Wastewater Treatment Methods Research Articles

Treated Wastewater by Selected Microalgae for Irrigation

Water is a major natural resource that supplies our demands in a precise manner. We must conserve and utilise every drop of water. Irrigation is considered the primary user of freshwater. Irrigation of land accounts for about 80% of overall freshwater usage. Reusing treated waste water could be an alternative method for increasing water resources. Many countries are using wastewater as an irrigation resource to meet urban demand and manage water scarcity. Microalgae-based water treatment is a viable bio refinery approach that promotes environmental and economic sustainability. Phycoremediation is a cost-effective, environmentally friendly, secure, and substitute method for wastewater treatment. In a polite lab experiment lasting 30 days, two microalgal strains Chlorella vulgaris and Trichormus variabilis were used as bioremediation agents for sewage water collected from Bahr El-Baqar, El- El-Sharkya Governorate, Egypt. The goal of the current study was to assess how inoculated microalgae (Chlorella vulgaris and Trichormus variabilis) contributed to the phycoremediation of sewage effluent, and then a pot experiment was conducted to test the water's potential for use in ornamental plant irrigation, due to decrease water consumption of fresh water. The study's findings revealed that sewage wastewater had a decrease in pH, electrical conductivity, total dissolved solids, phosphorous, potassium, ammonium, nitrate, biological oxygen demand, and chemical oxygen demand after 30 days of experimentation, some heavy metals were absorbed by both algal strains, while others were practically completely removed. Moreover, the treated waste water could be used for irrigation of ornamental plant.

Research on the Construction Technology of Intelligent Platform for Wastewater Treatment in Industrial Parks

With the rapid development of industrial parks, the problem of sewage and wastewater treatment is becoming increasingly prominent. This article focuses on the characteristics and needs of wastewater treatment in industrial parks, and conducts in-depth research on the construction technology of intelligent platforms for wastewater treatment. By analyzing the limitations of traditional wastewater treatment methods, the key technologies and construction elements of intelligent platforms are elaborated. Detailed introduction of the data architecture design, functional implementation, and application effects of the intelligent platform in practical cases. Finally, the future development direction of intelligent platform construction was discussed, providing new ideas and methods for the treatment of wastewater in industrial parks.

Sustainable Methylene Blue dye removal with activated carbon from Prosopis juliflora stem

This study addresses the environmental challenge posed by the invasive Prosopis juliflora plant by converting its stem into activated carbon for the adsorption of Methylene Blue dye from water. The goal is to create an effective and sustainable wastewater treatment solution. Prosopis juliflora stems were harvested, cleaned, dried, carbonized, and activated with zinc chloride to create Prosopis Juliflora Stem Activated Carbon. This activated carbon was characterized using Brunauer-Emmett-Teller surface area analysis, Fourier transform infrared spectroscopy, and scanning electron microscope imaging. Results revealed a significant surface area of 158.107 m2/g and the presence of functional groups essential for adsorption processes. Batch adsorption experiments were conducted to determine the efficiency of activated carbon in removing Methylene Blue dye at various dosages and contact times. The highest adsorption efficiencies were 73.5% at 80 min, 90.1% at 60 min, and 90.65% at 50 min for dosages of 80, 100, and 120 mg, respectively. These findings show that Prosopis Juliflora Stem Activated Carbon is highly effective at removing Methylene Blue dye, providing a cost-effective and environmentally friendly method of wastewater treatment.

