Emerging Contaminants In Water Research Articles

Dual-functional adsorptive membranes for PFAS removal: Mechanism, CFD simulation, and selective enrichment

The remediation of emerging water contaminants, particularly per- and polyfluoroalkyl substances (PFAS), presents challenges due to their refractory nature and the presence of competing substances. Dual-functional adsorptive membranes, with hydrophobic backbone and quaternary ammonium moieties, were thereby designed to selectively intercept organic competitors while enrich PFAS. A 96.8 % removal of perfluorooctanoic acid (PFOA) was achieved and this effective removal (>90 %) maintained across five reuse cycles with a total treatment capacity of 650 L m−2. Rather than the rejection mechanism of nanofiltration process, these adsorptive membranes utilize synergistic electrostatic attraction and hydrophobic interactions, leading to a greater enrichment factor of 18.5 (PFOA over humic acid) and a permeability of 34.6 L m-2h−1 bar−1 (1.9- and 4.5-fold higher than reported NF 270 membranes, respectively). Furthermore, computational fluid dynamics (CFD) modeling revealed that the sponge-like matrix effectively prevents channeling flow and enhance access to adsorption sites. Sensitivity analysis and the high Damkohler number indicated that the adsorption process is mass transfer-controlled, with the key parameters ranked in order of significance: residence time > fluid viscosity > intrinsic adsorption rate. With consistent removal performance with co-existing competitors, efficient regeneration, and reusability, the dual-functional adsorptive membranes offer promising practical efficacy for PFAS remediation.

Enhanced peroxymonosulfate activation for emerging contaminant degradation via defect-engineered interfacial electric field in FeNC

Peroxymonosulfate (PMS) activation technology has important application value in treating emerging contaminant (ECs), but it still faces challenges in achieving efficient electron transfer and metal valence cycling. In this study, the interfacial electric field characteristics of FeNC catalysts were adjusted by introducing NC defects to affect the electron transfer process, thereby enhancing the catalytic performance of PMS. It is found that in the FeNC structure, the shift of the charge generates an interfacial electric field, which can promote the directional transfer of electrons. Through quantitative structure–activity relationship (QSAR) analysis, it was confirmed that the defect played a decisive role in regulating the interfacial electric field and improving the catalytic reaction efficiency. The interfacial electric field-mediated superexchange interaction realizes the electron donor effect of organic pollutants and the effective electron transfer between the Fe site, accelerates the electron cycling of the Fe site, and realizes the rapid and stable catalysis of PMS. The increase of the occupancy state distribution of d orbitals near the Fermi level provides favorable conditions for electron transitions and catalytic activation of PMS. ECs can be converted into environmentally friendly, non-toxic and harmless substances through. This defect-controlled interface electric field strategy realizes rapid electron directional transfer, which provides a new solution for improving the catalytic efficiency of PMS and the safe treatment of ECs in water.

CYP2E1 in 1,4-dioxane metabolism and liver toxicity: insights from CYP2E1 knockout mice study.

1,4-Dioxane (DX), an emerging water contaminant, is classified as a Group 2B liver carcinogen based on animal studies. Understanding of the mechanisms of action of DX liver carcinogenicity is important for the risk assessment and control of this environmental pollution. Previous studies demonstrate that high-dose DX exposure in mice through drinking water for up to 3 months caused liver mild cytotoxicity and oxidative DNA damage, a process correlating with hepatic CYP2E1 induction and elevated oxidative stress. To access the role of CYP2E1 in DX metabolism and liver toxicity, in the current study, male and female Cyp2e1-null mice were exposed to DX in drinking water (5000 ppm) for 1 week or 3 months. DX metabolism, redox and molecular investigations were subsequently performed on male Cyp2e1-null mice for cross-study comparisons to similarly treated male wildtype (WT) and glutathione (GSH)-deficient Gclm-null mice. Our results show that Cyp2e1-null mice of both genders were resistant to DX-induced hepatocellular cytotoxicity. In male Cyp2e1-null mice exposed to DX for 3 months, firstly, DX metabolism to β-hydroxyethoxyacetic acid was reduced to ~ 36% of WT levels; secondly, DX-induced hepatic redox dysregulation (lipid peroxidation, GSH oxidation, and activation of NRF2 antioxidant response) was substantially attenuated; thirdly, liver oxidative DNA damage was at a comparable level to DX-exposed WT mice, accompanied by suppression of DNA damage repair response; lastly, no aberrant proliferative or preneoplastic lesions were noted in DX-exposed livers. Overall, this study reveals, for the first time, that CYP2E1 is the main enzyme for DX metabolism at high dose and a primary contributor to DX-induced liver oxidative stress and associated cytotoxicity. High dose DX-induced genotoxicity may occur via CYP2E1-independent pathway(s), potentially involving impaired DNA damage repair.

