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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Ion-imprinted no-core-fiber sensor for operando on-line monitoring of Cu²⁺ in environmental waters

Bing Xu,Feiyang Huang,Zhihui Luo,Changyan Ran

A compact optical fiber sensor based on a no-core fiber (NCF) segment functionalized with a Cu²⁺-imprinted chitosan/polyvinyl alcohol (CS/PVA) film was developed to enable operando on-line monitoring of Cu²⁺ with high selectivity and sensitivity in complex environmental water matrices. The optimal length of the NCF segment was determined to be 1 cm based on simulation and experimental evaluation, under which the highest sensitivity was achieved. The pseudo-second-order kinetic behavior of Cu²⁺ adsorption was first validated by analyzing the time-dependent shift of the interference valley, providing direct spectral evidence of a chemisorption-driven mechanism. A sensitivity of 0.0768 nm/μM and a detection limit of 0.1245 μM were obtained. A rapid response time of less than 20 s and excellent measurement repeatability, with strong specificity toward the target ion and relative standard deviation below 5 percent over five regeneration cycles, were also demonstrated. The sensor was further applied to spiked water samples from the Yangtze River and tap water. By integrating ion-imprinting technology with an optimized NCF-based fiber structure, a portable, cost-effective, and interference-resistant platform has been established for real-time and on-site monitoring of heavy metal ions in complex aquatic environments.

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2018 · IF 3.141

Significantly Enhancing Cu(II) Adsorption onto Zr-MOFs through Novel Cross-Flow Disturbance of Ceramic Membrane

Ke Wang,Zhaobin Tian,Na Yin

Novel cross-flow disturbance of ceramic membrane was used for the first time to enhance the adsorption of highly toxic Cu(II) onto Zr-based metal–organic frameworks (Zr-MOFs). Effects of temperature and pH were investigated on the adsorption process of Cu(II) onto the MOFs using the jar test. The results showed that the MOFs can well adsorb Cu(II) (59.8 mg g–1) at a pH of 6 and a temperature of 40 °C. On the basis of this, the MOFs were then added into a novel cross-flow ceramic membrane filtration system. Effects of the operation temperature and membrane pore size were also investigated on the adsorption process. The results showed that Zr-MOFs adsorption of Cu(II) increased with temperature. The ceramic membrane with a pore size of 200 nm exhibited better Cu(II) removal and membrane flux than did the 50 nm membrane, as well as better kinetic data fit of the pseudo-second-order model. With the aid of cross-flow disturbance of ceramic membrane, the capacity was incredibly increased to 988.2 mg g–1 at a pH of 6, temperature of 40 °C, cross-flow velocity of 4.5 m s–1, and trans-membrane pressure of 0.05 MPa. The principal advantages of this method are a significant enhancement of adsorption onto the Zr-MOFs in the removal of Cu(II) and convenient application in the continuous treatment of heavy metal wastewater. This can be used as an effective method in continuous adsorptive removal of heavy metals from wastewater.

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CELLULOSE · 2017 ·Vol. 25 ·期 1 ·735-751 · IF 3.417

Preparation of magnetic MnFe2O4-Cellulose aerogel composite and its kinetics and thermodynamics of Cu(II) adsorption

Cui Sheng,Wang Xue,Zhang Xin,Xia Wei,Tang Xianglong,Lin Benlan,Wu Qi,Zhang Xin,Shen Xiaodong

In this paper, a MnFe 2 O 4 -Cellulose magnetic composite aerogel (MnCA) with high adsorption capacity was fabricated by in situ incorporating MnFe 2 O 4 to regenerated cellulose hydrogel matrix, followed by CO 2 supercritical drying. A green synthetic strategy was performed by using renewable cellulose materials, environmentally benign cellulose solvents and facile synthetic conditions. The results showed that the obtained magnetic cellulose aerogel had a continuous and tiered three dimensional network with interconnected fibrils of about 30 nm in width, which was similar to those of cellulose aerogel prepared from NaOH/urea solution via CO 2 supercritical drying. Meanwhile, they had high specific surface areas of 236–288 m 2 /g and total pore volume of 0.55–0.88 cm 3 /g. In addition, the hybrid aerogel showed superparamagnetism with maximum saturation magnetization reaching up to 18.53 emu/g. The magnetic nanocomposite aerogel could be used for biological and environmental applications. The adsorption test showed that MnCA had rapid adsorption rate and excellent adsorption ability of removing heavy metal ions in aqueous solution which could attain to 63.3 mg/g within 100 min. Moreover, all the composite aerogels exhibited good reusability and could be easily reused from the water after adsorption.

