Organic Pollutants Research Articles

Seasonal Variation of Physicochemical Properties in the Lower River Benue, Nigeria

The study investigates the impact of seasonal changes on water quality in the River Benue, Nigeria. Conducted over eighteen months from January 2020 to June 2021, the research focuses on three locations: Ibi, Lau, and Mayo-Ranewo. Key physicochemical parameters such as temperature, pH, turbidity, conductivity, Biochemical Oxygen Demand (BOD), hardness, dissolved oxygen (DO), fluoride, and nitrate were measured to assess water quality. The findings reveal significant seasonal variations in these parameters, influenced by rainfall patterns, land use, and anthropogenic activities. Temperature ranged from 25.56°C to 30.70°C, remaining within acceptable limits for tropical waters, supporting stable biological processes. However, turbidity levels exceeded recommended values, indicating the presence of suspended solids that could impair water quality and harm aquatic life. Total dissolved solids (TDS) and conductivity showed potential contamination risks, likely due to agricultural runoff and urban discharges. Dissolved oxygen (DO) levels were generally adequate, especially during the wet season, enhancing oxygen content through increased photosynthetic activity and water inflows. However, BOD spiked with rainfall, signalling organic pollution and potential eutrophication risks. Seasonal shifts in pH and water hardness reflected changes in runoff and photosynthesis, with values largely within acceptable ranges for aquatic life. Fluoride and nitrate concentrations increased in the wet season, primarily due to agricultural runoff, highlighting the influence of land-based activities on water quality.

Aeration‐Free Photo‐Fenton‐Like Reaction Mediated by Heterojunction Photocatalyst toward Efficient Degradation of Organic Pollutants

The regulation of peroxymonosulfate (PMS) activation by photo‐assisted heterogeneous catalysis is under in‐depth investigation with potential as a replaceable advanced oxidation process in water purification, yet it remains a significant challenge. Herein, we demonstrate a strategy to construct polyethylene glycol (PEG) well‐coupled dual‐defect VO‐M‐Co3O4@CNx S‐scheme heterojunction to degrade organic pollutants without aeration, which dramatically provides abundant active sites, excellent photo‐thermal property, and distinct charge transport pathway for PMS activation. The degradation rate of VO‐M‐Co3O4@CNx in anaerobic conditions shows a higher efficient rate (4.58 min‐1 g‐2) than in aerobic conditions (1.67 min‐1 g‐2). Experimental evidence reveals that VO‐M‐Co3O4@CNx promotes more rapid redox conversion of photoexcited electrons induced by defects with PMS under anaerobic conditions compared to aerobic conditions. Additionally, in situ experiments and DFT provide mechanistic insights into the regulation pathway of PMS activation via synergistic defect‐induced electron, revealing the competitive effect between O2 and PMS over VO‐M‐Co3O4@CNx during the reaction process. The continuous flow reactor and flow cytometry results demonstrated that the VO‐M‐Co3O4@CNx/PMS/Vis system has remarkably enhanced stability and purification capability for removing organic pollutants. This work provides valuable insights into regulating the heterologous catalysis oxidation process without aeration through the photoexcitation synergistic PMS activation.

Aeration-Free Photo-Fenton-Like Reaction Mediated by Heterojunction Photocatalyst toward Efficient Degradation of Organic Pollutants.

The regulation of peroxymonosulfate (PMS) activation by photo-assisted heterogeneous catalysis is under in-depth investigation with potential as a replaceable advanced oxidation process in water purification, yet it remains a significant challenge. Herein, we demonstrate a strategy to construct polyethylene glycol (PEG) well-coupled dual-defect VO-M-Co3O4@CNx S-scheme heterojunction to degrade organic pollutants without aeration, which dramatically provides abundant active sites, excellent photo-thermal property, and distinct charge transport pathway for PMS activation. The degradation rate of VO-M-Co3O4@CNx in anaerobic conditions shows a higher efficient rate (4.58 min-1 g-2) than in aerobic conditions (1.67 min-1 g-2). Experimental evidence reveals that VO-M-Co3O4@CNx promotes more rapid redox conversion of photoexcited electrons induced by defects with PMS under anaerobic conditions compared to aerobic conditions. Additionally, in situ experiments and DFT provide mechanistic insights into the regulation pathway of PMS activation via synergistic defect-induced electron, revealing the competitive effect between O2 and PMS over VO-M-Co3O4@CNx during the reaction process. The continuous flow reactor and flow cytometry results demonstrated that the VO-M-Co3O4@CNx/PMS/Vis system has remarkably enhanced stability and purification capability for removing organic pollutants. This work provides valuable insights into regulating the heterologous catalysis oxidation process without aeration through the photoexcitation synergistic PMS activation.

