Sludge size affects sorption of organic micropollutants in full-scale aerobic granular sludge systems.

Aerobic granular sludge (AGS) is gaining popularity as an alternative to activated sludge for wastewater treatment. However, little information is available on AGS regarding the removal of organic micropollutants (OMPs) through sorption. In this study, the sorption behavior of 24 OMPs at environmentally relevant concentrations (1 µg/L) was investigated in six sludge fractions of varying sizes (>4 mm, 2-4 mm, 1-2 mm, 0.6-1 mm, 0.2-0.6 mm, and <0.2 mm) from a full-scale AGS reactor using batch experiments. Sorption was significant (removal efficiency >40 %) for 10 OMPs, including 4 zwitterionic and 6 positively charged pharmaceuticals, indicating the importance of electrostatic interaction for OMP sorption in AGS systems. Larger granules exhibited a higher sorption coefficient and capacity than smaller AGS fractions, probably due to increased extracellular polymeric substance content for larger granules. Equilibrium OMP sorption was only reached after 72 h in granules larger than 2 mm, indicating an effect of longer diffusion distance for OMPs into larger granules. Additionally, compared to activated sludge, AGS demonstrates a similar or even slightly higher sorption capacity for 10 OMPs at 1 µg/L. Overall, this study is the first to investigate the sorption behavior of six AGS size fractions for OMPs at environmentally relevant concentrations (1 µg/L) and propose the possible roles of different-sized sludge in OMP sorption in the full-scale AGS reactor.

Monitoring studies on contamination of urban runoff with hazardous benzotriazoles and bisphenols in one of the least polluted places worldwide.

Benzotriazoles (BTR) and bisphenols (BP) are artificial contaminants of emerging concern (CECs) commonly found in everyday products. This study focuses on urban runoff to investigate the occurrence of BTRs and BPs in Iceland, regarded as one of the least polluted places in the world, which made it reasonable to confirm or deny the presence of these micropollutants in its environment. Samples collected in February 2023 (SC1) and August 2024 (SC2) from seven locations along Iceland's Ring Road were evaluated to determine the occurrence of seven BTRs (1H-BTR, 4Me-BTR, 5Me-BTR, 5Cl-BTR, UV-P, UV-326, UV-329) and six BPs (BPF, BPE, BPA, BPZ, BPAP, BPM) in the runoff, using the ultrasound-assisted emulsification-microextraction for analytes isolation and gas chromatography-mass spectrometry for detection (USAEME-GC/MS). All locations showed detectable and varying levels of BTRs and BPs, with 5Cl-BTR (11.6 µg/L) and BPF (56.3 µg/L), both in SC1, demonstrating the highest concentrations, providing valuable insights into their prevalence and distribution. A correlational analysis investigated the connection between these pollutants and various characteristics associated with the locations along the Ring Road. This study contributes to the essential comprehension of these CECs, serving as input for future strategies for monitoring and mitigating their impact.

Removal of persistent and mobile organic micropollutants from drinking water utilizing a synthesized waste-derived adsorbent.

Persistent and mobile (PM) substances refer to a wide range of organic micropollutants (OMPs) with high persistence and mobility in water. So far, only a few methods have been explored for the removal of PM substances from drinking water. In this work, a new adsorbent based on spent coffee grounds and aluminum waste was synthesized and utilized to remove 25 OMPs, including 22 PM substances, from drinking water. Different characterization methods, including powder X-ray diffraction (XRD), analyses according to Brunauer-Emmett-Teller (BET), field-emission scanning electron microscopy (FE-SEM) and energy dispersive X-ray spectroscopy (EDS), were applied to describe the adsorbent's textural and structural characteristics. The results revealed that the adsorbent is highly effective in removing OMPs. Common OMPs (i.e. carbamazepine, sulfamethoxazole and diclofenac) were completely removed from drinking water. Also, many of the PM substances were removed by more than 80% using an adsorbent dosage of 0.1 g/L. A strong relation between abatement of ultraviolet light absorbance at 254 nm (UV254) and OMP removal was observed. Therefore, UV254 abatement is a useful surrogate for a quick estimation of OMP removals.

