nonmotofacient phase - vertaling naar arabisch
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nonmotofacient phase - vertaling naar arabisch

GENERAL PRINCIPLE IN THERMODYNAMICS REGARDING PVT SYSTEMS IN EQUILIBRIUM
Gibbs phase rule; Phase equilibria; Phase equilibrium; Phase Equilibria; Gibbs' Phase Rule; Gibb's phase rule; Phase Rule; Gibbs Phase Rule; Gibbs rule; Gibbs' phase rule; Gibbs's phase rule
  • critical point]] of carbon dioxide

nonmotofacient phase      
‎ الطَّورُ الغَيْرُ المُحْدِثِ للحَرَكَة‎
change of state         
  • A small piece of rapidly melting solid [[argon]] shows two concurrent phase changes. The transition from solid to liquid, and gas to liquid (shown by the white condensed water vapour).
  • Comparison of phase diagrams of carbon dioxide (red) and water (blue) explaining their different phase transitions at 1 atmosphere
  • the anomalous behavior of water]].
TRANSITIONS BETWEEN SOLID, LIQUID AND GASEOUS STATES OF MATTER, AND, IN RARE CASES, PLASMA
Phase transitions; Second order phase transition; First order phase transition; Order parameter; Phase Transition; Second-order phase transition; Phase changes; Phase transformation; Change of state; State change; Phase Transformation; First-order phase transition; First-order transition; Second-order transition; Continuous Phase Transitions; Second-Order Phase Transitions; Phase Transitions; Phase Change; Phase Changes; State Change; State Changes; Changes Of Phase; Change Of Phase; Changes Of State; Change Of State; Continuous phase transitions; Continuous phase transition; Change of phase; Order parameters; Transition of state
تغير او تغيير الحالة ، إستحالة
phase         
WIKIMEDIA DISAMBIGUATION PAGE
Phases; Phase (disambiguation); Phase (physics); Phases (album)
طَوْر

Definitie

phase angle
¦ noun
1. Physics a phase difference expressed as an angle, 360 degrees corresponding to one complete cycle.
2. Astronomy the angle between the lines joining a given planet to the sun and to the earth.

Wikipedia

Phase rule

In thermodynamics, the phase rule is a general principle governing "pVT" systems, whose thermodynamic states are completely described by the variables pressure (p), volume (V) and temperature (T), in thermodynamic equilibrium. If F is the number of degrees of freedom, C is the number of components and P is the number of phases, then

F = C P + 2 {\displaystyle F=C-P+2} : 123–125 

It was derived by American physicist Josiah Willard Gibbs in his landmark paper titled On the Equilibrium of Heterogeneous Substances, published in parts between 1875 and 1878. The rule assumes the components do not react with each other.

The number of degrees of freedom is the number of independent intensive variables, i.e. the largest number of thermodynamic parameters such as temperature or pressure that can be varied simultaneously and arbitrarily without determining one another. An example of one-component system is a system involving one pure chemical, while two-component systems, such as mixtures of water and ethanol, have two chemically independent components, and so on. Typical phases are solids, liquids and gases.