Water Treatment Technologies Research Articles

Facile and controlled dual-step modification with enhanced anti-fouling performance in polyvinylidene fluoride membranes

Water scarcity and pollution pose significant challenges, necessitating advancements in water treatment technologies. Among various solutions, ultrafiltration membranes, especially those crafted from polyvinylidene fluoride (PVDF), are favored for their mechanical robustness and chemical stability. However, their practical application is often limited by severe membrane fouling due to the inherent hydrophobicity of PVDF. This project introduces a straightforward, controlled method to enhance the anti-fouling properties of PVDF membranes, utilizing a blend of cellulose acetate (CA). The process involves a two-step modification of hydrolysis followed by quaternization, effectively increasing hydroxyl group presence and facilitating subsequent chemical reactions. The optimized membranes achieve a dynamic water contact angle of 0° within 30 s and maintain an electroneutral surface at pH 7.1. With a mean pore size reduction from 28.6 nm to 23.9 nm and an impressive drop in the irreversible fouling ratio from 36.9 % to 0.3 %, these modifications markedly improve the anti-fouling performance. This research demonstrates significant potential for enhancing the functionality of PVDF ultrafiltration membranes through post-fabrication modifications, offering significant benefits for water treatment applications.

Experimental and theoretical exploration of bactericidal and photo-catalytical activities of hierarchically porous AuNRs@CuO nanocomposite

In this study, a novel binary nanocomposite consisting of CuO nanosheets functionalized with gold nanorods (AuNRs@CuO), was successfully prepared using a two-step synthetic procedure and further investigated via Density Functional Theory. The physicochemical properties of prepared nanomaterials were analysed using Fourier transform infrared spectroscopy, X-ray diffraction, Field emission scanning electron microscopy, High-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy confirming successful fabrication with improved surface properties. Experimental analyses, including antibacterial assays and morphological studies of bacterial cells demonstrates superior bactericidal properties of AuNRs@CuO nanocomposite compared to pristine CuO nanosheets. Furthermore, molecular docking score provide theoretical insights into the underlying mechanism governing the enhanced antibacterial activity, highlighting the favorable interaction with the bacterial cells. The synergistic effect of CuO nanosheets and AuNRs further improves the photocatalytic efficacy, culminating in a high-yield photocatalyst that achieves 98.7% degradation for Indigo carmine under Xenon lamp irradiation compared to 40.8% and 62.4% for AuNRs and CuO nanosheets alone. Improved charge separation and generation of H+ as major reactive oxygen species from the nanocomposite to Indigo carmine was revealed by radical scavenger activity and photoluminescence studies. After cycles of operation, the morphology and surface state of the photocatalyst remained unchanged, as investigated by FESEM and HRTEM analysis. The novelty of this study lies in the integration of AuNRs and CuO nanosheets as an efficient photocatalytic material for the remediation of toxic organic dyes in wastewater, presenting a promising advancement in sustainable water treatment technologies.

Nanoparticle-Mediated remediation of wastewater contaminants: An inclusive analysis of glyphosate, Congo red and methyl orange

New techniques in purification are called for because, currently pollutants found within the wastewater sources are known to have adverse effects of man health, agricultural productivity and industrial applications. The purpose of this research was to assess the efficiency of different synthesized NPs in the rteutal of glyphosate, Congo red and MO from aqueous solution using a glass column. To determine the concentration of these contaminants, two analytical techniques namely High-Performance Liquid Chromatography (HPLC) and UV–Visible spectrophotometry were used. The findings revealed that the community removal rates differed depending on nanoparticle type, treatment time and light intensity. Zinc oxide nanoparticles (ZONPs) were found to reduce the glyphosate concentration by 56.81 % under 100-watt light after 120 minutes. Iron oxide nanoparticles (IONPs) on the other hand were found to eliminate 62.63 % of glyphosate without the application of light for the same length of time, this figure rose to 87 % when 100-watt light was applied. ZONPs also decolourized 59 % Congo red after 4 h and the decolorization efficiency increased to 86 % when exposed to 30 watt light. Further, magnetic iron oxide nanoparticles (MIONPs) reduced MO by 23.81 % under 100-watt light for 120 minutes. This research demonstrates that NPs may have a future in regard to water treatment as agents which are efficient to high degree; and in part, the ZONPs are more effective in elimination of glyphosate while the IONPs may be better suited for the removal of Congo red. The evidence suggest that more attention should be paid to the characteristic of NPs, the treatment time, and the light intensity in case of employing the technology in water treatment.

