Hamberg Lars, Walkenström Pernilla, Hermansson Anne-Marie
SIK, The Swedish Institute for Food and Biotechnology, P.O. Box 5401, Göteborg SE-40229, Sweden.
J Colloid Interface Sci. 2002 Aug 15;252(2):297-308. doi: 10.1006/jcis.2002.8511.
Shaping, defined as deformation in combination with gel formation of gelatine and kappa-carrageenan drops in an elongation flow, was studied. The focus was to investigate the possibility of shaping and fixating small drops in the diameter range 20 to 229 mum. In the shaping progress and the influence of experimental properties, the viscosity, temperature, and flow of the deforming fluid were examined on the final drop shape. In the experiments a hot emulsion of an aqueous biopolymer solution in silicone oil was injected into cold silicone oil where a deforming elongation flow field existed. After injection, a temperature decrease in the drops resulted in a gel formation of the biopolymer and a fixation of the deformed drop in the flow. The shape was measured and the effect on the drop aspect ratio was determined by image analysis. Over the total drop diameter range, kappa-carrageenan was more ellipsoid-shaped than gelatine, with a maximum aspect ratio of 6 compared to 4 for gelatine. For small drops, around 22 mum, it is possible to shape kappa-carrageenan, but for gelatine small drops tend to be unaffected. An increase in viscosity, temperature, and flow resulted in an increase in the final fixated shape of the drops. The differences in drop deformation between the biopolymers were explained by drop-viscosity/oil differences and differences in the kinetics of gel formation. The different gel formation kinetics resulted in a short, well-defined, shaping process for kappa-carrageenan, while for gelatine the process was more complex, with both deformation and relaxation present at different stages.
研究了成型过程,其定义为在拉伸流动中明胶和κ-卡拉胶液滴的变形与凝胶形成相结合的过程。重点是研究成型并固定直径范围为20至229微米的小液滴的可能性。在成型过程以及实验特性的影响方面,研究了变形流体的粘度、温度和流动对最终液滴形状的影响。在实验中,将生物聚合物水溶液在硅油中的热乳液注入存在变形拉伸流场的冷硅油中。注入后,液滴温度降低导致生物聚合物形成凝胶,并使变形后的液滴在流动中固定下来。通过图像分析测量形状并确定对液滴纵横比的影响。在整个液滴直径范围内,κ-卡拉胶比明胶更呈椭圆形,其最大纵横比为6,而明胶为4。对于约22微米的小液滴,可以使κ-卡拉胶成型,但明胶小液滴往往不受影响。粘度、温度和流动的增加导致液滴最终固定形状增加。生物聚合物之间液滴变形的差异由液滴粘度/油的差异以及凝胶形成动力学的差异来解释。不同的凝胶形成动力学导致κ-卡拉胶的成型过程短暂、明确,而对于明胶,该过程更为复杂,在不同阶段同时存在变形和松弛。