Abstract: Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

Abstract: The present disclosure refers to systems and methods for efficiently converting a C1-C3 alkane such as natural gas to a liquid C2-C10 product and hydrogen. Generally, the process comprises flowing the C1-C3 alkane through a plurality of tubes within a vessel wherein the tubes house a catalyst for converting the C1-C3 alkane to the liquid C2-C10 product and hydrogen. The C1-C3 alkane is heated under suitable conditions to produce the liquid C2-C10 product and hydrogen. Advantageously, the C1-C3 alkane is heated by burning a fuel outside the tubes in fuel burning nozzles configured to transfer heat from the burning through the tubes.

Abstract: Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

Abstract: The present disclosure refers to systems and methods for efficiently converting a C1-C3 alkane such as natural gas to a liquid C2-C10 product and hydrogen. Generally, the process comprises flowing the C1-C3 alkane through a plurality of tubes within a vessel wherein the tubes house a catalyst for converting the C1-C3 alkane to the liquid C2-C10 product and hydrogen. The C1-C3 alkane is heated under suitable conditions to produce the liquid C2-C10 product and hydrogen. Advantageously, the C1-C3 alkane is heated by burning a fuel outside the tubes in fuel burning nozzles configured to transfer heat from the burning through the tubes.

Abstract: The present disclosure refers to systems, methods, and catalysts for conversion of a hydrocarbon to hydrogen. The catalyst typically comprises a matrix comprising fused silica, quartz, glass, a zeolite, Si3N4, SiC, SiCxOy wherein 4x+2y =4, SiOaNb wherein 2a+3b =4, BN, TiO2, ZrO2, Al2O3, CeO2, Nb2O5, La2O3, a perovskite, or any mixture thereof. A metal dopant is embedded in the matrix. The metal dopant comprises Fe, Ni, Co, Cu, Zn, Mn, or any mixture thereof.

Abstract: The present disclosure refers to systems and methods for efficiently converting a C1-C3 alkane such as natural gas to a liquid C2-C10 product and hydrogen. Generally, the process comprises flowing the C1-C3 alkane through a plurality of tubes within a vessel wherein the tubes house a catalyst for converting the C1-C3 alkane to the liquid C2-C10 product and hydrogen. The C1-C3 alkane is heated under suitable conditions to produce the liquid C2-C10 product and hydrogen. Advantageously, the C1-C3 alkane is heated by burning a fuel outside the tubes in fuel burning nozzles configured to transfer heat from the burning through the tubes.

Abstract: The present disclosure refers to systems and methods for producing hydrogen among other products. In some embodiments the methods comprise sequentially conducting a cracking step in a fixed bed mode and conducting a flowing step in a fluidized bed mode. Such sequential processes may result in a number of advantages including, for example, regenerating the catalyst during the fluidized bed mode in a manner such that beneficial heat is generated for use in the endothermic cracking step.

Abstract: Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

Abstract: An improved method for recovering metals from spent catalysts, particularly from spent slurry catalysts, is disclosed. The method and associated processes comprising the method are useful to recover spent catalyst metals used in the petroleum and chemical processing industries. The method generally involves a combination of a pyrometallurgical and a hydrometallurgical method and includes forming a potassium carbonate calcine of a KOH leach residue of the spent catalyst containing an insoluble Group VIIIB/Group VIB/Group VB metal compound combined with potassium carbonate, and extracting and recovering soluble Group VIB metal and soluble Group VB metal compounds from the potassium carbonate calcine.

Abstract: A layered catalyst reactor system and process for hydrotreatment of hydrocarbon feedstocks. The layered catalyst system reactors comprise vertical bed layers including a demetallization catalyst layer, multiple layers of supported hydrotreating catalyst layer, and multiple alternating layers of supported hydrocracking catalysts and self-supported hydrotreating catalysts. The arrangement of the catalyst layers mitigates the risk of temperature run-aways, with improvements in hydrotreatment performance.

