Published July 2007 | Version v1
Journal article

Evidences for decarbonation and exfoliation of layered double hydroxide in N,N-dimethylformamide-ethanol solvent mixture

  • 1. Departamento de Quimica Fundamental, Instituto de Quimica, Universidade de Sao Paulo, CP 26077, CEP 05513-900, Sao Paulo, SP (Brazil)

Description

The behavior of a Hydrotalcite-like material (carbonate-containing Mg,Al-layered double hydroxide) in N,N-dimethylformamide (DMF)-ethanol mixture, at ambient temperature, has been investigated. The releasing of CO2 and production of a formate-containing material occurred mainly for 1:1 (v/v) solvent mixture. Decarbonation of Hydrotalcite is promoted by DMF hydrolysis followed by neutralization of brucite-like layers through HCOO- intercalation. Translucent colloidal dispersion of LDH nanoparticles from the formate-containing phase was characterized by transmission electron (TEM) and atomic force (AFM) microscopies. The absence of (00l) reflection at X-ray diffraction (XRD) pattern for dried colloidal dispersion indicated delamination of Hydrotalcite. The restacked sample exhibited broad reflections and typical hydroxide ordered layers non-basal (110) diffraction peaks. A LDH-HCOO- material was also prepared and characterized by FTIR and FT-Raman spectroscopies. Decarbonation and exfoliation of Hydrotalcite in N,N-dimethylformamide-ethanol mixed solvent provide an interesting method for preparation of new intercalated LDH materials. - Graphical abstract: Hydrotalcite suspended in 1:1 (v/v) N,N-dimethylformamide-ethanol solvent mixture, at ambient temperature, undergoes decarbonation and exfoliation. The process is promoted by DMF hydrolysis. Restacking of LDH layers is achieved by evaporating the solvent

Additional details

Identifiers

DOI
10.1016/j.jssc.2007.05.003;
PII
S0022-4596(07)00192-2;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
180
Journal Issue
7
Journal Page Range
p. 1967-1976
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.