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MATERIALS AND CORROSION-WERKSTOFFE UND KORROSION · 2019 ·Vol. 70 ·期 11 ·1964-1976 · IF 1.458

A novel process for copper protection in the simulated industrial cooling water based on click synthesis and self-assembling method

Jin Li,Daquan Zhang,Kai Zhang,Lixin Gao,Cheng Shi,Donghui Chen,Manhong Huang

The triazole inhibitor of 1-(p-tolylthio)-1H-1,2,3-triazole-4-carboxylic acid (TTC) was synthesized via the Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition reaction. The self-assembling method was performed to fabricate the self-assembled film of TTC on the copper surface. The electrochemical measurement results indicate that the TTC film can efficiently protect the copper from corrosion in high concentrated industrial cooling water. The protection efficiency of TTC film for copper is 92.2%. Surface characterizations imply that the copper with TTC film after corrosion is covered with multiple protective layers. It probably contains Cu(I) and Cu(II) complexes mixed with nitrogenous compound, Cl − and SO 4 2− . The result of quantum chemical calculation shows that the superior performance of TTC film is related to the adsorption of TTC molecules on copper surface horizontally. This kind of adsorption is mainly achieved via the adsorption centers of triazole ring and O atoms in TTC molecule.

CAS / MDL: 7440-50-8
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2018 · IF 3.141

High Thermal Conductivity and Mechanical Properties of Nanotube@Cu/Ag@Graphite/Aluminum Composites

Xiaopeng Han,Ying Huang,Qiao Gao,Meng Yu,Xuefang Chen

Weak interfacial bonding and the agglomeration of reinforcements are critical challenges for the expected performance in thermal management materials, hindering the extensive application of aluminum matrix composites. In this work, Cu particles, nanotubes, Ag-coated graphite flakes and films, urea, and starch were mixed together to fabricate porous preforms, which then were infiltrated by vacuum gas pressure at 720 °C. The effects of graphite film thickness on the microstructure and properties of thermal conductivity (TC) and coefficient of thermal expension were investigated. The nanotube@Cu/Ag@graphite/aluminum composites exhibited a high TC of 451 W/mK and excellent bending strength of 74 MPa, which were approximately increased by 48.8% and 126%, respectively, as compared with the samples without graphite film.

CAS / MDL: 7440-50-8
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ADVANCED POWDER TECHNOLOGY · 2018 · IF 2.943

Heterogeneity of grain refinement and texture formation during pulsed electric current sintering of conductive powder: A case study in copper powder

Kewei Li,Fei Gao

The heterogeneity of grain refinement and texture formation in conductive copper powder during pulsed electric current sintering have been investigated by means of microstructural analysis of the particle-contacting zone of the samples sintered with micron-sized powders. The particle-contacting region was indicated to experience a higher level of grain refinement than the particle center due to the inhomogeneous temperature distribution among the particle when pulsed electric current passed through. Meanwhile, two main textures of Cube (1 0 0)[0 0 1] texture and Goss (1 1 0)[0 0 1] texture were directly detected in the sintered Cu samples by a combination of electron backscatter diffraction and X-ray diffraction. Based on the experimental results, a feasible mechanism for the formation of texture during the pulsed electric current sintering has been proposed by considering the applied uniaxial pressure and pulsed electric current as well as the rearrangement of grains. In addition, the effects of heterogeneous grain refinement and texture formation on the tensile properties of the sintered Cu samples were also discussed based on the tensile properties and fractographic. These results would contribute to the basic understanding of the sintering mechanisms in pulsed electric current sintering process.

CAS / MDL: 7440-50-8
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CHEMOSPHERE · 2019 · IF 5.108

Efficient degradation of refractory organic contaminants by zero-valent copper/hydroxylamine/peroxymonosulfate process

Huizhong Chi,Xu He,Jianqiao Zhang,Jun Ma

Degradation of naproxen, bisphenol S and ibuprofen in a hydroxylamine enhanced zero-valent copper (Cu 0 ) catalyzed peroxymonosulfate system was investigated for the first time. We found that hydroxylamine addition accelerated the reduction of Cu 2+ to Cu + as well as the corrosion of Cu 0 , and environmental friendly gas nitrogen was the main product of hydroxylamine. Additionally, hydroxyl radical and sulfate radical were identified to be the dominant reaction species by competitive experiments. The degradation of naproxen, bisphenol S and ibuprofen kept highly efficient in the pH range of 3.0–7.0 in Cu 0 /hydroxylamine/peroxymonosulfate process, with their degradation products identified by HPLC-MS, which showed that Cu 0 /hydroxylamine/peroxymonosulfate system could be an alternative to remove non-steroidal antiinflammatory drugs or plasticizers in wastewater. Furthermore, the effects of Cu 0 , hydroxylamine and peroxymonosulfate dosage were studied and optimized by a BBD based response surface model. This study provided a method to solve the disadvantages of Cu 0 /peroxymonosulfate systems, and gave a promising method to enhance the efficiencies of ZVMs activated system such as iron, cobalt and copper.