Monte Carlo Simulations of Water Pollutant Adsorption at Parts-per-Billion Concentration: A Study on 1,4-Dioxane.

1,4-dioxane, an emerging water pollutant with high production volumes, is a probable human carcinogen. The inadequacy of conventional treatment processes demonstrates the need for an effective remediation strategy. Crystalline nanoporous materials are cost-effective adsorbents due to their high capacity and selective separation in mixtures. This study explores the potential of all-silica zeolites for the separation of 1,4-dioxane from water. These zeolites are highly hydrophobic and can preferentially adsorb nonpolar molecules from mixtures. We investigated six zeolite frameworks (BEA, EUO, FER, IFR, MFI, and MOR) using Monte Carlo simulations in the Gibbs ensemble. The simulations indicate high selectivity by FER and EUO, especially at low pressures, which we attribute to pore sizes and shapes with a greater affinity to 1,4-dioxane. We also demonstrate a Monte Carlo simulation workflow using gauge cells to model the adsorption of an aqueous solution of 1,4-dioxane at a 0.35 ppb concentration. We quantify 1,4-dioxane and water coadsorption and observe selectivities ranging from 1.1 × 105 in MOR to 8.7 × 106 in FER. We also demonstrate that 1,4-dioxane is in the infinite dilution regime in the aqueous phase at this concentration. This simulation technique can be extended to model other emerging water contaminants such as perfluoroalkyl and polyfluoroalkyl substances (PFAS), chlorofluorocarbons, and others, which are also found in extremely low concentrations.

Typical emerging contaminants in sewage treatment plant effluent, and related watersheds in the Pearl River Basin: Ecological risks and source identification

Emerging contaminants pose a potential risk to aquatic ecosystems in the Pearl River Basin, China, owing to the high population density and active industry. This study investigated samples from eight sewage treatment plants, and five surface water bodies of related watersheds. To screen the risk of emerging contaminants (ECs), and clarify their sources, this study calculated the risk quotient of detected chemical and performed source identification/apportionment using the positive matrix factorization method. In total, 149 organic pollutants were identified. Pharmaceuticals showed significant concentrations in sewage treatment plant samples (120.87 ng/L), compared with surface water samples (1.13 ng/L). The ecological risk assessment identified three chemicals with a heightened risk to aquatic organisms: fipronil sulfide, caffeine, and roxithromycin. Four principal sources of contaminants were identified: pharmaceutical wastewater, domestic sewage, medical effluent, and agricultural runoff. Pharmaceutical wastewater was the primary contributor (60.4 %), to the cumulative EC concentration and to ECs in sewage treatment plant effluent. Agricultural drainage was the main source of ECs in surface water. This study provides a strategy to obtain comprehensive information on the aquatic risks and potential sources of EC species in areas affected by artificial activities, which is of substantial importance to pollutant management and control.

Investigation of La-BiVO4/g-C3N4 photocatalytic system for efficient removal of hazardous water contaminants