In Situ Preparation of MnO2 on the Catechol/Silane-Coated Polypropylene Nonwoven Fabrics for Effective Removal of Cationic Dyes.

Previous studies have confirmed that MnOx removes heavy metal ions and organic pollutants from water with dual effects of adsorption and oxidation coupling, significantly improving the ability to remove impurities. Nanometal oxides have a highly reactive surface but tend to agglomerate during preparation and are challenging to recycle after use. A common method is to combine nano-MnO2 with Fe3O4 to prepare magnetic materials for easy recycling. Our previous research has confirmed that catechol (CA) and (3-aminopropyl) triethoxysilane (KH550) can be co-deposited on the surface of polypropylene nonwovens to form a stable CK coating under alkaline conditions. In addition, the coating has many active groups, including hydroxyl groups, amino groups, etc. This study further investigates the secondary reactivity of CK coatings. The coordination of catechol groups and metal ions was used to anchor manganese ions to the coating. Meanwhile, the hydroxyl and amino groups were used to reduce manganese ions to Mn4+ in situ to prepare PP-(CK-MnO2). We found that the sample had an excellent decolorization effect on cationic dyes but was limited to anionic dyes. The decolorization mechanism of cationic dyes was further discussed. The results showed that the decolorization of cationic dyes had a dual effect of adsorption and oxidative degradation. Under acidic conditions, its oxidation properties were enhanced. It can be used as a highly effective decolorizing agent for cationic dyes, and the decolorization behavior is consistent with the first-order kinetics. As the pH increases, its oxidation properties gradually decrease. Although the electrostatic adsorption effect was enhanced, the overall decolorization performance was significantly reduced. Recycling experiments have proved that it can maintain >90% removal rate after five cycles. This study also demonstrated that the CK coating has dopamine-like properties, which can coordinate with metal ions to prepare metal-organic hybrid materials.

Microwave-Assisted Synthesis of N, S Co-Doped Carbon Quantum Dots for Fluorescent Sensing of Fe(III) and Hydroquinone in Water and Cell Imaging

The detection of heavy metal ions and organic pollutants from water sources remains critical challenges due to their detrimental effects on human health and the environment. Herein, a nitrogen and sulfur co-doped carbon quantum dot (NS-CQDs) fluorescent sensor was developed using a microwave-assisted carbonization method for the detection of Fe3+ ions and hydroquinone (HQ) in aqueous solutions. NS-CQDs exhibit excellent optical properties, enabling sensitive detection of Fe3+ and HQ, with detection limits as low as 3.40 and 0.96 μM. Notably, with the alternating introduction of Fe3+ and HQ, NS-CQDs exhibit significant fluorescence (FL) quenching and recovery properties. Based on this property, a reliable “on-off-on” detection mechanism was established, enabling continuous and reversible detection of Fe3+ and HQ. Furthermore, the low cytotoxicity of NS-CQDs was confirmed through successful imaging of HeLa cells, indicating their potential for real-time intracellular detection of Fe3+ and HQ. This work not only provides a green and rapid synthesis strategy for CQDs but also highlights their versatility as fluorescent probes for environmental monitoring and bioimaging applications.

Cold Plasma for Enhanced Water Purification

Abstract Access to clean water remains a critical global challenge, with traditional water treatment methods often failing to eliminate complex pollutants such as pharmaceuticals, dyes, and antibiotics. Cold atmospheric plasma technology offers a promising solution by generating reactive oxygen and nitrogen species at room temperature, effectively degrading these contaminants and inactivating pathogens. Recent advancements in cold plasma have shown significant potential in water treatment applications. Cold plasma has demonstrated efficacy in disrupting bacterial biofilms, reducing antibiotic contaminants, and degrading complex organic pollutants, making it an innovative and eco-friendly alternative to conventional methods. This review examines the principles of plasma technology, evaluates its performance in water sanitation, and addresses the challenges of scalability and economic feasibility. By integrating cold plasma into existing water treatment systems and developing standardized protocols, this technology can significantly contribute to sustainable water management and public health, supporting the Sustainable Development Goals (SDGs).

