Poly applications potential

In the recent years, new markets have arisen for biodegradable polymers such as poly(butylene adipate-terephthalate), poly(lactide), poly(butylenesuccinate), or poly(3-hydroxybutyrate) and poly(carbonates). They constitute a new class of green polymers with wide application potential for packaging, clothing, carpets, applications in automotive engineering, foils, and utilities in agriculture. 

Rod—coil copolymers are a type of amphiphile that can self-assemble into a variety of ordered nanostructures in a selective solvent.36-37-71 In solvents that selectively dissolve only coil blocks, rod—coil copolymers can form well-defined nanostructures with rod domain consisting of the insoluble block. This results in an increase of the relative volume fraction of the coil segments relative to the rod segments, which gives rise to various supramolecular structures. Particularly, poly(alkylene oxide) as the coil block of rod—coil molecule has additional advantages due to complexation capability with alkali metal cation, which can provide an application potential for solid polyelectrolytes and induce various supramolecular structures.72-75... 

Graphene is considered bidimensional carbon nanofiller with a one-atom-thick planar sheet of sp -bonded carbon atoms that are densely packed in a honeycomb crystal lattice. It is regarded as one of the thinnest materials with tremendous application potential. Graphene and poly-mer/graphene nanocomposites have remarkable properties, among these ... 

Poly[3-hydroxybutyrate] was the first PHA to be produced on an industrial scale, but its brittle nature, its poor mechanical properties and its high production cost limited its application potential. In the early 1990s, Imperial Chemical Industries [ICI] started the production of poly[3-hydroxybutyrate-co-3-hydroxyvalerate] [P3HB3HV] under the trade name Biopol . This material showed lower degrees of crystallinity and superior mechanical properties. Later on, the production of Biopol was continued by Monsanto and subsequently followed up by Metabolix. PHAs were originally intended as bio-based alternatives for polyolefins used in plastic containers, films and bottles. Despite the large interest in PHAs, their application remains, however, limited due to their narrow processing window [84, 85]. 

T. Yoshida, T. Nagasawa, Epsilon-poly-L-lysine microbial production, biodegradation and application potential, Appl. Microbiol. 

R. Gangopadhyay, A. De, G. Ghosh, Polyaniline-Poly(vinyl Alcohol) Conducting Composite Material with Easy Processability and Novel Application Potential. Synth Met 2001,123,21-31. 

Alternating MA copolymers, including the styrene comonomer, have applications potential as detergent builders.In many cases, such copolymers improve the sequestering properties of the detergent formulation. SMA-Carbowax 350 (Union Carbide) combinations were shown useful modifiers for poly(vinyl alcohol) and cellulosic ether film packets for laundry detergents. 

Applications. Polymers with small alkyl substituents, particularly (13), are ideal candidates for elastomer formulation because of quite low temperature flexibiUty, hydrolytic and chemical stabiUty, and high temperature stabiUty. The abiUty to readily incorporate other substituents (ia addition to methyl), particularly vinyl groups, should provide for conventional cure sites. In light of the biocompatibiUty of polysdoxanes and P—O- and P—N-substituted polyphosphazenes, poly(alkyl/arylphosphazenes) are also likely to be biocompatible polymers. Therefore, biomedical appHcations can also be envisaged for (3). A third potential appHcation is ia the area of soHd-state batteries. The first steps toward ionic conductivity have been observed with polymers (13) and (15) using lithium and silver salts (78). 

Mention should also be made here of the extensive use of poly(vinyl alcohol) in potentially biodegradable applications. At appropriate hydroxyl contents these polymers will dissolve in water (see Chapter 14) and can apparently be conveniently washed away after use as a water-soluble packaging. Biodegradation does, however, appear to be slow and first requires an oxidative step involving enzymatic attack to a ketone such as polyenolketone, which then biodegrades more rapidly. 

