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Nano-ZrO_2 as hydrogenation phase in bi-functional catalyst for syngas aromatization

机译:纳米ZrO_2作为双功能催化剂加氢合成气芳构化的加氢相

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摘要

Oxide-zeolite bi-functional catalyst has shown promising potential in syngas aromatization. As hydrogenation phase in bi-functional catalyst, the preparation method of metal oxide will influence bi-functional catalyst properties. Herein, a series of nano-ZrO2 is successfully synthesized by using UiO-66 pyrolysis, hydrothermal, water/oil interface and sol-gel method. After thoroughly characterized through X-ray diffraction, transmission electron microscopy, N-2 adsorption, pyridine-adsorbed infrared spectroscopy, temperature programmed desorption of NH3/CO/H-2, X-ray photoelectron spectroscopy, electron paramagnetic resonance and temperature programmed reduction of H-2. We find ZrO2 preparation method directly influences its surface oxygen vacancy content, inducing the variation of acid amount and acid distribution over ZrO2 surface. Combine the result of density functional theory calculation with catalyst evaluation, the oxygen vacancy determines ZrO2 catalytic properties. As the catalytic site, oxygen vacancy is responsible for CO activation, and beneficial for the intermediates CH3OH formation. In this case, using hydro-ZrO2 as hydrogenation phase, adjusting the zeolite acidity and the ratio between metal oxide and zeolite, the derived bi-functional catalyst shows 21.59% CO conversion under 1200 ml/(g(cat).h), the aromatic selectivity reaches 95.13% in C-5(+). Furthermore, the catalyst shows excellent stability during a 120 h stability test.
机译:氧化物-沸石双功能催化剂在合成气芳构化中显示出有希望的潜力。作为双功能催化剂中的氢化相,金属氧化物的制备方法会影响双功能催化剂的性能。本文采用UiO-66热解,水热,水/油界面和溶胶-凝胶法成功合成了一系列纳米ZrO2。在通过X射线衍射,透射电子显微镜,N-2吸附,吡啶吸附的红外光谱,NH3 / CO / H-2的程序升温脱附,X射线光电子能谱,电子顺磁共振和程序升温还原进行了彻底表征后H-2。我们发现ZrO2的制备方法直接影响其表面氧空位含量,引起ZrO2表面酸量和酸分布的变化。将密度泛函理论计算的结果与催化剂评估相结合,氧空位决定了ZrO2的催化性能。氧空位作为催化位点,负责CO的活化,并有利于中间体CH3OH的形成。在这种情况下,使用氢化ZrO2作为氢化相,调节沸石的酸度和金属氧化物与沸石的比例,在1200 ml /(g(cat..h))下,衍生的双官能催化剂的CO转化率为21.59%。在C-5(+)中,芳烃的选择性达到95.13%。此外,该催化剂在120小时稳定性测试中显示出极好的稳定性。

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