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71.
Supramolecular polymer gels from polystyrene bearing cyclic amidine Group and acrylic acid/n‐butyl acrylate copolymers 下载免费PDF全文
Mina Sakuragi Naoto Aoyagi Yoshio Furusho Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2016,54(6):765-770
We have prepared supramolecular polymer gels by mixing solutions of a polystyrene bearing cyclic amidine pendant groups (Poly‐A) and copolymers of acrylic acid and n‐butyl acrylate (Poly‐C), followed by evaporation. FT‐IR analysis indicated that the gels were formed through three‐dimensional network of the amidinium‐carboxylate salt bridge. DSC study showed that the Poly‐A and the Poly‐C were miscible when the salt bridge content was high. On the other hand, the mixtures with small salt bridge content showed phase separation. Dynamic shear measurements showed that the gel prepared from Poly‐A and Poly‐C with acrylic acid unit content of 15% had G' higher than G″ over a temperature range of ?22 °C to 32 °C, in which the G' value reached almost 1 MPa. The gel had a crossover point of G' and G″ at 32 °C, very close to room temperature, which suggested facile processability. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 765–770 相似文献
72.
In this work, a bridge density functional approximation (BDFA) (J. Chem. Phys. 112, 8079 (2000)) for a nonuniform hard-sphere fluid is extended to a non-uniform hard-core repulsive Yukawa (HCRY) fluid. It is found that the choice of a bulk bridge functional approximation is crucial for both a uniform HCRY fluid and a non-uniform HCRY fluid. A new bridge functional approximation is proposed, which can accurately predict the radial distribution function of the bulk HCRY fluid. With the new bridge functional approximation and its associated bulk second order direct correlation function as input, the BDFA can be used to well calculate the density profile of the HCRY fluid subjected to the influence of varying external fields, and the theoretical predictions are in good agreement with the corresponding simulation data. The calculated results indicate that the present BDFA captures quantitatively the phenomena such as the coexistence of solid-like high density phase and low density gas phase, and the adsorption properties of the HCRY fluid, which qualitatively differ from those of the fluids combining both hard-core repulsion and an attractive tail. 相似文献
73.
P.?G.?ChufyrevEmail author N.?V.?Sidorov N.?N.?Mel'nik 《Journal of Applied Spectroscopy》2005,72(5):667-670
Using the Raman scattering spectra, we investigated the ordering of the structural units in the cation sublattice and the
photorefractive properties of lithium niobate single crystals of variable composition, i.e., nominally pure ones with different
Li/Nb ratios and those doped with the nonphotorefractive cations Mg2+, Gd3+, and Y3+. It is shown that at low concentrations of Mg2+, Gd3+, and Y3+ the magnitude of the photorefractive effect is substantially determined by the ordering of the structural units of the cation
sublattice. It has been found for the first time that the intensity of the line corresponding to the bridge valence vibrations
of oxygen atoms in the octahedrons of NbO6 is sensitive to the dipole ordering of the cation sublattice of the crystal.
__________
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 5, pp. 611–614, September–October, 2005. 相似文献
74.
Applying the time-dependent density functional theory (TD-DFT) method the design of molecular logical functions from the dithieno[3,2-b:2,3-d]thiophene (thiophene) and azo-dye Disperse Orange 3 (DO3) molecules joined with various electron-insulator bridges is performed. Based on the results of the investigations, the main design rules for the selection of the bridge fragment between a photo-acceptor and photo-donor of a charge transfer molecular device are proposed. 相似文献
75.
Simon A. King 《Transactions of the American Mathematical Society》2004,356(11):4519-4542
We introduce a numerical isomorphism invariant for any triangulation of . Although its definition is purely topological (inspired by the bridge number of knots), reflects the geometric properties of . Specifically, if is polytopal or shellable, then is ``small' in the sense that we obtain a linear upper bound for in the number of tetrahedra of . Conversely, if is ``small', then is ``almost' polytopal, since we show how to transform into a polytopal triangulation by local subdivisions. The minimal number of local subdivisions needed to transform into a polytopal triangulation is at least . Using our previous results [The size of triangulations supporting a given link, Geometry & Topology 5 (2001), 369-398], we obtain a general upper bound for exponential in . We prove here by explicit constructions that there is no general subexponential upper bound for in . Thus, we obtain triangulations that are ``very far' from being polytopal. Our results yield a recognition algorithm for that is conceptually simpler, although somewhat slower, than the famous Rubinstein-Thompson algorithm.
