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International Journal of Mining Science and Technology · 2013 · IF 0

Theoretical study of 2-mercaptobenzimidazole derivatives as chelating collectors in flotation separation of galena and pyrite

Qin Wei,Shengming Xu,Qiang Xie

Three 2-mercaptobenzimidazole derivatives, 1-ethyl-2-mercapto-benzimidazole (EMBI), 1-propyl-2-mercapto-benzimidazole (PMBI) and 1-benze-2-mercapto-benzimidazole (BMBI), were designed and synthesized in the paper, and their collecting behavior in flotation separation process of galena over pyrite was investigated by flotation tests on lab scale. Apart from this, density functional theory (DFT) calculation and molecular dynamics (MD) simulation were also used to elucidate their collecting mechanism. Results of flotation tests indicate that separation of galena over pyrite is feasible at pH 10, and BMBI has the best floatability among three collectors. DFT calculations show that BMBI has the highest occupied molecular orbital (HOMO) energy and strongest collecting efficiency. The adsorption mode of three collectors on mineral surface by MD method indicates that the combination processes of collectors with mineral are exothermic, and the higher the binding energy, the firmer the collector adsorbs on the mineral surface and the higher collecting capacity. The calculation results demonstrate that the floatability of three collectors follows the order: BMBI   >   PMBI   >   EMBI, which is highly consistent with the flotation tests.

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ELECTROCHIMICA ACTA · 2018 · IF 5.116

MOF-mediated synthesis of monodisperse Co(OH)2 flower-like nanosheets for enhanced oxygen evolution reaction

Cao Cui,Jingyun Wang,Zhenguo Luo,Jin Wang,Chunxia Li,Zhengquan Li

Cobalt hydroxide in α-form (α-Co(OH) 2 ) is an attractive electrocatalyst for oxygen evolution reaction (OER). Traditional preparation of α-Co(OH) 2 nanosheets often leads to a packing morphology after synthesis or post electrode fabrication, which severely limits the exposure of surface active sites. In this work, we report the synthesis of a self-supported 3D flower-like structure consisting of 2D α-Co(OH) 2 nanosheets through a metal-organic-framework (MOF)-mediated synthetic method. We found that the formation of MOF intermediates can produce dispersive α-Co(OH) 2 nanosheets with a stable 3D hierarchical structure which can effectively avoid the packing of individual nanosheets. The developed α-Co(OH) 2 nanosheets exhibit an obviously enhanced OER activity in comparison with the nanosheets prepared with traditional method. The prepared α-Co(OH) 2 nanosheets have been well characterized and their formation mechanism is proposed.

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OPTICS LETTERS · 2020 ·Vol. 45 ·期 5 ·1047-1050 · IF 3.714

Tm:YAG ceramic derived multimaterial fiber with high gain per unit length for 2 µm laser applications

Guoquan Qian,Wenlong Wang,Guowu Tang,Xianchao Guan,Wei Lin,Qi Qian,Dongdan Chen,Changsheng Yang,Jiantao Liu,Guiyao Zhou,Shanhui Xu,Zhongmin Yang

In this work, Tm:YAG (Tm:${{\rm Y}_3}{{\rm Al}_5}{{\rm O}_{12}}$) ceramic-derived multimaterial fiber was fabricated by using the molten core method, which has a high gain per unit length of 2.7 dB/cm at 1950 nm. To our knowledge, this is the highest gain per unit length at 2 µm band in similar Tm:YAG-derived multimaterial fibers. A distributed Bragg reflector (DBR) fiber laser was built based on a 10-cm-long as-drawn fiber. The achieved 1950 nm laser, which has a maximum output power of $\sim{240}\;{\rm mW}$ and a slope efficiency of 16.5%, was pumped by a self-developed 1610 nm fiber laser. What is more, an all-fiber-integrated passively mode-locked fiber laser based on the 10-cm-long as-drawn fiber was realized. The mode-locked pulses operate at 1950 nm with duration of $\sim{380}\;{\rm ps}$, and the repetition rate is 26.45 MHz. The results described here indicate that the Tm:YAG ceramic-derived multimaterial fiber with high gain per unit length has promising applications in 2 µm all-fiber fiber lasers.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2017 · IF 3.154

