4.8 Article

Solid-Phase Extraction of Aquatic Organic Matter: Loading-Dependent Chemical Fractionation and Self-Assembly

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 22, Pages 15495-15504

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c04535

Keywords

dissolved organic matter; fluorescence spectroscopy; EEMs; PARAFAC; RP-HPLC; scanning electron microscopy; polarized light microscopy; multilayer adsorption

Funding

  1. China Scholarship Council [201809370078]

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Dissolved organic matter (DOM) is a crucial component in marine and freshwater environments, playing a fundamental role in global biogeochemical cycles. The study found that increasing sorbent loading can reduce the extraction efficiencies of dissolved organic carbon (DOC), fluorescence, absorbance, and polar organic substances. Maintaining a similar relative DOC loading on the sorbent is crucial to avoid chemical fractionation and ensure accurate sample comparison.
Dissolved organic matter (DOM) is an important component in marine and freshwater environments and plays a fundamental role in global biogeochemical cycles. In the past, optical and molecular-level analytical techniques evolved and improved our mechanistic understanding about DOM fluxes. For most molecular chemical techniques, sample desalting and enrichment is a prerequisite. Solid-phase extraction has been widely applied for concentrating and desalting DOM. The major aim of this study was to constrain the influence of sorbent loading on the composition of DOM extracts. Here, we show that increased loading resulted in reduced extraction efficiencies of dissolved organic carbon (DOC), fluorescence and absorbance, and polar organic substances. Loading-dependent optical and chemical fractionation induced by the altered adsorption characteristics of the sorbent surface (styrene divinylbenzene polymer) and increased multilayer adsorption (DOM self-assembly) can fundamentally affect biogeochemical interpretations, such as the source of organic matter. Online fluorescence monitoring of the permeate flow allowed to empirically model the extraction process and to assess the degree of variability introduced by changing the sorbent loading in the extraction procedure. Our study emphasizes that it is crucial for sample comparison to keep the relative DOC loading (DOCload [wt %]) on the sorbent always similar to avoid chemical fractionation.

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