Patent classifications
B01J27/1853
4-WAY HYBRID BINARY CATALYSTS, METHODS AND USES THEREOF
The present disclosure describes hybrid binary catalysts (HBCs) that can be used as engine aftertreatment catalyst compositions, specifically 4-way catalyst compositions. The HBCs provide solutions to the challenges facing emissions control. In general, the HBCs include a porous primary catalyst and a secondary catalyst. The secondary catalyst partial coats the surfaces (e.g., the internal porous surface and/or the external surface) of the primary catalyst resulting in a hybridized composition. The synthesis of the HBCs can provide a primary catalyst whose entire surface, or portions thereof, can be coated with the secondary catalyst.
Mesoporous catalyst for hydroconversion of residues and method for preparing the latter
The invention relates to the preparation of a catalyst containing: a mainly aluminum oxide calcined support; a hydro-dehydrogenating active phase containing at least one metal of group VIB,
the process including:
a) a first precipitation step of at least one basic precursor and at least one acidic precursor,
b) a heating step,
c) a second precipitation step by addition to the suspension of at least one basic precursor and at least one acidic precursor,
d) a filtration step;
e) a drying step,
f) a moulding step,
g) a heat treatment step;
h) an impregnation step of the hydro-dehydrogenating active phase on the support obtained in the step g).
Catalyst and process for treatment of fluid comprising an oxidizable contaminant
Described is a process for treatment of a fluid comprising an oxidizable contaminant selected from one or both of a sulfide and a thiol, the process comprising the step of contacting the fluid with a first complex of ferric iron and a polyphosphate to oxidize the oxidizable contaminant and generate a second complex of ferrous ion and the polyphosphate.
Catalysts for the conversion of hydroxypropionic acid or its derivatives to acrylic acid or its derivatives
Catalysts for dehydrating hydroxypropionic acid, hydroxypropionic acid derivatives, or mixtures thereof to acrylic acid, acrylic acid derivatives, or mixtures thereof with high yield and selectivity, short residence time, and without significant conversion to undesired side products, such as, for example, acetaldehyde, propionic acid, and acetic acid, are provided. The catalysts are mixed condensed phosphates. Methods of preparing the catalysts are also provided.
Nickel Phosphide Catalysts for Direct Electrochemical CO2 Reduction to Hydrocarbons
Disclosed are cathodes comprising a conductive support substrate having a catalyst coating containing nickel phosphide nanoparticles. The conductive support substrate is capable of incorporating a material to be reduced, such as CO.sub.2 or CO. Also disclosed are electrochemical methods for generating hydrocarbon and/or carbohydrate products from CO.sub.2 or CO using water as a source of hydrogen.
TRI-FUNCTIONAL HETEROGENEOUS PHOTOCATALYST
A three-phase heterogeneous photocatalyst composition is provided for catalysing dry reforming reactions. The photocatalyst composition is comprised of a photochemically active component, a photothermal component, and a plasmonic material that function synergistically to catalyze dry reforming reactions.
A METHOD FOR CATALYTICALLY INDUCED HYDROLYSIS AND RECYCLING OF METAL BOROHYDRIDE SOLUTIONS
The process for obtaining M.sup.1BH.sub.4, the process comprising contacting M.sup.1-B0.sub.2 with a metal M.sup.2 in the presence of molecular hydrogen (H.sub.2) under conditions permitting the formation of M.sup.1-BH.sub.4 and M.sup.2-oxide, wherein the M.sup.1 is a metal selected from column I of the periodic table of elements or alloys of metals selected from column I of the periodic table of elements and M.sup.2 is a metal or an alloy of metals selected from column II of the periodic table of elements, provided that M.sup.2 is not Mg and M.sup.1 is different from M.sup.2.
CATALYST FOR DEHYDRATION OF GLYCERIN, PREPARATION METHOD THEREOF, AND PRODUCTION METHOD OF ACROLEIN USING THE CATALYST (AS AMENDED)
The present disclosure relates to a catalyst for dehydration of glycerin, a preparation method thereof, and a production method of acrolein using the catalyst.
Particularly, the catalyst according to an embodiment of the present disclosure is used in a dehydration reaction of glycerin to exhibit high catalytic activity, a high yield, and high selectivity to acrolein and acrylic acid, and has a longer lifetime compared to the conventional catalysts due to a characteristic that coke carbon cannot be easily deposited on the surface of the catalyst.
Catalyst for glycerin dehydration, preparation method therefor, and acrolein preparation method using catalyst
The present invention relates to: a catalyst for glycerin dehydration; a preparation method therefor; and an acrolein preparation method using the catalyst. According to one embodiment of the present invention, the catalyst is used in glycerin dehydration so as to exhibit high catalytic activity, a high yield and high acrolein selectivity, and has a characteristic in which carbon is not readily deposited, thereby having a long lifetime compared with that of a conventional catalyst.
Stable support for Fischer-Tropsch catalyst and methods for making and using
A process has been developed for preparing a Fischer-Tropsch catalyst precursor and a Fischer-Tropsch catalyst made from the precursor. The process includes preparing a catalyst precursor by contacting a boehmite material with a stabilizer containing vanadium-phosphorus. The boehmite material includes two or more different crystalline boehmites having the same average crystallite size to the nearest whole nanometer and having differing properties selected from surface area, pore volume, density and combinations thereof. The boehmite material is subjected to at least one heat treatment at a temperature of at least 500 C., either before or after the contacting step to obtain a stabilized catalyst support having a pore volume of at least 0.3 cc/g. A catalytic metal or a compound containing cobalt is applied to the stabilized catalyst support to form the catalyst precursor. Finally, the catalyst precursor is reduced to activate the catalyst precursor to obtain the Fischer Tropsch catalyst. The catalyst has enhanced hydrothermal stability as measured by losing no more than 6% of its pore volume when exposed to water vapor.