合成低聚甘油M/ZrO2催化剂的制备及性能
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广东工业大学轻工化工学院

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TQ426.94; TQ214

基金项目:

广东省植物资源生物炼制重点实验室资助项目(2021GDKLPRB10)


Preparation and Properties of M/ZrO2 Catalyst for Synthesis of Oligoglycerol
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School of Chemical Engineering and Light Industry Guangdong University of Technology

Fund Project:

Guangdong Provincial Key Laboratory of Plant Resources Biorefinery (2021GDKLPRB10)

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    摘要:

    为寻找一种可用于连续化生产低聚甘油的固体碱催化剂,采用共沉淀法将Na+、K+、Ca2+、Sr2+、Ba2+掺杂到ZrO2中,分别制得Na/ZrO2、K/ZrO2、Ca/ZrO2、Sr/ZrO2、Ba/ZrO2,同时将制得的催化剂用于合成低聚甘油。通过XRD、Raman、CO2-TPD等方法研究掺杂不同金属离子对催化剂结构及其表面碱度的影响。采用GC,ICP等方法研究催化剂的活性和稳定性。结果表明,Na/ZrO2,K/ZrO2为单斜相,Ba/ZrO2为四方相,Ca/ZrO2,Sr/ZrO2为立方相,且各催化剂表现出不同的碱性位点。五种催化剂中Ca/ZrO2表现出最佳的稳定性, Ca2+浸出量为0.003%,催化剂用量减半并循环4次后,甘油转化率保持在22%以上,催化剂回收率在95%以上。在Ca/ZrO2用量为1 g,甘油用量100 g,反应温度270 ℃,反应24 h的条件下,低聚甘油产率为73.05%,选择性为100%。

    Abstract:

    In order to find a solid base catalyst that can be used for the continuous production of oligoglycerol, Na+, K+, Ca2+, Sr2+, and Ba2+ were doped into ZrO2 by co-precipitation method to obtain Na/ZrO2, K/ZrO2, Ca/ZrO2, Sr/ZrO2, Ba/ZrO2, respectively, and the prepared catalyst was used to synthesize oligoglycerol. XRD, Raman, CO2-TPD and other methods were used to study the effects of doping different metal ions on the structure and surface alkalinity of the catalyst. GC, ICP and other methods were used to study the activity and stability of catalysts. The results showed that Na/ZrO2, K/ZrO2 were monoclinic phases, Ba/ZrO2 were tetragonal phases, Ca/ZrO2 and Sr/ZrO2 were cubic phases, and each catalyst showed different basic sites. Among the five catalysts, Ca/ZrO2 showed the best stability, Ca2+ leaching was 0.003%, and after halving the catalyst dosage and cycling for 4 times, the glycerol conversion rate remained above 22% and the catalyst recovery rate was above 95%. Under the conditions of Ca/ZrO2 dosage of 1 g, glycerol dosage of 100 g, reaction temperature of 270 °C, reaction temperature of 24 h, the yield of oligoglycerol was 73.05%, and the selectivity was 100%.

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  • 收稿日期:2022-11-24
  • 最后修改日期:2023-02-08
  • 录用日期:2023-02-13
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