Materials For Water Treatment Research Articles

Synthesis of Novel Fe-CNs-P/S Carbon Materials for Sustainable Water Treatment: Activation of Persulfate for Efficient Tetracycline Degradation

This study presents a novel Fe-CNs-P/S carbon composite material, synthesized by doping elements P and S into NH2-MIL-101 (Fe) using the carbonization method. The material’s application in sustainable water treatment was evaluated, focusing on its effectiveness in activating persulfate for pollutant degradation. The research thoroughly investigates the synthesis process, structural characteristics, and performance in degrading pollutants. The results indicate that Fe-CNs-P/S-5 with 50% P and S co-doping is higher than that of other samples, where the degradation rate of TC in 30 min is as high as 98.11% under the optimum conditions, that is temperature at 25 °C, 0.05 g/L of catalyst concentration, and 0.2 g/L of PMS concentration. The composite material demonstrates robust versatility and stability, maintaining high degradation efficiency across multiple organic pollutants, with no significant reduction in catalytic performance after four cycles. Furthermore, the free radical quenching experiments display that the singlet oxygen 1O2 is the main active species. It is demonstrated that the doping of P and S play a role in the enhancement of PMS activation over the Fe-CNs-P/S catalyst. This material demonstrates remarkable efficacy in treating a range of organic contaminants and exhibits excellent reusability, presenting a promising approach for enhancing sustainability in water treatment applications.

Advances in bimetallic metal organic frameworks (BMOFs) based photocatalytic materials for energy production and waste water treatment

Advances in bimetallic metal organic frameworks (BMOFs) based photocatalytic materials for energy production and waste water treatment

Vermiculite-derived MgFe nanosheet-enhanced hydrogel with dual photothermal and photocatalytic Fenton functions for solar water purification

The rapid expansion of industrial activities and urbanization has exacerbated environmental and water pollution. Solar water evaporation is a promising technique for water purification. Herein, an innovative dual-functional hydrogel that combines photothermal conversion with photocatalytic degradation was successfully prepared. The composited hydrogel (MF/CNTs-1) achieves a high-water evaporation rate of 2.23 kg·m−2·h−1 under 1 sun irradiation. Furthermore, two-dimensional MgFe nanosheets synthesized via alkali etching of vermiculite can generate highly reactive radicals through photo-Fenton reaction, facilitating efficient pollutants degradation. This dual-functional evaporator harnesses solar energy to enhance both water purification and pollutant degradation, providing valuable insights into designing vermiculite-derived materials for comprehensive water treatment and sustainable water purification.

Quantitative Analysis of Ferrate(VI) and Its Degradation Products in Electrochemically Produced Potassium Ferrate for Waste Water Treatment

Potassium ferrate(VI) (K2FeO4) as a particularly strong oxidant represents an effective and environmentally friendly waste water treatment material. When produced by anodic oxidation in highly alkaline aqueous solution, the K2FeO4 product is separated and sealed in inert plastic bags with the retention of some liquid phase with high pH. This method proved to be excellent for long-term storage at moderately low temperature (5 °C) for industrial applications. It is still imperative to check the ferrate(VI) content of the product whenever it is to be used. Fe-57 Mössbauer spectroscopy is an excellent tool for checking the ratio of ferrate(VI) to the degradation product iron(III) in a sample. For this purpose, normally the spectral areas of the corresponding subspectra are considered; however, this approximation neglects the possible differences in the corresponding Mössbauer–Lamb factors. In this work, we have successfully determined the Mössbauer–Lamb factors for the ferrate(VI) and for the most common iron(III) degradation products observed. We have found superparamagnetic behavior and low-temperature phase transformation for another iron(III) degradation product that made the determination of the Mössbauer–Lamb factors impossible in that case. The identities of a total of three different iron(III) degradation products have been confirmed.

