Abstract: There is provided a method for reducing the pour point of an alkyl aromatic lube base stock by hydroisomerizing alkyl side groups on alkyl aromatic compounds. The alkyl aromatic, compounds may be alkylated naphthalenes. The hydroisomerization reaction may take place over a catalyst comprising zeolite beta and platinum.

Abstract: A method is described for purifying an ultra-large pore crystalline material by contact with an aqueous solution having a hydroxyl concentration sufficient to solubilize an impurity phase but not the crystalline material. The purified crystalline material is also described, as is a hydrocarbon conversion process over the purified crystalline material.

Abstract: A process for the reforming of hydrocarbons is improved by the use of an enhanced nucleate boiling surface in a selected portion of the feed effluent heat exchanger. In a vertical type heat exchanger where the reforming feedstream enters at a lower end of the heat exchanger and is at least partially vaporized in the heat exchanger by contact with a reforming effluent stream that enters an upper end of the heat exchanger and is at least partially condensed therein, an enhanced nucleate boiling surface is formed on the heat exchange surface that is in contact with the entering liquid phase portion of the stream feed. The enhanced nucleate boiling surface increases the amount of condensing that takes place on the opposite side of the heat exchange surface in a boiling-condensing zone.

Abstract: Conversion of benzene to heavier aromatics by contact with alkyl polynucleararomatics, preferably FCC heavy cycle oil, in the presence of an alkylation/transalkylation catalyst is disclosed. Efficient conversion of relatively dilute benzene in reformate is possible. Use of alkyl polynucleararomatics as a source of alkyl groups, with reduced use of monocyclic alkyl aromatics, permits robust reaction conditions to be used without a net formation of benzene by dealkylation. The process preferably uses a solid zeolite based acidic catalyst disposed in a fixed, moving or fluid bed reactor. Preferred catalysts comprise MCM-22 or ZSM-5.

Abstract: A crystalline material having, in the dehydrated form, the empirical formula:m(M.sub.2/a O):X.sub.z O.sub.xz/2 :.sub.y YO.sub.2 (I)in which m is 0.5 to 1.5; M is a cation of valency a; X is a metal of valency x, selected from aluminium, boron, gallium, zinc, iron and titanium; z is 2 when x is an odd number, and z is 1 when x is an even number; y is at least 5; and Y is silicon or germanium; and having, in the calcined hydrogen form, an X-ray diffraction pattern including significant peaks substantially as shown in Table I herein. The material has been designated SUZ-2, and is used in the conversion of hydrocarbons or oxygenates.

Abstract: A process for reforming a hydrocarbon fraction having a limited proportion of C.sub.9 + hydrocarbons. A hydrocarbon fraction is separated into a light fraction and a heavy fraction, the light fraction containing less than 10% by volume of C.sub.9 + hydrocarbon. The light fraction is reformed in the presence of a monofunctional catalyst, and the heavy fraction is reformed in the presence of a bifunctional catalyst.

Abstract: This invention relates to acid catalysis, e.g. cracking, of organic compound feedstock, e.g. hydrocarbons, over catalyst material treated in a special way for increasing the acid catalytic activity thereof. In particular, a novel catalyst activation process is followed to enhance the alpha value of high-silica zeolite catalyst by contact with an ammoniacal solution of ammonium hydroxide and an alkali metal aluminate under appropriate conditions of time, temperature of pH.

Abstract: There is provided a catalytic composition which comprises a mixture of a crystalline chromosilicate and an oxide of chromium, said catalytic composition providing a specific X-ray diffraction pattern and having the following composition in terms of mole ratios of oxides:0.9.+-.0.2 M.sub.2/n O:Cr.sub.2 O.sub.3 :YSiO.sub.2 :ZH.sub.2 O,wherein M is at least one cation having a valence of n, Y is a value within the range of about 4 to about 500, and Z is a value within the range of about 0 to about 160. There is also provided a method for preparing such a catalytic composition.There is provided a process for the conversion of a hydrocarbon stream which comprises contacting said stream at conversion conditions with the above catalytic composition. In addition, there is provided a process for the isomerization of a xylene feed which comprises contacting said feed at isomerization conditions with the above catalytic composition.

