Limitations and high pressure behavior of MOF-5 for CO capture
Physical Chemistry Chemical Physics, ISSN: 1463-9076, Vol: 15, Issue: 34, Page: 14319-14327
2013
- 43Citations
- 93Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations43
- Citation Indexes43
- 43
- CrossRef40
- Captures93
- Readers93
- 93
Article Description
Porous network structures (e.g. metal-organic frameworks, MOFs) show considerable potential in dethroning monoethanol amine (MEA) from being the dominant scrubber for CO at the fossil-fuel-burning power generators. In contrast to their promise, structural stability and high-pressure behavior of MOFs are not well documented. We herein report moisture stability, mechanical properties and high-pressure compression on a model MOF structure, MOF-5. Our results show that MOF-5 can endure all tested pressures (0-225 bar) without losing its structural integrity, however, its moist air stability points at a 3.5 hour safety window (at 21.6°C and 49% humidity) for an efficient CO capture. Isosteric heats of CO adsorption at high pressures show moderate interaction energy between CO molecules and the MOF-5 sorbent, which combined with the large sorption ability of MOF-5 in the studied pressure-temperature ranges show the viability of this sorbent for CO capturing purposes. The combination of the physicochemical methods we used suggests a generalized analytical standard for measuring viability in CO capture operations. © the Owner Societies 2013.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84881393071&origin=inward; http://dx.doi.org/10.1039/c3cp51768c; http://www.ncbi.nlm.nih.gov/pubmed/23877231; https://xlink.rsc.org/?DOI=c3cp51768c; https://dx.doi.org/10.1039/c3cp51768c; https://pubs.rsc.org/en/content/articlelanding/2013/cp/c3cp51768c
Royal Society of Chemistry (RSC)
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