Hydrogenation of CO2 to Dimethyl Ether over Brønsted Acidic PdZn Catalysts
Author(s) -
Hasliza Bahruji,
Robert D. Armstrong,
Jonathan Ruiz Esquius,
Wilm Jones,
Michael Bowker,
Graham J. Hutchings
Publication year - 2018
Publication title -
industrial and engineering chemistry research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.878
H-Index - 221
eISSN - 1520-5045
pISSN - 0888-5885
DOI - 10.1021/acs.iecr.8b00230
Subject(s) - dimethyl ether , catalysis , methanol , chemistry , oxygenate , dehydration , ether , brønsted–lowry acid–base theory , inorganic chemistry , organic chemistry , biochemistry
Eschewing the common trend toward use of catalysts composed of Cu, it is reported that PdZn alloys are active for CO2 hydrogenation to oxygenates. It is shown that enhanced CO2 conversion is achievable through the introduction of Bronsted acid sites, which promote dehydration of methanol to dimethyl ether. We report that deposition of PdZn alloy nanoparticles onto the solid acid ZSM-5, via chemical vapor impregnation affords catalysts for the direct hydrogenation of CO2 to DME. This catalyst shows dual functionality; catalyzing both CO2 hydrogenation to methanol and its dehydration to dimethyl in a single catalyst bed, at temperatures of >270 °C. A physically mixed bed comprising 5% Pd 15% Zn/TiO2 and H-ZSM-5 shows a comparably high performance, affording a dimethyl ether synthesis rate of 546 mmol kgcat–1 h–1 at a reaction temperature of 270 °C.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom