Photocatalytic removal of ceftriaxone from wastewater using TiO2/MgO under ultraviolet radiation.

Pharmaceutical compounds are among the environmental contaminants that cause pollution of water resources and thereby threaten ecosystem services and the environmental health of the past decades. Antibiotics are categorized as emerging pollutants due to their persistence in the environment that are difficult to remove by conventional wastewater treatment. Ceftriaxone is one of the multiple antibiotics whose removal from wastewater has not been fully investigated. In this study, TiO2/MgO (5% MgO) the efficiency of photocatalyst nanoparticles in removing ceftriaxone was analyzed by XRD, FTIR, UV-Vis, BET, EDS, and FESEM. The results were compared with UVC, TiO2/UVC, and H2O2/UVC photolysis processes to evaluate the effectiveness of the selected methods. Based on these results, the highest removal efficiency of ceftriaxone from synthetic wastewater was 93.7% at the concentration of 400 mg/L using TiO2/MgO nano photocatalyst with an HRT of 120 min. This study confirmed that TiO2/MgO photocatalyst nanoparticles efficiently removed ceftriaxone from wastewater. Future studies should focus on the optimization of reactor conditions and improvements of the reactor design to obtain higher removal of ceftriaxone from wastewater.

Toxicity Effects of Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) on Two Green Microalgae Species.

Amongst per- and polyfluoroalkyl substances (PFAS) compounds, perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) have a high persistence in physicochemical and biological degradation; therefore, the accumulation of PFOS and PFOA can negatively affect aquatic organisms and human health. In this study, two microalgae species (Chlorella vulgaris and Scenedesmus obliquus) were exposed to different concentrations of a PFOS and PFOA mixture (0 to 10 mg L-1). With increases in the contact time (days) and the PFAS concentration (mg L-1) from 1 to 7, and 0.5 to 10, respectively, the cell viability, total chlorophyll content, and protein content decreased, and the decrease in these parameters was significantly greater in Scenedesmus obliquus. As another step in the study, the response surface methodology (RSM) was used to optimize the toxicity effects of PFAS on microalgae in a logical way, as demonstrated by the high R2 (>0.9). In another stage, a molecular docking study was performed to monitor the interaction of PFOS and PFOA with the microalgae, considering hydrolysis and the enzymes involved in oxidation-reduction reactions using individual enzymes. The analysis was conducted on carboxypeptidase in Chlorella vulgaris and on c-terminal processing protease and oxidized cytochrome c6 in Scenedesmus obliquus. For the enzyme activity, the affinity and dimensions of ligands-binding sites and ligand-binding energy were estimated in each case.

Removal of lead ions from wastewater using lanthanum sulfide nanoparticle decorated over magnetic graphene oxide.

In this study, the new lanthanum sulfide nanoparticle (La2S3) was synthesized and incorporated onto magnetic graphene oxide (MGO) sheets surface to produce potential adsorbent (MGO@LaS) for efficient removal of lead ions (Pb2+) from wastewater. The synthesized MGO@LaS adsorbent was characterized using Fourier transform infrared spectroscopy, field emission scanning electron microscopy and energy-dispersive X-ray spectroscopy. The effective parameters on the adsorption process including solution pH (~5), adsorbent dosage (20 mg), contact time (40 min), initial Pb2+ concentration and temperature were studied. The removal efficiency was obtained >95% for lead ions at pH 5 with 20 mg adsorbent. To validate the adsorption rate and mechanism, the kinetic and thermodynamic models were studied based on experimental data. The Langmuir isotherm model was best fitted to initial equilibrium concentration with a maximum adsorption capacity of 123.46 mg/g. This indicated a monolayer adsorption pattern for Pb2+ ions over MGO@LaS. The pseudo-second-order as the kinetic model was best fitted to describe the adsorption rate due to high R2 > 0.999 as compared first-order. A thermodynamic model suggested a chemisorption and physisorption adsorption mechanism for Pb2+ ions uptake into MGO@LaS at different temperatures; ΔG° < -5.99 kJ mol-1 at 20 °C and ΔG° -18.2 kJ mol-1 at 45 °C. The obtained results showed that the novel nanocomposite (MGO@LaS) can be used as an alternative adsorbent in wastewater treatment.

