Review
Frontiers in Environmental Engineering ·
Volume 5 - 2026 | https://doi.org/10.3389/fenve.2026.1847347
From conventional treatment to light-driven remediation: a review of strategies for treatment of dye-contaminated wastewater
- Aayushi1
- Shivam Pandey1*corresponding author
- Department of Chemistry, School of Applied and Life Sciences, Uttaranchal University, Dehradun, Uttarakhand, India
Abstract
Wastewater from textile and allied sectors offers nearly 15%–20% of global industrial water pollution, with dye concentrations generally ranging from 10 to 200 mg/L, making it a considerable environmental concern. Synthetic dyes are hazardous, prolonged, and toxic in nature. Conventional treatment procedures, such as physical, chemical, and biological processes, sometimes have issues, including being non-biodegradable, leading to secondary pollution such as sludge generation, production of toxic by-products, partial mineralization, and being cost-intensive. Photocatalysis has recently developed as an efficient advanced oxidation technique for dye degradation, employing semiconductor photocatalysts such as TiO 2, ZnO, and graphitic carbon nitride that are commonly used under light irradiation to produce reactive oxygen species that mineralize dyes into non-toxic byproducts. In comparison with conventional AOPs such as Fenton and ozonation, photocatalysis provides significant benefits, including lower chemical consumption, reduced sludge generation, catalyst reusability, and potential for solar-driven operation. The present review focuses on catalytic strategies, specifically on photocatalytic degradation of dyes, as a sustainable way for improving the environmental efficiency of textile processes. Major operational factors such as pH, catalyst loading, light intensity, and initial dye concentration are discussed in detail. The review highlights that advanced composite and immobilized photocatalysts demonstrate significantly upgraded degradation efficiency, enhanced charge separation, and better reusability as compared to single-component systems. Moreover, a comparative analysis of conventional and advanced treatment methods is presented, demonstrating that photocatalysis provides higher mineralization efficiency with reduced secondary pollution, making it a viable strategy for wastewater treatment.
Keywords
1 Introduction
The textile industry is one of the key contributors to water pollution due to the discharge of substantial quantities of dye-containing wastewater. These dyes possess complicated aromatic structures that grant high chemical stability, making them resistant to natural degradation processes (Armaković et al., 2022). Dyes are extensively used in textile, leather, paper, plastic, and cosmetic industries, and their complex aromatic structures impart high chemical stability and resistance to biodegradation (Wawrzkiewicz and Hubicki, 2015).
When dye-laden effluents are released into water systems, they block light, disrupt photosynthesis, and harm aquatic life and human health as these are toxic, mutagenic, and cancer-causing (Jabbar et al., 2024). Dyes provide water a strong color even at low levels, so removal of them is vital for the environment (Rauf and Ashraf, 2009). Biological procedure, adsorption, coagulation-flocculation, membrane filtration, and chemical oxidation are some of the usual ways to get dyes eliminated (Anwer et al., 2019). But these methods have problems like not breaking down completely, creating sludge, causing secondary pollution, and being expensive to run (Mirgane et al., 2020).
Photocatalysis has appeared as a transformative and sustainable technology for wastewater remediation due to its capability to achieve complete mineralization of organic pollutants under mild conditions. In contrast to conventional treatment methods, photocatalytic systems utilize semiconductor materials to harness solar or artificial light energy for the formation of highly reactive species such as hydroxyl radicals (•OH), enabling degradation of constant pollutants at the molecular level. Recent developments have demonstrated that photocatalysis can achieve degradation efficiencies exceeding 90% under optimized conditions, with slight sludge production and reduced secondary pollution. Moreover, the integration of visible-light-responsive and heterojunction photocatalysts has significantly increased solar utilization efficiency, making photocatalysis a promising candidate for large-scale and energy-efficient wastewater treatment applications (Shishir et al., 2025a).
Advanced oxidation processes have garnered considerable attention in recent times due to their ability to produce highly reactive radical species for the reduction of persistent organic pollutants (Zhang Q. et al., 2019). Among these processes, heterogeneous photocatalysis has emerged as an efficient and environmentally friendly approach for dye degradation in wastewater (Qasem et al., 2021). Photocatalytic degradation is based on the excitation of a semiconductor photocatalyst under light irradiation, resulting in the generation of electron–hole pairs. These photogenerated charge carriers initiate redox reactions leading to the formation of reactive oxygen species such as hydroxyl radicals and superoxide radicals (Park et al., 2015).
The generated reactive species are capable of oxidizing dye molecules and mineralizing them into simpler, non-toxic end products such as carbon dioxide and water. Semiconductor photocatalysts such as titanium dioxide (TiO2) and zinc oxide (ZnO) have been extensively investigated for dye degradation due to their high oxidative power, chemical stability, non-toxicity, and low cost (Pavel et al., 2023). TiO2 exists mainly in anatase, rutile, and brookite phases, among which anatase exhibits superior photocatalytic activity for dye degradation applications. ZnO has also demonstrated comparable photocatalytic efficiency and, in some cases, higher quantum efficiency than TiO2. Despite their advantages, the practical application of these photocatalysts is restricted due to rapid electron–hole recombination and limited utilization of visible light. Current studies have evidenced significant advancements in photocatalytic materials and reactor designs for dye degradation. For example, advanced heterojunction systems and nanocomposites have shown redefined visible-light activity and improved degradation efficiencies under real wastewater conditions (Kumari et al., 2024a; Kumari et al., 2025a; Kumari et al., 2024b; Kumari et al., 2025b; Kumari et al., 2023). These developments showcase the rising interest in sustainable and scalable photocatalytic technologies for environmental remediation. Compared to earlier reviews, this work provides a detailed analysis of conventional and advanced treatment techniques, with a particular focus on the adaptation of photocatalytic systems from single-component materials to advanced composite and immobilized structures, along with a consideration of operational parameters and scalability challenges.
2 Classifications of dyes
Based on their source of origin, dyes are typically classified as Natural and Synthetic dyes. Natural dyes are generally deemed less toxic; however, their safety depends on constituents and concentration, and some may still reveal environmental impacts. These are mainly derived from plants, animals, fungi or coloured ore-based sources. Indigo, betacyanin, curcumin, crocin, etc., are a few examples of natural dyes (Tan et al., 2018). Synthetic dyes are predominantly organic compounds; even so, certain dyeing processes may involve metal-based mordants or additives such as Pb, Hg, Cr, etc., that contribute to toxicity. (Alegbe and Uthman, 2024). Based on the type of fabric material on which the synthetic dyes are to be used, these are primarily classified into three distinct categories as seen in Figure 1 i.e.,. Cellulose fiber dyes, Protein fiber dyes and Synthetic fiber dyes (Singh, 2024b).

These are much more affordable than natural dyes and hence easily accepted by various industries. As some of these dyes contain heavy metal ions, these dyes cause a threat to the environment upon slipping into the food chain (Jarrar et al., 2024). For example, Blue 1, Red 40, Yellow 5, and Yellow six can potentially cause cancer in humans (Jarrar et al., 2024; Al-Hamdi et al., 2014; Hosseini et al., 2022; Fu et al., 2011). As a result, the removal of these materials is more worked upon when compared to their decomposition.
3 Methods for dye treatment
A variety of technologies have been employed for the efficient decolorization of dye-laden wastewater. Each treatment method possesses a unique operational approach; however, generally, the material interacts with the dye particles in the contaminated water, leading to a gradual reduction in dye concentration and the subsequent creation of clean water. At first, the decolorization process speeds up, then slows down, and finally stabilizes after a few minutes or hours. There are different ways through which dye-containing water can be treated, which are diagrammatically represented in Figure 2.

