Use este identificador para citar ou linkar para este item: http://hdl.handle.net/1843/61578
Tipo: Artigo de Periódico
Título: A soft chemistry approach to preparing (de)sodiated transition-metal hydroxy molybdates
Autor(es): Guilherme Mendes Martins
Roberto Luiz Moreira
Anderson Dias
Resumo: A soft chemistry approach was applied to synthesize de(sodiated) transition-metal hydroxy molybdates under hydrothermal conditions. Different NaM2(H3O2)(MoO4)2 and M2MoO4(OH)2 compositions (M = Ni, Zn) were prepared at mild temperatures (110–250 °C) for times ranging from 10 min to 24 h. Sodiated compounds were obtained after a microwave-assisted hydrothermal process at 150 °C (10–120 min) for zinc-based materials. Besides, conventional heating destabilized the sodiated NaZn2(H3O2)(MoO4)2 phase at 110 °C, thus increasing the amount of Zn2MoO4(OH)2 at temperatures up to 250 °C. NaNi2(H3O2)(MoO4)2 phases were noted only for 10 min under microwave irradiation, while longer times promoted a chemical reaction towards a new desodiated phase. This novel Ni2MoO4(OH)2 phase was also obtained by conventional hydrothermal processing (110–250 °C, 24 h). Slow precipitation rates yielded a hydrated nickel molybdate (triclinic, P[1 with combining macron]) after coprecipitation followed or not by microwave irradiation. Raman spectroscopy analysis results showed a good agreement with experimental results and group-theory calculations for both sodiated and desodiated materials. A temperature-induced polymorphic transformation was observed from NiMoO4·xH2O (triclinic, P[1 with combining macron]) to α-NiMoO4 (monoclinic, C2/m). For all the obtained polymorphs, the relevant Raman modes were depicted, allowing us to determine their spectroscopic fingerprints. The results constitute an important basis on the understanding of the synthesis of (de)sodiated transition-metal hydroxy molybdates under hydrothermal conditions.
Assunto: Ligas de metais de transição
Compostos de molibdênio
Microondas
Raman, Espectroscopia de
Polimorfismo (Cristalografia)
Idioma: eng
País: Brasil
Editor: Universidade Federal de Minas Gerais
Sigla da Instituição: UFMG
Departamento: ICX - DEPARTAMENTO DE FÍSICA
ICX - DEPARTAMENTO DE QUÍMICA
Tipo de Acesso: Acesso Restrito
Identificador DOI: https://doi.org/10.1039/C9CE01554J
URI: http://hdl.handle.net/1843/61578
Data do documento: 2020
metadata.dc.url.externa: https://pubs.rsc.org/en/content/articlelanding/2020/ce/c9ce01554j#!
metadata.dc.relation.ispartof: CrystEngComm
Aparece nas coleções:Artigo de Periódico

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