TY - JOUR
T1 - Study of Thermodynamics and Experiment on Direct Synthesis of Dimethyl Carbonate from Carbon Dioxide and Methanol over Yttrium Oxide
AU - Sun, Wen
AU - Zheng, Lan
AU - Wang, Yuqi
AU - Li, Dandi
AU - Liu, Zhiru
AU - Wu, Le
AU - Fang, Tao
AU - Wu, Jinqiao
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/3/11
Y1 - 2020/3/11
N2 - The thermodynamics on the direct synthesis of dimethyl carbonate (DMC) from CO2 and CH3OH was calculated and analyzed. Using Y(NO3)3·6H2O as the precursor, a series of Y2O3 were prepared through the one-pot calcination method, which were employed to catalyze DMC synthesis. The decomposition temperature of Y(NO3)3·6H2O was measured by thermogravimetric analysis, and Y2O3 was obtained after the precursor calcination at desired temperatures, denoted as Y2O3-T (°C). The catalysts were characterized by X-ray diffraction, Brunauer-Emmett-Teller method, transmission electron microscopy, NH3/CO2 temperature-programmed desorption, and X-ray photoelectron spectroscopy to detect the crystal phase, surface property, particle size, acidity-basicity amounts, and oxidation state, respectively. The characterization results indicated that Y2O3-750 can favor the formation of moderate acidic and basic sites and facilitate the activation of CO2 and CH3OH. The catalytic performance evaluation was experimentally investigated, and Y2O3-750 owned the highest DMC yield of 1.02 mmol/g·cat under 90 °C, 8 MPa, and 6 h, which also exhibited reliable recycle ability.
AB - The thermodynamics on the direct synthesis of dimethyl carbonate (DMC) from CO2 and CH3OH was calculated and analyzed. Using Y(NO3)3·6H2O as the precursor, a series of Y2O3 were prepared through the one-pot calcination method, which were employed to catalyze DMC synthesis. The decomposition temperature of Y(NO3)3·6H2O was measured by thermogravimetric analysis, and Y2O3 was obtained after the precursor calcination at desired temperatures, denoted as Y2O3-T (°C). The catalysts were characterized by X-ray diffraction, Brunauer-Emmett-Teller method, transmission electron microscopy, NH3/CO2 temperature-programmed desorption, and X-ray photoelectron spectroscopy to detect the crystal phase, surface property, particle size, acidity-basicity amounts, and oxidation state, respectively. The characterization results indicated that Y2O3-750 can favor the formation of moderate acidic and basic sites and facilitate the activation of CO2 and CH3OH. The catalytic performance evaluation was experimentally investigated, and Y2O3-750 owned the highest DMC yield of 1.02 mmol/g·cat under 90 °C, 8 MPa, and 6 h, which also exhibited reliable recycle ability.
UR - https://www.scopus.com/pages/publications/85080076391
U2 - 10.1021/acs.iecr.9b06092
DO - 10.1021/acs.iecr.9b06092
M3 - 文章
AN - SCOPUS:85080076391
SN - 0888-5885
VL - 59
SP - 4281
EP - 4290
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 10
ER -