2014
DOI: 10.1246/bcsj.20140124
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Adsorptive Removal of Pb(II) Ions from Aqueous Solution by (NH4)2S2O8 Oxidized Activated Carbons

Abstract: A commercially available activated carbon (AC) was oxidized using 1 M H 2 SO 4 solution containing 2 M (NH 4 ) 2 S 2 O 8 oxidant with the solution to carbon ratio of 50 cm 3 g ¹1 by changing oxidation period ranging 1 to 10 days at ambient temperatures of 20 or 30°C to introduce carboxy groups onto the carbon surface to capture Pb(II) ions. Adsorptive removal of Pb(II) ions from aqueous solution was also examined with the oxidized ACs. The Pb(II) ion adsorption progressed via ion exchange with protons of carbo… Show more

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Cited by 13 publications
(4 citation statements)
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References 30 publications
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“…The recovery could result from the estimation that the effect of pore entrance obstruction by surface functional groups was lessened because surface functional groups were eliminated during the outgassing, and the surface area in the inner part of the outgassed ACFs could be measured again by BET measurements using nitrogen gas. However, the pore diameter was still kept approximately 1.80 nm for all ACFs, which was different from our previous research [26], indicating that the decrease in surface area and total pore volume was not caused by the erosion of carbon during the oxidation procedure. This assumption was also supported by the calculated result that the decrease in carbon content by liberated CO and CO2 from the surface carboxy and lactone was only 0.83% in total.…”
contrasting
confidence: 99%
“…The recovery could result from the estimation that the effect of pore entrance obstruction by surface functional groups was lessened because surface functional groups were eliminated during the outgassing, and the surface area in the inner part of the outgassed ACFs could be measured again by BET measurements using nitrogen gas. However, the pore diameter was still kept approximately 1.80 nm for all ACFs, which was different from our previous research [26], indicating that the decrease in surface area and total pore volume was not caused by the erosion of carbon during the oxidation procedure. This assumption was also supported by the calculated result that the decrease in carbon content by liberated CO and CO2 from the surface carboxy and lactone was only 0.83% in total.…”
contrasting
confidence: 99%
“…There have been several attempts on heavy metal adsorption using activated carbons, and the reduction of adsorption amount under acidic conditions was observed as shown in the present study 27,28) . It is reported that the pK a value of benzoic acid is 4.2 29) , and carboxy groups as a main adsorption site would be negatively charged at pH > 4.2.…”
Section: Ph Dependence Of CD 2+ Adsorption On the Prepared Adsorbentsupporting
confidence: 63%
“…The pH pzc value of 7.1 for non-treated AC was decreased to 4.0 for Ox-9.5AG implying that positively charged N-Q species could be involved in the species on the carbon surface. Generally speaking, pH pzc of activated carbons is always decreased by oxidation 19,22) and it is increased by outgassing 23) and reduction. 24) In oxidation, carboxy groups play a decisive role to reduce pH pzc since carboxy groups easily discharge protons to aqueous phase generating negative charge of carbon surface, whereas in outgassing and reduction, acidic functional groups as carboxy and lactone are removed and/or transformed to basic functional groups such as carbonyl and quinone receiving protons resulting in positively charged carbon surface.…”
Section: Resultsmentioning
confidence: 99%
“…Elemental composition was measured by Perkin-Elmer PE2400 CHN analyzer. Since sulfur content has been already confirmed to be 0.02% or less for both AC and Ox, 19) oxygen content was determined by balance assuming all other elements except C, H and N would be O (oxygen). Adsorption experiments of nitrate were carried out using 15 mL NaNO 3 solution dosing 30 mg adsorbents of Ox-9.5AG and AC as a control.…”
Section: Methodsmentioning
confidence: 99%