Abstract

Vacuum-assisted evaporative concentration (VEC) was successfully applied and validated for the enrichment of 590 organic substances from river water and wastewater. Different volumes of water samples (6 mL wastewater influent, 15 mL wastewater effluent, and 60 mL river water) were evaporated to 0.3 mL and finally adjusted to 0.4 mL. 0.1 mL of the concentrate were injected into a polar reversed-phase C18 liquid chromatography column coupled with electrospray ionization to high-resolution tandem mass spectrometry. Analyte recoveries were determined for VEC and compared against a mixed-bed multilayer solid-phase extraction (SPE). Both approaches performed equally well (≥ 70% recovery) for a vast number of analytes (n = 327), whereas certain substances were especially amenable to enrichment by either SPE (e.g., 4-chlorobenzophenone, logDow,pH7 4) or VEC (e.g., TRIS, logDow,pH7 − 4.6). Overall, VEC was more suitable for the enrichment of polar analytes, albeit considerable signal suppression (up to 74% in river water) was observed for the VEC-enriched sample matrix. Nevertheless, VEC allowed for accurate and precise quantification down to the sub-nanogram per liter level and required no more than 60 mL of the sample, as demonstrated by its application to several environmental water matrices. By contrast, SPE is typically constrained by high sample volumes ranging from 100 mL (wastewater influent) to 1000 mL (river water). The developed VEC workflow not only requires low labor cost and minimum supervision but is also a rapid, convenient, and environmentally safe alternative to SPE and highly suitable for target and non-target analysis.

Highlights

  • Organic contaminants (OCs) are constantly emitted into the aquatic environment with urban wastewater (WW), industry, and agriculture as the major sources [1]

  • Monitoring and regulation gaps are both linked to underlying analytical issues, i.e., polar OCs have the potential to go unnoticed as they are hardly amenable to stateof-the art liquid chromatography mass spectrometry (LCMS) workflows currently and widely used for multiresidue trace organic analysis

  • Recent approaches that bypass or minimize this shortcoming include the following: (i) vacuum-assisted evaporative concentration (VEC) to dryness with subsequent hydrophilic interaction liquid chromatography (HILIC) [9], (ii) freeze-drying with subsequent mixedmode LC [10], (iii) freeze-drying followed by (HILIC)solid-phase extraction (SPE) and serial RPLC-HILIC or supercritical fluid chromatography (SFC) on a HILIC column [11], (iv) mixedbed multilayer SPE optimized for retention of polar OCs with subsequent polar RPLC [9, 12,13,14], or (v) largevolume direct injection [15, 16]

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Summary

Introduction

Organic contaminants (OCs) are constantly emitted into the aquatic environment with urban wastewater (WW), industry, and agriculture as the major sources [1]. Monitoring and regulation gaps are both linked to underlying analytical issues, i.e., polar OCs have the potential to go unnoticed as they are hardly amenable to stateof-the art liquid chromatography mass spectrometry (LCMS) workflows currently and widely used for multiresidue trace organic analysis These workflows often rely on pre-concentration by offline solid-phase extraction (SPE) with a single conventional sorbent material (e.g., C8, C18, mixed-mode) and LC on a reversed-phase (RP) stationary phase column [6,7,8]. Apart from these methods, chromatographic retention of polar OCs can be enhanced by ion chromatography (e.g. [17, 18]), two-dimensional LC approaches (e.g. [19,20,21]), or parallel LC, e.g., HILIC parallel to RPLC with post column combination of eluents [22]

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