Polyethylene defined

Fig. 4. Structure of orthorhombic polyethylene unit cell projected on the ab plane. The right-hand pictures define the setting angle .

The way in which these factors operate to produce Type III isotherms is best appreciated by reference to actual examples. Perhaps the most straightforward case is given by organic high polymers (e.g. polytetra-fluoroethylene, polyethylene, polymethylmethacrylate or polyacrylonitrile) which give rise to well defined Type III isotherms with water or with alkanes, in consequence of the weak dispersion interactions (Fig. S.2). In some cases the isotherms have been measured at several temperatures so that (f could be calculated in Fig. 5.2(c) the value is initially somewhat below the molar enthalpy of condensation and rises to qi as adsorption proceeds. In Fig. 5.2(d) the higher initial values of q" are ascribed to surface heterogeneity. 

Figure 2.5 shows some actual experimental data for versus 7, measured on a sample of polyethylene at 126°C. Note that the data are plotted on log-log coordinates. In spite of the different coordinates. Fig. 2.5 is clearly an example of pseudoplastic behavior as defined in Fig. 2.2. In this and the next several sections, we discuss shear-dependent viscosity. In this section the approach is strictly empirical, and its main application is in correcting viscosities measured...

Olefin fibers, also called polyolefin fibers, are defined as manufactured fibers in which the fiber-forming substance is a synthetic polymer of at least 85 wt % ethylene, propjiene, or other olefin units (1). Several olefin polymers are capable of forming fibers, but only polypropylene [9003-07-0] (PP) and, to a much lesser extent, polyethylene [9002-88-4] (PE) are of practical importance. Olefin polymers are hydrophobic and resistant to most solvents. These properties impart resistance to staining, but cause the polymers to be essentially undyeable in an unmodified form. 

High density polyethylene (HDPE) is defined by ASTM D1248-84 as a product of ethylene polymerisation with a density of 0.940 g/cm or higher. This range includes both homopolymers of ethylene and its copolymers with small amounts of a-olefins. The first commercial processes for HDPE manufacture were developed in the early 1950s and utilised a variety of transition-metal polymerisation catalysts based on molybdenum (1), chromium (2,3), and titanium (4). Commercial production of HDPE was started in 1956 in the United States by Phillips Petroleum Company and in Europe by Hoechst (5). HDPE is one of the largest volume commodity plastics produced in the world, with a worldwide capacity in 1994 of over 14 x 10 t/yr and a 32% share of the total polyethylene production. 

E] Ammonia absorption into water from air at 70 F. Gas-film resistance controls. Thin-waUed polyethylene Raschig rings and 1-inch Intalox saddles. Fit 25%. See Reiss for fit. Terms defined as above. 

Materials respond to stress by straining. Under a given stress, a stiff material (like steel) strains only slightly a floppy or compliant material (like polyethylene) strains much more. The modulus of the material describes this property, but before we can measure it, or even define it, we must define strain properly. 

For most practical purposes a polymer may be defined as a large molecule built up by repetition of small, simple chemical units. In the case of most of the existing thermoplastics there is in fact only one species of unit involved. For example the polyethylene molecule consists essentially of a long chain of repeating —(CH2)—(methylene) groups, viz. 

Although polyethylene is virtually defined by its very name as a polymer of ethylene produced by addition polymerisation, linear polymers with the formula (CH2), have also been prepared by condensation reactions. For example in 1898 von Pechmann produced a white substance from an ethereal solution of... 

In this review the definition of orientation and orientation functions or orientation averages will be considered in detail. This will be followed by a comprehensive account of the information which can be obtained by three spectroscopic techniques, infra-red and Raman spectroscopy and broad line nuclear magnetic resonance. The use of polarized fluorescence will not be discussed here, but is the subject of a contemporary review article by the author and J. H. Nobbs 1. The present review will be completed by consideration of the information which has been obtained on the development of molecular orientation in polyethylene terephthalate and poly(tetramethylene terephthalate) where there are also clearly defined changes in the conformation of the molecule. In this paper, particular attention will be given to the characterization of biaxially oriented films. Previous reviews of this subject have been given by the author and his colleagues, but have been concerned with discussion of results for uniaxially oriented systems only2,3). 

When X = Y, as in polyethylene, poly-(tetrafluoroethylene), polyisobutylene, and poly -(vinylidene chloride), the polymers are highly crystalline products with sharply definable melting points (except for polyisobutylene, which crystallizes readily on stretching but with difficulty on cooling). Oriented specimens of high strength may be obtained, exactly as in the crystalline condensation polymers. 

This system consists of an in situ polyethylene tank, an application system, and a bottom water recovery system.65 An underlying, permeable, water-bearing zone facilitates the creation of ingradient water flow conditions. The tank defines the treatment area, minimizes the potential for release of bacterial cultures to the aquifer, and maintains contaminant concentration levels that facilitate treatment. The ingradient conditions facilitate reverse leaching or soil washing and minimize the potential for outmigration of contaminants. 

The mechanisms described above tell us how heat travels in systems, but we are also interested in its rate of transfer. The most common way to describe the heat transfer rate is through the use of thermal conductivity coefficients, which define how quickly heat will travel per unit length (or area for convection processes). Every material has a characteristic thermal conductivity coefficient. Metals have high thermal conductivities, while polymers generally exhibit low thermal conductivities. One interesting application of thermal conductivity is the utilization of calcium carbonate in blown film processing. Calcium carbonate is added to a polyethylene resin to increase the heat transfer rate from the melt to the air surrounding the bubble. Without the calcium carbonate, the resin cools much more slowly and production rates are decreased. 

In the molten state polymers are viscoelastic that is they exhibit properties that are a combination of viscous and elastic components. The viscoelastic properties of molten polymers are non-Newtonian, i.e., their measured properties change as a function of the rate at which they are probed. (We discussed the non-Newtonian behavior of molten polymers in Chapter 6.) Thus, if we wait long enough, a lump of molten polyethylene will spread out under its own weight, i.e., it behaves as a viscous liquid under conditions of slow flow. However, if we take the same lump of molten polymer and throw it against a solid surface it will bounce, i.e., it behaves as an elastic solid under conditions of high speed deformation. As a molten polymer cools, the thermal agitation of its molecules decreases, which reduces its free volume. The net result is an increase in its viscosity, while the elastic component of its behavior becomes more prominent. At some temperature it ceases to behave primarily as a viscous liquid and takes on the properties of a rubbery amorphous solid. There is no well defined demarcation between a polymer in its molten and rubbery amorphous states. 

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... 

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