Microparticles of anthropogenic origin (microplastics and microfibers) in sandy sediments: A case study from calabria, italy.

Microparticles of anthropogenic origin, such as microplastics and microfibers, are pervasive pollutants in the marine environment of the world. These microparticles pollute water and can be ingested by biota; however, while microplastics are often monitored, very few studies focus on microfibers. Coastal areas, such as beaches, are more vulnerable to pollution due to their location between terrestrial and marine environments and their recreational and touristic functions. In this study, microparticle occurrence frequency was investigated along the Calabria coast, Italy, in one touristic beach in comparison with an unpopular one. High amounts of microparticles of anthropogenic origin were found in all sediment samples, despite the evident different tourist exploitation of the two examined beaches. Sediments of the most touristic beach had values between 729.5 ± 212.3 and 1327 ± 125.8 items/kg, instead, the less popular beach between 606.3 ± 102.8 and 1116.5 ± 226.9 items/kg (average and st. dev). Microparticle abundance varied before and after the touristic summer season, increasing in the most popular beach and decreasing in the unpopular one. Differences in microparticle abundance between foreshore and backshore were present too; however, statistical analyses did not show evident relations between microparticle abundance and the distance from the see. Grain size influenced the abundance of microparticles in sediments. Our results improve knowledge on microparticle pollution in marine environments, highlighting information about micropollution in coastal areas. Future studies are needed to understand better microparticle dynamics and ecological impacts in marine and terrestrial systems, implementing new strategies to monitor pollution state, enhancing the natural intermediate environments, and providing useful and sustainable measure of conservation.

Differentiated adsorption of acetaminophen and diclofenac via alkyl chain-modified quaternized SBA-15: Insights from molecular simulation.

The increasing presence of pharmaceuticals and personal care products (PPCPs) in aquatic systems pose significant environmental concerns. This study addresses this issue by synthesizing quaternized mesoporous SBA-15 (QSBA) with varied alkyl chain lengths of C1QSBA, C8QSBA, and C18QSBA. QSBA utilizes dual mechanisms: hydrophobic interactions via the alkyl chain and electrostatic attraction/ion exchange via the ammonium group. Diclofenac (DCF) and acetaminophen (ACT) were selected as target PPCPs due to their contrasting dissociation properties and hydrophobicity, which are the main characteristics of PPCPs. The adsorption of DCF and ACT revealed that longer alkyl chains enhanced the adsorption capacity of ACT through hydrophobic interactions, whereas dissociated DCF (DCF-) adsorption was superior owing to its high hydrophobicity (log Kow = 4.5) and electrostatic attraction. pH levels between 6 and 8 resulted in a high affinity for DCF-. Notably, among the three alkyl chains, only C18QSBA exhibited the most effective adsorption for DCF-. These PPCPs adsorption trends were confirmed through molecular simulations of adsorption under conditions in which competing ions coexisted. The molecular simulations show that while DCF- has lower adsorption energy than Cl-, OH-, and H3O+ ions in QSBA, enhancing its adsorption under various pH conditions. Conversely, ACT exhibits a higher adsorption energy, which reduces its adsorption efficiency. This suggests the potential application of QSBA with long alkyl chains in the treatment of highly hydrophobic and negatively charged PPCPs. Furthermore, this study emphasizes the importance of simulating adsorption under competing ion conditions.

Strategies for Removing Endocrine Disrupting Chemicals (EDCs) from Wastewater.

INTRODUCTION: Endocrine-disrupting drugs, also called endocrine disruptors or micropollutants, cause serious environmental and public health problems due to their ability to disrupt the endocrine functions of organisms and humans, even at low concentrations. This report provides a summary of current removal techniques, such as activated sludge processes, membrane filtration, adsorption, and membrane bioreactor techniques for endocrine-disrupting chemicals, including their efficiency, limitations, and practical implementation. METHODS: This review evaluates these methods by considering their treatment efficiency, costs, and environmental impact. To curb this menace, several developed countries have distinct strategies, such as physical remediation techniques, biological processes, phytoremediation, and chemical processes to remove endocrine disruptors. RESULTS: In developing nations, most conventional wastewater treatment plants do not even monitor those contaminants due to the low biodegradability and high complexity of such compounds. CONCLUSION: Hence, in this review work, potential endocrine-disrupting chemicals, their impacts, mechanisms of action, consequences for human health, and bio-mitigation strategies reported so far have been discussed in the context of the relevant literature.

