-diketone are shown in the patents FR2050841 and US4211535 respectively. However, the most surprising effect is claimed by the patent US4690687 where the effect of Mn added in gasoline as MMT is significantly intensified by the presence of β-diketones.
The main drawbacks of the diferrent typs of the octane-booster additives and the previous shown multi-component systems thereof are the following:
The organometallic octane - booster additives, especially those having high concentrations, alter the different parts of the engine; valves, ignition plugs, catalytic converter and can poluate the environment.
The octane - booster additives belonging to the oxygenated compounds class requires high concentrations into the gasoline, usually 5 -16% and, while increasing their concentrations, the the emission of volatile organic compounds and nitric oxides in the exhaust gases increase. The octane - booster additives belonging to the aromatic amines class have the drawback of a high cost, and at high concentrations, they can cause the semnificant increase of the nitric oxides emission in the exhaust gases.
The technical problem solved by the present invention is the preparation of the multi-component octane - booster additives having high effiency, based on the synergistic interaction of the organometallic compounds containing manganese, preferably as MMT with aromatic amines or mixtures of aromatic amines and oxygenated compounds, the ratio manganese / amines being in a well defined concentration range. The additive dosing is ground on the author's find that for weight ratios of >0-25 mg Mn/g aromatic amine, significant synergistic and demonstrable effects occur, their maximum intensity occurring in the composition range 0,5 - 1 ,0 mg Mn /g aromatic amine.
The characteristics of the reagents used for formulating the octane-booster additives used by the invention are shown in Table 1.
Table 1.
Reagent CAS# appereance purity density melt boiling
% 200C; point point kg/m3 C C
MMT 12108-13-3 liquid 97 1388 1.5 233
N-methyl aniline 100-61-8 liquid 98 989 -57 194-197
N,N-dimethyl 121-69-7 liquid 99 956 2 193 aniline m-toluidine 108-44-1 liquid 99 992 -32 Ia -30 203-204 p-toluidine 106-49-0 cryst. >99 973 42-44 199-202
3,5-dimethyl 108-69-0 liquid >97 971 9-11 220-221 aniline orto-toluidine 95-53-4 liquid 99 1004 -24 199-200
N,N-dimethyl-1 ,4- 99-98-9 solid 99 1030 34-36 262 phenylene diamine
MTBE 1634-04-4 liquid 99 742 -109 55-56
Ethanol 64-17-5 liquid 96 789 -130 78 anhydrous denatu rated
The gasoline used for experiments was refinery blending type whose characteristics are shown in Table 2
Table 2.
Characteristic UM Value Analysis standard density 15C kg/m3 732,0 SR EN ISO 3675:03
RON 91 ,6 SR EN ISO 5164:06
MON 80.8 SR EN ISO 5183:06 olefine % vol/vol 16.9 SR 1347:02 aromatics % vol/vol 33,2 SR EN 14517:05 sulfur content mg/kg 45,0 SR EN ISO 20846:04 evaporation at 1000C % vol/vol 59,2 SR EN ISO 3405:03 final boiling point C 202,0 SR EN ISO 3405:03 distillation residue % vol/vol 1.1 SR EN ISO 3405:03 gums mg/100mL 1.2 SR EN ISO 6246:00
Besides the addition of the synergistic octane-booster additives, the gasoline can be further added with deactivating metals, preferably N,N-disalicylidene-1 ,2-diaminopropane [CAS 94-91-7] and antioxidants belonging to the class of sterically hindered phenols, preferably 2,6-di-tert-butyl-p-cresol [CAS 128-37-0] in order to prevent the gums formation phenomena and the oxidation, processes catalyzed by the metals.
The main advantages of the present invention are as follows:
a. the optimization of the consumption of the octane - booster additives in the composition resulting to a reduction of 5 -25% of the consumption, for the same feats comparing with the individually used components. b. It decreases with 7 -22% the cost of the gasoline additives c. according to the invention, the concentration of the manganese in the gasoline is between 4 and 9 mg/L, thus eliminating the negative effects of the metals presence.