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Journal of Manufacturing Processes · 2020 · IF 4.086

Interfacial microstructure and mechanical properties of Ti/Cu joint manufactured by Ni-Al thermal explosion reaction

Xiaoping Cai,Keer Li,Changcheng Sang,Xuanru Ren,Leihua Xu,Peizhong Feng

The dissimilar metals joining of Ti/Cu was conducted using a rapid thermal explosion (TE) reaction. The Ni-Al powder mixture was used as TE reaction system, and the effect of temperature (600, 700, 800 and 900 °C) on interfacial diffusions, microstructure and mechanical properties of Ti/Cu joint were investigated. The maximum combustion temperature of Ni-Al interlayer during heating process was 720 °C and a significant exothermic phenomenon was observed for 5 s. The infiltration of melted Al into the Ti/Cu substrate and formed a continuous transition region at the interface of the joints were the dominant joining mechanisms. Microhardness of the interlayer after heated at 900 °C for 30 min possessed prominent improvement from 32.6 to 101.7 HV due to the completely phase transformation of Ni-Al interlayer, which composed of main phase NiAl and minor phase Ni 3 Al. The bond strength of the joint was checked to assess the joint quality. For the joint processed by 900 °C for 30 min, the maximum shear strength of Ti/NiAl and Cu/NiAl were 33.4 MPa and 39 MPa, respectively.

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ADVANCED ENGINEERING MATERIALS · 2024 ·Vol. 26 ·期 12 ·2400304 · IF 3.4

Influence of Macroscale Dimension on the Electrocrystallization of Cu Pad and Redistributed Layer in Advanced Packaging

Jin-Hao Liu,Yong-Qiang Wan,Li-Yin Gao,Xian-Wei Cui,Zhi-Quan Liu

Copper with equiaxed grains (EG Cu), copper with columnar nanotwinned grains (C-NT Cu), and copper with mixed equiaxed and columnar grains (MG Cu) are electroplated on pads and redistributed layers (RDLs) with different dimensions. When the diameters of pads increase from 40 to 105 μm, the flatness of pads decreases from 34.5% to 24.0%. The flatness gradually deteriorates from 16.5% to 34.4% with the increase of RDL width from 8 to 20 μm. In contrast, the flatness of C-NT Cu and MG Cu fluctuates between 1% and 5%, showing a weak correlation on the dimension. In terms of microstructure, the EG Cu and MG Cu has a weak correlation with size change, and the grain orientation shows a randomness. However, the (111) texture component of C-NT Cu differs greatly with different dimensions, especially in transition layer. The (111) texture component changes from 9.6% to 38.1% for ϕ 40–105 μm pad and from 14.3% to 18.9% for 8–20 μm-wide RDL. The study reveals the significant size effect on the deposited profile and microstructure of electrodeposited copper materials, which should give insights of the materials design in advanced packaging technology.

✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CHEMISTRY · 2023 ·Vol. 42 ·期 6 ·617-622 · IF 5.4

Synthesis, Structure and Chemical Bonding of Polyantimony Clusters Containing Coinage Metals [M2Sb14]4– (M = Cu, Ag)

Wei-Xing Chen,Yu-He Xu,Cui-Cui Wang,Lei Qiao,Zi-Yan Guo,Wen-Juan Tian,Zhong-Ming Sun

Comprehensive Summary Binary polyantimony clusters, namely [Cu 2 Sb 14 ] 4– and [Ag 2 Sb 14 ] 4– , containing coinage metals, were successfully synthesized and characterized, in which two homoatomic Sb 7 3– subunits are bridged by two coinage metals in η 4 : η 1 and η 1 : η 1 coordination modes, respectively. In [Cu 2 Sb 14 ] 4– , two bridging Cu ions and two Sb atoms form a planar rhombic unit, which was revealed to have antiaromatic properties by theoretical calculations. Further electron structure and bonding analysis confirmed the presence of delocalized bonds in the rhombic unit and the metallophilic interaction between two formal M + ions.

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ChemistrySelect · 2023 ·Vol. 8 ·期 19 ·e202300624 · IF 2.1

Effect of Basic-acidic Dopant over Cu/SiO2 Catalyst on Product Selectivity in Ethylene Carbonate Hydrogenation

Yaxin Chen,Xiaohua Cai,Yuxia Sun,Minxing Du,Jiaojiao Zhao,Yuehui Li

Cerium and boron are commonly used components to tune the acidic/basic property of catalysts in industry. In this work, cerium or boron-doped copper-based catalysts (xM−Cu/SiO 2 , M=Ce/B) were prepared with the ammonia-evaporation method. Both X-ray diffraction and Auger electron spectroscopy revealed that Cu + content increased along with the Ce-doping, but decreased by B-doping. NH 3 -Temperature Program Desorption results showed no change in the acidity of Ce-doped catalysts, while significant amounts of medium-strong acid sites appeared after B-doping. Application in ethylene carbonate hydrogenation indicates the promoting role of Ce-dopant in methanol production, while boron exhibits negative effects. The significant difference can be attributed to distinctive acidic/basic properties of Ce/B dopants, which affect the interaction between Cu and Si in the precursors, and thus adjust the ratio of Cu + /(Cu + +Cu 0 ). Graphical Ce promotes the interaction between copper and silicate, regulating the ratio of Cu + /(Cu + +Cu 0 ), and prompting the selectivity of methanol. On the contrary, B weakens the interaction and leads to poor catalytic performance.