The application of semiconductor photocatalysis powered by renewable energy sources for environmental remediation of emerging contaminants has gained significant research interest in recent years. Lanthanum-substituted bismuth vanadate (La-BiVO4)/graphitic carbon nitride (g-C3N4) heterojunctions were synthesized for the photocatalytic degradation of emerging water contaminants. Significantly, La³+ substitution serves as a model system for exploring the broader concept of cationic substitutions on BiVO4. By strategically replacing a portion of Bi(III) with various cations, we can potentially tailor the electronic structure of BiVO4 for enhanced photocatalytic performance. Photoelectrochemical analysis confirmed rapid charge separation and reduced resistance, leading to effective contaminant degradation. The La-BiVO4/g-C3N4 nanocomposite exhibited exceptional photocatalytic performance under simulated solar light irradiation (Xe-350W, AM 1.5 G), achieving 87.66% photooxidation of roxarsone within 150 min, surpassing g-C3N4, BiVO4, LaVO4, La-BiVO4, BiVO4/g-C3N4, and LaVO4/g-C3N4 by factors of 1.94, 1.26, 2.25, 1.39, 1.13, and 2.51, respectively. Moreover, it demonstrated 99.61% degradation of Cr(VI) after 60 min, outperforming g-C3N4, BiVO4, LaVO4, La-BiVO4, BiVO4/g-C3N4, and LaVO4/g-C3N4 by factors of 1.11, 1.81, 1.62, 1.67, 1.20, and 1.13, respectively. These findings underscore the superior photocatalytic efficacy of the La-BiVO4/g-C3N4 nanocomposite. The efficient photocatalytic activity of La-BiVO4/g-C3N4 type-II heterojunctions demonstrates its potential for real-world environmental remediation. This material offers a promising strategy for removing harmful water contaminants, thereby mitigating risks associated with water consumption.

First Direct Gravimetric Detection of Perfluorooctane Sulfonic Acid (PFOS) Water Contaminants, Combination with Electrical Measurements on the Same Device—Proof of Concepts

Perfluoroalkyl and polyfluoroalkyl substances (PFAS) are pollutants of concern due to their long-term persistence in the environment and human health effects. Among them, perfluorooctane sulfonic acid (PFOS) is very ubiquitous and dangerous for health. Currently, the detection levels required by the legislation can be achieved only with expensive laboratory equipment. Hence, there is a need for portable, in-field, and possibly real-time detection. Optical and electrochemical transduction mechanisms are mainly used for the chemical sensors. Here, we report the first gravimetric detection of small-sized molecules like PFOS (MW 500) dissolved in water. A 100 MHz quartz crystal microbalance (QCM) measured at the third harmonic and an even more sensitive 434 MHz two-port surface acoustic wave (SAW) resonator with gold electrodes were used as transducers. The PFOS selective sensing layer was prepared from the metal organic framework (MOF) MIL-101(Cr). Its nano-sized thickness and structure were optimized using the discreet Langmuir–Blodgett (LB) film deposition method. This is the first time that LB multilayers from bulk MOFs have been prepared. The measured frequency downshifts of around 220 kHz per 1 µmol/L of PFOS, a SAW resonator-loaded QL-factor above 2000, and reaction times in the minutes’ range are highly promising for an in-field sensor reaching the water safety directives. Additionally, we use the micrometer-sized interdigitated electrodes of the SAW resonator to strongly enhance the electrochemical impedance spectroscopy (EIS) of the PFOS contamination. Thus, for the first time, we combine the ultra-sensitive gravimetry of small molecules in a water environment with electrical measurements on a single device. This combination provides additional sensor selectivity. Control tests against a bare resonator and two similar compounds prove the concept’s viability. All measurements were performed with pocket-sized tablet-powered devices, thus making the system highly portable and field-deployable. While here we focus on one of the emerging water contaminants, this concept with a different selective coating can be used for other new contaminants.

Design of New Schiff Bases and Their Heavy Metal Ion Complexes for Environmental Applications: A Molecular Dynamics and Density Function Theory Study.

Schiff bases (SBs) are important ligands in coordination chemistry due to their unique structural properties. Their ability to form complexes with metal ions has been exploited for the environmental detection of emerging water contaminants. In this work, we evaluated the complexation ability of three newly proposed SBs, 1-3, by complete conformational analysis, using a combination of Molecular Dynamics and Density Functional Theory studies, to understand their ability to coordinate toxic heavy metal (HMs) ions. From this study, it emerges that all the ligands present geometries that make them suitable to complex HMs through the N-imino moieties or, in the case of 3, with the support of the oxygen atoms of the ethylene diether chain. In particular, this ligand shows the most promising coordination behavior, particularly with Pb2+.

