A constitutive theory is developed for shape memory polymers. It is to describe the thermomechanical properties of such materials under large deformations. The theory is based on the idea, which is developed in the work of Liu et al. [2006. Thermomechanics of shape memory polymers: uniaxial experiments and constitutive modeling. Int. J. Plasticity 22, 279-313], that the coexisting active and frozen phases of the polymer and the transitions between them provide the underlying mechanisms for strain storage and recovery during a shape memory cycle. General constitutive functions for nonlinear thermoelastic materials are used for the active and frozen phases. Also used is an internal state variable which describes the volume fraction of the frozen phase. The material behavior of history dependence in the frozen phase is captured by using the concept of frozen reference configuration. The relation between the overall deformation and the stress is derived by integration of the constitutive equations of the coexisting phases. As a special case of the nonlinear constitutive model, a neo-Hookean type constitutive function for each phase is considered. The material behaviors in a shape memory cycle under uniaxial loading are examined. A linear constitutive model is derived from the nonlinear theory by considering small deformations. The predictions of this model are compared with experimental measurements. 相似文献
Poisson mixtures are usually used to describe overdispersed data. Finite Poisson mixtures are used in many practical situations where often it is of interest to determine the number of components in the mixture. Identifying how many components comprise a mixture remains a difficult problem. The likelihood ratio test (LRT) is a general statistical procedure to use. Unfortunately, a number of specific problems arise and the classical theory fails to hold. In this paper a new procedure is proposed that is based on testing whether a new component can be added to a finite Poisson mixture which eventually leads to the number of components in the mixture. It is a sequential testing procedure based on the well known LRT that utilises a resampling technique to construct the distribution of the test statistic. The application of the procedure to real data reveals some interesting features of the distribution of the test statistic. 相似文献
We report on a rheooptical investigation of hairy-rod poly(p-phenylene) solutions at different concentrations and temperatures. These polymers have a reasonably high persistence length
(about 28 nm) and behave as worm-like chains in dilute solutions, whereas they form nearly spherical fractal aggregates with
internal anisotropy at higher concentrations. By exposing these systems to time-dependent simple shear and following the evolution
of birefringence in start-up and its subsequent relaxation upon the cessation of shear, we find a substantial broadening of
the cluster size distribution, resulting from flow-induced cluster deformation and break-up. In contrast to the very dilute
solutions, where polymers align in the flow direction, the deformed clusters main axes are aligned in the vorticity direction,
presumably due to their strong steric local pretransitional type of ordering, with the constituent polymers following the
velocity vector. At the highest concentration, which corresponds to a weak gel, shear is shown to break-up the gel and the
steady-state response of a broad-size aggregate suspension is eventually recovered.
Received: 18 February 1999/Accepted: 6 July 1999 相似文献
Depolarized light scattering of binary polymer blends in disordered state near the demixing critical point is considered both theoretically and experimentally. It is shown that the depolarized scattering in such systems is predominantly due to double scattering processes induced by composition fluctuations. For long enough polymer chains, this scattering is stronger than the contribution from intrinsic anisotropy fluctuations. The general equation for the static and dynamic double scattering function is obtained in terms of the system structure factor. The scattering functions are calculated both analytically and numerically (dynamic part) for polymer blends. We found that the depolarized intensity depends on the polymerization degree N and the relative distance from the critical point τ = 1 – χ*/χ (where χ is the Flory‐Huggins interaction parameter and χ* its critical value) as Ivh ∼︁ N2/τ2, which is in good agreement with the experimental data. It is also shown that the dynamic scattering function is decaying non‐exponentially. We calculate the relaxation rate and the non‐exponentiality parameter as functions of the scattering angle and τ. These theoretical predictions are compared with experimental data for three chemically different blends. 相似文献
Investigations of thermotropic phase transitions performed on organocyclosiloxanes [PhSi(O)OSiR]6, where R is Me3, Me2(CH2Cl) or Me2(CH≃CH2), have revealed that all these hexamers are mesomorphic compounds. The hexamers exhibit uncommon polymesomorphic behaviour forming two quite different mesomorphic structures. The molecular arrangement in the low temperature (LT) modification is characterized by two-dimensional (2D) long-range order with hexagonal packing. The X-ray diffraction pattern and peculiarities of molecular packing in the crystal lead us to suggest that the LT-mesophase is columnar, presumably of the Colhd type. The LT-mesophase is formed by dimeric moieties, which associate with each other in column-like substructures, the ring planes not orthogonal to the stack axis. The high temperature (HT) mesophase is a plastic crystal (3D-order), where molecules take up positions in a face-centred cubic lattice. This is a very uncommon example of thermal behaviour for plastic crystals that provides a unique opportunity to bridge the gap between plastic crystalline and liquid crystalline mesomorphic behaviour. The thermal and structural properties of the mesophases depend upon the type of side groups of the hexamers. The size of the ring also affects the phase behaviour and the mesomorphic structure. This conclusion is consistent with data obtained by us earlier for cyclotetrasiloxanes. 相似文献
Mesoporous solids which possess average pore diameters between 7 and 20 nm, depending on the composition, have been prepared. The solids have the general formula Al100PχM20 where M = Al or Fe, and χ = 0, 4.5, 9, 18, 36, 72 or 144. The initial addition of phosphorus as phosphate transforms the originally crystalline oxide/oxides into amorphous solids. These amorphous materials possess a narrow pore size distribution: 80–90% of the pores lie within 1–2 nm of the average pore diameter. Subsequent incremental amounts of phosphorus transform the material into a crystalline solid whilst the pore size distribution becomes much wider and the maximum moves towards larger pore diameters. Substitution of 20% of the aluminium by iron results, at a low phosphorus content, in pores with smaller pore volumes and smaller surface areas.
The data in the dVp/dDp = > Dp) graphs, where Vp is the incremental pore volume and Dp is the average pore diameter, can be approximated using an admixture of Gaussian and Lorentzian curves. For low phosphorus contents the dVp/dDp = (Dp) curves have a mainly Gaussian profile but the gradual addition of phosphorus transforms them to Lorentzian-type curves. An attempt to approximate the histograms dVp =(Dp) with the minimum number of distribution curves made up of the corresponding Gaussian and Lorentzian components indicates that each successive addition of phosphorus creates a dominant new pore component at a larger pore diameter. At the same time, the components at smaller pore diameters are diminished and eventually disappear as more phosphorus is added. 相似文献
This paper presents a new method for writing and erasing a birefringence in optical fibers by polarized ultra violet side-exposure.
This experiment gives new insight into the origin of the induced birefringence and some applications are outlined. 相似文献
An important question in discrete optimization under uncertainty is to understand the persistency of a decision variable, i.e., the probability that it is part of an optimal solution. For instance, in project management,
when the task activity times are random, the challenge is to determine a set of critical activities that will potentially
lie on the longest path. In the spanning tree and shortest path network problems, when the arc lengths are random, the challenge
is to pre-process the network and determine a smaller set of arcs that will most probably be a part of the optimal solution
under different realizations of the arc lengths. Building on a characterization of moment cones for single variate problems,
and its associated semidefinite constraint representation, we develop a limited marginal moment model to compute the persistency
of a decision variable. Under this model, we show that finding the persistency is tractable for zero-one optimization problems
with a polynomial sized representation of the convex hull of the feasible region. Through extensive experiments, we show that
the persistency computed under the limited marginal moment model is often close to the simulated persistency value under various
distributions that satisfy the prescribed marginal moments and are generated independently. 相似文献