Facile Synthesis of Novel Vanillin Derivatives Incorporating a Bis(2-hydroxyethyl)dithhioacetal Moiety as Antiviral Agents

Jian Zhang,Lei Zhao,Chun Zhu,Zengxue Wu,Guoping Zhang,Xiuhai Gan,Dengyue Liu,Jianke Pan,Deyu Hu,Baoan Song

A series of vanillin derivatives incorporating a bis(2-hydroxyethyl)dithioacetal moiety was designed and synthesized via a facile method. A plausible reaction pathway was proposed and verified by computational studies. Bioassay results demonstrated that target compounds possessed good to excellent activities against potato virus Y (PVY) and cucumber mosaic virus (CMV), of which, compound 6f incorporating a bis(2-hydroxyethyl)dithioacetal moiety, exhibited the best curative and protection activities against PVY and CMV in vivo, with 50% effective concentration values of 217.6, 205.7 μg/mL and 206.3, 186.2 μg/mL, respectively, better than those of ribavirin (848.0, 808.1 μg/mL and 858.2, 766.5 μg/mL, respectively), dufulin (462.6, 454.8 μg/mL and 471.2, 465.4 μg/mL, respectively), and ningnanmycin (440.5, 425.3 μg/mL and 426.1, 405.3 μg/mL, respectively). Current studies provide support for the application of vanillin derivatives incorporating bis(2-hydroxyethyl)dithioacetal as new antiviral agents.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Self-supported Hierarchical Fe(PO3)2@Cu3P nanotube arrays for efficient hydrogen evolution in alkaline media

Dongmei Dai,Bo Wei,Ying Li,Xiao Ma,Shuang Liang,Shuo Wang,Lingling Xu

Developing high-efficient and Earth-abundant electrocatalysts toward hydrogen evolution reaction (HER) is strongly desired for electrochemical water splitting but remains a considerable challenge. Herein, we propose a 3D hierarchical Fe(PO 3 ) 2 @Cu 3 P heterostructure nanotube arrays on Cu foams for promising HER catalysts. The HER performance can be tuned by changing FeCl 3 concentrations and the optimized cathode exhibits excellent HER activity in 1 M KOH with a low overpotentials of 108 mV @ 10 mA cm −2 and a small Tafel slope of 84 mV dec −1 . Furthermore, this electrode delivers high electrochemical durability with stable operation for 24 h. Such high performance can be ascribed to the unique hierarchical heterostructure with large electrochemical surface area, synergistic effect and fast electron transport . Our study can provide new inspiration for rational construction of copper-based hierarchical nanomaterials for HER electrodes and other energy-related applications.

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SCIENCE OF THE TOTAL ENVIRONMENT · 2022 · IF 10.753

Antibacterial polyvinyl alcohol nanofiltration membrane incorporated with Cu(OH)2 nanowires for dye/salt wastewater treatment

