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1.
Syntheses of Spinon Thermal Conductivity Materials in Sr–Cu–O System by Glass‐Ceramics Technique
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Nobuaki Terakado Yuudai Yokochi Kouki Watanabe Yoshihiro Takahashi Takumi Fujiwara 《Journal of the American Ceramic Society》2016,99(5):1565-1572
We have synthesized spinon thermal conductivity materials in Sr–Cu–O system by glass‐ceramics technique. The materials are promising for active control of thermal energy in microelectronic devices because of high and anisotropic thermal conduction, its controllability, and electric insulation. Nevertheless, research on these materials has been limited to that concerning theoretical perspectives and investigation of physical properties using large single crystals. In this study, we adopt glass‐ceramics technique to synthesize these materials: We prepared melt‐quenched multicomponent oxides including SrO and CuO, and checked its glass‐forming ability and crystallization behaviors by heating. As a result, we have found that SrCuO2 and Sr14Cu24O41, known as the spinon thermal conductivity materials, are synthesized using SrO–CuO–?Li2O–?Al2O3?–Ga2O3 system. This synthesis process for the system will provide practical application of the spinon thermal conductivity materials. 相似文献
2.
Minjie Wang Jianghua Shen Biao Chen Umeda Junko Katsuyoshi Kondoh Yulong Li 《金属学报(英文版)》2023,36(1):127
In this study, stress relaxation compression tests were performed to investigate the strain rate sensitivity, activation volume and mobile dislocations in carbon nanotubes/aluminum (CNTs/Al) composites. The results reveal that, with the addition of CNTs, the strain rate sensitivity of CNTs/Al increased. Meanwhile, a smaller V* of CNTs/Al compared with pure Al was attributed mainly to the CNT-Al interfaces and partly to the increased forest dislocations cutting activities in grain interior, which was related to the tendency of short ranges order formation during plastic deformation. The incorporation of CNTs also improved the dislocation storage capability and reduced the dislocation velocity, leading to a lower mobile dislocation exhaustion rate. 相似文献
3.
Gellan is an anionic extracellular bacterial polysaccharide discovered in 1978. Acyl groups present in the native polymer are removed by alkaline hydrolysis in normal commercial production, giving the charged tetrasaccharide repeating sequence: → 3)-β-d-Glcp-(1 → 4)-β-d-GlcpA-(1 → 4)-β-d-Glcp-(1 → 4)-α-l-Rhap-(1 →. Deacylated gellan converts on cooling from disordered coils to 3-fold double helices. The coil–helix transition temperature (Tm) is raised by salt in the way expected from polyelectrolyte theory: equivalent molar concentrations of different monovalent cations (Group I and Me4N+) cause the same increase in Tm; there is also no selectivity between different divalent (Group II) cations, but divalent cations cause greater elevation of Tm than monovalent. Cations present as counterions to the charged groups of the polymer have the same effect as those introduced by addition of salt. Increasing polymer concentration raises Tm because of the consequent increase in concentration of the counterions, but the concentration of polymer chains themselves does not affect Tm. Gelation occurs by aggregation of double helices. Aggregation stabilises the helices to temperatures higher than those at which they form on cooling, giving thermal hysteresis between gelation and melting. Melting of aggregated and non-aggregated helices can be seen as separate thermal and rheological processes. Reduction in pH promotes aggregation and gelation by decreasing the negative charge on the polymer and thus decreasing electrostatic repulsion between the helices. Group I cations decrease repulsion by binding to the helices in specific coordination sites around the carboxylate groups of the polymer. Strength of binding increases with increasing ionic size (Li+ < Na+ < K+ < Rb+ < Cs+); the extent of aggregation and effectiveness in promoting gel formation increase in the same order. Me4N+ cations, which cannot form coordination complexes, act solely by non-specific screening of electrostatic repulsion, and give gels only at very high concentration (above ∼0.6 M). At low concentrations of monovalent cations, ordered gellan behaves like a normal polymer solution; as salt concentration is increased there is then a region where fluid “weak gels” are formed, before the cation concentration becomes sufficient to give true, self-supporting gels. Aggregation and consequent gelation with Group II cations occurs by direct site-binding of the divalent ions between gellan double helices. High concentrations of salt or acid cause excessive aggregation, with consequent reduction in gel strength. Maximum strength with divalent cations comes at about stoichiometric equivalence to the gellan carboxylate groups. Much higher concentrations of monovalent cations are required to attain maximum gel strength. The content of divalent cations in commercial gellan is normally sufficient to give cohesive gels at polymer concentrations down to ∼0.15 wt %. Gellan gels are very brittle, and have excellent flavour release. The networks are dynamic: gellan gels release polymer chains when immersed in water and show substantial recovery from mechanical disruption or expulsion of water by slow compression. High concentrations of sugar (∼70 wt % and above) inhibit aggregation and give sparingly-crosslinked networks which vitrify on cooling. Gellan forms coupled networks with konjac glucomannan and tamarind xyloglucan, phase-separated networks with kappa carrageenan and calcium alginate, interpenetrating networks with agarose and gelling maltodextrin, and complex coacervates with gelatin under acidic conditions. Native gellan carries acetyl and l-glyceryl groups at, respectively, O(6) and O(2) of the 3-linked glucose residue in the tetrasaccharide repeat unit. The presence of these substituents does not change the overall double helix structure, but has profound effects on gelation. l-Glyceryl groups stabilise the double helix by forming additional hydrogen bonds within and between the two strands, giving higher gelation temperatures, but abolish the binding site for metal ions by changing the orientation of the adjacent glucuronate residue and its carboxyl group. The consequent loss of cation-mediated aggregation reduces gel strength and brittleness, and eliminates thermal hysteresis. Aggregation is further inhibited by acetyl groups located on the periphery of the double helix. Gellan with a high content of residual acyl groups is available commercially as “high acyl gellan”. Mixtures of high acyl and deacylated gellan form interpenetrating networks, with no double helices incorporating strands of both types. Gellan has numerous existing and potential practical applications in food, cosmetics, toiletries, pharmaceuticals and microbiology. 相似文献
4.
