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NANO · 2019 · IF 1.293

One-Step Hydrothermal Preparation of 1D α-MoO3 Nanobelt Electrode Material for Supercapacitor

Puhong Wen,Jingjing Guo,Lijun Ren,Chuanchuan Wang,Yuzhu Lan,Xiaowen Jiang

1D α α -MoO 3 nanobelts were prepared using ammonium heptamolybdate tetrahydrate [(NH 4 ) 6 4)6 Mo 7 O 2 4 ⋅ 4 24⋅4 H 2 O] as raw material by one-step hydrothermal method without template or guide agent at 180 ∘ C. The layered α α -MoO 3 nanobelt electrode has favorable electrochemical performance, and displays a fairly high specific capacitance, which can be up to 445 F/g at a current density of 0.5 A/g.

CAS / MDL: 7697-37-2
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ELECTROANALYSIS · 2019 ·Vol. 31 ·期 9 ·1809-1814 · IF 2.691

α-Fe2O3 Film with Highly Photoactivity for Non-enzymatic Photoelectrochemical Detection of Glucose

Fuyan Liu,Peng Wang,Qianqian Zhang,Zeyan Wang,Yuanyuan Liu,Zhaoke Zheng,Xiaoyan Qin,Xiaoyang Zhang,Ying Dai,Baibiao Huang

A non-enzyme photoelectrochemical (PEC) glucose sensor based on α-Fe 2 O 3 film is investigated. The α-Fe 2 O 3 film was fabricated via a simple spin coating method. The proposed glucose sensor exhibits good selectivity, a fast response time of <5 s, a linear range of 0.05 to 6.0 mM, sensitivity of 17.23 μA mM −1 cm −2 and a detection limit of 0.05 μM. Meanwhile, the excellent performances of the α-Fe 2 O 3 sensor were obtained in reproducibility and the long-term stability under ambient condition. The linear amperometric response of the sensor covers the glucose levels in physiological and clinical for diabetic patients. Therefore, this non-enzyme PEC sensor based on α-Fe 2 O 3 film has a great potential application in the development of glucose sensors.

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POLYMER · 2019 · IF 3.771

Chain-walking polymerization of 3-heptene with phenyl substituted α-diimine nickel catalysts

Fuzhou Wang,Guoyong Xu,Qingshan Li,Ryo Tanaka,Yuushou Nakayama,Takeshi Shiono

The first example of a 3-alkene polymerization has been successfully achieved with 3-heptene in the presence of phenyl-substituted α- diimine nickel precatalysts activated by dMMAO, and compared with the corresponding linear alkenes, i.e., 1-pentene, 2-hexene and 4-octene polymerizations. The microstructures of the produced poly(3-heptene), which consists of ethyl , propyl and butyl branches indicated the 3,4- and 4,3-insertion, followed by chain-walking, with incorporation of a small fraction of long methylene sequences of 1,7-enchainment via monomer-isomerization. Late-transition metal catalyzed polymerization reactions of internal alkenes to synthesize novel polyolefin materials are highly important and also highly challenging. Upon activation with dried modified methylaluminoxane (dMMAO), the first example of a 3-alkene polymerization has been successfully achieved for 3-heptene catalyzed by phenyl-substituted α- diimine nickel complexes in comparison, and compared with the polymerizations of the corresponding linear alkenes, i.e., 1-pentene, 2-hexene and 4-octene. The results indicate that the polymerization of 3-heptene was achieved via chain-walking to generate branched amorphous polymers with glass transition temperature of ca. −68 °C. The microstructures of the produced poly(3-heptene) indicated the 3,4- and 4,3-insertion followed by chain-walking, the latter being predominant. The NMR analyses of the polymers showed that the obtained poly(3-heptene) possessed ethyl, propyl and butyl branches and a small amount of the long methylene sequence of 1,7-enchainment via monomer-isomerization. The branches structures were significantly dependent on the polymerization temperature, and the content of propyl branches derived from 3,4-insertion decreased with an increase in the polymerization temperature.