Electrochemical Methods for Nutrient Removal in Wastewater: A Review of Advanced Electrode Materials, Processes, and Applications

In response to the increasing global water demand and the pressing environmental challenges posed by climate change, the development of advanced wastewater treatment processes has become essential. This study introduces novel electrochemical technologies and examines the scalability of industrial-scale electrooxidation (EO) methods for wastewater treatment, focusing on simplifying processes and reducing operational costs. Focusing on the effective removal of key nutrients, specifically nitrogen and phosphorus, from wastewater, this review highlights recent advancements in electrode materials and innovative designs, such as high-performance metal oxides and carbon-based electrodes, that enhance efficiency and sustainability. Additionally, a comprehensive discussion covers a range of electrochemical methods, including electrocoagulation and electrooxidation, each evaluated for their effectiveness in nutrient removal. Unlike previous studies, this review not only examines nutrient removal efficiency, but also assesses the industrial applicability of these technologies through case studies, demonstrating their potential in municipal and industrial wastewater contexts. By advancing durable and cost-effective electrode materials, this study emphasizes the potential of electrochemical wastewater treatment technologies to address global water quality issues and promote environmental sustainability. Future research directions are identified with a focus on overcoming current limitations, such as high operational costs and electrode degradation, and positioning electrochemical treatment as a promising solution for sustainable water resource management on a larger scale.

High-efficiency treatment of oily wastewater by photocatalytic in-situ Fenton oxidation under visible light

Oily wastewater poses a significant threat to environmental safety, and complex water environments have caused numerous disturbances in oil pollution treatment. Therefore, constructing composite systems is expected to improve oil pollution treatment efficiency. This study developed an efficient photocatalytic in-situ Fenton oxidation system, HTCC@ZnFe2O4/Ag3PO4 (HZFA), loaded onto polypropylene spheres (PP) for treating oily wastewater (diesel oil) in complex environments. The built-in electric field of HZFA promotes photogenerated carrier separation, enhancing photocatalytic effect. At a diesel concentration of 3.2 g/L, performance of HZFA degraded diesel in deionized water and artificial seawater (ASW) were 60.80 % and 52.62 %, respectively, much higher than a pure photocatalytic system (13.84 %). The dual system compensated for single system defects like instability and narrow application range, achieving 8 effective cycles in ASW. Experimental and computational results showed that high oxidation and reduction potentials in the dual system promoted hydrocarbon oxidative degradation and H2O2 production/activation. The amount of OH, O2−, and h+ produced in different environments is fundamental for the stabilization of catalytic degradation by HZFA. GC–MS and DFT analysis revealed potential oxidative chain-breaking processes for diesel components like alkanes, aromatics, alcohols, acids, aldehydes, and esters. This study offers a new method for green and efficient oily wastewater treatment, overcoming inherent defects of traditional Fenton, with broad application prospects.

Insights into sulfamethazine degradation by peroxymonosulfate activation using H2 reduced hematite in high-salinity wastewater: Performances and mechanisms

Sulfamethazine (SMT) is recognized as a persistent, bioaccumulate, and toxic antibiotic pollutant that is difficult to be completely eliminated through traditional wastewater treatment methods. Although advanced oxidation processes (AOPs) utilizing peroxymonosulfate (PMS) have demonstrated potential in degrading SMT, the lack of inexpensive and efficient PMS activators remains a significant obstacle for its practical application. In this study, we present the synthesis of a highly effective PMS activator, the naturally-occurring minerals-based material − H2– reduced hematite (HRH), on an industrial scale using a fluidized bed reactor. Impressively, within the PMS AOPs system, the synthesized HRH catalyst not only achieves 99.3 % degradation of SMT within 20 min, demonstrating a remarkable 10-fold increase in the degradation rate compared to pristine hematite, but also showcases excellent recyclability and durability. Additionally, this HRH/PMS system were proved to effectively remove SMT under high-salinity conditions. More importantly, through systematic characterization and theoretical calculations, an in-depth investigation into the primary activation mechanism and degradation pathway in this reaction process is provided. This work provided a highly feasible strategy for the application of natural mineral-based catalyst for the degradation of pollutants via PMS activation in high-salinity wastewater.