Innovative syntheses of immobilized CuxO semiconductors grown on 3D prints and their photoelectrochemical activity for sulfamethoxazole degradation

Traditional copper oxide manufacturing processes require high energy consumption, high synthesis temperatures, and long process times. This study proposes an innovative additive manufacturing process to support immobilized copper oxide, offering greater design flexibility and customization. CuxO semiconductors were synthesized on 3D-printed substrates via the anodization process and evaluated for their effectiveness in degrading sulfamethoxazole (SMX). XRD analysis of the samples revealed the presence of both CuO and Cu2O crystalline phases, this mixture of oxides helps to expand the absorption range of visible light. The immobilized CuxO semiconductors exhibited band gaps ranging between 1.6 and 1.8 eV. Negative current densities and Mott-Schottky analysis confirmed the nature of the p-type semiconductor. Semiconductors grown by 3D printing demonstrated remarkable degradation capacity for the antibiotic sulfamethoxazole (SMX), achieving 60% degradation after 360 minutes under visible light. Kinetic degradation tends to be a first-order and zero-order model. TOC analysis further revealed the formation of reaction intermediates during SMX degradation, ultimately leading to the mineralization of the contaminant. Based on these results, we report, for the first time CuxO semiconductors grown on large 3D-printed substrates as promising photocatalysts for the degradation of emerging water pollutants. Based on these results, we report, for the first time, that CuxO semiconductors grown on large 3D-printed substrates are promising photocatalysts for the degradation of emerging water contaminants. Furthermore, it should be emphasized that the proposed method is faster and does not require subsequent thermal treatments for its functionalization, making it attractive for various industrial applications.

Enhanced degradation of tetracycline by TiO2@MXene with peroxydisulfate under visible light irradiation

Photocatalysis and peroxydisulfate (PS) based advanced oxidation techniques are promising technologies in the field of water treatment that can be used to destroy increasingly persistent organic contaminants. The current work used a simple hydrothermal approach to synthesize a catalyst made of composites of TiO2 nanospheres and multi-layer Ti3C2Tx sheets (TiO2@MXene). Tetracycline (TC) was then effectively degraded by the TiO2@MXene material integrated with PS activation (300 mg/L). Under simulated sunlight (AM 1.5G, P = 2.8 W) irradiation, the combination method dramatically increases TC degradation. Following a 30-min treatment with 300 mg/L TiO2@MXene (wt.10 %), the optimal efficiency can reach 100 %. As the reactive functional species, holes (h+), SO4-•, •OH, and •O2− dominate the catalytic process. Furthermore, investigation was conducted into significant factors such as catalyst dosage, PS dosage, common anions, and TiO2 loading dosage. The TiO2@MXene material was demonstrated to be a feasible and sustainable strategy worth taking into consideration in the mitigation of emerging water contaminants due to its ease of recovery, stability of surface properties, and recyclability. Furthermore, the proposed degradation mechanism further demonstrated the viability of TiO2@MXene with PS in TC degradation. This, this study provides insights into the design of effective photocatalyst coupling PS activation for the efficient degradation of organic pollutants.

Sensors for Emerging Water Contaminants: Overcoming Roadblocks to Innovation.

Ensuring water quality and safety requires the effective detection of emerging contaminants, which present significant risks to both human health and the environment. Field deployable low-cost sensors provide solutions to detect contaminants at their source and enable large-scale water quality monitoring and management. Unfortunately, the availability and utilization of such sensors remain limited. This Perspective examines current sensing technologies for detecting emerging contaminants and analyzes critical barriers, such as high costs, lack of reliability, difficulties in implementation in real-world settings, and lack of stakeholder involvement in sensor design. These technical and nontechnical barriers severely hinder progression from proof-of-concepts and negatively impact user experience factors such as ease-of-use and actionability using sensing data, ultimately affecting successful translation and widespread adoption of these technologies. We provide examples of specific sensing systems and explore key strategies to address the remaining scientific challenges that must be overcome to translate these technologies into the field such as improving sensitivity, selectivity, robustness, and performance in real-world water environments. Other critical aspects such as tailoring research to meet end-users' requirements, integrating cost considerations and consumer needs into the early prototype design, establishing standardized evaluation and validation protocols, fostering academia-industry collaborations, maximizing data value by establishing data sharing initiatives, and promoting workforce development are also discussed. The Perspective describes a set of guidelines for the development, translation, and implementation of water quality sensors to swiftly and accurately detect, analyze, track, and manage contamination.

