SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2022
·
IF 4.831
Dianwei Zhang,Furui Zhang,Shengnan Wang,Sha Hu,Yonghong Liao,Fenghuan Wang,Huilin Liu
We constructed a smartphone-integrated optosensor with inexpensive, reversible, environmental friendly, and rapid adsorption to detect Cu(II) and L-cysteine (L-Cys). The key part of this study was to prepare a red-to-blue colorimetric probe from herbaceous andrographis paniculata using one-pot polymerization at room temperature. When Cu(II) existed, the red fluorescence on the surface of the core–shell probe was quenched, while the blue fluorescence of the core did not respond, because the colorimetric probe interacted with the Cu(II) on the surface of red CDs. After L-Cys added, it interacted with the Cu(II) to strip it from the surface of red CDs, resulting in the recovery of fluorescence response. Under optimal conditions, the detection limits of this method for Cu(II) and L-Cys were 71 nM and 12 nM, respectively. Further, the red-to-blue colorimetric probe was integrated into smartphone with a software application to convert fluorescent color images into specific red (R), green (G), and blue (B) values. The spiked recovery of Cu(II) and L-Cys in lake water was verified the feasibility of the developed optosensors with a recovery of 98.2–101.6 % and 103.3–121.6 %. This method for detecting Cu(II) and L-Cys can not only recognize metal ions from actual samples, but also effectively protect CDs from quenching and restore fluorescence.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2022
·
IF 24.319
Wenyang Fu,Yingying Du,Jiana Jing,Chunhong Fu,Minghua Zhou
Electrochemical reduction of nitrate to ammonia (ERNA) is a new process to recycle nitrogen resource from nitrate polluted wastewater. Nevertheless, how to optimize active sites on electrode to improve activity is a key challenge. Here, we proposed that building interfacial electric field could enhance ERNA. XPS analysis, DFT calculations and in-situ electrochemical measurements confirmed that high Fermi level of Cu (1.09 eV) and low valence band maximum of CoO (−0.23 eV) formed interfacial electric field in CoO/Cu electrode to transfer electron from Cu to CoO, resulting in positively charged Cu (+0.01 eV) increase nitrate adsorption, whereas negatively charged CoO (−0.007 eV) decrease NO adsorption, improving removal and selectivity greatly for boosting ERNA. Eventually, CoO/Cu foam (Co/Cu ratio of 3.05) achieved the highest ammonia yield of 4.3 mg cm −2 h −1 with faradic efficiency of 96.7 %, surpassing Cu foam (1.2 mg cm −2 h −1 ) and CoO/Ni foam (1.3 mg cm −2 h −1 ) electrodes.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
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IF 8.6
Yang Liu,Jun-xia Yu,Li Guo,Guoping Song,Xiaodi Li,Chunqiao Xiao,Fang Zhou,Ruan Chi,Guoqing Feng
A novel circulation system combined with coordination leaching and biosorption process was successfully used for the direct recycling of Cu 2+ from the electroplating sludge. Cu 2+ was firstly efficiently leached out from the sludge by the choosing organic acid, and then it was selectively adsorbed onto a modified sorbent from the lixivium containing other co-ions including Zn 2+ , Ca 2+ , Fe 3+ , Cr 3+ , and Mg 2+ under dynamic adsorption condition. The results of static leaching experiments and DFT calculations showed that citric acid showed the best leaching performance for Cu 2+ among the studied organic acids and the traditional inorganic acid (HCl). To selective recovery of Cu 2+ from the lixivium, ethylenediamine tetraacetic acid dianhydride (EDTAD) modified bagasse was prepared, and it had high adsorption capacity, selectivity, and good reusability toward Cu-citric acid complex. The adsorption isotherm for Cu matched with the Langmuir model with a maximum adsorption capacity of 52.2 mg/g. XPS and EXAFS analysis illustrated that the Cu-citric acid complex was broken by EDTA on the modified bagasse, and Cu 2+ enriched on the sorbent while citric acid was released into the lixivium again. In the combined leaching and sorption circulation system, Cu 2+ was simultaneously absorbed on the modified bagasse fixed bed column once it was leached out. Benefitting the recycling of citric acid and the continuous adsorbing of Cu of the circulation system, the leaching efficiency could be increased from 75.0 % to 92.4 %, even in the very dilute citric acid solutions (concentration of 0.01 mol/L). The combined methods could increase Cu recovery efficiency from the sludge at a low concentration of the leaching agent, which had great potential in the practical application.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2023
