Novel biomolecule-assisted interlayer anion-controlled layered double hydroxide as an efficient sorbent for arsenate removal

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 fr...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2017, Vol.5 (28), p.14783-14793
Hauptverfasser: Koilraj, Paulmanickam, Sasaki, Keiko, Srinivasan, Kannan
Format: Artikel
Sprache:eng
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Zusammenfassung: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 + ]-NO 3 − formation and thus produced pure NO 3 − -containing LDHs. Conversely, at temperatures above 115 °C, l -arginine decomposition occurred and produced NH 4 + and CO 2 , which resulted in CO 3 2− -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 CO 3 2− , 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 Mg 2.3 Al-LDH and Mg 2 Al-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 NO 3 − 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 NO 3 − that is present in the synthesis medium. The current synthesis method did not utilize a hazardous base during synthesis, and the [Arg + ]-NO 3 − byproduct can be used as a chemical source for health/skin care formulations with zero waste disposal, which offers great benefits.
ISSN:2050-7488
2050-7496
DOI:10.1039/C7TA03056H