Athmer Mathis, Röhnelt Anna M, Maas Torben J, Haderlein Stefan B, Karst Uwe
Institute of Inorganic and Analytical Chemistry, University of Münster, Münster, Germany.
Geo- and Environmental Research Center, Department of Geosciences, University of Tübingen, Tübingen, Germany.
J Chromatogr A. 2025 May 10;1748:465843. doi: 10.1016/j.chroma.2025.465843. Epub 2025 Mar 4.
Polyphosphonates (PPs) are increasingly used in detergents and as antiscalants in Europe, with an estimated 18,600 tons annually entering surface waters. Aminopolyphosphonates (APPs) can be readily transformed by environmental processes, contrary to previous beliefs about PP stability during wastewater treatment. Together with the identification of glyphosate as a minor transformation product (TP) of the widely used diethylenetriamine penta(methylenephosphonate) (DTPMP), this necessitates further detailed APP transformation studies. A novel speciation analysis method for phosphonates and several potential phosphorus-containing TPs was developed using a rapid ion chromatographic (IC) separation and element-specific detection by inductively coupled plasma-triple quadrupole-mass spectrometry (ICP-TQ-MS). Chromatographic separation was optimised with a five-step gradient, allowing the simultaneous analysis of a wide range of analytes with varying sizes and numbers of negative charges within a single chromatographic run. Nine phosphorus species including APPs, PPs, glyphosate, aminomethylphosphonic acid (AMPA) and phosphate can be analysed within a run time of 205 seconds. Excellent species-specific detection limits in the range of 0.06 to 0.73 µg/L of phosphorus were reached. Unidentified TPs could also be quantified by using a species-unspecific calibration approach to close the phosphorus mass balance (PMB). The method's applicability was successfully demonstrated by monitoring DTPMP transformation with MnO under environmentally relevant conditions. DTPMP and its TPs were identified and quantified over the course of the transformation experiment with PMB values ≥73 %. This rapid, straightforward, robust and highly sensitive approach offers an effective means of quantifying (aminopoly)phosphonates and their TPs, contributing to a better understanding of their environmental fate and impact.
在欧洲,聚膦酸盐(PPs)越来越多地用于洗涤剂中,并用作阻垢剂,估计每年有18600吨进入地表水。与之前关于聚膦酸盐在废水处理过程中稳定性的看法相反,氨基聚膦酸盐(APPs)很容易通过环境过程发生转化。随着草甘膦被鉴定为广泛使用的二乙烯三胺五(亚甲基膦酸)(DTPMP)的一种次要转化产物(TP),这就需要进一步开展详细的APP转化研究。利用快速离子色谱(IC)分离和电感耦合等离子体-三重四极杆质谱(ICP-TQ-MS)进行元素特异性检测,开发了一种用于膦酸盐和几种潜在含磷TPs的新型形态分析方法。采用五步梯度优化色谱分离,能够在一次色谱运行中同时分析多种大小和负电荷数量不同的分析物。在205秒的运行时间内可以分析包括APPs、PPs、草甘膦、氨基甲基膦酸(AMPA)和磷酸盐在内的9种磷形态。实现了0.06至0.73μg/L磷范围内出色的形态特异性检测限。未鉴定的TPs也可以通过使用非形态特异性校准方法来量化,以实现磷质量平衡(PMB)。通过在环境相关条件下监测DTPMP与MnO的转化,成功证明了该方法的适用性(在整个转化实验过程中,DTPMP及其TPs被鉴定和量化,PMB值≥73%)。这种快速、直接、稳健且高度灵敏的方法为定量分析(氨基聚)膦酸盐及其TPs提供了一种有效手段,有助于更好地了解它们的环境归宿和影响。