·Vol. 34
·期 24
·1-17
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IF 2.8
Fan Yan,Wang Lei,Sun Xueqin,Li Cuili,Liu Jiacheng
A series of UiO-66-NH 2 -CA-Cu/g-C 3 N 4 (UCC 1 /CN x ) heterogeneous photocatalysts were constructed via a facile physical mixing treatment of the covalently post-modified MOF (UiO-66-NH 2 -CA-Cu) and functional materials g-C 3 N 4 . The tetracycline removal by the photocatalysis coupled with persulfate activation were studied under white light irradiation. The optimal UCC 1 /CN 20 photocatalyst showed the best photocatalytic performance, in which 94.0% TC could be efficiently eliminated ( k = 0.08669 min −1 ) within 30 min. The satisfactory degradation performance could be ascribed to the effective separation of photogenerated electron-hole pairs over the heterogeneous binary structure, which were demonstrated by several characteristic technologies including photoluminescence spectra, electrochemical impedance spectroscopy, transient photocurrent response and Bader charge analysis based on density functional theory calculations. Moreover, a possible mechanism behind the photocatalytic degradation was proposed and further affirmed by the quenching experiments and electron spin resonance measurements. Our work may supply a feasible idea for treating wastewater contained organic pollutants based on the heterogeneous photocatalyst.
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Journal of Materials Chemistry C
·
2023
·Vol. 11
·期 38
·13047-13055
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IF 6.4
Xuemei Zhou,Lingmin Kong,Junkai Hao,Jing Feng,Shuo Sun,Chuanzhen Zhou,Yanmin Liu,Zhengquan Yan,Xiao Zhu,Lei Hu
To strengthen the enzyme-mimetic catalytic activity of the classical transition metal oxide of copper and iron, bimetal Cu–Fe oxide mesoporous nanoparticles (Cu–Fe MNPs) were prepared in one pot under microwave-assisted conditions. The proposed Cu–Fe MNPs possessed a well-distributed mesoporous structure with an average aperture of 3.91 nm and a high BET specific surface area of 197.93 m2 g−1. Their peroxidase-like kinetic parameters (Km/Vmax) toward catalyzing the redox reactions of TMB and H2O2 were 0.013 mM/3.01 × 10−8 M s−1 and 56.58 mM/4.12 × 10−8, respectively. In particular, both toxic o-aminophenol (o-AP) and bioactive glutathione (GSH) could deteriorate their peroxidase-like property with an obvious color change from blue to colorless in the proposed Cu–Fe MNPs-TMB-H2O2 system. Under optimized conditions, Cu–Fe MNPs-TMB-H2O2 showed selective response to o-AP and GSH with quite low detection limits of 1.57 × 10−8 mol L−1 (S/N = 3) and 3.35 × 10−8 mol L−1 (S/N = 3), respectively. When they were applied for the visual monitoring of o-AP and GSH in real aqueous, fruit juice and medicinal samples, the detection recovery (%) was between 96.8–101.4% for o-AP and 97.1–105.8% for GSH. The mechanisms of the synergetic enhancement of the peroxidase-like activity of Cu–Fe MNPs and the selective recognition of o-AP and GSH were investigated in detail.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Hui Yao,Wan-ting Zhang,Ting-yu Yan,Xiao-qin Li,Xiao-feng Wang
Metal-Organic Frameworks (MOFs) are promising materials in electrochemical sensor. Herein, Cu-doped zeolitic imidazolate framework (ZIF) was synthesized by hydrothermal method. The prepared composite was characterized by XRD, FTIR and SEM. Then the material was modified onto the surface of glass carbon electrode (GCE) with chitosan(CHIT) and Cytochrome C (cyt c ). The modified electrode showed good electrochemical activity toward the reduction of hydrogen peroxide (H 2 O 2 ). Under optimized conditions, the linear response of the sensor to H 2 O 2 ranges from 10～5200 μM, with a detection limit of 3.7 μM (S/N=3). Finally, the sensor was successfully applied to determine H 2 O 2 in water samples. Thus, the Cu-doped ZIF material has great potential for applications in electrochemical sensors.
