1,4-丁炔二醇选择性加氢催化剂:Pd/ZrO2及其碱金属改性
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1.四川大学 化学工程学院;2.重庆理工大学 化学化工学院;3.四川大学 新能源与低碳技术研究院

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Selective hydrogenation of 1,4-butynediol to 1,4-butenediol: Pd/ZrO2 catalyst and the effect of alkali metals
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1.School of Chemical Engineering, Sichuan University;2.School of Chemistry and Chemical Engineering, Chongqing University of Technolog;3.Institute of New Energy and Low-Carbon Technology, Sichuan University

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    摘要:

    本文以Zr(OH)4焙烧所得ZrO2为载体,采用等体积浸渍法制备了负载型Pd/ZrO2和碱金属改性的Pd/M/ZrO2催化剂,通过BET、XRD、CO2-TPD、XPS和TEM对催化剂结构和性质进行了表征,并对其在1,4-丁炔二醇(BYD)选择性加氢制1,4-丁烯二醇(BED)反应中的活性、选择性和稳定性进行了研究,考察了反应气氛、碱金属改性等对其活性和稳定性的影响。结果表明1.0% Pd/ZrO2在50 ℃,2.40 MPa H2下,能够催化1,4-丁炔二醇选择性加氢生成1,4-丁烯二醇,有较高的催化活性〔0.048 molBYD/(gPd·s)〕,在BYD完全转化的条件下,BED选择性为91.2%。反应体系中引入氨,能够显著抑制催化剂加氢活性,提高BED选择性。在BYD接近完全转化时,BED选择性可达95.6%。向ZrO2载体中引入少量的碱金属(Li、Na、K、Rb、Cs)能够提高BED选择性,其中Rb的影响最为显著,BED选择性可达94.1%。

    Abstract:

    Pd/ZrO2 and alkali metal doped Pd/M/ZrO2 catalysts were prepared by incipient-wetness impregnation with ZrO2 from Zr(OH)4 calcination as the support. These catalysts were applied to the selective hydrogenation of 1,4-butynediol (BYD) to 1,4-butenediol (BED). The structures and properties of the catalysts were characterized by BET, XRD, CO2-TPD, XPS, and TEM. The effects of reaction atmosphere and alkali metal dopant on the activity, selectivity and stability of the catalysts in hydrogenation of BYD to BED were investigated. 1.0% Pd/ZrO2 exhibited high catalytic activity (0.048 molBYD/(gPd·s)) and reasonable selectivity of BED (xBYD≈100%,SBED=91.2%) under the conditions of 50 ℃, 2.40 MPa H2 pressure. The presence of ammonia into the reaction mixture inhibits the hydrogenation activity but improves the selectivity of BED. 95.6% selectivity of BED was achieved with complete conversion of BYD. The doping of alkali metals (Li, Na, K, Rb, Cs) onto ZrO2 support improves the selectivity of BED, and Rb is the most effective dopant with BED selectivity up to 94.1%.

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周港,谭平华,吴潘,何坚,蒋 炜,刘长军,梁斌.1,4-丁炔二醇选择性加氢催化剂:Pd/ZrO2及其碱金属改性[J].精细化工,2024,41(3):

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  • 收稿日期:2023-03-26
  • 最后修改日期:2023-05-04
  • 录用日期:2023-05-08
  • 在线发布日期: 2024-03-07
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