Combined effects of polyamide microplastic and sulfamethoxazole in modulating the growth and transcriptome profile of hydroponically grown rice (Oryza sativa L.).

The use of reclaimed water from wastewater treatment plants for irrigation has a risk of introducing micropollutants such as microplastics (MPs) and antimicrobials (AMs) into the agroecosystem. This study was conducted to investigate the effects of single and combined treatment of 0.1 % polyamide (PA ∼15 µm), and varying sulfamethoxazole (SMX) levels 0, 10, 50, and 150 mg/L on rice seedlings (Oryza sativa L.) for 12 days. The study aimed to assess the impact of these contaminants on the morphological, physiological, and biochemical parameters of the rice plants. The findings revealed that rice seedlings were not sensitive to PA alone. However, SMX alone or in combination with PA, significantly inhibited shoot and root growth, total biomass, and affected photosynthetic pigments. Higher concentrations of SMX increased antioxidant enzyme activity, indicating oxidative stress. The roots had a higher SMX content than the shoots, and the concentration of minerals such as iron, copper, and magnesium were reduced in roots treated with SMX. RNA-seq analysis showed changes in the expression of genes related to stress, metabolism, and transport in response to the micropollutants. Overall, this study provides valuable insights on the combined impacts of MPs and AMs on food crops, the environment, and human health in future risk assessments and management strategies in using reclaimed water.

Assessment of contaminants of emerging concern and antibiotic resistance genes in the Mapocho River (Chile): A comprehensive study on water quality and municipal wastewater impact.

The primary objective of this study was to evaluate the persistence and elimination of Contaminants of Emerging Concern (CECs) in municipal wastewater treatment plants (MWWTPs) and their presence in the Mapocho River within the metropolitan area of Santiago, Chile. The use of advanced analytical techniques, based on liquid chromatography coupled to both low and high-resolution mass spectrometry, allowed a comprehensive overview on the presence of CECs in samples. Additionally, a preliminary assessment of the microbiological aspects aimed to determine the presence of indicator microorganisms of fecal contamination, such as Escherichia coli and total coliforms was conducted. Furthermore, a qualitative assessment of Antibiotic Resistant Genes (ARGs) was performed. No CECs were detected upstream to the MWWTPs. However, the results from various wastewater samples (influent, secondary, and tertiary effluents) revealed significant diversity, with 73 CECs detected alongside prevalent ARGs including sulI, sulfII, qnrB, and blaTEM. The presence of CECs and ARGs downstream of the MWWTP in the Mapocho River was mainly attributed to effluent discharge. On the other hand, typical values for a healthy river and a MWWTP with a final disinfection stage were found in terms of fecal contamination. Consequently, the imperative for developing tertiary or quaternary treatments capable of degrading CECs and ARGs to minimize environmental impact is underscored. These findings hold public health significance, offering insights into potential risks and influencing future legislative measures in Chile.

Electro-, photo-, and photoelectrochemical degradation of chloramphenicol on self-doping Ti nanotubes.

In this work, the photo-, electro-, and photo-electro-oxidation of chloramphenicol was investigated. The photo-experiments were carried out with different irradiation sources (an ultraviolet and a simulated solar source) using self-doped titanium nanotubes (SDTNT), a very promising and innovative material that deserves further investigations in the degradation of different pollutants. The photo-electrooxidation (j = 15 mA cm-2) under simulated solar irradiation presented the best efficiency, with ca. 100% degradation and kinetic constant of k = 0.04427 min-1. The FTIR analysis demonstrated a structural modification of the standard molecule occurred for all conditions used, suggesting a modification in functional groups responsible for the biological activity. Furthermore, the TOC analysis showed a significant mineralization of the pollutant (66% from the initial concentration). In addition, both photo-electrooxidation approaches have demonstrated a positive value of S, where the simulated solar irradiation reached the highest value S = 0.6960. The experimental results pointed out evidence that the methodology employed herein for chloramphenicol degradation is greatly interesting and the photo-electrooxidation under simulated solar irradiation is a promising approach for this purpose.

