TY - JOUR
T1 - Novel biomolecule-assisted interlayer anion-controlled layered double hydroxide as an efficient sorbent for arsenate removal
AU - Koilraj, Paulmanickam
AU - Sasaki, Keiko
AU - Srinivasan, Kannan
N1 - Publisher Copyright:
© 2017 The Royal Society of Chemistry.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - The synthesis of pure nitrate-containing layered double hydroxides (LDHs) via biomolecule-assisted methods is difficult to achieve without producing substantial waste. For the first time, we demonstrated the synthesis of LDHs with a controlled interlayer anion composition using an environmentally friendly l-arginine-assisted hydrothermal method with zero waste disposal. The mechanism of LDH formation was revealed through PXRD, FT-IR, XPS and ion chromatographic (IC) analyses. At low synthesis temperatures (90-110 °C), arginine-mediated water decomposition led to OH- and [Arg+]-NO3- formation and thus produced pure NO3--containing LDHs. Conversely, at temperatures above 115 °C, l-arginine decomposition occurred and produced NH4+ and CO2, which resulted in CO32--bearing LDHs. The FT-IR spectra of the solid residues, which were obtained at lower temperatures, indicated that several amino acids were functionalized on the surface of the LDHs and replaced by CO32-, which was produced at higher temperatures. The sorption of arsenate from an aqueous solution on the resulting LDHs showed maximum sorption capacity values of 1.675 and 1.972 mmol g-1 for Mg2.3Al-LDH and Mg2Al-LDH synthesised at 100 °C, respectively. The arsenate sorption capacity was enhanced by the functionalization of l-arginine compared with conventionally prepared LDHs. The mechanism of arsenate sorption was based on the ion-exchange of interlayer NO3- and functionalized arginine molecules. In summary, the chemical precursor l-arginine (utilized in this study) acts as a multifunctional reagent, including (i) a precipitant for the synthesis of LDH, (ii) an engineer for interlayer anion control, (iii) a functional reagent and (iv) a scavenger for free NO3- that is present in the synthesis medium. The current synthesis method did not utilize a hazardous base during synthesis, and the [Arg+]-NO3- byproduct can be used as a chemical source for health/skin care formulations with zero waste disposal, which offers great benefits.
AB - The synthesis of pure nitrate-containing layered double hydroxides (LDHs) via biomolecule-assisted methods is difficult to achieve without producing substantial waste. For the first time, we demonstrated the synthesis of LDHs with a controlled interlayer anion composition using an environmentally friendly l-arginine-assisted hydrothermal method with zero waste disposal. The mechanism of LDH formation was revealed through PXRD, FT-IR, XPS and ion chromatographic (IC) analyses. At low synthesis temperatures (90-110 °C), arginine-mediated water decomposition led to OH- and [Arg+]-NO3- formation and thus produced pure NO3--containing LDHs. Conversely, at temperatures above 115 °C, l-arginine decomposition occurred and produced NH4+ and CO2, which resulted in CO32--bearing LDHs. The FT-IR spectra of the solid residues, which were obtained at lower temperatures, indicated that several amino acids were functionalized on the surface of the LDHs and replaced by CO32-, which was produced at higher temperatures. The sorption of arsenate from an aqueous solution on the resulting LDHs showed maximum sorption capacity values of 1.675 and 1.972 mmol g-1 for Mg2.3Al-LDH and Mg2Al-LDH synthesised at 100 °C, respectively. The arsenate sorption capacity was enhanced by the functionalization of l-arginine compared with conventionally prepared LDHs. The mechanism of arsenate sorption was based on the ion-exchange of interlayer NO3- and functionalized arginine molecules. In summary, the chemical precursor l-arginine (utilized in this study) acts as a multifunctional reagent, including (i) a precipitant for the synthesis of LDH, (ii) an engineer for interlayer anion control, (iii) a functional reagent and (iv) a scavenger for free NO3- that is present in the synthesis medium. The current synthesis method did not utilize a hazardous base during synthesis, and the [Arg+]-NO3- byproduct can be used as a chemical source for health/skin care formulations with zero waste disposal, which offers great benefits.
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U2 - 10.1039/c7ta03056h
DO - 10.1039/c7ta03056h
M3 - Article
AN - SCOPUS:85025073130
SN - 2050-7488
VL - 5
SP - 14783
EP - 14793
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 28
ER -