Organic Pollutants Research Articles

3D Tremella‐Like g‐C3N4/TiO2/HNTs Heterojunction Photocatalyst for Enhanced Photocatalytic Degradation of Rhodamine B From Water

AbstractAmong the traditional treatment processes for purifying wastewater contaminated with Rhodamine B (RhB), semiconductor photocatalysis is the most effective technology because it can oxidize organic pollutants and convert them into CO2, H2O, and other harmless molecules in a safe and efficient manner. According to literature research, it is feasible to enhance the performance of g‐C3 N4 as a photocatalyst by constructing a heterojunction with other photocatalytic materials. Morphological regulation of carbon nitride (g‐C3N4) is a viable strategy for improving its photocatalytic activities. By controlling the morphology of g‐C3N4, factors such as light absorption, specific surface area, charge separation, and reaction sites can be optimized to enhance its photocatalytic efficiency. Three‐dimensional tremella‐like carbon nitride (3DT‐CN) and 3D‐CN/TiO2/HNTs (halloysite nanotubes) were prepared using bubble templates and an impregnation method respectively. The Z‐scheme heterojunction structure constructed by 3D‐CN and TiO2 promotes electron‐hole separation. Catalytic experiments demonstrated that under irradiation for 120 min, the 3D‐CN/TiO2/HNTs catalyst could eliminate 86.48 % of Rhodamine B (RhB). Additionally, active radicals such as e‐, h+, ⋅OH, and ⋅O2‐ are involved in RhB degradation. Therefore, the three‐dimensional tremella‐like 3D‐CN/TiO2/HNTs heterojunction photocatalyst has great potential for environmental purification.

Thymus vulgaris-assisted growth of nickel nanoparticles onto Luffa fibers: A robust and recyclable catalyst for the reduction of organic pollutants

A green and efficient synthetic pathway was developed to prepare nickel@Luffa nanocomposite. Thymus vulgaris extract was used to functionalize the surface of Luffa fibers with hydroxyl, carbonyl, and amide groups, which assisted in the adsorption of nickel ions. The scanning electron microscope images revealed that nickel nanoparticles grew as aggregates of semi-spherical particles and randomly dispersed on the Luffa fibers. The X-ray diffraction pattern of the nickel@Luffa nanocomposite showed the diffraction pattern of a face-centered cubic Ni crystal. XPS spectrum indicated the formation of metallic Ni at the Luffa surface. The prepared nickel@Luffa was used to catalyze the degradation of 4-nitrophenol, methyl orange, bromophenol blue and a mixture of both. The reaction rate constant for nickel@Luffa nanocomposite was calculated as 15.47 × 10−3 s−1 at pH = 10 and even after ten cycles its conversion was about 90%. The nickel nanoparticles could be recycled/reused for ten catalytic cycles with adequate catalytic activity. Such synthetic pathways encourage the application of renewable natural resources to fabricate separable/recyclable heterogeneous catalyst for many important reactions. The proposed nanocomposite is industrially applicable and environmentally-benign, fulfilling the requirements for the sustainable development.

Impact of Nitrate on the Removal of Pollutants from Water in Reducing Gas-Based Membrane Biofilm Reactors: A Review.

The membrane biofilm reactor (MBfR) is a novel wastewater treatment technology, garnering attention due to its high gas utilization rate and effective pollutant removal capability. This paper outlines the working mechanism, advantages, and disadvantages of MBfR, and the denitrification pathways, assessing the efficacy of MBfR in removing oxidized pollutants (sulfate (SO4-), perchlorate (ClO4-)), heavy metal ions (chromates (Cr(VI)), selenates (Se(VI))), and organic pollutants (tetracycline (TC), p-chloronitrobenzene (p-CNB)), and delves into the role of related microorganisms. Specifically, through the addition of nitrates (NO3-), this paper analyzes its impact on the removal efficiency of other pollutants and explores the changes in microbial communities. The results of the study show that NO3- inhibits the removal of other pollutants (oxidizing pollutants, heavy metal ions and organic pollutants), etc., in the simultaneous removal of multiple pollutants by MBfR.

