ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Yu Chen,Senqin Fan,Jiaojiao Chen,Lei Deng,Zeyi Xiao
A catalytic membrane nanoreactor (CMNR) with Cu–Agx (where x is the millimolar concentration of AgNO3) bimetallic catalysts immobilized in membrane pores has been fabricated via coupling flowing synthesis and replacement reaction. Surface characterization by transmission electron microscopy (TEM) gives obvious evidence of the formation of Cu–Ag bimetallic core–shell nanostructures with Ag islands deposited on the Cu core metal. An apparent high shift phenomenon for the Cu element and a low shift phenomenon for the Ag element was determined by X-ray photoelectron spectroscopy (XPS), indicating a close interaction with the transfer of electron density from the Cu atom to the Ag atom. The hydrogenation catalysis of p-nitrophenol (p-NP) was tested to evaluate the catalytic performance. During the catalytic process, the Cu core acts as an electron-deficient site to adsorb and activate the −NO2 group for p-NP, and the Ag shell is beneficial for enhancing active H spilling to the Cu surface and then performing hydrogenation. A volcano-shaped apparent reaction rate constant can be achieved, which rises initially with the increasing Ag content and subsequently drops with a further increase in the Ag content. The highest value of 1071 min–1 can be achieved for CMNR immobilized with Cu–Ag2 owing to the suitable adsorption activation behavior and the best hydrogen spillover behavior.
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JOURNAL OF MATERIALS PROCESSING TECHNOLOGY
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2022
·
IF 6.162
Lu Han,Jing Wang,Yuanyuan Chen,Zhang Liu,Yuan Huang,Dongguang Liu,Laima Luo,Chenxi Liu,Yongchang Liu,Zumin Wang
Metallurgical bonding was achieved between carbide-dispersion-strengthened Cu (CDS-Cu) and oxide-dispersion-strengthened W (ODS-W) after diffusion bonding via an interface tailoring method of anodization and deoxidation of ODS-W combined with the introduction of Cu wetting layer. The shear strength of the CDS-Cu/ODS-W joints fabricated by the interface-tailoring bonding is 124 MPa, which is higher than that of 99 MPa of the joint prepared by direct bonding. The increase in strength is due to the achievement of the metallurgical bonding between CDS-Cu/ODS-W, the increase of the debonding energy and the increase of propagation distance of the cracks. After metallurgical bonding, the second phase particles of WC in CDS-Cu and Y 2 O 3 in ODS-W were dispersed at the phase boundary to reduce the lattice strain energy. This work paves the way for the preparation of advanced plasma-facing components comprised of high-performance CDS-Cu and ODS-W for China Fusion Engineering Test Reactor (CFETR).
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Biomass Conversion and Biorefinery
·
2022
·Vol. 13
·期 15
·14049-14058
·
IF 4.05
Yan Mi,Zhang Yan,Grisdanurak Nurak,Wibowo Haryo,Yu Caimeng,Kanchanatip Ekkachai
One outstanding advantage of supercritical water gasification (SCWG) coupled with CO 2 capture and storage (CCS) technology is to realize the conversion of bio-waste into hydrogen-rich syngas. In this study, metal organic frameworks of copper benzene-1,3,5-tricarboxylate (Cu-BTC) were synthesized via solvothermal method with different synthesis time and used as adsorbent for capturing CO 2 from SCWG model syngas. The effect of synthesis time, adsorption temperature, and adsorption pressure on CO 2 adsorption capacity of Cu-BTC was evaluated using analysis of variance (ANOVA). The Pareto chart showed that adsorption pressure had significant effect on CO 2 adsorption capacity, and the surface plot indicated that CO 2 adsorption capacity increased with higher adsorption pressure and lower adsorption temperature. Cu-BTC with 48-h synthesis time had the largest specific surface area (1737 cm 2 /g) and pore volume (0.73 cm 3 /g), and it exhibited the highest CO 2 capacity of 19.83 mmol/g and 13.56 mmol/g at 0 °C and 25 °C, respectively. The adsorption results showed that CO 2 concentration in multi-component gas decreased from 48.75 to 12.9%, and H 2 concentration increased from 38.75 to 75.45%. Therefore, Cu-BTC has the potential for removal of CO 2 from SCWG syngas, and more work is necessary to further improve the adsorption capacity and selectivity. Graphical abstract
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ACS Biomaterials Science & Engineering
·
2022
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IF 5.395
Le Gao,Yibo Song,Jun Zhong,Xiaofeng Lin,Shu-Feng Zhou,Guowu Zhan
