TL;DR: Climate change and anthropogenic activities are severely impacting aquatic ecosystems, causing ocean acidification, habitat loss, and species decline, necessitating long-term monitoring, ecological indicators, and understanding biodiversity responses to global warming for mitigation.
Abstract: All living things depend on their natural environment, either directly or indirectly, for their high quality of life, growth, nutrition, and development. Due to the fast emissions of greenhouse gases (GHGs), the Earth's climate system is being negatively impacted by global warming. Stresses caused by climate change, such as rising and hotter seas, increased droughts and floods, and acrid waters, threaten the world's most populated areas and aquatic ecosystems. As a result, the aquatic ecosystems of the globe are quickly reaching hazardous conditions. Marine ecosystems are essential parts of the world's environment and provide several benefits to the human population, such as water for drinking and irrigation, leisure activities, and habitat for commercially significant fisheries. Although local human activities have influenced coastal zones for millennia, it is still unclear how these impacts and stresses from climate change may combine to endanger coastal ecosystems. Recent studies have shown that rising levels of greenhouse gases are causing ocean systems to experience conditions not seen in several million years, which may cause profound and irreversible ecological shifts. Ocean productivity has declined, food web dynamics have changed, habitat-forming species are less common, species ranges have changed, and disease prevalence has increased due to human climate change. We provide an outline of the interaction between global warming and the influence of humans along the coastline. This review aims to demonstrate the significance of long-term monitoring, the creation of ecological indicators, and the applications of understanding how aquatic biodiversity and ecosystem functioning respond to global warming. This review discusses the effects of current climate change on marine biological processes both now and in the future, describes present climate change concerning historical change, and considers the potential roles aquatic systems could play in mitigating the effects of global climate change.
TL;DR: This study reviews wastewater treatment for agricultural reuse, highlighting challenges and benefits of wastewater irrigation, and discusses the impact of combined conventional-advanced treatment processes on soil microbial activities and human health.
Abstract: Sustainable water recycling and wastewater reuse are urgent nowadays considering water scarcity and increased water consumption through human activities. In 2015, United Nations Sustainable Development Goal 6 (UN SDG6) highlighted the necessity of recycling wastewater to guarantee water availability for individuals. Currently, wastewater irrigation (WWI) of crops and agricultural land appears essential. The present work overviews the quality of treated wastewater in terms of soil microbial activities, and discusses challenges and benefits of WWI in line with wastewater reuse in agriculture and aquaculture irrigation. Combined conventional-advanced wastewater treatment processes are specifically deliberated, considering the harmful impacts on human health arising from WWI originating from reuse of contaminated water (salts, organic pollutants, toxic metals, and microbial pathogens i.e., viruses and bacteria). The comprehensive literature survey revealed that, in addition to the increased levels of pathogen and microbial threats to human wellbeing, poorly-treated wastewater results in plant and soil contamination with toxic organic/inorganic chemicals, and microbial pathogens. The impact of long-term emerging pollutants like plastic nanoparticles should also be established in further studies, with the development of standardized analytical techniques for such hazardous chemicals. Likewise, the reliable, long-term and extensive judgment on heavy metals threat to human beings's health should be explored in future investigations.
TL;DR: The use of AOP in conjunction with biological process has innumerous opportunities for not only wastewater treatment but also the production of high value by-products and their benefits needs to be explored in future towards achieving SDGs.
Abstract: Complexity of wastewater is the most challenging phenomenon on successful degradation of pollutant via any wastewater treatment regime. Upon availability of numerous techniques, Advanced Oxidation Processes (AOP) is the most promising technique for treating industrial wastewater. Higher operating cost is the most promising factor that possess challenge for the industrial scale usage of the AOP process. Combination of biological process with AOP helps in achieving sustainable degradation of toxic pollutant in the wastewater. AOP result in complete or partial degradation of toxic emerging pollutants with the help of free radicals like hydroxyl, superoxide, hydroperoxyl and sulphate radicals. In addition to this the presence of bio-enzymes and microorganisms helps in sustainable degradation of pollutant in an economical and environmentally friendly strategy. In this review, a detailed discussion was conducted on various AOP, focusing on catalytic ozonation, electrochemical oxidation, Sono chemical and photocatalytic processes. With the need for sustainable solutions for wastewater treatment, the use of AOP in conjunction with biological process has innumerous opportunities for not only wastewater treatment but also the production of high value by-products. Further, the effect of AOP combined biological processes needs to be analyzed in real time for the different concentration of industrial wastewater and their benefits needs to be explored in future towards achieving SDGs.
TL;DR: Fe3O4@NH2-MIL88B nanorods efficiently remove dexamethasone from aqueous solutions with 91% adsorption efficiency and 180.01 mg/g capacity, exhibiting spontaneous and endothermic adsorption, and promising reuse potential for environmental remediation.
