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AGET ATRP
APPLIED SURFACE SCIENCE · 2017 · IF 3.387

Design of UV-absorbing PVDF membrane via surface-initiated AGET ATRP

Li Dong,Xiangdong Liu,Zhengrong Xiong,Dekun Sheng,Yan Zhou,Changhong Lin,Yuming Yang

Herein, PVDF membranes with excellent UV-absorbing property were first synthesized through grafting the polymerizable low-molecular-weight organic UV-absorber 2-hydroxy-4-(3-methacryloxy-2-hydroxylpropoxy) benzophenone (BPMA) onto α-bromoester-functionalized PVDF membranes via the surface-initiated activator generated by electron transfer atom transfer radical polymerization (SI-AGET ATRP). The surface initiators were immobilized by the reaction between 2-bromoisobutyryl bromide (BIBB) and the hydroxylated PVDF membranes. PVDF-g-PBPMA membranes with different grafting densities were obtained by tuning the polymerization time and the modified membranes were characterized by 1 H-NMR, FT-IR, XPS, SEM, UV–vis Spectrophotometer, TGA and DSC. The experimental results indicated that PBPMA chains were successfully introduced onto PVDF membranes. Most importantly, the PVDF-g-PBPMA membranes exhibited outstanding UV-shielding property. UV–vis transmittance spectra showed that most UV light below 360 nm could be absorbed by PVDF-g-PBPMA membranes and the whole UV light region (200–400 nm) can be blocked with the reaction time increased.

研究领域: 材料科学 · 高分子化学
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APPLIED SURFACE SCIENCE · 2014 · IF 2.538

Optimizing conditions of preparation of thermoresponsive SiO2-POEGMA particles via AGET-ATRP

Zhiping Du,Xiaofeng Sun,Xiumei Tai,Guoyong Wang,Xiaoying Liu

Thermosensitive poly(ethylene glycol) methyl ether methacrylate (POEGMA) was grafted on SiO 2 nanoparticles using activators generated by electron transfer atom transfer radical polymerization (AGET-ATRP) technique. The effects of the amount of ligand, catalyst, ascorbic acid and monomer, as well as the reaction temperature and time were systematically investigated and optimized to get a high grafting density. The structure of the hybrid materials was characterized by Fourier transform infrared (FTIR) spectroscopy, and the morphology was characterized by transmission electron microscopy (TEM) observations. Thermosensitive properties of SiO 2 -POEGMA particles were investigated at different grafting densities by turbidity measurements.

研究领域: 材料科学 · 化学工程
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IRANIAN POLYMER JOURNAL · 2020 ·Vol. 29 ·期 3 ·275-286 · IF 1.707

Controlling gelation time of in situ polymerization of gel system through AGET ATRP principle

Shao Ming-lu,Yue Xiang-an,He Jie

To better control the gelation time of in situ polymerization of gel system in reservoir, an activator regenerated by AGET (activator generated by electron transfer) ATRP (atom transfer radical polymerization) initiating system was developed. The AGET ATRP initiating system was composed of an initiator 1,2-dibromoethane, a catalyst ferric chloride and a reducing agent vitamin C, and the effects of these three component proportions on the gelation time and gel viscosity were systematically investigated. Results of bottle tests indicated that the gelation time can even be more than 20 h at 60 °C at optimal concentration ratios. Moreover, the viscosity decreased and the gelation time increased with the increase of salinity and temperature. The gelation time of the core test was 1.5 times or even longer in comparison with that of the bottle test owing to the influences of dilution, adsorption, and rock skeleton isolation. It was also confirmed that the AGET ATRP initiating system can initiate the cross-link gelation of monomers in the core. The enhanced oil recovery result indicated that the oil recovery increased by 9.17% after the gelation of the gelling solutions, and final oil recovery was 40.05%. This research provided a brand-new method to control the gelation time of the in situ polymerization of gel system.

