Effect of palladium loaded activated carbons on hydrogen storage

Pd-loaded high surface area activated carbon (BAC-Pd) was produced from bamboo by carbonization and activation using potassium hydroxide with subsequent loading of palladium. The palladium loaded onto BACs appears to exist more in micropores. The Pd compounds exist mainly as amorphous PdCl₂ with Pd (0) structures in the whole surface of BAC-Pd. The hydrogen adsorption capability of BAC-Pd at 0.1?MPa and room temperature was evaluated for hydrogen storage. The amount of adsorbed hydrogen on BAC-Pd was the maximum among three Pd-loaded activated carbons because the physical properties and the Pd content are the highest among them. According to the effect of Pd content, the amounts of adsorbed hydrogen on BAC-Pd increased linearly as the Pd content increased, and the BET surface area of BAC-Pd decreased. BAC, which had the highest Pd contents in micropores, exhibited excellent adsorption ability for hydrogen at 298?K and 0.1?MPa. The amounts of chemisorbed hydrogen of BAC-Pd increased along with the increase in Pd content. Furthermore, the amount of adsorbed hydrogen of BAC-Pd is expected to increase in conditions with pressure higher than 0.1?MPa.     

Hexaphyrin as a Potential Theranostic Dye for Photothermal Therapy and 19F Magnetic Resonance Imaging

Two features of meso‐Aryl‐substituted expanded porphyrins suggest suitability as theranostic agents. They have excellent absorption in near infrared (NIR) region, and they offer the possibility of introduction of multiple fluorine atoms at structurally equivalent positions. Here, hexaphyrin (hexa) was synthesized from 2,6‐bis(trifluoromethyl)‐4‐formyl benzoate and pyrrole and evaluated as a novel expanded porphyrin with the above features. Under NIR illumination hexa showed intense photothermal and weak photodynamic effects, which were most likely due to its low excited states, close to singlet oxygen. The sustained photothermal effect caused ablation of cancer cells more effectively than the photodynamic effect of indocyanine green (a clinical dye). In addition, hexa showed potential for use in the visualization of tumors by ¹⁹F magnetic resonance imaging (MRI), because of the multiple fluorine atoms. Our results strongly support the utility of expanded porphyrins as theranostic agents in both photothermal therapy and ¹⁹F MRI.     

Photocatalytic inactivation and removal of algae with TiO<Subscript>2</Subscript>-coated materials

The capabilities of TiO₂-coated materials for the inactivation and removal of algae were investigated. As supports for TiO₂, non-woven fabric and Ni foam were chosen. To evaluate the ability of noble metal cocatalyst additions to facilitate the photocatalytic algal inhibition of TiO₂-coated materials, Pd nanoparticles were deposited on non-woven fabric-supported TiO₂ by photoelectrochemical deposition. The fabric-supported Pd/TiO₂ showed higher inhibition activity for algal growth compared to the fabric-supported TiO₂ without Pd. In addition, Ni foam-supported TiO₂ also showed high inhibition activity, both in laboratory-scale tests and open-air tests. Therefore, TiO₂-coated materials with suitable coating methods such as the use of cocatalysts or large surface area can substantially inhibit algal growth. The ability of the TiO₂-coated materials to inhibit algae correlated well with their activity for the photocatalytic decolorization of methylene blue, suggesting a nonspecific mechanism in the breakdown of cellular structures.     

High-Voltage Screening of Unidirectionally Surface-Ground Titania Ceramics

The effects of high-voltage screening were examined for perpendicularly and parallelly surface-ground titania rectangular bars. A screening field at or below which 30% of titania samples break electrically was applied to each group samples. After high-voltage screening, the surviving samples were subjected to mechanical strength measurement and the resultant strength distribution was compared with the original distribution. After screening, Weibull plots of perpendicularly ground samples bent to become convex curves while plots in the high-strength region remained almost the same, indicating that low-strength samples were selectively eliminated by the high-voltage screening. On the other hand, the screening effect on parallelly surface-ground samples was very small.     

Fouling reduction of a poly(ether sulfone) hollow‐fiber membrane with a hydrophilic surfactant prepared via non‐solvent‐induced phase separation

Membrane fouling is still a crucial problem, especially in applications for water treatment. When fouling takes place on membrane surfaces, it causes flux decline, leading to an increase in production cost due to increased energy demand. The selection of the right membrane material and a special treatment of the membrane are required to avoid membrane fouling. This article reports the fouling resistance of a poly(ether sulfone) (PES) hollow‐fiber membrane modified with hydrophilic surfactant Tetronic 1307. Experiments on several methods of fouling were carried out to investigate the effect of the addition of nonionic surfactant Tetronic 1307 on membrane fouling. The effectiveness of a chemical agent [sodium hypochlorite (NaClO)] in the reduction of bovine serum albumin (BSA) deposition on the membrane surface was also evaluated. Permeation results showed that the fouling of a PES blend membrane with Tetronic 1307 was lower than that of the original PES membrane in the case of BSA filtration. A treatment with a 100 ppm NaClO solution was capable of removing BSA cake formation and effective at improving the relative permeability. The permeability of a PES blend membrane with Tetronic 1307 was almost 2 times higher than the original permeability when the membrane was treated with a 100 ppm NaClO solution because both BSA and Tetronic 1307 could be decomposed. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and properties of liposomes composed of various phospholipids with different hydrophobic chains using a supercritical reverse phase evaporation method

