The present disclosure relates to a dehydrogenation catalyst for use in dehydrogenation of a branched light hydrocarbon gas, the catalyst including platinum, tin, and an alkali metal which are carried in a phase-changed carrier, in which platinum and tin form a single complex and are present in an alloy form within a predetermined thickness from the outer surface of the catalyst.

A process for dehydrogenating alkane or alkylaromatic compounds comprising contacting the given compound and a dehydrogenation catalyst in a fluidized bed. The dehydrogenation catalyst is prepared from an at least partially deactivated platinum/gallium catalyst on an alumina-based support that is reconstituted by impregnating it with a platinum salt solution, then calcining it at a temperature from 400° C. to 1000° C., under conditions such that it has a platinum content ranging from 1 to 500 ppm, based on weight of catalyst; a gallium content ranging from 0.2 to 2.0 wt %; and a platinum to gallium ratio ranging from 1:20,000 to 1:4. It also has a Pt retention that is equal to or greater than that of a fresh catalyst being used in a same or similar catalytic process.

A catalyst for dehydrogenation of hydrocarbons includes a support including zirconium oxide and alumina. A concentration of the zirconium oxide in the catalyst is in a range of from 1 weight percent (wt. %) to 20 wt. %. The catalyst includes from 0.01 wt. % to 2 wt. % of an alkali metal or alkaline earth metal. The catalyst includes from 1 wt. % to 2 wt. % of tin. The catalyst includes from 0.1 wt. % to 2 wt. % of a platinum group metal. The alkali metal or alkaline earth metal, tin, and platinum group metal are disposed on the support.

The present invention provides a catalyst for aromatization of a long-carbon chain alkane and a preparation method thereof. In the present invention, a molecular sieve containing a BEA structure is taken as an active component and mixed with a carrier, and then the mixture is formed, dried and calcined to obtain the catalyst for aromatization of a long-carbon chain alkane. The active component is prepared by taking a Naβ molecular sieve as a raw material and modifying through the following steps of: first obtaining an Hβ molecular sieve through ammonium ion-exchange, and then conducting dealumination and silicon insertion treatment of the Hβ molecular sieve through first hydrothermal treatment; forming a mesoporous structure in a molecular sieve framework through second hydrothermal treatment; reducing the acidity of the catalyst by potassium ion exchange, and finally using metal modification to improve the capability of the catalyst for catalyzing the aromatization of the long-carbon chain alkane and enhancing the toluene selectivity. The catalyst provided by the present invention shows high stability in the aromatization of the long-chain alkane and has a service life up to 170 h or above and aromatic hydrocarbon selectivity up to 80%, and the selectivity to toluene in aromatic hydrocarbon products can reach 85.5%.

The present invention concerns a method (100) for the production of a propylene product (9) in which a component mixture (2) containing propane, propylene and hydrogen is provided using a propane dehydrogenation (10) to which a reaction feed (1) containing propane and hydrogen is subjected, the component mixture (2) or a part thereof being subjected as a first separation feed to a first membrane separation (40), by means of which a first permeate (3) enriched in hydrogen with respect to the first separation feed and a first retentate (4) depleted in hydrogen with respect to the first separation feed and containing hydrogen, propane and propylene are formed, the first retentate (4) or part thereof being subjected to a second membrane separation (50) as a second separation feed, in which a second permeate (6) containing at least the predominant part of the hydrogen of the second separation feed and a second retentate containing at least the predominant part of the propane and the propylene of the second separation feed are formed, wherein the first membrane separation (40) is carried out using a sweep gas (5) containing propane and the first permeate (3) is obtained as a permeate (3) charged with propane of the sweep gas (5) and/or the second membrane separation (50) is carried out using the sweep gas (5) containing propane and the second permeate (6) is obtained as a permeate (6) charged with propane of the sweep gas (5), and wherein the first permeate (3) charged with propane of the sweep gas (5) and/or the second permeate (3) charged with propane of the sweep gas or one or more parts thereof is used in the formation of the reaction feed (1). A corresponding plant is also the subject of this invention.

