COLLOIDS AND SURFACES B-BIOINTERFACES
·
2012
·
IF 3.456
Wantong Song,Chunsheng Xiao,Liguo Cui,Zhaohui Tang,Xiuli Zhuang,Xuesi Chen
Construction of high density glycosylated surfaces is important in the investigation of interactions between pathogens and surface carbohydrates. In this work, we provided a flexible method for glycosyl surface fabrication by combination of surface-initiated atom transfer radical polymerization (SI-ATRP) and copper-catalyzed azide-alkyne 1,3-dipolar cycloaddition (CuAAC) reaction. Through this strategy, we got a very high surface glycosyl density of about 4 nmol/cm 2 with the surface “click” efficiency of nearly 50%. Then the carbohydrate decorated surfaces were used to mimic cell surfaces and specific recognition of mannose with Escherichia coli was observed. We believe the methodology provided here can be used as a facile way for construction of a wide range of functional biosurfaces.
研究领域:
生物化学
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材料科学
·
微生物学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
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2015
·Vol. 133
·期 1
·
IF 1.768
Caideng Yuan,Mingtong Cui,Longlong Feng,Jingpeng Wang,Yan Peng
An amino-functionalized nano-adsorbent (DETA-MNPs) was prepared by a process involving: (1) synthesis of superparamagnetic Fe 3 O 4 nanoparticles; (2) introduction of amino groups after which ATRP initiator was anchored; (3) grafting of glycidyl methacrylate (GMA) via SI-ATRP; and (4) ring-opening reaction of epoxy groups with diethylenetriamine (DETA). The nano-adsorbent was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM) and applied to remove Cu(II) in batch experiments. The effects of pH, Cu(II) concentrations, solution ionic strength, and contact time were investigated. The results show that the DETA-MNPs are spherical with cubic spine structure, high saturation magnetization (41.9 emu g −1 ), and an average diameter of 10 nm. The maximum Cu(II) adsorption capacity achieves 83.33 mg g −1 at pH 5.0 by Langmuir model. The adsorption process is highly pH-dependent and reaches equilibrium within 20 min. Furthermore, the DETA-MNPs exhibit excellent dispersibility and reusability. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 132 , 42859.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 8
·4226-4236
·
IF 3.108
Youning Chen,Wei Zhao,Juncai Zhang
The study focused on the preparation of a chelating resin with pyridine ring as the functional group. The 4VP monomer was directly grafted on the surface of CMPS resin via SI-ATRP, and the performance of adsorption of resin for Cr(VI), Pb(II), Cr(III), Zn(II), and Cd(II) was determined. With the extension of ATRP time and increase of 4VP consumption, the 4VP grafting rate was linearly increased, indicating an increase in the density of the pyridine ring on the resin surface. Adsorption experiments indicated that the adsorption capacity of the resin for the metal ions considerably improved when compared with that of those reported in literature, whereas the desorption rate and reusability were equivalent to those of the conventional resins. When the pH value was greater than 5.0, Pb(II), Cr(III), Zn(II), and Cd(II) ions could be adsorbed; however, when the pH value was less than 3.0, Cr(VI) could be selectively adsorbed. These results are indicative of a potential application of the resin in the treatment of heavy metal wastewater. Therefore, adoption of one-step SI-ATRP is one of the effective methods for preparing a chelating resin with high capacity via the selection of an appropriate functional monomer.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
POLYMER BULLETIN
·
2018
·Vol. 76
·期 3
·1081-1097
·
IF 1.589
Chen Youning,Zhao Wei,Yang Xiaoling,Li Yuhong