Stainless Steel Mesh in Electrochemistry: Comprehensive Applications and Future Prospects.

Stainless steel mesh (SSM) has emerged as a cornerstone in electrochemical applications owing to its exemplary versatility, electrical conductivity, mechanical robustness, and corrosion resistance. This state-of-the-art review delves into the diverse roles of SSM across a spectrum of electrochemical domains, including energy conversion and storage devices, water treatment technologies, electrochemical sensors, and catalysis. We meticulously explore its deployment in supercapacitors, batteries, and fuel cells, highlighting its utility as a current collector, electrode, and separator. The review further discusses the critical significance of SSM in water treatment processes, emphasizing its efficacy in supporting membranes and facilitating electrocoagulation, as well as its novel uses in electrochemical sensing and catalysis, which include electrosynthesis and bioelectrochemistry. Each section delineates the recent advancements, identifies the inherent challenges, and suggests future directions for leveraging SSM in electrochemical technologies. This comprehensive review showcases the current state of knowledge and articulates the novel integration of SSM with emerging materials and technologies, thereby establishing a new paradigm for sustainable and efficient electrochemical applications. Through critical analysis and insightful recommendations, this review positions itself as a seminal contribution, paving the way for researchers and practitioners to harness the full potential of SSM in advancing the electrochemistry frontiers.

Conductive Polymer Hydrogel-Derived 3D Nanostructures for Energy and Environmental Electrocatalysis.

Renewable energy and advanced water treatment technologies hold profound significance for driving sustainable development in modern society. Given the environmental friendliness and high efficiency of electrocatalysis processes, great expectations are placed on their applications in energy and water-related fields. However, the electrocatalysis is limited by the selectivity, activity, and durability of the electrocatalytic reactions. Hydrogels, with their hierarchical porous structure, compositional and structural tunability, and ease of functionalization, are bringing surprising advances in advanced energy and environment. Hydrogel catalysts, inheriting the advantages of hydrogel materials, hold promise for achieving significant breakthroughs in electrochemical performance. Here, the latest advancements in energy and environmental electrocatalytic fields are summarized based on the 3D nanostructured hydrogel catalysts. In addition, future potentials and challenges of continuing research on hydrogel materials for energy and environment are discussed.

Supramolecular Chemistry of Polymer-Based Molecular Tweezers: A Minireview

Polymer-based molecular tweezers have emerged as a prominent research area due to their enhanced ability to form host–guest complexes, driven by advancements in their design and synthesis. The impact of the spacer structure on the tweezers is predominant. They can be rigid, flexible, and stimuli-responsive. Herein, a new generation of molecular tweezers is introduced as polymer-based molecular tweezers. The integration of molecular tweezers onto biopolymers has significantly expanded their potential applications, making them promising candidates, especially in drug delivery, owing to their biocompatibility, adaptive structural features, and versatile interaction capabilities. The unique structure of polymer-based molecular tweezers, particularly when integrated with biopolymers, creates a unique nano-environment that enhances their interaction with guest molecules. This minireview focuses on the synthesis and applications of polymer-based molecular tweezers and examines how the incorporation of various spacers affects their binding affinity and specificity. These features highlight the advancement of these polymer-based systems, emphasizing their potential applications, particularly in drug delivery, water treatment technology, and future research opportunities.

Understanding the Selective Removal of Perfluoroalkyl and Polyfluoroalkyl Substances via Fluorine-Fluorine Interactions: A Critical Review.

As regulatory standards for per- and polyfluoroalkyl substances (PFAS) become increasingly stringent, innovative water treatment technologies are urgently demanded for effective PFAS removal. Reported sorbents often exhibit limited affinity for PFAS and are frequently hindered by competitive background substances. Recently, fluorinated sorbents (abbreviated as fluorosorbents) have emerged as a potent solution by leveraging fluorine-fluorine (F···F) interactions to enhance selectivity and efficiency in PFAS removal. This review delves into the designs and applications of fluorosorbents, emphasizing how F···F interactions improve PFAS binding affinity. Specifically, the existence of F···F interactions results in removal efficiencies orders of magnitude higher than other counterpart sorbents, particularly under competitive conditions. Furthermore, we provide a detailed analysis of the fundamental principles underlying F···F interactions and elucidate their synergistic effects with other sorption forces, which contribute to the enhanced efficacy and selectivity. Subsequently, we examine various fluorosorbents and their synthesis and fluorination techniques, underscore the importance of accurately characterizing F···F interactions through advanced analytical methods, and emphasize the significance of this interaction in developing selective sorbents. Finally, we discuss challenges and opportunities associated with employing advanced techniques to guide the design of selective sorbents and advocate for further research in the development of sustainable and cost-effective treatment technologies leveraging F···F interactions.

