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Material parameters defined by Equations (1.11) and (1.12) arise from anisotropy (i.e. direction dependency) of the microstructure of long-chain polymers subjected to liigh shear deformations. Generalized Newtonian constitutive equations cannot predict any normal stress acting along the direction perpendicular to the shearing surface in a viscometric flow. Thus the primary and secondary normal stress coefficients are only used in conjunction with viscoelastic constitutive models. [Pg.6]

Table 5.10 Behaviour of polymers subjected to high-energy radiation"... Table 5.10 Behaviour of polymers subjected to high-energy radiation"...
Figure 5.11 gives some comparative data for a selection of polymers subjected to tbe flaming condition mode. [Pg.109]

Thermoplastic polymers subjected to a continuous stress above the yield point experience the phenomenon of cold-drawing. At the yield point, the polymer forms a neck at a particular zone of the specimen. As the polymer is elongated further, so this neck region grows, as illustrated in Figure 7.7. [Pg.106]

Before fluorination, the dielectric constant ofpoly(bisbenzocyclobutene) was 2.8, and this value was reduced to 2.1 after plasma treatment. No data were reported in the paper on characterization of structure or properties, except for the dielectric constant of the modified poly(bisbenzocyclobutene). The authors did report that the thermal stability offluorinatedpoly(vinylidenefluoride) was inferior to the original poly(vinylidenefluoride) when treated in a similar way. One of the probable reasons for the low thermal stability is that the NF3 plasma degraded the polymer. According to their results, the thickness of fluorinated poly(bisbenzo-cyclobutene) was reduced by 30%. The same phenomenon was observed for other hydrocarbon polymers subjected to the NF3 plasma process. A remaining question is whether plasma treatment can modify more than a thin surface layer of the cured polymer Additionally, one of the side products generated was hydrogen fluoride, which is a serious drawback to this approach. [Pg.293]

P.R.277 is FDA compliant under 21 CFR Part 176.170C(c) at 2% by weight of the polymer subject to the provisions and definitions described in Title 21 CFR Part 178.3297. By virtue of this compliance, P.R.277 finds its way into many foodpackaging applications. In molding, P.R.277 has desirable low-warpage characteristics. [Pg.581]

For low radiation doses, peroxides accumulate almost linearly with dose. However, after a certain dose has been reached, their concentration tends to level off. This conclusion can be derived from the observed change in the rate of graft copolymerization initiated by polymers subjected to increasing doses of preirradiation in air. Figure 2 illustrates this effect in the case of grafting acrylonitrile onto polyethylene (2). The drop in the yield of peroxide production presumably results from the efficient radiation-induced decomposition of these peroxides. Peroxides are known to decompose under free radical attack, and selective destruction of peroxides under irradiation has been established experimentally (8). This decomposition can become autocatalytic, and sometimes the concentration of peroxides may reach a maximum at a certain dose and decrease on further irradiation. Such an effect was observed in the case of poly (vinyl chloride). Figure 3 shows the influence of preirradiation dose on the grafting ratio obtained with poly (vinyl chlo-... [Pg.39]

Fig. 4.25 Experimentally measured SANS patterns for an FCC micellar phase in a dPS-PI diblock (A/ = 55kgmor, 60wt% PS) in core contrast-matched decane/ d-decane mixtures (15wt% polymer) subject to steady shear in a Couette cell at different shear rates (McConnell et al. 1995) (a) y — 0.01 s aligned by inserting the stator (b) y=0.06s 1 (c) y = 0.66s 1 (d) y = 6.60s (e) y = 66.0 s (f) y = 200.0s-1. The wavevectors qv (horizontal) and qe (vertical) for these patterns range from —0.028 to 0.028 A. ... Fig. 4.25 Experimentally measured SANS patterns for an FCC micellar phase in a dPS-PI diblock (A/ = 55kgmor, 60wt% PS) in core contrast-matched decane/ d-decane mixtures (15wt% polymer) subject to steady shear in a Couette cell at different shear rates (McConnell et al. 1995) (a) y — 0.01 s aligned by inserting the stator (b) y=0.06s 1 (c) y = 0.66s 1 (d) y = 6.60s (e) y = 66.0 s (f) y = 200.0s-1. The wavevectors qv (horizontal) and qe (vertical) for these patterns range from —0.028 to 0.028 A. ...
The last two equations identify 0A(r) and average densities of A and B monomers at r, as calculated in an ensemble of non-interacting polymers subject to the fields wA(r) and WofV), which act on A and B monomers, respectively. Once the partition function of this problem is known, eqns A.7-A.11 can be solved and the free energy obtained. [Pg.414]

