Photocatalytic degradation of methylene blue and acetaldehyde by TiO<Subscript>2</Subscript>/glaze coated porous red clay tile

Nanosized TiO₂ sol synthesized by sol-gel method was successfully coated on the porous red clay tile (PRC tile) with micrometer sized pores. PRC tile was first coated with a low-firing glaze (glaze-coated PRC tile) and then TiO₂ sol was coated on the glaze layer. A low-fired glaze was prepared at various blending ratios with frit and feldspar, and a blending ratio glazed at 700 °C was selected as an optimum condition. Then TiO₂ sol synthesized from TTIP was dip-coated on the glazed layer (TiO₂/glaze-coated PRC tile), and it was calcined again at 500 °C. Here, these optimum calcination temperatures were selected to derive a strong bonding by a partial sintering between TiO₂ sol particles and glaze layer. Photocatalytic activity on the TiO₂/glaze-coated PRC tile was evaluated by the extent of photocatalytic degradation of methylene blue and acetaldehyde. Methylene blue with the high concentration of 150 mg/l on the surface of TiO₂/glaze-coated PRC tile was almost photodegraded within 5 hours under the condition of average UV intensity of 0.275 mW/cm₂, while no photodegradation reaction of methylene blue occurred on the glaze-coated PRC tile without TiO₂. Another photocatalytic activity was also evaluated by measuring the extent of photocatalytic degradation of gaseous acetaldehyde. The photodegradation efficiency in TiO₂/glaze-coated PRC tile showed about 77% photocatalytic degradation of acetaldehyde from 45,480 mg/l to 10,536 mg/l after the UV irradiation of 14 hours, but only about 16% in the case of the glaze-coated PRC tile.     

Resistance spot weldability of lightweight steel with a high Al content

Using alternating current (AC)- and direct current (DC)-type welders, the resistance spot weldability of lightweight steel was evaluated under various electrode forces, welding currents, and times. The acceptable welding conditions were specified; however, these had very narrow ranges and there was little difference between the conditions determined for the AC- and DC-type welding. In both types of welding with electrode forces of of 300 kg_f and 400 kg_f, the acceptable weld currents were 5.0 kA and 5.5 kA, respectively. Also, the nugget size increased with the welding current. Under the acceptable welding conditions, there were no significant changes in the maximum tensile shear strength and nugget size, as 6.4-6.6 kN and 4.1-4.3 mm, respectively. The microstructure of weld metals was consisted of martensite, austenite and ferrite. And the small fraction of martensite was founded in the heat affected zone (HAZ), therefore the weld metal had the greatest hardness, and HAZ softening did not occur in this study. Considering the fracture surface, cleavage and ductile fracture were investigated because of the existence of martensite and ferrite in the welds.     

Effect of the fluorine-addition order on the hydrodesulfurization activity of fluorinated NiW/Al2O3 catalysts

Fluorinated NiW/Al₂O₃ catalysts with different orders of fluorine addition have been prepared, tested for hydrodesulfurization (HDS) of thiophene, and characterized using nitric oxide chemisorption and temperature-programmed sulfidation. The catalyst surface area has been affected by fluorine addition but not by the order of fluorination. The fluorine addition-order does not affect the amount of fluorine retained in the catalysts after the calcination and the reaction steps, either. On the other hand, the order of fluorine addition changes the dispersion of the nickel and the tungsten species, incorporation of nickel with the tungsten edge sites, and consequently the HDS activity of the catalysts. The catalyst fluorinated in the last step, i.e., after addition of both tungsten and nickel, shows the highest activity in thiophene HDS, which is supported by other experimental results indicating the most nitric oxide chemisorption and the largest incorporation of nickel with the tungsten species. Accordingly, enhancement of the catalyst activity by fluorination is due to the repartition of the metal species rather than to partial solubilization of alumina in the fluorine-addition step.     

Synthesis of 1-phenyl-1-xylyl ethane by Friedel–Crafts alkylation of xylene with α-methylbenzyl alcohol over mordenite

In the Friedel–Crafts alkylation of xylene to prepare 1-phenyl-1-xylyl ethane (PXE), α-methylbenzyl alcohol was used as an alkylating agent over a mordenite catalyst. The catalyst was characterized by MAS-NMR, N₂ adsorption/desorption, NH₃-TPD, and various other techniques and was found to possess strong Brønsted acid sites. When temperature was low, the main product was bis-(α-methylbenzyl) ether. However, as the temperature went up, PXE and heavies, styrene trimers and heavier oligomers, became main products. The formation of PXE, occurring on strong acid sites, is favored by raising temperature, space velocity, pressure, and xylene/MBA ratio within the experimental ranges. As the catalyst deactivates, the selectivities to PXE and heavies decrease and those to linear dimer and styrene increase. A reaction mechanism is proposed.     

A study on magnetic abrasive deburring of dual micro pattern

Studies on dual micro pattern are not established because of difficulty of its fabrication and deburring technology. In this investigation, a dual micro pattern which consists of a net pattern and a lenticular pattern was fabricated on a cylindrical workpiece by turning process. Magnetic abrasive deburring (MAD) was proposed as a deburring process in this study. Burr height defined by difference of its height and theoretical pattern height was measured as about 1 μm. It is one of the non-traditional machining methods utilizing flexible tool which consists of ferrous particle and abrasive powder. Hence, the aim of this investigation is to remove generated burr on the dual micro pattern. Burr at the dual micro pattern was removed through MAD, and a prediction equation of machined pattern height was derived. A deburring condition was optimized and verified by experiments. As a result, it was confirmed that dual micro pattern which has high shape accuracy was fabricated using MAD.