76.
Existence results for some fourth-order nonlinear elliptic problems of local superlinearity and sublinearity 总被引:1,自引:0,他引:1
Guixiang Xu 《Journal of Mathematical Analysis and Applications》2003,281(2):633-640
In this paper we study the existence of positive solutions for the problem
(0.1) 相似文献
77.
Structural characteristics of the novel [fac-Re(CO)3L]Cl complex, where L denotes the N-methyl-2-pyridinecarboxyamide, are presented. Molecular structure of the complex has been established by means of X-ray single crystal diffraction and compared with quantum mechanical calculations. It has been shown that pyridinethioamide is softer base than pyridineamide. As a result of different ReI–S and ReI–O bond covalent shortenings (reflecting their diverse ionic/covalent character ratio) difference of the bond lengths decreases from a theoretical value of 0.45 Å to the value of 0.28 Å. 相似文献
78.
Gary R. Rodgers William J. P. Neish 《Monatshefte für Chemie / Chemical Monthly》1986,117(6-7):879-882
Expansion of the xanthine ring system has been accomplished by linear formation of a benzo, pyrido or pyrazino ring between the pyrimidine and imidazole portions.
Linear expandierte Xanthine (Kurze Mitteilung)
Zusammenfassung Durch Einbau eines Benzo-, Pyrido- oder Pyrazino-Ringes zwischen den Pyrimidin- und Imidazoleinheiten wurde die lineare Expansion des Xanthin-Ringsystems erreicht.相似文献
79.
The influence of the thickness of a covering liquid layer and its viscosity as well as the impact velocity on energy loss during the normal impact on a flat steel wall of spherical granules with a liquid layer was studied. Free-fall experiments were performed to obtain the restitution coefficient of elastic–plastic Al2O3 granules by impact on the liquid layer, using aqueous solutions of hydroxypropyl methylcellulose with different concentrations for variation of viscosity (1–300 mPa s). In the presence of a... 相似文献
80.
Guimei Zhang Xiaoxia Guo Jianhua Fang Kangcheng Chen Ken-ichi Okamoto 《Journal of membrane science》2009
A series of sulfonated copolyimides containing benzimidazole groups (SPIs) were synthesized by random copolymerization of 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA), 2-(4-aminophenyl)-5-aminobenzimidazole (APABI), 4,4′-diaminodiphenyl ether-2,2′-disulfonic acid (ODADS) and 9,9-bis(4-aminophenyl)fluorene (BAPF) in m-cresol in the presence of benzoic acid and triethylamine at 180 °C for 20 h. Membranes with good mechanical properties were prepared by solution cast method. Proton exchange treatment resulted in ionic cross-linking and the membranes were further covalently cross-linked by treating them in polyphosphoric acid (PPA) at 180 °C for 6 h. The covalently cross-linked membranes displayed slightly lower ion exchange capacities (IECs) and proton conductivities than the corresponding covalently uncross-linked ones because small part of the sulfonic acid groups had been consumed during the cross-linking process. Fenton’s test (3% H2O2 + 3 ppm FeSO4, 80 °C) revealed that benzimidazole groups played an important role in the radical oxidative stability of the membranes, while the cooperative effect of benzimidazole groups and covalent cross-linking led to much more significant enhancements in the radical oxidative stability of the membranes than each alone. The membrane 4 (ODADS/APABI/BAPF = 2/1/1, by mol), for example, after covalent cross-linking could maintain membrane form within 8 h measurement, which was much longer than that (3 h) before covalent cross-linking under the same conditions. The membrane 5 (ODADS/BAPF = 3/1, by mol) without benzimidazole groups, however, after covalent cross-linking started to break into pieces after 85 min measurement, which was only slightly longer than that (60 min) before cross-linking under the same conditions. 相似文献