Title of article :
Synthesis and properties of propene copolymers with ether comonomers
Author/Authors :
Ulrich Schulze، نويسنده , , Doris Pospiech، نويسنده , , Hartmut Komber، نويسنده , , Liane H?ussler، نويسنده , , Dieter Voigt، نويسنده , , Michael Eschner، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
10
From page :
694
To page :
703
Abstract :
The direct copolymerization of propene with polar comonomers using metallocene catalysts in solution was investigated. As comonomers, two ether compounds were used in comparison to 10-undecene-1-ol as well-investigated comonomer. The ether comonomers were diethylene glycol mono-10-undecenyl ether (DEGUE) and octaethylene glycol-10-undecenyl methyl ether (OEGUME). The influence of the different comonomers on the copolymerization behavior was studied. The copolymers were characterized with respect to their comonomer contents, molar masses, and thermal properties. The incorporation rate of DEGUE and OEGUME into the propene copolymers did not exceed 1.6 mol% for DEGUE and 0.31 mol% for OEGUME and was thus considerably lower than in the reference propene copolymerization with 10-undecene-1-ol. An uncompleted shielding of the oxygen atoms of the ether groups by triisobutyl aluminum (TIBA) to the metallocene catalyst is assumed to be responsible for this behavior. The crystallization kinetics in the copolymers with comparable molar masses is mainly influenced by the side chain density per 1000 propene units, n1000. The incorporation of hydrophilic comonomers into polypropene was expected to alter the surface properties. The slightly lowered water contact angles found on films of copolymers with higher comonomer content indicated the enhanced hydrophilicity of the polypropene copolymer surfaces compared to polypropene (PP).
Keywords :
Copolymerization , PP , Metallocene Catalysts , Functionalization , Polar comonomers
Journal title :
European Polymer Journal(EPJ)
Serial Year :
2008
Journal title :
European Polymer Journal(EPJ)
Record number :
1227558
Link To Document :
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