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81.
David R. Harding Holly Goodrich Aaron Caveglia Mitchell Anthamatten 《Journal of Polymer Science.Polymer Physics》2014,52(14):936-945
Knowing the mechanical properties of UV‐curable resins at cryogenic conditions is important to ongoing fusion‐energy research and to emerging aerospace applications. The tensile and interfacial shear strengths of two commercially available UV‐curable resins were measured at room‐temperature and cryogenic conditions for both bulk and reduced (subnanoliter) specimen volumes. The tensile properties of cured specimens are remarkably sensitive to both testing temperature and specimen size. For one type of resin, the cold (?150 °C) tensile strength of subnanoliter specimens is ~9× larger (179 ± 19 MPa) than bulk values at room temperature. The interfacial shear strength between SiC fibers and small volumes of resin volumes is comparable to the bulk, room‐temperature tensile strength, but it varies over a wide range at ?150 °C (15–53 MPa). All resins were fully cured, and an analysis of fractured surfaces revealed microstructural features. The enhanced strength in microscopic specimens may be related to inhomogeneous stress fields that develop during cure. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52, 936–945 相似文献
82.
Thode A Mellinger DK Stienessen S Martinez A Mullin K 《The Journal of the Acoustical Society of America》2002,112(1):308-321
Three-dimensional dive trajectories of three sperm whales in the Gulf of Mexico have been obtained by measuring the relative arrival times and bearings of the animals' acoustic multipath reflections, using two elements of a towed hydrophone array deployed at an unknown depth and orientation. Within the first 6-12 min of the start of a dive, the intervals between successive "clicks" of all three whales corresponded closely with the two-way travel time of an acoustic pulse traveling vertically between the animals' position and the ocean bottom. The click spectra contained multiple peaks, including a faint band of energy originally centered near 10 kHz. As the animals descended over 500 m in depth, the center frequency of this band shifted to nearly 15 kHz, but subsequently remained near this value during the rest of the dive. This frequency shift is consistent with that expected from energy scattering from an ensemble of incompressible small-scale air-filled resonators, with diameters on the order of 4 mm. One possible candidate for such an ensemble is proposed to reside in the collapsed frontal sac of the animal. A comparison of the received levels for the bottom and direct multipath arrivals indicates that the whales' acoustic directivity must range between 10-30 dB in the 5-20-kHz region. 相似文献
83.
Jayaprakash KN Gillepsie AM Gunnoe TB White DP 《Chemical communications (Cambridge, England)》2002,(4):372-373
Deprotonation of [TpRu(CO)(PPh3)(NHPh)][OTf]2 yields the thermally unstable d4 imido complex [TpRu-(CO)(PPh3)(NPh)][OTf]; a computational study of the bonding of the imido complex provides a foundation for discussion of its instability in terms of pi-conflict. 相似文献
84.
[formula: see text] Apoptolidin (1) is a novel oncolytic lead that induces apoptosis in transformed cell lines with exceptional selectivity. We report the isolation and characterization of a ring-expanded macrolide isomer of apoptolidin: isoapoptolidin (2). The solution conformation of isoapoptolidin is described. The rate of isomerization was measured under biologically relevant conditions and found to approach equilibrium within the time frame of most cell-based assays. Isoapoptolidin's ability to inhibit mitochondrial F0F1-ATPase is over 10-fold less than that of apoptolidin. 相似文献
85.
The dendrobatid alkaloid (-)-251F was synthesized. The key steps of the synthesis were (1) an asymmetric Diels-Alder reaction to establish four of the necessary stereocenters in the target, (2) a ring-opening/ring-closing metathesis reaction to establish a key [3.3.0] bicyclic intermediate, and (3) an intramolecular Schmidt reaction. 相似文献
86.
