期刊
CHEMISTRY OF MATERIALS
卷 30, 期 4, 页码 1265-1276出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.7b04598
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资金
- Tufts University
- Tufts Collaborates program
- National Science Foundation (NSF) [CBET-1703549, CBET-1553661]
- National Science Foundation under NSF [ECS-0335765]
- Directorate For Engineering [1553661] Funding Source: National Science Foundation
Hydrogels are promising materials as membrane selective layers due to their fouling-resistant nature, tunable mesh size, and functionalizability. These features are especially critical for protein purification applications. However, the fabrication of thin, uniform hydrogel membrane selective layers using a simple, scalable process is an unmet challenge. We demonstrate a new method, interfacially initiated free radical polymerization (IIFRP), for fabrication of ultrathin hydrogel selective layers on porous supports in a simple and reproducible process. This method utilizes segregation of the monomer and the photoinitiator into two separate, immiscible phases to form a very thin, uniform, and defect-free hydrogel layer at the interface upon photopolymerization. The resulting hydrogel-coated membranes have selective layers as thin as <100 nm, and can separate the proteins based on their size with a sharp molecular weight cutoff. The method is readily tunable for a broader range of separations simply by altering experimental parameters (e.g., UV exposure time, monomer concentration) or addition of inert porogens/comonomers. Membranes prepared using this method exhibit extremely high antifouling properties upon extended exposure to protein solution providing a promising approach for protein purification. Taken together, these findings illustrate a significant step toward simple, robust, and scalable fabrication of ultrathin, functional hydrogel selective layers in a controlled manner, with potential applications in bioseparations, wastewater treatment, and gas separation.
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