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Analytical Methods · 2019 ·Vol. 11 ·期 34 ·4382-4389 · IF 2.378

Copper-based metal–organic framework nanoparticles for sensitive fluorescence detection of ferric ions

Fanglin Ming,Jingzhou Hou,Danqun Huo,Jun Zhou,Mei Yang,Caihong Shen,Suyi Zhang,Changjun Hou

A luminescent amino-functionalized metal–organic framework (Cu–MOFs) was synthesized from 2-aminoterephthalic acid and Cu(II) ions by a solvothermal method. Cu–MOFs displayed blue fluorescence with a peak at 430 nm under 330 nm excitation. Its structure was characterized by FTIR, TEM, XRD, and XPS. The fluorescence of the Cu–MOFs was quenched by Fe3+ in aqueous solutions. The limit of detection was 0.5 μM, and the linear working range extended from 2 μM to 35 μM. Additionally, a good logarithmic relationship between relative fluorescence intensity (F/F0) and Fe3+ concentrations ranging from 2 to 180 μM was obtained with a detection limit of 1.56 μM (R2 = 0.9975). No clear interference was observed when challenged with a wide variety of cations and anions. The recoveries from spiked real water samples were in the range of 91.7–107.7%, and the detection results were consistent with inductively coupled plasma mass spectrometry (ICP-MS) results. Therefore, the fluorescent sensor has great potential in environmental monitoring.

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FOOD AND AGRICULTURAL IMMUNOLOGY · 2018 · IF 2.568

Development of a chemiluminescent enzyme immunoassay to detect cadmium in cereal samples

Zhi-Li Xiao,Wei Tian,Zhen-Lin Xu,Yuan-Ming Sun

In this study, we develop a sensitive indirect competitive chemiluminescent enzyme immunoassay (ic-CLEIA) to detect cadmium (Cd) in cereals. A luminol-hydrogen peroxide chemiluminescence system catalysed by horseradish peroxidase (HRP) was used as the signal detecting system. The method showed a half-maximal inhibition concentration (IC50) of 0.5 ng/mL and a limit of determination (LOD) of 0.06 ng/mL. The assay indicated an effective linear range from 0.16 to 1.56 ng/mL. There were no obvious cross-reactivities with other metal ions, including Hg2+, Pb2+, As2+, Ag+, Fe3+, Cu2+, Cr2+, Au3+, Ca2+, Mg2+, Mn2+ and Zn2+. Recovery rates ranged from 79.2% to 120.0% for rice, maize, wheat, brown rice and glutinous rice samples. Twenty-five practical cereal samples were analysed, and the comparative analysis of the results showed a strong correlation (r = 0.984) between the CLEIA and the GFAAS methods. The results indicated that the ic-CLEIA developed was acceptable to screen for cadmium in cereal samples.

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Journal of Biomedical Nanotechnology · 2017 ·Vol. 13 ·期 12 ·1631-1646 · IF 4.521

Curcumin-Loaded TPGS/F127/P123 Mixed Polymeric Micelles for Cervical Cancer Therapy: Formulation, Characterization, and In Vitro and In Vivo Evaluation

Wang Jiao,Liu Qiang,Yang Linnan,Xia Xiaofei,Zhu Rongrong,Chen Shengguang,Wang Mei,Cheng Liming,Wu Xianzheng,Wang Shilong

