Abstract
AbstractThe flow‐assisted degradation behavior of polystyrene was studied as a function of solvent, polymer concentration, molecular weight, and molecular weight distribution. To obtain data at concentrations as low as 100 parts per million by weight, turbulent drag reduction measurements were used to augment the usual analytical techniques of viscosity and gel permeation chromatography. Turbulent flow measurements were found to be a valuable technique for evaluating the effects of degradation: the drag reduction onset point provides information about the largest molecules in the sample while the flow rate dependence is related to the shape of the top part of the molecular weight distribution. For the polymers and flow conditions studied, the degradation causes a shift in the distribution to lower molecular weights with little change in the shape. This suggests a complex mechanism where the probability of bond scission is not random but varies along the polymer backbone.
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