The aim of the current study was to evaluate the effect of long-term (56 years) liming on changes in soil pH and aluminium (Al) forms in the soil profile compared with an unlimed soil in a sandy moraine loam of a Dystric Glossic Retisol. Long-term liming had a significant influence on soil acidity of the whole profile, causing increased pH values in the following horizons to 120 cm depth: the ploughing horizon (Ahp), where humus accumulates; the eluvial horizon (E), from which clay particles are leached; a horizon having retic properties and predominantly coarser-textured albic material (E/B); and a horizon with retic properties and predominantly finer-textured argic material (B/E). In the solid phase, non-crystalline Al in limed soil decreased in the Ahp horizon; meanwhile a decrease in total organically bound Al (Alp) and organo–Al complexes of low to medium stability was detected in the deeper El and ElBt horizons. High-stability Al complexes with organic matter were the predominant form of Alp in the unlimed and limed whole soil profile. The concentration of total water-soluble Al ranged from 0.61 to 0.80 mg/l in the limed soil profile but 0.62–1.15 mg/l in the unlimed soil. The highest concentration of exchangeable Al was determined in the upper horizons of the unlimed soil profile and the concentration decreased significantly in the same horizons of the limed soil profile. Long-term liming promoted changes in Al compounds throughout the soil profile.

Electrical power generation by means of electrochemical systems utilizing wastewaters is a global energy challenge tackling technique for which a creation of novel eco-friendly electrode materials is in high relevance. For this purpose a Rhodophyta algae derived activated biochar anode bound with a flaxseeds mucilage binder (5, 10, 20, 30 wt.%) was formed and characterized by thermogravimetric, Brunauer-Emmett-Teller (BET) analysis as well as conductivity and mechanical resistance determination. Activation technique with KOH prior to carbonization at 800 °C of algae was employed to obtain biocarbon with a large surface area. The highest specific surface area of 1298.49 m²/g was obtained with the binder-free sample and had a tendency to decrease with the increase of the binder content. It was estimated that biochar anodes are thermally stable at the temperature of up to 200 °C regardless of binder concentration. The concentration of the binder on the other hand had a significant influence in anodes mechanical resistance and electrical conductance: anode with 30 wt.% of the binder had the highest compressive strength equal to 104 bar; however, the highest conductivity was estimated in anode with 5 wt.% of the binder equal to 58 S/m. It is concluded that anode with 10 wt.% mucilage binder has the optimal properties necessary in MFC utilization.

Crude oil and petroleum products made from it are increasingly being extracted and consumed worldwide as an important energy source. During necessary transportation, e.g., by tanker, an oil spill might occur, which leads to water pollution by oil. One of the methods of cleaning up oil spills is to use sorbents, preferably made from natural materials. This study evaluates the remediation efficiency of brackish water polluted with crude oil, marine diesel oil (MDO) and lubricating oil. The experiment was performed with three different sorbents (straw, straw modified with methoxytrimethylsilanes (MTMS) and wood chip shavings) and without them. The evaporation loss and the dissolved and sorbed fractions of oil were measured by gas chromatography (GC) to evaluate remediation efficiency. Hydrophobization made the natural sorbents buoyant for the duration of the experiment, with only a slight increase in the maximum sorption capacity. The sorbents increased the evaporation of the oils and also of the water, reduced the proportion of the oil dissolved in water and retained the sorbed proportion for the lubricating oil and partly for the MDO, to such an extent that it could not be extracted entirely even after a 60-min extraction time.

Background: Oil spills can cause severe damage within a marine ecosystem. Following a spill, the soluble fraction of polycyclic aromatic hydrocarbons is rapidly released into the water column. These remain dissolved in seawater over an extended period of time, even should the insoluble fraction be removed. The vertical distribution of the aromatic hydrocarbon component and how these become transferred is poorly understood in brackish waters. This study examines the vertical distribution of polycyclic aromatic hydrocarbons having been released from a controlled film of spilled oil onto the surface of brackish water. Methods: The study was undertaken under controlled conditions so as to minimize the variability of environmental factors such as temperature and hydrodynamics. The distribution of polycyclic aromatic hydrocarbons was measured in the dissolved and suspended phases throughout the 1 m water column with different intensity of water sampling: 1, 2, 4, 7, 72, 120, 336, 504 and 984 h. Results: The total concentration of polycyclic aromatic hydrocarbons ranged from 19.01 to 214.85 ng L^–1 in the dissolved phase and from 5.14 to 63.92 ng L^–1 in the suspended phase. These hydrocarbons were released immediately following a controlled spill attaining 214.9 ng L^–1 in the dissolved phase and 54.4 ng L^–1 in the suspended phase near the cylinder bottom after 1–2 h. The 2–3 ring polycyclic aromatic hydrocarbons dominated in the dissolved phase (60–80%), whereas the greater amount of 4–6 ring polycyclic aromatic hydrocarbons (55–90%) occurred in the suspended phase. A relatively low negative correlation (r_S = –0.41) was determined between the concentration of phenanthrene and suspended matter, whereas a high negative correlation (r = − 0.79) was found between the concentration of pyrene and suspended matter. Despite the differences in the relationships between the concentration ratio and amount of suspended matter the obtained regressions allow roughly to predict the concentration of polycyclic aromatic hydrocarbons.

This study investigates the effects of immobilizing fungi on the straw’s performance as an oil sorbent. The buoyancy of the straw with fungi was found to be unaffected by the immobilization process. Even when sorbed with oil, the straw floated on the water’s surface throughout the 14-day test period. The sorption kinetics of the oil appeared similar in the straw with and without immobilized fungi, regardless of beaker shaking. However, the fraction of non-extractable oil was higher in the straw with fungi and shaking compared to the straw without shaking. This observation suggests the potential initiation of oil mining. Based on these results, it is suggested that instead of leaving the straw with fungi and oil in the water, removing it may be beneficial and allow for oil degradation and straw decomposition on land.

The slow pyrolysis of macroalgae at moderate temperatures in the reactor used resulted in an oil with a slightly better calorific value than that of the literature, but the other properties were not convincing. Therefore, co-pyrolysis with HDPE offers a way out in this study. However, this did not improve the property profile as a fuel, as the co-pyrolysate was incombustible due to its high water content. Only a mixture of the pyrolysis oil from algae and of the HDPE wax from the initial pyrolysis of HDPE resulted in a diesel-like product: the density was from 807 kg m⁻³, the viscosity 3.39 mm² s⁻¹, the calorific value was 46 MJ kg⁻¹, and the oxidation stability was 68 min. The isoparaffin index indicates only a low branching of the paraffins, and therefore a low research octane number of 80. The blend did not need any further stabilizing additives.