3.1 Adsorption and filtration
Adsorption is a widely used physical method for removing dye that relies on the binding of its molecules to a solid surface. Because they have a lot of surface area and can adsorb, carbon dioxide, zeolites, and other porous substances are often used as adsorbents (Khan et al., 2022). There are a number of things that impact the process, such as the adsorbent’s properties, the pH, the temperature, and the initial dye concentration. Adsorption may successfully decrease dye concentrations, making it ideal for both industrial and laboratory settings. Adjusted operational parameters help with problems like adsorbent regrowth and saturation (Al-Jabri et al., 2020). Whereas, in the process of filtering dye-containing water through an agent, the pigment particles are separated from the fluid phase. There are numerous methods to filter dye particles, depending on their size and type. Sand filtration captures dye particles within a sand bed (Althafiri, 2016); however, membrane filtration selectively isolates dye molecules from water through semi-permeable membranes with designated pore dimensions. The filtration process is based on the size of the dye molecules, the level of purification, and the parameters of the wastewater (Bhat et al., 2024). Such as activated carbon and biochar-based adsorbents have illustrated dye removal efficiencies exceeding 90% for methylene blue and congo red, although renewal and disposal of spent adsorbents remain significant challenges.
3.2 Sedimentation and photocatalysis
Sedimentation is the process that separates dye particles from water. It works by using gravity to settle the dye particles in a liquid (Carmen and Daniel, 2012). Larger, denser particles that have a tendency to sink to the bottom of a container are particularly well-suited for this technique because of their effectiveness. Coagulants or flocculants may be added to the mixture in order to improve particle aggregation and makes the sedimentation process more quickly. Sedimentation is an easy physical procedure; nevertheless, the effectiveness of this method is contingent on a number of parameters, including the size of the particles, the velocity at which they settle, and the presence of compounds that interfere with the process (Nguyen et al., 2018).
Photocatalysis is a complex physical method that speeds up the breakdown of dye molecules by using light-driven chemical reactions as seen in Figure 3. In this process, TiO2, also known as titanium dioxide, is a common photocatalyst (Bhat et al., 2024). When TiO2 is exposed to ultraviolet (UV) light, it makes reactive oxygen species (ROS) that speed up the breakdown of dye molecules into simpler, less harmful parts. Photocatalysis is very effective for organic dyes that do not respond well to other methods of treatment. Development in this field involves enhancing catalyst properties, light sources, and reactor designs to optimize the overall effectiveness of the photocatalytic process (Karimi-Maleh et al., 2020). Recent studies have reported that TiO2-based and g-C3N4-based photocatalysts can obtain degradation efficiencies above 85%–95% under optimized conditions, with nanocomposite systems showing improved performance due to strengthened charge separation and visible-light activity.

3.3 Electrochemical methods
Electrochemical techniques use an electric field or current to help dye ions move and be removed from water. For example, electrocoagulation makes use of electric current to destabilize charged particles, leading them to form aggregates that can be easily separated from the water (Tejero-Martin et al., 2019). Electrochemical technologies offer advantages such as ease of control, diminished chemical consumption, and the potential for metal recovery through electrodeposition. The effectiveness of the electric treatment is influenced by the choice of electrodes, voltage, and duration of the reaction (Zong et al., 2010).
3.4 Coagulation and flocculation
Flocculation and coagulation are chemical methods that use chemicals to group and destabilize dye particles, which makes it easier to get them out of water. Coagulants, such as aluminum sulfate (alum) or ferric chloride, cancel out the negative charges on dye particles. Polymers are the most common type of flocculant. They help bigger flocs stick together so that they can be easily separated from water. These technologies are widely used in industries that need to get rid of small, suspended particles, like dyes, quickly and effectively (Iwuozor, 2019). Coagulation and flocculation are used in municipal wastewater treatment plants and industries like textiles, paper, and tanneries. The effectiveness of coagulation and flocculation depends on factors like the type of dye, the pH, the temperature, and the amount of chemicals used. The best conditions are often different for each dye, so different strategies are needed. Residual coagulants and flocculants in treated water may pose challenges, underscoring the importance of effective post-treatment (Al-Hamdi et al., 2014).
3.5 Advanced oxidation processes (AOPs)
Advanced Oxidation Processes (AOPs) generate very reactive hydroxyl radicals (•OH) to break down and oxidize color molecules. Ozonation, Fenton’s reaction (Fe2+/H2O2), and photocatalysis using semiconductor materials like titanium dioxide (TiO2) activated by ultraviolet light are all common advanced oxidation processes (AOPs). AOPs are effective in treating stubborn and complicated dye compounds that do not respond to standard treatment methods (Hosseini et al., 2022). They are used to clean up industrial wastewater that has adamant dyes that will not go away easily. Advanced Oxidation Processes (AOPs) can use a lot of energy and make by-products, so they need to be carefully optimized. The efficiency depends on things like the type of dye, the setup of the reactor, and whether or not there are other organic or inorganic substances in the effluent (Fu et al., 2011). Advanced oxidation processes including Fenton and ozonation exhibit rapid dye degradation; however, they are linked with high chemical consumption, sludge generation, and operational costs, limiting their broad-scale application.
3.6 Biological treatment
Microorganisms are used in biological treatment methods to break down and degrade color compounds. Aerobic and anaerobic biodegradation are common methods. Microorganisms use oxygen to break down dyes in aerobic conditions, but they do not need oxygen to do so in anaerobic conditions. Biological treatment is particularly effective for the remediation of textile wastewater, which often contains complex dye chemicals (Chahal et al., 2022). Biological treatment methods involve constructed wetlands, activated sludge processes, and microbial fuel cells. Biological treatment may not work so well if the pH, temperature, or chemicals that stop it from working are present. The issues of slow degradation rates and the chance of biomass buildup are lessened by optimizing and making systems (Repeta et al., 2016).
Table 1 provides summary of biological catalytic methods for breaking down dyes using microorganisms and enzymes that are good for the environment. These methods let dyes change through metabolic and enzymatic pathways, but they get impacted by when they are used and usually take longer to work. Biological treatment methods are environmentally friendly; such as, their efficiency is frequently restricted to biodegradable dyes, and degradation rates are significantly lower rate compared to advanced oxidation processes.
TABLE 1. Catalytic degradation of dyes by biological methods.
| Biological method | Catalyst/Biological agent | Target Dye(s) | Degradation mechanism | Key outcomes | References |
|---|---|---|---|---|---|
| Bacterial degradation | Pseudomonas aeruginosa | Methylene Blue, Congo Red | Enzymatic reduction via azoreductase | High decolorization efficiency under aerobic conditions | Goodell et al. (2020) |
| Fungal degradation | Phanerochaete chrysosporium | Reactive Blue 19, Orange II | Ligninolytic enzymes (LiP, MnP, laccase) | Complete mineralization of complex dyes | Saggioro et al. (2016) |
| Algal degradation | Chlorella vulgaris | Methyl Orange | Biosorption followed by enzymatic breakdown | Eco-friendly and cost-effective process | Han et al. (2018) |
| Enzyme-based catalysis | Laccase (from white-rot fungi) | Acid Blue 25, Reactive Black 5 | Oxidative catalysis using oxygen as electron acceptor | Rapid dye oxidation at mild conditions | Zhang et al. (2019b) |
| Bacterial consortia | Mixed bacterial cultures | Azo dyes | Synergistic enzymatic action | Improved degradation compared to single strains | Zanon et al. (2011) |
| Immobilized enzymes | Immobilized peroxidase | Phenolic dyes | Catalytic oxidation | Enhanced stability and reusability | Mohamed and Awad (2021) |
| Yeast-based degradation | Saccharomyces cerevisiae | Basic dyes | Adsorption and enzymatic reduction | Moderate removal efficiency | Pavoković et al. (2020) |
| Plant-assisted biocatalysis | Horseradish peroxidase | Azo and anthraquinone dyes | H2O2-mediated catalytic oxidation | Efficient degradation at low enzyme dose | Harding, (2020) |
As soon as microorganisms break down dye compounds in an area with a lot of oxygen, rapid decay happens. Whenever bacteria are in the presence of oxygen, they use it to oxidize organic pollutants, which makes them into simpler and less harmful by-products (Thevarajah et al., 2005). Microorganisms that break out organic matter in the presence of oxygen include bacteria, fungi, and algae. Effluent from the textile and dyeing industries, which often contains azo dyes and other organic compounds, can be treated with aerobic methods. Dye properties, microbial activity, pH, and temperature are all things that can affect how well aerobic biodegradation works. Some dyes are very hard to break down, so they need more treatment (Xiao et al., 2018).
