Humic substances, including humin fraction, play a key role in the fate of organic and inorganic xenobiotics contaminating the environment. Humin is an important fraction of humic substances, which has been the least studied to date. This is due to the difficulties connected with its isolation that pose a number of methodological problems. Methods of humin fraction isolation can be divided into following main groups: (1) digestion of mineral soil components with HF/HCl followed by alkali extraction of HA and FA; (2) alkali extraction of HA and FA followed by extraction of humin by different organic solvents; and (3) alkali extraction of HA and FA followed by HF/HCl digestion of mineral soil components. Nevertheless, each of these methods has different limitations. We described in detail a useful procedure of humin isolation, in which this fraction was not extracted, but isolated from the soil by removing its soluble organic and mineral components. A modified method of HA and FA extraction with 0.1 M NaOH, according to the International Humic Substances Society, was used in the first step. Then, the mineral components in the residue were digested with the 10% HF/HCl. Unlike the procedures oriented to increase the concentration of organic matter, samples were treated several times with the HF/HCl mixture until the mineral fraction was almost completely digested. The main assumption of the method modification was to obtain the highest yield with the lowest possible ash content, but without affecting humin chemical structure. The results showed that the proposed procedure is characterized by a high efficiency and recovery and, therefore, it can be used to isolate high amounts of humin from soil.

Searching for a renewable phosphorus (P) source for agricultural soils has become a challenge of particular importance on a global scale. Depletion of the world’s phosphate resources as well as the risk of environmental problems caused by excessive P mobility have placed this topic among the most important environmental issues. The aim of this study was to analyse the transformation of phosphorus forms in municipal solid waste compost (MSWC) at different maturity stages, to assess the effects of their application on soil phosphorus status and to evaluate the suitability of MSWC for agricultural soils as a potential phosphorus source. The application of MSWC to the soil had a positive effect on the content of available P. The content of potentially mobile P forms increased significantly in the soil, primarily after the introduction of immature MSWC and confirmed by the significant correlations with the applied P indicators. However, the results indicate that the MSWC does not pose a serious environmental risk and could become a potential source of P in the soil, although the material used for this purpose should be mature. This study also indicated that the assessment of using compost as a P source should not be based on P total content alone, but should include the content of different P forms and specific P-related indicators, to reflect both the P availability and the potential environmental risks.

Currently, revealing soil management strategies that store the maximum atmospheric CO₂ in the soil is a major issue. This is best explored by investigating long-term experiments, like the Skierniewice (Poland) field trial, established in 1921 on sandy loam Luvisol. In this trial, the variants analyzed included control (CON), manure (MAN), legumes (LEG), and manure + legumes (MAN + LEG). Soil samples from the A horizon were analyzed for total organic carbon (TOC), carbon content of humic acids (HA), fulvic acids (FA), and humin (HUM), as well as for spectroscopic properties of bulk soil and isolated HUM. Compared to the control, all other treatments caused an increase in TOC, while the application of manure resulted in an increase in the amount of HUM. Legume application caused an increase in UV-Vis absorbance and fluorescence emission. Thermochemolysis and gas chromatography/mass spectrometry showed that HUM was enriched in carbohydrates in almost all pairs of soil and HUM. Compared to the CON, the largest proportion of carbohydrate in HUM was found in MAN + LEG. Different long-term soil management strategies not only altered TOC, but also, surprisingly, the chemical composition of HUM, which is considered to be particularly stable and a long-term sink of atmospheric carbon.

The constant influx of pesticides into soils is a key environmental issue in terms of their potential retention in the soil, thus reducing their negative impact on the environment. Soil organic matter (SOM) is an important factor influencing the environmental fate of these substances. Therefore, the aim of this research was to assess the chemical behavior of pesticides (flufenacet, pendimethalin, α-cypermethrin, metazachlor, acetamiprid) toward stable soil humin fractions (HNs) as a main factor affecting the formation of non-extractable residues of agrochemicals in soil. This research was conducted as a batch experiment according to OECD Guideline 106. For this purpose, HNs were isolated from eight soils with different physicochemical properties (clay content = 16–47%, pH_KCl = 5.6–7.7, TOC = 13.3–49.7 g·kg⁻¹, TN = 1.06–2.90 g·kg⁻¹, TOC/TN = 11.4–13.7) to reflect the various processes of their formation. The extraction was carried out through the sequential separation of humic acids with 0.1 M NaOH, and then the digestion of the remaining mineral fraction with 10% HF/HCl. The pesticide concentrations were detected using GC-MS/MS. The pesticides were characterized based on the different sorption rates to HNs, according to the overall trend: metazachlor (95% of absorbed compound) > acetamiprid (94% of absorbed compound) > cypermethrin (63% of partitioning compound) > flufenacet (39% of partitioning compound) > pendimethalin (28% of partitioning compound). Cypermethrin and metazachlor exhibited the highest saturation dynamic, while the other agrochemicals were much more slowly attracted by the HNs. The obtained sorption kinetic data were congruous to the pseudo-first-order and pseudo-second-order models related to the surface adsorption and interparticle diffusion isotherm. The conducted research showed that the processes of pesticide sorption, apart from physicochemical phenomena, are also affected by the properties of the pollutants themselves (polarity, K_OC) and the soil properties (SOM content, clay content, and pH_KCl).

The aim of this study was to assess the effect of long-term catch crop application on the structural properties of humin, which is considered the most recalcitrant fraction of soil organic matter. Soil samples from a 30-year field experiment on triticale cultivated with and without catch crops were analysed to determine the total organic carbon content and fractional composition of humic substances. Meanwhile, humin isolated from bulk soil was analysed to determine its elemental composition and spectroscopic properties measured with UV-Vis, fluorescence, and ¹³C-CPMAS-NMR. It was found that catch crop farming enhanced the formation of highly reactive humus substances, like low-molecular-weight fractions and humic acids, while decreasing the humin fraction. The higher H/C and O/C atomic ratios of humin and the UV-Vis, fluorescence, and ¹³C-CPMAS-NMR results confirmed a higher share of oxygen-containing functional groups in humin isolated from the soil with catch crop rotation, also corroborating its greater aliphatic nature. Under the conditions of our field experiment, the results indicated that organic residues from catch crops quickly undergo the decay process and are transformed mainly into highly reactive humus substances, which can potentially improve soil health, while mineral fertilisation alone without catch crops favours the stabilisation and sequestration of carbon.

The aim of the investigation was to determine the quantitative changes of selected organic compounds during composting of municipal solid wastes (MSWs). The object of the study was a differently matured compost produced according the to open pile/windrow semi-dynamic technology from selectively collected biodegradable municipal solid waste. During the experiment, the temperature and moisture of the composted wastes were monitored. In the collected samples—taken from differently matured compost—the total organic carbon (TOC) and total nitrogen (TN) were determined. The organic matter fractionation method described by Stevenson and Adani et al. was adopted, which allows to determine the carbon content of the following groups of organic compounds: hydrophobic (HSC), hydrophilic (WEOC), acidophilic (C_AC), cellulose (CCEL), core-HA (ligno-humic, CALK) and residual carbon (non-hydrolysing, CR). The TOC and TN content, as well as the origin and quality of the starting materials, allow the product tested to be classified for fertiliser purposes. The most intense changes were observed during the thermophilic composting phase. In spite of the optimal technological conditions of the process, the predominance of the CR and CCEL fraction was observed, and the share of humic compounds did not exceed 30% TOC. The investigated compost met legal, ecological and economic criteria for products of biological recycling, thus can be used as a good organic amendment to improve the soil organic matter balance, stimulate the soil biodiversity and carbon sequestration.