A novel electrochemical membrane filtration system operated with periodical polarity reversal for efficient resource recovery from nickel nitrate laden industrial wastewater

The economical and efficient removal of nickel nitrate from industrial wastewater remains a challenge. Herein, we developed an innovative electrochemical membrane filtration system that used a periodic polarity reversal process to adjust the acid-base environment near membrane interface for the recovery of nickel (II) and ammonia. The Ru based electrocatalytic layer could boost the selective reduction of nitrate to ammonia by generating atomic hydrogen, resulting in the precipitation of Ni2+ by the increasing pH at the membrane interface. Then, the precipitation of Ni(OH)2 could be effectively stripped and collected under the periodic polarity reversal process. In-situ interfacial measurements demonstrated that the polarity reversal process enabled a reversible transformation between strongly acidic (pH < 2) and alkaline (pH > 13) environments within a 200 µm range at the membrane interface. In continuous flow operation treating real industrial wastewater containing 96.7 mg-N L−1 nitrate and 135.0 mg L−1 Ni2+, the system demonstrated the capability to achieve 92.5 ± 2.6 % nitrate removal (with a recovery efficiency of 15.1 ± 1.9 g-NH3 kWh−1) and 99.7 ± 0.1 % Ni²⁺ removal (with a recovery efficiency of 24.9 ± 2.4 g-Ni kWh−1). Additionally, the specific treatment cost was approximately $0.17 m−3, attributed to the recovery of Ni(OH)₂ and ammonia. Furthermore, this system could deliver a significant economic benefit ($1.64 per m3) for treating a high concentration real wastewater (331.5 mg-N L−1 nitrate and 1496.3 mg L−1 Ni2+), outperforming traditional alkali precipitation and biological nitrification/denitrification processes. Overall, our study presents an economical and sustainable method for recovering valuable chemicals from wastewater containing heavy metals and inorganic nitrogen, potentially advancing cost-effective water treatment technologies.

Scaling-up the use of macroscopic photo-CWPO La1-xTixFeO3/SiC alveolar foam catalyst for solar water treatment against micropollutants

Current wastewater treatment plants are not prepared for the removal of micropollutants like phenol, pharmaceuticals and pesticides in water. As their release into the environment has adverse consequences towards the living organisms of ecosystems, the engineering of novel sustainable processes able to ultimately remove the emerging organic contaminants is an objective of paramount importance. Hereby we report for the first time on the successful scale-up of a macroscopic photo-CWPO La1-xTixFeO3/SiC alveolar foam catalyst used at the pilot-plant scale inside a Compound Parabolic Collectors based photoreactor. The removal of a span of organic micropollutants in water matrices of different complexity was efficiently realized under natural solar radiation using H2O2 or persulfates as oxidizing agent. The water matrix composition affected the efficiency of the degradation process. Using H2O2, for a collected energy of ca. 27 KJ/mol, the rate of micropollutant removal ranged from 53 % to 95 % in distilled water depending on the micropollutant in a cocktail configuration. It was lowered to the 17–66 % range in tap water, and to the 8–42 % range in simulated urban wastewater. The results demonstrated the promise of using sodium persulfate as oxidant instead of H2O2, with a better efficiency towards the removal of most of the micropollutants tested. The use of the sodium persulfate oxidant allows for overcoming the drawbacks associated to the treatment of real water matrices observed using H2O2, as better performances were reached when increasing the water matrix complexity. Complete removal of carbamazepine and diclofenac micropollutants was reached in tap water and simulated urban wastewater for ca. 27 KJ/mol of collected energy. The degradation performances combined to the catalyst robustness make this water treatment technology promising for operating in a continuous way under natural solar light.