Effects of Particle Shape and Surface Structure on the Adsorption Properties of Polystyrene Microplastics

Model spherical polystyrene particles are studied to understand the interactions of microplastics with organic pollutants. Analysis of the experimental results presented in the literature is complicated since researchers use different types and concentrations of particles, durations of tests, etc. In addition, there is little information on the effect of the structure of the surface layer of polystyrene particles on the processes under study, and the question of the effect of the shape of polystyrene particles remains open. Here, we present the first results of a model experiment to study the effect of the shape and structure of the surface layer of polystyrene microspheres and non-spherical particles of 2 to 5 μm in size on the sorption properties in relation to model molecules of rhodamine B as a model organic pollutant. The properties of both the initial model polystyrene particles and the modified ones were studied by optical, transmission electron, and atomic force microscopy, as well as using the Brunauer–Emmett–Teller method (BET). The sorption process was studied by spectrophotometry, and the analysis of sorption curves was carried out using the Langmuir model. It is shown that the shape of polystyrene model particles does not have a significant effect on the sorption capacity. At the same time, the sorption processes of rhodamine B molecules are determined by the structure of the surface layer, which can be changed, for example, by exposing the polystyrene microspheres to N,N′-dimethylformamide.

Machine Learning-Assisted Surface-Enhanced Raman Spectroscopy Detection for Environmental Applications: A Review.

Surface-enhanced Raman spectroscopy (SERS) has gained significant attention for its ability to detect environmental contaminants with high sensitivity and specificity. The cost-effectiveness and potential portability of the technique further enhance its appeal for widespread application. However, challenges such as the management of voluminous quantities of high-dimensional data, its capacity to detect low-concentration targets in the presence of environmental interferents, and the navigation of the complex relationships arising from overlapping spectral peaks have emerged. In response, there is a growing trend toward the use of machine learning (ML) approaches that encompass multivariate tools for effective SERS data analysis. This comprehensive review delves into the detailed steps needed to be considered when applying ML techniques for SERS analysis. Additionally, we explored a range of environmental applications where different ML tools were integrated with SERS for the detection of pathogens and (in)organic pollutants in environmental samples. We sought to comprehend the intricate considerations and benefits associated with ML in these contexts. Additionally, the review explores the future potential of synergizing SERS with ML for real-world applications.

Enhancing Manganese Peroxidase: Innovations in Genetic Modification, Screening Processes, and Sustainable Agricultural Applications.

Manganese peroxidase (MnP), a vital extracellular enzyme for the degradation of lignin and other organic pollutants, has demonstrated immense potential for agricultural and environmental applications, including straw pretreatment, feed fermentation, mycotoxin degradation, and water treatment. However, current research remains in its exploratory phase, with naturally sourced MnP unable to meet industrial-scale demands and no mature commercial enzyme preparations available on the market. This comprehensive review innovatively constructs a framework for MnP research, probing into its molecular conformation and catalytic principles, while providing an overview of the advancements in high-throughput screening and In silco designing strategies. Specifically, this review focuses on the practical applications of MnP in sustainable agriculture, elaborating on its potential and challenges in straw resource utilization, efficient feed fermentation, mycotoxin control, and water quality improvement. Furthermore, this review summarizes the recent achievements in optimizing MnP activity through enzyme engineering techniques and discuss customized mutation strategies tailored to specific agricultural and environmental requirements, thereby laying a solid theoretical foundation and scientific basis for the industrial production and commercialization of MnP.

Beyond the threshold - different accumulation of organochlorine compounds in common dolphins (Delphinus delphis) inhabiting continental and insular ecosystems in the Northeast Atlantic.

Assessing persistent organic pollutant (POP) levels across regions helps evaluate environmental health and determine ecological risks. As an apex predator, the common dolphin (Delphinus delphis) serves as an excellent model for understanding POP exposure and impact in Eastern North Atlantic marine ecosystems. In this study, we collected biopsy samples of common dolphins in two ecoregions, the pelagic system of Madeira Island (Portugal) (n = 30) and in the continental shelf of Northwest Portugal (n = 14) to analyse organochlorine concentrations (PCBs, DDTs, Mirex, HCB) from their blubber. For both ecoregions, PCBs comprised the largest proportion of the total measured organochlorines (60% in Madeira Island and 85% in Northwest Portugal), followed by DDTs, and lastly, HCB. Considerable differences in the organochlorine profile were identified between samples from Madeira and Northwest Portugal, with common dolphins showing higher PCB loads in Northwest Portugal (53 ± 37 μg.g-1 lw) compared to Madeira Island (11 ± 4.8 μg.g -1 lw). The high levels of PCBs found in individuals from mainland Portugal - reaching values up to 140 μg.g-1 lw - are some of the highest reported for the species worldwide, considerably exceeding toxicity thresholds. This is of particular concern as they may be potentially affecting important physiological processes of the animals. These results highlight the poor habitat quality in one of the studied regions, with potential impacts on ecosystem health, while offering valuable insights into the population structure of a species that remains understudied for effective management and conservation.

