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Seminar on Surface
and Interfacial
phenomenon
BY
GAJANAN V NAIK
M PHARM IST YEAR
Swami Ramanand teerth Marathwada University Nanded
School Of Pharmacy
UNDER GUIDANCE OF
DR. A. D. KSHIRSAGAR
ASS. PROFESSOR
What is micelle and how it forms?
• Ampiphile :
• A monomer is consist of
– Head : Hydrophilic
– Tail: Hydrophobic
What is micelle and how it forms?
• At low concentration: amphiphiles exist separately (subcolloidal
size)
• At high concentration: form aggregates or micelles (50 or more
monomers) (colloidalsize i.e. 50 Ǻ)
Micelle
At Low concentration
At High concentration
Bulk
interfaceinterface
What is micelle and how it forms?
• Critical micelle concentration (CMC ): The concentration of
monomer at which the micelles are formed.
• aggregation number : The number of monomers that aggregate
to form a micelle.
• From Gibbs equation of adsorption
Concentration Saturation Structure Surface tension
Below CMC Unsaturated Separated High
At CMC Saturated Micelles Reached final value
Above CMC More saturation Micelles Constant
Factors influencing CMC
• Structure of hydrophobic group. –
length of hydrocarbon chain is
Micelle size CMC
• Addition of Electrolyte
Micelle Size CMC
• Effect of Temperature
up to cloud point
Micelle Size CMC
Electrical Properties at Interfaces
• Particles dispersed in liquid media may become charged mainly
in one of two ways
– A. selective adsorption
– B. ionization of groups
• Two types of potential forms
– Nenrst
– Zeta
Zeta potential
• The zeta potential is defined as the
difference in potential between the
surface of the tightly bound layer
(shear plane) and the electroneutral
region of the solution.
• The potential located at the shear
plane bb’
Importance of Zeta potential
• The zeta potential has application in the stability of systems
containing dispersed particles.
• The zeta potential allows you to study the mechanism of
stabilization of a sample.
• The destruction of unwanted colloid.al dispersions
References
• A. N. Martin, Martin's Physical Pharmacy and Pharmaceutical
Sciences, 6th edition, p. 389-390.
• M.E. Aulton, Pharmaceutics science of dosage form design, 2nd
Edition, p. 88-89
• Leon Lachman, The Theory and Practice of Industrial Pharmacy,
3rd edition, p. 106
Seminar on surface and interfacial phenomenon

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Seminar on surface and interfacial phenomenon

  • 1. Seminar on Surface and Interfacial phenomenon BY GAJANAN V NAIK M PHARM IST YEAR Swami Ramanand teerth Marathwada University Nanded School Of Pharmacy UNDER GUIDANCE OF DR. A. D. KSHIRSAGAR ASS. PROFESSOR
  • 2. What is micelle and how it forms? • Ampiphile : • A monomer is consist of – Head : Hydrophilic – Tail: Hydrophobic
  • 3. What is micelle and how it forms? • At low concentration: amphiphiles exist separately (subcolloidal size) • At high concentration: form aggregates or micelles (50 or more monomers) (colloidalsize i.e. 50 Ǻ) Micelle At Low concentration At High concentration Bulk interfaceinterface
  • 4. What is micelle and how it forms? • Critical micelle concentration (CMC ): The concentration of monomer at which the micelles are formed. • aggregation number : The number of monomers that aggregate to form a micelle. • From Gibbs equation of adsorption Concentration Saturation Structure Surface tension Below CMC Unsaturated Separated High At CMC Saturated Micelles Reached final value Above CMC More saturation Micelles Constant
  • 5. Factors influencing CMC • Structure of hydrophobic group. – length of hydrocarbon chain is Micelle size CMC • Addition of Electrolyte Micelle Size CMC • Effect of Temperature up to cloud point Micelle Size CMC
  • 6. Electrical Properties at Interfaces • Particles dispersed in liquid media may become charged mainly in one of two ways – A. selective adsorption – B. ionization of groups • Two types of potential forms – Nenrst – Zeta
  • 7. Zeta potential • The zeta potential is defined as the difference in potential between the surface of the tightly bound layer (shear plane) and the electroneutral region of the solution. • The potential located at the shear plane bb’
  • 8. Importance of Zeta potential • The zeta potential has application in the stability of systems containing dispersed particles. • The zeta potential allows you to study the mechanism of stabilization of a sample. • The destruction of unwanted colloid.al dispersions
  • 9. References • A. N. Martin, Martin's Physical Pharmacy and Pharmaceutical Sciences, 6th edition, p. 389-390. • M.E. Aulton, Pharmaceutics science of dosage form design, 2nd Edition, p. 88-89 • Leon Lachman, The Theory and Practice of Industrial Pharmacy, 3rd edition, p. 106