Electrolytic coatings (layers) deposited from palladium(II) salts

1991 ◽  
Vol 56 (1) ◽  
pp. 167-177
Author(s):  
Jaromír Hlavatý ◽  
Jiří Volke

In contrast to a number of investigations concerning preparation of layers and coatings of palladium(II) oxides this communication describes a reproducible electrolytic preparation from activation baths containing Pd(II) ions of coatings with hydrated palladium oxides, in particular on platinum supports. The voltammetric curves of coatings formed in such a way are reproducible over the whole pH range and exhibit an irreversible cathodic-anodic couple of peaks. For the voltammetric curve on an active layer deposited on a platinum support from a solution of Pd(NO3)2 at pH 7.03 Ekp is + 0.02 V and Eap +0.33 V (vs SCE). The observed character of the pH dependences for the peak potentials and current densities with a similar, mostly linear, behaviour has been also observed with layers deposited on glassy carbon or nickel. The deposited layers containing hydrated palladium oxides exhibit oxidative activity as follows from voltammograms in slightly acidic to neutral and strongly alkaline region. These curves point to the ability to oxidize not only ethanol but also toluene used as a with difficulty oxidizable model substrate.

1990 ◽  
Vol 126 (2) ◽  
pp. 323-332 ◽  
Author(s):  
A. Ulloa-Aguirre ◽  
P. Damián-Matsumura ◽  
R. Espinoza ◽  
R. Dominguez ◽  
L. Morales ◽  
...  

ABSTRACT Anterior pituitary glands were removed from neonatally androgenized (100 μg testosterone propionate) female rats and normal controls at 5, 10, 18, 21, 30, 60 and 90 days of age, and the multiple forms of FSH present within them were separated by chromatofocusing (pH range 7·5–4·0). Additional pituitary glands from intact adult males (90 days old) were also studied for comparative purposes. All animal groups exhibited multiple forms of immunoactive FSH within a pH range of 7·5–4·0, as well as an additional FSH form obtained after the addition of 1·0 mol NaCl/l to the chromatofocusing column (salt peak). In animals 5–30 days old (controls and androgenized) the majority of FSH applied to the chromatofocusing columns was recovered within the salt peak (45-85% of total FSH immunoactivity recovered). However, as the animals aged, more FSH immunoactivity focused within less acidic regions (isoelectric point (pI) 5·9–5·0); pituitaries from animals 60 days old contained the greatest proportion of FSH focused within this pH range (controls, 39·2±0·6%; androgenized, 23·1 ±0·9% of total immunoactivity recovered; P < 0·03 vs animals 30 days old for both experimental groups). This shift towards less acidic FSH was attenuated in androgenized animals compared with the controls (P<0·01). In control adult rats, the chromatofocusing distribution pattern of pituitary FSH varied according to the day of the oestrous cycle. Pituitary extracts from control rats decapitated during the morning of pro-oestrus, oestrus and day 1 of dioestrus exhibited the highest proportion of immunoactive FSH (23·2–28·8% of total) focused within a pH range of 5·9–5·0, whilst only 10·4–11·6% of FSH from androgenized rats and those on day 1 of dioestrus was recovered within this pH range (P<0·05). In control animals decapitated during the morning of prooestrus and oestrus, 10–26% of FSH focused within the most alkaline region (pI 7·5–6·0); the chromatofocusing pattern of pituitary FSH from the neonatally androgenized animals was characteristic, in that no more than one peak (1·5±0·5% of total) was detected in this alkaline region. In the adult male rats, the majority of pituitary FSH eluted from the chromatofocusing columns within a pH of 4·9–4·0 (52·4±1·2% of total FSH immunoactivity) and the salt peak (pH <4·0) (33·1 ±2·4 of total). All FSH isoforms obtained after chromatofocusing represented α and β dimers as disclosed by size exclusion chromatography. The results strongly suggest that a cyclic or 'female' pattern of hypothalamic and gonadal secretion leads the anterior pituitary towards the production of less acidic FSH isoforms, whereas a tonic or 'androgenic' type of secretion, as that present in adult males and females with the androgen-induced anovulatory syndrome, leads more to the production of strongly acidic FSH isoforms. The finding of qualitative and quantitative differences among normally cycling and androgenized animals gives further support for the concept of the existence of a sexual dichotomy in terms of the type of FSH synthesized by the anterior pituitary gland. Journal of Endocrinology (1990) 126, 323–332


2020 ◽  
Vol 23 (10) ◽  
pp. 1002-1009
Author(s):  
Abd-Elgawad Radi ◽  
Hassan El-samboskany

Background: Rafoxanide (RFX) is an active agent against Fasciola hepatica, but it is prohibited for treatment of dairy animals whose milk is provided for human consumption. Objective: A reliable, fast, and simple method needs to be developed to monitor RFX residues in milk samples before distribution to consumers. Methods: In this work, the electrochemical oxidation of RFX was studied at glassy carbon electrodes (GCE) in Britton-Robinson buffer (BR) solutions over the pH range 2.0-12.0 using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The oxidation of the drug was accomplished in a single irreversible, adsorption-controlled step within the pH range 4.0-9.0. Therefore, the application of GCE for a sensitive and selective quantification of RFX by adsorptive stripping voltammetry was reported. The accumulation of the analyte was performed in Britton–Robinson buffer (pH 5.0) at a potential of -0.3 V (vs. Ag-AgCl-KClsat) for 300 s and the measurement was carried out, after medium exchange, in BR solution of pH 7.0 using DPV. Result and Conclusion: This format was satisfactorily applied for the determination of RFX in bovine milk. Limit of detection (LOD) of 1.25 µg kg -1 of milk and mean recoveries of 97.8 to 107.5% were achieved.


