Nash M J, Maskall J E, Hill S J
Department of Environmental Sciences, University of Plymouth, UK.
J Environ Monit. 2000 Apr;2(2):97-109. doi: 10.1039/a907875d.
Methodologies for the environmental analysis of total antimony and aqueous chemical speciation are critically reviewed, including preparation techniques for aqueous and solid matrices and the determination of solid state partitioning and recommendations are given for future research directions. Concentrations of total antimony commonly present in aqueous and solid environmental samples are readily determined using present day analytical techniques. This has resulted primarily from technological advances in microwave digestion for solid matrices and the development of plasma based analyte detection systems. ICP-AES and ICP-MS techniques are both utilised for the environmental analysis of total antimony concentrations. However, ICP-MS is increasingly favoured as a result of reduced spectral interferences and the potential for analyte detection in the pg mL(-1) range. Determination of aqueous antimony speciation presents a number of complex analytical challenges and highly selective separation and identification techniques are required prior to detection. The majority of published techniques including common applications of hydride generation are insufficiently selective for the determination of intrinsic chemical speciation and often only oxidation state data are obtained. The recent in-line applications of HPLC-ICP-MS offer the potential for highly selective separations of aqueous antimony species and determination of detailed chemical speciation data. However, considerable development work is required to optimise chromatographic separations and identify uncharacterised species resident in environmental systems. Analytical techniques to aid the determination of antimony's associations with solid environmental matrices include the application of chemical extraction procedures and leaching experiments. To date, this area of analytical research has received little attention and further studies are required to elucidate this aspect of antimony's environmental chemistry.
对总锑的环境分析方法和水相化学形态进行了严格审查,包括水相和固体基质的制备技术以及固态分配的测定,并给出了未来研究方向的建议。使用当今的分析技术可以很容易地测定水相和固体环境样品中常见的总锑浓度。这主要得益于固体基质微波消解技术的进步以及基于等离子体的分析物检测系统的发展。电感耦合等离子体发射光谱法(ICP - AES)和电感耦合等离子体质谱法(ICP - MS)技术都用于总锑浓度的环境分析。然而,由于光谱干扰减少以及在皮克每毫升(pg mL(-1))范围内检测分析物的潜力,ICP - MS越来越受到青睐。水相锑形态的测定面临许多复杂的分析挑战,在检测之前需要高度选择性的分离和鉴定技术。大多数已发表的技术,包括氢化物发生的常见应用,对于测定固有化学形态的选择性不足,通常只能获得氧化态数据。高效液相色谱法与电感耦合等离子体质谱联用(HPLC - ICP - MS)的最新在线应用为水相锑物种的高选择性分离和详细化学形态数据的测定提供了潜力。然而,需要进行大量的开发工作来优化色谱分离并识别环境系统中存在的未表征物种。有助于测定锑与固体环境基质结合情况的分析技术包括化学萃取程序和浸出实验的应用。迄今为止,这一分析研究领域很少受到关注,需要进一步研究以阐明锑环境化学的这一方面。