Abstract:
The invention relates to a nickel hexaaluminate-containing catalyst for reforming hydrocarbons, preferably methane, in the presence of carbon dioxide, comprising hexaaluminate in a proportion ranging from 65 to 95 wt.%, preferably from 70 to 90 wt.%, and a crystalline oxide secondary phase from the group consisting of LaAlO 3 , SrAl 2 O 4 , and/or BaAl 2 O 4 in a proportion ranging from 5 to 35 wt.%, preferably 10 to 30 wt.%. The BET surface of the catalyst is ≥ 5 m 2 /g, preferably ≥ 10 m 2 /g, the molar nickel content of the catalyst is ≤ 3 mol-%, preferably ≤ 2.5 mol-% and more preferably ≤ 2 mol-%, and the intermediate cations are preferably Ba and/or Sr. The method for producing the catalyst has the following steps: (i) producing a mixture of metal salts, preferably nitrate salts of Ni and Sr and/or La, and a nano-particulate aluminum source, (ii) molding, and (iii) calcining. In a reforming method, the catalyst according to the invention is brought into contact with hydrocarbons, preferably methane, and CO 2 , preferably at a temperature of > 800 °C. The catalyst is also characterized by preferable structural properties of the nickel, wherein the nickel particles mostly have a tetragonal shape, and the particles are ≤ 50 nm, preferably ≤ 40 nm and preferably ≤ 30 nm in particular, and are provided in a finely dispersed manner as a growth on hexaaluminate particles. The catalyst has only a very low tendency to form coke.
Abstract:
The invention relates to a process for obtaining isobutene from an isobutene containing C4-hydrocarbon mixture (1) in a plant comprising an etherification unit (3), a first distillation unit (5), an ether cleavage unit (8) and a second distillation unit (10), the process comprising: (a) contacting the C4-hydrocarbon mixture (1) with a primary alcohol (2) and reacting the mixture with the primary alcohol in the presence of an acidic catalyst to form the corresponding alkyl tert-butyl ether as an intermediate product and diisobutene as a byproduct in the etherification unit (3); (b) distilling the reaction mixture (4) from the etherification unit (3) in the first distillation unit (5), a C4-hydrocarbon raffinate being withdrawn as the overhead product (6), the alkyl tert-butyl ether and diisobutene being withdrawn as the liquid or vaporous bottom product (7), and vaporizing the bottom product (7) if it is withdrawn as a liquid; (c) reacting the vaporous bottom product (7) in the presence of an acidic catalyst obtaining isobutene and the primary alcohol as reaction products in the ether cleavage unit (8); (d) distilling the reaction mixture (9) from the ether cleavage unit (8) in the second distillation unit (10), isobutene being withdrawn as the overhead product (11), the primary alcohol and diisobutene being withdrawn as the bottom product (12) and being recycled to the etherification unit (3); the plant further comprising a byproduct separation unit (15) being fed by a bottom purge stream (13) of the first distillation unit (5) and/or by a part of the bottom product of the second distillation unit (10), wherein a diisobutene product stream rich in diisobutene is separated from this feed stream (13, 14).
Title translation:YTTRIUMHALTIGER催化剂用于高温KOHLENDIOXIDHYDRIERUNG,加之高温KOHLENDIOXIDHYDRIERUNG及改造和/或高温KOHLENDIOXIDHYDRIERUNG改革和方法,结合高温KOHLENDIOXIDHYDRIERUNG和重整和/或改革
Abstract:
The invention relates to a method for producing a catalyst for the high-temperature methods (i) carbon dioxide hydration, (ii) combined high-temperature carbon dioxide, and reforming and/or (iii) reforming of compounds containing hydrocarbons and/or carbon dioxide and to the use of the catalyst according to the invention in connection with the reforming and/or hydration of hydrocarbons, preferably methane, and/or carbon dioxide. For production of the catalyst a source of aluminium, which preferably comprises a water-soluble source of precursor, is brought into contact with an yttrium-containing metal salt solution, is dried, and calcined. The metal salt solution has, in addition to the yttrium species, at least one element from the group comprising cobalt, copper, nickel, iron, and zinc.
Abstract:
A plant for removing isobutene from an isobutene-containing C4-hydrocarbon mixture comprises an etherification unit containing moist acidic ion exchange resin, a first distillation unit, an ether cleavage unit, and a second distillation unit. A process for starting up the plant comprises: (a) filling the etherification unit with isobutanol; (b) filling the first distillation unit with C4-hydrocarbon and/or isobutanol, and operating the first distillation unit with total reflux; (c) filling the second distillation unit with C4-hydrocarbon and/or isobutanol, and operating the second distillation unit with total reflux; (d) withdrawing a bottom product of the second distillation unit, removing water from the bottom product and directing the bottom product to the etherification unit; (e) directing a discharge of the etherification unit to the first distillation unit; (f) directing a bottom product of the first distillation unit to the second distillation unit while bypassing the ether cleavage unit; (g) after the bottom product of the second distillation unit is essentially free of water, providing a flow of isobutene-containing C4-hydrocarbon mixture into the etherification unit and reacting the isobutene-containing C4-hydrocarbon mixture with isobutanol to form a mixture of IBTBE and unconverted hydrocarbons; (h) directing the mixture of IBTBE, unconverted hydrocarbons and unreacted isobutanol from the etherification unit to the first distillation unit and distilling the mixture to obtain a top product comprising the unconverted hydrocarbons, and a bottom product comprising IBTBE and unreacted isobutanol; (i) after IBTBE in the bottom product of the first distillation unit has reached a predetermined concentration, directing the bottom product of the first distillation unit to the ether cleavage unit to decompose the IBTBE to obtain isobutene and isobutanol; (i) directing the mixture of isobutene and isobutanol produced in step (j) to the second distillation unit and distilling the mixture of isobutene and isobutanol to obtain a top product comprising isobutene, and a bottom product comprising isobutanol and; (k) recycling the bottom product obtained in step (j) at least partially to the etherification unit. The stationary operation of the plant comprises (a) reacting an isobutene-containing C4-hydrocarbon mixture with isobutanol in the presence of an acidic ion exchange resin in an etherification unit to form a mixture of IBTBE and unconverted hydrocarbons; (b) distilling the reaction mixture in a first distillation unit to obtain a top product comprising the unconverted hydrocarbons, and a bottom product comprising IBTBE; (c) feeding the bottom product to a ether cleavage unit to decompose the IBTBE to obtain isobutene and isobutanol; (d) distilling the mixture of isobutene and isobutanol produced in step (c) in a second distillation unit to obtain a top product comprising isobutene, and a bottom product comprising isobutanol; and (e) recycling the bottom product of step (d) to step (a). A shutting down process comprises aa) taking the ether cleavage unit out of service and purging the ether cleavage unit with an inert gas; while the etherification unit, the first distillation unit and the second distillation unit stay in operation; bb) stopping the flow of isobutene-containing C4-hydrocarbon mixture into the etherification unit; cc) taking the etherification unit out of service; dd) operating the first distillation unit and the second distillation unit in total reflux mode; and ee) stopping the first distillation unit and the second distillation unit.