期刊
FOOD HYDROCOLLOIDS
卷 131, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2022.107777
关键词
Liquid-core alginate beads; Molecular structure; Thermal stability; Mechanical properties; Roughness
资金
- International S&T Innovation Cooperation Key Project [2017YFE0135400]
- National Natural Science Foundation of China [32072153]
- National First-class Discipline Program of Food Science and Technology [JUFSTR20180204]
- Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province China
Core-shell hydrogel beads have been increasingly studied due to their exciting texture and functional properties, but the thermal processing of these beads remains a challenge. In this study, liquid core gel beads were prepared from alginate with different molecular weights and M/G ratios. The results showed that the core and shell of the beads had a significant influence on their heat response. High G-content and high molecular weight contributed to improved mechanical properties of the beads at high temperatures. However, above the boiling point, the beads started to lose their original shape and the shell thickness was irregularly reduced. The water state and crosslinking of the chains were found to be the decisive factors for the beads' thermo-mechanical response. The study established a relationship between the beads' structural integrity, stability, and alginate's molecular composition during thermal treatment.
Core-shell hydrogel beads have recently drawn considerable attention to meet ever-changing consumer demand for exciting texture combined with functional properties. Still, the thermal processing of these types of beads remains insurmountable. In this paper, spherical liquid core gel beads were prepared from alginate with distinguishable Mw and M/G ratios and treated at temperatures varying from 60 to 121 degrees C. The core and the shell both had a precise response and influence towards heat. Improved mechanical properties were observed from beads up to 100 degrees C, figuring on hydrogels' network structure. High G-content and high molecular weight (Mw) contributed broadly up to a 50% increase in bursting force at high temperatures. Above the boiling point, beads started losing their original geometry since core materials diffused at an accelerated rate with a vapor pressure buildup. An irregular pattern of reduction in shell thickness, depending on crosslinking nature, was observed among alginate beads during heat treatment. A maximum 63.4% thickness reduction was recorded from low Mw alginate. Poorly constructed gel networks produced thermally vulnerable structures, predominantly by shorter chain length or higher M residue. Higher calcium concentration (up to a saturated crosslinking point) enhanced stability within the same alginate group. Heat treatment resulted in a compact shell microstructure with reduced pore size and a smoother surface. The water state and crosslinking of the chains were the decisive factors for the beads' thermo-mechanical response. Thus, a relationship was established between liquid-core beads' structural integrity, stability, and alginate's molecular composition concerning thermal treatment.
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