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A cooling curve of naphthalene from liquid to solid. A cooling curve is a line graph that represents the change of phase of matter, typically from a gas to a solid or a liquid to a solid. The independent variable (X-axis) is time and the dependent variable (Y-axis) is temperature. [1] Below is an example of a cooling curve used in castings.
The main feature of thermodynamic diagrams is the equivalence between the area in the diagram and energy. When air changes pressure and temperature during a process and prescribes a closed curve within the diagram the area enclosed by this curve is proportional to the energy which has been gained or released by the air.
Diffusional transformations like austenite transforming to a cementite and ferrite mixture can be explained using the sigmoidal curve; for example the beginning of pearlitic transformation is represented by the pearlite start (P s) curve. This transformation is complete at P f curve. Nucleation requires an incubation time.
Triple points mark conditions at which three different phases can coexist. For example, the water phase diagram has a triple point corresponding to the single temperature and pressure at which solid, liquid, and gaseous water can coexist in a stable equilibrium (273.16 K and a partial vapor pressure of 611.657 Pa).
There are two types of continuous cooling diagrams drawn for practical purposes. Type 1: This is the plot beginning with the transformation start point, cooling with a specific transformation fraction and ending with a transformation finish temperature for all products against transformation time for each cooling curve.
English: Example of a cooling curve of a pure metal or eutectic alloy, with various aspects pointed out. Based on image from Degarmo, E. Paul; Black, J T.; Kohser, Ronald A. (2003), Materials and Processes in Manufacturing (9th ed.), Wiley, ISBN 0-471-65653-4 .
The upper curve is the line of liquidus, and the lower curve is the line of solidus. In chemistry , materials science , and physics , the liquidus temperature specifies the temperature above which a material is completely liquid, [ 2 ] and the maximum temperature at which crystals can co-exist with the melt in thermodynamic equilibrium .
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]