Synthesis of graphene/tourmaline/TiO_2 composites with enhanced activity for photocatalytic degradation of 2-propanol

We report the construction of a graphene/tourmaline/TiO2(G/T/TiO2)composite system with enhanced charge‐carrier separation,and therefore enhanced photocatalytic properties,based on tailoring the surface‐charged state of graphene and/or by introducing an external electric field arising from tourmaline.A simple two‐step hydrothermal method was used to synthesize G/T/TiO2composites and poly(diallyldimethylammonium chloride)‐G/T/TiO2composites.In the photocatalytic degradation of2‐propanol(IPA),the catalytic activity of the composite containing negatively charged graphene was higher than of the composite containing positively charged graphene.The highest acetone evolution rate(223?mol/h)was achieved using the ternary composite with the optimum composition,i.e.,G0.5/T5/TiO2(0.5wt%graphene and5wt%tourmaline).The involvement of tourmaline and graphene in the composite is believed to facilitate the separation and transportation of electrons and holes photogenerated in TiO2.This synergetic effect could account for the enhanced photocatalytic activity of the G/T/TiO2composite.A mechanistic study indicated that O2??radicals and holes were the main reactive oxygen species in photocatalytic degradation of IPA.

Preparation and characterization of ZrO_2/TiO_2 composite photocatalytic film by micro-arc oxidation

ZrO2/TiO2 composite photocatalytic film was produced on the pure titanium substrate using in-situ Zr（OH）4 colloidal particle by the micro-arc oxidation technique and characterized by scanning electron microscope （SEM）, energy dispersive X-ray （EDX）, X-ray diffraction （XRD） and ultraviolet-visible （UV-Vis） spectrophotometer. The composite film shows a lamellar and porous structure which consists of anatase, futile and ZrO2 phases. The optical absorption edge of film is shifted to longer wavelength when ZrO2 is introduced to TiO2. Furthermore, the photocatalytic reaction rate constants of degradation of rhodamine B solution with ZrO2/TiO2 composite film and pure TiO2 film under ultraviolet irradiation are measured as 0.0442 and 0.0186 h 1, respectively.

Photocatalytic activity and kinetics for acid yellow degradation over surface composites of TiO_2-coated activated carbon under different photocatalytic conditions

TiO2-coated activated carbon surface （TAs） composites were prepared by a sol-gel method with supercritical pretreatment. The photocatalytic degradation of acid yellow （AY） was investigated under UV radiation to estimate activity of catalysts and determine the kinetics. And the effects of parameters including the initial concentration of AY, light intensity and TiO2 content in catalysts were examined. The results indicate that TAs has a higher efficiency in decomposition of AY than P25, pure TiO2 particles as well as the mixture of TiO2 powder and active carbon. The photocatalytic degradation rate is found to follow the pseudo-first order kinetics with respect to the AY concentration. The new kinetic model fairly resembles the classic Langmuir-Hinshelwood equation, and the rate constant is proportional to the square root of the light intensity in a wide range. However, its absorption performance depends on the surface areas of catalysts. The model fits quite well with the experimental data and elucidates phenomena about the effects of the TiO2 content in TAs on the degradation rate.

Thermal and Mechanical Properties of Isotactic Polypropylene/TiO_2 Particulate Composites

Particulate composites based on isotactic polypropylene(iPP) and titanium dioxide(TiO 2) have been prepared and their morphology and thermal behavior investigated by scanning electron microscopy(SEM), differential scanning calorimetry(DSC) and thermogravimetric analysis(TGA). Tensile tests were performed to assess the influence of TiO 2 on the mechanical properties of the iPP.

TiO_2/polyaniline composites:An efficient photocatalyst for the degradation of methylene blue under natural light

Polyaniline （PAn） sensitized nanocrystalline TiO2 composites （TiO2/PAn） were successfully prepared and used as an efficient photocatalyst for the degradation of dye methylene blue （MB）. The results showed that PAn was able to sensitize TiO2 efficiently and the composite photocatalyst could be activated by absorbing both the ultraviolet and visible light （λ： 190 ～ 800 nm）, whereas pure TiO2 absorbed ultraviolet light only （λ 〈 380 nm）. Under the irradiation of natural light, MB could be degraded more efficiently on the TiO2/PAn composites than on the TiO2 Furthermore, it could be easily separated from the solution by simple sedimentation.