Anaerobic biodegradation is a type of process which uses bacteria that do well in low oxygen environments. It turns color molecules into simpler chemicals and methane. Anaerobic biodegradation can break down wastewater that has dyes that are hard to get rid of. It works well on azo dyes, which are hard to break down. Process optimization and system design deal with how fast anaerobic degradation happens and how fast intermediate metabolites build up, adding co-substrates and controlling ambient parameters are two important things (Huang et al., 2021c).
3.7 Chemical precipitation
Chemical precipitation involves using reagents that react with dye ions to make precipitates that do not dissolve. Common precipitants are sodium carbonate, sodium hydroxide, and lime (calcium hydroxide) (Hao et al., 2021). Chemical precipitation is a method to remove heavy metal ions and certain dyes out of wastewater. It is easy to separate the precipitates that are made by sedimentation or filtration. The effectiveness of chemical precipitation depends on factors such as the solubility of the precipitate, the pH, and the reaction’s stoichiometry. System optimization takes into consideration the need for careful pH control and the amount of sludge produced (Fatima et al., 2020).
3.8 Constructed wetlands and microbial fuel cells (MFCs)
It uses natural processes in man-made systems to clean up wastewater that contains dyes. Plants and microorganisms that live in wetlands are very important for breaking down dye compounds. The wetland matrix is a good place for microbial communities to live. Constructed wetlands can be used to treat many different kinds of dye pollutants, making them a flexible and long-lasting option for treatment. They are especially good for distributed treatment in small to medium-sized facilities. The effectiveness of built wetlands is influenced by variables including plant selection, hydraulic retention time, and the properties of dye pollutants (Abdel et al., 2008). MFCs not only clean wastewater, but they also use the metabolic activity of microorganisms to make electricity. Microbial oxidation of organic molecules, releases electrons that help make power. Microbial fuel cells can make electricity and clean up wastewater at the same time. They can be used in decentralized applications because they can handle wastewater with low to moderate amounts of organic pollutants. MFCs have issues with reactor design, power output, and for making their technology work on a larger scale (Sharma and Bhattacharya, 2016).
3.9 Sequential batch reactors (SBRs)
In this method, a single reactor goes through the fill, react, settle, and decant phases over and over again. Microorganisms get used to certain dye chemicals during the react phase, which helps them break down the dye chemicals in a natural way. SBRs can clean up a wide range of dye pollutants because they can be used in many different ways. They are often used in treatment plants that are small to medium-sized, and they can be changed to work in different conditions. Some of the problems with SBRs are that they need to be monitored from time to time, they may not always work as well as they should, and they need to be controlled. To solve these problems, people use monitoring and advanced control methods (Kushwaha et al., 2022).
Conventional treatment methods such as adsorption, coagulation, and biological degradation exhibit dye removal optimization levels ranging between 60% and 90%; however, these ways often fail to achieve complete mineralization and create secondary waste such as sludge. For example, adsorption using activated carbon can achieve removal efficiencies above 90% but requires regular regeneration and disposal of spent adsorbents. Likewise, coagulation–flocculation is cost-effective but generates significant sludge, increasing post-treatment costs. On the other hand, photocatalytic processes demonstrate mineralization efficiencies exceeding 90%–95% under optimized conditions, transforming dyes into CO2 and H2O without secondary pollution. This clearly shows the superiority of light-driven processes over conventional treatment techniques.
Table 2 shows that among different dye treatment technologies photocatalytic degradation has superior mineralization efficiency with minimal secondary pollution.
TABLE 2. Comparative analysis of dye treatment technologies.
| Treatment method | Working principle | Removal efficiency (%) | Mineralization efficiency (%) | Typical treatment time | Sludge/Secondary pollution | Operational cost | Limitations | Advantages | References |
|---|---|---|---|---|---|---|---|---|---|
| Adsorption | Physical/chemical binding of dyes onto porous materials (e.g., activated carbon, biochar) | 70%–95% | ∼0% (no degradation) | Minutes–hours | High (spent adsorbent disposal) | Medium | No mineralization; regeneration issues; secondary waste | Simple, fast, effective for low concentrations | Kushwaha et al. (2022) |
| Biological Treatment | Microbial degradation under aerobic/anaerobic conditions | 40%–80% | 20%–50% | Hours–days | Low–moderate (biomass generation) | Low | Ineffective for non-biodegradable dyes; slow kinetics | Eco-friendly, low energy requirement | Sun et al. (2019) |
| Coagulation–Flocculation | Charge neutralization and aggregation using coagulants (e.g., alum, FeCl3) | 60%–85% | <20% | Minutes | High (∼0.3–0.6 kg sludge per m3 wastewater) | Low | High sludge generation; incomplete removal | Cost-effective, widely used | Chen et al. (2017) |
| Membrane Filtration | Size-based separation (UF/NF/RO membranes) | 85%–99% | ∼0% | Minutes–hours | Low (but concentrated reject stream) | High | Membrane fouling; high pressure/energy requirement | High removal efficiency, compact system | Gu et al. (2019) |
| Electrochemical Methods | Redox reactions induced by electric current | 70%–95% | 50%–80% | Minutes–hours | Moderate (electrode sludge possible) | High | High energy consumption; electrode corrosion | Controlled operation, effective for complex dyes | Deng and Zhao (2015) |
| Fenton Process | Fe2+/H2O2 generates •OH radicals | 80%–95% | 50%–80% | Minutes–hours | High (iron sludge generation) | Medium–High | Sludge disposal; narrow pH range (∼3) | Strong oxidation capability | Li et al. (2019) |
| Ozonation | O3 oxidation producing reactive oxygen species | 80%–95% | 60%–85% | Minutes | Low–moderate | High | High energy cost; ozone instability | Rapid oxidation, no sludge formation | Akpomie and Conradie (2023) |
| Photocatalysis | Light-induced generation of electron–hole pairs producing ROS (•OH, •O2-) | 85%–99% | 90%–100% | 30–120 min | Minimal (negligible sludge) | Medium (low if solar-driven) | Electron–hole recombination; catalyst recovery (in slurry systems) | Complete mineralization; reusable catalyst; solar-driven; low secondary pollution | Shu et al. (2017) |
4 Parameters affecting photocatalytic dye degradation
Photocatalytic dye degradation is firmly dependent on several operational parameters, each exhibiting an optimum range for maximum degradation efficiency. The optimum pH typically lies between five and 8, depending on the type of dye and catalyst, ensuring favorable electrostatic interactions and enhanced adsorption. Photocatalyst incorporation is generally optimized in the range of 0.5–1.5 g/L, where adequate active sites are available without causing light scattering or particle aggregation. The beginning dye concentration is ideally maintained between 10 and 50 mg/L, as higher concentrations restrict light penetration and reduce degradation efficiency. Temperature shows a medium influence, with optimal performance usually observed around 25 °C–40 °C, while excessive temperatures may encourage recombination of charge carriers. Light intensity must also be carefully handled, as an increase enhances electron–hole generation up to an optimum level, after which recombination effects dominate and reduce efficiency.
4.1 Effect of pH and temperature
The pH significantly impacts photocatalytic activity by changing the surface charge of the catalyst, ionization of the dye, way the dye molecules stick together, and the placement of the band edges. Electrostatic interactions between dye molecules, catalyst surfaces, and produced radicals control how well adsorption and degradation work (Priya et al., 2021). In acidic environments, cationic dyes are electrostatically pushed away from semiconductor surfaces that have a positive charge. This makes them less likely to stick and break down. Higher pH levels may lead to better adsorption, but having too much surface area can make photoexcitation less effective and block light absorption. So, very high or very low pH levels usually make breakdown less effective (Zhao et al., 2022). Temperature has a very small effect on it in the middle range (20 °C–80 °C). A minor rise in the rate of decomposition could happen because molecules are moving around more and colliding with each other more often. At high temperatures, less dissolved oxygen and contaminants coming off the catalyst surface make it easier for electrons and holes to recombine, which lowers activity (Niu et al., 2019).
4.2 Effect of light intensity and visible light irradiation
The charge of photons and the strength of the radiation affect how quickly dyes break down. Increasing the intensity of light speeds up degradation at first because it makes more electron-hole pairs. Further increase after optimal level show little or no effect, or even a negative effect, because of recombination processes and heat effects (Etacheri et al., 2015). Light-sensitive catalysts and heterojunction devices that respond to visible light make it possible for dyes to break down in sunlight or low-energy light sources.
