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Vinylidene fluoride thermal

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. [Pg.203]

Mihtary interest in the development of fuel and thermal resistant elastomers for low temperature service created a need for fluorinated elastomers. In the early 1950s, the M. W. Kellogg Co. in a joint project with the U.S. Army Quartermaster Corps, and 3M in a joint project with the U.S. Air Force, developed two commercial fluorocarbon elastomers. The copolymers of vinyUdene fluoride, CF2=CH2, and chlorotrifluoroethylene, CF2=CFC1, became available from Kellogg in 1955 under the trademark of Kel-F (1-3) (see Fluorine compounds, ORGANic-POLYcm.OROTRiFLUOROETHYLENE Poly(vinylidene) fluoride). In 1956, 3M introduced a polymer based on poly(l,l-dihydroperfluorobutyl acrylate) trademarked 3M Brand Fluorombber 1F4 (4). The poor balance of acid, steam, and heat resistance of the latter elastomer limited its commercial use. [Pg.508]

Vinylidene fluoride is produced by the thermal dehydrochlorination of 1-monochloro-1,1 -difluoroethane. [Pg.538]

Fluorocarbon elastomers represent the largest group of fluoroelastomers. They have carbon-to-carbon linkages in the polymer backbone and a varied amount of fluorine in the molecule. In general, they may consist of several types of monomers poly-vinylidene fluoride (VDF), hexafluoropropylene (HFP), trifluorochloroethylene (CTFE), polytetrafluoroethylene (TFE), perfluoromethylvinyl ether (PMVE), ethylene or propylene.212 Other types may contain other comonomers, e.g., 1,2,3,3,3-pentafluropropylene instead of HFP.213 Fluorocarbon elastomers exhibit good chemical and thermal stability and good resistance to oxidation. [Pg.108]

POLVINYLIDENE FLUORIDE. This product is made by the free-radical chain polymerization of vinylidene fluoride (H2C=CF2). This odorless gas which has a boiling point of —82°C is produced by the thermal dehydrochlorination of 1,1,1-chlorodifluoroethane or by the dechlorination of 1,2-dichloro-l.l-difluoro-ethane. As shown by the following equations, 1,1,1-chlorodifluoroethane may be obtained by the bydroflnorination and... [Pg.1358]

Poly(vinylidene fluoride) (PVDF) is the second most important thermoplastic within the fluoropolymer family after PTFE. Although, both the thermal and chemical stability of PVDF are somewhat lower compared to PTFE, the hydrogenated polymer can be more easily processed with conventional equipment, and it offers an advantageous compromise between quality and price. When the... [Pg.23]

The telomerisation of vinylidene fluoride (1,1-difluoroethylene) has been investigated by many authors. Almost all kinds of transfer agents have been used, as mentioned below, requiring various ways of initiation thermal, photochemical or from systems involving redox catalysts or radical initiators (Tables 3 and 4) and also hypofluorites as mentioned in Sect. 2.3.1. [Pg.182]

Table 3. Thermal and radical telomerisations of vinylidene fluoride (DTBP, DBP and sc-mean-ditertiarybutyl peroxide, dibenzoyl peroxide and supercritical, respectively) ... Table 3. Thermal and radical telomerisations of vinylidene fluoride (DTBP, DBP and sc-mean-ditertiarybutyl peroxide, dibenzoyl peroxide and supercritical, respectively) ...
The preceding structural characteristics dictate the state of polymer (rubbery vs. glassy vs. semicrystalline) which will strongly affect mechanical strength, thermal stability, chemical resistance and transport properties [6]. In most polymeric membranes, the polymer is in an amorphous state. However, some polymers, especially those with flexible chains of regular chemical structure (e.g., polyethylene/PE/, polypropylene/PP/or poly(vinylidene fluoride)/PVDF/), tend to form crystalline... [Pg.22]

Vinylidene fluoride is manufactured by the thermal elimination of hydrogen chloride from l-chloro-l,l-dilluoroe1hane. The starting material (1-chloro-1,1-difluoroethane) is manufactured by any of several different routes. [Pg.548]

