Abstract: Hydrocarbon feedstocks such as distillate fuel oils and gas oils are dewaxed by isomerizing the waxy components over a zeolite beta catalyst. The process may be carried out in the presence or absence of added hydrogen. Preferred catalysts have a zeolite silica:alumina ratio over 100:1.

Abstract: A process for the conversion of a hydrocarbon charge stock which comprises contacting said charge stock at hydrocarbon conversion conditions with a catalytic composite comprising a combination of a carrier material, a Group VIB metal component and Group VIII metal component wherein said Group VIB metal component and said Group VIII metal component are incorporated in said catalytic composite by means of a non-aqueous organic solution of a Group VIB metal compound and a Group VIII metal compound, wherein said non-aqueous organic solution comprises dimethylformamide, formamide, diethylformamide, ethylformamide, methylformamide, pyridine, aniline or toluene and wherein said catalytic composite is calcined in a non-oxidizing atmosphere.

Abstract: A method for producing branched aliphatic hydrocarbons by reacting H.sub.2 with a C.sub.1 -C.sub.6 alcohol and/or a C.sub.2 -C.sub.6 olefin in the presence of a cadmium component and a support which comprises an amorphous refractory inorganic oxide, a pillared smectite or vermiculite clay, a molecular sieve consisting essentially of unexchanged or cation-exchanged chabazite, clinoptilite, zeolite A, zeolite L, zeolite X, zeolite Y, ultrastable zeolite Y, or crystalline borosilicate molecular sieve, or a combination thereof.

Abstract: Isomerization is effected at improved conversion and selectivity by use of a 0.5 w %-2.5 w % platinum-palladium group metal on hydrogen mordenite catalyst, silica to alumina mole ratio in the range of 10:1 to 20:1, the catalyst having been calcined at 1200.degree. F.-1500.degree. F. prior to use whereby it acquires activated sites not present in mordenite calcined at lower temperature.

Abstract: A process for isomerization of paraffinic or olefinic hydrocarbons using as catalysts or as supports for catalysts bridged clays which are prepared by an aqueous clay suspension subjected to a dialysis.

Abstract: A shape selective catalyst useful in a variety of hydrocarbon conversion processes such as cracking, hydrocracking, hydrofining, isomerization, dewaxing, and the like, is obtained from the process which comprises steaming a precursor crystalline aluminosilicate in the hydrogen or ammonium form having a silica-alumina ratio greater than 12, a constraint index between about 1 and about 12 and an alpha value greater than about 20 in the presence of ammonia to provide a crystalline aluminosilicate having an alpha value of from about 10 to about 150 and thereafter ion-exchanging the steamed precursor with an alkali metal cation under conditions effective to further reduce the alpha value of the crystalline aluminosilicate to less than about 10.

Abstract: A new porous silico-crystal, designated as ZSM-48, a method of making same and the use thereof in catalytic conversion of organic compounds. The new product has a composition, expressed in terms of moles of anhydrous oxides per 100 moles of silica as follows:(0.05 to 5) N.sub.2 O:(0.1 to 10)M.sub.2 /.sub.n O:(0 to 4) Al.sub.2 O.sub.3 :(100) SiO.sub.2wherein M is at least one cation having a valence n, N is a mixture of C.sub.2 -C.sub.12 alkylamine and more preferably of C.sub.3 -C.sub.5 tetramethyl ammonium compound, and wherein the zeolite is characterized by the distinctive x-ray powder diffraction pattern shown in Table I.

Abstract: The liquid carrier in a Fischer-Tropsch synthesis slurry reactor system is periodically or continually separated and subjected to cracking and isomerization in the presence of suitable catalysts. The treated carrier is returned to the reactor system and the accumulation of high viscosity paraffin in the reactor slurry is minimized. Suitable catalysts include a mixture of cracking and isomerization catalysts.

Abstract: Hydrocarbon feedstocks such as distillate fuel oils and gas oils are dewaxed by isomerizing the waxy components over a zeolite beta catalyst. The process may be carried out in the presence or absence of added hydrogen. Preferred catalysts have a zeolite silica:alumina ratio over 100:1.

Abstract: A process for hydroisomerization of C.sub.4 -C.sub.7 paraffins with a nickel and/or cobalt synthetic mica-montmorillonite catalyst which has been pretreated with hydrogen at a temperature of at least 400.degree. C.

Abstract: Catalysts for the isomerization of n-paraffins are prepared by treating mordenite with an acid solution comprising Na- or K-ions and thereafter with a solution of an NH.sub.4 -compound, mixing the thus treated mordenite with an inert binder material on which a Group VIII noble metal has been deposited and finally shaping the resulting mixture under high pressure.

Abstract: Hydrocarbon conversion processes with crystalline silicates surrounded by an alumina containing isostructural shell are claimed.