4.3 Effect of photocatalyst dosage and initial dye concentration
Higher the concentration of photographic catalyst improves dye degradation by giving the dye more active sites and charge carriers. On the other hand, too much catalyst loading causes light to scatter, particles to clump together, and the solution to become cloudy, all of which make it harder for photons to get through and lower the active surface area, which lowers degradation efficiency (Yusoff et al., 2021). Moderate dye concentrations facilitate photocatalytic degradation by allowing for effective adsorption and surface interactions. Too much dye covering at higher concentrations slows down degradation rates by blocking active sites, making it harder for light to get through, and causing unwanted sensitization effects (Krishnan et al., 2016).
4.4 Effect of electron acceptors and intermediate species
Electron-hole recombination makes photocatalytic effectiveness very low. Electron acceptors like dissolved oxygen, hydrogen peroxide, persulfate, or bromate improve degradation efficiency by suppressing recombination. It is done by scavenging photogenerated electrons and encouraging the production of reactive oxygen species (Somsesta et al., 2019). Inorganic anions can pick up reactive radicals and stop degradation, while oxidants speed it up. It is important to keep an eye on reaction pathways and by-products because some degradation intermediates may be more harmful than the original dyes (Sasaki et al., 2016).
4.5 Effect of inorganic ions and photocatalyst morphology
Inorganic ions can either help or stop photocatalytic destruction, depending on what kind they are and how many there are. Some anions slow down degradation by getting rid of radicals or blocking active sites, while others speed it up by encouraging charge transfer (Qasem et al., 2021). These effects are additionally affected by pH-dependent ion speciation. The catalyst’s shape is essential for breaking down dyes. A high surface area, the right amount of porosity, beneficial crystallinity, and certain exposed facets all help with mass transfer, charge separation, and adsorption, which all improve photocatalytic performance (Kumar et al., 2019).
4.6 Photocatalyst resistance to photo-corrosion
Photocorrosion affects the long-term efficiency and lifespan of catalysts, especially in semiconductors like ZnO. Material modification and doping can make things more stable by stopping metal ions from leaking out, but they can also change the band structure and lower photocatalytic performance (Enaime et al., 2020). One of the most important problems is still finding the right balance between stability and efficiency.
Generally, the optimization of these parameters is critical for achieving maximum photocatalytic efficiency, as even marginal deviations from optimal conditions can significantly affect degradation kinetics and mineralization efficiency.
5 Composition of photocatalysts
A number of photocatalytic materials have been looked into to see if they can break down dyes in wastewater. These materials include metals, metal oxides, carbon-based materials, electronic quantum dots, magnetic composites, and metal-organic frameworks (Wu et al., 2015). Metal oxide-based photocatalysts remain the most extensively studied due to their effectiveness, stability, and availability. There are three main types of photocatalysts based on how complex their structure is and how well they work (Serrà et al., 2019). Figure 4, shows evaluation of photocatalysis from first generation to third generation system.

5.1 First-generation photocatalysts
First-generation photocatalysts are made up of single-component metal oxides like TiO2, ZnO, ZrO2, SnO2, ZnS, CuO, and NiO. When exposed to UV or UV-visible light, their photocatalytic activity depends on making electron-hole pairs (Bantawal et al., 2020). TiO2 and ZnO are the most commonly used of these compounds because they are chemically stable, not very toxic, cheap, and can mineralize a wide range of dyes. The three main types of TiO2 are anatase, rutile, and brookite. Anatase is the best choice because it can hold more and is more effective at photocatalysis. ZnO is also very easy to recycle and works very well at breaking down dyes. First-generation photocatalysts work, but they have some big problems. For example, they have wide band gaps that need to be activated by UV light, electrons and holes recombine quickly, and they can only be used with certain types of dyes (Ani et al., 2018).
5.2 Second-generation photocatalysts
Second-generation photocatalysts were made to fix the problems with single-component systems. Most of the time, these materials are made up of many parts that make up homojunction or heterojunction structures. Junctions effectively separate charges by directing photogenerated electrons and holes into separate areas and stopping them from recombining (Abarca et al., 2023).
Heterojunction photocatalysts, which are made up of two or more semiconductors with different band structures, work better as catalysts, transfer charge better, and absorb light when exposed to visible light. Adding metals or nonmetals and combining them with carbon-based materials makes degradation more effective and makes the material more responsive to light (Gong et al., 2021). Still, there are problems with recovering treated water, making the process more complicated, and raising operating costs. Composite photocatalysts illustrate advanced performance compared to single-component systems due to enhanced charge separation, extended light absorption range, and reduced electron–hole recombination, which substantively improve photocatalytic efficiency. Moreover, immobilized photocatalyst systems provide practical advantages over conventional slurry systems, including easy recovery, improved reusability, and reduced post-treatment separation costs. However, slurry systems may provide better degradation efficiency due to greater surface area exposure, showing a trade-off between operational efficiency and practical applicability.
5.3 Third-generation photocatalysts
The aim of third-generation photocatalysts is to address the challenges of catalyst recovery and reusability in suspended systems. Most of the time, these photocatalysts are stuck to solid membranes or supports, like composite frameworks, floating substrates, or polymer matrices. Immobilization makes it easy to separate, regenerate, and keep things stable over time without significantly reducing photocatalytic activity. The use of floating photocatalysts is a big step forward because they improve the interaction between surfaces and contaminants and solar energy use without needing to be moved around. These systems show that they are good for treating large amounts of wastewater because they are very good at breaking down waste, are stable in structure, and are good for large-scale use. Third-generation photocatalysts are very promising for cleaning up the environment because they have a large surface area, collect light well, and are easy to recover (Anwer et al., 2019; Liu et al., 2016; Sellet et al., 2023; Chandrapal et al., 2022; Medina-RamÃRez and Hernández-RamÃRez, 2014).
Table 3 briefs the major application areas of photocatalytic dye degradation systems as well as their advantages.
TABLE 3. Commonly used catalyst and their advantages.
| Application area | Wastewater source | Common dyes treated | Photocatalyst system used | Key advantage | References |
|---|---|---|---|---|---|
| Textile wastewater treatment | Textile dyeing and finishing units | Methylene Blue, Reactive Black 5, Congo Red | TiO2, ZnO, doped metal oxides | Complete mineralization without sludge formation | Ajmal et al. (2014) |
| Industrial effluent remediation | Paper, leather, printing industries | Acid dyes, Direct dyes, Azo dyes | Metal oxide heterojunctions (TiO2/ZnO, ZnO/g-C3N4) | Effective degradation of recalcitrant dyes | Aina et al. (2025) |
| Solar-driven wastewater treatment | Decentralized treatment systems | Mixed dye pollutants | Visible-light-active photocatalysts | Energy-efficient and sustainable process | Vajnhandl (2022) |
| Hybrid AOP systems | Industrial wastewater | Persistent synthetic dyes | Photocatalysis + oxidants (H2O2/persulfate) | Enhanced degradation kinetics | Fu and Amjad (2019) |
| Membrane-assisted photocatalysis | Continuous flow reactors | Reactive and basic dyes | Immobilized photocatalyst membranes | Easy catalyst recovery and reuse | Zeitoun and Selem (2023) |
| Floating photocatalytic systems | Surface water bodies | Low-concentration dyes | Floating TiO2/ZnO composites | Improved solar utilization | Saeedi et al. (2025) |
| Reusable catalyst systems | Large-scale reactors | Multiple dye classes | Magnetic/immobilized photocatalysts | Long-term operational stability | Glažar and Simončič (2023) |
| Eco-remediation of water bodies | Rivers and lakes near industries | Mixed dye contaminants | Biochar-based photocatalytic composites | Environment-friendly remediation | Aina et al. (2025) |
Table 4 analyzes commonly reported photocatalysts based on their degradation efficiency, highlighting the high-quality performance of composite and supported systems under visible and solar light conditions.
