Sliding Wear of the Hybrid Kevlar/PTFE Fabric Reinforced Phenolic Composite Filled with Nano-titania

The Kevlar/polytetrafluroethylene（Kevlar/PTFE） fabric composite can be used as a self-lubricating liner of the self-lubricating bearing.Many types of nano-particles can improve the tribological performance of the polymer-based composite.Unfortunately,up to now,published work on the effect of nano-particles on the tribological performance of the fabric composite which can be used as a self-lubricating liner is quite scarce.Therefore,for the purpose of exploring a way to significantly improve the tribological performance of the fabric composite,the tribological performance of the Kevlar/PTFE fabric composite filled with nano-titania is evaluated by using the block-on-ring wear tester.The scanning electron microscopy is utilized to observe the morphologies of worn surfaces of the fabric composites and the counterparts.The tensile properties of the composites are evaluated on the universal material testing machine.The test results show that the addition of nano-titania at a proper mass fraction of the matrix resin improves the wear resistance and the tensile strength,decreases the friction coefficient,and makes the wear volume of the composite reach a relative steady state more quickly;plastic deformation and microcutting are important for the wear of the fabric composite;a lubricating layer is formed on the worn surface of the composite during sliding,and the lubricating layer is critical for the tribological performance of the composite;the formation and properties of the lubricating layer are influenced by the nano-titania particles.The proposed study on the effect of nano-titania on the tribological performance of the Kevlar/PTFE fabric composite,especially on the evolution of the worn surface of the composite,provides the basis for further understanding of the influence mechanism of the nano-particles on the tribological performance of the composite and explores a method of improving the tribological performance of the composite.

Experimental Study on Indoor Air Cleaning Technique of Nano-Titania Catalysis Under Plasma Discharge

In this study, a new technique of air cleaning by plasma combined with catalyst was proposed, which consisted of electrostatic precipitation, volatile organic compounds （VOCs） decomposition and sterilization. A novel indoor air purifier based on this technique was adopted. The experimental results showed that formaldehyde decomposition by the plasma-catalyst hybrid system was more efficient than that by plasma only, Positive discharge was better than negative discharge in formaldehyde removal. Meanwhile, the outlet concentration of ozone byproduct was effectively reduced by the nano-titania catalyst.

Preparation and thermal decomposition mechanism of Mg,Al-hydrotalcite nano-crystals with titania doping

The highly pure nano-crystal Mg,Al-hydrotalcite with titania doping was synthesized by one-step liquid reaction method at atmospheric pressure. The preparation of the Mg,Al-hydrotalcite nano-crystal after doping titania was investigated according to the results of XRD, TEM, IR and DSC. Moreover, based on the DSC test results, the thermal mechanism functions of the Mg,Al-hydrotalcite with titania doping were studied after calculation and comparison.

Synthesis and Antimicrobial Activity of Boron-doped Titania Nano-materials

Antibacterial activity of boron-doped TiO2(B/TiO2) nano-materials under visible light irradiation and in the dark was investigated. A simple sol-gel method was used to synthesize TiO2 nano-materials. X-ray diffraction pattern of B/TiO2 nano-materials represents the diffraction peaks relating to the crystal planes of TiO2(anatase and rutile). X-ray photoelectron spectroscopy result shows that part of boron ions incorporates into TiO2 lattice to form a possible chemical environment like Ti O B and the rest exist in the form of B2O3. The study on antibacterial effect of B/TiO2 nano-materials on fungal Candida albicans(ATCC10231), Gram-negative Escherichia coli(ATCC25922) and Gram-positive Staphylococcus aureus(ATCC6538) shows that the antibacterial action is more significant on Candida albicans than on Escherichia coli and Staphylococcus aureus. Under visible light irradiation, the antibacterial activity is superior to that in the dark.

A ONE-STEP SURFACE MODIFICATION PROCEDURE TO PEG-GRAFTED NANO-TITANIA

PEG （Polyethylene Glycol）-grafted nano-titania has been obtained in a one-step procedure using hexamethylene diisocyanate as the coupling agent and dibutyltin dilaurate as the catalyst in toluene at 80℃ and characterized qualitatively by FTIR and quantitatively by elemental analysis and thermogravimetric analysis. A comparison of nano-titania with two other commonly used inorganic nanoparticles, nano-silica and nano-alumina, is made, revealing that reactivity order is nano- silica 〉 nano-alumina 〉 nano-titania in view of PEG grafting. Possible mechanism of PEG grafting is also discussed.