Resistome analysis of wastewater treatment plants in Agadir city, Morocco, using a metagenomics approach

Water scarcity has evolved into a pressing global issue, significantly impacting numerous regions worldwide. The use of treated wastewater stands out as a promising solution to this problem. However, the proliferation of various contaminants, primarily Antimicrobial Resistance Genes (ARGs), poses a significant challenge to its safe and sustainable use. In this study, we assessed the composition and abundance of 373 ARGs, corresponding to 31 different classes of antibiotics, in six wastewater treatment plants (WWTP) in Agadir city of Morocco. Influent and effluent samples were collected during the months of February and July in 2020, in addition to samples from the Atlantic Ocean. In total, 223 ARGs were uncovered, highlighting in particular resistance to aminoglycoside, macrolide lincosamide, beta-lactamase, chloramphenicol, sulfonamide, tetracycline, and other antibiotics. The mechanisms of action of these ARGs were mainly antibiotic inactivation, antibiotic target alteration, efflux pump and cellular protection. Mobile genetic elements (MGEs) were detected at high levels their co-occurrence with ARGs highlights their involvement in the acquisition and transmission of ARGs in microbial communities through horizontal gene transfer. While many wastewater treatment methods effectively reduce a large proportion of gene material and pathogens, a substantial fraction of ARGs and other contaminants persist in treated wastewater. This persistence poses potential risks to both human health and the environment, warranting the need of more effective treatment strategies.

Associative analysis of sludge microbiota and wastewater degradation efficacy within swine farm sludge systems

Industrial wastewater management is a significant global challenge. Sludge microbiota from swine farms may play a crucial role in enhancing wastewater treatment processes, thereby reducing water pollution from industrial activities. A deeper understanding of this complex community could lead to innovative approaches for improving wastewater treatment methods. Sludge samples were collected from the anaerobic, sedimentation, and thickening tanks of ten swine farms. The microbiota communities were analyzed using 16S rRNA full-length sequencing on the PacBio platform, with subsequent data analysis conducted on the QIIME2 platform utilizing the SILVA database. Compared to anaerobic and thickening tanks, the sedimentation tanks exhibited a unique profile of sludge microbiota, with higher abundances of the phyla Proteobacteria, Bacteroidota, and Caldatribacteriota. Additionally, sludges from farms already utilized in processing industrial water—specifically farms B, G, and J—contained higher concentrations of bacteria (>20 ng/μL), indicating the robustness of the bacterial load for practical industrial use. Furthermore, sludge from farms with higher alpha diversity, such as E, G, I, and J, exhibited enriched degradation profiles, including the degradation of aromatic compounds, polymers, industrial compounds, toluene, and vanillin. The farms were categorized based on wastewater ammonia nitrogen degradation levels, revealing a clustering effect of the microbiota from the sedimentation tanks in the Principal Coordinates Analysis (PCoA) plot. A higher relative abundance of the families Rhodocyclaceae, AKYH767, and Comamonadaceae, and a lower abundance of the families Anaerolineaceae and Christensenellaceae, were found in groups with high ammonia nitrogen reduction, suggesting potential targets for bioaugmentation strategies. In conclusion, this study underscores the critical role of microbial abundance, composition, and biodiversity in optimizing wastewater treatment and advocates for comprehensive microbiota analysis to identify suitable sludge for industrial applications.

On the Valorization of Olive Oil Pomace: A Sustainable Approach for Methylene Blue Removal from Aqueous Media.

