Patent classifications
C10G3/45
Systems and methods for renewable fuels
This application relates to production of renewable fuels, including a method of producing renewable fuels. The method comprises hydrotreating a biofeedstock by contacting reactants comprising a combined feedstock and hydrogen with a hydrotreating catalyst to produce normal paraffins. The combined feedstock comprises a biofeedstock and an additional feedstock. The biofeedstock has about 10% or more of each of metals, phosphorous, and chlorophyll than the additional feedstock. The biofeedstock comprises the metals in an amount of about 300 parts per million (ppm) or less, the phosphorous in an amount of about 300 ppm or less, and the chlorophyll in an amount of about 50 ppm or less. The method further comprises isomerizing at least a portion of the normal paraffins to produce branched paraffins in an isomerization effluent.
Method of obtaining liquid biohydrocarbons from oils of natural origin
In the method of obtaining liquid biohydrocarbons from oils of natural origin, in the first step, the oil and/or waste oil is/are heated in the presence of a mixture of hydrogen and carbon monoxide in the presence of a catalyst in the form of a metal oxide selected from a group comprising CoO, NiO, MoO.sub.3, ZrO.sub.2, or a mixture of such metal oxides, on an oxide support selected from a group comprising SiO.sub.2, Al.sub.2O.sub.3, TiO.sub.2, whereupon the product of the first step is contacted with hydrogen gas or with a mixture of hydrogen and carbon monoxide in the presence of a metallic catalyst selected from a group comprising Pd, Pt, Co/Mo, Ni/Mo, Zr on an oxide support selected from a group comprising SiO.sub.2, Al.sub.2O.sub.3, TiO.sub.2, P.sub.2O.sub.5, ZrO.sub.2 or on a mixture of such oxides.
HYDRODEOXYGENATION OF LIGNIN TO HYDROCARBONS USING BIMETALLIC CATALYSTS
Bimetallic catalysts for the hydrodeoxygenation (HDO) conversion of lignin into useful hydrocarbons are provided. The catalysts are bifunctional bimetallic ruthenium catalysts Ru-M/X.sup.+Y comprising a metal M such as iron (Fe), nickel (Ni), copper (Cu) or zinc (Zn), zeolite Y and cation X.sup.+ (e.g. H.sup.+) associated with zeolite Y.
PROCESSING BIOMASS
Techniques for processing biomass are disclosed herein. A method of preparing cellulosic ethanol having 100% biogenic carbon content as determined by ASTM 6866-18, includes treating ground corn cobs with electron beam radiation and saccharifying the irradiated ground corn cob to produce sugars. The method also includes fermenting the sugars with a microorganism. In addition, an unblended cellulosic-biomass derived gasoline with a research octane number of greater than about 87, as determined by ASTM D2699 is disclosed.
Metal phosphide catalysts and methods for making the same and uses thereof
The present disclosure relates to a method that includes heating a mixture that includes a metal phenylphosphine-containing precursor that includes at least one of Mo(PPh.sub.3).sub.2(CO).sub.4, Pd(PPh.sub.3).sub.4, Ru(PPh.sub.3).sub.3Cl.sub.2, Ru(PPh.sub.3).sub.2(CO).sub.2Cl.sub.2, Co(PPh.sub.3)(CO).sub.2(NO), and/or Rh(PPh.sub.3).sub.2(CO)Cl, a surfactant, and a solvent. The heating is to a target temperature to form a heated mixture containing a metal phosphide nanoparticle that includes at least one of MoP, Ru.sub.2P, Co.sub.2P, Rh.sub.2P, and/or Pd.sub.3P, and the metal phosphide nanoparticle is not hollow.
