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Differential scanning calorimetry (DSC) is a thermoanalytical technique in which the difference in the amount of heat required to increase the temperature of a sample and reference is measured as a function of temperature. [1] Both the sample and reference are maintained at nearly the same temperature throughout the experiment.
An example is oxidation induction time by differential scanning calorimetry which can determine the amount of oxidation stabiliser present in a thermoplastic (usually a polyolefin) polymer material. Compositional analysis is often made using thermogravimetric analysis, which can separate fillers, polymer resin and other additives.
This technique uses differential scanning calorimetry (DSC) to detect the phase changes. The signal detection relies on transient heat flows of latent heat of fusion at the phase changes, and thus the measurement can not be made arbitrarily slowly, limiting the resolution in pore size. There are also difficulties in obtaining measurements of ...
An example is a coffee-cup calorimeter, which is constructed from two nested Styrofoam cups, providing insulation from the surroundings, and a lid with two holes, allowing insertion of a thermometer and a stirring rod. The inner cup holds a known amount of a solvent, usually water, that absorbs the heat from the reaction.
where ln denotes the natural logarithm, is the thermodynamic equilibrium constant, and R is the ideal gas constant.This equation is exact at any one temperature and all pressures, derived from the requirement that the Gibbs free energy of reaction be stationary in a state of chemical equilibrium.
Characteristic DSC curve for a polyethylene, the OIT is measured. Oxidation induction time or OIT is a standardized test performed in a DSC which measures the level of thermal stabilization of the material tested. The time between melting and the onset of decomposition in isothermal conditions is measured.
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Differential thermal analysis (DTA) is a thermoanalytic technique that is similar to differential scanning calorimetry.In DTA, the material under study and an inert reference are made to undergo identical thermal cycles, (i.e., same cooling or heating programme) while recording any temperature difference between sample and reference. [1]