scholarly journals Hyper-crosslinked polymers with controlled multiscale porosity for effective removal of benzene from cigarette smoke

e-Polymers ◽  
2021 ◽  
Vol 22 (1) ◽  
pp. 19-29
Author(s):  
Xiaochen Xia ◽  
Peijian Sun ◽  
Xuehui Sun ◽  
Yipeng Wang ◽  
Song Yang ◽  
...  

Abstract A series of hyper-crosslinked polymers (HCPs) with connected hierarchical porous structures were synthesized from phenyl-based precursors of benzene (BEN), benzyl alcohol, aniline, biphenyl, and 1,3,5-triphenylbenzene (TPB) via the knitting method. The porous structures of the HCPs were greatly influenced by substituent groups and BEN ring number in the precursors. HCPs prepared from TPB had the largest surface area and pore volume with multiscale porosity. The porous structure of the HCPs could also be adjusted by the crosslinker amount. Insufficient crosslinking led to incomplete pore architecture, while excessive crosslinking resulted in a considerable decrease in the pore volume. With these HCPs as adsorbents, the BEN yield in the cigarette smoke could be largely reduced due to the connected multiscale porosity and π–π aromatic stacking interaction that facilitated the smoke aerosol passing and the small aromatic molecules absorbing, showing great potential of these HCPs as adsorbents for effective removal of BEN from cigarette smoke.

Author(s):  
Jinlong Hu ◽  
Lingzhi Zhang

Finding a tunable and facile method to make functional porous hollow carbons with ultrahigh-pore-volume hierarchical porous structures and well-designed functionalities has been challenging. Herein, we present a gas-solid interface reaction...


2016 ◽  
Vol 92 ◽  
pp. 345-355 ◽  
Author(s):  
Kathirvel Ganesan ◽  
Anne Dennstedt ◽  
Adam Barowski ◽  
Lorenz Ratke

RSC Advances ◽  
2017 ◽  
Vol 7 (52) ◽  
pp. 32795-32805 ◽  
Author(s):  
Xingxing Wu ◽  
Zhongwei Tian ◽  
Langqing Hu ◽  
Sha Huang ◽  
Jinjun Cai

Enteromorpha prolifera was converted into hierarchical carbons through the carbonization and activation with surface area and pore volume up to 3345 m2 g−1 and 1.94 cm3 g−1, showing excellent performance for H2 storage and supercapacitors.


2011 ◽  
Vol 115 (36) ◽  
pp. 17676-17681 ◽  
Author(s):  
Shunsuke Murai ◽  
Koji Fujita ◽  
Koji Iwata ◽  
Katsuhisa Tanaka

Small ◽  
2017 ◽  
Vol 13 (44) ◽  
pp. 1702474 ◽  
Author(s):  
Zhuangnan Li ◽  
Srinivas Gadipelli ◽  
Yuchen Yang ◽  
Zhengxiao Guo

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1331
Author(s):  
Siwei Zhao ◽  
Shaohua Jin ◽  
Huanmin Liu ◽  
Shengfu Li ◽  
Kun Chen

Due to their high absorption coefficient and long carrier lifetime, halide perovskites are promising candidates for photocatalysts. For this study, the antisolvent crystallization protocol and the colloidal crystal templating approach were combined to fabricate the highly crystalline cesium lead bromide perovskite with inverse opal morphology (IO-CsPbBr3). Scanning electron microscopy and transmission electron microscope images demonstrate the three-dimensional well-ordered porous structures of the IO-CsPbBr3 and their single-crystalline features. The presented approach not only provides hierarchical porous structures but also enhances overall crystallinity. When used as catalysts to promote the polymerization of 2,2′,5′,2″-ter-3,4-ethylenedioxythiophene, the highly crystalline IO-CsPbBr3 exhibits a superior photocatalytic performance compared to its polycrystalline counterpart. Furthermore, the morphology and the crystalline structure of the highly crystalline IO-CsPbBr3 are well preserved under photocatalytic conditions. This novel approach enables the preparation of a halide perovskite inverse opal with high crystallinity.


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