Abstract:
A method for washing a spent solid catalyst is disclosed which is characterized by washing the solid catalyst used for the reaction of generating an esterified compound in a device packed with the solid catalyst, distilling the cleaning fluid in a distilling part, and circulating the fraction obtained by the distillation to an esterification reactor. According to this invention, the existing apparatus used during the process for the production of an esterified compound can be adopted without any modification, the water by-produced in the reaction for production an esterified compound and an alcohol as the raw material for esterification can be used as the cleaning fluid, and these effective components can be recovered from the cleaning fluid. Thus, the stimulation from the offensive odor and the volatile component which has heretofore posed a problem during the removal of the solid catalyst is eliminated and the safety in terms of heath and in terms of operation is secured.
Abstract:
A process for the preparation of an alkylene glycol by reacting an alkylene oxide with water in the presence of a solid catalytic composition which includes a strongly basic ion exchange resin coordinated with one or more anions, and a stabilising additive which is an acidic ion exchange resin. Preferably the acidic ion exchange resin is of the weakly acidic methacrylate type.
Abstract:
Cobalt or rhodium carbonyl compounds are removed from an aqueous solution of 3-hydroxypropanal by a process comprising the steps of:(a) contacting the 3-hydroxypropanal solution with oxygen under acidic conditions at a temperature within the range of about 5 to about 45.degree. C. to produce an oxidation product mixture comprising an aqueous solution of 3-hydroxypropanal, one or more water-soluble cobalt or rhodium species, and byproduct carbon monoxide;(b) removing byproduct carbon monoxide from the oxidation product mixture as it is generated; and(c) passing the oxidation product mixture in contact with an acidic ion exchange resin maintained at a temperature less than about 45.degree. C. and removing at least a portion of the soluble metal compounds from the oxidation product mixture.Such a process is useful in, for example, the manufacture of 1,3-propanediol from ethylene oxide via an intermediate 3-hydroxypropanal solution containing residual carbon dioxide and insoluble cobalt or rhodium catalyst compounds.
Abstract:
The object of the present invention is a process of preparation of a graft copolymer obtained by pre-irradiation grafting of vinyl monomers onto polyolefins or fluorinated polyethylenes, in particular, of grafting acrylic or methacrylic acid onto polyethylene and/or polypropylene and subsequently loading a metal, such as a transition metal on the graft copolymer obtained. Such metal-loaded graft copolymers find use, especially as catalysts, e.g. for hydrogenation reactions.
Abstract:
A supported catalyst useful in the preparation of an electrode for an electrochemical cell which comprises the residue remaining after heating at about 500.degree. to about 800.degree. C. a transition metal and a polymer such as polyvinylpyridine all adsorbed on a support material. Useful electrodes are prepared by combining the supported catalyst with a current collector.
Abstract:
A series of new crystalline titanates (CT) are shown to have considerable potential as catalyst supports. For Pd supported catalyst, the catalytic activity for pyrene hydrogenation was substantially different depending on the type of CT, and one was substantially more active than Pd on hydrous titanium oxide (HTO). For 1-hexene hydrogenation the activities of the new CTs were approximately the same as for the hydrous metal oxide supports.
Abstract:
The invention is a process for making a high surface area, self-supporting catalyst suitable for use as an acid catalyst comprising:(a) at least partially polymerizing a perfluorinated monomer containing ion exchange groups convertible to an acid or salt form in a medium containing a gas-forming ingredient(s) which is present during polymerization and serves a polymerization enhancement purpose during polymerization; wherein the said gas-forming ingredient(s) is a material that will convert into a gaseous state and expand when heated; and(b) heating the polymer to a temperature sufficient to soften the polymer and sufficient to convert at least a portion of the gas-forming ingredient(s) into a gaseous state while the polymer is still in contact with at least a portion of the gas-forming ingredient(s), thereby converting the gas-forming ingredient(s) into a gas which expands the polymer and causes the formation of open and closed pores within the polymer.
Abstract:
A process for the removal of H.sub.2 S from a fluid stream whereby the H.sub.2 S is converted to soluble sulfur compounds by treatment with a solution of ferric chelates containing an oxidizing agent and a water soluble cationic polymeric catalyst such as poly(dimethyldiallyl ammonium chloride).
Abstract:
A catalyst suited for use in the sweetening of petroleum distillates (by oxidizing mercaptans to disulfides) which is formed of a metal complex of a polyaminoalkylpolycarboxylic acid deposited directly on a basic anion exchange resin. The method of making the source by exchanging a metal cation on an acidic resin; forming a complex by the action of a polyaminoalkylpolycarboxylic acid upon said resin; and exchanging the complex so formed on a basic anion exchange resin.
Abstract:
In a process for the preparation of an alkyl tert.-alkyl ether by reaction of an isoolefin branched at the double bond and an alkanol in the presence of a cation exchanger, the improvement which comprises:(a) Employing as the cation exchanger a macroporous or gelatinous acid cation exchanger in the H.sup.+ form which has been charged with 0.1 to 5 grams, per one liter of dry cation exchanger, of an elementary form of a metal of sub-groups VI, VII or VIII of the periodic table of elements (Mendeleev) which cation exchanger is crosslinked with the degree of crosslinking of 2 to 65% and has a specific surface area of 5 to 750 square meters per gram on the basis of dry cation exchange resin; and(b) The reaction is carried out in the liquid phase at a temperature of 30.degree. to 140.degree. C. at a pressure of 2 to 100 bars employing a molar ratio of isoolefin to alkanol of 0.1 to 5.