Specific Polymers

Coextrusion. An increasingly popular technique to produce tailored film or sheet products is to coextmde one or more polymer types in two or more layers of melt (6). In this fashion the benefits of specific polymer types or formulations may be combined. Thus high cost barrier resins may be combined with a low cost thicker layer of standard resin to achieve an optimum barrier film at lower cost. Thin sUp-control layers may be used on the surface of a bulk layer of opticaUy clear resin to obtain an aesthetic film with good handleabUity. Lower melting outer layers may be used to provide heat sealing for polymers that seal with difficulty by themselves. 

Noncrystalline aromatic polycarbonates (qv) and polyesters (polyarylates) and alloys of polycarbonate with other thermoplastics are considered elsewhere, as are aHphatic polyesters derived from natural or biological sources such as poly(3-hydroxybutyrate), poly(glycoHde), or poly(lactide) these, too, are separately covered (see Polymers, environmentally degradable Sutures). Thermoplastic elastomers derived from poly(ester—ether) block copolymers such as PBT/PTMEG-T [82662-36-0] and known by commercial names such as Hytrel and Riteflex are included here in the section on poly(butylene terephthalate). Specific polymers are dealt with largely in order of volume, which puts PET first by virtue of its enormous market volume in bottie resin. 

If deposits are minimized, the areas where caustic can be concentrated is reduced. To minimize the iron deposition in 6.895-12.07 x 10 Pa boilers, specific polymers have been designed to disperse the iron and keep it in the bulk water. As with phosphate precipitation and chelant control programs, the use of these polymers with coordinated phosphate—pH treatment improves deposit control. 

From a knowledge of various values of P it is possible to calculate F values for specific polymers and G values for specific gases if the G value for one of the gases, usually nitrogen, is taken as unity. These values are generally found to be accurate within a factor of 2 for gases but urtreliable with water vapour. Some... 

As has been mentioned in earlier chapters polymers vary enormously in their thermal stability. Before attempting to process any specific polymer compound its thermal stability characteristics should be considered. The most important questions to be answered are ... 

Although the properties of specific polymer/wall systems are no longer accessible, the various phase transitions of polymers in confined geometries can be treated (Fig. 1). For semi-infinite systems two distinct phase transitions occur for volume fraction 0 = 0 and chain length N oo, namely collapse in the bulk (at the theta-temperature 6 [26,27]) and adsorp-... 

Specific polymers discussed in this chapter and the type of column used for their characterization are summarized in Table 20.1. The polymers are categorized as nonionic, anionic, or cationic. The nomenclature (acronyms) used for the different polymer types are also listed in Table 20.1. 

The science and technology of conducting polymers are inherently interdisciplinary they fall at the intersection of three established disciplines chemistry, physics and engineering hence the name for this volume. These macromolccular materials are synthesized by the methods of organic chemistry. Their electronic structure and electronic properties fall within the domain of condensed matter physics. Efficient processing of conjugated polymer materials into useful forms and the fabrication of electronic and opto-electronic devices require input from engineering i. e. materials science (more specifically, polymer science) and device physics. 

The advances in polymer blending and alloying technology have occurred through three routes (1) similar-rheology polymer pairs, (2) miscible polymers such as polyphenylene oxide and polystyrene, or (3) interpenetrating polymer networks (IPNs). All these systems were limited to specific polymer combinations that have an inherent physical affinity for each other. However with... 

Adjuncts include antifoams and defoamers, some problem-specific polymers, and alkalinity boosters. 

Problem-specific polymers include terpolymers, used for iron dispersion, iron transport, and silica control. 

Stabilizers, transport agents, or problem-specific polymers to... 

Problem-specific polymer, function of all-organics 443 Problem-specific polymers, as adjuncts 389... 

The remainder of this introductory chapter covers a few general but important parameters of step-growth polymerization. References are provided throughout the chapter if further information is desired. Further details of specific polymers made by step-growth polymerization are provided in subsequent chapters within this book. 

The normalization method is the easiest and most straightforward to use but, unfortunately, it is also the least likely to be appropriate for most LC analyses. To be applicable, the detector must have the same response to all the components of the sample. An exceptional example, where the normalization procedure is frequently used, is in the analysis of polymers by exclusion chromatography using the refractive index detector. The refractive index of a specific polymer is a constant for all polymers of that type having more than 6 monomer units. Under these conditions normalization is the obvious quantitative method to use. 

The percentage x(p)% of any specific polymer (p) in a given polymer mixture can be expressed by... 

The development of commercial continuous processes involves the consideration of many factors associated with process design and product quality. Most of the factors discussed in this paper will be important. Other, equally significant parameters, may be important for specific polymer products. Failure to deal with any of these problems may mean failure to develop an economical process. 

Examination of the history of antioxidants such as hindered phenols and amines shows a move from low-MW products to higher-MW products. Specifically, polymer industries have abandoned the use of, e.g., butylated hydroxy toluene (BHT) in favor of tetrakismethylene (3,5-di-f-butyl-4-hydroxydrocinnamate)methane (see Figure 15.9). Likewise, polymeric HALS, like poly-methylpropyl-3-oxy-(4(2,2,6,6-tetramethyl)piperidinyl) siloxane, replaced the low-MW hindered amine Lowilite 77 (see Figure 15.10). The next obvious step was to produce a new class of stabilizers. 

Identity Sequence-specific polymers of amino acids Sequence-specific polymers of N-substituted glycines... 

At another level, water-soluble polyphosphazenes are of interest as plasma extenders. In addition, specific polymers with pendent imidazolyl units have been studied as carrier macromolecules for heme and other iron porphyrins (structures and (44,45). (In structures M and the ellipse and Fe symbol represent heme, hemin, or a synthetic heme analog.)... 

The solution to this problem has been to isolate the lactide and to polymerize this directly using a tin(ii) 2-(ethyl)hexanoate catalyst at temperatures between 140 and 160 °C. By controlling the amounts of water and lactic acid in the polymerization reactor the molecular weight of the polymer can be controlled. Since lactic acid exists as d and L-optical isomers, three lactides are produced, d, l and meso (Scheme 6.11). The properties of the final polymer do not depend simply on the molecular weight but vary significantly with the optical ratios of the lactides used. In order to get specific polymers for medical use the crude lactide mix is extensively recrystallized, to remove the meso isomer leaving the required D, L mix. This recrystallization process results in considerable waste, with only a small fraction of the lactide produced being used in the final polymerization step. Hence PLA has been too costly to use as a commodity polymer. 

Recently, Teymour and coworkers developed an interesting computational technique called the digital encoding for copolymerization compositional modeling [20,21], Their method uses symbolic binary arithmetic to represent the architecture of a copolymer chain. Here, each binary number describes the exact monomer sequence on a specific polymer chain, and its decimal equivalent is a unique identifier for this chain. Teymour et al. claim that the... 

Figures 5.3 and 5.4 are just two pieces of evidence that the bond fluctuation model is a reasonable starting point for describing the properties of polymer melts. Thus the next step has to be to incorporate suitable information about the chemical structure and the energetics of specific polymers into the model.

The Mapping Between Specific Polymers and the Bond Fluctuation Model... 

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