Abstract: The presence of pharmaceutical compounds in the environment poses a significant threat to human and aquatic animal health. Dexamethasone (DEX), a synthetic steroid hormone with endocrine-disrupting effects, is one such compound that needs to be effectively removed before discharging into the environment. This research presents a novel approach utilizing magnetically recyclable Fe3O4@NH2-MIL88B NRs as an efficient adsorbent for the treatment of DEX from aqueous solutions. The synthesized adsorbent was characterized by X-ray diffraction (XRD), scanning microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), diffuse reflectance spectra (DRS), and Fourier transform infrared spectroscopy (FTIR). Response surface methodology based on central composite design (RSM-CCD) was employed to optimize DEX removal efficiency by determining the optimal conditions, including pH, adsorbent dose, time, and DEX concentration. Under the optimized conditions (pH: 5.53, adsorbent dose: 0.185 g/L, time: 16.068 min, and DEX concentration: 33.491 mg/L), Fe3O4@NH2-MIL88B NRs revealed remarkable DEX adsorption efficiency of 91 ± 1.34% and adsorption capacity of 180.01 mg/g. The Langmuir isotherm and pseudo-second-order kinetic model were found to fit well with the experimental data, indicating a monolayer and chemical adsorption process. Thermodynamic analysis revealed that the adsorption process was spontaneous and endothermic. The study also investigated the inhibitory effect of background ions on DEX removal by Fe3O4@NH2-MIL88B NRs. Magnesium exhibited superior competitive ability with dexamethasone to occupy the active sites of the adsorbent compared to other background ions. The reuse of the adsorbent over ten consecutive cycles resulted in a 39.46% decrease in removal efficiency. The Fe3O4@NH2-MIL88B NRs are surrounded by abundant amounts of functional groups and π-electrons bands that can play a key role in the adsorption and separation of DEX from aqueous environments. The promising results obtained under real conditions highlight the potential of Fe3O4@NH2-MIL88B NRs as a practical and efficient adsorbent for the removal of DEX and other similar corticosteroids from aqueous solutions.
TL;DR: The mechanisms behind nano-enabled antioxidant enzyme-mediated plant tolerance, such as maintaining reactive oxygen species homeostasis, enhancing the capacity of plants to retain K+ and eliminate Na+, and increasing the production of nitric oxide are discussed, involving signaling pathways, and lowering lipoxygenase activities to lessen oxidative damage to membranes.
TL;DR: This review highlights recent advances in electro-oxidation, ozone oxidation, and other AOPs for treating pharmaceuticals, dyes, and pesticides in wastewater, emphasizing their efficiency, cost-effectiveness, and environmental acceptability.
Abstract: The existence of various pollutants in water environment contributes to global pollution and poses significant threats to humans, wildlife, and other living beings. The emergence of an effective, realistic, cost-effective, and environmentally acceptable technique to treat wastewater generated from different sectors is critical for reducing pollutant accumulation in the environment. The electrochemical advanced oxidation method is a productive technology for treating hazardous effluents because of its potential benefits such as lack of secondary pollutant and high oxidation efficiency. Recent researches on advanced oxidation processes (AOPs) in the period of 2018–2022 are highlighted in this paper. This review emphasizes on recent advances in electro-oxidation (EO), ozone oxidation, sonolysis, radiation, electro-Fenton (EF), photolysis and photocatalysis targeted at treating pharmaceuticals, dyes and pesticides polluted effluents. In the first half of the review, the concept of the AOPs are discussed briefly. Later, the influence of increasing current density, pH, electrode, electrolyte and initial concentration of effluents on degradation are discussed. Lastly, previously reported designs of electrochemical reactors, as well as data on intermediates generated and energy consumption during the electro oxidation and Fenton processes are discussed. According to the literature study, the electro-oxidation technique is more appropriate for organic compounds, whilst the electro-Fenton technique appear to be more appropriate for more complex molecules.
TL;DR: Straw-derived biochar (SBC) effectively removes antibiotics from water through adsorption and degradation mechanisms, with modified SBC achieving 1346.55 mg/g removal capacity and complete degradation within 6 minutes, but faces challenges in stability, cost, and recyclability.
Abstract: Antibiotics, a kind of containments with the properties of widely distributed and difficult to degrade, has aroused extensive attention in the world. As a prevalent agricultural waste, straws can be utilized to prepare biochar (straw-derived biochar, SBC) to remove antibiotics from aquatic environment. To date, although a number of review papers have summarized and discussed research on biochar application in wastewater treatment and soil remediation, there are few reviews on SBC for antibiotic removal. Due to the limitations of poor adsorption and degradation performance of the pristine SBC, it is necessary to modify SBC to improve its applications for antibiotics removal. The maximum antibiotic removal capacity of modified SBC could reach 1346.55 mg/g. Moreover, the adsorption mechanisms between modified SBC and antibiotics mainly involve π-π interactions, electrostatic interactions, hydrophobic interactions, and charge dipole interactions. In addition, the modified SBC could completely degrade antibiotics within 6 min by activating oxidants, such as PS, PDS, H2O2, and O3. The mechanisms of antibiotic degradation by SBC activated oxidants mainly include free radicals (including SO4•-, •OH, and O2•-) and non-free radical pathway (such as, 1O2, electrons transfer, and surface-confined reaction). Although SBC and modified SBC have demonstrated excellent performance in removing antibiotics, they still face some challenges in practical applications, such as poor stability, high cost, and difficulties in recycling. Therefore, the further research directions and trends for the development of SBC and biochar-based materials should be taken into consideration.
TL;DR: This comprehensive review assesses carbon capture methods and technologies, evaluating direct (pre-combustion, post-combustion, oxy-combustion) and indirect (reforestation, enhanced weathering, bioenergy with carbon capture) methods, highlighting post-combustion techniques' commercial viability and research gaps in solvent development and adsorption capacity improvement.
