Authors: Shi Bai, An Chun Mo, Su Qin Xian, Yi Zuo, Yu Bao Li, Wei Xu
Abstract: In this experiment, un-dried silver-hydroxyapatite-titania nanoparticles slurry was used to
make membrane with Polyamide-66 by co-polymerization method. The morphology, chemical
components and structures of the membrane were characterized by AAS, XRD, SEM and EDX. S.
aureus, E. eoli, P.gingivalis, F.nucleatum and S.mutans were utilized to test the antibacterial effect.
XRD results demonstrated that the membrane have characteristic diffraction peaks of pure HA. A
homogeneous distribution of the Ca, P, Ti, and Ag element in the membrane was confirmed by
EDX. Both surface and section showed porous structure which was confirmed by SEM and the
holes size was average 20-30μm. The bacteria assay reflects to the antibacterial effect, 56.31 % of
S. aureus and 50.10 % of E. eoli were killed after 24 hours incubation. However, 91.84 % of P.
gingivalis, 90.64 % of F. nucleatum and 90.49 % of S. mutans were killed and pictures of SEM
showed obviously fewer cells on the surface. So the nanocomposite membrane could be one of the
bioactive materials with antibacterial properties for oral GBR technique.
325
Authors: Juan Liao, An Chun Mo, Hong Kun Wu, Jing Chao Zhang, Yu Bao Li, Guo Yu Lv
Abstract: Since bacterial accumulation surrounding biomaterials has pathogens known to cause the
biomaterials centered infection, it may be important to develop some kind of biomaterial with
antibacterial activity as well as biocompatibility. This study focused on evaluating the antibacterial
activity of silver-hydroxyapatite/ Titania nanoparticles (Ag-nHA/nTiO2) against oral bacteria with
agar dilution method. Bacteria were seeded on agar plate containing antibacterial material with
different concentrations after incubation of 48 hours. The antibacterial activity was demonstrated by
MICs. The MICs of Ag-nHA/nTiO2 ranged between 1000μg/ ml and 7500μg /ml under anaerobic
conditions. And it also exhibited remarkable antibacterial activity to all the aerobe bacteria
(MIC≤500μg/ml). On the other hand, the antibacterial activities of Ag-nHA/nTiO2 differentiate to
some extent with the bacterial strains. This Ag-nHA/nTiO2 exhibited remarkable antibacterial
activity to anaerobic and aerobe bacteria. This antibacterial effect may reduce the potential for
bacterial colonisation of oral biomaterials with Ag-nHA/nTiO2.
299
Authors: S.H. Woo, Min Ku Lee, Chang Kyu Rhee
Abstract: In this study, the colloidal stability and sedimentation behavior of crystalline TiO2
particles (∼300nm) in various organic solvents have been investigated by means of a backscattered
light flux profile (Turbiscan) and a zeta potential measurement. The backscattered light flux profiles
revealed that the TiO2 nanoparticles were readily sedimented in water, methyl alcohol, and ethyl
alcohol due to a flocculation-induced particle growth, while a particle coalescence and a
sedimentation of the TiO2 nanoparticles were hardly observed in isopropyl alcohol. The measured ζ
potentials verified the differences of the colloidal stabilities of the TiO2 particles in the organic
solvents, showing a good correlation with the migration velocity.
267
Authors: Hiroki Tanaka, Shigeki Mouri, Kenji Nakahara, Hideaki Sano, Guo Bin Zheng, Yasuo Uchiyama
Abstract: The effect of TiC content on oxidation behavior of the sintered WC-TiC-TaC alloys with
2 mass% TaC and different TiC amount of 3-45 mass% was investigated through oxidation tests in
air at 973K in order to clarify their oxidation mechanism at high temperature. Based on the results
of mass change, SEM observation, elemental map analysis and composition analysis of the samples
before and after the oxidation test, it was revealed that with increasing TiC content in the alloys,
mass changes from oxidation and thickness of the oxidation scale decreased. Thus, it is considered
that the main component of the scales changed from WO3 to TiO2 gradually with increasing TiC
content in the alloys, and oxygen diffusing through the oxidation scale to the alloys was inhibited
more and more.
1173
Authors: Kyung Mo Kim, Eun Hee Lee, Uh Chul Kim
Abstract: Several chemicals were studied to suppress the damage due to stress corrosion cracking
(SCC) of steam generator (SG) tubes in nuclear power plants. The polarization curves showed that
the electrochemical properties on the surface of Alloy 600 MA changed with the addition of
inhibitors. The SCC tests were conducted by using a m-RUB specimen in a 10% NaOH solution at
a temperature of 315°C. The effects on the SCC of the compounds, TiO2, TyzorLA and CeB6, were
tested for several types of SG tubing materials. The test with the addition of TiO2 (P25) and CeB6
showed an effect in decreasing the SCC for the SG tubing material. However, CeB6 caused some
more SCC for Alloy 800. The penetration property into a crevice of the inhibitors was investigated
by using Alloy 600 specimens with different gap sizes and an AES analysis was performed on the
oxide layer of the specimen.
