Abstract: A strontium colloid system is introduced into a hydrocarbon conversion process to suppress the harmful effects of one or more metal contaminants in the hydrocarbon feedstock on the active component(s) of the catalyst used in said process. The strontium compound in the colloid system reacts with or traps the metal contaminants before they contact the active component(s) of said catalyst, thereby reducing catalyst deactivation, coke make and hydrogen production relative to that obtained had said compound been introduced into the process in non-colloid form. In a preferred embodiment, the strontium colloid system is introduced into the reaction zone of said process and, preferably, with at least a portion of the hydrocarbon feedstock to said process.

Abstract: A hydrocarbon conversion catalyst containing a Group VIB metal on a porous refractory oxide is prepared by impregnating support particles with a solution containing Group VIB metal components and citric acid, followed by drying and calcining. The catalyst is useful for promoting a number of hydrocarbon conversion reactions, particularly those involving hydrogenative desulfurization, demetallization and denitrogenation.

Abstract: A cobalt-molybdenum catalyst and a method for preparing same, said catalyst useful for the hydrodesulfurization (HDS) and hydrodenitrogenation (HDN) of distillates of petroleum. The catalyst is supported by aluminum phosphate or an aluminum borate. In a preferred embodiment the catalyst has a low cobalt content, between 0.5% and 2.0% by weight calculated as CoO, and a molybdenum content of between 10% and 20% by weight, calculated as MoO.sub.3. The phosphorus or boron compounds added to the aluminum before the impregnation of the active metals prevents the formation of undesirable compounds of the CoAl.sub.2 O.sub.4 type, which is inactive in HDS. It is for that reason that the catalyst has a formulation with 70% less cobalt than the previous state-of-the-art catalysts. Very small crystals, highly dispersed on the surface of the catalyst, whose formula is CoMoO.sub.4, are responsible for the stability and the high level of activity in HDS and HDN which results.

Abstract: This invention discloses processes for the treatment of coal and coal derivatives in order to remove contaminates to produce a high purity coal product. The processes generally comprise a sequential acid leaching in which a hydrofluoric acid leach is followed by a hydrochloric acid leach. The pyrite and other heavy metals from the coal are removed by physical separation, either gravity or magnetic separation. The leached coal is then treated either by a washing and drying step or by a heat treatment to remove volatile halides. The HF acid and the HCl acid leachates are recovered for regeneration of the respective leachates and are recycled for use in the leaching steps. In additional processing, the coal may be pre-treated by a mild HCl acid leach and by pre-drying or physical beneficiation of the coal feedstock.

Abstract: A hydrocarbon conversion catalyst containing a Group VIB metal on a porous refractory oxide is prepared by impregnating support particles with a solution containing Group VIB metal components and citric acid, followed by drying and calcining. The catalyst is useful for promoting a number of hydrocarbon conversion reactions, particularly those involving hydrogenative desulfurization, demetallization and denitrogenation.

Abstract: A process for the removal of H.sub.2 S from sour gaseous streams is disclosed in which the sour gaseous stream is contacted with a solution containing solubilized iron chelates of a specified organic acid or acids. The contacting is carried out in first and second contacting zones, the first being a gas-solution mixture formation zone and the second comprising a plurality of contacting sections adapted to provide reaction of the H.sub.2 S in the sour gaseous stream with the iron in the contacting solution without plugging due to deposition of sulfur.

Abstract: Procedure for hydrogenation of coal by means of liquid phase and fixed-bed catalyst hydrogenation whereby the head products of the high-temperature separator are led directly, and together with the entire high-pressure circuit gas, over a reactor with a rigidly installed catalyst; are separated from the exhaust products of this reactor by partial condensation of the cycle oil required for producing the coal paste and withdrawn from an intermediate separator; and are led again, together with the entire high-pressure circuit gas, over an additional reactor with a fixed-bed catalyst.

Abstract: We disclose a catalyst system which is capable of removing calcium from a hydrocarbon feed having at least 1 ppm oil-soluble calcium. It comprises a catalyst layer characterized as a fixed bed of catalyst particles, a high volume percent of their pore volume in the form of macropores above 1000 .ANG. in diameter, low surface area, and low hydrogenation activity. We also disclose a process of using the system.

Abstract: A process is disclosed for the thermal cracking of heavy oil containing nonvaporizable, high-molecular weight hydrocarbone in the presence of steam in one or more thermal cracking tubes or ducts, which process is characterized in that a fluid comprising steam and heavy oil is flowed through a thermal cracking tube such that thermal cracking is carried out under the following conditions:(a) temperature of the fluid in the thermal cracking tube: 800.degree. to 1100.degree. C.(b) pressure of the fluid in the thermal cracking tube: 0 to 50 kg/cm.sup.2 G(c) flow rate or velocity of fluid through the thermal cracking tube: 10 to 100 m/sec, and(d) residence time of the fluid in the thermal cracking tube: at least 0.2 seconds.