Further, 5 examples are shown.
Example 1 : Into the gasoline having the composition of table 2 with MMT is then added, at different concentrations, N-methyl aniline and finally mixtures of N-methyl aniline and MMT, followed by the measuring of the octane number according to the Standards SR EN ISO 5164:06; SR EN ISO 5183:06. The results of the individually adding of N-methyl aniline and MMT are shown in the tables 3 and 4 (ΔRON; ΔMON shows the increase of the octane number after adding the additives).
Table 3.
N-methyl aniline % wt 0,0 0,5 1,0 1,5 2,0 2,5
RON 91 ,6 92,5 93,5 94,4 95,2 95,8
ΔRON 0 0,9 1 ,9 2,8 3,6 4,2
Table 4.
Mn mg/kg 0 3 6 9 12 15 21
RON 91 ,6 91 ,9 92,1 92,4 92,5 92,6 93,0
ΔRON 0 0,3 0,5 0,8 0,9 1 1 ,4
Further, into the gasoline having the composition of table 2 are added different admixtures of N-methyl aniline (NMA) and MMT, than measuring the octane numbers according to the standards SR EN ISO 5164:06; SR EN ISO 5183:06 and the results are shown in table 5.
Table 5.
Mn mg/kg 3 6 9 12 15 18 21 24 30 42 N-methyl aniline 1% wt
RON 93,5 93,9 94,5 94,9 95 94,8 95,1
ΔRON 1 ,9 2,3 2,9 3,3 3,4 3,2 3,5
Σ(ΔRONMn + ΔRONNMA)* 1 ,9 2,2 2,4 2,7 2,8 2,9 3,3
ΔSRON 0,0 0,1 0,5 0,6 0,6 0,3 0,2
Mn/NMA mg/g 0 0,30 0,60 0,90 0,12 0,15 0,21
N-methyl aniline 2% Wt.
RON 95,2 95,5 96 96,5 97 96,8 97 97,1
ΔRON 3,6 3,9 4,4 4,9 5,4 5,2 5,4 5,5
Σ(ΔRONMn + ΔRONNMA)* 3,6 4,1 4,4 4,5 5 5,1 5,3 5,7
ΔSRON 0,0 -0,2 0 0,4 0,4 0,1 0,1 -0,2
Mn/NMA mg/g 0 0,30 0,45 0,60 0,90 0,12 0.15 0,21
The contribution of the individual effects
V
The data interpretation renders obvious the existence of the synergistic interactions. The range of synergism is maximum in the ratios range Mn/NMA 0,6 - 1 mg/kg N-methyl aniline. This range is suggestively shown in figure 1 , where the percentage increase of the synergistic additive efficiency %ΔE is shown comparing with the individual contribution of NMA and MMT, depending on the ratio Mn/ NMA expressed as mg/kg:
ΔE% =ΔSRON / ∑(ΔRONMn + ΔRONNMA)x100
The synergistic effect decreases while increasing the concentration of N-methyl aniline. When the concentration of N-methyl aniline is 1% wt., the synergism area is comprised between >0 and >2,2 mg Mn/g N-methyl aniline, while for a concentration of 2% wt. N-methyl aniline, the synergism area is diminished to the range 0,4 - 1 ,8 mg Mn/g N-methyl aniline, and its intensity is reduced to a half. For uses, the preferred range of the synergistic additives compositions is 0,5 - 1 ,0 mg Mn/g N-methyl aniline, range in which the synergistic effect intensity is maximum.
