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A Study of Mechanical Degradation of Polymer in High Performance GPC
16
Citations
2
References
1982
Year
Mechanical DegradationEngineeringMacromolecular ChemistryMechanical EngineeringMolecular WeightsChemistryPolymersChemical EngineeringPolymer ProcessingHigh PressureAnalytical ChemistryPlastic DegradationPolymer ChemistryChromatographyMaterials SciencePolymer StabilityPolymer EngineeringBiopolymersPolymer AnalysisHigh Performance GpcMacromolecular SciencePolymer SolutionPolymer SciencePolymer CharacterizationMolecular WeightMechanics Of Materials
Abstract Four narrow distribution polystyrene samples (M = 2.7 × 106, 6 × 106, 6.5 × 106, 7 × 106) were dissolved in tetrahydrofuran and the solutions were passed through a Shodex A-80M column at a concentration of approximately 1 × 10−3 g/ml, injection volume of 500 microliters, and a flow rate of 2 ml/min (i.e., maximun flow rate allowable for this column). Molecular weights of eluants were then determined by viscosity and laser light scattering methods; concentrations were determined by ultra-violet spectrophotometry. From the results of analysis of the eluate, it was shown that no significant degradation was detectable for all four samples in this colulmn which was packed with a cross-linked polystyrene gel. When a silica gel (irregular shaped) column was used, under same operating conditions, only sample PS-4, with a molecular weight of M = 7 × 106 underwent degradation up to 15%. High pressure exerted on the column is believed to be the main cause of the degradation.
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