4.6 Article

In situ evaluation of alginate-Ca2+ gelation kinetics

期刊

JOURNAL OF APPLIED POLYMER SCIENCE
卷 140, 期 32, 页码 -

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WILEY
DOI: 10.1002/app.54252

关键词

alginate; cross-linker; gelation; kinetics; reaction; rheology

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A customized parallel-plate rheometric setup was used for an in situ investigation on how the initial distribution of CaCl2 to alginate through micro-holes affects the gelation process. Increasing the number of suppliers (2-12) resulted in stiffer gels at the same probing time. The oscillation and different local distribution of cations into the biopolymer solution affected the development of the gel front, which was rheologically investigated through the temporal evaluation of complex modulus, G*. The alternative configurations of the same number of micro-holes also contributed significantly to this aspect. Additionally, a two-kernel equation was introduced to predict the alginate-Ca2+ gelation kinetics.
A thorough assessment of gelation progress requires real-time recording of biopolymer kinetics. In this study, an in situ investigation with a customized parallel-plate rheometric setup examines how the initial distribution of CaCl2 to alginate through micro-holes affects the process. At constant volume and concentration of reactants, stiffer gels are produced at the same probing time by increasing the number of suppliers (2-12). Due to the oscillation and the different local distribution of the cations into the biopolymer solution, the development of gel front is affected, which is for the first time in situ rheologically investigated by the temporal evaluation of complex modulus, G*. The alternative configurations of the same number of micro-holes have drastically contribution to this regard, too. Moreover, a two-kernel equation is introduced predicting the alginate-Ca2+ gelation kinetics. It represents the initial fast increase in G*, determined by the concentration of cross-linker, and the slow diffusion of cations to the assembled gelling structures depicted on the successive evolution of G* in longer times. Finally, a continuous and an intermittent oscillatory time sweep influence the diffusion of the cross-linking solution resulting in considerably different gelation curves for the same concentration of reactants.

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