High-Temperature Chemical Stability of Plasma-Sprayed Ca05Sr05Zr4P6O24 Coatings on Nicalon/SiC Ceramic Matrix Composite and Ni-Based Superalloy Substrates

The potential application of Ca05Sr05Zr4P6O24 (CS50) as a corrosion-resistant coating material for Si-based ceramics and as a thermal barrier coating material for Ni-based superalloys was explored. A ∼200 (xm thick CS50 coating was prepared by air plasma spray with commercially available powder. A Nicalon/SiC ceramic matrix composite and a Ni-based superalloy coated with a ∼200 (xm thick metallic bond coat layer were used as substrate materials. Both the powder and coating contained ZrP2O7 as an impurity phase, and the coating was highly porous as-deposited. The coating deposited on the Nicalon/SiC substrate was chemically stable upon exposure to air and Na2SO4/O2 atmospheres at 1000°C for 100 h. In contrast, the coating sprayed onto the superalloy substrate significantly reacted with the bond coat surface after similar oxidation in air.     

Continuous ethanol production from wood hydrolysate by chemostat and total cell retention culture

Chemostat and total cell retention cultures with internal filter system ofSaecharomyc.es cerevisiae H1-7 were carried out to produce ethanol from wood hydrolysate. Maximum ethanol productivity obtained in a chemostat with the aeration rate of 1 vvm was 3.79 g/(L·h). This was 20% higher than that in a chemostat without aeration. However, the substrate was not completely consumed at the dilution rate with the maximum productivity. The realistic productivity, which has higher than 99% conversion rate of substrate, was. 2.95 g/(L·h). The maximum productivity in the total cell retention culture was 6.65 g/(L·h) at the dilution rate of 0.19 h¹ and the residual glucose concentration was negligible.     

Decane reforming reaction over Pt,Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on Y-zeolite

Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on NaY- and HY-zeolite were examined as a catalyst for producing gasoline from n-decane via simultaneous reforming and cracking. The catalysts were prepared by calcining and reducing metal-ion-exchanged Y-zeolite with O₂ and H₂ at 300°C., respectively. Thus prepared catalysts were characterized by hydrogen chemisorption and temperature programmed desorption of ammonia. Pt-Ni/NaY and Pt-Ir/NaY bimetallic catalysts offered the improved activity maintenance compared to Pt/NaY monometallic catalyst. The catalysts supported on HY-zeolite showed higher selectivity toward C₅–C₇ and skeletal isomers of C₅–C₇- and C₈–C₁₀ than those of the catalysts supported on NaY-zeolite, which is a desired characteristic for increasing octane value of gasoline these days. However, deactivation with reaction time was much more pronounced on HY-zeolite-supported catalyst. When the catalyst was prcsulfided with H,S, the stability with time on stream was enhanced and the selectivity was quite different from that of the catalyst before presulfiding. The acidity of Y-zeolite and presulfiding of catalyst greatly influenced the activny, selectivity and stability of Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on Y-zeolite in n-decane reforming reaction.     

Thermistor behavior of PEDOT:PSS thin film

The temperature-dependent resistance changing characteristics (thermistor behaviors) of a poly(3,4-ethylenedioxythophene):poly(4-styrenesulfonate) (PEDOT:PSS) thin film are investigated in the 30–100 °C range using Greek-cross and bar patterns. The PEDOT:PSS film was spin-coated onto a Si wafer passivated with a SiO₂ layer, and a conventional dry etching technique was used to pattern the PEDOT:PSS film in conjunction with a nitride etch mask layer. Cr/Au was used for the electrode material. It was found that the characteristic temperature (T₀) and resistivity of the PEDOT:PSS film have an inversely proportional relationship with the number of coatings and the number of interfaces between multiply coated PEDOT:PSS layers. It was also found that as the number of coatings and the number of the interfaces increase, lower temperature-dependent resistance changes are observed. The temperature coefficient of resistance (TCR) value of 60 nm thick PEDOT:PSS film was slightly larger than or comparable to that of a conventional metal (Au or Pt) thermistor. The possibility of utilizing the PEDOT:PSS thin film in thermistor applications is discussed.     

Significant Enhancement of the Dielectric Constant through the Doping of CeO2 into HfO2 by Atomic Layer Deposition

Films of CeO₂ were deposited by atomic layer deposition (ALD) using a Ce(mmp)₄ [mmp = 1‐methoxy‐2‐methyl‐2‐propanolate] precursor and H₂O reactant. The growth characteristics and film properties of ALD CeO₂ were investigated. The ALD CeO₂ process produced highly pure, stoichiometric films with polycrystalline cubic phases. Using the ALD CeO₂ process, the effects of Ce doping into an HfO₂ gate dielectric were systematically investigated. Regardless of Ce/(Ce + Hf) composition, all ALD Ce_xHf_1?xO₂ films exhibited constant growth rates of approximately 1.3 Å/cycle, which is essentially identical to the ALD HfO₂ growth rates. After high‐temperature vacuum annealing at 900°C, it was verified, based on X‐ray diffraction and high‐resolution cross‐sectional transmission electron microscopy results, that all samples with various Ce/(Ce + Hf) compositions were transformed from nanocrystalline to stabilized cubic or tetragonal HfO₂ phases. In addition, the dielectric constant of the Ce_xHf_1?xO₂ films significantly increased, depending on the Ce doping content. The maximum dielectric constant value was found to be nearly 39 for the Ce/(Ce + Hf) concentration of ~11%.     

