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Hodges CS Looi L Cleaver JA Ghadiri M 《Langmuir : the ACS journal of surfaces and colloids》2004,20(22):9571-9576
A simple method for using the JKR model to determine interfacial adhesion between two ideal rough surfaces is demonstrated for individual asperity-asperity and asperity-flat contacts both in air and in water. The model takes into account the effect of a modified contact area at separation due to viscoelastic effects. The equilibrium version of the model significantly underestimates the measured adhesion, whereas the viscoelastic version of the model is much closer to the measured data. The asperity-flat geometry used with the viscoelastic version of the model seems to fit the experimental results best. This was thought to be due to the unlikely occurrence of direct asperity-asperity contacts. Instead, it would seem that the asperities have a far higher chance of fitting between each other on opposing surfaces, leading to correspondingly higher pull-off forces measured on separation. Many possible extensions to the roughness model described here may be made, allowing a much-improved understanding of the contact mechanics between two rough surfaces. 相似文献
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Scott W. Sides Gary S. Grest Mark J. Stevens Steven J. Plimpton 《Journal of Polymer Science.Polymer Physics》2004,42(2):199-208
The adhesion between a glassy polymer melt and substrate is studied in the presence of end‐grafted chains chemically attached to the substrate surface. Extensive molecular dynamics simulations have been carried out to study the effect of the areal density ∑ of tethered chains and tensile pull velocity v on the adhesive failure mechanisms. The initial configurations are generated using a double‐bridging algorithm in which new bonds are formed across a pair of monomers equidistant from their respective free ends. This generates new chain configurations that are substantially different than the original two chains such that the systems can be equilibrated in a reasonable amount of cpu time. At the slowest tensile pull velocity studied, a crossover from chain scission to crazing is observed as the coverage increases, while for very large pull velocity, only chain scission is observed. As the coverage increases, the sections of the tethered chains pulled out from the interface form the fibrils of a craze that are strong enough to suppress chain scission, resulting in cohesive rather than adhesive failure. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 199–208, 2004 相似文献
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S. Perutz E. J. Kramer J. Baney C.-Y. Hui C. Cohen 《Journal of Polymer Science.Polymer Physics》1998,36(12):2129-2139
The JKR technique was used to determine the source and nature of the adhesion hysteresis present in modified poly(dimethylsiloxane) (PDMS) networks. As controlled excess amounts of the tetrafunctional crosslinker were added to the networks, the adhesion hysteresis increased. It was found that by poisoning the catalyst with a thiol the hysteresis could be significantly lowered, and completely removed in some cases. We believe that the adhesion hysteresis in this system stems from a complexation between the excess crosslinker and the catalyst. We found that the work of adhesion in this case is a function of the unloading rate. The unloading rate dependence of this chemical adhesion hysteresis was attributed to the rate of bond dissociation. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2129–2139, 1998 相似文献
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Glassy polymers are considered as inhomogeneous with regions in which the gas sorption follows Henry's law and others where it follows Langmuir's law. It is assumed that the linear dimensions of these regions are small compared with the macroscopic length of interest but large compared with the mean free path of the penetrant gas molecules. Applying an homogenization method it is shown that the average flux is directly proportional to the concentration gradient in the polymer. This relationship can be expressed in terms of an effective diffusion coefficient Deff, which depends on the details of the microstructure. Deff is evaluated in the framework of the effective medium theory and compared with experimental data for diffusion of five vapors in ethylcellulose. 相似文献
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Choi J Cho SB Lee BS Joung YK Park K Han DK 《Langmuir : the ACS journal of surfaces and colloids》2011,27(23):14232-14239
A method of securing the adhesion of biodegradable polymer coating was investigated for drug-eluting metal stents, using surface-initiated ring-opening polymerization (SI-ROP) of L-lactide. Introduction of oligolactide on the stainless steel (SS) surface was successful and the thickness of the oligolactide grafts remained on the nanometer scale, as determined by ellipsometry. The presence of an oligolactide graft was also identified using attenuated total reflection-Fourier transform infrared (ATR-FTIR) and electron spectroscopy for chemical analysis (ESCA). On top of the grafts, poly(D,L-lactide-co-glycolide) (PLGA) coating was carried out on different substrates such as SS control, plasma-treated SS, and lactide-grafted (referred to as a nanocoupled) SS using electrospraying. When the adhesion forces were measured with a scratch tester, the nanocoupled SS showed the strongest interfacial adhesion between polymer coating layer and metal substrate. The outcome of the peel-off test was also consistent with the result of the scratch test. When degradation behavior of the polymer coating in vitro was examined for up to 4 weeks in a continuous fluid flow, the SEM images demonstrated that polymer degradation was obvious due to hydration and swelling of the polymer matrix. Although the matrix completely disappeared after 4 weeks for SS control and plasma-treated substrates, the nanocoupled SS was persistent with some polymer matrix. In addition, the release profiles of SRL-loaded PLGA coating appeared slightly different between control and nanocoupled groups. This work suggested that the concept of nanocoupling remarkably improved the interfacial adhesion stability between metal surface and polymer layer and controlled drug release, and showed the feasibility of drug-eluting stents. 相似文献
