Abstract: A process for making furfural, derivatives of furfural, or both from biomass is described. The biomass feed is optionally conditioned to obtain a moisture content of 25 wt % or less. The biomass feed is ground to form particles having a particle size in a range of 0.02 mm to 7 mm with 5 wt % or less being 75 microns or less, and an average aspect ratio of 0.4 or more. The ground biomass feed is blanketed with an inert gas having an oxidant or oxygen content of 5 mol % or less. The ground biomass feed is reacted in the presence of water, a water-immiscible organic solvent, and an acid catalyst to form a reaction product mixture comprising furfural, derivatives of furfural, or both.

Abstract: A catalytic composite comprises a first component selected from Group VIII noble metal components and mixtures thereof, a second component selected from one or more of alkali and alkaline earth metal components, and a third component selected from one or more of tin, germanium, lead, indium, gallium, and thallium, all supported on an alumina support comprising delta alumina having an X-ray diffraction pattern comprising at least three 2? diffraction angle peaks between 32.0° and 70.0°. The at least three 2? diffraction angle peaks comprise a first 2? diffraction angle peak of 32.7°±0.4°, a second 2? diffraction angle peak of 50.8°±0.4°, and a third 2? diffraction angle peak of 66.7°±0.8°, wherein the second 2? diffraction angle peak has an intensity of less than about 0.06 times the intensity of the third 2? diffraction angle peak.

Abstract: A catalytic composite comprises a first component selected from Group VIII noble metal components and mixtures thereof, a second component selected from one or more of alkali and alkaline earth metal components, and a third component selected from one or more of tin, germanium, lead, indium, gallium, and thallium, all supported on an alumina support comprising delta alumina having an X-ray diffraction pattern comprising at least three 2? diffraction angle peaks between 32.0° and 70.0°. The at least three 2? diffraction angle peaks comprise a first 2? diffraction angle peak of 32.7°±0.4°, a second 2? diffraction angle peak of 50.8°±0.4°, and a third 2? diffraction angle peak of 66.7°±0.8°, wherein the second 2? diffraction angle peak has an intensity of less than about 0.06 times the intensity of the third 2? diffraction angle peak.

Abstract: A process using a dealkylated aromatic liquid improves a heavy hydrocarbon liquid used for supporting molybdenum carbonized catalyst. Dealkylated aromatic liquid can be derived from heavy hydrocarbon materials that have been subjected to cracking, such as fluid catalytic cracking or slurry hydrocracking. The heavy hydrocarbon liquid can comprise a portion of resid SHC feed and a portion of a gas oil stream from SHC effluent.

Abstract: A process is disclosed for using an iron oxide and alumina catalyst with no more than more than about 55 wt % of the alumina in the diaspore phase or in the alpha phase in SHC. Alpha alumina is less effective catalyst component for slurry hydrocracking in terms of TIOR conversion. Drying procedures should avoid more than about 51 wt % of the alumina change to the alpha phase. The SHC catalyst is for converting heavy hydrocarbon feed into lighter hydrocarbon products.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process using a dealkylated aromatic liquid improves a heavy hydrocarbon liquid used for supporting molybdenum carbonized catalyst. Dealkylated aromatic liquid can be derived from heavy hydrocarbon materials that have been subjected to cracking, such as fluid catalytic cracking or slurry hydrocracking. The heavy hydrocarbon liquid can comprise a portion of resid SHC feed and a portion of a gas oil stream from SHC effluent.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process is disclosed for using an iron oxide and alumina catalyst with no more than more than about 55 wt % of the alumina in the diaspore phase or in the alpha phase in SHC. Alpha alumina is less effective catalyst component for slurry hydrocracking in terms of TIOR conversion. Drying procedures should avoid more than about 51 wt % of the alumina change to the alpha phase. The SHC catalyst is for converting heavy hydrocarbon feed into lighter hydrocarbon products.

Abstract: A process and catalyst is disclosed for converting a heavy hydrocarbon feed stream into lighter hydrocarbon products using a two component catalyst. The catalyst comprises iron and molybdenum containing catalyst. Alumina may be a third catalyst component. The molybdenum is present in the heavy hydrocarbon feed stream at about 500 wppm or less and the weight ratio of iron to the molybdenum is less than 5. Much lower concentrations of expensive molybdenum can be used due to the addition of iron in the catalyst.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process and catalyst is disclosed for converting heavy hydrocarbon feed into lighter hydrocarbon products using multifunctional catalysts. Multifunctional catalysts enable use of less expensive metal by substituting expensive metals for less expensive metals with no loss or superior performance in slurry hydrocracking. Less available and expensive ISM can be replaced effectively.

Abstract: A process of making terephthalic acid or a derivative of terephthalic acid is described. The process includes reacting a derivative of 2,5-dimethylfuran, with a dienophile containing an unsaturated 2-carbon unit, in the presence of a catalyst having Brönsted acidity to form a para-xylene derivative; and optionally reacting the para-xylene derivative to terephthalic acid.