Homopolymers examples

Fluoroplastic Homopolymer - A fluoropolymer entirely compiled of one monomer is called fluoroplastic homopolymer. Examples include poly-tetrafluoroethylene, polyvinylidene fluoride, and polyvinyl fluoride. 

Graft copolymers - These consist of two or more homopolymers, where one homopolymer is covalently attached or grafted as a long branch to the spine of another homopolymer. Examples are poly(acrylonitrile-graft-vinyl acetate) and poly(acrylonitrile-graft-methacrylie acid). 

Once the binary interaction parameters for the blend system are known, EOS theory can be used to predict phase separation behavior. Lower critical solution temperature (LCST) is the temperature above which a miscible system becomes immiscible. Upper critical solution temperature (UCST) is the temperature above which an immiscible polymer blend system becomes miscible. Some polymer-polymer systems exhibit either LCST or UCST or both or neither. Another set of phase separation can be obtained as shown in the copolymer-homopolymer example in Section 3.2 by varying the blend volume fraction. The Gibbs free energy of mixing per unit volume for a binary system of two polymers can be written as... 

Like polyamides, the polyester homopolymers are seldom used in hot melts. In most cases a better balance of properties such as melt point, flexibility, rate of crystallization, etc. is achieved with copolymers. As in polyamides, copolymerization can yield copolymers with a wide range of properties. Some copolymers have melt points below that of the lower melting homopolymer. Examples of copolymers with eutectics are shown in Figs. 6 and 7. ... 

Formaldehyde homopolymer is composed exclusively of repeating oxymethylene units and is described by the term poly oxymethylene (POM) [9002-81-7]. Commercially significant copolymers, for example [95327-43-8] have a minor fraction (typically less than 5 mol %) of alkyUdene or other units, derived from cycHc ethers or cycHc formals, distributed along the polymer chain. The occasional break in the oxymethylene sequences has significant ramifications for polymer stabilization. 

DMAC and nonpolar solvents form synergistic mixtures which dissolve high molecular weight vinyl chloride homopolymers. For example, a mixture of DMAC with an equal volume of carbon disulfide [75-15-0] a nonsolvent, dissolves 14 wt % of Geon 101 vinyl chloride homopolymer at room temperature, whereas the solubUity of Geon 101 ia DMAC alone is about 5 wt % (15). 

Manufacture of P-Silicon Carbide. A commercially utilized appHcation of polysdanes is the conversion of some homopolymers and copolymers to siHcon carbide (130). For example, polydimethyl silane is converted to the ceramic in a series of thermal processing steps. SiHcon carbide fibers is commercialized by the Nippon Carbon Co. under the trade name Nicalon (see Refractory fibers). 

Examples of the two macromolecular nomenclature systems are as foUows. For source-based names for homopolymers and copolymers polyacrylonitrile, poly(methyl methacrylate), poly(acrylainide- (9-vinylpyrroHdinone), polybutadiene- /oi / -polystyrene, and poly(propyl... 

Polypropylene polymers are typically modified with ethylene to obtain desirable properties for specific applications. Specifically, ethylene—propylene mbbers are introduced as a discrete phase in heterophasic copolymers to improve toughness and low temperature impact resistance (see Elastomers, ETHYLENE-PROPYLENE rubber). This is done by sequential polymerisation of homopolymer polypropylene and ethylene—propylene mbber in a multistage reactor process or by the extmsion compounding of ethylene—propylene mbber with a homopolymer. Addition of high density polyethylene, by polymerisation or compounding, is sometimes used to reduce stress whitening. In all cases, a superior balance of properties is obtained when the sise of the discrete mbber phase is approximately one micrometer. Examples of these polymers and their properties are shown in Table 2. Mineral fillers, such as talc or calcium carbonate, can be added to polypropylene to increase stiffness and high temperature properties, as shown in Table 3. 

Table 2. Examples of Random Copolymers That Form Miscible Blends with Other Polymers When Corresponding Homopolymers Do Not...

There are many examples known where a random copolymer Al, comprised of monomers 1 and 2, is miscible with a homopolymer B, comprised of monomer 3, even though neither homopolymer 1 or 2 is miscible with homopolymer 3, as illustrated by Table 2. The binary interaction model offers a relatively simple explanation for the increased likelihood of random copolymers forming miscible blends with other polymers. The overall interaction parameter for such blends can be shown (eg, by simplifying eq. 8) to have the form of equation 9 (133—134). 