Abstract: A majority of the primary contributors of carbon dioxide (CO2) emissions into the environment have really been out of human-made activities. The levels of CO2 in the atmosphere have increased substantially since the time of the industrial revolution. This has been linked to the use of fossil fuels for energy production, as well as the widespread production of some industrial components like cement and the encroaching destruction of forests. An extreme approach is now necessary to develop the right policies and address the local and global environmental issues in the right way. In this regard, CO2 capturing, utilization, and storage are reliable options that industrial facilities can initiate to overcome this problem. Therefore, we have evaluated the two leading technologies that are used for carbon capture: direct (pre-combustion, post-combustion, and oxy-combustion) and indirect carbon (reforestation, enhanced weathering, bioenergy with carbon capture, and agricultural practices) capturing to provide their current status and progresses. Among the considered processes, the post-combustion techniques are widely utilized on a commercial scale, especially in industrial applications. Technology readiness level (TRL) results have showed that amine solvents, pressure-vacuum swing adsorption, and gas separation membranes have the highest TRL value of 9. In addition, the environmental impact assessment methods have been ranked to evaluate their sustainability levels. The highest global warming potential of 219.53 kgCO2 eq./MWh has been obtained for the post-combustion process. Overall, through this comprehensive review, we have identified some critical research gaps in the open literature in the field of CO2-capturing methods where there are strong needs for future research and technology development studies, for instance, developing stable and cost-effective liquid solvents and improving the adsorption capacity of commercialized sorbents. Furthermore, some research areas, like novel process design, environmental and economic impact assessment of capturing methods with different chemicals and modeling and simulation studies, will require further effort to demonstrate the developed technologies for pilot and commercial-scale applications.
TL;DR: This review explores intelligent technologies for water and wastewater treatment, including nanofiltration, membrane filtration, and emerging technologies like nanochips and graphene, to mitigate pollution and achieve up to 95% water recovery.
Abstract: Water pollution poses significant threats to both ecosystems and human health. Mitigating this issue requires effective treatment of domestic wastewater to convert waste into bio-fertilizers and gas. Neglecting liquid waste treatment carries severe consequences for health and the environment. This review focuses on intelligent technologies for water and wastewater treatment, targeting waterborne diseases. It covers pollution prevention and purification methods, including hydrotherapy, membrane filtration, mechanical filters, reverse osmosis, ion exchange, and copper-zinc cleaning. The article also highlights domestic purification, field techniques, heavy metal removal, and emerging technologies like nanochips, graphene, nanofiltration, atmospheric water generation, and wastewater treatment plants (WWTPs)-based cleaning. Emphasizing water cleaning's significance for ecosystem protection and human health, the review discusses pollution challenges and explores the integration of wastewater treatment, coagulant processes, and nanoparticle utilization in management. It advocates collaborative efforts and innovative research for freshwater preservation and pollution mitigation. Innovative biological systems, combined with filtration, disinfection, and membranes, can elevate recovery rates by up to 90%, surpassing individual primary (<10%) or biological methods (≤50%). Advanced treatment methods can achieve up to 95% water recovery, exceeding UN goals for clean water and sanitation (Goal 6). This progress aligns with climate action objectives and safeguards vital water-rich habitats (Goal 13). The future holds promise with advanced purification techniques enhancing water quality and availability, underscoring the need for responsible water conservation and management for a sustainable future.
TL;DR: This review assesses recent advancements in phenol extraction, removal, and recovery from wastewater, highlighting challenges and future outlook, with a focus on adsorption techniques as a promising method for phenol removal using novel and low-cost adsorbents.
Abstract: Water pollution is the major problem seen in today's scenario and even pollutants at low concentration harms our environment. In industrial sector usage of phenol is seen even at low concentrations. The interaction of phenol in the environment provides adverse effects to living beings. This review focuses on the toxicity of phenol and its impact towards environment and human health. The treatment techniques such as distillation, extraction, wet air oxidation, membrane process, electrochemical oxidation, biological treatment and finally adsorption techniques were discussed. Among many treatment techniques so far utilized in the treatment of phenol, adsorption was considered as one of the best technique due to its advantages such as reusability, ease in operation, large availability etc., This review also highlights the adsorption technique for the cleaner removal of phenol from aqueous solution with novel as well as low-cost adsorbents in the removal of phenolic compounds. This review also discusses about the drawbacks and issues related with adsorption of phenolic compounds.
TL;DR: Climate policy uncertainty in China negatively affects corporate green technology innovation, impacting R&D investments and risk tolerance, but government subsidies can mitigate this effect, while environmental regulations exacerbate it.
Abstract: The frequent occurrence of extreme weather reminds us to focus more attention on sustainable development. A panel of Chinese A-share listed companies is selected as a research sample to explore how climate policy uncertainty has an effect on companies' green technology innovation. According to the empirical findings, corporate green technology innovation is negatively related to the uncertainty of climate policy. By affecting their R&D investments and risk tolerance, corporations' ability to develop in green technologies has been impacted by the uncertainty of climate policy. We also note that due to the nature of business ownership, the detrimental effect of uncertain climate policy on green technology innovation varies slightly between companies. While environmental regulations reinforce the negative impact of climate policy uncertainty, government subsidies can significantly mitigate this negative impact. These results have important theoretical and practical implications for the development of green economy theory and the realization of energy efficiency in various countries.
TL;DR: Wildfires have complex impacts on forests, altering vegetation, biodiversity, and greenhouse gas emissions, exacerbating climate change, and affecting animal habitats, with far-reaching ecological and climatic consequences, including biodiversity decline and increased CO2 emissions.
