二氧化钛纳米粒多孔膜增敏的石英微天平传感器

TiO2 纳米粒形成的纳微多孔膜具有比表面积高、透性好的特点。采用TiO2 纳微多孔膜作为基体 ,可将β 环糊精有效地固定在石英微天平表面 ,与聚苯乙烯包裹 β 环糊精的涂层相比 ,检测对硝基酚的灵敏度提高了 1 2倍。β 环糊精 TiO2 纳米粒多孔膜修饰的石英微天平传感器对邻、间、对硝基酚 3种异构体具有选择性响应。在pH 1 1、浓度范围 0 .6～ 2 0 μmol L内 ,其斜率分别是对硝基酚k=71 .9HzL μmol、邻硝基酚 4 9.1HzL μmol、间硝基酚 2 .8HzL μmol。TiO2

不同载药方法对介孔二氧化钛纳米粒载药及药物溶出速率的影响

目的考察不同载药方法对介孔二氧化钛纳米粒载药系统载药和溶出速率的影响。方法通过溶剂挥干法、熔融法、吸附平衡法分别将卡维地洛包载于介孔二氧化钛纳米粒中,用扫描电镜和透射电镜观测样品形貌,氮气吸附-解吸法测量载体的比表面积和孔体积,差示扫描量热法分析药物粒子的存在状态,X-射线衍射法进行物相分析,热失重法分析载药量,最后测定载药系统的溶出速率并进行长期稳定性试验。结果三种载药方法均能通过改变药物的存在状态使药物以非晶型存在于载体中而达到提高溶出速率的目的。其中溶剂挥干法所得的载药系统溶出速率提高显著,并且更具有长期稳定性。结论溶剂挥干法为介孔二氧化钛纳米粒载药的首选。

Preparation, Structures Nano TiO_2 Particles, and the properties of TiH_2 Coated with Nano TiO_2

The surface of Titanium Hydride (TiH 2) is coated by Nano Titanium Dioxide (TiO 2) particles prepared in both of methods of hydrolysis reaction of Ti(OC 4H 9) 4 and base precipitation reaction of Ti(SO 4) 2. TiH 2 coated with nano TiO 2 particles, in which there is an oxidation film on its surface, shown in the experiments, will obviously achieve good effects on releasing hydrogen slowly in high temperature. There are different structures and properties of TiH 2 coated by nano TiO 2 particles prepared in different ways in high temperature, which can influence on releasing hydrogen.

EFFECT OF INHALED NANO-TiO_2 ON LUNG AND SERUM BIOCHEMICAL INDEXES OF MICE

The effect of inhaled nano-TiO2 on lung histology and serum biochemical indexes is evaluated in healthy and adult Kunming mice（eight in each group）after exposure to TiO2 aerosols（1 500 mg/m3）in a sealed chamber.Another eight mice are exposed to indoor air to be served as a control group.Lung tissue and blood are collected after euthanizing the animals.The results show that lactate dehydrogenase（LDH）activity increases in all experimental groups.Alanine aminotransferase（ALT）activity and blood urea nitrogen（BUN）levels are increased in the group exposed to TiO2 aerosols for 28 d,and creatinine（Cr）levels are increased in 14 d and 28 d samples（P0.05）.No obvious changes are observed in other serum indexes.Lungs of mice exposed to 28 d exposure show significant but moderate increase in pulmonary inflammation,and many TiO2 particles are found in the interstitium of pulmonary alveoli.

Distance-Dependent Long-Range Electron Transfer in Protein:a Case Study of Photosynthetic Bacterial Light-Harvesting Antenna Complex LH2 Assembled on TiO 2 Nanoparticle by Femto-Second Time-Resolved Spectroscopy

