The aim of the research was to compare the effect of two types of organic sorbents—humic acid (HA) and biochar (BC)—in sorption-desorption processes of different polar pesticides, which residues are commonly present in arable soils and are potentially harmful for the environment. It also aims to advance the understanding of behavior of both ionizable and nonionizable pesticides in the presence of BC and HA in soils.

Biochar (BC) is often proposed as a tool for climate change mitigation, due to the expected long lifetime in the environment. However, BC’s stability can vary depending on feedstock type and the presence of labile carbon fractions. In this study, we verify the recent methods with new possible tools for biochar stability assessment on six different biochars derived from commonly available Europe biomass sources. Elemental composition (CHNO), dissolved organic carbon (DOC) and water-soluble carbonates content (WSC), volatile organic compounds (VOCs) composition, and mid-infrared spectra (MIR) were performed to estimate the persistence of biochars. Under similar conditions of pyrolysis, biochar properties can vary depending on a feedstock origin. Less aromatic structure and higher contents of labile carbon fractions (DOCs and WSC) in food waste biochars affected the lower stability, while biochars derived from high lignocellulose materials (straw, wood, and grass) were strongly carbonized, with persistent, aromatic structure. Labile carbon pool content (DOC, WSC) and spectral analysis can be useful tools for biochar stability assessment, giving similar information to the standard molar ratio method. Biochars obtained from agriculture and forestry management biomass should be considered as highly stable in soil and are appropriate for long-term carbon sequestration purposes.

The object of the experiment was to evaluate municipal solid waste (MSW) compost. Composting was carried out in a pile under aerobic conditions. Total content as well as water-extractable forms of macro and microelements were analysed during composting. Nutrient solubility indices were calculated for samples taken at various stages of maturity. The soluble forms of C, P, K, Ca and Mg decreased relatively to their total forms following maturation phases. For all micronutrients tested, a significant reduction in the proportion of soluble forms in relation to their total content was observed with an increase in composting time. In mature compost, low solubility were found for nitrogen, potassium, sodium and magnesium, which may indicate that the final product is a good source of these nutrients. The solubility index (percentage share of water-extractable forms of macro- and micronutrients in the total content) for iron indicates that the composting process does not affect its degree of solubility. Solubility index instead of the content of water-extractable forms of chosen macro- and microelements could be taken into account in determining the degree of MSW compost maturity.

Biochar activation methods have attracted extensive attention due to their great role in improving sorptive properties of carbon-based materials. As a result, chemically modified biochars gained application potential in the purification of soil and water from xenobiotics. This paper describes changes in selected physicochemical properties of high-temperature wheat-straw biochar (BC) upon its deashing. On the pristine and chemically activated biochar (BCd) retention of five pesticides of endocrine disrupting activity (carbaryl, carbofuran, 2,4-D, MCPA and metolachlor) was studied. Deashing resulted in increased sorbent aromaticity and abundance in surface hydroxyl groups. BCd exhibited more developed meso- and microporosity and nearly triple the surface area of BC. Hydrophobic pesticides (metolachlor and carbamates) displayed comparably high (88–98%) and irreversible adsorption on both BCs, due to the pore filling, whereas the hydrophilic and ionic phenoxyacetic acids were weakly and reversibly sorbed on BC (7.3 and 39% of 2,4-D and MCPA dose introduced). Their removal from solution and hence retention on the deashed biochar was nearly total, due to the increased sorbent surface area and interactions of the agrochemicals with unclogged OH groups. The modified biochar has the potential to serve as a superabsorbent, immobilizing organic pollutant of diverse hydrophobicity from water and soil solution.

Biochar seems to be a very promising material for remediation, reducing heavy metal mobility in contaminated sites. However, the effect of its application on soil depends on biochar origin, pyrolysis condition, soil type and properties like initial pH or cation exchange capacity, and also on metal form and interactions. This makes prediction about successful remediation with biochar more difficult and a lot of attention should be paid to choose the proper material appropriate to soil conditions. The aim of our study was to evaluate wheat straw biochar application on multi-contaminated soil, to decrease their mobility and minimize the risk of heavy metal occurrence in the area impacted by copper smelting processes. The results of this study indicate that wheat straw biochar application can potentially reduce Cu, Pb, Zn or Cd mobility only in sandy or acidified soils due to the liming effect. In alkaline soils the effect of biochar application on metal immobilization was imperceptible. The effect of wheat straw biochar on heavy metal immobilization in multi-contaminated soils is more complex and cannot be defined as all-purpose material in remediation procedures.

The majority of studies concerning the environmental behavior of hydrophobic pollutants in soil consider soil organic matter (SOM) content as a main factor influencing chemical retention, whereas the composition of SOM and its individual fraction share are often neglected. In the present paper, carbaryl, carbofuran and metolachlor retention by loamy sand and loam topsoil materials is compared and referred to humic acids (CHA) and the residual carbon (CR) content of SOM. Additionally, the sorption-desorption behavior of agrochemicals in soils was tested at a pH of three to seven. Calculated isothermal parameters point to favorable, spontaneous and physical pesticide sorption. Groundwater ubiquity score (GUS) indexes confirmed the low leaching ability of metolachlor on soils and moderate of carbofuran. The high affinity of carbaryl to CR may explain its pronounced sorption in loam soil and the lowest percolation potential. Carbofuran retention in soils was associated with montmorillonite (Mt) and CR fractions. Meanwhile, metolachlor uptake was related to humic acid and Mt content of the soils. Lower pH enhanced retention of the agrochemicals, except for carbaryl sorption in sandy loam soil. Results of this study highlight that SOM composition and mutual share of individual organic carbon fractions alongside pH may play a crucial role in predicting non-ionic pesticide behavior in soil.