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A method for the production of carbon water substance oils soluble, basic alkaline earth metal complex compounds of the carbon - and / or oelloeslichen organic sulfonic acids

机译:一种生产碳-和/或欧亚烯属有机磺酸的可溶于水的碱性碱土金属络合物的碳水物质油的方法

摘要

A lubricating composition comprises a major proportion of a lubricating oil and a minor proportion of an oil-soluble composition which comprises a carbonated, basic alkaline earth metal salt of a bright stock sulphonic acid (see Division C2), the metal salt having a metal ratio of at least about 3. The concentration of the carbonated, basic metal salts in the lubricating compositions may range from about 0.1% to about 30% by weight. The mineral oils useful as the lubricating oil base are preferably refined oils having viscosity values ranging from about 50 S.U.S. at 100 DEG F. to about 500 S.U.S. at 210 DEG F. If the carbonated, basic metal salt is prepared in a limited amount of mineral oil, the concentrate obtained may be diluted with additional amounts of mineral oil to give the required lubricating composition. The concentrate may also contain other additives. Other additives which may be present are supplementary detergent additives, rust-inhibiting agents, corrosion-inhibiting agents, extreme pressure agents, anti-foam agents, pour-point depressing agents, viscosity index improving agents, metal-deactivating agents, and oxidation-inhibiting agents. Group II metal phosphorodithioates are desirable for use in the lubricating compositions, the dialkylphosphorodithioates of zinc, calcium and barium being preferred. The alkyl radicals usually contain an average of at least 7.6 aliphatic carbon atoms per phosphorus atom. Other inhibiting agents include the oil-soluble alkaline earth metal salts of alkylated phenolic compounds such as alkyl-phenols, alkylnaphthols, sulphurized alkyl-phenols and naphthols, and condensation products of the alkylated phenolic compounds with aldehydes or ketones. The alkyl radical in the phenolic compounds should contain at least 7 carbon atoms. Also the basic metal salts of the above alkylated phenolic compounds, prepared by heating a mixture of an alkylated phenolic compound with an excess of an alkaline earth metal base or by carbonating at a temperature of about 100-250 DEG C. may be used. Other inhibiting agents useful are sulphurized or phosphosulphurized hydrocarbons or fatty materials such as dibutyl tetrasulphide, dipentyl disulphide, the reaction products of alphapinene with sulphur or P2S5, of terpentine with S or P2S5, of methyl oleate with P4S6 and of sperm oil with S. Organic phosphites such as dialkyl (including cycloalkyl) phosphites and diaryl phosphites are also useful. Further detergent additives