The function of protein in long-range biological electron transfer is a question of debate. We report some preliminary results in femtosecond spectroscopic study of photosynthetic bacterial light-harvesting antenna complex assembled onto TiO2 nanoparticle with an average size of 8 nm in diameter. Crystal structure shows that photosynthetic bacterial antenna complex LH2 has a ring-like structure composed by alpha- and beta-apoprotein helices. The alpha- and beta-transmembrance helices construct two concentric cylinders with pigments bacteriochlorophyll a (Bchl a) and carotenoid (Car) buried inside the protein. We attempt to insert TiO2 nanoparticle into the cavity of the inner cylindrical hollow of LH2 to investigate the nature of the electron transfer between the excited-state Bchl a and the TiO2 nanoparticle. A significant decrease in the ground state bleaching recovery time constant for Bchl a at 850 run (B850) in respect to that of the Bchl a in free LH2 has been observed. By using the relation of distance-dependent long-range electron transfer rate in protein, the distance between the donor B850 and the acceptor TiO2 nanoparticle has been estimated, which is about 0.6 nm. The proposed method of assembling proteins onto wide-gap semiconductor nanoparticle can be a promising way to determine the role of the protein playing in biological electron transfer processes.

Preparation and photocatalytic performance of Cu-doped TiO_2 nanoparticles

Cu-doped TiO2 nanoparticles with different doping contents from 0 to 2.0% （mole fraction） were synthesized through sol-gel method. X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and field emission scanning electron microscope （FE-SEM） were used to characterize the crystalline structure, chemical valence states and morphology of TiO2 nanoparticles. UV-Vis absorption spectrum was used to measure the optical absorption property of the samples. The photocatalytic performance of the samples was characterized by degrading 20 mg/L methyl orange under UV-Vis irradiation. The results show that the Cu-doped TiO2 nanoparticles exhibit a significant increase in photocatalytic performance over the pure TiO2 nanoparticles, and the TiO2 nanoparticles doped with 1.0% Cu show the best photocatalytic performance. The improvement in photocatalytic performance is attributed to the enhanced light adsorption in UV-Vis range and the decrease of the recombination rate of photoinduced electron-hole oair of the Cu-doped TiO2 nanoparticles.

Preparation of Nitrogen-doped TiO2 Nanoparticle Catalyst and Its Catalytic Activity under Visible Light

N-doped TiO2 nanoparticle photocatalysts were prepared through a sol-gel procedure using NH4C1 as the nitrogen source and followed by calcination at certain temperature. Systematic studies for the preparation parameters and their impact on the structure and photocatalytic activity under ultraviolet （UV） and visible light irra-diation were carried out. Multiple techniques （XRD, TEM, DRIF, DSC, and XPS） were commanded to characterize the crystal structures and chemical binding of N-doped TiO2. Its photocatalytic activity was examined by the deg- radation of organic compounds. The catalytic activity of the prepared N-doped TiO2 nanoparticles under visible light （λ〉400nm） irradiation is evidenced by the decomposition of 4-chlorophenol, showing that nitrogen atoms in the N-doped TiO2 nanoparticle catalyst are responsible for the visible light catalytic activity. The N-doped TiO2 nanoparticle catalyst prepared with this modified route exhibits higher catalytic activity under UV irradiation in contrast to TiO2 without N-doping. It is suggested that the doped nitrogen here is located at the interstitial site of TiO2 lattice.

Influence factors on thermal conductivity of ammonia-water nanofluids

In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with polyacrylic acid(PAA),TiO2 with polyethylene glycol(PEG 1000),and TiN,SiC,hydroxyapatite(noodle-like) with PEG 10000 to ammonia-water solution,respectively.The thermal conductivities were measured by using a KD2 Pro thermal properties analyzer.The influences of surfactant and ammonia on the dispersion stabilities of the binary nanofluids were investigated by the light absorbency ratio index methods.The results show that the type,content and size of nanoparticles,the temperature as well as the dispersion stability are the key parameters that affect the thermal conductivity of nanofluids.For the given nanoparticle material and the base fluid,the thermal conductivity ratio of the nanofluid to the ammonia-water liquid increases as the nanoparticle content and the temperature are increased,and the diameter of nanoparticle is decreased.Furthermore,the thermal conductivity ratio increases significantly by improving the stabilities of nanofluids,which is achieved by adding surfactants or performing the proper ammonia content in the fluid.

