Abstract: A method is described for rendering total liquid product hydroisomerates daylight stable and improving their oxidation stability, which method involves treating the hydroisomerate total liquid product with a Group VIII metal on refractory metal oxide catalyst or Group VIII metal on halogenated refractory metal oxide catalyst under mild conditions, which conditions are a temperature in the range of 170.degree. to 270.degree. C., a pressure in the range of 300 to 1500 psi H.sub.2, 0.25 to 10 v/v/hr and 500 to 10,000 SCF/B,H.sub.2.

Abstract: A novel zeolite hydrocracking catalyst which contains NH.sub.4.sup.+ sites, at ambient temperatures, and surface sites constituted of a chemisorbed silica-containing species, and process for producing said catalyst. The process for preparation of the catalyst includes a series of steps: an initial step wherein an acid zeolite, or acid zeolite hydrocracking catalyst, is treated with an agent, e.g., a nitrogen-containing compound, suitably ammonia, to convert the H.sup.+ sites throughout said zeolite framework to NH.sub.4.sup.+ sites, and a subsequent post treatment of said NH.sub.4.sup.+ zeolite with an organosilane to silylate, modify and form on the surface of said zeolite a chemisorbed silica species, e.g., --O--Si(CH.sub.3).sub.3. The surface silylated catalyst is useful for the production of high octane gasoline. When employed at elevated temperatures in a hydrocracking operation the catalyst will evolve ammonia and convert to a surface silylated H.sup.

Abstract: Fischer-Tropsch wax is converted to a lubricating oil having a high viscosity index and a low pour point by first hydrotreating the wax under relatively severe conditions and thereafter hydroisomerizing the hydrotreated wax in the presence of hydrogen on a particular fluorided Group VIII metal-on-alumina catalyst. The hydroisomerate is then dewaxed to produce a premium lubricating oil base stock.

Abstract: The present invention is directed to a process for the catalytic isomerization of waxes to liquid products, particularly to the production of high yields of liquid products boiling in the 370.degree. C..sup.+ range suitable for use as lube oil base stocks or blending stocks, said process employing as the catalyst a material made by depositing a hydrogenation metal component on a refractory metal oxide base, preferably alumina, fluoriding said metal loaded base using aqueous HF and subsequently crushing the fluorided metal loaded base to produce a sized material of 1/32 inch and less its largest cross-sectional dimension. Alternately the catalyst can be made by depositing a hydrogenation metal component on a refractory metal oxide base of 1/32 inch and less across its largest cross-sectional dimension and subsequently fluoriding said sized material using aqueous HF. In either case the catalyst is activated before being used by heating in a hydrogen atmosphere to from 350.degree. C. to 500.degree. C.

Abstract: A process is disclosed for the production of lube oil base stocks or blending stocks by the isomerization of waxes over isomerization catalysts containing a hydrogenating metal component on a fluorided alumina or material containing alumina.The present invention is also directed to a wax isomerization process which process employs a catalyst prepared by a process involving depositing a hydrogenation metal on alumina or material containing alumina support, calcining said metal loaded support and fluoriding said metal loaded support.

Abstract: A fluorided platinum-on-alumina catalyst for wax isomerization wherein the platinum is substantially uniformly distributed throughout the catalyst in the form of relatively small crystallites, of the total fluoride present in the catalyst very little is located on the outer surface of the catalyst and a significant concentration of the fluoride within the catalyst is present as aluminum fluoride hydroxide hydrate. The catalyst is prepared by contacting a platinum-on-alumina with a solution having a relatively high concentration of fluoride and drying the fluorided platinum-on-alumina catalyst at temperatures not in excess of 650.degree. F.

Abstract: A process for selectively producing middle distillate fuel products from paraffin waxes such as slack wax and Fischer-Tropsch wax by hydroisomerizing the wax to convert 60-95 weight percent per pass of the 700.degree. F..sup.+ fraction contained in said wax. The catalyst employed is a fluorided Group VIII metal-on-alumina catalyst where the fluoride within the catalyst is present predominately as aluminum fluoride hydroxide hydrate. The preferred Group VIII metal is platinum.

Abstract: An improved wax isomerization catalyst is described which is a hydrogenation metal on halogenated refractory metal oxide support catalyst characterized in that the catalyst is prepared by depositing the hydrogenation metal on the refractory metal oxide support followed by fluoriding using a low pH fluorine source such as aqueous HF. Thereafter the catalyst is crushed to expose inner surfaces, the crushed catalyst being sieved to remove fines, the catalyst charge having an average particle diameter of 1/32 inch and smaller across the longest continuous cross sectional dimension, preferably between 1/64 to 1/32". Alternatively, the catalyst is made by depositing a hydrogenation metal on a refractory metal support, crushing the material to a particle size of 1/32 inch and smaller across the longest continuous cross-sectional dimension and fluoriding said material using acidic fluorine source such as HF. Following sizing the sized catalyst is activated by heating in a hydrogen atmosphere.

