Green quantification of amino(poly)phosphonates using ion chromatography coupled to integrated pulsed amperometric detection.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Anna M Röhnelt, Philipp R Martin, Robert G H Marks, Daniel Buchner, Joachim Weiss, Torsten C Schmidt, Stefan B Haderlein
{"title":"Green quantification of amino(poly)phosphonates using ion chromatography coupled to integrated pulsed amperometric detection.","authors":"Anna M Röhnelt, Philipp R Martin, Robert G H Marks, Daniel Buchner, Joachim Weiss, Torsten C Schmidt, Stefan B Haderlein","doi":"10.1007/s00216-025-05747-w","DOIUrl":null,"url":null,"abstract":"<p><p>Aminopolyphosphonates (APPs) are widely used as chelating agents, and their increasing release into the environment has raised concerns due to their transformation into aminomethylphosphonic acid (AMPA) and glyphosate, compounds of controversial environmental impact. This transformation highlights the urgent need for detailed studies under controlled conditions. Despite the availability of various methods for quantifying individual aminopolyphosphonates and aminomonophosphonates, a green, low-cost approach for the simultaneous quantification of APPs and their transformation products in laboratory experiments has been lacking. In this study, we present a novel analytical method utilizing ion chromatography (IC) coupled to integrated pulsed amperometric detection (IPAD) to simultaneously quantify the six aminophosphonates: AMPA, glyphosate, iminodi(methylene phosphonate) (IDMP), aminotrismethylene(phosphonates) (ATMP), ethylenediamine tetra(methylene phosphonate) (EDTMP), and diethylenetriamine penta(methylene phosphonate) (DTPMP). This method achieves separation within a 35-min run time and method detection limits (MDLs) ranging from 0.014 μM for AMPA to 0.14 μM for DTPMP. The method's applicability was successfully shown by monitoring DTPMP, IDMP, and AMPA during DTPMP transformation on manganese dioxide. A key advantage of this method is its environmental friendliness compared to existing aminophosphonate quantification techniques. Next to the simultaneous analysis, it avoids the use of derivatization agents and organic solvents and employs an energy-efficient detector. While the method's limitations lie in the detector's inherent non-specific nature, it offers a low-cost and sustainable alternative to existing methods.</p>","PeriodicalId":462,"journal":{"name":"Analytical and Bioanalytical Chemistry","volume":" ","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical and Bioanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s00216-025-05747-w","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Aminopolyphosphonates (APPs) are widely used as chelating agents, and their increasing release into the environment has raised concerns due to their transformation into aminomethylphosphonic acid (AMPA) and glyphosate, compounds of controversial environmental impact. This transformation highlights the urgent need for detailed studies under controlled conditions. Despite the availability of various methods for quantifying individual aminopolyphosphonates and aminomonophosphonates, a green, low-cost approach for the simultaneous quantification of APPs and their transformation products in laboratory experiments has been lacking. In this study, we present a novel analytical method utilizing ion chromatography (IC) coupled to integrated pulsed amperometric detection (IPAD) to simultaneously quantify the six aminophosphonates: AMPA, glyphosate, iminodi(methylene phosphonate) (IDMP), aminotrismethylene(phosphonates) (ATMP), ethylenediamine tetra(methylene phosphonate) (EDTMP), and diethylenetriamine penta(methylene phosphonate) (DTPMP). This method achieves separation within a 35-min run time and method detection limits (MDLs) ranging from 0.014 μM for AMPA to 0.14 μM for DTPMP. The method's applicability was successfully shown by monitoring DTPMP, IDMP, and AMPA during DTPMP transformation on manganese dioxide. A key advantage of this method is its environmental friendliness compared to existing aminophosphonate quantification techniques. Next to the simultaneous analysis, it avoids the use of derivatization agents and organic solvents and employs an energy-efficient detector. While the method's limitations lie in the detector's inherent non-specific nature, it offers a low-cost and sustainable alternative to existing methods.

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信