Abstract: Wildfires have complex impacts on forests, including changes in vegetation, threats to biodiversity, and emissions of greenhouse gases like carbon dioxide, which exacerbate climate change. The influence of wildfires on animal habitats is particularly noteworthy, as they can lead to significant changes in native environments. The extent of these alterations in species and habitats plays a crucial role in shaping forest ecology. Drought, disease, insect infestations, overgrazing, or their combined effects can amplify the negative effects on specific plant genera and entire ecosystems. In addition to the immediate consequences of plant mortality and altered community dynamics, forest fires have far-reaching implications. They often increase flowering and seed production, further influencing ecological communities. However, one concerning trend is the decline in the diversity of forest biological species within fire-affected areas. Beyond their ecological impacts, wildfires emit substantial quantities of greenhouse gases and fine particulates into the atmosphere, triggering profound changes in climate patterns and contributing to global warming. As vegetation burns during these fires, the carbon stored within is released, rendering large forest fires detrimental to biodiversity and the emission of CO2, a significant contributor to global warming. Measuring the global impact of wildfires on ecological communities and greenhouse gas emissions has become increasingly vital. These research endeavors shed light on the intricate relationships and feedback loops linking wildfires, ecosystem inhabitants, and the evolving climate landscape.
TL;DR: This study examines the effects of informal environmental regulation on carbon emissions in China, finding significant reductions in emissions, particularly in eastern cities, pilot cities, and cities with long-term governor's tenure, through industrial structure transition and renewable energy substitution.
Abstract: Against the backdrop of the global carbon peak and carbon neutrality goals, the role of informal environmental regulation, epitomized by public engagement, is assuming an increasingly pivotal position within the realm of environmental management. By contrast, amidst the prevailing landscape dominated by formal environmental regulation (command-and-control and market-driven approaches), the environmental effects of informal environmental regulation on carbon emissions have received scant attention. Consequently, we examine the net, nonlinear, and mediation effects of informal environmental regulation on carbon emissions using panel data from 30 provinces in China, from 2003 to 2019. We find that informal environmental regulation has a significant effect on regional carbon emission reduction, especially in the eastern cities, pilot cities, and cities with long-term governor's tenure. Its U-shaped effect is confirmed by changes in environmental decentralization. The key points remain valid after the robustness test and the endogenous processing. The mechanism analysis shows that informal environmental regulation can reduce carbon emissions in the dual channels by improving industrial structure transition and renewable energy substitution. Therefore, this study assesses the management effectiveness of informal environmental regulation and determines the underlying mechanism between it and regional carbon emission reduction to provide a reference and an empirical basis for other countries regarding environmental improvement.
TL;DR: The design and testing of a new biosensor based on a graphene oxide (GO) nanocomposite for the exact measurement of carcinoembryonic antigen (CEA), a well-known biomarker for colorectal cancer, is described.
Abstract: Colorectal cancer is still a major global health concern, and early detection and accurate biomarker analyses are critical to its successful management. This paper describes the design and testing of a new biosensor based on a graphene oxide (GO) nanocomposite for the exact measurement of carcinoembryonic antigen (CEA), a well-known biomarker for colorectal cancer. The current study attempted to create a highly sensitive immunosensor for sensitive measurement of CEA based on a polypropylene-imine-dendrimer (PPI) and GO nanocomposite on GCE (PPI/GO/GCE). The PPI/GO nanocomposite served as an appropriate biocompatible nanostructure with a large surface area for immobilizing carcinoembryonic antigen (anti-CEA) and bovine serum albumin (BSA) molecules (BSA/anti-CEA/PPI/GO/GCE), thereby promoting the selectivity of electrochemical immunosensors, according to structural and electrochemical studies. Results showed that the BSA/anti-CEA/PPI/GO/GCE as a selective, sensitive, and stable immunosensor revealed a wide linear response from 0.001 to 2000 ng/mL, and a limit of detection of 0.3 pg/mL, which indicated comparable or better performance towards the CEA immunosensors in recent reports in the literature. This was due to the synergetic effect of the GO nanosheets and PPI with porous structure and more conductivity. Analytical results showed values of RSD (4.49%–5.04%) and recovery (90.00%–99.98%) are suitable for effective and accurate practical assessments in CEA in clinical samples. The capacity of the BSA/anti-CEA/PPI/GO/GCE to determine CEA in human blood was studied.
TL;DR: This study examines the global relationship between climate change, greenhouse gas emissions, and agriculture greening, finding a robust positive association between climate and GHG emissions, with projected increases in emissions by 2100 in most countries, except the UK.
Abstract: Climate change due to increased greenhouse gas emissions (GHG) in the atmosphere has been consistently observed since the mid-20th century. The profound influence of global climate change on greenhouse gas (GHG) emissions, encompassing carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O), has established a vital feedback loop that contributes to further climate change. This intricate relationship necessitates a comprehensive understanding of the underlying feedback mechanisms. By examining the interactions between global climate change, soil, and GHG emissions, we can elucidate the complexities of CO2, CH4, and N2O dynamics and their implications. In this study, we evaluate the global climate change relationship with GHG globally in 246 countries. We find a robust positive association between climate and GHG emissions. By 2100, GHG emissions will increase in all G7 countries and China while decreasing in the United Kingdom based on current economic growth policies, resulting in a net global increase, suggesting that climate-driven increase in GHG and climate variations impact crop production loss due to soil impacts and not provide climate adaptation. The study highlights the diverse strategies employed by G7 countries in reducing GHG emissions, with France leveraging nuclear power, Germany focusing on renewables, and Italy targeting its industrial and transportation sectors. The UK and Japan are making significant progress in emission reduction through renewable energy, while the US and Canada face challenges due to their industrial activities and reliance on fossil fuels.
