4.3 Article

Direct analysis of biodegradable chelating agents based on liquid chromatography/electrospray ionization mass spectrometry using a metal-free hydrophilic interaction liquid chromatographic column

Journal

ANALYTICAL SCIENCES
Volume 39, Issue 5, Pages 663-670

Publisher

SPRINGERNATURE
DOI: 10.1007/s44211-022-00247-8

Keywords

Biodegradable chelating agent; Metal-free column; Hydrophilic interaction liquid chromatography; Liquid chromatography; electrospray ionization mass spectrometry; Biodegradation; Photodegradation

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This article describes a direct analytical method for biodegradable chelating agents using ultra-performance liquid chromatography/electrospray ionization quadrupole/time-of-flight mass spectrometry. The method offers the advantages of quickness, sensitivity, and requires no complicated pretreatment steps, making it suitable for practical analysis of chelating agents in environmental water samples.
Recently, biodegradable aminopolycarboxylic acid chelating agents have attracted attention as an alternative to environmentally persistent chelating agents such as ethylenediamine-N,N,N',N'-tetraacetic acid. However, the detection of chelating agents requires complexation with metals or derivatization by esterification reagents, and their direct detection using the currently available analytical methods still represents a challenge. Herein, we describe a direct analytical method for the biodegradable chelating agents ethylenediamine-N,N'-disuccinic acid, 3-hydroxy-2,2 & PRIME;-iminodisuccinic acid, methylglycine-N,N'-diacetic acid, and N,N-bis(carboxymethyl)-l-glutamic acid, via ultra-performance liquid chromatography/electrospray ionization quadrupole/time-of-flight mass spectrometry. Satisfactory retention and separation with a good peak shape were successfully achieved using a metal-free hydrophilic interaction liquid chromatographic column. The calibration curves showed good linearity in the range of 1.0-50 mu M with correlation coefficients greater than 0.9988. The detection limits ranged from 0.04 to 0.12 mu M. Furthermore, the developed method could be applied to the quantitative analysis of the four chelating agents in biodegradation and photodegradation experiments at the laboratory level. The proposed method, which offers the advantages of quickness, sensitivity, and requiring no complicated pretreatment steps, is expected to contribute significantly to the practical analysis of chelating agents in environmental water samples.

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