Abstract: A process for the conversion of a feed rich in fused two-ring aromatic and fused two-ring hydroaromatic hydrocarbons, notably light cat cycle oil, furnance oils, coal liquids, tar sands liquids, shale oil liquids, and the like to high density jet fuels. Sulfur or nitrogen, or both are removed from said feed and a hydrodesulfurized/hydrodenitrogenated liquid product separated therefrom is hydrotreated in a second stage over a highly active fluorided Group VIII metal-on-alumina catalyst at conditions sufficient to selectively hydrogenate and saturate the fused two-ring aromatics and/or partially saturated fused two-ring hydroaromatics at high selectivity to naphthenes without any significant conversion thereof to lower molecular weight hydrocarbons. High density jet fuels having an API gravity ranging from about 25 to about 35, with a total aromatic content well below about 50 percent, preferably 5 percent to about 30 percent, are produced.

Abstract: A process for producing a pumpable syncrude from a Fischer-Tropsch wax by fractionating the wax into relatively low boiling fraction containing oxygenate compounds and a relatively high boiling fraction which is substantially free of oxygenate compounds and thereafter isomerizing/hydrocracking the low boiling fraction in the presence of hydrogen and a fluorided Group VIII metal-on-alumina catalyst. The preferred Group VIII metal is platinum.The pumpable syncrude is thereafter fractionated to produce a low boiling fraction which is thereafter isomerized/hydrocracked in the presence of hydrogen and a fluorided Group VIII metal-on-alumina catalyst to produce upgraded middle distillate fuel products. The preferred catalyst for middle distillate production is a fluorided platinum-on-alumina catalyst where a major portion of the fluoride within the catalyst is present as aluminum fluoride hydroxide hydrate.

Abstract: A process for improving the color and oxidation stability of feed characterized as an admixture of liquid hydrocarbon compounds, inclusive of fused multi-ring aromatic and hydroaromatic hydrocarbons. This feed, which boils within a range of from about 224.degree. C. to about 538.degree. C. and contains moderate to high concentrations of organic sulfur and organic nitrogen compounds, is (1) hydrotreated over a hydrotreating catalyst at hydrotreating conditions, or (2) hydrotreated over a hydrotreating catalyst at hydrotreating conditions and the high boiling product therefrom hydrocracked over a hydrocracking catalyst at hydrocracking conditions, to obtain a low sulfur, low nitrogen product which is contacted as a feed in the presence of hydrogen, over a catalyst comprised of elemental iron and one or more alkali or alkaline-earth metals components at hydrogen partial pressure and temperature sufficient to improve product color, or stablize the product against light and oxygen degradation, or both.

Abstract: A process for the conversion of fused two-ring aromatic and fused two-ring hydroaromatic hydrocarbons into lower boiling aromatics, particularly alkylbenzenes of higher octane values. Such feeds are contacted in the presence of hydrogen over an iron catalyst at temperature sufficient to selectively hydrogenate and hydrocrack said fused two-ring aromatic hydrocarbon compound, or fused two-ring hydroaromatic hydrocarbon compounds, or both, to produce lower molecular weight, higher octane components suitable for direct blending with gasoline.

Abstract: A process for hydrocracking a hydrocarbon feedstock having a propensity to form polynuclear aromatic hydrocarbon compounds to suppress fouling the processing unit. The hydrocracking method includes contacting the hydrocarbon feedstock with a crystalline zeolite hydrocracking catalyst, contacting at least a portion of the resulting unconverted hydrocarbon oil containing polynuclear aromatic compounds with an iron catalyst in the presence of hydrogen to hydrogenate and hydrocrack the polynuclear aromatic hydrocarbon compounds, and recycling unconverted hydrocarbon oil having a reduced concentration of polynuclear aromatic compounds to the hydrocracking zone.

Abstract: A process wherein a feed comprising an admixture of liquid hydrocarbon compounds which includes a polynuclear aromatic hydrocarbon compound, or compounds (PNA's) is contacted in the presence of hydrogen over an iron catalyst at temperature sufficient to selectively hydrogenate and hydrocrack, or destroy the PNA's of the admixture without excessively hydrogenating and hydrocracking the non-PNA's of said feed. The process is particularly applicable for the removal of PNA's from reformates, processed naphthas, and other hydroprocessed streams or the like to achieve a lower and more favorable distribution of PNA's in a motor gasoline pool, and further to remove PNA's from prime fuels and heavier hydrocarbon mixtures.

