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921.
922.
Masataka Sugimoto Keisuke Sakai Yuji Aoki Takashi Taniguchi Kiyohito Koyama Toshihiro Ueda 《Journal of Polymer Science.Polymer Physics》2009,47(10):955-965
The effect of hydrocarbon oil incorporation on the rheological and phase behaviors of poly(styrene‐b‐(ethylene‐co‐butylene)‐b‐styrene) (SEBS) has been investigated. SEBS‐A1 (neat SEBS) shows a presence of very long relaxation time mode even at the highest temperature carried out here. On the other hand, G′ of SEBS‐A3 (oil concentration = 50 wt %) drastically decreases with increase of temperature at a critical temperature, which can be assigned to be order–disorder transition (ODT). The critical temperature was determined by two rheological criteria. Incorporation of hydrocarbon oil affects the ODT temperature. The rheological response is very sensitive to a few temperature increases around the ODT temperature. Above the critical temperature, G′ finally yields the terminal flow in the low frequency range. The morphological observation at various temperatures was determined using atomic force microscopy (AFM) equipped with environmental controller. This enabled in situ observation of structural change of SEBS induced by temperature and phase transition. We found that the layered texture, mostly aligned along the surface can be seen for SEBS‐A1 ranging from room temperature to 230 °C, though the image contrast reduced by an increase of temperature. SEBS‐A3 showed sphere domains at room temperature and also remains the structure at a critical temperature. The phase separated structure disappeared almost completely above ODT temperature, which was confirmed by the rheologial criteria. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 955–965, 2009 相似文献
923.
Reforming of dimethyl ether with carbon dioxide into synthesis gas has been carried out over a mixed catalyst containing Cu-based methanol decomposition catalyst and alumina. The catalyst is found to show a high activity and selectivity. Catalyst stability and deactivation mechanism was also examined. 相似文献
924.
A novel design is described for an amperometric biosensor based on NAD(P)-dependent glucose dehydrogenase (GDH) combined with a plasma-polymerized thin film (PPF). The GDH is sandwiched between several nanometer thick acetonitrile PPFs on a sputtered gold electrode (PPF/GDH/PPF/Au). The lower PPF layer plays the role as an interface between enzyme and electrode because it is extremely thin, adheres well to the substrate (electrode), has a flat surface and a highly-crosslinked network structure, and is hydrophilic in nature. The upper PPF layer (overcoating) was directly deposited on immobilized GDH. The optimized amperometric biosensor characteristics covered 2.5-26 mM glucose concentration at +0.6 V of applied potential; the least-squares slope was 320 nA mM(-1) cm(-2) and the correlation coefficient was 0.990. Unlike conventional wet-chemical processes that are incompatible with mass production techniques, this dry-chemistry procedure has great potential for enabling high-throughput production of bioelectronic devices. 相似文献
925.
926.
Ken Hatano Tetsuya Yamazaki Koji Yoshino Naoto Ohyama Tetsuo Koyama Koji Matsuoka Daiyo Terunuma 《Tetrahedron letters》2008,49(39):5593-5596
A novel O-protected lactose (Galβ1→4Glcβ1-) derivative bearing trimethoxysilyl group at the aglycon was developed as a silane coupling agent. Reaction of the coupling agent with tris(2,2′-bipyridine)ruthenium (II) dichloride (Rubpy) doped silica particle gave a Rubpy-doped silica particle peripherally functionalized with O-protected lactose derivative. De-O-protection of the particle with aqueous ammonia provided lactose-coating Rubpy-doped silica particles, combining luminophor encapsulated in silica matrix and carbohydrate having lectin-recognition ability. Specific adhesion of fluorescein isothiocyanate-labeled peanut agglutinin (FITC-PNA) to the lactose-coating Rubpy-doped silica particles was confirmed by fluorescence microscopic analysis. 相似文献
927.
Shin-ya Koyama 《Journal of Number Theory》2008,128(6):1769-1774
We construct the multiple Eisenstein series and we show a relation to the multiple cotangent function. We calculate a limit value of the multiple Eisenstein series. 相似文献
928.
929.
Prof. Dr. Munenori Numata Daiki Kinoshita Naoya Hirose Dr. Tomohiro Kozawa Prof. Hitoshi Tamiaki Yoshihiro Kikkawa Dr. Masatoshi Kanesato 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(5):1592-1598
Developing new strategies for controlling polymer conformations through precise molecular recognition can potentially generate a machine‐like motion that is dependent on molecular information—an important process for the preparation of new intelligent nanomaterials (e.g., polymer‐based nanomachines) in the field bordering between polymer chemistry and conventional supramolecular sciences. Herein, we propose a strategy to endow a helical polymer chain with dynamic spring‐like (contraction/expansion) motion through the one‐dimensional self‐assembly (aggregation/disaggregation) of peripheral amphiphilic molecules. In this developing system, we employed a semi‐artificial helical polysaccharide presenting peripheral amphiphilic chlorophyll units as a power device that undergoes contractive motion in aqueous media, driven by strong π–π interactions of its chlorophyll units or by cooperative molecular recognition of bipyridyl‐type ligands through pairs of chlorophyll units, thereby converting molecular information into the regulated motion of a spring. In addition, this system also undergoes expansive motion through coordination of pyridine. We anticipate that this strategy will be applicable (when combined with the established wrapping chemistry of the helical polysaccharide) to the development of, for example, drug carriers (e.g., nano‐syringes), actuators (stimuli‐responsive films), and directional transporters (nano‐railways), thereby extending the frontiers of supramolecular science. 相似文献
930.
Hisanori Sugiura Yoshiaki Saklrai Yoshihide Masuda Hitoshi Takeda Shigekazu Kusabayashi Shunsuke Takenaka 《Liquid crystals》2013,40(3):441-450
Abstract The thermal properties of 4-octyloxyphenyl 4-(4-R-3-nitrobenzoyloxy) benzo-ates (1) and 4-(4-octyloxybenzoyloxy)phenyl 4-R-3-nitrobenzoates (2) have been examined, where R = hydrogen, halogens, alkyl and alkoxy groups. The derivatives of compound 1 incorporating hydrogen, halogens, methoxy and nitro groups show a smectic A phase having a bilayer arrangement, and the others with a long alkoxy group show the SA phase with the monolayer arrangement. The derivatives of compound 2 incorporating halogens, and the nitro group show the SA phase with the monolayer arrangement. The alkoxy derivatives show a smectic C phase as well as the nematic phase. The nitro group at the lateral position tends to increase the ratio of the SA-N transition temperature to the N-I. The effect of the nitro group on the smectic properties has been discussed in terms of the structural and electrostatic nature of the nitro group. 相似文献