Figure 1
0 0.2 0,4 0,6 0.8 1 1 ,2 1 ,4 1 ,6 1.8 2 2,2 Mii/N-metlιyl aniline ing/g
Example 2: 97g of N-methyl aniline was admixed to homogenization with 3g of N,N- dimethyl aniline, resulting 100g solution containing 97% wt. N-methyl aniline (NMA) and 3% wt. N,N-dimethyl aniline (NNDMA). 0,52 g MMT was admixed with 9,48g solution 97% wt. aniline and 3% wt. N,N-dimethyl aniline previously prepared, resulting a 13,16 mg/g Mn solution. 2,5 g of solution containing 13,16 mg/g Mn was admixed with 47,5g of
a 97% wt NMA and 3% m/m NNDMA solution resulting a synergistic multi-component octane-booster additive composition containing 0,65 mg Mn/kg, further named additive A. In a next step, to the gasoline whose composition is shown in table 2, the solution containing NMA - NNDMA and the additive A at different concentrations were added, measuring the octane numbers according to the Standards mentioned in example 1. The comparative results are shown in table 6.
Table 6. Comparation between the efficiency as octane- booster additive of the 97% NMA - 3% NNDMA solution solutiei and the additive A
Concentration % wt. 97% NMA - 3% NNDMA Solution
0 0,5 1 1 ,5 2
ΔRON 0 1 ,2 2,3 3,3 3,9
ΔMON 0 0,8 1 ,6 2,0 2,4
Additive A (97% NMA - 3% N1NDMA + 0,65mg Mn/kg
Solution)
ΔRON 0 1 ,9 3,3 4,7 5,3
ΔMON 0 1 ,3 2,3 3,1 3,3
The interpretation of the data of table 6 and their graphical representation in figure 2. obviously show the synergism phenomena.
Figure 2
0 0,2 0,4 0,6 0,8 1 1 ,2 1 ,4 1 ,6 1 ,8 2 2,2 additive A % wt.
Example 3: Following the procedure of example 2 the admixtures I - IX having octane - booster properties and representing the comparison standard and the multi-component synergistic additives I-Mn - IX-Mn having the content of Mn within the synergism range of 0,6 - 1 mgMn/g were prepared. For the additives VII-Mn si IX-Mn, the Mn concentrations were calculated so they be within the range 0,6 - 1 mg Mn/g N-methyl aniline. All these compositions are shown in table 7. The additives prepared in this way were dosed up into the basic gasoline having the composition of table 2 and the octane numbers were measured according to the Standards mentioned in example 1 ; the test results are shown in table 8.
Table 7
( anhydrous denaturated ethanol with 4,2% isopropanol
(2) 8,3 mg Mn/ g N- methyl aniline
(3) 7,5 mg Mn/ g N- methyl aniline
Table 8
Example 4: 1kg of multi-component synergistic additive was prepared by admixing and homogenizing 929g N-methyl aniline; 29,7g N,N-dimethyl aniline; 29,7g anisole; 3,6 g MMT; 4g N,N-disalicylidene-1 ,2-diaminopropane [CAS 94-91-7]; 4g 2,6-di-tert-butyl-p- cresol [CAS 128-37-0]. The resulted amount of multi-component synergistic additive was admixed and homogenized with 99kg gasoline having the composition of table 2, resulting 100 kg of gasoline RON 95, whose octane numbers were measured according to the Standards mentioned in example 1 ; the results are shown in table 9.
Table 9.
Characteristic Unit Value Standard for analysis density 15C kg/m3 734,2 SR EN ISO 3675:03
RON 95,2 SR EN ISO 5164:06
MON 83,7 SR EN ISO 5183:06 final boiling point C 202,0 SR EN ISO 3405:03 distillation residue % v/v 1 ,10 SR EN ISO 3405:03 gums mg/10OmL 2,5 SR EN ISO 6246:00 manganese mg/L 6,5 SR EN 14517:05
Example 5: 6,5kg of multi-component synergistic additive were prepared by admixing and homogenizing 1891g N-methyl aniline; 58,5g N,N-dimethyl aniline; 450Og anhydrous denaturated ethanol; 3,8 g MMT; 4g N,N-disalicylidene-1 ,2-diaminopropane 4g 2,6-di-tert- butyl-p-cresol. The resulted amount of multi-component synergistic additive was admixed and homogenized with 99kg gasoline having the composition of table 2, resulting 100 kg
of gasoline RON 95, whose octane numbers were measured according to the Standards mentioned in example 1 ; the results are shown in table 10.
