Over 95% of large-scale length uniformity in template-assisted electrodeposited nanowires by subzero-temperature electrodeposition

In this work, we report highly uniform growth of template-assisted electrodeposited copper nanowires on a large area by lowering the deposition temperature down to subzero centigrade. Even with highly disordered commercial porous anodic aluminum oxide template and conventional potentiostatic electrodeposition, length uniformity over 95% can be achieved when the deposition temperature is lowered down to -2.4°C. Decreased diffusion coefficient and ion concentration gradient due to the lowered deposition temperature effectively reduces ion diffusion rate, thereby favors uniform nanowire growth. Moreover, by varying the deposition temperature, we show that also the pore nucleation and the crystallinity can be controlled.     

非晶态催化剂Cu-ZnO-Al2O3MnO2/HZSM-5二氧化碳加氢制备二甲醚的研究

考察了MnO2对CO2加氢直接合成二甲醚催化剂Cu-ZnO-A12O3/HZSM-5的影响.采用固定床反应装置对CO2加氢直接合成二甲醚的活性进行考察,并运用XRD、HZ-TPR技术对催化剂结构及表面性质进行研究.实验结果表明,催化剂中加入MnO2能显著提高Cu-ZnO-Al2O3/HZM-5催化剂的稳定性,促进催化剂...     

Theoretical and practical investigations of copper ion selective electrode with polymeric membrane based on N,N′-(2,2-dimethylpropane-1,3-diyl)-bis(dihydroxyacetophenone)

A novel ion-selective poly(vinyl chloride) (PVC) membrane sensor for Cu²⁺ ions based on N,N′-(2,2-dimethylpropane-1,3-diyl)-bis(dihydroxyacetophenone) (NDHA) as a new ionophore was prepared and studied. The best performance was observed for the membrane composition, including 30:65:1:4 (wt%) = PVC:DBP:KTpClPB:NDHA. The electrode showed a good Nernstian slope of 30.0 ± 0.5 mV/decade in a wide linear range activity of 3.0 × 10⁻⁷ to 1.0 × 10⁻² mol dm⁻³ Cu(NO₃)₂ with limit of detection 2.5 × 10⁻⁷. Sensor exhibited a fast response time (t_95% < 10 s) and could be used for about 4 months in the pH range of 3.0–7.4. The proposed potentiometric sensor was found to work satisfactorily in partially non-aqueous media up to 30 (vol%) content of methanol, ethanol and acetone. Applications of this electrode for the determination of copper in real samples, and as an indicator electrode for potentiometric titration of Cu²⁺ ion using EDTA, were reported. In order to predict the extraction ability of NDHA for different metallic ions, the complexes [M(NDHA)] and [M(H₂O)₆] (where M = Cu²⁺, Co²⁺, Hg²⁺, Pb²⁺, Ag⁺, Mg²⁺, Ca²⁺, Mn²⁺, Zn²⁺, Cd²⁺, K⁺ and Al³⁺) were investigated using ab initio theoretical calculations. The metal binding capability was evaluated using the binding energy. Results of our study could be useful for prediction of the extraction power of this Schiff base and could play a guiding role in planning experiments.     

Effect of copper pretreatment on the zincate process and subsequent electroplating of a protective copper/nickel deposit on the AZ91D magnesium alloy

To obtain a durable Ni coating with excellent adhesion strength on an AZ91D Mg alloy, a pretreatment was performed with a small amount of Cu²⁺ ions added to the activation bath used in the pretreatment prior to the plating process. In the pretreatment activation process, a high density Cu layer was deposited on both the α-phase and β-phase areas of the substrate accompanied with Mg dissolution. The Cu deposit acted as nucleation seeds for the Zn deposition in the following zincate process which provided a uniform and dense Zn layer almost completely covering the substrate. Then a thin Cu layer was electroplated on this zincated substrate as an undercoating for the succeeding electroplating with Ni. Cross-sectional scanning electron microscopy observations showed that the Cu deposited by the pretreatment enabled the deposition of a protective Ni layer with few defects. This structure also contributed to the improvement of adhesion strength and corrosion resistance as compared with the non-Cu added sample.     