A Mini Review on the Opportunities for Membrane Pervaporation Technology for Energy-efficient Removal of Dispersed Oil and Dissolved Hydrocarbons from Produced Water

Produced water is reported to have the largest volume of waste stream associated with hydrocarbon recovery. It was estimated to increase from 250 million B/D in 2007 to more than 300 million B/D between 2010 and 2012. Market research conducted by Adroit put the globally produced water treatment market at a value of USD 5.10 billion in 2022. This value is anticipated to be USD 9.80 billion in 2032 at a compound annual growth rate (CAGR) of 5.80% over the prediction period. Oil and gas companies have been mandated to comply with the newly enacted environmental regulations that require extensive treatment of this water before discharge or reuse. The limited quantity of freshwater resources coupled with the increasing oil and gas production activities has made it necessary for all stakeholders to look for sustainable management of this water. Presently, a certain percentage of produced water is reused while the rest is discharged into the ocean. In both cases, the water needs to be thoroughly treated. The choice of technologies for produced water treatment depends on numerous factors, such as the chemical composition of the water and the level of purity that must be attained before disposal, recycling, or re-use. Some of the technologies used for produced water treatment include physical separation methods such as gravity, adsorption, filtration, coalescence, cyclones, flotation, centrifuges, membranes, and oxidation. There are also chemical and biological separation methods. Contaminants such as small droplets of dispersed oil and dissolved hydrocarbons (DODHs) are very challenging to remove using the above-listed water treatment technologies. Moreover, the use of membrane technology has been limited only to the use of reverse osmosis and membrane filtration for removing salinity, metals, and other inorganics. This article highlights the opportunities for the use of membrane vapor permeation and pervaporation for the removal of the small droplets of DODHs, which have been reported to be very challenging contaminants to remove. The use of 3D printing technology for the fabrication of membrane materials was reviewed. The 3D membrane development method can be used to fabricate almost any shape of the material in a highly customized manner using computer-aided design. The information presented in this article will serve as a useful reference for the technologies used for a sustainable water treatment strategy in the oil and gas industry.

Synthesis of high-value porous carbon from waste plastics and structure regulation promote solar interface water evaporation

Water scarcity and waste plastics elimination are long-term problems facing sustainable development, and solar interface evaporation to produce clean water is regarded as a promising water treatment technology. Herein, we report on low-cost waste plastic bottles synthetic carbon-based photothermal materials. By KOH activation and perforation, the surface crack structure of porous carbon is formed to facilitate multi-stage reflection of solar light, and significantly improve the solar light absorbance and photothermal conversion ability. Three-dimensional solar evaporators with low thermal conductivity and super hydrophilic wood sponge are fabricated, and the rectangular hole is designed to regulate water movement and prevent heat dissipation. When exposed to 1 sun illumination (1 kW/m2), an evaporation rate of 1.59 kg·m-2·h-1 is achieved, along with an energy conversion efficiency of 88.49 %. In addition, different micro-surface rough structures are constructed to boost the solar light absorption, thereby enhancing the photothermal conversion ability, among which the micro-cone structure increased the evaporation rate to 1.93 kg·m−2·h−1, demonstrating excellent stability over 15 cycles. In the simulated sewage purification process, the removal rate of pollutants is 99.9 %, and the evaporator without obvious salt accumulation in the seawater for 24 h, showing good salt resistance and self-cleaning ability. This research has important reference value for high-value preparation of carbon-based photothermal materials from waste plastics, extraction of clean water and environmental sustainable protection.

Exploring of novel reverse thermally induced phase separation process based on preparation and characterization of polysulfate ultrafiltration membranes with bicontinuous structure

AbstractContaminated water sources from various industries pose severe environmental challenges due to their complex compositions, high toxicity, and fluctuating qualities. This study introduces a groundbreaking strategy for fabricating advanced polysulfate (PSE) ultrafiltration membranes using a novel reverse thermally induced phase separation (RTIPS) process. By manipulating the cloud point through the DMAc/DEG solvent/nonsolvent system, our work innovatively controls membrane microstructure, overcoming limitations of conventional nonsolvent‐induced phase separation (NIPS). Our findings reveal that RTIPS, when employed above the cloud point, yields PSE membranes with a unique bicontinuous sponge‐like structure, significantly improving upon conventional NIPS products. Specifically, the optimized RTIPS membranes exhibit enhanced pure water flux (916.23 vs. 336.23 LMH), larger pore sizes (0.083 vs. 0.054 μm), increased tensile strength (1.32 vs. 0.84 MPa), and improved fouling resistance (FRR 65.5% vs. 55.2%). This research pioneers a facile yet potent method for tailoring membrane properties, achieving a balance between permeability, mechanical stability, and filtration efficacy. The demonstrated success of RTIPS in enhancing PSE membrane performance not only contributes to the development of high‐performance water treatment technologies but also charts a new course in membrane science, offering a promising avenue for sustainable wastewater management solutions.