Preparation of amphiphilic TiO_2 Janus particles with highly enhanced photocatalytic activity

Stearic-acid-modified TiO2 (STA-TiO2) particles were prepared via the impregnation approach and used as a precursor for preparing TiO2 Janus particles. The morphology, structure, and properties of the TiO2 Janus particles were characterized using Fourier-transform infrared spectroscopy, ultraviolet- visible diffuse reflectance spectroscopy, thermogravimetric analysis, fluorescence microscopy, high-resolution transmission electron microscopy, contact angle analysis, dynamic light scattering, biological microscopy, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy measurements. The results show that TiO2 Janus particles can be successfully prepared via toposelective surface modification. STA grafted on the surface of TiO2 enhances its hydrophobicity, promotes charge separation, and improves its adsorption capacity for organic compounds. The TiO2 Janus particles strongly adsorb on an oil-water interface to form a stable Pickering emulsion. The degradation rates of high-concentration kerosene and nitrobenzene wastewaters when the photocatalyst is pure TiO2, STA-TiO2, or TiO2 Janus particles are discussed and compared. The degradation rates were determined using an ultraviolet-visible spectrophotometer. It was found that the Pickering emulsion stabilized by the TiO2 Janus particles exhibited the best photocatalytic performance;these Janus particles show promising potential for catalytic application.

Study on Properties of Composite Oxides TiO_2/SiO_2

The nanometer particles of TiO_2 and TiO_2/SiO_2 oxides wereprepared by sol-gel supercritical fluid drying method. The propertiesof TiO_2 and TiO_2/SiO_2 were characterized by means of BET(Brunner-Emmett- Teller method), TEM (transmission electronmicroscopy), SEM (scanning electron microscopy), XRD (X-ray diffrac-tion) and FTIR (Fourier transform-infrared) techniques. The effectsof different preparation route, prehydrolysis and non-prehydrolysis,on the properties of TiO_2/SiO_2 oxide were also examined.

Facet-dependent anchoring of gold nanoparticles on TiO2 for CO oxidation

The interfacial perimeter of gold nanocatalysts is popularly viewed as the active sites for a number of chemical reactions,while the geometrical structure of the interface at atomic scale is less known.Here,TiO2-nanosheets and nanospindles were adapted to accommodate Au particles(~2.2 nm),forming Au-TiO2{001}and Au-TiO2{101}interfaces.Upon calcination at 623 K in air,HAADF-STEM images evidenced that the Au particles on TiO2{101}enlarged to 3.1 nm and these on TiO2{001}remained unchanged,suggesting the stronger metal-support interaction on TiO2{001}.Au/TiO2{001}was more active for CO oxidation than Au/TiO2{101}system.

TiO_2 composite nanotubes embedded with CdS and upconversion nanoparticles for near infrared light driven photocatalysis

We report a colloidal process to coat a layer of TiO2onto SiO2composite nanofibers containing embedded CdS and upconversion nanoparticles(UCNPs).The SiO2composite nanofibers were fabricated by electrospinning.To improve the energy transfer efficiency,UCNPs and CdS nanoparticles were bound in close proximity to each other within the SiO2matrix.β‐NaYF4:Yb(30%),Tm(0.5%)@NaYF4:Yb(20%),Er(2%)core–shell nanoparticles were used as nanotransducers for near infrared light.These nanoparticles exhibited enhanced upconversion fluorescence compared withβ‐NaYF4:Yb(30%),Tm(0.5%)orβ–NaYF4:Yb(30%),Tm(0.5%)@NaYF4nanoparticles.The morphologies,size and chemical compositions have been extensively investigated using field emission scanning electron microscopy(FESEM),transmission electron microscopy(TEM),X‐ray diffraction(XRD)and X‐ray photoelectron spectra(XPS),respectively.The TEM images showed that the TiO2composite nanotubes were embedded with a large amount of UCNPs and CdS nanoparticles.The composite TiO2nanotubes degraded more than90%of rhodamine B(RhB)dye during20min of irradiation by simulated solar light.In particular,more than50%of RhB was decomposed in70min,under irradiation of near infrared light(NIR).This high degradation was attributed to the full spectrum absorption of solar light,and the enhanced transfer efficiency for near infrared light.The as‐prepared nanostructures can harness solar energy,and provide an alternative to overcome energy shortages and environmental protection.

