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    • 1. 发明申请
    • GASOLINE ALKYLATE RVP CONTROL
    • 汽油烷基酯RVP控制
    • US20090306448A1
    • 2009-12-10
    • US12134652
    • 2008-06-06
    • Lawrence A. Smith, JR.Abraham P. GelbeinWilliam M. Cross, JR.
    • Lawrence A. Smith, JR.Abraham P. GelbeinWilliam M. Cross, JR.
    • C07C2/02
    • C07C9/02C07C2/62
    • A process for producing an alkylate having a low Reid vapor pressure, the process including: contacting a C6+-containing hydrocarbon stream with a mixture of isopentane and isobutane in the presence of an acid catalyst in an alkylation reactor to form a dilute alkylate product, wherein the C6+-containing hydrocarbon stream includes at least one of oligomers of C3 to C5 olefins and a dilute alkylate produced by contacting an isoparaffin with at least one of C3 to C5 olefins and oligomers of C3 to C5 olefins; fractionating the dilute alkylate product to form an isobutane-rich fraction, a n-butane-rich fraction, a fraction containing isopentane, and an alkylate product having a Reid vapor pressure less than 0.35 bar (5 psi); recycling at least a portion of the fraction containing isopentane to the alkylation reactor.
    • 一种制备具有低Reid蒸气压的烷基化物的方法,该方法包括:在烷基化反应器中,在酸催化剂存在下,将含C 6+的烃物流与异戊烷和异丁烷的混合物接触以形成稀烷基化物产物,其中 含有C 6 +的烃物流包括C 3 -C 5烯烃的低聚物和通过使异链烷烃与C 3至C 5烯烃中的至少一种和C 3至C 5烯烃的低聚物接触而产生的稀烷基化物中的至少一种; 分馏稀烷基化产物以形成富含异丁烷的馏分,富含正丁烷的级分,含有异戊烷的级分和具有Reid蒸汽压小于0.35巴(5psi)的烷基化物产物; 将至少一部分含有异戊烷的级分再循环至烷基化反应器。
    • 3. 发明授权
    • Paraffin alkylation
    • 石蜡烷基化
    • US07250542B2
    • 2007-07-31
    • US10793028
    • 2004-03-04
    • Lawrence A. Smith, Jr.Mitchell E. LoescherJohn R. AdamsAbraham P. Gelbein
    • Lawrence A. Smith, Jr.Mitchell E. LoescherJohn R. AdamsAbraham P. Gelbein
    • C07C6/00C07C2/58C07C2/62
    • C07C2/62C07C11/02C07C2527/054C10G29/205C10G2300/1081C10G2300/1088
    • A process for the alkylation of alkane with olefin or olefin precursor such as an oligomer of tertiary olefin comprising contacting a liquid system comprising acid catalyst, isoparaffin and olefin in concurrent downflow into contact in a reaction zone with a disperser mesh under conditions of temperature and pressure to react said isoparaffin and said olefin to produce an alkylate product is disclosed. Preferably, the liquid system is maintained at about its boiling point in the reaction zone. Unexpectedly, the olefin oligomers have been found to function as olefin precursors and not as olefins in the reaction. Thus, for example, a cold acid alkylation using an oligomer of isobutene (principally dimer and trimer) with isobutane produces isooctane with the isobutane reacting with the constituent isobutene units of the oligomers on a molar basis. The product isooctane is essentially the same as that produced in the conventional cold acid process.
