Abstract:
A process for producing a Fischer-Tropsch synthesis catalyst according to the present invention comprises a step of calcining a carrier precursor containing silica calcined at a temperature T1 and a zirconium compound at a temperature T2 to obtain a carrier; and a step of calcining a catalyst precursor containing the carrier and a cobalt compound and/or a ruthenium compound at a temperature T3, wherein the content of the zirconium compound in the carrier precursor is 0.01 to 7% by mass in terms of zirconium oxide based on the total mass of the catalyst, and T1, T2, and T3 satisfy conditions represented by expressions (1) to (3): T1≧T3 (1) 250° C.≦T2≦450° C. (2) 250° C.≦T3≦450° C. (3).
Abstract:
A catalyst composition contains an inorganic porous material with pore diameters of at least 2 nm and of crystals of molecular sieve. The crystals of molecular sieve have an average diameter, measured by scanning electron microscopy, not bigger than 50 nm. The catalyst composition has a concentration of acid sites ranges from 50 to 1200 μmol/g measured by TPD NH3 adsorption. An XRD pattern of the catalyst composition is the same as an XRD pattern of the inorganic porous material.
Abstract:
The present application describes a catalyst that is suitable for the CO2 reforming of methane-rich gases, such as biogas, that is resistant to poisoning by sulfur. The catalyst comprises from about 5 wt % to about 20 wt % Ni and 0 wt % to about 10 wt % Co supported on a support having a formula selected from: (a) Al2O3; (b) M1aOb—Al2O3; and (c) M1aOb—ZrO2—Al2O3, where M1aOb is either CaO or MgO.
Abstract translation:本申请描述了一种适用于耐甲烷中毒的富甲烷气体如沼气的二氧化碳重整的催化剂。 催化剂包含约5重量%至约20重量%的Ni和0重量%至约10重量%的Co负载在具有选自以下的式的载体上:(a)Al 2 O 3; (b)M1aOb-Al2O3; 和(c)M1aOb-ZrO2-Al2O3,其中M1ab是CaO或MgO。
Abstract:
Novel catalysts comprising nickel oxide nanoparticles supported on alumina nanoparticles, methods of their manufacture, heavy oil compositions contacted by these nanocatalysts and methods of their use are disclosed. The novel nanocatalysts are useful, inter alia, in the upgrading of heavy oil fractions or as aids in oil recovery from well reservoirs or downstream processing.
Abstract:
In accordance with the present subject matter there is provided a process for catalytic decomposition of lower hydrocarbons to produce carbon oxides free hydrogen and bamboo shaped carbon nanotubes over a catalyst composition. The process for catalytic decomposition of lower hydrocarbons comprises contacting lower hydrocarbon over a catalyst composition, where the catalyst composition comprising, a catalyst, at least one modifying agent and a support material.
Abstract:
The catalytic composition for the electrochemical reduction of carbon dioxide is a metal oxide supported by multi-walled carbon nanotubes. The metal oxide may be nickel oxide (NiO) or tin dioxide (SnO2). The metal oxides form 20 wt % of the catalyst. In order to make the catalysts, a metal oxide precursor is first dissolved in deionized water to form a metal oxide precursor solution. The metal oxide precursor solution is then sonicated and the solution is impregnated in a support material composed of multi-walled carbon nanotubes to form a slurry. The slurry is then sonicated to form a homogeneous solid solution. Solids are removed from the homogeneous solid solution and dried in an oven for about 24 hours at a temperature of about 110° C. Drying is then followed by calcination in a tubular furnace under an argon atmosphere for about three hours at a temperature of 450° C.
Abstract:
A method of operating a fuel cell having an anode, a cathode and a polymer electrolyte membrane disposed between the anode and the cathode, includes feeding the anode with an impure hydrogen stream having low levels of carbon monoxide up to 5 ppm, and wherein the anode includes an anode catalyst layer including a carbon monoxide tolerant catalyst material, wherein the catalyst material includes: (i) a binary alloy of PtX, wherein X is a metal selected from the group consisting of Ti, V and Cr, and wherein the atomic percentage of platinum in the alloy is from 45 to 80 atomic % and the atomic percentage of X in the alloy is from 20 to 55 atomic %; and (ii) a support material on which the PtX alloy is dispersed; wherein the total loading of platinum in the anode catalyst layer is from 0.01 to 0.2 mgPt/cm2.
Abstract translation:一种操作具有设置在阳极和阴极之间的阳极,阴极和聚合物电解质膜的燃料电池的方法包括向阳极供给具有低至5ppm的一氧化碳含量低的不纯氢气流,并且其中阳极 包括含有一氧化碳耐受性催化剂材料的阳极催化剂层,其中催化剂材料包括:(i)PtX的二元合金,其中X是选自Ti,V和Cr的金属,其中原子百分比 的合金中的铂为45〜80原子%,合金中的X的原子百分比为20〜55原子%。 和(ii)分散有PtX合金的载体材料; 其中铂在阳极催化剂层中的总负载量为0.01至0.2mgPt / cm 2。
Abstract:
Provided is an improved alkylation process using a delaminated SSZ-70 catalyst. The process comprises contacting a hydrocarbon feedstock comprising olefins and isoparaffins with a catalyst comprising delaminated SSZ-70 under alkylating reaction conditions. The delaminated SSZ-70 offers a zeolite layer with a single unit cell of thickness in one dimension, allowing an elimination of mass transfer in comparison with regular SSZ-70. This prevents coke formation inside zeolite channels and improves catalyst stability.
Abstract:
A composition that comprises a support material having incorporated therein a metal component and impregnated with an additive compound that is an acetoacetic acid compound. The composition includes the support material that is impregnated with the additive compound and is useful in the hydroprocessing of hydrocarbon feedstocks, especially in the denitrogenation and desulfurization of distillate feedstocks to make ultra low sulfur diesel.
Abstract:
A catalyst system and a process for methanol to light olefin conversion with enhanced selectivity towards propylene. The catalyst system comprises a honeycomb monolith catalyst support coated with nanozeolite catalysts on the edges and inside the channels of the support structure. The nanozeolite catalysts have been pre-modified with metal. The catalyst system gives higher hydrothermal stability to the catalyst compared to randomly packed pellet catalyst and allows methanol to be converted to predominantly propylene at a low temperature, with decreased selectivity towards C2, higher olefins and paraffinic hydrocarbons.