The Wiley Database of Polymer Properties 1999
DOI: 10.1002/0471532053.bra029
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Physical Constants of Poly(vinyl acetate)

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Cited by 4 publications
(3 citation statements)
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“…5 displays the DSC traces and the glass transition temperatures (T g ) of the pure homopolymers and the copolymers synthesized in the presence of various amounts of thiocol. The T g s determined for both thiocol (T g = À56.1°C) and PVAc (T g = 30.4°C) were in good agreement with the values reported in literature for these polymers [1,30], while in the case of the copolymers, the DSC analysis revealed only one glass transition in each case, placed in-between those of pure homopolymers. The T g of the copolymers diminished as F VAc decreased, as encountered in the case of statistical copolymers.…”
Section: Ss ð%þ ¼supporting
confidence: 88%
“…5 displays the DSC traces and the glass transition temperatures (T g ) of the pure homopolymers and the copolymers synthesized in the presence of various amounts of thiocol. The T g s determined for both thiocol (T g = À56.1°C) and PVAc (T g = 30.4°C) were in good agreement with the values reported in literature for these polymers [1,30], while in the case of the copolymers, the DSC analysis revealed only one glass transition in each case, placed in-between those of pure homopolymers. The T g of the copolymers diminished as F VAc decreased, as encountered in the case of statistical copolymers.…”
Section: Ss ð%þ ¼supporting
confidence: 88%
“…The conversion between vol% and wt% was carried out by using the values of 1.19 and 1.50 g/cm 3 for PVAc (Lindemann 1989) and sisal whisker (Gindl and Keckes 2004), respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The value of k −C O has not been measured in PVAc or in ethyl acetate. Because the relative permittivities (Riddick et al 1986, Lindemann 1999 of isooctane (ε = 1.94), ethyl acetate (ε = 6.02), and PVAc films (ε = 3.5 at 50 • C) are similar, we use k −C O in isooctane for the values in ethyl acetate and PVAc. As mentioned above, radicals in both of the radical pairs can diffuse from their initial solvent cages and undergo out-of-cage reactions that result in fragmentation products (3-5), radical pair B-like combination products (2, 2BN, and 4BN but from different original partners), and a crossed combination product, 2,3-diphenylbutane (6) (Scheme 2).…”
Section: Combinations Of Radical Pairs a And B From (R)-1 General Comentioning
confidence: 99%