may be acylated alkylene amines. A preferred class of acylated amines are the reaction products of an ethylene amine such as ethylene diamine, diethylene triamine, tetraethylene pentamine, hexamethylene heptamine, or triethylene tetramine with a hydrocarbon substituted succinic acid or anhydride in which the hydrocarbon substituent contains at least 50 aliphatic carbon atoms. In the examples, the concentrate of the carbonated, basic calcium bright stock sulphonate is blended with (1) SAE20 mineral oil, (2) SAE30 mineral oil and zinc di-octylphosphorodithioate, (3) SAE90 mineral oil, zinc dicyclohexylphosphorodithioate and an acylated amine obtained by heating 1 mole of a polyisobutene (M.W. of 1000)-substituted succinic anhydride with 0.4 mole of tetraethylene pentamine at 150-220 DEG C. and removing the water formed thereby; (4) SAE30 mineral oil, calcium salt of 2,21-methylene - bis - (4 - heptylphenol), and polyisobutene (M.W. of 750)-substituted succinimide of N-aminoethyl piperazine; (5) SAE10 mineral oil and di-benzyl disulphide; (6) SAE30 mineral oil; and (7) SAE40 mineral oil, dibutyl tetrasulphide, an ashless detergent obtained by heating equi-molar amounts of polyisoprene (M.W. of 1500)-substituted succinic acid and ethylene diamine at 150-250 DEG C. and removing the water formed thereby.ALSO:The invention comprises an oil-soluble composition suitable for use as a detergent in lubricating oils comprising a carbonated, basic alkaline earth metal salt of a bright stock sulphonic acid, or of a mixture of at least 50% by weight of a bright stock sulphonic acid and not more than 50% of a carboxylic acid having at least 12 aliphatic carbon atoms, the metal salt having a metal ratio of at least 3. The term " metal ratio " is used to designate the ratio of the total equivalents of the metal in the metal salt to the equivalents of metal in the form of a normal salt. It may be obtained by carbonating a substantially anhydrous mixture of the acid reactant with at least about three equivalents of an alkaline earth metal base per equivalent of acid in the presence of a promoting agent. The metal base may be an alkaline earth metal oxide, hydroxide, bicarbonate, sulphide, mercaptide, hydride, alcoholate or phenate. The alkaline earth metal may be Mg, Ca, Sr, or Ba, but is preferably calcium. The carboxylic acids which may be used together with the bright stock sulphonic acids may be substituted, unsubstituted aliphatic, or aliphatically substituted aromatic acids having at least 12 aliphatic carbon atoms, such as palmitic acid, stearic acid, myristic acid, oleic acid, linoleic acid, behenic acid, hexatria-contanoic acid, stearyl benzoic acid, wax (eicosane) substituted naphthoic acid, dilauryl decahydronaphthalene