Thermoplastic polymer examples

In practice, synthetic polymers are sometimes divided into two classes, thermosetting and thermo-plMtic. Those polymers which in their original condition will fiow and can be moulded by heat and pressime, but which in their finished or cured state cannot be re softened or moulded are known as thermo setting (examples phenol formaldehyde or urea formaldehyde polymer). Thermoplastic polymers can be resoftened and remoulded by heat (examples ethylene polymers and polymers of acrylic esters). 

Examples of plasticizers include adsorbed water and ethylene glycol for vinyl binders, stearic acid and oleic acid for wax binders, glycerine and ethylene glycol for clay bodies, and molten oils and waxes for thermoplastic polymers used in injection mol ding. 

One of the most attractive features of TLCPs is their ability to alter the rheology of bulk thermoplastic polymers. Most reports in the academic literature are concerned with viscosity reduction. For example, Siegmann et al. [1] observed a steep viscosity drop when a TLCP... 

Ethylene reacts by addition to many inexpensive reagents such as water, chlorine, hydrogen chloride, and oxygen to produce valuable chemicals. It can be initiated by free radicals or by coordination catalysts to produce polyethylene, the largest-volume thermoplastic polymer. It can also be copolymerized with other olefins producing polymers with improved properties. Eor example, when ethylene is polymerized with propylene, a thermoplastic elastomer is obtained. Eigure 7-1 illustrates the most important chemicals based on ethylene. 

A copolymer, on the other hand, results from two different monomers hy addition polymerization. For example, a thermoplastic polymer with better properties than an ethylene homopolymer comes from copolymerizing ethylene and propylene ... 

Tetrazole, DNA synthesis and, 1115 Thermal cracking, 173-174 Thermodynamic control, 491 Thermoplastic polymer, 1216 characteristics of, 1216 examples of. 1216 Tg of, 1216 uses of, 1216... 

For the most part, plastics are man-made since very few plcistlcs are natural, i.e.- nature-made. Natural plastics include large molecular-wei t proteins and similar molecules. Man-made plastics can be classified as either thermoplastic or thermosetting. Each class derives its physical properties from the effects of application of heat, the former becoming "plastic" (that is- it becomes soft and tends to flow) while the latter becomes less "plastic" and tends to remain in a softened state. This difference in change of state derives from the actual nature of the chemical bonds in the polymer. Thermoplastic polymers generally consist of molecules composed of many monomeric units. A good example is that of polyethylene where the monomeric unit is -(CH2-CH2)-. The molecule is linear... 

We can create thermoplastic polymers by chain growth or step growth reactions. In either case the polymer chains consist of a string of monomer residues, each of which is attached to two other monomer residues. The polyethylene molecule shown in Fig. 1.1 is an example of a thermoplastic polymer made via chain growth polymerization, as shown in Fig. 1.7,... 

Thermosets differ molecularly from thermoplastics in that their individual chains are anchored to one another through crosslinks. The resulting network creates cohesive materials that demonstrate better thermal stability, rigidity, and dimensional stability than thermoplastics. Some examples of traditional thermosets are melamine-formaldehyde resins, which are used to treat fabrics to make them wrinkle-free, and Bakelite (a phenol-formaldehyde resin), a historically important polymer used in many applications, such as costume jewelry, electrical switches, and radio casings. 

Thermoplastic polymer macromolecules usually tend to become oriented (molecular chain axis aligns along the extrusion direction) upon extrusion or injection moulding. This can have implications on the mechanical and physical properties of the polymer. By orienting the sample with respect to the coordinate system of the instrument and analysing the sample with polarised Raman (or infrared) light, we are able to get information on the preferred orientation of the polymer chains (see, for example, Chapter 8). Many polymers may also exist in either an amorphous or crystalline form (degree of crystallinity usually below 50%, which is a consequence of their thermal and stress history), see, for example, Chapter 7. 

