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101.
In this work, the so-called natural or passive ventilation drag reduction method is investigated experimentally and numerically. Passive ventilation is performed by directly connecting the high pressure region at the front of a body to the lower pressure in the near wake using a venting duct; in this manner, a net mass flux is established within the wake. In particular, in aerodynamic applications it appears suitable to attain a global reduction in the drag of a body moving in a fluid and a reduction in turbulence levels by means of a global modification of the body wake. Velocity field investigations using particle image velocimetry measurements and a Reynolds averaged numerical code are employed at moderately high Reynolds numbers to clarify the effectiveness of drag reduction on a vented bluff body. The numerical and experimental results agree qualitatively, but the amount of reduction for the vented body (about 10%) is underestimated numerically. The effectiveness of drag reduction has been proved both for smooth and rough (single strip) models. Direct balance measurements are used for comparisons.  相似文献   
102.
The large and reversible photoinduced linear and circular birefringences in azo‐compounds are at the basis of the interest in these materials, which are potentially useful for several applications. Since the onset of the linear and circular anisotropies relies on orientational processes, which typically occur on the molecular and supramolecular length scale, respectively, a circular birefringence at least one order of magnitude lower than the linear one is usually observed. Here, the synthesis and characterization of an amorphous polymer with a dimeric repeating unit containing a cyanoazobenzene and a cyanobiphenyl moiety are reported, in which identical optical linear and circular birefringences are induced for proper light dose and ellipticity. A pump‐probe technique and an analytical method based on the Stokes–Mueller formalism are used to investigate the photoinduced effects and to evaluate the anisotropies. The peculiar photoresponse of the polymer makes it a good candidate for applications in smart functional devices.

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103.
104.
Dendrimersomes are stable, monodisperse unilamellar vesicles self-assembled in water from amphiphilic Janus dendrimers. Their size, stability, and membrane structure are determined by the chemical structure of Janus dendrimer and the method of self-assembly. Comparative analysis of the periodic arrays in bulk and dendrimersomes assembled by ethanol injection in water of 11 libraries containing 108 Janus dendrimers is reported. Analysis in bulk and in water was performed by differential scanning calorimetry, X-ray diffraction, dynamic light scattering, and cryo-TEM. An inverse proportionality between size, stability, mechanical properties of dendrimersomes, and thickness of their membrane was discovered. This dependence was explained by the tendency of alkyl chains forming the hydrophobic part of the dendrimersome to produce the same local packing density regardless of the branching pattern from the hydrophobic part of the dendrimer. For the same hydrophobic alkyl chain length, the largest, toughest, and most stable dendrimersomes are those with the thinnest membrane that results from the interdigitation of the alkyl groups of the Janus dendrimer. A simplified spherical-shell model of the dendrimersome was used to demonstrate the direct correlation between the concentration of Janus dendrimer in water, c, and the size of self-assembled dendrimersome. This concentration-size dependence demonstrates that the mass of the vesicle membrane is proportional with c. A methodology to predict the size of the dendrimersome based on this correlation was developed. This methodology explains the inverse proportionality between the size of dendrimersome and its membrane thickness, and provides a good agreement between the experimental and predicted size of dendrimersome.  相似文献   
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106.
The principles of self-assembly of tapered exo-receptors constructed from monodendrons containing crown-ether, oligooxyethylenic groups and polymer backbones as endo-receptors into tubular supramolecular architectures are described with selected examples. In the case of polymers with flexible backbones it is suggested that a helical chain conformation is induced during the assembly of its own tapered side groups. This mechanism is supported by the enhanced self-assembling ability of tapered side groups attached to a backbone with rigid helical conformation.  相似文献   
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108.
Journal of Thermal Analysis and Calorimetry - The investigation of radiation effects on ethylene–propylene–diene terpolymer (EPDM) loaded with trifunctional monomer (trimethylolpropane...  相似文献   
109.
The aim of this work is to the study the influence of the isomer structures of butyl acrylate monomer on the single‐electron transfer/degenerative chain transfer mediated living radical polymerization (SET‐DTLRP). The kinetic of isobutyl acrylate is determined for the first time by SET‐DTLRP in water catalyzed by sodium dithionite. The plots of number‐average molecular weight versus conversion and ln([M]0/[M]) versus time are linear, demonstrating a controlled polymerization. The influence of the isomer t‐butyl, i‐butyl, and n‐butyl on the kinetics, properties, and stereochemistry of the reactions was assessed. To the best of our knowledge, there is no previous report dealing with the synthesis of PiBA by any LRP approach in aqueous medium. The results presented in this work suggest that the stability provided by the acrylate side group has an important influence in the polymerization process. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6542–6551, 2008  相似文献   
110.
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