Chp 8: Surface Active Agents (Surfactants)
Introduction to Surface Active Agents
- Definition: Surface active agents, also known as surfactants, are molecules or ions that adsorb at interfaces, lowering the surface tension between liquids or between liquids and solids.
- Amphiphiles: Surfactants are amphiphilic, possessing both hydrophilic (polar) and hydrophobic (non-polar) regions, allowing them to interact with both polar and non-polar solvents.
- Applications: Used in pharmaceuticals as:
- Wetting agents
- Emulsifiers
- Solubilizing agents
- Antifoaming agents
Surfactant Behavior at Interfaces
- Air-water Interface: Lipophilic chains of surfactants orient upwards into the air.
- Oil-water Interface: Surfactant chains associate with the oil phase.
Classification of Surfactants
- Anionic Surfactants: E.g., Sodium dodecyl sulfate (SDS®)
- Cationic Surfactants: E.g., Cetyl trimethyl ammonium bromide (CTAB®)
- Ampholytic (Zwitterionic) Surfactants: E.g., Phospholipids
- Non-ionic Surfactants: E.g., Polyoxyethylene (Tween®)
Hydrophilic-Lipophilic Balance (HLB)
- HLB Scale: Measures the hydrophilicity and lipophilicity of emulsifying agents.
- Higher HLB indicates greater hydrophilicity.
- Spans (sorbitan esters) have low HLB (lipophilic).
- Tweens (polyoxyethylene derivatives of Spans) have high HLB (hydrophilic).
Micelles and Critical Micelle Concentration (CMC)
- Amphiphilic Characteristics: Molecules contain both hydrophilic and hydrophobic parts.
- Low Concentration: At low surfactant concentrations, amphiphiles exist as individual molecules.
- Critical Micelle Concentration: As concentration increases, aggregation occurs forming micelles, which can contain 50 or more monomers.
- Micelle Size: Each micelle has a diameter of about 50 Å, classifying it as colloidal.
- Micelles: Formed in aqueous solutions from lipid molecules.
- Structure: Spherical due to the amphipathic nature (both hydrophilic head and hydrophobic tail).
- Role of Micelles: Increase solubility of materials that are normally insoluble or slightly soluble in the dispersion medium through solubilization.
Shapes of Micelles
- Spherical Micelle
- Cylindrical Micelle
- Bilayer (Laminar Micelle)
Experimental Work
- Materials Required:
- Salicylic acid powder, Tween 60, distilled water, phenol red indicator, volumetric and conical flasks, graduated pipettes, burette, filter paper, funnel, balance, NaOH solution (0.05N).
- Objective: Investigate the effect of Tween concentration on the solubility of salicylic acid.
- Critical Micelle Concentration (CMC): Concentration of monomers at which micelles form, crucial for understanding surfactant efficiency.
Procedure Overview
- Prepare Tween 60 solutions at varying concentrations (0%, 0.05%, 0.5%, 1%, 2%, 3%) using the stock solution (5%).
- Combine 25 mL of Tween 60 solutions with 0.25g salicylic acid in conical flasks.
- Shake each flask for 10 minutes and allow to settle for another 10 minutes.
- Filter if necessary, then titrate 10 mL of each filtrate with 0.05N NaOH using phenol red as an indicator. Record color change from yellow to pink as the endpoint.
- Plot salicylic acid solubility (mg/mL or g/100mL) against Tween 60 concentration.
Calculations
- Molecular Weight: 138.1 g for salicylic acid corresponds to 1L of 1N NaOH.
- Equivalence Calculations: 0.0069 g of salicylic acid is determined as the chemical factor for calculations.
- Final Calculation: Chemical factor multiplied by endpoint gives the amount of salicylic acid dissolved per 10 mL medium.