BRPI0617637A2 - Two-stroke gasoline engine oil, method for reducing the observable smoke emitted from a two-stroke gasoline engine, and use of a lubricant - Google Patents

Two-stroke gasoline engine oil, method for reducing the observable smoke emitted from a two-stroke gasoline engine, and use of a lubricant Download PDF

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BRPI0617637A2
BRPI0617637A2 BRPI0617637-2A BRPI0617637A BRPI0617637A2 BR PI0617637 A2 BRPI0617637 A2 BR PI0617637A2 BR PI0617637 A BRPI0617637 A BR PI0617637A BR PI0617637 A2 BRPI0617637 A2 BR PI0617637A2
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oil
base oil
lubricant
gtl base
cst
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BRPI0617637-2A
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Portuguese (pt)
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Jacob J Habeeb
Paul J Berlowitz
Richard A Mcevoy
Daniel F Ryan
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Exxonmobil Res & Eng Co
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Publication of BRPI0617637A2 publication Critical patent/BRPI0617637A2/en

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/10Lubricating oil
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
    • C10M2205/163Paraffin waxes; Petrolatum, e.g. slack wax used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/17Fisher Tropsch reaction products
    • C10M2205/173Fisher Tropsch reaction products used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/02Viscosity; Viscosity index
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/50Emission or smoke controlling properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/25Internal-combustion engines
    • C10N2040/255Gasoline engines
    • C10N2040/26Two-strokes or two-cycle engines

Abstract

<B>óLEO DE MOTOR A GASOLINA DE DOIS TEMPOS, MéTODO PARA REDUZIR A FUMAçA OBSERVáVEL EMITIDA DE UM MOTOR A GASOLINA DE DOIS TEMPOS, E, USO DE UM LUBRIFICANTE<D>O índice de fumaça de um motor de dois tempos é melhorado pela utilização com o lubrificante de motor de um óleo de motor de dois tempos que compreende uma quantidade maior de um óleo de base GTL.<B> TWO-STROKE GASOLINE ENGINE OIL, METHOD TO REDUCE THE OBSERVABLE SMOKE EMITTED FROM A TWO-STROKE GASOLINE ENGINE, AND USE OF A LUBRICANT <D> The smoke index of a two-stroke engine is improved by use with the engine lubricant of a two-stroke engine oil that comprises a larger quantity of a GTL base oil.

Description

"ÓLEO DE MOTOR A GASOLINA DE DOIS TEMPOS, MÉTODO PARAREDUZIR A FUMAÇA OBSERVÁVEL EMITIDA DE UM MOTOR AGASOLINA DE DOIS TEMPOS, E, USO DE UM LUBRIFICANTE"Campo da Invenção"TWO-TIME GAS ENGINE OIL, METHOD TO STOP OBSERVABLE SMOKE ISSUED FROM A TWO-TIME AGASOLINE ENGINE, AND USE OF A LUBRICANT" Field of the Invention

Esta invenção refere-se a uma composição lubrificante útilcomo um óleo lubrificante de motor de dois tempos. Mais particularmente,esta invenção refere-se a um óleo lubrificante de dois tempos caracterizadopor suas características de geração de fumaça baixa.This invention relates to a lubricating composition useful as a two stroke engine lubricating oil. More particularly, this invention relates to a two-stroke lubricating oil characterized by its low smoke generation characteristics.

Fundamentos da InvençãoBackground of the Invention

Motores a gasolina de dois tempos têm encontrado uso amploem uma grande variedade de equipamento de jardim e de recreação. Porexemplo, motores de dois tempos são usados em cortadores de grama, cerrasde corrente, cortadores de corda, motocicletas, veículos motorizados paraneve e motores externos marinhos para mencionar uns poucos.Two-stroke petrol engines have found wide use in a wide variety of garden and recreational equipment. For example, two-stroke engines are used in lawnmowers, chain saws, rope cutters, motorcycles, paranight motor vehicles and outboard marine engines to name a few.

Motores a gasolina de dois tempos são operados usando umamistura de gasolina e um lubrificante em proporções determinadas.Two-stroke gasoline engines are operated using a gasoline mixture and a lubricant in specified proportions.

Lubrificantes de motor de dois tempos são tipicamenteformulados com um óleo mineral lubrificante ou óleo de base sintético, umavariedade de aditivos para melhorar as características de desempenho e umsolvente para melhorar a miscibilidade do lubrificante com gasolina.Two-stroke engine lubricants are typically formulated with a lubricating mineral oil or synthetic base oil, a variety of additives to improve performance characteristics, and a solvent to improve gasoline miscibility.

