CATALYSIS LETTERS
·
2019
·Vol. 150
·期 1
·178-184
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IF 2.372
Li Zhi-Xin,Wei Xian-Yong,Yang Zheng,Zhang Min,Meng Xing-Long,Niu Shuo,Zhang Di,Zong Zhi-Min
Abstract Highly selective hydrogenation of furfural to furan-2-ylmethanol (FM) in isopropanol was achieved over a novel magnetic Cu–Co/C derived from zeolitic imidazolate frameworks prepared by galvanic replacement reaction. Furfural conversion and FM selectivity (FMS) are 100% and 97.2%, respectively, at 200 °C. FMS was held around 95% after 5-times recycle of the Cu–Co/C. In addition, cinnamaldehyde was completely converted with 96.8% of phenylpropanol selectivity over the Cu–Co/C at 150 °C. Graphic Abstract
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SEPARATION AND PURIFICATION TECHNOLOGY
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2021
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IF 7.312
Bingzhi Liu,Haitao Lu,Shenyu Wu,Zizeng Wang,Li Feng,Huaili Zheng
Conventional flocculants are difficult to effectively remove dissolved ions and organic matter from water. This work aims to develop an environmentally friendly and renewable core–shell type flocculant (MCHS-g-P(AM-IA)) with octopus tentacle-like strong adsorption structure. The organic shell hydrolyses into molecular chains like octopus tentacles and adsorb dissolved ions/organic macromolecules through suckers-like functional groups, while the magnetic core acts as the growth center of flocs. Configuration and physical/chemical properties of the flocculant were analyzed by a series of characterization methods. Set Cu(II) and malachite green (MG) as models of heavy metal and organic pollutants separately, the removal capacity of MCHS-g-P(AM-IA) for water contaminants was studied in single-contaminant system and binary-contaminant system. The flocculation behavior and mechanism of MCHS-g-P(AM-IA) were deeply investigated by analysis of pH-dependence, background cationic influence and flocculation kinetics and SEM-EDS/XPS analysis of flocs. Furthermore, the flocculation performance in actual water matrix and regeneration tests of MCHS-g-P(AM-IA) were carried out to evaluate the applicable feasibility of flocculants for purification of complex wastewater in single stage water treatment.
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TALANTA
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2016
·
IF 4.035
Xiangheng Niu,Jianming Pan,Fengxian Qiu,Xin Li,Yongsheng Yan,Libo Shi,Hongli Zhao,Minbo Lan
Enzyme-free electrochemical detection of glucose in alkaline media with favorable properties has been acquired by fabricating a robust and large-surface sensing platform, which is composed of anneal-shrinked Cu 2 O dendrites grown on porous Cu foam. On the one hand, the good compatibility of electrodeposited Cu 2 O architectures and Cu foam substrate, together with a post-deposition anneal at 200 °C, offers a mechanically stable interface for glucose determination. On the other hand, the macropores of Cu foam that is decorated with unique Cu 2 O dendrites provide large active surface for electrocatalytic reaction and mass transport. As a result, selective sensing of glucose in the linear concentration range of 0.001–1.4 mM was achieved on the fabricated sensor, with a sensitivity of as high as 5.04 mA cm −2 mM −1 and a detection limit of 0.13 μM. Desired long-term performance stability was obtained, partially due to the strong adhesion of Cu 2 O microstructures to the Cu foam support after annealing. Practical monitoring of glucose in serum samples was also demonstrated on the proposed sensor.
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JOURNAL OF RARE EARTHS
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2020
·
IF 3.104
Di Deng,Shujun Deng,Dandan He,Zhiheng Wang,Zhipeng Chen,Yi Ji,Guoping Yan,Guangjin Hou,Licheng Liu,Hong He
Ce- or La-doped Cu/SSZ-13 catalysts were prepared by a hydrothermal method and Cu, Ce or La ions were incorporated through stepwise ion exchange. The catalyst activity was measured for the ammonia selective catalytic reduction reaction. The structure and composition of catalyst were characterized by using X-ray diffraction, scanning electron microscopy, inductively coupled plasma mass spectrometry solid-state NMR, NH 3 -TPD techniques, and the active components were examined by XPS and XANES . The results indicate that the Ce and La doping can both completely preserve the SCR activity of Cu/SSZ-13 above 300 °C, but there is also a decrease of activity below 200 °C. On the other hand, Ce doping is beneficial to the formation of framework aluminum , stabilizes molecular sieve framework and Cu active sites of Cu/SSZ-13, thereby improves the catalyst hydrothermal stability. But La doping will decrease the amount of framework aluminum and Cu active sites of Cu/SSZ-13 after hydrothermally aging, even destroy zeolite CHA structure. This is quite harmful to the catalyst hydrothermal stability.