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Literature data on structural rearrangements taking place in amorphous glassy polymers upon their plastic deformation are analyzed. This deformation is shown to be primarily accompanied by polymer self-dispersion into fibrillar aggregates composed of oriented macromolecules with a diameter of 1—10 nm. The above structural rearrangements proceed independently of the deformation mode of polymers (cold drawing, crazing, or shear banding of polymers under the conditions of uniaxial drawing or uniaxial compression). Principal characteristics of the formed fibrils and the conditions providing their development are considered. Information on the properties of the fibrillated glassy polymers is presented, and the pathways of their possible practical application are highlighted. 相似文献
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T. S. Chow 《Journal of Polymer Science.Polymer Physics》1987,25(1):137-148
This paper reports the theoretical prediction and experimental verification of the connection between the yield stress of amorphous polymers and the physical aging phenomenon. The analysis reveals the existence of a fundamental relationship between the nonequilibrium glassy state and the thermally activated process controlling viscoelastic and plastic deformation. The results show that the volume relaxation and deformation kinetics share the same relaxation times, and that the activation energy for deformation below Tg is much smaller than previously mentioned in the literature. This indicates that the phenomenon of physical aging plays a very important role in the deformation and processing of polymers at low temperatures. The effect of quenching and annealing on the yield stress is described in terms of the mean energy of hole formation, the departure of volume from its equilibrium state, the distribution of hole energies, and lattice volume. The same set of molecular parameters obtained from the molecular kinetic theory of the glass transition and volume relaxation predicts the yield stress as a function of cooling rate, annealing time, temperature, and strain rate. 相似文献
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Interfacial tensions γ were measured for mixtures of poly(methylphenylsiloxane) (4 kg/mol) and poly(dimethylsiloxane) (24 kg/mol) in the absence and in the presence of small amounts of the random copolymer poly(dimethylsiloxane-ran-methylphenylsiloxane) (89 mol-% of dimethylsiloxane units, 28 kg/mol) from 25 to 110°C. Approximately 1 wt.-% of the copolymer additive suffices to reduce γ from ca. 2.2 to 1.6 mN/m. The time dependence of the apparent γ value in the course of the attainment of equilibria also indicates surface acivity. The hypothesis is formulated that the efficiency of the random copolymer for a reduction of γ is bound to the condition that it is only sparingly soluble in both blend components. 相似文献
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Bilayer film Fourier transform infrared (FTIR) model experiments are designed to provide a well-defined interface for study which can be probed by infrared spectroscopy during the interdiffusion and reaction of two reactive polymers. This provides a model experiment to determine the kinetics and extent of reaction between functionalized polymers during reactive polymer blending. This type of experiment provides data on the reaction at a stagnant interface which is necessary for the analysis of the interface while it is simultaneously undergoing deformation. It is also useful as a screening or preliminary experiment on reactive blending systems in that the extent of reaction may be followed for different systems at different temperatures. Experiments reported here trace the reaction of a styrene–maleic anhydride copolymer with two different amine terminated polymers. Results are obtained for the interdiffusion and reaction of a styrene-maleic anhydride copolymer with two amine terminated polymers: a butadiene-acrylonitrile copolymer and Nylon 11. The kinetics from these experiments include contributions due to both interdiffusion and chemical reaction. The chemical reaction kinetics may be isolated from the diffusion kinetics by performing experiments on well-mixed systems which are prepared by casting films of the polymer mixtures from a mutual solvent. © 1994 John Wiley & Sons, Inc. 相似文献
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Yuri M. Boiko 《Colloid and polymer science》2011,289(17-18):1847-1854