Abstract: A process for the production of jet fuels, diesel fuels, multi-purpose fuels meeting the specifications for both high grade jet fuels and diesel fuels, and high quality blending components useful for the production of such fuels; and the compositions produced thereby. In accordance with the process, a multi-reactor system, inclusive of a first reactor and a second reactor are connected through a first distillation column which separates the product of the first reactor into two or more fractions to provide a heavy feed fraction which is charged to the second reactor, wherein the heavy feed is hydroselectively cracked. The product from the second reactor is fractionated to produce high quality jet and diesel fuels, multi-purpose jet and diesel fuels, or provide a major blending component for the production of such fuels, or fuel components.

Abstract: A catalyst support is prepared by grinding a calcined alumina to a powder, compacting the powder at an elevated pressure, recracking the compressed powder to a predetermined size particle and acid extracting the particle. The support can be composited with catalytic components such as hydrogenation components and/or zeolites and used in a variety of hydrocarbon treating processes, such as hydrorefining, hydrodesulfurization, hydroconversion, reforming, and catalytic cracking.

Abstract: A process for the production of low sulfur, low nitrogen fuels at low hydrogen consumption by splitting a feed into two components, a high boiling component, suitably a 1050.degree. F.+ fraction, and a low boiling component, suitably a 1050.degree. F.- fraction, and processing the two different components over two different types of catalysts, at different severities. Suitably, on the one hand, the high boiling component is treated over a large pore metal hydrogenation catalyst at severity sufficient to convert at least 30 percent, preferably at least 50 percent of the feed, based on the weight of the feed, to a 1050.degree. F.- product. The 1050.degree. F.- product from the conversion over the large pore metal hydrogenation catalyst is then blended with the low boiling component split from the original feed, and the blended low boiling material is then treated at low severity over a small pore metal hydrogenation catalyst to hydrodesulfurize and hydrodenitrogenate said low boiling components.

Abstract: A hydrodesulfurization process (and catalyst) wherein a sulfur-containing hydrocarbon feed is contacted, in the presence of hydrogen, with a catalyst having greater than 50 percent of its total pore volume of absolute diameter ranging from about 70A to about 160A. Preferably, the total pore volume of the catalyst contains greater than 70 percent of its total pore volume within the 70A to 160A pore diameter range, and more preferably greater than 90 percent of its total pore volume is within the 70A to 160A pore diameter range, with pore diameters below 70A and above 160A being minimized. The pore volume of such catalysts range between about 0.3 cc/g and 1.0 cc/g (B.E.T.), and preferably from about 0.4 cc/g to about 0.8 cc/g. The surface area of such catalysts range between about 150 m.sup.2 /g and 450 m.sup.2 /g, preferably from about 200 m.sup.2 /g to about 400 m.sup.2 /g.

Abstract: This invention relates to novel catalysts, of two distinct types, useful for the catalytic hydroconversion of the 1050.degree. F.+ hydrocarbon materials contained in heavy crudes and residua such that the resulting product will be suitable for further processing in conventional refinery operations allowing maximization of clean liquid products. Catalysts, which include Group VIB and Group VIII metals, preferably in admixture, and preferably including a Group IVA metal, notably germanium, having certain critical ranges of physical characteristics inclusive of large uniform pore sizes, are used for the conversion, these having been shown to possess improved catalytic activity and selectively for the hydroconversion of the 1050.degree. F.+ materials of the heavy feeds and residua. Novel methods are described for the preparation of such catalysts, as well as for the use of such catalysts. One of the catalysts, i.e.

Abstract: This invention relates to novel catalysts, of two distinct types, useful for the catalytic hydroconversion of the 1050.degree. F.+ hydrocarbon material contained in heavy crudes and residua such that the resulting product will be suitable for further processing in conventional refinery operations allowing maximization of clean liquid products. Catalysts, which include Group VIB and Group VIII metals, preferably in admixture, and preferably including a Group IVA metal, notably germanium, having certain critical ranges of physical characteristics inclusive of large uniform pore sizes, are used for the conversion, these having been shown to possess improved catalytic activity and selectivity for the hydroconversion of the 1050.degree. F.+ materials of the heavy feeds and residua. Novel methods are described for the preparation of such catalysts, as well as for use of such catalysts. One of the catalysts, i.e.