C10G35/09

PROCESS FOR THE PREPARATION OF A CATALYST SUPPORT
20180099266 · 2018-04-12 ·

Process for preparing a catalyst support which process comprises a) mixing pentasil zeolite having a bulk silica to alumina molar ratio in the range of from 20 to 150 with water, a silica source and an alkali metal salt, b) extruding the mixture obtained in step (a), c) drying and calcining the extrudates obtained in step (b), d) subjecting the calcined extrudates obtained in step (c) to ion exchange to reduce the alkali metal content, and e) drying the extrudates obtained in step (d); process for preparing a catalyst by furthermore impregnating such support with platinum in an amount in the range of from 0.001 to 0.1 wt % and tin in an amount in the range of from 0.01 to 0.5 wt %, each on the basis of total catalyst; ethylbenzene dealkylation catalyst obtainable thereby and a process for dealkylation of ethylbenzene which process comprises contacting feedstock containing ethylbenzene with such catalyst.

Process for the preparation of a catalyst support

Process for preparing a catalyst support which process comprises a) mixing pentasil zeolite having a bulk silica to alumina molar ratio in the range of from 20 to 150 with water, a silica source and an alkali metal salt, b) extruding the mixture obtained in step (a), c) drying and calcining the extrudates obtained in step (b), d) subjecting the calcined extrudates obtained in step (c) to ion exchange to reduce the alkali metal content, and e) drying the extrudates obtained in step (d); process for preparing a catalyst by furthermore impregnating such support with platinum in an amount in the range of from 0.001 to 0.1 wt % and tin in an amount in the range of from 0.01 to 0.5 wt %, each on the basis of total catalyst; ethylbenzene dealkylation catalyst obtainable thereby and a process for dealkylation of ethylbenzene which process comprises contacting feedstock containing ethylbenzene with such catalyst.

UNIT FOR PRODUCING AND SEPARATING AROMATICS WITH RECOVERY OF AN EXTRACT AND/OR RAFFINATE FROM A LIQUID-LIQUID EXTRACTION PROCESS

The invention relates to a production and separation device and method wherein: a reforming effluent (40) is produced and fractionated in a separation unit (1) and a fractionation train (5-6-7) for extracting benzene (22), toluene (23), xylenes (24) and C9-10 aromatics; aromatics are extracted from a feedstock (41) in a liquid-liquid extraction unit (14) to produce a first raffinate (43) and a first extract (42), the first extract (42) being sent to a benzene-toluene fractionation device (5); the xylenes are separated in a xylene separation unit (10) to produce a second extract (31) containing para-xylene, and a second raffinate (32) containing ortho-xylene and meta-xylene; and the second raffinate is isomerised in an isomerisation unit (11) so as to produce an isomerate (34) enriched in para-xylene sent to a fractionation train (5-6-7).

UNIT FOR PRODUCING AND SEPARATING AROMATICS WITH RECOVERY OF AN EXTRACT AND/OR RAFFINATE FROM A LIQUID-LIQUID EXTRACTION PROCESS

The invention relates to a production and separation device and method wherein: a reforming effluent (40) is produced and fractionated in a separation unit (1) and a fractionation train (5-6-7) for extracting benzene (22), toluene (23), xylenes (24) and C9-10 aromatics; aromatics are extracted from a feedstock (41) in a liquid-liquid extraction unit (14) to produce a first raffinate (43) and a first extract (42), the first extract (42) being sent to a benzene-toluene fractionation device (5); the xylenes are separated in a xylene separation unit (10) to produce a second extract (31) containing para-xylene, and a second raffinate (32) containing ortho-xylene and meta-xylene; and the second raffinate is isomerised in an isomerisation unit (11) so as to produce an isomerate (34) enriched in para-xylene sent to a fractionation train (5-6-7).

Naphtha reforming process

The present disclosure relates to a naphtha reforming process for obtaining reformed naphtha comprising contacting naphtha with a catalyst, the catalyst comprising a chloride free zeolite coated alumina support impregnated with 0.01 wt % to 0.5 wt % active metal and 0.01 wt % to 0.5 wt % promoter metal, wherein the thickness of the zeolite coating on the alumina support ranges from 100 m to 200 m, which results in formation of reformed products of naphtha and ethylbenzene formed in-situ.

