Titania Loading Research Articles

Enhanced super-ultra-deep photocatalytic oxidative desulfurization by titanium-activated metal-organic frameworks nanophotocataltyst

Addressing the escalating global demand for fossil fuels and the urgent environmental concerns associated with their use necessitates the development and implementation of efficient and cost-effective techniques for the removal of sulfur compounds. In this study, titanium-activated MIL-101(Fe) was utilized for the removal of organosulfur compounds through the photocatalytic oxidation desulfurization (PODS) process. The coexistence of active sites with titanium and iron resulted in an ultra-deep desulfurization. The impact of titanium loading was assessed, with TxML representing the ratio of Ti to Fe (x = 1, 1.5, and 2, respectively). Nanophotocatalysts were fabricated by solvothermal method. The physicochemical properties of the new materials were investigated by performing XRD, TEM, FT-IR, FESEM, EDX, UV–Vis DRS, PL, GC–MS, ESR, TGA, transient photocurrent, and nitrogen adsorption–desorption analyses. The effect of titanium loading on the structure, and performance of photocatalysts in the PODS reaction was investigated. The reaction parameters were optimized for maximum efficiency. Under optimal conditions of T2ML loading at 1.5 g/L, a volumetric solvent to fuel ratio (S/F) of 1, and a temperature of 50 ℃, T2ML shows the best performance by removing 100 % of dibenzothiophene.Kinetic experiments revealed that the PODS reaction obeys a pseudo-first order equation, and activation energy is 47.08 kJ.mol−1.

Strongly reinforced mechanical and thermal properties of polyamide 66 by high loading titanium dioxide whiskers

Of large length-to-diameter ratio and specific area, inorganic whiskers were widely applied for polymer reinforcement. As a well-known nanofiller, titanium dioxide (TiO2) has been welcome by polymer engineering, mostly for whitening with spherical shapes favored. To date, there have been no TiO2 whiskers reported for polymer reinforcement. In this work, a rutile type TiO2 whisker was compounded with polyamide 66 (PA66) to prepare nanocomposites with surficial modification being conducted to further improve the compatibility between them. It was found that the rutile-type TiO2 whisker significantly improves the mechanical properties of PA66 at high loadings and the performance went better when surficial modification for it was applied. Under 50 wt% addition of TiO2 whisker either modified or not, the tensile strength, tensile modulus, flexural strength, flexural modulus, impact strength and heat deformation temperature of prepared PA66 composites were respectively increased by 52 %, 279 %, 44 %, 313 %, 20 %, 199 % and 84 %, 279 %, 88 %, 303 %, 114 %, 207 %, comparing with the pristine PA66. The mechanism regarding the overall reinforcement was analyzed, which was attributed to the shape-relevant multiple interactions between TiO2 and PA66. Besides, the improved adhesion due to strong stable chemical bonding by surficial modification of fillers, is also accountable.

Synergistic catalytic effect of titanium and iron incorporated to spherical MCM-41 in selective catalytic oxidation of diphenyl sulphide with H2O2

Spherical mesoporous silicas of MCM-41 type modified with titanium, iron or both these metals were prepared by co-condensation method and tested in the role of catalysts for selective oxidation of diphenyl sulphide with H2O2 to diphenyl sulphoxide and diphenyl sulphone. The monometallic catalysts containing titanium or iron were found to be active catalysts of diphenyl sulphide mainly to diphenyl sulphoxide. A very significant increase in catalytic activity was observed for the bimetallic samples, containing both titanium and iron. Moreover, in the case of bimetallic catalysts with higher titanium loading, diphenyl sulphone is a dominating reaction product. The increased activity of the bimetallic catalysts has been related to the synergistic operation of titanium and iron in conversion of hydrogen peroxide into reactive species, which in the next step oxidise diphenyl sulphoxide.

High-Performance Lithium-Ion Batteries with High Stability Derived from Titanium-Oxide- and Sulfur-Loaded Carbon Spherogels.