Clearly, the hardnesses of thermoplastic polymers are not intrinsic. They depend on various extrinsic factors. Only trends can be cited. For example, as the molecular weight in polyethylene materials increases, they become harder. And, as the molecular aromaticity increases, a polymeric material becomes harder. Thus, higher molecular weight anthracene is harder than napthalene and more aromatic Kevlar is harder than polymethacrylate. 

Safety precautions Before this experiment is carried out, Sect. 2.2.5 must be read as well as the material safety data sheets (MSDS) for all chemicals and products used. This example describes the concept of core/shell impact modifiers for thermoplastic polymers (see Sect. 5.51). 

Little is known about the mass transport properties of reinforced-composite materials. Certainly, there are no new relations or concepts that govern estimations of diffusiv-ities that have not already been discussed. In most polymer-matrix composites, the transport properties of the polymer play an important role in diffusion through the composite. For example, hydrophilic polymers such as epoxy readily absorb water from the atmosphere. Thermoplastic polymers absorb relatively little moisture since they are more hydrophobic, but are more susceptible to uptake of organic solvents. 

A case of application of fractional replica 27-3 of a full factorial experiment on studying adhesion of thermoplastic polymer and fiber has been analyzed earlier in Example 2.33. Tensile strength of adhesion has been measured as the system response. The experiment included seven factors, with the nature of fiber being a qualitative-categorical factor. The regression coefficient values and method of steepest ascent are shown Table 2.188. 

Examples of various thermoplastics are discussed in detail in the literature [6,10] and can be found in commercial materials data banks [1], Examples of the most common thermoplastic polymers, with a short summary, are given below. Ranges of typical processing conditions... 

Continuity can also be reached by polymerizing one of the components within the other. In such a case the blend is called an IPN, an interpenetrating network it is, in most cases formed by a thermoset in a thermoplastic polymer. An example is a compound built-up from 50% of a thermoplast (polycarbonate or polysulphone), and 50% of a cross-linked polymer on the basis of dicyanate bisphenol-A. The skeleton... 

The above thermal analysis studies demonstrated the enhanced thermal stability of POSS materials, and suggested that there is potential to improve the flammability properties of polymers when compounded with these macromers. In a typical example of their application as flame retardants, a U.S. patent39 described the use of preceramic materials, namely, polycarbosilanes (PCS), polysilanes (PS), polysilsesquioxane (PSS) resins, and POSS (structures are shown in Figure 8.6) to improve the flammability properties of thermoplastic polymers such as, polypropylene and thermoplastic elastomers such as Kraton (polystyrene-polybutadiene-polystyrene, SBS) and Pebax (polyether block-polyamide copolymer). 

All polymers can be divided into two major groups thermoplastics and thermosets) based on their thermal processing behavior. Thermoplastics soften and flow when heated. Upon cooling, thermoplastic polymers harden and assume the shape of the mold. Examples of commercial thermoplastics include polystyrene, polyolefins (e.g. polyethylene and polypropylene), nylon, poly(vinyl) chloride (PVC), and poly (ethylene) terephthalate (PET). Thermoplastics make up 80% of the plastic produced today and these polymers are linear or branched in their structure. 

A condensation polymer is one in which the repeating unit lacks certain atoms which were present in the monomer(s) from which the polymer was formed or to which it can be degraded by chemical means. Condensation polymers are formed from bi- or polyfunctional monomers by reactions which involve elimination of some smaller molecule. Polyesters (e.g., 1-5) and polyamides like 1-6 are examples of such thermoplastic polymers. Phenol-formaldehyde resins (Fig. 5-1) are thermosetting condensation polymers. All these polymers are directly synthesized by condensation reactions. Other condensation polymers like cellulose (1-11) or starches can be hydrolyzed to glucose units. Their chemical structure indicates that their repealing units consist of linked glucose entities which lack the elements of water. They are also considered to be condensation polymers although they have not been synthesized yet in the laboratory. 

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