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.

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.

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.

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.

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.

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.

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.

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.

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.

Ammonia removal from industrial effluent using zirconium oxide and graphene-oxide nanocomposites.

The present study developed and evaluated nano-adsorbents based on zirconium oxide and graphene oxide (ZrO2/GO) as a novel adsorbent for the efficient removal of ammonia from industrial effluents. Fourier transform infrared (FTIR) spectroscopy, Field Emission Scanning Electron Microscope, Energy-dispersive X-ray Spectroscopy, and X-ray diffraction were used to evaluate and identify the novel adsorbent in terms of morphology, crystallography, and chemical composition. The pH (7), adsorbent quantities (20 mg), adsorbent contact time (30 min) with the sample, and initial ammonia concentration were all tuned for ammonia uptake. To validate ammonia adsorption on the ZrO2/GO adsorbent, several kinetic models and adsorption isotherms were also utilized. The results showed that the kinetics of ammonia adsorption are of the pseudo-second order due to high R2 (>0.99) value as compared first-order (R2 = 0.52). The chemical behavior and equilibrium isotherm were analyzed using the isotherm models and Langmuir model provided high R2 (>0.98) as compared Freundlich (>0.96). Hence, yielding a maximum uniform equilibrium adsorption capacity of 84.47 mg g-1. The presence of functional groups on the surface of graphene oxide and ZrO2 nanoparticles, which interact efficiently with ammonia species and provide an efficient surface for good ammonia removal, is most likely to be responsible.

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.

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.

Pharmaceuticals and personal care products in aquatic environments and their removal by algae-based systems.

The consumption of pharmaceuticals and personal care products (PPCPs) has been widely increasing, yet up to 90-95% of PPCPs consumed by human are excreted unmetabolized. Moreover, the most of PPCPs cannot be fully removed by wastewater treatment plants (WWTPs), which release PPCPs to natural water bodies, affecting aquatic ecosystems and potentially humans. This study sought to review the occurrence of PPCPs in natural water bodies globally, and assess the effects of important factors on the fluxes of pollutants into receiving waterways. The highest ibuprofen concentration (3738 ng/L) in tap water was reported in Nigeria, and the highest naproxen concentration (37,700 ng/L) was reported in groundwater wells in Penn State, USA. Moreover, the PPCPs have affected aquatic organisms such as fish. For instance, up to 24.4 × 103 ng/g of atenolol was detected in P. lineatus. Amongst different technologies to eliminate PPCPs, algae-based systems are environmentally friendly and effective because of the photosynthetic ability of algae to absorb CO2 and their flexibility to grow in different wastewater. Up to 99% of triclosan and less than 10% of trimethoprim were removed by Nannochloris sp., green algae. Moreover, variable concentrations of PPCPs might adversely affect the growth and production of algae. The exposure of algae to high concentrations of PPCPs can reduce the content of chlorophyll and protein due to producing reactive oxygen species (ROS), and affecting expression of some genes in chlorophyll (rbcL, psbA, psaB and psbc).

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.

The Potential of Chaetoceros muelleri in Bioremediation of Antibiotics: Performance and Optimization.

Antibiotics are frequently applied to treat bacterial infections in humans and animals. However, most consumed antibiotics are excreted into wastewater as metabolites or in their original form. Therefore, removal of antibiotics from aquatic environments is of high research interest. In this study, we investigated the removal of sulfamethoxazole (SMX) and ofloxacin (OFX) with Chaetoceros muelleri, a marine diatom. The optimization process was conducted using response surface methodology (RSM) with two independent parameters, i.e., the initial concentration of antibiotics and contact time. The optimum removal of SMX and OFX were 39.8% (0.19 mg L-1) and 42.5% (0.21 mg L-1) at the initial concentration (0.5 mg L-1) and contact time (6.3 days). Apart from that, the toxicity effect of antibiotics on the diatom was monitored in different SMX and OFX concentrations (0 to 50 mg L-1). The protein (mg L-1) and carotenoid (µg L-1) content increased when the antibiotic concentration increased up to 20 mg L-1, while cell viability was not significantly affected up to 20 mg L-1 of antibiotic concentration. Protein content, carotenoid, and cell viability decreased during high antibiotic concentrations (more than 20 to 30 mg L-1). This study revealed that the use of Chaetoceros muelleri is an appealing solution to remove certain antibiotics from wastewater.