Structure transition of nano-titania during calcination

In order to study the structure transition during calcination, nano-titania powders prepared by hydrolyzing precipitation approach and calcined at 300, 400, 500, 600 and 700 ℃ were characterized by XRD, TEM and electron diffraction(ED), respectively. The results show that titania powders calcined below 500 ℃ are almost composed of anatase, rutile appears below 500 ℃ and its ratio increases gradually with increase of calcin temperature; nano-titania particles are smaller than 40 nm mostly and the dispersion is related to calcining temperature; the inter-planar distances of nano-anatase single crystalline change gradually when calcing temperature increases to 500 ℃; so do that of nano-rutile single crystalline when calcining temperature charges from 600 to 700 ℃. The conclusions can be drawn that the temperature of transformation from anatase to rutile is below 500 ℃ and the process carries on gradually. Both inter-planar distances and the structure of nano-titania transform gradually with increasing calcing temperature.

Synthesis of rutile from high titania slag by pyrometallurgical route

A new technique was developed for the conversion of high titania slag,containing 70%-75% TiO2 and with MgO,FeO,CaO,Al2O3 and SiO2 as main impurities,into a synthetic rutile,90%-95% TiO2,which satisfies the requirements for fluidizing chlorination process with respect to impurity contents.After a pre-oxidation at around 1 042 ℃ and a heat-treatment above 1 510 ℃,the Ti components in high titania slag can be enriched into the rutile phase which can precipitate and grow,and can be separated with dilute hydrochloric and sulfuric acid,respectively.The results show that the average crystal size of rutile phase is over 25 μm,and the synthetic rutile containing more than 95% TiO2 can be produced by selective leaching.

Synthesis of C-Cl-codoped titania/attapulgite composites with enhanced visible-light photocatalytic activity

We demonstrate the synthesis of C-Cl-codoped titania/attapulgite（TiO2/ATT） composites containing a mixture of TiO2 phases by a facile sol-gel method at 70 ℃ using titanium tetraisopropoxide as the TiO2 precursor and ATT as a support for the TiO2 nanoparticles.The photocatalytic activity of the C-Cl-codoped TiO2/ATT composites with mixed anatase/brookite/rutile phases obtained at pH= 3.0 was much higher than that of commercially available Degussa P25 for the photocatalytic degradation of acid red G under visible-light irradiation.The excellent photocatalytic activity of the developed composite originates from the nonmetal codoping,which extends the absorption edge of TiO2 into visible region,and the presence of multiple phases,which slow the recombination of photoexcited electron/hole pairs.The formation of hydroxyl radicals during the photocatalytic degradation process was detected by photoluminescence probing using terephthalic acid.A mechanism for photocatalysis over the C-Cl-codoped TiO2/ATT composites was proposed.

High temperature oxidation behavior of electroconductive TiN/O′-Sialon ceramics prepared from high titania slag-based mixture

The oxidation behavior of electroconductive TiN/O′-Sialon ceramics prepared using high titania slag as main starting material was studied at 1 200-1 300 °C in air. The isothermal and non-isothermal oxidation processes were investigated by DTA-TG. Phase compositions and morphologies of the oxidized products were analyzed by XRD, SEM and EDS. The results indicate that the oxidation of TiN and O′-Sialon occurs at about 500 °C and 1 050 °C, respectively. After oxidation at 1 200-1 300 °C, a protective scale that consists of Fe2MgTi3O10, SiO2 and TiO2 is formed on the surface of the materials, which effectively prevents the oxidation process. The formation of a protective scale is relative to TiN content and apparent porosity of the samples, the amount of SiO2 and amorphous phase in the oxidation product. At the initial oxidation stage, the oxidation kinetics of the materials follows perfectly the linear law with the apparent activation energy of 1.574×105 J/mol, and at the late-mid stage, the oxidation of the samples obeys the parabolic law with the apparent activation energy of 2.693×105 J/mol. With the increase of TiN content, mass gain of the materials increases significantly.

Preparation of bismuth oxide/titania composite particles and their photocatalytic activity to degradation of 4-chlorophenol

Bismuth oxide/titania, one interfacial composite semiconductor with high photocatalytic activity under solar light, was prepared at low temperature. The structure was characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, brunauer-emmett-teller （BET）, X-ray photoelectron spectroscopy （XPS） and diffuse reflection spectra （DRS）. The results indicate that deposited titania nanoparticles on bismuth oxide surface have micro-nano structure, and this composite material exhibits porosity and increased surface hydroxyl groups. Furthermore, the as-prepared photocatalyst shows higher photocatalytic activity to the degradation of 4-chlorophenol than pure titania or P25 under sunlight.

