Combustion synthesis of AlN doped with carbon and oxygen

Carbon-and-oxygen-doped AlN specimens were prepared by combustion synthesis using Al, graphite, and AlN. Graphite addition changed the product color from white to blue. By XRD, the lattice constant increased slightly with increasing carbon content. Blue AlN powder was synthesized with a molar ratio of the diluent AlN of 0.2-0.5 with a fixed graphite content of 0.05. At an AlN molar ratio exceeding 0.6, carbon was not successfully incorporated due to the lower reaction temperature. Calcination at 800°C in air removed residual graphite without changing the crystal structure or product color. Oxygen, nitrogen, and carbon analyses revealed that blue AlN powders contained 0.45-0.54 mass% carbon and 1.4-1.6 mass% oxygen, while the undoped AlN contained 0.021 mass% carbon and 0.94 mass% oxygen. The origin of the white-to-blue color change was investigated via reflection measurements. Blue AlN exhibits an absorption peak at 634 nm (1.96 eV). From first-principles electronic structure calculations, the C-doped AlN and carbon-and-oxygen-doped AlN with a 1:1 ratio could be classified as p-type, whereas the O-doped AlN and 1:3 carbon-and-oxygen-doped AlN were n-type. One reason for the absorption peak at 634 nm may be a transition from the conduction band to an upper unoccupied state. These results suggest the possible control of optical and electronic properties of AlN via carbon-and-oxygen doping.     

Size-dependent separation of graphene oxide by deformation of packed-gel in a chromatographic column

ABSTRACT

A deformable gel-packed chromatographic column was used to separate as-synthesized graphite oxide with different sizes. The synthesized gel (56 µm) was deformed by pressure of the fluid flow and the gaps in the gels showed a range of sizes. A suspension of graphene oxide (0.1 g/L, 10 mL) was injected, and graphene oxide in the elution had a size at 0.56 μm and 0.14 μm, whereas in half upper and bottom domain of the gel layer graphene oxide had a size at 33 µm and 2.9 µm, respectively, demonstrating that graphene oxide suspension was separated by size through gel layer.     

Feasibility of zeolites in converting butyric acid into propylene for biorefineries

The biorefinery has been recognized as a new industry to produce both energy and chemical materials such as olefins and BTX from renewable resources. In this context the conversion of butyric acid over zeolites was investigated for establishing a new production route of propylene. Propylene was mainly generated by decarbonylation and dehydration of butyric acid. Our study proved that H-ZSM-5 (750) and silicalite were the best industrial catalyst among the tested ones. For H-ZSM-5 (750), the selectivity of propylene reached 64.2 C% and the ratio of the yield for propylene to theoretical yield (75 C%) became 85.6%.     

Main‐chain smectic liquid crystalline polymer exhibiting unusually high thermal conductivity in an isotropic composite

The thermal conductivity (TC) of an isotropic composite comprising of a main‐chain smectic liquid crystalline PB‐10 polyester and 50‐μm‐sized roughly spherical magnesium oxide (MgO) particles is investigated. The increase in the composite TC with higher MgO fractions is steeper than that expected by Bruggeman's theory for the TC of a polydomain PB‐10 polyester (0.52 W m^?1 K^?1). When the filler content is larger than 30 vol %, the composite TC approaches a value that can be explained only if the polyester functions as a matrix with 1.0 W m^?1 K^?1, which is five times as high as those of isotropic common polymers (0.2 W m^?1 K^?1). Such an unusually high TC for a polymer matrix is attributed to some polymer lamellae that lie parallel to the particle surface and are stacked toward neighboring particles, thus creating effective heat paths between the particles and a continuous thermal network in a composite. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 39896.     

The correlation between the ionic degree of covalent bond comprising polymer main chain and the ionic yield due to mechanical fracture

The mechanical force to polymeric materials in vacuum at 77 K produces mechano radicals, mechano anions and mechano cations due to homogeneous and heterogeneous scissions of the covalent bonds comprising polymer main chain. The ionic degree of the covalent bond was estimated by calculating the “absolute ΔMulliken atomic charge,” which was defined as the difference between the Mulliken atomic charges of the two adjacent atoms comprising the covalent bond of the polymer main chain. The ionic yield of the covalent bond increased with increasing the absolute ΔMulliken atomic charge. The empirical formula for the ionic yield was obtained with the absolute ΔMulliken atomic charge, and indicates that the ionic yield could be estimated from its chemical structure.     

