A novel hydrocracking Ni-W binary catalyst was tentatively designed and prepared by means ofimpregnation on mixed supports of modified Y zeolite and amorphous aluminosilicate . The structure andproperties of catalyst ...A novel hydrocracking Ni-W binary catalyst was tentatively designed and prepared by means ofimpregnation on mixed supports of modified Y zeolite and amorphous aluminosilicate . The structure andproperties of catalyst were extensively characterized by XRD, NH3-TPD, IR and XRF techniques. The perfor-mance of catalyst was evaluated by a 100-ml hydrogenation laboratory test unit with two single-stage fixed-bedreactors connected in series. The characterization results showed that the catalyst has a developed and con-centrated mesopores distribution, suitable acid sites and acid strength distribution, and uniform and highdispersion of metal sites. Under a high conversion rate of 73.8% with the >350℃ feedstock, a 98.1m% of C5+yield and 83.5% of middle distillates selectivity were obtained. The yield of middle distillates boiling between140℃and 370℃ was 68.70m% and its quality could meet the WWFC category III specification. It means thatthis catalyst could be used to produce more high quality clean middle distillates derived from heavy oilhydrocracking. The potential aromatic content of heavy naphtha from 65℃ to 140℃ was 37.5m%. The BMCIvalue of >370℃ tail oil was 6.6. The heavy naphtha and tail oil are premium feedstocks for catalytic reformingand steam cracker units.展开更多
Batch extractive distillation was studied in a column with amiddle vessel. The process was simulated by a constant holdup modeland solved by two point implicit method. Acetone and methanol mixturewas separated in such...Batch extractive distillation was studied in a column with amiddle vessel. The process was simulated by a constant holdup modeland solved by two point implicit method. Acetone and methanol mixturewas separated in such a setup using water as solvent. The simulationagrees well with experimental results. The experimental andsimulation results show that the solvent at the bottom and theproduct at the top of the column can be withdrawn simulataneously fora long period of time. It needs more time for the solvent to reachhigh purity than that required for the more volatile component toreach high purity, so that the time to withdraw solvent from thebottom is delayed.展开更多
文摘A novel hydrocracking Ni-W binary catalyst was tentatively designed and prepared by means ofimpregnation on mixed supports of modified Y zeolite and amorphous aluminosilicate . The structure andproperties of catalyst were extensively characterized by XRD, NH3-TPD, IR and XRF techniques. The perfor-mance of catalyst was evaluated by a 100-ml hydrogenation laboratory test unit with two single-stage fixed-bedreactors connected in series. The characterization results showed that the catalyst has a developed and con-centrated mesopores distribution, suitable acid sites and acid strength distribution, and uniform and highdispersion of metal sites. Under a high conversion rate of 73.8% with the >350℃ feedstock, a 98.1m% of C5+yield and 83.5% of middle distillates selectivity were obtained. The yield of middle distillates boiling between140℃and 370℃ was 68.70m% and its quality could meet the WWFC category III specification. It means thatthis catalyst could be used to produce more high quality clean middle distillates derived from heavy oilhydrocracking. The potential aromatic content of heavy naphtha from 65℃ to 140℃ was 37.5m%. The BMCIvalue of >370℃ tail oil was 6.6. The heavy naphtha and tail oil are premium feedstocks for catalytic reformingand steam cracker units.
文摘Batch extractive distillation was studied in a column with amiddle vessel. The process was simulated by a constant holdup modeland solved by two point implicit method. Acetone and methanol mixturewas separated in such a setup using water as solvent. The simulationagrees well with experimental results. The experimental andsimulation results show that the solvent at the bottom and theproduct at the top of the column can be withdrawn simulataneously fora long period of time. It needs more time for the solvent to reachhigh purity than that required for the more volatile component toreach high purity, so that the time to withdraw solvent from thebottom is delayed.