Currently, industrial water pollution represents a significant global challenge, with the potential to adversely impact human health and the integrity of ecosystems. The continuous increase in global consumption has resulted in an exponential rise in the use of dyes, which have become one of the major water pollutants, causing significant environmental impacts. In order to address these concerns, a number of wastewater treatment methods have been developed, with a particular focus on physicochemical approaches, such as adsorption. The objective of this study is to investigate the potential of a bio-based material derived from olive oil pomace (OOP) as an environmentally friendly bio-adsorbent for the removal of methylene blue (MB), a cationic dye commonly found in textile effluents. The biobased material was initially characterized by determining the point of zero charge (pHpzc) and using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). Subsequently, a comprehensive analysis was conducted, evaluating the impact of specific physicochemical parameters on MB adsorption, which included a thorough examination of the kinetic and thermodynamic aspects. The adsorption process was characterized using Langmuir, Freundlich, Brunauer-Emmett-Teller (BET), and Dubinin Radushkevich (D-R) isotherms. The results suggest that the equilibrium of adsorption is achieved within ca. 200 min, following pseudo-second-order kinetics. The optimal conditions, including adsorbent mass, temperature, bulk pH, and dye concentration, yielded a maximum adsorption capacity of ca. 93% (i.e., 428 mg g-1) for a pomace concentration of 450 mg L-1. The results suggest a monolayer adsorption process with preferential electrostatic interactions between the dye and the pomace adsorbent. This is supported by the application of Langmuir, BET, Freundlich, and D-R isotherm models. The thermodynamic analysis indicates that the adsorption process is spontaneous and exothermic. This work presents a sustainable solution for mitigating MB contamination in wastewater streams while simultaneously valorizing OOP, an agricultural by-product that presents risks to human health and the environment. In conclusion, this approach offers an innovative ecological alternative to synthetic adsorbents.

Degradation of piroxicam and celecoxib from aqueous solution by high-energy electron beam as a Sustainable method

Non-steroidal anti-inflammatory drugs (NSAIDs) are one of the most commonly prescribed drugs that can reduce pain. This study aimed to measure the concentration of piroxicam and celecoxib in Iranian hospitals, as well as the effect of electron beam irradiation on the degradation of these pollutants in synthetic and real samples. The high-performance liquid chromatography (HPLC) was used to detect the residual analytes in the samples. The Response Surface Methodology (RSM) was used to design the experiment conditions that investigate the effect of electron beam irradiation on degradation of piroxicam and celecoxib from synthetic samples, and then according to the optimum condition, the experiments were carried out for real wastewater samples. The results of wastewater analysis shown that the mean concentration of PIRO and CELE were 6.32 ± 2.5 and 11.5 ± 3.2 μg/L, respectively. Also, the findings show that 98.98 % and 97.62 % of piroxicam and celecoxib was degraded, respectively, when the optimum conditions (pH = 4, electron beam irradiation = 8 kGy, and concentrations of 60 μg/L for piroxicam and 50 μg/L for celecoxib) were applied. Results show that the degradation rates of piroxicam and celecoxib in the real wastewater sample at optimum condition were 89.6 % and 84.25 %, respectively. So, electron beam irradiation is a long-lasting and promising method for removal emerging contaminants from wastewater, like non-steroidal anti-inflammatory drugs, that can't be removed by conventional wastewater treatment methods; so, it can be used in combination with conventional wastewater treatment methods.

Bio-inspired fabrication of Ag-ZnO nanoparticle decorated Nylon 11 nanofibers: Multifunctional membrane for environmental remediation

Traditional wastewater treatment methods using nanoparticles (NPs) encounter challenges with catalyst recovery. In this study, we fabricated a Nylon 11 nanofibrous membrane (NFM) via electrospinning and functionalized it with polydopamine (PDA) to immobilize Ag-ZnO NPs for photocatalytic degradation of organic pollutants. The Nylon 11 NFM was treated with a dopamine tris buffer solution for PDA coating, which facilitated mussel-inspired attachment of the ZnO NPs. These NPs served as a nucleation site for the biomimetic nucleation of Ag-ZnO NPs during the hydrothermal process. The synthesized composite membrane was characterized by various microscopic and spectroscopic techniques. The water contact angle decreased from 135° (Nylon 11 NFM) to 41° (PDA/Nylon 11 NFM) and the filtration efficiency improved 10 folds (from 15.92 Lm-2h−1 to 170.60 Lm−2 h−1) at ambient conditions. The Ag-ZnO/PDA/Nylon 11 NFM showed strong antimicrobial activity against different bacterial strains and excellent photocatalytic degradation for methyl orange with a rate constant of 0.0431 min−1, significantly surpassing other configurations. The membrane exhibited excellent stability, reusability and consistent photocatalytic efficiency over multiple cycles. It is easily recoverable from the reaction mixture, and suitable for repeated use, making it a promising candidate for environmental remediation due to its antibacterial properties, photocatalytic activity, enhanced filtration efficiency, and reusability.