Non‑Magnetic Bimetallic MOF‑Derived Porous Carbon‑Wrapped TiO2/ ZrTiO4 Composites for Efficient Electromagnetic Wave Absorption

Modern communication technologies put forward higher requirements for electromagnetic wave(EMW)absorption materials.Metal-organic framework(MOF)derivatives have been widely concerned with its diverse advantages.To break the mindset of magneticderivative design,and make up the shortage of monometallic non-magnetic derivatives,we first try non-magnetic bimetallic MOFs derivatives to achieve efficient EMW absorption.The porous carbon-wrapped TiO2/ZrTiO4 composites derived from PCN-415(TiZr-MOFs)are qualified with a minimum reflection loss of−67.8 dB(2.16 mm,13.0 GHz),and a maximum effective absorption bandwidth of 5.9 GHz(2.70 mm).Through in-depth discussions,the synergy of enhanced interfacial polarization and other attenuation mechanisms in the composites is revealed.Therefore,this work confirms the huge potentials of nonmagnetic bimetallic MOFs derivatives in EMW absorption applications.

TiO2-PES Fibrous Composite Material for Ammonia Removal Using UV-A Photocatalyst

This study focused on the development and characterization of TiO2-PES composite fibers with varying TiO2 loading amounts using a phase inversion process. The resulting composite fibers exhibited a sponge-like structure with embedded TiO2 nanoparticles within a polymer matrix. Their photocatalytic performance for ammonia removal from aqueous solutions under UV-A light exposure was thoroughly investigated. The findings revealed that PeTi8 composite fibers displayed superior adsorption capacity compared to other samples. Moreover, the study explored the impact of pH, light intensity, and catalyst dosage on the photocatalytic degradation of ammonia. Adsorption equilibrium isotherms closely followed the Langmuir model, with the results indicating a correlation between qm values of 2.49 mg/g and the porous structure of the adsorbents. The research underscored the efficacy of TiO2 composite fibers in the photocatalytic removal of aqueous under UV-A light. Notably, increasing the distance between the photocatalyst and the light source resulted in de-creased hydroxyl radical concentration, influencing photocatalytic efficiency. These findings contribute to our understanding of TiO2 composite fibers as promising photocatalysts for ammonia removal in water treatment applications.

Characterization of Calcined Kaolin/TiO_2 Composite Particle Material Prepared by Mechano-Chemical Method

Calcined kaolin/TiO2 composite particle material （CK/TCPM） was prepared with TiO2 coating on the surfaces of calcined kaolin particles by the mechano-chemical method. X-ray diffraction （XRD） and scanning electron microscope （SEM） were used to investigate the microstructures and morphologies, respectively. The mechanism of the mechano-chemical reaction between calcined kaolin and TiO2 was studied by infrared spectra （IR）. The results show that TiO2 coats evenly on the surfaces of calcined kaolin particles by Si-O-Ti and Al-O-Ti bonds on their interfaces. The hiding power and whiteness of CK/TCPM are 17.12 g/m^2 and 95.7%, respectively, presenting its similarity to TiO2 in pigment properties.

The Effects of TiO2 Particle Size on the Properties of PTFE/TiO2 Composites

TiO2 filled polytetrafluoroethylene (PTFE) composite were fabricated for microwave circuit applications. PTFE/TiO2 composites were prepared by cold pressing and hot treating. The particle size of TiO2 varied from 5 μm to 11 μm.TiO2 powders with different sizes were prepared by the solid state ceramic route. The effects of TiO2 particle size on the microstructure, density, moisture absorption, thermal conductivity and microwave dielectric properties of PTFE/TiO2 composites were investigated. The density showed an increasing trend as the TiO2 particle size increased, while the dielectric loss (tanδ) and moisture absorption decreased with the increase of TiO2 particle size. The dielectric constant (εr) and thermal conductivity (λ) decreased up to D50 = 6.5 μm and then sharply increased. Good properties with values of εr = 6.8, tanδ = 0.0012 and λ = 0.533 W?m?1?K?1 were obtained in PTFE/TiO2 composites when the particle size of TiO2 was 11 μm.

