戊二醛
吸附
聚合物
乙二醛
聚乙烯亚胺
铜
动力学
扫描电子显微镜
化学
反应速率常数
核化学
无机化学
材料科学
色谱法
有机化学
复合材料
生物化学
转染
物理
基因
量子力学
作者
Azekah Yashna Swamy,Shelvin Prasad,Xun Pan,Mats R. Andersson,Desta Gedefaw
标识
DOI:10.1002/slct.202104318
摘要
Abstract The water body can potentially be contaminated with heavy metals such as Cu 2+ ions which beyond a certain concentration could impact human and animal health. In the past, different techniques have been developed to remove Cu 2+ ions from water. In this study, polyethlenimine (PEI) was crosslinked with glutaraldehyde and glyoxal to yield three polymers (P1‐P3). P3 consists of hydroxypropyl methylcellulose (HPMC) as a template to decrease the size of the crosslinked polymer particles. The polymer powders were used to adsorb Cu 2+ from CuSO 4 water solutions. The addition of 50, 100 and 150 mg of P3 removed 25, 32 and 38 mg of Cu 2+ , respectively, from 0.075 M (10 mL) of CuSO 4 solution, after stirring at room temperature for 24 h. In comparison, P1 and P2 removed a lower amount. The better performance of P3 arises from the larger surface area of the polymer powder compared to P1 and P2 as revealed from scanning electron microscopy (SEM) images. Kinetic studies indicated that the polymers remove a larger amount of Cu 2+ during the first 3 h with a slower rate of adsorption continuing until 12 h. The adsorption kinetics were fitted with Elovich and Pseudo second order models to understand the adsorption mechanism. The higher R 2 (∼0.99) value of the linear plots signifies the adsorption is likely to follow a Pseudo second order kinetics, with P3 showing a rate constant of 8.43x10 −5 g mg −1 min −1 . The Cu 2+ loaded polymers (100 mg) were soaked in 10 mL of 2 % HNO 3 for 24 h for the desorption of Cu 2+ , where 12, 10 and 16 mg of Cu 2+ desorbed from P1, P2 and P3, respectively. This indicates the polymers could potentially be reused to adsorb another batch of Cu 2+ from water to maximize an economic benefit.
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