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Effect of Functional Group Density of Anion Exchange Resins on Removal of p-Toluene Sulfonic Acid from Aqueous Solution
Adsorption using anion exchange resins is an efficient method for the removal of aromatic sulfonic acids (ASAs) from industrial wastewater. In this study, a series of weak-base anion exchangers (SD1–SD5) were synthesized to investigate the effect of functional group density of resins on the adsorpti...
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Published in: | Applied sciences 2020-01, Vol.10 (1), p.1 |
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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: | Adsorption using anion exchange resins is an efficient method for the removal of aromatic sulfonic acids (ASAs) from industrial wastewater. In this study, a series of weak-base anion exchangers (SD1–SD5) were synthesized to investigate the effect of functional group density of resins on the adsorption of ASAs from wastewater containing competitive inorganic anions. p-Toluene sulfonic acid (PTSA) was selected as a target pollutant, and Na2SO4 was chosen as the competitive inorganic salt because of its widespread existence in industrial wastewater. Adsorption performances of these resins were evaluated and compared in terms of selectivity, kinetics, isotherms, regeneration, and dynamic adsorption behavior. Importantly, the PTSA uptake increased with the raising content of functional groups on resins in the absence of Na2SO4; however, in the presence of a high level of Na2SO4 (for example, ≥1%), a decrease in the functional group density could improve the adsorption capacity of resins for PTSA. Moreover, desorption and fixed bed column experiments were conducted in all resins, thereby confirming the effect of functional group density of resins on the PTSA adsorption in actual application. In brief, this research will provide a better understanding for the design and preparation of anion exchangers for the effective removal of ASA from wastewater. |
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ISSN: | 2076-3417 2076-3417 |
DOI: | 10.3390/app10010001 |