Modeling of reverse osmosis flux of aqueous solution containing glucose

The aim of the paper is to model the permeate flux during reverse osmosis (RO) of a highly concentrated glucose solution using the osmotic pressure model. Such a model accounts for the effect of the concentration polarization phenomenon on the permeate flux. To apply this model the viscosity, the osmotic pressure of solution and the diffusion coefficient of glucose were estimated. Using mathematical simulation software, the values of mass transfer coefficient for different concentrations of glucose (5, 10, 15 and 20 wt%) and at different feed flow rate were determined. The experimental permeate flux values conducted on flat RO membranes (Type HR-99) agreed well with the values calculated by the osmotic pressure model, as shown by statistical analysis.     

Hydrolysis of polyurea under high pressure of carbon dioxide

A chemical decomposition of polyurea (PUA) by hydrolysis under high pressure of carbon dioxide (CO₂) was proposed. The hydrolysis of PUA was carried out at 190 °C for 2 h under 7.0 MPa of CO₂ in the presence of water. The hydrolysis reaction gave white residual solid and water soluble compound. The white residual solid was characterized to be degraded PUA by FT-IR spectrum and elemental analysis. ¹H-NMR spectra of the water soluble compound revealed that the hydrolysis of PUA produced diamine only from repeating unit of PUA, which was a component of PUA. This hydrolysis gave the corresponding diamine for quantitative yields.     

Investigation of electron trapping behavior in n-channel organic thin-film transistors with ultrathin polymer passivation on SiO2 gate insulator

Electron trapping behavior at the interface between N,N′-ditridecyl-3,4,9,10-perylene tetracarboxylic diimide (PTCDI-C13) film and thermal SiO₂ was investigated by utilizing ultrathin poly(methyl methacrylate) (PMMA) gate passivation layers. From the capacitance–voltage analysis for the PTCDI-C13/PMMA/SiO₂ interface, it is found that the electron tunneling appeared with PMMA thinner than 0.8 nm, and that the thickness of the gate passivation layer should be at least 1 nm for preventing injection-type hysteresis in the capacitance–voltage curve. The effective electron mobility of organic thin-film transistors (OTFTs) based on PTCDI-C13 with SiO₂ gate insulator was increased by suppressing shallow-level interface traps on SiO₂ with the PMMA layer, which can be partially accounted for by the multiple trap and release model. In this work, the thickness and the density of the PMMA layers were precisely controlled with a simple spin-coating process. Even 1.3-nm thick PMMA layer caused the improvements of the electron mobility and the air stability of the n-channel conduction.     

Study on dominant mechanism of high-cycle fatigue life in 6061-T6 aluminum alloy through microanalyses of microstructurally small cracks

The mechanism controlling the fatigue life of a precipitation-hardened Al–Mg–Si alloy (6061-T6) at a high-cycle fatigue (HCF) regime of over 10⁷ cycles was investigated in detail. It was found that over 90% of the total fatigue life was occupied by the growth process of a microstructurally small crack at relatively low stress amplitude. The small crack was often found to be arrested and halted for a long period (more than 10⁶ cycles) before it began to grow again, which resulted in a significantly slow growth process. The small crack was then analyzed not only by the conventional fractography but also by the cross-sectional observation of the crack tip region using a focused ion beam and transmission electron microscopy. These observations, supplemented also by a grain orientation analysis using electron backscattered diffraction, explicitly revealed the following points: (i) the small crack growth observed on the specimen surface is primarily related to facet-type cracking that occurs exclusively at the specimen surface; (ii) the growth direction of the small crack has strong anisotropy (i.e. surface-induced growth); (iii) the facet-type cracking is related to the formation of persistent fine slip bands that accompany no structural change of the matrix. On the basis of these results, the micromechanism of small crack growth and its relation to the concept of fatigue limit at the HCF regime is discussed in detail.     

Oxygen Uptake and Release Mechanism of Lithium Manganese Ferrite in the Low Temperature Range of 573–773 K

Oxygen uptake and release of (Li,Mn) ferrite [LMF; (Li_0.60Mn_1.20Fe_1.20)_1−δO₄; δ= 0.007 to 0.033] was investigated concerning the relations between redox reactions of ferrite and cation migration. Mössbauer spectroscopy and X-ray diffractometry showed that some of the Li⁺ and Fe³⁺ ions migrated from the A sites to the B sites of the spinel-type structure and Mn⁴⁺ ions migrated from the B sites to the A sites during oxygen uptake at 573 K. The cation-deficient LMF formed by the oxygen uptake released oxygen molecules in He gas only at 660 K. The cation migration during the oxygen release was in the opposite direction of the movement during oxygen uptake at 573 K.     