TL;DR: Despite the efforts made to better understand PFAS toxicokinetics, further studies are needed to identify important characteristics of these persistent chemicals, including the variability among the investigated populations.
Abstract: Per- and polyfluoroalkyl substances (PFAS) constitute a heterogeneous group of synthetic compounds widely used in industrial applications. The estimation of PFAS half-life (t1/2) is essential to quantify their persistence, their toxicity and mechanism of action in humans. The purpose of this review is to summarize the evidence on PFAS half-lives in humans from the available literature, and to investigate the limitations and uncertainties characterizing half-life estimation. The search was conducted on PubMed, Scopus, and Embase databases up to July 03, 2023 and was aimed at identifying all papers that estimated PFAS half-life in human populations. We excluded studies on temporal trends or providing estimates of half-life based solely on renal clearance. As persistent and ongoing exposures can influence half-life estimation, we decided to include only studies that were conducted after the main source of exposure to PFAS had ceased. A random-effects meta-analysis was conducted on studies that reported perfluorooctanoic acid (PFOA), perfluorooctane sulfonic acid (PFOS) or perfluorohexanesulfonic acid (PFHxS) half-life estimation. Risk of bias was evaluated using the OHAT tool. A total of 13 articles were included in the review, with 5 studies conducted in exposed general populations and 8 studies conducted in exposed workers; the estimated mean half-life ranged from 1.48 to 5.1 years for PFOA, from 3.4 to 5.7 years for total PFOS, and from 2.84 to 8.5 years for PFHxS. High heterogeneity among studies was observed; potential reasons include the variability among the investigated populations, discrepancies in considering ongoing exposures, variability in PFAS isomeric compositions, accounting for background exposure, time since exposure stopped and methods used for half-life estimation. Despite the efforts made to better understand PFAS toxicokinetics, further studies are needed to identify important characteristics of these persistent chemicals. Biomonitoring studies should focus on persistent and unaccounted sources of exposure to PFAS and on individual characteristics potentially determining half-life, to ensure accurate estimates.
TL;DR: This study investigates the two-step pyrolytic preparation of biochar for tetracycline adsorption in water, demonstrating improved adsorption capacity and regeneration capabilities compared to one-step pyrolysis biochar, with maximum adsorption capacities ranging from 142.56 to 158.93 mg/g.
Abstract: In this study, cow dung biomass was converted into biochar (BC). BC900 was obtained through one-step pyrolysis at 900 °C, while BC700–900 and BC900–700 were obtained via two-step pyrolysis at temperature ranges of 700–900 °C and 900-700 °C, respectively. The primary objective was to investigate the adsorption performance and application value of BCs for tetracycline (TC) in water. The samples underwent characterization using scanning electron microscopy and mapping analysis, Fourier transform infrared spectroscopy, X-ray diffraction, and thermogravimetric analysis. Subsequently, the effects of reaction time, adsorbent dosage, temperature, pH, and ionic strength were analyzed. Based on the fitting results of adsorption kinetics, the pyrolytic BCs exhibited a better fit with the pseudo-secondary kinetic model. The adsorption isotherm indicated monolayer adsorption on the surface of the adsorbents, with maximum adsorption capacities of 158.93 mg/g for BC900–700, 150.15 mg/g for BC700–900, and 142.56 mg/g for BC900, respectively. Furthermore, results from simulated wastewater and regeneration experiments demonstrated that BC900–700 exhibited not only excellent adsorption performance in wastewater but also remarkable regeneration capabilities. The two-step pyrolysis BCs in this study displayed a higher adsorption capacity compared to the one-step pyrolysis BCs in practical applications. These findings provide insights for further exploring the adsorption mechanism and optimizing the process.
TL;DR: A bimetallic Mo and Ni co-doped g-C3N4 composite catalyst effectively degrades phenol by activating PMS through a non-free radical 1O2 mechanism, achieving 95% degradation within 20 min at neutral pH and 90% degradation across a pH range of 3-11.
Abstract: The application of bimetal supported graphite phase carbon nitride in activated peroxymonosulfate (PMS) process has become a research hotspot in recent years. In this study, 8-g C3N4/Mo/Ni composite catalyst material was successfully prepared by doping Mo and Ni in graphite phase carbon nitride. The bimetallic active sites were formed in the catalyst, and PMS was activated by the metal valence Mo6+/Mo4+ and Ni2+/Ni(0) through redox double cycle to effectively degrade phenol. When pH was neutral, the degradation rate of 20 mg/L phenol solution with 8-g C3N4/Mo/Ni (0.35 g/L) and PMS (0.6 mM) could reach 95% within 20 min. The degradation rate of 8-g C3N4/Mo/Ni/PMS catalytic system could reach more than 90% within 20min under the condition of pH range of 3–11 and different anions. Meanwhile, the degradation effects of RhB, MB and OFX on different pollutants within 30min were 99%, 100% and 82%, respectively. Electron spin resonance and quenching experiments showed that in 8-g C3N4/Mo/Ni/PMS system, the degradation mechanism was mainly non-free radicals, and the main active species in the degradation process was 1O2. This study provides a new idea for the study of bimetal supported graphite phase carbon nitride activation of PMS and the theoretical study of degradation mechanism.