Yingdong Chen,Rongze Sun,Wentao Yan,Mengyao Wu,Yong Zhou,CongJie Gao

In many important industries, such as the textile printing industry, a large amount of dye/salt wastewater is often discharged, which can destroy the ecological environment of the water body. Membrane technology has a great potential in the treatment of environmental problems caused by dye/salt wastewater. Polyvinyl alcohol (PVA) nanofiltration (NF) membrane has a bright future in dye/salt wastewater treatment , however, works on this are rare. Herein, antibacterial PVA NF membrane incorporated with Cu(OH) 2 nanowires for the dye/salt wastewater treatment is reported. The membrane was prepared via coating the solutions containing PVA, glutaraldehyde and Cu(OH) 2 nanowires on the polyethersulfone ultrafiltration membrane. Cu(OH) 2 nanowires has a diameter of 60 nm and was successfully introduced into the membrane. The introduction of nanowires improved the membrane hydrophilicity and roughness, which is conducive to the improvement of membrane flux. Membrane separation performance for one component solution and dye/salt solution were investigated. The introduction of Cu(OH) 2 increases the flux of the membrane obviously (the highest increase is 178.78% (from 21.49 to 38.42 L·m −2 ·h −1 ·bar −1 , for NaCl solution as the feed). Besides, the membrane doped with nanowires also possessed a high dye/salt selectivity . For one component solution, the dye removal rate was over 97.00% while the salt rejection was low (the lowest was 13.18% (NaCl)). For the dye/salt solution, the dye (Congo Red) rejection kept at a high level (98.91%) and the salt (NaCl) rejection was still low (13.71%), while the flux was also high (37.56 L·m −2 ·h −1 ·bar −1 ). The performance is superior to that of many membranes reported in previous works. Moreover, the Cu(OH) 2 nanowires endowed the membrane with an improved and high antibacterial property. The sterilization rate of Escherichia coli and Staphylococcus aureus reached more than 99.99%.

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JOURNAL OF ORGANIC CHEMISTRY · 2019 · IF 4.745

Lewis Acids Promoted 3 + 2 Cycloaddition of Oxaziridines and Cyclic Allylic Alcohols through Carbonyl Imine Intermediates

Erbao Zhao,Feilong Zhou,Yujun Zhao

Syntheses of isoxazolidines through the carbonyl imine intermediates are currently limited to monosubstituted olefin substrates. Herein, we reported syntheses of novel bicyclic isoxazolidine-containing compounds through 1,3-dipolar cycloaddition reactions using cyclic allylic alcohols as substrates, which proved challenging in previous reports. Generally, the reaction yields range from good to high, and the reaction substrates tolerate various functional groups, including the cyclopropyl and amine groups. Mechanistic studies suggest that an allylic cation and a carbonyl imine intermediate are involved and responsible for the observed stereochemistry and diastereoselectivity.

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JOURNAL OF CHEMICAL RESEARCH · 2018 · IF 0.668

Cu(OAc)2/Malononitrile/Water: A Simple Reaction System for Synthesis of Aromatic Nitriles from Aldoximes

Xiaoyun Ma,Daqin He,Zhengjian Chen

A simple method for the preparation of nitriles in moderate to good yield has been achieved by treatment of aromatic and heterocyclic aldoximes with malononitrile in water at reflux in the presence of copper acetate as catalyst. Arylaldoximes with an electron-donating group showed the highest reactivity, their conversion being achievable at room temperature.

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JOURNAL OF COORDINATION CHEMISTRY · 2014 · IF 2.212

Diverse structures, weak interactions, and catalytic properties of three palladium 2-sulfobenzoate complexes with 1,10-phenanthroline

Xiao-Li Tang,Ai-Qing Ma,Guo-Qiang Cai,Long-Guan Zhu

Three complexes with same components, PdII, 2-sulfobenzoate and 1,10-phenanthroline, [Pd(phen)2]⋅2(2-Hsb) (1), [Pd(phen)2](2-Hsb)⋅(2-Hsb)⋅2H2O (2), and [Pd(phen)2]⋅[Pd(phen)(2-sb)2]⋅6H2O (3), where 2-H2sb is 2-sulfobenzoic acid and phen is 1,10-phenanthroline, were synthesized and characterized by IR spectra, elemental analyses, thermogravimetric analyses, UV–vis absorption spectra and powder X-ray analysis. Single X-ray crystal structural analyses showed that 1 and 2 are ionic species, while 3 is a dimer through weak bonding interactions. In 1 and 2, 2-Hsb− ligands are partly deprotonated and it is fully deprotonated in 3. In 2 and 3 there are hydrogen bonds and π–π interactions. Extended hydrogen bonding structures for 2 and 3 are 1-D and 3-D architectures, respectively. The oxidation of methyl phenyl sulfide by 1-3 as homogeneous catalysts gave high conversion and selectivity in methanol. The addition of 2-sulfobenzoic acid in the catalytic reaction further promotes the conversion.

