AL

Liquids: Surface Tension, Viscosity, Capillary Action, Vapor Pressure, Boiling Point

Learning Objectives

  • Describe, measure, and explain the macroscopic properties of liquids:
    • \text{viscosity}
    • \text{surface tension}
    • \text{capillary action}
    • \text{vapor pressure}
    • \text{boiling point}
    • \Delta H_{vap} (molar heat of vaporization)
  • Perform guided-inquiry experiments that reveal each property (paper-clip flotation, “vanishing water,” etc.).
  • Relate observable behavior to the type & strength of intermolecular forces (IMF): hydrogen bonding, dipole–dipole, London dispersion.
  • Appreciate real-life significance in biology, medicine, environmental science, and industry.

Key Properties of Liquids (overview)

  • Surface Tension – energy cost to create new surface; resistance of the surface to external force.
  • Viscosity – internal resistance to flow (not illustrated in transcript, but part of objective).
  • Capillary Action – spontaneous rise or fall of a liquid in a narrow tube (implied link to surface tension & adhesion).
  • Vapor Pressure – pressure exerted by vapor in equilibrium with its liquid/solid.
  • Boiling Point – temperature where P{vapor} = P{external}.
  • Heat of Vaporization – enthalpy required to vaporize 1\,\text{mol} at the boiling point.

Surface Tension

  • Definition: \gamma = \dfrac{\text{energy}}{\text{area}} needed to expand surface; measured in \text{J m}^{-2} or \text{N m}^{-1}.
  • Cohesive forces pull molecules inward; surface behaves like a stretched elastic membrane.
  • Water’s high surface tension due to an extensive hydrogen-bonding network.

Molecular View: Surface vs. Bulk

  • Bulk interior: molecules experience symmetric IMF in all directions ⇒ net force =0.
  • Surface layer: molecules lack neighbors above; net inward force shortens area.
  • Diagrams (Pages 3–5) show surface layer (label “1”) vs. interior; arrows denote stronger inward bonds, especially hydrogen bonds.

Demonstration: Floating Paper Clips (Page 6)

  • Untouched water: paper clip can rest on the surface because \gamma{\text{H}2\text{O}} is high.
  • Adding dishwashing liquid (surfactant) lowers \gamma ⇒ paper clip sinks.
    • Conclusion: surfactants disrupt hydrogen bonding, reduce cohesive tension.

Surfactants & Detergent Molecule (Pages 7–8)

  • Amphiphilic structure (Fig 3):
    • Hydrophilic ionic head (often \text{–SO}_3^-\,\text{Na}^+)
    • Hydrophobic tail (long hydrocarbon chain)
  • In water, tails orient away from H₂O, heads stay in contact ⇒ adsorb at interface, lower \gamma.
  • Practical outcome: creates “low surface tension” water enabling wetting & cleaning (Page 8 comparison diagram).

Factors Affecting \gamma

  • Intermolecular force strength ↑ ⇒ \gamma ↑.
  • Temperature ↑ ⇒ molecules gain KE, more escape to vapor, hydrogen bonds break ⇒ \gamma ↓ (Page 10).

Viscosity (mentioned, not detailed in transcript)

  • Definition: internal frictional resistance; symbol \eta.
  • Correlates with IMF strength & molecular shape (long chains ↑ tangling).

Capillary Action (mentioned, not detailed)

  • Combination of cohesive (liquid–liquid) & adhesive (liquid–wall) forces.
  • When F{adhesion} > F{cohesion}, liquid rises in tube; otherwise it depresses.

Vapor Pressure (Pages 11–12)

  • Vaporization (liquid → gas) occurs when surface molecules escape.
  • At equilibrium: \text{rate}{\text{evap}} = \text{rate}{\text{cond}} ⇒ constant P_{vapor}.
  • Stronger IMF ⇒ fewer molecules escape ⇒ lower P_{vapor}.
  • “Vanishing Water” station: Different containers lose water at different rates.
    1. Container with larger exposed area or higher T loses more water.
    2. Difference caused by faster evaporation (higher vapor pressure).
    3. Higher P_{vapor} accelerates mass loss.

Boiling Point (Pages 13)

  • Boiling when P{vapor} = P{external}.
  • Normal Boiling Point: value measured at P_{external}=760\,\text{mm Hg} (1 atm).
  • Lower external pressure ⇒ liquid boils at lower T (e.g., high altitude cooking); higher pressure ⇒ higher B.P. (pressure cookers).

Heat of Vaporization \left(\Delta H_{vap}\right) (Pages 14–15)

  • Definition: heat required to vaporize one mole at its B.P.
  • Units: \text{kJ mol}^{-1}.
  • Reflects IMF strength; larger \Delta H_{vap} ⇒ stronger forces.
  • Data table (Page 15):
    • Argon: \Delta H_{vap}=6.3\,\text{kJ mol}^{-1}, BP=-186^\circ\text{C} (weak dispersion).
    • Pentane \left(\text{C}5\text{H}{12}\right): 26.5\,\text{kJ mol}^{-1}, BP=36.1^\circ\text{C}.
    • Acetone \left(\text{CH}3\text{COCH}3\right): 30.3\,\text{kJ mol}^{-1}, BP=56.5^\circ\text{C} (dipole-dipole).
    • Ethanol \left(\text{C}2\text{H}5\text{OH}\right): 39.3\,\text{kJ mol}^{-1}, BP=78.3^\circ\text{C} (hydrogen bonding).
  • Trend: BP \uparrow as \Delta H_{vap} \uparrow since more energy needed to overcome IMF.

Real-World Relevance

  • Biology: surface tension enables insects to walk on water; capillary action drives water movement in xylem of plants.
  • Medicine: pulmonary surfactants reduce alveolar surface tension, preventing lung collapse.
  • Environment: volatility (linked to vapor pressure) influences pollutant dispersion and atmospheric chemistry.
  • Industry: detergents, paints, ink-jet printing rely on controlled surface tension; pressure cooking leverages boiling-point elevation.

Guided-Inquiry & Experimental Connections

  • Paper-clip float test demonstrates cohesive force vs. surfactant disruption.
  • “Vanishing Water” compares evaporation rates, linking to vapor pressure & temperature.
  • Suggested extensions: measure capillary rise of various liquids; time viscosities with a falling-ball viscometer.

Conceptual & Mathematical Relationships

  • P{vapor} \propto e^{-\frac{\Delta H{vap}}{RT}} (Clausius–Clapeyron, optional advanced link).
  • Surface energy change: \Delta E = \gamma \Delta A.
  • Boiling criterion: P{vapor}(T{boil}) = P_{atm}.

Summary

  • Surface tension, vapor pressure, boiling point, and \Delta H_{vap} are macroscopic manifestations of molecular-level IMF.
  • Manipulating temperature, pressure, or chemical additives (surfactants) allows control of liquid behavior in technology and nature.
  • Mastery of these concepts provides predictive power for laboratory work, engineering design, and understanding everyday phenomena.