This study presents a novel approach to developing high-performance lithium-ion battery electrodes by loading titania-carbon hybrid spherogels with sulfur. The resulting hybrid materials combine high charge storage capacity, electrical conductivity, and core-shell morphology, enabling the development of next-generation battery electrodes. We obtained homogeneous carbon spheres caging crystalline titania particles and sulfur using a template-assisted sol-gel route and carefully treated the titania-loaded carbon spherogels with hydrogen sulfide. The carbon shells maintain their microporous hollow sphere morphology, allowing for efficient sulfur deposition while protecting the titania crystals. By adjusting the sulfur impregnation of the carbon sphere and varying the titania loading, we achieved excellent lithium storage properties by successfully cycling encapsulated sulfur in the sphere while benefiting from the lithiation of titania particles. Without adding a conductive component, the optimized material provided after 150 cycles at a specific current of 250 mA g-1 a specific capacity of 825 mAh g-1 with a Coulombic efficiency of 98%.

Ultra-deep photocatalytic oxidative desulfurization of liquid fuels by Ti@CeO2/ZnO nanophotocatalyst under visible light and mild operating conditions

Herein, various Ti@CeO2/ZnO nanophotocatalysts (TxCZ, x: the molar ratio of Ti to Ce and Zn) were synthesized using the solvothermal method in two stages. After that, the effectiveness of the fabricated catalysts in the photocatalytic oxidative desulfurization (PODS) reaction were assessed. The physicochemical properties of the synthesized samples were analyzed through the implementation of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS), photoluminescence spectroscopy (PL), and electron paramagnetic resonance (EPR) techniques. The study evaluated the impact of varying levels of titanium loading on the physicochemical characteristics of nanoparticles and the elimination of sulfur compounds. Under the optimal reaction conditions of T = 50 °C, 1.5 g/L of photocatalyst dosage, an oxidant to sulfur molar ratio of 6, and a solvent to fuel volume ratio of 1, the TxCZ sample exhibited superior performance by completely removing dibenzothiophene (DBT) from the model fuel. Kinetic studies indicate that the PODS reaction adheres to the pseudo-first-order kinetic model, with an observed activation energy of 69.25 kJ/mol−1.

Fe-NC nanozymes-loaded TiO2 nanotube arrays endow titanium implants with excellent antioxidant capacity for inflammation inhibition and soft tissue integration

Titanium (Ti) and its alloys have been widely used as percutaneous and subcutaneous implants due to their excellent mechanical properties and biocompatibility. However, the aggregation of reactive oxygen species (ROS) and persistent inflammatory responses at the implant site severely affect the soft tissue integration of Ti implants, causing a series of biological complications. To address this issue, in this study, Fe-nitrogen-doped carbon single-atom nanozymes (Fe-NC nanozymes) loaded titanium oxide nanotube arrays (Fe-NC@TNT) were constructed by anodic oxidation and solvothermal method on medical titanium surfaces. The surface morphology, physical composition, enzyme-like catalytic activity, inflammatory response, and soft tissue compatibility of Fe-NC@TNT were investigated. The unique nanotube array fully exposes the catalytic active sites of Fe-NC nanozymes and significantly enhances their enzyme-like catalytic performance to eliminate superoxide anion, hydrogen peroxide, and more toxic hydroxyl radicals, which could effectively reduce the intracellular ROS levels of macrophages and fibroblasts, thereby inhibiting the inflammatory responses of macrophages and promoting the functional expression of fibroblasts. In vivo animal experiments have further demonstrated that Fe-NC@TNT can effectively regulate the immune response and promote the integration between the implant and the surrounding soft tissues.

Iron-doped titania nanoparticles supported on polystyrene for photocatalytic treatment of contaminated water in a continuous system

A visible-light active photocatalyst based on Fe-doped TiO2 and supported by polystyrene pellets (PS) was synthesized for wastewater treatment. “Solid-state” synthesis and doping were carried out and optimized, and the catalyst was characterized by scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), UV–Vis-DRS and X-ray diffraction (XRD) analysis. A heat treatment method was developed to support the Fe/TiO2 onto 1 and 3 mm polystyrene pellets without waste production, and photocatalytic activity was investigated on methylene blue and rhodamine B at titania loading up to 50 wt%, both in batch and in a continuous system. Smaller pellets (1 mm) with low titania loading (4 wt%) proved to be the most efficient photocatalyst.Furthermore, the PS-Fe/TiO2 catalyst was easily separated from treated wastewater and reused for up to ten cycles without any loss of catalyst content and activity. The results showed the feasibility of scaling up a laboratory-scale water treatment into a continuous system.

