Current Understanding of Cu-Exchanged Chabazite Molecular Sieves for Use as Commercial Diesel Engine DeNOx Catalysts

Selective catalytic reduction (SCR) of NO_x with ammonia using metal-exchanged molecular sieves with a chabazite structure has recently been commercialized on diesel vehicles. One of the commercialized catalysts, i.e., Cu-SSZ-13, has received much attention for both practical and fundamental studies. For the latter, the particularly well-defined structure of this zeolite is allowing long-standing issues of the catalytically active site for SCR in metal-exchanged zeolites to be addressed. In this review, recent progress is summarized with a focus on two areas. First, the technical significance of Cu-SSZ-13 as compared to other Cu ion-exchanged zeolites (e.g., Cu-ZSM-5 and Cu-beta) is highlighted. Specifically, the much enhanced hydrothermal stability for Cu-SSZ-13 compared to other zeolite catalysts is addressed via performance measurements and catalyst characterization using several techniques. The enhanced stability of Cu-SSZ-13 is rationalized in terms of the unique small pore structure of this zeolite catalyst. Second, the fundamentals of the catalytically active center; i.e., the chemical nature and locations within the SSZ-13 framework are presented with an emphasis on understanding structure–function relationships. For the SCR reaction, traditional kinetic studies are complicated by intra-crystalline diffusion limitations. However, a major side reaction, nonselective ammonia oxidation by oxygen, does not suffer from mass-transfer limitations at relatively low temperatures due to significantly lower reaction rates. This allows structure–function relationships that are rather well understood in terms of Cu ion locations and redox properties. Finally, some aspects of the SCR reaction mechanism are addressed on the basis of in situ spectroscopic studies.     

Correcting veiling glare of refined CIECAM02 for mobile display

Small displays are widely used; they are small enough to be carried around and are often viewed under extreme surround conditions. Under bright illumination, mobile display users experience “veiling glare” caused by bright ambient lighting. A refined version of CIECAM02 called “Refined CIECAM02 and original CIECAM02” were tested to predict visual results in terms of lightness (J), colourfulness (M), and brightness (Q) on a 2‐inch sized display (2″) mobile phone under four surround conditions; dark (0 cd/m²), dim (5 cd/m²), average (1000 cd/m²), and bright (10,000 cd/m²). Other than the two versions of CIECAM02 using the original data, a correction to the models' predicted lightness J and a black correction to the original data were developed. Overall, the refined CIECAM02 plus the J correction performed the best for predicting the lightness, brightness and colourfulness under all the viewing conditions, especially for bright surround condition. Furthermore, another experiment was carried out using complex images to verify different versions of CIECAM02. The images were reproduced using JMh (lightness, colourfulness, and hue) spaces from the modified CIECAM02 versions. The experiment was conducted by comparing original images viewed under dim, average, or bright surround conditions and the predicted images were viewed under dark surround condition on two identical mobile displays. The different versions of the CIECAM02 showed similar results to each other for dim and average surround conditions but large differences when predicting the images under bright surround condition. The refined CIECAM02 with the J′ formula performed the best amongst all four CIECAM02 versions. © 2011 Wiley Periodicals, Inc. Col Res Appl, 2013.     

Effect of reaction kinetics of polymer electrolyte on the ion‐conductive behavior for poly(oligo oxyethylene methacrylate)–LiTFSI mixtures

The effect of the reaction kinetics on the ionic conductivity for a comblike‐type polyether (MEO) electrolyte with lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) was characterized by DSC, complex impedance measurements, and ¹H pulse NMR spectroscopy. The ionic conductivity of these electrolytes was affected by the reaction condition of the methacrylate monomer and revealed by the glass transition temperature (T_g), spin–spin relaxation time (T₂), steric effects of the terminal groups, and the number of charge carriers indicated by the VTF kinetic parameter. In this system, the electrolytes prepared by the reaction heating rate of 10°C/min of MEO–H and 15°C/min of MEO–CH₃ showed maximum ionic conductivity, σ_i, two to three times higher in magnitude than that of the σ_i of the others at room temperature. As experimental results, the reaction kinetic rate affected the degree of conversion, the ionic conductivity, and the relaxation behaviors of polyether electrolytes. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2149–2156, 2003     

Effect of slot-die configurations on coating gap dependence of maximum and minimum wet thicknesses

The dependence of the maximum and minimum wet thicknesses on the coating gap is derived for the slot-die coating process, under different slot-die configurations. Analytical expressions for the wet thickness and its derivative with respect to the coating gap are obtained using a simple flow model. The results indicate that, as expected, the minimum wet thickness increases linearly with the coating gap; however, the maximum wet thickness demonstrates a counterintuitive trend of decreasing as the coating gap increases, when a specific slot-die configuration is assumed. Moreover, the results are also validated by numerically solving the complete two-dimensional (2D) Navier–Stokes equation.     

Frequency response of continuous-flow adsorber for multicomponent system

In this paper, we present a theoretical analysis of the frequency response of a continuous-flow adsorber with periodic modulation of the inlet flow-rate to measure multicomponent diffusion kinetics in porous media. Micropore diffusion kinetics is assumed for the intraparticle mass transfer mechanism and three different shapes of microparticle are considered: slab, cylinder, and sphere. Simulation results for a binary system show that the frequency response of the faster diffusing component is strongly influenced by the slower component. The out-of-phase characteristic function of the frequency response of the faster diffusing component shows maximum and minimum points. The deviation between these maximum and minimum values becomes smaller when the cross-terms of diffusivity go to zero, while the deviation becomes larger when the cross-terms of the adsorption equilibrium constant go to zero. Contrary to the behaviour of the out-of-phase function of the faster diffusing component, the out-of-phase function of the slower diffusing component shows no extrema at all. The in-phase characteristic function of the frequency response of the continuous-flow adsorber is not affected by the overflow parameter.     

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.     

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.     

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.     

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.