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J. C. Meiners A. Ritzi M. H. Rafailovich J. Sokolov J. Mlynek G. Krausch 《Applied Physics A: Materials Science & Processing》1995,61(5):519-524
We have used atomic force microscopy to study the adsorption of PolyStyrene-Poly(VinylPyridine) (PS-PVP) block copolymers from a selective solvent onto atomically smooth mica surfaces. At certain copolymer concentrations, we observe a highly regular array of spherical surface micelles covering macroscopic areas of the substrate surface. Evidence is given for a thin homogeneous layer underneath the micelles which is probably due to adsorption of free copolymer chains and brush formation prior to the formation of the micellar structures. We discuss the quality of the self-assembled structures regarding different types of defects and try to identify means for improving the long range periodicity of the structures. 相似文献
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Lorenzo CaggianoDamiano Castoldi Raphael BeumerPau Bayón Joachim TelserCesare Gennari 《Tetrahedron letters》2003,44(43):7913-7919
During the course of our synthetic studies towards simplified eleuthesides, we have found that p-methoxyphenyl (PMP) protected allylic alcohols are compatible with the RCM reaction and can give better yields than the corresponding free allylic alcohols. 相似文献
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The “Thermo-Stat” — a new device for the determination of catalyticaily active substancesA device for the determination of catalytically active substances, called a “ThermoStat”, is described. An additional heater is used to keep constant an arbitrarily preset temperature gradient between the reaction mixture and a cooling coil. Any heat produced by the catalysed reaction induces a deviation from the preset parameter and thus cuts out the additional heater. These breaks are plotted versus time by an integrating recorder. The slope of the reaction curve obtained is a measure of the concentration of the catalyst. As examples, determinations of copper in the range 0.1–2.0μg and molybdenum in the range 5–50 μg are discussed. 相似文献
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Based on theoretical thermodynamic principles, the possibility of environmental degradation of polyacrylamide to its starting monomer was investigated. Theoretical electronic structure studies on the geometry and fragmentation energy of acrylamide and N,N‐dimethyl acrylamide tetramer models were carried out using a first principles gradient corrected density functional approach. Thermal degradation to form a radical would require the cleavage of carbon–carbon bonds in the polymer chain; the energy needed for this cleavage was found to depend on the structure of the repeat unit which ranged from low of 72.5 kcal for a rare head‐to‐head construct to 86.2 kcal for a normal head‐to‐tail polymer construct (therefore, for the cleavage of a normal head‐to‐tail repeat unit, temperatures of approximately 450°C would be required). The thermodynamics of the unzipping, disproportionation, and back‐biting reactions in the resulting radical fragments were also investigated; the back‐biting process was found to require the least energy and provided the most stable radical fragment with a low probability for disproportionation or releasing of monomer to occur. The effect of solvation on the hydrogen‐bonding network in the acrylamide tetramer was studied by adding explicit molecules of water to the tetramer models. The addition of water had a significant effect on the stability of the model polymer slightly stabilizing the head‐to‐head polymer, and slightly destabilizing the head to tail polymer. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
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The iodine—azide reaction catalyzed by sulphur-containing compounds is followed simultaneously by optical and thermometric measurements in closed and flowing systems. In the closed system, thiosulphate can be determined in the range 32.4–324 μg ml-1, by observing the turbidity caused by the nitrogen formed during the reaction and the temperature changes. With the flow apparatus, thiosulphate can be determined in the range 112–1120 μg ml-1 by continuously mixing the sample and reagent solutions. H2S in nitrogen 5–100 ppm) is measured by sweeping the gas into the reaction Cuvette. In a third flow procedure, H2S is liberated continuously from sodium sulphide solutions (0.1–10 μg S2- ml-1) by ascorbic acid, and swept to the measuring cuvette with nitrogen. 相似文献
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Luís Antônio Dantas Silva Fernanda Vieira Teixeira Raphael Caixeta Serpa Najla Locatelli Esteves Rayane Ramos dos Santos Eliana Martins Lima Marcílio Sérgio Soares da Cunha-Filho Adriano Antunes de Souza Araújo Stephânia Fleury Taveira Ricardo Neves Marreto 《Journal of Thermal Analysis and Calorimetry》2016,123(3):2337-2344
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