A method for converting an alcohol to a hydrocarbon fraction reduced in gaseous hydrocarbon content, the method comprising: (i) contacting said alcohol with a metal-loaded zeolite catalyst under conditions suitable for converting said alcohol to a first hydrocarbon fraction containing liquid hydrocarbons having at least five carbon atoms along with gaseous hydrocarbons having less than five carbon atoms, wherein said metal-loaded zeolite catalyst is catalytically active for converting said alcohol to said first hydrocarbon fraction; and (ii) selectively removing said gaseous hydrocarbons from the first hydrocarbon fraction and contacting said gaseous hydrocarbons with a metal-loaded zeolite catalyst under conditions suitable for converting said gaseous hydrocarbons into liquid hydrocarbons having at least five carbon atoms to produce a second hydrocarbon fraction reduced in gaseous hydrocarbon content, wherein the metal-loaded zeolite catalyst in steps (i) and (ii) are the same or different.

The present invention provides a delayed coking process comprising a step of subjecting a mixed feed comprises residual heavy hydrocarbon feedstock and bio oil obtained from fast pyrolysis of lignocellulosic biomass of one or more of Jatropha, Cashew nut, Karanjia and Neem to a delayed coking process and a system for the delayed coking process.

A process is provided for the catalytic cracking of a glyceride oil feedstock with a catalyst composition containing a deactivated phosphorus-containing ZSM-5 light olefins selective additive.

The present invention describes a process for the production of biofuel, said process comprising, pretreating a feedstock, mixing a catalyst with said feedstock, transferring the mixture of catalyst and feedstock into a reactor, and subjecting said mixture to a heating sequence by applying microwave energy thereto, wherein the catalyst comprises an aluminosillicate mineral, the percentage of aluminosillicate mineral in the catalyst-feedstock mixture is less than 10% (w/w), and the temperature of the mixture of catalyst and feedstock is no higher than 450° C. during the process.

Systems and methods are provided for performing hydrodeoxygenation of bio-derived feeds while maintaining the hydrodeoxygenation catalyst in a sulfided state. During hydrodeoxygenation, a hydrogen-containing stream is provided to the hydrodeoxygenation reactor as a hydrogen treat gas to provide hydrogen for the reaction. In some aspects, the hydrogen treat gas used for hydrodeoxygenation can be formed at least in part from hydrogen that has been used as a stripping gas for removing H.sub.2S from a rich amine stream. In other aspects, H.sub.2S can be stripped using water vapor, and a resulting overhead HS stream can be compressed prior to incorporation of the H.sub.2S into a hydrogen-containing stream. The resulting hydrogen-containing stream can include sufficient H.sub.2S to substantially maintain the catalyst in the hydrodeoxygenation stage in a sulfided state.

A method may include: hydropyrolyzing a bio feedstock in a hydropyrolysis unit to produce at least a hydropyrolysis oil; introducing at least a portion of the hydropyrolysis oil with a hydrocarbon co-feed into a fluidized catalytic cracking unit; and cracking the hydropyrolysis oil in the fluidized catalytic cracking unit to produce at least fuel range hydrocarbons.

The invention relates to methods for converting algal biomass into a gas or into biocrude comprising (a) gasification or hydrothermal liquefaction of an algal biomass in at least one first reactor, (b) separation of the gas or biocrude produced thereby from the aqueous effluents and the CO.sub.2 produced, at the outlet of the first reactor, (c) recovery of the aqueous effluents, and (d) oxidation of the aqueous effluents in at least one second reactor. Continuous processes for culture of algal biomass and conversion of the algal biomass cultivated into a gas or into a biocrude are also disclosed.

A system for processing a renewable bio-based material comprising: a reactor, a feedstock substantially renewable and comprising triglycerides and free fatty acids, with hydrogen in the presence of a catalyst in a reactor to form a treated oil; a heat exchanger for receiving the treated oil from the reactor and reducing its temperature to a predetermined temperature; a high-pressure separator followed by a low-pressure separator; and (i) a distillation unit for passing the treated oil through to form green diesel and an adsorption unit for passing the green diesel through; or (ii) at least one distillation column to separate the treated oil into at least one component and an adsorption column for passing the at least one component through; wherein the reactor comprises a cooling function for controlling the temperature of the reactor; wherein the cooling function is an internal cooling function comprising adding a cooling substance into the reactor.

A process is disclosed for producing distillate range hydrocarbons using MTW and/or SSZ-41x catalysts.

A method of hydroprocessing is performed wherein non-petroleum feedstocks, such as those containing from about 10% or more olefinic compounds or heteroatom contaminants by weight, are treated in a first reaction zone to provide reaction products. The process involves introducing the feedstock along with diluents or a recycle and hydrogen in a first reaction zone and allowing the feed and hydrogen to react in a liquid phase within the first reaction zone to produce reaction products. The reaction products are cooled and/or water is removed from the reaction products. At least a portion of the cooled and/or separated reaction product are introduced as a feed along with hydrogen into a second reaction zone containing a hydroprocessing catalyst. The feed and hydrogen are allowed to react in a liquid phase within the second reaction zone to produce a second-reaction-zone reaction product.