We employ density functional and quantum Monte Carlo calculations to show that significant changes occur in the gap of fully hydrogenated nanoclusters when the surface contains passivants other than hydrogen, in particular atomic oxygen. In the case of oxygen, the gap reduction computed as a function of the nanocluster size provides a consistent interpretation of several recent experiments. Furthermore, we predict that other double bonded groups also significantly affect the optical gap, while single bonded groups have a minimal influence. 相似文献
87.
We present a model of leptogenesis that preserves lepton number. The model maintains the important feature of more traditional leptogenesis scenarios: The decaying particles that provide the CP violation necessary for baryogenesis also provide the explanation for the smallness of the neutrino Yukawa couplings. This model clearly demonstrates that, contrary to conventional wisdom, neutrinos need not be Majorana in nature in order to help explain the baryon asymmetry of the universe. 相似文献
88.
Jean-Jacques Aaron Zouhair Mechbal Alain Adenier Cyril Parkanyi Vaclav Kozmik Jiri Svoboda 《Journal of fluorescence》2002,12(2):231-239
The structural and solvent effects on the electronic absorption and fluorescence spectra, and fluorescence quantum yields, of four new fused benzothiophene derivatives, including benzothieno[3,2b]-thiophene (BTT), benzothieno[3,2-b]benzothiophene (BTBT), 6-methoxy[1]benzothieno[3,2b]-thiophene (MeOBTT), and benzothieno[3,2-b]indole (BTI) were investigated at 295 K. The luminescence properties of the corresponding conductive oligomers, poly(BTT) and poly (MeOBTT), electrosynthesized in acetonitrile, were also studied. Satisfactory McRae, Suppan, and Kawski-Chamma-Viallet solvatochromic correlations were established for the four monomers in most solvents. A weak negative solvatochromic behavior was found for these compounds, indicating that their dipole moments are slightly lower in the excited singlet state than in the ground state. Kamlet-Abboud-Taft multiparametric correlations were also obtained for absorption and fluorescence wave numbers and quantum yields, demonstrating the existence of specific solute-solvent interactions. In the case of the oligomers, important red-shifts of the fluorescence emission maxima ( 90–110 nm) relative to the corresponding monomers were observed, which shows the extent of conjugated segments in the oligomer chains. 相似文献
89.
Yao-Yi Cheng Peggy Cebe Malcolm Capel Heidi Schreuder-Gibson Aaron Bluhm Walter Yeomans 《Journal of Polymer Science.Polymer Physics》1995,33(17):2331-2341
Crystallization and melting behavior are studied by small-angle X-ray scattering (SAXS) for a series of recently synthesized monotropic liquid crystalline polycarbonates based on α-methyl stilbene mesogen and methylene flexible spacer. The one-dimensional electron density correlation function is used to obtain long period, crystal thickness, and linear crystallinity from the Lorentz-corrected SAXS intensity. Changes in these parameters during nonisothermal crystallization and melting are explained by a model of dual crystal populations. The primary crystals form first using the liquid crystalline phase as crystal nuclei, while smaller and less perfect crystals form later from the isotropic phase at low temperature. The results of the real-time SAXS study of isothermal crystallization also support the view that the nematic phase serves as crystal nuclei for fast crystallization. An odd-even effect in crystal thickness and linear crystallinity is observed in all the SAXS experiments mentioned above. The results of this study and our complementary wide-angle X-ray scattering (WAXS) investigation show clearly that the difference in the position of the neighboring carbonate dipoles on a chain affects structural organization both at the unit cell level and at the level of the crystal in these monotropic LCPs. © 1995 John Wiley & Sons, Inc. 相似文献
90.
Abstract— A methodology for the determination of chemiluminescence quenching terms is given. By using the oxidation of tetrakis(dimethylamino)ethylene as an example, it is shown how the nature and magnitude of the quenching terms help to elucidate the reaction mechanism, or how ignoring them can lead to false impressions. It is shown that chemiluminescence quenching effects need not be the same as those for photoluminescence of the same electronically excited species. 相似文献