Preparation and characterization of trilobal activated carbon fibers

The objective of this research was to evaluate the effectiveness of several different methods for controlling the pore size and pore size distribution in activated carbon fibers. Variables studied included fiber shape, activation time, and the addition of small amounts of silver nitrate. Pure isotropic pitch and the same isotropic pitch containing 1 wt.% silver were melt spun to form fibers with round and trilobal cross sections. These fibers were then stabilized, carbonized, and activated in carbon dioxide. Field emission scanning electron microscopy (FE SEM), electron dispersive spectra (EDS), and wavelength dispersive spectra (WDS) were used to monitor the size and distribution of the silver particles in the fibers before and after activation. Each of these analyses showed that the distribution of silver particles was extremely uniform before and after activation. The fibers were also weighed before and after activation to determine the percent burn-off. The BET specific surface areas of the activated fibers were determined from N₂ adsorption isotherms measured at −196 °C. The results showed that round and trilobal fibers with equivalent cross-sectional areas yielded similar burn-off values and specific surface areas after activation. Also, activation rates were found to be independent of CO₂ flow rate. The porosity of the activated fibers depended on the total time of activation and the cross-sectional area of fibers. The N₂ adsorption measurements showed that the activated fibers had extremely high specific surface areas (greater than 3000 m²/g) and high degrees of meso- and macro-porosity. FE SEM was also used to investigate surface texture and size of pore openings on the surfaces of the activated fibers. The photos showed that silver particles generated surface macro- and mesopores, in agreement with the inferences from N₂ adsorption measurements.     

Protein Ligation-Assisted Reconstitution of Split HRP Fragments for Facile Production of HRP Fusion Proteins in E. coli

Horseradish peroxidase (HRP) is a pivotal biocatalyst for biosensor development and fine chemical synthesis. HRP proteins are mostly extracted and purified from the roots of horseradish because the solubility and productivity of recombinant HRP in bacteria are significantly low. In this study, we investigate the reconstitution system of split HRP fragments to improve its soluble expression levels in E. coli allowing the cost-effective production of bioactive HRPs. To promote the effective association between two HRP fragments (HRPn and HRPc), we exploit SpyTag-SpyCatcher chemistry, a versatile protein coupling method with high affinity and selectivity. Each HRP fragment was genetically fused with SpyTag and SpyCatcher, respectively, exhibiting soluble expression in the E. coli cytoplasm. The engineered split HRPs were effectively and irreversibly reconstituted into a biologically active and stable assembly that can catalyze intrinsic enzymatic reactions. Compared to the chaperone co-expression system, our approach shows that the production yield of soluble HRP is comparable, but the purity of the final product is relatively high. Therefore, our results can be applied to the high-yield production of recombinant HRP variants and other difficult-to-express proteins in bacteria without complex downstream processes.     

Fabrication and Characterization of Nanoscale Ferroelectric Honeycombs

Nanoscale ferroelectric honeycombs, comprised of vertically aligned PbTiO₃ nanotubes, are fabricated by vapor phase reaction between lead acetate‐infiltrated TiO₂ nanotubes and PbO vapor. PbTiO₃ nanohoneycombs converted by vapor phase reaction at 550°C showed well‐aligned nanoscale structure with alignment angle less than 1° and well‐defined ferroelectric properties with the effective piezoelectric coefficient of 44 pm/V. This novel nanoscale structure is expected to facilitate high efficiency sensing of electromechanical and electrochemical stimuli.     

Lower Tropospheric Aerosol Measurements by MAX-DOAS During Severe Asian Dust Period

