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More rapid sample heating and cooling rates by RHDSC (CAT#: STEM-MB-0505-WXH)

Introduction

IR-heated DSC is a heat-flux DSC, which is comprised of a DSC sensor assembly for receiving a sample that is installed in a cavity within an elongated cylinder and an IR lamp assembly disposed of circumferentially around the elongated cylinder having a length substantially similar to that of the cylinder.
This type of DSC is configured to provide more rapid sample heating and cooling rates in comparison with conventional systems. IR-heated DSC is also named as rapid-heating DSC (RHDSC). The calorimeter can offer heating rates up to 2000°C/min, providing a new opportunity to characterize unstable polymorphs as a result of the likelihood that form changes can be inhibited at higher heating rates.




Principle

Calorimetry is a primary technique for measuring the thermal properties of materials to establish a connection between temperature and specific physical properties of substances and is the only method for direct determination of the enthalpy associated with the process of interest. Calorimeters are used frequently in chemistry, biochemistry, cell biology, biotechnology, pharmacology, and recently, in nanoscience to measure thermodynamic properties of the biomolecules and nano-sized materials.
Amongst various types of calorimeters, differential scanning calorimeter (DSC) is a popular one. DSC is a thermal analysis apparatus measuring how physical properties of a sample change, along with temperature against time.1In other words, the device is a thermal analysis instrument that determines the temperature and heat flow associated with material transitions as a function of time and temperature. During a change in temperature, DSC measures a heat quantity, which is radiated or absorbed excessively by the sample on the basis of a temperature difference between the sample and the reference material.

Applications

Providing more rapid sample heating and cooling rates in comparison with conventional systems.
Providing a new opportunity to characterize unstable polymorphs.

Procedure

1. Instrument Start-up
2. Sample Preparation
(1) Dialyze the sample against the buffer that will be used as the reference for the experiment.
(2) Determine the concentration of the protein sample using the most suitable protein concentration determination method.
(3) Degas the sample and reference buffer in vacuum to get rid of microbubbles that can cause volume inaccuracy.
(4) load the samples and their respective buffer in pairs into 96 well plates compatible with the instrument.
(5) Place the plate in the sample holding compartment in the proper orientation.
3. Experimental Parameter Setup
Set the starting temperature, final temperature and the scan rate of the experiment.
4. Data Analysis

Materials

Differential Scanning Calorimeters
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