Enhanced degradation of micropollutants using In situ electrogenerated sulfate radical at high flux.

The degradation of micropollutants via in situ-generated reactive species from coexisting substances in water is a promising approach for advanced water treatment. However, treatment efficiency and practical applications are hindered by limited operation conditions and prohibitive costs, respectively. Herein, we report an upgraded electrochemical filtration system that is chemical-free and made efficient by achieving in situ SO4•- generation at enhanced flux and in complicated water matrices. The ion transport was enhanced by coupled electric and flow fields, providing an outstanding performance in removing micropollutants. At the optimized conditions, the proposed system degraded 90.5% of bisphenol A (BPA) in 40 min and its degradation kinetics was 14.7 times that of the batch mode, and the treatment efficiency of the proposed system was 2.5 times more efficient than our previous design because of the enhanced flux. Quenching experiments indicate that indirect oxidation by SO4•- and •OH as well as direct electron transfer play critical roles during the BPA degradation. Importantly, the proposed system does not need any added chemicals and uses only the ubiquitous SO42- and electricity. From an environmental point of view, its energy conservation and the lack of additional chemicals ensure its applicability for purifying micropollutants.

Investigation of the Effect of Oxide Additives on the Band Gap and Photocatalytic Efficiency of TiO2 as a Fixed Film.

The effects of various additives (Y2O3, Ga2O3, and WO3) on photocatalytic degradation efficiency under UV light-emitting diodes (LEDs) and the optical properties of TiO2 Degussa P25 were investigated using ketoprofen and diclofenac, two non-steroidal anti-inflammatory drugs commonly detected in German rivers. Experimental results demonstrated that thin films containing these additives exhibited similar photocatalytic degradation efficiencies as pure TiO2, achieving a 30% degradation of ketoprofen over 150 min. In contrast, the Y2O3/TiO2 thin film showed significantly improved performance, achieving a 46% degradation of ketoprofen in 180 min. Notably, the Y2O3/TiO2 system was three times more effective in degrading diclofenac compared to pure TiO2. Additionally, the Y2O3/TiO2 photocatalyst retained its activity over three successive cycles with only a slight decrease in efficiency. The photocatalytic degradation of both organic pollutants followed first-order kinetics with all photocatalysts. The investigation included SEM imaging to assess the surface homogeneity of the thin films and UV-vis solid-state spectroscopy to evaluate the impact of the additives on the energy band gap of TiO2.

VUV Activated Fe(VI) by Promoting the Generation of Intermediate Valent Iron and Hydroxyl Radicals.

In this study, vacuum ultraviolet (VUV) was first proposed to activate ferrate (Fe(VI)) for degrading micropollutants (e.g., carbamazepine (CBZ)). Results indicated that VUV/Fe(VI) could significantly facilitate the CBZ degradation, and the removal efficiencies of VUV/Fe(VI) were 30.9-83.4% higher than those of Fe(VI) at pH = 7.0-9.0. Correspondingly, the degradation rate constants of VUV/Fe(VI) were 2.3-36.0-fold faster than those of Fe(VI). Free radical quenching and probe experiments revealed that the dominant active species of VUV/Fe(VI) were •OH and Fe(V)/Fe(IV), whose contribution ratios were 43.3 to 48.6% and 48.2 to 46.6%, respectively, at pH = 7.0-9.0. VUV combined with Fe(VI) not only effectively mitigated the weak oxidizing ability of Fe(VI) under alkaline conditions (especially pH = 9.0) but also attenuated the deteriorating effect of background constituents on Fe(VI). In different real waters (tap water, river water, WWTPs effluent), VUV/Fe(VI) retained a remarkably enhanced effect on CBZ degradation compared to Fe(VI). Moreover, VUV/Fe(VI) exhibited outstanding performance in the debasement of CBZ and sulfamethoxazole (SMX), as well as six other micropollutants, displaying broad-spectrum capability in degrading micropollutants. Overall, this study developed a novel oxidation process that was efficient and energy-saving for the rapid removal of micropollutants.