CAS / MDL: 14686-14-7
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ACS Applied Materials & Interfaces · 2019 · IF 8.456

Bifunctional Hybrid Enzyme-Catalytic Metal Organic Framework Reactors for α-Glucosidase Inhibitor Screening

Yingying Zhong,Linjin Yu,Qiyi He,Qiuyan Zhu,Chunguo Zhang,Xiping Cui,Junxia Zheng,Suqing Zhao

The screening strategy based on α-glucosidase inhibition has been widely employed for the discovery of antidiabetic drugs, but it still faces some challenges in practical applications, such as poor stability of enzyme, high consumption of test compounds, low sensitivity of screening methods and so on. In this work, a bifunctional hybrid enzyme-catalytic metal organic framework reactor (GAA@GOx@Cu-MOF) with a flower-shaped globular structure was innovatively prepared via self-assembling of α-glucosidase (GAA), glucose oxidase (GOx), Cu2+, and 4,4′-bipyridine. It was found that GAA@GOx@Cu-MOF not only enjoyed merits of high stability, selectivity, and sensitivity but also possessed the character of assembly line work, with about 4.58 times enhanced enzyme activity compared with the free enzyme system. Based on the above characteristics, a highly sensitive screening of GAA inhibitors could be achieved with the detection limit of 7.05 nM for acarbose. Furthermore, the proposed method was successfully applied to the screening of oleanolic acid derivatives as potential antidiabetic drugs. Therefore, it was expected that this work could provide new insights and inspirations for the screening of clinical antidiabetic drugs and for further exploration of functional MOF composites.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2018 ·Vol. 25 ·期 23 ·22455-22463 · IF 2.8

Improving photoelectrochemical reduction of Cr(VI) ions by building α-Fe2O3/TiO2 electrode

Wang Pingping,Dong Faqin,Liu Mingxue,He Huichao,Huo Tingting,Zhou Lei,Zhang Wei

Photoelectrochemical process is an environmentally friendly technology and has a wide application in the control of environmental pollutants. Efficient nanophotocatalysts responsive to visible light are still highly attractive. In this work, α-Fe 2 O 3 /TiO 2 were grown on fluorine doped tin oxide (FTO) substrates by hydrothermal method for photoelectrochemical reduction of Cr(VI). Compared with the separate α-Fe 2 O 3 and TiO 2 electrodes, the composite α-Fe 2 O 3 /TiO 2 electrodes show higher photocurrent density. Under visible light irradiation, 100% removal efficiency of Cr(VI) was obtained after 40 min treatment. The composite α-Fe 2 O 3 /TiO 2 electrodes showed an enhanced absorbance in visible light region and had good stability to photoelectrochemical reduction of Cr(VI). The role of hole scavengers (citric acid and oxalic acid) and pH values was systematically investigated. This novel intensification approach provides new insight on the application of photoelectrochemical reduction in environmental remediation.

CAS / MDL: 10025-77-1 57-13-6
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CHEMOSPHERE · 2018 · IF 4.427

EDDS enhanced Shewanella putrefaciens CN32 and α-FeOOH reductive dechlorination of carbon tetrachloride

Li Yang Zhou,Shuai Chen,Hui Li,Shu Guo,Yong Di Liu,Jie Yang

S,S-ethylenediamine-N,N-disuccinic acid (EDDS) enhanced reductive dissolution of α-FeOOH by Shewanella putrefaciens CN32 (CN32), resulting in formation of surface-bound Fe(II) species ( Fe II EDDS) to improve reductive dechlorination of carbon tetrachloride (CT). The pseudo-first-order rate constants for bio-reduction extents of α-FeOOH by CN32 in the presence of 1.36 mM EDDS was 0.023 ± 0.0003 d −1 which was higher than without EDDS. The enhancement mechanism of bio-reduction was attributed to the strong complexation ability of EDDS to formed Fe III EDDS, which could be better utilized by CN32. The dechlorination kinetic of CT by Fe II EDDS (2.016 h −1 ) in the presence of 1.36 mM EDDS was 24 times faster than without EDDS. Chloroform were detected as main products for the degradation of CT. The chemical analyses and morphological observation showed that combination between EDDS and Fe 2+ produced Fe II EDDS complex, which had a reductive potential of −0.375 V and significantly enhanced CT dechlorination. The results showed that EDDS played an important role in enhancing the bio-reduction of α-FeOOH to accelerate reductive dechlorination of CT.

