建立了离子色谱一氢化物发生原子荧光光谱联用分离4神常见有毒砷化合物的方法。二者通过内径0.25min的PEEK管直接相连。实验对影响分离度和测定灵敏度的参数进行了优化。在优化条件下,质量浓度均为50μg/L的4种砷化合物混合标准溶液平行7次进样,得到DMA、As(Ⅲ)、MMA和As(V)的色谱峰面积的相对标准偏差(RSD)为2.8~3.0%。250μL进样的线性范围为5-1000μL,检出限为0.8~1.2μg/L(三倍基线噪音峰高)。用建立的方法测定了砷处理后的水稻木质部伤流液中的砷量,4种砷化合物的加标回收率为89%-105%。该装置接口简单,方法分离度好。灵敏度高,可用于实际样品中痕量砷化合物的形态分析。
A method has been developed for the speciation of dimethylarsinic (DMA), arsenite As( Ⅲ ), monomethyl- arsonic (MMA) and arsenite As( V ) by ion chromatography coupled hydride generation-atomic fluorescence spectrometry. The eluent gradient of IC and the parameters influencing AFS detection were discussed. Under the optimized experimental conditions, the relative standard deviation (RSD) is 2.8 % - 3.0% (n = 7). The linear ranges for the four species are all between 5 and 1000 lxg/L, while the detection limits are between 0.8 and 1.2 μg/L. The method has been applied to the speciation of arsenic in rice xylem samples and the range of recoveries is 89% - 105%. This simple method, with high sensitivity and low detection limit, can be applied to practical environmental samples.