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ACS Applied Materials & Interfaces
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2021
·
IF 9.229
Yingying Zhong,Tiantian Wang,Zhiting Lao,Minglei Lu,Shan Liang,Xiping Cui,Qing-lan Li,Suqing Zhao
Herein, a Au-Au/IrO2 nanocomposite with tandem enzyme-mimicking activity was innovatively synthesized, which can show outstanding glucose oxidase (GOx)-like activity and peroxidase-like activity simultaneously under neutral conditions. Moreover, a Au-Au/IrO2@Cu(PABA) reactor was prepared via encapsulation of the Au-Au/IrO2 nanocomposite in a Cu(PABA) metal organic framework. The reactor not only exhibits excellent organic solvent stability, acid resistance, and reusability but also displays better cascade reaction catalytic efficiency (kcat/Km = 148.86 min–1 mM–1) than the natural free enzyme system (GOx/HRP) (kcat/Km = 98.20 min–1 mM–1) and Au-Au/IrO2 nanocomposite (kcat/Km = 135.24 min–1 mM–1). In addition, it is found that the reactor can catalyze glucose or dissolved oxygen to produce active oxygen species (ROS) including HO, 1O2, and O2–· through its enzyme-mimicking activity. Finally, the novel reactor was successfully used in organic dye degradation and antibacterial application. The results show that it can effectively degrade methyl orange, methylene blue, and rhodamine B, which all can reach a degradation rate of nearly 100% after interacting with Au-Au/IrO2@Cu (PABA) for 3.5 h. Furthermore, the reactor also exhibits excellent antibacterial activity, so as to achieve a complete bactericidal effect to Staphylococcus aureus and Escherichia coli at a concentration of 12.5 μg mL–1.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2022
·
IF 4.326
Xiaoxian Li,Yuanzhe Gong,Qi Lu,Min Lin,Jian Liu,Yulong Wu
In this work, the hierarchical pore HZSM-5 zeolite was synthesized by the method of alkali treatment, and the bimetallic loading of Mo and Cu was investigated for the hydrothermal aromatization of stearic acid. After alkali treatment, the pore size of HZSM-5 increased, but the acid sites decreased. The metal loading reintroduced the Lewis acid sites, greatly increasing the ratio to Brönsted acid sites. Therefore, the treated catalyst achieved higher hydrothermal stability while maintaining the high activity of hydrothermal aromatization of stearic acid. Mo0.02Cu0.01/Z-0.2M achieved excellent activity in the stearic acid hydrothermal aromatization with a high overall TEX (toluene, ethylbenzene, and xylenes) yield of 50.19 wt %, including 10.30 wt % toluene, 3.82 wt % ethylbenzene, and 36.07 wt % xylene. In addition, Mo0.02Cu0.01/Z-0.2M still showed excellent catalytic activity while applied in the system of the simulated microalgal bio-oil. As the reactant changed to the mixture of stearic acid and hexadecanamide, an overall TEX yield of 34.11 wt % was obtained at 450 °C. These results demonstrate the excellent hydrothermal aromatization ability of the MoCu-supported hierarchical pore ZSM-5 zeolite, which provides the potential to produce value-added chemicals from algal biomass.
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MICROCHIMICA ACTA
·
2017
·Vol. 184
·期 10
·3817-3823
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IF 4.58
Li Jingjing,Wang Yuxian,Jiao Yunfei,Jia Ru,Chen Zhengbo
Under normal circumstances, chromate ions cannot oxidize core-shell Cu-Au nanoparticles (NPs) because the standard redox potential of the Cr(VI)/Cr(III) system is lower than that of Au(I)/Au. However, in the presence of a certain concentration of hydrogen bromide, the Nernst potential becomes higher than that of Au(I)/Au and Cu(II)/Cu (as calculated by the Nernst equation). Based on this finding, a colorimetric method was developed that is based on oxidative etching of Cu@Au NPs by chromate. The Cu-Au NPs have a light red color in the presence of 5 mM HBr. On addition of Cr(VI), the gold shell is rapidly etched from the surface of the Cu-Au NPs, and this is accompanied by a color change to blue. The color changes were characterized by UV-vis spectroscopy. The absorbance at 526 nm changes in the 0.4 nM to 1 μM chromate concentration range, and the detection limit is 0.21 nM.