Optical Amplification at 1.3 μm in a Praseodymium-Doped Sulfide-Glass Fiber

Praseodymium-doped glasses were prepared in the Ga-Na-S (GNS) system and their optical properties were studied. A single-mode fiber with an attenuation loss of 1.2 dB/m at a wavelength of 1.31 μm was fabricated using an extrusion method, and the amplification characteristics were measured in the bidirectional pumping configuration. We demonstrated a gain coefficient of 0.81 dB/mW at a wavelength of 1.34 μm, which is the highest we have ever reported, and achieved a net gain of 32 dB for a pump power of 90 mW. Highly efficient optical amplification at a wavelength of 1.3 μm was demonstrated in the praseodymium-doped GNS fiber.     

Effect of Hydrogen Atmosphere on Pyrolysis of Cured Polycarbosilane Fibers

SiC-based fibers with various chemical compositions were synthesized using an irradiation-curing process. Polycarbosilane (PCS) fibers were cured by irradiation with an electron beam in a helium atmosphere. The cured PCS fibers were pyrolyzed at 1300°C under controlled hydrogen or argon atmospheres, and SiC fibers with C/Si of 0.84 to 1.56 were obtained. The fibers consisted of <1.0 wt% O, <0.2 wt% N, <0.1 wt% H, with the balance being Si and C. The mechanism of pyrolytic transformation of cured PCS to SiC-based ceramics was investigated using TG/DTA analysis. Greater mass losses were observed during pyrolysis in a hydrogen atmosphere than in argon. This result suggests that the hydrogen atmosphere suppresses H₂ evolution and helps to remove excess carbon as CH₄ during pyrolysis. The microstructure and mechanical properties of the resulting SiC-based fibers were found to be very dependent on their C/Si chemical compositions.     

Magnetic properties of metal layer deposited by reduction of metal ions contained in polymer with applying magnetic field

Metal layer was deposited by the reduction of NiCl₂ and CoCl₂ in polyacrylonitrile film after applying an external magnetic field in directions parallel and perpendicular to the surface of the film; the magnetic properties of the metal-deposited film were investigated. When the parallel magnetic field was applied, the values of coercivity (H_c), remanent flux density (B_r) and maximum flux density (B_s) increased regardless of the composition of the metal ions, compared with the case without the application of the magnetic field. From the scanning electron micrographs and X-ray diffraction analyses, it was shown that the growth of crystalline orientation in the deposited metals was enhanced by applying a parallel magnetic field.     

Wavelength-dependent switching of the photocurrent direction at the surface of molecular semiconductor electrodes based on orbital-confined excitation and transfer of charge carriers from higher excited states

Photoelectrochemical experiments are performed at evaporated thin films of unsubstituted phthalocyanines (Pc) and derivatives with electronegative substituent groups in the ligand. Light absorption in the B-band leads to occupation of a higher excited singlet state S₂ relative to the first excited singlet state S₁ that is populated by Q-band absorption. Charge carriers in S₂ can have sufficient lifetime to be transferred to adsorbed reactants at the electrode surface despite the competing relaxation into S₁ and to the ground state S₀. The assignment of the well-defined B- and Q-bands in the solid state to transitions between distinct molecular orbitals is thereby proven to be of practical relevance. If a material of a suitable position of energy levels is chosen, the direction of charge transfer can be switched by illumination with light of the two different wavelengths. According to the separate pathways of reaction starting from the S₂ and S₁ excited states different quantum efficiencies are obtained following absorption in either the B- or Q-band. Surface traps in the different reactions of charge transfer to the electrolyte are detected by charging and discharging photocurrent spikes. Implications of the present findings for the fundamental discussion of electrical and electrochemical properties involving illumination of molecular modified electrodes which are in part also of technical significance due to the related phenomena of photoconduction (photocopiers, laser printers), light emission (organic light emitting diodes) and charge transfer (solar energy conversion) are discussed.     

Preparation of Ultrafine Fe–Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis

We prepared ultrafine Fe–Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength) using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe–Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5–3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III) acetylacetonate compared with Pt(II) acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe–Pt nanoparticles and UV–visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe–Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.