Two-dimensional (2D) metal–organic frameworks (MOFs) could serve as multifunctional nanoplatforms to load small-molecule drugs and enzyme-mimicking nanoparticles (NPs) with a high efficiency for combined cancer therapy. Herein, we have prepared novel 2D Cu-tetrakis (4-carboxyphenyl) porphyrin (TCPP) nanosheets with an average thickness of 1.2 ± 0.1 nm using Cu2O nanocubes (50 nm) as a template and solid copper ion supplier. Cu2O nanocubes can be consumed and hybridized with the obtained Cu-TCPP, depending on the molar ratio of Cu2O and TCPP linker. The resultant Cu2O/Cu-TCPP could serve as nanoplatforms for co-loading of Pt and Au NPs to construct multifunctional Cu2O/Cu-TCPP/(Pt–Au) nanomedicines, which showed a superior anticancer effect via multiple therapeutic modes. For instance, Cu(II)-TCPP can produce 1O2 in the presence of acidic H2O2 by the Russell mechanism and the intrinsic Cu(I) ions (derived from the residual Cu2O) could mediate a Fenton-like reaction in tumorous tissues to generate toxic hydroxyl radicals (•OH). Moreover, the loaded Pt NPs with catalase (CAT)-mimic activity could decompose hydrogen peroxide (H2O2) into O2 within the tumor cells, increasing the local O2 concentration, modulating the tumorous hypoxia atmosphere, and promoting the O2-dependent glucose oxidation reaction. Furthermore, Au NPs with glucose oxidase (GOx)-mimic activity could accelerate the consumption of glucose and cut nutrient supply to induce starvation therapy. Consequently, our designed 2D MOF-based therapeutic nanomedicines would be a promising candidate for future smart and combined cancer therapy.
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Acta Biomaterialia
·
2023
·
IF 9.7
Haotian Tian,Jianqin Yan,Wei Zhang,Huaixu Li,Shouwei Jiang,Haisheng Qian,Xulin Chen,Xingliang Dai,Xianwen Wang
During the past few years, bacterial infection and oxidative stress have become important issues for wound healing. However, the emergence of numerous drug-resistant superbugs has had a serious impact on the treatment of infected wounds. Presently, the development of new nanomaterials has become one of the most important approaches to the treatment of drug-resistant bacterial infections. Herein, coordination polymer copper-gallic acid (Cu-GA) nanorods with multi-enzyme activity is successfully prepared for efficient wound treatment of bacterial infection, which can effectively promote wound healing. Cu-GA can be efficiently prepared by a simple solution method and had good physiological stability. Interestingly, Cu-GA shows enhanced multienzyme activity (peroxidase, glutathione peroxidase , and superoxide dismutase), which can produce a large number of reactive oxygen species (ROS) under acidic conditions while scavenging ROS under neutral conditions. In acidic environment, Cu-GA possesses POD (peroxidase)-like and glutathione peroxidase (GSH-Px)-like catalytic activities that is capable of killing bacteria ; but in neutral environment, Cu-GA exhibits superoxide dismutase (SOD)-like catalytic activity that can scavenge ROS and promote wound healing. In vivo studies show that Cu-GA can promote wound infection healing and have good biosafety. Cu-GA contributes to the healing of infected wounds by inhibiting bacterial growth, scavenging reactive oxygen species, and promoting angiogenesis . Statement of significance Cu-GA-coordinated polymer nanozymes with multienzyme activity were successfully prepared for efficient wound treatment of bacterial infection, which could effectively promote wound healing. Interestingly, Cu-GA exhibited enhanced multienzyme activity (peroxidase, glutathione peroxidase, and superoxide dismutase), which could produce a large number of reactive oxygen species (ROS) under acidic conditions and scavenge ROS under neutral conditions. In vitro and in vivo studies demonstrated that Cu-GA was capable of killing bacteria, controlling inflammation, and promoting angiogenesis.
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DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 33
·11441-11450
·
IF 4
Defeng Hu,Zhongqiao Sun,Yide Han,Hao Meng,Xia Zhang
Considering the surface affinity of MOFs and separation advantages of polymer membranes, herein, a one-step interface synthesis strategy is used in the construction of Cu-BTC/PVDF hybrid membranes, in which Cu2+ ions and 1,3,5-benzenetricarboxylic acid (H3BTC) were dissolved in ionized water and n-octanol separately, and polyvinylidene fluoride (PVDF) films were laid at the interface of two immiscible solvents. As a result, Cu-BTC was generated and readily self-assembled inside the PVDF films. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA) and the Brunauer–Emmett–Teller (BET) method were used to characterize Cu-BTC/PVDF hybrid membranes, and Congo red (CR) was selected as the target dye to evaluate the surface adsorption activity of the hybrid membranes. Batch adsorption tests under various conditions were conducted to optimize the adsorption capacity, adsorption kinetics, isotherms and thermodynamics, which were analyzed to further explore the adsorption behavior. Based on this, the adsorption mechanism was discussed. It is worth noting that because of the π–π stacking interaction and hydrogen bonding, an extraordinary adsorption capacity of CR was achieved, and the good separation advantage and the cyclic adsorption performances endow the resulting Cu-BTC/PVDF hybrid membranes with promising applications in the removal of organic dyes from practical wastewater.
