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51.
An efficient solution-processable route employing Pb(Ac)2 as lead source and anti-solvent treatment to achieve fully covered and homogenous perovskite films is reported. 相似文献
52.
Production of submicron-sized multihollow polymer particles by alkali/cooling method 总被引:5,自引:0,他引:5
Submicron-sized styrene-methacrylic acid copolymer particles, which were produced by emulsion copolymerization, were changed to those having multihollow structure by treating stepwise the emulsion as follows. First alkali treatment was carried out at higher temperature than the glass transition temperature and subsequently the emulsion was cooled by keeping it at room temperature. This was named alkali/cooling method. The effects of methacrylic acid content, pH, time and temperature in the alkali treatment on the formation of multihollow structure were clarified.Part CLV of the series Studies on suspension and emulsion 相似文献
53.
Summary A polystyrene sample obtained by free radical polymerization has been fractionated by preparative scale GPC and the structure and morphology of the fractions have been studied by13C-NMR spectroscopy, DSC and X-ray measurements. No changes in morphology in the course of fractionation have been obeyed. A distribution of syndiotacticity within the molecular weight distribution does not exist.
List of abbrevations and symbols AIBN a, a-Azo-bis-(iso-butyronitrile) - D Dispersity, M w /M n - DSC Differential scanning calorimetry - EF Efficiency of fractionation - GPC Gel permeation chromatography - m mass of the fraction - M mass of the fractionated polymer sample - MWD Molecular weight distribution - P r content of racemic dyads - PS Polystyrene - THF Tetrahydrofuran - U D-1 - U ss U of the starting sample - U f U of the fraction Auszug aus der Dissertation von U.-D. Standt: Zur Morphologie von Polystyrol, TU Braunschweig 1981. 相似文献
Zusammenfassung Eine Polystyrolprobe, die durch radikalische Polymerisation hergestellt wurde, wurde mit Hilfe der präparativen Gelpermeationschromatographie fraktioniert; die Struktur und Morphologie der Fraktionen wurde mit13C-NMR-Spektroskopie, DSC und Röntgenbeugung untersucht. Im Verlauf der Fraktionierung traten keine Änderungen der Morphologie der Fraktionen auf. Innerhalb der Molekulargewichtsverteilung existiert keine Verteilung der Syndiotaktizität.
List of abbrevations and symbols AIBN a, a-Azo-bis-(iso-butyronitrile) - D Dispersity, M w /M n - DSC Differential scanning calorimetry - EF Efficiency of fractionation - GPC Gel permeation chromatography - m mass of the fraction - M mass of the fractionated polymer sample - MWD Molecular weight distribution - P r content of racemic dyads - PS Polystyrene - THF Tetrahydrofuran - U D-1 - U ss U of the starting sample - U f U of the fraction Auszug aus der Dissertation von U.-D. Standt: Zur Morphologie von Polystyrol, TU Braunschweig 1981. 相似文献
54.
René Androsch 《European Polymer Journal》2007,43(1):93-108
The melt-crystallization of an oligo[(R)-3-hydroxybutyrate] with five repeating units has been analyzed using standard and temperature-modulated calorimetry, optical microscopy, and atomic force microscopy. Specimens of different crystallinity and supermolecular structure were generated by variation of the rate of cooling of a quiescent melt, or by variation of the temperature of isothermal crystallization. Completely amorphous samples can be obtained by cooling of the melt at a rate of 40 K min−1, or faster, to a temperature lower than the glass transition. The crystallinity depends on the crystallization temperature. The maximum enthalpy-based crystallinity of about 40-45% is obtained by crystallization at temperatures lower than the temperature of the maximum crystallization rate, which is between 310 and 320 K. Analysis of the apparent heat capacity in metastable structural equilibrium reveals reversible melting at temperatures between 320 and 370 K by observation of an excess heat capacity above the level of the vibrational heat capacity, i.e., in the temperature range of irreversible reorganization and melting. The reversible melting is discussed in the context of coupling of the crystalline and amorphous phases, and compared to earlier studies on oligoethylene and oligo(oxyethylene). The presence of crystals causes formation of a rigid amorphous fraction of about 30% at a crystallinity of 40%. Optical and atomic force microscopy reveal spherulitic crystallization. At relatively high crystallization temperature, and in the early stage of the crystallization process, dendrites are observed which finally yield spherulites of decreased perfection. Larger spherulites of higher perfection grow at relatively low crystallization temperature, as deduced from the appearance of the Maltese cross, and the regularity of banding. The band spacing is less than 5 μm, as is accurately determined by atomic force microscopy. The temperature dependence of the spherulitic growth rate is in accord with the calorimetric analysis of the crystallization rate. 相似文献
55.