Mechanical properties developing at the contact zone of two samples of linear amorphous polymers with vitrified bulk have been employed to analyze the process of segmental diffusion of reptating chains across polymer?Cpolymer interfaces. The diffusion coefficients (D) of this process have been estimated for polymers with different chain architecture and investigated with respect to healing temperature (T). It has been shown that logD????1/T at $ T < T_{\text{g}}^{\text{bulk}} $ ( $ T_{\text{g}}^{\text{bulk}} $ is the glass transition temperature of the polymer bulk), which implies that the process of segmental diffusion under healing conditions investigated is a thermally activated Arrhenius-like process describing as D?=?D 0 exp[?E a/(RT)], where D 0 and E a are the activation energy and the pre-exponential factor, respectively. It has been found that logD 0????E a, which points to the validity of the so-called kinetic compensation effect for the interdiffusion process at the contact zones of polymers with glassy bulk when an increase in E a is ??compensated?? by the corresponding increase in D 0. 相似文献
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A. P. Safronov A. S. Istomina T. V. Terziyan Yu. I. Polyakova I. V. Beketov 《Polymer Science Series A》2012,54(3):214-223
For composites based on polystyrene, the styrene-butadiene copolymer, and polybutadiene filled with various kinds of zinc
oxide powder, the enthalpy of mixing is calculated in the entire range of filler contents on the basis of calorimetric measurements
with the use of the thermochemical cycle. It is shown that, when the polymer is in excess in the composites based on polystyrene
and its copolymer, the enthalpy of mixing is negative, whereas at a high content of the filler, this value is positive. The
alternating-sign pattern of the concentration dependence of the enthalpy of mixing is interpreted in terms of the superposition
of the negative contribution of the enthalpy of the interfacial-adhesion interaction of a polymer matrix with the filler and
the positive contribution due to a gain in the level of nonequilibrium of the glassy matrix near the surface. A thermodynamic
model that makes it possible to separate these contributions and to describe the experimental curves of the enthalpy of mixing
for the composites is advanced. 相似文献
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C. Bauwens-Crowet J. C. Bauwens G. Homs 《Journal of Polymer Science.Polymer Physics》1969,7(4):735-742
It is shown that, at the yield stress, glassy polymers exhibit viscous flow which is in agreement with the generalized theory of Eyring. The study of the yield stress over a wide range of temperatures and strain rates provides evidence on the secondary transitions found by other methods. From our measurements we conclude that every secondary transition corresponds to the liberation of one of the degrees of freedom of a segment of the main chain. 相似文献
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A mathematical model is formulated for solvent dissolution of rubbery and glassy polymers. An exact solution to the problem is derived for the constant diffusivity case, and a weighted residual solution is developed for the case of a concentration-dependent diffusion coefficient. The solution is used to calculate concentration profiles, dissolution curves, dissolution half-times, and pseudointerface positions at various times. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2607–2614, 1998 相似文献
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Kei-Ichi Akabori Daisuke Baba Kazuhiro Koguchi Keiji Tanaka Toshihiko Nagamura 《Journal of polymer science. Part A, Polymer chemistry》2006,44(24):3598-3604
Polystyrene (PS) bilayers were prepared and were adhered at a temperature between the surface and bulk glass-transition temperatures for a given time. Then, the interfacial adhesion strength (GL) was examined with a conventional lap-shear measurement. GL first increased with increasing adhesion time and then reached a constant value. This result implied that the segments moved across the interface, to a certain depth, even at a temperature below the bulk glass-transition temperature. To confirm this, the interfacial evolution for the PS/deuterated PS bilayers was examined with dynamic secondary-ion mass spectrometry. The GL value was linearly proportional to the thickness of the interfacial adhesion layer. Finally, we propose a strategy for regulating the adhesion strength based on the chain-end chemistry. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3598–3604, 2006 相似文献
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M. Kitagawa 《Journal of Polymer Science.Polymer Physics》1977,15(9):1601-1611
The published data on the yielding of glassy polymers under a variety of testing conditions reveal that the yield stress increases with the elastic modulus. However, fundamental understanding of the interrelation has not yet been established. In this paper, a power law relation between the shear yield stress τy and the shear modulus G is presented: T0τy/Tτy0 = (T0G/TG0)n, where T is the absolute temperature, T0. is reference temperature, and τy0 and G0 are, respectively, the shear yield stress and the shear modules at T0. The exponent n takes a value 1.63 for amorphous polymers without exception, whereas it is about 0.8–0.9 for crystalline polymers. The exponent 1.63 for amorphous polymers is in good agreement with the value derived from the approximation of the Bowden–Raha dislocation analog. This law may enable us to investigate a model for the yielding of glassy polymers. 相似文献
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[reaction: see text] A new method is presented for the measurement of enantiomeric excess (ee) utilizing molecularly imprinted polymers (MIPs). The method is demonstrated to be accurate and rapid, as the ee values can be calculated from straightforward concentration measurements. The MIP-based assay can also be adapted to measure the ee of samples of differing initial concentrations. 相似文献