The surface electron transfer strategy promotes the hole of PDI release and enhances emerging organic pollutant degradation

In semiconductor photocatalysts, the easy recombination of photogenerated carriers seriously affects the application of photocatalytic materials in water treatment. To solve the serious problem of electron−hole pair recombination in perylene diimide (PDI) organic semiconductors, we loaded ferric hydroxyl oxide (FeOOH) on PDI materials, successfully prepared novel FeOOH@PDI photocatalytic materials, and constructed a photo-Fenton system. The system was able to achieve highly efficient degradation of BPA under visible light, with a degradation rate of 0.112 min−1 that was 20 times higher than the PDI system, and it also showed universal degradation performances for a variety of emerging organic pollutants and anti-interference ability. The mechanism research revealed that the FeOOH has the electron trapping property, which can capture the photogenerated electrons on the surface of PDI, effectively reducing the compounding rate of photogenerated carriers of PDI and accelerating the iron cycling and H2O2 activation on the surface of FeOOH at the same time. This work provides new insights and methods for solving the problem of easy recombination of carriers in semiconductor photocatalysts and degrading emerging organic pollutants.

Polymer-grafted silica based hybrid macrobeads for Pb(II) and Cr(VI) removal from water

The presence of heavy metals in water deters its usability for drinking purposes. Indiscriminate disposal of industrial effluent into water bodies further complicates the situation. Accordingly, there is a dire need for a treatment system that can effectively remove the contaminants from water. Although there are solutions like the utilization of membrane and other powder-based adsorbers, challenges like high cost, fouling, scaling, the generation of a new class of waste (post usage), and limited recyclability often limit their usage. Hence, there is a critical need to develop a system that demonstrates high adsorption capacity, is reusable, and is easy to develop. Accordingly, we synthesized silylated polyethyleneimine, grafted it onto silica particles, and tested its efficacy in removing heavy metal contaminants like lead and hexavalent chromium from water. The resultant modified polyethyleneimine modified silica particles (termed as SiEP) outperformed many adsorber materials, including metal–organic framework, zeolite, clay, etc., and it demonstrated a staggering adsorption capacity (Langmuir) of 442 mg/g (pH 6) and 182 mg/g (pH 5) for lead and chromium, respectively at 30 °C. The developed nanopowder was further encapsulated inside polyacrylonitrile macrobeads and tested for its efficacy. Although the encapsulation resulted in a decrease in adsorption capabilities, common problems like high-pressure build-up and inefficient contact associated with powder-based adsorber were avoided upon encapsulation. The macrobeads exhibited 37 mg/g and 20 mg/g adsorption capacities for lead and chromium, respectively. For both the powder and the macrobeads, the adsorption capacity was tested in the presence of mixed ions and both the adsorber demonstrated their unique capability to be selective against targeted ions. They were further tested against a real groundwater matrix synthetically spiked with lead and chromium. Such findings open up a new avenue to developing water treatment materials that demonstrate selectivity and recyclability, indicating their potential for large-scale water treatment applications in industrial settings.

Optimization of synthesis of cationic starches for wastewater sludge and microalgae separation

The implementation of stricter water protection legislation requires the development of novel environmentally friendly water treatment materials. A new method for the preparation of water soluble cationic starch flocculants using potato starch, 3-chloro-2-hydroxypropyltrimethylammonium chloride and CaO additive was developed and surface response methodology was successfully utilized for the optimization of degree of substitution in the cationization of potato starch with and without CaO additive. Based on the results of destabilization studies of model kaolin, wastewater sludge, and microalgae dispersion systems, optimized conditions ware proposed for obtaining an efficient, soluble, and biodegradable cationic starch flocculant with optimal structure. The duration of starch etherification reaction was reduced to <12 h to obtain soluble cationic starch derivatives with a degree of substitution of quaternary ammonium groups of 0.25, which retained the granular structure during synthesis. An efficient flocculation technology using anionic polymer and high content of biodegradable cationic flocculant was proposed. The highly efficient flocculation of microalgae suspensions using developed cationic starch derivative with the degree of substitution of cationic groups of 0.25 has been also achieved. The developed environmentally friendly cationic starches with tailored flocculation properties proofed to have a great potential in various water cleaning and separation technologies with prospects in wastewater treatment, agriculture or energy sectors.

Preparation and characterization of hierarchically porous hybrid gels for efficient dye adsorption.

