4.8 Article

Facile Preparation of Methyl Phenols from Ethanol over Lamellar Ce(OH)SO4•xH2O

期刊

ACS CATALYSIS
卷 11, 期 10, 页码 6162-6174

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c01096

关键词

lamellar rare earth material; ethanol transformation; methyl phenols; kinetics; rate-determining step

资金

  1. 111 Project of China [B18030]
  2. Fundamental Research Funds for the Central Universities, Nankai University [63201071, ZB19500202]
  3. open foundation of Key Laboratory of Industrial Ecology and Environmental Engineering of Ministry of Education, Dalian University of Technology [KLIEEE-19-07]
  4. Natural Science Foundation of Tianjin [19JCYBJC20500]
  5. National Key R&D Program of China [2017YFA0208000]
  6. National Natural Science Foundation of China [21971117, 21771156]
  7. State Key Laboratory of Rare Earth Resource Utilization [RERU2019001]
  8. Beijing-Tianjin-Hebei Collaborative Innovation Project [63201058]

向作者/读者索取更多资源

This study demonstrates the high efficiency of a novel Ce(OH)SO4•xH2O catalyst for the selective upgrading of ethanol transformation, especially for high weight molecules. Combining kinetic, thermodynamic, and in situ spectroscopy measurements provided insights into the key reaction intermediates and mechanisms during the catalysis, as well as the active species and their mechanisms of action.
Ethanol transformation with high product selectivity is a great challenge, especially for high weight molecules. Here, we show a combination study of kinetic, thermodynamic, and in situ spectroscopy measurements to probe the selective upgrading of ethanol over lamellar Ce(OH)SO4 center dot xH(2)O catalysts, with 60-70% Ce3+ preserved during the catalysis. High methyl phenols (MPs) selectivity at similar to 80% within condensation products was achieved at similar to 50% condensation yield (3.0 kPa C2H5OH, 15 kPa H-2, Ar balanced, 693 K, 1 atm, gas hourly space velocity (GHSV) similar to 5.4 min(-1)), with acetaldehyde, acetone, 4-heptanone, and 2-pentanone as the key reaction intermediates. Kinetic measurements with the assistance of isotope labeling proved that MPs generated from the kinetically relevant step (KRS) of C-C bond coupling of enolate nucleophilically attacks surface C2H4O following a Langmuir-Hinshelwood model. Low ethanol and water pressures and high acetaldehyde and hydrogen pressures were proved to be favored for MPs generation rather than dehydration, in which hydrogen could reduce the amount of lattice oxygen and facilitate the preparation of MPs while water and ethanol both compete with acetaldehyde for active sites during catalysis. On the basis of in situ X-ray diffraction (XRD), quasi-in situ X-ray photoelectron spectroscopy (XPS), and Raman characterizations, the Ce(OH)SO4 crystal structure was proved to be maintained along with ethanol activation, and the Ce3+-OH Lewis acid-base pair was proved to be the active species for the selective C-C bond coupling. The KRS assumption was also supported by the apparent activation energy assessment within the reaction network on dehydration, dehydrogenation, aldol condensation, and cyclization and a series of negligible kinetic isotope effects (KIEs). This system can be easily extended to some other systems related to C-C bond coupling and is attracting attention on converting oxygenate platform molecules over lanthanide species.

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