Self-powered organic pollutants degradation in wastewater by photocatalytic ozonation based on triboelectric nanogenerator

It is of great significance to explore innovative ways to degrade organic pollutants in wastewater. Here, for the first time, we report a self-powered photocatalytic ozonation water purification system for removing organic pollutants in aquatic environment. A rabbit fur-based rotary triboelectric nanogenerator (RR-TENG) is designed as the power supply of water purification system. As a new TENG-based ozone generation method, spark-surface dielectric barrier discharge (Spark-SDBD) is proposed, which is composed of spark discharge device and surface dielectric barrier discharge (SDBD) device in series and can generate ozone to a maximum concentration of 36.4 mg/m3. Rhodamine B and ciprofloxacin, two typical organic compounds, are selected as simulated pollutants in wastewater, and P25 particles loaded on nickel foam are used as the photocatalyst. Ozone is continuously introduced into the polluted solution through an aeration device, coupled with photocatalysis. Within 80 minutes, it can be observed that Rhodamine B has 100% decolorization and ciprofloxacin is degraded to 99%. This work broadens the field of water purification and provides an effective way to create a cleaner and safer aquatic environment.

Development of Magnetic Solid Phase Micro-Extraction (MSPE) Method for the Extraction and Preconcentration of the Selected β-Blockers in the Environmental Wastewaters

AbstractEmerging organic pollutants s have always been the greatest environmental concern due to their ubiquity and distinguished adverse effects. These are mostly water-bone pollutants flagged as endocrine disruptors and can greatly inconvenience the ecosystem. Among others, β-blockers have also been detected in the environment at various concentrations that threaten the well-being of humans and animals. In this work, NH2-MIL-101(Cr) doped magnetic nanoparticles nanocomposite was successfully synthesised and characterised using analytical techniques such as X-ray diffraction spectroscopy (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) and transmission electron microscopy (TEM). The Fe3O4@NH2-MIL-101(Cr) was then used as an adsorbent to extract the selected β-blockers in the environmental wastewater. The selected β-blockers were quantified using a high-performance liquid chromatography-diode array detector (HPLC-DAD). Parameters affecting the extraction were screened and optimised using fractional factorial design (FFD) and central composite design (CCD), respectively. Under optimum conditions, the LODs were 0.057 and 0.065 µg L− 1, and LOQs were 0.19 and 0.22 µg L− 1 for acebutolol (ACE) and metoprolol (MET), respectively. The calibration curve exhibited the linearity range of 0.2–1200 µg L− 1 with correlation coefficients of 0.9987 and 0.9968 for ACE and MET, respectively. Repeatability studies demonstrated the %RSD of 0.63 and 0.74% for MET and ACE. At the same time, reproducibility studies displayed the %RSD of 1.057 and 1.178% for MET and ACE, respectively. Spike recovery experiments were carried out to assess the performance of MSPE in real samples, and over 88% of both analytes were recovered. This indicated that the MSPE method could enrich various organic pollutants from different environmental matrices.

Multiple-component covalent organic frameworks for simultaneous extraction and determination of multitarget pollutants in sea foods

Persistent organic pollutants (POPs), such as perfluoroalkyl and polyfluoroalkyl substances (PFASs), polychlorinated biphenyls (PCBs), and bisphenols (BPs), have been raising global concerns due to their toxic effects on environment and human health. The monitoring of residues of POPs in seafood is crucial for assessing the accumulation of these contaminants in the study area and mitigating potential risks to human health. However, the diversity and complexity of POPs in seafood present significant challenges for their simultaneous detection. Here, a novel multi-component fluoro-functionalized covalent organic framework (OH-F-COF) was designed as SPE adsorbent for simultaneous extraction POPs. On this basis, the recognition and adsorption mechanisms were investigated by molecular simulation. Due to multiple interactions and large specific surface area, OH-F-COF displayed satisfactory coextraction performance for PFASs, PCBs, and BPs. Under optimized conditions, the OH-F-COF sorbent was employed in a strategy of simultaneous extraction and stepwise elution (SESE), in combination with HPLC−MS/MS and GC−MS method, to effectively determined POPs in seafood collected from coastal areas of China. The method obtained low detection limits for BPs (0.0037 −0.0089 ng/g), PFASs (0.0038 −0.0207 ng/g), and PCBs (0.2308 −0.2499 ng/g), respectively. This approach provided new research ideas for analyzing and controlling multitarget POPs in seafood. Environmental implicationsPersistent organic pollutants (POPs), such as perfluoroalkyl and polyfluoroalkyl substances (PFASs), polychlorinated biphenyls (PCBs), and bisphenols (BPs), have caused serious hazards to human health and ecosystems. Hence, there is a need to develop a quantitative method that can rapidly detect POPs in environmental and food samples. Herein, a novel multi-component fluorine-functionalized covalent organic skeletons (OH-F-COF) were prepared at room temperature, and served as adsorbent for POPs. The SESE-SPE strategy combined with chromatographic techniques was used to achieve a rapid detection of POPs in sea foods from the coastal provinces of China. This method provides a valuable tool for analyzing POPs in environmental and food samples.