A recently developed aerosol retrieval algorithm based on O₄ slant column densities (SCDs) measured at a visible wavelength (476 nm) was utilized to derive aerosol information (e.g., aerosol optical depth (AOD) and vertical distributions of aerosol extinction coefficients (AECs)) in the lower troposphere during a severe Asian dust period. The MAX-DOAS measurements were carried out at Gwangju, Korea for nearly three months from February through May 2008. Comparison with AOD and surface PM₁₀, measured by collocated sunphotometer and beta gauge sampler, were made to validate the retrieved AODs and AECs in the atmospheric layer surface to 1 km height above ground. On the Asian dust days, temporal variations of the AODs retrieved from MAX-DOAS measurements show similar patterns, but with reduced magnitudes, to those measured by sunphotometer whereas similar AOD magnitude and temporal variation was observed between MAX-DOAS and sunphotometer measurements during the non-episodic days. Smaller correlation was observed between the surface PM₁₀ and AECs at 0.5 km during the Asian dust period compared to the correlation obtained for the non episodic days. This study demonstrates the ability of MAX-DOAS as a remote sensing technique for surface aerosol measurements under conditions of homogeneously distributed pollution in the planetary boundary layer. However, for the measurement of significantly enhanced aerosol loads with heterogeneous vertical distribution (e.g., Asian dust), measured AODs and AECs are underestimated at altitudes above 1 km due to decreased sensitivity of MAX-DOAS measurements at high altitudes.     

Novel High‐Temperature Antiferroelectric‐Based Dielectric NaNbO3–NaTaO3 Solid Solutions Processed in Low Oxygen Partial Pressures

The (1?x)NaNbO₃–(x)NaTaO₃ solid solution was investigated for x ≤ 0.4 in terms of new high‐temperature and high‐permittivity dielectric system that is suitable for base metal inner electrode capacitor applications. The addition of Ta significantly enhanced the resistivity of the dielectric, resulting in superior resistivity than the dielectrics‐formulated BaTiO₃ systems that dominate the multilayer ceramic capacitor dielectric devices. The voltage dependence of the permittivity was also superior to BaTiO₃‐based materials, providing higher capacitance at higher temperatures. A transmission electron microscopy study illustrated that the grains had so‐called core‐shell structure. According to the electron diffraction analysis, the core region had an inhomogeneous structure between antiferroelectric and ferroelectric phases, and shell region had an incommensurate ferroelectric‐like structure. The core and shell region had Nb‐ and Ta‐rich composition, respectively, and their interface was compositionally sharp, implying that shell region was formed via a liquid phase during the sintering process with an incongruent Ta dissolution reprecipitation. We anticipate that these or similar materials based on the alkali‐niobate perovskites can be further enhanced to provide capacitor solutions from 150°C to 250°C, which is an important range for a number of new AC–DC invertor and engine control units.     

Preparation of a high hydrophobic aluminium surface by double zincating process

In this present study, an efficient method has been proposed to develop a high hydrophobic zincated coating on the eva-core aluminium (Al) alloy surface. The double zincating method (Z2) was utilized to develop the required roughness on the Al surface. To control the surface energy, lauric acid (LA) was coated on the surface using the liquid self-assembled monolayers (L-SAMs) method. Surface morphology, the chemical composition of the treated and untreated Al alloy has been studied using scanning electron microscopy (SEM), atomic force microscopy (AFM), optical microscopy and X-ray diffraction (XRD), respectively. The hydrophobicity of the substrates has also been analysed using a contact angle measurement (CA). AFM micrographs show the surface roughness of the Al alloy has been drastically increased with chemical treatments from 0.071 to 0.32 μm. XRD shows the percentage crystallinity of the Al alloy is decreased with double zincating and LA coating from 56.8 to 22.7%. As a result, a high hydrophobicity of Al alloy was induced with a contact angle of 150° upon the double zincating method and L-SAMs coating.     

Flavonoids from Orostachys japonicus A. Berger Inhibit the Invasion of LnCaP Prostate Carcinoma Cells by Inactivating Akt and Modulating Tight Junctions

Tight junctions (TJs) are a mode of cell-to-cell adhesion in epithelial or endothelial cells, and serve as a physical barrier to maintenance of homeostasis in body by controlling paracellular transport. Claudins are the most important molecules of the TJs, but paradoxically these proteins are frequently over-expressed in cancers and their overexpression is implicated in the invasive potential of cancer. Hence, we investigated the effects of flavonoids extracted from Orostachys japonicus A. Berger (FEOJ) on TJs and the expression of claudins as well as cancer invasion along with in LnCaP human prostate cancer. FEOJ suppressed cancer cell motility and invasiveness at the concentrations where FEOJ did not show anti-proliferative activity. FEOJ increased transepithelial electrical resistance (TER) associated with tightening TJs, and suppressed expression of claudin proteins. Furthermore, FEOJ suppressed the activities of MMP-2 and -9 in a dose-dependent manner, which came from the activation of tissue inhibitor of metalloproteinases (TIMPs) by FEOJ. FEOJ suppressed migration and invasion by suppressing PI3K/Akt signaling pathway. Taken together, this study suggest that FEOJ suppresses cancer migration and invasion by tightening TJs through the suppression of claudin expression, and by suppressing MMPs in LnCaP human prostate cancer cells, which at least in part results from the suppression of PI3K/Akt signaling pathway.     

