Biological materials play a significant role in the treatment of heavy metal-contaminated soil and wastewater. In this study, the Pb²⁺ biosorption potential of lichen Evernia prunastri, extensively available at a forest in Bilecik-Turkey, was investigated at batch-scale level. The optimal conditions were determined and the adsorption isotherms, kinetics, and thermodynamic calculations were also done. In order to have detailed knowledge about metal biosorption, SEM, FTIR, and BET analyses were carried out before and after the biosorption process. The optimal pH was found pH 4 and the maximum metal uptake capacity was found as 0.067 mol kg⁻¹. The results of this study indicate that the lichen was effectively applied to the removal of Pb²⁺ process as an inexpensive biosorbent from industrial wastewater.

A new adsorbent poly-3-hydroxybutyrate-2-(dodecylthiocarbonothioylthio)-2-methylpropionate triester (PH-DTT-MPT) was first time loaded in a micropipette tip for speciation of chromium in different water samples. Total chromium (Cr), trivalent chromium (Crᴵᴵᴵ), and hexavalent chromium (Crⱽᴵ) in different natural water samples were determined by electrothermal atomic absorption spectrometry. Known concentration of Crᴵᴵᴵ and Crⱽᴵ was passed through a biodegradable polymer for investigation of the behavior of the newly used adsorbent. The newly used copolymer absorbed the Crᴵᴵᴵ on surface of the PH-DTT-MPT at pH 7.0, while Crⱽᴵ was not adsorbed in desired pH value. After passing the real and standard solutions through the micropipette, then 2.0 mol L⁻¹ HCl was used for elution of Crᴵᴵᴵ from the biodegradable polymer. Total Cr was calculated after reducing Crⱽᴵ into Crᴵᴵᴵ by specific concentration of hydroxy ammonium chloride (HONH₂·HCl). The concentration of Crⱽᴵ in different natural water samples was estimated after back calculation of Crᴵᴵᴵ from total chromium. Effect of analytical parameters like adsorbent, pH, eluent, sample volume, flow rates, and interfering ions was also studied. The LOD, LOQ, RSD, and EF of the developed method were calculated as 6.1 ng L⁻¹, 20 ng L⁻¹, 1.17%, and 90, respectively. Validation of developed method was checked by certified reference materials and spiking addition method. The developed method was successfully applied for determination of total Cr, Crᴵᴵᴵ, and Crⱽᴵ in various natural water ecosystems.

The study investigated the sorption capacity of biosorbent-raphia sp. against ammonia. Raphia fibers were used without and with the modification of its surface with NaCl, NaNO₃, and K₂SO₄. The data was analyzed in the state of equilibrium using four isotherm models such as Langmuir, Freudlich, Temkin, and Dubinin-Radushkevich. The equilibrium of ammonia sorption for all studied systems was best described by the Freudlich isotherm model. On its basis, it can be assumed that the studied process is of chemical nature, which results from the value of the coefficient 1/n < 1. In order to confirm the sorption mechanism, analysis of the kinetics of the ammonia sorption process on raphia fibers was performed. Four kinetic models of sorption were calculated: pseudo-first-order model, pseudo-second-order model, Elovich model, and Webber-Morris intermolecular diffusion model. The sorption kinetics of the modeled ammonia waste were carried out using unmodified palm fibers and all kinds of surface modification. This process was best described by the pseudo-second-order sorption model, which can be considered as a confirmation of the chemical nature of ammonia sorption on raphia sp. fibers.

The present work aimed to evaluate the effects of commercial fungicides containing the active compounds from the triazole group—tebuconazole (TBZ) and difenoconazole (DFZ)—and dicarboximide group—procymidone (PRD) and iprodione (IPD) on the mitotic cycle of the plant model Lactuca sativa L. These active compounds have been present in foods sampled at different Brazilian’s states and amounted higher than recommended by law. The bioassay with L. sativa was applied to access the toxicity and better understand the mechanisms of action of these compounds in living beings. The active principles IPD and DFZ presented mitodepressive effect, statistically reducing the MI at all applied concentrations in comparison to the negative control. TBZ was the most cytotoxic active compound tested inhibited in 77% mitotic active in the lowest concentration applied. PRD alter the frequency of mitotic cells only in the concentration above that recommended by the manufacture. C-metaphase and adherent chromosomes were the most frequent cell cycle alteration observed on the treated cells, followed by bridges and lost chromosomes. Therefore, the mechanism of action was mainly aneugenic (70%). For TBZ, the frequency of condensed nucleus was very expressive (313 higher than the negative control).

