儿茶酚
动力学
胺气处理
机制(生物学)
材料科学
化学工程
有机化学
纳米技术
化学
量子力学
认识论
物理
工程类
哲学
作者
Wen‐Ze Qiu,Guang‐Peng Wu,Zhi‐Kang Xu
标识
DOI:10.1021/acsami.7b18934
摘要
Bioinspired polyphenol/polyamine codeposition has been demonstrated by the competence for surface modification; however, the reaction processes including mechanism and kinetics remain superficially understood. In this work, the catechol (CA)-amine reaction has been thoroughly investigated by using CA and two amines m-phenylenediamine and piperazine. We verify that both primary and secondary amines are prone to link with CA through Michael addition to form polyphenol/polyamine oligomers under aerobic and mild-alkaline conditions. Molecular simulations indicate that the Michael addition products are dominant for both aromatic and aliphatic amines with CA, which supports the durable chem- and phystability of the codeposited coatings. The aggregation kinetics of polyphenol/polyamine is provided for the first time, and the formed aggregates show high-adhesive properties, which can be deposited as the skin layers for high-performance nanofiltration membranes.
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