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非均相催化剂羰基合成醋酐工艺研究 被引量:3
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作者 吴良彪 冷宝林 王建荣 《广州化工》 CAS 2013年第18期93-95,共3页
以醋酸甲酯、甲醇和一氧化碳为原料,选用铑系催化剂,碘甲烷、醋酸锂为助催化剂,选用高压釜,非均相羰基合成醋酐,为进一步研究中试放大,对羰基合成小试工艺进行研究。对小试提供的最佳工艺条件进行研究考核,结果表明:在温度190~... 以醋酸甲酯、甲醇和一氧化碳为原料,选用铑系催化剂,碘甲烷、醋酸锂为助催化剂,选用高压釜,非均相羰基合成醋酐,为进一步研究中试放大,对羰基合成小试工艺进行研究。对小试提供的最佳工艺条件进行研究考核,结果表明:在温度190~200℃下,压力5~5.5 MPa,催化剂质量分数20%~25%,碘甲烷浓度3mol/L,醋酸锂浓度1mol/L,反应时间80-100min的工艺条件下,按醋酐选择性为96%,CO转化率为97%,羰基产物醋酐收率为94%,醋酐的时空收率为460molAc_2O/(molRh·h)。此工艺数据的可以指导中试放大,并为工业化生产提供基础数据。 展开更多
关键词 非均相羰基化 醋酐 醋酸甲酯 铑系催化剂 碘甲烷
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Study on Direct Synthesis of Diphenyl Carbonate with Heterogeneous Catalytic Reaction (V) Screening Catalysts and Optimizing Synthesis Conditions 被引量:7
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作者 张光旭 吴元欣 +4 位作者 马沛生 田崎峰 吴广文 李定或 王存文 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2003年第5期526-530,共5页
Pd/LaxPbyMnOz, Pd/C, Pd/molecular sieve and Pd-heteropoly acid catalysts for direct synthesis of diphenyl carbonate (DPC) by heterogeneous catalytic reaction were compared and the results of DPC synthesis indicated th... Pd/LaxPbyMnOz, Pd/C, Pd/molecular sieve and Pd-heteropoly acid catalysts for direct synthesis of diphenyl carbonate (DPC) by heterogeneous catalytic reaction were compared and the results of DPC synthesis indicated that the catalyst Pd/LaxPbyMnOz had higher activity. The Pd/LaxPbyMnOz catalyst and the support was characterized by XRD, SEM and TEM, the main phase was Lao.szPbo.asMnOa and the average diameter could be about 25.4nm. The optimuna conditions for synthesis of DPC with Pd/LasPbyMnOz were determined by orthogonal experiments and the experimental results showed that reaction temperature was the first factor of effect on the selectivity and yield of DPC, and the concentration of O2 in gas phase also had significant effect on selectivity of DPC. The optimum reaction conditions were catalyst/phenol mass ratio l to 50, pressure 4.5MPa, volume concentration of O2 25%, reaction temperature 60℃ and reaction time 4 h. The maximum yield and average selectivity could reach 13% and 97% respectively in the batch operation. 展开更多
关键词 diphenyl carbonate supported catalyst heterogeneous catalytic reaction optimum conditions
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Acid‐promoted Ir‐La‐S/AC‐catalyzed methanol carbonylation on single atomic active sites 被引量:4
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作者 Zhou Ren Yuan Lyu +2 位作者 Siquan Feng Xiangen Song Yunjie Ding 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2018年第6期1060-1069,共10页
Highly active Ir‐La‐S/AC catalyst was successfully prepared by co‐impregnation of an activated carbon(AC) carrier with a sulfuric acid solution of Ir and La species and compared with a tradition‐ally prepared Ir... Highly active Ir‐La‐S/AC catalyst was successfully prepared by co‐impregnation of an activated carbon(AC) carrier with a sulfuric acid solution of Ir and La species and compared with a tradition‐ally prepared Ir‐La/AC catalyst. High angle annular dark‐field‐scanning transmission electron mi‐croscopy(HAADF‐STEM) measurement results show that most of the Ir species on Ir‐La‐S/AC exist as single atomic sites, while those on Ir‐La/AC exist as nanoparticles with an average diameter of 1.5 nm. Evaluation of Ir‐La‐S/AC as a catalyst for heterogeneous carbonylation of methanol to acetyl gave a maximum TOF (turn‐over‐frequency) of 2760 h^–1, which was distinctly higher than that achieved by the Ir‐La/AC catalyst(approximately 1000 h^-1). Temperature‐programmed desorption of ammonia(NH3‐TPD) result shows that the addition of sulfuric acid during the preparation pro‐cedure results in significantly more acidic sites on Ir‐La‐S/AC than those on Ir‐La/AC, which plays a key role in the enhancement of CO insertion as the rate‐determining step. Tempera‐ture‐programmed reduction(TPR) and in situ X‐ray photoelectron spectroscopy reveal that Ir spe‐cies are more reducible, and that more Ir^+ might be formed by activation of Ir‐La‐S/AC than those on the Ir‐La/AC catalyst, which is thought to be beneficial for reductive elimination of AcI from Ir^3+ species as an essential step for CH3I regeneration and acetyl formation. 展开更多
关键词 Heterogeneous METHANOL carbonylationIr‐La‐S/ACcatalyst BIFUNCTIONAL catalyst Single‐atomic active site Co‐impregnation
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武汉化工学院攻克非光气法制PC的技术难关
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《甲醛与甲醇》 2003年第4期40-40,共1页
关键词 武汉化工学院 非光气法 制备 PC 光盘级 聚碳酸酯 原料 碳酸二苯酯 非均相催化氧化羰基化
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