The present invention concerns a method (100) for the production of a propylene product (9) in which a component mixture (2) containing propane, propylene and hydrogen is provided using a propane dehydrogenation (10) to which a reaction feed (1) containing propane and hydrogen is subjected, the component mixture (2) or a part thereof being subjected as a first separation feed to a first membrane separation (40), by means of which a first permeate (3) enriched in hydrogen with respect to the first separation feed and a first retentate (4) depleted in hydrogen with respect to the first separation feed and containing hydrogen, propane and propylene are formed, the first retentate (4) or part thereof being subjected to a second membrane separation (50) as a second separation feed, in which a second permeate (6) containing at least the predominant part of the hydrogen of the second separation feed and a second retentate containing at least the predominant part of the propane and the propylene of the second separation feed are formed, wherein the first membrane separation (40) is carried out using a sweep gas (5) containing propane and the first permeate (3) is obtained as a permeate (3) charged with propane of the sweep gas (5) and/or the second membrane separation (50) is carried out using the sweep gas (5) containing propane and the second permeate (6) is obtained as a permeate (6) charged with propane of the sweep gas (5), and wherein the first permeate (3) charged with propane of the sweep gas (5) and/or the second permeate (3) charged with propane of the sweep gas or one or more parts thereof is used in the formation of the reaction feed (1). A corresponding plant is also the subject of this invention.

Hydrocarbon composition plays vital role in fuel quality. For gasoline/motor spirit applications the hydrocarbon should have more octane-possessing molecules from the groups of aromatics, naphthenics and isoparaffins, while n-paraffins are not preferred due to their poor octane. Among the high-octane groups, again aromatics occupy the top but not more than 35 vol % aromatics can be mixed in gasoline for engine applications to avoid harmful emission, But there is no single process that addresses so far the issue of co-producing all the desired hydrocarbon components in a single process. Thus, it is interesting to have a single once-through process working on single catalyst system to produce mixture of all three high-octane molecules namely, aromatics, naphthenics and isoparaffins directly from low-value, low-octane n-paraffin feed. Herein, we report a novel single-step catalytic process for the simultaneous production of aromatics, naphthenics and isoparaffins for gasoline and petrochemical applications.

New/fresh catalyst is added to a dehydrogenation unit and aged catalyst is removed from the dehydrogenation unit on a continuous or semi-continuous basis while the dehydrogenation unit is in operation. The conversion achieved by the higher activity catalyst results in the production rate of olefin product being maintained at near start-of-run production for longer, with a slower rate of decline. The higher activity catalyst extends run time, reduces feed consumption for each unit of olefin product, and minimizes fresh catalyst expenses.

New/fresh catalyst is added to a dehydrogenation unit and aged catalyst is removed from the dehydrogenation unit on a continuous or semi-continuous basis while the dehydrogenation unit is in operation. The conversion achieved by the higher activity catalyst results in the production rate of olefin product being maintained at near start-of-run production for longer, with a slower rate of decline. The higher activity catalyst extends run time, reduces feed consumption for each unit of olefin product, and minimizes fresh catalyst expenses.

Provided is a continuous process for converting waste plastic into a feedstock for polyethylene polymerization. The process comprises selecting waste plastics containing polyethylene and/or polypropylene, and then passing the waste plastics through a pyrolysis reactor to thermally crack at least a portion of the polyolefin waste and produce a pyrolyzed effluent. The pyrolyzed effluent is then separated into offgas, a pyrolysis oil comprising a naphtha/diesel/heavy fraction, and char. The pyrolysis oil is passed to a crude unit in a refinery from which a naphtha fraction (C.sub.5-C.sub.8), or a propane and butane (C.sub.3-C.sub.4) fraction, is recovered. The naphtha fraction, or propane and butane (C.sub.3-C.sub.4) fraction, is then passed to a steam cracker for ethylene production.