Patent classifications
B01J37/20
DLM-1 Molecular Sieve, Process for Preparing the Same, and Use Thereof
A DLM-1 molecular sieve, a process for preparing the molecular sieve, and use thereof in treating an organic substance are provided. The DLM-1 molecular sieve is an Al-SBA-15 molecular sieve, and has a schematic chemical composition as represented by the formula “first oxide*second oxide”. The first oxide is silica, the second oxide is alumina, and the content by mass percent of alumina in the schematic chemical composition is 2% to 85%. The DLM-1 molecular sieve is suitable for the hydrodenitrogenation reaction of heavy distillate oil, and is favorable for improving the hydrodenitrogenation activity.
Multi-metallic bulk hydroprocessing catalysts
Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, copper, and optionally, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.
Multi-metallic bulk hydroprocessing catalysts
Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, copper, and optionally, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.
Multi-metallic bulk hydroprocessing catalysts
Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, yttrium, and optionally, copper, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.
Multi-metallic bulk hydroprocessing catalysts
Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, yttrium, and optionally, copper, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.
COBALT CATALYST AND PREPARATION METHOD THEREOF
A cobalt catalyst and a preparation method thereof are provided. The cobalt catalyst includes a carrier and a catalytically active substance; the carrier is a cobalt-based substrate material; the catalytically active substance is grown on the surface of the carrier, and the catalytically active substance has a morphology of hydrangea-shaped nanospheres. The cobalt catalyst is an autogenously grown monolithic nanosphere catalyst with a three-dimensional structure assembled by nano-sheets on the catalyst surface. The cobalt catalyst has a high specific surface area and can fully expose the catalytically active sites to enhance the catalytic efficiency. Compared to a nanowire catalyst, the cobalt catalyst has better self-supporting properties, and the active components are not easily aggregated nor fall off during a use process. Therefore, the cobalt catalyst has a longer service life.
Rare-earth metal vanadates catalysts for NO.SUB.x .reduction at low temperatures
Provided are catalysts for reduction of nitrogen oxides including an active site including lanthanum vanadate represented by at least one of Formula 1 and Formula 2 and a support carrying the active site.
LaVO.sub.4 (wherein LaVO.sub.4 is polymorphous and has a tetragonal or monoclinic crystal structure) Formula 1
LaV.sub.3O.sub.9 (wherein LaV.sub.3O.sub.9 has a monoclinic crystal structure) Formula 2.
Rare-earth metal vanadates catalysts for NO.SUB.x .reduction at low temperatures
Provided are catalysts for reduction of nitrogen oxides including an active site including lanthanum vanadate represented by at least one of Formula 1 and Formula 2 and a support carrying the active site.
LaVO.sub.4 (wherein LaVO.sub.4 is polymorphous and has a tetragonal or monoclinic crystal structure) Formula 1
LaV.sub.3O.sub.9 (wherein LaV.sub.3O.sub.9 has a monoclinic crystal structure) Formula 2.
Process and Materials for Trim Dewaxing of Distillates
Described herein are novel and inventive dewaxing processes that employ dewaxing catalysts which are co-extrusions of two different zeolites, particularly two different 10MR zeolites or a co-extrusion of a 10MR zeolite and a 12MR zeolite in combination with a hydrogenation component. The hydrogenation component can be a mixture of non-noble metal components or a mixture of noble metal components. This novel and inventive process demonstrated a significant activity boost (as measured by increased cloud point reduction) and/or selectivity boost (as measured by reduced diesel loss) compared to either single zeolite component.
Process and Materials for Trim Dewaxing of Distillates
Described herein are novel and inventive dewaxing processes that employ dewaxing catalysts which are co-extrusions of two different zeolites, particularly two different 10MR zeolites or a co-extrusion of a 10MR zeolite and a 12MR zeolite in combination with a hydrogenation component. The hydrogenation component can be a mixture of non-noble metal components or a mixture of noble metal components. This novel and inventive process demonstrated a significant activity boost (as measured by increased cloud point reduction) and/or selectivity boost (as measured by reduced diesel loss) compared to either single zeolite component.