Life Cycle Impact Assessment (LCIA), A Decision Making Approach in Waste Water Treatment Plant: A Case Study

Environmental foot print of a waste water treatment plant is an important criterion to assess the performance of treatment unit. The novel waste water treatment technology was used to clean waste water up to a certain limit. Therefore, in whole process, beginning from electricity production to final disposal of water these treatment technologies can affect our environment. This environmental foot print can be determined by using CML 2000 guideline. In final performance of a waste water treatment plant environmental ill effects should also be incorporated instead of only using treatment efficiency, CML 2000 gives environmental performance. In this study four waste water treatment technologies namely Activated Sludge Process, up flow Anaerobic Sludge Blanket, Membrane Biofilm Bioreactor, Fluidized Aerobic Bed were taken. The environmental performance of all these novel technologies was assessed on the basis of eutrophication, global warming potential and removal efficiency, characterization factors are normalized by using CML 2000 guideline. The maximum and minimum results of Acidification was obtained as 0.2215 &amp; 0.0569 in UASB and FAB respectively. The maximum and minimum results of Eutrophication was attained as 0.564 &amp; 0.055 in MBBR and ASP respectively.

Which organic contaminants should be paid more attention: Based on an improved health risk assessment framework

The increasing chemical pollution of the drinking water is widely concerned. Large number of organic contaminants cannot be removed by conventional water treatment technology due to their low concentration, and long-term exposure may pose significant risks to human health. Which organic contaminants in drinking water should be given more attention has been a topic of great concern in recent years. To identify the organic contaminants that need attention, this research proposes an improved health risk screening method to quantitatively analyze the risks of accumulation, persistence, toxicity, and antibiotic resistance. Compared with conventional method, 26 compounds were added to the improved screening list, including 9 DBPs (e.g., NDMA), 3 antibiotics (e.g., oxytetracycline), PFNA and other compounds. Overall, antibiotics and plasticizers rose in the risk rankings. From the perspective of the proportion of total risk value, a single risk plays a decisive role (more than 99%) in the ranking. This change suggests that antibiotic resistance and the accumulation of organic matter are as important as their toxic risks to humans. 58 compounds were recommended for the priority control organic contaminants list in drinking water. This list provides the necessary information for authoritative regulations to monitor, control, assess, and manage the risks of environmentally relevant compounds in drinking water in China.

Real-time induced magnetic vibrational based antifouling mechanism for ultrafiltration (UF) membrane

Despite the widespread adoption of membrane technologies for efficient water treatment, membrane fouling remains a significant challenge, reducing separation efficiency, shortening lifespan, and increasing operational costs. Various studies have explored chemical membrane modifications to mitigate fouling, often resulting in adverse effects on flux and selectivity. Based on numerical modeling and experimental investigation, this work introduces real-time induced magnetic vibration as a sustainable approach for membrane antifouling without compromising permeability and selectivity. By preventing or delaying particle deposition on the membrane surface, magnetic vibration reduces fouling intensity. Experimental results demonstrated that different frequencies of magnetic vibration influenced the deposition of foulants (Humic Acid and Sodium Alginate) on the membrane surface. Notably, vibrating the membrane at 10 Hz with centrally attached iron particles led to a 22.4 % reduction in flux when treated with Humic Acid, compared to a 33.9 % reduction without vibration. Exposure to vibrations at the resonance frequency (5 Hz) for 6 h resulted in only a 10 % reduction in flux, effectively preventing the formation of a dense cake layer. Similarly, in the case of Sodium Alginate, a 10 Hz vibration for 2 h decreased the flux reduction from 21.4 % without vibration to 7.3 %, suggesting the preventive effect of vibration on aggregated SA deposition or facilitating continuous displacement for flux retention. Moreover, the study examined the influence of the configuration of iron particles attached to the membranes on the effectiveness of vibration. The study revealed that a striped configuration was more effective than a centralized configuration, owing to the distributed vibration effect across each part of the membrane. Furthermore, the fouling mechanism and rejection percentage were further investigated to enhance understanding of the fouling processes.

