Graft copolymerization of styrene onto cellulose acetate p-nitrobenzoate by chain transfer reaction

Styrene was grafted onto cellulose acetate p-nitrobenzoate (CANB) by chain transfer reaction of growing polymer radicals to the pendant nitro groups of CANB. A copolymer with a branch for every 17.2 nitro groups was obtained. This result indicates that the pendant aromatic nitro group is more effective in obtaining a graft copolymer by radical mechanism than pendant double bond on the trunk polymer previously reported, where graft copolymers with a branch for several hundred of double bonds are produced.     

One-Step Synthesis of Luminescent Nanoparticles of Complex Oxide, Strontium Aluminate

An organic aqueous solution of metal acetylacetonate precursors was subjected to spray pyrolysis in order to fabricate SrAl₂O₄:Eu (SAO) nanoparticles. Non-agglomerated luminescent SAO nanoparticles, having a spherical shape with a size of 10–30 nm, were achieved in a single step, while only submicrometer-sized SAO particles were obtained from the conventional ultrasonic pyrolysis of the metal nitrates. Without any post-annealing process, the as-prepared SAO nanoparticles were observed to exhibit a strong photoluminescence, which is comparable with that of the submicrometer-sized SAO particles. A mechanism for the formation of the nanoparticles is also discussed.     

Electro-rheological effect and dynamic rheological properties of a blend composed of two liquid crystalline materials with different molecular weight

Electro-rheological (ER) effect of a blend composed of two liquid crystalline materials with different molecular weights is described in this article. The results indicated that ER effect of the blend was observed at the temperature range where each neat sample did not show ER effect. Furthermore, both storage modulus (G′) and loss modulus (G″) decreased drastically at the temperature range for the blend in dynamic viscoelastic measurements. We show that steady ER effect could be obtained by using a blend made up of two liquid crystalline components, whereas remarkable increment in shear stress was not observed for each component under applied electric field.     

Numerical analysis of particle mixing in a rotating fluidized bed

This paper describes the numerical analysis of particle mixing in a rotating fluidized bed (RFB). A two-dimensional discrete element method (DEM) and computational fluid dynamics (CFD) coupling model were proposed to analyze the radial particle mixing in the RFB. Spherical polyethylene particles (Geldart group B particles) were used as model particles under the assumptions that they were cohesionless and mono-disperse with their diameter of 0.5 mm.The validity of the proposed model was confirmed by the comparison between the calculated degree of particle mixing and the experimental one, which was obtained by measuring the lightness of the recorded image taken by a high-speed video camera. Effects of the operating parameters (gas velocity, centrifugal acceleration, particle bed height, and vessel radius) on the radial particle mixing rate were numerically analyzed. The radial particle mixing rate was found to be strongly affected by the bubble characteristics, especially by the bubble size. The mathematical model for the rate coefficient of particle mixing as functions of operating parameters was empirically proposed. The radial particle mixing rate in a RFB could be well correlated by the three dimensionless numbers: dimensionless acceleration (Ac), bubble Froude number (Fr_b), and dimensionless radius on the surface of particle bed (β_s).     

Study on ketalization reaction of poly(vinyl alcohol) by ketones. IV. Reaction between poly(vinyl alcohol) and aliphatic ketones and behavior of polyvinylketal in water

Ketalization reaction of poly(vinyl alcohol) (PVA) by aliphatic ketones, dimethylsulfoxide (DMSO) as solvent, under the presence of acidic catalyst, in homogeneous system was carried out and the synthesis of polyvinylketals were successfully performed. The equilibrium constant at 40°C is ca. 0.07 in the case of methyl n-propyl ketone (nPK) and methyl n-butyl ketone (nBK), but is ca. 0.05 in the case of methyl i-propyl ketone (iPK) and ca. 0.01 in the case of methyl i-butyl ketone (iBK) and methyl t-butyl ketone (tBK), respectively. Moreover, the ketalization degree of polyvinylketal by iBK and tBK reached to only ca. 35 mol % as the maximum. It seems that these were due to steric hindrance of bulky side chain of ketones. But the heat of reaction is 7.5 kcal/mol in all aliphatic ketones, it seems to proceed the same ketalization reaction mechanism. Films prepared from the polyvinylketals were soaked in water and degree of swelling, solubility, and hydrolysis of films were measured. The reaction of film with water, in acidic side, at first the film swells, and then, as the deketalization reaction proceeds, the film dissolves in water. The dissolution time is controlled by the kind of ketones, ketalization degree, and pH of water which reveals that deketalization reaction proceeds proportional to proton concentration. It is more difficult to dissolve highly ketalized polyvinylketals obtained by propyl ketones and butyl ketones than that by acetone. The hydrolysis of polyvinylketal film proceeds in the order as follows: acetone > MEK > nPK > iPK ≒ nBK > iBK > tBK. This phenomenon seems to be affected by hydrophobicity of the film surface which depends upon the kind of the original ketones.     