TABLE 4. Comparative efficiency of photocatalysts for dye degradation.
| Photocatalyst | Dye | Light source | Degradation efficiency (%) | Time (min) | References |
|---|---|---|---|---|---|
| TiO2 (P25) | Methylene Blue | UV | 85%–90% | 60–120 | Karthik et al. (2024) |
| ZnO | Rhodamine B | UV | 80%–88% | 60–100 | Mallah et al. (2024) |
| g-C3N4 | Congo Red | Visible | 75%–85% | 90–150 | Ravichandran et al. (2024) |
| TiO2/g-C3N4 composite | Methylene Blue | Visible | 90%–95% | 60–90 | Prabakaran and Pillay (2025) |
| Biochar-supported TiO2 | Reactive Dyes | Solar | 85%–92% | 80–120 | De Rivas et al. (2011) |
| Ag–TiO2 | Rhodamine B | Visible | 92%–98% | 60–80 | Wang et al. (2010) |
| ZnO/Graphene | Methylene Blue | UV–Vis | 90%–96% | 50–90 | Zhao et al. (2015) |
| BiVO4 | Congo Red | Visible | 85%–92% | 90–120 | Xia et al. (2015) |
| Fe2O3/TiO2 | Reactive Dyes | Solar | 88%–94% | 80–110 | Eblagon and Tsang (2014) |
| CdS/g-C3N4 | Methylene Blue | Visible | 93%–97% | 60–110 | Saeed et al. (2024) |
6 Characterization techniques for photocatalysts
Photocatalysts are characterized using various techniques to recognize their structural, morphological, and optical properties. X-ray diffraction (XRD) is used to identify crystal structure, while scanning electron microscopy (SEM) and transmission electron microscopy (TEM) give morphological details. Brunauer–Emmett–Teller (BET) analysis evaluates surface area, and X-ray photoelectron spectroscopy (XPS) recognizes elemental composition and oxidation states. UV–Vis spectroscopy is used to evaluate optical absorption properties, while Fourier transform infrared spectroscopy (FTIR) identifies functional groups. These characterization techniques are important for correlating material properties with photocatalytic performance (Shishir et al., 2025b; Bayzid et al., 2025).
7 Challenges and future perspectives
In spite of significant advancements, photocatalytic dye degradation faces several challenges that restrict its large-scale application. One of the main limitations is the rapid recombination of photogenerated electron–hole pairs, which lowers efficiency. In addition, many conventional photocatalysts are only UV-active, restricting solar energy utilization. Catalyst recovery and stability, especially in slurry systems, also remain critical challenges. Moreover, the formation of intermediate by-products during degradation escalates concerns regarding toxicity and requires further investigation. Future research should target the development of visible-light-active and heterojunction photocatalysts with enhanced charge separation efficiency. The framework of immobilized and magnetic photocatalysts can address recovery and reusability issues. Integration of photocatalysis with other advanced oxidation processes and the operation of artificial intelligence for process optimization are emerging trends. Furthermore, pilot-scale studies and real wastewater treatment investigations are essential to bridge the gap between laboratory research and industrial application.
8 Conclusion
Chemically stable and toxic dyes are still very hard for the environment to get rid of from wastewater. Even though traditional methods are widely used, their flaws show that we need better and more effective methods. Photocatalytic degradation is a good option because it lets dye mineralization happen in a way that is safe for the environment. The performance of photocatalytic systems relies on their operational mechanisms and the characteristics of the catalyst, particularly metal oxide photocatalysts, which are crucial. New ways to change and fix catalysts have made them more stable, reusable, and better at using light. Photocatalytic systems need to keep getting better at being efficient and long-lasting if they are going to be useful for treating large amounts of wastewater. From an economic and sustainability perspective, photocatalysis provides benefits such as low chemical consumption, potential solar energy utilization, and reduced sludge generation, making it a favourable alternative for long-term wastewater treatment solutions.
Generative AI statement
The author(s) declared that generative AI was used in the creation of this manuscript. The authors used large language model, i.e., chatgpt to make images and for literature survey. The authors take full responsibility of the work.
Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Footnotes
Edited by: Jianhua Zhang, Victoria University, Australia
Reviewed by: Sheetal Kumari, Harbin Institute of Technology, China
Md. Khalid Hossain Shishir, Chittagong University of Engineering & Technology, Bangladesh
Statements
- Conflict of interest
The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
- Funding
The author(s) declared that financial support was not received for this work and/or its publication.
- Author contributions
Ayushi: Data curation, Investigation, Writing – original draft. SP: Conceptualization, Formal Analysis, Supervision, Writing – original draft, Writing – review and editing.
References
- Abarca J. A., Díaz-Sainz G., Merino-Garcia I., Irabien A., Albo J. (2023). Photoelectrochemical CO2 electrolyzers: from photoelectrode fabrication to reactor configuration. J. Energy Chem. 85, 455 – 480. doi:10.1016/j.jechem.2023.06.032
- Abdel A. A., Barakat M. A., Mohamed R. M. (2008). Electrophoreted Zn-TiO2-ZnO nanocomposite coating films for photocatalytic degradation of 2 chlorophenol. Appl. Surf. Sci. 254 (15), 4577 – 4583. doi:10.1016/j.apsusc.2008.01.049
- Aina A. R. N., Patel H., Aich S., Roy B., Samanta N. S., Pal B. (2025). Recent advances in ZnO-based photocatalysts for industrial dye degradation. Discov. Appl. Sci. 7, 977. doi:10.1007/s42452-025-07530-z
- Ajmal A., Majeed I., Malik R. N., Idriss H., Nadeem M. A. (2014). Principles and mechanisms of photocatalytic dye degradation on TiO 2 -based photocatalysts: a comparative overview. RSC Adv. 4, 37003 – 37026. doi:10.1039/C4RA06658H
- Akpomie K. G., Conradie J. (2023). Efficient adsorptive removal of paracetamol and thiazolyl blue from polluted water onto biosynthesized copper oxide nanoparticles. Sci. Rep. 13 (1), 859. doi:10.1038/s41598-023-28122-0
- Al-Hamdi A. M., Sillanpää M., Dutta J. (2014). Photocatalytic degradation of phenol in aqueous solution by rare earth-doped SnO2 nanoparticles. J. Mat. Sci. 49, 5151 – 5159. doi:10.1007/s10853-014-8223-2
- Al-Jabri H., Das P., Khan S., Thaher M., AbdulQuadir M. (2020). Treatment of wastewaters by microalgae and the potential applications of the produced biomass—A review. Water 13 (1), 27. doi:10.3390/w13010027
- Alegbe E. O., Uthman T. O. (2024). A review of history, properties, classification, applications and challenges of natural and synthetic dyes. Heliyon 10 (13), e33646. doi:10.1016/j.heliyon.2024.e33646
- Althafiri F. S. (2016). “ Treatment of endocrine disrupting chemicals using the downflow gas contractor reactor,” in University of Birmingham Institutional Research Archive (University of Birmingham). Available online at:.
