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Combination of Cu/ZnO methanol synthesis catalysts and ZSM-5 zeolites to produce oxygenates from CO2 and H2 - data

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posted on 2024-09-18, 10:58 authored by Anisa Tariq, Jonathan Ruiz EsquiusJonathan Ruiz Esquius, Thomas DaviesThomas Davies
<p>Cu/ZnO methanol catalysts were deposited over several ZSM-5 acid zeolites (Si/Al = 30, 50 and 80) to directly synthesise oxygenates (methanol and dimethyl ether) from a CO<sub>2</sub>/H<sub>2</sub> feed. Catalysts were prepared by two different preparation methodologies: chemical vapour impregnation (CZZ-CVI) and oxalate gel precipitation (CZZ-OG). Chemical vapour impregnation led to Cu/ZnO being unevenly deposited on the zeolite surface, whilst oxalate gel precipitation led to the formation of Cu/ZnO agglomerates.</p><p>For both sets of catalysts a higher concentration of mild and strong acid sites were produced, compared to the parent ZSM-5 zeolites, and CZZ-CVI had a higher concentration of acid sites compared to CZZ-OG. Nevertheless, CZZ-OG shows considerably higher oxygenate productivity, 1322 mmol Kg<sub>cat</sub><sup>-1</sup> h<sup>-1</sup>, compared to 192 mmol Kg<sub>cat</sub><sup>-1</sup> h<sup>-1</sup> over CZZ-CVI (ZSM-5(50), 250 °C, 20 bar, CO<sub>2</sub>/H<sub>2</sub>=1/3, 30 ml min<sup>-1</sup>), which could be assigned to a combination of smaller particle size and enhanced methanol mass transfer within the zeolites.</p><p>Increasing the concentration of Al on the zeolite led to a greater productivity of by-products, formed through the methanol/DME-to-hydrocarbons process (MTH/DMTH).</p><p>Catalysts were characterised by XRD, TEM, N<sub>2</sub> absorption and NH<sub>3</sub>-TPD.</p><p>Research results based upon these data are published at http://doi.org/10.1007/s11244-021-01447-8<br></p><p><br></p>

Funding

Flexible routes to liquid fuels from co2 by advanced catalysis and engineering (2016-03-31 - 2020-09-30); Hutchings, Graham. Funder: Engineering and Physical Sciences Research Council:IRIS 130635/54

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  • English-Great Britain (EN-GB)

Data-collection start date

2019-02-01

Data-collection end date

2021-02-22

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