Silica-titania mesoporous silicas of MCM-41 type as effective catalysts and photocatalysts for selective oxidation of diphenyl sulfide by H2O2

Abstract Spherical Ti-MCM-41, synthetized by co-condensation method, presented very promising activity in catalytic and photocatalytic oxidation of diphenyl sulfide with H2O2 to obtain diphenyl sulfoxide and diphenyl sulfone. Mesoporous silica materials with various titanium content were analyzed with respect to chemical composition (inductively coupled plasma optical emission spectrometry), structure properties (X-ray diffraction), textural properties (low-temperature N2 adsorption–desorption), morphology (scanning electron microscopy), forms and aggregation introduced titanium species (diffuse reflectance spectroscopy, Raman spectroscopy), and surface acidity (NH3-TPD). Titanium introduced in the samples was present mainly in the form of highly dispersed species, presenting catalytic and photocatalytic activities in diphenyl sulfide oxidation with H2O2. Efficiency of the reaction increased with an increase in titanium loading in the samples and was significantly intensified under UV irradiation. The role of various Ti species in diphenyl sulfide oxidation was presented and discussed.

Colloidal solution combustion synthesis of am-TiO2/o-YFeO3 nanocomposites: effect of titania loading on the photo-Fenton-like activity

Colloidal solution combustion synthesis of am-TiO2/o-YFeO3 nanocomposites: effect of titania loading on the photo-Fenton-like activity

Effects of Coupled-/soluble-Copper, Generating from Copper-doped Titanium Dioxide Nanotubes on Cell Response.

Endothelialization in vitro is a very common method for surface modification of cardiovascular materials. However, mature endothelial cells are not suitable because of the difficulty in obtaining and immunogenicity. In this patent work, we determined the appropriate amount of copper by constructing a copper- loaded titanium dioxide nanotube array that can catalyze the release of nitric oxide, compared the effects of coupled-/soluble-copper on stem cells, and then induced stem cells to differentiate into endothelial cells. The results showed that it had a strong promotion effect on the differentiation of stem cells into endothelial cells, which might be used for endothelialization in vitro. SEM and EDS results prove that a high content of copper ions are indeed doped onto the surface of nanotubes with small amounts of Cu release. The release of NO confirms that the release of several samples within a period of time is within the physiological concentration.

UV-modified and dual-catalytic Cu porphyrin-loaded TiO2 nanotubes with enhanced hemocompatibility and prevention of stent restenosis

Implanting vascular stents is regarded as a ground-breaking technique for treating cardiovascular disorders. Thus, advancements in vascular stent technology and stent materials have significant social and economic implications. The development of a surface with bionic endothelial function of nitric oxide (NO) release is always an ideal direction for cardiovascular material modification. However, The NO-release stents will face severe challenges in the oxidative stress microenvironment of atherosclerotic lesions. Excessive reactive oxygen species (ROS) can delay scaffold surface re-endothelialization by causing rapidly oxidative inactivation of NO and by causing endothelial cells (ECs) to undergo apoptosis. Regulating the oxidative stress microenvironment is crucial to address the aforementioned issues. In this study, a composite material that contains ultraviolet (UV)-modified and Copper (II) meso-tetra(4-carboxyphenyl) porphine (CuTPP)-loaded titanium dioxide nanotubes (NTs) was presented. CuTPP can efficiently catalyze the decomposition of ROS and also decompose GSNO into NO. As a unique technique, UV irradiation was used to enhance the anticoagulant properties of the CuTPP-loaded NTs (NTs@Cu). In vivo and in vitro results demonstrated that UV treated NTs@Cu maintained strong biocompatibility, anti-thrombosis, ECs and smooth muscle cells (SMCs) regulation, and anti-inflammatory capabilities. This technique might present a fresh idea for developing brand-new NO-release scaffolds.

A Flexible Lithium-Ion-Conducting Membrane with Highly Loaded Titanium Oxide Nanoparticles to Promote Charge Transfer for Lithium-Air Battery.