Liposomes were prepared by the supercritical reverse phase evaporation method developed in our laboratory using various phospholipids with different hydrocarbon chains. The effects of the length of alkyl chain and number of unsaturated bonds of phospholipids on the properties of liposomal membranes were examined through trapping efficiency measurements, transmission electron microscopic observations, and osmotic response measurements. The trapping efficiency for water-soluble drugs of liposomes prepared by our method was greatly higher than that of liposomes prepared by the conventional Bangham method. Liposomes prepared using unsaturated phospholipids showed a high trapping efficiency compared with those prepared using saturated phospholipids. In addition, the trapping efficiency of liposomes prepared using 1-palmitoyl-2-oleoyl phosphatidylcholine (POPC), a complex phospholipid with both saturated and unsaturated alkyl groups, had a value intermediate between L-alpha-dipalmitoyl-phosphtidylcholine (DPPC), a saturated phospholipid, and L-alpha-dioleoylphosphatidylcholine (DOPC), an unsaturated phospholipid. That is, the trapping efficiency of liposomes was dependent on the number of unsaturated bonds rather than the alkyl chain length of phospholipid molecule and it increased with increasing bulkiness of the molecule. The osmotic response was higher for liposomes prepared using unsaturated phospholipids than for those formed by saturated phospholipids.     

Preparation and luminescent properties of Eu-doped transparent mica glass–ceramics

Eu-doped transparent mica glass–ceramics were prepared, the influence of Eu-doping on the crystallization of the parent glasses was investigated and the luminescent properties of the parent glasses and the glass–ceramics were estimated. A small additive amount of Eu element was very effective in preparing transparent mica glass–ceramics. However, the excess addition led to the coarsening of phase separation in the glass phase and the separation of unidentified crystal phases and β-eucryptite during heating of the parent glasses, which caused white opaque at lower heating temperatures. When mica crystals were separated, Eu ions entered the interlayers of mica crystals. The observed emission and excitation spectra showed that parts of Eu³⁺ ions which were added as Eu₂O₃ were reduced to Eu²⁺ ions during melting of the starting materials and heating the parent glasses in air and the energy transfer from Eu²⁺ to Eu³⁺ ions occurred.     

Cutting characteristics of PVD-coated tools deposited by filtered arc deposition (FAD) method

The cutting characteristics of novel physical vapor deposition (PVD)-coated tools deposited using filtered arc deposition (FAD) method are investigated. The TiCN-coated films are extremely smooth without any droplets. They exhibit superior hardness and adherence and a favorable cutting performance for the high-speed milling of a prehardened stainless steel. The availability of a newly proposed VN film is also examined. Owing to the good lubrication and tribological properties of the VN coating film, the lower cutting force, flank wear with, and cutting temperature than those of the TiN-coated tool are obtained in milling of the prehardened steel.     

Pressureless Sintering of Carbon Nanofibre/SiC Composites and Their Properties

To enhance the fracture toughness of silicon carbide (SiC) ceramics and prevent the generation of cracks and chippings in the SiC ceramics during machining process, carbon nanofibres (CNFs) were compounded with SiC. The densification and microstructure development of the CNFs/SiC composites pressureless sintered in Ar atmosphere were investigated. The fracture toughness of SiC ceramics was enhanced by the addition of 1–3 wt% CNFs, which resulted from the pullout and/or bridging effect of CNFs bonded much more closely with SiC. The addition of 3 wt% CNFs prevented the chippings from generating in the composite during precision machining process.     

Palladium on Carbon‐Catalyzed Cross‐Coupling using Triarylbismuths

Simple and efficient protocols for the 10% palladium on carbon (Pd/C)‐catalyzed cross‐coupling reactions between triarylbismuths and aryl halides have been developed. A variety of iodo‐ and bromobenzenes possessing an electron‐withdrawing group on the aromatic nucleus were smoothly cross‐coupled in the presence of 10% Pd/C, sodium phosphate dodecahydrate (Na₃PO₄⋅12 H₂O) and 1,4‐diazabicyclo[2.2.2]octane (DABCO) in heated N‐methyl‐2‐pyrrolidone (NMP) as the solvent. For the arylations of iodobenzenes, the reactions effectively proceeded under the combined use of caesium fluoride (CsF) and 2,2′‐biquinoline. Furthermore, a ligand‐free 10% Pd/C‐catalyzed cross‐coupling reaction between the aryl iodides and triarylbismuths was also established by the addition of tetra‐n‐buthylammonium fluoride trihydrate (TBAF⋅3 H₂O) in which the palladium metals were hardly leached from the catalyst into the reaction media.