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Journal of CO2 Utilization · 2016 · IF 4.764

Protic ionic liquids-promoted efficient synthesis of quinazolines from 2-aminobenzonitriles and CO2 at ambient conditions

Xian-Dong Lang,Yi-Chen Yu,Zheng-Ming Li,Liang-Nian He

Despite recent renaissance of CO 2 chemistry, transformation of CO 2 at ambient conditions remains still of great challenge. In this work, an easily prepared protic ionic liquid e.g. 1,1,3,3-tetramethylguanidinium imidazolide [HTMG][Im] was developed as highly efficient, recyclable and bifunctional catalyst for the carboxylative cyclization of 2-aminobenzonitriles with CO 2 at atmospheric pressure and room temperature. The catalytic protocol was found to be applicable to various 2-aminobenzonitriles bearing electron-withdrawing or electron-donating substituents, affording the corresponding quinazoline-2,4(1H,3H)-diones in moderate to excellent yields. In addition, the catalyst could be conveniently recovered and reused for five cycles with almost consistent activity. Consequently, this process represents an alternative approach for the efficient and greener chemical fixation of CO 2 to afford valuable heterocycles.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Phosphorus-induced reconstruction of Sub‐2 nm ultrafine spinel type CoO nanosheets for efficient water oxidation

Yang Zhu,Tongfeng Cai,Huangping Rui,Xiangyao Gu,Xueqin Mu,Yu Tong,Haibao Duan,Changyun Chen,Suli Liu,Shichun Mu

The surface configuration of low‐cost spinel oxides for oxygen evolution reaction (OER) can significantly affect the electrochemical behavior by generating a thin oxyhydroxide layer and other structures on the surface. Herein, we design and construct phosphorus (P)-activated ~1.0 nm ultrathin CoO nanosheets (devoted as P x -CoO NSs) with enriched P-O bonds and high valence state Co active sites, which is beneficial to the OER process due to the balance with Co 3+ and oxygen vacancies on the reconstructed surface/interface. In addition, such an ultrathin nanosheet structure is also benefit to expose more active sites and improve the intrinsic electronic conductivity. As a result, the surface reconstructed P x -CoO NSs show superior OER activity compared with pure CoO and IrO 2 as benchmark. Furthermore, P 1 -CoO NSs demonstrate intrinsically high mass activity of 6.8 A g Co −1 at an overpotential of 270 mV, large turnover frequency of 0.0024 s −1 at an overpotential of 300 mV, and strong cycling stability in 0.1 M KOH solutions. Structural analysis further reveals that, as compared with CoO, the P-substitution not only induces the surface reconstruction into active Co oxyhydroxides under OER conditions, but also enhances the reaction kinetics. Undoubtedly, this work enriches the ways to prepare high-performance transition-metal-oxide-based catalyst for practical applications.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Pumpkin-derived N-doped porous carbon for enhanced liquid-phase reduction of 2-methyl-4-nitrophenol

Lixia Wang,Rongfei Ye,Panming Jian,Jiangyong Liu

Metal-free catalysts with environmental friendless, cost-competitiveness and less susceptibility to leaching and poisoning over metal-based catalysts, have revolutionized in the catalysis domain. In this respect, we herein report the first application of cheap and abundant pumpkin-derived N -doped porous carbon for the reduction of 2-methyl-4-nitrophenol assisted by NaBH 4 . The obtained catalyst is cost-competitive, efficient and robust, with an attractive mass-normalized rate constant of 4.73 s −1 g −1 and good recycling performance. Systematical analyses demonstrate that the 2-methyl-4-nitrophenol reduction reaction catalyzed by the N -doped carbon proceeds through the Langmuir–Hinshelwood kinetics and the performance enhancement benefits from the strong adsorption and activation of the substrates induced by the electronic modulation in the carbon framework via N -doping. This study opens up new avenues for the high-value use of pumpkin as well as the development of metal-free strategy in more catalytic applications.

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