Application of Highly Functional Ti-Oxide-Based Photocatalysts in Clean Technologies

Various Ti-oxide based photocatalysts such as the highly dispersed Ti-oxide species within zeolite frameworks, TiO₂ nano-particles hybridized with hydrophobic zeolite adsorbents as well as visible light responsive TiO₂ thin films have been successfully prepared. Characterization studies at the molecular level, such as X-ray absorption fine structure (XAFS) and photoluminescence (PL), revealed that the highly dispersed Ti-oxide species within the nano-spaces of zeolites possess a tetrahedral coordination and that they demonstrate unique and high performance for the photocatalytic decomposition of NOx and the photocatalytic reduction of CO₂ with H₂O. A high photocatalytic reactivity for the TiO₂ semiconducting photocatalysts could be achieved by blending them with hydrophobic siliceous zeolites which was equal to the performance of TiO₂ deposited with expensive Pt particles. The role of the siliceous zeolites can be described as a so-called “catch and release effect of organic compounds”, i.e., (i) the condensation of the reactants within the hydrophobic cavities of zeolites and; (ii) the efficient diffusion of the reactant onto the TiO₂ photocatalytic sites. Furthermore, a novel photocatalytic system which can convert abundant solar energy into renewable H₂ energy by the decomposition of H₂O into H₂ and O₂ can also be achieved by using visible light responsive TiO₂ thin film photocatalysts prepared by a RF-magnetron sputtering deposition method. The conversion efficiency of solar energy into H₂ energy may be estimated at ca. 0.1% from the initial rate of H₂ evolution.     

Morphologic Control of Pt Supported Titanate Nanotubes and Their Photocatalytic Property

Morphologic control of Pt supported titanate nanotubes was attempted by the hydrothermal hot-pressing (HHP) technique in order to improve the handleability as a photocatalyst. The bulk of Pt-nanocrystal supported titanate nanotubes was successfully fabricated without the H₂ reduction process by applying the HHP technique. The bulky Pt-nanocrystal supported titanate nanotubes possessed dense microstructures, significantly sharp distributions of mesopores, and high Brunauer–Emmett–Teller (BET) surface area. Furthermore, the bulky Pt-nanocrystal supported titanate nanotubes showed the photocatalytic degradation activities of 2-propanol aqueous solution under UV-light irradiation.     

Enhancement of the photocatalytic reactivity of TiO2 nano-particles by a simple mechanical blending with hydrophobic mordenite (MOR) zeolite

The photocatalytic oxidation of gaseous acetaldehyde with O₂ on commercial TiO₂ nano-particles could be successfully enhanced by a simple mechanical blending with a high-silica mordenite (MOR) zeolite, the surface of which showed high hydrophobic properties. When the TiO₂ nano-particles of ca. 5–20 wt% were mixed with the MOR zeolite powders in an agate mortar for only 5 min, the blended TiO₂/MOR samples showed higher photocatalytic reactivity as compared to the pure TiO₂ nano-particles. Since the high-silica zeolite powders are highly transparent in UV light regions, the incident UV light is effectively irradiated onto the whole part of the TiO₂ nano-particles without any loss of light intensity. Furthermore, the siliceous MOR zeolite powders effectively adsorb the gaseous acetaldehyde molecules and supply them onto the surfaces of the blended TiO₂ nano-particles, resulting in an enhancement of the photocatalytic reactivity.     

Potential estimation of hourly blank storage space and charge loads of EVs using road traffic census and vehicles status

If both EVs (Electric Vehicles, includes plug‐in hybrid electric vehicles) and renewable energies spread in large quantities, it is possible to control the supply fluctuation of renewable energies using the storage battery of EVs. This research sought to show the charge load potential of EVs based on the state of the Japanese passenger car using traffic census results, etc. Furthermore, it tried to show the trend of the storage battery capacity according to time. From the estimated results: (1) the charge electricity of low and middle distance gets a majority of the total charge demand, (2) charge load changes according to time several times, and the minimum load is the number of gigawatt‐hours at early morning, (3) if night charge is assumed, the standby charge demand of noon will reach tens of gigawatt‐hours, it may have sufficient scale for supply fluctuation control of PVs. Although the present EV is not suitable for long‐distance running, these are expected to be 30 or less percent of the total charge demand. The estimated storage capacity potential in this research will not change numbers of times. © 2012 Wiley Periodicals, Inc. Electr Eng Jpn, 182(3): 30–38, 2013; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.22352     

Reusable Floating Beads with Immobilized Xylose-Fermenting Yeast Cells for Simultaneous Saccharification and Fermentation of Lime-Pretreated Rice Straw

