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Hexane diol diacrylate

PU-based acrylate-terminated polymers have also been introduced for use in UV-cured or electron beam (EB)-cured elastomer coatings. They are usually used in conjunction with di- or trifunctional acrylate resins such as 1,6-hexane diol diacrylate (HDDA) (Fig. 12.8) whose function is to control hardness and flexibility in the final elastomeric lacquer. A series of these special monomers and urethane oligomers is marketed under the trade name Photomer (Harcross Chemicals). [Pg.352]

Rolla et ah, used microwave dielectric measurements to monitor the polymerization process of mono functional n-butyl acrylate as well as 50/50 w/w blends with a difunctional hexane-diol diacrylate that gave highly cross-linked networks. In these real time cure experiments the decreasing acrylate monomer concentration was studied via a linear correlation with the dielectric loss index at microwave frequencies. This correlation is a result of the largely different time scales for dipolar polarization in the monomer on one hand and in the polymerized reaction product on the other hand. [Pg.186]

Poly(vinyl chloride) 40 36 Hexane diol diacrylate (HDDA)... [Pg.154]

H (xi, X2,. Xs) Hamiltonian function HDDA hexane-l,6-diol diacrylate... [Pg.322]


See other pages where Hexane diol diacrylate is mentioned: [Pg.113]    [Pg.246]    [Pg.352]    [Pg.113]    [Pg.65]    [Pg.399]    [Pg.146]    [Pg.246]    [Pg.352]    [Pg.54]    [Pg.25]    [Pg.399]    [Pg.350]    [Pg.9]    [Pg.85]   
See also in sourсe #XX -- [ Pg.214 ]

See also in sourсe #XX -- [ Pg.246 ]




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Diacrylate

Diacrylates

Hexane-1,6-diol

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