METHOD FOR PRODUCING HYDROCARBON LIQUID FUEL
A method for producing a hydrocarbon liquid fuel including hydrocracking a raw material oil in the presence of a hydrocracking catalyst, at a supplying pressure of hydrogen of from 0.1 to 1.0 MPa, a liquid space velocity of liquid volume of the raw material oil of from 0.05 to 10.0 hr.sup.1, and a flow rate of the hydrogen from 50 to 3,000 NL per 1 L of the raw material oil, wherein the hydrocracking catalyst is produced by a method including stirring a sulfur compound and a cracking catalyst in an aqueous medium to allow liquid-solid separation (step 1); stirring a solid product obtained in the step 1 and a metal component in an aqueous medium to allow liquid-solid separation (step 2); baking a solid product obtained in the step 2 (step 3); and reducing a solid product obtained in the step 3, or reducing a solid product obtained in the step 3, and then subjecting a reduced product to sulfurization treatment (step 4). According to the present invention, the hydrocracking of a raw material oil such as fats and oils and biomass retort oils, or a hydrocarbon or the like in petroleum oils, in a given composition can be accomplished by supplying a low-pressure hydrogen of a normal pressure or so.
Catalyst Compositions Comprising Small Size Molecular Sieves Crystals Deposited on a Porous Material
Catalyst compositions comprising an inorganic porous material with pore diameters of at least 2 nm and of crystals of molecular sieve, characterized in that the crystals of molecular sieve have an average diameter, measured by scanning electron microscopy, not bigger than 50 nm, and in that the catalyst composition presents a concentration of acid sites ranges from 50 to 1200 mol/g measured by TPD NH3 adsorption; and the XRD pattern of said catalyst composition is the same as the X ray diffraction pattern of said inorganic porous material.
PHOSPHORUS-DOPED NICKEL ALUMINUM OXIDE, AND PREPARATION METHOD THEREFOR AND USE THEREOF
The present invention relates to the technical field of new catalytic materials, and specifically relates to a phosphorus-doped nickel-aluminum oxide, its preparation method and the application thereof. Said preparation method comprises: the nickel-aluminum-based layered double hydroxide is subjected to high-temperature aerobic calcination to obtain nickel-aluminum oxide, the nickel-aluminum oxide obtained thereby is mixed with a phosphorus source and heated in an inert gas atmosphere or in vacuum conditions to dope phosphorus into the nickel-aluminum oxide, whereby the final phosphorus-doped nickel-aluminum oxide is obtained. In the present invention the NiAl interactions are constructed by subjecting the nickel-aluminum based layered double hydroxides to aerobic calcination at high temperature. The NiP interactions are constructed by doping P into nickel-aluminum oxides. Thus, the synergistic interactions of NiAl and NiP achieve regulating the electron density around the P-active metals, wherein the active metal is in an intermediate phase between metal and metal phosphide, which suppresses the factors leading to deactivation of the catalyst, such as metal agglomeration, carbon deposition, and phase transformation, demonstrating excellent catalytic activity, selectivity and stability.
CONVERSION OF BIOMASS INTO A LIQUID HYDROCARBON MATERIAL
A process for producing liquid hydrocarbon products from a biomass feedstock is provided. The process comprises:
contacting the feedstock with one or more hydropyrolysis catalyst compositions and molecular hydrogen to produce a product stream comprising hydropyrolysis product that is at least partially deoxygenated;
hydroconverting said hydropyrolysis product in the presence of one or more hydroconversion catalyst compositions to produce a vapour phase product comprising substantially fully deoxygenated hydrocarbon product,
wherein one or both of the hydropyrolysis catalyst composition and the hydroconversion catalyst composition is produced in a process comprising incorporating one or more metals selected from those of groups 6, 9, and 10 of the periodic table, into a shaped support; and incorporating one or more coordinating organic compounds into said shaped support, thus forming a catalyst precursor; and then either (i) treating the catalyst precursor in the presence of hydrogen and sulfiding it or (ii) calcining the catalyst precursor.
Mild catalytic reduction of C—O bonds and C═O bonds using a recyclable catalyst system
A method of reducing a CO bond to the corresponding CH bond in a substrate, which could be a benzylic alcohol, allylic alcohol, ester or an ether bond beta to a hydroxyl group or alpha to a carbonyl group using a recyclable metal catalyst system. The recyclable catalyst system is also applicable to reducing a CO bond to the corresponding COH bond and then CH bond. These methodologies can be linked in one-pot to selective oxidation and depolymerizations of aromatic polyols such as lignin.