Thermal and Structural Analyses of PMMA/TiO₂Nanoparticles Composites

In the present work, composites of poly (methyl methacrylate)/titanium oxide nanoparticles (100/0, 97.5/2.5, 95/5, 92.5/7.5, 90/10 and 0/100 wt/wt%)were prepared to be used as bioequivalent materials according to their importance broad practical and medical applications. Thermal properties as well as X-ray diffraction analyses were employed to characterize the structure properties of such composite. The obtained results showed variations in the glass transition temperature (Tg), the melting temperature (Tm), shape and area of thermal peaks which were attributed to the different degrees of crystallinity and the existence of interactions between PMMA and TiO2 nanoparticle molecules. The XRD patterns showed sharpening of peaks at different concentrations of nano-TiO2 powder with PMMA. This indicated changes in the crystallinity/amorphosity ratio, and also suggested that the miscibility between the amorphous components of homo- polymers PMMA and nano-TiO2 powder is possible.The results showed that nano-TiO2 powder mix with PMMA can improve the thermal stability of the homo-polymer under investigation, lead- ing to interesting technological applications.

Facile fabrication of TiO_2 nanoparticle–TiO_2 nanofiber composites by co-electrospinning–electrospraying for dye-sensitized solar cells

We report a facile method for the fabrication of TiO2 nanofiber-nanoparticle composite （FP） via. simulta- neous electrospraying and electrospinning for dye-sensitized solar cell （DSC） applications. The loading of nanoparticles on the fibers is controlled by varying their feed rates during electrospinning. The FP composites having three different particle loading are prepared by the methodology and the FP with the highest particle loading （denoted as FP-3 in the manuscript） showed the best overall efficiency of 9.15% in comparison to the other compositions of the FP （FP-2, 8.15% and FP-1, Z51%, respectively） and nanofibers （F） and nanoparticles （P） separately （7.21 and 7.81, respectively）. All the material systems are characterized by spec- troscopy, microscopy, surface area measurements and the devices are characterized by current-voltage （I-V）, incident photon-to-current conversion efficiency （IPCE）, electrochemical impedance measurements, etc. I-V, dye-loading and reflectance measurements throw light on the overall performance of the DSC devices.

Analysis and characterization of microstructures of a TiO_2/bamboo charcoal composite and modified poplar veneer

A type of TiO/bamboo charcoal composite made by a dip-dry method was loaded onto wood veneer with a vacuum- pressure method in order to prepare modified poplar veneer. The pore structure parameters and surface morphology of the TiO2/ bamboo charcoal composite were determined and analyzed by means of a porosimetry analyzer and SEM. The results show that the surface morphology of the composite does not change after being loaded with nano TiO2. However, its specific surface area （359.814 m^2·g^-1）, pore volume （0.317 cm^3.g^-1） and average pore diameter （3.526 nm） increased; particularly the cumulative volume of pores was increased by 65.83%. In addition, the distribution range of the pores was wider than that of the bamboo charcoal. Combining the SEM of unmodified and modified poplar veneer, the results of X-ray photoelectron spectroscopy revealed that actually some TiOz compounds, i.e., 4.08%, are imbedded in the modified poplar veneer.

