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Heat-treated Saccharomyces cerevisiae for antimony speciation and antimony(III)preconcentration in water samples

机译:热处理的酿酒酵母用于水样中的锑形态和锑(III)富集

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摘要

An analytical method was developed for antimony speciation and antimony(III)preconcentration in water samples.The method is based on the selective retention of Sb(III)by modified Saccharomyces cerevisiae in the presence of Sb(V).Heat,caustic and solvent pretreatments of the biomass were investigated to improve the kinetics and thermodynamics of Sb(III)uptake process at room temperature.Heating for 30min at 80 °C was defined as the optimal treatment.Antimony accumulation by the cells was independent of pH(5-10)and ionic strength(0.01-0.1 molL~(-1)).140 mg of yeast and 2h of contact were necessary to ensure quantitative sequestration of Sb(III)up to 750mu gL~(-1).In these conditions,Sb(V)was not retained.Sb(V)was quantified in sorption supernatant by inductively coupled plasma mass spectrometry(ICbeta-MS)or inductively coupled plasma optical emission spectrometry(ICP-OES).Sb(III)was determined after elution with 40mmolL~(-1)thioglycolic acid at pH 10.A preconcentration factor close to nine was achieved for Sb(III)when 100 mL of sample was processed.After preconcentration,the detection limits for Sb(III)and Sb(V)were 2 and 5ngL~(-1),respectively,using ICbeta-MS,7 and 0.9 mu g L~(-1)using ICbeta-OES.The proposed method was successfully applied to the determination of Sb(III)and Sb(V)in spiked river and mineral water samples.The relative standard deviations(n=3)were in the 2-5% range at the tenth mu gL~(-1)level and less than 10% at the lowest Sb(III)and Sb(V)tested concentration(0.1 mu gL~(-1)).Corrected recoveries were in all cases close to 100%.
机译:建立了一种分析水样中锑形态和锑(III)富集的分析方法,该方法基于修饰的酿酒酵母在Sb(V)存在下对Sb(III)的选择性保留。热,苛性碱和溶剂预处理为了提高室温下Sb(III)吸收过程的动力学和热力学,对生物量进行了研究。在80°C下加热30分钟被定义为最佳处理方法。细胞中锑的积累与pH(5-10)无关离子强度(0.01-0.1 molL〜(-1))。140 mg酵母和2h的接触时间才能确保Sb(III)定量螯合到750μgL〜(-1)。在这些条件下,Sb(保留了V)。通过电感耦合等离子体质谱(ICbeta-MS)或电感耦合等离子体发射光谱(ICP-OES)在吸附上清液中对Sb(V)进行定量。用40mmolL洗脱后测定Sb(III)〜 pH值为10的(-1)巯基乙酸当处理100 mL样品时,Sb(III)达到了ne。预浓缩后,使用ICbeta-MS对Sb(III)和Sb(V)的检出限分别为2和5ngL〜(-1)。并用ICbeta-OES测定0.9μg L〜(-1)。该方法成功地用于测定加标河流和矿泉水样品中的Sb(III)和Sb(V)。相对标准偏差(n = 3)在第十μgL〜(-1)浓度范围内为2-5%,在最低Sb(III)和Sb(V)测试浓度(0.1μgL〜(-1))下小于10%。在所有情况下,校正后的回收率均接近100%。

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