In this research, we aim to investigate a flexible composite lithium-ion-conducting membrane (FC-LICM) consisting of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and titanium dioxide (TiO2) nanoparticles with a TiO2-rich configuration. PVDF-HFP was selected as the host polymer owing to its chemically compatible nature with lithium metal. TiO2 (40-60 wt%) was incorporated into the polymer matrix, and the FC-LICM charge transfer resistance values (Rct) were reduced by two-thirds (from 1609 Ω to 420 Ω) at the 50 wt% TiO2 loading compared with the pristine PVDF-HFP. This improvement may be attributed to the electron transport properties enabled by the incorporation of semiconductive TiO2. After being immersed in an electrolyte, the FC-LICM also exhibited a Rct that was lower by 45% (from 141 to 76 Ω), suggesting enhanced ionic transfer upon the addition of TiO2. The TiO2 nanoparticles in the FC-LICM facilitated charge transfers for both electron transfer and ionic transport. The FC-LICM incorporated at an optimal load of 50 wt% TiO2 was assembled into a hybrid electrolyte Li-air battery (HELAB). This battery was operated for 70 h with a cut-off capacity of 500 mAh g-1 in a passive air-breathing mode under an atmosphere with high humidity. A 33% reduction in the overpotential of the HELAB was observed in comparison with using the bare polymer. The present work provides a simple FC-LICM approach for use in HELABs.

Variation in Metal-Support Interaction with TiO2 Loading and Synthesis Conditions for Pt-Ti/SBA-15 Active Catalysts in Methane Combustion.

The control of catalytic performance using synthesis conditions is one of the main goals of catalytic research. Two series of Pt-Ti/SBA-15 catalysts with different TiO2 percentages (n = 1, 5, 10, 30 wt.%) were obtained from tetrabutylorthotitanate (TBOT) and peroxotitanate (PT), as titania precursors and Pt impregnation. The obtained catalysts were characterized using X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM), N2 sorption, Raman, X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS), hydrogen temperature-programmed reduction (H2-TPR) and H2-chemisorption measurements. Raman spectroscopy showed framework titanium species in low TiO2 loading samples. The anatase phase was evidenced for samples with higher titania loading, obtained from TBOT, and a mixture of rutile and anatase for those synthesized by PT. The rutile phase prevails in rich TiO2 catalysts obtained from PT. Variable concentrations of Pt0 as a result of the stronger interaction of PtO with anatase and the weaker interaction with rutile were depicted using XPS. TiO2 loading and precursors influenced the concentration of Pt species, while the effect on Pt nanoparticles' size and uniform distribution on support was insignificant. The Pt/PtO ratio and their concentration on the surface were the result of strong metal-support interaction, and this influenced catalytic performance in the complete oxidation of methane at a low temperature. The highest conversion was obtained for sample prepared from PT with 30% TiO2.

Titanium porous-transport layers for PEM water electrolysis prepared by tape casting

While the porous-transport layer (PTL) is a key component in PEM electrolyzers, it is one of the most underexplored due to limited available structures. In this work, we present a novel PTL design for PEM water electrolyzers enabled by a cost-effective, scalable tape-casting technique. A precise control of the PTL pore structure is achieved by incorporating poreformers of various sizes, and by varying the titanium and poreformer ratio. The structures are characterized with SEM and synchrotron X-ray computed tomography imaging techniques. Comprehensive electrochemical performance analysis demonstrates that higher titanium loading provides improved contact at the catalyst-layer/PTL interface but suffers from severe mass-transport losses due to gas bubbles. We solve this mass-transport problem by mixing in large poreformer beads that produce a highly porous structure with excellent gas removal properties yet still maintaining mechanical integrity. The PTL fabricated with 60:40 Ti:PMMA ratio and 60 μm PMMA bead size outperformed the standard commercial Ti powder-based PTL by 62 mV at 4 A/cm2.

Structural Characterization of Polycrystalline Titania Nanoparticles on C. striata Biosilica for Photocatalytic POME Degradation.