研究领域: 化学工程 · 石油工程
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E-POLYMERS · 2019 ·Vol. 19 ·期 1 ·323-329 · IF 1.491

γ-valerolactone (GVL) as a bio-based green solvent and ligand for iron-mediated AGET ATRP

XianRong Shen,DengZhou Xia,YiXin Xiang,JianGang Gao

In this paper, γ-valerolactone (GVL), a bio-based polar solvent, was applied as green solvent for iron(III)-catalyzed AGET ATRP without any external ligand. GVL is a fully degradable, non-toxic green solvent and has complex ability to iron halide complexes through –OCO- group. GVL as the solvent and the ligand for AGET ATRP of MMA in a controlled manner, as proved by kinetic study, the low PDI values and the increase in polymer molecular weight versus monomer conversion. Chain re-initiation experiments and 1 HNMR characterization were conducted to further confirm the living feature. Graphical

CAS / MDL: 80-62-6
研究领域: 材料科学 · 化学工程
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POLYMER SCIENCE SERIES B · 2016 ·Vol. 58 ·期 3 ·313-320 · IF 0.737

Synthesis and surface properties of a new fluorinated acrylic diblock copolymer via AGET ATRP

Guo Yanjuan,Liu Weiqu

A series of fluorinated diblock copolymers poly(2,2,3,4,4,4-hexafluorobutyl methacrylate)- b -poly(glycidyl methacrylate) PHFMA- b -PGMA with different fluorine content were synthesized by activator generated by electron transfer atom transfer radical polymerization (AGET ATRP). FTIR, 1 H NMR and GPC data verified feasibility and controllability of the synthesis. In order to evaluate the effect of chain structure on the surface properties, corresponding homopolymer poly(2,2,3,4,4,4-hexafluorobutyl methacrylate) and random copolymer copoly(2,2,3,4,4,4-hexafluorobutyl methacrylate- r -glycidyl methacrylate) were also comparatively studied. Contact angle measurements indicated that the water and ethyleneglycol contact angles of block- and random copolymers increased with increase of fluorine content, but in different manner. This difference comes from different surface energy at the same fluorine content on film surface. The surface stability of block-copolymer was obviously better than that of random copolymer; the same results were observed in heat resistance tests.

研究领域: 材料科学 · 高分子化学
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APPLIED SURFACE SCIENCE · 2011 · IF 1.795

Facile surface glycosylation of PVDF microporous membrane via direct surface-initiated AGET ATRP and improvement of antifouling property and biocompatibility

Jing Yuan,Jian-qiang Meng,Yin-lin Kang,Qi-yun Du,Yu-feng Zhang

This paper describes a facile and novel approach for the surface glycosylation of poly(vinylidene difluoride) (PVDF) microporous membrane. A glycopolymer poly( d -gluconamidoethyl methacrylate) (PGAMA) was tethered onto the membrane surface via activators generated by electron transfer atom transfer radical polymerization (AGET ATRP) directly initiated from the PVDF surface. Chemical changes of membrane surface were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). It was revealed that PGAMA was successfully grafted onto the membrane surface and its grafting density can be modulated in a wide range up to 2.4   μmol/cm 2 . The effects of glycosylation on membrane morphology, flux and surface hydrophilicity were investigated. Field emission scanning electron microscopy (FESEM) results indicated shrinkage of the surface pore diameters and the growth of the glycopolymer layer on the membrane surface. The static water contact angle (WCA) of the membrane surface decreased from 110° to 30.4° with the increase of grafting density, indicating that the PGAMA grafts dramatically improved the surface hydrophilicity. The protein adsorption and platelets adhesion experiments indicated that the grafted PGAMA could effectively improve the membrane antifouling property and biocompatibility.