Water treatment faces significant challenges due to the increasing complexity of pollutants and the need for more efficient, sustainable treatment methods. However, current adsorbent materials often struggle with issues such as low adsorption capacity, slow kinetics, and poor reusability, limiting their practical application. In this study, we developed a novel hierarchical porous hybrid gel (HPHG) for water treatment to address the limitations of conventional adsorbents. The HPHG features a multi-level porous structure (from 48 ± 28 nm to 4385 ± 823 nm) that significantly enhances its porosity and specific surface area. We systematically investigated the relationship between the material's structure and its adsorption performance. Kinetic studies revealed a tendency towards a pseudo-second-order adsorption model, attributed to the material's unique structural features that facilitate rapid mass exchange channels inside HPHG and provide abundant active sites for pollutant adsorption. Reusability tests demonstrated that the material retained 85.4% of its initial adsorption capacity after five adsorption-desorption cycles, highlighting its potential for practical applications. This study provides valuable insights into structure-performance relationships in advanced water treatment materials, offering a promising approach for designing next-generation adsorbents with superior efficiency and sustainability.

Chemical and Physical Characterization of Three Oxidic Lithological Materials for Water Treatment

Water treatment necessitates the sustainable use of natural resources. This paper focuses on the characterization of three oxidic lithological materials (OLMs) with the aim of utilizing them to prepare calcined adsorbent substrates for ionic adsorption. The three materials have pH levels of 7.66, 4.63, and 6.57, respectively, and organic matter contents less than 0.5%. All of the materials are sandy loam or loamy sand. Their electric conductivities (0.18, 0.07, and 0.23 dS/m) show low levels of salinity and solubility. Their CEC (13.40, 13.77, and 6.76 cmol(+)kg) values are low, similar to those of amphoteric oxides and kaolin clays. Their aluminum contents range from 7% up to 12%, their iron contents range from 3% up to 7%, their titanium contents range from 0.3% to 0.63%, and their manganese contents range from 0.007% up to 0.033%. The amphoteric oxides of these metals are responsible for their ionic adsorption reactions due to their variable charge surfaces. Their zirconium concentrations range from 100 to 600 mg/g, giving these materials the refractory properties necessary for the preparation of calcined adsorbent substrates. Our XRD analysis shows they share a common mineralogical composition, with quartz as the principal component, as well as albite, which leads to their thermal properties and mechanical resistance against abrasion. The TDA and IR spectra show the presence of kaolinite, which is lost during thermal treatments. The results show that the OLMs might have potential as raw materials to prepare calcined adsorbent substrates for further applications and as granular media in the sustainable treatment of both natural water and wastewater.

Engineering mineralized interlayers for enhanced nanofiltration: Synergistic modulation of polyamide layer structure and catalytic self-cleaning performance

High permselectivity and antifouling/self-cleaning nanofiltration (NF) membranes are ideal materials for water treatment, and this vision is expected to be reached through the design of multifunctional self-cleaning interfaces. In this study, we employed metal - polyphenol network (MPN) to mediate in situ mineralization of porous substrates, enabling simultaneous modulation of interfacial polymerization (IP) and catalytic self-cleaning. The findings demonstrate that the mineralized layers employ an interlayer modulation strategy to produce a polyamide (PA) layer that is more hydrophilic, thinner, and structurally denser. As a result, the resulting PA-Fe3O4-PSF membrane exhibited a 2.5-fold increase in permeance (19.2 L m−2 h−1 bar−1) and a 7.3-fold enhancement in Cl−/SO42− selectivity (66.4), compared to the control membrane (PA-PSF). Additionally, its highly polarized membrane surface significantly improved its antifouling performance. Compared to membranes with mineralized layers on the surface (Fe3O4-PA-PSF), PA-Fe3O4-PSF constructs a confined space that facilitates more efficient regeneration through in situ catalytic self-cleaning and ensures greater stability during multiple fouling-regeneration cycle operations. This study paves the way for fabricating multifunctional NF membranes with sustainable applications in material concentration, wastewater treatment, and environmental remediation.

Investigation of the efficacy of graphite-sulfur iron tailing composite catalysts for activation of peroxydisulfate for rhodamine B degradation.

Herein, a novel graphite/sulfur iron tailing composite was applied as a peroxydisulfate (PDS) activator for rhodamine B (RhB) degradation in the water. The superior catalytic efficiency of graphite/sulfur iron tailing was achieved through radical (SO4•- and •OH) and non-radical (1O2) processes according to the radical quenching experiments and electron paramagnetic resonance analysis. The carbonyl group and Fe species were the main active sites on the surface of graphite/sulfur iron tailing, which was demonstrated by combining Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and reaction kinetic experiments, and a possible degradation mechanism was also proposed. Overall, activated with 0.30g/L of C-1, PDS achieved a 94.8% removal rate for RhB and maintained a removal rate of over 85% even after five consecutive operation cycles, and this study will benefit the application of iron/carbon composite materials in practical water treatment.