Using SI-ATRP technique, 1-vinylimidazole (VI) monomer was directly modified onto the surface of CMPS resin to prepare a chelating resin (PVI-g-PS) with imidazole ring as functional group. The adsorption properties of Cd(II), Ni(II), Pb(II) and Cu(II) were studied. It was found that with the increase in ATRP time and the amount of VIM, the graft ratio of VIM increased linearly, which indicated that the density of imidazole ring on the surface of resin increased. Adsorption experiments showed that the resin has good adsorption properties for Cd(II), Ni(II), Pb(II) and Cu(II). At pH 5.0, the static saturated adsorption amount of PVIM-g-PS for Cd(II), Ni(II), Pb(II) and Cu(II) was 2.82, 1.77, 1.22 and 0.83 mmol g −1 , respectively. The adsorption model could be described by Langmuir isothermal adsorption and the adsorption process accorded with quasi-first-order kinetic equation. In addition, the resin has good desorption rate and reusability. These findings suggest that the resin can be potentially applied to the efficient removal of heavy metal ions from wastewater.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
CARBOHYDRATE POLYMERS
·
2021
·
IF 9.381
Ming Li,Shiyu Fu
Wood is actually a natural polymers composite that is easy to process, mainly constituted of cellulose, hemicellulose and lignin. However, most wood-based functional materials are prepared by physical methods, which undoubtedly limit the application of wood-based materials. Herein, the wood aerogel (WA) was obtained from wood by delignification and freezing dried. The WA then was fabricated into an unexpected photochromic wood aerogel (PWA) via surface-initiated atom transfer radical polymerization (SI-ATRP) covalently grafting poly{6-[4-(4-methoxyphenyl-azo)phenoxy]hexyl methacrylate} (PMAZOM). Both WA and PWA showed good compression resilience. The hydrophobicity of PWA was obviously enhanced because of the surface modification. The color of PWA can change from yellow to orange-red after being irradiated by UV light for 30 s. The color of sample can be reversibly changed to yellow under sunlight for 200 s. The lightweight and photosensitive wood aerogel is potential to apply for optical information storage materials and photosensitive devices.
研究领域:
材料科学
·
高分子化学
·
纳米材料
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智能材料
·
可持续材料
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
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2023
·Vol. 47
·期 20
·9905-9912
·
IF 3.3
Jun Tian,Yi Pang,Hongjuan Gu,Dongyan Tang,Zaiqian Yu
Nanoscale molecularly imprinted polymers (MIPs) could offer high binding capacity and fast mass transfer, but their removal after adsorption is costly and time-consuming. In this paper, Fe3O4@SiO2 nanoparticles were synthesized and a lysozyme-imprinted polymer was synthesized via surface initiated atom transfer polymerization on the surface of Fe3O4@SiO2. Temperature-controlled adsorption and desorption of lysozyme were measured, and the adsorption kinetics and isothermal adsorption were determined. The results indicate that the synthesized Fe3O4 has an inverse spinel crystalline structure and Fe3O4@SiO2 is a core–shell structured nanoparticle. The adsorption kinetics followed the Langmuir EXT1 model, and the equilibrium adsorption capacity of the Fe3O4@SiO2@MIP at 40 °C was 117.12 mg g−1 with an imprinting factor of 1.51. SDS-PAGE electrophoresis confirmed the specific adsorption of lysozyme, and 86% of the adsorbed lysozyme could be released by changing the temperature.
研究领域:
生物化学
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材料科学
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产品关联
DOI
高影响因子
CELLULOSE
·
2017
·Vol. 24
·期 10
·4189-4203
·
IF 3.417
Zhang Xiuqiang,Zhang Jinlong,Dong Lili,Ren Suxia,Wu Qinglin,Lei Tingzhou
We report a series of thermoresponsive cellulose nanocrystals (CNCs) decorated with poly(poly(ethylene glycol) methylacrylate) copolymers (poly(PEGMA)- g -CNCs) synthesized by surface initiated-atom transfer radical polymerization (SI-ATRP). The chemical structures and surface morphologies were subsequently confirmed by FT-IR, XPS, and AFM measurements. With regard to thermally responsive behavior, poly(PEGMA)- g -CNCs show tunable lower critical solution temperature (LCST) values in the range of 34–66 °C by varying the feeding ratios of comonomers. The reversible morphological transformation from individual nano-rod structures to larger globule aggregates was further verified by AFM during the LCST transition. These functionalized CNCs have potential as smart film filters and biosensors.
