Thorough Validation of Optimized Size Exclusion Chromatography-Total Organic Carbon Analysis for Natural Organic Matter in Fresh Waters

Author:

Laforce Elien1ORCID,Dejaeger Karlien234ORCID,Vanoppen Marjolein23ORCID,Cornelissen Emile235ORCID,De Clercq Jeriffa1,Vermeir Pieter6ORCID

Affiliation:

1. Industrial Catalysis and Adsorption Technology (INCAT), Department of Materials, Textiles and Chemical Engineering, Faculty of Engineering and Architecture, Ghent University, 9000 Ghent, Belgium

2. PaInT, Particle and Interfacial Technology Group, Department of Green Chemistry and Technology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000 Ghent, Belgium

3. Centre for Advanced Process Technology for Urban Resource Recovery (CAPTURE), Frieda Saeysstraat 1, 9052 Ghent, Belgium

4. CNRS, UMR 8516—LASIRE—Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l’Environnement, Université de Lille, 59000 Lille, France

5. KWR Water Research Institute, Groningenhaven 7, 3433 PE Nieuwegein, The Netherlands

6. Laboratory for Chemical Analysis (LCA), Department of Green Chemistry and Technology, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium

Abstract

Size exclusion chromatography with total organic carbon detection (HPSEC-TOC) is a widely employed technique for characterizing aquatic natural organic matter (NOM) into high, medium, and low molecular weight fractions. This study validates the suitability of HPSEC-TOC for a simplified yet efficient routine analysis of freshwater and its application within drinking water treatment plants. The investigation highlights key procedural considerations for optimal results and shows the importance of sample preservation by refrigeration with a maximum storage duration of two weeks. Prior to analysis, the removal of inorganic carbon is essential, which is achieved without altering the NOM composition through sample acidification to pH 6 and subsequent N2-purging. The chromatographic separation employs a preparative TSK HW-50S column to achieve a limit of detection of 19.0 µgC dm−3 with an injection volume of 1350 mm−3. The method demonstrates linearity up to 10,000 µgC dm−3. Precision, trueness and recovery assessments are conducted using certified reference materials, model compounds, and real water samples. The relative measurement uncertainty in routine analysis ranges from 3.22% to 5.17%, while the measurement uncertainty on the bias is 8.73%. Overall, the HPSEC-TOC represents a reliable tool for NOM fractions analysis in both treated and untreated ground and surface water.

Funder

European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie

Publisher

MDPI AG

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