Protective Effects of Polysaccharide of Atractylodes Macrocephala Koidz against Porcine Aortic Valve Endothelial Cells Damage Induced by di (2-ethylhexyl) Phthalate.

The activation, injury, and dysfunction of endothelial cells are considered to be the initial key events in the development of atherosclerosis. Di (2-ethylhexyl) phthalate (DEHP), a prevalent organic pollutant, can cause damage to multiple organs. Polysaccharide of Atractylodes macrocephala Koidz (PAMK) is a bioactive compound extracted from A. macrocephala Koidz with various biological activities. This study investigates the protective effects of PAMK on porcine aortic valve endothelial cells (PAVEC) damaged by DEHP. PAVECs treated with DEHP alone or with PAMK showed reduced cell apoptosis and death in PAMK-pretreated cells. PAMK up-regulated Bcl-2 expression and down-regulated Bax protein, suppressing apoptosis. Flow cytometry analysis demonstrated that PAMK protected PAVECs from DEHP-induced damage. These findings suggest that PAMK inhibits cell apoptosis and protects against DEHP damage in endothelial cells.

Interactions of Brominated Flame Retardants with Membrane Models of Dehalogenating Bacteria: Langmuir Monolayer and Grazing Incidence X-ray Diffraction Studies.

Brominated flame retardants (BFRs) are small organic molecules containing several bromine substituents added to plastics to limit their flammability. BFRs can constitute up to 30% of the weight of some plastics, which is why they are produced in large quantities. Along with plastic waste and microplastic particles, BFRs end up in the soil and can easily leach causing contamination. As polyhalogenated molecules, multiple BFRs were classified as persistent organic pollutants (POPs), meaning that their biodegradation in the soils is especially challenging. However, some anaerobic bacteria as Dehaloccocoides can dehalogenate BFRs, which is important in the bioremediation of contaminated soils. BFRs are hydrophobic, can accumulate in plasma membranes, and disturb their function. On the other hand, limited membrane accumulation is necessary for BFR dehalogenation. To study the BFR-membrane interaction, we created membrane models of soil dehalogenating bacteria and tested their interactions with seven legacy and novel BFRs most common in soils. Phospholipid Langmuir monolayers with appropriate composition were used as membrane models. These membranes were doped in the selected BFRs, and the incorporation of BFR molecules into the phospholipid matrix and also the effects of BFR presence on membrane physical properties and morphology were studied. It turned out that the seven BFRs differed significantly in their membrane affinity. For some, the incorporation was very limited, and others incorporated effectively and could affect membrane properties, while one of the tested molecules induced the formation of bilayer domains in the membranes. Thus, Langmuir monolayers can be effectively used for pretesting BFR membrane activity.

Pollution characteristics and risk assessment of organophosphate esters (OPEs) in typical industrial parks in Southwest China.