Abstract: A novel catalytic absorbent composition is prepared with a synthetic copper or silver carbonate-containing material. The absorbent is useful for removing hydrogen sulfide and mercaptan sulfur from hydrocarbon oils, especially from feedstreams to a reformer.

Abstract: Process for the production of a liquid effluent comprising at least 75% of aromatic hydrocarbons from a naphtha feed charge of high sulfur, nitrogen or oxygen content; said process comprises two steps: (a) hydrotreatment of the charge to decrease its sulfur, nitrogen or oxygen content to selected values, and (b) dehydrogenation of the product of step (a) in the presence of a supported catalyst whose neutralization heat by ammonia adsorption is lower than about 40 joules per gram at 300 mm Hg.

Abstract: A process for preparing diesel fuel from coal-derived light fuel oils by alkylating said coal-derived light fuel oils with olefins and hydrotreating said alkylated product.

Abstract: Residual oils from steam-cracking or catalytic cracking, oils from coal liquefaction and oils from bituminous sands and shales are converted to gasoline by a process comprising the fractionation of the feed charge to a naphtha and a middle distillate: the naphtha, admixed with a gasoline cut "E", is hydrotreated and then dehydrogenated to gasoline; the middle distillate is hydrotreated and fractionated to gasoline and a heavier fraction, the heavier fraction is hydrocracked and fractionated, thus producing a gasoline cut which constitutes the above cut "E".

Abstract: A process for the catalytic conversion of aromatic fractions additionally containing variable proportions of C.sub.5 to C.sub.11 non-aromatic hydrocarbons, to obtain substantially pure benzene and hydrogen, by water dealkylation of the aromatic hydrocarbons and simultaneous reforming of the non-aromatic hydrocarbons, characterized in that aromatic fractions having boiling points which may be varied depending on the yield of hydrogen desired, are treated by steam at temperatures from 350.degree. C. to 600.degree. C., at a pressure of 1 to 80 bars, a volume of liquid passed per unit volume of catalyst of 0.1 to 10 and a water/hydrocarbon charge flow rate ratio of 0.2 to 4, in the presence of a dealkylation catalyst selected from at least one group VIII metal, on a support selected from a sieve L, a pretreated gamma alumina, and a mixed spinel (M.sub.x M'.sub.1-x) Al.sub.2 O.sub.4, M being a non-noble group VIII metal, and M' being selected from the group consisting of magnesium, manganese, and copper.

Abstract: A process for effecting an endothermic and an exothermic reaction, under conversion conditions, in a single reaction zone wherein ethane is endothermically converted to C.sub.3 + hydrocarbons, and wherein an unconverted portion of ethane is simultaneously exothermically hydrogenated to methane in the presence of a catalyst system comprising a crystalline aluminosilicate zeolite having a uniform structure characterized by pores, the major dimension of which is less than 6 Angstroms and ZSM-5 type aluminosilicate zeolite, containing a minor amount of Zn in combination with a Group VIII noble metal or a Group IB metal, the exothermic reaction providing sufficient heat to maintain the reaction zone at a temperature capable of sustaining the endothermic reaction.

Abstract: A process for treating a hydrocarbon composition containing both straight chain and non-straight chain hydrocarbons in which said hydrocarbon composition is separated into a straight chain hydrocarbon-rich fraction and a non-straight chain hydrocarbon-rich fraction, non-aromatics in said non-straight chain hydrocarbon-rich fraction are converted to aromatics, and at least a portion of the straight chain hydrocarbon-rich fraction is passed in combination with steam over a steam active catalyst comprising at least one Group VIII metal and a tin modified Group II metal aluminate under conditions such that aromatics are produced.

Abstract: A saturated hydrocarbon charge containing both butane and isobutane is subjected to selective hydrogenolysis in the presence of a catalyst comprising a specific carrier and 0.1 - 10 % b.w. of rhodium. Butane is thus selectively converted to ethane and propane, while isobutane is preserved or formed and can be recovered from the reaction product.