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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2013 ·Vol. 51 ·期 6 ·1468-1474 · IF 3.543

“Nascent” Cu(0) nanoparticles-mediated single electron transfer living radical polymerization of acrylonitrile at ambient temperature

Yun-Hai Yu,Xiao-Hui Liu,Di Jia,Bo-Wen Cheng,Fei-Jun Zhang,Hui-Na Li,Peng Chen,Shan Xie

Zn(0)/ppm concentrations of CuBr 2 from 10 to 50 ppm was firstly used to catalyze radical polymerization of acrylonitrile at ambient temperature. The polymerization displayed typical living radical polymerization (LRP) characteristics, as evidenced by pseudo first-order kinetics of polymerization, linear increase of number-average molecular weight, and low polydispersity index (PDI) value. Effects of solvent, copper concentration, and initiator concentration on the polymerization reaction and molecular weight as well as PDI were investigated in detail. EC excelled NMP, DMF, and DMSO in terms of rate of polymerization as well as control of molecular weight and PDI. The increase of the copper concentration from 2.5 to 50 ppm leads to a higher rate of polymerization and a better control over the polymerization reaction. 1 H NMR and GPC analyses as well as chain extension reaction confirmed the very high chain-end functionality of the resultant polymer. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

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Nano Energy · 2026 · IF 16.7

Chemical-pressure-enhanced Jahn-Teller distortion in (Cu, Cr, Mn)3O4 spinel for high-temperature broadband emissivity

Yan Zheng,Linjing Qiao,Zhongyang Wang,Hao Gong,Boyu Liu,Jiajun Wang,Liping Tong,Zhiyuan Zhao,Xiao Zhou,Tongxiang Fan

Chemical pressure engineering of Jahn-Teller distortion enables broadband high emissivity. • A quantitative Jahn-Teller distortion index ( Q OJT ) is established to correlate structure with emissivity. • Ca 2+ doping (Cu, Cr, Mn) 3 O 4 spinel achieves an emissivity of 0.947 across the 0.4–25 μm range. • Exceptional thermal stability is demonstrated with less than 1.4% degradation at 1673 K. • An 11% enhancement in heating rate is achieved in practical radiative heating tests. Infrared radiation materials with broadband emissivity and high thermal stability are highly desirable for energy saving and thermal management applications. However, achieving high emissivity across the visible to mid-infrared range (0.4–25.0 μm) remains challenging due to the discontinuous absorption mechanisms in ceramics. Herein, a strategy based on promoting Jahn-Teller (JT) distortion is proposed to enhance the broadband emissivity of (Cu, Cr, Mn) 3 O 4 spinel. Substituting Cu 2+ with alkaline-earth ions (Mg 2+ , Ca 2+ , Sr 2+ ) introduces tunable chemical pressure, which modifies the local electric field and valence state distribution, thereby regulating the JT structural evolution. An octahedral JT structural descriptor ( Q OJT ) is developed to quantitatively compare JT structural evolution among different compositions. The Q OJT values show a positive correlation with broadband emissivity. The optimized JT structural evolution simultaneously enhances electronic transition, carrier and lattice vibration absorption, enabling synergistic regulation of broadband emissivity across the entire 0.4–25.0 μm spectral range. Among the investigated compositions, Ca 2+ -doped (Cu, Cr, Mn) 3 O 4 exhibits a broadband emissivity of 0.947 and maintains excellent stability under a simulated hypersonic environment at 1673 K. In radiative heating test, it achieves a heating rate approximately 11% higher than that of Al 2 O 3 . These findings demonstrate that chemical pressure provides an effective strategy for regulating JT structural evolution and designing broadband thermal radiation ceramics for high temperature applications. Download: Download high-res image (225KB) Download: Download full-size image Chemical-pressure-tuned Jahn-Teller distortion in (Cu, Cr, Mn) 3 O 4 spinel enables broadband high emissivity (0.947, 0.4–25.0 μm) and exceptional thermal stability up to 1673 K. A quantitative octahedral Jahn-Teller distortion index ( Q OJT ) correlates directly with emissivity performance. The optimized material achieves a 11% acceleration in heating rate, demonstrating its potential for high-temperature radiative transfer and thermal management applications.