Change in the molecular weight distribution of poly(ethylene oxide) caused by the complexation with poly(acrylic acid)

The complexation between poly(ethylene oxide) (PEO) and poly(acrylic acid) (PAA) was made by using double the molar quantity of either polymer component at pH 2 where the resulting complex completely precipitates. After the removal of the precipitate, PEO or PAA remaining in the supernatant was subjected to gel permeation chromatography to investigate the change in the molecular weight distribution (MWD) caused by the complexation. No remarkable difference is observed in the MWD curves for PEO[1] (M_w=1.37 × 10⁴) before and after the complexation with PAA[1] (M_w=1.10 × 10³) and PAA[2] (M_w=4.16 × 10⁵). However, the MWD curves of PEO[2] (M_w=1.26 × 10⁵) and PAA[2] become shortened and shift to the low molecular weight side after the complexation with PAA[1] or [2] and PEO[2], respectively. This tendency is enhanced by increasing the complexation temperature. From these results, it is indicated that the complexation between PEO and PAA deals with an equilibrium reaction, and the equilibrium constant is dependent on the chain length of both polymer components and also on the complexation temperature.     

Additional kernel observer: privilege escalation attack prevention mechanism focusing on system call privilege changes

International Journal of Information Security - Cyberattacks, especially attacks that exploit operating system vulnerabilities, have been increasing in recent years. In particular, if administrator...     

Effect of Computational Constraints on Zero-Dimensional Computations for the Nanosecond-Order Ignition Process of the CH4/Air Mixture

Combustion, Explosion, and Shock Waves - Zero-dimensional computations of nanosecond-order ignition using a nanosecond discharge are performed with two constraints. The effects of these constraints...     

Experimental design to evaluate properties of electrospun fibers of zein/poly (ethylene oxide) for biomaterial applications

The production of polymer fibers from the combination of zein and PEO might have great potential in the field of biomaterial. Zein/PEO fibers were obtained in this work through solution electrospinning. An experimental design, 2^4-1, was used for evaluating the influences of PEO content in the blend, distance from the needle tip to the collector, applied electric voltage and solution flow for average fiber diameter and relative-yield process. Beyond this, the relationship between PEO content in the blend and the fiber properties were evaluated through FTIR, DSC, TG, tensile tests, and cytotoxic tests. The factor that exerts the greatest effect on the average fiber diameter response was the electrical voltage. The increase in PEO content in the blend decreased the thermal stability and increased the degree of the fibers' crystallinity. The mechanical tests showed that fibers with higher elongation were obtained at richer PEO blends. The fibers presented cytocompatible characteristics.     

Hydrogen absorption characteristics of Pd1−xLix (x = 0.055 and 0.072) alloys and ordered Pd7Li

Thermodynamic quantities were determined for the absorption of hydrogen in Pd-5.5at.%Li and Pd-7.2at.%Li alloys, the latter alloy being in the two-phase field of saturated -Pd(Li,s) solid solution and the ordered Pd₇Li phase. Data were also determined for the Pd-10.6at.%Li alloy which consists only of the ordered Pd₇Li phase. The data were determined from measurements of pressure-composition isotherms at temperatures between 273 K and 463 K and hydrogen pressures up to 1000 Torr. The Pd---Li alloys dissolve considerable amounts of hydrogen and form a more stable hydride phase than Pd despite the lattice contraction which occurs on alloying Pd with Li. The hydrogen solubility in the ordered Pd₇Li phase alone is a little smaller than that in the two-phase mixture. The large hydrogen absorption of Pd---Li alloys, which does not depend on the presence of ordered Pd₇Li, may be attributed to (i) an attractive H---Li pair interaction, (ii) a decrease in the strain energies necessary for hydrogen occupation of the interstices, because of the similar lattice parameters of the -Pd(Li,s) and ordered Pd₇Li phases, and the large compressibility of Pd---Li alloys, and (iii) the valence of 1 of Li in Pd compared with 3 for, for example, Y in Pd.