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    • 3. 发明授权
    • Process for converting methane into ethane
    • 将甲烷转化为乙烷的方法
    • US07473814B2
    • 2009-01-06
    • US10517212
    • 2003-06-04
    • Jean-Marie BassetPhilippe BresChristophe CoperetBarry Martin MaundersDaravong SoulivongMostafa TaoufikJean Thivolle-Cazat
    • Jean-Marie BassetPhilippe BresChristophe CoperetBarry Martin MaundersDaravong SoulivongMostafa TaoufikJean Thivolle-Cazat
    • C07C2/00
    • C07C2/76C07C2531/12Y10S585/943C07C9/06
    • The invention relates to a process for producing ethane comprising contacting methane with a metal catalyst selected from metal hydrides, metal organic compounds and mixtures thereof. It also relates to a process for the conversion of methane to carbon-containing products comprising contacting methane with a metal catalyst comprising at least one metal, Me, chosen from the lanthanides, the actinides and the metals from Groups 2 to 12 of the Periodic Table of the Elements, so as to produce ethane in a proportion of at least 65%, especially at least 98% or 99% by weight with respect to carbon-containing products formed in the process. The process can be a single-step process, preferably carried out under conditions involving a non-oxidative catalytic coupling of methane, in particular under operating conditions maintained substantially constant, preferably continuously, during the ethane production, e.g. at a temperature ranging from −30° C. to +80° C., preferably from 20° C. to 500° C., under a total absolute pressure ranging from 10−3 to 100 MPa, preferably from 0.1 to 50 MPa. The metal catalyst may be chosen from metal catalysts supported on and preferably grafted to a solid support. One of the main advantages of the present invention is to produce ethane with a very high selectivity.
    • 本发明涉及一种生产乙烷的方法,包括使甲烷与选自金属氢化物,金属有机化合物及其混合物的金属催化剂接触。 它还涉及将甲烷转化为含碳产物的方法,包括使甲烷与包含至少一种金属的金属催化剂接触,所述金属催化剂选自镧系元素,锕系元素和元素周期表第2至12族中的金属 的元素,以便相对于在该方法中形成的含碳产品,以至少65重量%,特别是至少98重量%或99重量%的比例制备乙烷。 该方法可以是单步骤方法,优选在涉及甲烷的非氧化催化偶合的条件下进行,特别是在乙烷生产期间,优选连续保持基本上恒定的操作条件下,例如乙烷生产。 在-30℃至+ 80℃,优选20℃至500℃的温度下,在绝对压力范围为10-3-100MPa,优选0.1-50MPa的温度下进行。 金属催化剂可以选自负载在并优选接枝到固体载体上的金属催化剂。 本发明的主要优点之一是以非常高的选择性生产乙烷。
    • 5. 发明授权
    • Process for the preparation of mono-olefins from paraffinic hydrocarbons
    • 从链烷烃制备单烯烃的方法
    • US06555721B2
    • 2003-04-29
    • US10093725
    • 2002-03-11
    • David Charles GriffithsBarry Martin MaundersWilliam Terence Woodfin
    • David Charles GriffithsBarry Martin MaundersWilliam Terence Woodfin
    • C07C100
    • C07C5/48C07C1/0485C07C29/1518C10G2/30C10G2400/20Y02P20/132Y02P30/40Y02P30/42C07C11/02C07C31/04
    • Process for producing a mono-olefin from a feedstock containing a paraffinic hydrocarbon comprising feeding a gaseous paraffinic hydrocarbon-containing feedstock and a molecular oxygen-containing gas to an autothermal cracker wherein they are reacted in the presence of a catalyst capable of supporting combustion beyond the normal fuel rich limit of flammability to produce a product comprising one or more mono-olefin(s) and synthesis gas, and wherein the autothermal cracker is operated at a temperature greater than 650° C. and at a pressure of greater than 5 bar absolute. The product is separated into a high pressure fuel gas stream comprising methane, carbon monoxide and hydrogen and a stream comprising one or more olefins and recovering the one or more olefin(s). The high pressure fuel gas stream comprising methane, carbon monoxide and hydrogen separated in the second step is passed to a Fischer-Tropsch reactor containing a Fischer-Tropsch catalyst, wherein the stream is converted to hydrocarbons and wherein the Fischer-Tropsch is operated at a pressure of between 5-50bar absolute. Thereafter at least part of the hydrocarbon product is recovered.
