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991.
Qi Kang RAN 《数学学报(英文版)》2005,21(4):705-714
In this paper, we prove that the weak solutions u∈Wloc^1, p (Ω) (1 〈p〈∞) of the following equation with vanishing mean oscillation coefficients A(x): -div[(A(x)△↓u·△↓u)p-2/2 A(x)△↓u+│F(x)│^p-2 F(x)]=B(x, u, △↓u), belong to Wloc^1, q (Ω)(A↓q∈(p, ∞), provided F ∈ Lloc^q(Ω) and B(x, u, h) satisfies proper growth conditions where Ω ∪→R^N(N≥2) is a bounded open set, A(x)=(A^ij(x)) N×N is a symmetric matrix function. 相似文献
992.
A novel process was developed to fabricate biodegradable polymer scaffolds for tissue engineering applications, without using organic solvents. Solvent residues in scaffolds fabricated by processes involving organic solvents may damage cells transplanted onto the scaffolds or tissue near the transplantation site. Poly(L-lactic acid) (PLLA) powder and NaCl particles in a mold were compressed and subsequently heated at 180 degrees C (near the PLLA melting temperature) for 3 min. The heat treatment caused the polymer particles to fuse and form a continuous matrix containing entrapped NaCl particles. After dissolving the NaCl salts, which served as a porogen, porous biodegradable PLLA scaffolds were formed. The scaffold porosity and pore size were controlled by adjusting the NaCl/PLLA weight ratio and the NaCl particle size. The characteristics of the scaffolds were compared to those of scaffolds fabricated using a conventional solvent casting/particulate leaching (SC/PL) process, in terms of pore structure, pore-size distribution, and mechanical properties. A scanning electron microscopic examination showed highly interconnected and open pore structures in the scaffolds fabricated using the thermal process, whereas the SC/PL process yielded scaffolds with less interconnected and closed pore structures. Mercury intrusion porosimetry revealed that the thermally produced scaffolds had a much more uniform distribution of pore sizes than the SC/PL process. The utility of the thermally produced scaffolds was demonstrated by engineering cartilaginous tissues in vivo. In summary, the thermal process developed in this study yields tissue-engineering scaffolds with more favorable characteristics, with respect to, freedom from organic solvents, pore structure, and size distribution than the SC/PL process. Moreover, the thermal process could also be used to fabricate scaffolds from polymers that are insoluble in organic solvents, such as poly(glycolic acid). Cartilage tissue regenerated from thermally produced PLLA scaffold. 相似文献
993.
Two new isostructural tellurites, Pb(4)Te(6)M(10)O(41) (M = Nb(5+) or Ta(5+)), have been synthesized by standard solid-state techniques using PbO, Nb(2)O(5) (or Ta(2)O(5)), and TeO(2) as reagents. The structures of Pb(4)Te(6)Nb(10)O(41) and Pb(4)Te(6)Ta(10)O(41) were determined by single-crystal and powder X-ray diffraction. The materials exhibit a three-dimensional framework consisting of layers of corner-shared NbO(6) octahedra connected by TeO(3) and PbO(6) polyhedra. The Nb(5+), Te(4+), and Pb(2+) cations are in asymmetric coordination environments attributable to second-order Jahn-Teller effects. The Nb(5+) cations undergo an intraoctahedral distortion either toward a face or a corner, whereas the Te(4+) and Pb(2+) cations are in distorted environments attributable to their lone pair. In addition, the TeO(3) polyhedra strongly influence the direction of the Nb(5+) intraoctahedral distortion. Infrared and Raman spectroscopy, thermogravimetric analysis, and dielectric measurements are also presented. Crystal data: Pb(4)Te(6)Nb(10)O(41), monoclinic, space group C2/m (No. 12), with a = 23.412(3) A, b = 20.114(3) A, c = 7.5008(10) A, beta = 99.630(4) degrees, V = 3482.4(8) A(3), and Z = 4; Pb(4)Te(6)Ta(10)O(41), monoclinic, space group C2/m (No. 12), with a = 23.340(8) A, b = 20.068(5) A, c = 7.472(2) A, beta = 99.27(3) degrees, V = 3453.8(2) A(3), and Z = 4. 相似文献
994.
From the stem bark of Albizzia julibrissin DURAZZ (Leguminosae), two new phenolic glycosides (albibrissinosides A and B) were isolated. Their structures were determined by spectroscopic analysis. The albibrissinoside B was found to be a radical scavenger on the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical. 相似文献
996.
997.
998.
Xiaofeng Luo Naiwen Kang Lei Li Jianping Deng Wantai Yang 《Journal of polymer science. Part A, Polymer chemistry》2010,48(7):1661-1668
This article reports a class of nanoscale materials, that is, optically active nanoparticles consisting of helical‐substituted polyacetylenes. Such nanoparticles were prepared via aqueous catalytic miniemulsion polymerization, by which nanoparticles with a wide range of size (diameter: 60–400 nm) can be easily prepared. The nanoparticles could be obtained in quantitative monomer conversions. Large specific rotations and intense circular dichroism effects demonstrated that the nanoparticles possessed large optical activities; moreover, the optical activities were found to increase with a decrease in particle size. From the obtained polymer nanoparticles and with poly(vinyl alcohol) (PVA) as supporting material, composite films were further prepared and also exhibited considerable optical activities. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1661–1668, 2010 相似文献
999.
The mononuclear complex Fe(II)(mtq)2{P(OCH3)3}2 (Hmtq = 8-Mercaptoquinoline) with mixed N-heterocyclic thiolato and phosphite ligands was synthesized and characterized by X-ray crystallography and cyclic voltammetric measurement. The title complex crystallizes in the triclinic space group P-1 with a = 8.929(4), b = 9.965(3), c = 16.913(11) Å, α = 76.21(10), β = 80.89(10), γ= 68.010(10)°, V = 1351.2(11) Å3. The Fe(II) atom exhibits an elongated octahedral geometry composed of N2S2P2 donors. The equatorial plane is made up of two cis-oriented N donors from the thiolato ligands and two cis-oriented monodentate P(OCH3)3 ligands. The apical sites are occupied by two trans-oriented S atoms from the mtq? ligands. The thione form is predominant coordination mode of 8-mercaptoquinoline with the N and S donors bound to the Fe(II) to form five-membered chelate rings. The structural feature of the mononuclear Fe(II) complex with mixed phosphite and thiolate ligands is summarized. 相似文献
1000.