Electrochemical Preparation of Ce-Mg-Ni Alloy Film in Acetamide-Urea-NaBr Melting System

2011 ◽  
Vol 311-313 ◽  
pp. 798-804
Author(s):  
Cheng Yu Guo ◽  
Jian Chao Wang ◽  
Bi Qing Chen ◽  
Shu Hai Wang ◽  
Mei Feng Yun
Keyword(s):  
Electron Transfer ◽  
Diffusion Coefficient ◽  
Alloy Film ◽  
Molar Ratio ◽  
Cathode Potential ◽  
Pt Electrode ◽  
Electrochemical Preparation ◽  
Ni Alloy ◽  
One Step ◽  
Alloy Increase

Ni(Ⅱ) was reduced to Ni atom irreversibly by a one-step reaction in acetamide-urea-NaBr melt at 353K. The electron-transfer coefficient, and the diffusion coefficient, D0 were determined to be 0.21 and 1.15×10-8 cm2.s-1 on Pt electrode. Although the Ce（Ⅲ）and the Mg（Ⅱ）cannot be reduced to Ce and Mg alone, they can be inductively codeposited with Ni（Ⅱ）to obtain an amorphous Ce-Mg-Ni alloy film by potentiostatic electrolysis. The content of Ce in the alloy increase with the increasing of the molar ratio of Ce（Ⅲ）/Ni（Ⅱ） and reaches to the maximum of 49.70 wt%. The content of Mg in the alloy increase with the increasing of the cathode potential and the maximum was 4.558wt%.

scholarly journals One-step synthesis of nitrogen-grafted copper-gallic acid for enhanced methylene blue removal

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shella Permatasari Santoso ◽  
Vania Bundjaja ◽  
Artik Elisa Angkawijaya ◽  
Chintya Gunarto ◽  
Alchris Woo Go ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Gallic Acid ◽  
Synthesis Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
One Step ◽  
Detailed Assessment ◽  
Higher Temperature

AbstractNitrogen-grafting through the addition of glycine (Gly) was performed on a metal- phenolic network (MPN) of copper (Cu2+) and gallic acid (GA) to increase its adsorption capacity. Herein, we reported a one-step synthesis method of MPN, which was developed according to the metal–ligand complexation principle. The nitrogen grafted CuGA (Ng-CuGA) MPN was obtained by reacting Cu2+, GA, and Gly in an aqueous solution at a molar ratio of 1:1:1 and a pH of 8. Several physicochemical measurements, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), N2 sorption, X-ray diffraction (XRD), and thermal gravimetry analysis (TGA), were done on Ng-CuGA to elucidate its characteristics. The analysis revealed that the Ng-CuGA has non-uniform spherical shaped morphology with a pore volume of 0.56 cc/g, a pore size of 23.25 nm, and thermal stability up to 205 °C. The applicational potential of the Ng-CuGA was determined based on its adsorption capacity against methylene blue (MB). The Ng-CuGA was able to adsorb 190.81 mg MB per g adsorbent at a pH of 6 and temperature of 30 °C, which is 1.53 times higher than the non-grafted CuGA. Detailed assessment of Ng-CuGA adsorption properties revealed their pH- and temperature-dependent nature. The adsorption capacity and affinity were found to decrease at a higher temperature, demonstrating the exothermic adsorption behavior.

Synergistic effect of co-reactant promotes one-step oxidation of cyclohexane into adipic acid catalyzed by manganese porphyrins

2015 ◽  
Vol 93 (7) ◽  
pp. 696-701 ◽  
Author(s):  
Hui Li ◽  
Yuanbin She ◽  
Haiyan Fu ◽  
Meijuan Cao ◽  
Jing Wang ◽  
...  
Keyword(s):  
Synergistic Effect ◽  
Co Oxidation ◽  
Adipic Acid ◽  
Molar Ratio ◽  
Reaction Conditions ◽  
Catalyst Structure ◽  
Manganese Porphyrins ◽  
Co Oxidation Reaction ◽  
One Step ◽  
Acid Catalyzed

The synergistic effect of cyclohexane and cyclohexanone promoted synthesis of adipic acid catalyzed by [MnIIIT(p-Cl)PP]Cl with cyclohexane and cyclohexanone as co-reactants. The results showed that the conversions of cyclohexane and cyclohexanone were significantly enhanced because of the cyclohexanone synergistic effect, and the higher selectivity to adipic acid was obtained with dioxygen as an oxidant. The studies indicated that the co-oxidation of cyclohexane and cyclohexanone was influenced by the initial molar ratio of cyclohexanone and cyclohexane, catalyst structure, catalyst concentrations, and reaction conditions. The preliminary mechanism of the co-oxidation reaction of cyclohexane and cyclohexanone using [MnIIIT(p-Cl)PP]Cl as the catalyst was proposed.

