Phase diagram H2O saturation pressure

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SUMMARY

The discussion focuses on the thermodynamic behavior of 2 kg of H2O at 200°C and 300 kPa, specifically examining the changes in volume, internal energy, and enthalpy as the temperature increases to 400°C at constant pressure. The saturation pressure of H2O at 200°C is 1.5536 MPa, indicating that the process occurs in the superheated region rather than the compressed liquid region. The participant emphasizes the importance of understanding phase diagrams and the unique properties of different substances, noting that while water behaves predictably, other chemicals may require distinct p-v diagrams or steam tables for accurate phase determination.

PREREQUISITES
  • Understanding of thermodynamic principles, specifically the ideal gas law and phase changes.
  • Familiarity with p-v diagrams and steam tables for H2O.
  • Knowledge of internal energy and enthalpy calculations in thermodynamics.
  • Experience with constant pressure processes in thermodynamic systems.
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  • Learn about the construction and interpretation of phase diagrams for various substances.
  • Explore the differences in behavior between saturated and superheated vapor states in thermodynamics.
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Homework Statement


Suppose 2 kg of H2O at 200 C and 300 kPa are contained in a weighted piston cylinder assembly. As a result of heating at constant pressure, the temperature of the H2O increases to 400 C. Determine the change in volume, the change in internal energy, and the change in enthalpy of the H2O for this process.


Homework Equations


By consulting water table, at 200 C the pressure of H2O is 1.5536 MPa.


The Attempt at a Solution


This is a textbook example, so the answer is already known. However, my question is in regards to the concept.

I have attached a figure, and everything in it is correct EXCEPT the brown line with a arrow in the left side (this is my own work). Everything else is copied direct from the book. The blue arrow is the actual process of this problem.

By consulting the table, 300 kPa is obviously smaller than the saturation pressure of 1.5 MPa, and since we know Pressure is constant, this process must proceed at a pressure lower than P saturation. My question is why can't this process occur in the compressed liquid region (brown arrow)? Why the superheated region? Obviously since this is H2O, I know that's physically not possible at 200 C, but what if the substance were to be changed into something I don't know about? For example if a unknown chemical substance was used instead, and the only thing I can go by to determine its phase is the pressure difference, how do I determine whether it is in the super-heated vapor region or compressed liquid region?
 

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You're told it's water. Believe it! Other substances behave differently, some extremely differently, and you'd need separate p-v diagrams or steam tables for all of them.

With 2kg of water at p = 300 kPa and T = 200C there is one and only one place on your p-v diagram where your point 1 could be. That is as shown by the left end of your blue line.

(Replace v by V = 2000v to get your actual volume on your p-v chart, then it's obvious).

I don't understand your reference to 'saturation pressure'.
 

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