Novel sustainable porous organic polymer for multifunctional water treatment: Adsorption and disinfection applications

The removal of dyes and bacteria from wastewater is crucial for environmental remediation and public health protection. The discharge of untreated wastewater containing dyes and bacteria can lead to water pollution, ecosystem disruption, and human health risks. In this context, we report the development of a sustainable gallic acid-based porous organic polymer (GA-azo-DADPM POP) for multifunctional water treatment applications. The polymer was characterized using 13C CP/MAS NMR, ATR-FTIR, SEM, and TEM, confirming its formation and revealing its agglomerate morphology, porous nature, and stacked sheet-like structure. The polymer exhibited a high BET surface area of 402 m2/g and a pore size distribution in the range of 2–20 nm, indicating its mesoporous nature. The adsorption studies demonstrated a maximum methylene blue dye removal capacity of 141.94 mg/g, while the antibacterial performance showed effective disinfection against E. coli. The adsorption studies followed the Freundlich isotherm and Pseudo second-order kinetic model. These results highlight the potential of GA-azo-DADPM POP for simultaneous dye removal and bacterial disinfection in wastewater treatment. In conclusion, this study demonstrates a novel, sustainable, and multifunctional material for water treatment, offering a promising solution for environmental restoration. The development of such materials can contribute significantly to the advancement of water treatment technologies, ensuring a safer and more sustainable future.

Ibuprofen removal by modified natural zeolite: characterization, modeling, and adsorption mechanisms

AbstractBACKGROUNDDeveloping robust technologies to remove emerging pollutants from water is urgent since conventional treatments are not technically prepared to remove them. This paper investigated the ibuprofen (IBU) adsorption capacity onto natural zeolite (NZ) and hydrothermally modified zeolite in an acidic medium followed by impregnation with the cationic surfactant cetyltrimethylammonium bromide (CTAB) (MZHT‐CTAB). The materials characterization included scanning electron microscopy (SEM), X‐ray diffraction (XRD), atomic absorption spectroscopy (AAS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA/DTG), N2 adsorption/desorption isotherm (BET), Zeta Potential (ZP), and Point of Zero Charge (pHPZC). The adsorptive capacity studies were carried out by varying the pH solution, a kinetic study at three concentrations (25, 50, and 100 mg L−1), and the contaminant concentration influence (5–100 mg L−1).RESULTSThe results showed that the MZHT‐CTAB obtained both the highest removal efficiency (~ 37%) and the highest adsorption capacity (~ 14 mg g−1) at pH 5.0. The Pseudo Second‐Order (PSO) model, which showed the best fit to the experimental data, is significant as it indicates the reliability of our results. The maximum adsorption capacity for the concentration of 100 mg L−1 was 11.93 mg g−1. According to Giles's classification, the isotherm was classified as S‐3 type, indicating the competition between the adsorbate and water molecules for the active sites on the adsorbent surface.CONCLUSIONThe adsorption studies demonstrate that the novel adsorbent (MZHT‐CTAB) is highly effective in removing IBU, presenting a significant removal capacity and feasibility. This promising result contributes to the ongoing search for alternative materials for water treatment. © 2024 Society of Chemical Industry (SCI).

Adsorption studies of methylene blue on cation-modified graphene oxide and graphene oxide/MXene membranes

Membranes prepared from graphene oxide (GO) have greater advantages over traditional materials for water treatment, while MXene is a good candidate for pollutant removal. However, the effect of different cations introduced into the prepared GO membranes on their adsorption performance must be further explored. In this study, a series of cation-modified GO and GO/MXene membranes were prepared based on the self-assembly of GO. Na+-modified membranes were found to be more effective at removing methylene blue (MB) than multivalent cation-modified GO membranes. However, the cation-modified GO/MXene membranes improved the MB adsorption efficiency, and the higher the ionic valence, the more pronounced the effect. In addition, the effects of the pH, temperature, contact time and initial concentration of MB on the adsorption performance of the membranes were investigated. The best removal of MB was achieved under neutral conditions, and the adsorption process was consistent with quasi-secondary kinetics and Langmuir isotherm models. The fitting results of the Langmuir isotherm model showed that the maximum adsorption capacities of the cation-modified GO membranes for MB were 654.9, 319.8, and 246.3 mg/g, respectively. The maximum adsorption capacities of the cation-modified GO/MXene membranes for MB were 687.3, 497.6, and 772.4 mg/g, respectively. Furthermore, the results of the intraparticle diffusion model revealed that the entire adsorption process was controlled by both external and internal diffusion. The thermodynamic analysis results indicated that the entire adsorption process was a heat-absorbing process and could proceed spontaneously. That the findings suggest that the Na+-modified GO and Al3+-modified GO/MXene membranes demonstrate the best adsorption effects and are promising adsorbents for MB removal.

