TY - JOUR
T1 - Self-Reducible Conjugated Microporous Polyaniline for Long-Term Selective Cr(VI) Detoxication Driven by Tunable Pore Dimension
AU - Chen, Jie
AU - Wang, Yubing
AU - Ye, Changshen
AU - Lyu, Wei
AU - Zhu, Jinwei
AU - Yan, Wei
AU - Qiu, Ting
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/6/24
Y1 - 2020/6/24
N2 - A simple methodology to controllably tune the pore size and Cr(VI) adsorption capacity was reported herein to synthesize a new series of conjugated microporous polyaniline (CMPA) networks. The well-ordered micropore was acquired through our very recent Bristol-Xi'an Jiaotong method, and the pore size was fine-tuned to increase with the increasing length of linkers, mimicking covalent organic frameworks and metal organic frameworks very much. A selective ultrahigh adsorption capacity of 520.8 mg/g was achieved by CMPA-1 in a very fast manner, with a systematically gradual decrease to 173.9 mg/g of CMPA-3 by enlarging the pore size of the networks, featuring tunable adsorption capacity through molecular-size-recognition mechanism. Additionally, our robust CMPA networks, which were constructed by Buchwald-Hartwig chemistry, showed the complete function of polyaniline and were capable of providing, besides large storage capacity for Cr(III), at least 10 reductant/desorption-free cycles for effective Cr(VI) reduction and detoxication through their novel self-reducible redox states. Outcomes showed that our CMPAs could be applied as new self-healing scavengers in the next generation for Cr(VI) storage and detoxication.
AB - A simple methodology to controllably tune the pore size and Cr(VI) adsorption capacity was reported herein to synthesize a new series of conjugated microporous polyaniline (CMPA) networks. The well-ordered micropore was acquired through our very recent Bristol-Xi'an Jiaotong method, and the pore size was fine-tuned to increase with the increasing length of linkers, mimicking covalent organic frameworks and metal organic frameworks very much. A selective ultrahigh adsorption capacity of 520.8 mg/g was achieved by CMPA-1 in a very fast manner, with a systematically gradual decrease to 173.9 mg/g of CMPA-3 by enlarging the pore size of the networks, featuring tunable adsorption capacity through molecular-size-recognition mechanism. Additionally, our robust CMPA networks, which were constructed by Buchwald-Hartwig chemistry, showed the complete function of polyaniline and were capable of providing, besides large storage capacity for Cr(III), at least 10 reductant/desorption-free cycles for effective Cr(VI) reduction and detoxication through their novel self-reducible redox states. Outcomes showed that our CMPAs could be applied as new self-healing scavengers in the next generation for Cr(VI) storage and detoxication.
KW - conjugated microporous polyanilines
KW - Cr(VI) selective detoxication
KW - molecular-size-recognition
KW - self-reducible redox states
KW - tunable pore dimension
UR - https://www.scopus.com/pages/publications/85087111411
U2 - 10.1021/acsami.0c07059
DO - 10.1021/acsami.0c07059
M3 - 文章
C2 - 32479056
AN - SCOPUS:85087111411
SN - 1944-8244
VL - 12
SP - 28681
EP - 28691
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 25
ER -