scholarly journals Reusable Surface-Modified Bacterial Cellulose Based on Atom Transfer Radical Polymerization Technology with Excellent Catalytic Properties

Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1443 ◽  
Author(s):  
Xin Li ◽  
Quan Feng ◽  
Dawei Li ◽  
Narh Christopher ◽  
Huizhen Ke ◽  
...  

The high catalytic activity of membrane-binding gold nanoparticles (AuNPs) makes its application in oxidation or reduction an attractive challenge. Herein, surface-functionalized bacterial cellulose (BC-poly(HEMA)) was successfully prepared with 2-hydroxyethyl methacrylate (HEMA) as monomers via the atom transfer radical polymerization (ATRP) method. BC-poly(HEMA) was further utilized as not only reducing agent but also carrier for uniform distribution of the AuNPs in the diameter of about 8 nm on the membrane surface during the synthesis stage. The synthesized AuNPs/BC-poly(HEMA) exhibited excellent catalytic activity and reusability for reducing 4-nitrophenol (4-NP) from NaBH4. The results proved that the catalytic performance of AuNPs/BC-poly(HEMA) was affected by the surrounding temperature and pH, and AuNPs/BC-poly(HEMA) maintained the extremely high catalytic activity of AuNPs/BC-poly(HEMA) even after 10 reuses. In addition, no 4-NP was detected in the degradation solution after being stored for 45 days. The reusable catalyst prepared by this work shows a potential industrial application prospect.

Membranes ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 417
Author(s):  
Lehui Ren ◽  
Meng Ping ◽  
Xingran Zhang

A facile approach to fabricate antibiofouling membrane was developed by grafting quaternary ammonium compounds (QACs) onto polyvinylidene fluoride (PVDF) membrane via surface-initiated activators regenerated by electron transfer atom-transfer radical-polymerization (ARGET ATRP) method. During the modification process, a hydrophilic silica nanoparticle layer was also immobilized onto the membrane surface as an interlayer through silicification reaction for QAC grafting, which imparted the membrane with favorable surface properties (e.g., hydrophilic and negatively charged surface). The QAC-modified membrane (MQ) showed significantly improved hydrophilicity and permeability mainly due to the introduction of silica nanoparticles and exposure of hydrophilic quaternary ammonium groups instead of long alkyl chains. Furthermore, the coverage of QAC onto membrane surface enabled MQ membrane to have clear antibacterial effect, with an inhibition rate ~99.9% of Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive), respectively. According to the batch filtration test, MQ had better antibiofouling performance compared to the control membrane, which was ascribed to enhanced hydrophilicity and antibacterial activity. Furthermore, the MQ membrane also exhibited impressive stability of QAC upon suffering repeated fouling–cleaning tests. The modification protocols provide a new robust way to fabricate high-performance antibiofouling QAC-based membranes for wastewater treatment.


2010 ◽  
Vol 150-151 ◽  
pp. 565-570 ◽  
Author(s):  
Yong Bo Shen ◽  
Ya Tao Zhang ◽  
Jian Hua Qiu ◽  
Yan Wu Zhang ◽  
Hao Qin Zhang

Hydrophilic poly((poly(ethylene glycol) methyl ether methacrylate) (P(PEGMA)) brushes were grafted from chloromethylated polyethersulfone (CMPES) hollow fiber membrane surface by surface-initiated atom transfer radical polymerization(SI-ATRP) to improve the membrane’s hydrophilic property. The CMPES hollow fiber membrane was prepared by phase inversion process. The benzyl chloride groups on the CMPES membrane surface could afford effective macroinitiators for grafting the well-defined polymer brushes. Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy confirmed the grafting of P (PEGMA) chains. Field emission scanning electron microscopy (FESEM) was used to characterize the surface morphology of the CMPES membrane and modified membrane. The grafting yield of P (PEGMA) was determined by weight gain measurement. The results showed that the number-average molecular weight (Mn) of P (PEGMA) increased with the polymerization time. It was found that the grafting of P (PEGMA) brought higher pure water flux, improved water uptake ratio and better anti-protein absorption ability to CMPES membrane after modification.


RSC Advances ◽  
2016 ◽  
Vol 6 (66) ◽  
pp. 61434-61442 ◽  
Author(s):  
Dapeng Liu ◽  
Jing Zhu ◽  
Ming Qiu ◽  
Chunju He

Antifouling PVDF membranes were fabricated through the covalent binding of lysine methacrylamide (LysAA) brushes on the membrane surface via mussel-inspired surface-initiated atom transfer radical polymerization (SI-ATRP).


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Liang Li ◽  
Guoping Yan ◽  
Jiangyu Wu ◽  
Xianghua Yu ◽  
Qingzhong Guo

AbstractA simple one-step method for the chloromethylation of polyethersulfone (PES) under mild conditions provided surface benzyl chloride groups as the active initiators for the surface-initiated atom-transfer radical polymerization (ATRP) to tailor the functionality of the PES membrane. Functional hydrophilic polymer brushes of poly(ethylene glycol)monomethacrylate (PEGMA) and sodium 4- styrenesulfonate (NaStS), as well as their block copolymer brushes, were prepared via surface initiated ATRP from the chloromethylated PES surfaces. X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) were used to characterize the surface-modified membranes. The PEGMA-grafted PES membranes showed great protein resistance to protein adsorption compared to the pristine PES surface.


2016 ◽  
Vol 7 (5) ◽  
pp. 1037-1048 ◽  
Author(s):  
So-ichiro Nakanishi ◽  
Mitsunobu Kawamura ◽  
Yusuke Sunada ◽  
Hideo Nagashima

A new Fe(ii) complex, (Me3TACN)FeBr2(κ-NCMe), was prepared as an efficient and reusable catalyst for atom transfer radical polymerization.


2014 ◽  
Vol 50 (66) ◽  
pp. 9266-9269 ◽  
Author(s):  
Xiangyang Du ◽  
Jinlong Pan ◽  
Mengting Chen ◽  
Lifen Zhang ◽  
Zhenping Cheng ◽  
...  

A thermo-regulated phase separable catalysis (TPSC) system for AGET ATRP based on a thermo-regulated ionic liquid was developed for the first time. The corresponding transition metal catalysts could be easily recovered and reused several times with negligible loss of catalytic activity.


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