Novel bioreactor beads for simultaneous saccharification and fermentation (SSF) of lime-pretreated rice straw (RS) into ethanol were prepared. Genetically modified Saccharomyces cerevisiae cells expressing genes encoding xylose reductase, xylitol dehydrogenase, and xylulokinase were immobilized in calcium alginate beads containing inorganic lightweight filler particles to reduce specific gravity. For SSF experiments, the beads were floated in slurry composed of lime-pretreated RS and enzymes and incubated under CO₂ atmosphere to reduce the pH for saccharification and fermentation. Following this reaction, beads were readily picked up from the upper part of the slurry and were directly transferred to the next vessel with slurry. After 240 h of incubation, ethanol production by the beads was equivalent to that by free cells, a trend that was repeated in nine additional runs, with slightly improved ethanol yields. Slurry with pre-saccharified lime-pretreated RS was subjected to SSF with floating beads for 168 h. Although higher cell concentrations in beads resulted in more rapid initial ethanol production rates, with negligible diauxic behavior for glucose and xylose utilization, no improvement in the ethanol yield was observed. A fermentor-scale SSF experiment with floating beads was successfully performed twice, with repeated use of the beads, resulting in the production of 40.0 and 39.7 g/L ethanol. There was no decomposition of the beads during agitation at 60 rpm. Thus, this bioreactor enables reuse of yeast cells for efficient ethanol production by SSF of lignocellulosic feedstock, without the need for instruments for centrifugation or filtration of whole slurry.     

Manufacture of organic transistors on large‐area flexible substrate using direct imaging exposure system by wet process suitable for roll‐to‐roll production

Organic thin‐film transistors (OTFTs) can be fabricated via a wet process and have exceptionally high flexibility. Therefore, production using the roll‐to‐roll (RtoR) method is expected. We succeeded in developing a new OTFT wet fabrication process adaptable to the RtoR process. Utilizing the electroless plating method for wiring formation, all materials can be formed in a wet process and can be patterned using the photolithography process. In addition, we succeeded in fabricating OTFT on an A4‐type flexible substrate using RtoR direct imaging exposure system.     

Preparation of transparent ts-1 zeolite film and its photocatalytic isomerization under uv irradiation

TS-1 zeolite film has been prepared by using nano sized TS-1 zeolite particles for the photocatalytic isomerization of cis-2-butene. TS-1 zeolite film showed optical transparent property and the thickness of film was 0.7 μm. UV irradiation of TS-1 zeolite film in the presence ofcis-2-butene leads to the photocatalytic isomerization ofcis-2-butene intotrans-2-butene at the temperature of 275 K. The yield oftrans- 2-butene was linearly increased with UV-irradiation time.     

Photocatalytic oxidation of CO with various oxidants by Mo oxide species highly dispersed on SiO2 at 293 K

The photocatalytic oxidation of CO into CO₂ with oxidants such as NO, N₂O and O₂ proceeded efficiently on a Mo/SiO₂ with high Mo dispersion under UV light irradiation. It was found that the reaction rate greatly depended on the kind and concentration of the oxidant. Photoluminescence investigations reveal the close relationship between the reaction rate and the relative concentration of the photo-excited Mo⁶⁺-oxide species, i.e. charge transfer–excited–triplet state (Mo⁵⁺–O⁻)^*, under steady-state reaction conditions. Moreover, the photocatalytic oxidation of CO with O₂ in excess H₂ was carried out to test suitability for applications to supplying pure H₂. This reaction was seen to proceed efficiently on Mo/SiO₂ with a high CO conversion of 100% and CO selectivity of 99% after 180 min under UV light irradiation, showing higher photocatalytic performance than TiO₂ (P-25) photocatalyst. UV–vis, XAFS, photoluminescence and FT-IR investigations revealed that the high reactivity of the charge transfer–excited–triplet state (Mo⁵⁺–O⁻)^*, with CO as well as the high reactivity of the photoreduced Mo-oxide species (Mo⁴⁺-species) with O₂ to produce the original Mo-oxide species (Mo⁶⁺O²⁻), played a crucial role in the reactions.     

Polymerization of [2,5-bis(trifluoromethyl)phenyl]acetylene and polymer properties

Summary [2,5-Bis(trifluoromethyl)phenyl]acetylene [BTFPA; HCCC₆H₃-2, 5-(CF₃)₂]polymerized with W, Mo, and Nb catalysts to produce methanol-insoluble polymers in high yields. The poly(BTFPA) produced by the W(CO)₆-based catalyst at 30 °C was soluble in p-(CF₃)₂C₆H₄, and had relatively high molecular weight ([]=0.352 dL/g in p-(CF₃)₂C₆H₄). The main chain of the polymer was composed of alternating double bonds, and the polymer was a dark brown solid. The temperature at which the weight loss of the polymer started was higher than 300 °C. The polymerization behavior and polymer properties for BTFPA are compared with those for phenylacetylene and [o-(trifluoromethyl)phenyl]acetylene.