Synthesis of activated carbon-supported nano copper oxide and its inactivation performance on Escherichia coli in water

Copper oxide (CuO) is limited in inactivating bacteria due to the deficiency of active Cu(I) that can catalyze dissolved oxygen to produce reactive oxygen radicals. A novel sterilization agent was developed to inactivate Escherichia coli (E. coli) by loading nano copper oxide onto activated carbon (nCuO/AC) with a facile impregnation method. Surface techniques proved that CuO with a size of 100–200 nm was evenly loaded on AC surface, which improved its dispersity and reactivity. XPS analysis further revealed a cycle of surface-bonded Cu(II) to Cu(I) in the nCuO matrix that was driven by reducing groups on AC surface such as hydroxyl. The resultant Cu(I) activated dissolved oxygen to produce reactive oxygen species for bacterial inactivation. Superoxide radical (•O2–) was proved to be the primarily oxidative species during the sterilization process by EPR analysis and quenching investigations. Therefore, the nCuO/AC achieved an enhanced inactivation efficiency of 6.0 log CFU/mL as compared to those of 1.1 and 0.4 log CFU/mL by the nCuO and AC, respectively. The above sterilization reaction was pH-dependent and high inactivation efficiency could be achieved under neutral conditions. Additionally, the nCuO/AC exhibited excellent stability with an inactivation efficiency of 5.4 log CFU/mL after 4 cycles. Spent nCuO/AC showed great potential in renewability because it could inactivate 5.5 log CFU/mL of E. coli by peeling off residual nCuO on AC surface with sulfuric acid and reloading new nCuO through impregnation, with a regeneration rate up to 97.2 %. The above results demonstrated that nCuO/AC could be a promising bactericidal material for water treatment.

Exploring the Potential of Natural Materials in Water Treatment

Exploring the Potential of Natural Materials in Water Treatment

Unveiling the efficiency of peanut shell-derived porous composite for water denitrification: Characterization, kinetic, isotherm and thermodynamic studies

This research investigated the valorization of peanut shell (PS) waste to produce a ZnO-modified activated carbon composite ZnO@PS-AC for water denitrification. The composite was synthesized through chemical activation with ZnCl₂ followed by pyrolysis at 700 °C. Characterization techniques revealed a highly porous structure with over 79 % carbon content and successful ZnO formation, indicating the effectiveness of the synthesis process. Batch adsorption experiments were conducted to evaluate nitrate removal under various conditions. The adsorption process demonstrated rapid kinetics, reaching equilibrium within 60 min. Isotherm studies showed a maximum adsorption capacity of 17.9 mg/g, while kinetic analysis revealed significant nitrate removal within the first 5 min. Phenomenological modelling suggested that adsorption onto active sites was the rate-limiting step in the process. Thermodynamic analysis indicated an exothermic, physical adsorption process, providing insights into the nature of the nitrate-adsorbent interactions. The study highlights ZnO@PS-AC’s potential as an eco-friendly, cost-effective adsorbent for nitrate removal from water. Its porous structure facilitates rapid uptake and efficient removal, making it a promising solution for water treatment applications. These findings demonstrate the viability of valorizing agricultural waste into effective water treatment materials, contributing to both waste management and environmental remediation efforts.