Abstract: A process is provided for effecting hydroisomerization of a C.sub.4 -C.sub.8 paraffin by contacting the same under hydroisomerization conditions with a catalyst comprising a porous crystalline zeolite characterized by a silica/aluminum mole ratio of greater than 12 and a constraint index within the approximate range of 1 to 12, which zeolite has undergone controlled pretreatment by contact with water to enhance the acid activity thereof, expressed as alpha, to greater than about 300. The catalyst also comprises, intimately combined therewith, a minor proportion of a Group VIII metal.

Abstract: A new porous zeolite, a method of making same and the use thereof in catalytic conversion of organic compounds. The new product has a composition, expressed in terms of moles of anhydrous oxides per 100 moles of silica as follows:(0-2.5)M.sub.2/n O:(0- 2.5)Al.sub.2 O.sub.3 :(100)SiO.sub.2wherein M is at least one cation having a valence n and wherein the zeolite is characterized by the distinctive X-ray powder diffraction pattern as shown in Table 1 herein. The new zeolite is prepared from a reaction mixture comprising a source of silica, a source of organic compounds of Group VB, alkali metal cations, water and with or without a source of alumina.

Abstract: Dewaxed lube base stock oil which forms a wax haze on storage at a temperature above its cloud point is treated by contacting the oil and hydrogen with a zeolite catalyst such as ZSM-5 to eliminate the wax-haze formation. The method may be used to reclaim wax-contaminated lube base stock oils and other wax-contaminated hydrocarbon oils.

Abstract: An amorphous aluminosilicate sol with uniform size particles and a porous amorphous aluminosilicate powder are useful as catalyst in petroleum cracking. Water is removed from the sol without gelling so that the particles become uniformly packed into aggregates having pores of substantially uniform size and coating said powder with a surface layer 0 to 15% by weight of a metal or metal oxide, said powder having a specific surface area of 30 to 750 m.sup.2 /g, a bulk density of 0.5 g/cc or more and substantially uniform size pore diameters of from 20 A to 250 A, with pore diameters of 20 A to 45 A having a uniformity such that at least 90% of the pore volume is made up of pores of from 0.6D to 1.4D and pore diameters of 45 A to 250 A having a uniformity such that at least 80% of the pore volume is made up of pores of from 0.6D to 1.4D, where D is the median pore diameter.

Abstract: A new crystalline zeolite, designated ZSM-43, a method of making same and the use thereof in catalytic conversion of organic compounds is the subject of this application. The new zeolite has a composition, in the anhydrous state, expressed in terms of mole ratios of oxides, as follows:(0.6 to 2.1)M.sub.2/n O:Al.sub.2 O.sub.3 :xSiO.sub.2wherein M is at least one cation having a valence n and x is at least 5, and is characterized by a specified X-ray powder diffraction pattern.

Abstract: Isomerization process for petroleum light hydrocarbons with a boiling point within the range of from about 100.degree. F. (38.degree. C.) to about 210.degree. F. (99.degree. C.) wherein said process comprises contacting said hydrocarbons with a catalyst consisting essentially of an ultrastable, large pore crystalline zeolite aluminosilicate material containing less than 1 (wt)% alkali metal and characterized by well-defined hydroxyl infra-red bands and a maximum unit cubic cell dimension of 24.55 A and a metal component selected from the metals, oxides or sulfides of the Group VIII elements of the Periodic Table, under suitable isomerization conditions.

Abstract: Ammonia exchanged large port mordenite, which is subsequently mildly acid leached, and calcined, in which at least 95% of the exchangeable sodium has been removed and having from 0.38 to 0.8 milliequivalents of acid sites at least as strong as 48% sulfuric acid per gram (as measured by titration with butylamine, and employing dicinnamalacetone indicator) has been found to be highly active hydrocarbon isomerization catalyst. Incorporation of noble metal, e.g. palladium, on the catalyst improves the selectivity for isomerization of normal pentane to isopentane for highly active catalysts at high conversion rates.

Abstract: A process for virtually complete isomerization of the normal paraffin hydrocarbons contained in a feed stream consisting essentially of mixed normal and non-normal hydrocarbons, wherein the feedstock is first passed through an isomerization reactor and the hydrocarbons in the effluent from the reactor are passed through an adsorption section wherein the normals are adsorbed and the non-normals passed out of the system as an isomerate product. The fresh feed is controllably flow blended with the variable desorption effluent from the adsorber beds containing desorption normals and hydrogen purge gas in order to provide a constant flow of combined feed to the isomerization reactor.

Abstract: Low-octane C.sub.5 -C.sub.6 gasoline pool mixtures or components are upgraded into improved-octane gasoline blendstock by (1) catalytically converting a minor yet significant portion of the C.sub.6 -fraction into a relatively high-octane stock using a unique crystalline aluminosilica zeolite catalyst, (2) isomerizing the C.sub.5 -fraction plus the remainder of the C.sub.6 -fraction, and (3) blending the converted C.sub.6 -portion with the C.sub.5 -C.sub.6 isomerizate.