Fabrication of ultrafine Pd nanoparticles on 3D ordered macroporous TiO_2 for enhanced catalytic activity during diesel soot combustion

Nanocatalysts consisting of three‐dimensionally ordered macroporous(3DOM)TiO2‐supported ultrafine Pd nanoparticles(Pd/3DOM‐TiO2‐GBMR)were readily fabricated by gas bubbling‐assisted membrane reduction(GBMR)method.These catalysts had a well‐defined and highly ordered macroporous nanostructure with an average pore size of 280 nm.In addition,ultrafine hemispherical Pd nanoparticles(NPs)with a mean particle size of 1.1 nm were found to be well dispersed over the surface of the 3DOM‐TiO2 support and deposited on the inner walls of the material.The nanostructure of the 3DOM‐TiO2 support ensured efficient contact between soot particles and the catalyst.The large interface area between the ultrafine Pd NPs and the TiO2 also increased the density of sites for O2 activation as a result of the strong metal(Pd)‐support(TiO2)interaction(SMSI).A Pd/3DOM‐TiO2‐GBMR catalyst with ultrafine Pd NPs(1.1 nm)exhibited higher catalytic activity during diesel soot combustion compared with that obtained from a specimen having relatively large Pd NPs(5.0 nm).The T10,T50 and T90 values obtained from the former were 295,370 and 415°C.Both the activity and nanostructure of the Pd/3DOM‐TiO2‐GBMR catalyst were stable over five replicate soot oxidation trials.These results suggest that nanocatalysts having a 3DOM structure together with ultrafine Pd NPs can decrease the amount of Pd required,and that this approach has potential practical applications in the catalytic combustion of diesel soot particles.

Analysis of Percolation of the Stabilized Suspensions of TiO2 and SiO2 Nanoparticles in Soil Columns Simulating Landfill Layers

It studied the behavior of transport and stability of TiO2 and SiO2 nanoparticles suspensions percolating through soil columns aiming at simulating municipal waste landfills covering soil layers performance. Experimental columns were constructed with landfill soils and water suspensions with nanoparticles percolation runs were carried out. The experimental columns were constructed with 100 mm and 200 mm of diameter and height, respectively. Outlet concentrations were measured along the percolation time using ICP-OES and nanoparticles tracking analyzer. It was observed that SiO2 nanoparticles acts as a stabilizer of TiO2 nanoparticles suspensions and promotes its transport through the soil columns, which simulates the conditions of the controlled landfills layers. The interaction of the suspensions of SiO2 nanoparticles with nanoparticles of TiO2, promote a high stability of the emulsions, which confers the high zeta potential present in SiO2 suspensions, promoting greater mobility and transport through the soil columns. The experimental results demonstrated that TiO2 nanoparticles were kept suspended, even after 10 days, which indicates good stability. It was observed that both TiO2 and SiO2 were kept in suspensions with negligible nanoparticles clustering and decantation. It was confirmed that the TiO2 and SiO2 of the outflow of soil columns are strongly affected by the soil pH, organic carbon and clay content of the soils. It was observed that the soil columns behave as a retention barrier for both TiO2 and SiO2 nanoparticles.

Synthesis of Three-Dimensional Agaric-like Biomorphic TiO_2 by a Facile Method with Coscinodiscus sp.Frustule

The paper aims to expand the application of natural marine algae. Marine diatoms, which have intricate frustule struc- tures, can serve as bio-template for preparing three-dimensional materials. A simple and effective approach to synthesize the corru- gated agaric-like biomorphic TiO2 templated with frustule of Coscinodiscus sp. is reported. In the sol-gel preparation process, the titania-coating on the frustule is prepared through the deposition and condensation with the aid of acetylacetone （acac） as a control- ling agent to make the precursor Ti（BuO）4 hydrolyze slowly. The as-prepared titania-coated frustule and biomorphic TiOz is charac- terized by scanning electron microscopy （SEM） attached with energy dispersive X-ray spectrometer （EMAX） and X-ray diffraction （XRD）. The microstructure of the corresponding titania nanoparticles appears to be sphere with the diameters distributed around 10-20nm. The templating process is repeated for three cycles. Subsequently, the three-dimensional freestanding corrugated aga- ric-like biomorphic TiO2 structure is obtained by a selective removal in the NaOH solution. As far as we known, the 3D freestanding corrugated agaric-like biomorphic TiOz with greatly increased surface area is obtained for the first time.