Simultaneous extraction and determination of lead, cadmium and copper in rice samples by a new pre-concentration technique: Hollow fiber solid phase microextraction combined with differential pulse anodic stripping voltammetry

In the present work, a novel solid phase microextraction (SPME) technique using a hollow fiber-supported sol–gel combined with multi-walled carbon nanotubes, coupled with differential pulse anodic stripping voltammetry (DPASV) was employed in the simultaneous extraction and determination of lead, cadmium and copper in rice. In this technique, an innovative solid sorbent containing mixture of carbon nanotube and a composite microporous compound was developed by the sol–gel method via the reaction of tetraethylorthosilicate (TEOS) with 2-amino-2-hydroxymethyl-propane-1,3-diol (TRIS). The growth process was initiated in basic condition (pH 10–11). Afterward this sol was injected into a polypropylene hollow fiber segment for in situ gelation process. The main factors influencing the pre-concentration and extraction of the metal ions; pH of the aqueous feed solution, extraction time, aqueous feed volume, agitation speed, the role of carbon nanotube reinforcement (as-grown and functionalized MWCNT) and salting effect have been examined in detail. Under the optimized conditions, linear calibration curves were established for the concentration of Cd(II), Pb(II) and Cu(II) in the range of 0.05–500, 0.05–500 and 0.01–100 ng mL⁻¹, respectively. Detection limits obtained in this way are, 0.01, 0.025 and 0.0073 ng mL⁻¹ for Cd(II), Pb(II) and Cu(II), respectively. The relative standard deviations (RSDs) were found to be less than 5% (n = 5, conc.: 1.0 ng mL⁻¹).     

Monitoring Cu nodule formation using Ni marker layers

We have used Ni marker layers to study the evolution of the characteristic spheroidal nodule morphology in electrodeposited Cu films. Ultrathin Ni layers were electrodeposited in-between Cu layers, and cross sections prepared by electrochemical polishing. During growth of a typical spheroidal feature, the edge (i.e. where there is a discontinuity in the surface slope) traces out a straight line in the cross-sectional image. At high overpotential, the cross-sections show nodule-on-nodule growth, giving rise to the well known cauliflower morphology. Rotating disk electrode studies reveal that, surprisingly, the absolute diffusion layer thickness does not appear to play a major role in the development of spheres.     

Effect of Al2Cu precipitates size and mass transport on the polarisation behaviour of age-hardened Al–Si–Cu–Mg alloys in 0.05 M NaCl

The electrochemical behaviour of age-hardened Al–Si–Cu–Mg alloys was investigated in a 0.05 M NaCl solution under controlled mass transport conditions using a rotating disk electrode. This work aimed at getting better understanding of the effect of the alloy microstructure, in particular the size distribution of Al₂Cu phase, on the corrosion behaviour of the alloy. Three different size distributions of the Al₂Cu phase were obtained through appropriate heat treatments. The cathodic reduction of oxygen was found to occur mainly on the Al₂Cu phases acting as preferential cathodes. Small sized Al₂Cu phases were found to promote at high rotation rates a transition from a 4 electron to a 2 electron dominated oxygen reduction mechanisms.     

