The present disclosure provides compositions and methods for use with hydrogen gas. A method may include adding hydrogen gas to a medium and adding a production chemical to the medium. As examples, the production chemical may be a corrosion inhibitor, an anti-foulant, a hydrate anti-agglomerate, a kinetic hydrate inhibitor, an amine for gas sweetening, a regenerable H.sub.2S scavenger, a non-regenerable H.sub.2S scavenger, an alcohol for gas dehydration, an alcohol for hydrate control, a thermodynamic hydrate inhibitor, or any combination thereof. The present disclosure also provides test methods to determine the susceptibility of a production chemical to reaction with hydrogen gas.

The present invention relates to a process and system for forming a hydrocarbon feedstock from a biomass material, and the hydrocarbon feedstock formed therefrom. The present invention also relates to a process and system for forming a bio-derived naphtha fuel from a hydrocarbon feedstock, and the bio-derived naphtha fuel formed therefrom, as well as intermediate treated hydrocarbon feedstocks formed during the process.

This invention relates to a catalyst system comprising (a) at least one layer of a first catalyst comprising a dehydrogenation active metal on a solid support; (b) at least one layer of a second catalyst comprising a metal oxide; and (c) at least one layer of a third catalyst comprising a transition metal on an inorganic support; wherein the at least one layer of a second catalyst is sandwiched between the at least one layer of a first catalyst and the at least one layer of a third catalyst; and a process comprising contacting a hydrocarbon feed with the catalyst system.

Systems and methods are provided for reducing the end point of distillate fuel boiling range fractions while reducing or minimizing conversion of the distillate fuel to naphtha or light ends. To perform end point reduction, a distillate boiling range fraction is exposed to a conversion catalyst that has a total surface area of at least 200 m.sup.2/g, an average pore size of 12 Angstroms or more, and/or a low acidity, where the conversion catalyst includes a supported Group 8-10 metal, such as a supported Group 8-10 noble metal. Such a conversion catalyst can have improved activity for reducing end point of a distillate fuel fraction while reducing or minimizing conversion relative to 177 C. Performing end point reduction using such a catalyst can allow for increased yields of distillate fuel boiling range products by allowing increased amounts of heavy feed components to be included in the input to a distillate fuel processing train.

A new family of crystalline microporous silicometallophosphate designated SAPO-69 has been synthesized. These silicometallophosphate are represented by the empirical formula of:
R.sup.p+.sub.rM.sub.m.sup.+E.sub.xPSi.sub.yO.sub.z
where M is an alkali metal such as potassium, R is an organoammonium cation such as ethyltrimethylammonium and E is a trivalent framework element such as aluminum or gallium. The SAPO-69 family of materials represent the first phosphate-based molecular sieves to have the OFF topology and have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

The present disclosure relates to catalyst systems which may be useful for the dehydrogenation of hydrocarbons. According to one or more embodiments, the catalyst systems may include a zincosilicate support material, one or more alkali or alkaline earth metals, and one or more platinum group metals. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc. The present disclosure also relates to methods for the production of such catalyst systems as well as methods for the use of such catalyst systems for the dehydration of hydrocarbons.

The present disclosure relates to catalyst systems which may be useful for the dehydrogenation of hydrocarbons. According to one or more embodiments, the catalyst systems may include a zincosilicate support material, one or more alkali or alkaline earth metals, and one or more platinum group metals. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc. The present disclosure also relates to methods for the production of such catalyst systems as well as methods for the use of such catalyst systems for the dehydration of hydrocarbons.

According to one or more embodiments presently disclosed, one or more reactant hydrocarbons may be dehydrogenated by a method that includes contacting the one or more reactant hydrocarbons with a catalyst system to dehydrogenate at least a portion of the reactant hydrocarbons. The catalyst system may include a zincosilicate support material that includes an MFI framework type structure incorporating at least silicon and zinc. The catalyst system may further include one or more alkali or alkaline earth metals, and one or more platinum group metals.

According to one or more embodiments presently disclosed, a catalyst system may be made by a method that includes introducing one or more alkali or alkaline earth metals to a zincosilicate support material, and introducing one or more platinum group metals to the zincosilicate support material. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc.

Systems and methods are provided for slurry hydroconversion of a heavy oil feed, such as an atmospheric or vacuum resid. The systems and methods allow for slurry hydroconversion using catalysts with enhanced activity and/or catalysts that can be recycled as a side product from a complementary refinery process.