Abstract

Abstract. Although column experiments are frequently used to investigate the transport of organic micropollutants, little guidance is available on what they can be used for, how they should be set up, and how the experiments should be carried out. This review covers the use of column experiments to investigate the fate of organic micropollutants. Alternative setups are discussed together with their respective advantages and limitations. An overview is presented of published column experiments investigating the transport of organic micropollutants, and suggestions are offered on how to improve the comparability of future results from different experiments. The main purpose of column experiments is to investigate the transport and attenuation of a specific compound within a specific sediment or substrate. The transport of (organic) solutes in groundwater is influenced by the chemical and physical properties of the compounds, the solvent (i.e., the groundwater, including all solutes), and the substrate (the aquifer material). By adjusting these boundary conditions a multitude of different processes and related research questions can be investigated using a variety of experimental setups. Apart from the ability to effectively control the individual boundary conditions, the main advantage of column experiments compared to other experimental setups (such as those used in field experiments, or in batch microcosm experiments) is that conservative and reactive solute breakthrough curves can be derived, which represent the sum of the transport processes. There are well-established methods for analyzing these curves. The effects observed in column studies are often a result of dynamic, non-equilibrium processes. Time (or flow velocity) is an important factor, in contrast to batch experiments where all processes are observed until equilibrium is reached in the substrate-solution system. Slight variations in the boundary conditions of different experiments can have a marked influence on the transport and degradation of organic micropollutants. This is of critical importance when comparing general results from different column experiments investigating the transport behavior of a specific organic compound. Such variations unfortunately mean that the results from most column experiments are not transferable to other hydrogeochemical environments but are only valid for the specific experimental setup used. Column experiments are fast, flexible, and easy to manage; their boundary conditions can be controlled and they are cheap compared to extensive field experiments. They can provide good estimates of all relevant transport parameters. However, the obtained results will almost always be limited to the scale of the experiment and are not directly transferrable to field scales as too many parameters are exclusive to the column setup. The challenge for the future is to develop standardized column experiments on organic micropollutants in order to overcome these issues.

Highlights

  • The presence of organic micropollutants in aquatic environments has been of great concern worldwide for a number of years and increasing numbers of compounds continue to be detected in all kinds of waterbodies

  • An overview is presented of published column experiments investigating the transport of organic micropollutants, and suggestions are offered on how to improve the comparability of future results from different experiments

  • Apart from the ability to effectively control the individual boundary conditions, the main advantage of column experiments compared to other experimental setups is that conservative and reactive solute breakthrough curves can be derived, which represent the sum of the transport processes

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Summary

Introduction

The presence of organic micropollutants in aquatic environments has been of great concern worldwide for a number of years and increasing numbers of compounds continue to be detected in all kinds of waterbodies. Even irradiation with UV light (Bergheim et al, 2015) or ozonation (Favier et al, 2015) can lead to the formation of metabolites with higher ecotoxicity than their parent compounds This implies that organic micropollutants are still continuously released into the aquatic environment and concentrations in aquatic environments are increasing rather than decreasing. The number of investigations into organic micropollutants has increased in line with continuing improvements in analytical techniques, such as the use of mass spectrometry (and enhancements) and solid-phase extraction methods These organic compounds can be quantified down to low ng L−1 values (e.g., Nödler et al, 2010), which has opened up new possibilities for research into organic micropollutants, including, for example, their use as anthropogenic indicators or tracers in aquatic systems. Nödler et al (2013) used a combination of micropollutants that had originated from wastewater (carbamazepine and acesulfame) or treated wastewater (valsartan acid) to determine the sources of groundwater in a karst spring (leaking sewer or rain-induced overflow of untreated sewage vs. outflow from a wastewater treatment plant). Zirlewagen et al (2016) used artificial sweeteners to identify and quantify different sources as well as to estimate the residence times of wastewater contamination. Jekel et al (2015) presented a schema for identifying processes and sources in the anthropogenic water cycle using different organic micropollutants that degrade differently and have dif-

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