微波辐射KF/nano-γ-Al_2O_3催化的Gewald反应研究

以KF/nano-γ-Al2O3为碱性催化剂,在微波辐射作用下发生三组分Gewald反应,合成了一类2-氨基噻吩类化合物,并探索了不同反应条件对收率的影响。实验结果表明,该方法具有催化剂廉价高效、反应时间短、产品收率高、后处理简便等优点。

Preparation and photocatalytic activity of neodymium doping titania loaded to silicon dioxide

Neodymium doping titania was loaded to silicon dioxide to prepare Nd/TiO2-SiO2 by sol-gel method and Nd/TiO2-SiO2 was characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform-infrared spectroscopy （FT-IR） and diffuse reflectance spectra （DRS）. Photocatalytic activities of Nd/TiO2-SiO2 with different neodymium contents were evaluated by degradation of methyl orange. The light absorption of Nd/TiO2-SiO2 increased with increasing doping neodymium in a visible light range of 388-619 nm, and Nd doping was in favor of decreasing the recombination of photo-generated electrons with holes. Nd and SiO2 improved the photocatalytic activity of TiO2. The optimal molar fraction of Nd to Ti was 0.1%, and the optimum calcination temperature was 600 ℃. The highest degradation rate of methyl orange was 82.9% after irradiation for 1 h.

Investigation on Quick Surface Metallization of Nano Titania Powder

Quick surface metallization of titania powder was carried out by electrolesschemical deposition of nickel. The fabricated product was characterized by XRD, SEM, FTIR andcross-section metallography. The analysis results show that titania particles are completely coatedby a thin nickel shell about 600 nm thick composed of nano-sized crystalline nickel particles.Mechanism of nickel chemical deposition on nano powder is proposed.

Preparation, Characterization, Photocatalytic Activity of S and Ag co-Doped Mesoporous Titania Photocatalysts

In order to improve the photocatalytic performance of mesoporous titania under visible light, a series of photocatalysts of S and Ag co-doped mesoporous titania have been successfully prepared by template method using thiourea, AgNO3 and tetrabutyl titanate as precursors and Pluronic P123 （EO20PO70EO20） as template. Scanning electron microscopy （SEM）, X-ray diffraction （XRD）, nitrogen adsorption-desorption measurements, and UV-visible spectroscopy （UV-Vis） were employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The microcrystal of the photocatalysts consisted of anatase phase and was approximately present in the form of spherical particle. The photocatalytic performance was studied by photodegradation methyl orange （MO） in water under UV and visible light irradiation. The calcination temperature and the doping content influenced the photoactivity. In addition, the possibility of cyclic usage of co-doped mesoporous titania was also confirmed, the photocatalytic activity of mesoporous titania remained above 89% of that of the fresh sample after being used four times. It was shown that the co-doped mesoporous titania could be activated by visible light and could thus be potentially applied for the treatment of water contaminated by organic pollutants. The synergistic effect of sulfur and silver co-doping played an important role in improving the photocatalytic activity.

Chemical equilibrium controlled synthesis of polyoxymethylene dimethyl ethers over sulfated titania

The chemical equilibrium and reaction kinetic behavior in the synthesis of polyoxymethylene dimethyl ethers （DMMn） were investigated over sulfated titania in order to reveal the decisive factor controlling the reaction. The results showed that the molar ratio of adjacent DMMn products in equilibrium solution had the same value, which depended absolutely on the reaction temperature. Meanwhile, the reactions had the same DMMn products distributions under varied reaction conditions. The equilibrium constants of the related step-wise reactions for DMMn formation were equal, which were calculated based on the bulk compositions of the reaction solution. And thus, the selectivity to DMMn was mainly controlled by the chemical equilibrium, i.e., thermodynamic control. In brief, the present results provide some guidance for future synthesis of DMMn.

Enhancement of formaldehyde degradation by amine functionalized silica/titania films

Doping amine functional groups into SiO2/TiO2 films for enhancing the decomposition of formaldehyde has been investigated using the modified sol-gel method to prepare organic-inorganic hybrid photocatalysts via the co-condensation reaction of methyltrimethoxysilane （MTMOS） and amine functional groups, n-（2-Aminoethyl）-3-aminopropyl-trimethoxysilane （AEAPTMS） and 3-aminopropyl-trimethoxysilane （APTMS） were selected to study the effect of amine functional groups on the enhancement of formaldehyde adsorption and degradation under a UV irradiation process. Physicocbemical properties of prepared photocatalysts were characterized with nitrogen adsorption-desorption isotherms measurement, X-ray diffraction （XRD） and Fourier transform infrared （FT-IR） spectroscopy. The results indicated that the APTMS/SiO2/TiO2 film demonstrated a degradation efficiency of 79% superior to those of SiO2/TrO2 and AEAPTMS/SiO2/TiO2 films due to the synergetic effect of adsorption and photocatalytic properties. The APTMS/SiO2/TiO2 film can be recycled with about 7% decreasing of degradation efficiency after seven cycles.