Cu–Co bimetallic organic framework as effective adsorbents for enhanced adsorptive removal of tetracycline antibiotics

In this study, the removal effect of a new MOF-on MOF adsorbent based on Cu–Co bimetallic organic frameworks on tetracycline antibiotics (TCs) in water system was studied. The adsorbent (Cu-MOF@Co-MOF) were synthesized by solvothermal and self-assembly method at different concentrations of Co2+/Cu2+. The characterization results of SEM, XRD, XPS, FTIR and BET indicated that the MOF-on MOF structure of Cu-MOF@Co-MOF exhibited the best recombination and physicochemical properties when the molar ratio of Co2+: Cu2+ is 5:1. In addition, the Cu-MOF@Co-MOF have a high specific surface area and bimetallic clusters, which can achieve multi-target synergistic adsorption of TCs. Based on above advantages, Cu-MOF@Co-MOF provided a strong affinity and could efficiently adsorb more than 80% of pollutants in just 5 to 15 min using only 10 mg of the adsorbent. The adsorption capacity of tetracycline and doxycycline was 434.78 and 476.19 mg/g, respectively, showing satisfactory adsorption performance. The fitting results of the experimental data were more consistent with the Langmuir isotherm model and pseudo-second-order kinetic model, indicating that the adsorption process of TC and DOX occurred at the homogeneous adsorption site and was mainly controlled by chemisorption. Thermodynamic experiments showed that Cu-MOF@Co-MOF was thermodynamically advantageous for the removal of TCs, and the whole process was spontaneous. The excellent adsorption capacity and rapid adsorption kinetics indicate the prepared MOF-on MOF adsorbent can adsorb TCs economically and quickly, and have satisfactory application prospects for removing TCs in practical environments. The results of the study pave a new way for preparing novel MOFs-based water treatment materials with great potential for efficient removal.

Multifunctional bacterial cellulose-bentonite@polyethylenimine composite membranes for enhanced water treatment: Sustainable dyes and metal ions adsorption and antibacterial properties

Developing multifunctional materials for water treatment remains a significant challenge. Bacterial cellulose (BC) holds immense potential as an adsorbent with high pollutant-binding capacity, hydrophilicity, and biosafety. In this study, N-acetylglucosamine was used as a carbon source to ferment BC, incorporating amide bonds in situ. Bentonite, renowned for its adsorption properties, was added to the culture medium, resulting in BC-bentonite composite membranes via a one-step fermentation process. Polyethyleneimine (PEI) was crosslinked with amide bonds on the membrane via glutaraldehyde through Schiff base reactions to enhance the performance of the composite membrane. The obtained membrane exhibited increased hydrophilicity, enhanced active adsorption sites, and enlarged specific surface area. It not only physically adsorbed contaminants through its unique structure but also effectively captured dye molecules (Congo red, Methylene blue, Malachite green) via electrostatic interactions. Additionally, it formed stable complexes with metal ions (Cd²⁺, Pb²⁺, Cu²⁺) through coordination and effectively adsorbed their mixtures. Moreover, the composite membrane demonstrated the broad-spectrum antibacterial activity, effectively inhibiting the growth of tested bacteria. This study introduces an innovative method for fabricating composite membranes as adsorbents for complex water pollutants, showing significant potential for long-term wastewater treatment of organic dyes, heavy metal ions, and pathogens.

Influence of yttrium doping on the photocatalytic behaviour of lanthanum titanate: a material for water treatment

Abstract Remediating water contamination greatly benefits from the removal of chemical as well as microbiological contaminants using the same substance. Yttrium-doped Lanthanum Titanate (LaY x Ti1−x O3, where x = 0 (LTO) and 0.05 (LYTO)) nanoparticles (NPs) synthesized by the auto-combustion method were already proven to have better antibacterial activities. The current study aims to investigate the photocatalytic degradation efficiency of the same sample for the organic pollutant Methylene Blue (MB) dye. Here, two vital and decisive characterization methods were employed: Raman spectroscopy for chemical and morphological features and X-ray photoelectron spectroscopy (XPS) for surface phase identification. The oxidation states of La3+ and Ti3+ ions have been deduced using XPS. The HRTEM reveals the nano-structure with SAED pattern is supporting with XRD data. LaTiO3 (LTO) and LaY0.05Ti0.95O3 (LYTO) nanoparticles showed degradation efficiencies of 40.26 % and 86.24 %, respectively, at degrading methylene blue (MB) dye after a reaction time of 90 min. The degradation efficiency of LTO increased to 87.19 % after a reaction time of 150 min. The introduction of yttrium doping into lithium titanate demonstrates promise as a material for mitigating water treatment, as it augments the material’s antibacterial and photocatalytic characteristics.