Enhanced degradation of Procion Red MX-5B using Fe-doped corn cob ash and Fe-doped g-C3N4

ABSTRACT Procion Red MX-5B (PRM) is harmful to both human health and the environment, and it is resistant to degradation through conventional wastewater treatment methods. In this study, solar-Fenton-like oxidation was used to treat it, employing Fe-doped corn cob ash and Fe-doped g-C₃N₄ (CN) photocatalysts. First, a characterization study (SEM, XRD, BET, PL, and XPS) was performed and its results proved that they were successfully synthesized and the most promising one was 20 wt. % Fe containing Fe/g-C3N4 ;(%20FeCN). Then, the influence of reaction parameters was studied and the optimal conditions were determined to be 0.2 g/L of %20FeCN, 10 mm of HPC, and pH = 3. At these reaction conditions, complete degradation of PRM was observed. Lastly, a kinetic study was performed and the reaction was found to follow the first-order kinetics, with an activation energy calculated to be 40.88 kJ/mol. This suggests that the 20% FeCN catalyst is highly effective and holds great promise for PRM degradation.

Removal of Methylene Blue from Aqueous Solution through Adsorption and Heterogeneous Fenton Reaction using Iron Oxides Produced by Different Methods

Direct discharge of industrial wastewater containing dyes into water bodies has contributed to the scarcity of drinking water. As environmental legislation becomes stricter, it is increasingly important to develop efficient methods for wastewater treatment. Traditional methods are commonly costly and have limited efficiency. This study aimed to prepare iron oxides via different synthetic routes and evaluate the effect of synthesis method on the efficiency of these materials as adsorbents and heterogeneous Fenton catalysts for the removal of methylene blue from aqueous solution. Iron oxides were synthesized by non-hydrolytic sol–gel (NHSG) and co-precipitation (CP) methods, followed by hydrothermal treatment for different times. CP oxides demonstrated high efficiency in dye adsorption, particularly the sample subjected to hydrothermal treatment for 6 h (CP-R6). This sample achieved 94.04% removal in 120 min. NHSG materials, by contrast, were less effective. The CP series of materials showed superior catalytic performance in heterogeneous Fenton experiments, with CP-R6 reaching 98.79% decolorization in 240 min. X-ray diffraction analysis indicated that iron oxides were composed of crystalline hematite and maghemite. Scanning electron microscopy revealed that CP materials were more porous and homogeneous than NHSG materials. The results demonstrated the efficiency of the developed iron oxides in removing methylene blue via adsorption and heterogeneous Fenton degradation and clarified how synthesis method influences adsorptive and catalytic properties.

Constructing Stable Nitrogen-Rich Core-Shell CdS@MC for Photocatalytic Reduction of U(VI) in Air without Sacrificial Agent.

Photocatalytic reduction of uranium from U(VI) to U(IV) has been recognized as an effective treatment method for uranium wastewater. However, most photocatalysts have to be reduced under inert gas and sacrificial agent. Here, a class of nitrogen-rich core-shell photocatalysts (CdS@MC) with high stability was successfully prepared by modifying CdS with melamine and cyanuric chloride condensation. When the initial concentration of U(VI) was 100 mg/L and the solid-liquid ratio was 0.2 g/L, the removal of U(VI) by CdS@MC without sacrificial agent under air could reached 95%. The removal rate was still above 80% after five cycles with good stability and good removal rate of U(VI) at high salt concentration. CdS@MC not only efficiently generates electrons for photocatalytic reduction of U(VI), but also generates H2O2 from O2, which then reacts with uranyl ions to produce metastudtite. This study provides a new direction for the study of efficient uranium removal photocatalysts without sacrificial agent in air environment.