Adsorption and desorption behavior of arsenite and arsenate at river sediment-water interface.

The adsorption of inorganic arsenic (As) plays an important role in the mobility and transport of As in the river environment. In this work, the adsorption and desorption of arsenite [As(III)] and arsenate [As(V)] on river sediment were conducted under different pH, initial As concentrations, river water and sediment composition to assess As adsorption behavior and mechanism. Both adsorption kinetics and equilibrium results showed higher adsorption capacity of sediment for As(V) than As(III). Adsorption of As(III) and As(V) on river sediment was favored in acidic to neutral conditions and on finer sediment particles, while sediment organic matter marginally reduced adsorption capacity. In addition, higher adsorption affinity of As(III) and As(V) in river sediment was observed in deionised water than in river water. For the release process, the desorption of both As(III) and As(V) followed nonlinear kinetic models well, showing higher amount of As(III) release from sediment than As(V). Adsorption isotherm was well described by both Langmuir and Freundlich models, demonstrating higher maximum adsorption capacity of As(V) at 298.7 mg/kg than As(III) at 263.3 mg/kg in deionised water, and higher maximum adsorption capacity of As(III) of 234.3 mg/kg than As(V) of 206.2 mg/kg in river water. The XRD showed the changes in the peaks of mineral groups of sediment whilst FTIR results revealed the changes related to surface functional groups before and after adsorption, indicating that Fe-O/Fe-OH, Si(Al)-O, hydroxyl and carboxyl functional groups were predominantly involved in As(III) and As(V) adsorption on sediment surface. XPS analysis evidenced the transformation between these As species in river sediment after adsorption, whilst SEM-EDS revealed higher amount of As(V) in river sediment than As(III) due to the lower signal of Al.

Advances in As contamination and adsorption in soil for effective management.

Arsenic (As) is a heavy metal that causes widespread contamination and toxicity in the soil environment. This article reviewed the levels of As contamination in soils worldwide, and evaluated how soil properties (pH, clay mineral, organic matter, texture) and environmental conditions (ionic strength, anions, bacteria) affected the adsorption of As species on soils. The application of the adsorption isotherm models for estimating the adsorption capacities of As(III) and As(V) on soils was assessed. The results indicated that As concentrations in contaminated soil varying significantly from 1 mg/kg to 116,000 mg/kg, with the highest concentrations being reported in Mexico with mining being the dominating source. Regarding the controlling factors of As adsorption, soil pH, clay mineral and texture had demonstrated the most significant impacts. Both Langmuir and Freundlich isotherm models can be well fitted with As(III) and As(V) adsorption on soils. The Langmuir adsorption capacity varied in the range of 22-42400 mg/kg for As(V), which is greater than 45-8901 mg/kg for As(III). The research findings have enhanced our knowledge of As contamination in soil and its underlying controls, which are critical for the effective management and remediation of As-contaminated soil.

Cross-linked chitosan/zeolite as a fixed-bed column for organic micropollutants removal from aqueous solution, optimization with RSM and artificial neural network.

Organic micropollutants (MPs) in low concentrations can affect aquatic ecosystems and human health. Adsorption technique is one of the promising methods to remove MPs. Chitosan and zeolites are environmentally friendly and low-cost adsorbents. Thus, removal of organic MPs (such as bisphenol A (BPA), carbamazepine (CBZ), ketoprofen (KTF) and tonalide (TND) from aqueous solution via cross-linked chitosan/zeolite, as a fixed-bed column, was investigated in the current study. Hydraulic retention time was set at 0.8 h pH and concentration of organic MPs ranged from 4 to 8 and 0.50 mg/L to 2.0 mg/L, and they were considered as factors in optimizing the removal of pollutants via response surface methodology (RSM). Approximately 1.4560 mg/L (89.0%) of BPA, 1.4724 mg/L (90.0%) of CBZ, 1.4920 mg/L (91.2%) of KTF and 1.4118 mg/L (86.3%) of TND were removed at 5.1 pH and 1.636 mg/L initial concentration as the optimum removal efficiency on the basis of RSM. Artificial neural network (ANN) was used to optimise removal effectiveness for each MP. The high R2 values and reasonable mean squared errors indicated that ANN optimized MP removal in a logical aspect. Adsorption isotherm studies revealed that organic MP removal through chitosan/zeolite could be explained with Freundlich and Langmuir isotherms.

