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Biosorption of Cu2+ by a novel modified spent Chrysanthemum:kinetics, isotherm and thermodynamics
The present study explored the ability of a novel spent chrysanthemum adsorbent prepared from acid acetaldehyde for the removal of Cu2+ from an aqueous solution. The effect of various parameters, including solution pH, adsorbent dosage, contact time and temperature on adsorption of Cu2+ were studied...
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Published in: | Journal of environmental chemical engineering 2017-08, Vol.5 (4), p.4151-4156 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The present study explored the ability of a novel spent chrysanthemum adsorbent prepared from acid acetaldehyde for the removal of Cu2+ from an aqueous solution. The effect of various parameters, including solution pH, adsorbent dosage, contact time and temperature on adsorption of Cu2+ were studied by batch experiments. According to the experimental results, the optimal pH range and optimum dosage were found to be 3.0–5.0 and 6.0g/L, respectively. The adsorption amount at equilibrium decreased with the increase of temperature. Freudlich model provided better correlation for the adsorption of Cu2+ by modified spent Chrysanthemum (MSC) (R=0.99)and spent Chrysanthemum (SC)(R=0.98). Adsorption capacity of MSC was 692mg/g at 293K, but it was 400mg/g at 293K for SC. The adsorption process on Cu2+ proceeded rapidly and almost reached adsorption equilibrium within 20min. The kinetics data of MSC were analyzed using the pseudo-first-order equations and pseudo-second-order equations. The pseudo-second-order equation fitted the experimental data very well (R=0.99). The adsorption amount at equilibrium decreased with the increase of temperature. The thermodynamic parameters showed that the biosorption was exothermic and spontaneous. Experimental results showed that MSC could be used as an effective biosorbent for Cu2+ removal from aqueous solutions. |
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ISSN: | 2213-3437 2213-3437 |
DOI: | 10.1016/j.jece.2017.07.077 |