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首页> 外文期刊>Analytica chimica acta >Microvolume turbidimetry for rapid and sensitive determination of the acid labile sulfide fraction in waters after headspace single-drop microextraction with in situ generation of volatile hydrogen sulfide
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Microvolume turbidimetry for rapid and sensitive determination of the acid labile sulfide fraction in waters after headspace single-drop microextraction with in situ generation of volatile hydrogen sulfide

机译:微量浊度法可快速灵敏地测定顶空单滴微萃取并原位生成挥发性硫化氢后水中的酸性不稳定硫化物组分

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摘要

In this work, we demonstrate the feasibility of applying headspace single-drop microextraction with in-drop precipitation for the quantitative determination of the acid labile sulfide fraction (H2S, HS~-, and S~(2-) (free sulfide), amorphous FeS and some metal sulfide complexes-clusters as ZnS) in aqueous samples by microvolume turbidimetry. The methodology lies in the in situ hydrogen sulfide generation and subsequent sequestration into an alkaline microdrop containing ZnO_2~(2-) and exposed to the headspace above the stirred aqueous sample. The ZnS formed in the drop was then determined by microvolume turbidimetry. The optimum experimental conditions of the proposed method were: 2 μ L of a microdrop containing 750 mg L~(-1) Zn(II) in 1 mol L~(-1) NaOH exposed to the headspace of a 20-mL aqueous sample stirred at 1600 rpm during 80 s after derivatization with 1 mL of 6 mol L~(-1) HCl. An enrichment factor of 1710 was achieved in only 80s. The calibration graph was linear in the range of 5-100 μ g L~(-1) with a detection limit of 0.5 μg L~(-1). The repeatability, expressed as relative standard deviation, was 5.8% (N=9). Finally, the proposed methodology was successfully applied to the determination of the acid labile sulfide fraction in different natural water samples.
机译:在这项工作中,我们证明了应用顶空单滴微滴加滴内沉淀法定量测定酸不稳定的硫化物馏分(H2S,HS〜-和S〜(2-)(游离硫化物),无定形的可行性。用微量比浊法测定水性样品中的FeS和一些金属硫化物络合物-ZnS)该方法在于原位生成硫化氢,然后隔离到含有ZnO_2〜(2-)的碱性微滴中,并暴露于搅拌的水样上方的顶部空间。然后通过微量比浊法测定液滴中形成的ZnS。该方法的最佳实验条件为:2μL的微滴,其中的750 mg L〜(-1)Zn(II)在1 mol L〜(-1)NaOH中暴露于20 mL水样的顶部空间在用1 mL 6 mol L〜(-1)HCl衍生化后的80秒钟内以1600 rpm的转速搅拌。仅80年代就实现了1710的富集因子。校正曲线在5-100μg L〜(-1)范围内呈线性,检出限为0.5μgL〜(-1)。以相对标准偏差表示的重复性为5.8%(N = 9)。最后,该方法成功地用于测定不同天然水样中酸不稳定的硫化物含量。

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