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用于选择性萃取UO₂²⁺的UO₂²⁺离子印迹聚合物的合成与表征

Synthesis and characterization of UO(2)(2+)-ion imprinted polymer for selective extraction of UO(2)(2+).

作者信息

Singh Dhruv K, Mishra Shraddha

机构信息

Analytical Research Laboratory, Department of Chemistry, Harcourt Butler Technological Institute, Kanpur 208002, India.

出版信息

Anal Chim Acta. 2009 Jun 30;644(1-2):42-7. doi: 10.1016/j.aca.2009.04.020. Epub 2009 Apr 19.

DOI:10.1016/j.aca.2009.04.020
PMID:19463560
Abstract

Ion-imprinted polymers (IIPs) were prepared for uranyl ion (imprint ion) by formation of binary (salicylaldoxime (SALO) or 4-vinylpyridine (VP)) or ternary (salicylaldoxime and 4-vinylpyridine) complex in 2-methoxy ethanol (porogen) following copolymerization with methacrylic acid (MAA) as a functional monomer and ethylene glycol dimethacrylate (EGDMA) as crosslinking monomer using 2,2'-azobisisobutyronitrile as initiator. Control polymers (CPs) were also prepared under identical experimental conditions without using imprint ion. The above synthesized polymers were characterized by surface area measurement, microanalysis and FT-IR analysis techniques. The imprinted polymer formed with ternary complex of UO(2)(2+)-SALO-VP (1:2:2, IIP3) showed quantitative enrichment of uranyl ion from dilute aqueous solution and hence was chosen for detailed studies. The optimal pH for quantitative enrichment is 3.5-6.5. The adsorbed UO(2)(2+) was completely eluted with 10 mL of 1.0 M HCl. The retention capacity of IIP3 was found to be 0.559 mmol g(-1). Further, the distribution ratio and selectivity coefficients of uranium and other selected inorganic ions were also evaluated. Five replicate determinations of 25 microg L(-1) of uranium(VI) gave a mean absorbance of 0.032 with a relative standard deviation of 2.20%. The detection limit corresponding to three times the standard deviation of the blank was found to be 5 microg L(-1). IIP3 was tested for preconcentration of uranium(VI) from ground, river and sea water samples.

摘要

通过在2-甲氧基乙醇(致孔剂)中形成二元(水杨醛肟(SALO)或4-乙烯基吡啶(VP))或三元(水杨醛肟和4-乙烯基吡啶)配合物,随后与作为功能单体的甲基丙烯酸(MAA)和作为交联单体的乙二醇二甲基丙烯酸酯(EGDMA)使用2,2'-偶氮二异丁腈作为引发剂进行共聚,制备了用于铀酰离子(印迹离子)的离子印迹聚合物(IIP)。还在不使用印迹离子的相同实验条件下制备了对照聚合物(CP)。通过表面积测量、微量分析和傅里叶变换红外光谱(FT-IR)分析技术对上述合成的聚合物进行了表征。由UO(2)(2 +)-SALO-VP的三元配合物(1:2:2,IIP3)形成的印迹聚合物显示出从稀水溶液中定量富集铀酰离子,因此被选用于详细研究。定量富集的最佳pH为3.5 - 6.5。用10 mL 1.0 M HCl可将吸附的UO(2)(2 +)完全洗脱。发现IIP3的保留容量为0.559 mmol g(-1)。此外,还评估了铀和其他选定无机离子的分配比和选择性系数。对25 μg L(-1)的铀(VI)进行五次重复测定,平均吸光度为0.032,相对标准偏差为2.20%。发现对应于空白标准偏差三倍的检测限为5 μg L(-1)。对IIP3进行了从地下水、河水和海水样品中预富集铀(VI)的测试。

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