Emissões de hidrocarboneto dos motores de dois tempos,em virtude de seu projeto básico, tendem a ultrapassar emissões demotor de quatro ciclos comparáveis. Além disso, os avançostecnológicos para reduzir emissões dos motores de quatro ciclos não têmsido bem sucessivamente adaptados nos motores de dois tempos. Comoconseqüência, há uma preocupação crescente sobre as emissões, talcomo fumaça visível, produzidas pelos motores a gasolina de doistempos.Hydrocarbon emissions from two-stroke engines, by virtue of their basic design, tend to exceed comparable four-cycle engine emissions. In addition, advances in technology to reduce emissions from four-cycle engines have not been successively adapted to two-stroke engines. As a result, there is growing concern about the emissions, such as visible smoke, produced by two-time gasoline engines.

Poucos aditivos redutores de fumaça estão comercialmentedisponíveis para formuladores de lubrificantes de dois tempos. Alguns, comoaqueles que contêm metais, são ambientalmente indesejáveis; e outros, comopoliisobutilenos, contribuem para depósitos e obstrução em porta de exaustãoo que resulta em desgaste por atrito e perda de potência. Matérias-primas basesintéticas conhecidamente reduzem fumaça em motores de dois tempos, massão ineficazes em termos de custo.Few smoke reducing additives are commercially available for two-stroke lubricant formulators. Some, such as those containing metals, are environmentally undesirable; and others, such as polyisobutylenes, contribute to deposits and exhaust port obstruction resulting in frictional wear and power loss. Synthetic base materials are known to reduce smoke in cost-effective two-stroke engines.

Assim há uma necessidade de uma composição de lubrificantede motor a gasolina de dois tempos que atenda aos critérios de desempenhopadrão, seja efetivo em termos de custo e possua boas características deemissão de fumaça.Sumário da InvençãoThus there is a need for a two-stroke gasoline engine lubricant composition that meets the standard performance criteria, is cost effective and has good smoke emission characteristics.

Basicamente, a presente invenção é predicada sobre adescoberta de que um óleo de motor de dois tempos que compreende umaquantidade de óleo de base GTL possui um índice de fumaça maior do quecerca de 75.Basically, the present invention is predicated upon the discovery that a two-stroke engine oil comprising a GTL base oil amount has a smoke index greater than about 75.

Conseqüentemente, uma modalidade da invenção é umacomposição de óleo de motor de dois tempos compreendendo uma quantidademaior de um óleo de base lubrificante GTL e uma quantidade efetiva de pelomenos um aditivo selecionado do grupo consistindo de aditivos de pressãoextrema, agentes antiespumantes, depressores de ponto de fluidez, inibidoresde ferrugem, antioxidantes, detergentes, dispersantes e solventes dehidrocarboneto.Accordingly, one embodiment of the invention is a two-stroke motor oil composition comprising a larger amount of a GTL lubricating base oil and an effective amount of at least one additive selected from the group consisting of extreme pressure additives, defoaming agents, pour point depressants. , rust inhibitors, antioxidants, detergents, dispersants and hydrocarbon solvents.

Outra modalidade da invenção é um método para reduzir afumaça observável emitida de um motor a gasolina de dois tempos pelo usode um lubrificante compreendendo um óleo de base GTL.Another embodiment of the invention is a method for reducing observable fumes emitted from a two-stroke gasoline engine by the use of a lubricant comprising a GTL base oil.

Estas e outras modalidades tornar-se-ão evidentes a partir dadescrição detalhada que segue.Descrição Detalhada da InvençãoThese and other embodiments will become apparent from the following detailed description. Detailed Description of the Invention

Os óleos base GTL de acordo com a invenção são materiais deviscosidade lubrificante que são geralmente derivados de hidrocarbonetos, porexemplo, hidrocarbonetos sintéticos cerosos, que são eles mesmos derivadosde compostos contendo carbono gasosos mais simples, compostos contendohidrogênio, e/ou elementos como alimentações. Óleos base e matérias-primasbase GTL incluem isomeratos de cera, compreendendo, por exemplo,hidrocarbonetos cerosos sintetizados hidroisomerizados ou iso-removidos decera, material de Fischer-Tropsch (F-T) hidroisomerizado ou iso-removidosde cera (i.e., hidrocarbonetos, hidrocarbonetos cerosos, ceras e oxigenadosanálogos), preferivelmente hidrocarbonetos cerosos F-T hidroisomerizados ouiso-removidos de cera, ou ceras sintetizadas hidroisomerizadas ou iso-removidos de cera, ou misturas dos mesmos.GTL base oils according to the invention are lubricating viscosity materials which are generally derived from hydrocarbons, for example waxy synthetic hydrocarbons, which are themselves derived from simpler gaseous carbon-containing compounds, hydrogen-containing compounds, and / or feedstocks. GTL base oils and base materials include wax isomerates, comprising, for example, hydroisomerized or iso-removed synthesized waxy hydrocarbons, hydroisomerized or iso-removed Fischer-Tropsch (FT) material (ie, hydrocarbons, waxy hydrocarbons, waxes and oxygenated analogs), preferably hydroisomerized or iso-removable wax WT hydrocarbons, or hydroisomerized or iso-removed synthesized wax waxes, or mixtures thereof.