Singlet oxygen dominant-activation by hollow structural cobalt-based MOF/peroxymonosulfate system for micropollutant removal.

Despite the keen interest in potentially using the metal-organic framework (MOF) in advanced oxidation processes (AOPs), their application for environmental abatement and the corresponding degradation mechanisms have remained largely elusive. This study explores the use of cobalt-based MOF (CoMOF) for peroxymonosulfate (PMS) activation to remove tetracycline (TC) from water resources. Under optimal conditions, the given catalytic system could achieve a TC removal of 83.3%. Radical quenching tests and EPR analysis revealed that SO4•-, HO•, •O2-, and 1O2 could participate in the catalytic degradation, but the discernible removal mechanism was mainly ascribed to the nonradical pathway induced by 1O2. At only 5 mg/L of CoMOF, the performance of the catalytic system was superior to that of PMS alone for different types of micropollutants. The CoMOF/PMS system could also reliably deal with typical anions in water, such as Cl-, SO42-, HCO3-, and PO43-. The MOF catalyst could last for four cycles with a minor decrease in reactivity of ∼30%. However, the removal performance decreased markedly when aromatic natural organic matter (NOM) were present in the water bodies, and the effectiveness was lower in alkaline or acidic environments. Our work offers insights into the catalytic degradation of CoMOF/PMS applied in contaminated water remediation and serves as a baseline for fabricating an efficient MOF with enhanced catalytic performance and stability.

Hybrid packed bed bioreactor using combined biodegradation and ozonation to enhance nitrogen and micropollutants removal from landfill leachate.

Landfill leachate contains ammonium and micropollutants. Ammonium can be biologically removed but bio-recalcitrant micropollutants removal requires post-treatment like ozonation. This study developed an expanded clay aggregates packed biofilm column (EBC) and demonstrated its feasibility of coupling biodegradation and ozonation (CBAO) to simultaneously remove nitrogen and bio-recalcitrant micropollutants. The first 60 days only had biodegradation process to start the bioreactor. 51 % nitrogen was biologically removed but the removal of micropollutant carbamazepine (CBZ) was only 30 %. From 61 d to 150 d, both biodegradation and ozonation were performed in the EBC. After 48 h-biodegradation, ozone gas was introduced and bubbling through EBC for 30 min to further remove residual micropollutants. At 0.4 gO3/gCOD, CBZ were completely removed. The average nitrogen removal efficiency (85 %) was increased by 34 % because the increased abundance of nitrifying and denitrifying bacteria in EBC. This study confirmed the promising potential of the CBAO process for treating landfill leachte.

Fate of persistent and mobile chemicals in the water cycle: From municipal wastewater discharges to river bank filtrate.

