The invention provides a modified zeolite, a method of preparing the modified zeolite and a method of one cycle alkylating benzene in presence of one of an unmodified and modified zeolite catalyst. The modified zeolite catalyst includes zeolite with ratio of silica to alumina ranging between 5% to 95% of silica and 95% to 5% alumina, kaolinite and a binder, wherein the zeolite is modified with one or more metal oxides of Lanthanide-series of the Periodic Table. The method of alkylating benzene is one cycle process in presence of a catalyst that includes charging benzene and ethylene gas feedstock to an alkylation zone. Heated benzene and the ethylene gas feedstock are contacted in a fixed bed reactor in the alkylation zone. The catalyst for alkylating benzene is added in a catalyst zone of the fixed bed reactor.

The invention provides a modified zeolite, a method of preparing the modified zeolite and a method of one cycle alkylating benzene in presence of one of an unmodified and modified zeolite catalyst. The modified zeolite catalyst includes zeolite with ratio of silica to alumina ranging between 5% to 95% of silica and 95% to 5% alumina, kaolinite and a binder, wherein the zeolite is modified with one or more metal oxides of Lanthanide-series of the Periodic Table. The method of alkylating benzene is one cycle process in presence of a catalyst that includes charging benzene and ethylene gas feedstock to an alkylation zone. Heated benzene and the ethylene gas feedstock are contacted in a fixed bed reactor in the alkylation zone. The catalyst for alkylating benzene is added in a catalyst zone of the fixed bed reactor.

The present disclosure relates to a process for preparing linear alkyl benzne (LAB). The process comprises alkylation of benzene with an alkylating agent in the presence of an ionic liquid to obtain a first product mixture comprising a first organic phase and a first aqueous phase comprising first partially spent ionic liquid. The first organic phase is deacidified and fractionally distilled to obtain a fraction comprising LAB and a fraction comprising HAB. The fraction comprising HAB is transalkylated with benzene in the presence of the ionic liquid to obtain a second product mixture comprising a second organic phase comprising LAB and a second aqueous phase comprising second partially spent ionic liquid. The partially spent ionic liquids are regenerated, and reused in the steps of alkylation or transalkylation for at least 6 cycles.

The present disclosure relates to a process for preparing linear alkyl benzne (LAB). The process comprises alkylation of benzene with an alkylating agent in the presence of an ionic liquid to obtain a first product mixture comprising a first organic phase and a first aqueous phase comprising first partially spent ionic liquid. The first organic phase is deacidified and fractionally distilled to obtain a fraction comprising LAB and a fraction comprising HAB. The fraction comprising HAB is transalkylated with benzene in the presence of the ionic liquid to obtain a second product mixture comprising a second organic phase comprising LAB and a second aqueous phase comprising second partially spent ionic liquid. The partially spent ionic liquids are regenerated, and reused in the steps of alkylation or transalkylation for at least 6 cycles.

The present disclosure relates to a process for preparing linear alkyl benzne (LAB). The process comprises alkylation of benzene with an alkylating agent in the presence of an ionic liquid to obtain a first product mixture comprising a first organic phase and a first aqueous phase comprising first partially spent ionic liquid. The first organic phase is deacidified and fractionally distilled to obtain a fraction comprising LAB and a fraction comprising HAB. The fraction comprising HAB is transalkylated with benzene in the presence of the ionic liquid to obtain a second product mixture comprising a second organic phase comprising LAB and a second aqueous phase comprising second partially spent ionic liquid. The partially spent ionic liquids are regenerated, and reused in the steps of alkylation or transalkylation for at least 6 cycles.

A process for producing alkylaromatic compounds is described. The process involves utilizing at least a portion of the aromatic compound used to regenerate the alkylation catalyst in a spent alkylation reaction zone as a reactant in the active alkylation reaction zone.

A process for producing alkylaromatic compounds is described. The process involves utilizing at least a portion of the aromatic compound used to regenerate the alkylation catalyst in a spent alkylation reaction zone as a reactant in the active alkylation reaction zone.

A process for producing alkylaromatic compounds is described. The process involves utilizing at least a portion of the aromatic compound used to regenerate the alkylation catalyst in a spent alkylation reaction zone as a reactant in the active alkylation reaction zone.

The present invention relates to an integrated process for increasing the research octane number (RON) of FCC gasoline with simultaneous reduction in benzene content. In this process, benzene rich gasoline fraction is reacted with light olefin rich gaseous streams like FCC off gas/dry gas, coker off gas to produce alkyl aromatics using FCC catalyst system containing ZSM-5 zeolite. The catalyst is continuously drawn from the FCC regenerator by suitably placing the alkylation reactor in communication with the FCC regenerator. The product stream of the alkylation reactor is routed to main fractionator for separation of off gas and benzene lean gasoline. This integrated process not only improves the octane number of gasoline but also lowers the gasoline benzene content. Further the integrated alkylation reactor system acts as a heat sink lowering the FCC regenerator temperature and enables the FCC unit to process high CCR feeds.

A method is provided for predicting conjunct polymer concentration in spent ionic liquid during a continuous hydrocarbon conversion process.