Enhanced Fenton-like process over Cu/L(+)-ascorbic acid co-doping mesoporous silica for toxicity reduction of emerging contaminants

Effective removal of emerging contaminants (ECs) to minimize their impacts on human health and the natural environment is a global priority. For the removal of ECs in water, we fabricated a seaweed spherical microsphere catalyst with Cu cation-π structures by in situ doping of Cu species and ascorbic acid in mesoporous silica (Cu-C-MSNs) via a hydrothermal method. The results indicate that bisphenol A (BPA) is substantially degraded within 5 min under natural conditions, with its biological toxicity considerably weakened. Moreover, industrial wastewater could also be effectively purified by Cu-C-MSNs/H2O2 system. The presence of metal sites and the complexation of ECs via cation-π interaction and π-π stacking on the catalyst surface were directly responsible for the polarization distribution of electrons, thus activating H2O2 and dissolved oxygen (DO). The removal of contaminants could be attributed primarily to 1) the activation of H2O2 into •OH to attack the contaminants and 2) self-cleavage because of the transfer of electrons from the contaminants to the catalysts. This study provides an innovative solution for the effective treatment of ECs and has positive implications for easing global environmental crises.

Removal of Inorganic Pollutants from Wastewater: Innovative Technologies and Toxicity Assessment

In the past decade, a sudden increase in the number and kind of emerging water contaminants has been observed. The emerging contaminants can be categorized as organic or inorganic. Organic contaminants have been known for years, and techniques for their detection and remediation have been developed. However, inorganic pollutants are much more common. This is because they are detected in very low or negligible concentrations and are equally toxic as organic pollutants at higher concentrations. To boost the research on inorganic pollutant contamination, advancements in detection and quantification techniques are required. The presented paper discusses major inorganic pollutants such as metals and their salts, inorganic fertilizers, sulfides, acids and bases, and ammonia and oxides of nitrogen. In addition, it discusses the inorganic toxicants’ toxicity to organisms and the environment, upgraded quantification methods, and advancements in inorganic toxicant mitigation. Moreover, the major bottlenecks in the quantification and removal of inorganic pollutants are discussed at the end.

Occurrence and risks of pharmaceuticals, personal care products, and endocrine-disrupting compounds in Chinese surface waters

The continuous and rapid increase of chemical pollution in surface waters has become a pressing and widely recognized global concern. As emerging contaminants (ECs) in surface waters, pharmaceutical and personal care products (PPCPs), and endocrine-disrupting compounds (EDCs) have attracted considerable attention due to their wide occurrence and potential threat to human health. Therefore, a comprehensive understanding of the occurrence and risks of ECs in Chinese surface waters is urgently required. This study summarizes and assesses the environmental occurrence concentrations and ecological risks of 42 pharmaceuticals, 15 personal care products (PCPs), and 20 EDCs frequently detected in Chinese surface waters. The ECs were primarily detected in China's densely populated and highly industrialized regions. Most detected PPCPs and EDCs had concentrations between ng/L to µg/L, whereas norfloxacin, caffeine, and erythromycin had relatively high contamination levels, even exceeding 2000 ng/L. Risk evaluation based on the risk quotient method revealed that 34 PPCPs and EDCs in Chinese surface waters did not pose a significant risk, whereas 4-nonylphenol, 4-tert-octylphenol, 17α-ethinyl estradiol, 17β-estradiol, and triclocarban did. This review provides a comprehensive summary of the occurrence and associated hazards of typical PPCPs and EDCs in Chinese surface waters over the past decade, and will aid in the regulation and control of these ECs in Chinese surface waters.

Deep mining of reported emerging contaminants in China's surface water in the past decade: Exposure, ecological effects and risk assessment.

The identification and management of high-risk contaminants have raised great concern from governments. Facing the growing amount of data on the occurrence of emerging contaminants (ECs) in surface water, a deep mining and quality control strategy was developed to integrate data on all reported ECs in Chinese surface water over the past decade, and an exposure and effect database was further built. In addition, multilevel risk characterization was carried out to prioritize high-risk areas, contaminants and endpoints. A total of 1038 ECs, mainly pharmaceutical and personal care products (PPCPs) and industrial chemicals, were curated, with concentrations ranging from 0.02 pg/L to 533µg/L. For individual risk, all the provinces had acceptable risks except for Henan, which was characterized with a medium chronic risk. Nine ECs, including 4-nonylphenol and estrone, dominated individual risks. Conversely, for multisubstance risk, 76.20% and 73.87% of aquatic organisms were affected acutely and chronically at the national level, with acute and chronic risks exceeding the safety threshold of 5% in 11 and 19 provinces, respectively. Nineteen ECs, including sitosterol and chyfluthrin, dominated the multisubstance risk. In addition, 9 MoAs mainly inducing electron transfer inhibition, neurotoxicity and narcosis toxicity are high-risk endpoints. The study revealed the ecological risk status and key risk entities of Chinese surface waters, which provided the latest data to support the control of ECs in China.