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Mengzhen Song,Jingru Han,Yingzhi Wang,Lungang Chen,YanYan Chen,Xiaoyuan Liao
Fe-based MOFs (Fe-MOFs) are deemed promising Fenton-like catalysts due to their well-developed pores and accessible active sites. However, their inferior catalytic activity, iron leaching, and low H2O2 utilization always hinder their application as Fe-based MOF catalysts. In this work, we manipulated the structure of Fe-oxo nodes in MIL-88B(Fe) via a CuI species substitution method, affording a mixed-valence (Cu-incorporated Fe-MOFs) with highly improved Fenton-like performance. It is found that the CuI serves as a shuttle to promote transfer between FeII/FeIII, inducing the formation of a larger amount of stable FeII sites, which was proven by experimental and DFT calculation results. A linear relationship was observed for the Fenton-like performance and the amount of CuI species for the catalysts. The corresponding value of the •OH formation is 2.17 eV for Cu-incorporated MIL-88B(Fe), which is significantly lower than that of MIL-88B(Fe) (2.69 eV). Meanwhile, the enriched CuI species suppress Fe species leaching during the catalytic reaction. The Fe-ion leakage of 0.4Cu@MIL-88B is very tiny (0.01–0.03 mg/L), significantly less than that of MIL-88B (2.00–3.02 mg/L). At the same time, H2O2 utilization for 0.4Cu@ MIL-88B(Fe) is 88%, which is almost 4.4 times that of pure MIL-88B(Fe). This work provides insights into the rational design of Fe-MOFs as promising Fenton-like catalysts for wastewater treatment.
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ENERGY & FUELS
·
2023
·
IF 5.3
Yi Ren,Yujia Bai,Genxiang Wang,Yijian Liu,Chuancheng Mou,Jiayu Chen,Baohuan Wei,Hui Wang,Yuhan Sun
Efficient conversion of CO2 to value-added fuels or chemicals using electricity from renewable sources is an appealing approach to realize carbon neutrality. Under this background, it is crucial to design efficient and low-cost catalysts for CO2 electroreduction. Herein, we fabricated an electrocatalyst with the structure of Cu–Ni alloy nanoparticles grown on nitrogen-doped carbon nanotubes (CuxNi/NCNT, x = 2.4, 1, and 0.36) for electrochemical CO2 reduction reaction (CO2RR) via a hydrothermal method followed by pyrolysis. The optimized CuNi/NCNT demonstrates a favorable CO2RR performance with a CO Faradaic efficiency (FECO) of 94.8% and a current density of 26.6 mA cm–2 at −0.9 V versus the reversible hydrogen electrode (vs RHE) in the H-cell, far superior to those of single metal counterparts. Density functional theory (DFT) calculations unravel that the Cu–Ni alloys possess much lower free energy changes for the formation of the key COOH* intermediate than those of the Cu metal, thereby facilitating CO2 reduction into CO. Additionally, the CO2RR performance of CuNi/NCNT was further evaluated in the gas diffusion electrode (GDE) involved in the flow cell to examine the practical application of the prepared catalyst, which can deliver a current density of 124.6 mA cm–2 with a FECO of 92.8% at −1.1 V vs RHE. This work enriches electrocatalysts for highly efficient CO2 electroreduction to CO.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2023
·
IF 5.2
Wei Zhang,Ping Xiong,Qiao Li,Jiansheng Li,Jinyou Shen,Pengyu Zhu,Xiuyun Sun,Jingyu Lu,Ya Hu
EDTA-complexed heavy metals (EDTA-CHMs), one of the typical contaminants in industrial effluents , present challenges for wastewater purification because of their stability and high solubility over a wide pH range. Selective adsorption of various EDTA-CHMs coexisting in industrial wastewater is crucial for the recovery of heavy metal resources. Hence, investigating the competitive behavior and selective adsorption mechanisms of coexisting EDTA-CHMs during the effluent removal process is worthwhile. In this study, we chose Ferrihydrite (Fh) as the adsorbent and focused on the competitive adsorption behavior of two common EDTA-CHMs (EDTA-Cu(Ⅱ) and EDTA-Cr(Ⅲ)) on the Fh surface, as well as their removal mechanisms. For binary systems (EDTA-Cu(Ⅱ) and EDTA-Cr(Ⅲ)), the maximum adsorption capacity of Fh for EDTA-Cu(Ⅱ) was 17.32 mg/g, but because of the coexisting EDTA-Cu(Ⅱ), adsorption of EDTA-Cr(Ⅲ) by Fh was severely inhibited. In a competition experiment with binary contaminants of different EDTA complexes, Fh consistently exhibited stronger adsorption performance on EDTA-Cu(Ⅱ) when the ratio and addition order of EDTA-Cu(Ⅱ) and EDTA-Cr(Ⅲ) in the coexisting system was changed, and the valence state of the EDTA-CHMs was the key factor. The adsorption mechanism indicated that Fh could directly adsorb EDTA-CHMs through electrostatic interaction and surface complexation. The recycling rate of EDTA-Cu(Ⅱ) was still approximately 70.63% after five cycles of treatment with Na 2 SO 4 solution. This study provides new insights into the adsorption behavior of coexisting EDTA-CHMs on adsorbents and the selective removal of related pollutants.
