Thermal Analysis
Thermal analysis provides very useful and relevant information for a number of various materials. By utilizing various techniques, H&M can determine the melting point, glass transition temperature, weight loss, specific heat and other material properties. This is achieved by employing 2 different but complimentary characterization techniques, thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC).
Thermal Gravimetric Analysis
TGA can measure the changes in a samples weight in a controlled environment as a function of either temperature or time. The weight loss occurs due to the changing of chemical or physical properties and can be detected down to fractions of a micro-gram. Based on the type of sample and information that’s required, the test can be performed by fixing the temperature over a range of time or by ramping the temperature over a fixed time period. Both of these methodologies provide information of thermal stability.
Differential Scanning Calorimetry
DSC consists of exposing a small quantity of a sample, typically 0.5 to 100 mg, to a controlled heating program with a known reference material in the chamber in order to measure the temperature difference between them. If the sample undergoes a thermal event that absorbs more heat than the reference, this corresponds to a decrease in the heat flow on the DSC and is called an endothermic process. An example of this behavior is once a material reaches its melting point. The opposite reaction is called an exothermic event and this occurs when the DSC displays an increase in heat flow compared to the reference. An example of this behavior is a crystallization point for a specified material. Determining the exact point of these transitions is important in evaluating the presence of a polymorph in pharmaceutical samples or identifying an unknown material or phase. Standard steady state heating cycles, multiple heating or cooling ramps, and isothermal holds can be utilized to study different thermal events.
Main Applications of Thermal Analysis
TGA
- Thermal stability of a solid or liquid
- Decomposition kinetics of volatile materials
- Absorbed moisture content
- Screening of additives
DSC
- Characterization of phase transitions in glasses and other materials
- Determining the heat capacity
- Oxidative stability
- ID of unknown impurities in materials
- Characterizing polymorphic materials
Detailed Analysis
Technical Specifications of Equipment
TGA
- Signal detected: Mass and temperature change
- Sample size range: 10 mg to 1 g
- Temperature range: Ambient to 1000°C
- Controlled heating rate: 0.01 to 100°C/minute
- Weighing precision: +/- 0.01%
DSC
- Temperature range: -40°C to 400°C
- Controlled heating rate: 0.01 to 200°C/minute
- Temperature accuracy: +/- 0.1°C
- Temperature precision: +/- 0.05°C
- Sample size Range: 0.5 mg to 100 mg
Key Markets Served
- Pharmaceuticals
- Semiconductors
- Coatings and Adhesives
- Glass Manufacturing
- Polymers & Plastics
- Aerospace
- Solar and Lighting
- Defense
- Data Storage
- Raw Chemicals
- Personal Care
- Packaging
- Life Sciences
- Law and Litigation



