4.7 Article

Aminoalkyl-organo-silane treated sand for the adsorptive removal of arsenic from the groundwater: Immobilizing the mobilized geogenic contaminants

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 425, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.jhazmat.2021.127916

关键词

Mono and di-aminosilane; Chemisorption; Ion-dipole; Triethoxy; And methoxyorganosilane

资金

  1. Tawata Technologies, GIDC, Ahmedabad, Gujarat

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The study demonstrates the effectiveness of impregnating organosilane into quartz sand particles for treating arsenic-polluted water, with increased removal efficiency through chemisorption. The optimal dosage of adsorbent is 10 g/L, and chemical adsorption and charge/ion-dipole interaction are found to be possible mechanisms for arsenate removal.
Arsenic (As), a geogenic legacy pollutant can be present in environmental matrices (water, soil, plants, or animal) in two redox states (As(III) or As(V)). In the present study, charged mono-and di-amino functionalized triethoxy and methoxyorganosilane (TT1 and TT2-1% and 5%) were impregnated with quartz sand particles for the treatment of As polluted water. Spectroscopic characterization of organosilane treated sand (STS) indicated the co-existence of minerals (Mg, Mn, Ti), amide, and amidoalkyl groups, which implies the suitability of silanized materials as a metal(loids) immobilization agent from water. Changes in peaks were observed after As sorption in Fourier thermal infrared and EDS images indicating the involvement of chemisorption. Batch sorption studies were performed with the optimized experimental parameters, where an increased removal (>20% for TT2-1% and >60% for TT1-1%) of As was observed with sorbate concentration (50 mu g L-1), temp. (25 +/- 2 degrees C) and sorbent dosages (of 10 g L-1) at 120 min contact time. Among the different adsorbent dosages, 10 g L-1 of both TT1 and TT2 was selected as an optimum dosage (maximum adsorption capacity approximate to 2.91 mu g g(-1)). The sorption model parameters suggested the possibility of chemisorption, charge/ion-dipole interaction for the removal of arsenate.

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