Surface Modification of Epoxy Resin with Silicone-containing Block Copolymers

In order to improve oil and water repellency, silicone-containing block copolymers, composed of methylmethacrylate (MMA), glycidylmethacrylate (GMA), and polydimethylsiloxanemethacrylate (SMA), were blended in an epoxy resin. It was expected that the low surface energy dimethylsiloxane segments would adsorb and orient at the exterior of the resin to make a thin surface phase and the glycidyl groups would mesh with the epoxy resin by primary bonding. The techniques of X-ray photoelectron spectroscopy (ESCA), dynamic contact angle (DCA) and peel strength measurements of pressure sensitive adhesives were used to characterize the modified epoxy resin surface phases. The amount of Si_2p obtained via angular dependent ESCA investigation in the near surface region of the modified resin increased with decreasing sampling depth. With an increase in modifier content, both the amount of Si_2p and O_1s also increased. Both advancing and receding contact angles for an aluminum plate coated with modified resin, measured by dipping into and out of water, increased with the addition of these modifiers. The peel strength of a pressure sensitive adhesive tape affixed to the modified epoxy resin decreased dramatically with increasing modifier content. It was found that these copolymers were good surface modifiers to improve oil and water repellency and that they acted as release agents.     

Positron lifetime calculations on vacancy clusters and dislocations in Ni and Fe

Positron lifetime calculations have been performed on vacancy clusters (stacking fault tetrahedra (SFT), vacancy loops), such clusters on dislocation line, interstitial clusters, such clusters on a dislocation line and dislocation line itself in order to investigate the so-called intermediate lifetimes observed in the experiments, namely, positron lifetimes between that at a matrix and that at a single vacancy. Before lifetime calculations, various defects were constructed in the model lattices and were relaxed completely to obtain the stable atomic structure by using N-body potentials. Then positron lifetime calculation was carried out for each defect. It was shown that positron lifetime for a SFT in Ni dependes on its size and becomes smaller with increasing the size. The positron wave function is mainly localized at the corner of a SFT, which gives rather lifetime, e.g., 130 ps for V₂₈, but when the cluster size is small, e.g., less than 10 vacancies, it gives a rather longer lifetime, e.g., 177 ps for V₆ because of the wave function localized at the inner space of a cluster. These behaviours are consistent with the experimental results. It was also found that the positron lifetime on a dislocation line and that at a jog are short (113 and 119 ps, respectively for Ni, 117 and 117 ps, respectively for Fe), close to the lifetime at matrix (110 ps for both Ni and Fe) and in these cases trapping potentials for a positron are shallow both for Ni and Fe.     

Tolerance of point substitution of methionine for isoleucine in hen egg white lysozyme

X-ray structure determination of proteins by using the multiple-wavelengthanomalous dispersion method targeting selenomethionine is nowwidely employed. Isoleucine was examined for the second choiceof the `safe' substitution of methionine next to leucine. Weperformed a systematic mutational study of the substitutionsof methionine for isoleucine. All mutated lysozymes were lessstable than the wild-type by about 1 kcal/mol and it is suggestedthat this instability was caused by the change in residual hydrophobicityfrom isoleucine to methionine. The X-ray structures of all mutantlysozymes were very similar to that of the wild-type. In addition,both the accessible surface areas and the conformation of theside chain of methionine in all mutant lysozymes were similarto those of the side chain at the respective isoleucine in thewild-type. Therefore, it is suggested that the mutation fromisoleucine to methionine in a protein can be considered as a`safe' substitution.     

The corrosion behaviour of Zr-based bulk metallic glasses in 0.5 M NaCl solution

The corrosion behaviour of eutectic Zr₅₀Cu₄₀Al₁₀ and hypoeutectic Zr₇₀Cu₆Al₈Ni₁₆ bulk metallic glasses (BMGs) was studied by electrochemical measurements, scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS). Zr₅₀Cu₄₀Al₁₀ BMG was highly susceptible to pitting corrosion in naturally aerated 0.5 M NaCl solution at 30 °C. In contrast, Zr₇₀Cu₆Al₈Ni₁₆ BMG passivated spontaneously under the same condition. EDX results for Zr₅₀Cu₄₀Al₁₀ indicated that enrichment of Cu, Cl and O occurred in the pitted region, while for Zr₇₀Cu₆Al₈Ni₁₆ BMG, no significant difference was found in the surface composition from the specimens before and after immersion in the solution. XPS analysis including angle-resolved measurements for Zr₇₀Cu₆Al₈Ni₁₆ BMG revealed that zirconium cation (Zr⁴⁺) was highly concentrated in both air-formed and passive films. Furthermore, the concentration of Zr⁴⁺ ions after immersion for 24 h or more showed tendency to increase with decreasing take-off angle, indicating that the exterior part of the passive film consisted exclusively of zirconium oxyhydroxide. The high corrosion resistance of Zr₇₀Cu₆Al₈Ni₁₆ BMG was attributed to the formation of homogeneous and stable passive film enriched with zirconium.     

Influence of humidity and of the electric and magnetic microwave radiation fields on the remediation of TCE-contaminated natural sandy soils

The influence of moisture content (15% w/w) on the remediation (vaporization) of trichloroethylene (TCE) present in natural sands, chosen as a TCE-polluted model system for soils, was investigated with regard to applied microwave power levels, the depth of the sand sample, and the dielectric factors. The heating process occurring in the sand samples arises through the microwave conduction loss heating and dielectric loss heating mechanisms. The characteristic relevance of the electric and magnetic microwave radiation fields to the heating mechanisms was also examined. Heating by the magnetic microwave radiation field was considerable when magnetite was added to the dry and wet sand samples as the microwave absorber. Optimal microwave conditions are reported for a single-mode microwave applicator. Near-quantitative elimination of the TCE contaminant was achieved for sandy soils within a very short time.     

Chiral Homobimetallic Palladium(II) Complexes Composed of Chirality-Organized Quinonediimines Bearing Amino Acid Moieties

The chirality-organized quinonediimine derivatives bearing amino acid moieties were demonstrated to react with 2 molar equiv. of Pd(OAc)₂, resulting in the formation of the chiral homobimetallic palladium(II) complexes. The crystal structures of the chiral conjugated complexes revealed the coordination of the quinonediimine nitrogen to a palladium center and a chiral propeller twist conformation of the π-conjugated backbone. The mirror image relationship of the CD signals around the quinonediimine moieties in acetonitrile was observed between l- and d-derivatives, indicating the preservation of the chirality-organized structures even in a solution.     

Enhanced mixing of Newtonian fluids in a stirred vessel using impeller speed modulation

This paper reports on an experimental study of mixing intensification using speed modulation of a six‐blade Rushton turbine in a stirred vessel. Mixing times were measured using a non‐intrusive technique based on direct visualisation of an acid‐base reaction in a Newtonian fluid. The impeller speed modulation was achieved by using two waveforms: a square wave and a sine wave. The amplitude was fixed between a maximum Reynolds number of Re_max = 60 and minimum Reynolds numbers of Re_min = 40 or 30. The wave periods were varied (10, 20, or 40 s) in order to compare the effects of unsteady stirring on mixing performance. It was observed that a square wave protocol with the shortest wave period and the larger amplitude resulted in the shortest time to destroy the observed isolated mixing regions (IMRs), which are known to exist in stirred vessels operating at low Reynolds number. However, the sine wave protocol led to a slow diffusive mechanism in which IMR structures reached an asymptotic volume and remained visible even after several hours. The results are presented and discussed using digital photographs taken at different time intervals during experimentation.