Pollutants removal from synthetic wastewater by the combined electrochemical, adsorption and sequencing batch reactor (SBR).

Wastewater filtration is considered the main solution to water shortages. Here, we treated synthetic wastewater by combining treatment techniques, namely, electrochemical oxidation and adsorbent added sequencing batch reactor (SBR). One beaker with a working value of 1500 mL was applied in this contemporary study. In the upper part of the beaker, an anode and a cathode (Ti/RuO2-IrO2) were arranged in parallel for the electrochemical oxidation process. Sodium sulfate (Na2SO4) with a concentration of 2.5 g/L was added as the electrolyte. The voltage and current were set to 7.50 V and 0.40 A, respectively. Aeration was conducted at the bottom of the beaker. Then, 15% working value of the reactor was filled by activated sludge, and 85% working value of the reactor was added with synthetic wastewater. In addition, 1.50 g/L of powdered cockleshell was added in the reactor. Response surface methodology was used for statistical analysis. In synthetic wastewater, concentrations of COD, ammonia, phenols and chromium were 2500 mg/L, 2500 mg/L, 100 mg/L and 100 mg/L, respectively. pH and reaction time (h) were considered as independent factors. A total of 2430 mg/L biochemical oxygen demand, 2500 mg/L ammonia, 90.0 mg/L phenols, and 84.0 mg/L chromium were eliminated at the optimum reaction time (72.9 min) and pH (6.5). The energy consumption value was 6.5 (kWh kg-1) at the optimum operating conditions. This study indicated that this combined treatment system exhibited high performance.

Ammonia, phosphate, phenol, and copper(II) removal from aqueous solution by subsurface and surface flow constructed wetland.

Water pollution is a global problem. During current study, ammonia, phosphate, phenol, and copper(II) were removed from aqueous solution by subsurface and surface flow constructed wetland. In current investigation, distilled water was polluted with four contaminants including ammonia, phosphate, copper (Cu), and phenol. Response surface methodology and central composite design were applied to optimize pollutant removal during treatment by subsurface flow constructed wetland (SSFCW). Contact time (12 to 80 h) and initial pollutant concentration (20 to 85 mg/L) were selected as independent factors; some upper and lower ranges were also monitored for accuracy. In SSFCW, water hyacinth transplanted in two substrate layers, namely zeolite and cockle shell. SSFCW removed 87.7, 81.4, 74.7, and 54.9% of ammonia, phosphate, Cu, and phenol, respectively, at optimum contact time (64.5 h) and initial pollutant concentration (69.2 mg/L). Aqueous solution was moved to a surface flow constructed wetland (SFCW) after treating via SSFCW at optimum conditions. In SFCW, Typha was transplanted to a fixed powdered substrate layer, including bentonite, zeolite, and cockle shell. SFCW could develop performance of this combined system and could improve elimination efficacy of the four contaminants to 99.99%. So this combined CW showed a good performance in removing pollutants. Graphical abstract Wetlands arrangement for treating aqueous solution in current study.

Co-treatment of landfill leachate and municipal wastewater using the ZELIAC/zeolite constructed wetland system.

Constructed wetland (CW) is a low-cost alternative technology to treat wastewater. This study was conducted to co-treat landfill leachate and municipal wastewater by using a CW system. Typha domingensis was transplanted to CW, which contains two substrate layers of adsorbents, namely, ZELIAC and zeolite. Response surface methodology and central composite design have been utilized to analyze experimental data. Contact time (h) and leachate-to-wastewater mixing ratio (%; v/v) were considered as independent variables. Colour, COD, ammonia, nickel, and cadmium contents were used as dependent variables. At optimum contact time (50.2 h) and leachate-to-wastewater mixing ratio (20.0%), removal efficiencies of colour, COD, ammonia, nickel, and cadmium contents were 90.3%, 86.7%, 99.2%, 86.0%, and 87.1%, respectively. The accumulation of Ni and Cd in the roots and shoots of T. domingensis was also monitored. Translocation factor (TF) was >1 in several runs; thus, Typha is classified as a hyper-accumulator plant.

