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Blue hydrochars formed on hydrothermal carbonization of glucose using an iron catalyst
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0001-8225-9670
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0001-7286-1211
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0002-7284-2974
2022 (English)In: Carbon Trends, ISSN 2667-0569, Vol. 8, article id 100172Article in journal (Refereed) Published
Abstract [en]

We hypothesized that the morphology of the hydrochar from hydrothermal carbonization of glucose would be affected by Fe2+; and indeed, with such ions, large pieces of hydrochar formed that comprised aggregated spherical particles and blue and thin films. Thin carbonized films formed at the bottom of the autoclave liners or on TeflonTM tape used as a template. Free-standing films could be prepared by stretching the TeflonTM tape after the synthesis. The carbonized films that formed at the bottom of the autoclave adhered to spherical hydrochar particles. The blueness was ascribed to thin-film interference under white-light irradiation and related to the film thickness, which was about 200 nm. Analysis of transmission electron microscopy (TEM) images showed that the films consisted of a layered amorphous carbon. The amorphous and thin films were more carbonized than the amorphous carbon of the TEM grid, as derived via electron energy loss spectroscopy (EELS). Additional analysis of one of the thin films by X-ray photoelectron spectral analysis showed a higher carbon fraction than for bulk hydrochar, supporting the EELS analysis. We believe that the synthesis of thin films of hydrochar can open up new colloidal processing pathways, which could be useful in the preparation of carbon-based materials and alike.

Place, publisher, year, edition, pages
2022. Vol. 8, article id 100172
Keywords [en]
Hydrothermal carbonization, Glucose, Iron sulfate, Carbon spheres, Thin films, Thin film interference
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:su:diva-206189DOI: 10.1016/j.cartre.2022.100172Scopus ID: 2-s2.0-85128535062OAI: oai:DiVA.org:su-206189DiVA, id: diva2:1675085
Funder
Mistra - The Swedish Foundation for Strategic Environmental Research, 2015/31Available from: 2022-06-22 Created: 2022-06-22 Last updated: 2024-04-22Bibliographically approved
In thesis
1.
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2. From blue hydrochars to activated carbons: Hydrothermal carbonization, chemical activation and gas adsorption
Open this publication in new window or tab >>From blue hydrochars to activated carbons: Hydrothermal carbonization, chemical activation and gas adsorption
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Hydrothermal carbonization (HTC) of carbohydrates and biomass is a straightforward method for preparing hydrochars at low temperatures of 180-250 °C. Hydrochars are more carbonized than their precursors. Increasing the carbonization degree of hydrochars at hydrothermal temperatures is a scientific quest that is addressed in this thesis. Hydrochars are known to have a spherical or irregular morphology. Here we address thin film hydrochars for the first time.  Hydrochars themselves are carbon precursors for preparing activated carbons. Activated carbons are porous materials that can be used for gas adsorption applications. In this thesis, enhanced adsorption of VOCs at low pressures is addressed by using iron phosphate impregnated activated carbons. Finaly, any chemical process or product including those in this thesis such as HTC, activation, hydrochar and activated carbons may contribute to the issue of environmental degradation positively or negatively. Such environmental impacts are addressed by life cycle assessment of processes of HTC and activation and their related products in the last paper of this thesis. Briefly mentioned, in my first study (Paper I), I focused on the HTC of glucose in the presence of iron (II) sulfate. By changing the concentration of iron (II) sulfate, with a catalytic amount, blue hydrochars were formed at the bottom of the autoclave. The blueness was related to thin film interference. The thin film hydrochars were more carbonized than spherical hydrochars and the yield of HTC has increased in the presence of iron (II) sulfate. The second study (Paper II) is focused on the activation of hydrochars with H3PO4 and H3PO4+FeCl3. We showed that ultramicroporosity and impregnated iron phosphate species enhance the adsorption of VOCs at low pressure. The ACs were impregnated with Fe (PO3)2 and it was shown that Fe (PO3)2 acts as an activation agent which opens up for future studies. In the third study (Paper III), H3PO4-activated carbons were prepared and modified with FeS and FeSe and it was shown that the ACs were also impregnated with Fe2P, in the case of AC-FeS/Fe2P. FeSe and FeS were not detected by XRD. Only large crystals of Fe2P were detected in the sample AC-FeS/Fe2P. In the last study (Paper IV), prickly pear seed biomass from the agro sector in Tunisia was hydrothermally carbonized. The hydrochars were then activated into ACs by CO2 activation. The life cycle assessment of the HTC and activation process was investigated.  

Place, publisher, year, edition, pages
Department of Materials and Environmental Chemistry, Stockholm University, 2024. p. 51
Keywords
hydrochars, activated carbons, hydrothermal carbonization, chemical activation, gas adsorption
National Category
Materials Chemistry
Research subject
Materials Chemistry
Identifiers
urn:nbn:se:su:diva-228549 (URN)978-91-8014-797-2 (ISBN)978-91-8014-798-9 (ISBN)
Public defence
2024-06-14, online via Zoom, public link is available at the department website, Stockholm, 13:00 (English)
Opponent
Supervisors
Available from: 2024-05-22 Created: 2024-04-22 Last updated: 2024-05-13Bibliographically approved

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Saadattalab, VahidJansson, KjellTai, Cheuk WaiHedin, Niklas

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