Oleaginous microalgae and yeast are the two major propitious factories which are sustainable sources for biodiesel production, as they can accumulate high quantities of lipids inside their bodies. To date, various microalgal and yeast species have been exploited singly for biodiesel production. However, despite the ongoing efforts, their low lipid productivity and the high cost of cultivation are still the major bottlenecks hindering their large-scale deployment. Co-culturing of microalgae and yeast has the potential to increase the overall lipid productivity by minimizing its production cost as both these organisms can utilize each other’s by-products. Microalgae act as an O₂ generator for yeast while consuming the CO₂ and organic acids released by the yeast cells. Further, yeast can break complex sugars in the medium, which can then be utilized by microalgae thereby opening new options for copious and low-cost feedstocks such as agricultural residues. The current review provides a historical and technical overview of the existing studies on co-culturing of yeast and microalgae and elucidates the crucial factors that affect the symbiotic relationship between these two organisms. Furthermore, the review also highlighted the advantages and the future perspectives for paving a path towards a sustainable biodiesel product.

Electronic waste (e-waste) has been widely studied by scholars all over the world, but the research topics and development trends in this field are still unclear. This study aimed to explore the status quo, hot topics, and future prospects in the field of e-waste. Data of publications were downloaded from the Web of Science Core Collection. We used CiteSpace V, Histcite, and VOSviewer to analyze literature information. A total of 2800 papers in e-waste research were identified, and the number of publications increased rapidly after 2004. Six thousand five hundred seventy-three authors participated in the e-waste research, but 70.01% of the authors published only 1 article. The most productive country in this field was China (1146 publications), and the most productive institution was the Chinese Academy of Sciences (370 publications). The Waste Management (225 publications) was the most productive journal, and Environment Science & Technology (9704 co-citations) was the most co-cited journal. The main hot topics in e-waste field were management and recycling of e-waste in developing countries, health risk assessment after exposure to organic pollutants, degradation and recovery of waste metal materials, and impact of heavy metals on children’s health. The frontier topic was degradation.

Nowadays, widespread application of engineered nanoparticles (ENPs) inevitably leads to their release into the environment. Soils are regarded as the ultimate sink for ENPs. The study on mobility of ENPs in soils is important in the assessment of potential risks related to their toxicity. The behavior of ENPs is dependent not only on parameters of soil but also on exposure scenarios, namely, the amount of ENPs trapped in soil. In the present work, the mobility of cerium dioxide nanoparticles (nCeO₂) in soils at different exposure scenarios has been studied. The relationship between mobility of nCeO₂ and their concentration in soil in the range from 1 to 1000 μg g⁻¹ is evaluated. It is shown that the mobility of nCeO₂ decreases with decreasing their concentration in soil and attains the minimum value at the concentration of nCeO₂ below 10 μg g⁻¹. In relative terms, only about 0.1–0.2% of nCeO₂ at their concentration in soil 10–1000 μg g⁻¹ are mobile and can migrate in soil profile under saturated conditions. The major portion of nCeO₂ (about 99.8%) remains immobile in soil. Evidently, the vertical transport of nCeO₂ in soil profile should depend on volume of released suspensions. In the case of small or moderate wet deposition, nanoparticles will accumulate in upper soil horizons, where biological activity is highest, and affect the soil inhabitants (plant roots, earthworms, insects, microorganisms, etc.).

