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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 PDF

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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
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gasoline
octane
manganese
additives
synergistic
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PCT/RO2009/000015
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French (fr)
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WO2010077161A3 (en
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Constantin-Marius Vladulescu
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Marine Resources Exploration International B.V.
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/10Use of additives to fuels or fires for particular purposes for improving the octane number
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/183Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom
    • C10L1/1832Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom mono-hydroxy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1852Ethers; Acetals; Ketals; Orthoesters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/223Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino group bound to an aromatic carbon atom
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/228Organic 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
    • C10L1/2283Organic 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/30Organic compounds compounds not mentioned before (complexes)
    • C10L1/305Organic 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.

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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:
Figure imgf000004_0001
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
Figure imgf000010_0001
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
Figure imgf000011_0001
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
Figure imgf000012_0001
( 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
Figure imgf000013_0001
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.
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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

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