TL;DR: This review explores sustainable utilization of coal gasification slag, highlighting its volcanic ash characteristics and residual carbon potential, and reviews existing methods, including building materials, carbon-ash separation, and high-value applications like activated carbon and zeolite production.
Abstract: Currently, the storage of coal gasification slag (CGS) is continuously increasing, as the coal gasification technology develops, posing significant environmental hazards. Due to its volcanic ash characteristics and rich residual carbon, CGS has great potential for resource utilization, which has attracted the attentions of many scholars. This paper firstly introduces the compositions and properties of CGS. Then, it reviews the existing utilization methods of CGS, including Preparation of building materials, carbon-ash separation technology, ecological restoration, and cyclic blending. The advantages and disadvantages of various methods are compared. Subsequently, some high-value utilization methods of coal gasification slag are introduced, such as the preparation of high-performance activated carbon and zeolite, of which the feasibility and advantages are evaluated. Finally, some suggestions are put forward for future developing technologies. This paper aims to provide some references and inspiration for the utilization and environmental protection of CGS.
TL;DR: This review explores arsenic contamination in the environment, its impact on human health and ecosystems, and existing treatment systems. It highlights the potential of hydrochar-nanoparticle integration for efficient arsenic removal from wastewater, exceeding 99% efficiency, and emphasizes the need for advanced treatment technologies and public awareness.
Abstract: Arsenic (As) contamination poses a significant threat to human health, ecosystems, and agriculture, with levels ranging from 12 to 75% attributed to mine waste and stream sediments. This naturally element is abundant in Earth's crust and gets released into the environment through mining and rock processing, causing ≈363 million people to depend on As-contaminated groundwater. To combat this issue, introducing a sustainable hydrochar system has achieved a remarkable removal efficiency of over 92% for arsenic through adsorption. This comprehensive review presents an overview of As contamination in the environment, with a specific focus on its impact on drinking water and wastewater. It delves into the far-reaching effects of As on human health, ecosystems, aquatic systems, and agriculture, while also exploring the effectiveness of existing As treatment systems. Additionally, the study examines the potential of hydrochar as an efficient adsorbent for As removal from water/wastewater, along with other relevant adsorbents and biomass-based preparations of hydrochar. Notably, the fusion of hydrochar with nanoparticle-centric approaches presents a highly promising and environmentally friendly solution for achieving the removal of As from wastewater, exceeding >99% efficiency. This innovative approach holds immense potential for advancing the realms of green chemistry and environmental restoration. Various challenges associated with As contamination and treatment are highlighted, and proposed solutions are discussed. The review emphasizes the urgent need to advance treatment technologies, improve monitoring methods, and enhance regulatory frameworks. Looking outlook, the article underscores the importance of fostering research efforts, raising public awareness, and fostering interdisciplinary collaboration to address this critical environmental issue. Such efforts are vital for UN Sustainable Development Goals, especially clean water and sanitation (Goal 6) and climate action (Goal 13), crucial for global sustainability.
TL;DR: A CuFe2O4/SiO2/ZnO nanocomposite exhibits 90% metronidazole decontamination within 120 minutes under optimized conditions, utilizing photocatalytic ozonation and hydroxyl radicals as major oxidative species, demonstrating a promising method for eliminating pharmaceutical contaminants from aqueous environments.
Abstract: The increasing use of pharmaceuticals and the ongoing release of drug residues into the environment have resulted in significant threats to environmental sustainability and water safety. In this sense, developing a robust and easy-recovered magnetic nanocomposite with eminent photocatalytic activity is very imperative for detoxifying pharmaceutical compounds. Herein, a systematic study was conducted to investigate the photocatalytic ozonation for eliminating metronidazole (MET) from aqueous media utilizing the CuFe2O4/SiO2/ZnO heterojunction under simulated sunlight irradiation. The composite material was fabricated by a facile hydrothermal method and diagnosed by multiple advanced analytical techniques. Modelling and optimization of MET decontamination by adopting the central composite design (CCD) revealed that 90 % of MET decontamination can be achieved within 120 min of operating time at the optimized circumstance (photocatalyst dose: 1.17 g/L, MET dose: 33.20 mg/L, ozone concentration: 3.99 mg/min and pH: 8.99). In an attempt to scrutinize the practical application of the CuFe2O4/SiO2/ZnO/xenon/O3 system, roughly 56.18% TOC and 73% COD were removed under the optimized operational circumstances during 120 min of degradation time. According to the radical quenching experiments, hydroxyl radicals (HO•) were the major oxidative species responsible for the elimination of MET. The MET degradation rate maintained at 83% after seven consecutive runs, manifesting the efficiency of CuFe2O4/SiO2/ZnO material in the MET removal. Ultimately, the photocatalytic ozonation mechanism over the CuFe2O4/SiO2/ZnO heterojunction of the fabricated nanocomposites was rationally proposed for MET elimination. In extension, the results drawn in this work indicate that integrating photocatalyst and ozonation processes by the CuFe2O4/SiO2/ZnO material can be applied as an efficient and promising method to eliminate tenacious and non-biodegradable contaminants from aqueous environments.
TL;DR: ZIF-8 nanoparticles effectively remove tetracycline from aqueous solution, achieving a 90.59% removal rate, with a maximum adsorption capacity of 359.61 mg/g at 303K, driven by electrostatic and π-π stacking interactions.
