Structure Evolution of Gelatin Particles Induced by pH and Ionic Strength

被引:4
|
作者
Xu, Jing [1 ,2 ]
Li, Tianduo [1 ,2 ]
Tao, Furong [2 ]
Cui, Yuezhi [2 ]
Xia, Yongmei [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Dept Appiled Chem, Wuxi 214122, Peoples R China
[2] Shandong Polytech Univ, Key Lab Fine Chem Shandong Prov, Jinan 250353, Peoples R China
关键词
gelatin; aggregate; pH; ionic strength; electrostatic repulsion; ANGLE NEUTRON-SCATTERING; SODIUM DODECYL-SULFATE; CROSS-LINKING; MECHANICAL-PROPERTIES; LIGHT-SCATTERING; AQUEOUS-SOLUTION; AGGREGATION; POLYELECTROLYTE; HYDROGELS; FILMS;
D O I
10.1002/jemt.22164
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Microstructure of gelatin particles played a key role in determining the physicochemical properties of gelatin. Ionic strength and pH as systematic manners were considered to affect gelatin particles structure on the micrometer scale. Scanning electron microscopy was used for depicting the morphologies of gelatin particles. Increasing pH to 10.0 or decreasing pH to 4.0, spherical, spindle, and irregular aggregates of gelatin particles at 2, 6, 10, and 14% solution (w/w) were all transformed to spindle aggregates. When NaCl was added to the system, the molecular chains of gelatin possibly rearranged themselves in a stretched state, and the ribbon aggregates was observed. The structural transitions of gelatin aggregates were strongly depended on the electrostatic repulsion. In the gelatinsodium dodecyl sulfate (SDS) case, the micrometer scale of aggregates was larger and the different degrees of cross-links were induced through hydrophobic interaction and electrostatic repulsion. Microsc. Res. Tech. 76:272281, 2013. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:272 / 281
页数:10
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