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Biocatalytic PVDF composite hollow fiber membranes for CO2 removal in gas-liquid membrane contactor.

Authors :
Xu, Yilin
Lin, Yuqing
Chew, Nick Guan Pin
Malde, Chandresh
Wang, Rong
Source :
Journal of Membrane Science. Feb2019, Vol. 572, p532-544. 13p.
Publication Year :
2019

Abstract

Abstract A highly efficient biocatalytic carbonic anhydrase (CA)-polydopamine (PDA)/polyethylenimine (PEI)-polyvinylidene fluoride (PVDF) (referred to as CA-m-PVDF) composite membrane was fabricated for CO 2 conversion and capture in the gas-liquid membrane contactor (GLMC) process. The co-deposition of PDA/PEI with amino functional groups was employed to amine-functionalize a PVDF substrate as support for subsequent in-situ CA immobilization by cross-linking with glutaraldehyde. This enhances the enzyme stability and prolongs its lifespan, thus facilitates CO 2 hydration efficiency in the GLMC process. In this work, different immobilization CA protocols were compared based on the CA activity and activity recovery. For biocatalytic CA-m-PVDF membranes, the best activity of 498 U m−2 (membrane) and a corresponding activity recovery of 31.5% were achieved (m(5 h)-PVDF as support, 0.67 (v/v)% GLU as cross-linking agent, 600 μg mL−1 CA solution, pH 8.0, temperature at 25 °C, and 24 h reaction time). By using water as absorbent with a liquid velocity of 0.25 m s−1 in a bench-scale GLMC setup, a high-efficiency CO 2 absorption flux of 2.5 × 10−3 mol m−2 s−1 was obtained, which was ~165% higher than that of the non-biocatalytic m-PVDF membrane. The long-term stability test showed a good enzyme activity for CO 2 hydration capacity for the CA-m-PVDF membranes during 40 days of test duration. Overall, the results achieved in this work may provide promising insights into enzyme immobilization on polymeric supports for the development of high-efficiency biocatalytic membranes for CO 2 capture in GLMC applications. Highlights • A highly efficient biocatalytic composite membrane was fabricated for CO 2 conversion and capture. • PDA/PEI with amino functional groups was co-deposited to amine-functionalize a PVDF substrate. • Subsequent in-situ carbonic anhydrase (CA) immobilization was conducted by cross-linking. • The resultant membrane shows a high CO 2 absorption flux of 2.5 × 10-3 mol m-2 s-1 in the gas-liquid membrane contactor. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03767388
Volume :
572
Database :
Academic Search Index
Journal :
Journal of Membrane Science
Publication Type :
Academic Journal
Accession number :
133599226
Full Text :
https://doi.org/10.1016/j.memsci.2018.11.043