假单胞菌MBR还原钛(Ⅳ)合成钛纳米粒子

研究了一株假单胞菌MBR（Pseudomonas sp.MBR）在好氧环境下,以有机碳源为电子供体,将氟钛酸盐还原为钛单质的特性及影响还原的因素.结果表明,该菌还原氟钛酸盐初始浓度范围为0.5~8.0 mmol/L,最适pH值为7.0,柠檬酸钠为最佳碳源供给物,并且在电子供体和钛的摩尔比为100：1时还原效果最好.扫描电子显微镜和透射电子显微镜观察显示加氟钛酸盐后细胞的形态并没有发生变化,还原的Ti单质以纳米粒子形式积累在细胞内.

聚酰亚胺/纳米钛系粒子杂化膜制备与性能

采用原位聚合法和流延成膜法制备了系列纳米钛系粒子含量的聚酰亚胺(PI)/TiO_(2)和PI/BaTiO_(3)杂化膜,以γ-巯丙基三甲氧基硅烷偶联剂(KH590)对纳米钛系粒子进行表面处理以提高有机-无机相之间的界面相容性,通过傅里叶变换红外光谱、广角X射线衍射对杂化膜的结构进行研究,同时分析了TiO_(2)和BaTiO_(3)对杂化膜热性能、亲水性、介电性和力学性能的影响。杂化膜结构研究表明,原位聚合法成功地将纳米钛系粒子引入PI基体中,纳米钛系粒子的掺杂没有破坏PI分子链的有序排列;PI/TiO_(2)杂化膜的热失重5%温度(T5%)较纯PI膜都有所降低,而PI/BaTiO_(3)杂化膜的T5%普遍高于纯PI膜,纳米钛系粒子质量分数达到5%时,PI/TiO_(2)和PI/BaTiO_(3)杂化膜的T5%达到最大,分别为540℃和584℃。杂化膜的亲水性和介电强度较纯膜均得到了较大提高,但力学性能均有不同程度的降低,当纳米钛系粒子质量分数为15%时,PI/TiO_(2)和PI/BaTiO_(3)杂化膜的接触角最小,分别为79.3°和77.3°,且PI/BaTiO_(3)杂化膜的力学性能、亲水性和介电强度均高于PI/TiO_(2)杂化膜。

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.

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.

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.

Preparation and Characterization of Nano-Particles PZT Ferroelectric Thin Films by RF-Magnetron Sputtering

Pt/Ti bottom electrodes were fabricated on SiO2/Si substrates by magnetron dual-facingtarget sputtering system. Lead zirconate titanate（PZT） thin films were deposited on Pt/Ti/SiO2/Si substrates by radio frequency （RF） magnetron sputtering system. The thickness of PZT thin films which were deposited for 5 h was about 800 nm. XRD spectra show that PZT thin films deposited in Ar ambience and rapid-thermal-annealed for 20 min at 700 ℃ have good crystallization behavior and perovskite structure. AFM micrographs show that mean diameter of crystallites is 70 nm and surface structures of PZT thin films are uniform and dense. Raw mean, root mean square roughness and mean roughness of PZT thin films are 34..357 rim, 2. 479 nm and 1. 954 nm respectively. As test frequency is 1 kHz, dielectric constant of PZT thin films is 327.5. Electric hysteresis loop shows that coercive field strength, residual polarization strength and spontaneous polarization strength of PZT thin films are 50 kV/cm, 10μC/cm^2 and 13μC/cm^2 respectively.

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.

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.

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.

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.

Tradeoffbetween Narrowing Optical Band Gap and Enhancing Electrical Conductivity of the Metal Nanoparticles-Modified Titanium Oxide Films

The n-type semiconducting titanium oxide thin films are well-known as electron transporting interlayer in photovoltaic cells. The favorable characteristics of interlayers in photovoltaics are high optical transmittance （T%）, wide band gap energy （Eg） and high electrical conductivity （σ）. Modifying titanium oxide films with metal nanoparticles would increase electrical conductivity but reduce optical band gap energy. We developed the sol-gel derived titanium suboxide （TiOx） films modified with silver （Ag） or gold （Au） or copper （Cu） nanoparticles （NPs）. This study explores a tradeoff between narrowing optical band gap and enhancing electrical conductivity of nanostructured TiOx films by controlling the Au- or Ag- or Cu-NPs loading concentrations （mol%） in titania. The Au- and Cu-NPs loading concentration of 4 mol% should meet a tradeoff which yields the higher T%, wider Eg and higher compared to those of pure TiOx films. In addition, since the pure Cu is not thermodynamically stable in ambience as compared to Au and Ag, the stability of as-obtained colloidal CuNPs is also examined. A careful examination of the time evolution of surface plasmon resonance （SPR） bands of CuNPs indicates that their stability is only up to 4 h.

Enhanced Photocatalytic Activity of TiO2 Nanofibers and Their Flexible Composite Films： Decomposition of Organic Dyes and Efficient H2 Generation from Ethanol-Water Mixtures

TiO2 nanofibers decorated with Pt and Pd nanoparticles have been synthesized and studied in various photocatalytic processes. Excellent photocatalytic behavior in the decomposition of organic dyes in water, degradation of organic stains on the surface of flexible freestanding cellulose/catalyst composite films and in generation of hydrogen from ethanol using both suspended and immobilized catalysts are demonstrated. The performance of the nanofiber-based TiO2 materials is competitive with and in some cases outperforms--their conventional nanoparticle-based counterparts. In all cases, Pd-decorated TiO2 nanoparticles and nanofibers proved to be more efficient than their Pt-based counterparts, which could be explained on the basis of the formation of nano-sized Schottky interfaces at the contacts between TiO2 and metal nanoparticles. The feasibility of forming cellulose/catalyst composites provides a novel way of utilizing photocatalyst materials in large-area coatings and freestanding films.