Powdered ZELIAC augmented sequencing batch reactors (SBR) process for co-treatment of landfill leachate and domestic wastewater.

Sequencing batch reactor (SBR) is one of the various methods of biological treatments used for treating wastewater and landfill leachate. This study investigated the treatment of landfill leachate and domestic wastewater by adding a new adsorbent (powdered ZELIAC; PZ) to the SBR technique. ZELIAC consists of zeolite, activated carbon, lime stone, rice husk ash, and Portland cement. The response surface methodology and central composite design were used to elucidate the nature of the response surface in the experimental design and describe the optimum conditions of the independent variables, including aeration rate (L/min), contact time (h), and ratio of leachate to wastewater mixture (%; v/v), as well as their responses (dependent variables). Appropriate conditions of operating variables were also optimized to predict the best value of responses. To perform an adequate analysis of the aerobic process, four dependent parameters, namely, chemical oxygen demand (COD), color, ammonia-nitrogen (NH3-N), and phenols, were measured as responses. The results indicated that the PZ-SBR showed higher performance in removing certain pollutants compared with SBR. Given the optimal conditions of aeration rate (1.74 L/min), leachate to wastewater ratio (20%), and contact time (10.31 h) for the PZ-SBR, the removal efficiencies for color, NH3-N, COD, and phenols were 84.11%, 99.01%, 72.84%, and 61.32%, respectively.

Identification of influential parameters and conditions in heavy metals adsorption onto Cal-LDH-PC using optimization approaches of RSM and Taguchi.

Adsorption process plays an important role in the remediation of heavy metals (HMs) from wastewater. A laboratory trial was conducted to investigate effective parameters for improving the bio-adsorption removal of HMs. SEM, EDX, BET, and FTIR techniques were applied to characterize the calcined layer double hydroxide (Cal-LDH), pectin (PC), and Cal-LDH-PC composite prepared from Licorice pomace. The adsorption of zinc (Zn) cadmium, nickel (Ni) and lead (Pb) onto the most efficient sorbent was investigated using RSM methodology with operational factors such as concentration, reaction time, sorbent dose, and pH. The results related to FTIR showed that Cal-LDH-PC had the highest number of functional groups. Based on the SEM results Cal-LDH had a low surface area (9.36 m2 g-1) and a small pore size (9.22 nm). After the modification process (Cal-LDH-PC), the values of surface area and pore size increased by 13-fold (120 m2 g-1) and 1.5-fold (18 nm), respectively. Cal-LDH had high adsorption performance, more cavities, stability, various functional groups, and excessive carbon and oxygen content, which make it efficient and powerful in removing HMs from wastewater. The optimal condition for achieving the removal efficiency (RE%) values of metals was determined to be 80.79 mg L-1, 100 min, 0.167 g L-1, and 9 for concentration, reaction time, sorbent dose, and pH, respectively. Maximum adsorption capacity and RE (%) were 300 mg g-1 and 99% for Zn. According to the results concentration had a major impact on RE% (except for Ni), while for Ni, adsorbent dose had the most significant impact. The present study introduced Cal-LDH-PC prepared from Licorice pomace as a capable, useful and economical sorbent for HMs removal from polluted environments. Taguchi's statistical method is distinguished as an economic method with easier interpretation, while the RSM approach is more accurate, and it can also check the interaction of parameters.

Sorption-based atmospheric water harvesting for continuous water production in the built environment: Assessment of water yield and quality.