Naphtha reforming process

The present disclosure relates to a naphtha reforming process for obtaining reformed naphtha comprising contacting naphtha with a catalyst, the catalyst comprising a chloride free zeolite coated alumina support impregnated with 0.01 wt % to 0.5 wt % active metal and 0.01 wt % to 0.5 wt % promoter metal, wherein the thickness of the zeolite coating on the alumina support ranges from 100 m to 200 m, which results in formation of reformed products of naphtha and ethylbenzene formed in-situ.

Method for regenerating semi-regenerated reforming catalyst

This disclosure describes a method for regenerating a semi-regenerated reforming catalyst. The method comprises adjusting the reaction temperature to 250-480 C., introducing a sulfur-containing naphtha into the reforming reactor, or stopping introducing a feedstock into the reforming reactor, and introducing a sulfur-containing hydrogen into a recycle gas, until the sulfur content in the catalyst is 0.32-0.8 mass %, then the catalyst is subject to coke-burning, oxychlorination and reduction. Alternatively, the method first subjects the spent catalyst to coke-burning followed by introducing sulfate ions thereinto; and then performing oxychlorination and reduction. Disclosed is still another method for regenerating a platinum-rhenium reforming catalyst, which comprises coke-burning the spent catalyst; introducing sulfur and chlorine in the catalyst by impregnation; and then drying, calcinating and reducing.

Method for regenerating semi-regenerated reforming catalyst

This disclosure describes a method for regenerating a semi-regenerated reforming catalyst. The method comprises adjusting the reaction temperature to 250-480 C., introducing a sulfur-containing naphtha into the reforming reactor, or stopping introducing a feedstock into the reforming reactor, and introducing a sulfur-containing hydrogen into a recycle gas, until the sulfur content in the catalyst is 0.32-0.8 mass %, then the catalyst is subject to coke-burning, oxychlorination and reduction. Alternatively, the method first subjects the spent catalyst to coke-burning followed by introducing sulfate ions thereinto; and then performing oxychlorination and reduction. Disclosed is still another method for regenerating a platinum-rhenium reforming catalyst, which comprises coke-burning the spent catalyst; introducing sulfur and chlorine in the catalyst by impregnation; and then drying, calcinating and reducing.

PROCESS FOR THE PREPARATION OF A CATALYST SUPPORT
20170182483 · 2017-06-29 ·

Process for preparing a catalyst support which process comprises a) mixing pentasil zeolite having a bulk silica to alumina molar ratio in the range of from 20 to 150 with water, a silica source and an alkali metal salt, b) extruding the mixture obtained in step (a), c) drying and calcining the extrudates obtained in step (b), d) subjecting the calcined extrudates obtained in step (c) to ion exchange to reduce the alkali metal content, and e) drying the extrudates obtained in step (d); process for preparing a catalyst by furthermore impregnating such support with platinum in an amount in the range of from 0.001 to 0.1 wt % and tin in an amount in the range of from 0.01 to 0.5 wt %, each on the basis of total catalyst; ethylbenzene dealkylation catalyst obtainable thereby and a process for dealkylation of ethylbenzene which process comprises contacting feedstock containing ethylbenzene with such catalyst.

CATALYST, A PROCESS FOR PREPARATION OF THE CATALYST AND APPLICATION THEREOF

The present disclosure relates to a composition, wherein the composition is a catalyst comprising support matrix, active metal, promoter metal and halide, wherein the support matrix is additionally subjected to a modifier to obtain a modified support matrix. The catalyst in the reaction reduces the percentage coke formation and provides for an enhanced reformate yield having an increase total aromatic yield and C8 aromatic yield when compared to the known/commercially available catalyst for naphtha reforming process, and also improves the quality of reformate obtained at end of the reaction. The disclosure further relates to process of preparation of the catalyst, the catalyst of the present disclosure derived from the process described, displays lower deactivation during the reaction demonstrating increased stability and reduction in the regeneration frequency and thereby making the catalyst economically feasible.