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71.
Joichi Koga Keisuke Taguchi Nobuhiko Kuroki Kenzo Konishi 《Colloid and polymer science》1967,215(1):45-47
Summary Some organic acids, alcohol and amine which have an asymmetric carbon atom were used for an investigation of asymmetric absorption
on wool. Racemic mixture of hydratropic acid, mandelic acid andα-phenethylamine have shown the selective absorption on wool from their aqueous and alcoholic aqueous solutions and S-form
of their diastereoisomers preferentially absorbed on wool. According to the results we obtained so far, it is concluded that
the preferential absorption strongly depends on the configuration of the substance of which wool is composed. 相似文献
72.
Some years ago, Atiyah and Manton described a method to construct approximate Skyrmion solutions from Yang-Mills instantons. Here we present a dynamical realization of this construction using domain walls in a five-dimensional gauge theory. The non-Abelian gauge symmetry is broken in each vacuum but restored in the core of the domain wall, allowing instantons to nestle inside the wall. We show that the world volume dynamics of the wall is given by the Skyrme model, including the four-derivative term, and the instantons appear as domain wall Skyrmions. 相似文献
73.
[reaction: see text] Concise synthesis of defucogilvocarcin M was achieved via the [2 + 2 + 2] approach to beta-phenylnaphthalene structure. 相似文献
74.
Direct observation of the antiferro (AF) magnetic domain structures of a NiO (0 0 1) surface is found to be possible using a spectroscopy photoelectron low-energy electron microscope (SPELEEM) and a commercial UV Hg excitation light source without using any polarizers. The principle is based on the magnetic linear dichroism (MLD) effect, where different domain contrasts are produced according to the relative angle between the antiferromagnetic axis and the linearly polarized light. The observed AF magnetic domain structures are strongly affected by both bulk AF magnetic domain structures and the stresses induced during the sample cleaving process. Moreover, the AF magnetic domain structures are found to be irreversible when the sample is heated to over its Néel temperature and then cooled. The possibility of imaging AF magnetic domain structures without using synchrotron radiation or a polarizer is attractive. 相似文献
75.
傅元勇 周书华T. Koike S. Kinoshita Y. Ma Y. Miura K. Miwa Y. Miyagi K. Shirotori T. Suzuki H. Tamura K. Tsukada M. Ukai K. Futatsukawa K. Hosomi M. Kawai M. Mimori N. Terada N. Maruyama K. Aoki H Fujioka Y Kakiguchi T. Nagae D. Nakajima H Noumi T Takahashi T.N. Takahashi A. Toyota M. Dairaku T. Fukuda S. Minami W. Imoto S. Aiimura K. Tanida 《中国物理快报》2007,24(8):2216-2218
From the ^12 C(π^+,K^+)^12 AC reaction the γ -rays of 261.6±0.24 ke V(7/2^+ →5/2^+)and 1481.7±0.7 ke V(1/2^+ →5/2^+) of ^11 A B,and 2667.3±2.8 keV(1^- 2 → 2^- 1)of ^12 A C hypernuclei have been identified using a large germanium detector array Hyperball2 at K6 beam line of KEK. The observed energies of the transitions 1481.7keV and 261.6 keV are significantly different from the values predicted by the shell model using the △ and SN parameters determined from the ^7 △ Li data. 相似文献
76.
Hiroto Murakami Keisuke Futashima Minoru Nanchi Shin’ichiro Kawahara 《European Polymer Journal》2011,(3):378-384
An acrylic pressure-sensitive adhesive (PSA), bearing octadecyl acrylate, methyl acrylate and acrylic acid groups, and crosslinked by aluminum acetylacetonate (AlACA), displayed behavior unique among acrylic PSAs in that its adhesion, which decreases with an increase in temperature, began to increase again from around 150 °C. In order to understand this behavior, the structure and thermal properties of the PSA were investigated in detail, along with another PSA crosslinked by a covalent crosslinking agent (Az). From thermal mechanical analysis, the PSA with ionic crosslinks (AlACA) showed three softening points at 20, 60, and 160 °C. In comparison, the PSA covalently crosslinked by Az only exhibited two softening points (at 20 and 60 °C). The softening point at 160 °C is clearly related to ionic chelate crosslinking. DSC measurements indicated that the softening point at 20 °C resulted from melting of the ordered octadecyl group, and the softening point at 60 °C was due to an increase in the mobility of the main chain. The temperature dependence of viscoelastic measurements revealed that the viscosity of the PSA crosslinked by AlACA increased at around 160 °C. From these results, we considered that the distinctive adhesion of the PSA crosslinked by AlACA could be due to ligand exchange at the aluminum crosslinking points, which are chelated by carboxy groups built in the main chain. 相似文献
77.
78.
79.
Keisuke Akita Youhi Morii Hisashi Nakamura Takuya Tezuka Kaoru Maruta 《Proceedings of the Combustion Institute》2021,38(2):2247-2255
Two-dimensional axisymmetric numerical simulation reproduced flames with repetitive extinction and ignition (FREI) in a micro flow reactor with a controlled temperature profile with a stoichiometric n-heptane/air mixture, which have been observed in the experiment. The ignition of hot flame occurred from consumption reactions of CO that was remained in the previous cycle of FREI. Between extinction and ignition locations of hot flames, several other heat release rate peaks related to cool and blue flames were observed for the first time. After the extinction of the hot flame, cool flame by the low-temperature oxidation of n-heptane appeared first and was stabilized in a low wall temperature region. In the downstream of the stable cool flame, a blue flame by the consumption reactions of cool flame products of CH2O and H2O2 appeared. After that, the hot flame ignition occurred from the remaining CO in the downstream of the blue flame. Then after the next hot flame ignition, the blue flame was swept away by the propagating hot flame. Soon before the hot flame merged with the stable cool flame, the hot flame propagation was intensified by the cool flame. After the hot flame merged with the stable cool flame, the hot flame reacted with the incoming fresh mixture of n-C7H16 and O2. 相似文献
80.
Yoshimasa Makita Tomofumi Danno Keisuke Ikeda Hsien-Han Lee Taro Abe Kento Sogawa Akihiro Nomoto Shin-ichi Fujiwara Akiya Ogawa 《Tetrahedron letters》2017,58(48):4507-4509
Hemicryptophanes are covalent molecular cages, constructed from a cyclotriveratrylene-based host unit and a functional unit linked by covalent spacers, which have been designed to accommodate endohedral functionalities in the cavity. In this study, the synthesis and characterization of the rigid, biphenyl-linked hemicryptophane 1 were investigated by NMR, ESI-MS, and X-ray crystallography. The structure of the inclusion complex, in which a dichloromethane molecule was constructed encapsulated within 1, was characterized by X-ray crystallography. An endohedral, cobalt(II) hemicryptophane complex 2 was also synthesized and characterized ESI-MS and X-ray crystallography. The X-ray crystal structure of 2 showed that the biphenyl-linked hemicryptophane had three components—a molecule each of chloroform and acetonitrile, and a cobalt(II) ion—within its cavity. 相似文献