Solutions. Types of disperse systems. True solutions. Water as most widespread solvent in pharmacy. Solvatation and heat effect of solubility process. Solubility of solid, liquids and gases (Henry law).concentration units. - PowerPoint PPT Presentation

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Solutions. Types of disperse systems. True solutions. Water as most widespread solvent in pharmacy. Solvatation and heat effect of solubility process. Solubility of solid, liquids and gases (Henry law).concentration units.

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Title: Solutions. Types of disperse systems. True solutions. Water as most widespread solvent in pharmacy. Solvatation and heat effect of solubility process. Solubility of solid, liquids and gases (Henry law).concentration units.


1
LECTURE 1
Solutions. Types of disperse systems. True
solutions. Water as most widespread solvent in
pharmacy. Solvatation and heat effect of
solubility process. Solubility of solid, liquids
and gases (Henry law).concentration units.
ass. prof. Ye. B. Dmukhalska
2
PLAN
  • Solubility. The mechanism of dissolving.
  • Solubility of gases in liquids. The Henrys law.
  • Colligative properties
  • a) osmosis. The vant-Hoffs law. Hemolysis and
    plasmolysis
  • b) vapor-pressure lowering of solution. A
    Raoults law
  • c) boiling-point elevation
  • d) freezing-point depression.

3
Water main solvent
  • The water - main component of organisms and
    medium, in which lives the person. The main
    properties of water that in water can solubility
    a different matters.
  • In the human, animal, plant organisms the water
    is main part, a constituent solvent and it
    participates in exchange reactions of matters
    (hydrolysis, hydration, swelling, digestion).
  • In a human organism are about 70 - 80 of water.

4
The mechanism of dissolving
5
  • (- )Polar molecule
  • (-) Negative ion
  • () Positive ion
  • (-)Water dipole

6
  • The dissolving depends primarily on the relative
    strengths of three attractive forces
  • the forces between the particles of the solute
    before it has dissolved solute-solute forces),
  • the forces between solvent particles before
    dissolution has taken place (solvent-solvent
    forces),
  • the forces that are formed between solute and
    solvent particles during the dissolving process
    (solute-solvent forces).

7
Type of solution
  • A saturated solution is one that is in
    equilibrium with excess undissolved solute, or
    would be in equilibrium if excess solute were
    present. The term saturated denotes the highest
    concentration of solute which a solution can have
    and be in equilibrium with any undissolved solute
    with which it is placed in contact.
  • An unsaturated solution is one in which the
    concentration of solute is less than its
    concentration in a saturated solution.
  • A supersaturated solution is one in which the
    concentration of solute is greater than its
    concentration in a saturated solution.
  • A supersaturated solution is unstable and its
    solute tends eventually to crystallize out of
    solution, much as a super cooled liquid tends
    eventually to crystallize.

8
  • Gas solution is not possible to prepare a
    heterogeneous mixture of two gases because all
    gases mix uniformly with each other in all
    proportions. Gaseous solutions have the structure
    that is typical of all gases. Air, the gaseous
    solution with which we come in closest contact,
    is composed primarily of N2 (78 by volume), O2
    (21 ), and Ar (1 ), with smaller concentrations
    of CO2, H2O, Ne, He, and dozens of other
    substances at very low levels.
  • Liquid solutions have the internal structure that
    is typical of pure liquids closely spaced
    particles arranged with little order. Unlike a
    pure liquid, however, a liquid solution is
    composed of different particles. Much of this
    chapter is devoted to the properties of liquid
    solutions, and special emphasis is given to
    aqueous solutions, in which the major component
    is water.
  • Two kinds of solid solutions are common. The
    first, the substitutional solid solution,
    exhibits a crystal lattice that has structural
    regularity but in which there is a random
    occupancy of the lattice points by different
    species.

9
Disperse systems
  • Disperse systems are called systems, which
    consist of two phases, one of which is scattered
    or dispersed in other.
  • The disperse phase - phase which is scattered
    (dispersed) in medium.
  • The disperse medium - phase in which dispersion
    done.

10
Classification disperse systems
  • By stat of dispersed phase and dispersed medium

11
  • By size of dispersed phase

12
  • Colloidal solutions are disperse systems, which
    have dispersed phase particle, which size between
    10-9 to 10-7m or 1 nm to 100 nm.

13
Concentration units of solution
  • Mass fraction (?i) of solute in solution is the
    ratio of the mass solute (mi) to the mass of
    solution mi ms ms- mass of a solvent
  • Percentage by weight (mass) or mass percent, is
    the quantity of one component of a solution
    expressed as a percentage of the total mass
  • where ?m - percent by mass,
  • mA, mB, mC - mass of components in the solution.

14
  • Mass concentration, titer (T) is number grams of
    solute (m) per one milliliter of solution (V). Or
    it is the ratio of the quantity grams of solute
    and volume solution
  • T m .
  • V
  • Molarity (CM), or molar concentration, is the
    number of moles of solute dissolved per liter of
    solution.
  • CM ? m .
  • V MV
  • where CM - molarity (by mole of solute per
    liter of a solution)
  • ? - number mole solute
  • m - mass solute, grams
  • M - molar mass solute, in grams/mole
  • V - volume of the solution
  • Molality is defined as the number of moles (?) of
    solute dissolved per kilogram of solvent. Thus,
    the molality of solute in a solution is
  • Cm ? msolute
  • msolvent M solute msolvent
  • when Cm molality (by mole of solute per
    kilogram of solvent)
  • ? - number of moles of solute
  • m mass of solvent.