Poly(vinyl alcohol) used to manufacture the poly(vinyl acetal)s is made from poly(vinyl acetate) homopolymer (see Vinyl polymers, vinyl alcohol polymers Vinyl POLYMERS, vinyl acetate polymers). Hydrolysis of poly(vinyl acetate) homopolymer produces a polyol with predominandy 1,3-glycol units. The polyol also contains up to 2 wt % 1,2-glycol units that come from head-to-head bonding during the polymeri2ation of vinyl acetate monomer. Poly(vinyl acetate) hydrolysis is seldom complete, and for some appHcations, not desired. For example, commercial PVF resins may contain up to 13 wt % unhydroly2ed poly(vinyl acetate). Residual vinyl acetate units on the polymer help improve resin solubiHty and processibiHty (15). On the other hand, the poly(vinyl alcohol) preferred for commercial PVB resins has less than 3 wt % residual poly(vinyl acetate) units on the polymer chain. 

Copolymers wet and adhere well to nonporous surfaces, such as plastics and metals. They form soft, flexible films, in contrast to the tough, horny films formed by homopolymers, and are more water-resistant. As the ratio of comonomer to vinyl acetate increases, the variety of plastics to which the copolymer adheres also increases. Comonomers containing functional groups often adhere to specific surfaces for example, carboxyl containing polymers adhere well to metals. 

The Chemical Abstracts Services Registry Number and lUPAC nomenclature for PVP are [9003-39-8] and l-ethenyl-2-pyrrohdinone homopolymer, respectively however, it is known by a variety of approved names by foreign and domestic regulatory authorities. For example ... 

The glass-transition temperature in amorphous polymers is also sensitive to copolymerization. Generally, T of a random copolymer falls between the glass-transition temperatures of the respective homopolymers. For example, T for solution-polymerized polybutadiene is —that for solution-polymerized polystyrene is -HlOO°C. A commercial solution random copolymer of butadiene and styrene (Firestone s Stereon) shows an intermediate T of —(48). The glass-transition temperature of the random copolymer can sometimes be related simply as follows ... 

Another important feature of some random copolymers is the abihty to achieve miscibility in either a homopolymer or a second random copolymer. This "copolymer effect" has been shown empirically for quite some time, eg, PVC is miscible with random copolymers of ethylene and vinyl acetate (52). Such systems are effective because repulsions between the dissimilar segments in the copolymer are enough to overcome the repulsions between these segments and those of the second component in the mixture. In other words, in the above example, the ethylene units "hate" vinyl acetate units more than either of them "hate" PVC. Thus there is a net negative interaction energy and the two materials are miscible (53). 

Whilst the Vicat test usually gives the higher values the differences are quite modest with many polymers (e.g. those of types A, B and C). For example, in the case of the polycarbonate of bis-phenol A (Chapter 20) the heat distortion temperatures are 135-140°C and 140-146°C for the high and low stress levels respectively and the Vicat softening point is about 165°C. In the case of an acetal homopolymer the temperatures are 100, 170 and 185°C respectively. With nylon 66 the two ASTM heat distortion tests give values as different as 75 and 200°C. A low-density polyethylene may have a Vicat temperature of 90°C but a heat distortion temperature below normal ambient temperatures. 

As with poly(ethylene terephthalate) PBT-based copolymers have been introduced to overcome some of the deficiencies of the homopolymer. For example, the rather low notched impact strength of unreinforced grades has been overcome by partial replacement of the terephthalic acid with a longer chain aliphatic dicarboxylic acid. Improved toughness has also been obtained by grafting about 5% of ethylene and vinyl acetate onto the polyester backbone. 

Should it be capable of reacting with both phases, there is nothing to preclude a functional homopolymer from being an effective coupling agent. For example. 

In a somewhat wider sense, one can define amphiphiles as molecules in which chemically very different units are linked together. For example, the structures formed by A B block copolymers in demixed A and/or B homopolymer melts and their phase behavior are very similar to those of classical amphiphiles in water and/or oil [13,14]. Copolymers are used not only to disperse immiscible homopolymer phases in one another, but also to create new, mesoscopically structured materials with unusual and interesting properties [15]. 

In general, as the ion content is raised, the modulus or stiffness of the ionomer is increased, as shown by the data in Fig. 2. While the increase is much greater in the elevated temperature range, where the polymer is acting more like a crosslinked rubber, there is still a significant increase in the glassy modulus below Tg. For example, for the PMMA-based ionomer of Fig. 2, the modulus at 30°C is almost 20% above that of the homopolymer for an ionomer having an ion content of 12.4 mol%. For the... 

In most ionomers, it is customary to fully convert to the metal salt form but, in some instances, particularly for ionomers based on a partially crystalline homopolymer, a partial degree of conversion may provide the best mechanical properties. For example, as shown in Fig. 4, a significant increase in modulus occurs with increasing percent conversion for both Na and Ca salts of a poly(-ethylene-co-methacrylic acid) ionomer and in both cases, at a partial conversion of 30-50%, a maximum value, some 5-6 times higher than that of the acid copolymer, is obtained and this is followed by a subsequent decrease in the property [12]. The tensile strength of these ionomers also increases significantly with increasing conversion but values tend to level off at about 60% conversion. 

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