- Ani I., Akpan U., Olutoye M., Hameed B. (2018). Photocatalytic degradation of pollutants in petroleum refinery wastewater by TiO2- and ZnO-based photocatalysts: recent development. J. Clean. Prod. 205, 930 – 954. doi:10.1016/j.jclepro.2018.08.189
- Anwer H., Mahmood A., Lee J., Kim K., Park J., Yip A. C. K. (2019). Photocatalysts for degradation of dyes in industrial effluents: opportunities and challenges. Nano Res. 12 (5), 955 – 972. doi:10.1007/s12274-019-2287-0
- Armaković S. J., Savanović M. M., Armaković S. (2022). Titanium dioxide as the most used photocatalyst for water purification: an overview. Catalysts 13 (1), 26. doi:10.3390/catal13010026
- Bantawal H., Shenoy U. S., Bhat D. K. (2020). Vanadium-Doped SrTiO3 Nanocubes: insight into role of vanadium in improving the photocatalytic activity. Appl. Surf. Sci. 513, 145858. doi:10.1016/j.apsusc.2020.145858
- Bayzid T., Shishir M. K. H., Akand M. S., Sohage M. S. P., Alam M. A., Karim M. M. (2025). Crystallographic analysis of silk sericin-stabilized zinc oxide nanoparticles with enhanced antimicrobial and photocatalytic properties. Inorg. Chem. Commun. 178, 114481. doi:10.1016/j.inoche.2025.114481
- Bhat S. A., Kumar V., Li F., Verma P., Egea-Corbacho A., Franco A. A. (2024). Detection and Treatment of Emerging Contaminants in Wastewater. IWA Publishing eBooks. doi:10.2166/9781789063752
- Carmen Z., Daniel S. (2012). “ Textile organic dyes – characteristics, polluting effects and separation/Elimination procedures from industrial effluents – a critical overview,” in Intech Ebooks. doi:10.5772/32373
- Chahal S., Phor L., Singh S., Singh A., Malik J., Goel P. (2022). An efficient and unique method for the growth of spindle-shaped Mg-doped cerium oxide nanorods for photodegradation of p-Nitrophenol. Ceram. Int. 48 (19), 28961 – 28968. doi:10.1016/j.ceramint.2022.04.145
- Chandrapal R. R., Bharathkumar S., Bakiyaraj G., Ganesh V., Archana J., Navaneethan M. (2022). Hydrothermally synthesized strontium-modified ZnO hierarchical nanostructured photocatalyst for second-generation fluoroquinolone degradation. Appl. Nanosci. 12 (6), 1869 – 1884. doi:10.1007/s13204-022-02414-9
- Chen L., Shi G., Shen J., Peng B., Zhang B., Wang Y. (2017). Ion sieving in graphene oxide membranes via cationic control of interlayer spacing. Nature 550 (7676), 380 – 383. doi:10.1038/nature24044
- De Rivas B., López-Fonseca R., Gutiérrez-Ortiz M. A., Gutiérrez-Ortiz J. I. (2011). Impact of induced chlorine-poisoning on the catalytic behaviour of Ce0.5Zr0.5O2 and Ce0.15Zr0.85O2 in the gas-phase oxidation of chlorinated VOCs. Appl. Catal. B Environ. 104 (3–4), 373 – 381. doi:10.1016/j.apcatb.2011.03.003
- Deng Y., Zhao R. (2015). Advanced Oxidation Processes (AOPs) in wastewater treatment. Curr. Pollut. Rep. 1 (3), 167 – 176. doi:10.1007/s40726-015-0015-z
- Eblagon K. M., Tsang S. (2014). Structure-reactivity relationship in catalytic hydrogenation of heterocyclic compounds over ruthenium black-part A: effect of substitution of pyrrole ring and side chain in N-heterocycles. Appl. Catal. B Environ. 160–161, 22 – 34. doi:10.1016/j.apcatb.2014.04.044
- Enaime G., Baçaoui A., Yaacoubi A., Lübken M. (2020). Biochar for wastewater Treatment—Conversion technologies and applications. Appl. Sci. 10 (10), 3492. doi:10.3390/app10103492
- Etacheri V., Di Valentin C., Schneider J., Bahnemann D., Pillai S. C. (2015). Visible-light activation of TiO2 photocatalysts: advances in theory and experiments. J. Photochem. Photobiol. C Photochem. Rev. 25, 1 – 29. doi:10.1016/j.jphotochemrev.2015.08.003
- Fatima R., Warsi M. F., Zulfiqar S., Ragab S. A., Shakir I., Sarwar M. I. (2020). Nanocrystalline transition metal oxides and their composites with reduced graphene oxide and carbon nanotubes for photocatalytic applications. Ceram. Int. 46 (10), 16480 – 16492. doi:10.1016/j.ceramint.2020.03.213
- Fu Y., Amjad Z. (2019). Combined photocatalytic and biological process for textile wastewater treatments. Water Environ. Fed. (WEF).
- Fu M., Li Y., Wu S., Lu P., Liu J., Dong F. (2011). Sol gel preparation and enhanced photocatalytic performance of Cu-doped ZnO nanoparticles. Appl. Surf. Sci. 258 (4), 1587 – 1591. doi:10.1016/J.APSUSC.2011.10.003
- Glažar D., Simončič B. (2023). TiO 2 and ZnO as advanced photocatalysts for effective dye degradation in textile wastewater. Tekstilec 66 (3), 178 – 198. doi:10.14502/tekstilec.66.2023045
- Gong E., Ali S., Hiragond C. B., Kim H. S., Powar N. S., Kim D. (2021). Solar fuels: research and development strategies to accelerate photocatalytic CO2 conversion into hydrocarbon fuels. Energy and Environ. Sci. 15 (3), 880 – 937. doi:10.1039/d1ee02714j
- Goodell B., Winandy J. E., Morrell J. J. (2020). Fungal degradation of wood: emerging data, new insights and changing perceptions. Coatings 10 (12), 1210. doi:10.3390/coatings10121210
- Gu T., Wang Y., Lu Y., Cheng L., Feng L., Zhang H. (2019). Platinum nanoparticles to enable electrodynamic therapy for effective cancer treatment. Adv. Mater. 31 (14), e1806803. doi:10.1002/adma.201806803
- Han L., Zhang H., Chen D., Li F. (2018). Protein‐Directed metal oxide nanoflakes with Tandem enzyme‐like characteristics: colorimetric glucose sensing based on One‐Pot Enzyme‐free Cascade catalysis. Adv. Funct. Mater. 28 (17), 1800018. doi:10.1002/adfm.201800018
- Hao M., Qiu M., Yang H., Hu B., Wang X. (2021). Recent advances on preparation and environmental applications of MOF-Derived carbons in catalysis. Sci. Total Environ. 760, 143333. doi:10.1016/j.scitotenv.2020.143333
- Harding T. (2020). “ A prototype dynamic model for the co-treatment of a high strength simple-organic industrial effluent and coal-mine drainage,” in Belarusian State Pedagogical University Repository (Belarusian State Pedagogical University). Available online at:.