Characteristics, prediction, and risk assessment of phthalates, organophosphate esters, and polycyclic aromatic hydrocarbons in vegetables from plastic greenhouses of Northeast China.

We investigated the contaminations of phthalates (PAEs), organophosphate esters (OPEs), and polycyclic aromatic hydrocarbons (PAHs) in the vegetables and their corresponding soils from 26 plastic greenhouses of Northeast China. PAEs, OPEs, and PAHs in the edible portion of vegetables were in the range of 2620-21800, 115-852, and 32.4-602 ng/g, while the levels of these chemicals in the greenhouse soils were 5770-18800, 196-935, and 109-1600 ng/g, respectively. PAEs are the main organic pollutants in greenhouses, which were 1-2 orders of magnitude higher than that of OPEs and PAHs. Leafy vegetables showed the highest contamination level, which is ∼1-3 times that of root and fruit vegetables. Bioaccumulation factors (BAFs) of chemicals are significantly negatively correlated with their physicochemical properties, e.g., octanol-water partition coefficient and organic carbon partition coefficient. The partition-limited model can accurately predict the contamination level of greenhouse vegetables to a certain extent based on the chemical's concentration in the corresponding soil. We assessed the hazard quotients of target compounds through daily intake of greenhouse vegetables, and found a low risk for di(2-ethylhexyl) phthalate. This research emphasized the potential dietary exposure risks caused by greenhouse leafy vegetables, and proposed a method for evaluating the risk of greenhouse vegetables through soil monitoring.

The definition of chemical contaminants in food: ambiguity and consequences.

Consumers may be exposed via foods to a diverse range of substances that could be considered as contaminants. However, it is not always straightforward to understand the definition of a 'contaminant'. The present review evaluates how various categories of food-relevant substances are considered in terms of being 'contaminants'. To this end these categories of food borne constituents are evaluated against the various criteria encountered in the available definitions of a food contaminant, including unintentional presence, harmful, existence of regulatory limits, and stakeholder perception. The categories of chemicals considered include: phytotoxins, mycotoxins, (heavy) metals, persistent organic pollutants (POPs), processing aids, process related contaminants, food contact materials (FCMs), pesticides and veterinary drugs. The evaluation revealed that usage of the term appears complex, and may differ between stakeholders. A common proposed definition of the term 'contaminant' could be 'a substance considered to require control measures due to the unacceptability of its context within a food'. Use of a dimension of harm results in equivocal outcomes because risk depends on the level of exposure. As the term 'contaminant' has influence on risk management including public policy, the motivations for applying the term should be subject to more detailed analysis and understanding.

Biological importance and environmental quality of the Laguna Santa Ana in Zacatecas, Mexico

Objective: To determine the environmental quality and diversity of the waterfowl species of the Laguna Santa Ana, located in the municipality of Fresnillo, Zacatecas. Design/Methodology/Approach: A physicochemical analysis of the water was carried out to determine its organic matter pollution. In addition, the Bradford method was applied to establish protein levels, and an optical emission spectrometry was conducted to detect heavy metals. The Shannon-Weiner diversity index (H’) was carried out to identify and count the populations of the lagoon. Results: The physicochemical analysis of water recorded 55 and 230.6 mg/L BOD5 and COD, respectively. High protein levels (0.27-2.95 mL/mL) indicated organic pollution and high arsenic levels. The Shannon-Weiner index (2.7) recorded a high waterfowl diversity. Study Limitations/Implications: Biological abundance was not determined, as a result of the sample size. The changes regarding waterfowl diversity may be the consequence of the seasonal conditions. Findings/Conclusions: The Laguna de Santa Ana has a high waterfowl diversity, including species of international interest; however, organic pollution has caused a a significant environmental deterioration.

