A calorimeter is a device used for calorimetry, the science of measuring the heat of chemical reactions or physical changes as well as heat capacity. The word calorimeter is derived from the Latin word calor, meaning heat. The constant-volume calorimeter is the most common type of calorimeter.
A bomb calorimeter is a type of constant-volume calorimeter capable of withstanding the large pressure and force of explosive reactions.
Inevitably there will always be some heat loss from a calorimeter. One method of accounting for this is to use an electrical heater to produce the same temperature change over the same time period in the calorimeter as the reaction being measured. The electrical energy supplied to produce the temperature change is equal to the energy change that occurred in the reaction. Another method is to keep the temperature of the water surrounding the reaction vessel constant by heating or cooling it, and to measure the energy that is required to do this. This can then be used in calculations to produce extremely accurate results for energy changes.
An example is a coffee-cup calorimeter, which is constructed from two nested Styrofoam cups and holes through which a thermometer and a stirring rod can be inserted. The inner cup holds the solution in which the reaction occurs, and the outer cup provides insulation.
In a heat flux DSC, both pans sit on a small slab of material with a known (calibrated) heat resistance K. The temperature of the calorimeter is raised linearly with time (scanned), i.e., the heating rate dT/dt = β is kept constant. This time linearity requires good design and good (computerized) temperature control. Of course, controlled cooling and isothermal experiments are also possible.
Heat flows into the two pans by conduction. The flow of heat into the sample is larger because of its heat capacity Cp. The difference in flow dq/dt induces a small temperature difference ΔT across the slab. This temperature difference is measured using a thermocouple. The heat capacity can in principle be determined from this signal:
Note that this formula (equivalent to Newton's law of heat flow) is analogous to, and much older than, Ohm's law of electric flow: ΔV = R dQ/dt = R I.
When suddenly heat is absorbed by the sample (e.g., when the sample melts), the signal will respond and exhibit a peak.
From the integral of this peak the enthalpy of melting can be determined, and from its onset the melting temperature.
Differential scanning calorimetry is a workhorse technique in many fields, particularly in polymer characterization.
A modulated temperature differential scanning calorimeter (MTDSC) is a type of DSC in which a small oscillation is imposed upon the otherwise linear heating rate. This has a number of advantages. It facilitates the direct measurement of the heat capacity in one measurement, even in (quasi-)isothermal conditions. It permits the simultaneous measurement of heat effects that are reversible and not reversible at the timescale of the oscillation (reversing and non-reversing heat flow, respectively). It increases the sensitivity of the heat capacity measurement, allowing for scans at a slow underlying heating rate.
The technique is gaining in importance particularly in the field of biochemistry, because it facilitates determination of substrate binding to enzymes.
Measuring instruments | Laboratory equipment
Каларыметры | Kalorimetr | Kalorimeter | Calorímetro | Calorimetro | קלורימטר | Calorimeter | Kalorymetr | Calorimeter | Kalorimetre
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