Tabluel 10.
Characteristic Unit Value Standard for analysis density 150C kg/m3 739,1 SR EN ISO 3675:03
RON 98,1 SR EN ISO 5164:06
MON 86,7 SR EN ISO 5183:06 final boiling point C 201 ,0 SR EN ISO 3405:03 distillation residue % v/v 1 ,3 SR EN ISO 3405:03 gums mg/100ml_ 2,8 SR EN ISO 6246:00 manganese mg/L 6,7 SR EN 14517:05
Content of oxygen % m/m 1 ,6 SR EN 13132:01 ethanol % v/v 3,2 SR EN 13132:01 isopropanol % v/v 0,1 SR EN 13132:01
References:
1 EP0235280
2 EP0466511
3 EP0476197
4 FR1255840
5 FR2050841
6 GB252019
7 GB334181
8 GB530597
9 RU2005138060
10 RU2110561
11 RU2117691
12 RU2129141
13 RU2152981
14 RU2184767
15 RU2203927
16 RU2235117
17 US2819953
18 US3770397
19 US3794473
20 US4036605
21 US4139349
22 US4280458
23 US4690687
24 US5118325
25 US5470358
26 WO0116257
27 WO2005087901
28 WO2006076020
29 WO2007105982
30 WO2007117176
31 WO2008076759
Mohammad Ashraf SIi, Halim Hamid, Mohammad Ashraf AIi in "Handbook of MTBE and Other Gasoline Oxygenates" Printed in USA, Marcel Dekker
32 Inc, New York.Basel;1979
Claims
1. A process for obtaining synergistic octane - booster additives containing manganese and gasoline comprising thereof, characterized in that the synergistic octane - booster additives are obtained from aromatic amines, preferably N-methyl aniline and organometallic compounds comprising manganese, preferably methylcyclopentadienyl manganese (II) tricarbonyl, dozed so that the weight ratio between Mn and amine or aromatic amines is in the range >0 - 2,6 mg Mn/g aromatic amines, preferably 0,5 - 1 ,0 mg Mn/g aromatic amines.
2. The process according to claim 1 , characterized in that the synergistic octane - booster additives can be formulated also by admixing oxygenated organometallic compounds, such as ethers from alcohols, ethers from phenols or alcohols.
3. The process according claim to 1 , characterized in that, for obtaining gasoline by adding synergistic octane - booster additives, also organometallic compounds belonging to the metal deactivator class, such as N,N-disalicylidene-1 ,2-diaminopropane and antioxidants belonging to the class of sterically hindered phenols, such as 2,6-di-tert- butyl-p-cresol, can be added, either included in the additive compositions or separately added.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ROA200800919 | 2008-11-21 | ||
RO200800919 | 2008-11-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2010077161A2 true WO2010077161A2 (en) | 2010-07-08 |
WO2010077161A3 WO2010077161A3 (en) | 2010-09-23 |
Family
ID=42310440
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/RO2009/000015 WO2010077161A2 (en) | 2008-11-21 | 2009-11-20 | Synergistic octane booster additives containing aromatics amines and manganese and gasoline resulted from their usage |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2010077161A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012023872A3 (en) * | 2010-02-10 | 2012-04-12 | Marine Resources Exploration International B.V. | Synergistic compositions of anti-explosive additives for gasolines |
WO2014160802A1 (en) * | 2013-03-27 | 2014-10-02 | Motor Sports Fuel And Equipment | Fuel additive and fuel composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE590314A (en) * | 1960-05-02 | |||
RU2009176C1 (en) * | 1992-09-18 | 1994-03-15 | Акционерное общество "Сигма-Гикон" | Multifunctional additive for liquid fuels |
CN1218096A (en) * | 1997-11-26 | 1999-06-02 | 孙乐之 | Multifunctional additive for liquid fuel |