Photocatalytic and Thermal Insulating Performances of Fiber Reinforced Hierarchical TiO_2/SiO_2 Xerogel Composites Synthesized by Ambient Drying Route

Silica( SiO_2) based aerogel/xerogel materials have been received ever-growing attentions for versatile applications. However,the widespread applications are narrowed by the inert properties,fragile and brittle natureof silica materials and cumbersome preparation processes. In this paper,titania( TiO_2) was introduced into SiO_2 matrix to form photocatalytic hybrid gels. The TiO_2/SiO_2 composites were then reinforced by the impregnation of various fibrillary reinforcements,such as glass,mullite mineral and ceramic fibers. The properties of the composites were studied systematically in terms of fiberstability,microstructure,chemical interaction and thermal conductivity. The final xerogel composites displayed improved monolithic geometry,satisfied thermal conductivity(0. 09-0. 25 W·m^(-1)·K^(-1)) and optimized photocatalytic performance(85% removal of model pollutant of methyl orange( Mo)),which could be expected to be a feasible route to multi-functional building facades in the future.

TiO2-Loaded WO3 Composite Films for Enhancement of Photocurrent Density

Titanium dioxide （TiO2） loaded tungsten trioxide （WO3） composite films are prepared by an E-beam vapor system. Associated with the existence of a heterojunction at the interface of TiO2 and WO3, the prepared TiO2-WO3 composite film shows enhanced photocurrent density, four times than the pure WO3 film illuminated under xenon lamp, and higher incident-photon-to-current conversion e^ciency. By varying the initial TiO2 film thickness, such composite structures could be optimized to obtain the highest photocurrent density. We believe that thin TiO2 films improve the light response and increase the surface roughness of WO3 films. Furthermore, the existence of the heterojunction results in the e^cient charge carriers＇ separation, transfer process, and a lower recombination of electron-hole pairs, which is beneficial for the enhancement of photocurrent density.

Effects of CaTiO3 Loading on the Properties of PTFE/TiO2 Composites

In this paper, a detailed study was carried out on the PTFE reinforced with TiO2 and CaTiO3. The filler content of ceramic powder was a fixed value of 61 wt% and the content of CaTiO3 in PTFE matrix varied from 0 wt% to 16 wt% with a step size of 4 wt%. The effects of CaTiO3 loading on the density, moisture absorption, thermal expansion, microstructure and microwave dielectric properties were investigated. As CaTiO3 loading content increased from 0 wt% to 16 wt%, the thermal expansion initially displayed a sharp increase, and showed a slight enhancement when the content of CaTiO3 exceeded 12 wt%. The density experienced a continuous decrease with the addition of CaTiO3. The moisture absorption displayed a steady increase with the increasing CaTiO3 loading amount. The changing of dielectric constant (εr) and loss tangent (tanδ) were similar to that of the moisture absorption in a manner. Good dielectric properties with values of εr = 11.60, tanδ = 0.002 were obtained in the PTFE matrix with 16 wt% CaTiO3 and 45 wt% TiO2.

Preparation and Characterization of Tetracomponent ZnO/SiO₂/SnO₂/TiO₂Composite Nanofibers by Electrospinning

[Zn(CH3COO)2 + PVP]/[C2H5O)4Si + PVP]/[SnCl4 + PVP]/[Ti(OC4H9)4 + CH3COOH + PVP] precursor composite fibers have been fabricated through self-made electrospinning equipment via electrospinning tech-nique. ZnO/SiO2/SnO2/TiO2 composite nanofibers were obtained by calcination of the relevant precursor composite fibers. The samples were characterized by thermogravimetric-differential thermal analysis (TG-DTA), X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and Scanning electron microscopy (SEM). TG-DTA analysis reveals that solvents, organic compounds and inorganic in the precursor composite fibers are decomposed and volatilized totally, and the mass of the samples kept constant when sintering temperature was above 900?C, and the total mass loss percentage is 88%. XRD results show that the precursor composite fibers are amorphous in structure, and pure phase ZnO/SiO2/SnO2/TiO2 com-posite nanofibers are obtained by calcination of the relevant precursor composite fibers. FTIR analysis manifests that pure inorganic oxides are formed. SEM analysis indicates that the width of the precursor composite fibers is ca. 1.485 ± 0.043 μm. The width of the ZnO/SiO2/SnO2/TiO2 composite nanofibers is ca. 1145.098 ± 68.093 nm.