     

Advancement in the Hydrogen Absorbing and Releasing Kinetics of MgH<Subscript>2</Subscript> by Mixing with Small Percentages of Zn(BH<Subscript>4</Subscript>)<Subscript>2</Subscript> and Ni

Zn(BH₄)₂ made in our former investigation and Ni were mixed with MgH₂ to promote the hydrogen absorption and release features of Mg. A 96 w/o MgH₂ + 2 w/o Ni + 2 w/o Zn(BH₄)₂ sample [named MgH₂–4NZ] was prepared by milling in a planetary ball mill in a hydrogen atmosphere. The proportion of the additive was small (4 w/o) in order to increase hydrogen absorbing and releasing rates without majorly sacrificing the hydrogen-storage capacity. The hydrogen absorption and release features of the MgH₂–4NZ were inspected in detail and compared with those of 99 w/o MgH₂ + 1 w/o Zn(BH₄)₂ [named MgH₂–1Z] and 95 w/o MgH₂ + 2.5 w/o Ni + 2.5 w/o Zn(BH₄)₂ [named MgH₂–5NZ] samples. The activation of the MgH₂–4NZ was not required. The MgH₂–4NZ had a useful hydrogen-storage capacity (the quantity of hydrogen absorbed after 60 min) of about 5.5 w/o at the first cycle. At the first cycle, the MgH₂–4NZ absorbed 3.84 w/o hydrogen after 5 min and 5.47 w/o hydrogen after 60 min at 593 K in 12 bar hydrogen. The MgH₂–4NZ had a higher releasing rate, larger amounts of hydrogen absorbed and released after 60 min, and a better cycling capability than the MgH₂–1Z. Staying of Ni (as Mg₂Ni) and a larger amount of Zn among particles is believed to have led to the better cycling capability of the MgH₂–4NZ.     

Direct evidence for the formation of ordered carbides in a ferrite-based low-density Fe–Mn–Al–C alloy studied by transmission electron microscopy and atom probe tomography

We study the structure and chemical composition of the κ-carbide formed as a result of isothermal transformation in an Fe–3.0Mn–5.5Al–0.3C alloy using transmission electron microscopy and atom probe tomography. Both methods reveal the evolution of κ-particle morphology as well as the partitioning of solutes. We propose that the κ-phase is formed by a eutectoid reaction associated with nucleation growth. The nucleation of κ-carbide is controlled by both the ordering of Al partitioned to austenite and the carbon diffusion at elevated temperatures.     

Applications of Mesenchymal Stem Cells in Skin Regeneration and Rejuvenation

Mesenchymal stem cells (MSCs) are multipotent stem cells derived from adult stem cells. Primary MSCs can be obtained from diverse sources, including bone marrow, adipose tissue, and umbilical cord blood. Recently, MSCs have been recognized as therapeutic agents for skin regeneration and rejuvenation. The skin can be damaged by wounds, caused by cutting or breaking of the tissue, and burns. Moreover, skin aging is a process that occurs naturally but can be worsened by environmental pollution, exposure to ultraviolet radiation, alcohol consumption, tobacco use, and undernourishment. MSCs have healing capacities that can be applied in damaged and aged skin. In skin regeneration, MSCs increase cell proliferation and neovascularization, and decrease inflammation in skin injury lesions. In skin rejuvenation, MSCs lead to production of collagen and elastic fibers, inhibition of metalloproteinase activation, and promote protection from ultraviolet radiation-induced senescence. In this review, we focus on how MSCs and MSC-derived molecules improve diseased and aged skin. Additionally, we emphasize that induced pluripotent stem cell (iPSC)-derived MSCs are potentially advanced MSCs, which are suitable for cell therapy.     

Continuous viscosity measurement of non-Newtonian fluids over a range of shear rates using a mass-detecting capillary viscometer

A newly designed mass-detecting capillary viscometer uses a novel concept to continuously measure non-Newtonian fluids viscosity over a range of shear rates. A single measurement of liquid-mass variation with time replaces the flow rate and pressure drop measurements that are usually required by capillary tube viscometers. Using a load cell and a capillary, we measured change in the mass flow rate through a capillary tube with respect to the time,m(t), from which viscosity and shear rate were mathematically calculated. For aqueous polymer solutions, excellent agreement was found between the results from the mass-detecting capillary viscometer and those from a commercially available rotating viscometer. This new method overcomes the drawbacks of conventional capillary viscometers meassuring non-Newtonian fluid viscosity. First, the mass-detecting capillary viscometer can accurately and consistently measure non-Newtonian viscosity over a wide range of shear rate extending as low as 1 s⁻¹. Second, this design provides simplicity (i. e., ease of operation, no moving parts), and low cost.     

Improved Emotion Recognition With a Novel Speaker-Independent Feature

Emotion recognition is one of the latest challenges in human-robot interaction. This paper describes the realization of emotional interaction for a Thinking Robot, focusing on speech emotion recognition. In general, speaker-independent systems show a lower accuracy rate compared with speaker-dependent systems, as emotional feature values depend on the speaker and their gender. However, speaker-independent systems are required for commercial applications. In this paper, a novel speaker-independent feature, the ratio of a spectral flatness measure to a spectral center (RSS), with a small variation in speakers when constructing a speaker-independent system is proposed. Gender and emotion are hierarchically classified by using the proposed feature (RSS), pitch, energy, and the mel frequency cepstral coefficients. An average recognition rate of 57.2% (plusmn 5.7%) at a 90% confidence interval is achieved with the proposed system in the speaker-independent mode.