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排序方式: 共有235条查询结果,搜索用时 46 毫秒
1.
J. Podeva P. pa
ek A. Sikora A. F. Podol'Skii 《Journal of polymer science. Part A, Polymer chemistry》1984,22(11):3343-3350
An initiation system of the anionic polymerization, intended for the syntheses of homopolymers and block copolymers with narrow molar mass distribution, was tested with styrene and isoprene. The actual initiating species, viz., the oligomeric α-methylstyryl anion, originates by the reaction of n-butyllithium with α-methylstyrene in a benzene/diethyl ether 1:1 (v:v) solvent mixture at room temperature. The homopolymers and two-block copolymers of styrene and isoprene, prepared by using this system, were characterized by light scattering, membrance osmometry, GPC, and 1H NMR spectroscopy. By using the suggested initiation system, it is possible to synthesize well-defined homopolymers and block copolymers with low polydispersity (as judged by the shape of the GPC peaks and by the values of the polydispersity index), especially in a molar mass region between 4 × 104 and 1.5 × 105 g/mol. Above the upper limit of this interval, an appropriate decrease of the diethyl ether/benzene volume ratio is recommended, though the polymerization time must then be prolonged. 相似文献
2.
Y.A DemchenkoA Razina Z SedlákovaA Sikora J BaldrianM Ilavský 《European Polymer Journal》2002,38(12):2333-2341
Thermotropic polyesters based on 4,4′-alkane-1-ω-diylbis(4-hydroxybenzoic acid) and 4,4′-(pentane-1,5-diyloxy)dibenzoic acid were studied by dynamic mechanical spectroscopy, X-ray scattering, differential scanning calorimetry and polarizing microscopy. The effect of structure changes in the mesogenic group as well as in the flexible spacer, in particular the incorporation of Cl atoms into the mesogen, introduction of ether oxygen into spacer and the number of CH2 groups in spacer was investigated. More complex mechanical and thermal behaviour was found on second heating scan than on first cooling of the isotropic melt; higher values of mechanical functions were observed in the isotropic state than in the nematic state of melts. While an even number of CH2 groups and the presence of ether oxygen in spacer shifts the transition temperatures to higher values, the incorporation of Cl atoms into the mesogen leads to disappearance of ordered structure and the polymers behave as amorphous materials. 相似文献
3.
Battle PD Blundell SJ Brooks ML Hervieu M Kapusta C Lancaster T Nair SP Oates CJ Pratt FL Rosseinsky MJ Ruiz-Bustos R Sikora M Steer CA 《Journal of the American Chemical Society》2004,126(39):12517-12527
The temperature dependence of the crystal structure and electronic properties of brownmillerite-like Ca(2.5)Sr(0.5)GaMn(2)O(8) has been studied by neutron powder diffraction and muSR spectroscopy. The results show that short-range 2D magnetic order begins to develop within the perovskite-like bilayers of MnO(6) octahedra approximately 50 K above the 3D Néel temperature of approximately 150 K. The bilayers show a structural response to the onset of magnetism throughout this temperature range whereas the GaO(4) layers that separate the bilayers only respond below the 3D ordering temperature. XANES spectroscopy shows that the sample contains Mn(3+) and Mn(4+) cations in a 1:1 ratio, and the behavior in the region of the Néel transition is interpreted as a local charge ordering. Electron diffraction and high-resolution electron microscopy have been used to show that the local microstructure is more complex than the average structure revealed by neutron diffraction, and that microdomains exist in which the GaO(4) tetrahedra show different orientations. It is argued that the bonding requirements of diamagnetic gallium control the electronic behavior within the perovskite-like bilayers. 相似文献
4.
Crystallization behaviour of blends of poly(N-methyldodecano-12-lactam) (PMDL) with statistical copolymer poly(styrene-stat-acrylic acid) (PSAA) has been studied by the DSC and WAXD methods. The blend films prepared from dioxane solutions were crystallized at laboratory temperature for five days. Approximate crystallinities of as-prepared neat lower- PMDL 5 and higher-molecular weight PMDL 45 were 28% and 19%, respectively. With increasing PSAA content in the blends the crystallinities decreased sharply. The melting point of the primary crystalline structure of PMDL showed a decreasing dependence on PSAA content in the blends, confirming miscibility of the PMDL-PSAA pair. Recrystallization was strongly suppressed in the blends. The lower-melting endotherm appearing at about 10-15 °C above the crystallization temperature was attributed to melting to less perfect structures formed during secondary crystallization. In neat PMDL, the extent of secondary crystallization was approximately 5-10%. In the blends containing 20% PSAA approximate relative proportion of secondary crystallites on total crystallinity was 40% and 60% for the blends with PMDL 5 and PMDL 45, respectively. WAXD measurements did not reveal any change in crystal modification on blending. Increased Tg in blends of flexible PMDL cannot play a significant role in suppression of primary in favour of secondary crystallization. This was attributed to low mobility of PMDL chains due to dilution effect and specific interactions with the amorphous copolymer component, and, in case of the higher-molecular-weight PMDL, a greater involvement of entanglements. Higher Tg of blends was involved in retardation of non-isothermal crystallization on cooling and subsequent cold crystallization. 相似文献
5.
