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Vapor pressure

Vapor pressure is a physics topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Vapor pressure rather than just read about it. In short: Vapor pressure or equilibrium vapor pressure is the pressure exerted by a vapor in thermodynamic equilibrium with its condensed phases (solid or liquid) at a given temperature in a closed system. The equilibrium vapor pressure is an indication of a liquid's thermodynamic tendency to evaporate.

Vapor pressure — main illustration
Vapor pressure — illustration

Key takeaways

  • Vapor pressure belongs to physics; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Vapor pressure to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Vapor pressure from memory before moving on to harder problems.

Reference excerpt

Vapor pressure or equilibrium vapor pressure is the pressure exerted by a vapor in thermodynamic equilibrium with its condensed phases (solid or liquid) at a given temperature in a closed system. The equilibrium vapor pressure is an indication of a liquid's thermodynamic tendency to evaporate. It relates to the balance of particles escaping from the liquid (or solid) in equilibrium with those in a coexisting vapor phase. A substance with a high vapor pressure at normal temperatures is often referred to as volatile. The pressure exhibited by vapor present above a liquid surface is known as vapor pressure. As the temperature of a liquid increases, the attractive interactions between liquid molecules become less significant in comparison to the entropy of those molecules in the gas phase, increasing the vapor pressure. Thus, liquids with strong intermolecular interactions are likely to have smaller vapor pressures, with the reverse true for weaker interactions. The vapor pressure of any substance increases non-linearly with temperature, often described by the Clausius–Clapeyron relation. The atmospheric pressure boiling point of a liquid (also known as the normal boiling point) is the temperature at which the vapor pressure equals the ambient atmospheric pressure. With any incremental increase in that temperature, the vapor pressure becomes sufficient to overcome atmospheric pressure and cause the liquid to form vapor bubbles. Bubble formation in greater depths of liquid requires a slightly higher temperature due to the higher fluid pressure, due to hydrostatic pressure of the fluid mass above. More important at shallow depths is the higher temperature required to start bubble formation. The surface tension of the bubble wall leads to an overpressure in the very small initial bubbles.

Measurement and units Vapor pressure is measured in the standard units of pressure. The International System of Units (SI) recognizes pressure as a derived unit with the dimension of force per area and designates the pascal (Pa) as its standard unit. One pascal is one newton per square meter (N·m−2 or kg·m−1·s−2). Experimental measurement of vapor pressure is a simple procedure for common pressures between 1 and 200 kPa. The most accurate results are obtained near the boiling point of the substance; measurements smaller than 1kPa are subject to major errors. Procedures often consist of purifying the test substance, isolating it in a container, evacuating any foreign gas, then measuring the equilibrium pressure of the gaseous phase of the substance in the container at different temperatures. Better accuracy is achieved when care is taken to ensure that the entire substance and its vapor are both at the prescribed temperature. This is often done, as with the use of an isoteniscope, by submerging the containment area in a liquid bath. Very low vapor pressures of solids can be measured using the Knudsen effusion cell method. In a medical context, vapor pressure is sometimes expressed in other units, specifically millimeters of mercury (mmHg). Accurate knowledge of the vapor pressure is important for volatile inhalational anesthetics, most of which are liquids at body temperature but have a relatively high vapor pressure.

Estimating vapor pressures with Antoine equation The Antoine equation is a pragmatic mathematical expression of the relation between the vapor pressure and the temperature of pure liquid or solid substances. It is obtained by curve-fitting and is adapted to the fact that vapor pressure is usually increasing and concave as a function of temperature. The basic form of the equation is:

log ⁡ P = A − B C + T {\displaystyle \log P=A-{\frac {B}{C+T}}}

and it can be transformed into this temperature-explicit form:

T = B A − log ⁡ P − C {\displaystyle T={\frac {B}{A-\log P}}-C}

where:

P {\displaystyle P} is the absolute vapor pressure of a substance

T {\displaystyle T} is the temperature of the substance

A {\displaystyle A} , B {\displaystyle B} and C {\displaystyle C} are substance-specific coefficients (i.e., constants or parameters)

log {\displaystyle \log } is typically either log 10 {\displaystyle \log _{10}} or log e {\displaystyle \log _{e}}

A simpler form of the equation with only two coefficients is sometimes used:

log ⁡ P = A − B T {\displaystyle \log P=A-{\frac {B}{T}}}

which can be transformed to:

T = B A − log ⁡ P {\displaystyle T={\frac {B}{A-\log P}}}

… excerpt ends here. Continue reading the full article.

Illustrations

Vapor pressure: The microscopic process of evaporation and condensation at the liquid surface.
The microscopic process of evaporation and condensation at the liquid surface.
Vapor pressure: If vapor pressure exceeds the thermodynamic equilibrium value, condensation occurs in presence of nucleation sites. This principle is indigenous in cloud chambers, where ionized particles form condensation tracks when passing through.
If vapor pressure exceeds the thermodynamic equilibrium value, condensation occurs in presence of nucleation sites. This principle is indigenous in cloud chambers, where ionized particles form condensation tracks when passing through.
Vapor pressure: A log-lin vapor pressure chart for various liquids
A log-lin vapor pressure chart for various liquids
Vapor pressure: Vapor pressure of liquid and solid benzene
Vapor pressure of liquid and solid benzene
Vapor pressure: Graph of water vapor pressure versus temperature. At the normal boiling point of 100 °C, it equals the standard atmospheric pressure of 760 torr or 101.325 kPa.
Graph of water vapor pressure versus temperature. At the normal boiling point of 100 °C, it equals the standard atmospheric pressure of 760 torr or 101.325 kPa.

Worked examples

Example 1 — a first encounter with Vapor pressure

Start with the simplest possible case. Write down what Vapor pressure claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In physics, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Vapor pressure before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Vapor pressure ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Vapor pressure

In research
Vapor pressure appears in physics research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Vapor pressure in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Vapor pressure is common in secondary-school and first-year university syllabi. It links to neighbouring topics Engineering thermodynamics, Gases, Meteorological concepts, so understanding it makes those chapters shorter.
In everyday life
Look for Vapor pressure outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Vapor pressure in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Vapor pressure means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Vapor pressure out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Vapor pressure in simple terms?

Vapor pressure or equilibrium vapor pressure is the pressure exerted by a vapor in thermodynamic equilibrium with its condensed phases (solid or liquid) at a given temperature in a closed system. The equilibrium vapor pressure is an indication of a liquid's thermodynamic tendency to evaporate.

Why does Vapor pressure matter?

Because it connects several physics ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Vapor pressure?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Vapor pressure.

Tags

  • Engineering thermodynamics
  • Gases
  • Meteorological concepts
  • Meteorological quantities
  • Pressure
  • Thermodynamic properties

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