Abstract: An improved process is disclosed for the removal of nitrogen compounds from light hydrocarbon streams. Such nitrogen removal enhances the performance of catalytic processes which upgrade light hydrocarbons, especially light olefins, such as isomerization and etherification. The nitrogen-removal process can usefully be combined with steps for removal of sulfur compounds and highly unsaturated compounds in a process combination for upgrading the light hydrocarbons.

Abstract: This invention deals with a process for converting aliphatic C.sub.2 -C.sub.6 hydrocarbons into C.sub.6.sup.+ aromatics and C.sub.3.sup.= /C.sub.4.sup.= olefins. The process involves combining dehydrocyclodimerization (DHCD) with dehydrogenation. Thus, the feedstream is first sent to a DHCD zone which produces an effluent stream which contains C.sub.6.sup.+ aromatics along with C.sub.1 -C.sub.5 hydrocarbons. This effluent stream is separated into a stream containing C.sub.1 -C.sub.4 hydrocarbons and one containing C.sub.6.sup.+ aromatics. The C.sub.1 -C.sub.4 containing stream is flowed to a dehydrogenation zone to produce C.sub.3.sup.= /C.sub.4.sup.= olefins.

Abstract: This invention relates to a process for convening C.sub.5 /C.sub.6 hydrocarbons to aromatic products, e.g., benzene, toluene, etc. The process involves first flowing the C.sub.5 /C.sub.6 feedstream to a first reaction zone where the C.sub.5 /C.sub.6 feed is convened to aromatics and C.sub.3 /C.sub.4 products which are then flowed to a second reaction zone where the C.sub.3 --C.sub.4 compounds are convened to aromatic compound along with formation of hydrogen and fuel gas products. The product stream from the second reaction zone is combined with the products from the first conversion zone and the entire stream separated into the desired components.

Abstract: The present invention is an integrated catalytic reforming/hydrodealkylation process that maximizes benzene recovery by incorporating refrigeration and pressure swing adsorption separation units. In the refrigeration separation unit, liquid reformate is used as a sponge oil to recover benzene from a hydrodealkylation purge gas stream, which in the past has been vented. The pressure swing adsorption unit remove impurities from a hydrogen-rich gas stream prior to use in the hydrodealkylation unit.

Abstract: A process is disclosed for the conversion of light aliphatic hydrocarbons such as propane into aromatic hydrocarbons and especially high purity benzene. The feed hydrocarbon is converted to aromatic hydrocarbons in a dehydrocyclodimerization zone. The product stream from the dehydrocyclodimerization zone which contains benzene, toluene, xylenes and C.sub.6 -C.sub.10 non-aromatics are separated into an overhead stream which contains the non-aromatic hydrocarbons and a small fraction of the benzene and a bottoms stream which contains the remainder of the benzene and other aromatic components. The overhead stream is then flowed to a conversion zone where the C.sub.6 -C.sub.7 non-aromatic hydrocarbons are cracked and the benzene is combined with the bottoms stream and further separated to give a high purity benzene product stream and a toluene, xylenes and C.sub.9 + product stream. The toluene, xylenes and C.sub.9 + product stream may further be separated into a toluene and xylenes product and a C.sub.

Abstract: A process for converting C.sub.2 to C.sub.6 aliphatic hydrocarbons to aromatics is described. The process uses a catalyst which contains a zeolite, an aluminum phosphate binder and a gallium component. Examples of zeolites which can be used are the ZSM family of zeolites, with ZSM-5 being a specific example. The catalyst is characterized in that it is tolerant to exposure to hydrogen at temperatures of about 500.degree. to about 700.degree. C. The catalyst's tolerance to hydrogen exposure is the result of treating the catalyst with an aqueous solution of a weakly acidic ammonium salt or a dilute acid solution at a temperature of about 50.degree. to about 100.degree. C. for a time of about 1 to about 48 hours, followed by calcination.

Abstract: This invention relates to a process for reactivating a dehydrocyclodimerization catalyst. Dehydrocyclodimerization catalysts which contain an aluminum phosphate binder can be deactivated when they are exposed to hydrogen at temperatures above 500.degree. C. The instant process restores substantially all of the catalyst's lost activity. The process involves treating the catalyst with an aqueous solution of a weakly acidic ammonium salt or a dilute acid solution at a temperature of about 50.degree. to about 100.degree. C. for a time of about 1 to about 48 hours. An ammonium nitrate solution is preferred. Next the catalyst is calcined at a temperature of about 500.degree. to about 700.degree. C. for a time of about 1 to about 15 hours to provide a reactivated catalyst. The catalyst can be reactivated several times using this process.

Abstract: A catalyst for converting C.sub.2 to C.sub.6 aliphatic hydrocarbons to aromatics is described. The catalyst contains a zeolite, an aluminum phosphate binder and a gallium component. Examples of zeolites which can be used are the ZSM family of zeolites, with ZSM-5 being a specific example. The catalyst is characterized in that it is tolerant to exposure to hydrogen at tempertures of about 500.degree. to about 700.degree. C. The catalyst's tolerance to hydrogen exposure is the result of treating the catalyst with an aqueous solution of a weakly acidic ammonium salt or a dilute acid solution at a temperature of about 50.degree. to about 100.degree. C. for a time of about 1 to about 48 hours, followed by calcination. A process for preparing the catalyst is also described.

Abstract: A combination process for the conversion of C.sub.2 -C.sub.6 aliphatic hydrocarbons into easily transportable hydrocarbons of greater molecular weight. The combination process comprises converting the C.sub.2 -C.sub.6 aliphatic hydrocarbons to aromatic hydrocarbons in a dehydrocyclodimerization reaction zone after which the aromatic product is isomerized in the presence of hydrogen from the dehydrocyclodimerization reaction step to produce transportable aliphatic hydrocarbons.

Abstract: A dehydrocyclodimerization process employing a catalyst comprising a crystalline aluminosilicate and a metal oxide component is started-up by contacting the catalyst with a start-up gas that contains less than 50 mole percent hydrogen. The catalyst is exposed to the gaseous atmosphere containing less than 50 mole percent hydrogen until a C.sub.2 -C.sub.5 aliphatic hydrocarbon feedstock is contacted with the catalyst at dehydrocyclodimerization reaction conditions at which point hydrogen is generated as a dehydrocyclodimerization reaction product and displaces the non-hydrogen start-up gas from the process.

Abstract: A combination process for the conversion of C.sub.2 -C.sub.6 aliphatic hydrocarbons into easily transportable hydrocarbons of greater molecular weight. The combination process comprises converting the C.sub.2 -C.sub.6 aliphatic hydrocarbons to aromatic hydrocarbons in a dehydrocyclodimerization reaction zone after which the aromatic is directly hydrogenated in the presence of hydrogen from the dehydrocyclodimerization reaction step to produce large transportable aliphatic hydrocarbons. It is also an aspect of the invention that the hot hydrogenation reaction zone product stream is used to preheat the feed stream to the dehydrocyclodimerization reaction zone.