Horhold found that the action spectrum of phenyl-substituted polyarylene-vinylenes shifts substantially to longer wavelengths when the photoconductor probe is simultaneously irradiated by UV light from another source31. The action spectrum of photoconductivity of the polymer subjected to UV radiation is the same as the action spectrum of photoconductivity of the cation radical of the same polymer... [Pg.18]

Pruitt L, Hermann R, Suresh S (1992) Fatigue crack growth in polymers subjected to fully compressive cyclic loads. J Mater Sci 27(6) 1608-1616... [Pg.151]

The two modeling elements, spring and dash pot, are combined in various ways to demonstrate the deformation of a polymer subjected to the application of stress as shown in Fig. 14.19. [Pg.558]

It has already been mentioned above, however, that we should distinguish between the true anisotropy and induced, unstable, anisotropy especially for superconcen-trated solutions and a solid polymer subjected to mechanical effects. [Pg.89]

A very frequently described family of polymers subjected to simple coacervation are cellulose derivatives, particularly ethyl cellulose (EC). ° While most cellulose ethers are soluble in water, EC and the cellulose esters are insoluble or only partly soluble in water, e.g., as a function of pH. For coacervation of EC, toluene is a preferred good solvent and cyclohexane a poor solvent. Gradual addition of cyclohexane to a solution of EC desolvates the polymer. Alternatively, EC can be dissolved in hot cyclohexane cooling to room temperature induces polymer phase separation. In both these cases, the coacervate film or droplets can be hardened by exposing the coacervate to a large volume of cyclohexane, whereby physical cross-links are formed. [Pg.604]

Since the parameters utilized in the development of the relationship between Tg and M by Fox and Loshaek are somewhat inconvenient to apply to the polyphosphate system, this relationship will be rederived here to make its application somewhat more convenient for polymers subject to random reorganization at elevated temperatures, for which data are usually given in terms of the concentration of ends, middles, branches, etc. (67). Since it is very convenient to determine the specific volume of the pol3q)hosphates at room temperature, and since the... [Pg.67]

IV. Viscoelasticity of Ionic Polymers Subject to Bond Interchange (2i, 22)... [Pg.94]

It is advisable to review very briefly the preceeding work done on the viscoelastic properties of polymers subject to multiple relaxation mechanisms, as well as previous solution studies of phosphates in the presence of lanthanum on the basis of these studies La" was chosen as the ion most likely to lead to bond interchange. [Pg.95]

Primary bonds in high MW polymers subjected to high-shear or extensional flows, such as in pumps, contraction or expansion flows, break up and the degradation is permanent. The microstructures of surfactant solutions also break up under strong shear, but they self-assemble soon after the shear is released recovering their microstructures. ... [Pg.773]

Gusev, A.A. and Suter, U.W. Dynamics of small molecules in polymers subject to thermal motion, /. Chem. Phys., 99, 2228, 1993. [Pg.163]


See other pages where Polymers Subjects is mentioned: [Pg.483]    [Pg.488]    [Pg.515]    [Pg.235]    [Pg.235]    [Pg.264]    [Pg.580]    [Pg.581]    [Pg.582]    [Pg.35]    [Pg.85]    [Pg.109]    [Pg.7]    [Pg.696]    [Pg.65]    [Pg.58]    [Pg.170]    [Pg.446]    [Pg.471]    [Pg.69]    [Pg.602]    [Pg.169]    [Pg.605]    [Pg.1235]    [Pg.121]    [Pg.652]   
See also in sourсe #XX -- [ Pg.301 ]




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Block, polymer synthesis 296 Subject

CROSS-LINKED POLYMERS Subject

Carbon nanotube -polymers Subject

Cumulative Subject polymers

Heterocyclic polymers Subject

Ionic Polymers Subject to Bond Interchange

PYRROLE POLYMER Subject

Polymer network systems Subject

Polymer phase Subject

Polymer resin Subject

Polymer systems 226 Subject

Polymer-drug conjugates Subject

Polymer-surfactant Subject

Polymers Related Subjects)

Polymers Specific Subjects)

SYNTHETIC POLYMERS , l. Brief introduction to subject

Subject backbone polymers

Subject bending type polymer

Subject blend polymer coating

Subject cationic polymers

Subject hydrocarbon polymers

Subject inorganic-organic polymers

Subject nanocomposite polymer

Subject natural polymers

Subject polymer alloy

Subject polymer blends

Subject polymer chains

Subject polymer conductivity

Subject polymer content

Subject polymer films

Subject polymer matrix

Subject polymer matrix surface

Subject polymer mixture

Subject polymer-analogous

Subject polymer-analogous reactions

Subject polymer-controlled

Subject polymers, flow characteristics

Subject rubber/polymer materials

Subject rubbery polymers

Subject synthetic polymers

Subject wrapping with polymers

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