TiO_2 nanoparticles' effects on properties of concrete using ground granulated blast furnace slag as binder

In the present study, compressive strength, pore structure, thermal behavior and microstrncture characteristics of concrete containing ground granulated blast furnace slag and TiO2 nanoparticles as binder were investigated. Portland cement was replaced by different amounts of ground granulated blast furnace slag and the properties of concrete specimens were investigated. Al- though it negatively impacts the properties of concrete at early ages, ground granulated blast furnace slag up to 45 wt% was found to improve the physical and mechanical properties of concrete at later ages. TiO2 nanoparticles with the average particle size of 15 nm were partially added to concrete with the optimum content of ground granulated blast furnace slag and physical and mechanical properties of the specimens were measured. TiO2 nanoparticle as a partial replacement of cement up to 3 wt% could accelerate C-S-H gel formation as a result of increased crystalline Ca（OH）2 amount at the early age of hydration and hence increase compressive strength of concrete. The increased TiO2 nanoparticles＇ content of more than 3 wt% may cause reduced compressive strength because of the decreased crystalline Ca（OH）2 content required for C-S-H gel formation and unsuitable dispersed nanoparticles in the concrete matrix. TiO2 nanoparticles could improve the pore structure of concrete and shift the distributed pores to harmless and less-harm pores.

Fe3O4-nanoparticle-decorated TiO2 nanofiber hierarchical heterostructures with improved lithium-ion battery performance over wide temperature range

A facile strategy was designed for the fabrication of Fe3O4-nanoparticle- decorated TiO2 nanofiber hierarchical heterostructures （FTHs） by combining the versatility of the electrospinning technique and the hydrothermal growth method. The hierarchical architecture of Fe3O4 nanoparticles decorated on TiO2 nanofibers enables the successful integration of the binary composite into batteries to address structural stability and low capacity. In the resulting unique architecture of FTHs, the 1D heterostructures relieve the strain caused by severe volume changes of Fe3O4 during numerous charge-discharge cycles, and thus suppress the degradation of the electrode material. As a result, FTHs show excellent performance including higher reversible capacity, excellent cycle life, and good rate performance over a wide temperature range owing to the synergistic effect of the binary composition of TiO2 and Fe304 and the unique features of the hierarchical nanofibers.

A Comparative Study of TiO_2 Nanoparticles Synthesized in Premixed and Diffusion Flames

Previous studies have been shown that synthesis of titania （TiO2） crystalline phase purity could be effectively controlled by the oxygen concentration through titanium tetra-isopropoxide （TTIP） via premixed flame from a Bunsen burner. In this study, a modified Hencken burner was used to synthesize smaller TiO2 nanoparticles via short diffusion flames. The frequency of collisions among particles would decrease and reduce TiO2 nanoparticle size in a short diffusion flame height. The crystalline structure of the synthesized nanoparticles was characterized by X-ray diffraction （XRD）, transmission electron microscope （TEM）, Barrett-Joyner- Halenda （BJH） and Brnnauer-Emmett-Teller （BET） measurements. The characteristic properties of TiO2 nanoparticles synthesized from a modified Hencken burner were compared with the results from a Bunsen burner and commercial TiO2 （Degussa P25）. The results showed that the average particle size of 6.63 nm from BET method was produced by a modified Hencken burner which was smaller than the TiO2 in a Bunsen burner and commercial TiO2. Moreover, the ruffle content of TiO2 nanoparticles increased as the particle collecting height increased. Also, the size of TiO2 nanoparticles was highly dependent on the TTIP loading and the collecting height in the flame.

Flower-like Au/Ag/TiO2 nanocomposites with enhanced photocatalytic efficiency under visible light irradiation

Uniform flower-like TiO2 coated Au nanostars and core-shell Au@Ag nanostars with different amounts of Ag coating were prepared through a facile method by hydrolysis of TiF4 under an acidic environment. The photocatalytic capability of these flower-like nanocomposites under visible light irradiation was found to be enhanced by up to 4.7-fold compared to commercial P25 TiO2 nanoparticles. The enhanced photocatalytic activity was ascribed to improved light absorption and hot electron inj ection from the photo-excited Au@Ag core to the TiO2 shell.

Multicycle photocatalytic reduction of Cr(Ⅵ) over transparent PVA/TiO_2 nanocomposite films under visible light

Photocatalytic reduction of hexavalent chromium in wastewater has been widely investigated as an attractive treatment method. In this work, we reported an efficient method for photocatalytic reduction of Cr（VI） over transparent polyvinyl alcohol/titanium dioxide （PVA/TiO2） nanocomposite films under sunlight irradiation. The trans- parent PVA/TiO2 nanocomposite films were prepared by a simple hydrothermal method combined with a solution casting process. The results revealed that the anatase TiO2 nanoparticles with size less than 10 nm were in-situ generated in PVA matrix, which endowed the films with high trans- parency. Photocatalytic reduction of Cr（VI） over PVA/TiO2 nanocomposite films exhibited superior visible light pho- tocatalytic activity. Mechanism investigation demonstrated that the PVA acted not only as a transparent support for TiO2 nanoparticles, but also as holes scavengers simultaneously to improve the separation of photogenerated holes and elec- trons. Meanwhile, the transparent PVA/TiO2 nanocomposite films displayed remarkable stability and excellent recyclabil- ity during multicycle Cr（VI） photoreduction. Furthermore, the PVA/TiO2 nanocomposite films showed selective adsorp- tion ability for Cr（III）, and thus totally removal of Cr（VI） was achieved after photoreduction process.