56.
J. B. Miller 《Journal of Thermal Analysis and Calorimetry》1997,49(1):521-524
Nuclear magnetic resonance (NMR) spectroscopy has been used to study the morphology and dynamics in semicrystalline polymers. Dynamics may be observed through NMR relaxation rates that are sensitive to motions in the 1–108 Hz range, or through modulation of anisotropic magnetic interactions, such as the chemical shift and dipole-dipole interactions. Morphological structure may be inferred through NMR measurements of polymer dynamics or investigated directly through studies of the magnetic interactions. Here, we discuss the study of morphological structure in semicrystalline polymers using NMR, and review results on poly(ethylene terephthalate) that address the question of the number of phases in this semicrystalline polymer.This work was funded by the Office of Naval Research. 相似文献
57.
Poly(L -lactide-co-β-malic acid) was obtained after the hydrogenolysis of the copolymer of L -lactide (L-LA) and β-benzyl malate (MA). 1H-NMR demonstrated that the composition of the copolymer was identical to the feeding dose. Thermal property study revealed the morphology of the copolymer could be changed from semi-crystalline to amorphous with increasing hydrophilic β-malic acid content. The copolymers with 8 and 13 mol% β-malic acid content possessed enough mechanical property for fabricating cell scaffold. Degradation result demonstrated that most of the hydrophilic β-malic acid units broke down from the copolymer within 1 week and the ester bond between L -lactide and β-malic acid hydrolyzed prior to the inner ester bond of poly(L -lactide) (PLLA). Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
58.
CuO超细粉体的形貌与红外特性研究 总被引:16,自引:0,他引:16
CuO作为一种多功能精细无机材料,在印染、陶瓷、玻璃及医药等领域的应用已有数十年的历史,作为催化剂的主要活性成分,近年来在氧化、加氢、C1化学合成、NOx还原、CO及碳氢化合物燃烧、精细化工等多种催化反应中也得到了广泛的应用。可以推测,当CuO材料的粒度达到纳米级时,将使它的功能更加独特,应用更为广泛。因此CuO纳米材料的制备方法、聚集状态、与其他组分或载体的作用状况及催化活性等成为当前功能材料发展的研究热点之一犤1~8犦。我们在前文中报道了直接热解Cu2(OH)2CO3所得CuO粒径小、分布均匀、比表面积大,… 相似文献
59.
Silicon nitride powders were synthesized in an atmospheric-pressure convection-stabilized arc using silicon and ammonia as reactants. The morphology and particle size distributions of the silicon nitride particles were characterized by SEM, TEM, and electron diffraction analyses. The silicon nitride particles collected in the plasma reactor were formed by either gas-condensed phase reactions or chemical vapor reactions. The morphologies of the particles formed by gas-condensed phase reactions consisted of -Si3N4 prisms, -Si3N4 matte, -Si3N4 needles, and spaghetti-like whiskers. For the homogeneously nucleated particles, the morphologies included dendrites, needles, platelets, and amorphous particles. Most of the particles formed were aggregates with particle size distributions ranging from 500 to 1500 Å depending on the location of injection of the reactants. 相似文献
60.
Tarek M. Madkour Rasha A. Azzam 《Journal of polymer science. Part A, Polymer chemistry》2002,40(14):2526-2536
Polyurethane elastomers of a controlled molecular architecture were synthesized using a two‐step polymerization technique. The building blocks of the elastomeric materials included urea–urethane prepolymers end‐capped with diisocyanate groups and had an exact number of urea groups at both ends. Two‐dimensional bifurcated hydrogen‐bonding networks incorporating the urea groups were, with differential scanning calorimetric and dynamic mechanical thermal analyzer techniques, responsible for the increase in the glass‐transition temperature (Tg) of the hard block and sharp interface morphology between the pure “hard” domains and pure “soft” domains. The higher extent of the phase separation between the two phases contributed to higher elastic moduli for the hard blocks and higher tensile strength for the elastomeric samples. Higher elongation values were attributed to the liberation of the elastomeric chain ends that otherwise would have been constrained in the interface region. The higher Tg values of the hard blocks corresponded to an increase in the hardness values and a decrease in the tear‐strength values. The increase in the amount of urea groups within the hard segments, as a result of the increased amount of water and blowing catalyst, resulted in elastomeric foams with higher open‐cell content. This resulted in lower resilience values as measured using the pendulum rebound test and was attributed to the ability of the open cells to absorb and dissipate energy. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2526–2536, 2002 相似文献