Abstract: A system is provided for passivating metals, such as vanadium, deposited on a catalyst during a conversion reaction. Spent catalyst particles containing the metal deposits are introduced into a regenerator, and passivating particles containing the passivating materials are also introduced into the regenerator. The passivating particles and the catalyst particles are separated after they have exited from the regenerator. At least a portion of the separated passivating particles are recycled to the regenerator, and the regenerated, separated catalyst particles are reintroduced into a reaction zone, such as a riser conversion zone.

Abstract: Porous materials having a dual surface are disclosed. Also disclosed is a method for their preparation. An example of such a material is a silica gel reacted with a reactive silane intermediate such as (CH.sub.3).sub.2 Si.dbd.O and then, with a reactive silane such as ##STR1## to give a dual treated material having --((CH.sub.3).sub.2 SiO).sub.x H on the exterior surface and ##STR2## on the interior surface of the pores.

Abstract: This support is constituted by a crosslinked polyvinyl alcohol hydrogel, whereof at least part of the --OH groups have been replaced by --OSO.sub.3 H groups. The crosslinked polyvinyl alcohol hydrogel comprises 70 to 95% by weight of chains derived from polyvinyl alcohol and 5 to 30% by weight of chains derived from crosslinking monomers, such as triethylene glycol diacrylate and tetraethylene glycol triacrylate.These supports can be used for the ex-vivo purification of the blood plasma in pocket 31 or 33.

Abstract: Mono- or multi-metal microaggregates in a monodisperse phase in a solid or liquid medium and of a size uniformly less than 5 nm. The microaggregates are obtained by irradiation of a metal salt or a mixture of salts, by means of an ionizing radiation source, comprising dissolving a metal salt or a mixture of metal salts, in an appropriate solvent, in the presence of an oxidizing radical scavenger, and a surfactant, a support or both a surfactant and a support, and then carrying out irradiation. The metal microaggregates are useful for catalysis of various reactions, in particular, the photoreduction of water.

Abstract: A method for applying porous, preferably catalytically active metal oxide coatings to relatively non-porous substrates in a fibrous form, and the catalyst materials thereby obtained. A solution is formed of one or more hydrolyzable precursors of metal oxides, in an anhydrous, organic solvent. The substrate to be coated, having active surface hydroxyl groups and preferably being glass or ceramic, is dipped into the solution and thereafter removed, drained and dried in an atmosphere containing water vapor so as to form a uniform, and at least partially hydrolyzed metal hydroxide/alkoxide coating on the substrate. The thus coated substrate is cured by heating in one or more stages at temperatures in the range of between about 250.degree. and 500.degree. C. to form an adherent, highly porous coating of the corresponding metal oxide.

Abstract: A new method is described for the in situ activation of catalysts. Conductive catalysts or catalyst compositions are treated by applying a relatively high (up to 3,000 vdc), substantially electrostatic, potential to the catalyst while the surface of the catalyst is exposed to an ionizable gas. Activation is observed only when the catalyst is biased negatively with respect to a remote counter electrode. The activation persists even after the electrical potential is removed. This activation and, in some cases, catalyst regeneration is believed to arise from the production of cation radicals which react with and remove inactivating deposits on the catalytic surface. The process is demonstrated on the nickel-catalyzed hydrogenolysis of ehtane and ethylene.

Abstract: A process for the production of a solid, particulate immobilized extractant, which process comprises adsorbing (a) a liquid extractant which is not homopolymerizable onto (b) a porous, solid, particulate, substrate; adsorbing (c) a monomer onto the substrate; and polymerizing the adsorbed monomer (c) thereby entrapping the liquid extractant (a) on substrate (b).

Abstract: This invention relates to a finely divided iron carbide-first row transition metal-based catalyst which is produced by a gas phase pyrolytic decomposition reaction driven by a laser. The catalysts may be used to produce various hydrocarbons, including olefins, from CO.sub.2 and H.sub.2.

Abstract: This invention relates to a finely divided iron carbide-based catalyst which is produced by a gas phase pyrolytic decomposition reaction driven by a laser. The catalysts may be used to produce various hydrocarbons, including olefins, from CO and H.sub.2.

Abstract: This invention relates to a promoted finely divided or supported iron carbide-based catalyst which is produced by a gas phase pyrolytic decomposition reaction driven by a laser and the use of such a catalyst to produce various heavier hydrocarbons from CO and H.sub.2.

Abstract: There is provided a process for producing a catalyst to convert carbon monoxide in a gas into carbon dioxide. The process comprises causing activated carbon to absorb an aqueous solution of chloroplatinic acid, reducing the absorbed chloroplatinic acid to platinum with a reducing agent, and decomposing an excess of the reducing agent with hydrogen peroxide. The catalyst contains at least 6 mg of platinum per gram of activated carbon.

Abstract: The invention relates to metal microaggregates.The monodisperse of the invention are non-noble metal microaggregates in a monodispersed form in a solid or liquid medium and of a size uniformly less than 5 nm. They are obtained by irradiation of a metal salt or a mixture of salts, by means of an ionizing radiation source, by dissolving a non-noble metal salt or a mixture of metal salts, at least one of which is a non-noble metal, in an appropriate solvent, in the presence of an oxidizing radical scavenger and a surfactant and/or a support, and then by carrying out irradiation.Application is for catalysis of various reactions, in particular the photoreduction of water into hydrogen.

Abstract: Fly ash is activated by heating a screened magnetic fraction of the ash in a steam atmosphere and then reducing, oxidizing and again reducing the hydrothermally treated fraction. The activated fly ash can be used as a carbon monoxide disproportionating catalyst useful in the production of hydrogen and methane.

