Abstract
Lower critical solubility temperatures ( LCST) of linear polyethylene (PE), isotactic polypropylene (PP) and of five random ethylene-propylene (EP) copolymers of different composition have been measured in (i) five linear alkanes (n-C 5 to n-C 9); (ii) sixteen branched alkanes and (iii) four cycloalkanes. The effect of correlations of molecular orientations ( CMO) on the LCST was investigated. The main results of this work are the following: (1) the LCST for PE are much lower than those for PP although the expansion coefficients of the two polymers are similar. Calculations using the van der Waals model for a liquid would predict them 10° to 20° apart while the experimental difference can reach 90°. (2) In PE solutions, the linear alkanes are much better solvents than those which are branched. This constitutes a rare example in non-polar solutions in which the magnitude of the equation of state term is not sufficient to predict or even to compare the LCST. The importance on x of polymer-segment and solvent shapes even above the boiling point of the solvent is to be noted. (3) The LCST of the five copolymer samples are almost a linear function of their composition over all the composition range. (4) These results can be understood if the existence of CMO between the (CH 2Ch 2) sequences is assumed in the pure PE melt and in the copolymers but not between the CH(CH 3)CH 2 sequences. CMO in solution between the polymeric chains and the linear alkanes make the linear alkanes better solvents than the branched ones. From LCST data in n-C 7 and its isomers, the temperature to which CMO in PE disappear can be estimated to be above 170°C, a value which is consistent with those found for long linear alkanes. (5) Branched volatile alkanes such as 2,2-dimethylpentane appear to be a good choice for dosage of the ethylene content of an EP copolymer because of the large interval of LCST between PP and PE in such solvents. LCST measurements could become a sensitive and routine analytical tool for polymer and copolymer characterization for some polymers in well-chosen solvents.
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