Abstract: In this study, ZIF-8 nanoparticles were synthesized using a simple method at room temperature. The ZIF-8 nanoparticles were then characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), BET (Brunauer-Emmett-Teller) specific surface area, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA) and zeta potential. Subsequent batch adsorption experiments evaluated the adsorption performance of ZIF-8 on tetracycline, examining key pa-rameters like reaction time, pH, temperature, and adsorbent dosage. The results revealed a removal rate for TC of up to 90.59%. The adsorption data aligned with the Sips model, showcasing a maximum adsorption capacity of 359.61 mg/g at 303K. Further, the adsorption kinetics adhered to the pseudo-second-order kinetic model with an equilibrium adsorption capacity of 90 mg/g at 303K. The considerable specific surface area of ZIF-8, standing at 1674.169 m2/g, likely enhances the adsorption efficacy. Analysis using XRD and FTIR confirmed the adsorption of TC on the ma-terial's surface. Overall, the predominant driving forces behind the adsorption process were identified as electrostatic interactions and π-π stacking interactions.
TL;DR: The existing understanding of prevalent EDCs that impact women's health and involvement in female reproductive dysfunction is summarized and the need for more research on potential mechanisms of action is highlighted.
Abstract: An Endocrine Disrupting Chemical (EDC) is any compound that disrupts the function of the endocrine system in humans and is ubiquitous in the environment either as a result of natural events or through anthropogenic activities. Bisphenol A, phthalates, parabens, pesticides, triclosan, polychlorinated biphenyls, and heavy metals, which are frequently found in the pharmaceutical, cosmetic, and packaging sectors, are some of the major sources of EDC pollutants. EDCs have been identified to have a deteriorating effect on the female reproductive system, as evidenced by the increasing number of reproductive disorders such as endometriosis, uterine fibroids, polycystic ovary syndrome, premature ovarian failure, menstrual irregularity, menarche, and infertility. Studying EDCs in relation to women's health is essential for understanding the complex interactions between environmental factors and health outcomes. It enables the development of strategies to mitigate risks, protect reproductive and overall health, and inform public policy decisions to safeguard women's well-being. Healthcare professionals must know the possible dangers of EDC exposure and ask about environmental exposures while evaluating patients. This may result in more precise diagnosis and personalized treatment regimens. This review summarises the existing understanding of prevalent EDCs that impact women's health and involvement in female reproductive dysfunction and underscores the need for more research. Further insights on potential mechanisms of action of EDCs on female has been emphasized in the article. We also discuss the role of nutritional intervention in reducing the effect of EDCs on women's reproductive health. EDC pollution can be further reduced by adhering to strict regulations prohibiting the release of estrogenic substances into the environment.
TL;DR: This review critically aims to advance mechanistic understanding related to the reduction of phytotoxicity of pesticides via the use of microbe-mediated remediation techniques leading to crop optimization in pesticide-stressed soils.
Abstract: Reclamation of pesticide-polluted lands has long been a difficult endeavour. The use of synthetic pesticides could not be restricted due to rising agricultural demand. Pesticide toxicity has become a pressing agronomic problem due to its adverse impact on agroecosystems, agricultural output, and consequently food security and safety. Among different techniques used for the reclamation of pesticide-polluted sites, microbial bioremediation is an eco-friendly approach, which focuses on the application of resilient plant growth promoting rhizobacteria (PGPR) that may transform or degrade chemical pesticides to innocuous forms. Such pesticide-resilient PGPR has demonstrated favourable effects on soil-plant systems, even in pesticide-contaminated environments, by degrading pesticides, providing macro-and micronutrients, and secreting active but variable secondary metabolites like-phytohormones, siderophores, ACC deaminase, etc. This review critically aims to advance mechanistic understanding related to the reduction of phytotoxicity of pesticides via the use of microbe-mediated remediation techniques leading to crop optimization in pesticide-stressed soils. The literature surveyed and data presented herein are extremely useful, offering agronomists-and crop protectionists microbes-assisted remedial strategies for affordably enhancing crop productivity in pesticide-stressed soils.
TL;DR: This review examines the adverse effects of excessive insecticide use on agriculture and the environment, proposing eco-friendly remediation strategies, including integrated pest management, selective insecticides, and precision farming to minimize chemical usage and promote sustainable agriculture practices.
Abstract: Insecticides are indispensable for modern agriculture to ensuring crop protection and optimal yields. However, their excessive use raises concerns regarding their adverse effects on agriculture and the environment. This study examines the impacts of insecticides on agriculture and proposes remediation strategies. Excessive insecticide application can lead to the development of resistance in target insects, necessitating higher concentrations or stronger chemicals, resulting in increased production costs and disruption of natural pest control mechanisms. In addition, non-target organisms, such as beneficial insects and aquatic life, suffer from the unintended consequences of insecticide use, leading to ecosystem imbalances and potential food chain contamination. To address these issues, integrated pest management (IPM) techniques that combine judicious insecticide use with biological control and cultural practices can reduce reliance on chemicals. Developing and implementing selective insecticides with reduced environmental persistence is crucial. Promoting farmer awareness of responsible insecticide use, offering training and resources, and adopting precision farming technologies can minimize overall insecticide usage.