Abstract: Synthesis gas comprising a mixture of carbon monoxide and hydrogen is derived from fossil fuels and catalytically converted in a first reaction zone to a mixture of methanol and dimethyl ether which in turn is converted in a separate reaction zone in contact with a crystalline aluminosilicate zeolite catalyst having a silica to alumina ratio of at least about 12 and a constraint index of about 1 to 12, and preferably a crystal density in the hydrogen form of not substantially below about 1.6 grams per cubic centimeter to a product which is resolved into a high octane gasoline fraction, a light hydrocarbon gas fraction which may be liquefied and a hydrogen-rich gaseous by-product which is recycled to the conversion of fossil fuels to synthesis gas or may be otherwise used.

Abstract: This invention relates to a method of dehydrocyclizing aliphatic hydrocarbons to form corresponding aromatic hydrocarbons. According to the invention, a batch of aliphatic hydrocarbons, in the presence of hydrogen at a temperature of 430.degree. to 550.degree. C is passed over a catalyst consisting essentially of a type L zeolite having exchangeable cations of which at least 90% are alkali metal ions selected from the group consisting of ions of sodium, lithium, potassium, rubidium and caesium and containing at least one metal selected from the group which consists of metals of groups VIII of the periodic table of elements, tin and germanium, said metal or metals including at least one metal from group VIII of said periodic table having a dehydrogenating effect, so as to convert at least part of the batch into aromatic hydrocarbons. The aliphatic hydrocarbons preferably contain 6 - 10 carbon atoms.

Abstract: Alkanes are catalytically converted employing a catalyst comprising at least one alkaline earth oxide together with a promoting amount of manganese oxide and/or rhenium oxide. When the catalyst is treated with an oxygen-containing gas, such as air, prior to contacting the alkanes conversion by cracking is favored. When the catalyst is treated with hydrogen prior to contacting the alkanes dehydrocyclization is favored. A composition of matter is disclosed suitable for use as a catalyst for converting alkanes.

Abstract: High temperature chemical reaction processes utilizing fluid-wall reactors can be conducted in fluid-wall reactors by a process which includes the steps of (a) generating a shell of a refractory material which reflects radiation, the volume enclosed by the shell constituting a black body cavity; (b) generating within the black body cavity an annular envelope of an inert fluid which is substantially transparent to radiation, the envelope having substantial axial length and the interior of the envelope defining a reaction chamber; (c) passing at least one reactant into the black body cavity and through the reaction chamber along a predetermined path substantially coincident with the longitudinal axis of the envelope, the reactants being confined within the reaction chamber; and (d) directing high intensity radiant energy into the reaction chamber to coincide with at least a portion of the predetermined path of the reactants, sufficient radiant energy being absorbed within the reaction chamber to raise the tempe

Abstract: A method for effecting chemical reactions of aliphatic hetero compounds comprising alcohols, halides mercaptans, sulfides, amines, ethers and carbonyl compounds with crystalline zeolite catalysts of the ZSM-5 type in a fluid catalyst operation is described.

Abstract: The product of Fischer-Tropsch Synthesis is separated to recover a C.sub.5 -400.degree. F liquid fraction which is thereafter contacted with a ZSM-5 type zeolite in the presence of added hydrogen under conditions of elevated temperature and pressure so as to obtain gasoline of a higher octane rating.

Abstract: The conversion of methanol to gasoline boiling hydrocarbons in a thermally balanced operation with a special group of zeolite catalysts having a constraint index of 1 to 12, a silica to alumina ratio of at least about 12 and a crystal density of not substantially lower than about 1.6 grams per cubic centimeter is described. The steady state operation of the process is improved by feeding methanol preheated to a selected temperature proximate to its boiling point so that the heat required thereafter to vaporize the feed and to raise its temperature to conversion temperature is substantially equal to the exothermicity of the conversion itself.

Abstract: High temperature chemical reaction processes utilizing fluid-wall reactors can be conducted in fluid-wall reactors by a process which includes the steps of (1) generating a shell of a refractory material which reflects radiation, the volume enclosed by the shell constituting a black body cavity; (2) generating within the black body cavity an annular envelope of an inert fluid which is substantially transparent to radiation, the envelope having substantial axial length and the interior of the envelope defining a reaction chamber; (3) passing at least one reactant into the black body cavity and through the reaction chamber along a predetermined path substantially coincident with the longitudinal axis of the envelope, the reactants being confined within the reaction chamber; and (4) directing high intensity radiant energy into the reaction chamber to coincide with at least a portion of the predetermined path of the reactants, sufficient radiant energy being absorbed within the reaction chamber to raise the tempe