Oleos base e matérias-primas base GTL derivados de materiaisGTL, especialmente óleos base e matérias-primas base derivados de materialF-T hidroisomerizado/ iso-removidos de cera são caracterizados tipicamentecomo possuindo viscosidades cinéticas a 100°C de cerca de 2 cSt a cerca de50 cSt, preferivelmente de cerca de 3 cSt a cerca de 30 cSt, maispreferivelmente de cerca de 3,5 cSt a cerca de 25 cSt, como exemplificadopor um matéria-prima base GTL derivado por iso-remoção de cera F-T, quepossui uma viscosidade cinemática de cerca de 4 cSt a 100°C e um índice deviscosidade de cerca de 130 ou maior. Referência aqui à viscosidadecinemática refere-se a uma medição feita pelo método ASTM D445.GTL base oils and base materials derived from GTL materials, especially base oils and base materials derived from hydroisomerized / iso-removed F-T material are typically characterized as having kinetic viscosities at 100 ° C of about 2 cSt to about 50 ° C. cSt, preferably from about 3 cSt to about 30 cSt, more preferably from about 3.5 cSt to about 25 cSt, as exemplified by an FT wax iso-removal based GTL base material, which has a kinematic viscosity of about 4 cSt at 100 ° C and a viscosity index of about 130 or greater. Reference herein to kinematic viscosity refers to a measurement made by the ASTM D445 method.

Oleos base e matérias-primas base GTL derivados de materiaisGTL, especialmente óleos base e matérias-primas base derivados de materialF-T hidroisomerizado/iso-removido de cera são adicionalmente caracterizadoscomo possuindo pontos de fluidez de cerca de -5°C ou menor,preferivelmente de cerca de -10°C ou menor, mais preferivelmente de cercade -15°C ou menor, ainda mais preferivelmente de cerca de -20°C ou menor,e sob algumas condições podem possuir pontos de fluidez vantajosos de cercade -25°C ou menor, com pontos de fluidez úteis de cerca de -3O°C a cerca de -40°C ou menor. Referências aqui ao ponto de fluidez referem-se à mediçãofeita por ASTM D97 e pelas versões automatizadas similares.Base oils and base materials GTL derived from GTL materials, especially base oils and base materials derived from hydroisomerized / iso-removed F-T material are further characterized as having pour points of about -5 ° C or less, preferably about -10 ° C or below, more preferably about -15 ° C or below, even more preferably about -20 ° C or below, and under some conditions may have advantageous pour points around -25 ° C. or less, with useful pour points of from about -30 ° C to about -40 ° C or less. References herein to the pour point refer to the measurement made by ASTM D97 and similar automated versions.

Os óleos base e matérias-primas base GTL derivados demateriais F-T, especialmente óleos base e matérias-primas base derivados dematerial F-T hidroisomerizado/iso-removido de cera também sãocaracterizados como possuindo índices de viscosidade de 80 ou maior,preferivelmente 100 ou maior, e mais preferivelmente 120 ou maior.Adicionalmente, em certos casos particulares, o índice de viscosidade destasmatérias-primas base pode ser preferivelmente de 130 ou maior, maispreferivelmente de 135 ou maior, e ainda mais preferivelmente de 140 oumaior. Por exemplo, Óleos base e matérias-primas base GTL que derivadosde materiais GTL preferivelmente materiais F-T especialmente cera F-Tgeralmente possuem um índice de viscosidade de 130 ou maior. Referênciasaqui ao índice de viscosidade referem-se ao método ASTM D2270.GTL base oils and base materials derived from FT materials, especially base oils and base materials derived from hydroisomerized / iso-removed FT material are also characterized as having viscosity indices of 80 or greater, preferably 100 or greater, and more. preferably, in particular, the viscosity index of these base raw materials may preferably be 130 or greater, more preferably 135 or greater, and even more preferably 140 or greater. For example, Base oils and GTL base raw materials which are derived from GTL materials preferably F-T materials especially F-T wax generally have a viscosity index of 130 or greater. References herein to the viscosity index refer to the ASTM D2270 method.