Sorption-based atmospheric water harvesting (SAWH) is a promising solution for localized high-quality water production. Application of SAWH indoors offers dual benefits of on-site water generation and humidity control. This study evaluated the use of SAWH for water production in residential or office buildings, employing a portable zeolite-based SAWH device. Over the twelve-month testing period in the arid southwestern USA, the device achieved a median water yield of 3.6 L/day at a cost 30 % less than bottled water sold in the U.S. A mathematical model was developed for predicting water yield under different temperature and relative humidity (RH) conditions. Daily water yields were well fitted with the modified Langmuir model, with absolute humidity serving as the only prediction variable. Water extracted from a well-ventilated office building generally met the drinking water standards set by USEPA. However, elevated levels of dissolved organic carbon (DOC) were detected in the samples collected from the residential house (median = 32.6 mg/L), emphasizing the influence of human activities (e.g., cooking) on the emission of volatile and semi-volatile organic compounds in the air, which consequently reside in harvested water. Aldehydes and volatile fatty acids (formate, acetate) comprised roughly 50 % of the DOC found in the AWE water. A carbon fiber filter was not effective at removing these substances, highlighting the need for further research into effective treatment methods for DOC management before the safe use of AWE water. Overall, this study provides critical insights for the practical application of indoor SAWH as a decentralized source of high-quality water and emphasizes the need to identify and manage DOC for its safe use.

Plastic pollution and degradation pathways: A review on the treatment technologies.

In recent years, the production of plastic has been estimated to reach 300 million tonnes, and nearly the same amount has been dumped into the waters. This waste material causes long-term damage to the ecosystem, economic sectors, and aquatic environments. Fragmentation of plastics to microplastics has been detected in the world's oceans, which causes a serious global impact. It is found that most of this debris ends up in water environments. Hence, this research aims to review the microbial degradation of microplastic, especially in water bodies and coastal areas. Aerobic bacteria will oxidize and decompose the microplastic from this environment to produce nutrients. Furthermore, plants such as microalgae can employ this nutrient as an energy source, which is the byproduct of microplastic. This paper highlights the reduction of plastics in the environment, typically by ultraviolet reduction, mechanical abrasion processes, and utilization by microorganisms and microalgae. Further discussion on the utilization of microplastics in the current technologies comprised of mechanical, chemical, and biological methods focusing more on the microalgae and microbial pathways via fuel cells has been elaborated. It can be denoted in the fuel cell system, the microalgae are placed in the bio-cathode section, and the anode chamber consists of the colony of microorganisms. Hence, electric current from the fuel cell can be generated to produce clean energy. Thus, the investigation on the emerging technologies via fuel cell systems and the potential use of microplastic pollutants for consumption has been discussed in the paper. The biochemical changes of microplastic and the interaction of microalgae and bacteria towards the degradation pathways of microplastic are also being observed in this review.

Impact of polystyrene microplastics on the growth and photosynthetic efficiency of diatom Chaetoceros neogracile.

The increasing prevalence of microplastic pollution in aquatic environments has raised concerns about its impact on marine life. Among the different types of microplastics, polystyrene microplastics (PSMPs) are one of the most commonly detected in aquatic systems. Chaetoceros neogracile (diatom) is an essential part of the marine food web and plays a critical role in nutrient cycling. This study aimed to monitor the ecotoxicological impact of PSMPs on diatoms and observe enzymatic interactions through molecular docking simulations. Results showed that diatom growth decreased with increasing concentrations and exposure time to PSMPs, and the lowest photosynthetic efficiency (Fv/Fm) value was observed after 72 and 96 h of exposure to 200 mg L-1 of PSMPs. High concentrations of PSMPs led to a decrease in chlorophyll a content (up to 64.4%) and protein content (up to 35.5%). Molecular docking simulations revealed potential interactions between PSMPs and the extrinsic protein in photosystem II protein of diatoms, suggesting a strong affinity between the two. These findings indicate a detrimental effect of PSMPs on the growth and photosynthetic efficiency of diatoms and highlight the need for further research on the impact of microplastics on marine microbial processes.

Regeneration of exhausted adsorbents after PFAS adsorption: A critical review.