CAS / MDL: 74-87-3 75-09-2 67-66-3
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Catalytic reduction of α-pinene using Ru nanoparticles stabilized by modified carboxymethyl cellulose

Li Qu,Hailong Yu,Fengli Yu,Bing Yuan,Congxia Xie,Shitao Yu

A new and environmental friendly route has been developed to hydrogenate α-pinene to cis -pinane. The α-pinene was hydrogenated using ruthenium (Ru) nanoparticles that were stabilized by modified carboxymethyl cellulose in aqueous medium. The conversion of α-pinene reached 96.6% and the selectivity of cis -pinane was 98.4%. Ru nanoparticles could be recycled 18 times. Ru nanoparticles and micelles were characterized by transmission electron microscopy (TEM), confocal laser scanning microscopy (CLSM), dynamic light scattering (DLS), X-ray diffraction (XRD), and other detection techniques. Ru nanoparticles (3.2 nm) had a good stability and uniform distribution, the reaction was divided into micelles that appeared to act as “microreactors”, and the micelle size was increased in the absence of sodium carbonate. The good stability of the Ru nanoparticles could be attributed to electrostatic and steric stabilization.

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Nanomaterials · 2018 ·Vol. 8 ·期 5 ·326 · IF 3.504

Borylation of α,β-Unsaturated Acceptors by Chitosan Composite Film Supported Copper Nanoparticles

Wu Wen,Biao Han,Feng Yan,Liang Ding,Bojie Li,Liansheng Wang,Lei Zhu

We describe here the preparation of copper nanoparticles stabilized on a chitosan/poly (vinyl alcohol) composite film. This material could catalyze the borylation of α,β-unsaturated acceptors in aqueous media under mild conditions. The corresponding organoboron compounds as well as their converted β-hydroxyl products were all obtained in good to excellent yields. It is noteworthy that this catalyst of copper nanoparticles can be easily recycled eight times and remained catalytically reactive. This newly developed methodology provides an efficient and sustainable pathway for the synthesis of organoboron compounds and application of copper nanoparticles.Keywords:chitosan composite film;copper nanoparticles;organoboron compounds;easily recyclable

CAS / MDL: 9012-76-4
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2018 ·Vol. 56 ·期 20 ·2280-2285 · IF 2.588

α-Fe2O3/Attapulgite-mediated reaction of benzyl chloride: Synthesis of poly(phenylene methylene)

Dao-Guang Teng,Xian-Yong Wei,Zheng Yang,Zhi-Min Zong

Thermostable and fluorescent poly(phenylene methylene) (PPM) was synthesized via α-Fe 2 O 3 /attapulgite (α-Fe 2 O 3 / A )-mediated polymerization of benzyl chloride (BC) in CCl 4 in good yields. A carbocationic mechanism was proposed based on the controlling experiment. The structure and properties of PPM were characterized by Fourier transform infrared spectrometry, 1 H and 13 C nuclear magnetic resonance spectrometry, thermogravimetric analysis, elemental analysis, gel permeation chromatography, and UV–vis and fluorescence spectrometry. The results show that PPM possesses outstanding homoconjugation fluorescence and excellent thermal stability with onset decomposition temperature of ca. 420 °C. Recycled α-Fe 2 O 3 / A proved to be still highly active for BC polymerization. Moreover, the strategy features low-cost and readily accessible starting materials, simple one-pot operation, and recyclable catalyst, facilitating future applications. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56 , 2280–2285

CAS / MDL: 56-23-5 67-56-1 98-95-3
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Royal Society Open Science · 2018 ·Vol. 5 ·期 6 · IF 2.504

Benzothiazole heterogeneous photodegradation in nano α-Fe2O3/oxalate system under UV light irradiation