电沉积HA/TiO_2复合涂层的结合强度和热稳定性研究

HA/TiO 2 composite coating were fabricated via adding TiO 2 powder in the electrolyte by electrodeposition.The influence of current dens ity and deposition time on the content of TiO 2 in the coating,the influence of the content of TiO 2 in the coating on the bonding strength of coating and the influence of sinte ring temperature on the structure and the bonding strength of coating were inves tigated.The experiment results show that the content of TiO 2 in the coating increase with reducing the current density and prolonging the deposition time,the bonding strength improve with increasing the content of TiO 2 in the coating,which can obtain18.7MPa when the weight percent TiO 2 in the coating attain72.2%.The addition of TiO 2 in the coating reduces the thermal expansion co - efficient of the coating,improves the bonding strength of coating and change s the fracture mechanism of the coat - ing from adhesion failure to cohesive failure.HA in the composite coatings i s decomposed by the catalysis reac - tion of TiO 2 at the temperature of sinter850 ℃ .Differential scanning calorimetry and X - ray diffractometry analy - ses showed that the chemical reaction between HA and TiO 2 lead to the product are α- TCP and CaTiO 3 at the temperature of sinter1200 ℃ .In order to prevent the coating from decomposing and attain hign bonding st rength,the sintering temperature should be less than820 ℃ .

射频磁控溅射TiO_2/HA复合生物膜的制备与表征

将水热合成的羟基磷灰石(HA)粉与20wt%Ti粉混合,冷压烧结成靶材。采用射频磁控溅射方法,在工业纯钛基体上沉积TiO2/HA生物薄膜,通过扫描电镜(SEM)及其能谱(EDS)、X射线衍射(XRD)和差热分析仪(TDA)对膜层进行了表征,探讨了溅射膜的晶化工艺。结果表明:由于选择溅射和OH-损失,溅射膜由TiO2晶体颗粒和非晶钙磷化合物组成,且其Ca/P比降低。经700℃,0.5h水蒸气处理,非晶钙磷化合物结晶度大大提高,并部分转化为HA晶体,且处理后的溅射膜与基体间无裂纹。

Carbon-13 Solid State NMR Techniques to Evaluate the Morphology of PP/TiO2 Composites

Solid state NMR was successfully used to determine the proton spin-lattice relaxation time in the rotating frame (T1ρH) for systems based on polypropylene (PP) and PP with titanium dioxide (TiO2) organically modified or unmodified incorporated, in order to understand the molecular behavior of these systems. These techniques were employed in the samples organically modified and unmodified TiO2 to investigate the effect of organic modification on the dispersion and distribution of the particles in the PP matrix. The results were analyzed in terms of the effect of the particles organic modified or not according to the intermolecular interaction in the composites. According to the T1ρH values, all composites showed at least two domains: the short values were related to the rigid part, which included the crystalline and amorphous phase constricted in it, while the longer times were attributed to the amorphous region, which had higher molecular mobility compared to the rigid region of the materials. The increase in the relaxation time parameter in the composites compared to the pure PP was associated to the strong interaction between titanium dioxide particles and the polymer chains. This effect was more pronounced for the systems containing organically modified TiO2. According to the results, it could be inferred that intermolecular interaction occurred in the CH2 and CH groups, being more intense with CH2 groups. Finally, the solid state NMR techniques were able to evaluate the molecular dynamics of those systems.

具有多孔结构的HA/TiO_2生物材料的制备工艺研究

以聚氨酯为造孔支架模板,采用有机泡沫法与高温烧结法,制备了多孔HA/TiO2陶瓷支架材料。讨论了烧结保温时间、PVB含量、TiO2含量等对材料结构与性能的影响。研究表明:较佳的烧结工艺为1 200℃烧结3 h,烧结后样品主要是HA、TiO2相。多孔HA/TiO2陶瓷拥有大孔径300～1 000μm,也有50～300μm的小孔径,具有较好的孔连通性与孔结构,有利于细胞和组织的生长以及营养输送。TiO2具有增强效应,其含量增加,材料压缩强度提高,但TiO2含量过高会增加其脆性,最佳含量为5%,此时材料力学性能接近于人体松质骨。