The adsorption process efficiently removes per- and polyfluoroalkyl substances (PFAS) from water, but managing exhausted adsorbents presents notable environmental and economic challenges. Conventional disposal methods, such as incineration, may reintroduce PFAS into the environment. Therefore, advanced regeneration techniques are imperative to prevent leaching during disposal and enhance sustainability and cost-effectiveness. This review critically evaluates thermal and chemical regeneration approaches for PFAS-laden adsorbents, elucidating their operational mechanisms, the influence of water quality parameters, and their inherent advantages and limitations. Thermal regeneration achieves notable desorption efficiencies, reaching up to 99% for activated carbon. However, it requires significant energy input and risks compromising the adsorbent's structural integrity, resulting in considerable mass loss (10-20%). In contrast, chemical regeneration presents a diverse efficiency landscape across different regenerants, including water, acidic/basic, salt, solvent, and multi-component solutions. Multi-component solutions demonstrate superior efficiency (>90%) compared to solvent-based solutions (12.50%), which, in turn, outperform salt (2.34%), acidic/basic (1.17%), and water (0.40%) regenerants. This hierarchical effectiveness underscores the nuanced nature of chemical regeneration, significantly influenced by factors such as regenerant composition, the molecular structure of PFAS, and the presence of organic co-contaminants. Exploring the conditional efficacy of thermal and chemical regeneration methods underscores the imperative of strategic selection based on specific types of PFAS and material properties. By emphasizing the limitations and potential of particular regeneration schemes and advocating for future research directions, such as exploring persulfate activation treatments, this review aims to catalyze the development of more effective regeneration processes. The ultimate goal is to ensure water quality and public health protection through environmentally sound solutions for PFAS remediation efforts.

Optimization of LDO-Pectin Synthesis Conditions for the Removal of Metals from Wastewater: A Comparison of Response Surface Methods and Taguchi Approaches.

With the continuous growth of industrialization, the presence of heavy metals (HMs) in the environment has become a critical issue, necessitating cost-effective and efficient techniques for their removal. The present study aimed to determine the optimal preparation conditions for synthesizing pectin (PC) as a polymer sorbent, combined with Magnesium (Mg) Aluminum (Al) layered double oxides (LDOs), using a fast and facile co-precipitation method. Both the response surface method (RSM) and the Taguchi method were employed to optimize the influence of key independent variables, including the molar ratio of cations Mg:Al, the ratio of pectin to LDO, and the temperature for removing multiple elements from wastewater. The results indicated that RSM is more accurate and examines more interactions, while Taguchi reduces the number of tests and is more economical than RSM. However, both statistical methods showed good potential for predicting the adsorption capacity (Qe) of HMs. The optimal preparation conditions were identified as a molar ratio of 3:1, a ratio of pectin to LDO of 7% w/w, and a temperature of approximately 600 °C. In conclusion, the application of RSM and Taguchi approaches was found to be feasible and effective in optimizing the preparation conditions of modified LDO, which can be utilized as a potential adsorbent for removing multiple elements from wastewater.

Occurrence of per- and polyfluoroalkyl substances in aquatic environments and their removal by advanced oxidation processes.

Per- and polyfluoroalkyl substances (PFAS), one of the main categories of emerging contaminants, are a family of fluorinated organic compounds of anthropogenic origin. PFAS can endanger the environment and human health because of their wide application in industries, long-term persistence, unique properties, and bioaccumulation potential. This study sought to explain the accumulation of different PFAS in water bodies. In aquatic environments, PFAS concentrations range extensively from <0.03 (groundwater; Melbourne, Australia) to 51,000 ng/L (Groundwater, Sweden). Additionally, bioaccumulation of PFAS in fish and water biota has been stated to range from 0.2 (Burbot, Lake Vättern, Sweden) to 13,900 ng/g (Bluegill samples, U.S.). Recently, studies have focused on PFAS removal from aqueous solutions; one promising technique is advanced oxidation processes (AOPs), including microwaves, ultrasound, ozonation, photocatalysis, UV, electrochemical oxidation, the Fenton process, and hydrogen peroxide-based and sulfate radical-based systems. The removal efficiency of PFAS ranges from 3% (for MW) to 100% for UV/sulfate radical as a hybrid reactor. Therefore, a hybrid reactor can be used to efficiently degrade and remove PFAS. Developing novel, efficient, cost-effective, and sustainable AOPs for PFAS degradation in water treatment systems is a critical area of research.