Persistent and mobile (PM) chemicals are considered detrimental for drinking water resources as they may pass through all barriers protecting these resources against pollution. However, knowledge on the occurrence of PM chemicals in the water cycle, that make their way into drinking water resources, is still limited. The effluents of six municipal wastewater treatment plants (WWTPs, n = 38), surface water of two rivers (n = 32) and bank filtrate of one site (n = 15) were analyzed for 127 suspected PM chemicals. In the rivers, median concentrations of 92 detected analytes ranged from 0.3 ng/L to 2.6 µg/L (tetrafluoroborate, BF4). Lower than average dilution from WWTP effluent to surface water of 43 PM chemicals suggests significant discharge from other sources. Many of these compounds were industrial chemicals, including cyanoguanidine, trifluoromethanesulfonic acid and BF4. River bank filtration (RBF) reduced the total concentration of 40 quantified compounds by 60 % from 19.5 µg/L in surface water to 8.4 µg/L in bank filtrate, on average. Of these, 20 compounds showed good removal (> 80 %), 14 intermediate (80 - 20 %) and 6 no removal (≤ 20 %), among them carbamazepine, hexafluorophosphate, and 2-pyrrolidone. 13 substances occurred at concentrations ≥ 0.1 µg/L in bank filtrate; for six of them toxicological data were insufficient for a health-based risk assessment. The regulatory definition of P and M chemicals, if used together with existing data on environmental half-lives (P) and Koc (M), showed little power to discriminate between chemicals well removed in RBF and those that were hardly removed. This comprehensive field study shows that RBF is a useful but incomplete barrier to retain PM chemicals from surface water. Thus, PM chemicals are, indeed, a challenge for a sustainable water supply.

Co-occurrence and spatial distribution of organic micropollutants in surface waters of the River Aconcagua and Maipo basins in Central Chile.

Organic Micropollutants (OMPs) might pose significant risks to aquatic life and have potential toxic effects on humans. These chemicals typically occur as complex mixtures rather than individually. Information on their co-occurrence and their association with land use is largely lacking, even in industrialized countries. Furthermore, data on the presence of OMPs in freshwater ecosystems in South America is insufficient. Consequently, we assessed the co-occurrence and distribution of OMPs, including pharmaceuticals, pesticides, personal care products, surfactants, and other industrial OMPs, in surface waters of two river basins in central Chile. We focused on identifying and ranking quantified chemicals, classifying their mode of actions, as well as correlating their occurrence with distinct land uses. We identified and quantified 311 compounds that occurred at least once in the River Aconcagua and River Maipo basins, encompassing compounds from urban, agricultural, industrial, and pharmaceutical sectors. Pharmaceuticals were the most frequently occurring chemicals, followed by pesticides, personal care and household products. OMPs with neuroactive properties dominated surface waters in Central Chile, along with OMPs known to alter the cardiovascular and endocrine systems of humans and aquatic animals. Finally, we observed positive correlations between agricultural and urban land uses and OMPs. Our findings represent a step forward in extending current knowledge on the co-occurrence patterns of OMPs in aquatic environments, particularly in developing countries of the southern hemisphere.

Effects of functional groups of polyfluoroalkyl substances on their removal by nanofiltration.

Determining the reliability of nanofiltration (NF) membranes for the removal of contaminants of emerging concern, including polyfluoroalkyl substances (PFASs), pharmaceuticals, and personal care products (PPCPs), is important for ensuring drinking water safety. This study aimed to clarify the factors that influence the removal of nine major PFASs during submerged NF treatment via extrapolation based on the factors that influence PPCP removal. The rejection of nine PFASs in ultra-filtered dam water by a polypiperazine-amide (NF270) membrane increased from 71 % to 94 % at a low permeate flux of 5 L/m2 h as the PFAS molecular dimensions increased. PFASs with a carboxylic acid (-CO2H) were rejected to a greater extent than PFASs with a sulfo group (-SO3H). Further, negatively charged PFASs or PPCPs were rejected to a greater extent than uncharged and positively charged PPCPs. Our findings suggest that the rejection of PFASs can vary because of the (i) clearance distance between the PFASs' molecular dimensions and NF membrane pore diameter and (ii) intensity of electrostatic repulsion between the PFASs' functional groups and NF membrane surface. Our study indicates that submerged NF can achieve high PFAS rejection; however, variations in rejection among PFASs can become more prominent owing to a low permeate flux.

Trace Elements Anomalous Concentrations in Building Materials-The Impact of Secondary Mineralisation Processes.

