Abstract:
Additives for mixing with the catalyst inventory in process units for fluid catalytic cracking (FCC) for maximizing the production of LPG and light olefins are described. Said additives comprise a matrix that incorporates a zeolite of type MFI, preferably zeolite ZSM-5, a zeolite of type Y, and a source of phosphorus, in a single particle. Mixing of the additive in proportions from 1.0 to 40 wt. % with the equilibrium catalyst of an FCC unit maximizes the production of LPG and light olefins, chiefly propylene.
Abstract:
The invention realizes a catalyst which is hardly deteriorated even when volatile catalyst-poisoning compounds such as P and As are accumulated and which can reduce the rate of oxidation of SO2 to a level as low as a fraction of that of the catalyst in the prior art, and provides an exhaust gas purification catalyst which can maintain a high activity and a low rate of oxidation of SO2 for a long time even with any diversified coal, a method of producing the same, and an exhaust gas purification method using the same. Disclosed is an exhaust gas purification catalyst having a composition comprising oxides of titanium (Ti), molybdenum (Mo) and/or tungsten (W), vanadium (V) and bismuth (Bi), wherein the atomic ratio of Ti:(Mo and/or W):V is 75 to 98.9:1 to 0.1 to 10 and the atomic ratio of Bi/(Mo and/or W) is 0.1 to 0.8.
Abstract:
A fuel cell reforming catalyst includes a platinum-group metal; an inorganic oxide selected from CeO2, Pr6O11, and combinations thereof; a strong acid ion; and a carrier. The fuel cell reforming catalyst has high activity for the reforming reaction at low temperatures and low space velocities.
Abstract translation:燃料电池重整催化剂包括铂族金属; 选自CeO 2,Pr 6 O 11的无机氧化物及其组合; 强酸离子; 和载体。 燃料电池重整催化剂在低温下的重整反应活性高,空速低。
Abstract:
The present invention concerns doped catalysts on an alumino-silicate support with an adapted macropore content and hydrocracking/hydroconversion and hydrotreatment processes employing them. The catalyst comprises at least one hydrodehydrogenating element selected from the group formed by elements from group VIB and group VIII of the periodic table, a controlled quantity of phosphorus (optionally in combination with boron and/or silicon) as a doping element, and a non-zeolitic support based on alumina-silica containing a quantity of more than 5% by weight and 95% by weight or less of silica (SiO2).
Abstract:
The TiO2 catalyst structure consisting of TiO2 nano-particles in the anatase crystal form, doped with 0.05-5 wt % phosphorus on the TiO2 basis, organized in the circular planar aggregates with the specific surface area ranging from 40 to 120 m2/g, suitable for catalytic processes at the temperature up to 800° C., and the TiO2 catalyst structure of with the morphology of the aggregated compact particles, with the specific surface area from 20 to 40 m2/g, suitable for the catalytic processes at the temperature up to 1000° C. Active substances selected from the group consisting of silver, copper, gold, platinum metals, nickel, molybdenum and metal oxides except for alkaline metals oxides can be applied onto the surface of both types of the structure.
Abstract:
The present invention relates to a process for producing light olefins from a synthesis gas with significantly improved conversion and selectivity for C2-C4 light olefins in general and propylene in particular, as compared to a conventional process, through a sequential two-step process comprising preparing olefin compounds from a synthesis gas in the presence of an iron catalyst by the Fischer-Tropsch reaction followed by cracking the olefin compounds in the presence of a zeolite catalyst.
Abstract:
According to one embodiment of the present invention, an enhanced NH3 adsorbing automotive exhaust composition including a catalyst composition suitable for use in a selective catalytic reduction (SCR) system and an acidified support composition for enhancing NH3 adsorption capacity of the automotive exhaust composition is disclosed.
Abstract:
The invention concerns a process for preparing a hydrotreatment catalyst, comprising the following steps: a) at least one step for impregnation of a calcined and/or dried catalytic precursor containing at least one element from group VIII and/or at least one element from group VIB and an amorphous support, using an impregnation solution constituted by at least one phosphorus-containing compound in solution in at least one polar solvent with a dielectric constant of more than 20; b) a step for maturing said impregnated catalytic precursor from step a); c) a step for drying, without a subsequent calcining step, said catalytic precursor from step b).
Abstract:
The present invention relates to a cobalt/phosphorus-alumina catalyst in which cobalt is supported as an active component on a phosphorus-alumina support wherein phosphorus is supported on alumina surface. With a bimodal pore structure of pores of relatively different pore sizes, the catalyst provides superior heat- and matter-transfer performance and excellent catalytic reactivity. Especially, when Fischer-Tropsch (F-T) reaction is performed using the catalyst, deactivation by the water produced during the F-T reaction is inhibited and, at the same time, the dispersion and reducing property of cobalt and other active component are improved. Therefore, the cobalt/phosphorus-alumina catalyst for F-T reaction in accordance with the present invention provides good carbon monoxide conversion and stable selectivity for liquid hydrocarbons.
Abstract:
Hydrogenation processes using a catalyst composition which, preferably comprises a glass substrate, with one or more functional surface active constituents integrated on and/or in the substrate surface. A substantially nonporous substrate has (i) a total surface area between about 0.01 m2/g and 10 m2/g; and (ii) a predetermined isoelectric point (IEP) obtained in a pH range greater than 0, preferably greater than or equal to 4.5, or more preferably greater than or equal to 6.0, but less than or equal to 14. At least one catalytically-active region may be contiguous or discontiguous and has a mean thickness less than or equal to about 30 nm, preferably less than or equal to 20 nm and more preferably less than or equal to 10 nm. Preferably, the substrate is a glass composition having a SARCNa less than or equal to about 0.5.