As alternative substances of PBDEs, organophosphate esters (OPEs), an emerging organic pollutant, were increasingly produced and used in many kinds of industries and consumer products. However, OPEs also have various adverse toxic effects. Information on the pollution levels and exposure to OPEs in related industries is still limited. This study presented data on OPE contamination in the soil, leaf, and river water samples from seven typical industrial parks in Southwest China. Total concentration of seven OPEs (Σ7OPE) including tri-n-butyl phosphate (TnBP), tris-(2-ethylhexyl) phosphate (TEHP), tris-(2-butoxyethyl) phosphate (TBEP), tris-(2-carboxyethyl) phosphine (TCEP), triphenyl phosphate (TPhP), tris-(1,3-dichloro-2-propyl) ester (TDCPP), and tris-(chlorisopropyl) phosphate (TCPP) in the soil samples (36.2 ~ 219.7 ng/g) and the surrounding river water samples (118.9 ~ 287.7 ng/L) were mostly lower than those in other studies, while the Σ7OPE level in the leaves (2053.3 ~ 8152.7 ng/g) was relatively high. There were significant differences in the concentration and distribution of OPEs in the surrounding environment of different industrial parks. TDCPP, TnBP, and TCPP could be used as the characteristic compound in soil samples from auto industrial park, river samples from shoe making industrial park, and leaf samples from logistics park, respectively. The parameter m (the content ratio of chlorinated OPEs to alkyl OPEs) was suggested to distinguish the types of industrial park preliminary. When m ≥ 1, it mainly refers to heavy industries sources such as automobiles, electronics, and machinery, etc. When m<1, it mainly for the light industrial sources such as textile industry, transportation services, and resources processing, etc. For logistics park, furniture park and Wuhou comprehensive industrial park, the volatilization of materials was the main sources of OPEs in the surrounding environment, while more effort was required to strengthen the pollution control and management of the waste water and soil in the pharmacy industrial park, shoe making industrial park and auto industrial park. Risk assessment showed that there was a negligible non-cancer and carcinogenic risk in the soil, while high attention should be paid to the non-cancer risk for children.

Improvement of the treatment of cork boiling wastewater by solar photo-Fenton process

The manufacturing process of cork generate a high volume of industrial wastewater which presents a significant organic pollution and low biodegradability. Solar photo-Fenton has been investigated for the remediation of these effluents with good reductions of organic load and demonstrating to be an efficient alternative and allowing the possibility to combine with other processes. This work proposes a treatment line for the improvement of this process based on an innovative solar prototype which optimizes the solar irradiation for improving the removal rate of pollutants. Additionally, efficient and green physicochemical technologies using decantation and NaHCO3 were put into practice and evaluated.After the solar photo-Fenton process, chemical oxygen demand and total phenolic compounds decreased by 48–91 % and 45–96 %, respectively, with a relatively short illumination time. With the subsequent physicochemical treatment performed after photo-Fenton process, the minimum thresholds of reductions increase by more than 25 % with respect to the application of only photo-Fenton treatment: increase of 48 %–75 % reduction for chemical oxygen demand and 45 %–75 % removal for total phenolic compounds. Therefore, costs savings were achieved by avoiding more sophisticated treatments.

A New Strategy for the Treatment of Old Corrugated Container Pulping Wastewater by the Ozone-Catalyzed Polyurethane Sponge Biodegradation Process.

Old Corrugated Container (OCC) pulping wastewater has a complex organic composition and high levels of biotoxicity. The presence of dissolved and colloidal substances (DCSs) is a major limiting factor for pulp and paper companies to achieve closed-water recycling. In order to solve this problem, the coupled ozone-catalyzed oxidation and biodegradation (OCB) method was used to treat OCC pulping wastewater in this study. A polyurethane sponge was used as the basic skeleton, loaded with nano TiO2 and microorganisms, respectively, and then put into a reactor. After an 8-min ozone-catalyzed oxidation reaction, a 10-h biological reaction was carried out. The process was effective in removing organic pollutants such as COD and BOD5 from OCC paper whitewater. The removal rates of COD and BOD5 were 81.5% and 85.1%, respectively. By using the polyurethane sponge to construct a microenvironment suitable for microbial growth and metabolism, this study successfully applied and optimized engineered bacteria-white rut fungi (WRF)-in the system to achieve practical degradation of OCC pulping wastewater. Meanwhile, the biocompatibility of different microbial communities on the polyurethane sponge was analyzed by examining the degradation performance of OCC pulping wastewater. The structure of microbial communities loaded on the polyurethane sponge was analyzed to understand the degradation mechanism and microbial reaction behavior. White-rot fungi (Phanerochaete) contributed more to the degradation of OCC wastewater, and new strains adapted to OCC wastewater degradation were generated.

Effects of PFAS on human liver transporters: implications for health outcomes.

