常用酸和阴离子对铁(Ii)从水溶液中萃取到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)氯仿溶液中的影响

J. Godwin, A. Inengite, U. Chukwu
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引用次数: 3

摘要

研究了常用酸、阴离子和辅助络合剂对水溶液中Fe2+的溶剂萃取作用,考察了在1-(3-羟基-5-甲基-2-苯基-2-苯基-2,3-二氢- 1h -吡唑-4-基)和1-(3-羟基-5-甲基-2-苯基-2,3-二氢- 1h -吡唑-4-基)丁醇-1-酮(HBuP)存在的氯仿溶液中,4,4′-(1E,1E′)-1,1′-(乙烷-1,2-二基-1-二基)(H2BuEtP)。采用1,10-菲罗啉比色法测定萃取后水溶液中Fe2+的浓度,采用差值法测定萃取百分比。利用前人的研究数据计算分离因子βXY,用相同的有机相确定从Ni2+、Pb2+和UO22+中分离Fe2+的理论条件。在HNO3和H3PO4的混合配体H2BuEtP/HBuP有机体系中,在0.01M和0.1M的浓度下,所有酸对Fe2+的提取率最高,分别为99.93%。在配体H2BuEtP单独体系中,H3PO4在0.1M下的提取率为99.3%。虽然研究中所使用的阴离子在两种有机相中不同浓度下对Fe2+的萃取率都达到了90%以上,但CHCOO-、PO43-、Br-和酒石酸盐离子对H2BuEtP萃取Fe2+的效果最好。酸和阴离子在不同浓度下起盐渍剂或掩蔽剂的作用。计算得到的分离因子βXY表明,仅用H3PO4分离Fe2+和Ni2+,用H3PO4、HCl和EDTA单独用H2BuEtP分离Fe2+和Pb2+在理论上是可行的。用混合配体H2BuEtP/HBuP计算分离因子βXY表明,HNO3和H3PO4可以分离Ni2+中的Fe2+, HCl和草酸盐可以分离Pb2+中的Fe2+, CHCOOH、PO43-、Br-和草酸盐可以分离U(VI)中的Fe2+。还计算并显示了实现99.9%分离所需的萃取批次数n。
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Effect of Common Acids and Anions on the Extraction of Iron (Ii) from Aqueous Solutions into Chloroform Solution Of 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)
The effect of common acids, anions, and auxiliary complexing agents in the solvent extraction of Fe2+ from aqueous solutions into chloroform solutions of 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) alone and in the presence of of 1-(3-hydroxy-5-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl) butan-1-one (HBuP) was studied. Colorimetric method of analysis using 1,10-phenanthroline was used to determine concentrations of Fe2+ in aqueous solutions after extraction and percentage extraction determined by difference. Separation factors βXY were calculated using data from previous studies using same organic phases to determine theoretical conditions for separating Fe2+ from Ni2+, Pb2+, and UO22+. All acids gave > 90% extraction of Fe2+ at most concentrations with HNO3 and H3PO4 giving the highest percentage extraction of 99.93% at 0.01M and 0.1M respectively in the mixed ligands H2BuEtP/HBuP organic system. H3PO4 also gave best extraction of 99.3% at 0.1M in ligand H2BuEtP alone system. Although all anions used for study also gave > 90% extraction of Fe2+ at different concentration in both types of organic phases, CHCOO-, PO43-, Br- and tartrate ions gave the best extraction of Fe2+ with H2BuEtP. Acids and anions behave as salting out agents or masking agents at different concentrations. Calculated separation factors βXY indicated that it was theoretically possible to separate Fe2+ from Ni2+ with H3PO4 only and Fe2+ from Pb2+ with H3PO4, HCl, and EDTA with H2BuEtP alone. With mixed ligands H2BuEtP/HBuP, calculated separation factors βXY showed that it was possible to separate Fe2+ from Ni2+ with HNO3 and H3PO4, Fe2+ from Pb2+ with HCl and oxalate, and Fe2+from U(VI) with CHCOOH, PO43-, Br- and oxalate. The number of batches of extraction n needed to achieve 99.9% separations are also calculated and shown.
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