Schematic of a highly sensitive and selective colorimetric method for detection of chromate based on the redox etching of Cu@Au nanoparticles induced by Cr(VI). The presence of HBr enables Cu@Au NPs to be oxidized by Cr 6+ .
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Inorganic and Nano-Metal Chemistry
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2021
·
IF 1.716
Weiqiang Xu,KaiKai Hu,Shouwen Jin,Yuting Zhang,Daqi Wang
Transition metal carboxylates with O- and N-donor ligands are interesting for their structural features. Seven novel isonicotinamide(inic)-based metal complexes of [Cd(inic)2(L1)2(H2O)2] · 2H2O (1) (L1 = 2-chloronicotinate), [Cd(inic)2(L2)2(H2O)2] (2) (L2 = 2,4-dichlorobenzoate), [Cu(inic)2(L3)2] (3) (L3 = 4-chlorophenoxyacetate), [Cu3(inic)6(L4)2(HL4)2(H2O)2] · 2H2O (4) (L4 = azelate), [Zn(inic)2(L1)2(H2O)2] · (inic) · H2O (5), [Zn(inic)(L5)(H2O)4] (6) (L5 = 3-nitrophthalate) and [Zn2(inic)2(L6)2] · 5H2O (7) (L6 = 1,4-cyclohexanedicarboxylate) have been obtained by the introduction of the carboxylates by the common solution method and are structurally featured by different techniques of EA, IR spectra, TG and SCXRD analysis. The X-ray studies told that these complexes display mononuclear to trinuclear structures with octahedral/square-pyramidal geometry around the Zn2+, trigonal bipyramidal/octahedral at the Cu2+ and octahedral for the Cd2+. The inic in 1–7 are coordinated only in monodentate fashion with its ring N, while 5 has the lattice inic. The carboxylates coordinated to the metal in monodentate, chelating bidentate and bridging bidentate fashions. The pair of complementary N-H···O H-bonds from the CONH2 of the inic were found in all compounds except 7. Except 1 and 2, all other compounds bear the CH-O contacts from the pyridine CH of the inic. The intricate intra- and intermolecular classical H-bonds, CH-N, CH-O, CH-Cl, CH2-O, O-N, O-O, Cl-O, Cl-Cl, CH-π, CH2-π, C-π, N-π, Cl-π and π-π associations are elucidated by the X-ray crystallographic studies, which push the discrete complexes into high-dimensional ordered supramolecular structures.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
·
IF 8.128
Haitao Xu,Dianhua Song,Jiao Li,Yan Zhao,Ruijie Yang,Jingzhe Zhao
The demand for sustainable energy sources urges the development of efficient and earth-abundant electrocatalysts . Herein, chlorine assisted ion-exchange and in-situ sulfurization processes were combined to construct CuCo 2 S 4 @(Cu,Co) 2 Cl(OH) 3 heterostructures from Cu(OH) 2 nanoarrays. Chlorine element in the cobalt source stimulated the formation of (Cu,Co) 2 Cl(OH) 3 precursor, and further facilitated partial transformation of the precursor to CuCo 2 S 4 on the surface to achieve composite structure. The mixed valences of Co element (Co 3+ in CuCo 2 S 4 and Co 2+ in (Cu,Co) 2 Cl(OH) 3 ) and O S interpenetrated nanointerface in the composite catalysts provided low electron transfer resistance for good alkaline oxygen evolution reaction (OER) activities. In 1 mol L −1 KOH electrolyte, the overpotentials of the optimal composite catalyst reached 253 and 290 mV respectively at the current density of 20 and 50 mA cm −2 , which is comparable to the activity of commercial Ir/C (281 mV@20 mA cm −2 ). These findings could provide opportunities for designing effective and inexpensive composite electrocatalysts through nanointerface engineering strategy.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2019
·
IF 6.361
Yuanli Liu,Jiang Xu,Zhen Cao,Ruiqi Fu,Chuchen Zhou,Zheni Wang,Xinhua Xu
