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Efficient and synergistic removal of tetracycline and Cu(II) using novel magnetic multi-amine resins

机译:使用新型磁性多胺树脂高效协同去除四环素和铜(II)

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摘要

A series of magnetic multi-amine resins (MMARs, named E1D9-E9D1) was proposed for the removal of tetracycline (TC) and Cu(II) in sole and binary solutions. Results showed that the N content of the resins increased sharply from 1.7% to 15.49%, and the BET surface areas decreased from 1433.4 m2/g to 8.9 m2/g with methyl acrylate ratio increasing from E1D9 to E9D1. Their adsorption capacities for TC and Cu(II) could reach 0.243 and 0.453 mmol/g, respectively. The adsorption isotherms of TC onto MMARs transformed from heterogeneous adsorption to monolayer-type adsorption with DVB monomer ratio in resin matrix decrease, suggesting the dominant physical adsorption between TC and benzene rings. TC adsorption capacity onto E9D1 was higher than that onto E7D3 when the equilibrium concentration of TC exceeded 0.043 mmol/L because the electrostatic interaction between negatively charged groups of TC and protonated amines of adsorbents could compensate for the capacity loss resulting from BET surface area decrease. In the binary system, the electrostatic interaction between negatively charged TC-Cu(II) complex and protonated amines of adsorbents was responsible for the synergistic adsorption onto E7D3 and E9D1. The XPS spectra of magnetic resins before and after adsorption were characterized to prove the probable adsorption mechanisms. This work provides alternative adsorbent for the efficient treatment of multiple pollution with different concentrations of organic micropollutants and heavy metal ions.
机译:提出了一系列磁性多胺树脂(MMAR,称为E1D9-E9D1),用于去除单一溶液和二元溶液中的四环素(TC)和Cu(II)。结果表明,树脂的N含量从1.7%急剧增加到15.49%,BET表面积从1433.4 m 2 / g降低到8.9 m 2 / g丙烯酸甲酯的比例从E1D9增加到E9D1。它们对TC和Cu(II)的吸附能力分别达到0.243和0.453 mmol / g。在树脂基体中DVB单体比例从非均相吸附转变为单层型吸附的TC对TC的TC吸附等温线减少,表明TC与苯环之间的物理吸附占主导地位。当TC的平衡浓度超过0.043 / mmol / L时,TC对E9D1的吸附能力高于E7D3,这是因为TC的带负电基团与吸附剂的质子化胺之间的静电相互作用可以弥补BET表面积降低导致的容量损失。在二元系统中,带负电的TC-Cu(II)配合物与质子化吸附剂胺之间的静电相互作用是E7D3和E9D1协同吸附的原因。表征了吸附前后磁性树脂的XPS光谱,证明了可能的吸附机理。这项工作为有效处理具有不同浓度的有机微污染物和重金属离子的多种污染提供了替代吸附剂。

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