Improving soil aquifer treatment efficiency using air injection into the subsurface

Abstract. Soil aquifer treatment (SAT) is an effective and sustainable technology for wastewater or stormwater treatment, storage, and reuse. During SAT, the vadose zone acts as a pseudo-reactor in which physical and biochemical processes are utilized to improve the infiltrated-water quality. Dissolved oxygen (DO) is necessary for aerobic microbial oxidation of carbon and nitrogen species in the effluent. Therefore, to enhance aeration, SAT is generally operated in flooding and drying cycles. While long drying periods (DPs) lead to better oxidizing conditions and improve water quality, they reduce recharge volumes. As the population grows, the quantity of effluent directed to SAT sites increases, and increasing recharge volumes become a concern and often a limiting factor for SAT usage. In this study, direct subsurface air injection SAT (Air-SAT) was tested as an alternative to long-DP operation. Six long-column experiments were conducted (2 m column) that aimed to examine the effect of air injection on the soil's water content, oxidation–reduction potential (ORP), DO concentrations, infiltrated amounts, and ultimate outflow quality. In addition to basic parameters, such as dissolved organic C (DOC) and N species, the effluent quality analysis also included an examination of three emerging water contaminants: ibuprofen, carbamazepine, and 1H-benzotriazole. Pulsed-air-injection experiments were conducted during continuous flooding using different operation modes (i.e., air pulse durations, frequencies, and airflow rates). Our results show that Air-SAT operation doubled the time during which infiltration was possible (i.e., the infiltration was continuous with no downtime) and allowed up to a 46 % higher mean infiltration rate in some cases. As a result, the infiltration volumes in the Air-SAT modes were 47 %–203 % higher than conventional flooding–drying operation (FDO). A longer air pulse duration (60 min vs. 8 min) and higher airflow rate (∼2 L min−1 vs. ∼1 L min−1) led to a higher mean infiltration rate, whereas a high pulse frequency (4.5 h−1) led to a lower mean infiltration rate compared with low-frequency operation (24 h−1). Air injection also allowed good recovery of the ORP and DO levels in the soil, especially in the high-frequency Air-SAT experiments, where steady aerobic conditions were maintained during most of the flooding. Consequently, the mean DOC, total Kjeldahl N (TKN), and ibuprofen removal values in these experiments were up to 9 %, 40 %, and 65 % higher than those with FDO, respectively. However, high-frequency Air-SAT during continuous flooding also led to significant deterioration of the mean infiltration rate, probably due to enhanced biological clogging. Hence, it may be more feasible and beneficial to combine it with conventional FDO, allowing a steady infiltration rate and increased recharge volumes while sustaining high effluent quality. While these results still need to be verified at full scale, they highlight the possibility of using air injection to minimize the DP length and alleviate the pressure on existing SAT sites.

Adsorption behavior of triclosan on microplastics and their combined acute toxicity to D. magna

Microplastics (MP) have been recently identified as emerging water contaminants in worldwide. Owing to its physicochemical properties, MP have been considered as a vector of other micropollutants and may affect their fate and ecological toxicity in the water environment. In this study, triclosan (TCS), which is a widely-used bactericide, and three frequently found types of MP (PS-MP, PE-MP, and PP-MP) were investigated. The adsorption behavior of TCS on MP was investigated by the effect of reaction time, initial concentration of TCS, and other water chemistry factors. Elovich model and Temkin model are the most fitted well with kinetics and adsorption isotherms, respectively. The maximum TCS adsorption capacities were calculated for PS-MP (9.36 mg/g), PP-MP (8.23 mg/g), and PE-MP (6.47 mg/g). PS-MP had higher affinity to TCS owing to hydrophobic and π-π interaction. The TCS adsorption on PS-MP was inhibited by decreasing concentrations of cations, and increasing concentration of anion, pH, and NOM concentration. At pH 10, only 0.22 mg/g of adsorption capacity was obtained because of the isoelectric point (3.75) of PS-MP and pKa (7.9) of TCS. And almost no TCS adsorption occurred at NOM concentration of 11.8 mg/L. Only PS-MP had no acute toxic effect on D. magna, whereas TCS showed acute toxicity (EC50,24h of TCS = 0.36 ± 0.4 mg/L). Although survival rate increased when TCS with PS-MP due to lower the TCS concentration in solution via adsorption, PS-MP was observed in intestine and body surface of D. magna. Our findings can contribute to understanding the combined potential effects of MP fragment and TCS to aquatic biota.

