Polycarbonate chemical functionalization

Hole transport in polymers occurs by charge transfer between adjacent donor functionalities. The functionalities can be associated with a dopant molecule, pendant groups of a polymer, or the polymer main chain. Most literature references are of doped polymers. The more common donor molecules include various arylalkane, arylamine, enamine, hydrazone, oxadiazole, oxazole, and pyrazoline derivatives. Commonly used polymers are polycarbonates, polyesters, and poly(styrene)s. Transport processes in these materials are unipolar. The mobilities are very low, strongly field and temperature dependent, as well as dependent on the dopant molecule, dopant concentration, and the polymer host This chapter reviews hole transport in polymers and doped polymers of potential relevance to xerography. The organization is by chemical classification. The discussion mainly includes molecularly doped, pendant, and... 

The sol-gel method is a low temperature synthesis route for complex oxides [42]. It can be used to make complex functional oxide nanowires inside the pores of templates. In addition to the sol-gel method precursor-based solution deposition routes can also be used for nanostructure formation [43]. In both cases a postdeposition high temperature anneal (>500-600 °C) is needed to form the required stoichiometric phase. Due to the requirement of a high temperature anneal, alumina templates are used as the polycarbonate membranes decompose at a much lower temperature. For chemical solution deposition the membrane is dipped directly into the precursor solution. For sol-gel growth generally the required sol is prepared and the template is put into the sol for a required period (e.g. 0.5-1 h). After removing the membrane from the sol it is dried and then annealed at higher temperature before the required phase is formed. A schematic of the sol-gel route is shown in Figure 21.10. 

A large diffusion may be found also for composite materials, carbon, or metal based. In the first case different types of polymeric resins (thermoplastics, such as polypropylene, polyethylene, and PVDF, or thermosettings, such as epoxies and phenolics) are filled with carbonaceous powders (graphite or carbon blacks), to provide a material characterized by very high chemical stability in the fuel cell environment and satisfactory properties of electrical conductivity, but which cannot offer sufficient robustness at thickness lower than 2 mm. The metal composite plates are essentially based on combinations (sandwiches of different layers) of stainless steel, porous graphite, and polycarbonates, with the aim to exploit the characteristics of different materials. Their fabrication can be more complex but this is compensated by the possibility to incorporate other functional components, such as manifolds, seals, and cooling layers. 

Fig. 10.26. Carbon-observe, fluorine-dephase REDOR NMR spectra of a heterogeneous blend of [carbonyl- CJpolycarbonate and poly(p-fluorostyrene-co-styrene) as a function of the number of rotor cycles of 5 kHz magic-angle spinning. The natural-abundance background has been subtracted from both the top and bottom sets of spectra. The REDOR difference (top) arises exclusively from the polycarbonate carbons at the interface. (Reprinted with permission from Ref. [153]. 1995 American Chemical Society, Washington, DC.)...

The author worked for many years at BP Research on the synthesis of LCPs and devised an empirical method called the Mesogenic Index, which employs functional group contributions on an additive score basis to predict whether a particular random copolymer is likely to exhibit a mesophase (subject to the polymer being soluble or fusible). This chapter explores the general features and theoretical aspects of the chemical structures of main chain LCPs and describes the Mesogenic Index and how it was successfully applied to polyesters, polyamides and polycarbonates. The final section describes the extension of the MI empirical method to the various types of LC polyimides reported in recent years. 

Bisphenol A phenoxy polymers and bisphenol A polycarbonates were blended in solution. Chemical changes from aromatic to aliphatic carbonate groups were monitored by FTIR as a function of time and temperature (348). 

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