717
Authors: Shin Hyuk Kang, Beom Seob Kim, Deug Joong Kim
Abstract: The carbothermal reduction synthesis process of titanium diboride (TiB2) particles was
studied. In the synthesis of TiB2 using carbothermal reduction from a mixture of TiO2, B2O3 and
carbon, solid-solid reactions occur. TiO2 particles rapidly react with carbon to TiC, which then
reacts with boron oxide and carbon to TiB2. In the vacuum condition, TiB2 particles were formed
within 10 minutes at temperature of 1300oC. It seems that a high exothermic reaction eventually
results in the increase of reaction rate. In flowing argon atmosphere, TiB2 particles were formed at
temperature of 1550oC after a reaction of 0 minute and it showed a finer particle size than that in
the vacuum condition. This is attributed to the faster heat elimination due to the flowing argon. In
high atmospheric pressure of argon gas such as 20 atm in reaction or cooling state, the synthesized
TiB2 particles shows a mixture of diverse sized particles.
145
Authors: Beom Seob Kim, Young Chul Woo, Deug Joong Kim
Abstract: Synthesis of nano TiC powder by carbothermal reduction procedure of TiO2 was
investigated. TiO2 was mixed with resin or carbon powder as reduction agent and was reacted at
1500oC for 0 ~ 45 minutes under Ar atmosphere. Conglomeration of the powders mixed with TiO2
and resin were observed in the initial stage of the reduction and the unreacted TiO2 was not found
even after 5 minutes elapsed. The fine TiC particles with a size of 80 nm were formed by complete
reaction between Ti, a reduction product, and C after 15 minutes. However, the conglomerated
particles were not the powders added with carbon powder as carbon source in the initial stage. The
unreacted TiO2 particles were kept for 15 minutes. Finally, TiC particles were formed and were
partially grown after 20 minutes.
141
Authors: Jong Oh Kim, Jong Tae Jung, Won Youl Choi
Abstract: This study was conducted to evaluate the applicability of photocatalytic metal membrane
system for the treatment of humic acid and heavy metals in aqueous solution. The catalysts, TiO2
powder P25 Degussa and metal membrane with 0.5 μm nominal pore size were used for
experiments. Removal efficiency of humic acid and heavy metals increased with the increase of
TiO2 dosage, however decreased over 0.3 g/L of TiO2 dosage. The addition of H2O2 as an oxidation
reagent had a positive effect for the removal rate of humic acid and heavy metals. Metal membrane
with stainless steel seemed to be quite stable to UV light with oxidation reagent in long-term
operational periods over 6 months. Moreover, TiO2 particles can be effectively separated from the
treated water by membrane rejection and the permeation flux was also enhanced by the combination
of photocatalytic reaction.
1317
Authors: A.P.P. Fontanesi, J.M. Cavenaghi, Vania Caldas de Sousa
Abstract: Dopants such as Ta2O5 play a major role in the formation of barriers at the grain
boundary in TiO2 varistors, increasing their nonlinear coefficient and decreasing their
breakdown electric field. This paper discusses the microstructural and physical properties of
Ta- and Cr-doped TiO2 systems in which imported tantalum oxide was replaced with an
equivalent Brazilian raw material. Preliminary results confirm that this national oxide can be
utilized to obtain electroceramics such as varistors.
444
Authors: Masahiro Toyoda, Beata Tryba, Fumi Koujin, Tomoki Tsumura, Michio Inagaki
Abstract: Carbon-coated TiO2 photocatalysts were prepared by a simple heat treatment of the powder mixtures
of anatase-type TiO2 with PVA at a temperature of 700 and 900 oC in a N2 atomosphere. Diffuse optical
reflectance spectra for carbon-coated TiO2 showed the absorption edge for anatase structure clearly, overlapping
with absorption due to coated carbon over whole range of wavelegth. These carbon-coated TiO2 photocatalysts
had relatively high apparent BET surface area, from 50 to 170 m2/g, which suggested the formation of porous
carbon layers, and showed relatively high adsorption of various pollutants, methylene blue (MB), reactive black
(RB-5), phenol (Ph) and iminoctadine triacetate (IT), in water. Photocatalytic activity of carbon-coated TiO2 thus
prepared was evaluated through the determination of the rate constant for the decomposition of different
pollutants in water. Rate constant values were strongly depend on the pollutants, but their dependence on the
crystallinity of TiO2 phase. The relations between adsorptivity and rate constant for four pollutants looked
similar with each other, and the pollutants adsorbed in the larger amount was decomposed with the higher rate.
Adsorptivity of carbon-coated TiO2 photocatlysts was determined and discussed on the relations to BET surface
area, amount of carbon coated and also rate constant k for the decomposition of MB, RB5, Ph and IT.
Adsorptivity of carbon-coated catalysts depends strongly on the adsorbate (pollutant) but also on the surface
nature of carbon layer on TiO2 particles. The relations between adsorptivity and rate constant k for four
pollutants looked similar, suggesting that the pollutant adsorbed in the larger amount being decomposed with the
higher rate.
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