Abstract

The synthesis and optical properties of Mg-Al layered double hydroxide (LDH) precursor powders were investigated using X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), selected area electron diffraction (SAED), high-resolution TEM (HRTEM), UV-transmission spectrometer, and fluorescence spectrophotometer. The FT-IR results show that the intense absorption at around 1363–1377 cm-1 can be assigned to the antisymmetric ν3 mode of interlayer carbonate anions because the LDH phase contains some CO32-. The XRD results show that all of the Mg-Al LDH precursor powders contain only a single phase of [Mg0.833Al0.167(OH)2](CO3)0.083·(H2O)0.75 but have broad and weak intensities of peaks. All of Mg-Al LDHs precursor powders before calcination have the same photoluminescence (PL) spectra. Moreover, these spectra were excited at λex = 235 nm, and the broad emission band was in the range 325-650 nm. In the range, there were relatively strong intensity at around 360, 407 and 510 nm, respectively.

Highlights

  • The general formula of layered double hydroxide (LDH) can be represented as follows (Khan and O’Hare 2002; Costa et al.2005; Goh et al 2008):[M21+-xP3x+ (OH)2]ξ+(Anξ-/n) mH2O (1)where M2+ is a divalent metal ion such as Mg2+, Zn2+, and so on, while P3+ is a trivalent ion such as Al3+, Cr3+, and so on

  • The Mg-Al LDH precursors were synthesized by a coprecipitation route with various processes

  • The following analytical grade preliminary materials were used as reagents for the synthesis of the MgAl LDH precursors: Mg(NO3)2·6H2O, Al(NO3)3·9H2O, NaOH, and Na2CO3

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Summary

Introduction

The general formula of LDHs can be represented as follows (Khan and O’Hare 2002; Costa et al.2005; Goh et al 2008):[M21+-xP3x+ (OH)2]ξ+(Anξ-/n) mH2O (1)where M2+ is a divalent metal ion such as Mg2+, Zn2+, and so on, while P3+ is a trivalent ion such as Al3+, Cr3+, and so on. LDHs have applications as ion-exchangers (Dimotakis and Pinnavaia 1990; You et al 2002), absorbents (Hermosin et al 1996; Huston et al 2004), pharmaceutics (Hwang et al 2001; Wang et al 2005), catalysts or catalyst supports (Choudary et al 2002; Motokura et al 2004), and sunscreens for cosmetic use (Cursino et al 2013)

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