淀粉
肺表面活性物质
皮克林乳液
胶束
化学工程
化学
透射电子显微镜
吸附
粒子(生态学)
生物高聚物
琥珀酸酐
材料科学
乳状液
结晶学
高分子化学
有机化学
纳米技术
水溶液
生物化学
工程类
地质学
聚合物
海洋学
作者
Wei Liu,Yue Li,H. Douglas Goff,John Nsor‐Atindana,Jianguo Ma,Fang Zhong
出处
期刊:Langmuir
[American Chemical Society]
日期:2019-03-04
卷期号:35 (13): 4702-4709
被引量:30
标识
DOI:10.1021/acs.langmuir.9b00069
摘要
The mechanisms of granular octenyl succinate anhydride (GOSA) and dissolved OSA (DOSA) starches in emulsion stabilization were investigated. In general, DOSA starch offered better emulsification activity by generating greater ζ-potential, lower particle size as well as long-term stability in comparison to GOSA starch of close degree of substitution (DS). A compact interface in DOSA starches was determined, resulting from an increased surface loading value of 2.37 mg/m2 in comparison to that of GOSA of 1.6 mg/m2. Additionally, the irreversibly adsorbed and predominantly elastic interface of both DOSA and GOSA starches indicated that the DOSA starch may be a Pickering emulsifier rather than a biopolymer surfactant. This assumption was confirmed by transmission electron microscopy. Spherical micelles with average diameters of 100 nm were observed above the critical micelle concentration of 1 mg/mL. Moreover, samples G28 (representing DS of 0.028), D28, G16, and D16 could reach equilibrium interfacial tensions of 19.4, 16.5, 20.0, and 19.3 mN/m, respectively. However, due to the misleading contact angle as a result of rough surfaces and nonignorable gravity of GOSA starch, the energy escape equation failed to be employed in this study.
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