Abstract: A layered catalyst reactor system and process for hydrotreatment of hydrocarbon feedstocks. The layered catalyst system reactors comprise vertical bed layers including a demetallization catalyst layer, multiple layers of supported hydrotreating catalyst layer, and multiple alternating layers of supported hydrocracking catalysts and self-supported hydrotreating catalysts. The arrangement of the catalyst layers mitigates the risk of temperature run-aways, with improvements in hydrotreatment performance.

Abstract: An improved method for recovering metals from spent catalysts, particularly from spent slurry catalysts, is disclosed. The method and associated processes comprising the method are useful to recover catalyst metals used in the petroleum and chemical processing industries. The method generally involves a pyrometallurgical method and a hydrometallurgical method and includes forming a soda ash calcine of a caustic leach residue of the spent catalyst containing an insoluble Group VIII/Group VIB/Group VB metal compound combined with soda ash, and extracting and recovering soluble Group VIB metal and soluble Group VB metal compounds from the soda ash calcine.

Abstract: Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

Abstract: A process is disclosed for opening naphthenic rings of naphthenic ring-containing compounds. Naphthene ring opening is achieved using a self-supported mixed metal sulfide catalyst comprising nickel sulfide, molybdenum sulfide, tungsten sulfide and an organic complexing agent. The catalyst is characterized as having a composition of metal components, in terms of molar ratios; as follows: 0.25?Ni/(Ni+Mo+W)?0.80; 0<Mo/(Ni+Mo+W)?0.25; 0.12?W/(Ni+Mo+W)?0.50; and 1.5?W/Mo?3.0.

Abstract: Disclosed herein is a process for preparing an isomeric mixture comprising a major amount of a para-branched mono-alkyl-substituted hydroxyaromatic compound.

Abstract: In a process for forming a bulk hydroprocessing catalyst by sulfiding a catalyst precursor made in a co-precipitation reaction, up to 60% of the metal precursor feeds do not react to form catalyst precursor and end up in the supernatant as metal residuals. In the present disclosure, the metals can be recovered in a chemical precipitation step, wherein the supernatant is mixed with at least one of an acid, a sulfide-containing compound, a base, and combinations thereof to precipitate at least 50% of metal ions in at least one of the metal residuals, wherein the precipitation is carried out at a pre-select pH. The precipitate is isolated and recovered, yielding an effluent stream. The precipitate and/or the effluent stream can be further treated to form at least a metal precursor feed which can be used in the co-precipitation reaction. The process generates an effluent to waste treatment containing less than 50 ppm metals.

Abstract: A hydroprocessing co-catalyst composition may comprise in an embodiment a first component comprising co-catalyst particles and a liquid carrier, and a second component comprising a dispersant and a dispersant diluent. The co-catalyst particles may be in the micron size range, and the dispersant may promote dispersion of the co-catalyst particles in materials such as the liquid carrier, the dispersant diluent, and combinations thereof. Methods of introducing a hydroprocessing co-catalyst composition into a hydroprocessing system are also disclosed.

Abstract: The present invention relates to a new process which comprises the steps of hydrotreating, paraffin disproportionation and hydroisomerization to convert biological hydrocarbonaceous oxygenated oils comprising triglycerides into biologically-derived paraffinic jet/diesel fuels, solvents and base oils. A combination of conventional hydrogenation/dehydrogenation catalysts, such as Pt/Al2O3, and conventional olefin metathesis catalysts, such as WO3/SiO2, or inexpensive variations thereof, is generally employed in the paraffin disproportionation step.

Abstract: A hydroprocessing co-catalyst composition may comprise in an embodiment a first component comprising co-catalyst particles and a liquid carrier, and a second component comprising a dispersant and a dispersant diluent. The co-catalyst particles may be in the micron size range, and the dispersant may promote dispersion of the co-catalyst particles in materials such as the liquid carrier, the dispersant diluent, and combinations thereof. Methods of introducing a hydroprocessing co-catalyst composition into a hydroprocessing system are also disclosed.

Abstract: The invention provides complexes in which a calixarene-related compound is coordinated to an iridium-containing metal colloid. The complexes can be immobilized on a substrate. The complexes of the invention are useful as tunable and highly robust isolated metal colloids that find use in binding of molecules and catalysis of chemical reactions.