Stretched polymer

Q are the absorbance and wavenumber, respectively, at the peak (center) of the band, p is the wavenumber, and y is the half width of the band at half height. Liquid band positions ate usually shifted slightly downward from vapor positions. Both band positions and widths of solute spectra are affected by solute—solvent interactions. Spectra of soHd-phase samples are similar to those of Hquids, but intermolecular interactions in soHds can be nonisotropic. In spectra of crystalline samples, vibrational bands tend to be sharper and may spHt in two, and new bands may also appear. If polarized infrared radiation is used, both crystalline samples and stressed amorphous samples (such as a stretched polymer film) show directional effects (28,29). 

The photoelectron spectra of pyridazine have been interpreted on the basis of many-body Green s function calculations both for the outer and the inner valence region. The calculations confirm that ionization of the first n-electron occurs at lower energy than of the first TT-electron (79MI21201). A large number of bands in the photoelectron spectrum of 3,6-diphenylpyridazine in stretched polymer sheets have been assigned to transitions predicted... 

Stretched Polymers MF membranes rnav be made bv stretching... 

When —CO—CH=CH—COOH groups bonded to the aromatic ring of PS, the physico-mechanic, thermal, and adhesion properties increased from 4.5 mol% to 20.0 mol%. This caused the following changes the resistance of PS increased from 14.0 to 19.2 kJ/m, the resistance to stretch polymer material itself increased from 35.0 to... 

Stretched Polymers MF membranes may be made by stretching (Fig. 20-68). Semicrystalline polymers, if stretched perpendicular to the axis of crystallite orientation, may fracture in such a way as to make reproducible microchannels. Best known are Goretex produced from Teflon , and Celgard produced from polyolefin. Stretched polymers have unusually large fractions of open space, giving them very high fluxes in the microfiltration of gases, for example. Most such materials are very hydrophobic. 

Voids within a sample are a major cause of internal haze. We see the effect of voiding when we stretch polymers, such as high density polyethylene and isotactic polypropylene, that have distinct yield points and clearly defined necks (as discussed earlier in this chapter). The... 

The parameters K1/ K2/ and K3 are defined by the refractive indices of the crystal and sample and by the incidence angle [32]. If the sample has uniaxial symmetry, only two polarized spectra are necessary to characterize the orientation. If the optical axis is along the plane of the sample, such as for stretched polymer films, only the two s-polarized spectra are needed to determine kz and kx. These are then used to calculate a dichroic ratio or a P2) value with Equation (25) (replacing absorbance with absorption index). In contrast, a uniaxial sample with its optical axis perpendicular to the crystal surface requires the acquisition of spectra with both p- and s-polarizations, but the Z- and X-axes are now equivalent. This approach was used, through dichroic ratio measurements, to monitor the orientation of polymer chains at various depths during the drying of latex [33]. This type of symmetry is often encountered in non-polymeric samples, for instance, in ultrathin films of lipids or self-assembled monolayers. 

EW Thulstrup and J Michl, A critical comparison of methods for analysis of linear dichroism of solutes in stretched polymers, J. Phys. Chem., 84 82-93, 1980. 

The base resin contains a styrene-divinylbenzene polymer, DVB. If styrene alone were used, the long chains it formed would disperse in organic solvents. The divinylbenzene provides cross-linking between the chains. When the cross-linked structure is immersed in an organic solvent, dispersion takes place only to the point at which the osmotic force of solvation is balanced by the restraining force of the stretched polymer structure. 

The fiberlike crystalline structures (shish) are highly stable to the point that they can be superheated [31]. Therefore, it is believed that the core of the shish is formed by crystallization of completely stretched polymer chains. The kebabs are believed to be folded-chain lamellar structures. The direction of growth of the kebabs is normal to the shish. The chain ahgnment in the kebabs is believed to be parallel to the shish. Similar structures are obtained by crystalhzation in polymer melt films exposed to orientational deformation [32,33]. These two-dimensional shish-kebabs also consist of a central fiber, shish, and periodically attached linear kebabs, with growth direction normal to the shish. 

Calculate the values of d for all observed equatorial reflections for the bulk polymer and the stretched polymer sample (Notes 2 and 3). 

A good elastomer should not undergo plastic flow in either the stretched or relaxed state, and when stretched should have a memory of its relaxed state. These conditions are best achieved with natural rubber (ds-poIy-2-methyl-1,3-butadiene, ds-polyisoprene Section 13-4) by curing (vulcanizing) with sulfur. Natural rubber is tacky and undergoes plastic flow rather readily, but when it is heated with 1-8% by weight of elemental sulfur in the presence of an accelerator, sulfur cross-links are introduced between the chains. These cross-links reduce plastic flow and provide a reference framework for the stretched polymer to return to when it is allowed to relax. Too much sulfur completely destroys the elastic properties and produces hard rubber of the kind used in cases for storage batteries. 

For a more comprehensive list, see reference 1. b Feirocenyl polymer (3.63), where OR = OCH2CF3. c Varies with ratio of side groups. d Complex melting phenomena. e For the stretched polymer. 

J. F. Tassin and L. Monnerie, A fluorescence polarization study of matrix molecular weight on the relaxation of a labeled molecule in a stretched polymer melt, J. Polym. Sci. Polym. Phys. Ed., 21,1981 (1983). 

A neutral collapsed polymer chain can be considered in a first approximation as a liquid drop which undergoes the Rayleigh instability when it becomes charged [64, 66]. The various daughter drops are however linked into a chain and the daughter drops cannot separate from each other. They remain linked by stretched polymer strands. The picture that is obtained for a polymer chain in a poor solvent is thus that of a necklace of collapsed globules, the pearls, connected by the strands that are stretched by the electrostatic interactions between the pearls. 

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