NiO/vermiculite composites prepared for photocatalytic degradation of methanol-water solution and hydrogen generation
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F24%3A10255443" target="_blank" >RIV/61989100:27710/24:10255443 - isvavai.cz</a>
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S0169131724002576" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0169131724002576</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.clay.2024.107509" target="_blank" >10.1016/j.clay.2024.107509</a>
Alternative languages
Result language
angličtina
Original language name
NiO/vermiculite composites prepared for photocatalytic degradation of methanol-water solution and hydrogen generation
Original language description
A novel eco-friendly NiO/Vm clay based photocatalysts were synthesized from two vermiculites (Vm1 and Vm2) and nickel(II) nitrate hexahydrate (Ni(NO3)2.6H2O salt precursor by the chemical precipitation without and with the sodium hydroxide (NaOH) or ammonium hydroxide (NH4OH, 28% NH3 in H2O) as precipitation agents (Synthesis A) in comparison with the solid-state thermal decomposition (Synthesis B) at 600 oC. Structural properties of all specimens were characterized by X-ray fluorescence, scanning electron microscopy, X-ray diffraction, infrared (IR) and Raman spectroscopy. The photocatalytic performance of NiO/Vm composites was evaluated under UV radiation (λ = 254 nm) for decomposition of methanol-water to hydrogen over 4-h and the stable yield of hydrogen over the 24-h periods. The NaOH and NH4OH affected the NiO crystallite size and therefore the photocatalytic activity during 4 h. Different 2:1 layer charge of Vm1 (0.82 eMINUS SIGN ) and Vm2 (0.40 eMINUS SIGN ) and the specific surface area of Vm1 (about 43 m2/g) and Vm2 (about 34 m2/g) supported H2 yield of 628.2 μmol/gcat. and 596.8 μmol/gcat., close to 657.0 μmol/gcat. produced in the presence of commercial photocatalyst TiO2 Evonik P25. Crystalline NiO precipitated and anchored in NiO/Vm composites contained smaller crystallites than those in free NiO. Vermiculite silica surface supports coverage of NiO by hydrogen bonding to Si-OH groups influencing the geometry of the NiO crystal structure (disorder NiO(X)). The heterojunction with Si-O-Ni bonding, at which electrons transfer from Vm to NiO cause enriching electron density in NiO and favoring its photocatalytic activity. Photocatalytic hydrogen generation from methanol-water mixture at the presence of all specimens indicated the main product H2 and minimum by-products CH4 and CO. The stable hydrogen production for 24 h was confirmed only in the presence NiO/Vm1-24 while maintaining the NiO(X) in small crystallites. The thermal solid-state procedure provided the gradual dehydration of vermiculites and Ni(NO3)2.6H2O to the same amount and crystallinity of NiO in NiO/Vm1 and NiO/Vm2 composites. The results of this work confirm that vermiculites mixed layer structures with different negative layer charge play a dominant role as semiconductors for anchored NiO. The photocatalytic activity of NiO/vermiculite composites can be harnessed to treat wastewater containing organic contaminants. (C) 2024 Elsevier B.V.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
20402 - Chemical process engineering
Result continuities
Project
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Continuities
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Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Applied Clay Science
ISSN
0169-1317
e-ISSN
1872-9053
Volume of the periodical
259
Issue of the periodical within the volume
October
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
11
Pages from-to
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UT code for WoS article
001282586800001
EID of the result in the Scopus database
2-s2.0-85199677555