Per- and polyfluoroalkyl substances (PFAS) have become internationally recognized over the past three decades as persistent organic pollutants used in the production of various consumer and industrial goods. Research efforts continue to gauge the risk that historically used, and newly produced, PFAS may cause to human health. Numerous studies report toxic effects of PFAS on the human liver as well as increased serum cholesterol levels in adults. A major concern with PFAS, also dubbed "forever chemicals", is that they accumulate in liver and kidney and persist in serum. The mechanisms responsible for their disposition and excretion in humans are poorly understood. A better understanding of the interaction of PFAS with liver transporters, as it pertains to the disposition of PFAS and other xenobiotics, could provide mechanistic insight into human health effects and guide efforts toward risk assessment of compounds in development. This review summarizes the current state of the literature on the emerging relationships (e.g., substrates, inhibitors, modulators of gene expression) between PFAS and specific hepatic transporters. The adaptive and toxicological responses of hepatocytes to PFAS that reveal linkages to pathologies and epidemiological findings are highlighted. The evidence suggests that our understanding of the molecular landscape of PFAS must improve to determine their impact on the expression and function of hepatocyte transporters that play a key role in PFAS or other xenobiotic disposition. From here, we can assess what role these changes may have in documented human health outcomes.

Sulfonated cobalt phthalocyanine/NH2-MIL-125 heterojunction modified electrospun nanofiber membrane for emulsion separation and PMS-photocatalysis synergistic degradation

Membrane technology for wastewater remediation has generated significant interest, however, the single functionality, dull wettability and easy fouling property of the membrane hinder its practical application. Herein, a self-cleaning and multi-use superwetting nanofiber membrane was prepared by electrospinning and subsequent spraying technique. The sulfonated cobalt phthalocyanine/NH2-MIL-125 (CoPcS/NMIL) heterojunction was uniformly enrobed over polyethylene terephthalate (PET) electrospun membrane derived from waste PET bottles. The unique CoPcS/NMIL heterojunction exhibited a dual driving effect in photocatalytic activity and membrane wettability. Therefore, the fabricated CoPcS/NMIL@PET composite membrane demonstrated its capability to address complex water pollution issues effectively. The composite membrane exhibited notable flux permeation ability (538–3180 L m−2 h−1) and achieved excellent separation efficiency of over 99 % for diverse oil-in-water emulsions under the gravity filtration condition. Notably, the membrane can efficiently deal with stubborn high-viscosity crude oil fouling profiting from the photocatalytic self-cleaning function. A high flux recovery ratio of 93.6 % and a low irreversible fouling resistance ratio of 6.4 % can be obtained after 30 min of visible light irradiation. Impressively, CoPcS/NMIL@PET membrane exhibited enhanced permeation flux, separation efficiency and self-cleaning capacity compared to NMIL@PET membrane. Meanwhile, the CoPcS/NMIL@PET-activated peroxomonosulfate (PMS) system exhibited extremely high degradation performance for RhB under visible light with the degradation efficiency of 98 % within 10 min, suggesting its potential in the rapid purification of water-soluble organic pollutants. In addition, the CoPcS/NMIL@PET membrane has good chemical stability and mechanical properties for potential long-term use. Moreover, the demulsification mechanism in oil-water separation and PMS-photocatalysis synergetic mechanism over the fabricated CoPcS/NMIL@PET membrane were also investigated in detail. The research offers a promising approach for the design and fabrication of novel nanofiber membranes that incorporate photosensitizers and MOFs functional surfaces to address the challenges associated with such wastewater treatment.

Solar-driven Bi6O5(OH)3(NO3)5(H2O)3/Bi2WO6 heterojunction for efficient degradation of organic pollutants: Insights into adsorption mechanism, charge transfer and degradation pathway

Actualizing controllable construction of efficient heterojunction nanocomposites remains a challenge in the field of photocatalytic water remediation, which can be got over through exploiting in-situ attachment approaches between different semiconductors. Based on this, we successfully fabricated a unique separable Z-scheme Bi6O5(OH)3(NO3)5(H2O)3/Bi2WO6 (BON/BW) nanoflowers by an in-situ growth strategy. The profitable photogenerated carriers transfer mediated by Z-scheme heterojunction greatly accelerated the generation of •O2– and •OH. The strong adsorption of 4-nitrophenols (4-NP) with parallel configuration on side Bi2WO6 in BON/BW nanocomposites also provides great convenience for subsequent degradation steps. By optimizing multiple steps in the photocatalytic reaction process, BON/BW showed far superior photodegradation performance compared to single components. The causes and consequences of 4-NP photodegradation were explored through LC-MS tests, theoretical calculations, and toxicity analysis, and a green and safe degradation pathway was proposed. More experiments have confirmed that the synthesized BON/BW composites also have excellent degradation ability against other pollutants under sunlight, demonstrating excellent universality. With any luck, the logical design of heterojunction photocatalysts for effective photocatalytic water remediation should be aided by this study.