Aptamer-modified magnetic nanoprobe for molecular MR imaging of VEGFR2 on angiogenic vasculature

Nucleic acid-based aptamers have been developed for the specific delivery of diagnostic nanoprobes. Here, we introduce a new class of smart imaging nanoprobe, which is based on hybridization of a magnetic nanocrystal with a specific aptamer for specific detection of the angiogenic vasculature of glioblastoma via magnetic resonance (MR) imaging. The magnetic nanocrystal imaging core was synthesized using the thermal decomposition method and enveloped by carboxyl polysorbate 80 for water solubilization and conjugation of the targeting moiety. Subsequently, the surface of the carboxylated magnetic nanocrystal was modified with amine-functionalized aptamers that specifically bind to the vascular growth factor receptor 2 (VEGFR2) that is overexpressed on angiogenic vessels. To assess the targeted imaging potential of the aptamer-conjugated magnetic nanocrystal for VEGFR2 markers, the magnetic properties and MR imaging sensitivity were investigated using the orthotopic glioblastoma mouse model. In in vivo tests, the aptamer-conjugated magnetic nanocrystal effectively targeted VEGFR2 and demonstrated excellent MR imaging sensitivity with no cytotoxicity.     

Latent catalyst effects in halogen‐free epoxy molding compounds for semiconductor encapsulation

Latent catalyst effects were investigated to improve the physical properties of halogen‐free epoxy molding compounds (EMCs) for semiconductor encapsulation. In this study, biphenyl‐type resins were used as the epoxy and hardener resin for halogen‐free EMCs to obtain high flame‐retardant properties and high filler contents. Latent catalyst effects were examined with two kinds of EMC compositions, halogen‐free EMCs and conventional EMC compositions. We used triphenylphosphine‐benzoquinone salt (TPP‐BQ) as a latent catalyst. Spiral flow and gel time were measured to investigate the change in moldability with the latent catalyst. We measured package fail, moisture absorption, and delamination for reliability evaluation and flexural strength, flexural modulus, and adhesion for mechanical properties to examine latent catalyst effects. An improvement in moldability, reliability, and the mechanical properties were observed in two types of halogen‐free EMCs with TPP‐BQ as a latent catalyst. These phenomena were seen in conventional EMCs, including o‐cresol novolac epoxy resin. The cure kinetics of these systems were investigated by differential scanning calorimetry with an isothermal approach to explain these phenomena. The results indicate that the improvement in moldability in halogen‐free EMCs with TPP‐BQ was due to the low conversion rate of this system, and the increase in mechanical properties was attributed to the high conversion of curing reaction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2287–2299, 2005     

Apatite Induction on Ca-Containing Titania Formed by Micro-Arc Oxidation

Ca-containing, particularly CaTiO₃, titania films were prepared by micro-arc oxidation (MAO) of Ti in an electrolytic solution containing calcium acetate monohydrate (CA), and their apatite-inducing ability was evaluated in a simulated body fluid (SBF). The phase, Ca content, and morphology of the films were found to be strongly dependent on the applied voltage. The CaTiO₃-embedded titania was obtained at higher voltages (>300 V). When immersed in SBF, no apatite was induced in all the MAO specimens irrespective of the presence of CaTiO₃, which has been claimed to be an apatite inducer. However, after a hydrothermal treatment at 250°C, apatite was formed on the surfaces of the CaTiO₃-embedded titania after 28 days, which was closely related to the formation of amorphous Ca(OH)₂ and presumably surface Ti–OH groups.