JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
·
2019
·Vol. 107
·期 10
·2310-2326
·
IF 3.221
Bailong Tao,Maowen Chen,Chuanchuan Lin,Lu Lu,Zhang Yuan,Ju Liu,Qiang Liao,Zengzilu Xia,Zhihong Peng,Kaiyong Cai
The poor osseointegration and postoperative bacterial infection are prominently responsible for the failure of titanium (Ti)-based implant in clinic. To address above issues, methacryloyl modified graphene oxide (GOMA) as zinc ions (Zn 2+ ) reservoir and release platform was fabricated on the Ti substrates with cathode electrophoresis deposition (EPD). Afterward, phenylboronic acid (PBA) functionalization methacryloyl-gelatin (GelMA-PBA) was reacting with GOMA through in situ free-radical polymerization to prepare GO-Zn/GelMA-PBA coating. The obtained coating was confirmed by scanning electron microscopy, X-ray photoelectron spectroscopy, and Zn ions release property, respectively. in vitro cellular experiments including cell activity, alkaline phosphatase, collagen secretion, extracellular matrix (ECM) mineralization, osteogenic genes and proteins, revealed that GO-Zn/GelMA-PBA coating was beneficial for enhancing the adhesion, proliferation, and differentiation of osteoblasts. The positive results were related to the existence of gelatin, formation of boronic ester between PBA groups, and carbohydrates of osteoblasts surface. Meanwhile, antibacterial assay against Staphylococcus aureus and Pseudomonas aeruginosa confirmed that GO-Zn/GelMA-PBA coating on Ti substrates had superior antibacterial capacity, availably inhibited the bacterial adhesion, and prevented formation of biofilm. Hence, the study provides a promising strategy for designing pro-osteogenesis and antibacterial coating on Ti substrates for orthopedic applications.
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INORGANICA CHIMICA ACTA
·
2019
·
IF 2.433
Lixia Liu,Xuefang Shang,Ruiqi He,Jie Li,Yanmei Chen,Hongli Chen,Tianyun Wang
A zinc(II) complex–based selective colorimetric chemosensor for H 2 S was synthesized. The ligand and complex crystals were obtained, and the molecular structures were confirmed by single-crystal X-ray diffraction analysis in addition to electrospray ionization high resolution mass spectrometer, as well as elemental analysis . The photo-physical and recognition properties toward HS – were examined. The complex indicated the presence of HS – with an obvious color change from yellow to red, based on zinc ion displacement mechanism. However no obvious changes were observed in the presence of other anions (AcO − , H 2 PO 4 − , F − , Cl − , Br − , I − and SO 3 2− ). In addition, the chemosensor was applied to assess HeLa cell cytotoxicity. Our inorganic-reaction based sensor for HS – is simple, easily prepared and efficient. The complex has many potential chemical and analytical applications for the sensing of H 2 S.
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JOURNAL OF MATERIALS RESEARCH
·
2019
·Vol. 34
·期 14
·2445-2455
·
IF 1.982
Uwamahoro Evariste,Guohua Jiang,Bo Yu,Yongkun Liu,Zheng Huang,Qiuling Lu,Pianpian Ma
In this work, hierarchical mesoporous Zn–Ni–Co–S–rGO/NF microspheres have been prepared by hydrothermal, sulfurization, and subsequent calcination process. The effect of different sulfurization time on the morphology and capacitance of composites was tested. The high electrochemical performance of (Zn–Ni–Co–S–rGO/NF) composite was obtained when the sulfurization time was 3 h (Zn–Ni–Co–S–rGO/NF-3h), where a specific capacitance of 627.7 F/g at 0.25 A/g and excellent rate capability of about 97.8% capacitance retention at 2 A/g after 4000 cycles were achieved. Moreover, an asymmetric supercapacitor fabricated by (Zn–Ni–Co–S–rGO/NF-3h) composite and activated carbon (AC) as the positive and the negative electrodes, respectively, showed a high energy density of 75.96 W h/kg at a power density of 362.49 W/kg with a remarkable cycle stability performance of 91.2% capacitance retention over 5000 cycles. This incredible electrochemical behavior illustrates that the hierarchical mesoporous Zn–Ni–Co–S–rGO/N-3h microsphere electrodes are promising electrode materials for application in high-performance supercapacitors.