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ENVIRONMENTAL RESEARCH · 2026 · IF 8.2

Fabrication of hierarchically porous Cu/PVDF/CeO2 membranes via synergistic NIPS-spraying for robust oil-water separation

Junjie Zhang,Jiayuan Xu,Jijun Ding,Haixia Chen

High-efficiency oil-water separation membranes based on low-mesh copper mesh offer advantages in cost-effectiveness, scalability, and adaptability to complex separation scenarios. However, their inherently large pore size usually results in insufficient separation precision. In this work, the Cu/PVDF/CeO 2 composite membrane is fabricated on the copper mesh substrate by combining the non-solvent induced phase separation method with spraying and immersion techniques. By adjusting the porogen content, the pore size of the composite membrane is effectively regulated, leading to enhanced separation efficiency. This strategy aims to simultaneously achieve superhydrophobicity and high-precision oil-water separation on low-mesh-number copper mesh substrates. The Cu/PVDF/CeO 2 composite membrane achieves a maximum water contact angle of 158.7°, exhibiting superhydrophobicity. In oil-water separation tests, the membrane demonstrates a separation efficiency exceeding 98.5% for all tested oil-water mixtures. Optimal performance is observed in the separation of the immiscible mixture of dichloromethane and water, where the membrane achieves a separation efficiency of 99.83% alongside a high separation flux of 79138.4 L m −2 ·h −1 . Additionally, the composite membrane exhibits excellent long-term stability and cycling stability. This study provides a feasible method for the preparation of high-efficiency oil-water separation composite membranes based on copper mesh substrates, with potential applications in industrial wastewater treatment and environmental remediation.

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Journal of Environmental Chemical Engineering · 2026 ·Vol. 14 ·期 5 ·124128 · IF 7.5

Cu-based MOFs@TiO2/PVDF composite membrane for efficient oil-water separation and bacterial isolation and sterilization

Lin-Lin Liu,Xue-Ling Zeng,Xuan Shi,Yu-Zhuo Fan,Wen-Yan Zeng,Ze-Hui Bai,Rong-Ke You,Xue-Qin Zhan,Fang-Chang Tsai,Ning Ma

Developing a multifunctional composite membrane with efficient oil-water separation, antifouling, stability, bacterial filtration, and antibacterial functions is essential for treating oily and organic medical wastewater. In this study, a PVDF/TA/APTES/CMCS/Cu-BTC@TiO 2 membrane was fabricated using mussel-inspired surface chemistry and dip-coating. Hydrophilic tannic acid (TA) and carboxymethyl chitosan (CMCS) enhanced membrane hydrophilicity, while hydrolyzed γ-aminopropyl triethoxysilane (APTES) formed a thin SiO 2 network layer that improved the stability of the deposited coating. Photocatalytic TiO 2 and biocompatible Cu-BTC contributed to the membrane’s photothermal response, antibacterial activity, and bacterial filtration. The membrane exhibited superhydrophilicity (water contact angle 10.3°), underwater oleophobicity (oil contact angle 153.9°), high water flux (5963.33 L·m −2 ·h −1 ), and 98.85% separation efficiency. It also achieved 99.99% bacterial filtration efficiency, 99.9% photothermal antibacterial rate, 99.99% photocatalytic sterilization, and self-cleaning ability. This multifunctional membrane shows great promise for oil-water separation and medical wastewater treatment.

CAS / MDL: 9003-39-8
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2026 · IF 9.2

Interfacial electronic coupling tunes d-band center in a sulfur-modulated NiFe–Cu catalyst for glycerol electrooxidation

Zhicong Hu,Guannan Li,Wenfu Xie,Jing Liu,Qiang Wang,Jiandu Lei

Coupling glycerol oxidation with hydrogen production offers a promising approach to reducing the energy consumption of hydrogen production and upgrading biomass. However, the catalytic performance is often limited by insufficient interfacial charge transfer and poorly defined active sites. Herein, we report a sulfur-modulated NiFe layered double hydroxide catalyst integrated with a Metal-organic frameworks (MOF)-derived Cu framework on nickel foam, in which well-defined heterogeneous interfaces are deliberately constructed to regulate the local electronic structure and catalytic microenvironment. Sulfur incorporation reconstructs the metal coordination environment and induces electron redistribution. As a result, the catalyst exhibits outstanding glycerol oxidation performance toward formate with high selectivity over a broad potential window, along with remarkable durability at high current densities. In situ Fourier transform infrared (FTIR) spectroscopy identifies the key intermediates involved in glycerol oxidation, while density functional theory (DFT) calculations reveal that sulfur-induced electronic coupling lowers the reaction energy barrier and facilitates charge transfer.

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