Abstract: A process for producing an antimony-containing oxide catalyst with improved strength is described, by the steps of preparing a slurry containing an antimony compound, a polyvalent metal compound and a silica sol as the essential ingredients, adjusting the pH of the slurry to 7 or less, heat treating the slurry at a temperature of 40.degree. C. or higher, and thereafter drying the slurry and calcining the dried particles, wherein said slurry is irradiated with ultrasonic waves during the pH adjustment, or after the pH adjustment and before completion of the heat treatment.

Abstract: This invention relates to a process for the desorption of spent solid adsorbent through heating the latter to desorption temperature by means of a hot granular heat carrier medium; particularly of activated coal or activated coke used for flue gas purification by adsorption in power plants, for example.

Abstract: A process and apparatus for the transportation and heating of granulated materials, particularly of solid particles of catalyst used for hydrocarbon conversion which must be activated or regenerated. The process comprises moving a bed of catalyst particles on travelling bands or floor plates passing through an elongate chamber and eventually inclined to the axis. The bands are subjected to vibrations imparting to said bed an unidirectional motion, and said bed on said bands being exposed to heating by means of electromagnetic radiations of a wave length range from 0.38 .mu.m to 50 mm.

Abstract: The instant invention is directed to a process for the continuous manufacturing of carbon molecular sieves having average effective pore diameters of from 2 to 15 Angstroms which comprises continuously feeding a charred naturally occurring substrate to a means for heating said substrate and heating said substrate under non-activation conditions, without the use of an externally added pore blocking substance, at a temperature range of about 900.degree. F. (482.degree. C.) to 2000.degree. F. (1093.degree. C.) for a time period of about 5 to 90 minutes.The instant invention is also directed to a carbon molecular sieve, useful for separating gas or liquid mixtures containing components of at least two different molecular diameters, molecular weights or molecular shapes which has the following physical characteristics:(a) an apparent density of from 0.60 to 0.70 g/cc,(b) an oxygen diffusivity (.times.10.sup.-8) of from 500 to 900 cm.sup.2 /sec,(c) an oxygen/nitrogen selectivity ratio of from 5.0 to 8.

Abstract: A catalyst is disclosed wherein a particulate catalyst support has cosputtered on its surface a mixture of a catalytically active metal such as Pt, Pd, Ag, Au, Re, Rh, Ru or Ir and a cosputtered support material which preferably is the same material as the catalyst support.

Abstract: A process for hydrocracking hydrocarbons for residuum conversion in the presence of a fluidized catalyst, which is characterized by extracting at least part of the fluidized catalyst from the reaction system as a spent catalyst, subjecting at least part of the spent catalyst to hydrotreatment for solubilizing toluene-insoluble carbonaceous materials deposited on the catalyst thereby regenerating the spent catalyst, and recycling the regenerated catalyst to the hydrocracking step. According to this process, the spent catalyst is recycled to the hydrocracking step in a highly activated state after the regenerative hydrotreatment, so that it becomes possible to suppress the coke production within the reactor to a considerable degree, to maintain the coke level of the catalyst below a predetermined value and to preclude the contamination of the reactor walls with coke.

Abstract: A solid catalyst material is evaporated from a coating on a transparent solid substrate and is condensed onto a solid polymeric organic catalyst carrier or into a liquid, by passing a laser beam through said solid transparent substrate and onto the back of said coating and contacting said catalyst carrier or liquid with the evaporated catalyst material. Suitably, the laser source is a ruby or a rhodamine dye laser; a suitable catalyst material is rhodium metal; and a suitable solid polymeric organic catalyst carrier is polystyrene crosslinked by divinyl benzene and a suitable liquid is aqueous polyvinyl alcohol. The process minimizes the exposure to heat of the catalyst carrier or suspending liquid.

Abstract: Finely divided, hydrogen-activated catalyst compositions comprising iron, silicon and carbon or iron and silicon that selectively convert gaseous mixtures of CO and H.sub.2, at a temperature of about 150.degree.-450.degree. C. and at pressures of about 10-2000 kPa, into reaction mixture containing at least about 75% C.sub.2 -C.sub.6 alkenes and no more than about 25% of CH.sub.4 and undesirable CO.sub.2 by-products are disclosed. A wide range of iron/silicon-based catalyst compositions are conveniently prepared by laser pyrolysis and hydrogen-pretreatment and readily reactivated with hydrogen at elevated temperatures.

Abstract: A heterogeneous catalyst formed by the steps of:(a) irradiating an organic macromolecular substrate or a metal substrate with ionizing or U.V. radiation in the presence of a monomer selected from the group comprising o-, m-, or p- styryl diphenyl phosphine or o-, m-, or p- phenyl acrylyl diphenyl phosphine to graft the monomer to the substrate, and(b) reacting the graft copolymer with a homogeneous catalyst selected from the group consisting of catalytic metal salts and catalytic organometallic complexes such that the monomer-substrate conjugate becomes a ligand of the catalyst.These catalysts have particular activity in hydrogenation reactions, hydroformylation reactions, isomerization reactions, cracking reactions and dehydrogenation reactions of organic compounds.

Abstract: A process for regenerating a spent copper-porous refractory metal oxide carrier composite for sorbing sulfur compounds from hydrocarbons in which the spent sorbent is stripped of hydrocarbons, oxidized to convert absorbed sulfur to a sulfate form, and then extracted with a liquid solvent to remove the sulfate and reduce the sulfur content of the sorbent.