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ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Haoqing Ji,Mengfan Wang,Sisi Liu,He Sun,Jie Liu,Tao Qian,Chenglin Yan
Pyridinic and graphitic nitrogen are recognized as the most promising dopants for promoting oxygen reactions since they are beneficial to the formation of corresponding C–N bonds as efficient active sites. However, complete control of such efficient nitrogen-doping sites in carbon materials is difficult to realize in practice in a pyrolysis process . Here, we present maximized pyridinic and graphitic nitrogen-doped oxygen electrode via the precise use of nitrogen-containing precursors and carbonization temperature. The critical roles of pyridinic and graphitic nitrogen dopants in enhancing oxygen reaction activity are unraveled and this highly active material exhibits a remarkable half-wave potential of 0.89 V versus the reversible hydrogen electrode (vs. RHE) for oxygen reduction reaction (ORR) and a small potential gap of 0.78 V between ORR and oxygen evolution reaction (OER) in 0.1 M KOH, which is one of the best to date among metal-free bifunctional electrocatalysts . Both zinc-air batteries using liquid electrolytes and the all-solid-state batteries assembled with such air cathodes exhibit excellent cycle performance and reversibility, which can be expressly observed by in-situ X-ray diffraction (XRD) characterization. This nitrogen dopants engineering strategy gives an effective methodology to make full use of nanocarbon materials for their practical applications in next-generation powerful and durable energy devices.
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CLAYS AND CLAY MINERALS
·
2019
·Vol. 67
·期 4
·325-333
·
IF 1.835
Guo Yu-Hua,Pan Guo-Xiang,Xu Min-Hong,Wu Tao,Wang Yong-Ya
Adsorption desulfurization is a potential new method for deep desulfurization of fuel oil. The development of adsorbents with high adsorption capacity and selectivity is the core of deep adsorption desulfurization. The adsorption behavior of thiophene in MCM-41 mesoporous materials modified by various metal ions was studied in order to understand the adsorption desulfurization process of molecular sieves. The Fe-, Co-, and Zn-modified MCM-41 materials were prepared using a one-step in situ hydrothermal synthesis method. The modified MCM-41 molecular sieves maintained the mesoporous structure, and the metal ions had specific dispersion on the surface of the molecular sieves. Adsorption of thiophene on the surfaces of molecular sieves had both physical and chemical characteristics. The adsorption desulfurization performance of the modified molecular sieve was superior to that of the pure silica molecular sieve. In the simulated gasoline with sulfur content of 220 μg/g, when the amount of adsorbent used was 100 mg, the adsorptive desulfurization performance tended to be in equilibrium, and the optimum adsorption temperature was 30°C. Fe-MCM-41 and MCM-41 molecular sieves reached adsorption equilibrium after ~60 min, but the desulfurization rate of Co-MCM-41 and Zn-MCM-41 still increased slightly. The kinetic simulation results indicated that the pseudo-second-order kinetics adsorption model described well the adsorption process of thiophene on molecular sieves. The molecular sieve Fe-MCM-41 had the best desulfurization performance with an equilibrium adsorption capacity of 14.02 mg/g and the desulfurization rate was ~90%.
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ANALYTICA CHIMICA ACTA
·
2018
·
IF 5.123
Yuanyuan Li,Xue Hu,Xiaodan Zhang,Haiyan Cao,Yuming Huang
Contrary to organic solvent-induced aggregation of Au nanoclusters (AuNCs), herein, we reported aggregation induced emission enhancement (AIEE) of AuNCs in an aqueous media through confinement of AuNCs by in situ formed Zn-MOF for detecting Zn 2+ . Glutathione capped AuNCs (GSH-AuNCs) was synthesized through reduction of Au 3+ by glutathione. Zn 2+ could significantly enhance the fluorescence of GSH-AuNCs upon addition of 2-methylimidazole, which was attributed to the formation of Zn-MOF. XRD and TEM were used to characterize the in situ formed Zn-MOF. Zn 2+ induced aggregation was demonstrated by dynamic light scattering and TEM. The quantum yields (QYs) of AuNCs after aggregation induced by in situ formed Zn-MOF attained to 36.6%, which was nearly 9 times that of the sole AuNCs. On this basis, a fluorogenic sensor was reported for Zn 2+ detection with a linear range from 12.3 nM to 24.6 μM and a detection limit of 6 nM (S/N = 3). The proposed sensor was successfully applied to assay the content of zinc in human serum, milk, water, and zinc sulfate syrup oral solution samples. The novel strategy proposed in this work may open a new window of interest in an unconventional application of gold nanoclusters/MOF nanoscale platform for metal ion detection and nutritional assessment of food.