Abstract: A process for the hydrogenolysis of a coal liquid bottom containing benzene-insoluble components and having a boiling point of at least 420.degree. C., which comprises:(a) hydrogenating the coal liquid bottom at a temperature of not higher than 350.degree. C. in the presence of a catalyst comprising an alkali metal and/or an alkaline earth metal and a metal of Group VI A of the Periodic Table to reduce the content of the benzene-insoluble components in the fraction having a boiling point of at least 420.degree. C., to a level of not higher than 10% by weight, and then(b) subjecting the product to hydrogenolysis at a temperature of higher than 350.degree. C. and not higher than 450.degree. C. in the presence of a catalyst comprising a metal of Group VI A of the Periodic Table.

Abstract: Pyrolysis tars are upgraded by hydrotreatment thereof in the presence of an acidic catalyst. The treated pyrolysis tars are used to produce premium cokes useful in the production of graphite electrodes.

Abstract: High efficiency scrubbing of SO.sub.2 from stack gases by contact with a sodium based liquor is achieved by adjusting the pH of the scrubber liquor supplied to be in the range of 7.00 to 8.00; and a source of such liquor in a dual alkali system is disclosed in which a mixture of slaked lime and limestone is reacted with spent liquor in two stages one of which is at pH above 8.00, the other of which is at a pH below about 6.8 and the pH of the resulting regenerated liquor is adjusted to the desired pH range.

Abstract: A continuous multi-stage catalytic process for converting ethene-rich lower olefinic feedstock to heavier liquid hydrocarbon product, comprising the steps ofcontacting ethene-rich feedstock at elevated temperature and moderate pressure in a primary stage reaction zone with a first catalyst comprising shape selective medium pore zeolite to convert at least a portion of the lower olefinic components to intermediate olefinic hydrocarbons;cooling primary stage reaction effluent by introducing a stream of cold water sufficient to reduce the primary stage effluent to second stage reaction temperature; andcontacting unreacted ethene and at least a portion of the intermediate olefinic hydrocarbons from the primary stage with nickel-containing shape selective medium pore zeolite oligomerization component at elevated temperature to provide a heavier hydrocarbon effluent stream comprising gasoline and/or distillate range hydrocarbons.

Abstract: Methods and compositions are provided for the removal of rosin soldering flux and adhesive tape residues from printed circuit and/or wiring boards, and for testing the quality of curing of U.V.-cured soldermask on such boards. The compositions of the invention contain terpene compounds, preferably in combination with terpene emulsifying surfactants to facilitate removal by rinsing in water.

Abstract: Disclosed herein are catalyst compositions comprised of:(a) from about 15 to about 85 wt. % of crystallites selected from the group consisting of (i) crystallites of one or more transition metals and (ii) crystallites of reducible transition metal carbides and nitrides, and mixtures thereof, said transition metal being selected from those reducible metals from Groups IB, IIB, VIB, VIIB, and VIII of the Periodic Table of the Elements, wherein at least 80% of the crystallities have a diameter, d, between about 25 .ANG. and 500 .ANG. with the proviso that the crystallite size distribution of at least about 80% of these be expressed by the relationship 0.5D<d<2D where D is the median of the diameters of this 80%.(b) from about 15 to about 85 wt.

Abstract: Catalysts having as their active component sulfides of vanadium, molybdenum and tungsten are contacted with ammonia or with an amine which in aqueous solution has a basic ionization constant greater than that of ammonium hydroxide to suppress deactivation of the catalysts by exposure to the atmosphere.

Abstract: Heavy oils are simultaneously subjected to cracking and dewaxing in the absence of added hydrogen using a catalyst comprising Zeolite Beta and an X or Y or other faujasite zeolite. The process is able to effect a bulk conversion of the oil, while, at the same time, yielding a higher octane gasoline, increased yields of C.sub.3 and C.sub.4 olefins, and a low pour point distillate product.

Abstract: An aqueous solution of a heteropolysaccharide comprising glucose, galactose, pyruvic and succinic acid, is prepared by mixing a concentrate of said heteropolysaccharide with a saline aqueous medium containing from 12 to 30% w of at least one salt, and by shearing the mixture obtained.

Abstract: A catalyst consisting essentially of a nickel component, a molybdnemum component, a phosphorus component on a heterogeneous support containing alumina matrix is employed to mildly hydrocrack a hydrocarbon oil.

Abstract: A hydroprocessing catalyst contains nickel, phosphorus and about 19 to about 21.5 weight percent of molybdenum (MoO.sub.3) components on a porous refractory oxide. The catalyst has a narrow pore size distribution wherein at least 75 percent of the pore volume is in pores of diameter from about 50 to about 110 angstroms, at least 10 percent of the pore volume in pores of diameter less than 70 angstroms and at least 60 percent of the pore volume in pores of diameter within about 20 angstroms above or below the average pore diameter. The catalyst is employed to hydroprocess a hydrocarbon oil, especially those oils containing sulfur and nitrogen components.