首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Inorganic arsenic speciation analysis of water samples by trapping arsine on tungsten coil for atomic fluorescence spectrometric determination
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Inorganic arsenic speciation analysis of water samples by trapping arsine on tungsten coil for atomic fluorescence spectrometric determination

机译:水样中砷的捕集钨线圈上无机砷形态的原子荧光光谱法测定。

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摘要

Arsine trapping on resistively heated tungsten coil was investigated and an analytical method for ultra-trace arsenic determination in environmental samples was established. Several chemical modifiers. including Re, Pt, Mo, Ta and Rh, were explored as permanent chemical modifiers for tungsten coil on-line trapping and Rh gave the best performance. Arsine was on-line trapped on Rh-coated tungsten coil at 640 degrees C, then released at 1930 degrees C and subsequently delivered to an atomic fluorescence spectrometer (AFS) by a mixture of Ar and H-2 for measurement. In the medium of 2% (v/v) HCl and 3% (m/v) KBH4, arsine can be selectively generated from As(III). Total inorganic arsenic was determined after pre-reduction of As(V) to As(III) in 0.5% (m/v) thiourea-0.5% (m/v) ascorbic acid solution. The concentration of As(V) was calculated by difference between the total inorganic arsenic and As(III), and inorganic arsenic speciation was thus achieved. With 8 min on-line trapping, the limit of detection was 10 ng L-1 for As(III) and 9 ng L-1 for total As: and the precision was found to be <5% R.S.D. (n = 7) for 0.2 ng mL(-1) As. The proposed method was successfully applied in total arsenic determination of several standard reference materials and inorganic arsenic speciation analysis of nature water samples.
机译:研究了电阻加热钨线圈上的砷捕获,并建立了测定环境样品中痕量砷的分析方法。几种化学改性剂。包括Re,Pt,Mo,Ta和Rh在内的化合物被用作钨线圈在线捕集的永久化学改性剂,Rh表现最佳。 s在640摄氏度时在线捕获在涂有Rh的钨线圈上,然后在1930摄氏度下释放,然后通过Ar和H-2的混合物输送到原子荧光光谱仪(AFS)中进行测量。在2%(v / v)HCl和3%(m / v)KBH4的介质中,可以从As(III)选择性生成a。在0.5%(m / v)硫脲-0.5%(m / v)的抗坏血酸溶液中将As(V)预还原为As(III)后,测定总无机砷。通过总无机砷和As(III)之差计算As(V)的浓度,从而获得无机砷形态。在线捕获时间为8分钟,As(III)的检出限为10 ng L-1,总As:的检出限为9 ng L-1,发现精密度小于5%R.S.D. (n = 7)对于0.2 ng mL(-1)As该方法成功地用于几种标准参考物质的总砷测定和自然水样品的无机砷形态分析。

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