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CATALYSIS COMMUNICATIONS
·
2018
·
IF 3.463
Qinqin Wang,Mingyuan Zhu,Haiyang Zhang,Caixia Xu,Bin Dai,Jinli Zhang
Zr-modified ZSM-5 zeolite was successfully prepared, and Zn/Zr-ZSM-5 was employed as a catalyst for the acetylene hydration reaction. High catalytic activity, above 96% C 2 H 2 conversion, was achieved at 260 °C with a feed reactant ratio of H 2 O/C 2 H 4 = 4 and a GHSV of 90 h −1 . To understand the influence of zirconium addition in the zeolite, Fourier-transform infrared spectroscopy, X-ray diffraction, surface texture analysis (BET method), transmission electron microscopy, temperature programmed desorption of NH 3 , temperature programmed reduction by hydrogen and X-ray photoelectron spectroscopy techniques were used. The incorporation of zirconium in the zeolite enhanced Zn metal dispersion and metal–support interactions. Moreover, an enhanced concentration of weak acid sites and active catalytic sites were found to be responsible for the high catalytic activity of Zn/Zr-ZSM-5 for the acetylene hydration.
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Chemical Engineering and Processing-Process Intensification
·
2018
·
IF 2.826
Yanyan Guo,Chengna Dai,Zhigang Lei
A series of Pd-La/SiO 2 /cordierite (cordierite = COR) and Pd-Zn/SiO 2 /COR bimetallic monolithic catalysts were prepared, characterized, and tested for the hydrogenation of 2-ethylanthraquinone (eAQ) as the key step of anthraquinone method for production of H 2 O 2 . It was found that the metal particle size is remarkably dependent on the Pd/M (M = La, and Zn) mass ratio of bimetallic monolithic catalysts. By virtue of its small metal particle size and the strong interaction, the 0.8% Pd-0.4% La/SiO 2 /COR monolithic catalyst presents the highest H 2 O 2 yield (7.7 g L −1 ) and selectivity toward active quinones (95%), which is attributed to the addition of La leading to the synergistic effect between Pd and La. Moreover, the density functional theory (DFT) calculations for the adsorption of eAQ over the surface of Pd-La/SiO 2 /COR and Pd-Zn/SiO 2 /COR bimetallic monolithic catalysts have been conducted to further understand the mechanism of molecule–surface interactions between eAQ and the PdM(1 1 1) or Pd(1 1 1) surfaces. Detailed studies showed that the high catalytic activity of Pd-La/SiO 2 /COR bimetallic monolithic catalyst is attributed to the stronger adsorption between Pd 3 La 1 (1 1 1) and the carbonyl group of eAQ.