RU2161639C1 (en) * | 2000-07-17 | 2001-01-10 | Закрытое акционерное общество Научно-производственное объединение "Химсинтез" | Gasoline additive and composition containing thereof |
RU2260034C1 (en) * | 2004-05-05 | 2005-09-10 | Открытое акционерное общество "Пигмент" | Motor gasoline additive |
RU2276683C1 (en) * | 2005-01-25 | 2006-05-20 | Общество с ограниченной ответственностью "РЕССЕЛЛ ГРУП" | Additive to motor gasoline |
US8715373B2 (en) * | 2007-07-10 | 2014-05-06 | Afton Chemical Corporation | Fuel composition comprising a nitrogen-containing compound |
-
2009
- 2009-11-20 WO PCT/RO2009/000015 patent/WO2010077161A2/en active Application Filing
Non-Patent Citations (1)
Title |
---|
None |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012023872A3 (en) * | 2010-02-10 | 2012-04-12 | Marine Resources Exploration International B.V. | Synergistic compositions of anti-explosive additives for gasolines |
WO2014160802A1 (en) * | 2013-03-27 | 2014-10-02 | Motor Sports Fuel And Equipment | Fuel additive and fuel composition |
US9644162B2 (en) | 2013-03-27 | 2017-05-09 | Motor Sports Fuel And Equipment | Fuel additive and fuel composition |
Also Published As
Publication number | Publication date |
---|---|
WO2010077161A3 (en) | 2010-09-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6761745B2 (en) | Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines | |
US6767372B2 (en) | Aviation gasoline containing reduced amounts of tetraethyl lead | |
AU782062B2 (en) | Method of reducing the vapour pressure of ethanol-containing motor fuels for spark ignition combustion engines | |
AU2014206195B2 (en) | High octane unleaded aviation gasoline | |
GB2515202A (en) | High octane unleaded aviation gasoline | |
US20050229479A1 (en) | Fuel compositions and methods thereof | |
CN106687566A (en) | Aviation fuel with a renewable oxygenate | |
CN104711049A (en) | Nonmetallic gasoline antiknock | |
CN112004917A (en) | High power and economical friendly fuel composition | |
US20010034966A1 (en) | Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines | |
RU2263135C2 (en) | Multifunctional additive for the motor fuel | |
EP0667387B1 (en) | Reducing exhaust emissions from Otto-cycle engines | |
WO2014168513A1 (en) | Multifunctional additive for hydrocarbonaceous fuel and a fuel composition containing same | |
WO2010077161A2 (en) | Synergistic octane booster additives containing aromatics amines and manganese and gasoline resulted from their usage | |
RU2246527C1 (en) | Multifunctional motor fuel antiknock additive | |
WO2001038464A1 (en) | Fuel additive, additive-containing fuel compositions and method of manufacture | |
US8147566B2 (en) | Fuel additive, additive-containing fuel compositions and method of manufacture | |
SA519402550B1 (en) | Alcohol and ether fuel additives for unleaded gasoline | |
US3976437A (en) | Composition comprising a methyl phenol and an ether for gasoline fuels | |
WO2012023872A2 (en) | Synergistic compositions of anti-explosive additives for gasolines | |
WO1989005339A1 (en) | Octane improving gasoline additives | |
CN107849469B (en) | Gasoline composition with improved octane number | |
RU2061736C1 (en) | Hydrocarbon composition for engines of internal combustion having spark ignition | |
CN109852445A (en) | An environmentally friendly vehicle gasoline component that replaces MTBE | |
CA2785026A1 (en) | Liquid fuel compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09821413 Country of ref document: EP Kind code of ref document: A2 |
|
DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 09821413 Country of ref document: EP Kind code of ref document: A2 |