Dana Kubies Jaroslav Š?udla Rudolf Puffr Antonín Sikora Josef Baldrian Jana Ková?ová Miroslav Šlouf František Rypá?ek 《European Polymer Journal》2006,42(4):888-899
Poly(ε-caprolactone) (PCL) masterbatches with the intercalated and the exfoliated morphology were prepared by ring opening polymerization of ε-caprolactone in the presence of organomodified montmorillonite (MMT) Cloisite 30B. Poly(l-lactide) (PLLA) nanocomposites with Cloisite 30B or PCL masterbatches were prepared by melt blending. The effects of the silicate type, MMT content and the nanocomposite morphology on thermal and mechanical properties of PLLA nanocomposites were examined. The montmorillonite particles in PLLA/Cloisite 30B and PLLA/intercalated masterbatch nanocomposites were intercalated. In contrary to expectations, the exfoliated silicate layers of exfoliated masterbatch were not transferred into the PLLA matrix. Due to a low miscibility of PCL and PLLA, MMT remained in the phase-separated masterbatch domains. The stress-strain characteristics of PLLA nanocomposites, Young modulus E, yield stress σy and yield strain εy, decreased with increasing MMT concentration, which is associated with the increase in PCL content. The expected stiffening effect of MMT was low due to a low aspect ratio of its particles and was obscured by both plastifying effects of PCL and low PLLA crystallinity. Interestingly, in contrast to the neat PLLA, ductility was enhanced in all PLLA/Cloisite 30B materials and in PLLA/masterbatch nanocomposites with low MMT concentrations. 相似文献
6.
7.
The blends of poly(N-methyldodecano-12-lactam) (MPA) with poly(styrene-co-acrylic acid) (PSAA) prepared from dioxane solutions were studied by differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). The experimental DSC data of glass transition temperature Tg as a function of composition of amorphous phase were fitted for the as-prepared and re-scanned samples using theoretical approaches. The as-prepared blends show monotonic single-Tg dependence. The values of the Gordon-Taylor coefficient not far from unity suggest miscibility of the blend system in amorphous phase in the whole concentration range. As documented by FTIR, this miscibility is associated with hydrogen bonds between COOH groups of the acrylic acid units in PSAA molecules acting as the H-bond donor and CO groups of MPA acting as the H-bond acceptor. The Tg-dependencies obtained form the second runs have a profound sigmoid character. The Schneider treatment induced an idea of partial limited miscibility in the MPA/PSAA blends caused by prevalence of homogeneous contacts. The difference in Tg between the first and second run can partly be attributed to higher crystallinities in the former. 相似文献
8.
9.
We study the one-dimensional symmetry of solutions to the nonlinear Stokes equation which are periodic in the d − 1 last variables (living on the torus 𝕋d−1) and globally minimize the corresponding energy in Ω = ℝ × 𝕋d−1, i.e., Namely, we find a class of nonlinear potentials W ≥ 0 such that any global minimizer u of E connecting two zeros of W as x1 → ± ∞ is one-dimensional; i.e., u depends only on the x1 -variable. In particular, this class includes in dimension d = 2 the nonlinearities with w being a harmonic function or a solution to the wave equation, while in dimension d ≥ 3 , this class contains a perturbation of the Ginzburg-Landau potential as well as potentials W having d + 1 wells with prescribed transition cost between the wells. For that, we develop a theory of calibrations relying on the notion of entropy (coming from scalar conservation laws). We also study the problem of the existence of global minimizers of E for general potentials W providing in particular compactness results for uniformly finite energy maps u in Ω connecting two wells of W as x1 → ± ∞ . © 2019 Wiley Periodicals, Inc. 相似文献