MICROPLASTICS IN LANDFILL LEACHATES IN THREE NORDIC COUNTRIES

We investigated the occurrence of microplastics (size range 5,000-50 µm) in leachates at 11 landfills of different age and operational status in Finland, Iceland and Norway. Collective sampling was carried out by pumping leachate with a stainless-steel submergible pump through a custom-made, stainless-steel filter unit containing filter plates with decreasing pore sizes (5,000, 417 and 47 µm, respectively). Samples were pre-treated and split into particles size classes above 500 μm and above 50 μm, and screened for occurrence of microplastics made of PE, PP, PVC, PS, PET, PA, PU, PC, PMMA, POM, SBR (rubber) or PMB (polymer modified bitumen). Samples were analysed by FT-IR spectroscopy, both to identify and to count microplastic particles (SBR and PMB were merely identified). Most samples tested positive for multiple microplastics. Three leachates, including drinking water (blank), tested positive for SBR particles and/or PMB only. Treated leachate samples exhibited lower total microplastic’s counts than untreated, up to several orders of magnitude. National waste management practices over time, landfill age or operational status do not seem to explain differences in microplastic abundance or counts between leachates. Particle count and calculated loads of microplastic emissions through leachates differed several orders of magnitude between landfills. Results indicate that landfill leachates might be a relatively small source of microplastics (>50 µm) to surface waters compared to untreated and treated sewage or road runoff. Continued data acquisition, improved sample preparation and understanding of variability of microplastics in landfill leachate are necessary, including particles smaller than 50 µm.

A Review on the Application of Isotopic Techniques to Trace Groundwater Pollution Sources within Developing Countries

Owing to a lack of efficient solid waste management (SWM) systems, groundwater in most developing countries is found to be contaminated and tends to pose significant environmental health risks. This review paper proffers guidelines on the application of isotopic techniques to trace groundwater pollution sources from data spanning from 2010 to 2020 within developing countries. Earlier groundwater studies in those countries were mainly focused on using hydrochemical and geophysical techniques. The limitation of these techniques is that they can only monitor the concentration of pollutants in the water bodies and possible leachate infiltration but cannot determine the specific sources of the pollution. Stable isotopes of δ18O, δ2H and δ13C can confirm leachate migration to water bodies due to methanogenesis. The high tritium in landfill leachates is useful to identify leachate percolation in groundwater. The δ15N technique has been used to distinguish between synthetic and organic nitrogen sources but its application is limited to differentiating between atmospheric vs. inorganic nitrogen sources. The use of a dual isotope of δ15N–NO3− and δ18O–NO3− is beneficial in terms of identifying various sources of nitrogen such as atmospheric and inorganic fertilizers but is yet to be used to differentiate between nitrogen pollution sources from dumpsites, sewage and animal manure. The coupling of the 11B isotope with δ15N–NO3− and δ18O–NO3− and other hydrochemical parameters has proven to be effective in distinguishing between nitrate fertilizer, animal manure, seawater contamination and sewage. Therefore, in areas affected by agricultural activities, landfill leachates, domestic or sewage effluent and seawater intrusion, it is incumbent to couple hydrochemical (Cl−, NO3−, B, DO) and isotope techniques (δ18O, 2H, δ13C, δ18O–NO3−, δ15N–NO3−, δ11B and 3H) to effectively determine pollution sources of groundwater in developing countries. The foregoing review will provide guidelines for studies that may aim to critically distinguish between seawater intrusion, dumpsites, sewage and septic leachates.

Kinetics of the Organic Compounds and Ammonium Nitrogen Electrochemical Oxidation in Landfill Leachates at Boron-Doped Diamond Anodes

Electrochemical oxidation (EO) of organic compounds and ammonium in the complex matrix of landfill leachates (LLs) was investigated using three different boron-doped diamond electrodes produced on silicon substrate (BDD/Si)(levels of boron doping [B]/[C] = 500, 10,000, and 15,000 ppm—0.5 k; 10 k, and 15 k, respectively) during 8-h tests. The LLs were collected from an old landfill in the Pomerania region (Northern Poland) and were characterized by a high concentration of N-NH4+ (2069 ± 103 mg·L−1), chemical oxygen demand (COD) (3608 ± 123 mg·L−1), high salinity (2690 ± 70 mg Cl−·L−1, 1353 ± 70 mg SO42−·L−1), and poor biodegradability. The experiments revealed that electrochemical oxidation of LLs using BDD 0.5 k and current density (j) = 100 mA·cm−2 was the most effective amongst those tested (C8h/C0: COD = 0.09 ± 0.14 mg·L−1, N-NH4+ = 0.39 ± 0.05 mg·L−1). COD removal fits the model of pseudo-first-order reactions and N-NH4+ removal in most cases follows second-order kinetics. The double increase in biodegradability index—to 0.22 ± 0.05 (BDD 0.5 k, j = 50 mA·cm−2) shows the potential application of EO prior biological treatment. Despite EO still being an energy consuming process, optimum conditions (COD removal > 70%) might be achieved after 4 h of treatment with an energy consumption of 200 kW·m−3 (BDD 0.5 k, j = 100 mA·cm−2).