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 |
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Hauptverfasser: | , , |
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. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C7TA03056H |