Cloud point extraction of heavy metal ions for wastewater remediation: an equilibrium and kinetic study

Abstract Surfactants offer a promising alternative for the efficient and environmentally friendly removal of organic pollutants and toxic heavy metal ions from various media. Their high efficiency and environmental compatibility make them a valuable option for remediation efforts. This study focuses on the cloud point extraction (CPE) of ions from aqueous solutions using biodegradable nonionic surfactants combined with ionic surfactants instead of chelating agents. Phase diagrams of binary surfactant/water systems were first constructed. The effects of salt, inorganic contaminants, and ionic surfactants on the cloud point (Tc) were then investigated. At temperatures above the cloud point, two distinct phenomena were observed and monitored over time: phase separation and phase clarification. The kinetic process was studied using the Turbiscan Lab Expert. Extraction results were evaluated based on four responses: extraction yield (E%), residual concentrations of solute (Xs,w) and surfactant (Xt,w) in the dilute phase, and volume fraction of coacervate at equilibrium (Φ C). Empirical modelling gives a satisfactory agreement between experimental and calculated values. The capacity of CPE to simultaneously remove an organic pollutant and a toxic heavy metal was demonstrated.

Green Synthesis of New Spiropyrrole Derivatives by Employing Activated Carbonyl Compounds and Graphen Oxide Decorated on Ag@CuO/ZnO NPs or CuO/ZnO NPs: Theoretical and Biological Study

ABSTRACTThis study focused on investigating the synthesis of new spiropyrrole derivatives with high yields. The two nanocatalyst CuO/ZnO@Graphen Oxide nanocomposites (CuO/ZnO@GO NCs) and Ag/CuO/ZnO@Graphen Oxide (Ag@CuO/ZnO@GO NCs) were employed in a multicomponent reaction at room temperature to synthesize new compounds. The reaction involved isatins, N‐alkyl isatins, and ninhydrin as activated carbonyl compounds, ammonium acetate, ethyl 2‐arylamino‐4‐dioxo‐4‐arylbutanoates, hydrazonoyl chloride, or ethylbromopyruvate in water. Also, the catalytic activity of the green synthesized CuO/ZnO@GO and Ag@CuO/ZnO@GO was evaluated in the reduction of organic pollutants such as 4‐nitrophenol (4‐NP) in water at mild conditions. The results indicated that the biosynthesized MNCs have very high and effective catalytic activity for organic pollutants within a few seconds. The newly synthesized spiro compounds demonstrate antioxidant activity as a result of two assessment processes conducted by its NH group. In addition, the antibacterial activity of newly created spiro compounds was assessed using a disk distribution method, involving two types of Gram‐negative bacteria. These compounds were found to limit the growth of Gram‐positive bacteria as well. Also, to better understand the reaction mechanism, density functional theory (DFT)–based quantum chemical methods have been applied. The advantages of this technology encompass rapid response times, high product yields, and uncomplicated catalyst and product separation via simple procedures.

Harnessing natural light: Novel nanoheterojunction photocatalyst NaGdF4:Yb,Tm@TiO2/Cu2(OH)2CO3 for actual wastewater remediation

This study introduces NaGdF4:Yb,Tm@TiO2/Cu2(OH)2CO3 (UTCu), an innovative nanophotocatalyst designed to address global energy crises and water contamination issues. Our developed photocatalyst, NaGdF4:Yb,Tm@TiO2/0.5mol%Cu2(OH)2CO3 (UTCu0.5), demonstrated exceptional efficiency, degrading 96.3% of malachite green (MG) within 2 h under Xenon lamp irradiation. The photocatalytic degradation rate of UTCu0.5 surpassed those of UT, Cu2(OH)2CO3, and P25 (Commercial TiO2) by 3.3, 9, and 2.8 times, respectively. The process effectively mineralized MG into less harmful compounds, marking its potential for eco-friendly wastewater treatment. Furthermore, UTCu0.5 exhibited robust degradation capabilities across various organic dyes and maintained its efficacy in mixed dye systems. Detailed mechanistic analysis revealed that the ·OH and ·O2− radicals play pivotal roles in the degradation process, facilitated by the formation of heterojunctions that enhance carrier separation and photocatalytic performance. Theoretical studies supported the significance of S-scheme heterojunctions in boosting the photocatalytic activity of UTCu0.5. Additionally, the catalyst was effective in degrading organic pollutants in different water matrices under both Xenon lamp irradiation and direct sunlight. Remarkably, it achieved a 77.4% removal rate of NH4⁺-N in real municipal wastewater under natural sunlight, with a selective conversion rate of 95.3% to N2, underscoring its practical applicability in environmental remediation. This research not only progresses photocatalysis technology but also provides vital insights for enhancing natural condition wastewater treatment strategies.