Em adição, os óleos base e matérias-primas base sãotipicamente elevadamente parafínicos (>90% saturados), e podem contermisturas de monocicloparafinas e multicicloparafinas em combinação comisoparafinas não-cíclicas. A razão de conteúdo naftênico (i.e., cicloparafina)em tais combinações varia com o catalisador e a temperatura usados.Ademais, os óleos base e matérias-primas base GTL tipicamente possuemconteúdo de nitrogênio e de enxofre muito baixo, geralmente contendo menosdo que cerca de 10 ppm, e mais tipicamente menos do que cerca de 5 ppm decada um destes elementos. O conteúdo de nitrogênio e de enxofre de óleo debase e matéria-prima base GTL obtidos pela hidroisomerização/iso-remoçãode cera de material F-T, especialmente cera F-T é essencialmente zero.In addition, base oils and base raw materials are typically highly paraffinic (> 90% saturated), and may contain mixtures of monocycloparaffins and multicycloparaffins in combination with non-cyclic paraffins. The naphthenic content ratio (ie, cycloparaffin) in such combinations varies with the catalyst and temperature used. In addition, base oils and GTL base raw materials typically have very low nitrogen and sulfur content, usually containing less than about 10 ppm, and more typically less than about 5 ppm each of these elements. The nitrogen and sulfur content of base oil and GTL base raw material obtained by hydroisomerization / iso-removal of F-T material, especially F-T wax is essentially zero.

Composições úteis de óleos base e matérias-primas base GTL,óleos base e matérias-primas base derivados de material F-Thidroisomerizado ou iso-removido de cera, óleos base e matérias-primas basehidroisomerizados/iso-removidos de cera derivados de cera, tais comoisomeratos/iso-removidos de cera de cera, são citados em Patentes U.S.6.080.301 e 6.165.949 por exemplo.Useful compositions of base oils and base materials GTL, base oils and base materials derived from F-Hydroisomerized or iso-removed wax material, base oils and wax-based hydroisomerized / iso-removed raw materials such as such as isomerates / iso-removed from wax, are cited in U.S. Patent Nos. 6,080,301 and 6,165,949 for example.