Carbon nanotubes: properties,synthesis, purification,and medical applications

Current discoveries of different forms of carbon nanostructures have motivated research on their applications in various fields. They hold promise for applications in medicine, gene, and drug delivery areas. Many different production methods for carbon nanotubes (CNTs) have been introduced; functionalization, filling, doping, and chemical modification have been achieved, and characterization, separation, and manipulation of individual CNTs are now possible. Parameters such as structure, surface area, surface charge, size distribution, surface chemistry, and agglomeration state as well as purity of the samples have considerable impact on the reactivity of carbon nanotubes. Otherwise, the strength and flexibility of carbon nanotubes make them of potential use in controlling other nanoscale structures, which suggests they will have a significant role in nanotechnology engineering.     

Water-soluble PPV and C60 nanocomposite with enhanced miscibility and enhanced photo-induced charge transfer through ground state electrostatic interactions

We report the preparation of highly charged nanocomposites comprised of water-soluble, anionic fullerene and cationic poly-phenylenevinylene (PPV) derivatives. The nanocomposites display high fluorescence quenching efficiency (99%) presumably due to enhanced miscibility between cationic PPV and anionic C₆₀ via electrostatic interactions. We show that complexation between the cationic PPV and anionic C₆₀ derivatives leads to formation of nanocomposites with optical and electronic properties distinct from individual components without preferential electrostatic interactions. Photo-induced charge transfer quenches fluorescence from the PPV component is consistent with the frontier energy offsets of PPV and C₆₀, and cyclic voltammetry and UV–Vis spectroscopy measurements. This result confirms high miscibility between donor and acceptor and resonance Raman spectra indicate a conformational changes of the PPV backbone upon complex formation.     

Charge Density Influences C1 Domain Ligand Affinity and Membrane Interactions

The C1 domain, which represents the recognition motif on protein kinase C for the lipophilic second messenger diacylglycerol and its ultrapotent analogues, the phorbol esters, has emerged as a promising therapeutic target for cancer and other indications. Potential target selectivity is markedly enhanced both because binding reflects ternary complex formation between the ligand, C1 domain, and phospholipid, and because binding drives membrane insertion of the C1 domain, permitting aspects of the C1 domain surface outside the binding site, per se, to influence binding energetics. Here, focusing on charged residues identified in atypical C1 domains which contribute to their loss of ligand binding activity, we showed that increasing charge along the rim of the binding cleft of the protein kinase C δ C1 b domain raises the requirement for anionic phospholipids. Correspondingly, it shifts the selectivity of C1 domain translocation to the plasma membrane, which is more negatively charged than internal membranes. This change in localization is most pronounced in the case of more hydrophilic ligands, which provide weaker membrane stabilization than do the more hydrophobic ligands and thus contributes an element to the structure–activity relations for C1 domain ligands. Coexpressing pairs of C1‐containing constructs with differing charges each expressing a distinct fluorescent tag provided a powerful tool to demonstrate the effect of increasing charge in the C1 domain.     

Fretting corrosion of tin-plated contacts

The susceptibility of tin-plated contacts to fretting corrosion is a major limitation for its use in electrical connectors. The present paper evaluates the influence of a variety of factors, such as, fretting amplitude (track length), frequency, temperature, humidity, normal load and current load on the fretting corrosion behaviour of tin-plated contacts. This paper also addresses the development of fretting corrosion maps and lubrication as a preventive strategy to increase the life-time of tin-plated contacts. The fretting corrosion tests were carried out using a fretting apparatus in which a hemispherical rider and flat contacts (tin-plated copper alloy) were mated in sphere plane geometry and subjected to fretting under gross-slip conditions. The variation in contact resistance as a function of fretting cycles and the time to reach a threshold value (100 mΩ) of contact resistance enables a better understanding of the influence of various factors on the fretting corrosion behaviour of tin-plated contacts. Based on the change in surface profile and nature of changes in the contact zone assessed by laser scanning microscope (LSM) and surface analytical techniques, the mechanism of fretting corrosion of tin-plated contacts and fretting corrosion maps are proposed. Lubrication increases the life-time of tin-plated contacts by several folds and proved to be a useful preventive strategy.     

A study on performance optimization of a toilet by measuring accumulated flow rate of a trapway

When water shortages occur, toilet water-saving becomes an effective way to solve the problem. We developed a new method that utilizes the accumulated flow rate to predict the flushing performance and to obtain design data for the development of high-efficiency toilets. The results showed that the length and shape of the trapway are the most important factors for flushing performance, and additional water saving can be achieved by delaying the opening of the trapway outlet valve. In addition, the tank water level in the water tank needs to be optimized considering siphon intensity as well as siphon duration. In conclusion, the toilet was optimized up to 6.5 kg of water using 60 mm diameter flexible tube by the method of accumulated flow rate measurement. In the future, the development of an ultra high efficiency toilet below 4.5 kg will be tried utilizing the method.