    • 一种烷烃与烯烃或烯烃前体烷基化的方法,例如叔烯烃的低聚物,包括使含有酸催化剂,异链烷烃和烯烃的液体体系同时向下流动,在温度和压力条件下在分散网中与反应区接触 使所述异链烷烃和所述烯烃反应生成烷基化物产物。 优选地,液体系统保持在反应区域的大约沸点。 出乎意料地,已经发现烯烃低聚物作为烯烃前体而不是反应中的烯烃。 因此,例如,使用异丁烯(主要是二聚体和三聚体)的低聚物与异丁烷的冷酸烷基化产生异辛烷,异丁烷与摩尔的低聚物的组分异丁烯单元反应。 产物异辛烷基本上与常规冷酸法中产生的相同。
    • 5. 发明授权
    • Process for the synthesis of aliphatic alcohol-containing mixtures
    • 用于合成含脂肪醇的混合物的方法
    • US4477594A
    • 1984-10-16
    • US450341
    • 1982-12-16
    • Marvin I. GreeneAbraham P. Gelbein
    • Marvin I. GreeneAbraham P. Gelbein
    • B01J23/80B01J23/86C07C29/154C07C27/06C07C31/00
    • C07C29/154B01J23/80B01J23/868Y02P20/52
    • A process for the synthesis of mixtures which include saturated aliphatic alcohols is disclosed. In the first step of the process, the first catalyst activation stage, a catalyst, which comprises the oxides of copper, zinc, aluminum, potassium and one or two additional metals selected from the group consisting of chromium, magnesium, cerium, cobalt, thorium and lanthanum, is partially activated. In this step, a reducing gas stream, which includes hydrogen and at least one inert gas, flows past the catalyst at a space velocity of up to 5,000 liters (STP) per hour, per kilogram of catalyst. The partially activated catalyst is then subjected to the second step of the process, second-stage catalyst activation. In this step, the catalyst is contacted by an activation gas stream comprising hydrogen and carbon monoxide present in a volume ratio of 0.5:1 and 4:1, respectively, at a temperature of 200.degree. to 450.degree. C. and a pressure of between 35 and 200 atmospheres. The activation gas flows at a space velocity of from 1,000 to 20,000 liters (STP) per hour, per kilogram of catalyst. Second-stage activation continues until the catalyst is contacted with at least 500,000 liters (STP) of activation gas per kilogram of catalyst. The fully activated catalyst, in the third step of the process, contacts a synthesis gas stream comprising hydrogen and carbon monoxide.
    • 公开了一种合成包含饱和脂族醇的混合物的方法。 在该方法的第一步中,第一催化剂活化阶段是一种催化剂,其包含选自铬,镁,铈,钴,钍中的铜,锌,铝,钾和一种或两种另外的金属的氧化物 和镧,部分活化。 在该步骤中,包括氢气和至少一种惰性气体的还原气流以每千克催化剂每小时高达5000升(STP)的空间速度流过催化剂。 然后将部分活化的催化剂进行该过程的第二步骤,第二阶段催化剂活化。 在该步骤中,催化剂在200℃至450℃的温度下分别以0.5:1和4:1的体积比分别包含氢和一氧化碳的活化气流接触, 35和200大气压。 活化气体以每千克催化剂每小时1,000至20,000升(STP)的空间速度流动。 继续进行第二阶段活化,直到催化剂与每千克催化剂至少500,000升(STP)的活化气体接触。 在该方法的第三步中,完全活化的催化剂与包含氢气和一氧化碳的合成气流接触。
    • 7. 发明授权
    • Paraffin alkylation
    • 石蜡烷基化
    • US07319180B2
    • 2008-01-15
    • US10973746
    • 2004-10-26
    • Lawrence A. Smith, Jr.Mitchell E. LoescherJohn R. AdamsAbraham P. Gelbein
    • Lawrence A. Smith, Jr.Mitchell E. LoescherJohn R. AdamsAbraham P. Gelbein
    • C07C2/54
    • C07C2/62C07C11/02C07C2527/054C10G29/205C10G2300/1081C10G2300/1088
    • A process for the alkylation of alkane with olefin or olefin precursor such as an oligomer of tertiary olefin comprising contacting a liquid system comprising acid catalyst, isoparaffin and olefin in concurrent downflow into contact in a reaction zone with a disperser mesh under conditions of temperature and pressure to react said isoparaffin and said olefin to produce an alkylate product is disclosed. Preferably, the liquid system is maintained at about its boiling point in the reaction zone. Unexpectedly, the olefin oligomers have been found to function as olefin precursors and not as olefins in the reaction. Thus, for example, a cold acid alkylation using an oligomer of isobutene (principally dimer and trimer) with isobutane produces isooctane with the isobutane reacting with the constituent isobutene units of the oligomers on a molar basis. The product isooctane is essentially the same as that produced in the conventional cold acid process.
