A method of producing p-xylene comprising the steps of separating the reformate feed in the reformate splitter to produce a benzene stream, a combined heavy stream, a xylene stream, and a toluene stream, converting the C9+ aromatic hydrocarbons in the presence of a dealkylation catalyst in the dealkylation reactor to produce a dealkylation effluent, separating the dealkylation effluent in the dealkylation splitter to produce a C9 stream and a C10+ stream, reacting the C9 stream, the toluene stream, the benzene stream, and the hydrogen stream in the presence of a transalkylation catalyst in the transalkylation reactor to produce a transalkylation effluent, separating the p-xylenes from the xylene stream in the p-xylene separation unit to produce a p-xylene product and a p-xylene depleted stream, converting the m-xylene and o-xylene in the p-xylene depleted stream in the isomerization unit to produce an isomerization effluent.

A method of producing p-xylene comprising the steps of separating the reformate feed in the reformate splitter to produce a benzene stream, a combined heavy stream, a xylene stream, and a toluene stream, converting the C9+ aromatic hydrocarbons in the presence of a dealkylation catalyst in the dealkylation reactor to produce a dealkylation effluent, separating the dealkylation effluent in the dealkylation splitter to produce a C9 stream and a C10+ stream, reacting the C9 stream, the toluene stream, the benzene stream, and the hydrogen stream in the presence of a transalkylation catalyst in the transalkylation reactor to produce a transalkylation effluent, separating the p-xylenes from the xylene stream in the p-xylene separation unit to produce a p-xylene product and a p-xylene depleted stream, converting the m-xylene and o-xylene in the p-xylene depleted stream in the isomerization unit to produce an isomerization effluent.

To provide a hydrocarbon adsorbent having high hydrocarbon adsorbing properties even after exposed to a high temperature/high humidity reducing atmosphere. A hydrocarbon adsorbent, which includes a FAU type zeolite having a lattice constant of at least 24.29 Å and containing copper. Such a hydrocarbon adsorbent may be used for a method for adsorbing hydrocarbons to be exposed to a high temperature/high humidity environment, and may be used particularly for a method for adsorbing hydrocarbons in an exhaust gas of an internal combustion engine, such as an automobile exhaust gas.

To provide a hydrocarbon adsorbent having high hydrocarbon adsorbing properties even after exposed to a high temperature/high humidity reducing atmosphere. A hydrocarbon adsorbent, which includes a FAU type zeolite having a lattice constant of at least 24.29 Å and containing copper. Such a hydrocarbon adsorbent may be used for a method for adsorbing hydrocarbons to be exposed to a high temperature/high humidity environment, and may be used particularly for a method for adsorbing hydrocarbons in an exhaust gas of an internal combustion engine, such as an automobile exhaust gas.

The present invention discloses a method of separating C8 aromatic hydrocarbon isomers. The anion-pillared metal-organic framework materials with a pore diameter of 5-10 Å is used as adsorbents to achieve selective adsorption and separation of C8 aromatic hydrocarbon isomers by contacting the C8 aromatic hydrocarbon isomers with the adsorbents; the anion-pillared microporous materials are porous materials formed by metal ion M, inorganic anion A and organic ligand L through coordination bonds, with the general formula of [MAL.sub.2].sub.n, where n>4 and n is an integer; the descried “metal ion M” is Fe.sup.2+, Co.sup.2+, Ni.sup.2+, Cu.sup.2+; the descried “inorganic anion A” is SiF.sub.6.sup.2−, NbOF.sub.5.sup.2−, TaF.sub.7.sup.2−, ZrF.sub.6.sup.2−, TiF.sub.6.sup.2−, GeF.sub.6.sup.2−, SO.sub.3CF.sub.3.sup.−, NbF.sub.6.sup.−; the descried “organic ligand L” is selected from any of the following:

