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101.
102.
Dynamics of a Cubic Nonlinear Vibration Absorber 总被引:1,自引:0,他引:1
We study the dynamics of a nonlinear active vibration absorber. We consider a plant model possessing curvature and inertia nonlinearities and introduce a second-order absorber that is coupled with the plant through user-defined cubic nonlinearities. When the plant is excited at primary resonance and the absorber frequency is approximately equal to the plant natural frequency, we show the existence of a saturation phenomenon. As the forcing amplitude is increased beyond a certain threshold, the response amplitude of the directly excited mode (plant) remains constant, while the response amplitude of the indirectly excited mode (absorber) increases. We obtain an approximate solution to the governing equations using the method of multiple scales and show that the system possesses two possible saturation values. Using numerical techniques, we perform stability analyses and demonstrate that the system exhibits complicated dynamics, such as Hopf bifurcations, intermittency, and chaotic responses. 相似文献
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104.
Chin‐San Wu 《Journal of polymer science. Part A, Polymer chemistry》2005,43(8):1690-1701
In this study, a silicic acid and tetra isopropyl ortho titanate ceramic precursor and a metallocene polyethylene‐octene elastomer (POE) or acrylic acid grafted metallocene polyethylene‐octene elastomer (POE‐g‐AA) were used in the preparation of hybrids (POE/SiO2? TiO2 and POE‐g‐AA/SiO2? TiO2) using an in situ sol‐gel process, with a view to identifying a hybrid with improved thermal and mechanical properties. Hybrids were characterized using Fourier transform infrared spectroscopy, 29Si solid‐state nuclear magnetic resonance (NMR), X‐ray diffraction, differential scanning calorimetry, thermogravimetry analysis, dynamic mechanical thermal analysis, and Instron mechanical testing. Properties of the POE‐g‐AA/SiO2? TiO2 hybrid were superior to those of the POE/SiO2? TiO2 hybrid. This was because the carboxylic acid groups of acrylic acid acted as coordination sites for the silica‐titania phase to allow the formation of stronger chemical bonds. 29Si solid‐state NMR showed that Si atoms coordinated around SiO4 units were predominantly Q3 and Q4. The 10 wt % SiO2? TiO2 hybrids gave the maximum values of tensile strength and glass transition temperature in both POE/SiO2? TiO2 and POE‐g‐AA/SiO2? TiO2. It is proposed that above this wt %, excess SiO2? TiO2 particles caused separation between the organic and inorganic phases. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1690–1701, 2005 相似文献
105.
Fang‐Chyou Chiu Chin‐Yu Kan Jen‐Chang Yang 《Journal of Polymer Science.Polymer Physics》2009,47(15):1497-1510
The thermal properties and phase morphology of poly(L ‐lactide) (PLLA)‐based blends have been studied. Two poly(ethylene glycol)s (PEGs) with molecular weight (MW) of about 1,500 (1.5k) g/mol and 2,000,000 (2M) g/mol, respectively, were used as counterparts. The blends were annealed at a preselected temperature of 200 °C for either 2 min or 30 min before the characterizations. Both PEGs were determined to enhance the crystallizability of PLLA. After a 2‐min process of annealing, the PEG(1.5k)'s crystallization efficiency on PLLA has been noted to increase with the increase of its content. Conversely, PEG(2M)'s crystallization efficiency declined with the increase of its content. Extending the annealing time has evidently changed the PEGs' crystallization effect on PLLA. Moreover, the PEG(1.5k) has, to a greater extent, brought about the depression of PLLA's melting temperature by increasing its content, and this depression increased with the annealing time. The blends exhibited lower thermal stability than those of the parent components, particularly for the PEG(1.5k)‐included system with a higher PEG content. Regardless of the annealing time, the PEG(1.5k)‐included blends have shown homogeneous melt morphology under light microscope, whereas the PEG(2M)‐included blends have displayed phase‐separated melt morphology. In addition to the composition, PEG's MW and annealing time influence the crystalline morphology of the blends. The ringed PLLA spherulites have appeared mostly in the 2‐min annealed PEG(1.5k)‐included blends. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1497–1510, 2009 相似文献
106.
Xinjian Cheng Sie Chin Tjong Qiang Zhao Robert K. Y. Li 《Journal of polymer science. Part A, Polymer chemistry》2009,47(18):4547-4554
This article presents a facile method to prepare silver/polystyrene composite microspheres. In this approach, monodispersed polystyrene (PS) particles were synthesized with carboxyl acid groups on the surfaces of the PS particles via dispersion polymerization at first. With the addition of [Ag(NH3)2]+ to the PS dispersion, [Ag(NH3)2]+ was absorbed to the surfaces of the PS particles, and then by heating the system, [Ag(NH3)2]+ complex ions were reduced to silver to form the Ag/PS composite microspheres. In the synthesis of PS dispersion, PVP was used as dispersant to stabilize the PS particles, it also acted as reducing agent in the reduction of [Ag(NH3)2]+ complex ions to silver, so no additional reducing agent was needed. The resulting composite microspheres were characterized by TEM, SEM, XPS, and XRD. The catalytic properties and surface‐enhance Raman scattering (SERS) was studied as well. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4547–4554, 2009 相似文献
107.
Starting from one fullerene, the three geometric transformations, cap, face dual and edge dual produce series of carbon clusters and deltahedra. The geometric relation between these polyhedra implies that their topological matrices and eigenvalue spectra must be relative. We have developed a matrix algebra method to research some polyhedra with high symmetry and one kind, two or three kinds of equivalent vertices such as C60(Ih), resolve their exact eigenvalues, and proved this point. 相似文献
108.
109.
110.
Hui H. Chin Leonid V. Azroff Agya R. Saini Robert W. Lenz 《Journal of Polymer Science.Polymer Physics》1989,27(10):2001-2009
Semiflexible thermotropic aromatic polyesters with lateral groups were aligned magnetically and mechanically in monodomains after separation into high-molecular-weight (polymer) and low-molecular-weight (oligomer) fractions. Based on the x-ray intensity distributions recorded for a series of seven different substituents in the arylsulfonyl substituted group, a novel smectic structure was determined for H, F, Cl, OCH3, and CH3 in the para position while a normal nematic alignment prevailed when it contained Br or NO2. 相似文献