A Hybrid Dielectric Ink Consisting of up to 50 wt% of TiO2 Nanoparticles in Polyvinyl Alcohol （PVA）

PVA （Polyvinyl Alcohol） is a water soluble organic dielectric, easily solution processed to fabricate films by spin coating, dip coating or inkjet printing. It has been used as a dielectric layer in OTFTs （organic thin film transistors）, and its dielectric constant is around 3.5-10. For OTFTs operating at lower voltage, it is desirable to increase the dielectric constant. Here, we report a technique to incorporate upto 50 wt% of TiO2 nanoparticles （15-25 nm） in PVA to increase its dielectric constant. Rutile phase of TiO2 is used, because of its higher dielectric constant （e = 114） compared to anatase phase （E = 31）. We have made inks containing 10 and 50 wt% （of PVA） TiO2 nanoparticles, which is stable upto six months. PVA-TiO2 dispersions and PVA （without TiO2） were spin coated on indium tin oxide coated polyethylene terephthalate substrate. Film structure was studied using SEM （scanning electron microscopy）. Absorption study of the films confirms presence of TiO2 nanoparticles. M-I-M capacitors were fabricated by thermally evaporating aluminium on top of the dielectric films. We observed enhancement in dielectric constant by a factor of 2 for PVA containing 50 wt% TiO2 in comparison to PVA＇s dielectric constant. There is no concomitant increase in the leakage current.

Surface Structure, Spectroscopic and Photocatalytic Activity Study of Polyaniline/TiO2 Nanocomposites

PANI （polyaniline） as a promising conducting polymer and photosensitizer has been used to prepare PANI/TiO2 （polyaniline/TiO2） nanocomposite as photocatalyst. TiO2 nanoparticles with size of 5-100 nm were encapsulated by PANI via the ＂in situ＂ polymerization of aniline on the surface of TiO2 nanoparticles. IR, SEM, EPR techniques were used to characterize the mechanism of electron interaction in PANI/TiO2 nanocomposite. The resulting PANI-modified TiO2 composites exhibit significantly higher photocatalytic activity than that of neat PANI on degradation of MB （methylen blue） aqueous solution under UV irradiation.

Decomposition of formaldehyde based on gold-coated TiO2 nanoparticles

The synthesis of gold nanoparticles caped with visible light-responsible TiO2 nanoparticles. was prepared by using electrochemical Oxidation-Reduction Cycles （ORC） in 0.1 M HCI aqueous solution containing 60 mM visible light-responsible TiO2 nanoparticles. Firstly, an Au substrate was cycled in a deoxygenated aqueous solution containing 0.1 M HCI and 60 mM anatase TiO2 nanoparticles from -0.28 to ＋1.22 V vs Ag/AgCI at 500 mV/s with 25 scans. The durations at the cathodic and anodic vertexes are 10 and 5 s, respectively. After this process, Au-and TiO2-containing complexes were left in the solution. Then a Pt electrode immediately replaced the Au working electrode, and a cathodic overpotential of 0.6 V from the Open Circuit Potential （OCP） was applied under sonification to synthesize Au nanoparticles. Encouragingly, the prepared Au nanoparticles caped with visible light-responsible TiO2 nanoparticles are more active for the decomposition of formaldehyde than pure visible light-responsible TiO2 nanoparticles are in the same condition. After 5 days testing, the formaldehyde was decomposed ca. 35% in containing Au nanoparticles caped with visible light-responsible TiO2 nanoparticles, but the formaldehyde was decomposed only ca. 25% in containing pure visible light-responsible TiO2 nanoparticles.

Comparative study on photocatalytic properties of TiO_2 nanoparticles prepared in acidic medium and basic medium by hydrothermal method

In order to investigate the difference of phtotocatalytic properties of TiO2 samples prepared in different pH conditions, TiO2 nanopartieles were prepared in acidic medium and basic medium by a hydrothermal process, respectively. The samples were characterized using XRD, TEM, BET, XPS, surface photovoltage spectroscopy （SPS） and field-induced surface photovohage spectroscopy （FISPS）. Effects of temperature and pH in the hydrothermal process on particle sizes, specific surface areas, and photoeatalytic properties of the TiO2 nanoerystalline were investigated. The experimental results indicate that the photocatalysis activity of TiO2 nanoparticles prepared in basic medium （ B-TiO2 ） is superior to that in acidic medium （ A-TiO2 ）, which is ascribed to the difference of surface state between A-TiO2 and B-TiO2.