界面聚合
膜
化学工程
石墨烯
氧化物
材料科学
聚酰胺
扩散
相(物质)
海水淡化
薄膜复合膜
聚合
纳米复合材料
高分子化学
反渗透
化学
纳米技术
聚合物
复合材料
有机化学
单体
生物化学
工程类
热力学
物理
冶金
作者
Biqin Wu,Na Zhang,Mengling Zhang,Shuhao Wang,Xiaoxiao Song,Zhou Yong,Saren Qi,Congjie Gao
出处
期刊:Membranes
[Multidisciplinary Digital Publishing Institute]
日期:2021-06-29
卷期号:11 (7): 488-488
被引量:14
标识
DOI:10.3390/membranes11070488
摘要
In this paper, we used an octadecylamine functionalized graphene oxide (ODA@GO) to induce the confined growth of a polyamide nanofilm in the organic and aqueous phase during interfacial polymerization (IP). The ODA@GO, fully dispersed in the organic phase, was applied as a physical barrier to confine the amine diffusion and therefore limiting the IP reaction close to the interface. The morphology and crosslinking degree of the PA nanofilm could be controlled by doping different amounts of ODA@GO (therefore adjusting the diffusion resistance). At standard seawater desalination conditions (32,000 ppm NaCl, ~55 bar), the flux of the resultant thin film nanocomposite (TFN) membrane reached 59.6 L m−2 h−1, which was approximately 17% more than the virgin TFC membrane. Meanwhile, the optimal salt rejection at seawater conditions (i.e., 32,000 ppm NaCl) achieved 99.6%. Concurrently, the boron rejection rate was also elevated by 13.3% compared with the TFC membrane without confined growth.
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