Patent classifications
C07C15/073
PROCESS FOR PRODUCING PARA-XYLENE AND ETHYLBENZENE FROM C8 AROMATICS CONTAINING ETHYLBENZENE
A process for producing para-xylene and ethylbenzene from C.sub.8 aromatics containing ethylbenzene includes the steps of sending C.sub.8 aromatics containing ethylbenzene to an ethylbenzene liquid-phase adsorption separation device, wherein a suction liquid containing ethylbenzene and a suction residual liquid are obtained after the adsorption separation, and the desorbents in the suction liquid and the suction residual liquid are removed to obtain ethylbenzene and a suction residual oil; sending the suction residual oil to a para-xylene adsorption separation device, and unadsorbed components are discharged as a raffinate from the adsorbent bed; the adsorbent bed is rinsed with a desorbent to desorb the para-xylene therein and obtain an extract; the desorbents in the extract and the raffinate are respectively removed to obtain para-xylene and a raffinate oil; sending the raffinate oil to a xylene isomerization device to carry out xylene isomerization, and the isomerization product is fractionated.
PROCESS FOR PRODUCING PARA-XYLENE AND ETHYLBENZENE FROM C8 AROMATICS CONTAINING ETHYLBENZENE
A process for producing para-xylene and ethylbenzene from C.sub.8 aromatics containing ethylbenzene includes the steps of sending C.sub.8 aromatics containing ethylbenzene to an ethylbenzene liquid-phase adsorption separation device, wherein a suction liquid containing ethylbenzene and a suction residual liquid are obtained after the adsorption separation, and the desorbents in the suction liquid and the suction residual liquid are removed to obtain ethylbenzene and a suction residual oil; sending the suction residual oil to a para-xylene adsorption separation device, and unadsorbed components are discharged as a raffinate from the adsorbent bed; the adsorbent bed is rinsed with a desorbent to desorb the para-xylene therein and obtain an extract; the desorbents in the extract and the raffinate are respectively removed to obtain para-xylene and a raffinate oil; sending the raffinate oil to a xylene isomerization device to carry out xylene isomerization, and the isomerization product is fractionated.
METHOD FOR SEPARATING C8 AROMATIC HYDROCARBON ISOMER MIXTURE
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##
METHOD FOR SEPARATING C8 AROMATIC HYDROCARBON ISOMER MIXTURE
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##
METHOD FOR PREPARING A CATALYST CONTAINING AN ACTIVE NICKEL PHASE DISTRIBUTED IN A SHELL AND A NICKEL-COPPER ALLOY
A process for preparing a catalyst comprising nickel and copper, comprising the following steps: impregnating the porous support with a volume of a butanol solution of between 0.2 and 0.8 times the total pore volume of the support; maturing the impregnated porous support for 0.5 to 40 hours; impregnating the matured impregnated support with a solution comprising a precursor of the nickel active phase; impregnating the support with a solution containing a copper precursor and a nickel precursor.
METHOD FOR PREPARING A CATALYST CONTAINING AN ACTIVE NICKEL PHASE DISTRIBUTED IN A SHELL AND A NICKEL-COPPER ALLOY
A process for preparing a catalyst comprising nickel and copper, comprising the following steps: impregnating the porous support with a volume of a butanol solution of between 0.2 and 0.8 times the total pore volume of the support; maturing the impregnated porous support for 0.5 to 40 hours; impregnating the matured impregnated support with a solution comprising a precursor of the nickel active phase; impregnating the support with a solution containing a copper precursor and a nickel precursor.
METHOD FOR PREPARING A CATALYST COMPRISING AN ACTIVE NICKEL PHASE DISTRIBUTED IN A SHELL
A process for preparing a catalyst comprising an active phase based on nickel and an alumina support, which process comprises the following steps: a) said support is impregnated with a volume V1 of a butanol solution of between 0.2 and 0.8 times the total pore volume TPV of said support in order to obtain an impregnated support; b) the impregnated support obtained at the end of step a) is left to mature for 0.5 to 40 hours; c) the matured impregnated support obtained at the end of step b) is impregnated with a solution comprising at least one precursor of the nickel active phase in order to obtain a catalyst precursor; d) the catalyst precursor obtained at the end of step c) is dried at a temperature below 250° C.
METHOD FOR PREPARING A CATALYST COMPRISING AN ACTIVE NICKEL PHASE DISTRIBUTED IN A SHELL
A process for preparing a catalyst comprising an active phase based on nickel and an alumina support, which process comprises the following steps: a) said support is impregnated with a volume V1 of a butanol solution of between 0.2 and 0.8 times the total pore volume TPV of said support in order to obtain an impregnated support; b) the impregnated support obtained at the end of step a) is left to mature for 0.5 to 40 hours; c) the matured impregnated support obtained at the end of step b) is impregnated with a solution comprising at least one precursor of the nickel active phase in order to obtain a catalyst precursor; d) the catalyst precursor obtained at the end of step c) is dried at a temperature below 250° C.
USE OF MAGNETIC MESOPOROUS POLY(IONIC LIQUID) INTERFACIAL CATALYST IN HYDROGENATION REACTION AND PREPARATION OF BIODIESEL
The disclosure provides use of an efficient, recyclable, green and friendly catalyst to realize a method of hydrogenation of an unsaturated alkene, and a method for preparing biodiesel through the transesterification of soybean oil with ethanol. The method of hydrogenation of the unsaturated alkene comprises performing a hydrogenation reaction of an unsaturated alkene at ambient temperature and atmospheric pressure by using a CO.sub.2 and magnetic dual-responsive mesoporous poly(ionic liquid) as a catalyst I, and using n-hexane and water as a solvent, to obtain a corresponding saturated alkane. The method for preparing biodiesel through transesterification of soybean oil with ethanol comprises performing a transesterification reaction of soybean oil with ethanol at a temperature of 25-90° C. and atmospheric pressure by using a CO.sub.2 and magnetic dual-responsive mesoporous poly(ionic liquid) as a catalyst II, to obtain the biodiesel.
USE OF MAGNETIC MESOPOROUS POLY(IONIC LIQUID) INTERFACIAL CATALYST IN HYDROGENATION REACTION AND PREPARATION OF BIODIESEL
The disclosure provides use of an efficient, recyclable, green and friendly catalyst to realize a method of hydrogenation of an unsaturated alkene, and a method for preparing biodiesel through the transesterification of soybean oil with ethanol. The method of hydrogenation of the unsaturated alkene comprises performing a hydrogenation reaction of an unsaturated alkene at ambient temperature and atmospheric pressure by using a CO.sub.2 and magnetic dual-responsive mesoporous poly(ionic liquid) as a catalyst I, and using n-hexane and water as a solvent, to obtain a corresponding saturated alkane. The method for preparing biodiesel through transesterification of soybean oil with ethanol comprises performing a transesterification reaction of soybean oil with ethanol at a temperature of 25-90° C. and atmospheric pressure by using a CO.sub.2 and magnetic dual-responsive mesoporous poly(ionic liquid) as a catalyst II, to obtain the biodiesel.