Em uma modalidade preferida o material GTL é um materialderivado de processo de síntese de F-T. Em um processo de síntese de F-T5 um gás de síntese compreendendo uma mistura de H2 e CO é cataliticamenteconvertido em hidrocarbonetos e preferivelmente hidrocarbonetos líquidos. Arazão em moles de hidrocarboneto para monóxido de carbono pode variaramplamente de cerca de 0,5 a 4, mas está tipicamente dentro da faixa de cercade 0,7 a 2,75 e preferivelmente de cerca de 0,7 a 2,5. Como é bem sabido, os processos de síntese F-T incluem processos nos quais o catalisador está naforma de um leito fixo, um leito fluidizado ou como uma lama de partículasde catalisador em um líquido de lama de hidrocarboneto. A razão em molestequiométrica para uma reação de síntese de F-T é 2,0, mas por motivospara uso de uma razão diferente da estequiométrica como é sabido por aquelas pessoas experientes na arte. Em um processo de síntese de hidrocarboneto emlama de cobalto a razão em mol de alimentação de H2 para CO é tipicamentede cerca de 2,1/1. O gás de síntese compreendendo uma mistura de H2 e CO éborbulhado para dentro do fundo da lama e reage na presença do catalisadorparticulado de síntese de F-T no líquido de lama em condições efetivas para formar hidrocarbonetos, cuja uma porção é líquida nas condições de reação eque compreende o líquido de lama de hidrocarboneto. O líquido dehidrocarboneto sintetizado é separado das partículas de catalisador comofiltrado por meio tal como filtração, embora outro meio de separação tal comocentrifugação possa ser usado. Alguns dos hidrocarbonetos sintetizados sai no topo do reator de síntese de hidrocarboneto como vapor, juntamente com gásde síntese não reagido e outros produtos de reação gasosos. Alguns destesvapores de hidrocarboneto no topo são tipicamente condensados para líquidoe combinados com o filtrado líquido de hidrocarboneto. Assim, o ponto deebulição inicial do filtrado pode variar dependendo de se ou não um poucodos vapores de hidrocarboneto condensados tem sido combinado com ele.Condições de processo de síntese de hidrocarboneto em lama podem variarum pouco dependendo do catalisador e dos produtos desejados. Condiçõestípicas efetivas para formar hidrocarbonetos compreendendo em sua maiorparte parafinas C5+, (e.g., C5+-C2oo) e preferivelmente parafinas Cio+, em umprocesso de síntese de hidrocarboneto em lama empregando um catalisadorcompreendendo um componente cobalto suportado incluem, por exemplo,temperaturas, pressões e velocidades espaciais horárias dentro da faixa decerca de 160-454°C, 551-4.137 kPa e 100-40.000 V/h/N, expressada comovolumes padrão de mistura gasosa de CO e H2 (0°C, 101,3 kPa) por hora porvolume de catalisador, respectivamente. É preferido que a reação de síntesede hidrocarboneto seja conduzida sob condições nas quais nenhuma reação dedeslocamento de gás de água ocorre ou ocorre reação de deslocamento de gásde água apenas limitada e mais preferivelmente sem ocorrência de reação dedeslocamento de gás de água durante a síntese de hidrocarboneto. Também épreferido conduzir a reação sob condições para alcançar um alfa de pelomenos 0,85, preferivelmente pelo menos 0,9 e mais preferivelmente pelomenos 0,92, de modo a sintetizar mais dos hidrocarbonetos de peso molecularmais alto mais desejáveis. Isto tem sido alcançado em um processo em lamausando um catalisador contendo um componente cobalto de catalisador.Aquelas pessoas experientes na arte sabem que pelo alfa quer-se dar osignificado de alfa cinético de Schultz-Flory. Embora tipos adequados decatalisador de reação de F-T compreendam, por exemplo, um ou mais metaiscatalíticos do Grupo VIII tais como Fe, Ni, Co, Ru e Re, é preferido que ocatalisador compreenda um componente catalítico de cobalto. Em umamodalidade o catalisador compreende quantidades cataliticamente efetivas deRe, Ru, Fe, Ni, Th, Zr, Hf, U, Mg e La sobre um material de suporteinorgânico, preferivelmente um que compreende um ou mais óxidos de metalrefratários. Suportes preferidos para catalisadores contendo cobaltocompreendem particularmente titânico. Catalisadores úteis e sua preparaçãosão conhecidos e ilustrativos, mas exemplos não limitantes podem serencontrados, por exemplo, em Patentes U.S. 4.568.663; 4.663.305; 4.542.122;4.621.072 e 5.545.674.In a preferred embodiment the GTL material is an F-T synthesis process derivative material. In an F-T5 synthesis process a synthesis gas comprising a mixture of H2 and CO is catalytically converted to hydrocarbons and preferably liquid hydrocarbons. The molar ratio of hydrocarbon to carbon monoxide may vary from about 0.5 to 4, but is typically within the range of about 0.7 to 2.75 and preferably about 0.7 to 2.5. As is well known, F-T synthesis processes include processes in which the catalyst is in the form of a fixed bed, a fluidized bed or as a catalyst particle slurry in a hydrocarbon slurry liquid. The molestequiometric ratio for an F-T synthesis reaction is 2.0, but for reasons of using a different stoichiometric ratio as is known to those skilled in the art. In a cobalt emlama hydrocarbon synthesis process the molar ratio of H2 to CO feed is typically about 2.1 / 1. The synthesis gas comprising a mixture of H2 and CO is bubbled into the bottom of the slurry and reacts in the presence of the particulate FT synthesis catalyst in the slurry liquid under conditions effective to form hydrocarbons, a portion of which is liquid under reaction conditions and comprising the hydrocarbon slurry liquid. The synthesized hydrocarbon liquid is separated from the filtrated catalyst particles by means such as filtration, although other separation means such as centrifugation may be used. Some of the synthesized hydrocarbons come out on top of the hydrocarbon synthesis reactor as steam, along with unreacted synthesis gas and other gaseous reaction products. Some of these top hydrocarbon vapors are typically liquid condensed and combined with the liquid hydrocarbon filtrate. Thus, the initial melting point of the filtrate may vary depending on whether or not a few condensed hydrocarbon vapors have been combined with it. Slurry hydrocarbon synthesis process conditions may vary slightly depending on the catalyst and desired products. Effective typical conditions for forming hydrocarbons comprising mostly C5 + paraffins (eg C5 + -C20) and preferably C10 + paraffins in a slurry hydrocarbon synthesis process employing a catalyst comprising a supported cobalt component include, for example, temperatures, pressures and spatial velocities 160-454 ° C, 551-4,137 kPa and 100-40,000 V / h / N, expressed as standard CO and H2 gas mixture volumes (0 ° C, 101.3 kPa) per hour per volume. catalyst, respectively. It is preferred that the hydrocarbon synthesis reaction is conducted under conditions in which no water gas displacement reaction occurs or only limited water gas displacement reaction occurs and more preferably no water gas displacement reaction occurs during hydrocarbon synthesis. It is also preferred to conduct the reaction under conditions to achieve an alpha of at least 0.85, preferably at least 0.9 and more preferably at least 0.92, in order to synthesize more of the most desirable higher molecular weight hydrocarbons. This has been achieved in a slurry process using a catalyst containing a cobalt catalyst component. Those skilled in the art know that by alpha is meant the Schultz-Flory kinetic alpha. While suitable F-T reaction catalyst types comprise, for example, one or more Group VIII catalytic metals such as Fe, Ni, Co, Ru and Re, it is preferred that the catalyst comprises a cobalt catalytic component. In one embodiment the catalyst comprises catalytically effective amounts of Re, Ru, Fe, Ni, Th, Zr, Hf, U, Mg and La on an inorganic support material, preferably one comprising one or more metallo-refractory oxides. Preferred supports for cobalt-containing catalysts comprise particularly titanic. Useful catalysts and their preparations are known and illustrative, but nonlimiting examples can be found, for example, in U.S. Patent 4,568,663; 4,663,305; 4,542,122; 4,621,072 and 5,545,674.