The biosilica shell of marine diatoms has emerged as a unique matrix for photocatalysis, owing to its sophisticated architecture with hierarchical nanopores and large surface area. Although the deposition of titania nanoparticles on diatom biosilica has been demonstrated previously, their photocatalytic activity has been tested only for degradation of pure compounds, such as dyes, nitrogen oxide, and aldehydes. The efficiency of such photocatalysts for degradation of mixtures, for instance, industrial wastewaters, is yet to be investigated. Furthermore, reports on the lattice structures and orientation of nanotitania crystals on biosilica are considerably limited, especially for the underexplored tropical marine diatoms. Here, we report an extensive characterization of titania-loaded biosilica from the tropical Cyclotella striata diatom, starting from freshly grown cell cultures to photodegradation of wastewaters, namely, the palm oil mill effluent (POME). As Indonesia is the largest palm oil producer in the world, photocatalytic technology could serve as a sustainable alternative for local treatment of POME. In this study, we achieved a 54% loading of titania on C. striata TBI strain biosilica, as corroborated by XRF analyses, which was considerably high compared to previous studies. Through visualization using HR-TEM, supported by SAED and XRD analyses, nanocrystal TiO2 appeared to be trapped in an anatase phase with polycrystalline characteristics and distinct crystallographic orientations. Importantly, the presence of C. striata biosilica lowered the band gap of titania from 3.41 eV to around 3.2 eV upon deposition, enabling photodegradation of POME using a broad-range xenon lamp as the light source, mimicking the sunlight. Kinetic analyses revealed that POME degradation using the photocatalysts followed quasi-first-order kinetics, in which the highest titania content resulted in the highest photocatalytic activity (i.e., up to 47% decrease in chemical oxygen demand) and exhibited good photostability throughout the reaction cycles. Unraveling the structure and photoactivity of titania-biosilica catalysts allows transforming marine diatoms into functional materials for wastewater photodegradation.

Kinetics of TiCl4 Vapor Phase Infiltration (VPI) into PMMA and the Resulting Thermophysical and Optical Properties of the TiOx -PMMA Hybrids

Vapor phase infiltration (VPI) is a post-polymerization modification technique that imbues inorganic materials into polymers to create organic-inorganic hybrid materials with new properties distinct from the parent polymer. While several VPI precursor-polymer chemistries have been explored, a lack of chemical intuition remains for fully understanding the thermodynamics and kinetics that govern the VPI process. This study seeks to continue to build this knowledge by examining the VPI process kinetics for TiO2 infiltration into PMMA via the use of TiCl4 and H2O precursors. In this research, polymethylmethacrylate / TiO2 hybrid materials are prepared using VPI. The depth of infiltration of the TiO2species into ~200 nm PMMA thin films is studied using x-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy and spectroscopic ellipsometry. The kinetics for TiCl4 infiltration increases with both VPI process temperature and TiCl4 exposure time. However, the rates of infiltration are considerably slower than those observed in the more commonly studied trimethylaluminum (TMA) / PMMA system. Even at 150 °C, process times of at least 12 hours are required to fully infiltrate a 200 nm PMMA film whereas using TMA similar films are fully infiltrated within 1 hour at the same process temperature. Films that we believe to be fully infiltrated at 150 °C and 24 hours of TiCl4 exposure have a 6 at% Ti in the innermost bulk, as determined by XPS. Interestingly, unlike AlOx-PMMA hybrids, these TiOx – PMMA hybrids exhibit significant changes in their optical properties. Increased titanium loading leads to a 4% increase in refractive index and increased UV absorbance in the UV range of 270-350nm. Furthermore, films infiltrated at 150 °C and 24 hours of TiCl4 exposure had a 50 % and 70 % reduction in coefficients of thermal expansion (CTE) below and above Tg respectively. Reduced CTE trends with increased titanium loading. We will discuss possible opportunities to use these new properties for various applications.This project is supported by the Laboratory Directed Research and Development program at Sandia National Laboratories, a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia LLC, a wholly owned subsidiary of Honeywell International Inc. for the U.S. Department of Energy’s National Nuclear Security Administration under contract DE-NA0003525.

Optimization of Preparation Conditions of F-N-TiO2/AC Composite Photocatalyst for Degradation of Printing and Dyeing Wastewater

Abstract A novel composite photocatalyst loading titanium dioxide particles onto activated carbon and co-doping with fluorine and nitrogen (F-N-TiO2/AC) was synthesized using the impregnation-hydrothermal method for the degradation of printing and dyeing wastewater. The optimal preparation conditions of the composite photocatalyst were determined using orthogonal experiments. Through range analysis and variance analysis, the optimal preparation conditions were as follows: a molar ratio of anhydrous ethanol, glacial acetic acid, and tetrabutyl titanate of 3:175:100, and hydrothermal temperature of 150°C and hydrothermal time of 12 h. The catalyst prepared under these conditions showed high catalytic activity, with 100 % degradation of methyl orange when irradiated with a xenon lamp light source for 60 min, and the preparation conditions were feasible. The F-N-TiO2/AC composite photocatalysts were characterized using x-ray diffraction and nitrogen adsorption–desorption measurements. On the basis of this analysis, it was found that the doping of fluorine and nitrogen did not change the anatase structure of titanium dioxide but affected the grain growth and changed the structural properties of the F-N-TiO2/AC photocatalyst. Good reusability properties were also found.

