化学
延伸率
膜
离子
化学工程
大小排阻色谱法
分子动力学
表面电荷
色谱法
无机化学
材料科学
物理化学
计算化学
有机化学
冶金
生物化学
工程类
极限抗拉强度
酶
作者
Yifeng Chen,Jiaheng Teng,Baoqiang Liao,Renjie Li,Hongjun Lin
出处
期刊:Chemosphere
[Elsevier BV]
日期:2019-10-26
卷期号:242: 125232-125232
被引量:83
标识
DOI:10.1016/j.chemosphere.2019.125232
摘要
Molecular mechanisms responsible for the filtration behaviors of sodium alginate (SA) in presence of different iron(III) ion concentration were explored in this study. It was found that specific filtration resistance (SFR) of alginate mixtures (1.0 gSA/L) firstly increased and then decreased to a trough with iron(III) concentration increase from 0 to 2.5 mM. Alginate mixture interacting with 0.1 mM iron(III) possessed an SFR as high as 1.65 × 1014 m kg−1, which could be explained by Flory-Huggins lattice theory related with gel filtration. Optical observation showed significant morphology transition (from gel to granular solids) of foulant layers with iron(III) concentration increase. A series of characterizations indicated the change of microstructure, pH and surface charge of alginate mixture with iron(III) concentration. Density functional theory (DFT) simulation suggested that iron(III) ion preferentially forms coordination bonds with three terminal carboxyl groups of alginate chains, facilitating elongation and cross-linking of alginate chains. Such a coordination mode induces formation of a slime and homogeneous gel, corresponding to high SFR. Continuous increase in iron(III) concentration leads to non-terminal coordination, which makes alginate chains more clustered and coiled. This effect, together with effects of the reduced surface charge and electric double layer compression, significantly decrease SFR of alginate mixtures. This study provided deep molecular insights into effects of iron(III) ions on alginate fouling.
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