carboxylic acid, dido-decyltetralin carboxylic acid, dioctyl-cyclohexane carboxylic acid, the acids obtained by hydrolysis of sperm oil, tall oil or other fatty esters, alkenyl succinic acids or anhydrides in which the alkenyl group contains at least 12 carbon atoms such as the product of the reaction of maleic acid or anhydride with a polyisobutene having a M.W. of about 700-1000. The promoting agent may be an alcohol including polyhydric alcohols and heterocyclic alcohols or a phenol. Alcohols having up to 12 carbon atoms, phenols and alkylated phenols having one to three alkyl substituents each of which has up to 50 carbon atoms and mixtures thereof are preferred. The amount of promoting agent to be used may be from 0.1 to 10 equivalents or more per equivalent of the acid reactant, preferably from about 0.25 to 5 equivalents. It is desirable to use the above hydroxy compounds in combination with from about 0.1% to 5% based on the weight of the carbonation mixture of an inorganic halide such as ammonium chloride or bromide, or an alkali metal or alkaline earth metal halide. The carbonation temperature depends on the promoting agent, when a phenol is used the temperature may be from 80 DEG to 300 DEG C. preferably from 100 DEG to 200 DEG C., and when an alcohol is used a temperature from 20 DEG to 100 DEG C. is generally suitable. The promoting agent may be removed by distillation, after carbonation, if it is a volatile substance otherwise it is allowed to remain in the product. Generally, it is convenient to prepare the carbonated, basic metal salt in a mineral oil so that the product is a fluid oil solution or concentrate which readily mixes with additional quantities of mineral oil to give the required lubricating composition. The carbonation may be carried out in a solvent such as mineral oil, hexane, naphtha, dodecane, benzene, toluene, xylene. It may also be a polar substituted hydrocarbon such as chlorobenzene, diphenyl oxide or nitrobenzene. Examples are given for the carbonation of calcium bright stock sulphonate (1) in toluene as solvent in the presence of methanol, isooctanol and ammonium chloride as promoter (2) as in (1) except that ammonium chloride is replaced by calcium chloride (3) as in (2) except that the calcium hydroxide is added in stages to the bright stock sulphonic acid, (4) as in (3) except that lime is added in 4 portions followed by carbonation (5) in admixture with distilled tall oil acid, in mineral oil as solvent, in the presence of methanol, octanol and calcium chloride as promoter, the alkaline earth metal base being calcium hydroxide (6) as in (5) except that toluene is present in addition as solvent (7) as in (6) except that naphthenic acid is used in place of distilled tall oil acid and (8) as in (1) except that ammonium chloride is absent. The products may be used as additives for lubricating oils (see Division C5).