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SENSORS AND ACTUATORS B-CHEMICAL
·
2023
·
IF 8.4
Xin Chen,Xiao-Zhen Feng,Tao Zhan,Yu-Ting Xue,Hai-Xiang Li,Guo-Cheng Han,Zhencheng Chen,Heinz-Bernhard Kraatz
Three enzyme-free electrochemical glucose (GLU) sensors with bimetallic structures were constructed by electrodeposition of gold and copper nanoparticles (AuNPs/CuNPs), nickel and copper nanoparticles (NiNPs/CuNPs), and a copper-based metal-organic framework (Cu-MOF) combined with PtNPs , respectively. Amongst, the Cu-MOF/PtNPs on a gold electrode (GE) exhibited the best catalytic performance for GLU oxidation due to the synergistic amplification. The relevant electrochemical behaviour of GLU showed that two OH - and two electrons were involved in the process. The differential pulse voltammetry (DPV) enables the establishment of linearity in the concentration of 0.40–25.00 mM, with a detection limit (LOD) of 0.06 mM and a sensitivity of 158.41 µA·mM −1 cm −2 . In addition, the Cu-MOF/PtNPs/GE sensor was used to detect GLU in oral liquid as well as human serum samples with a recovery rate of 97.00–103.98% and RSD less than 3.59%. Finally, a portable electrochemical detection system based on the STM32F103C8T6 microcontroller , obtained a GLU concentration 5.24 mM while detecting in a diluted injection where the value 5.40 mM was recorded by a commercial meter to show the system has very broad application prospects in the point-of-care setting.
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POLYHEDRON
·
2023
·
IF 2.6
Zhwan Naghshbandi,Mohammad Gholinejad,José M. Sansano
In recent years, the excellent pore volume, huge specific surface area, and easy functionalizable zeolitic imidazolate frameworks (ZIFs), as new type of porous materials, attracted the attention of scientists. In this work, the new Co-based trimetallic Cu-Ni@ZIF-67 was synthesized using embedded the Cu-Ni precursor in ZIF-67. The structure, morphology and properties of Cu-Ni@ZIF-67 was characterized by the various analysis. The catalytic performance of Cu-Ni@ZIF-67 was investigated for tetracycline (TC) degradation and nitroarenes reduction at room temperature. The resultant catalyst was demonstrated excellent TC degradation efficiency by persulfate (PS) activation in the water during 30 min, and Cu-Ni@ZIF-67 was displayed superior catalytic activity for nitroarenes reduction in the presence of NaBH 4 . Comparing catalytic activity of Cu-Ni@ZIF-67 with Cu/ZIF-67, Ni/ZIF-67, Cu-Ni and ZIF-67 indicated higher activity of Cu-Ni@ZIF-67. Moreover, the recyclability and stability of this catalyst were surveyed.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Saif Ullah,Rooh Ullah,Rasha M.K. Mohamed,Gang Hu,Ateeq ur rehman,Muhammad Yasir Nawabi,Asif Hayat,Ata Ur Rehman,Mehboob Hassan,Ikram Uddin,Syed Attaullah Shah,Muhammad Zahir Shah,Jimei Song
An appropriate analytical technique for determination of kaempferol (KMF) by its perturbation effect on Belousov-Zhabotinskii (B-Z) oscillating system was reported. The macrocyclic copper (II) complex [CuL] (ClO 4 ) 2 ] was used as a catalyst while malic acid as substrate in B-Z system. The ligand L in the macrocyclic-complex is 5, 7, 7, 12, 14, 14-hexamethyl-1, 4, 8, 11-tetraazacyclotetradeca-4, 11-diene. Experimental outcomes shown the perturbation effect of KMF could cause the change in the amplitude of oscillation (ΔA) which was directly related to its concentration (2.5 × 10 -6 to 3.0 × 10 -4 mol/L) with correlation coefficient of 0.99315. The calculated relative standard deviation (RSD) is 3.1 % by eight samples (1.8 × 10 -5 mol/L) and the observed lower limit of detection is 1.25 × 10 -6 mol/L. The cyclic voltammetry (CV) experiments were used to confirm the redox reaction between kaempferol and sodium bromate. Furthermore, the reaction perturbation mechanism was derived from the well-known FKN (Field-Koros-Noyes) oscillation mechanism.