Development of highly flexible PVDF-TiO2 nanocomposites for piezoelectric nanogenerator applications

Polyvinylidene fluoride (PVDF) thin films have a wide prospect in energy harvesting applications due to flexible design and presence of electroactive phase. Despite massive work in this domain, commercial applications are very rare since PVDF based thin films have low piezoresponse. In this paper, the piezoelectric output voltage of the PVDF films is further enhanced by loading Titanium dioxide (TiO2) nanofillers into the viscous PVDF solution using solvent casting approach. Tensile strength, elastic modulus, and storage modulus of PVDF-TiO2 nanocomposite films showed significant enhancement compared to pure PVDF. PVDF-TiO2 films showed about 143% increment in dielectric constant (ε) and 214% increment in AC conductivity (σac) than pure PVDF. PVDF-TiO2 films showed significant increment in remnant polarization (Pr) values which is indicating enhanced piezoelectric performance. The piezoelectric output voltage of TiO2 reinforced nanocomposite films also showed significant improvement.

Fast Removal of Methylene Blue via Adsorption-Photodegradation on TiO2/SBA-15 Synthesized by Slow Calcination.

TiO2/SBA-15 photocatalysts were successfully prepared by impregnating low loading titania to SBA-15 via slow calcination. The photocatalyst is efficient for fast methylene blue removal via adsorption and photodegradation methods. The impregnation of low TiO2 loading via slow calcination enhanced TiO2 dispersion that preserved the SBA-15 porosity and uniform morphology. High interfacial interaction of TiO2/SBA-15 improves TiO2 photoresponse by narrowing the bandgap, resulting in a stronger redox ability. The methylene blue removal on 10%TiO2/SBA-15 followed the pseudo-second-order kinetic model that reached 67% removal efficiency in 90 min. The synergy between adsorption and photodegradation is responsible for the fast methylene blue removal. These results indicate the importance of maintaining the adsorption capacity in SBA-15 after impregnation with TiO2 for efficient adsorption-photodegradation processes, which can be achieved by controlling the deposition of TiO2 on SBA-15. A low titania loading further reduced the cost of photocatalysts, thus becoming a potential material for environmental pollution treatment.

Photocatalytic Degradation Performance of Fluorine and Nitrogen Co‐doped TiO2/AC Composites over Printing and Dyeing Wastewater under Visible‐Light Irradiation

AbstractPrinting and dyeing wastewater is one of the difficult wastewater to treat because of its complex composition, difficult degradation, high color and high concentration of organic matter. At present, photocatalysis, a chemical treatment method, is playing an increasingly important role in the field of printing and dyeing wastewater treatment. To improve the photocatalytic degradation efficiency of TiO2 on printing and dyeing wastewater, F−N‐TiO2/AC composite photocatalysts were prepared by loading titanium dioxide (TiO2) particles onto activated carbon (AC) using an impregnation‐hydrothermal method and co‐doping with fluorine and nitrogen. The characterization results showed that the TiO2 particles were loaded onto the surface and pores of AC, which increased the specific surface area of the composite and the average particle size of the TiO2 particles was reduced by the co‐doping of fluorine and nitrogen. Using methyl orange solution to simulate dye wastewater, the highest degradation efficiency (100 %) of methyl orange was achieved via F−N‐TiO2/AC composite photocatalysts when the F/TiO2 molar ratio was 0.3 and N/TiO2 molar ratio was 0.5. The rate of adsorption reaction for methyl orange by F−N‐TiO2/AC followed the pseudo second‐order kinetic. The effects of the catalyst dosage, environmental pH and interferences in water on the degradation efficiency of the F−N‐TiO2/AC composite photocatalyst were then investigated. The photocatalytic degradation of methyl orange is well fitted by a first‐order kinetic model and the degradation rate is 0.09616 min−1, which is about 6 times higher than that of TiO2/AC composites. Meanwhile, the F−N‐TiO2/AC composite photocatalyst had good recycling performance and the degradation efficiency toward methyl orange was still >80 % after five times of repeated use.