机译:润滑组合物包含主要比例的润滑油和次要比例的油溶性组合物,所述油溶性组合物包含光亮的磺酸的碳酸碱金属碱土金属盐(参见C2部分),该金属盐具有金属比润滑组合物中碳酸碱性金属盐的浓度可为约0.1重量%至约30重量%。用作润滑油基础油的矿物油优选是粘度值在约50S.U.S.范围内的精制油。在100°F至约500 S.U.S.如果在有限量的矿物油中制备碳酸的碱性金属盐,则可在210°F下将所得的浓缩物用附加量的矿物油稀释以得到所需的润滑组合物。浓缩物还可包含其他添加剂。可能存在的其他添加剂是补充洗涤剂添加剂,防锈剂,缓蚀剂,极压剂,消泡剂,降凝剂,粘度指数改进剂,金属灭活剂和氧化抑制剂代理商。 II族金属二硫代磷酸酯是理想的用于润滑组合物中,锌,钙和钡的二烷基二硫代磷酸酯是优选的。烷基通常每个磷原子平均包含至少7.6个脂肪族碳原子。其他抑制剂包括烷基化酚化合物如烷基酚,烷基萘酚,硫化烷基酚和萘酚的油溶性碱土金属盐,以及烷基化酚化合物与醛或酮的缩合产物。酚类化合物中的烷基应包含至少7个碳原子。也可以使用上述烷基化酚化合物的碱性金属盐,该碱金属盐是通过加热烷基化酚化合物与过量碱土金属碱的混合物或在约100-250℃的温度下碳化而制得的。其他有用的抑制剂是硫化的或磷硫化的碳氢化合物或脂肪物质,例如二丁基四硫化物,二戊基二硫化物,αpinenene与硫或P2S5的反应产物,松节油与S或P2S5的反应产物,油酸甲酯与P4S6的反应以及精油与S的反应。亚磷酸酯如亚磷酸二烷基酯(包括环烷基)和亚磷酸二芳基酯也是有用的。其他洗涤剂添加剂可以是酰化的亚烷基胺。一类优选的酰化胺是亚乙基胺如乙二胺,二亚乙基三胺,四亚乙基五胺,六亚甲基庚胺或三亚乙基四胺与烃取代的琥珀酸或酸酐的反应产物,其中烃取代基包含至少50个脂肪族碳。原子。在实施例中,将碳酸的碱性光亮磺酸钙磺酸盐的浓缩物与(1)SAE20矿物油,(2)SAE30矿物油和二辛基磷酸二硫代锌盐,(3)SAE90矿物油,二环己基磷酸二硫合锌和酰化胺混合。通过在150-220℃下加热1摩尔的聚异丁烯(MW为1000)-取代的琥珀酸酐与0.4摩尔的四亚乙基五胺加热并除去由此形成的水而获得; (4)SAE30矿物油,2,21-亚甲基-双-(4-庚基苯酚)的钙盐和N-氨基乙基哌嗪的聚异丁烯(M.W.为750)取代的琥珀酰亚胺; (5)SAE10矿物油和二苄基二硫化物; (6)SAE30矿物油; (7)SAE40矿物油,四硫化二丁酯,一种无灰的去污剂,其通过在150-250℃下加热等摩尔量的聚异戊二烯(MW为1500)取代的琥珀酸和乙二胺并除去由此形成的水而获得。 :本发明包括一种油溶性组合物,其适合用作润滑油中的去污剂,其包含光亮磺酸或至少50重量%光亮磺酸的混合物的碳酸化碱金属碱土金属盐酸和不超过具有至少12个脂肪族碳原子的羧酸的50%,金属盐的金属比至少为3。术语“金属比”用于表示金属的总当量之比在金属盐中的含量相当于正盐形式的金属的当量含量。它可以通过在促进剂的存在下,将酸反应物的基本上无水的混合物与每当量的酸至少约三当量的碱土金属碱碳化来获得。金属碱可以是碱土金属氧化物,氢氧化物,碳酸氢盐,硫化物,硫醇盐,氢化物,醇盐或酚盐。碱土金属可以是Mg,Ca,Sr或Ba,但优选为钙。可以与光亮磺酸一起使用的羧酸可以是取代的,未取代的脂肪族,或具有至少12个脂肪族碳原子的脂肪族取代的芳族酸,例如棕榈酸,硬脂酸,肉豆蔻酸,油酸,亚油酸,山acid酸,六三-十六烷酸,硬脂基苯甲酸,蜡(二十烷)取代的萘甲酸,二月桂基十氢萘甲酸,二癸基四氢萘甲酸,二辛基-环己烷甲酸,通过精油,妥尔油或其他脂肪酸酯水解得到的酸,烯基琥珀酸或其中烯基含有至少12个碳原子的酸酐例如马来酸或酸酐与MW为约700-1000的聚异丁烯反应的产物。促进剂可以是包括多元醇和杂环醇的醇或酚。优选具有至多12个碳原子的醇,具有1-3个烷基取代基的酚和烷基化的酚,它们各自具有至多50个碳原子,及其混合物。每当量酸反应剂,助催化剂的用量可以为0.1-10当量或更多,优选约0.25-5当量。理想的是将上述羟基化合物与约0.1%至5%的无机卤化物(如氯化铵或溴化物)或碱金属或碱土金属卤化物的碳酸化混合物的重量结合使用。碳酸化温度取决于促进剂,当使用苯酚时,温度可以为80-300℃,优选为100-200℃,而当使用醇时,温度为20-100℃。 C.通常是合适的。碳酸化后,如果是挥发性物质,可以通过蒸馏除去促进剂,否则可以保留在产物中。通常,方便的是在矿物油中制备碳酸的碱金属盐,使得产物是流体油溶液或浓缩物,其易于与额外量的矿物油混合以得到所需的润滑组合物。碳酸化可在溶剂如矿物油,己烷,石脑油,十二烷,苯,甲苯,二甲苯中进行。它也可以是极性取代的烃,例如氯苯,二苯醚或硝基苯。如(1)中所述,给出了在甲醇,异辛醇和氯化铵作为促进剂(2)的存在下,在甲苯中作为溶剂的光亮磺酸钙磺酸盐(1)的碳酸化的实例,除了用氯化钙(3)代替氯化铵以外。除了将氢氧化钙分阶段添加到光亮磺酸中外,其余与(2)相同,除了如(3)中一样将氢氧化钙分阶段添加到(4)中,不同之处在于,将石灰分四部分添加,然后碳酸化(5)与蒸馏妥尔油酸混合在作为溶剂的矿物油中,在甲醇,辛醇和氯化钙作为促进剂的存在下,碱土金属碱是如(5)中的氢氧化钙(6),不同之处在于,除了甲苯还作为溶剂(7)存在之外, (6)除了使用环烷酸代替蒸馏妥尔油酸外,(8)与(1)相同,不同之处在于不存在氯化铵。该产品可用作润滑油的添加剂(请参阅C5部分)。

著录项

  • 公开/公告号DE1221226B

    专利类型

  • 公开/公告日1966-07-21

    原文格式PDF

  • 申请/专利权人 LUBRIZOL CORP;

    申请/专利号DE1964L047014

  • 发明设计人 GREENWALD RUDOLPH;

    申请日1964-02-11

  • 分类号C07G99;C10M159/20;C10M159/24;

  • 国家 DE

  • 入库时间 2022-08-23 15:01:12

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