The role of TiO2 and gC3N4 bimetallic catalysts in boosting antibiotic resistance gene removal through photocatalyst assisted peroxone process

Antibiotics are extensively used in human medicine, aquaculture, and animal husbandry, leading to the release of antimicrobial resistance into the environment. This contributes to the rapid spread of antibiotic-resistant genes (ARGs), posing a significant threat to human health and aquatic ecosystems. Conventional wastewater treatment methods often fail to eliminate ARGs, prompting the adoption of advanced oxidation processes (AOPs) to address this growing risk. The study investigates the efficacy of visible light-driven photocatalytic systems utilizing two catalyst types (TiO2-Pd/Cu and g-C3N4-Pd/Cu), with a particular emphasis on their effectiveness in eliminating blaTEM, ermB, qnrS, tetM. intl1, 16 S rDNA and 23 S rDNA through photocatalytic ozonation and peroxone processes. Incorporating O3 into photocatalytic processes significantly enhances target removal efficiency, with the photocatalyst-assisted peroxone process emerging as the most effective AOP. The reemergence of targeted contaminants following treatment highlights the pivotal importance of AOPs and the meticulous selection of catalysts in ensuring sustained treatment efficacy. Furthermore, Polymerase Chain Reaction-Denaturing Gradient Gel Electrophoresis (PCR-DGGE) analysis reveals challenges in eradicating GC-rich bacteria with TiO2 and g-C3N4 processes, while slight differences in Cu/Pd loadings suggest g-C3N4-based ozonation improved antibacterial effectiveness. Terminal Restriction Fragment Length Polymorphism analysis highlights the efficacy of the photocatalyst-assisted peroxone process in treating diverse samples.

Non-radical oxidation driven by iron-based materials without energy assistance in wastewater treatment.

Chemical oxidation is extensively utilized to mitigate the impact of organic pollutants in wastewater. The non-radical oxidation driven by iron-based materials is noted for its environmental friendliness and resistance to wastewater matrix, and it is a promising approach for practical wastewater treatment. However, the complexity of heterogeneous systems and the diversity of evolutionary pathways make the mechanisms of non-radical oxidation driven by iron-based materials elusive. This work provides a systematic review of various non-radical oxidation systems driven by iron-based materials, including singlet oxygen (1O2), reactive iron species (RFeS), and interfacial electron transfer. The unique mechanisms by which iron-based materials activate different oxidants (ozone, hydrogen peroxide, persulfate, periodate, and peracetic acid) to produce non-radical oxidation are described. The roles of active sites and the unique structures of iron-based materials in facilitating non-radical oxidation are discussed. Commonly employed identification methods in wastewater treatment are compared, such as quenching, chemical probes, spectroscopy, mass spectrometry, and electrochemical testing. According to the process of iron-based materials driving non-radical oxidation to remove organic pollutants, the driving factors at different stages are summarized. Finally, challenges and countermeasures are proposed in terms of mechanism exploration, detection methods and practical applications of non-radical oxidation driven by iron-based materials. This work provides valuable insights for understanding and developing non-radical oxidation systems.

Sustainable Solutions for Industrial Wastewater Remediation by KBiFe2O5 Under Visible‐Light Irradiation

AbstractIndustrial wastewater poses a serious threat to human health and the environment. The rising demand for an easy, efficient, environment‐friendly, and cost‐effective method for wastewater treatment has paved the way for the photocatalytic degradation of wastewater. Organic dyes, which comprise a major portion of organic pollutants in industrial wastewater, are highly toxic and carcinogenic. The hydrothermal method, being economical, easily available, and environmentally friendly, is used to prepare the time‐varying KBiFe2O5 samples. KBiFe2O5 is a lead‐free (nonhazardous), low‐bandgap brownmillerite‐structured crystalline material that can use a wide range of solar spectrum. Their phase purity is also confirmed by powder X‐ray diffraction (XRD), UV–Vis diffuse reflectance spectrophotometer (UV–Vis DRS) is done to confirm the bandgap value and Fourier transform infrared (FTIR) spectroscopy is performed to identify the chemical bonds in the material. Degrading textile organic effluent methylene blue (MB) dye under visible light and comparing its photodegradation performance are conducted to investigate the synthesized samples’ photocatalytic properties. The photocatalytic activity is relatively enhanced by adding H2O2 in a precise amount. So, the synthesized samples effectively demonstrate photocatalytic behavior, which has been used for wastewater remediation purposes.