- Hosseini Z. S., Haghparast F., Masoudi A. A., Mortezaali A. (2022). Enhanced visible photocatalytic performance of un-doped TiO2 nanoparticles thin films through modifying the substrate surface roughness. Mat. Chem. Phys. 279, 125530. doi:10.1016/J.MATCHEMPHYS.2021.125530
- Huang D., Zhang G., Yi J., Cheng M., Lai C., Xu P. (2021c). Progress and challenges of metal organic frameworks-based materials for SR-AOPs applications in water treatment. Chemosphere 263, 1 – 25. doi:10.1016/j.chemosphere.2020.127672
- Iwuozor K. O. (2019). Prospects and Challenges of Using coagulation-Flocculation method in the treatment of effluents. Adv. J. Chemistry-Section A, 105 – 127. doi:10.29088/sami/ajca.2019.2.105127
- Jabbar Z. H., Graimed B. H., Ammar S. H., Sabit D. A., Najim A. A., Radeef A. Y. (2024). The latest progress in the design and application of semiconductor photocatalysis systems for degradation of environmental pollutants in wastewater: mechanism insight and theoretical calculations. Mater. Sci. Semicond. Process. 173, 108153. doi:10.1016/j.mssp.2024.108153
- Jarrar R., Abbas M. K. G., Al-Ejji M. (2024). Environmental remediation and the efficacy of ceramic membranes in wastewater treatment—a review. Emergent Mater. 7 (4), 1295 – 1327. doi:10.1007/s42247-024-00687-0
- Karimi-Maleh H., Karimi F., Orooji Y., Mansouri G., Razmjou A., Aygun A. (2020). A new nickel-based co-crystal complex electrocatalyst amplified by NiO dope Pt nanostructure hybrid; a highly sensitive approach for determination of cysteamine in the presence of serotonin. Sci. Rep. 10 (1), 11699. doi:10.1038/s41598-020-68663-2
- Karthik A., Senthil S., Tamilselvi D., Rathinam R., Jeevanantham V. (2024). Nitrogen doped TIO2/g-C3N4 nanocatalyst for photodegradation of methylene blue dye. J. Indian Chem. Soc. 101 (11), 101424. doi:10.1016/j.jics.2024.101424
- Khan M., Ali S. W., Shahadat M., Sagadevan S. (2022). Applications of polyaniline-impregnated silica gel-based nanocomposites in wastewater treatment as an efficient adsorbent of some important organic dyes. Green Process. Synthesis 11 (1), 617 – 630. doi:10.1515/gps-2022-0063
- Krishnan J., Kishore A. A., Suresh A., Madhumeetha B., Prakash D. G. (2016). Effect of pH, inoculum dose and initial dye concentration on the removal of azo dye mixture under aerobic conditions. Int. Biodeterior. and Biodegrad. 119, 16 – 27. doi:10.1016/j.ibiod.2016.11.024
- Kumar V., Kumar P., Singh J. (2019). Contaminants in Agriculture and Environment: Health Risks and Remediation. Agro Environ Media - Agriculture and Ennvironmental Science Academy, 1 – 301. doi:10.26832/aesa-2019-cae
- Kumari S., Chowdhry J., Sharma P., Agarwal S., Garg M. C. (2023). Integrating artificial neural networks and response surface methodology for predictive modeling and mechanistic insights into the detoxification of hazardous MB and CV dyes using Saccharum officinarum L. biomass. Chemosphere 344, 140262. doi:10.1016/j.chemosphere.2023.140262
- Kumari S., Singh S., Lo S., Sharma P., Agarwal S., Garg M. C. (2024a). Machine learning and modelling approach for removing methylene blue from aqueous solutions: optimization, kinetics and thermodynamics studies. J. Taiwan Inst. Chem. Eng. 166, 105361. doi:10.1016/j.jtice.2024.105361
- Kumari S., Singh R., Jahangeer J., Garg M. C. (2024b). Innovative strategies for dye removal from textile wastewater: a comprehensive review of treatment approaches and challenges. Water Air and Soil Pollut. 235 (11), 720. doi:10.1007/s11270-024-07532-4
- Kumari S., Agarwal S., Kumar M., Sharma P., Kumar A., Hashem A. (2025a). An exploration of RSM, ANN, and ANFIS models for methylene blue dye adsorption using Oryza sativa straw biomass: a comparative approach. Sci. Rep. 15 (1), 2979. doi:10.1038/s41598-025-87274-3
- Kumari S., Chowdhry J., Uppaluri R. V., Patel P. K. (2025b). Chitosan-based materials: bridging the gap between pollutant removal and sustainability. Process Saf. Environ. Prot. 202, 107671. doi:10.1016/j.psep.2025.107671
- Kushwaha A., Goswami L., Singhvi M., Kim B. S. (2022). Biodegradation of poly(ethylene terephthalate): mechanistic insights, advances, and future innovative strategies. Chem. Eng. J. 457, 141230. doi:10.1016/j.cej.2022.141230
- Li X., Zhang W., Cui W., Li J., Sun Y., Jiang G. (2019). Reactant activation and photocatalysis mechanisms on Bi-metal@Bi2GeO5 with oxygen vacancies: a combined experimental and theoretical investigation. Chem. Eng. J. 370, 1366 – 1375. doi:10.1016/j.cej.2019.04.003
- Liu G., Zhao G., Zhou W., Liu Y., Pang H., Zhang H. (2016). In situ bond modulation of graphitic carbon nitride to construct p–n homojunctions for enhanced photocatalytic hydrogen production. Adv. Funct. Mater. 26 (37), 6822 – 6829. doi:10.1002/adfm.201602779
- Mallah A., Abdelrahman E. A., Raza N., Alqarni L. S., Ismail M., Modwi A. (2024). Boosting of photocatalytic degradation of malachite green dye on facile synthesized highly active Ca@TiO2@g-C3N4 photocatalyst: photocatalytic mechanism and kinetics. Inorg. Chem. Commun. 170, 113464. doi:10.1016/j.inoche.2024.113464
- Medina-RamÃRez I., Hernández-RamÃRez A. (2014). Photocatalytic Semiconductors. doi:10.1007/978-3-319-10999-
- Mirgane N. A., Shivankar V. S., Kotwal S. B., Wadhawa G. C., Sonawale M. C. (2020). Degradation of dyes using biologically synthesized zinc oxide nanoparticles. Mater. Today Proc. 37, 849 – 853. doi:10.1016/j.matpr.2020.06.037
- Mohamed E. F., Awad G. (2021). Hollow N-TiO2/MnO2 nanocomposite based yeast biomass for gaseous formaldehyde degradation under visible light. J. Industrial Eng. Chem. 98, 366 – 374. doi:10.1016/j.jiec.2021.03.028
- Nguyen C. H., Fu C., Juang R. (2018). Degradation of methylene blue and methyl orange by palladium-doped TiO2 photocatalysis for water reuse: efficiency and degradation pathways. J. Clean. Prod. 202, 413 – 427. doi:10.1016/j.jclepro.2018.08.110
- Niu L., Liu J., Liang X., Wang S., Lei A. (2019). Visible light-induced direct α C–H functionalization of alcohols. Nat. Commun. 10 (1), 467. doi:10.1038/s41467-019-08413-9
- Park H., Kim H., Moon G., Choi W. (2015). Photoinduced charge transfer processes in solar photocatalysis based on modified TiO2. Energy and Environ. Sci. 9 (2), 411 – 433. doi:10.1039/c5ee02575c
- Pavel M., Anastasescu C., State R., Vasile A., Papa F., Balint I. (2023). Photocatalytic degradation of organic and inorganic pollutants to harmless end products: assessment of practical application potential for water and air cleaning. Catalysts 13 (2), 380. doi:10.3390/catal13020380
- Pavoković D., Košpić K., Panić M., Redovniković I. R., Bubalo M. C. (2020). Natural deep eutectic solvents are viable solvents for plant cell culture-assisted stereoselective biocatalysis. Process Biochem. 93, 69 – 76. doi:10.1016/j.procbio.2020.03.020
- Prabakaran E., Pillay K. (2025). Silver and titanium oxides coated on G-C3N4 nanocomposite for photocatalytic degradation of mixture of brilliant Green-congo red dyes and ciprofloxacin antibiotic under visible light irradiation. Water Conservation Sci. Eng. 10 (1), 9. doi:10.1007/s41101-024-00323-2
- Priya, Naveen, Kaur K., Sidhu A. K. (2021). Green synthesis: an eco-friendly route for the synthesis of iron oxide nanoparticles. Front. Nanotechnol. 3, 655062. doi:10.3389/fnano.2021.655062
- Qasem N. a. A., Mohammed R. H., Lawal D. U. (2021). Removal of heavy metal ions from wastewater: a comprehensive and critical review. Npj Clean. Water 4 (1), 36. doi:10.1038/s41545-021-00127-0
- Rauf M., Ashraf S. S. (2009). Fundamental principles and application of heterogeneous photocatalytic degradation of dyes in solution. Chem. Eng. J. 151 (1–3), 10 – 18. doi:10.1016/j.cej.2009.02.026
- Ravichandran K., Suvathi S., Kavitha P., Kaleeswaran B., Vasuki M., Mahalakshmi G. (2024). Photocatalytic dye decomposition by bio-enzyme enriched TiO2/g-C3N4 nanocomposite and assessment of toxicity of resultant water using Catla catla fish. Biocatal. Agric. Biotechnol. 58, 103135. doi:10.1016/j.bcab.2024.103135
- Repeta D. J., Ferrón S., Sosa O. A., Johnson C. G., Repeta L. D., Acker M. (2016). Marine methane paradox explained by bacterial degradation of dissolved organic matter. Nat. Geosci. 9 (12), 884 – 887. doi:10.1038/ngeo2837
- Saeed M., Asghar H., Khan I., Akram N., Usman M. (2024). Synthesis of TiO2-g-C3N4 for efficient photocatalytic degradation of Congo Red dye. Catal. Today 447, 115154. doi:10.1016/j.cattod.2024.115154
- Saeedi S. N., Rasoulifard M. H., Dorraji M. S. S., Douroudgari H., Sehati N. (2025). Enhanced photocatalytic degradation of organic pollutants using a TiO 2 –clay nanocomposite in a rotary photoreactor with experimental and theoretical insights. Sci. Rep., 15 (1), 38193. doi:10.1038/s41598-025-22099-8
- Saggioro E. M., Oliveira A. S., Moreira J. C. (2016). Heterogeneous photocatalysis remediation of wastewater polluted by indigoid dyes. Text Wastewater Treat 93, 93 – 114. doi:10.5772/63790
- Sasaki S., Drummen G. P. C., Konishi G. (2016). Recent advances in twisted intramolecular charge transfer (TICT) fluorescence and related phenomena in materials chemistry. J. Mater. Chem. C 4 (14), 2731 – 2743. doi:10.1039/c5tc03933a
- Sellet N., Clement‐Comoy L., Elhabiri M., Cormier M., Goddard J. (2023). Second generation of near-infrared Cyanine‐Based photocatalysts for faster organic transformations. Chem. - a Eur. J. 29 (68), e202302353. doi:10.1002/chem.202302353
- Serrà A., Zhang Y., Sepúlveda B., Gómez E., Nogués J., Michler J. (2019). Highly active ZnO-based biomimetic fern-like microleaves for photocatalytic water decontamination using sunlight. Appl. Catal. B Environ. 248, 129 – 146. doi:10.1016/j.apcatb.2019.02.017
- Sharma S., Bhattacharya A. (2016). Drinking water contamination and treatment techniques. Appl. Water Sci. 7 (3), 1043 – 1067. doi:10.1007/s13201-016-0455-7
- Shishir M. K. H., Akand M. S., Maola M., Monira M. F., Rifat M., Sayeem N. R. (2025a). Photocatalytic removal of textile dyes: analytical strategies for post-degradation evaluation. Desalination 617, 119437. doi:10.1016/j.desal.2025.119437
- Shishir M. K. H., Alam M. A., Bishwas R. K., Karim M. M., Alam S. N., Khan G. M. A. (2025b). Crystallographic insights into copper oxide nanoparticles synthesized via a unique sol-gel method: antibacterial activity and photocatalytic evaluation. South Afr. J. Chem. Eng. 55, 162 – 179. doi:10.1016/j.sajce.2025.11.006
- Shu X., Zhang K., Zhang Q., Wang W. (2017). Response of soil physico-chemical properties to restoration approaches and submergence in the water level fluctuation zone of the danjiangkou Reservoir, China. Ecotoxicol. Environ. Saf. 145, 119 – 125. doi:10.1016/j.ecoenv.2017.07.023
- Singh P. (2024b). Dye Pollution from Textile Industry: Challenges and Opportunities for Sustainable Development. Springer.
