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    钠基体匹配法-电感耦合等离子体原子发射光谱法测定土壤中6种金属元素的含量

    Determination of 6 Metal Elements in Soil by Inductively Coupled Plasma Atomic Emission Spectrometry with Sodium Matrix Matching Method

    • 摘要: 在特定的波长下,比较了不同质量浓度的土壤基体和易电离元素对电感耦合等离子体原子发射光谱法(ICP-AES)测定锌、锰、铜、镍、钴、钒等6种金属元素的影响。结果显示,土壤基体干扰与易电离元素干扰存在一定相关性,对6种金属元素均存在负干扰,其中对铜、镍、钴的干扰明显大于锌、钒。选择钠质量浓度为1 000 mg·L−1的氯化钠溶液为绘制校准曲线溶液的基体,可以校正称样量为0.3 g的土壤基体干扰,进而获得准确的测定结果。采用钠基体匹配法,6种金属元素的质量浓度在一定范围内与对应的发射强度呈线性关系,检出限(3.14s)为0.1~0.5 mg·kg−1;对6个土壤成分分析标准物质进行准确度试验,测定值的相对误差为−3.8%~4.0%;对土壤成分分析标准物质GSS20进行精密度试验,测定值的相对标准偏差(n=6)为1.8%~4.0%。方法用于3个不同的环境土壤样品分析,得到的测定结果与波长色散X射线荧光光谱法一致。

       

      Abstract: At specific wavelengths, the effects of different mass concentrations of soil matrix and easily ionizable elements on determination of 6 metal elements (zinc, manganese, copper, nickel, cobalt, and vanadium) by inductively coupled plasma atomic emission spectrometry (ICP-AES) were compared. As shown by the results, a certain correlation between soil matrix interference and easily ionizable element interference. Negative interference was observed for all 6 metal elements, with significantly greater interference on copper, nickel and cobalt compared to zinc and vanadium. By selecting the sodium chloride solution with sodium mass concentration of 1 000 mg·L−1 as the matrix for drawing calibration curves, the interference from the soil matrix with a sample mass of 0.3 g could be calibrated, thereby achieving accurate determination results. Using the sodium matrix matching method, linear relationships between the corresponding emission intensities and mass concentrations of 6 metal elements were found in definite ranges, with detection limits (3.14s) in the range of 0.1-0.5 mg·kg−1. Accuracy tests were conducted on 6 soil composition analysis standard materials, and the relative errors of the determined values ranged from -3.8% to 4.0%. Precision test was conducted on the soil composition analysis standard material GSS20, and RSDs (n=6) of the determined values ranged from 1.8% to 4.0%. This method was applied to analysis of 3 different environmental soil samples, and the obtained results were consistent with those of wavelength dispersive X-ray fluorescence spectrometry.

       

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