##STR00001##

The present invention discloses a method of separating C8 aromatic hydrocarbon isomers. The anion-pillared metal-organic framework materials with a pore diameter of 5-10 Å is used as adsorbents to achieve selective adsorption and separation of C8 aromatic hydrocarbon isomers by contacting the C8 aromatic hydrocarbon isomers with the adsorbents; the anion-pillared microporous materials are porous materials formed by metal ion M, inorganic anion A and organic ligand L through coordination bonds, with the general formula of [MAL.sub.2].sub.n, where n>4 and n is an integer; the descried “metal ion M” is Fe.sup.2+, Co.sup.2+, Ni.sup.2+, Cu.sup.2+; the descried “inorganic anion A” is SiF.sub.6.sup.2−, NbOF.sub.5.sup.2−, TaF.sub.7.sup.2−, ZrF.sub.6.sup.2−, TiF.sub.6.sup.2−, GeF.sub.6.sup.2−, SO.sub.3CF.sub.3.sup.−, NbF.sub.6.sup.−; the descried “organic ligand L” is selected from any of the following:

##STR00001##

The present invention discloses a method of separating C8 aromatic hydrocarbon isomers. The anion-pillared metal-organic framework materials with a pore diameter of 5-10 Å is used as adsorbents to achieve selective adsorption and separation of C8 aromatic hydrocarbon isomers by contacting the C8 aromatic hydrocarbon isomers with the adsorbents; the anion-pillared microporous materials are porous materials formed by metal ion M, inorganic anion A and organic ligand L through coordination bonds, with the general formula of [MAL.sub.2].sub.n, where n>4 and n is an integer; the descried “metal ion M” is Fe.sup.2+, Co.sup.2+, Ni.sup.2+, Cu.sup.2+; the descried “inorganic anion A” is SiF.sub.6.sup.2−, NbOF.sub.5.sup.2−, TaF.sub.7.sup.2−, ZrF.sub.6.sup.2−, TiF.sub.6.sup.2−, GeF.sub.6.sup.2−, SO.sub.3CF.sub.3.sup.−, NbF.sub.6.sup.−; the descried “organic ligand L” is selected from any of the following:

##STR00001##

The present invention discloses an integrated process and an apparatus for production of various alcohols and Oligomerization of Olefinic feed stocks comprising butylenes and mixture thereof. In this process the combined light olefinic hydrocarbon feedstock is divided into two streams and contacted in two different reaction zones, viz. hydration and oligomerization. The mixture of alcohols and oligomer product from hydration reaction is separated and the bottom stream from separator is routed to oligomerization reaction zone in a controlled quantity as selectivity enhancer. Both the reaction zones are operated at different conditions. The product from oligomerization zone is further separated in to lighter and heavier components. Each reaction zone may comprise series of reactors filled with acidic catalysts comprising ion exchange resins.

The present invention discloses an integrated process and an apparatus for production of various alcohols and Oligomerization of Olefinic feed stocks comprising butylenes and mixture thereof. In this process the combined light olefinic hydrocarbon feedstock is divided into two streams and contacted in two different reaction zones, viz. hydration and oligomerization. The mixture of alcohols and oligomer product from hydration reaction is separated and the bottom stream from separator is routed to oligomerization reaction zone in a controlled quantity as selectivity enhancer. Both the reaction zones are operated at different conditions. The product from oligomerization zone is further separated in to lighter and heavier components. Each reaction zone may comprise series of reactors filled with acidic catalysts comprising ion exchange resins.

The present invention discloses an integrated process and an apparatus for production of various alcohols and Oligomerization of Olefinic feed stocks comprising butylenes and mixture thereof. In this process the combined light olefinic hydrocarbon feedstock is divided into two streams and contacted in two different reaction zones, viz. hydration and oligomerization. The mixture of alcohols and oligomer product from hydration reaction is separated and the bottom stream from separator is routed to oligomerization reaction zone in a controlled quantity as selectivity enhancer. Both the reaction zones are operated at different conditions. The product from oligomerization zone is further separated in to lighter and heavier components. Each reaction zone may comprise series of reactors filled with acidic catalysts comprising ion exchange resins.