    • 一种烷烃与烯烃或烯烃前体烷基化的方法,例如叔烯烃的低聚物,包括使含有酸催化剂,异链烷烃和烯烃的液体体系同时向下流动,在温度和压力条件下在分散网中与反应区接触 使所述异链烷烃和所述烯烃反应生成烷基化物产物。 优选地,液体系统保持在反应区域的大约沸点。 出乎意料地,已经发现烯烃低聚物作为烯烃前体而不是反应中的烯烃。 因此,例如,使用异丁烯(主要是二聚体和三聚体)的低聚物与异丁烷的冷酸烷基化产生异辛烷,异丁烷与摩尔的低聚物的组分异丁烯单元反应。 产物异辛烷基本上与常规冷酸法中产生的相同。
    • 8. 发明授权
    • Process for making dialkyl carbonates
    • 制备碳酸二烷基酯的方法
    • US07314947B2
    • 2008-01-01
    • US11358671
    • 2006-02-21
    • J. Yong RyuAbraham P. Gelbein
    • J. Yong RyuAbraham P. Gelbein
    • C07C67/18
    • C07C68/00C07C69/96
    • A process for the production of dialkyl carbonates from the reaction of alcohol, for example C1-C3 alcohols, with urea is disclosed wherein the water and ammonium carbamates impurities in the feed are removed in a prereactor. The water is reacted with urea in the feed to produce ammonium carbamate which is decomposed along with the ammonium carbamates originally in the feed to ammonia and carbon dioxide. In addition some of the urea is reacted with the alcohol in the first reactor to produce alkyl carbamate which is a precursor to dialkyl carbonate. Dialkyl carbonates are produced in the second reaction zone. The undesired by-product N-alkyl alkyl carbamates are continuously distilled off from the second reaction zone along with ammonia, alcohol and dialkyl carbonates under the steady state reactor operation. N-alkyl alkyl carbamates can be converted to heterocyclic compounds in a third reaction zone to remove as solids from the system.
    • 公开了一种由醇(例如C 1 -C 3 -C 3醇)与脲的反应制备碳酸二烷基酯的方法,其中水和氨基甲酸铵在 饲料在预反应器中被去除。 水与进料中的尿素反应生成氨基甲酸铵,氨基甲酸铵与原料在氨和二氧化碳中的氨基甲酸铵一起分解。 此外,一些尿素与第一反应器中的醇反应以产生作为碳酸二烷基酯的前体的氨基甲酸烷基酯。 在第二反应区产生碳酸二烷基酯。 在稳态反应器操作下,不需要的副产物N-烷基烷基氨基甲酸酯与第二反应区连同蒸馏出氨,醇和碳酸二烷基酯。 N-烷基烷基氨基甲酸烷基酯可以在第三反应区转化为杂环化合物,以从体系中作为固体除去。
    • 9. 发明授权
    • Production of epoxy compounds from olefinic compounds
    • 从烯烃化合物生产环氧化合物
    • US4443620A
    • 1984-04-17
    • US35557
    • 1979-05-03
    • Abraham P. GelbeinArthur S. Nislick
    • Abraham P. GelbeinArthur S. Nislick
    • C07D301/26
    • C07D301/26
    • Chlorine and tertiary alkanol dissolved in an inert organic solvent are reacted with calcium oxide in aqueous calcium chloride to produce tertiary alkyl hypochlorite which is recovered in the organic solvent and reacted with water and olefinically unsaturated compound to produce chlorohydrin and tertiary alkanol. Chlorohydrin and tertiary alkanol recovered in the organic solvent are contacted with calcium oxide in aqueous calcium chloride to produce the epoxy compound, and tertiary alkanol recovered in the organic solvent is recycled to hypochlorite production. Calcium chloride produced as by-product in the hypochlorite production and saponification is recovered as an aqueous solution having a calcium chloride concentration of at least 25 wt. % to provide calcium chloride in a usable form.
    • 溶解在惰性有机溶剂中的氯和叔烷醇与氧化钙在氯化钙水溶液中反应,生成叔烷基次氯酸盐,将其回收到有机溶剂中,并与水和烯属不饱和化合物反应产生氯代醇和叔链烷醇。 在有机溶剂中回收的氯代醇和叔链烷醇与氯化钙水溶液中的氧化钙接触以产生环氧化合物,并将在有机溶剂中回收的叔烷醇再循环至次氯酸盐生产。 在次氯酸盐生产和皂化中作为副产物生产的氯化钙作为氯化钙浓度至少为25重量%的水溶液回收。 %以提供可用形式的氯化钙。