Charged ultrafiltration membranes based on TEMPO-oxidized cellulose nanofibrils/poly(vinyl alcohol) antifouling coating

被引:38
作者
Aguilar-Sanchez, Andrea [1 ]
Jalvo, Blanca [1 ]
Mautner, Andreas [2 ]
Rissanen, Ville [3 ]
Kontturi, Katri S. [3 ]
Abdelhamid, Hani Nasser [1 ]
Tammelin, Tekla [3 ]
Mathew, Aji P. [1 ]
机构
[1] Stockholm Univ, Div Mat & Environm Chem, Frescativagen 8, S-10691 Stockholm, Sweden
[2] Univ Vienna, Inst Mat Chem & Res, Fac Chem, Polymer & Composite Engn Grp, Wahringer Str 42, A-1090 Vienna, Austria
[3] VTT Tech Res Ctr Finland, Solut Nat Resources & Environm, POB 1000, FIN-02044 Espoo, Finland
基金
欧盟地平线“2020”;
关键词
Pore structure - Cellulose - Nanofibers - Ultrafiltration - Coatings - Thickness measurement;
D O I
10.1039/d0ra10220b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study reports the potential of TEMPO-oxidized cellulose nanofibrils (T-CNF)/poly(vinyl alcohol) (PVA) coatings to develop functionalized membranes in the ultrafiltration regime with outstanding antifouling performance and dimensional/pH stability. PVA acts as an anchoring phase interacting with the polyethersulfone (PES) substrate and stabilizing for the hygroscopic T-CNF via crosslinking. The T-CNF/PVA coated PES membranes showed a nano-textured surface, a change in the surface charge, and improved mechanical properties compared to the original PES substrate. A low reduction (4%) in permeance was observed for the coated membranes, attributable to the nanometric coating thickness, surface charge, and hydrophilic nature of the coated layer. The coated membranes exhibited charge specific adsorption driven by electrostatic interaction combined with rejection due to size exclusion (MWCO 530 kDa that correspond to a size of similar to 35-40 nm). Furthermore, a significant reduction in organic fouling and biofouling was found for T-CNF/PVA coated membranes when exposed to BSA and E. coli. The results demonstrate the potential of simple modifications using nanocellulose to manipulate the pore structure and surface chemistry of commercially available membranes without compromising on permeability and mechanical stability.
引用
收藏
页码:6859 / 6868
页数:10
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