Sadtler Véronique M, Imbert Pascal, Dellacherie Edith
Laboratoire de Chimie Physique Macromoléculaire, UMR CNRS-INPL 7568 Groupe ENSIC, 1 rue Grandville, BP 451, Nancy Cedex, 54001, France.
J Colloid Interface Sci. 2002 Oct 15;254(2):355-61. doi: 10.1006/jcis.2002.8624.
The stability of oil-in-water emulsions prepared using dextran, a natural polysaccharide, hydrophobically substituted with phenoxy groups, was studied. The evolution of the emulsion droplet size was investigated as a function of polymer concentration (Cp=0.2 to 1% w/w in a water phase) and the degree of phenoxy substitution (tau=4.2 to 15.7%). For the highest tau values, emulsions, which presented submicrometer droplets, were stable over more than 4 months at room temperature. The most substituted polymers clearly showed a better efficiency to lower the surface tension at the oil/water interface. DexP did not induce real viscosification of the continuous phase. The linearity of the particle volume variation with time, and the invariability of the volume distribution function, proved that Ostwald ripening was the main destabilization mechanism of the phenoxy dextran emulsions. The nature of the oil dispersed phase drastically affected the behavior of emulsions. While the emulsions prepared with n-dodecane presented a particle growth with time, only few size variations occurred when n-hexadecane was used. Furthermore, small ratios of n-hexadecane in n-dodecane phase reduced the particle growth due to the lower solubility and lower diffusion coefficient in water of n-hexadecane, which acted as a ripening inhibitor.
研究了用苯氧基疏水取代的天然多糖葡聚糖制备的水包油乳液的稳定性。研究了乳液滴尺寸随聚合物浓度(水相中Cp = 0.2至1% w/w)和苯氧基取代度(tau = 4.2至15.7%)的变化。对于最高的tau值,呈现亚微米级液滴的乳液在室温下4个多月内保持稳定。取代度最高的聚合物在降低油/水界面表面张力方面效率明显更高。葡聚糖苯醚(DexP)不会引起连续相真正的增粘。颗粒体积随时间变化的线性以及体积分布函数的不变性证明,奥斯特瓦尔德熟化是苯氧基葡聚糖乳液的主要失稳机制。分散油相的性质极大地影响了乳液的行为。用正十二烷制备的乳液颗粒随时间增长,而使用正十六烷时尺寸变化很小。此外,正十二烷相中少量的正十六烷由于正十六烷在水中的溶解度较低和扩散系数较低,起到了熟化抑制剂的作用,从而减少了颗粒的生长。