研究领域:
材料科学
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高分子化学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2015
·Vol. 5
·期 76
·62024-62032
·
IF 3.84
Qian Feng,Dongyan Tang,Haitao Lv,Weile Zhang,Wenbo Li
Well fabricated ZnO nanorods (ZnO NRs) arrays with preferred-orientation that grown on pre-deposited ZnO seed layers substrate were selected to graft thermo-responsive polymers of poly(N-isopropylacrylamide) (PNIPAM) by surface-initiated atom transfer radical polymerization (SI-ATRP). As a controlled/“living” radical polymerization, SI-ATRP could endow the systems with the characteristics of the grafted PNIPAM, meanwhile, with the maintaining of the properties of the ZnO NRs. The structures of ZnO and the grafted polymer with the relatively high molecular weights (Mn, 24 300) and narrow molecular weight distributions (Mw/Mn, 1.19) that determined by GPC detection, were characterized by XRD and FT-IR. The graft amount of PNIPAM on ZnO NRs and the interactions between the two components were determined by TG and XPS, respectively. The relatively thin layers of PNIPAM (∼15 nm) formed around NRs via SI-ATRP method were observed by SEM. And the temperature-sensitivity of the grafted nanorods were proved by contact angles measurements. Furthermore, photodegradation of Rhodamine B (Rh-B) by the grafted nanorods revealed that ZnO NRs–PNIPAM exhibited photocatalysis and temperature responsibility characteristics, indicating the significant potential applications with tunable responsiveness by changing the environmental conditions.
研究领域:
材料科学
·
高分子化学
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产品关联
DOI
高影响因子
Polymer Chemistry
·
2013
·Vol. 5
·期 3
·882-891
·
IF 5.231
Ping Wang,Yin-Ning Zhou,Jiang-Shui Luo,Zheng-Hong Luo
In this study, a novel kind of organic–inorganic core–shell SiO2-poly(p-vinylbenzyl) trimethylammonium tetrafluoroborate (SiO2–P[VBTMA][BF4]) nanoparticle was well designed and successfully synthesized via surface-initiated atom transfer radical polymerization (SI-ATRP). Fourier transform infrared spectroscopy (FT-IR), 1H nuclear magnetic resonance (1H NMR), X-ray photoelectron spectroscopy (XPS), dynamic light scattering (DLS) and scanning electron microscopy (SEM) were used to confirm the formation of the core–shell nanoparticles and the surface modification. In order to overcome the challenge of the characterization of the number average molecular weight of poly(ionic liquid)s, “sacrificial initiator” method was used here employing a trimethylsilyl (TMS)-labeled initiator as the NMR marker for integration. In addition, good thermal stability of the new hybrid polyelectrolyte was proved by thermogravimetric analysis. The electrochemical impedance measurements revealed that the room temperature conductivity reached 10−4 S cm−1, which is much higher than that of the pure poly(ionic liquid)s and varies with the amount of the grafted polymer and the test temperature. The X-ray diffraction (XRD) tests further investigated the crystal structure of the nanocomposite and pure P[VBTMA][BF4]. The temperature dependence of ionic conductivity conforms to Arrhenius behavior for both of the nanocomposites and the pure polymer. The results indicated that the SI-ATRP approach provided a simple and versatile route to tune the ionic conductivity of the hybrid nanoparticles by changing the chain length of the grafted polymer, which can be potentially used in a variety of electrochemical devices.
