Structures fluorocarbon monomer

A variety of ionomers have been described in the research literature, including copolymers of a) styrene with acrylic acid, b) ethyl acrylate with methacrylic acid, and (c) ethylene with methacrylic acid. A relatively recent development has been that of fluorinated sulfonate ionomers known as Nafions, a trade name of the Du Pont company. These ionomers have the general structure illustrated (10.1) and are used commercially as membranes. These ionomers are made by copolymerisation of the hydrocarbon or fluorocarbon monomers with minor amounts of the appropriate acid or ester. Copolymerisation is followed by either neutralisation or hydrolysis with a base, a process that may be carried out either in solution or in the melt. 

In the addition to homo-PVF2, a large number of copolymers have also been synthesized which allow to optimize the mechanical properties of fluoropolymers. Most common are copolymers with vinyl fluoride, trifluoroethylene, tetrafluoroethylene, hexafiuoropropy-lene, hexafluoroisobutylene, chlorotrifluoroethylene, and pentafiuoro-propene [521,535, 559-562]. Copolymerization with nonfluorinated monomers is possible [563] in principle but has not yet found commercial use. Fluorocarbon monomers that can help to retain or enhance the desirable thermal, chemical, and mechanical properties of the vinylidene structure are more interesting comonomers. Copolymerization with hexafluoropropylene, pentafluoropropylene, and chlorotrifluoroethylene results in elastomeric copolymers [564]. The polymerization conditions are similar to those of homopoly(vinylidene fluoride) [564]. The copolymers have been well characterized by x-ray analysis [535], DSC measurements [565], and NMR spectroscopy [565,566]. 

Potentially, this direct fluorination process is a new approach to the synthesis of fluorocarbon polymers. Polyethylene, polypropylene, polystyrene, polyacrylonitrile, polyacrylamide, resor phenol formaldehyde resin, and ethylene propylene copolymer have been fluorinated to produce perf1uorocarbon polymers which are structurally similar to the hydrocarbon starting materials and have physical properties similar to known structurally related fluorocarbon polymers obtained by polymerization of fluorocarbon monomers. High yield of fluorocarbon polymers approaching 100 have been obtained. This direct technique used for fluorination of hydrocarbons and polymers is called the LaMar process and has been previously described in connection with the direct fluorination of Lt ver molecular weight species ". ... 

In this work we have demonstrated that a new class of heavily fluorinated acrylic and methacrylic resins can be efficiently synthesized and then cured to solid form with radical initiator at elevated temperatures. These cured resins were found to have low dielectric constants, which are close to the minimum known values for Teflon and Teflon AF. In contrast to tetrafluoroethylene, our monomers are processable owing to the fact that they are liquids or low-melting solids, and moreover are soluble in common organic solvents. Lower dielectric constants are obtained as fluorine contents on the polymer backbone or side chain increase, when acrylate is replaced by methacrylate, when ether linkages are present in the fluorocarbon, and when aromatic structure is symmetrically meta-substituted. 

In this context, by the term fluorosilicone are meant polymers containing C-F bonds and Si-O bonds with hydrocarbon entities between them. Thus, the repeating structure may be generally written as [RfX (CH J (CH,)vSiOz, where Rf is the fluorocarbon group.59 Commercially available fluorosilicones are based on polymethyltri-fluoropropylsiloxane (PMTFPS), or more accurately poly[methyl (3,3,3-trifluoropropyl)siloxane]. In some cases PMTFPS is copolymerized with polydim-ethyl siloxane (PDMS) for cost/benefit balance.60 The manufacture of monomers for fluorosilicones is discussed in some detail in Reference 60. Fluorosilicone elastomers... 

The family of FPs, also called fluorocarbon plastics, is based on polymers made of monomers composed of fluorine and carbon may also include chlorine atoms in their structure. Specific types include polytetrafluoroethylene (PTFE), polytetrafluoroethylene-cohexafluoro-propylene or fluorinated ethylene propylene (FEP), polytrafluoroethylene-coperfluoropropylvinyl ether (PFA), ethylenetetrafluoroethylene (ETFE). polychlorotrifluoroethylene (PCTFE), ethylene-chlorotri-fluoroethylene (ECTFE), polyvinylidene fluoride (PVDF), polyvinyl fluoride (PVF), perfluoromethylvinylether (PFMV), perfluoroalkoxy (PFA), etc. 

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