2003
DOI: 10.1016/s1383-5866(03)00006-6
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Removal of chromates from drinking water by anion exchangers

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Cited by 68 publications
(42 citation statements)
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“…The toxicity of such metal ions arise due to their non-biodegradable nature thereby accumulating in the living cells and impairing the normal functions of various organs of living beings. Technologies like chemical precipitation, electrochemical separation, membrane separation, reverse osmosis, ion exchange and adsorption resins though effective for metal remediation, yet are not competitive in industrial application [9][10][11][12][13][14][15][16][17][18][19][20][21][22]. Such methods involve either large capital or operational costs, and are not effective in removing metal ions present in ppm levels [12,18].…”
Section: Introductionmentioning
confidence: 99%
“…The toxicity of such metal ions arise due to their non-biodegradable nature thereby accumulating in the living cells and impairing the normal functions of various organs of living beings. Technologies like chemical precipitation, electrochemical separation, membrane separation, reverse osmosis, ion exchange and adsorption resins though effective for metal remediation, yet are not competitive in industrial application [9][10][11][12][13][14][15][16][17][18][19][20][21][22]. Such methods involve either large capital or operational costs, and are not effective in removing metal ions present in ppm levels [12,18].…”
Section: Introductionmentioning
confidence: 99%
“…chromium(VI) is a highly toxic metal that has been linked to cancer in humans following prolonged inhalation, and is toxic to aquatic life at relatively low concentrations (US Environmental Protection Agency (EPA), 1998). The maximum permitted level of chromium for drinking water is 0.05 mg/L [2,3].…”
Section: Introductionmentioning
confidence: 99%
“…We also concluded that the active form of Cr(VI) that could be adsorbed by POT/Pmc and P2ClAn/Pmc was HCrO Pmc and P2ClAn/Pmc composites, which was attributed to the stronger electrostatic attraction. 39,41,42 Another explanation could have been that at very low pH values, the surface of the sorbent was also surrounded by the hydronium ions, which enhanced Cr(VI) interaction with the binding sites of the sorbent by greater attractive forces. As the pH increased, however, the overall surface charge on the sorbents became negative and sorption decreased.…”
Section: Effect Of Phmentioning
confidence: 99%