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31.
There are several developments taking place in the field of sensors driven by the world today requirements. One of the most important novelties of the last two decades in the field is represented by the hydrogel-based sensors which constitute a wide family of innovative smart sensing devices relevant for many different applications. Hydrogels in fact are hydrophilic, biocompatible and highly water swellable polymer networks able to convert chemical energy into mechanical energy, with the great peculiarity to be able to respond to external stimuli. These characteristics have ensured them considerable recognition as valuable tool for smart sensing and diagnostics. The aim of this review is to focus on the advances obtained in the field in the last ten years. 相似文献
32.
A novel silane coupling agent bearing sulfobetaine group, N,N-diethyl-N-(3-sulfopropyl)-aminopropyl- trimethoxysilane (DESATS), was first designed, synthesized and characterized. Its solution property was studied by means of dynamic light scattering. DESATS was successfully bonded onto the surface of the glass and proved by ESCA. Platelet adhesion assay in vitro indicated that the nonthrombogenicity of glass slide modified with DESATS is greatly improved. 相似文献
33.
Jean-Yves Sanchez Fannie Alloin Cristina Iojoiu 《Journal of fluorine chemistry》2006,127(11):1471-1478
This contribution has been partly adapted from a special lecture intended to commemorate the Nobel prize, awarded one century ago, to Henri Moissan. It, is focused on fluorinated and perfluorinated molecules and macromolecules used in electrochemical energy sources, i.e. storage and conversion of energy. The latter, which figure indisputably among New Energy Technologies, include lithium batteries and fuel cells based on polymeric membranes both of which have tremendous development potential in terms of performances, safety and cost reductions. The advantages inherent in fluorine, in particular its electron-withdrawing effect and the oxidation stability that it provides to the carbon-fluorine bond, make it an asset in the search for new organic molecular and macromolecular anions with extensive delocalization of the negative charge, usable both in lithium batteries and fuel cells. As for fluorinated and perfluorinated macromolecule backbones, they are currently the reference material in fuel cell ionomeric membranes but some of them are also good candidates for use in lithium-ion batteries. This paper, far from being exhaustive, also emphasizes the economic aspects that influence material selection and also govern the future of basic research. 相似文献
34.
The lithium ion conducting solid polymer electrolytes (SPE) based on PVAc-LiClO4 of various compositions were prepared by solution casting technique. Structure and surface morphology characterization were studied by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM) measurements, respectively. Thermal and conductivity behavior of polymer-salt complexes were studied by employing differential scanning calorimetry (DSC) and ac impedance measurements, respectively. XRD and SEM analyses indicate the amorphous nature of the polymer-salt complexes. DSC measurements show decrease in Tg with the increase in LiClO4 concentrations. The bulk conductivity of the PVAc:LiClO4 polymer electrolytes was found to vary between 7.6×10−7 and 6.2×10−5 S cm−1 at 303 K with the increase in salt concentration. The temperature dependence of the polymer electrolyte complexes appear to obey Arrhenius law. 相似文献
35.
The Maxwell-Wagner-Sillars (MWS) relaxation is studied for semi-crystalline polymers poly (ether ether ketone) (PEEK), in the range 20 Hz-1 MHz and temperature varying from 80 to 330 °C. The parameter is the crystallization condition in the case of PEEK, which is a semi-crystalline polymer considered as a particulate composite. The relaxation found in the semi-crystalline polymers above the α relaxation of the PEEK is ascribed to the trapping of conductive carriers at the interface between crystalline lamellae and the amorphous matrix. The study of PEEK microstructure is based on differential calorimetry and X-rays diffraction. Two lamellae populations have been detected, that depends on the crystallization temperature and its duration. The crystallinity rate is increasing with crystallization temperature and duration. In dielectric studies, the use of the electric modulus instead of permittivity allows us to minimize the ionic conduction and then leads to the appearance of the interfacial relaxation. According to our measurements, the crystallinity rate is not the main factor of the interfacial relaxation intensity, which also depends on the nature and degree of perfection of the lamellae. 相似文献
36.
Living polymers are formed by reversible association of primary units (unimers). Generally the chain statistical weight involves
a factor σ < 1 suppressing short chains in comparison with free unimers. Living polymerization is a sharp thermodynamic transition
for σ ≪ 1 which is typically the case. We show that this sharpness has an important effect on the kinetics of living polymerization
(one-dimensional association). The kinetic model involves i) the unimer activation step (a transition to an assembly-competent
state); ii) the scission/recombination processes providing growth of polymer chains and relaxation of their length distribution.
