Abstract
Abstract A method of molecular weight calibration was devised for various substituted liquid crystalline polymers with substantial molecular weight repeat units. With the use of gel permeation chromatography, oligomer peak separation was achieved offering a method for self calibration for molecular weight distribution determinations. Employing an overlay of a low molecular weight polystyrene standard, a retention time marker was utilized as a source from which to mark an oligomer peak. The calibration plot produced using this technique showed much better correlation coefficients than that of the polystyrene calibration plot. In addition, molecular weight determinations made from the two techniques yielded two distinct molecular weight averages and distributions, indicating polystyrene to be a poor relative calibration method for the liquid crystalline polymers tested. The technique illustrates the utility of alternative calibration methods when samples show certain physical characteristics.
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