Efficient removal of Cd2+ by dialdehyde phenylhydrazine starch from aqueous solution

苯肼 吸附 水溶液 化学 水溶液中的金属离子 核化学 弗伦德利希方程 金属 无机化学 放热反应 淀粉 有机化学
作者
Rou Wang,Zhengping Dong,Ren‐Qi Wang,Xin Tian,Chunyang Li,Rong Li
出处
期刊:RSC Advances [Royal Society of Chemistry]
卷期号:3 (43): 20480-20480 被引量:7
标识
DOI:10.1039/c3ra42670j
摘要

Three similar adsorbents were prepared via the conjugation of o-phenylenediamine (PDA), m-phenylenediamine (MPA) and phenylhydrazine (PH) with dialdehyde starch (DAS) and designated as DASPDA, DASMPA, DASPH, respectively. The adsorption properties of the three adsorbents toward metal ions were determined, and the results indicated that DASPH had a good adsorbability to Cd2+ among different metal ions. The DASPH was characterized by elemental analysis, BET, FT-IR spectra and SEM. FT-IR of DASPH revealed the incorporation of the C=N group (1601.1 cm(-1)) and the disappearance of the C=O (carbonyl) group (1733.4 cm(-1)). DASPHs with different degrees of substitution (0.48, 0.72 and 0.86) of phenylhydrazine were prepared and their adsorption properties for Cd2+ from aqueous solution were investigated. Adsorption of Cd2+ towards DASPH was optimized by pH, contact time, initial Cd2+ concentration and temperature. The adsorption capacity increased with the increasing DS (degree of substitution) of the DASPH, and reached 4.021, 4.034 and 4.163 mmol g(-1), respectively, for DASPH(1), DASPH(2) and DASPH(3). The adsorption equilibrium data were correlated well with the Freundlich isotherm model. The present adsorption system can be described more favorably by the pseudo-second-order kinetic model. Moreover, lower temperature was preferable for the process as it was exothermic.
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