Removal of Herbicides from Landfill Leachate in Biofilters Stimulated by Ammonium Acetate

At a former Danish polluted landfill, a field experiment using biofilters as an ex-situ remediation strategy for leachate water was carried out. The leachate water was polluted with phenoxy acids, mecoprop, dichlorprop, and their impurities originated from previous years of disposal of production wastes. Three individual biofilters were set up and each was filled with different a support material, e.g., sand, stonewool, and peat amended sand. The sand biofilter was spiked with ammonium acetate in pulses lasting a week to stimulate biomass growth and thereby enhance the removal of the phenoxy acids. The effects on removal and enantioselectivity were studied during a 69-day sampling campaign. Results showed that stimulation of the microbial community with ammonium acetate provided a boost, hence removal in the sand biofilter increased after the dosing whereas the stonewool and peat biofilters showed generally low removal. The highest removal was observed after stimulation in the sand biofilter for both herbicides. After a starting period, the removal was compound-specific but ranged from 60–100%. The final concentrations exceeded the drinking water limits slightly (0.25 µg L−1) (mecoprop and 2-(2/4-chlorophenoxy)propanoic acid), while it was considerably below the limit for all other compounds (2-(2-methylphenoxy)propanoic acid and dichlorprop). Enantioselective fractions were already 0.41, and 0.75 for mecoprop and dichlorprop, respectively, in the inlet, probably due to in-situ degradation in the landfill—Mecoprop showed some enrichment of the (R)-enantiomer in the sand biofilter whereas no real trends were seen in the stonewool and peat biofilter. Only minor alterations in enantiomeric fractions were observed for dichlorprop in all three biofilters. This experiment shows that it is feasible to remove micropollutants from landfill leachates and it is possible to stimulate biomass and thereby initiate and obtain increased removal faster.

Retention Modelling of Phenoxy Acid Herbicides in Reversed-Phase HPLC under Gradient Elution

Phenoxy acid herbicides are used worldwide and are potential contaminants of drinking water. Reversed phase high-performance liquid chromatography (RP-HPLC) is commonly used to monitor phenoxy acid herbicides in water samples. RP-HPLC retention of phenoxy acids is affected by both mobile phase composition and pH, but the synergic effect of these two factors, which is also dependent on the structure and pKa of solutes, cannot be easily predicted. In this paper, to support the setup of RP-HPLC analysis of phenoxy acids under application of linear mobile phase gradients we modelled the simultaneous effect of the molecular structure and the elution conditions (pH, initial acetonitrile content in the eluent and gradient slope) on the retention of the solutes. In particular, the chromatographic conditions and the molecular descriptors collected on the analyzed compounds were used to estimate the retention factor k by Partial Least Squares (PLS) regression. Eventually, a variable selection approach, Genetic Algorithms, was used to reduce the model complexity and allow an easier interpretation. The PLS model calibrated on the retention data of 15 solutes and successively tested on three external analytes provided satisfying and reliable results.

Occurrence and transformation of phenoxy acids in aquatic environment and photochemical methods of their removal: a review

The article presents the behavior of phenoxy acids in water, the levels in aquatic ecosystems, and their transformations in the water environment. Phenoxy acids are highly soluble in water and weakly absorbed in soil. These highly mobile compounds are readily transported to surface and groundwater. Monitoring studies conducted in Europe and in other parts of the world indicate that the predominant phenoxy acids in the aquatic environment are mecoprop, 4-chloro-2-methylphenoxyacetic acid (MCPA), dichlorprop, 2,4-dichlorophenoxyacetic acid (2,4-D), and their metabolites which are chlorophenol derivatives. In water, the concentrations of phenoxy acids are effectively lowered by hydrolysis, biodegradation, and photodegradation, and a key role is played by microbial decomposition. This process is determined by the qualitative and quantitative composition of microorganisms, oxygen levels in water, and the properties and concentrations of phenoxy acids. In shallow and highly insolated waters, phenoxy acids can be decomposed mainly by photodegradation whose efficiency is determined by the form of the degraded compound. Numerous studies are underway on the use of advanced oxidation processes (AOPs) to remove phenoxy acids. The efficiency of phenoxy acid degradation using AOPs varies depending on the choice of oxidizing system and the conditions optimizing the oxidation process. Most often, methods combining UV radiation with other reagents are used to oxidize phenoxy acids. It has been found that this solution is more effective compared with the oxidation process carried out using only UV.

MINI REVIEW ON THERAPEUTIC PROFILE OF PHENOXY ACIDS AND THIER DERIVATIVES

<p>Phenoxy acids and their derivatives are associated with a variety of biological activities such as antihyperlipidemic, hypoglycemic, antimicrobial, antiviral, antitubercular, anti-inflammatory, analgesic, antioxidant, anticancer and antihypertensive activities. This mini review outlines diverse biological properties of phenoxy acids and their derivatives. </p>