Research on the treatment and secondary fluid mixing technology for oil-containing drilling wastewater in gas fields

Drilling operations in oil and gas fields will generate a large amount of highly polluted and difficult to degrade drilling wastewater. Oil drilling wastewater mainly includes diluted drilling fluid mud, heavy metals and radioactive substances. At present, the treatment methods for oily drilling wastewater mainly include reinjection into the formation, recycling and discharge after standard treatment, but the treatment effect is not good. This article describes the treatment of oily drilling wastewater through wastewater oxidation, flocculation, mechanical dehydration, intermediate water oxidation, flocculation and filtration. The experimental results show that the RR of the wastewater can reach 93.50 %, the maximum oil recovery rate (ORR) can reach 89.56 %, the light transmittance (LT) of the purified water can reach 98.40 %, the suspended solids (SS) can be reduced to 46.12 mg/L, the HBO2- content can be reduced to 4.20 mg/L. The water quality meets the requirements of DB61/T 1248–2019. Indoor technology was used for on-site testing, and the lowest reduction rate (RR) and ORR after wastewater treatment were 87.64 % and 84.21 %, respectively. Comparing the cost of treating the same type of wastewater, the treatment cost of the process in this article can be reduced by 1.87 USD/m3, which has higher economic benefits.

Spent Tea Leaves as an Adsorbent Material: Preparation, Characterization, and Application

The adsorption of Congo Red (CR) on the surface of Spent Tea Leaves (STL) was evaluated in an aqueous system. The study was carried out for the establishment of a standard wastewater treatment method that would remove reactive dyes by employing spent tea leaves as a bio-adsorbent. The effect of various parameters like amount of adsorbent, contact time, concentration of dye, and pH on the adsorption was studied. The adsorption capacity was monitored with a UV-visible spectrophotometer. The maximum adsorption of dye was observed at adsorbent mass of 3.5g /100 mL, at 8×10-5 M CR concentration, at pH = 9.72 and 50 minutes of contact time. The experimental results suggest that the adsorption of CR on the surface of STL is an exothermic process. The adsorption of CR on STL is found to follow pseudo first order kinetics. Based on the findings, it’s feasible to draw the conclusion that spent tea leaves would be a better adsorbent for the removal of reactive dyes from the wastewater.

N vacancies and OH/C=O co-modified g-C3N4 photoactivated peroxymonosulfate for the degradation of tetracycline: Synergistic promotion effect between excitons and carriers

Activation of peroxymonosulfate (PMS) to generate reactive oxygen species (ROS) for pollutant degradation via metal-free photocatalysts is an important green wastewater treatment and remediation method, but the pathway for generating ROS via exciton effects in catalysts is often overlooked. In this study, OH/C=O co-modified N-defective rod-shaped carbon nitride (Nv-CN-O) was designed and synthesized by soft template and alkali hydrothermal method. In the Nv-CN-O/PMS/Light system, there was a synergistic degradation of tetracycline (TC) by carriers and excitons, with a degradation rate 2.15 times higher than that of CN/PMS/Light. N vacancies and OH/C=O enhanced the adsorption to PMS, accelerated the charge transfer process, and activated PMS to generate ·O2− dominated reactive species. The functional group OH/C=O promoted the production of triplet excitons that through the energy transfer pathway to promote the production of 1O2. Abundant ROS were involved in the TC degradation process, and three possible TC degradation pathways were proposed. Nv-CN-O has strong anti-interference ability in actual water bodies, shows a promoting effect on the degradation of TC, which has practical application potential.