Naoki Izawa Tomoko Hanamizu Toshiro Sone Katsuyoshi Chiba 《Journal of Bioscience and Bioengineering》2010,109(4):356-360
To increase the hyaluronic acid (HA) yield from Streptococcus thermophilus YIT 2084, fermentation conditions (pH, temperature, agitation, aeration) were optimized in milk-based medium, and the effects of supplemental soybean peptides, which have different molecular weight distributions, were determined. HA production was enhanced to approximately 100 mg/l at pH 6.8 and 33–40 °C. Agitation speed and aeration rate slightly affected HA production. Soybean peptides including those of high molecular weight (approximately 27 to 130 kDa) further increased HA production to 208 mg/l under the optimal condition (pH 6.8, 35 °C, 100 rpm), which was 20-fold greater than non-optimal condition. HA production was no longer related to the specific growth rate. The HA produced under the optimal condition included a large amount of high-molecular-weight fraction of 100 to 2000 kDa, compared with under the basal condition without optimization. 相似文献
5.
Takahiro Funami Sakie Noda Makoto Nakauma Sayaka Ishihara Rheo Takahashi Saphwan Al-Assaf Shinya Ikeda Katsuyoshi Nishinari Glyn O. Phillips 《Food Hydrocolloids》2009,23(2):548-554
Aqueous solutions of gellan gum with comparable molecular mass but with different acyl contents were investigated by atomic force microscopy and rheological measurements in the presence of sodium chloride (NaCl). Results obtained were discussed in relation to our previous report using potassium chloride (KCl) as an added salt. For a low-acyl sample, continuous fibrous network structures were identified microscopically as in the case of KCl. The network structures were more heterogeneous than those formed with KCl in terms of the height distribution of molecular assemblies. Rheological thermal hysteresis between sol–gel transitions was detected as in the case of KCl. The storage modulus (G′) of the gelled system was ca. 15% of the corresponding data with KCl at 20 °C. For a high-acyl sample, no continuous network structures were identified but branches with observable ends were identified as in the case of KCl. The hysteresis was less evident than the corresponding data with KCl and for the low-acyl sample with NaCl. Also, G′ values at 20 °C were ca. 30% and 20% of the corresponding data with KCl and for the low-acyl sample with NaCl, respectively. Continuousness and homogeneity of network structures related to the hysteresis and elasticity of the system, respectively. 相似文献
6.
7.
Kenta Arima Katsuyoshi Endo Toshihiko Kataoka Kikuji Hirose Hidekazu Goto Yasushi Oshikane Haruyuki Inoue Yoshitaka Tatara Yuzo Mori 《Computational Materials Science》1999,14(1-4):236-240
Local density of states (LDOS) is obtained by the first principles calculation based on the density functional theory on the Si(0 0 1)2 × 1 surface and on the surface with an Al dimer. At an Al dimer, LDOS has a high intensity in the conduction band region, which cannot be seen on the Si(0 0 1)2 × 1 surface. This tendency is observed in STS measurements as well. The possibility for a microelementary analysis is presented by applying this method to other metal atoms on the Si surface. Furthermore, it is pointed out that STS measurements should be always performed at the same tip-sample separation to obtain reproducible STS spectrums. 相似文献
8.
9.
Hiroyuki Fukuda Katsuyoshi KondohJunko Umeda Bunshi Fugetsu 《Materials Letters》2011,65(11):1723-1725
The mechanical behavior of the non-aged and the aged Al-Mg-Si alloy composites reinforced with CNTs was evaluated with tensile test and Vickers hardness test. The composites showed higher mechanical strength than the pristine Al alloy before the aging, although exhibiting lower mechanical strength after the aging. The aging treatment was ineffective to strengthen the Al-Mg-Si alloy composites reinforced with CNTs. EDS elemental mapping clarified the Mg and O concentration around CNTs. The reduction of Al oxide species formed around CNTs facilitated the Mg concentration. Due to the Mg consumption around CNTs, Mg elements in Al matrix decreased, and resulted in the incomplete matrix strengthening after the aging. 相似文献
10.
Rapid solidification magnesium alloy powders produced by spinning water atomization process were hot extruded into rectangular bars, from which tensile and compression samples have been cut at 0°, 45° and 90° angles from the extrusion direction to study their anisotropy. Electron back-scattered diffraction analysis has been used to investigate the texture evolution during the extrusion process. Texture parameters like the Schmid factor and the intensity of (0 0 0 1) basal plane in the pole figure have been evaluated and correlated to the mechanical properties. Results have shown that the extruded rods exhibited high strength and relatively less anisotropy compared to other previously reported values for wrought magnesium alloys. Tensile and compression yield stresses have shown very similar values to each other at all loading directions. This limited anisotropy could be linked to both the fine grained and inter-metallic-compound-dispersed microstructure of the extruded alloys. Dynamic recrystallization behavior during hot extrusion has also been investigated in the present study. 相似文献