Cervical cancer is the fourth most common cancer in women worldwide, and existing treatments cause severe side effects and great burdens. Thus, the development of safe, inexpensive therapeutic agents is necessary. Curcumin (Cur), a well-known natural product, exerts promising anti-cancer activities against various cancer types. However, its therapeutic efficacy is severely restrained due to rapid degradation, poor aqueous solubility, and low bioavailability. The objective of this study was to investigate the therapeutic potential of novel curcumin-loaded TPGS/F127/P123 mixed polymeric micelles (Cur@NPT100) for cervical cancer treatment. The Cur@NPT100 exhibited an average size of approximately 19 nm, a zeta potential of around –4 mV, a drug loading of 8.18 ± 0.36%, and an encapsulation efficiency of 79.38 ± 4.65%. Unlike free Cur, Cur@NPT100 are readily dispersed in aqueous medium, showing enhanced stability and a sustained release profile over a 6-day period. In vitro cell culture experiments revealed that TPGS/F127/P123 mixed polymeric micelles (NPT100) based nanocarriers substantially promoted the selective cellular uptake of Cur into HeLa cells rather than by non-cancerous NIH3T3 cells, inducing higher cytotoxicity and greater apoptosis and significantly increasing the percentage of cells arrested at the G2/M phase of the cell cycle. Additionally, the Cur@NPT100 facilitated more Cur accumulation in the mitochondria and decreased the mitochondrial membrane potential. In addition, western blot assays demonstrated that Cur@NPT100 were more potent than free Cur at activating the mitochondria-mediated apoptosis pathway. In vivo results further confirmed that Cur@NPT100 exhibited a much higher antitumor efficacy than free Cur and had excellent biocompatibility. In conclusion, Cur@NPT100 might be an effective therapeutic agent for cervical cancer.

CAS / MDL: 7440-50-8 9002-96-4
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JOURNAL OF ELECTRONIC MATERIALS · 2017 ·Vol. 47 ·期 2 ·1705-1712 · IF 1.579

Effects of Grain Orientation on Cu6Sn5 Growth Behavior in Cu6Sn5-Reinforced Composite Solder Joints During Electromigration

Han Jing,Wang Yan,Tan Shihai,Guo Fu

Electromigration is a major reliability problem in composite solder joints. Due to the anisotropy of the β -Sn crystal structure, the Sn grain orientations present in the solder matrix dominate the principal failure mechanism in solder joints under electric current stressing. In this work, the Cu 6 Sn 5 growth behavior in Cu 6 Sn 5 -reinforced composite solder joints with three different Sn grain orientations was investigated at current density of 10 4  A/cm 2 at room temperature. Micron-sized Cu particles were added to Sn-3.5Ag solder at 2% volume fraction using an in situ method. After current stressing for 528 h, the polarity effect in the composite solder joint was greatest for an angle ( θ ) between the c -axis and electron flow direction of 30°, resulting in higher growth rate of Cu 6 Sn 5 in the solder matrix compared with composite solder joints with θ of 60° or 90°. There were no noticeable changes in the composite solder joint with θ of 90°. The growth behavior of Cu 6 Sn 5 , Cu atomic motion, and Cu diffusivity in the composite solder joints with different Sn grain orientations were analyzed in detail.

CAS / MDL: 7440-50-8
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MICROCHEMICAL JOURNAL · 2025 · IF 5.1

A colorimetric sensor of functionalized gold nanoparticles for the identification of copper and magnesium ions based on SPR and Gaussian calculations

Xueqi Duan,Xing Li,Qingya Yang

Due to the serious threat of excessive copper and magnesium ions to human health, it is crucial to detect copper and magnesium ions in aquatic environments. In this study, we propose a colorimetric strategy – gold nanoparticles (AuNPs) modified by 5-(3-aminophenyl)-1H-tetrazole (TA@AuNPs) for the rapid and portable identification of copper and magnesium ions in water. As the concentration of the target metal ions increases, the colorimetric principle (TA@AuNPs) causes the aggregation of the AuNPs system, shifts of the surface plasma resonance (SPR) absorption peak, and a change of system colors (wine-red to gray-blue). The advantages of this work: 1) the detection process is simple without complex pretreatment; 2) the concentration of the target ions could be quickly detected within 3 min by Standard Color Cards; 3) it can selectively detect two kinds of metal ions (Cu 2+ and Mg 2+ ) with high specificity in the presence of other interfering ions; 4) It eliminates the interference of calcium ions in the detection of magnesium ions; 5) It has excellent linearity and low detection limit (for Cu 2+ : R 2  = 0.94, LOD = 30.0 μM by the naked eye and 0.229 μM through ultraviolet–visible spectroscopy; for Mg 2+ : R 2  = 0.96, LOD = 300 μM by the naked eye and 0.653 μM through ultraviolet–visible spectroscopy). Furthermore, the colorimetric mechanism of the present work has been comprehensively demonstrated through DLS, TEM, zeta potential analysis, FT-IR, UV–vis and Gaussian calculations.

