Polymer materials for

C. P. Wong, Improved Eoom-Temperature Wulconicyed Silicone Elastomers as Integrated Circuit Encapsulants, Polymer Materials for Electronics Applications, American Chemical Society Symposium Series, Washington, D.C., Nos. 184, 171, 1982. 

Fig. 7 gives an example of such a comparison between a number of different polymer simulations and an experiment. The data contain a variety of Monte Carlo simulations employing different models, molecular dynamics simulations, as well as experimental results for polyethylene. Within the error bars this universal analysis of the diffusion constant is independent of the chemical species, be they simple computer models or real chemical materials. Thus, on this level, the simplified models are the most suitable models for investigating polymer materials. (For polymers with side branches or more complicated monomers, the situation is not that clear cut.) It also shows that the so-called entanglement length or entanglement molecular mass Mg is the universal scaling variable which allows one to compare different polymeric melts in order to interpret their viscoelastic behavior. 

When estimating the remaining service life of a polymer material for a particular application, the limiting value should be established of some material property such as tensile strength, elongation at break, electrical conductivity, permeability to low molar mass compounds, the average polymerization degree, etc., at which the polymer does not fail. 

Approaches to make a polymeric membrane selective to C02 attempt to enhance the solubility selectivity of the polymer material for C02 and reduce the diffusivity selectivity of the polymer that favors smaller hydrogen molecule. The permeability of a polymer membrane for species A, PA, is often expressed as (Ghosal and Freeman, 1994)... 

Reichmanis,E. Wilkens,C.W. In Polymer Materials for Electronic Applications American Chemical Society Symposium Series Washington, DC, 1983 Vol.184, p.30. 

Roziere, J. and Jones, D. 2003. Nonfluorinated polymer materials for proton exchange membrane fuel cells. Annual Review of Materials Research 33 503-555. 

The Maxwell model can also guide the selection of a proper polymer material for a selected zeolite at a given volume fraction for a target separation. For most cases, however, the Maxwell model cannot be applied to guide the selection of polymer or zeolite materials for making new mixed-matrix membranes due to the lack of permeabihty and selectivity information for most of the pure zeolite materials. In addition, although this Maxwell model is well-understood and accepted as a simple and effective tool for estimating mixed-matrix membrane properties, sometimes it needs to be modified to estimate the properties of some non-ideal mixed-matrix membranes. 

Fisher, M. and C. Cumming. Utilization of novel fluorescent polymer materials for trace level vapor-phase detection of nitroaromatic explosives, in Proceedings of the... 

In Polymer Materials for Electt onic Applications Feit, E., et al. ... 

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