Abstract: A process for reforming with hydrogen, or hydroforming, a naphtha in a cyclic reforming unit which contains a plurality of catalyst-containing on stream reactors in series, and a catalyst-containing swing reactor manifolded therewith which can be periodically placed in series and substituted for an on stream reactor while the latter is removed from series for regeneration and reactivation of the catalyst contained therein. In the process, a reactor which is next scheduled for regeneration and reactivation of its near deactivated catalyst is located immediately downstream next in series with a reactor which contains freshly regenerated, reactivated catalyst at the time the latter is initially put on stream so that sulfur released by the freshly regenerated, reactivated catalyst which occurs a short time after the upstream reactor has been returned to service, is adsorbed by the near deactivated catalyst of the reactor next requiring removal from the series for catalyst regeneration and reactivation.

Abstract: An improved hydrocarbon reforming process comprising:1. contacting a hydrocarbon feed with a platinum group metal, rhenium-containing catalyst in the presence of hydrogen in at least one reaction zone at a temperature in the range of about 500.degree. F. to about 650.degree. F. for a time sufficient to improve the catalytic activity stability of the catalyst; and thereafter,2. contacting the hydrocarbon chargestock with the catalyst in the presence of hydrogen at hydrocarbon reforming conditions including a higher temperature than the temperature at which step (1) occurred.

Abstract: An improved moving bed contacting design is disclosed, which is especially useful for moving bed reforming. A moving catalyst bed is contained in a single, downflowing annular bed. Multiple feed inlet and outlet locations, and baffles on screens containing the catalyst, permit radial flow operation through a single bed of catalyst to simulate several distinct catalyst beds. Some gas may flow up or down, instead of radially to increase or decrease the loading of the catalyst bed.

Abstract: Synthetic natural gas and high octane motor fuel blending stock is produced by catalytically reforming naphtha at low severity to maximize production of aromatics and minimize hydrocracking, and then converting the remaining paraffins to methane in a methanation zone. The effluent from the methanation zone is separated into synthetic natural gas and motor fuel blending stock.

Abstract: A multiple-stage catalytic conversion system in which a hydrocarbon charge stock is countercurrently reacted in a plurality of catalytic reaction zones, in all of which the catalyst particles are downwardly movable via gravity-flow. The charge stock, in the absence of added, or recycled hydrogen, is reacted serially in the reaction zones in the order of increasing catalyst loading, the product ultimately being recovered from the effluent emanating from that reaction zone (1) into which fresh, or regenerated catalyst particles are introduced and, (2) which contains the greatest quantity of catalyst particles. Catalyst particles are transferred from one reaction zone to another in the order of decreasing catalyst loading, ultimately being withdrawn from the system through the reaction zone containing the least amount of catalyst particles.

Abstract: A multiple-stage catalytic conversion system in which a hydrocarbonaceous charge stock is reacted in a plurality of catalytic reaction zones, through all of which the catalyst particles flow downwardly via gravity-flow. The charge stock, in the absence of added, or recycled hydrogen, is reacted in the last reaction zone, from which deactivated catalyst particles are withdrawn for regeneration. The reaction product effluent emanating therefrom is further reacted in an intermediate reaction zone. Additional reaction of the product effluent, from the intermediate zone, is effected in the first reaction zone, through which fresh, or regenerated catalyst particles are introduced into the system. The effluent from the first reaction zone is separated to recover the intended product. The system may comprise three or more reaction zones in side-by-side relationship, with the catalyst particles being transported from the lower end of one zone to the upper end of the next succeeding reaction zone.

Abstract: A multiple-stage catalytic conversion system in which a hydrocarbonaceous charge stock is reacted in a plurality of stacked catalytic reaction zones through which catalyst particles flow downwardly via gravity-flow. The charge stock, in the absence of added, or recycle hydrogen, is reacted first in the lowermost reaction zone, from which deactivated catalyst particles are withdrawn from the system. Resulting reaction zone effluent is further reacted in the uppermost reaction zone, through which fresh, or regenerated catalyst particles are introduced into the system, and serially in one or more subsequent, lower reaction zones. Product effluent from the reaction zone immediately above the lowermost zone is separated to recover the desired normally liquid product.

Abstract: Naphthas are upgraded in a two-stage process to give improved yields of high octane gasoline. The first stage operates at low temperatures of 100.degree.-300.degree. F using a highly active chlorinated alumina containing a metal of the platinum group, while the second stage operates at high temperatures using a reforming catalyst.

Abstract: A reforming operation is described which incorporates a zeolite selective conversion catalyst as a final catalyst composition contacted under temperature conditions controlled by quench gas as a function of product and seasonal demands. Preferably the zeolite catalyst is included as a separate downstream bed of catalyst in an enlarged final reactor of a three reactor reforming operation.

Abstract: Process for producing aromatic hydrocarbons, particularly benzene and/or toluene from a feed charge containing saturated and unsaturated hydrocarbons, by catalytic treatment of said charge with hydrogen, fractionation of the resulting product to separate a fraction containing benzene and/or toluene, extractive distillation of at least one aromatic hydrocarbon in a column, by means of an extraction solvent from which said hydrocarbon is subsequently separated, and recycling to the reaction zone of at least one portion of the products recovered at the top of said extractive distillation column and containing essentially C.sub.6 and C.sub.7 saturated hydrocarbons.

Abstract: An improved vapor phase catalytic isomerization of a hydrocarbon fraction containing C.sub.5 and C.sub.6 isomerizable hydrocarbons is obtained by subjecting the hydrocarbon fraction in the presence of gaseous hydrogen to a plural stage, such as a dual stage, catalytic isomerization operation preferably employing a chlorinated platinum-containing alumina catalyst wherein the hydrocarbon fraction undergoing isomerization is supplied sequentially and serially from the first stage through to the last stage of the plural stage isomerization operation and wherein the first stage of the plural stage isomerization operation is supplied with the hydrocarbon fraction at a temperature in the range about 300.degree.-305.degree.F. and recovered from the first stage at a temperature in the range about 310.degree.-335.degree.F. The last stage of the plural stage isomerization operation is supplied with the hydrocarbon fraction at a temperature in the range about 315.degree.-350.degree.F.

Abstract: Upgrading a full boiling range naphtha by the combination of reforming only a low boiling portion of the naphtha followed by contacting the reformate product thereof combined with the high boiling portion of the naphtha over a ZSM-5 type catalyst conversion operation is described.

Abstract: The catalyst comprises a Group-VIII-noble-metal hydrogenation component and a small amount of zirconium on a solid catalytic support comprising a porous refractory inorganic oxide. The zirconium may be present either in the elemental form or as compounds. The preferred hydrogenation component is platinum and the preferred porous refractory inorganic oxide is a catalytically active alumina.The reforming process comprises contacting a petroleum hydrocarbon stream in a reforming zone under reforming conditions and in the presence of hydrogen with the above-described catalyst. In one embodiment, the process comprises contacting a partially-reformed hydrocarbon stream in a reforming zone under reforming conditions and in the presence of hydrogen with the above catalyst. In another embodiment, the process comprises contacting a naphtha in a reforming zone under reforming conditions and in the presence of hydrogen with the above catalyst.