Sensitizer created defective metal organic framework as a new platform for boosting visible-light photocatalysis of g-C3N4

We developed herein for the first time a sensitizer created defective MOF (SCD-MOF), simultaneously possessing sensitizers and defects as visible-light harvester and electron trapper, respectively, which can synergistically improve the visible-light photocatalysis of polymeric graphitic carbon nitride (g-C3N4). Based on this discovery, the resulting 5.0 wt% FeTCPP⊂UiO-66@g-C3N4 shows a significant 6.6 and 3.9 times improvement in catalytic efficiency compared with its parent materials of FeTCPP⊂UiO-66 and g-C3N4 in degrading organic pollutants. Moreover, it shows a 10.4 times enhancement in catalytic efficiency compared with commercial TiO2 (P25). Mechanism studies suggest that sensitizer molecules and defects in SCD-MOF can synergistically improve photocatalytic efficiency because of broadening the visible-light response and strengthening the charge carrier separation. This work illustrates a remarkably triple synergetic effect among visible-light harvester, electron/hole separator, and semiconductor and thus established SCD-MOF as a class of new platform to greatly improve the visible-light photocatalytic performance of conventional semiconductors.

Bifunctional titanium boron-phosphate glass containing Ag nanoparticles for the detection and photocatalysis of organic compounds

This study delves into the structural characterization of a composition comprising Ag-NPs/phosphate plasmonic glass. Additionally, it explores two applications aimed at addressing one of the numerous challenges facing the modern world. The continuous technological progress of society has led to the proliferation of chemicals in natural water sources, posing a significant threat to ecosystems due to their low concentrations, making them difficult to detect and remove. The findings presented herein showcase the potential of Ag-NPs/sodium/titanium-phosphate glasses as a promising solution for detecting and degrading organic pollutants in freshwater. To achieve this, Ag nanoparticles were integrated into the glass surface via the ion exchange method, followed by thermal treatment. Subsequently, the detection of crystal violet solutions, applied dropwise onto the sample surface, was successfully carried out using surface-enhanced Raman spectroscopy, reaching a detection limit as low as 10−6 M. Furthermore, the glass composition demonstrated heterogeneous photocatalytic properties for UV degradation of methylene blue, with enhanced photoactivity attributed to the presence of silver nanoparticles, resulting in a 111 % increase in the kinetic constant compared to unmodified glass. Thus, these newly developed Ag-NPs sodium titanium-phosphate glasses exhibit remarkable bifunctional capabilities, offering improved optical detection and efficient photodegradation of organic molecules.

MOF-derived CuO@CB@CF cathode for O2 activation to generate ROSs for efficient electro-Fenton-catalysis

The generation of reactive radicals by molecular oxygen activation has become an important advanced oxidation technique. The combination of highly active carbon materials and stable transition metal oxides can activate molecular oxygen to produce hydrogen peroxide and further produce active free radicals at the same time, which is an efficient way for the removal of organic pollutants by heterogeneous electro-Fenton (HEF) system. In this study, a novel metal organic framework (MOF) derived CuO-carbon black-carbon felt (CuO@CB@CF) composite catalytic electrode has been prepared, which can generate H2O2 efficiently by selective O2 reduction through two-electron pathway with high pollutant removal efficiency. By optimizing the calcination temperature of MOF and loading capacity, the MOF-derived CuO@CB@CF has demonstrated excellent performance as a HEF catalytic electrode. Meanwhile, the effects of applied voltage, pH value, electrode area and aeration conditions have been studied. The excellent performance of MOF-derived CuO@CB@CF provides new insights into the removal of organic pollutants through electro-Fenton processes of transition metal oxide and carbon-based catalysts.

