The present disclosure provides production processes that can include exposing a carbon-based material to liquid media to form hydrocarbon fuel. Waste to fuel conversion processes as well as waste material processing reactors are provided that can be configured to convert waste to fuel. Heat exchangers, power generation processes and combustion turbine exhaust apparatus are also provided. Fuel generation processes and generation systems are provided. Reaction media conduit systems as well as processes for servicing reactant media pumps coupled to both inlet and outlet conduits containing reactant media, are also provided.

The present invention provides a catalytic fast pyrolysis process for the production of fuel blendstocks and chemicals. In addition, the invention provides compositions of renewable blendstocks, compositions of renewable fuel blends, and compositions of 100 percent renewable fuels compatible with gasoline specifications and regulations.

The present invention provides a catalytic fast pyrolysis process for the production of fuel blendstocks and chemicals. In addition, the invention provides compositions of renewable blendstocks, compositions of renewable fuel blends, and compositions of 100 percent renewable fuels compatible with gasoline specifications and regulations.

This disclosure pertains to the use of black liquors from kraft pulp mills as a source of catalysts for the thermochemical conversion of organic matter feedstocks to bio oils. More particularly, some embodiments pertain to integrated kraft pulp mill and thermochemical conversion systems, which include: a Kraft pulp mill comprising a digester for digesting a lignocellulosic material with white liquor to produce pulp and black liquors; a thermochemical conversion subsystem comprising: at least one mixing tank for combining pulping liquors received from the pulp mill with an organic matter feedstock and water to produce a reaction mixture; a reactor vessel for treating the reaction mixture received from the mixing tank at a reaction temperature and pressure suitable for conversion of all or a portion of the organic matter in the reaction mixture into a product mixture comprising a bioproduct and an aqueous stream containing both organic and inorganic compounds; and a depressurizer for depressurizing product mixture received from the reactor vessel; and one or more conveyors for conveying the pulping liquors from the pulp mill to the mixing tank.

Pyrolysis processes comprise contacting a waste polyolefin with a solid catalyst at a pyrolysis temperature to form a pyrolysis product containing C.sub.1-C.sub.10 hydrocarbons. In some instances, the solid catalyst can be a silica-coated alumina, a fluorided silica-coated alumina, or a sulfated alumina, while in other instances, the solid catalyst can be any suitable solid oxide or chemically-treated solid oxide that is characterized by a d50 average particle size from 5 to 12 ?m and a particle size span from 0.7 to 1.7. Hydrocarbon compositions are formed from the pyrolysis of waste polyolefins with specific amounts of methane and higher carbon number hydrocarbons.

The present subject matter describes a method and apparatus for operating a delayed coker. The method comprises contacting a vapour produced in a delayed coker-drum with a catalyst maintained in form of a bed, and maintaining a level of said catalyst-bed within pre-defined limits during catalytic-cracking of the vapour. Thereafter, the cracked-vapour is routed to a coker-fractionator column to trigger conversion into one or more hydrocarbon products.

Systems and methods are provided for block operation during lubricant and/or fuels production from deasphalted oil. During block operation, a deasphalted oil and/or the hydroprocessed effluent from an initial processing stage can be split into a plurality of fractions. The fractions can correspond, for example, to feed fractions suitable for forming a light neutral fraction, a heavy neutral fraction, and a bright stock fraction, or the plurality of fractions can correspond to any other convenient split into separate fractions. The plurality of separate fractions can then be processed separately in the process train (or in the sweet portion of the process train) for forming fuels and/or lubricant base stocks. This can allow for formation of unexpected base stock compositions.

Disclosed is a process for the one-pot liquefaction of a biomass or coal and a biomass, the process comprising: first preparing a slurry containing a catalyst, a vulcanizing agent and a biomass (and coal), and then introducing hydrogen gas into the slurry to carry out a reaction. Preparing the slurry comprises: subjecting a biomass (and coal) sequentially to drying, a first pulverization, compression and a second pulverization, then mixing same with a catalyst and a vulcanizing agent to obtain a mixture, and adding the mixture to an oil product for grinding and pulping to obtain a biomass slurry. By means of the treatment process of subjecting the straw firstly to compression and then to a second pulverization, the volume of the straw is greatly reduced, thereby facilitating the dispersion thereof in the oil product, increasing the concentration of the reaction material, and improving the delivery amount of the biomass per unit time by means of a pump; Furthermore, the conversion rate of the biomass is also improved.

The present disclosure relates to a process for producing crude bio oil from biomass. The process involves hydrothermally liquefying a biomass in presence of a catalyst at a temperature in the range of 250 C. to 400 C. and at a pressure in the range of 70 bar to 225 bar, to obtain a product mixture comprising crude bio-oil. This product mixture comprising crude bio-oil is cooled to obtain a cooled mixture; the oil is then separated from the cooled mixture to obtain crude bio-oil and a residue containing the catalyst. Carbon content of crude bio-oil is in the range of 60 wt % to 85 wt %.

Process for chemically treating scrap tyres, comprising the steps of: a) grinding the tyres and removing the inorganic material; b) melting the material from step a); c) devulcanizing the molten material from step b) according to the reaction R1

R1:[CH.sub.2-]n-S[CH.sub.2-]m+H.sub.2=[CH.sub.2-].sub.n*[CH.sub.2-]m*H.sub.2S where m and n indicate non-identical lengths of the macromolecules in terms of carbon atoms and the asterisk indicates the possible presence of at least one ethylene unsaturation, said reaction R1 being possibly associated with the saturation reaction R2 of said possible at least one ethylene unsaturation:

R2:[CH.sub.2-]n*+[CH.sub.2-]m*+H 2=[CH.sub.2-]n+[CH.sub.2]m d) converting the plastics from step c) into products of commercial value. wherein step c): is carried out in the presence of catalysts based on cobalt oxide or molybdenum oxide possibly supported on alumina; and comprises a hydrogen sulphide splitting step to create hydrogen and sulphur according to the reaction R3:

R3:H.sub.2S=H.sub.2+1/XSx and the formed hydrogen is recycled to step c).