Removal of Pharmaceutical Micropollutants with Integrated Biochar and Marine Microalgae.

Using microalgae to remove pharmaceuticals and personal care products (PPCPs) micropollutants (MPs) have attracted considerable interest. However, high concentrations of persistent PPCPs can reduce the performance of microalgae in remediating PPCPs. Three persistent PPCPs, namely, carbamazepine (CBZ), sulfamethazine (SMT) and tramadol (TRA), were treated with a combination of Chaetoceros muelleri and biochar in a photobioreactor during this study. Two reactors were run. The first reactor comprised Chaetoceros muelleri, as the control, and the second reactor comprised Chaetoceros muelleri and biochar. The second reactor showed a better performance in removing PPCPs. Through the response surface methodology, 68.9% (0.330 mg L-1) of CBZ, 64.8% (0.311 mg L-1) of SMT and 69.3% (0.332 mg L-1) of TRA were removed at the initial concentrations of MPs (0.48 mg L-1) and contact time of 8.1 days. An artificial neural network was used in optimising elimination efficiency for each MP. The rational mean squared errors and high R2 values showed that the removal of PPCPs was optimised. Moreover, the effects of PPCPs concentration (0-100 mg L-1) on Chaetoceros muelleri were studied. Low PPCP concentrations (<40 mg L-1) increased the amounts of chlorophyll and proteins in the microalgae. However, cell viability, chlorophyll and protein contents dramatically decreased with increasing PPCPs concentrations (>40 mg L-1).

Removal performance and optimisation of pharmaceutical micropollutants from synthetic domestic wastewater by hybrid treatment.

Occurrence of pharmaceutical micropollutants in aquatic environments has been one amongst serious environmental problems. During this study, two reactors, including a sequencing batch reactor (SBR) + powdered composite adsorbent (CA) (first reactor, SBR + CA) and a sequencing batch reactor (second reactor, SBR), were designed to treat synthetic wastewater. Powdered CA was added with a dosage of 4.8 g L-1 to the first reactor. Tap water was contaminated with chemical oxygen demand (COD), ammonia and three pharmaceuticals, namely, atenolol (ATN), ciprofloxacin (CIP) and diazepam (DIA) to produce synthetic wastewater. The SBR + CA illustrated a better performance during synthetic municipal wastewater treatment. Up to 138.6 mg L-1 (92.4%) of COD and up to 114.2 mg L-1 (95.2%) of ammonia were removed by the first reactor. Moreover, optimisation of pharmaceuticals removal was conducted through response surface methodology (RSM) and artificial neural network (ANN). Based on the RSM, the best elimination of ATN (90.2%, 2.26 mg L-1), CIP (94.0%, 2.35 mg L-1) and DIA (95.5%, 2.39 mg L-1) was detected at the optimum initial concentration of MPs (2.51 mg L-1) and the contact time (15.8 h). In addition, ANN represented a high R2 value (>0.99) and a rational mean squared error (<1.0) during the optimisation of micropollutants removal by both reactors. Moreover, adsorption isotherm study showed that the Freundlich isotherm could justify the abatement of micropollutants by using CA better than the Langmuir isotherm.

Effects of glyphosate on germination, photosynthesis and chloroplast morphology in tomato.

The adverse effects of glyphosate herbicide on plants are well recognised, however, potential hormetic effects have not been well studied. This study aimed to use tomato as a model organism to explore the potential hormetic effects of glyphosate in water (0-30 mg L-1) and in compost soil (0-30 mg kg-1). The growth-promoting effects of glyphosate at concentrations of 0.03-1 mg L-1 in water or 0.03-1 mg kg-1 in compost were demonstrated in tomato for the first time. These hormetic effects were manifest as increased hypocotyl and radicle growth of seedlings germinated on paper towel soaked in glyphosate solution and also in crops which had been sprayed with glyphosate. Increased rates of photosynthesis (up to 2-fold) were observed in 4-week old crops when seeds were sown in compost amended with glyphosate and also when leaves were sprayed with glyphosate. The examination of chloroplast morphology using transmission electron microscopy revealed that the hormetic effects were associated with elongation of chloroplasts, possibly due to lateral expansion of thylakoid grana.