- Somsesta N., Sricharoenchaikul V., Aht-Ong D. (2019). Adsorption removal of methylene blue onto activated carbon/cellulose biocomposite films: equilibrium and kinetic studies. Mater. Chem. Phys. 240, 122221. doi:10.1016/j.matchemphys.2019.122221
- Sun H., Jiao R., Xu H., An G., Wang D. (2019). The influence of particle size and concentration combined with pH on coagulation mechanisms. J. Environ. Sci. 82, 39 – 46. doi:10.1016/j.jes.2019.02.021
- Tan L. T., Chan K., Chan C. K., Khan T. M., Lee L., Goh B. (2018). Antioxidative potential of a streptomyces sp. MUM292 isolated from mangrove soil. BioMed Res. Int. 2018, 1 – 13. doi:10.1155/2018/4823126
- Tejero-Martin D., Rad M. R., McDonald A., Hussain T. (2019). Beyond traditional coatings: a review on thermal-sprayed functional and smart coatings. J. Therm. Spray Technol. 28 (4), 598 – 644. doi:10.1007/s11666-019-00857-1
- Thevarajah S., Huston T. L., Simmons R. M. (2005). A comparison of the adverse reactions associated with isosulfan blue versus methylene blue dye in sentinel lymph node biopsy for breast cancer. Am. J. Surg. 189, 236 – 239. doi:10.1016/J.AMJSURG.2004.06.042
- Vajnhandl S. (2022). Photocatalytic degradation of disperse azo dyes in textile wastewater using green zinc oxide nanoparticles: a critical review. J. Water Process Eng. 47, 102705. doi:10.1016/j.jwpe.2022.102705
- Wang K., Hu N., Xu G., Qi Y. (2010). Stable superhydrophobic composite coatings made from an aqueous dispersion of carbon nanotubes and a fluoropolymer. Carbon 49 (5), 1769 – 1774. doi:10.1016/j.carbon.2010.12.063
- Wawrzkiewicz M., Hubicki Z. (2015). “ Anion exchange resins as effective sorbents for removal of acid, reactive, and direct dyes from textile wastewaters,” in Intech Ebooks. doi:10.5772/60952
- Wu X., Liu C., Li X., Zhang X., Wang C., Liu Y. (2015). Effect of morphology on the photocatalytic activity of g-C3N4 photocatalysts under visible-light irradiation. Mater. Sci. Semicond. Process. 32, 76 – 81. doi:10.1016/j.mssp.2014.11.047
- Xia S., Yao L., Zhao Y., Li N., Zheng Y. (2015). Preparation of graphene oxide modified polyamide thin film composite membranes with improved hydrophilicity for natural organic matter removal. Chem. Eng. J. 280, 720 – 727. doi:10.1016/j.cej.2015.06.063
- Xiao C., Li J., Zhang G. (2018). Synthesis of stable burger-like a -Fe2O3 catalysts: formation mechanism and excellent photo-Fenton catalytic performance. J. Clean. Prod. 180, 550 – 559. doi:10.1016/j.jclepro.2018.01.127
- Yusoff N. R. N., Lim P. W., Azmi N. a. B., Yusoff M., Muhammad M. (2021). Effect of photocatalyst dosage and air loading in photocatalytic degradation of metamifop. IOP Conf. Ser. Earth Environ. Sci. 842 (1), 012061. doi:10.1088/1755-1315/842/1/012061
- Zanon N. C., Oliveira O. N., Caseli L. (2011). Immbolization of uricase enzyme in Langmuir and langmuir-blodgett films of fatty acids: possible use as a uric acid sensor. J. Colloid Interface Sci. 373 (1), 69 – 74. doi:10.1016/j.jcis.2011.07.095
- Zeitoun Z., Selem N. Y. (2023). A comprehensive review on textile wastewater treatment by coupling TiO 2 with PVDF membrane. Bull. Natl. Res. Centre 47, 153. doi:10.1186/s42269-023-01131-9
- Zhang Q., He D., Li X., Feng W., Lyu C., Zhang Y. (2019a). Mechanism and performance of singlet oxygen dominated peroxymonosulfate activation on CoOOH nanoparticles for 2,4-dichlorophenol degradation in water. J. Hazard. Mater. 384, 121350. doi:10.1016/j.jhazmat.2019.121350
- Zhang B., Li W., Guo Y., Zhang Z., Shi W., Cui F. (2019b). Microalgal-bacterial consortia: from interspecies interactions to biotechnological applications. Renew. Sustain. Energy Rev. 118, 109563. doi:10.1016/j.rser.2019.109563
- Zhao L., Gao M., Yue W., Jiang Y., Wang Y., Ren Y. (2015). Sandwich-structured Graphene-FE3O4@Carbon nanocomposites for High-Performance Lithium-Ion batteries. ACS Appl. Mater. and Interfaces 7 (18), 9709 – 9715. doi:10.1021/acsami.5b01503
- Zhao J., Wu Q., Tang Y., Zhou J., Guo H. (2022). Tannery wastewater treatment: conventional and promising processes, an updated 20-year review. J. Leather Sci. Eng. 4 (1), 10. doi:10.1186/s42825-022-00082-7
- Zong L., Ramanathan S., Chen C. (2010). Predicting thermophysical properties of Mono- and diglycerides with the chemical constituent fragment approach. Industrial and Eng. Chem. Res. 49 (11), 5479 – 5484. doi:10.1021/ie901948v
Citation
Aayushi, & Pandey, S. (2026). From conventional treatment to light-driven remediation: a review of strategies for treatment of dye-contaminated wastewater. Frontiers in Environmental Engineering, Volume 5. https://doi.org/
- Received
- Accepted
- Published
- Volume
- 5 - 2026
Copyright
Copyright © 2026 Aayushi and Pandey.
License: https://creativecommons.org/licenses/by/4.0/
*Correspondence: Shivam Pandey
Article metrics
- Views
- 0
- Downloads
- 0
- Citations
- 0
- Shares
- 0