Preparation of nitrogen-doped titania and its photocatalytic activity

Yellowish nitrogen-doped titania was produced through sol-gel method in mild condition, with the elemental nitrogen derived from aqua ammonia. The titania catalysts were characterized using XRD, BET, TEM, XPS, and UV-Vis diffuse reflectance spectrophotometer, and their photocatalytic activities were evaluated under UV and visible light, respec tively. The XRD results showed that all titania catalysts were anatase. More significantly, the crystallite size of nitrogen-doped titania increased with an increase in N/Ti proportion, and the doping of nitrogen could extend the absorption shoulder into the visible-light region, thus it possessed a higher visible-light activity illustrated by decolorization of methyl orange （65.3%） under the irradiation of visible light, whereas pure titania showed little of such kind of visible light activity. The UV-light activity of nitrogen-doped titania catalysts was worse than that of pure titania and Degussa P25. In the range of N/Ti proportion of 4-10 mol%, the activity of nitrogen-doped titania weakened appreciably in the visible-light region as the N/Ti proportion increased, whereas a reverse relationship existed under the irradiation of UV light.

Molybdosphoric Acid Mixed with Titania Used as a Catalyst to Synthesize Diphenyl Carbonate via Transesterification of Dimethyl Carbonate and Phenol

The 12-molybdosphoric acid mixed with titania （MPA-TiO2） was found to be a novel and efficient catalyst for the synthesis of diphenyl carbonate （DPC） via transesterification of dimethyl carbonate （DMC） and phenol. The X-ray diffraction （XRD） and infrared （IR） techniques were employed to characterize the prepared catalysts. The effect of the weight ratio of the 12-molybdosphoric acid to titania on the transesterification was investigated. A 13.1% yield of DPC and an 11.6% yield of methyl phenyl carbonate （MPC） were obtained over MPA-TiO2 with the weight ratio of MPA to TiO2 as 5：1.

Synthesis and Characterization of Co-Doped Brookite Titania Photocatalysts with High Photocatalytic Activity

Transition metal-doping could effectively extend the light response range of TiO _2 photocatalysts from the ultraviolet(UV)to the visible region.Co-doped brookite titanium dioxide(Co–TiO_2)photocatalysts were synthesized via the hydrothermal method with titanium tetrachloride as the raw material and cobalt chloride hexahydrate as the dopant.The prepared Co–TiO_2 photocatalysts were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),Raman spectroscopy,X-ray photoelectron spectroscopy(XPS)and UV–Vis diffuse reflectance spectroscopy(UV–Vis DRS).The photocatalytic activities of Co–TiO _2 photocatalysts were evaluated by photocatalytic degradation of isopropanol alcohol(IPA),a typical volatile organic compound(VOC),under visible light.The influences ofdifferent Co doping rates,initial concentrations of IPA gas and the amounts of photocatalyst addition were also studied.At the same time,the enhancement mechanism ofcobalt ions as a trap for photogenerated holes was discussed.Thus,we found the optimum doping rate,initial concentration of IPA gas and amount of photocatalyst to add.The results show that the mesoporous Co–TiO _2 photocatalysts possess smaller size particles,larger specific surface area,lower forbidden bandgap energy(Eg)and better photocatalytic activity than pure brookite TiO _2.When the doping of Co was 7% by mass,the initial concentration ofIPA gas was 1.0×10^(-6 )mol/L and the addition of Co–TiO_2 photocatalysts was 50 mg,the best photocatalytic activity was achieved.Furthermore,the degradation rate ofIPA was up to 91%,which shows great potential for waste water treatment.

Synthesis of Nanoscale Shell-core Titania Coated Silica Particles in the Presence of Polyether Polyamine and the Phase Transition

The nanoscale titania coated silica was prepared via a two-step precipitating approach, where the nanoscale silica nuclei were first prepared by passing an aqueous solution of sodium silicate through an ion-exchange resin bed, then coated with the precipitation from hydrolyzed butyl titanate in an ethanol-hexane mixture at a low pH value in the presence of poly(ethylene oxide) polyamine salt(PPA) at a high temperature of 90 ℃. In the second-step precipitating process, the spontaneously precipitated titania shell on the silica nuclei was stabilized in the suspension solution with the help of the adsorption of PPA on the particles. A possible precipitating mechanism was suggested. Furthermore, the amorphous titania shell could undergo crystallization from the amorphous to the anatase structure at a high temperature of 650 ℃, and a further phase transition from the anatase to the rutile structure in the different sintering processes at a rising temperature of 750 ℃.