Patent classifications
B01J27/10
Process for preparing a chlorine comprising catalyst, the prepared catalyst, and its use
The invention concerns a process for preparing a chlorine comprising catalyst by (a) providing a Fischer-Tropsch catalyst comprising titania and at least 5 weight percent cobalt; (b) impregnating the catalyst with a solution comprising chloride ions; and (c) heating the impregnated catalyst at a temperature in the range of between 100 and 500° C. for at least 5 minutes up to 2 days. The prepared catalyst preferably comprises 0.13-3 weight percent of the element chlorine. The invention further relates to the prepared catalyst and its use.
A METHANE OXIDATION CATALYST AND A METHOD OF MAKING AND USING THEREOF
A sulfur-resistant, high activity methane oxidation catalyst for use in removing methane from gas streams having a concentration of methane by oxidizing the methane. The methane oxidation catalyst is especially useful in processing gas streams that also have a concentration of a sulfur compound. The sulfur-resistant methane oxidation catalyst includes a unique multi-crystalline zirconia as a support for a platinum component and a ruthenium component. The multi-crystalline zirconia contributes to the excellent properties of the catalyst. The platinum and ruthenium components can be included in the methane oxidation catalyst in a specific weight ratio that also contributes to the enhanced properties of the catalyst. The sulfur-resistant methane oxidation catalyst may also include a chloride component that contributes to enhanced properties of the catalyst.
LIGAND COMPOUND, CATALYST SYSTEM FOR OLEFIN OLIGOMERIZATION, AND METHOD FOR OLIGOMERIZING OLEFINS USING THE SAME
The present invention relates to a compound represented by the chemical formula 1, a catalyst system for olefin oligomerization comprising the same, and a method for oligomerizign olefins using the same, and the catalyst system for olefin oligomerization according to the present invention has excellent catalytic activity as well as high selectivity for 1-hexene or 1-octene, thereby enabling more efficient preparation of alpha-olefins.
A process for preparation of amides and esters of 2-((2-hydroxypropanoyl)oxy)propanoic acid
The present invention describes method of preparation of esters or amides of lactyl lactates of general formula I, where Z denotes to group of R—O or RR′—N and R represent alkyl, aryl or H from lactide and the lactide is in contact with a hydrocarbyl alcohol and a hydrolyzable halide in a non-chlorinated organic solvent, or an amine initiated by a hydrolysable halide or hydrogen halide solution or an ammonium hydrohalide, wherein the hydrocarbyl alcohol or amine is either aliphatic or aromatic and containing 1 to 1000 carbon atoms, preferably 1 up to 150 carbon atoms, and optionally one or more, preferably 1 to 5, —CH.sub.2— groups may be replaced by —O— groups.
Structure for annotation
##STR00001##
A process for preparation of amides and esters of 2-((2-hydroxypropanoyl)oxy)propanoic acid
The present invention describes method of preparation of esters or amides of lactyl lactates of general formula I, where Z denotes to group of R—O or RR′—N and R represent alkyl, aryl or H from lactide and the lactide is in contact with a hydrocarbyl alcohol and a hydrolyzable halide in a non-chlorinated organic solvent, or an amine initiated by a hydrolysable halide or hydrogen halide solution or an ammonium hydrohalide, wherein the hydrocarbyl alcohol or amine is either aliphatic or aromatic and containing 1 to 1000 carbon atoms, preferably 1 up to 150 carbon atoms, and optionally one or more, preferably 1 to 5, —CH.sub.2— groups may be replaced by —O— groups.
Structure for annotation
##STR00001##
Silica-coated alumina activator-supports for metallocene catalyst compositions
Silica-coated alumina activator-supports, and catalyst compositions containing these activator-supports, are disclosed. Methods also are provided for preparing silica-coated alumina activator-supports, for preparing catalyst compositions, and for using the catalyst compositions to polymerize olefins.
REGENERATION VESSEL ADSORPTION ZONE AND PROCESS FOR ADSORBING HALOGEN-CONTAINING MATERIAL AND SAMPLING CATALYST
A regenerator vessel for adsorbing halogen-containing material from a regenerator vent gas stream has a plurality of catalyst nozzles disposed at a top portion of the regenerator vessel. A first gas outlet is associated with a chlorination zone, and a second gas outlet associated with a combustion zone. A drying zone is in fluid communication with an air heater and the drying zone located in a bottom portion of the regenerator vessel. The first gas outlet is configured to withdraw a first gas stream from the chlorination zone and the second gas outlet is configured to withdraw a second gas stream from the combustion zone. The top portion of the regenerator vessel has an adsorption zone having a vent gas inlet port, a vent gas outlet port, and a portion of an annular catalyst bed.
Oxygen absorbing and carbon dioxide emitting composition
A composition that absorbs oxygen and emits carbon dioxide in response to absorbing oxygen including ascorbic acid, an organic acid, a catalyst that promotes oxidation of the organic acid and emission of carbon dioxide and a soluble transition metal salt characterized by multiple oxidation states.
Oxygen absorbing and carbon dioxide emitting composition
A composition that absorbs oxygen and emits carbon dioxide in response to absorbing oxygen including ascorbic acid, an organic acid, a catalyst that promotes oxidation of the organic acid and emission of carbon dioxide and a soluble transition metal salt characterized by multiple oxidation states.
Methods of Preparing an Aromatization Catalyst
Catalysts and method of preparing the catalysts are disclosed. One of the catalysts includes a zeolite support, a Group VIII metal on the zeolite support, and at least two halides bound to the zeolite support, to the Group VIII metal, or to both, and can have an average crush strength greater than 11.25 lb based on at least two samples of pellets of the catalyst measured in accordance with ASTM D4179.