Strengthened ozone adsorption through positive electric field-induced charge migration on various TiO2 crystal surfaces: A mechanistic and theoretical study

This study investigates the enhancement of ozone adsorption on diverse TiO2 crystal interfaces through an innovative electrochemical modulation approach. The research focuses on the effects of applied electric field strength and reaction sites on ozone interfacial adsorption energies for Ti/Anatase TiO2 (0 0 1) and Ti/Rutile TiO2 (1 1 0) interfaces. The findings reveal that positive electric fields significantly enhance ozone adsorption on both interfaces, with adsorption energies increasing by up to 18% for Ti/Anatase TiO2 (0 0 1) and 15% for Ti/Rutile TiO2 (1 1 0). Notably, double water molecule sites (≡(H2O)2) play a crucial role in this enhancement process. The study demonstrates that the applied electric field alters the charge distribution at the TiO2 catalytic interface, thereby increasing interfacial charge density and promoting charge migration to ozone. Furthermore, this process leads to enhanced overlap and hybridization between ≡(H2O)2 sites and the s and p orbitals of ozone molecules, resulting in the formation of chemical bonds with lower Fermi levels. These comprehensive results demonstrate the broad applicability of the electrochemical interfacial ozone adsorption enhancement method across different crystal types and surfaces. Consequently, this study provides essential data to support the advancement of greener and more energy-efficient heterogeneous catalytic ozonation processes, potentially contributing to significant improvements in ozone-based water treatment technologies.

Photosensitive and high temperature resistant polyamide composite nanofiltration membranes with high flux and stable retention

Currently, most commercial membranes are used at temperatures below 50 °C. For high temperature water treatment, nanofiltration membranes with good thermal stability are highly sought after. In order to construct a novel polyamide thin-film composite nanofiltration (TFC NF) membrane, Congo red (CR) as monomer was introduced to the aqueous phase and the chemical structure of the selective layer was changed. Next, a thorough investigation was conducted into the impacts of the piperazine (PIP) to CR ratio on the surface morphology, separation efficiency and chemical structure of the membranes. The TFC NF membrane prepared after parameter optimization exhibited high retention (Na2SO4, >98 %) and flux up to 30 L·m−2·h−1·bar−1 at room temperature. Moreover, the Na2SO4 retention of the TFC NF membrane decreased by less than 1 % when used at 90 °C, demonstrating excellent heat resistance. Meanwhile, the incorporation of CR allowed the structure of the TFC NF membranes to be altered under UV irradiation conditions, which provided new insights into the optical modulation of the composite membrane properties. A promising and reproducible methodology for the development of high flux TFC NF membrane with thermal stability was offered, achieving a breakthrough in water treatment technology under high-temperature conditions.

Advanced membrane technologies for water treatment: utilization of nanomaterials and nanoparticles in membranes fabrication

Advanced membrane technologies for water treatment: utilization of nanomaterials and nanoparticles in membranes fabrication

Geochemical Insights into Heavy Metal Contamination and Health Hazards in Palar River Basin: A Pathway to Sustainable Solutions

The pollution of groundwater by heavy metals is becoming an increasingly urgent problem due to the rapid growth of industrialization and urbanization. A detailed geochemical investigation of physicochemical properties and heavy metal contamination was conducted on 140 groundwater samples in the Vellore district around the Palar River, Tamil Nadu, India, to assess the metal index risk in groundwater. The water quality is significantly contaminated with Cr, Co, Cu, Cd, and Fe, and moderately contaminated with Mn, Ni, and Zn, according to the groundwater assessment using the heavy metal index, contamination factor, and Igeo index. This contamination is associated with various health problems, including mental illness, stomach and skin cancer, liver failure, and kidney damage. Based on contour maps created with GIS, most of the region is heavily contaminated with heavy metals, rendering the groundwater unfit for human consumption. The Health Risk Assessment Index (HRAI) rose to 9028.6, indicating an extremely high health risk. In addition to identifying the extent of contamination, the study also proposes sustainable solutions to mitigate these risks. These include the adoption of advanced water treatment technologies, the promotion of green chemistry practices in local industries, the establishment of stricter regulatory frameworks, and the implementation of community-based water management strategies. These measures are essential to ensuring safe drinking water and achieving Sustainable Development Goal 6 (SDG 6). The findings underscore the urgent need for comprehensive monitoring and proactive remediation strategies in industrially contaminated regions.

Predominant Drinking Water Treatment Technologies in Urban Areas of Myanmar: Challenges and Solutions. A Review

Predominant Drinking Water Treatment Technologies in Urban Areas of Myanmar: Challenges and Solutions. A Review