4,4-(1e,1e)-1,1-(乙烷-1,2-二基双(azan -1- yl- 1- ylidene)) -(5-甲基-2-苯基-2,3-二氢-1h-吡唑-3-醇)(H2BuEtP)评价络合剂在多金属萃取中的潜力

G. Jackson, Yameso Abasi Cyprian, Newton Ebelegi Augustus
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引用次数: 0

摘要

重金属的毒性导致人们不断研究新的和有效的方法来从环境中去除重金属。采用溶剂萃取法研究了辅助络合剂乙二胺四乙酸(EDTA)、草酸盐(c4h4o62 -)、硫氰酸盐(SCN -)和酒石酸盐(c4h4o62 -)离子在同时萃取镉、铁、用有机萃取剂4,4′-(1 E,1 E′)-1,1′-(乙烷-1,2-二基双(氮-1-基-1-乙烷))-(5-甲基-2-苯基-2,3-二氢-1 H-吡唑-3-醇)(H 2 BuEtP)或在4-丁基-2-4-二氢-5-甲基-2-苯基-3-吡唑-3-酮(HBuP)存在下,将水溶液中的镍和铅缓冲至pH为4.75或7.5。辅助络合剂用量为0.001 ~ 0.1 M,平衡时间为60 min。利用萃余物和金属标准吸光度计算分布比和提取率。EDTA、草酸盐和硫氰酸盐离子在pH为4.75时不适合多金属的提取,因为这些辅助络合剂离子形成非常稳定的配合物,掩盖了金属的提取,尽管从统计学上看,在大多数情况下,两种缓冲液中金属的提取没有显著差异。单独使用配体h2 BuEtP,缓冲液pH为7.5,酒石酸盐为0.001 M,理论上需要7批萃取才能达到99.9%的同时萃取四种金属的最佳效果;使用混合配体h2 BuEtP/HBuP有机萃取剂体系,0.001 ~ 0.005 M酒石酸盐需要7批萃取,0.05 M酒石酸盐需要5批萃取,0.01 M酒石酸盐需要4批萃取效果最佳。统计上,两种有机相之间没有显著差异,除了缓冲液pH为7.5的硫氰酸盐对镍有轻微的HBuP协同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the potentials of complexing agents in multi-metal extractions using 4,4-(1e,1e)-1,1-(Ethane-1,2-Diylbis(Azan-1-Yl-1ylidene))Bis(5-Methyl-2-Phenyl-2,3-Dihydro-1h-Pyrazol-3-Ol) (H2BuEtP)
Heavy metals toxicity has led to the continuous study of new and efficient methods for their removal from the environment. Solvent extraction method was used to study the potentials of the auxiliary complexing agents Ethylenediaminetetraacetic acid (EDTA), Oxalate (C 2 O 42- ), Thiocyanate (SCN - ) and Tartrate (C 4 H 4 O 62- ) ions in the simultaneous extraction of Cadmium, Iron, Nickel and Lead from aqueous solutions buffered to either pH 4.75 or 7.5 using the organic extractant 4,4´-(1 E ,1 E ´)-1,1´-(ethane-1,2-diylbis(azan-1-yl-1ylidene))bis(5-methyl-2-phenyl-2,3-dihydro-1 H -pyrazol-3-ol) (H 2 BuEtP) alone or in the presence 4-butanoyl-2-4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one (HBuP). 0.001 to 0.1 M of the auxiliary complexing agents and equilibration time of 60 min was used. Distribution ratios and percentage extraction was calculated using raffinates and metal standard absorbances. EDTA, Oxalate and Thiocyanate ions and pH 4.75 was found not suitable for the multi-metal extraction of the four metals attributed to the formation of very stable complexes with these auxiliary complexing agents’ ions masking the extraction of the metals, although statistically, there were no significant differences in most cases between the extractions of the metals in the two buffers. Using the ligand H 2 BuEtP alone with a buffer of pH 7.5 and 0.001 M Tartrate, 7 batches of extraction are theoretically required to achieve 99.9% simultaneous extraction of the four metals as the best result while with the mixed ligands H 2 BuEtP/HBuP organic extractant system, 7 batches are required for 0.001 to 0.005 M Tartrate, 5 batches for 0.05 M Tartrate and 4 batches for 0.01 M Tartrate as the best results. Statistically, there was no significant difference between the two organic phases with the exception being Thiocyanate for Nickel with buffer of pH 7.5 that showed slight synergic effect of HBuP.
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