The Pb, Cr, Cd, Ni, Zn, Cu, Co, As, Sr, Ba, and Zr content has been determined in the tested rock raw materials. The concentration of cadmium (Cd) was found to be elevated in all types of rock materials and was found on average to be: 1.39 mg/kg in limestones, 0.86 mg/kg-sandstones, 0.44 mg/kg-diatomites, 0.55 mg/kg-opoka rocks, 0.89 mg/kg-marls, 0.21 mg/kg-gaizes 0.42 mg/kg-kaolin clays, and 2.13 mg/kg-decalcified opoka rocks. Higher concentrations of arsenic (As) have also been recorded in sandstones and diatomites, as well as lead (Pb) in limestones and sandstones. The results obtained indicate that the anomalous level of elements is of natural origin and the results of identified secondary mineralisation processes that have affected the tested materials. Pyritization and sulfatization processes have been detected. Mineralogical research has shown that these processes can be associated with the activity of biochemical processes caused by the decomposition of the soft tissues of animal organisms and the organic substances of plant origin that fill the stylolites. It has been shown that the content of strontium (Sr) increases in geologically older Jurassic formations compared to younger Cretaceous formations, which can be used in the monitoring of building materials.

Perspectives for Photocatalytic Decomposition of Environmental Pollutants on Photoactive Particles of Soil Minerals.

The literature shows that both in laboratory and in industrial conditions, the photocatalytic oxidation method copes quite well with degradation of most environmental toxins and pathogenic microorganisms. However, the effective utilization of photocatalytic processes for environmental decontamination and disinfection requires significant technological advancement in both the area of semiconductor material synthesis and its application. Here, we focused on the presence and "photocatalytic capability" of photocatalysts among soil minerals and their potential contributions to the environmental decontamination in vitro and in vivo. Reactions caused by sunlight on the soil surface are involved in its normal redox activity, taking part also in the soil decontamination. However, their importance for decontamination in vivo cannot be overstated, due to the diversity of soils on the Earth, which is caused by the environmental conditions, such as climate, parent material, relief, vegetation, etc. The sunlight-induced reactions are just a part of complicated soil chemistry processes dependent on a plethora of environmental determinates. The multiplicity of affecting factors, which we tried to sketch from the perspective of chemists and environmental scientists, makes us rather skeptical about the effectiveness of the photocatalytic decontamination in vivo. On the other hand, there is a huge potential of the soils as the alternative and probably cheaper source of useful photocatalytic materials of unique properties. In our opinion, establishing collaboration between experts from different disciplines is the most crucial opportunity, as well as a challenge, for the advancement of photocatalysis.

Relationship among micro-pollutants, economic growth, renewable energy, nanotechnology and ecological foot prints of China: evidence from panel data analysis.

An important concern is the availability of clean drinking water, which is an essential need for human survival. This issue arises due to the existence of hazardous micropollutants originating from various emission sources. Nanotechnology aids in the mitigation of micropollutants by assimilating and counteracting their effects, hence diminishing their influence on water and other ecosystems. The study investigates the relationship between nanotechnological progress, the adoption of renewable energy, environmental consequences, and economic growth in China, using the Environmental Kuznets Curve theory as a conceptual framework. The study employs panel cointegration tests to analyze structural breaks from 2000 to 2020. Nanotechnology is expected to reduce environmental degradation and the presence of micro-pollutants by increasing the use of renewable energy and promoting energy conservation. Nanotechnology is crucial for mitigating micro-pollutants and advancing sustainable development in this specific context. However, the literature also highlights the harmful consequences of nanoparticle emissions caused by nanotechnology on human and environmental health for a long duration, requiring more examination. This research is the first empirical inquiry into the relationship between improvements in nanotechnology, the use of renewable energy, economic growth, and ecological effect, all within the context of the Environmental Kuznets Curve theory. The results confirm the successful incorporation of all components with a focus on long-term outcomes. The findings suggest that the EKC hypothesis is relevant in China. In China, advancements in nanotechnology have a moderating effect on environmental degradation. The use of renewable energy sources in China enhances environmental circumstances. Given the offered empirical evidence, it is advisable for the government to have a leading role in the development of innovative nanotechnologies that have low emissions of nanoparticles. By using this approach, it will be possible to encourage the conservation of energy and the use of renewable sources in a more secure way, hence improving the effectiveness of sustainable development initiatives.