Metal-organic frameworks/cellulose hybrids with their modern technological implementation towards water treatment

Metal-organic frameworks (MOFs) are amongst the most attractive porous polymeric networks with appealing properties. However, their inherent fragility, powder nature, low processibility, and handling present some exceptional challenges for high-tech commercial applications. Currently, economic and environmental concerns drive the development of some bioinspired polymeric matrices containing MOFs. As an artifact, the availability of previously unattainable properties is negotiated by conjugating cellulosic materials with crystalline MOFs. Thus, multi-dimensional organic-inorganic hybrid composites are formed with high electrical, optical, mechanical, and thermal features. These MOF/cellulose hybrids, known as CelloMOFs (cellulose MOFs), have remarkable mechanical properties with tunable porosities, specific surface area and accessible active sites, making them ideal for real-world troubleshooting applications such as wastewater treatment, chemical sensing, energy storage, and so on. In this review, current state-of-the-art strategic synthesis routes for fabrication of MOF/cellulose composites with a specific focus on CelloMOFs as a potential tool for mitigation of the targeted emerging water contaminants have been done under the same umbrella, which has previously been less explored. Streamlining discussions on general properties such as raw material selection, structural analysis of cellulose, availability of surface functional groups, cellulose-metal node interactions, cellulose charging, and so on have been emphasized, as has integration with robust MOFs. A better understanding of these fundamental properties is critical because they will have a significant impact on the performance of MOF/cellulose composites in a variety of applications. Furthermore, at the end of this review, the challenges and perspectives of using CelloMOFs have been discussed in a concise manner in order to improve their practical utility rather than just concept mapping.

ZnHCF@PB nanoparticles with reduced bandgap as a promising photocatalyst for the degradation of conventional and emerging water contaminants

The photocatalytic degradation of conventional and emerging pollutants (i.e., methyl, ethyl, and butyl parabens) was investigated under light irradiation with 315–1050 nm wavelength using core–shell zinc doped hexacyanoferrate@Prussian blue nanoparticles. Different synthesis parameters including precursors loading, drying temperature and different metal ions precursors were studied. The ten different composite systems obtained, were investigated for the photodegradation of methylene blue in deionized water. The optimal performance photocatalyst (20 mg/L) photodegrade 94% of 10 ppm methylene blue within 24 min. The optimized sample was further used for the photodegradation of methylene blue in municipal wastewater matrix; it completely degraded the methylene blue after 51 min. Finally, the developed nanoparticles were investigated for the photodegradation of parabens. The chemical oxygen demand showed 30% of parabens was degraded in the municipal wastewater matrix. The results of this research show that ZnHCF@PB nanoparticles could be used for the effective photocatalytic remediation of conventional and emerging pollutants, i.e., parabens. Statement of environmental implicationThrough this study, it is anticipated that ZnO-derived ZnHCF@PB NPs can achieve a bandgap of 1.11 eV, which is much lower than that of ZnO NPs (3.15 eV). Interestingly, ZnHCF@PB NPs were efficiently used for the degradation of conventional (i.e., dyes) and emerging contaminants (i.e., parabens) in deionized water and municipal wastewater matrices to mimic industrial wastewater.

Acute Toxicity of a Marine Emerging Pollutant (Promethazine Hydrochloride) on Artemia sp.

Recently, there has been a worrying increase in the pollution of the aquatic ecosystem caused by emerging contaminants (ECs) detected in wastewater effluent discharges. Although traces of ECs in waters have been found in low concentrations, it leads to negative effects for nontarget organisms. Antihistamines are a class of drugs largely used, whose metabolites are widespread in the aquatic ecosystem. The aim of the study was to evaluate the short-term effects of promethazine hydrochloride on nauplii of Artemia sp. A high percentage of mortality and morphological alterations were found. The results suggest a possible correlation between exposure to antihistamine and an acceleration of larval development.