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11.
Hajime Miyama Kouichi Tanaka Yoshio Nosaka Nobuyuki Fujii Hiroshi Tanzawa Shoji Nagaoka 《应用聚合物科学杂志》1988,36(4):925-933
Polyacrylonitrile-g-poly(N,N-dimethylaminoethyl methacrylate) was synthesized photochemically and quaternized. The positively charged membranes made from the quaternized graftcopolymer showed high ultrafiltration rate for water by adding poly(vinyl alcohol) to casting solution and washing it out after the casting. In buffered saline solution, the permeability of the membranes was very small at pH below isoelectric point of albumin but increased markedly at higher pH. On the other hand, the permeability for γ-globulin was very small and did not show any pH dependence. 相似文献
12.
Single-walled carbon nanotube networks grown on SiO2 pillars were studied by means of scanning photoemission microscopy. The individual nanotubes or nanotube bundles growing from the pillar tops were observed in C 1s images. Band bending near catalytic Fe/nanotube contacts in an end-bonded configuration was studied by measuring C 1s spectra along the tube axes. Within our experimental resolution, no band bending was observed. This implies that the depletion width is less than the spatial resolution of the scanning photoemission microscope (90 nm) or that the amount of the band bending is less than 0.1 eV. 相似文献
13.
Fumiaki Kobayashi Toru Ogawa Mitsuo Akabori Yoshio Kato 《Journal of the American Ceramic Society》1995,78(8):2279-2281
Uranium-plutonium nitride is a candidate fuel for fast reactors, but its major drawback is 14 C formation from natural nitrogen. One would probably have to use highly 15 N-enriched nitrogen. A pyrochemical process with molten-salt electroreflning has been proposed as a means to increase the nuclear proliferation resistance of the fuel cycle. Molten-salt electroreflning could also be applied to nitride fuels to make possible the recycling of 15 N. The anodic dissolution behavior of UN in LiCI-KCI melt was studied to provide the basis for a feasibility study of electroreflning of irradiated nitride fuels. 相似文献
14.
The O-methylation of phenol with dimethyl carbonate proceeds selectively in the vapor phase over alkali ion exchanged X-zeolites. Thus, a 76% yield of anisole was obtained with a 93% selectivity over NaX at 553 K. The participation of basic sites in the O-methylation is suggested. 相似文献
15.
Ki Soo ParkMyung Hun Cho Sang Ho ParkKee Suk Nahm Yang Kook SunYun Sung Lee Masaki Yoshio 《Electrochimica acta》2002,47(18):2937-2942
Layered Li0.7[M1/6Mn5/6]O2 (M=Li, Ni) was synthesized using a sol-gel method. P2-Na0.7[M1/6Mn5/6]O2 precursor was first synthesized by a sol-gel method, and then O2-Li0.7[M1/6Mn5/6]O2 was prepared by an ion exchange of Li for Na in P2-Na0.7[M1/6Mn5/6]O2 precursor. From charge/discharge curves, it was seen that Li0.7[Li1/6Mn5/6]O2 has two plateaus similar to those observed from a spinel structure, but Li0.7[Ni1/6Mn5/6]O2 holds a single plateau as observed from a typical layered structure. It was considered that Li0.7[Li1/6Mn5/6]O2 undergoes a phase transformation from layered to spinel structure during the charge/discharge cycle, but Li0.7[Ni1/6Mn5/6]O2 maintains O2-layered structure after the cycles. Li0.7[Ni1/6Mn5/6]O2 was higher in discharge capacity and retention rate than Li0.7[Li1/6Mn5/6]O2. 相似文献
16.
ihiro Kasuga † ‡ Tatsuya Inoue† Kenji Tsuji† Yoshio Ota† § Yoshihiro Abe † 《Journal of the American Ceramic Society》1995,78(1):245-247
High-strength calcium metaphosphate fibers for biomedical applications are extracted from crystallized products of calcium ultraphosphate glasses by aqueous leaching. In the present work, new types of porous ceramics with a skeleton composed of the crystalline fibers are prepared by heating the fibrous products extracted. The fibers in the ceramic are interlinked to each other by glassy phases formed during the heating. This porous material has a large porosity of >60%. The surface of the skeleton can be successfully converted into new calcium phosphate phases such as apatite by heating the porous material treated with a molten salt mixture of CaCl2 -Ca(NO3 )2 . 相似文献
17.