研究领域: 材料科学 · 生物医学工程
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2014 ·Vol. 52 ·期 7 ·1020-1027 · IF 3.245

Iron-mediated AGET ATRP of methyl methacrylate in the presence of polar solvents as ligands

Danfeng Yang,Dan He,Yonggui Liao,Zhigang Xue,Xingping Zhou,Xiaolin Xie

The polar solvents, N -methylpyrrolidone (NMP), N , N -dimethylformamide (DMF), and acetonitrile (CH 3 CN) were used as ligands for iron(III)-mediated activators generated by electron transfer atom transfer radical polymerizations (AGET ATRPs) of methyl methacrylate (MMA) with various initiators and reducing agents. Polymerizations were conducted with a molar ratio of [MMA] 0 /[initiator] 0 /[FeBr 3 ] 0 /[reducing agent] 0 = 100:1:1:0.5 and a volume ratio of MMA/solvent = 2:1 at 60 °C to investigate the effects of initiator, solvent and reducing agent, and most of the systems showed the typical features of “living”/controlled radical polymerization. In order to get a deeper understanding of the mechanism, the amount of the reducing agent was changed to study the polymerization behavior. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52 , 1020–1027

研究领域: 高分子化学 · 材料科学
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POLYMER SCIENCE SERIES B · 2023 ·Vol. 65 ·期 2 ·103-110 · IF 1.2

Iron-Mediated AGET ATRP of Methyl Methacrylate in Green Polar Ethyl Lactate Solvent without any External Ligand

Tianchen Song,Xiang Yixin,Gao Jiangang,Shen Xianrong

Abstract In this paper, ethyl lactate was used as a green solvent for iron(III)-catalyzed activators generated by electron transfer atom transfer radical polymerizations of methyl methacrylate in the absence of any external ligand. The effects of amount and type of solvent were investigated. Most of the systems showed the typical features of reversible deactivation radical polymerization. The polymerization of methyl methacrylate with ethyl lactate as a solvent and a ligand proceeded in a controlled manner as demonstrated by the first-order kinetic plot, low dispersity of polymers, an increase in polymer molecular weight with rise of the monomer conversion and by chain extension experiments.

研究领域: 材料科学 · 聚合物化学
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CELLULOSE · 2022 ·Vol. 30 ·期 2 ·1087-1102 · IF 6.123

Phytic acid-assist for self-healing nanocomposite hydrogels with surface functionalization of cellulose nanocrystals via SI-AGET ATRP

Li Chunyu,Hou Zehua,Li Pan,Zhang Guomin,Bai Liangjiu,Wang Wenxiang,Chen Hou,Yang Huawei,Yang Lixia

Cellulose nanocrystals (CNCs) have been widely used in the surface modification and construction of nanocomposites due to their excellent surface activity and high tensile strength. In this manuscript, nanocomposite hydrogels were prepared by implanting poly(glycidyl methacrylate)-modified CNCs (CNCs@PGMA) and biomass phytic acid (PA). After extracting CNCs from microcrystalline cellulose, PGMA was successfully grafted on the surface of CNCs by surface-initiated Activator Generated by Electron Transfer Atom Transfer Radical Polymerization (SI-AGET ATRP). With the assistance of PA, the reversible hydrogen bonding interaction between the internal structures of the matrix was promoted to construct the CNCs@PGMA/PA self-healing nanocomposite hydrogels. The obtained hydrogels by using CNCs@PGMA and PA as additives have excellent mechanical properties (tensile strength of 1.39 MPa) and self-healing ability (91.4% after 6 h). This study develops a facile method for the preparation of nanocomposite hydrogels with excellent self-healing properties. Graphical abstract

CAS / MDL: 83-86-3
研究领域: 材料科学 · 化学工程 · 纳米技术
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Materials Science & Engineering C-Materials for Biological Applications · 2012 ·Vol. 32 ·期 6 ·1699-1703 · IF 2.686

Use of Yb-based catalyst for AGET ATRP of acrylonitrile to simultaneously control molecular mass distribution and tacticity

Jing Ma,Hou Chen,Min Zhang,Chunhua Wang,Ying Zhang,Rongjun Qu

Yb-based catalyst was used for the first time for atom transfer radical polymerization using activators generated by electron transfer (AGET ATRP) of acrylonitrile (AN) with 2-bromopropionitrile (BPN) as initiator, 2, 2′-bipyridine (bipy) as ligand, and tisn(II) bis(2-ethylhexanoate) (Sn(EH) 2 ) as reducing agent in the presence of air. With respect to AGET ATRP of AN catalyzed by CuBr 2 , an evident increase of polymer tacticity was observed for AGET ATRP of AN. The increase of syndiotacticity became more and more pronounced than the increase of isotacticity of polyacrylonitrile (PAN) along with YbBr 3 content. The block copolymer PAN-b-PMMA with molecular weight at 60,000 and polydispersity at 1.36 was successfully prepared.