Abstract: Method for the dehydrogenation or dehydrocyclization of paraffins, for dehydrogenation of olefins with from 2 to 20 carbon atoms, and for hydrodealkylation of naphthalene homologs at temperatures ranging from 300.degree. to 650.degree. C a catalyst comprising a palladium base alloy containing rhenium, tungsten or a combination of tungsten and ruthenium.The method can find application in the production of monomers, such as isoprene, for synthetic materials, pharmaceuticals, in processing petroleum hydrocarbons and natural gas.

Abstract: This invention relates to a process for producing aromatic hydrocarbons, particularly xylenes, by dehydrocyclodimerization of a C.sub.4 feedstock in the presence of a catalyst comprising alumina promoted by zinc or a zinc compound.

Abstract: Reacting mixtures of difficultly convertible aliphatic organic oxygenate compounds, such as short chain aldehydes, carboxylic acids or carbohydrates with easily convertible aliphatic alcohols, ethers, acetals and analogs thereof over a crystalline aluminosilicate zeolite having a silica to alumina ratio of at least about 12 and a constraint index of about 1 to 12, at elevated temperatures, 0.5 to 50 LHSV and 1 to 200 atmospheres to produce a product comprising water, full range highly aromatic hydrocarbon gasoline and light aliphatic hydrocarbon gases having an improved production of C.sub.6 and C.sub.10 monocyclic aromatic hydrocarbons.

Abstract: In the dewaxing of gas oils for the purpose of pour point reduction by catalytic hydrodewaxing using a catalyst comprising a crystalline aluminosilicate zeolite having a high silica to alumina ratio of at least 12 and a constraint index of about 1 to 12, carrying out the process at elevated temperature and pressure, including providing a hydrogen atmosphere in a preferred process configuration, the improvement of using a catalyst comprising said zeolite in microcrystalline from having a maximum crystal size of about 0.05 microns (M); and of operating the process at low pressures of up to about 500 psig, whereby not only is the catalytic activity increased but the catalyst aging rate is decreased and the product distribution is varied such that the process does not consume hydrogen but rather produces hydrogen or is at least neutral in this respect.

Abstract: Foots oil, the by-product left when high quality wax is recovered by a solvent dewaxing process, is usually used as cracker feed stock. There is disclosed a method of converting it to higher quality lubricant base stock by subjecting such to catalytic hydroprocessing utilizing a ZSM-5 or similarly behaving zeolite catalyst under hydrogen pressure followed by distillation of the product to remove light products such as naphtha, LPG and No. 2 fuel oil therefrom.

Abstract: A method for the operation of a hydrodewaxing unit wherein a petroleum distillate is separated into two streams, one having a pour point of above about 30.degree.F, and the other having a pour point of less than about 30.degree.F., the 30.degree.F plus pour point fraction is treated in a hydrodewaxing unit with a ZSM-5 type catalyst under hydroprocessing conditions while the 30.degree.F. minus pour point portion is untreated and combined with the hydrodewaxed product. The process yields a net production of hydrogen, and exhibits excellent catalyst aging characteristics.

Abstract: The octane number of a hydrocarbon fraction boiling below 425.degree.F is improved by a cracking-isomerization procedure. The C.sub.5 + portion of the resulting product may be used as a motor fuel or as a blending component for motor fuels.

Abstract: A process for producing high octane low lead content or unleaded gasoline from a hydrocarbon feedstock by hydrocracking the hydrocarbon feedstock; fractionating the hydrocracking effluent in a fractionation zone, thereby obtaining a stream rich in singly branched hexanes; isomerizing the singly branched hexanes to doubly branched hexanes in an isomerization zone operated at a reaction temperature below 300.degree.F.; and combining the doubly branched hexanes with C.sub.7 + hydrocarbons derived from the hydrocracking effluent, thereby obtaining a high octane gasoline or gasoline blending stock. In a preferred embodiment, the isomerization zone effluent is fractionated to give a cyclohexane-rich stream which stream is catalytically reformed and then the reformate is combined with the doubly branched hexanes from the isomerization zone.