High-performance internal circulation anaerobic granular sludge reactor for cattle slaughterhouse wastewater treatment and simultaneous biogas production

This research investigates the efficacy of a high-performance pilot-scale Internal Circulation Anaerobic Reactor inoculated with Granular Sludge (ICAGSR) for treating cattle slaughterhouse wastewater while concurrently generating biogas. The primary objective is to assess the efficiency and performance of ICAGSR in terms of organic pollutant removal and biogas production using granular anaerobic sludge. The research methodology entails operating the ICAGSR system under ambient conditions and systematically varying key parameters, including different Hydraulic Retention Times (HRTs) (24, 12, and 8 h) and Organic Loading Rates (OLRs) (3.3, 6.14, and 12.83 kg COD/m³. d). The study focuses on evaluating pollutants’ removal and biogas production rates. Results reveal that the ICAGSR system achieves exceptional removal efficiency for organic pollutants, with Chemical Oxygen Demand (COD) removal exceeding 74%, 67%, and 68% at HRTs of 24, 12, and 8 h, respectively. Furthermore, the system demonstrates stable and sustainable biogas production, maintaining average methane contents of 80%, 76%, and 72% throughout the experimental period. The successful operation of the ICAGSR system underscores its potential as a viable technology for treating cattle slaughterhouse wastewater and generating renewable biogas. In conclusion, this study contributes to wastewater treatment and renewable energy production by providing a comprehensive analysis of the ICAGSR system’s hydrodynamic properties. The research enhances our understanding of the system’s performance optimization under varying conditions, emphasizing the benefits of utilizing ICAGSR reactors with granular sludge as an effective and sustainable approach. Identifying current gaps, future research directions aim to further refine and broaden the application of ICAGSR technology in wastewater treatment and renewable energy initiatives.

The enhanced degradation of Bi4O5I2 photocatalyst to the various organic pollutants through the upconversion luminescence of Yb3+/Er3+

The types of pollutants in water environment are very complex, so it is very important to develop a photocatalyst that can have universal applicability to a variety of pollutants. In this study, Bi4O5I2 was modified by Yb3+ and Er3+ doping, and an efficient photocatalyst with upconversion luminescence was found. After heat treatment, the sample was transformed from BiOI to Bi4O5I2 (BI), and the crystallite size of BI was significantly reduced and the porosity increased, which provided more active sites for the photocatalytic reaction, and the photocatalytic performance of BI samples was greatly improved. Compared with Er3+ single doped samples (BIE), Yb3+ and Er3+ co-doping (BIYE) effectively promotes the photogenerated carrier migration. Under simulated sunlight, BiOI, BI, BIE and BIYE degraded 30.1%, 62.2%, 72.6% and 92.1% of RhB solution within 30 min of illumination, respectively. In addition, the degradation of MB, MO, carmine, phenol and TC by BIYE were also tested. The results show that BIYE has a good ability to degrade a variety of organic pollutants that are difficult to degrade. The results of photocurrent response test show that BIYE has a stable photocurrent response signal to near-infrared light, which means that BIYE can respond to near-infrared light. The upconversion luminescence of the sample was further investigated. The energy transfer between Yb3+ and Er3+ enhances the upconversion luminescence of Er3+, that is, the conversion of near-infrared light into visible light, which can be absorbed and utilized by Bi4O5I2 matrix. The degradation of RhB solution was tested under near-infrared conditions, and the results show that BIYE also has excellent photocatalytic ability under near-infrared light.

Ultrafast catalytic reduction of organic pollutants using ternary zinc–copper–nickel layered double hydroxide

Water is the utmost essential commodity for the support of life process in animals. In recent decades, rapid industrialization and uncontrolled agricultural practices have led to increased level of toxic pollutants in groundwater, including organic pollutants (dyes, nitroarene compounds, antibiotics, etc.), inorganic pollutants (heavy metals, nanoparticles, etc.), and pesticides, posing a serious threat to human health and the environment. Although various technologies such as adsorption, photocatalysis, reverse osmosis, filtration, sedimentation, flocculation, and precipitation are available for the elimination of toxic pollutants from wastewater, issues such as their cost and efficacy limit their usage. Recently, catalysis has been found to be the most effective approach since it exhibits significant capability to eliminate almost all the pollutants and offers the benefit of simple design and low initial cost. In the present study, ternary zinc–copper–nickel layered double hydroxide (ZnCuNi‐LDH) synthesized using facile acid hydrolysis method was employed as an efficacious heterogeneous catalyst for the reduction of NACs (para‐nitrophenol and para‐nitroaniline) and degradation of organic azo dyes (methyl orange, amaranth, and brilliant black). ZnCuNi‐LDH exhibited superior catalytic activity for the reduction of all five model pollutants with reduction efficiency of more than 95% within a short time span of 5 min. Therefore, keeping in view the layered structure, high specific surface area, and remarkable catalytic performance, ZnCuNi‐LDH holds immense potential for the large‐scale catalytic degradation of refractory pollutants.