    • 包括从包含链烷烃的原料生产单烯烃的方法,包括将含有含链烷烃的原料和含分子氧的气体进料到自热裂化器中,其中它们在能够支持燃烧的催化剂存在下反应, 正常燃料浓度极限的可燃性,以产生包含一种或多种单烯烃和合成气的产物,并且其中自热裂化器在大于650℃的温度和大于5巴的绝对压力下操作 。 将产物分离成包含甲烷,一氧化碳和氢气的高压燃料气流和包含一种或多种烯烃的流并回收一种或多种烯烃。 包含在第二步骤中分离的甲烷,一氧化碳和氢气的高压燃料气流被送入包含费 - 托催化剂的费 - 托反应器,其中流转化为烃,其中费 - 托在 压力在5-50bar之间绝对。 此后回收至少部分烃产物。
    • 6. 发明申请
    • PROCESS FOR PRODUCING TRIPTANE
    • 生产TRIPTANE的方法
    • US20100240938A1
    • 2010-09-23
    • US12734673
    • 2008-11-07
    • Berian John DanielDavid John LawBarry Martin MaundersJohn Glenn SunleyJan Cornelis van der Waal
    • Berian John DanielDavid John LawBarry Martin MaundersJohn Glenn SunleyJan Cornelis van der Waal
    • C07C1/00C07C1/04
    • C07C29/151C07C1/20C07C2529/08C07C2529/12C07C2529/14C07C2529/16C07C2529/18C07C2529/40C07C2529/44C07C2529/46C07C2529/48C07C2529/70C07C2529/74C07C2529/76C07C2529/78Y02P20/52C07C9/16C07C11/02C07C31/04C07C31/08C07C31/10C07C31/12
    • A process for producing triptane and/or triptene from methanol and/or one or more derivatives thereof, and optionally one or more further alcohols and/or derivatives thereof at a temperature in the range of from 150 to 400° C., in the presence of a zeolite catalyst having Brønsted acidity, in which all the carbon atoms in the triptane and/or triptene are derived from the methanol and/or one or more derivatives thereof and the optional further alcohols and/or derivatives thereof, the zeolite catalyst being selected from: i. zeolites having frameworks comprising silicon and aluminium atoms at a Si:Al mole ratio of greater than (2), which zeolites also have a channel structure comprising a ring size of (12) or more non-oxygen atoms in (2) or (3) dimensions; and ii. zeolites having frameworks comprising silicon and aluminium atoms, and which have a framework ring comprising (12) or more non-oxygen-atoms accessible on the external surface of the zeolite and a pore structure in which all of the channels have a ring-size of less than (12) non-oxygen atoms. There is also described a process for producing triptane and/or triptene wherein the zeolite catalyst is zeolite X, the reaction composition additionally comprises a C3 alcohol and/or one or more derivatives thereof, in which the mole ratio of C3 alcohol:methanol present in the reaction composition, or derivable from the one or more derivatives thereof present in the reaction composition, is greater than 0.23:10, and the temperature of the process is in the range of greater than 200° to 400° C.
    • 在150-400℃的温度下,在甲醇和/或其一种或多种衍生物和任选的一种或多种其它醇和/或其衍生物的存在下,在存在 具有布朗斯台德酸性的沸石催化剂,其中所述三庚烷和/或三丁烯中的所有碳原子来自甲醇和/或其一种或多种衍生物和任选的其它醇和/或其衍生物,选择沸石催化剂 从:我 具有Si:Al摩尔比大于(2)的硅和铝原子的骨架的沸石,该沸石还具有在(2)或(3)中具有包含(12)以上非氧原子的环尺寸的通道结构 )尺寸; 和ii。 具有包含硅和铝原子的框架的沸石,并且具有包含可在沸石的外表面上的(12)或更多个非氧原子的骨架环和其中所有通道的环尺寸为 小于(12)个非氧原子。 还描述了一种制备三庚烷和/或三丁烯的方法,其中沸石催化剂是沸石X,反应组合物另外包含C3醇和/或其一种或多种衍生物,其中存在的C3醇:甲醇的摩尔比 反应组合物或可衍生自存在于反应组合物中的一种或多种衍生物的反应组合物大于0.23:10,并且该方法的温度在大于200℃至400℃的范围内。