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利用超高分辨率质谱结合负离子和正离子电喷雾电离对地下水溶解有机物的分子特征进行补充阐释

Complementary Elucidation of the Molecular Characteristics of Groundwater Dissolved Organic Matter Using Ultrahigh-Resolution Mass Spectrometry Coupled with Negative- and Positive-Ion Electrospray Ionization.

作者信息

Zhou Ziqi, Fu Qing-Long, Fujii Manabu, Waite T David

机构信息

School of Environmental Studies, China University of Geosciences, Wuhan 430078, China.

UNSW Water Research Centre, School of Civil and Environmental Engineering, The University of New South Wales, Sydney, New South Wales 2052, Australia.

出版信息

Environ Sci Technol. 2023 Mar 21;57(11):4690-4700. doi: 10.1021/acs.est.2c08816. Epub 2023 Mar 11.

Abstract

The formula assignment of the Fourier transform ion cyclotron resonance mass spectrometry coupled with positive-ion electrospray ionization [ESI(+)-FT-ICR MS] is challenging because of the extensive occurrence of adducts. However, there is a paucity of automated formula assignment methods for ESI(+)-FT-ICR MS spectra. The novel automated formula assignment algorithm for ESI(+)-FT-ICR MS spectra developed herein has been applied to elucidate the composition of dissolved organic matter (DOM) in groundwater during air-induced ferrous [Fe(II)] oxidation. The ESI(+)-FT-ICR MS spectra of groundwater DOM were profoundly impacted by [M + Na] adducts and, to a lesser extent, [M + K] adducts. Oxygen-poor and N-containing compounds were frequently detected when the FT-ICR MS was operated in the ESI(+) mode, while the components with higher carbon oxidation states were preferentially ionized in the negative-ion electrospray ionization [ESI(-)] mode. Values for the difference between double-bond equivalents and the number of oxygen atoms from -13 to 13 are proposed for the formula assignment of the ESI(+)-FT-ICR MS spectra of aquatic DOM. Furthermore, for the first time, the Fe(II)-mediated formation of highly toxic organic iodine species was reported in groundwater rich in Fe(II), iodide, and DOM. The results of this study not only shed light on the further algorithm development for comprehensive characterization of DOM by ESI(-)-FT-ICR MS and ESI(+)-FT-ICR MS but also highlight the importance of appropriate treatment of specific groundwater prior to use.

摘要

傅里叶变换离子回旋共振质谱联用正离子电喷雾电离[ESI(+)-FT-ICR MS]的分子式归属具有挑战性,因为加合物广泛存在。然而,针对ESI(+)-FT-ICR MS谱图的自动化分子式归属方法却很匮乏。本文开发的用于ESI(+)-FT-ICR MS谱图的新型自动化分子式归属算法已被应用于阐明空气诱导亚铁[Fe(II)]氧化过程中地下水中溶解有机物(DOM)的组成。地下水中DOM的ESI(+)-FT-ICR MS谱图受到[M + Na]加合物的显著影响,在较小程度上也受到[M + K]加合物的影响。当FT-ICR MS以ESI(+)模式运行时,经常检测到贫氧且含氮的化合物,而具有较高碳氧化态的组分在负离子电喷雾电离[ESI(-)]模式下优先被电离。针对水生DOM的ESI(+)-FT-ICR MS谱图的分子式归属,提出了双键当量与氧原子数之差在-13至13之间的值。此外,首次报道了在富含Fe(II)、碘化物和DOM的地下水中Fe(II)介导形成剧毒有机碘物种。本研究结果不仅为通过ESI(-)-FT-ICR MS和ESI(+)-FT-ICR MS对DOM进行全面表征的进一步算法开发提供了思路,还强调了在使用前对特定地下水进行适当处理的重要性。

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