This work aimed to develop a feasible technology to reuse dead pig biowaste for heavy metals removal , which was first carbonized into pig bone char (PBC) after pyrolysis and further functionalized with amino ( NH 2 ) to improve its affinity with heavy metals. The application of PBC after NH 2 -functionalization for aqueous heavy metals removal was explored, including Pb 2+ , Cu 2+ , and different complex Cu(II) species. PBC@SiO 2 -NH 2 showed comparable performance with AC@SiO 2 -NH 2 . The adsorption capacity of Pb 2+ and Cu 2+ by PBC@SiO 2 -NH 2 was 120 and 30 mg g −1 , respectively. The NH 2 functionalization enhanced the adsorption of complex Cu(II) species, and PBC@SiO 2 -NH 2 exhibited good performance under a wide pH range and coexisting ions. The adsorption of Cu(II) EDTA species with an EDTA/Cu(II) molar ratio of 1.0 by PBC would be enhanced ~3 times and ~6 times after NH 2 functionalization and further addition of Fe 3+ , respectively. The results of EDX , elemental mapping, and XPS confirmed the adsorption of Cu(II) species. The adsorption kinetics , isotherm, and thermodynamics of different Cu(II) species by PBC@SiO 2 -NH 2 were investigated. The regeneration of PBC@SiO 2 -NH 2 was easily performed via acidic wash. These results suggested the application potential of the reuse of biowaste, which could be a promising adsorbent for aqueous heavy metals after specific functionalization.
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iScience
·
2022
·
IF 6.107
Tongyang Song,Yuanyuan Qi,Chen Zhao,Peng Wu,Xiaohong Li
Summary An ultrastable and efficient Cu@C/SiO 2 nanocatalyst was fabricated for the hydrogenation of ethylene carbonate, in which Cu nanoparticles are encapsulated by sorbitol-derived graphitized carbon overlayers. During the calcination of Cu-sorbitol/SiO 2 precursors under N 2 atmosphere, sorbitol decomposed to CO and CO 2 . The in situ generated CO not only reduced Cu 2+ to Cu 0 /Cu + , but also formed graphitized carbon overlayers on the Cu surface via the disproportionation of CO. The Cu@C/SiO 2 catalyst exhibited superior catalytic performance (91% MeOH yield and 43.6 h −1 TOF) at a H 2 /EC molar ratio of 20. Of particular note, the Cu@C/SiO 2 catalyst showed remarkable long-term stability during 736 h time-on-stream test without any deactivation. The graphitized carbon overlayers on the surface of Cu nanoparticles not only functioned synergistically with the surface Cu 0 /Cu + sites to promote the EC hydrogenation but also suppressed the sintering of Cu nanoparticles. Furthermore, the interaction of Cu nanoparticles and graphitized carbon overlayers stabilized the surface Cu + /(Cu 0 +Cu + ) ratio.
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BIORESOURCE TECHNOLOGY
·
2018
·
IF 5.807
Zheng-Zhe Zhang,Ya-Fei Cheng,Lian-Zeng-Ji Xu,Jing Wu,Yu-Hui Bai,Jia-Jia Xu,Zhi-Jian Shi,Ren-Cun Jin
Metal and metal oxide nanoparticles (NPs) show differences in antimicrobial activity due to different chemical and physical properties. Using copper as a representative example, this study compared the NP effects on anaerobic ammonium oxidation (anammox) bacteria in wastewater treatment. Long-term exposure to 5 mgCu L −1 CuNPs reduced the physiological activity and abundance of anammox bacteria, thereby causing deterioration of reactor performance. However, anammox granules exhibited stronger resistance and resilience to perturbation by 1–160 mgCu L −1 CuONPs, and no adverse effects on performance were observed. Moreover, the level of Cu(II) released from NPs in the influent exhibited good correlations with variations of the community structure and sludge properties. Therefore, the effects of Cu-based NPs on anammox sludge properties are dependent on their forms and levels, and their discrepant effects are partially attributed to their ability to release ionic copper.
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