Summary Well-defined living polymers of isobutyl vinyl ether were obtained in the polymerization initiated with ethylaluminum dichloride (EtAlCl2) in conjunction with a stoichiometric excess of dioxane (5–10 vol%) in n-hexane at 0°C. Under these conditions, the number-average molecular weight of the polymers increased in direct proportion to monomer conversion, while the molecular weight distribution stayed narrow (Mw/Mn = 1.1–1.25). In sharp contrast, the EtAlCl2-initiated polymerization in the absence of dioxane led to non-living polymers with a broad molecular weight distribution. It was concluded that the propagating carbocation is stabilized not by the counteranion but by an externally added basic compound (dioxane) that strongly interacts with the active end. 相似文献
18.
Sittidej Teekateerawej Junichi Nishino Yoshio Nosaka 《Journal of Applied Electrochemistry》2005,35(7-8):693-697
Two kinds of porous ceramic disks, having through-holes with diameters of 0.1 and 0.05 mm, were coated with TiO2 using two different starting solutions: titanyl(IV)acetylacetonate and a commercial titania sol (STS-01). The morphology
of these porous ceramics before and after TiO2 coating was observed by SEM. The TiO2-coated porous ceramics were examined as honeycomb photocatalytic microreactors. The photocatalytic activity was evaluated
using the decomposition of methylene blue solution for radiation angles of 0° and 10° with respect to the pore axis. The highest
photocatalytic activity was obtained for the porous ceramic having the pore diameter of 0.1 mm, coated with titanyl(IV)acetylacetonate
and irradiated with a light angle of 0° with respect to the pore axis. 相似文献
19.
Processing of Silicon Carbide-Mullite-Alumina Nanocomposites 总被引:2,自引:0,他引:2
Yoshio Sakka Donald D. Bidinger Ilhan A. Aksay 《Journal of the American Ceramic Society》1995,78(2):479-486
Nanocomposite materials in the form of nanometer-sized second-phase particles dispersed in a ceramic matrix have been shown to display enhanced mechanical properties. In spite of this potential, processing methodologies to produce these nanocomposites are not well established. In this paper, we describe a new method for processing SiC-mullite-Al2 O3 nanocomposites by the reaction sintering of green compacts prepared by colloidal consolidation of a mixture of SiC and Al2 O3 powders. In this method, the surface of the SiC particles was first oxidized to produce silicon oxide and to reduce the core of the SiC particles to nanometer size. Next, the surface silicon oxide was reacted with alumina to produce mullite. This process results in particles with two kinds of morphologies: nanometer-sized SiC particles that are distributed in the mullite phase and mullite whiskers in the SiC phase. Both particle types are immersed in an Al2 O3 matrix. 相似文献
20.
Toshihiro Nagao Yuji Shimada Yoshie Yamauchi-Sato Takaya Yamamoto Masaaki Kasai Kentaro Tsutsumi Akio Sugihara Yoshio Tominaga 《Journal of the American Oil Chemists' Society》2002,79(3):303-308
A commercial product of CLA contains almost equal amounts of cis-9,trans-11 (c9,t11)-CLA and trans-10,cis-12 (t10,c12)-CLA. We attempted to enrich the two isomers by a two-step selective esterification using Candida rugosa lipase that acted on c9,t11-CLA more strongly than on t10,c12-CLA. An FFA mixture containing CLA isomers was esterified with an equimolar amount of lauryl alcohol in a mixture of 20%
water and the lipase. When the esterification of total FA reached 50%, two isomers were fractionated in a good yield: t10,c12-CLA was enriched in FFA, and c9,t11-CLA was recovered in lauryl esters. The FFA were esterified again to enrich t10,c12-CLA. At 27.3% esterification of total FA, the t10,c12-CLA content in FFA increased to 64.8 wt% with 89.3% recovery: The ratio of the content of t10,c12-CLA to that of two isomers was 95.9%. Lauryl esters obtained by the single esterification were employed for enrichment
of c9,t11-CLA. After the esters were hydrolyzed, the resulting FFA were esterified again with lauryl alcohol. At 62.0% esterification
of total FA, the c9,t11-CLA content in lauryl esters increased to 73.3 wt% with 79.4% recovery: The ratio of the content of c9,t11-CLA to that of two isomers was 95.6%. In a 600-g-scale purification, molecular distillation was effective in separating
the reaction mixture into lauryl alcohol, FFA, and lauryl ester fractions. 相似文献