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Polymers
·
2018
·Vol. 10
·期 12
·1383
·
IF 2.935
Jian Shen,Nan Wang,Yang Guang Wang,Di Yu,Xiao–kun Ouyang
Composite adsorption materials combine the advantages of various adsorptive materials and compensate for the defects of single adsorbents. Magnetic montmorillonite (MMMT) shows good adsorption properties for Pb(II). In order to further improve the adsorption properties of MMMT, in this work, Zn-BDC, a kind of metal–organic framework (MOF), was modified onto the surface of MMMT by in situ polymerization. The composite material MMMT@Zn-BDC was characterized by Zetasizer, SEM, TEM, FTIR, XRD, VSM, and XPS. The influence of adsorption conditions on the adsorption capacity of MMMT@Zn-BDC for Pb(II) was examined, including the adsorbent dosage, pH of Pb(II) solution, initial concentration of Pb(II), and the temperature and adsorption time. Also, the adsorption mechanism was studied. The results of this study show that MMMT@Zn-BDC adsorbs Pb(II) via chemisorption. In addition, MMMT@Zn-BDC exhibits good potential for adsorbing Pb(II), including its high adsorption capacity (724.64 mg/g) and good recyclability.Keywords:Zn-BDC;magnetic montmorillonite;Pb(II);adsorption
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ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
·
2015
·Vol. 641
·期 11
·1953-1958
·
IF 1.16
Yunsheng Liu,Dajiang Mei,Jingli Xu,Yuandong Wu
Sodium magnesium selenite NaMg 2 (OH)(SeO 3 ) 2 and rubidium zinc selenite RbZn 2 (OH)(SeO 3 ) 2 were prepared by hydrothermal reactions. The crystal structures of the title compounds were determined by single-crystal X-ray diffraction. NaMg 2 (OH)(SeO 3 ) 2 crystallizes in the orthorhombic space group Pnma (no. 62) with lattice parameters a = 13.1919(10), b = 6.0415(4), c = 8.2182(6) Å, and Z = 4 and RbZn 2 (OH)(SeO 3 ) 2 crystallizes in the triclinic space group P (no. 2) with lattice parameters a = 4.8698(5), b = 7.3446(8), c = 11.7796(12) Å, α = 82.554(3), β = 78.456(2), γ = 71.603(3)°,and Z = 2. The structure of NaMg 2 (OH)(SeO 3 ) 2 is a three-dimensional framework consisting of edge-sharing MgO 6 octahedra and trigonal pyramidal SeO 3 2– groups, whereas the structure of RbZn 2 (OH)(SeO 3 ) 2 is a two-dimensional layers structure consisting of corner-sharing [Zn 2 O 7 ] dimers linked by trigonal pyramidal SeO 3 2– groups. The compounds were characterized by the solid state UV/Vis/NIR diffuse reflectance, and FT-IR spectroscopy.
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ELECTROPHORESIS
·
2013
·Vol. 34
·期 6
·846-853
·
IF 3.261
Haizhi Zhang,Li Qi,Ying Shen,Juan Qiao,Lanqun Mao
Amino acid ionic liquids (AAILs) with l -lysine ( l -Lys) as anion were synthesized and applied as new chiral ligands in Zn(II) complexes for chiral ligand-exchange CE. After effective optimization, baseline enantioseparation of seven pairs of dansylated amino acids was achieved with a buffer of 100.0 mM boric acid, 5.0 mM ammonium acetate, 3.0 mM ZnSO 4 , and 6.0 mM [C 6 mim][ l -Lys] at pH 8.2. To validate the unique behavior of AAILs, a comparative study between the performance of Zn(II)- l -Lys and Zn(II)-[C 6 mim][ l -Lys] systems was conducted. In Zn(II)-[C 6 mim][ l -Lys] system, it has been found that the improved chiral resolution could be obtained and the migration times of the three test samples were markedly prolonged. Then the separation mechanism was further discussed. The role of [C 6 mim][ l -Lys] indicated clearly that the synthesized AAILs could be used as chiral ligands and would have potential utilization in separation science in future.
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SENSORS AND ACTUATORS B-CHEMICAL
·
2014
·
IF 3.84
Yang Zhang,Jinchao Shen,Hong Yang,Yan Yang,Zhiguo Zhou,Shiping Yang
A magnetic sensor for Cd 2+ has been developed based on (Zn, Mn)-doped iron oxide nanoparticles [(Zn, Mn)Fe 3 O 4 NPs], which was modified by ethyl 1-(2-(3′,4′-dihydroxyphenyl)-2-oxoethyl)-1H-1,2,3-triazole-4-carboxylate (ETC). ETC provided the binding sites to Cd 2+ to induce the transformation of (Zn, Mn)Fe 3 O 4 NPs from a dispersed to an aggregated state with a corresponding increase in the transverse relaxation time ( T 2 ) of surrounding water protons. Owing to the special strong interaction between ETC and Cd 2+ , ETC coordinated (Zn, Mn)Fe 3 O 4 [(ETC-(Zn, Mn)Fe 3 O 4 )] NPs exhibited a low limit of detection of Cd 2+ of 3.5 nM and a high selectivity over other metal ions . Furthermore, ETC-(Zn, Mn)Fe 3 O 4 NPs can be used to detect Cd 2+ in living cells by magnetic resonance (MR) imaging.
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