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Development of Absorbent Using Amylose-Graphite Composite Electrode for Removal of Heavy Metals
Amylose of captures heavy metals in a box consisting of sugar chains. However, its absorption rate is low in the period of the month scale. Therefore, the electrochemical driving force was used to promote the absorption rate in this research. Amylose was doped with TiO porous graphite electrode. The...
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Published in: | Membranes (Basel) 2021-11, Vol.11 (12), p.930 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Amylose of
captures heavy metals in a box consisting of sugar chains. However, its absorption rate is low in the period of the month scale. Therefore, the electrochemical driving force was used to promote the absorption rate in this research. Amylose was doped with TiO
porous graphite electrode. The composted absorbent was characterized using XRD(X-ray diffraction), SEM (Scanning Electrode Microscopy), Raman spectroscopy, and electrochemical methods. The affinity and maximum absorption amount were calculated using the isotherm method. In this study, Pb
, Cu
, Cd
, and Cr
were chosen to demonstrate because these heavy metals are significant pollutants in Japan's surface water. It was found that the maximum absorption was Cu
(56.82-mg/L) > Pb
(55.89-mg/L) > Cr
(53.97-mg/L) > Cd
(52.83.68-mg/L) at -0.5 V vs. Ag/AgCl. This is approximately the same order as the hydration radius of heavy metals. In other words, the absorption amounts were determined by the size of heavy metal ions. Subsequently, the mixed heavy metal standard solution was tested; the maximum absorption amount was 21.46 ± 10.03 mg/L. It was inferred that the electrochemical driving force could be shown as the ion size effect in the mixed solution. Despite there being no support for this hypothesis at this time, this study succeeded in showing that the electrochemical driving force can improve the ability of the absorbent. |
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ISSN: | 2077-0375 2077-0375 |
DOI: | 10.3390/membranes11120930 |