CAS / MDL: 7440-50-8 7439-95-4
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JOURNAL OF MOLECULAR STRUCTURE · 2024 · IF 4

An eco-friendly colorimetric strategy based on gold nanoparticles modified with 3-pyridinylboronic acid for detecting copper ions

Xueqi Duan,Guona Li,Zhijian Jia,Hongzhen Xie,Xing Li

Copper is an essential element in the human body. Excess accumulations of copper, however, would become a potential threat. Therefore, it is of great significance to detect copper ions. Owing to their controllable morphology, dispersal characteristics, high extinction coefficient, and easily functionalized surfaces, gold nanoparticles (AuNPs) have been highly employed as attractive sensing probes for environmental and biological analyses. We herein propose an eco-friendly colorimetric strategy based on AuNPs modified with 3-pyridinylboronic acid (PA) for sensitive and selective detection of copper ions (Cu 2+ ) in water at trace level. The color changes of the system from wine-red to gray-blue with increasing amounts of copper ions is due to the binding of AuNPs modified with 3-pyridinylboronic acid to copper ions, which in turn leads to the aggregation of AuNPs with fine anti-interference. Strengths of the work: 1) rapid response time without complex pre-treatment; 2) high sensitivity with low limit of detection (LOD) and the good linear relationship ( R 2 = 0.98, LOD = 3.0 μM by the naked eye and 72 nM by ultraviolet-visible spectroscopy); 3) high selectivity under other interfering ions. In addition, the detection mechanism of this work has been successfully confirmed by density functional theory (DFT), transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), Zeta potential analysis and ultraviolet-visible spectroscopy (UV–vis).

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Analytical Methods · 2012 ·Vol. 4 ·期 8 ·2441-2446 · IF 1.547

Determination of polycyclic aromatic hydrocarbons from soil samples using selective pressurized liquid extraction

Qian Zhang,Tao Liang,Lingqing Wang,Hongying Cao

A selective pressurized liquid extraction (SPLE) method has been optimized for the determination of polycyclic aromatic hydrocarbons (PAHs) in soil samples. The method comprises a fully automated extraction and on-line clean-up procedure by inclusion of sorbents in the extraction cells. The contributing parameters of SPLE including type of solvent, static extraction time, number of extractions, extraction temperature, nature and amount of sorbents were investigated. The optimal extraction was performed at 70 °C for 10 min (static extraction time) cycled once using n-hexane/methylene chloride (50 : 50, v/v) and the sorbents in the extraction cells were 3 g of alumina and 2 g of silica gel. The collected extracts from the cells, after pre-concentration, were clean enough for direct injection into GC-MS. Validation of the SPLE technique was performed, with the recovery rates for 16 PAHs in the range of 75–103%, and the relative standard deviation (RSD) was generally less than 10%. Method detection limits (MDL) were in the ranges of 0.001–0.080 μg kg−1 for the GC-MS analyses. Finally, the method was successfully used to evaluate the cultivated soils in Beijing, China.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2015 · IF 2.999

Superior critical current density obtained in Mg11B2 low activation superconductor by using reactive amorphous 11B and optimizing sintering temperature

Fang Cheng,Yongchang Liu,Zongqing Ma,Huijun Li,M. Shahriar Al Hossain

The un-doped Mg 11 B 2 and Cu-doped Mg 11 B 2 bulks using 11 B as a boron precursor were fabricated by solid-state reaction and sintered at different temperature in present work. By analyzing the sintering process, it was found that 11 B original powder is more reactive and can react with Mg severely even at low temperature before Mg melting, which leads to the formation of refined Mg 11 B 2 grains. Consequently, the critical current density of Mg 11 B 2 sample prepared in this work is higher than that of natural MgB 2 . Furthermore, it was found that proper Cu addition could obviously accelerate the reaction between Mg and 11 B and promote the formation of Mg 11 B 2 due to the appearance of Mg–Cu liquid at low sintering temperature before Mg melting. On the other hand, Cu addition also introduced more MgCu 2 impurity, leading to a relatively lower critical current density on the whole. Interestingly, the critical current density of the Cu doped sample sintered at 800 °C is surprisingly enhanced at the low field, compared with that of the corresponding un-doped one. This is due to the peritectic reaction which generated small-sized MgCu 2 occurred that at 800 °C, providing MgCu 2 pinning centers well-distributed in the MgB 2 matrix.

CAS / MDL: 7440-50-8
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