One-pot epoxide-driven synthesis of M2Al(OH)6Cl·1.5H2O layered double hydroxides: Precipitation mechanism and relative stabilities

A family of single-crystalline particles of M2Al(OH)6Cl·1.5H2O layered double hydroxides (LDH) with M(II) a transition-metal cation were obtained by a one-pot room-temperature homogeneous alkalinization driven by glycidol ring opening. In contrast with traditional homogeneous methods, LDH phases are...

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Autor principal: Oestreicher, V.
Otros Autores: Fábregas, I., Jobbágy, M.
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Lenguaje:Inglés
Publicado: American Chemical Society 2014
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100 1 |a Oestreicher, V. 
245 1 0 |a One-pot epoxide-driven synthesis of M2Al(OH)6Cl·1.5H2O layered double hydroxides: Precipitation mechanism and relative stabilities 
260 |b American Chemical Society  |c 2014 
270 1 0 |m Jobbágy, M.; INQUIMAE-DQIAQF, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos AiresArgentina 
506 |2 openaire  |e Política editorial 
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520 3 |a A family of single-crystalline particles of M2Al(OH)6Cl·1.5H2O layered double hydroxides (LDH) with M(II) a transition-metal cation were obtained by a one-pot room-temperature homogeneous alkalinization driven by glycidol ring opening. In contrast with traditional homogeneous methods, LDH phases are obtained in the exchangeable chloride-containing form. The main precipitation steps were assessed by continuous measurement of pH profiles, field emission scanning electron microscopy, and powder X-ray diffraction, revealing the heterogeneous nucleation of LDH phase over previously formed nano-Al(OH)3 seeds. The precipitation pH plateau of each LDH follows the trend of the inherent solubility of the single M(II) phases obtained under alkalinization. A linear free-energy relation links the solubility of the bare M(II) hydroxides with the correspondent M(II)-Al(III) LDH, in good agreement with previously reported thermochemical models. © 2014 American Chemical Society.  |l eng 
593 |a INQUIMAE-DQIAQF, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, C1428EHA, Argentina 
593 |a Division of Porous Materials, UNIDEF, CONICET, S.J.B de la Salle 4397, Villa Martelli, Buenos Aires, B1603ALO, Argentina 
593 |a Centro Interdisciplinario de Nanociencia y Nanotecnologiía, Argentina 
690 1 0 |a CHLORINE COMPOUNDS 
690 1 0 |a FIELD EMISSION MICROSCOPES 
690 1 0 |a FREE ENERGY 
690 1 0 |a SCANNING ELECTRON MICROSCOPY 
690 1 0 |a SOLUBILITY 
690 1 0 |a TRANSITION METALS 
690 1 0 |a X RAY DIFFRACTION 
690 1 0 |a CONTINUOUS MEASUREMENTS 
690 1 0 |a FIELD EMISSION SCANNING ELECTRON MICROSCOPY 
690 1 0 |a HETEROGENEOUS NUCLEATION 
690 1 0 |a HOMOGENEOUS ALKALINIZATION 
690 1 0 |a LAYERED DOUBLE HYDROXIDES 
690 1 0 |a POWDER X RAY DIFFRACTION 
690 1 0 |a PRECIPITATION MECHANISM 
690 1 0 |a THERMOCHEMICAL MODELS 
690 1 0 |a ALUMINUM 
700 1 |a Fábregas, I. 
700 1 |a Jobbágy, M. 
773 0 |d American Chemical Society, 2014  |g v. 118  |h pp. 30274-30281  |k n. 51  |p J. Phys. Chem. C  |x 19327447  |t Journal of Physical Chemistry C 
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