研究领域: 高分子化学 · 材料科学 · 催化化学 · 聚合物合成 · 功能材料
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RSC Advances · 2015 ·Vol. 5 ·期 22 ·17194-17201 · IF 3.84

Synthesis of hybrid silica nanoparticles grafted with thermoresponsive poly(ethylene glycol) methyl ether methacrylate via AGET-ATRP

Zhiping Du,Xiaofeng Sun,Xiumei Tai,Guoyong Wang,Xiaoying Liu

Thermosensitive SiO2 nanoparticles were prepared with graft-on poly(ethylene glycol) methyl ether methacrylate (POEGMA, Mn ∼ 300 or 500 g mol−1) via atom transfer radical polymerization with activators generated through electron transfer (AGET ATRP). CuBr2/PMDETA and ascorbic acid (AA) were employed as the catalyst and reducing agent respectively in the fabrication process. The structure and surface composition of our hybrid materials were analyzed using Fourier Transform Infrared (FTIR) spectroscopy and X-ray Photoelectron Spectroscopy (XPS) in detail. The results of Thermogravimetric Analysis (TGA) show that AGET-ATRP could provide a higher surface grafting density to get more pronounced thermosensitive properties. The morphology of our hybrid SiO2 nanoparticles was characterized by Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM). measurements of turbidity, Dynamic Light Scattering (DLS), and phase transfer were conducted to investigate the thermal responses of the hybrid material. In addition, Pickering emulsions were prepared using such hybrid SiO2-POEGMA as an emulsifier. Moreover, its fast de-emulsification above a lower critical solution temperature (LCST) may be exploited for the efficient separation and recycling of catalysts in future.

研究领域: 材料科学 · 化学工程 · 纳米技术
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REACTIVE & FUNCTIONAL POLYMERS · 2019 · IF 3.074

Fabrication of nanoprobe via AGET ATRP and photocatalytic modification for highly sensitive detection of Hg(II)

Xiaoqing Zhao,Na Wang,Hou Chen,Liangjiu Bai,Hui Xu,Wenxiang Wang,Huawei Yang,Donglei Wei,Lixia Yang

In this paper, a functional nanoprobe based on graphene oxide (GO) composites was successfully prepared for detection of mercury ion (Hg(II)) with high sensitivity. GO as a substrate was modified and used for the growth of polymer chains to synthesize polyacrylonitrile-grafted GO (PAN- g -GO) by activator generated by electron transfer atom transfer radical polymerization (AGET ATRP). Under the condition of visible light shines, the PAN- g -GO was further modified to prepare [poly(acrylonitrile- co -vinyl(diphenyl pyridine))]-grafted GO (P(AN- co -PHPY)- g -GO) nanomaterial by one-step synthesis. Finally, P(AN- co -PHPY)- g -GO as a nanoprobe was dropped to the surface of the glassy carbon electrode and assembled to the electrochemical sensor . Moreover, it can effectively improve the enrichment capacity of mercury ions and increase the electron transfer rate on the electrode surface. Differential pulse anodic stripping voltammetry (DPASV) was used to evaluate the electrochemical performance. Under optimum conditions, the response of Hg(II) at this resulting sensor was linear in the range of 2.0 μM~0.1 nM with a detection limit of 0.06 nM. Additionally, this sensor showed excellent reproducibility, selectivity and stability.

CAS / MDL: 600-00-0
研究领域: 纳米技术 · 材料科学 · 分析化学 · 环境科学
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