Journal
MACROMOLECULES
Volume 39, Issue 17, Pages 5760-5767Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ma060340q
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A comparative study on the influence of chemical structure and solubility of a series of low molecular-weight 1,4-phenylene-bisamides in isotactic polypropylene (i-PP) was conducted to explore their performance as nucleating agents and electret additives. The series consists of three isomers of dicyclohexylsubstituted 1,4-phenylene-bisamide and three asymmetrically substituted cyclohexyl/n-alkyl-1,4-phenylenebisamides with different chain lengths. The symmetry of the molecules, the type of substitution and the length of the alkyl chain influence the solubility in the i-PP melt, the nucleation efficiency, the ratio of the alpha-to beta-crystal modification and the charge storage properties. The best,beta-nucleating efficiency was observed for the symmetrically substituted compounds, whereas the nucleation efficiency was substantially reduced in the presence of n-alkylsubstituents. The charge storage behavior of i-PP was improved only for the three dicyclohexyl-substituted 1,4phenylene bisamides at concentrations of 100 ppm and even below. For example, a film comprising 10 ppm additive displayed charge retention of 90% after an accelerated aging (annealing for 24 h at 90 degrees C).
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