Feasibility of using U to reconstruct close-in fallout deposition from the Hiroshima atomic bomb

The first results on the feasibility of using ²³⁶U to reconstruct the level and spatial distribution of close-in fallout deposition from the Hiroshima A-bomb are reported, coupled with the use of global fallout ¹³⁷Cs and ^239 + 240Pu. The results for global fallout ²³⁶U in soil samples (0-30 cm) from Ishikawa prefecture showed that the deposition density of ²³⁶U from the global fallout can be accurately evaluated using AMS. All deposited ²³⁶U, ¹³⁷Cs and ^239 + 240Pu appeared to have been recovered using 30-cm cores. It was also noted from the depth profiles for ²³⁶U/^239 + 240Pu and ²³⁶U/¹³⁷Cs ratios that the downward behavior of ²³⁶U in the soil was apparently similar to that of ^239 + 240Pu, while the ¹³⁷Cs was liable to be retained in upper layers compared with ²³⁶U and ^239 + 240Pu. The accumulated levels were 1.78 × 10¹³ atoms m^− 2 for ²³⁶U, 4340 Bq m^− 2 for ¹³⁷Cs and 141 Bq m^− 2 for ^239 + 240Pu. The ratios of ²³⁶U/¹³⁷Cs and ²³⁶U/^239 + 240Pu were (4.10 ± 0.12) × 10⁹ and (1.26 ± 0.04) × 10¹¹ atoms Bq^− 1, respectively. Results of ²³⁶U, ¹³⁷Cs and ^239 + 240Pu measurements for the seven soil cores (0-30 cm) from Hiroshima were discussed on the basis of ratios of ²³⁶U/¹³⁷Cs and ²³⁶U/^239 + 240Pu by comparing with those from the background area in Ishikawa, indicating that the global fallout dominates the current level of ²³⁶U accumulation in soil in the Black-rain area around Hiroshima after the Hiroshima bomb, and the contribution of the close-in fallout ²³⁶U produced by the Hiroshima A-bomb seems difficult to observe.     

Effect of drawing condition on mechanical properties and molecular orientation of self-reinforced poly(lactic acid) screws

Effects of extrusion ratio (ER) during extruding on mechanical properties of poly(lactic acid) (PLA) screws were investigated in terms of shear and twist strength. Shear strength increased by drawing, while twist strength decreased. This might be due to orientation of molecular chains during drawing. In order to evaluate orientation of molecular chains, orientation function in extruded billets was measured as a function of ER. Since orientation function increased with ER, drawing is effective method to improve shear strength of screw, where fibrous structure which was formed during extruding resisted shear stress in cross-section perpendicular to screw axis. Although orientation functions for billet extruded at ER 1.3–4 were equivalent, both strengths changed for the screw extruded at the range of this ER. Infrared spectra suggested transforming from α to β crystal for the billet extruded at the range of this ER. This result suggested that mechanical properties of screw also depended on the crystal forms.     

Optimized ANN model for predicting rock mass quality ahead of tunnel face using measure-while-drilling data

Bulletin of Engineering Geology and the Environment - Rock mass quality assessment has a vital influence on the excavation of tunnels and caverns in rock mass. For this purpose, extensive field...     

Formation of macroporous organic‐inorganic polymer hybrids using tea extract

Macroporous organic–inorganic polymer hybrids were prepared from poly(vinyl pyrrolidone), and inorganic alkoxides. To a reaction mixture of poly(vinyl pyrrolidone) and tetramethoxysilane, extract from tea leafs and HCl aqueous solution in methanol were added. The resulting mixture was constantly stirred at room temperature for 1 h and heated at 60°C for two weeks. Consequently, the corresponding polymer hybrid became a macroporous material having a pore size from 3.26 to 20.86 μm. We succeeded in finding that the pruned tea leafs were able to utilize the synthesis of novel macroporous materials. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Inserting polyoxomolybdate cluster into poly(?-caprolactone) to create a class of new heteropolymer: Synthesis and supramolecular structures

In the present work, we report our work concerning the synthesis of heteropolymers of poly(?-caprolactone)-polyoxomolybdate-poly(?-caprolactone) using ring-opening polymerization (ROP) of ?-caprolactone monomer initiated by two hydroxyl groups attached on the two sides of a polyoxomolybdate cluster which was organically modified using pentaerythritols. Since the hydroxyl groups on polyoxomolybdate macroinitiator are less reactive, ring-opening polymerization were finally carried out by using 4,4′-(dimethylamino) pyridine to activate ?-caprolactone monomer. The polyoxomolybdate-containing heteropolymers were confirmed in detail by ¹H NMR, FT-IR, GPC, TGA and XPS methods. Although the size of polyoxomolybdate cluster is extremely small compared to PCL chains, it was also found that POM played an important role in crystallization process. Self-assembly of such heteropolymers in mixed solvents were investigated and the analysis of formed spherical aggregates with multiple concaves on the surface was supported by TEM results and 3D electron tomography.