Analyzing the polymerization with no chains but unimers at t = 0 , with initial concentration of unimers M ≳ M
* (M* is the critical polymerization concentration), we determine the time evolution of the chain length distribution and find
that: 1) for M
* ≪ M ≪ M
*/σ the kinetics is characterized by 5 distinct time stages demarcated by 4 characteristic times t1, t2, t3 and t*; 2) there are transient regimes (t
1 ≲ t ≲ t
3) when the molecular-weight distribution is strongly non-exponential; 3) the chain scissions are negligible at times shorter
than t2. The chain growth is auto-accelerated for t
1 ≲ t ≲ t
2 : the cut-off chain length (= polymerization degree 〈n〉w
N
1 ∝ t
2 in this regime. 4) For t
2 < t < t
3 the length distribution is characterized by essentially 2 non-linear modes; the shorter cut-off length N1 is decreasing with time in this regime, while the length scale N2 of the second mode is increasing. (5) The terminal relaxation time of the polymer length distribution, t*, shows a sharp maximum in the vicinity of M*; the effective exponent
is as high as ∼ σ-1/3 just above M*. 相似文献
37.
Summary We discuss some recent theoretical studies of the kinetics of the collapse transition in homopolymers. An isolated polymer
is modelled using computer simulation, and a time-dependent mean-field theory. The mean-field theory is analysed analytically
for early stages, and for short polymers the equations are studied numerically. The results of simulation and theory are compared
yielding, we argue, a consistent physical picture. Quantitative comparisons are not yet given, but seem relatively promising.
Paper presented at the I International Conference on Scaling Concepts and Complex Fluids, Copanello, Italy, July 4– 1994. 相似文献
38.
John F. Nagle 《Journal of statistical physics》1985,38(3-4):531-540
It has been suggested that some lattice models of polymers, especially ones that incorporate more realistic excluded volume interactions extending to further neighbors, may be subject to gridlock. A model is defined to have the property of gridlock if it cannot melt at any temperature unless a density decrease is allowed. Classical theories of polymer melting are incompatible with the property of gridlock. This paper proves rigorously that a two-dimensional square-lattice model of polymer chains that have nearest-neighbor excluded volume interactions (called the X1S model) has the gridlock property. The proof uses elementary concepts from graph theory. Also, different interpretations of the X1S model are given in terms of real polymers. This leads to a discussion of a number of different classes of melting depending upon whether the intramolecular rotameric energies and the attractive intermolecular energies are antagonistic to or supportive of the melting transition. 相似文献
39.
Basu A Joanny JF Jülicher F Prost J 《The European physical journal. E, Soft matter》2008,27(2):149-160
We discuss general features of noise and fluctuations in active polar gels close to and away from equilibrium. We use the
single-component hydrodynamic theory of active polar gels built by Kruse and coworkers to describe the cytoskeleton in cells.
Close to equilibrium, we calculate the response function of the gel to external fields and introduce Langevin forces in the
constitutive equations with correlation functions respecting the fluctuation-dissipation theorem. We then discuss the breakage
of the fluctuation-dissipation theorem due to an external field such as the activity of the motors. Active gels away from
equilibrium are considered at the scaling level. As an example of application of the theory, we calculate the density correlation
function (the dynamic structure factor) of a compressible active polar gel and discuss possible instabilities. 相似文献
40.
Gravimetry experiments in a well-controlled environment have been performed to investigate aging for a glassy PMMA/toluene
film. The temperature is constant and the control parameter is the solvent vapor pressure above the film (i.e. the activity). Several experimental protocols have been used, starting from a high activity where the film is swollen and
rubbery and then aging the film at different activities below the glass transition. Desorption and resorption curves have
been compared for the different protocols, in particular in terms of the softening time, i.e. the time needed by the sample
to recover an equilibrium state at high activity. Non-trivial behaviors have been observed, especially at small activities
(deep quench). A model is proposed, extending the Leibler-Sekimoto approach to take into account the structural relaxation
in the glassy state, using the Tool formalism. This model well captures some of the observed phenomena, but fails in describing
the specific kinetics observed when aging is followed by a short but deep quench. 相似文献