Polycarbonateurethane films containing complex of copper(II) catalyzed generation of nitric oxide

Nitric oxide (NO) is a well known potent antiplatelet agent, and its continuous release will effectively prevent the adhesion of platelets on artificial blood vessel walls. In this paper, polycarbonateurethane (PCU) with lipophilic Cu(II)‐complex (Cu(II)‐DTTCT) blending films were prepared and used as catalyst to generate NO from nitrite. The mechanical properties of PCU films blended with Cu(II)‐DTTCT were characterized by tensile strength measurement. The tensile stress and Young's modulus of PCU films blending with Cu(II)‐DTTCT increased, however, the elongation at break decreased compared with corresponding PCU films. The NO generation was investigated in vitro in the presence of NaNO₂ and ascorbic acid in PBS (pH = 7.4) at 37°C. The flux of NO generation was quantitatively measured by Griess assay. NO flux and velocity increased with the increase of NaNO₂ concentration, the concentration of ascorbic acid in PBS and the amount of Cu(II) in the films. The loss of Cu(II) from blending film surfaces was found during the in vitro NO generation experiments, which resulted in the decrease of NO flux in the second run. The PCU film could catalyze continually generation of NO for two days, which will provide a promising approach that enable endogenous NO generation on the surface of the medical devices. The generation of biologically active level of NO at the blood/polymer interface can reduce the risk of thrombosis on the implants. Polycarbonateurethane films with NO generation function may be used as high thromboresistant blood contacting materials or coating. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation of Cu(II)‐chelated poly(vinyl alcohol) nanofibrous membranes for catalase immobilization

Poly(vinyl alcohol) (PVA) nanofibers were formed by electrospinning. Metal chelated nanofibrous membranes were prepared by reaction between Cu(II) solution and nanofibers, and which were used as the matrix for catalases immobilization. The constants of Cu(II) adsorption and properties of immobilized catalases were studied in this work. The Cu(II) concentration was determined by atomic absorption spectrophotometer (AAS), the immobilized enzymes were confirmed by the Fourier transform infrared spectroscopy (FTIR), and the amounts of immobilized enzymes were determined by the method of Bradford on an ultraviolet spectrophotometer (UV). Adsorption of Cu(II) onto PVA nanofibers was studied by the Langmuir isothermal adsorption model. The maximum amount of coordinated Cu(II) (q_m) was 2.1 mmol g⁻¹ (dry fiber), and the binding constant (K_l) was 0.1166 L mmol⁻¹. The immobilized catalases showed better resistance to pH and temperature inactivation than that of free form, and the thermal and storage stabilities of immobilized catalases were higher than that of free catalases. Kinetic parameters were analyzed for both immobilized and free catalases. The value of V_max (8425.8 μmol mg⁻¹) for the immobilized catalases was smaller than that of the free catalases (10153.6 μmol mg⁻¹), while the K_m for the immobilized catalases were larger. It was also found that the immobilized catalases had a high affinity with substrate, which demonstrated that the potential of PVA‐Cu(II) chelated nanofibrous membranes applied to enzyme immobilization and biosensors. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Full‐visible spectrum emitting Zn–In–S:Cu/ZnS nanocrystals based on varying Cu concentrations and its application in white LEDs

A series of high‐quality Cu‐doped Zn–In–S nanocrystals (d‐NCs) were prepared by a conventional hot injection process. The full‐visible spectrum emission from 480 to 648 nm can be easily achieved by adjusting the Cu doping concentration in the Zn–In–S system, but not by varying the ratio of In/Zn in the alloyed host material. After wrapping the ZnS shell around the Zn–In–S:Cu d‐NCs core, the resultant Zn–In–S:Cu/ZnS core/shell d‐NCs not only exhibited an enhanced prominent photoluminescent quantum yield (PLQY) up to 65% but also possessed the excellent thermal, photochemical stability, and longer PL lifetime. Furthermore, high color rendition white light was generated from a single color converter Zn–In–S:Cu/ZnS core/shell NCs‐assisted white light‐emitting diodes (LEDs). Under operation of 38 mA forward bias current, the fabricated white LEDs emitted bright natural white light with a luminous efficiency of 62 lm/W, and the correlated color temperature of 5658 K. Simultaneously, the good color stability was accompanied by the CIE color coordinates of (0.3287, 0.3527) under different forward bias currents.