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Synthesis of chelating resins with iminodiacetic acid and its wastewater treatment application
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Citations
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References
2002
Year
Wastewater Treatment ApplicationEngineeringWastewater TreatmentChemical EngineeringMetal Ion AdsorptionSustainable SynthesisPlatform ChemicalIminodiacetic AcidIon ExchangeChemisorptionAdsorptionIndustrial WastewaterAdsorption IsothermsWaste ManagementEnvironmental EngineeringAdsorption BehaviorWater PurificationRecyclingSynthetic Chemistry
Abstract The chelating resins have high potential applications for the selective removal and recovery of metal ions from industrial waste solutions. The hydrophilic acrylate monomer with the iminodiacetic acid chelating group was prepared from glycidyl methacrylate and iminodiacetic acid at 60°C. The microbeads, prepared from acrylate monomer with the iminodiacetic acid chelating group, were employed by inversion suspension polymerization. In the pH range of 2–6, a reasonably good equilibrium sorption capacity is maintained for Cr 3+ (ca. 2.7 mmol/g) and Cu 2+ (ca. 1.8 mmol/g) in the chelating resins. The adsorption of Cd 2+ and Pb 2+ on microbeads is clearly affected by the pH of the solution, such that these ions' adsorption capacity increased with the pH of the aqueous solution. The adsorption of Cd 2+ (ca. 1.25–1.87 mmol/g) and Pb 2+ (ca. 0.99–1.89 mmol/g) showed a maximum at approximately pH = 5 and 6, respectively. The adsorption isotherms of Cr 3+ and Cu 2+ adsorbed on microbeads were following the Langmuir isotherm, but the adsorption behavior of Cd 2+ and Pb 2+ were not. The concentration of alkaline earth–metal cations on the range of 0–200 ppm had no influence on metal ions adsorbed capacity of chelating resins. Additionally, NTA (nitrilotriacetic acid) had no significant influence on metal ion adsorption by chelating resins. Furthermore, phenol pollutant can be adsorbed effectively by metal ions chelated microbeads; therefore, the microbeads were useful not only in recovering metal ions but also in the treating phenol pollutants in wastewater. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1353–1362, 2002; DOI 10.1002/app.10243
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