Less common in practice is poly(trifluoroethylene). Poly(trifluoroethylene) behaves during thermal decomposition similarly to poly(vinylidene fluoride). A study on thermal decomposition of this polymer between 380° C and 800° C showed the formation of high yields of HF and of some nonvolatile products [42]. [Pg.291]

Difluoroethylene is used in the manufacture of poly-vinylidene fluoride, which is used as a thermal. [Pg.854]

Another example of the use of polarized radiation in imaging studies is the analysis of poly(vinylidene fluoride)(PVDF) films, which have been uniaxially elongated at different temperatures. Depending on the thermal, mechanical and electrical pretreatment, PVDF can exist in different modifications [59]. The crystal structure of the cmmpled 11(a) modification can be converted into the aU-tra s 1(P) form by tensile stress below 140°C (see Figure 9.27a). Figure 9.27b shows the stress-strain diagrams of PVDF films in the 11(a) form which have been elongated to 400 % strain at 100 and 150°C. The observed decrease in stress upon elevation of the... [Pg.324]

This paper presents details of a new, low-cost, continuous process in which pellets of poly(vinylidene fluoride) (PVDF) are directly converted into piezoelectric tube. Kawai s paper in 1969 (1 ) described a batch process for making PVDF piezoelectric by stretching filmB at an elevated temperature and subsequently applying a high electric field to the electroded and heated films (thermal poling). Since then many variations of this technique have been described. Southgate in 1976 (2) demonstrated that... [Pg.399]

Vinylidene Fluoride Hexafluoropropylene Copolymer - Thermoplastic copolymer of vinylidene fluoride and hexafluoropropylene. Has better thermal stability, antistick, dielectric, and antifriction properties, and chemical resistance, but lower mechanical strength at room temperature and creep resistance, compared to incompletely fluorinated fluoropolymers. Processing by conventional thermoplastic techniques is difficult due to its high melt viscosity. Uses include chemical apparatus, containers, films, and coatings. Also called TAM... [Pg.547]

Chiu (116) used the apparatus previously described to study the thermal decomposition of selected polymers such as polyethylene terephthalate), po y(vinyl fluoride), po y(vinylidene fluoride), and others. The dielectric constant curves of a group of fluorocarbon polymers are shown in Figure 11.33. As illustrated, the more polar polymers such as poly(vinylidinefiuoride) (PVDF) and poly(vinyl fluoride) (PVF) show characteristic dielectric loss peaks that are distinguishable from the relatively featureless and low-loss curves of the other polymers. For PVF, the low-temperature process is due... [Pg.724]

Loufakis K, Wunderlich B (1987) Thermal analysis of the conformational disorder in semicrystalline poly(vinylidene fluoride) and polytrifluoroethylene. Macromolecules, 20 2474... [Pg.112]

Ghasem, N., Al-Marzouqi, M., Duaidar, A. 2011. Effect of quenching temperature on the performance of poly(vinylidene fluoride) microporous hollow fiber membranes fabricated via thermally induced phase separation technique on the removal of CO2 from C02-gas mixture. Int. J. Greenh. Gas Control 5 1550-1558. [Pg.785]

Synonyms FPM Vinylidenefluoride/hexafluoropropylene copolymer IMinUon Elastomer consisting of 60-85% vinylidene fluoride gt thermal props, and chem. resist. [Pg.1137]


See other pages where Vinylidene fluoride thermal is mentioned: [Pg.639]    [Pg.360]    [Pg.70]    [Pg.220]    [Pg.294]    [Pg.115]    [Pg.294]    [Pg.109]    [Pg.22]    [Pg.17]    [Pg.152]    [Pg.150]    [Pg.320]    [Pg.63]    [Pg.123]    [Pg.332]    [Pg.100]    [Pg.173]    [Pg.289]    [Pg.299]    [Pg.2384]    [Pg.377]    [Pg.109]    [Pg.451]    [Pg.212]    [Pg.45]    [Pg.330]    [Pg.831]    [Pg.153]   
See also in sourсe #XX -- [ Pg.211 ]




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