Abstract: The development of composites for food packaging that have good mechanical and antimicrobial characteristics is still a major challenge. In applications like food packaging, the usage of poly (butylene adipate-co-terephthalate) (PBAT), which has an adversative effect on the environment and reduces petroleum resources, has grown widespread. The present work reveals PBAT composites reinforced with CNPs at a few percentages up to 5.0 wt %. The PBAT/CNPs composites were produced using the solvent casting method. The results of TGA studies, CNPs significantly enhanced the thermal stability of composites using PBAT. The mechanical strength of the PBAT composites was improved by increasing CNPs concentration. Tensile strength increased from 7.38 to 10.22 MPa, respectively. The oxygen transmission rate (OTR) decreased with increasing the CNPs concentrations. The barrier properties (H2O and O2) of PBAT were improved by the presence of CNPs. WVTR was calculated to be 108.6 ± 1.8 g/m2/day for PBAT. WVTR reduced when CNPs concentration in PBAT increased. The PCN-5.0 film sample had the lowest WVTR value, 34.1 ± 3.1 g/m2/day. For PCN-3.0, WVTR dropped by 45.39%, indicating and even with a 3.0 wt% loading of CNPs in PBAT, the rise is noticeable. Contact angle measurements indicate that PBAT/CNPs composites becomes hydrophobic after reinforcing. Gram-positive (S. aureus) and Gram-negative (E. coli) food-borne pathogenic microorganisms showed enhanced antimicrobial activity against the developed PBAT composites. The carrot pieces preserved their freshness for an extended period of 12 days while packaged in the PBAT/CNPs composite film, indicating that the film is an effective and excellent packaging for food materials.
TL;DR: This study synthesizes sulphuric acid-activated coffee husk carbon, optimizing its adsorption of methylene blue dye, with 99.48% removal at 4.83 g/L dosage, 30°C, and pH 8.12, exhibiting spontaneity and enthalpy-driven process.
Abstract: In the current study, an attempt was made to synthesize coffee husk (CH) activated carbon by chemical modification approach (sulphuric acid-activated CH (SACH) activated carbon) and was used as a valuable and economical sorbent for plausible remediation of Methylene blue (MB) dye. Batch mode trials were carried out by carefully varying the batch experimental variables: SACH activated carbon (SACH AC) dosage, pH, initial dye concentration, temperature, and contact time. The optimum equilibrium time for adsorption by SACH activated carbon was obtained as 60 min, and the maximum adsorption took place at 30 °C. Morphological and elemental composition, crystallinity behaviour, functional groups, and thermal stability were examined using SEM with EDX, XRD, FTIR, BET, TGA, and DTA and these tests showed successful production of activated carbon. The outcomes showed that chemical activation enhanced the number of pores and roughness which possibly maximized the adsorptive potential of coffee husk. The Box-Benken design (BBD) was used to optimize the MB dye adsorption studies and 99.48% MB dye removed at SACH AC dosage of 4.83 g/L at 30 °C for 60 min and pH 8.12, and the maximum adsorption was yielded for sulphuric acid-activated coffee husk carbon carbon with 88.1 mg/g maximum MB adsorption capacity. Langmuir- Freundlich model deliberately provided a better fit to the equilibrium data. The SACH AC-MB dye system kinetics showed a high goodness-of-fit with pseudo second order model, compared to other studied models. Change in Gibbs's free energy (ΔGo) of the system indicated spontaneity whereas low entropy value (ΔSo) suggested that the removal of MB dye on the SACH activated carbon was an enthalpy-driven process. The exothermic nature of the sorption cycle was affirmed by the negative enthalpy value (ΔHo). The adsorptive-desorptive studies reveal that SACH AC could be restored with the maximum adsorption efficiency being conserved after the fifth cycles. Overall, the outcomes revealed that sulphuric acid-activated coffee husk activated carbon (SACH AC) can be used as prompt alternative for low-cost sorbent for treating dye-laden synthetic wastewaters.
TL;DR: Researchers develop a high-temperature post-treatment to create g-C3N4 nanosheets with crystalline/amorphous interfaces, enhancing photocatalytic H2 and H2O2 evolution efficiency by 5.8 times under visible light, with a new-emerged n→π* transition improving light utilization.
Abstract: Photocatalystic evolution of H2O2 from water and oxygen has attracted significant attention because of environmentally friendly. The absorption in visible and hydrophilic feature of graphitic carbon nitride (g-C3N4) make it a good candidate. In this paper, a rapid post-treatment at high temperature was developed to obtain g-C3N4 nanosheets with abundant crystalline/amorphous interfaces to form homojunctions, which optimized uniplanar carrier mobility dynamics. The conversion from bulk to two-dimensional g-C3N4 resulted from the breakage of interplanar hydrogen bonds and interlayer Van der Waals force. The unique morphology not only rendered photocatalyst with larger specific surface area but also inhibited the robust volume recombination of charge carriers. The accelerated charge carriers flow at the interface, interplane and interlayer together ameliorated the separation and transfer of electrons and holes. A new-emerged n→π* transition ameliorated the poor light utilization efficiency. Beyond the increased photocatalytic H2 evolution property (779.2 μmol g−1 h−1), optimized sample displayed a H2O2 evolution activity as high as 4877.1 μM g−1 h−1 under visible light illumination, which was ∼5.8 times of that of bulk g-C3N4. Detailed photocatalytic mechanism investigation manifested that the two-step single-electron oxygen reduction process occupied the dominant status in H2O2 evolution. This work proposed a novel strategy for obtaining g-C3N4 homojunctions as a promising bi-functional metal-free catalyst to be applied in clean energy production field.