Alkaline thermal treatment of seaweed for high-purity hydrogen production with carbon capture and storage potential
Nature Communications, ISSN: 2041-1723, Vol: 11, Issue: 1, Page: 3783
2020
- 52Citations
- 133Captures
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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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations52
- Citation Indexes51
- 51
- CrossRef20
- Policy Citations1
- Policy Citation1
- Captures133
- Readers133
- 133
Article Description
Current thermochemical methods to generate H include gasification and steam reforming of coal and natural gas, in which anthropogenic CO emission is inevitable. If biomass is used as a source of H, the process can be considered carbon-neutral. Seaweeds are among the less studied types of biomass with great potential because they do not require freshwater. Unfortunately, reaction pathways to thermochemically convert salty and wet biomass into H are limited. In this study, a catalytic alkaline thermal treatment of brown seaweed is investigated to produce high purity H with substantially suppressed CO formation making the overall biomass conversion not only carbon-neutral but also potentially carbon-negative. High-purity 69.69 mmol-H/(dry-ash-free)g-brown seaweed is produced with a conversion as high as 71%. The hydroxide is involved in both H production and in situ CO capture, while the Ni/ZrO catalyst enhanced the secondary H formation via steam methane reforming and water-gas shift reactions.
Bibliographic Details
Springer Science and Business Media LLC
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