TY - JOUR
T1 - Facile bio-functionalized design of thermally responsive molecularly imprinted composite membrane for temperature-dependent recognition and separation applications
AU - Wu, Yilin
AU - Yan, Ming
AU - Lu, Jian
AU - Wang, Chen
AU - Zhao, Juan
AU - Cui, Jiuyun
AU - Li, Chunxiang
AU - Yan, Yongsheng
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - It is becoming significant needed that ‘smart membranes’ with specific recognition sites can rapidly change flow rates in response to external stimuli. Herein, inspired by a mussel-inspired two-step surface synthesis methodology, we have reported a novel system for harvesting thermally responsive molecularly imprinted composite membranes (TMICMs) with excellent selective adsorption and separation performance toward template molecules. A self-polymerized polydopamine coating process was initially conducted to obtain the highly adjustable active surfaces. The TMICMs were then prepared through an in situ photoinitiated ATRP method by using N-isopropylacrylamide (NIPAm) as the thermo-responsive backbone monomer. Attributing to the formation of the polydopamine coating surfaces, remarkably enhanced rebinding capacity (2.343 mmol cm−2) was obtained. Importantly, the as-prepared TMICMs with thermo-responsive “specific recognition sites” also exhibited excellent temperature-dependent switching modes for selective recognition and separation of the template molecule (ciprofloxacin). Meanwhile, this bioinspired thermo-responsive method could not only present an outstanding permselectivity property (separation factor β was more than 4.0), but also showed excellent structural stability and adsorption regeneration performance (the TMICMs could still possessed 92.74% of the maximum adsorption capacity after four adsorption/desorption cycles). Finally, we envision that the developed bio-adhesive platform synthesis strategy employed in this case can be utilized in a broad range of applications and will have a great impact on the fields of fluid handling, thermo-responsive sensors, membrane-based drug delivery and separation.
AB - It is becoming significant needed that ‘smart membranes’ with specific recognition sites can rapidly change flow rates in response to external stimuli. Herein, inspired by a mussel-inspired two-step surface synthesis methodology, we have reported a novel system for harvesting thermally responsive molecularly imprinted composite membranes (TMICMs) with excellent selective adsorption and separation performance toward template molecules. A self-polymerized polydopamine coating process was initially conducted to obtain the highly adjustable active surfaces. The TMICMs were then prepared through an in situ photoinitiated ATRP method by using N-isopropylacrylamide (NIPAm) as the thermo-responsive backbone monomer. Attributing to the formation of the polydopamine coating surfaces, remarkably enhanced rebinding capacity (2.343 mmol cm−2) was obtained. Importantly, the as-prepared TMICMs with thermo-responsive “specific recognition sites” also exhibited excellent temperature-dependent switching modes for selective recognition and separation of the template molecule (ciprofloxacin). Meanwhile, this bioinspired thermo-responsive method could not only present an outstanding permselectivity property (separation factor β was more than 4.0), but also showed excellent structural stability and adsorption regeneration performance (the TMICMs could still possessed 92.74% of the maximum adsorption capacity after four adsorption/desorption cycles). Finally, we envision that the developed bio-adhesive platform synthesis strategy employed in this case can be utilized in a broad range of applications and will have a great impact on the fields of fluid handling, thermo-responsive sensors, membrane-based drug delivery and separation.
KW - Bioinspired self-polymerization coating
KW - Ciprofloxacin
KW - Molecular imprinting
KW - Selective recognition and separation
KW - Thermo-responsive membrane
UR - http://www.scopus.com/inward/record.url?scp=84991449951&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2016.10.023
DO - 10.1016/j.cej.2016.10.023
M3 - 文章
AN - SCOPUS:84991449951
SN - 1385-8947
VL - 309
SP - 98
EP - 107
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -