SURFACE & COATINGS TECHNOLOGY
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2022
·
IF 4.865
Shuhan Dong,Yang Yang,Ruina Ma,An Du,Mingxu Yang,Yongzhe Fan,Xue Zhao,Xiaoming Cao
A Cu/Ni–B 4 C superhydrophobic coating was fabricated on the surface of Q235 steel under different current density via electrodeposition . The distribution of electric field influenced by current density controls the growth of rough structure. Therefore, the effect of current density was measured by the morphology and wettability of coating and analyzed by Electric field distribution model. The coating surface demonstrates the most uniform and compact rough structure at a current density of 3 A/dm 2 (M C-3 ) obtaining contact angle 160 ± 2° after the surface energy reduced by stearic acid. The self-cleaning performance and mechanical stability of M C-3 coating were studied. The potentiodynamic polarization curve (PPC) and electrochemical impedance spectroscopy (EIS) were used to measure the anti-corrosion and protection performance of the coatings with different morphology and contact angle. The protective performance of M C-3 coating soaked in 3.5 wt% NaCl solution for different time was studied by EIS. The wetting stability of different coatings was studied by single frequency impedance spectroscopy. Then the double protective mechanism of superhydrophobic coating was described and the corresponding model was established.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 38
·18251-18261
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IF 3.925
Jiabao Sun,Qiang Li,Dajie Zhang,Dongsheng Xia
Oxytetracycline (OTC) is a typical antibiotic that poses a serious threat to the environment. However, traditional treatment methods suffer from low treatment efficiencies and potential secondary contamination. Therefore, there is a need to develop efficient, convenient, and environmentally friendly removal technology. In this paper, magnetic nano-Cu/Fe composites were successfully synthesized and used as the activator of peroxymonosulfate (PMS) to degrade OTC. The obtained catalysts with different ratios showed excellent degradation effects, especially the Cu/Fe-1 catalysts. The highest removal efficiency of OTC (93%) was achieved with 0.2 g L−1 PMS and 0.1 g L−1 catalyst in 60 min. The impacts of the catalyst and PMS dosages, initial temperature and pH, coexisting anions, microplastics, and real-life water samples were investigated. To explore the mechanism for OTC degradation, radical scavenging and electron spin resonance (EPR) experiments were carried out, and non-radical 1O2 was identified to be the main radical. TEM and XRD results show the presence of CuFe2O4 composites in Cu/Fe-1, which can promote the production of 1O2 and thus improve the OTC degradation efficiency. This work provides a new efficient, stable, low-cost, and environmentally friendly approach for the degradation of oxytetracycline.
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Molecular Catalysis
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2022
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IF 5.089
Pan Pan,Mingming Li,Yuxin Liu,Yisi Feng,Xinglong Li
2,5-diformylfuran (DFF) is a multifunctional intermediate, which can be used in drugs, functional polymers, fluorescent materials and surfactants. In this paper, a TEMPO-assisted magnetic Fe 3 O 4 @SiO 2 @mSiO 2 -NH 2 -Cu(II) catalytic system was developed for the selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran. The structure of Fe 3 O 4 @SiO 2 @mSiO 2 -NH 2 -Cu(II) was double-layer shell-core spherical structure with uniform ordered mesoporous on the surface, amino groups and Cu were evenly distributed in the outer mesoporous. The catalyst was characterized by FT-IR, TEM, EDS, SEM, XRD, BET and VSM. The effects of reaction conditions were investigated in detail. The conversion of HMF was 98.9% and the highest DFF yield was 92.4% under atmospheric oxygen in toluene solvent. The catalytic activity did not decrease significantly after 5 cycles. The catalytic system had good substrate adaptability for benzyl alcohols and aromatic alcohols with satisfactory yield of corresponding aldehydes (91.3–100%). A possible reaction mechanism was also proposed and found that bis(μ-hydroxy) double copper (II) may be the active reactant in oxidation reaction. The system provides a promising industrialized preparation method for DFF.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2022
·
IF 4.326
Xiao Chen,Wenqi Liu,Jingjie Luo,Hongyu Niu,Rongrong Li,Changhai Liang
The hydrogenation of furfural containing multifunctional group often needs the high-efficiency cooperation of multiple catalytic active centers, which is greatly determined by the regulation of the surface and interface structure of multicomponent catalytic materials. Based on such circumstance, a series of highly dispersed supported bimetallic Cu–Ni catalysts prepared by the in situ topological transformation of layered double hydroxides have been investigated for the one-pot hydrogenation of furfural. Compared with the supported monometallic Cu and Ni catalysts, the optimized bimetallic Cu1Ni3/MgAlO catalyst presents highly efficient and good selectivity in the hydrogenation of furfural at the bath reactor. The selectivity to tetrahydrofurfuryl alcohol reaches 94.0% with a complete conversion of furfural at 110 °C under 3 MPa of H2 for 3 h. The results of TEM and in situ FT-IR confirm that the Ni-rich Cu–Ni alloy in the Cu1Ni3/MgAlO catalyst generates a strong synergistic effect, which shifts the adsorption configuration of furfural from parallel or vertical adsorption to tilted adsorption so as to significantly improve the catalytic performance. The intrinsic catalytic performances of CuxNiy/MgAlO catalysts indicate that the TOFC═O and TOFC═C values can be balanced through construction of the structure of the catalyst for achieving the synergistic effect between Cu and Ni significantly to enhance the one-pot selective hydrogenation of furfural to tetrahydrofurfuryl alcohol. Additionally, the Cu1Ni3/MgAlO catalyst presents excellent reusability by six-cycle testing. The above results indicate that the Cu1Ni3/MgAlO with the cooperation of multiple catalytic active centers is a promising catalyst for the selective hydrogenation of furfural.
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APPLIED ORGANOMETALLIC CHEMISTRY
·
2022
·Vol. 36
·期 10
·e6833
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IF 4.072
Jing Hu,Yun Luo,Min Hou,Jia Jia Qi,Li Li Liang,Wen Ge Li
Two dinuclear complexes [Cu 2 (LO) 2 ] and [Ni 2 L 2 Cl 2 (C 2 H 5 OH) 2 ] derived from (5-chlorosalicylaldehyde)-4-aminoantipyrine (HL) were synthesized and characterized by infrared (IR) spectroscopy，thermogravimetric analysis, and powder X-ray diffraction. Molecular structures of the Cu (II) and Ni (II) complexes were determined by single-crystal X-ray diffraction. Their cytotoxicity was evaluated by methyl thiazolyl tetrazolium assay against human tumor cells, such as lung carcinoma A549, lung adenocarcinoma H1975, breast carcinoma MDA-MB-231, and nasopharyngeal carcinoma CNE-2Z cell lines. The results showed that the Cu (II) complex had much better anticancer activity than the Ni (II) complex, especially for MDA-MB-231 and CNE-2Z cells. The reason may be that they have different structures. The methyl group on the (5-chlorosalicylaldehyde)-4-aminoantipyrine (HL) was oxidized to the hydroxymethyl group, herein, namely LO, which is difficult to achieve in the normal chemical synthesis process. However, we did it by a solvothermal method at low temperature. It provides a new way of thinking and synthesis. The anticancer activity of the copper complex was next only to cisplatin, and the copper complex was nontoxic for the human normal cell lines. The experiment results also showed that the copper complex could inhibit tumor cell proliferation through the cell cycle and cell apoptosis.
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 29
·13931-13939
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IF 3.925
Nan Sun,Yuhan Jing,Yong Zhang,Xinru Li,Yaoning Bai,Yuwei Yan,Taoyuan Ouyang,Honglin Tan,Xiaoming Cai,Jinming Cai
Copper-based photocatalysts have attracted much attention because of their great prospects in photochemical conversion. However, the preparation of highly stable copper-based photocatalysts is a challenge. In this study, copper nanoparticles (Cu NPs) wrapped in graphitized polyacrylonitrile (g-PAN) were prepared by a two-step sintering method. Even if Cu@g-PAN is placed in the air for one month, the Cu NPs were still not oxidized. Furthermore, we succeeded in further introducing graphitized carbon nitride (g-C3N4) into the g-PAN shell structure, which was confirmed using a Scanning Transmission Electron Microscope (STEM), FT-IR, and UV-Vis absorption spectra. Cu@g-PAN/g-C3N4 can degrade 88.61% of methylene blue (MB) in one hour, showing a higher catalytic activity than Ag@g-PAN/g-C3N4 (55.18%). XPS and Auger electron spectroscopy tests of catalyzed Cu@g-PAN/g-C3N4 show that Cu is not oxidized. We have proposed a possible mechanism for charge separation and transformation in the Cu@g-PAN/g-C3N4 composites to explain the enhanced photocatalytic performance. This work provides a new method to protect Cu NPs and demonstrates the prospect of rational design of copper-based photocatalysts with high stability and efficiency.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Xianda Han,Zhigang Yu,Yangkejia Xiang,Fengqin Li,Xiaoping Tan,Lan Xu,Guiling Zhang
An electrochemical fabrication method of Ru[bpy] 3 2+ @Cu-MOF(-SH)/Au (MOF = metal–organic framework) was developed with a photo/electrochemical information characterization and a DNA-based biosensing validation for the proposed interface. Applying an anodic synthesis method, a modification layer of Ru[bpy] 3 2+ encapsulated with MOF was formed on the Au electrode surface to fabricate an interface with photo/electrochemical dual-signal response. Combining the scanning electrochemical microscopy (SECM) imaging technology with electrochemical and electrochemiluminescence (ECL) detection, the information about the interfacial photo/electrochemical bi-functional properties was explored from three aspects of the parameter variable, intensity variable, and morphology variable. The results show that the effect of parameter variables on the interfacial response follows an “interference effect” mechanism. Under the optimized conditions, the background and the saturation ECL intensities are 610.0 and 24.0 with a quenching efficiency of 96.1% and a detection limit of 30 fM. The saturation current is 48.8 µA with a detection limit of 330.0 nM. Both ECL and electrochemical imaging methods can corroborate each other, validating the logical correlation between the interface fabrication and the response performance in the regional interfacial distribution and laying a methodological foundation for evaluating the interface fabrication quality based on imaging morphology qualitatively. The proposed interface can construct photo/electrochemical dual-signal DNA-based biosensors.
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Analytical Methods
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2022
·Vol. 14
·期 33
·3153-3159
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IF 3.532
Ling Mei,Tiantian Si,Shuai Wang,Jie Zhu,Hao Tang,Xiaojing Liang
The TiO2@MOF-919(Fe–Cu) solid-phase extraction material was prepared by growing MOF-919(Fe–Cu) in situ on three-dimensional radial TiO2 microspheres by a simple solvothermal method. This combination drew on both the resources of good single dispersion and extraction rate, which made it a better extraction material. It was accompanied with high-performance liquid chromatography (SPE–HPLC) for the separation and determination of four benzoylurea pesticides (triflumuron, chlorbenzuron, teflubenzuron and diflubenzuron) in afforestation irrigation water and juice samples (grape, peach and apple juices). Under the optimal conditions, the linearity of the method ranged from 1 to 400 μg L−1 with a correlation coefficient (R2) ≥ 0.9994, while the detection limit was in the range of 0.40–0.56 μg L−1 for the four pesticides. The adopted material showed good reusability and can be used no less than 10 times. The intra-day and inter-day precision were in the range of 1.78–3.24% and 4.06–5.08%, respectively. The proposed method was then successfully applied for the detection of benzoylurea pesticides in the spiked samples with good recoveries (72.3–108.4%) and good precision (5.15%) due to π–π and hydrophobic interactions between the analytes and adsorbent. The results show that the composite had the potential to be used as a SPE adsorbent for the enrichment and extraction of benzene ring structures containing imide groups in actual samples.
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PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2021
·
IF 8.128
Ben Chen,Jin Zhang,Jing Yu,Rui wang,Beibei He,Jun Jin,Huanwen Wang,Yansheng Gong
Poor visible light utilization and charge separation efficiency of TiO 2 restrict its extensive application in the photocatalytic field. Herein, a specific Z-scheme TiO 2-x /Cu/ZnO heterojunction was successfully constructed by atomic layer deposition (ALD) technique and spray pyrolysis technology. Benefited from the surface plasmon resonance (SPR) effect of Cu and Z-scheme heterojunction, the visible light absorption capacity was greatly enhanced. Meanwhile, ZnO nanolayer coating, prepared by ALD technique, protects Cu element to hinder its oxidation, thus enhancing the separation efficiency of photogenerated carriers. Therefore, the photocatalytic hydrogen production performance was significant improved, exhibiting a maximum value of 342.0 µmol·g −1 ·h −1 for the optimal B-T-0.1C-10Z (black TiO 2 /0.1Cu/10 nm ZnO) sample without any noble-metal cocatalyst, which is higher than pure TiO 2 (310.7 µmol·g −1 ·h −1 , with 3 wt% Pt) synthesized by spray pyrolysis method under equal conditions. In addition, a possible mechanism for the enhanced performance was briefly discussed based on the experimental results.
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PubMed
高影响因子
TALANTA
·
2021
·
IF 6.057
Rongrong Wang,Yong Cao,Hao Qu,Yanbo Wang,Lei Zheng
Copper sulfate is a widely used agent to control insects, bacteria and algae for fishery. However, excess amount of copper ions in water accumulate in aquatic products through the ecological cycle system, highly threatening food safety and public health. Therefore, it is urgent to develop a rapid and efficient method for the determination of copper content in aquatic products. In this study, we developed a label-free biosensor for Cu(II) based on a graphene field-effect transistor gated by structure-switching aptamer probes (SSA-GFET) against Cu(II) we obtained before. The detection mechanism of the biosensor is attributed to the surface charge shift and the potential change of the gate electrode upon the specific binding of Cu(II). The SSA-GFET biosensor has a low detection limit of 10 nM and a linear range of 10 nM to 3 μM to Cu(II). In addition to the excellent selectivity to Cu(II), the biosensor also showes the advantage of high recovery rate for detection of Cu(II) in real fish samples. Because of the detection characteristics of label-free SSA-GFET, it has great advantages in the field of food safety and environmental detection.
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高影响因子
ANALYTICA CHIMICA ACTA
·
2021
·
IF 6.558
Yawen Wu,Xiaolong Chen,Xiaogang Luo,Mei Yang,Changjun Hou,Danqun Huo
Carcinoembryonic antigen (CEA) is a key serum tumor marker which is overexpressed in all types of adenocarcinomas. Therefore, establish the ultrasensitive, accurate and rapid method for CEA detection is essential for reducing the mortality of cancer. Here, a bimetallic organic framework Cu/UiO-66 was synthesized through the simple two-step hydrothermal method and used to construct a “fluorescence turn-on” analytical method for CEA detection. Cu/UiO-66 can adsorb CEA aptamers modified with FAM (CEA/FAM-Apt) and take place photoinduced electron transfer (PET) between Cu/UiO-66 and FAM, resulting in the fluorescence of the FAM is quenched. When CEA is present, CEA and CEA/FAM-Apt are tightly combined, making CEA/FAM-Apt far away from the Cu/UiO-66 surface. As a result, the fluorescence intensity of the system was significantly restored. Under optimal conditions, the proposed “fluorescence turn-on” method can detect CEA as low as 0.01 ng mL −1 in a range of 0.01–0.3 ng mL −1 . Besides, this analytical method owns good selectivity , reproducibility and serum applicability, which provides a new platform for the direct detection of clinical diagnosis-related markers.
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高影响因子
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2021
·
IF 6.064
Yafei Li,Xiaocheng Lan,Boyang Liu,Tiefeng Wang
A stable and highly efficient supported Cu-Ni catalysts for the conversion of ethyl levulinate (EL) to γ-valerolactone (GVL) was developed. The catalysts were characterized by XRD, TEM, TPD, TPR, and XPS. The support effect of metal oxides (Al 2 O 3 , SiO 2 , ZrO 2 , and TiO 2 ) revealed that Cu-Ni supported on Al 2 O 3 showed the highest activity for EL hydrogenation to ethyl 4-hydroxypentanoate (EHP) and the subsequent intramolecular esterification of EHP to GVL. EHP intramolecular esterification to GVL in the ethanol solution was a reversible reaction with an equilibrium constant of 24 at 453 K. A simplified reaction kinetic network was established. The solvent had a significant influence on the reaction equilibrium and the catalyst stability. Cu-Ni/Al 2 O 3 in n-hexane solvent gave a higher GVL yield than that in ethanol solvent, and showed better recyclability than that in toluene solvent. With optimizing the conditions, Cu-Ni/Al 2 O 3 gave 99.9% conversion and 98% selectivity to GVL with a space–time yield of 1.13 g GVL g cat -1 h −1 in n-hexane solvent with good recyclability.
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