Increasing applications of rare earth elements (REEs) and improving technologies have led to increased demand. Because of their limited availability and depletion of most resources, the recovery of these elements from waste has become important. The use of cost-effective materials for this purpose and the high value that can potentially be recovered would be beneficial and attractive to many industries using REEs. In this study, natural zeolite and bentonite were used in batch studies to recover REEs (La, Y, Lu, Sm, Pr, Tm, Ce, Nd, Yb, Gd, Eu, Er, Ho, Dy, and Sc) from aqueous solutions. The effect of adsorbent dosage, pH, concentration, contact time, and competing ions on recovery was investigated. Desorption studies were conducted using ammonium sulphate. Adsorption onto zeolite was found to increase with pH, whereas uniform adsorption was observed for bentonite, except at pH 2 (16% less efficiency). The pH values of 6.2 and 3.2 were selected as the optimum for zeolite and bentonite, respectively. For zeolite, the average adsorption efficiencies for REEs at 0.5, 1.0, 2.0, 5.0, and 10 mg L⁻¹ were found to be 91, 96, 89, 40, and 20% respectively but, > 98% adsorption efficiencies were achieved with bentonite at all concentrations. The zeolite and bentonite adsorption data were better described by Langmuir though, for bentonite, the coefficients of determination (R² values) for the Freundlich and Dubinin-Radushkevich isotherm models were also significant. There was no significant difference (p > 0.05) on the adsorption of the elements in the presence of competing ions. Bentonite proved to perform better, most likely as a result of its higher surface area. Generally, the good adsorption performance of both adsorbents in their natural forms makes them an attractive and potential cheap option for the recovery of REEs from wastewaters.

Adsorption plays an important role in removing cadmium (Cd²⁺) from water, and magnetic adsorbents are increasingly being used due to their ease of separation and recovery. Magnetic Fe₃O₄–coated hydroxyapatite (HAP) nanoparticles (nHAP-Fe₃O₄) were developed by co-precipitation and then used for the removal of Cd²⁺ from water. The properties of these nanoparticles were characterized by transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and magnetization curves. Experiments were conducted to investigate the effects of adsorption and mechanisms. Results illustrated that kinetic data were well fitted by a pseudo-second-order model. The adsorption capacity of nHAP-Fe₃O₄ was 62.14 mg/g. The mechanisms for the adsorption of Cd²⁺ on nHAP-Fe₃O₄ included rapid surface adsorption, intraparticle diffusion, and internal particle bonding, with the ion exchange with Ca²⁺ and chemical complexation being the most dominant. The regeneration efficiency and recovery rate of nHAP-Fe₃O₄ eluted by EDTA-Na₂ after the fifth cycle were 63.04% and 40.2%, respectively. Results revealed that the feasibility of nHAP-Fe₃O₄ as an adsorbent of Cd²⁺ and its environmental friendliness make it an ideal focus for future research.

For a long-period comparative analysis of air pollution in coastal and inland cities, we analyzed the continuous Morlet wavelet transform on the time series of a 5274-day air pollution index in Shanghai and Lanzhou during 15 years and studied the multi-scale variation characteristic, main cycle, and impact factor of the air pollution time series. The analysis showed that (1) air pollution in the two cities was non-stationary and nonlinear, had multiple timescales, and exhibited the characteristics of high in winter and spring and low in summer and autumn. (2) The monthly variation in air pollution in Shanghai was not significant, whereas the seasonal variation of air pollution in Lanzhou was obvious. (3) Air pollution in Shanghai showed an ascending tendency, whereas that in Lanzhou presented a descending tendency. Overall, air pollution in Lanzhou was higher than that in Shanghai, but the situation has reversed since 2015. (4) The primary cycles of air pollution in these two cities were close, but the secondary cycles were significantly different. The aforementioned differences were mainly due to the impact of topographical and meteorological factors in Lanzhou, the weather process and the surrounding environment in Shanghai. These conclusions have reference significance for Shanghai and Lanzhou to control air pollution. The multi-timescale variation and local features of the wavelet analysis method used in this study can be applied to varied aspects of air pollution analysis. The identification of cycle characteristics and the monitoring, forecasting, and controlling of air pollution can yield valuable reference.