Preferivelmente, o material ceroso de F-T é um possuindo umponto de ebulição inicial dentro da faixa de cerca de 3430C a 3710C epreferivelmente ferve continuamente até um ponto final de pelo menos565,6°C.Preferably, the F-T waxy material is one having an initial boiling point within the range of about 3430 ° C to 3710 ° C and preferably boils continuously to an end point of at least 565.6 ° C.

O material ceroso é hidroprocessado para produzir um óleo debase GTL. Tais técnicas de hidroprocessamento são bem conhecidas na arte.Com relação a isto veja, por exemplo, outros catalisadores de isomerização eprocessos para hidrocraqueamento/hidroisomerização/iso-remoção de cera demateriais GTL e/ou de materiais cerosos em óleo de base ou matéria-primabase são descritos, por exemplo em Patentes U.S. 2.817.693; 4.900.407;4.937.399; 4.975.177; 4.921.594; 5.059.299; 5.200.382; 5.516.740;5.182.248; 5.290.426; 5.580.442; 5.976.351; 5.935.417; 5.885.438;5.965.475; 6.190.532; 6.375.830; 6.332.974; 6.103.099; 6.025.305;6.080.301; 6.096.940; 6.620.312; 6.676.827; 6.383.366; 6.475.960;5.059.299; 5.977.425; 5.935.416; 4.923.588; 5.158.671; e 4.897.178; EP0324528 (131), EP 0532116 (BI), EP 0532118 (BI), EP 0537815 (BI), EP0583836 (B2), EP 0666894 (132), EP 0668342 (131), EP 0776959 (A3), WO97/031693 (Al), WO 02/064710 (A2), WO 02/064711 (Al), WO 02/070627(A2), WO 02/070629 (Al), WO 03/033320 (Al) bem como em PatentesBritânicas 1.429.494; 1.350.257; 1.440.230; 1.390.359; WO 99/45085 e WO99/20720. Processos particularmente favoráveis são descritos em Pedidos dePatente Européia 464546 e 464547. Processos usando alimentações de cera F-T são descritos em Patentes U.S. 4.594.172; 4.943.672; 6.046.940; 6.475.960;6.103.099; 6.332.974; e 6.375.830.The waxy material is hydroprocessed to produce a GTL base oil. Such hydroprocessing techniques are well known in the art. In connection with this see, for example, other isomerization catalysts and processes for hydrocracking / hydroisomerization / iso-removal of GTL dematerials and / or waxy materials in base oil or base material. are disclosed, for example, in US Patents 2,817,693; 4,900,407; 4,937,399; 4,975,177; 4,921,594; 5,059,299; 5,200,382; 5,516,740; 5,182,248; 5,290,426; 5,580,442; 5,976,351; 5,935,417; 5,885,438; 5,965,475; 6,190,532; 6,375,830; 6,332,974; 6,103,099; 6,025,305; 6,080,301; 6,096,940; 6,620,312; 6,676,827; 6,383,366; 6,475,960; 5,059,299; 5,977,425; 5,935,416; 4,923,588; 5,158,671; and 4,897,178; EP 0324528 (131), EP 0532116 (BI), EP 0532118 (BI), EP 0537815 (BI), EP 0583836 (B2), EP 0666894 (132), EP 0668342 (131), EP 0776959 (A3), WO97 / 031693 ( Al), WO 02/064710 (A2), WO 02/064711 (Al), WO 02/070627 (A2), WO 02/070629 (Al), WO 03/033320 (Al) as well as in British Patents 1,429,494; 1,350,257; 1,440,230; 1,390,359; WO 99/45085 and WO99 / 20720. Particularly favorable processes are described in European Patent Applications 464546 and 464547. Processes using F-T wax feeds are described in U.S. Patent 4,594,172; 4,943,672; 6,046,940; 6,475,960; 6,103,099; 6,332,974; and 6,375,830.