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DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 32
·11213-11221
·
IF 4
Yingying Wang,Yue Cao,Yan Hai,Xinyan Wang,Senda Su,Wenming Ding,Zhenyu Liu,Xiaoman Li,Min Luo
Electrocatalytic nitrate reduction to ammonia, which removes nitrates from aquatic ecosystems, is a potential alternative to the classical Haber–Bosch process. Nevertheless, the selectivity of ammonia is often affected by the toxic by-product nitrite. Here, the polyhedral-supported Cu nanoparticle binder-free monolithic electrode (Cu-BTC-Cu) is synthesized by the in situ electroreduction of Cu metal–organic framework (Cu-MOF) precursors. The Cu-BTC-Cu displays a high ammonia yield of 4.00 mg h−1 cm−2cat and a faradaic efficiency of 83.8% in 0.05 M K2SO4 (pH = 7), greatly outperforming the rod-supported (Cu-BTEC-Cu) and unsupported (Cu-BDC-Cu) Cu nanoparticle monolithic electrodes. Impressively, the Cu-BTC-Cu can inhibit significantly the release of by-product NO2− and present favourable stability after 10 consecutive cycles. These preeminent properties can be attributed to the polyhedral structure, which enables better dispersion of Cu nanoparticles and brings more active sites. Moreover, the reaction mechanism of Cu-BTC-Cu is analysed by electrochemical in situ characterization and several key intermediates are captured. This work provides new insights into the modification of the electrocatalytic nitrate reduction activity of Cu-based catalysts and ideas for the design of high-efficiency electrodes.
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Catalysis Science & Technology
·
2022
·Vol. 12
·期 21
·6416-6426
·
IF 6.177
Binxiong Guang,Wei Zhang,Yiwei Zhang,Yahui Xiao,Yong Liu
A novel, efficient and economical process of cyclohexanol (CHOL) production based on cyclohexene esterification–hydrogenation has become a research hotspot in recent years. Wherein, hydrogenation of cyclohexyl acetate (CHA) derived from the esterification of cyclohexene with acetic acid is a crucial step. Combining the advantages of metal complexes and heterogeneous catalysts, the robust Cu(I) coordinated amino-functionalized poly(ionic liquid)s (PILs-Cu(I)) were, in this research, synthesized for use in the mild and highly selective hydrogenation of CHA to CHOL. The results of FT-IR, UV-vis, BET, XPS and SEM-EDS confirmed that the Cu(I) was dominant in the PILs-Cu(I), and was homogeneously and stably coordinated on the amino-functionalized poly(ionic liquid)s. Benefiting from that, the PILs-Cu(I) was endowed with an unprecedented performance in the mild and highly selective hydrogenation of CHA to CHOL. Specifically, 95.6% CHA conversion with 96.6% selectivity of CHOL, and 97.0% selectivity of ethanol was obtained under extremely mild conditions of 80 °C and 2 MPa H2. Furthermore, no significant activity loss was observed over the PILs-Cu(I) after recycling for at least five times, delivering excellent stability and reusability.
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JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
·
2022
·
IF 4.383
Xiao-qi Chen,Zhi Huang,Yan-ying Liu,Qian Zhang,Jun-ming Hong
Conventional metal–organic frameworks (MOFs) used for electrocatalytic applications have the drawbacks of poor conductivity and instability. Herein, a Cu–1,2,3,4,5,6-benzenehexamine (Cu-HAB)/graphene oxide (GO) composite was prepared for the electrocatalytic degradation of tetracycline hydrochloride (TCH). Our characterization results show that Cu-HAB/GO has more active sites ( I D / I G = 1.0030), larger surface area (S BET = 395.3441 m 2 /g), and faster electron transport (Rct = 20.69) than Cu-HAB. Simultaneously, the improvement in the number of active sites, surface area and electron transport leads to a superior TCH electrocatalytic degradation efficiency. The reaction rate constant (0.70575 min −1 ) of the composite was higher with a 51.81% improvement observed when compared to Cu-HAB under the optimum conditions of 1 g/L NaCl, 20 mA, and 20 °C. In addition, 100% of the degradation efficiency was maintained after five cycles. A detailed study of the mechanism revealed that 1 O 2 and active chlorine were the critical active species for the degradation of TCH via quenching and electron paramagnetic resonance (EPR) studies. The possible TCH degradation pathway has been proposed. This study provides a novel and feasible method for the preparation of MOF-based electrocatalysts to expand their application to environmental fields.
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