Oxidation Kinetics of Cu-Ni Alloy Observed by in situ UHV-TEM

2007 ◽  
Vol 1026 ◽  
Author(s):  
Li Sun ◽  
John E. Pearson ◽  
Judith C. Yang
Keyword(s):  
High Vacuum ◽  
Alloy Film ◽  
Ultra High Vacuum ◽  
Cross Sectional ◽  
Primary Mechanism ◽  
Transmission Electron ◽  
Ni Alloy ◽  
Cu Oxidation ◽  
Kinetics Of

AbstractThe nucleation and growth of Cu2O and NiO islands due to oxidation of Cu-24%Ni(001) films were monitored at various temperatures by in situ ultra-high vacuum (UHV) transmission electron microscopy (TEM). In remarkable contrast to our previous observations of Cu and Cu-Au oxidation, irregular-shaped polycrystalline oxide islands were observed to form with respect to the Cu-Ni alloy film, and an unusual second oxide nucleation stage was noted. Similar to Cu oxidation, the cross-sectional area growth rate of the oxide island is linear indicating oxygen surface diffusion is the primary mechanism of oxide growth.

scholarly journals Poly(3,4-ethylenedioxythiophene)-tosylate (PEDOT-Tos) electrodes in thermogalvanic cells

2017 ◽  
Vol 5 (37) ◽  
pp. 19619-19625 ◽  
Author(s):  
Kosala Wijeratne ◽  
Mikhail Vagin ◽  
Robert Brooke ◽  
Xavier Crispin
Keyword(s):  
Electron Transfer ◽  
Waste Heat ◽  
Pt Electrode

The interest in thermogalvanic cells (TGCs) has grown because it is a candidate technology for harvesting electricity from natural and waste heat. The polymer electrode PEDOT is investigated as potential material to replace Pt electrode in TGCs. The power of the TGC increases with thickness and PEDOT provides an efficient electron transfer to Fe(CN)63−.

Volumes of activation for electrode processes of various charge-types in nonaqueous solvents

2001 ◽  
Vol 79 (12) ◽  
pp. 1864-1869 ◽  
Author(s):  
Mitsuru Matsumoto ◽  
Delanie Lamprecht ◽  
Michael R North ◽  
Thomas W Swaddle
Keyword(s):  
Electron Transfer ◽  
Reaction Rate ◽  
Electrode Reaction ◽  
State Theory ◽  
Exchange Reactions ◽  
Pt Electrode ◽  
Electrode Processes ◽  
Solvent Dynamics ◽  
The Mean ◽  
Dynamical Control

Volumes of activation (ΔV‡el) are reported for electron transfer at a Pt electrode of Mn(CN-cyclo-C6H11)62+/+ in acetonitrile, acetone, methanol, and propylene carbonate, and of Fe(phen)33+/2+ in acetonitrile. In all cases, ΔV‡el is markedly positive, whereas for the homogeneous self-exchange reactions of these couples in the same solvents the corresponding parameter is known to be strongly negative. The rate constants for the electrode reactions correlate loosely with the mean reactant diffusion coefficients (i.e., with solvent fluidity) and the ΔV‡el values with the volumes of activation for diffusion (i.e., for viscous flow), consistent with solvent dynamical control of the electrode reaction rate in organic solvents. A detailed analysis of ΔV‡el values of the kind presented for a couple with an uncharged member (Zhou and Swaddle, Can. J. Chem. 79, 841 (2001)) fails, however, either because of ion-pairing effects with these more highly charged couples or because of breakdown of transition-state theory in predicting the contribution of the activational barrier. Attempts to measure ΔV‡el for the oxidation of the uncharged molecule ferrocene at various electrodes in acetonitrile were unsuccessful, although ΔV‡el was again seen to be clearly positive.Key words: electrode kinetics, volumes of activation, nonaqueous electron transfer, solvent dynamics.

scholarly journals Preparation and Study of Sulfonated Co-Polynaphthoyleneimide Proton-Exchange Membrane for a H2/Air Fuel Cell

Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5297
Author(s):  
Ulyana M. Zavorotnaya ◽  
Igor I. Ponomarev ◽  
Yulia A. Volkova ◽  
Alexander D. Modestov ◽  
Vladimir N. Andreev ◽  
...  
Keyword(s):  
Diffusion Coefficient ◽  
Proton Exchange Membrane ◽  
Maximum Output Power ◽  
Exchange Capacity ◽  
Proton Exchange ◽  
Molar Ratio ◽  
Disulfonic Acid ◽  
Membrane Electrode ◽  
Maximum Output ◽  
Practical Applications

The sulfonated polynaphthoyleneimide polymer (co-PNIS70/30) was prepared by copolymerization of 4,4′-diaminodiphenyl ether-2,2′-disulfonic acid (ODAS) and 4,4’-methylenebisanthranilic acid (MDAC) with ODAS/MDAC molar ratio 0.7/0.3. High molecular weight co-PNIS70/30 polymers were synthesized either in phenol or in DMSO by catalytic polyheterocyclization in the presence of benzoic acid and triethylamine. The titration reveals the ion-exchange capacity of the polymer equal to 2.13 meq/g. The membrane films were prepared by casting polymer solution. Conductivities of the polymer films were determined using both in- and through-plane geometries and reached ~96 and ~60 mS/cm, respectively. The anisotropy of the conductivity is ascribed to high hydration of the surface layer compared to the bulk. SFG NMR diffusometry shows that, in the temperature range from 213 to 353 K, the 1H self-diffusion coefficient of the co-PNIS70/30 membrane is about one third of the diffusion coefficient of Nafion® at the same humidity. However, temperature dependences of proton conductivities of Nafion® and of co-PNIS70/30 membranes are nearly identical. Membrane–electrode assemblies (MEAs) based on co-PNIS70/30 were fabricated by different procedures. The optimal MEAs with co-PNIS70/30 membranes are characterized by maximum output power of ~370 mW/cm2 at 80 °C. It allows considering sulfonated co-PNIS70/30 polynaphthoyleneimides membrane attractive for practical applications.

Electrochemical Preparation of Fe-Mn Alloy Film in Organic Bath

2019 ◽  
Vol 2 (3) ◽  
pp. 393-400
Author(s):  
Gregory A. Hope ◽  
Peng Liu ◽  
Qiqing Yang ◽  
Gaoren Li ◽  
Yexiang Tong
Keyword(s):  
Alloy Film ◽  
Electrochemical Preparation
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