Vinylidene copolymer

Dichloroethylene (1,1-DCE) is nsed to produce vinylidene copolymers for films and coatings. 

A series of vinylidene copolymers are sold commercially as Saran. These are random copolymers of vinylidene chloride with vinyl chloride (88 mol % vinylidene chloride, M =100 kg mol Tg=7 C) 4, acrylonitrile (>80% vinylidene... 

Perfluorinated copolymers, Nafion (DuPont), are the current fuel cell PEM materials of choice. They are chemically very stable and have good proton conductivity. Conversely, Nafion and similar perfluorinated vinylidene copolymers have several limitations, some of which include (1) low modulus as well as modest glass-transition temperatures (2) reduced conductivity at temperatures above 80°C and (3) relatively high methanol permeability, which limits efficient applications for direct methanol fuel cells. They are also recognized to be currently quite expensive. 

As a substimte to Nafion impregnation into a fluoropolymer matrix, solution cast films have been prepared from blends of Nafion and vinylidene fluoride-hex-afluoropropylene copolymer [16]. Upon addition of 20 60% vinylidene copolymer, a steep decrease in proton conductivity was observed, from 10 " S cm to 10 -10 S cm , which was accompanied by a significant decrease in methanol permeability. In a more recent paper [27], Si et al. solution cast membranes composed of Nafion and poly(vinylidene fluoride), henceforth denoted as PVDF, where characterized where the PVDF content was varied from 0 to 65 wt%. As expected, the conductivity and methanol permeability decreased with inaeasing PVDF content, with a much more dramatic drop in transport parameters when the PVDF content was >50%. From proton conductivity and methanol permeability data, the relative selectivity can be determined ... 

Partially fluorinated oligomers derived from hexafluoropropylene oxide je.g., F[C(CF3)FCF20]9C(CF3)FC00CH2CH2(0CH2CH2)60CH3 lower the critical surface tension of polymers on which they are adsorbed [e.g., polystyrene, poly (methyl methacrylate), and a vinyl chloride-vinylidene copolymer] [282]. 

B.p. — 29X. Monomer used to form polymers (only under rather drastic conditions) or copolymers with C2F4 and vinylidene fluoride, CH2 = CF2. Hexafluoropropene may be prepared by thermal decomposition of CF3CF2CF2C02Na or is prepared commercially by low pressure pyrolysis of C2F4. 

Polymeric vinylidene chloride generally produced by free radical polymerization of CH2 = CCl2. Homopolymers and copolymers are used. A thermoplastic used in moulding, coatings and fibres. The polymers have high thermal stability and low permeability to gases, and are self extinguishing. 

Vinylidene chloride and vinyl chloride lead to the copolymer known as Saran. Other commercial copolymers are produced from vinyl chloride and acrylonitrile (Dynel), and from maleic anhydride and styrene. 

Acrylonitrile-butadiene-styrene (ABS) copolymer Poly(vinylidene chloride)... 

Fluorinated ethylene-propylene resin Poly(vinylidene fluoride) Ethylene-tetrafluoroethylene copolymer Ethylene- chlorotrifluoro- ethylene copolymer Cellulose- filled Glass-fiber- reinforced... 

U.S. demand for [CPD OROC ARSONS AND CPD OROHYDROC ARSONS - SURVEY] (Vol5) Vinylidene chloride-acrylomtrile copolymers [9010-76-8]... 

The equimolar copolymer of ethylene and tetrafluoroethylene is isomeric with poly(vinyhdene fluoride) but has a higher melting point (16,17) and a lower dielectric loss (18,19) (see Fluorine compounds, organic-poly(VINYLIDENE fluoride)). A copolymer with the degree of alternation of about 0.88 was used to study the stmcture (20). Its unit cell was determined by x-ray diffraction. Despite irregularities in the chain stmcture and low crystallinity, a unit cell and stmcture was derived that gave a calculated crystalline density of 1.9 g/cm. The unit cell is befleved to be orthorhombic or monoclinic (a = 0.96 nm, b = 0.925 nm, c = 0.50 nm 7 = 96%. 

Vinylidene chloride copolymers were among the first synthetic polymers to be commercialized. Their most valuable property is low permeabiUty to a wide range of gases and vapors. From the beginning in 1939, the word Saran has been used for polymers with high vinylidene chloride content, and it is still a trademark of The Dow Chemical Company in some countries. Sometimes Saran and poly (vinylidene chloride) are used interchangeably in the Hterature. This can lead to confusion because, although Saran includes the homopolymer, only copolymers have commercial importance. The homopolymer, ie, poly (vinylidene chloride), is not commonly used because it is difficult to fabricate. 

Table 5. Common Solvents for Vinylidene Chloride Copolymers...

Fig. 4. Oxygen permeability in a vinylidene chloride copolymer film at selected levels of plasticizer (Citroflex A-4). Plasticizer level in parts pet hundred resin...

Vinylidene Chloride Copolymer Latex. Vinyhdene chloride polymers are often made in emulsion, but usuaUy are isolated, dried, and used as conventional resins. Stable latices have been prepared and can be used direcdy for coatings (171—176). The principal apphcations for these materials are as barrier coatings on paper products and, more recently, on plastic films. The heat-seal characteristics of VDC copolymer coatings are equaUy valuable in many apphcations. They are also used as binders for paints and nonwoven fabrics (177). The use of special VDC copolymer latices for barrier laminating adhesives is growing, and the use of vinyhdene chloride copolymers in flame-resistant carpet backing is weU known (178—181). VDC latices can also be used to coat poly(ethylene terephthalate) (PET) bottles to retain carbon dioxide (182). 

Table 19. Film Properties of Vinylidene Chloride Copolymer Latex ...

Vinylidene Chloride Copolymer Foams. Low density, fine-celled VDC copolymer foams can be made by extmsion of a mixture of vinylidene chloride copolymer and a blowing agent at 120—150°C (190). The formulation must contain heat stabilizers, and the extmsion equipment must be made of noncatalytic metals to prevent accelerated decomposition of the polymer. The low melt viscosity of the VDC copolymer formulation limits the size of the foam sheet that can be extmded. 

Expandable VDC copolymer microspheres are prepared by a microsuspension process (191). The expanded microspheres are used in reinforced polyesters, blocking multipair cable, and in composites for furniture, marble, and marine appHcations (192—195). Vinylidene chloride copolymer microspheres are also used in printing inks and paper manufacture (196). 

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