O óleo de base GTL compreende uma quantidade maior dacomposição total da invenção. Tipicamente, compreenderá mais do que 55por cento em volume da composição e preferivelmente mais do que cerca de60 por cento em volume da composição.GTL base oil comprises a larger amount of the total composition of the invention. Typically, it will comprise more than 55 percent by volume of the composition and preferably more than about 60 percent by volume of the composition.

Em adição a compreender uma quantidade maior de um óleode base GTL, a composição de lubrificante inclui aditivos de desempenho dedois tempos conhecidos na arte e selecionados do grupo consistindo deaditivos de pressão extrema, agentes antiespumantes, depressores de ponto defluidez, inibidores de ferrugem, antioxidantes, detergentes, dispersantes esolventes de hidrocarboneto. Tais aditivos são usados em quantidadesefetivas, tipicamente dentro da faixa de 0,1 por cento em peso a cerca de 15,0por cento em peso baseado no peso total da composição.In addition to comprising a larger amount of a GTL base oil, the lubricant composition includes two-time performance additives known in the art and selected from the group consisting of extreme pressure deadeners, defoamers, pour point depressants, rust inhibitors, antioxidants, detergents, hydrocarbon solvent dispersants. Such additives are used in effective amounts, typically within the range of 0.1 weight percent to about 15.0 weight percent based on the total weight of the composition.

Quando misturada com em uma quantidade efetiva comgasolina e alimentada a um motor de dois tempos, a composição delubrificante resulta em emissões de motor possuindo fumaça observávelreduzida. De fato, uso das composições da invenção proporcionará emissõesde motor possuindo um índice de fumaça maior do que cerca de 75 conformemedido pelo teste JASO M 342-92. Este teste foi estabelecido pela Society ofAutomotive Engineers of Japan (JSAE) para motores de dois tempos epublicado pela Japan Automotive Standards Organization (JASO).When mixed with an effective amount of gasoline and fed to a two-stroke engine, the lubricant composition results in engine emissions having reduced observable smoke. In fact, use of the compositions of the invention will provide engine emissions having a smoke index greater than about 75 as measured by the JASO M 342-92 test. This test was established by the Society ofAutomotive Engineers of Japan (JSAE) for two-stroke engines and published by the Japan Automotive Standards Organization (JASO).

Os exemplos que seguem servem para ilustrar a invenção.The following examples serve to illustrate the invention.

ExemplosExamples

Dois óleos foram avaliados para propriedades de geração defumaça de acordo com o teste JASO M 342-92. Neste teste o resultado éexpressado como um índice de Fumaça e é referido contra um óleo de doistempos padrão com um índice de fumaça de 100. Quanto maior o índice defumaça, maior é a redução nas emissões de fumaça. O óleo de base GTLusado tinha um VI de 142, uma KV @ 40°C de 23,99 e @ 100°C de 5,05 eum ponto de fluidez de -24°C.Two oils were evaluated for smoke generation properties according to the JASO M 342-92 test. In this test the result is expressed as a Smoke index and is referred to against a standard two-stroke oil with a smoke index of 100. The higher the smoke index, the greater the reduction in smoke emissions. The GTLused base oil had an IV of 142, a KV @ 40 ° C of 23.99 and> 100 ° C 5.05 and a pour point of -24 ° C.

A composição dos óleos de teste é dada na Tabela 1 abaixo.TABELA 1The composition of the test oils is given in Table 1 below. TABLE 1

<table>table see original document page 10</column></row><table><table> table see original document page 10 </column> </row> <table>

As viscosidades cinemáticas das composições são dadas naThe kinematic viscosities of the compositions are given in

TABELA 2.TABLE 2

<table>table see original document page 10</column></row><table><table> table see original document page 10 </column> </row> <table>

O índice de fumaça para a composição convencionalcomparativa verificado foi de 65, enquanto que aquele para a composição deExemplo verificado foi significativamente melhor a 78.The smoke index for the verified comparative conventional composition was 65, while that for the verified Example composition was significantly better at 78.

