POLYMER ANALYSIS SOLUTIONS
Guides | 2016 | PerkinElmerInstrumentation
Dynamic Scanning Calorimetry (DSC) is widely used to study thermal transitions in polymers and pharmaceuticals, but conventional DSC methods (10–40 °C/min) can lack sensitivity, distort weak transitions, and require lengthy runs. HyperDSC, a fast-scanning power-compensation DSC technique (up to 500 °C/min heating and cooling), provides up to 10× increased throughput, higher sensitivity for minute samples, and suppression of kinetic artifacts (re-crystallization or decomposition).
• Ultra-low-mass, rapid-response furnaces enable controllable scan rates of 100–500 °C/min under true power compensation.
• Direct heat-flow measurement (mW) eliminates heat-flux DSC mathematical corrections.
• Fast cooling/heating minimizes sample reorganization before thermal events, preserving true as-received behavior.
• Glass-transition detection: Polypropylene Tg (~0 °C) obscured at 10 °C/min emerges clearly at 150 °C/min in <2 min.
• Polymorphic analysis: Carbamazepine exhibits two thermal events; the minor dehydration peak is distinguished from the polymorphic transition, independent of scan rate.
• Crystallization study: Cooling polyethylene blends at 150 °C/min alters crystallization behavior, revealing distinct peaks vs. slow cooling.
• Film characterization: Biaxial-oriented PP films show distinct melting shifts (157 °C vs. 166 °C) at 200 °C/min, versus overlapping peaks at 10 °C/min.
• Multilayer and thin samples: HyperDSC can analyze microgram-scale materials (coatings, laminates) with enhanced sensitivity.
• Calibration: Use indium and lead standards; verify baseline stability before/after runs.
• Sample size: 1–10 mg for typical measurements; smaller masses yield higher signal/noise at fast rates.
• Cooling accessories: Intracooler (N₂) or CryoFill (LN₂) enable fast controlled cooling.
• Data analysis: Second derivative curves highlight closely spaced transitions at high scan rates.
HyperDSC uniquely combines speed, sensitivity, and artifact suppression to accelerate DSC analysis and reveal fine thermal transitions otherwise masked in conventional DSC. It enables high-throughput screening, accurate polymorphic and crystallization studies, and direct analysis of process-conditioned materials. This makes it an indispensable tool for polymers, pharmaceuticals, and advanced materials development, reducing time-to-market and ensuring deeper insight into material behavior.
• Integration with kinetic modeling for lifetime predictions under realistic thermal profiles.
• Coupling HyperDSC with in-situ spectroscopy or rheometry for simultaneous thermal, structural, and mechanical analysis.
• Expanded use in additive manufacturing (3D printing) to optimize layer crystallization during rapid heating cycles.
• Application to nanocomposites and ultrathin films (<1 μm) for electronics and barrier coatings.
1. Pijpers et al., Macromolecules, 2002, 35, 3601–3613.
2. Ford & Mann, TAC2002, UK.
3. Eder & Janeschitz-Kriegl, Processing of Polymers, VCH, 1997.
4. Mathot, Calorimetry and Thermal Analysis of Polymers, Hanser, 1994.
5. Wunderlich, Macromolecular Physics Vol. 3, Academic Press, 1980.
GC/MSD, HeadSpace, GC/SQ
IndustriesEnergy & Chemicals
ManufacturerPerkinElmer
Summary
Importance of HyperDSC in Material Characterization
Dynamic Scanning Calorimetry (DSC) is widely used to study thermal transitions in polymers and pharmaceuticals, but conventional DSC methods (10–40 °C/min) can lack sensitivity, distort weak transitions, and require lengthy runs. HyperDSC, a fast-scanning power-compensation DSC technique (up to 500 °C/min heating and cooling), provides up to 10× increased throughput, higher sensitivity for minute samples, and suppression of kinetic artifacts (re-crystallization or decomposition).
Principles of HyperDSC
• Ultra-low-mass, rapid-response furnaces enable controllable scan rates of 100–500 °C/min under true power compensation.
• Direct heat-flow measurement (mW) eliminates heat-flux DSC mathematical corrections.
• Fast cooling/heating minimizes sample reorganization before thermal events, preserving true as-received behavior.
Applications and Benefits
• Glass-transition detection: Polypropylene Tg (~0 °C) obscured at 10 °C/min emerges clearly at 150 °C/min in <2 min.
• Polymorphic analysis: Carbamazepine exhibits two thermal events; the minor dehydration peak is distinguished from the polymorphic transition, independent of scan rate.
• Crystallization study: Cooling polyethylene blends at 150 °C/min alters crystallization behavior, revealing distinct peaks vs. slow cooling.
• Film characterization: Biaxial-oriented PP films show distinct melting shifts (157 °C vs. 166 °C) at 200 °C/min, versus overlapping peaks at 10 °C/min.
• Multilayer and thin samples: HyperDSC can analyze microgram-scale materials (coatings, laminates) with enhanced sensitivity.
Practical Considerations
• Calibration: Use indium and lead standards; verify baseline stability before/after runs.
• Sample size: 1–10 mg for typical measurements; smaller masses yield higher signal/noise at fast rates.
• Cooling accessories: Intracooler (N₂) or CryoFill (LN₂) enable fast controlled cooling.
• Data analysis: Second derivative curves highlight closely spaced transitions at high scan rates.
Conclusion
HyperDSC uniquely combines speed, sensitivity, and artifact suppression to accelerate DSC analysis and reveal fine thermal transitions otherwise masked in conventional DSC. It enables high-throughput screening, accurate polymorphic and crystallization studies, and direct analysis of process-conditioned materials. This makes it an indispensable tool for polymers, pharmaceuticals, and advanced materials development, reducing time-to-market and ensuring deeper insight into material behavior.
Future Trends and Applications
• Integration with kinetic modeling for lifetime predictions under realistic thermal profiles.
• Coupling HyperDSC with in-situ spectroscopy or rheometry for simultaneous thermal, structural, and mechanical analysis.
• Expanded use in additive manufacturing (3D printing) to optimize layer crystallization during rapid heating cycles.
• Application to nanocomposites and ultrathin films (<1 μm) for electronics and barrier coatings.
References
1. Pijpers et al., Macromolecules, 2002, 35, 3601–3613.
2. Ford & Mann, TAC2002, UK.
3. Eder & Janeschitz-Kriegl, Processing of Polymers, VCH, 1997.
4. Mathot, Calorimetry and Thermal Analysis of Polymers, Hanser, 1994.
5. Wunderlich, Macromolecular Physics Vol. 3, Academic Press, 1980.
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