Exploring into a light-avoided environment: Mechanical-thermal coupled conditions responsible for the aging behavior of plastic waste in landfills.

Plastics in landfills undergo a unique micronization process due to multi-factor and light-avoided conditions, but their aging process in such a typical environment remains unexplored. This study investigated the aging behavior of polyethylene plastics, representative of landfills, under simulated dynamic mechanical forces and high temperature-two prevalent environmental factors in landfills. The study explored the individual and combined contributions of these factors to the aging process. Results indicated that high temperature played a primary role in aging plastics by depolymerization and degradation through ·OH production, while mechanical forces contributed mainly to surface structure breakdown. The combined effect leads to more serious surface damage, creating holes, cracks, and scratches that provide access for free radical reactions to plastic bulk, thereby accelerating the aging and micronization process. The resulting microplastics were found to be 14.25 ± 0.53 µg L-1. Aged plastics exhibit a rapid aging rate of depolymerization and oxidation compared to virgin plastics due to their weak properties, suggesting a higher potential risk of microplastic generation. This study fills a knowledge gap regarding the aging behavior of plastics under complex and light-avoided landfill conditions, emphasizing the need for increased attention to the evolution process of microplastics from aged plastic waste in landfills.

Lead and Zinc Uptake and Toxicity in Maize and Their Management.

Soil contamination with heavy metals is a global problem, and these metals can reach the food chain through uptake by plants, endangering human health. Among the metal pollutants in soils, zinc (Zn) and lead (Pb) are common co-pollutants from anthropogenic activities. Thus, we sought to define the accumulation of Zn and Pb in agricultural soils and maize. Concentrations of Pb in agricultural soil (in Namibia) could reach 3015 mg/Kg, whereas concentrations of Zn in soil (in China) could reach 1140 mg/Kg. In addition, the maximum concentrations of Zn and Pb were 27,870 and 2020 mg/Kg in maize roots and 4180 and 6320 mg/Kg in shoots, respectively. Recent studies have shown that soil properties (such as organic matter content, pH, cation exchange capacity (CEC), texture, and clay content) can play important roles in the bioavailability of Zn and Pb. We also investigated some of the genes and proteins involved in the uptake and transport of Zn and Pb by maize. Among several amendment methods to reduce the bioavailability of Zn and Pb in soils, the use of biochar, bioremediation, and the application of gypsum and lime have been widely reported as effective methods for reducing the accumulation of metals in soils and plants.

Occurrence, impact, toxicity, and degradation methods of microplastics in environment-a review.

Microplastic defines as a tiny plastic particle that has a size of less than 5 mm and is ubiquitous in the environment. Due to the tiny size, this microplastic adversely affected the environment, notably aquatic life via ingestion, choking, and entanglement. This microplastic is arduous to degrade as it takes a thousand years due to the properties of plastic itself and consequently remains in nature. In dealing with microplastic issues, this paper reflects the occurrence, impact, toxicity, and degradation methods of microplastics in the environment including physical, chemical, and biological treatments. Here, the physical treatment methods include incineration treatment, ultraviolet (UV), and photocatalytic. The incineration process contributes to environmental pollution due to the release of toxic gases into the atmosphere. In addition, chemical treatments for plastic waste are the degradation process involving chemical additives such as ethylene glycol (EG), nano-magnesium oxide (MgO), diethylene glycol (DEG), and calcium or zinc (Ca/Zn) stearate as a catalyst. These treatments depend on the chemicals that can affect human health and the ecosystem. The biodegradation treatment using bacterial and fungal species can consume the microplastic without disrupting the surrounding environment and biota. It includes recent findings on the biodegradation of microplastic under aerobic and anaerobic conditions. Thus, biodegradation can be considered the best option to degrade microplastic as green and sustainable technology.