15
  • In measure analysis for the characteristic the
    composition of solution will use molar mass of an
    equivalent (equivalent mass)
  • Molar mass of an equivalent of element is the
    mass of the element which combines with or
    displaces 1.008 parts by mass of hydrogen or 8
    part by mass of oxygen or 35.5 parts by mass of
    chlorine E fequivalence MB
  • The factor of equivalence (fequiv) - number,
    which is demonstrated which part of matter
    (equivalent) can react with one atom of Hydrogen,
    or one electron in reduction reactions.
  • Molar concentration of an equivalent (normal
    concentration), normality is quantity
    gram-equivalent of solute per one liter of
    solution (V)
  • Ceq ?eq m .
  • V E V
  • where CM - molarity (by mole of solute per
    liter of a solution)
  • ?eq - number mole-equivalent of solute
  • m - mass solute, grams
  • E - molar mass of an equivalent solute
    (equivalent mass of solute)
  • V - volume of the solution

16
Henry's Law
  • The solubility of a gas dissolved in a liquid is
    proportional to the partial pressure of the gas
    above the liquid.
  • This is a statement of Henry's law, which can be
    written
  • X KP
  • X is the equilibrium mole fraction of the gas in
    solution (its solubility)
  • P is its partial pressure in the gas phase
  • K - constant of proportionality or Henry's-law
    constant.
  • The partial pressure is a part of common
    pressure, which one is a share of each gas in gas
    mixture.

17
  • Properties of a solution which depend only on
    the concentration of the solute and not upon its
    identity are known as colligative properties.
  • vapor-pressure lowering
  • boiling-point elevation
  • freezing-point depression
  • osmotic pressure.

18
  • The spontaneous mixing of the particles of the
    solute (present in the solution) and the solvent
    (present above the solution) to form ?
    homogeneous mixture is called diffusion, just as
    the term is used for the spontaneous mixing of
    gases to form homogeneous mixtures.
  • A semi-permeable membrane - ? membrane which
    allows the solvent molecules to pass through but
    not the solute particles.
  • The net spontaneous flow of the solvent molecules
    from the solvent to the solution or from a less
    concentrated solution to ? more concentrated
    solution through ? semi-permeable membrane is
    called osmosis (Greek push).

19
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20
  • The osmotic pressure of ? solution may thus be
    defined as the equivalent of excess pressure
    which must be applied, to the solution in order
    to prevent the passage of the solvent into it
    through ? semi-permeable membrane separating the
    two, i.e. the solution and the pure solvent.
  • Osmotic pressure may be defined as the
    equilibrium hydrostatic pressure of the column
    set up as ? result of osmosis.
  • ? ?? ?? ? ???? or PR?C?T
  • PV nRT vant Hoff equation for dilute
    solutions

21
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22
  • Laws of osmotic pressure - These are the same as
    gas laws and apply to dilute solutions which
    occur in the living body

23
  • The effect of hypertonic and hypotonic solutions
    on animal cells.
  • (?) Hypertonic solutions cause cells to shrink
    (crenation)
  • (b) hypotonic solutions cause cell rupture
  • (c) isotonic solutions cause no changes in cell
    volume.

24
  • The partial vapor pressure of a component in
    liquid solution is proportional to the mole
    fraction of that component, the constant of
    proportionality being the vapor pressure of the
    pure component.
  • Raoult's law can be written as
  • P1 X1 P10
  • where P1 and P10 are the vapor pressure of the
    solution and that of the pure solvent,
    respectively,
  • X1 is the mole fraction of the solvent in the
    solution.
  • P1 is the total vapor pressure of the solution.
  • X2 1 - X2,
  • P1 (1- X2)P10
  • P10 - P1 is the vapor-pressure lowering
  • P10 - P1
  • ---------- X2 fractional vapor-pressure
    lowering
  • P10
  • which can be seen to be equal to the mole
    fraction of the solute - X2.

25
  • The relationship between boiling-point elevation
    and solute concentration it can be shown that in
    dilute solutions the boiling-point elevation is
    proportional to the molality of the solute
    particles.
  • if ?Tb, represents the boiling-point elevation
  • ?Tboiling Tboiling (solution) - Tboiling
    (solvent),
  • ?Tb KbCm
  • Cm molality, number of mole of solute per one
    kilogram of solvent
  • Where Cm - molality of the solute in solution
  • Kb- proportionality constant known as the molal
    boiling-point elevation constant.

26
  • The relationship between freezing-point
    depression and molality in dilute solutions is a
    direct proportionality
  • ?Tf Tfreezing(solvent) - Tfreezing(solution)
    - freezing-point depression
  • ?Tfreezing KfCm
  • Where Cm - molality of solute
  • Kf - molal freezing-point depression constant

27
Thank you for attention
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