Another interesting applications area for fullerenes is based on materials that can be fabricated using fullerene-doped polymers. Polyvinylcarbazole (PVK) and other selected polymers, such as poly(paraphcnylene-vinylene) (PPV) and phenylmethylpolysilane (PMPS), doped with a mixture of Cgo and C70 have been reported to exhibit exceptionally good photoconductive properties [206, 207, 208] which may lead to the development of future polymeric photoconductive materials. Small concentrations of fullerenes (e.g., by weight) lead to charge transfer of the photo-excited electrons in the polymer to the fullerenes, thereby promoting the conduction of mobile holes in the polymer [209]. Fullerene-doped polymers also have significant potential for use in applications, such as photo-diodes, photo-voltaic devices and as photo-refractive materials. 

The study of acid-base interaction is an important branch of interfacial science. These interactions are widely exploited in several practical applications such as adhesion and adsorption processes. Most of the current studies in this area are based on calorimetric studies or wetting measurements or peel test measurements. While these studies have been instrumental in the understanding of these interfacial interactions, to a certain extent the interpretation of the results of these studies has been largely empirical. The recent advances in the theory and experiments of contact mechanics could be potentially employed to better understand and measure the molecular level acid-base interactions. One of the following two experimental procedures could be utilized (1) Polymers with different levels of acidic and basic chemical constitution can be coated on to elastomeric caps, as described in Section 4.2.1, and the adhesion between these layers can be measured using the JKR technique and Eqs. 11 or 30 as appropriate. For example, poly(p-amino styrene) and poly(p-hydroxy carbonyl styrene) can be coated on to PDMS-ox, and be used as acidic and basic surfaces, respectively, to study the acid-base interactions. (2) Another approach is to graft acidic or basic macromers onto a weakly crosslinked polyisoprene or polybutadiene elastomeric networks, and use these elastomeric networks in the JKR studies as described in Section 4.2.1. 

Figure 12.30 Potential uses of polyphosphazenes (a) A thin film of a poly(aminophosphazene) sueh materials are of interest for biomedical applications, (b) Fibres of poly[bis(trifluoroethoxy)phosphazene] these fibres are water-repellant, resistant to hydrolysis or strong sunlight, and do not burn, (c) Cotton cloth treated with a poly(fluoroalkoxyphosphazene) showing the water repellaney eonferred by the phosphazene. (d) Polyphosphazene elastomers are now being manufaetured for use in fuel lines, gaskets, O-rings, shock absorbers, and carburettor eomponents they are impervious to oils and fuels, do not bum, and remain flexible at very low temperatures. Photographs by eourtesy of H. R. Allcock (Pennsylvania State University) and the Firestone Tire and Rubber Company.

Polyacetylene is considered to be the prototypical low band-gap polymer, but its potential uses in device applications have been hampered by its sensitivity to both oxygen and moisture in its pristine and doped states. Poly(thienylene vinylene) 2 has been extensively studied because it shares many of the useful attributes of polyacetylene but shows considerably improved environmental stability. The low band gap of PTV and its derivatives lends itself to potential applications in both its pristine and highly conductive doped state. Furthermore, the vinylene spacers between thiophene units allow substitution on the thiophene ring without disrupting the conjugation along the polymer backbone. 

There have been a number of different synthetic approaches to substituted PTV derivatives proposed in the last decade. Almost all focus on the aromatic ring as the site for substitution. Some effort has been made to apply the traditional base-catalyzed dehydrohalogenation route to PTV and its substituted analogs. The methodology, however, is not as successful for PTV as it is for PPV and its derivatives because of the great tendency for the poly(u-chloro thiophene) precursor spontaneously to eliminate at room temperature. Swager and co-workers attempted this route to synthesize a PTV derivative substituted with a crown ether with potential applications as a sensory material (Scheme 1-26) [123]. The synthesis employs a Fager condensation [124] in its initial step to yield diol 78. Treatment with a ditosylate yields a crown ether-functionalized thiophene diester 79. This may be elaborated to dichloride 81, but pure material could not be isolated and the dichloride monomer had to be polymerized in situ. The polymer isolated... 

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