Structural modifications of BiOBr nanoplates by electron beam irradiation

Abstract In this study, BiOBr nanoplates are synthesized through the hydrothermal method, then samples have been irradiated by an electron beam of 10 MeV energy to deliver doses of 100 kGy and 500 kGy. XRD and Raman investigations corroborated the presence of a pure phase in all nanoplate samples. The sharp and narrow peaks in XRD indicate well crystalline in nature of the samples, which decreases with increasing the electron dose as confirmed by the decay in peak intensity. Conversely, the peak position shifts at lower angle with increasing the electron dose. Structural factors including lattice parameter, dislocation density, cell volume, microstrain, as well as stacking fault have been found to change due to electron beam irradiation. We employed the Debey-Scherrer formula (D-S), Size Strain Plot method (SSP), and Halder Wagner (H-W) methods to determine the crystal size and strain of purified and irradiated BiOBr nanoplates. It has been found that the size of the crystallites increases nonlinearly as the irradiation dose increases. All three of the aforementioned calculation methods have observed this trend. Strain and dislocation density exhibited the opposite trend of crystallite size, as they decreased as the irradiation dose increased. The dislocation density, strain, and crystallite size values are nearly identical for the SSP and H-W procedures, while the D-S method exhibits values with deviation. The tetragonal structure and the Raman active mode, which we have identified as closely resembling those in other literature of this composition, are discussed in the respective section. Because of their intriguing phase strength, the synthesized nanoplates may be suitable for the degradation of organic pollutants and the separation of water through photo-electrocatalysis.

Visible Light-Driven Photocatalysis of Al-Doped SrTiO3: Experimental and DFT Study

Environmental problems associated with water pollution caused by organic dyes have raised serious concerns. In this context, photocatalytic processes have proven to be promising and environmentally friendly methods for water purification utilising abundant solar energy. In this study, a SrTiO3-based photocatalyst was modified by doping with Al ions and the deposition of dual co-catalysts (Rh/Cr2O3 and CoOOH) to enhance the photocatalytic decomposition efficiency of methylene blue (MB). Pure perovskite SrTiO3 was synthesised by chemical precipitation followed by calcination at 1100 °C. Al-doped SrTiO3 with deposited co-catalysts showed 3.2 times higher photocatalytic activity compared to unalloyed SrTiO3 with co-catalysts in MB decomposition under visible radiation. This study highlights the effectiveness of using dual co-catalysts and low-valence metal doping to enhance the efficiency of the photocatalytic decomposition of organic pollutants. The density functional theory analysis results show that the Al doping of SrTiO3 improves charge separation and increases the lifetime of photogenerated electrons and holes while maintaining the size of the forbidden band, which confirms its effectiveness for enhancing photocatalytic activity.

Editorial: Biosurfactants - next-generation biomolecules for enhanced biodegradation of organic pollutants, volume II

Editorial: Biosurfactants - next-generation biomolecules for enhanced biodegradation of organic pollutants, volume II

Visible light responsive heterophase Titania monoliths for the fast and efficient photocatalytic decontamination of organic pollutants

The article reports the synthesis of an ordered mesoporous network of heterophase TiO2 monoliths as a visible light-responsive photocatalyst using tri-block copolymers of Pluronic F108, P123 and F127 as structure-directing agents (SDAs) and temperature-controlled calcination (450–650 °C) has been carried out by direct templating-assisted hydrothermal approach. The structural/surface morphology and topographical properties of the photocatalyst are characterized using FE-SEM-EDAX, HR-TEM-SAED, p-XRD, VB-XPS, PLS, TG/DTA, UV-Vis-DRS, BET/BJH and zeta potential analysis. The undoped heterophase mesoporous TiO2 monoliths with in-built lattice/surface defects exhibit visible light photocatalytic properties, successfully dissipating Reactive Brown 10 (RB-10) dye. The influence of physicochemical parameters, such as SDAs, temperature, pH, dye concentration, catalyst dosage, photosensitizers and light intensities, are optimized for maximum photocatalytic performance at a shorter timespan. The F127-assisted mesoporous TiO2 monolith (550 °C) exhibits superior degradation kinetics (15 min) for RB-10 dye solution (20 ppm) at pH 2.0–3.0 using a photocatalyst dosage of 50 mg and 2 mM of KBrO3, irradiated with 150 W/cm2 tungsten lamp. The photocatalysts are fabricated without complicated chemical modifications and display topmost efficiency in quickly decontaminating persistent pollutants. The photoproducts from RB-10 photocatalytic degradation are investigated using HR-MS analysis. The photocatalyst can be reused efficiently for six cycles, even under extreme conditions.