Xiangyun Han,Xi Zhang,Lei Zhang,Mei Pan,Jinlong Yan

The photodegradation of benzothiazole (BTH) in wastewater with the coexistence of iron oxides and oxalic acid under UV light irradiation was investigated. Results revealed that an effective heterogeneous photo-Fenton-like system could be set up for BTH abatement in wastewater under UV irradiation without additional H2O2, and 88.1% BTH was removed with the addition of 2.0 mmol l−1 oxalic acid and 0.2 g l−1 α-Fe2O3 using a 500 W high-pressure mercury lamp (365 nm). The degradation of BTH in the photo-Fenton-like system followed the first-order kinetic model. The photoproduction of hydroxyl radicals (·OH) in different systems was determined by high-performance liquid chromatography. Identification of transformation products by using liquid chromatography coupled with high resolution tandem mass spectrometry provided information about six transformation products formed during the photodegradation of BTH. Further insight was obtained by monitoring concentrations of the sulfate ion (SO42−) and nitrate ion (NO3−), which demonstrated that the intermediate products of BTH could be decomposed ultimately. Based on the results, the potential photodegradation pathway of BTH was also proposed.

CAS / MDL: 144-62-7
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Infection and Drug Resistance · 2018 · IF 3.443

Two residues in Staphylococcus aureus α-hemolysin related to hemolysis and self-assembly

Yufeng Du,Li Liu,Chunping Zhang,Yani Zhang

Staphylococcus aureus is becoming increasingly intractable because of its ability to acquire antimicrobial resistance and secrete numerous virulence factors that can exacerbate inflammation. Alpha-hemolysin (Hla) is a pore-forming virulence factor produced by S. aureus that can self-assemble into heptameric mushroom-structured pores in target cell membranes, leading to cell lysis and death. In the present study, we sought to better understand the mechanism underlying hemolysis and the oligomerization of Hla by creating nine mutants with single amino acid changes in different positions of the Hla protein: N17C, T18C, P103C, N105C, M113C, T117C, N121C, D128C, and T129C. The results showed that the P103C and N105C mutations, which are located in the triangle region, significantly diminished hemolysis and heptamer formation when compared with the wild-type Hla protein. This suggests that the P103 and N105 residues play key roles in the assembly of the Hla pore. These results improve our understanding of the mechanism underlying the pore-forming ability of Hla.

CAS / MDL: 9048-46-8
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International Journal of Applied Ceramic Technology · 2019 ·Vol. 16 ·期 6 ·2173-2180 · IF 1.074

Fabrication of α-Si3N4-nanowire/γ-Y2Si2O7 composite superhydrophobic membrane for membrane distillation

Ming-Ye Yang,Bin-Bin Dong,Fei-Hong Wang,Xin Xu,Simeon Agathopoulos

This paper reports on the successful fabrication of α -Si 3 N 4 -nanowire/Y 2 Si 2 O 7 composite membranes with superhydrophobic properties, aiming to achieve a high performance in membrane distillation. The starting powder mixture of 87 wt% γ -Y 2 Si 2 O 7 , 5 wt% Si, 3 wt% LiYO 2 , and 5 wt% ferrocene catalyst was dispersed in a stable suspension, and after being tape-casted, it was sintered at 1300°C for 4 hours in order to obtain the composite membrane. α -Si 3 N 4 nanowires with a diameter of about 50 nm were formed, distributed uniformly on the surface and in the pores of the membrane and their presence greatly favored superhydrophobicity. After surface modification with a robust hydrophobic layer of SiNCO nanoparticles, strongly adhered to the surface of the produced membrane, a water contact angle of 153 o , was measured. Water desalination experiments, using a sweeping gas membrane distillation (SGMD) device, were conducted. High water flux of 11.91 L/m 2 /h was achieved for a 4 wt% NaCl feeding solution at 90°C. Stable water flux and rejection rates were recorded in long-term experiments (>500 hours) using the produced superhydrophobic composite membrane.

CAS / MDL: 75-78-5 75-54-7
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