Pluronicf127辅助水热法制备CexZr1−xOy室温催化氧化甲醛

Pluronic F127-assisted hydrothermal synthesis of CexZr1−xOy for room-temperature catalytic oxidation of formaldehyde

  • 摘要: 以阴离子表面活性剂F127为结构导向剂,辅助水热法制备具有介孔结构的催化剂FCexZr1-xOy用于室温下催化氧化甲醛,考察了不同F127添加量及不同铈锆掺杂比例、烧结温度对室温下催化氧化甲醛效果的影响,并采用BET、SEM、IR、XPS、XRD、N2吸附脱附对催化剂进行表征,结果表明,当F127添加量为1.5 g、焙烧温度为500 ℃时,不同Ce/Zr掺杂比例使催化剂的晶粒尺寸、Ce3+含量、比表面积等存在明显差异,其中FCe0.5Zr0.5催化剂的Ce3+含量最高,具有最大比表面积111 m2/g和孔容0.124 cm³·g−1,6 h内表现出甲醛最佳转化率,为84.69%. 反应后催化剂氧空位吸附氧和比表面积大幅降低,晶格氧含量升高,催化剂失活.

     

    Abstract: Using the anionic surfactant F127 as a structure-directing agent, a mesoporous-structured catalyst FCexZr1-xOy was prepared via a hydrothermal method. This catalyst was employed for the catalytic oxidation of formaldehyde at room temperature. The effects of different F127 addition amounts, cerium-zirconium doping ratios, and calcination temperatures on the catalytic oxidation performance of formaldehyde at room temperature were investigated. The catalyst was characterized using BET, SEM, IR, XPS, XRD, and N2 adsorption-desorption techniques. The results showed that when the F127 addition amount was 1.5 g and the calcination temperature was 500 ℃ different Ce/Zr doping ratios led to significant differences in the catalyst's grain size, Ce3+ content, and specific surface area. Among them, the FCe0.5Zr0.5 catalyst exhibited the highest Ce3+ content, the largest specific surface area of 111 m²/g, and the highest pore volume, as well as the best formaldehyde conversion rate within six hours. After the reaction, the oxygen vacancies, adsorbed oxygen, and specific surface area of the catalyst decreased significantly, while the lattice oxygen content increased, leading to catalyst deactivation.

     

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