Claims (11)

1. Óleo de motor a gasolina de dois tempos, caracterizado pelofato de compreender:uma quantidade maior de óleo de base GTL; euma quantidade efetiva de pelo menos um aditivo selecionadodo grupo consistindo de aditivos de pressão extrema, agentes antiespumantes,depressores de ponto de fluidez, inibidores de ferrugem, antioxidantes,detergentes, dispersantes e solventes de hidrocarboneto.1. Two-stroke gasoline engine oil, characterized by the understanding: a larger amount of GTL base oil; an effective amount of at least one additive selected from the group consisting of extreme pressure additives, defoaming agents, pour point depressants, rust inhibitors, antioxidants, detergents, dispersants and hydrocarbon solvents. 2. Oleo de acordo com a reivindicação 1, caracterizado pelofato de que o óleo de base GTL possui uma viscosidade cinemática a IOO0Cde cerca de 2 cSt a cerca de 50 cSt e um VI maior do que 80.Oil according to Claim 1, characterized in that the GTL base oil has a kinematic viscosity at 100 ° C of about 2 cSt to about 50 cSt and a VI of greater than 80. 3. Óleo de acordo com a reivindicação 2, caracterizado pelofato de que óleo de base GTL é derivado de uma cera F-T.Oil according to claim 2, characterized in that the GTL base oil is derived from an F-T wax. 4. Oleo de acordo com a reivindicação 3, caracterizado pelofato de que o óleo de base GTL contém misturas de cicloparafinas.Oil according to Claim 3, characterized in that the GTL base oil contains mixtures of cycloparaffins. 5. Oleo de acordo com a reivindicação 3, caracterizado pelofato de que o citado óleo possui um índice de fumaça maior do que cerca de-75.Oil according to Claim 3, characterized in that the said oil has a smoke index of greater than about -75 ° C. 6. Método para reduzir a fumaça observável emitida de ummotor a gasolina de dois tempos, caracterizado pelo fato de compreender:proporcionar o motor sob condições de uso com uma gasolinae uma composição de lubrificante na qual a composição de lubrificantecompreende uma quantidade maior de um óleo de base lubrificante GTL.6. A method for reducing the observable smoke emitted from a two-stroke petrol engine, comprising: providing the engine under conditions of use with a petrol and a lubricant composition in which the lubricant composition comprises a larger amount of a GTL lubricant base. 7. Método de acordo com a reivindicação 6, caracterizado pelofato de que o óleo de base GTL possui uma viscosidade cinemática a IOO0Cdecerca de 2 cSt a cerca de 50 cSt e um VI maior do que cerca de 80.A method according to claim 6, characterized in that the GTL base oil has a kinematic viscosity at 100 ° C of about 2 cSt to about 50 cSt and a VI greater than about 80. 8. Método de acordo com a reivindicação 6, caracterizado pelofato de que o óleo de base GTL é derivado de uma cera F-T.Method according to claim 6, characterized in that the GTL base oil is derived from an F-T wax. 9. Motor de combustão interna de dois tempos compreendendoum lubrificante, caracterizado pelo fato de que compreende:uma quantidade maior de um óleo de base GTL; umaquantidade efetiva de pelo menos um aditivo selecionado do grupoconsistindo de aditivos de pressão extrema, agentes antiespumantes,depressores de ponto de fluidez, inibidores de ferrugem, antioxidantes,detergentes, dispersantes e solventes de hidrocarboneto; e na qual o índice defumaça resultante do lubrificante é maior do que cerca de 75.9. Two-stroke internal combustion engine comprises a lubricant, characterized in that it comprises: a larger quantity of a GTL base oil; an effective amount of at least one group-selected additive consisting of extreme pressure additives, defoaming agents, pour point depressants, rust inhibitors, antioxidants, detergents, dispersants and hydrocarbon solvents; and wherein the resulting smoke index of the lubricant is greater than about 75. 10. Motor de acordo com a reivindicação 9, caracterizado pelofato de que o óleo de base GTL possui uma viscosidade cinemática a 100°Cdecerca de 2 cSt a cerca de 50 cSt e um VI maior do que cerca de 80.Engine according to claim 9, characterized in that the GTL base oil has a kinematic viscosity at 100 ° C of about 2 cSt to about 50 cSt and a VI of greater than about 80. 11. Motor de acordo com a reivindicação 10, caracterizadopelo fato de que o óleo de base GTL é derivado de uma cera F-T.Engine according to claim 10, characterized in that the GTL base oil is derived from an F-T wax.
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