研究领域:
材料科学
·
电化学
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产品关联
DOI
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 74
·46812-46822
·
IF 3.108
Chunmiao Bo,Yinmao Wei
Mixed-mode chromatographic (MMC) stationary phases must be functionalized with at least two functional groups to yield multiple interactions. The present study proposed a novel approach of grafting copolymers with monomers with different properties via surface initiated-atom transfer radical polymerization (SI-ATRP) for the development of MMC stationary phases. In the synthesis, block copolymers and random copolymers containing sodium 4-styrenesulfonate (NASS) and dimethylaminoethyl methacrylate (DMAEMA) units were controllably grafted onto a silica surface via SI-ATRP for the preparation of hydrophilic/ion-exchange stationary phases. Upon investigation of their retention behaviors under different chromatographic conditions (i.e. water content, salt concentration and pH in mobile phase, column temperature) compared to a typical diol column, both the block and random copolymer stationary phases presented mixed-mode retention mechanisms involving hydrophilic and ion-exchange interactions. Furthermore, various solutes, such as basic β-agonists, strong polar nucleosides, organic acids, and a real sample of safflower injection, were employed to evaluate the separation selectivities of the stationary phases; similar selectivities and good separation efficiencies were achieved on the two copolymer columns. In conclusion, the method of surface-grafted copolymers via SI-ATRP possesses potential for further applications in the development of various MMC stationary phases.
研究领域:
分析化学
·
材料科学
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产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2013
·
IF 3.172
Zhihua Fu,Na Zhang,Jie Liu,Tiesheng Li,Wenjian Xu,Fei Wang,Tao Wang,Zhen Zhai,Linlin Liu,Luyan Mao,Yangjie Wu
Poly (N-hydroxy methyl acrylamide)-grafted silicon, glass, and quartz surfaces were successfully prepared by surface-initiated atom transfer radical polymerization (SI-ATRP) with methyl alcohol/water mixtures as solvents and CuCl/2,2-dipyridyl as a catalyst. The modified surfaces were characterized by water contact angle, atomic force microscope (AFM), Fluorescence spectrophotometer, Low-angle X-ray diffraction (LAXRD), and X-ray Photoelectron Spectroscopy (XPS). The results showed that the homogeneous and well hydrophilic N-hydroxymethyl acrylamide polymer brushes (NHAM-brushes), which had high hydrophilic properties and the added advantage of providing 3-D coatings with higher binding capacities, were obtained successfully. Cyclopalladated arylimine functionalized polymer brushes were also obtained by reacting HAM-brushes with N,N′-Carbonyldiimidazole (CDI) and cyclopalladated arylimine. The catalyst functionalized PHAM-brushes had good catalytic activity in heterogeneous compared to homogeneous catalyst and exhibited much improved stability and recyclability over time in Suzuki cross-coupling reaction.
研究领域:
材料科学
·
化学工程
·
表面化学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2017
·
IF 4.233
Qiang Huang,Meiying Liu,Liucheng Mao,Dazhuang Xu,Guangjian Zeng,Hongye Huang,Ruming Jiang,Fengjie Deng,Xiaoyong Zhang,Yen Wei
Monodispersed SiO 2 particles functionalized with cationic polymers poly-((3-acrylamidopropyl)trimethylammonium chloride) (PAPTCl) were prepared using mussel inspired surface modification strategy and surface initiated atom transfer radical polymerization (SI-ATRP). Fourier transform infrared spectroscopy, transmission electron microscope, thermogravimetric analysis, X-ray photoelectron spectroscopy, and zeta potential were employed to characterize these SiO 2 samples. The adsorption performance of the functionalized SiO 2 (donated as SiO 2 -PDA-PAPTCl) towards anionic organic dye Congo red (CR) was investigated to evaluate their potential environmental applications. We demonstrated that the surface of SiO 2 particles can be successfully functionalized with cationic PAPTCl. The adsorption capability of as-prepared SiO 2 was found to increases from 28.70 and 106.65 mg/g after surface grafted with cationic polymers. The significant enhancement in the adsorption capability of SiO 2 -PDA-PAPTCl is mainly attributed to the introduction of cationic polymers. More importantly, this strategy is expected to be promising for fabrication of many other functional polymer nanocomposites for environmental applications due to the universality of mussel inspired chemistry and well designability and good monomer adaptability of SI-ATRP.
研究领域:
材料科学
·
环境工程
·
聚合物化学
✓ 已验证
DOI
PubMed
高影响因子