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ACS Applied Nano Materials
·
2023
·
IF 5.9
Hanxu Lu,Zhe Hu,Hong Liu,Zizhao Fu,Hanqing Dai,Wanlu Zhang,Ruiqian Guo
Transition-metal-ion-doped quantum dots (QDs) are promising candidates to fabricate full-spectrum white-light-emitting diodes (WLEDs). In this work, a series of efficient white-light-emitting Cu,Mn-codoped ZnGaS/ZnS (Cu,Mn:ZnGaS/ZnS) QDs were synthesized by controlling the Zn/Ga molar ratio and the amounts of Mn dopants. After ZnS shelling, the photoluminescence quantum yield reached 58% and the spectrum almost covered the whole visible spectrum. Further, the stepwise doping process was investigated, which had considerable reference value to subsequent research. The Cu,Mn:ZnGaS/ZnS QDs were employed to fabricate WLEDs displaying a color rendering index of 94 and CIE coordinates of (0.34, 0.35).
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MATERIALS RESEARCH BULLETIN
·
2021
·
IF 4.641
Chuanfu Song,Kunyuan Chen,Xin Jin,Xinyu Zhao,Guangrong Liu,Feifei He,Qiang Huang
The biochar-supported Cu 2 O/Cu composite (Cu 2 O/Cu/BC) was fabricated by direct pyrolysis of hemp hurds pretreated with KOH and CuCl 2 , in which the synchronous carbonization-activation-functionalization was achieved to produce copper-modified biochars. Cu 2 O/Cu/BCs were characterized by XRD , Raman, XPS , SEM and N 2 adsorption-desorption techniques. The adsorption methyl orange by Cu 2 O/Cu/BCs showed that the incorporation of Cu 2 O/Cu has improved the adsorption capacity. The adsorption obeyed the pseudo-second-order kinetic model and Langmuir isotherm. The maximum adsorption capacity reached 379.4 mg∙g -1 at 303.5 K. Furthermore, assisted with the photoactivity of Cu 2 O/Cu heterojunction the saturated adsorbent can be regenerated under simulated sunlight, and the re-adsorption capacity was still as high as 77.1% of the fresh adsorbent after six cycles. The regeneration efficiency was much better than traditional thermal regeneration and solvent treatment. This work should allow to provide a convenient preparation of functionalized biochars and to develop solar-driven, self-regenerative sorbents for water decontamination with high efficiency.
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RSC Advances
·
2021
·Vol. 12
·期 1
·602-610
·
IF 3.361
Yingxin Liu,Kai Liu,Meihua Zhang,Kaiyue Zhang,Jiao Ma,Shuwen Xiao,Zuojun Wei,Shuguang Deng
Highly active and thermally stable Cu–Re bimetallic catalysts supported on TiO2 with 2.0 wt% loading of Cu were prepared via an incipient wetness impregnation method and were applied for liquid phase selective hydrogenation of levulinic acid (LA) to γ-valerolactone (GVL) in H2. The effect of the molar ratios of Cu : Re on the physico-chemical properties and the catalytic performance of the Cu–Re/TiO2 catalysts was investigated. Moreover, the influence of various reaction parameters on the hydrogenation of LA to GVL was studied. The results showed that the Cu–Re/TiO2 catalyst with a 1 : 1 molar ratio of Cu to Re (Cu–Re(1 : 1)/TiO2) exhibited the highest performance for the reaction. Complete conversion of LA with a 100% yield of GVL was achieved in 1,4-dioxane solvent under the reaction conditions of 180 °C, 4.0 MPa H2 for 4 h, and the catalyst could be reused at least 6 times with only a slight loss of activity. Combined with the characterization results, the high performance of the catalyst was mainly attributed to the well-dispersed Cu–Re nanoparticles with a very fine average size (ca. 0.69 nm) and the co-presence of Cu–Re bimetal and ReOx on the catalyst surface.
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