4.3 Article

Preparation of W/O (water-in-oil) emulsions using a PTFE (polytetrafluoroethylene) membrane - A new emulsification device

Journal

JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY
Volume 24, Issue 2, Pages 249-257

Publisher

MARCEL DEKKER INC
DOI: 10.1081/DIS-120019976

Keywords

membrane emulsification; PTFE (polytetrafluoroethylene) membrane; SPG (Shirasu porous glass) membrane; W/O (water-in-oil) emulsion; emulsification apparatus

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The potential of polytetrafluoroethylene (PTFE) membranes as water-in-oil (W/O) emulsification devices was investigated to obtain uniformly sized droplets and to convert them into microcapsules and polymer particles via subsequent treatments. Uniform W/O emulsion droplets have not been achieved using glass membranes unless the membrane was rendered hydrophobic by treatment with silanes. If a PTFE membrane is capable of providing uniform droplets for a W/O emulsion, a coordinated membrane emulsification system can be established since glass membranes have been so successful for O/W (oil-in-water) emulsification. In order to examine the feasibility of PTFE membrane emulsification, O/W and W/O emulsion characteristics prepared using PTFE membranes were compared with those prepared by the conventional SPG (Shirasu porous glass) membrane emulsification method. A 3 wt.% sodium chloride solution was dispersed in kerosene using a low HLB surfactant. Effects of the membrane pore size, permeation pressure, and the type of emulsifiers and concentration on the droplet size and on the size distribution (CV, coefficient of variation) were investigated. The CV of the droplets was fairly low, and the average droplet size was correlated with the critical permeation pressure of the dispersed phase, revealing that the PTFE membrane could be used as a one-pass membrane emulsification device. Low CV values were maintained with a Span 85 (HLB = 1.8) concentration, 0.2-5.0 wt.% and a range of HLB from 1.8-5.0. For a brief demonstration of practical applications, nylon-6,10 microcapsules prepared by interfacial polycondensation and poly(acrylamide) hydrogels from inverse suspension polymerization are illustrated.

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