1995 ◽  
Vol 73 (2) ◽  
pp. 176-180 ◽  
Author(s):  
Rajeev Jain ◽  
M. Damodharan

Electrochemical behaviour of the medicinally important 4-(4′-sulphonamoyl)hydrazono-1-phenyl-3-methyl-2-pyrazolin-5-ones has been studied at d.m.e. and glassy carbon electrodes. At d.m.e., all six compounds exhibited a single, well-defined, four-electron wave in the pH range 2.5–12.0. Polarographic four-electron wave was found to be diffusion-controlled and irreversible. Similarly, cyclic voltammetry of these compounds at glassy carbon electrode exhibited a single peak. Peak potential shows shifts towards negative potential with pH, with linear segments up to pH 8.2 and are practically pH independent at higher pH values. An anodic peak at far-off positive potential was observed in the reverse scan, indicating the irreversible nature of the electrode process. Controlled potential electrolysis and coulometric studies gave the value of n as 4.0 ± 0.1 in the pH range 2.5 to 10.0. Out of the two major end products formed, one was identified as sulphanilamide and the other as 1-phenyl-3-methyl-4-amino-2-pyrazolin-5-one on the basis of IR and NMR studies. On the basis of DCP, LSV, CV, CPE, coulometry and spectral analysis, a mechanism has been postulated for the reduction of these compounds at d.m.e. and glassy carbon electrodes. Keywords: polarography, cyclic voltammetry, antibacterials, pyrazolin-5-ones.


Catalysts ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 130 ◽  
Author(s):  
Lijuan Han ◽  
José Ramón Galán-Mascarós

The lack of an earth-abundant, robust, and fast electrocatalyst for the oxygen evolution reaction (water oxidation) is a major bottleneck for the development of an scalable scheme towards the production of electrolytic hydrogen and other synthetic fuels from renewable energy and natural feedstocks. While many transition metal oxides work reasonably well in basic media, very few alternatives are available in neutral or acidic media. One promising candidate comes from the Prussian blue family, cobalt hexacyanoferrate. This electrocatalyst offers robust activity in a large pH range ( 0 < pH < 13 ), although current densities are limited due to slow charge transfer kinetics. Herein, we report how the partial substitution of catalytically active Co centres by additional Fe boosts current densities, reaching over 100 mA/cm 2 , more than double the performance of the parent Co 2 [Fe(CN) 6 ]. Those new results clearly increase the opportunity for this catalyst to become relevant in industrial-ready electrolyser architectures.


2010 ◽  
Vol 76 (1) ◽  
pp. 13-25 ◽  
Author(s):  
Abd-Elgawad M. Radi ◽  
Shimaa H. Eissa

The electrochemical behavior of a hypoglycemic drug, glimepiride (GM), was studied at glassy carbon (GCE) and carbon paste (CPE) electrodes in phosphate buffer over the pH range of 2.7–11.7 using cyclic and differential pulse voltammetry. Oxidation of the drug was shown to be an irreversible and diffusion-controlled process. Using differential pulse voltammetry (DPV), the drug yielded a well-defined voltammetric peak in phosphate buffer pH 6.4 at +1.16 V and pH 7.0 at +1.07 V (vs Ag|AgCl) on glassy carbon and carbon paste electrodes, respectively. This process could be used to determine glimepiride concentrations in the range from 1.0 × 10–5 to 3.2 × 10–5 mol l–1 with a detection limit of 2.0 × 10–6 mol l–1 in case of the glassy carbon electrode and in the range of 2.0 × 10–6 to 1.5 × 10–5 mol l–1 with a detection limit of 7.5 × 10–7 mol l–1 in case of the carbon paste electrode. The method was successfully applied to the determination of the drug in a tablet dosage form. Next, the formation of an inclusion complex of glimepiride with β-cyclodextrin (β-CD) in phosphate buffer (pH 7.0):methanol (90:10 (v/v)) has been investigated by differential pulse voltammetry as well as UV spectrophotometry and its stability constant was determined by both methods to be 202.0 and 197.9 l mol–1, respectively.


RSC Advances ◽  
2018 ◽  
Vol 8 (23) ◽  
pp. 12526-12534 ◽  
Author(s):  
Hsi-Kuei Lin ◽  
Jia-Xing Li ◽  
Hao-Cheng Wang ◽  
Yu-Wei Su ◽  
Kaung-Hsiung Wu ◽  
...  

In photovoltaic devices, more effective transfer of dissociated electrons and holes from the active layer to the respective electrodes will result in higher fill factors and short-circuit current densities and, thus, enhanced power conversion efficiencies (PCEs).


Author(s):  
W.R. Bottoms ◽  
G.B. Haydon

There is great interest in improving the brightness of electron sources and therefore the ability of electron optical instrumentation to probe the properties of materials. Extensive work by Dr. Crew and others has provided extremely high brightness sources for certain kinds of analytical problems but which pose serious difficulties in other problems. These sources cannot survive in conventional system vacuums. If one wishes to gather information from the other signal channels activated by electron beam bombardment it is necessary to provide sufficient current to allow an acceptable signal-to-noise ratio. It is possible through careful design to provide a high brightness field emission source which has the capability of providing high currents as well as high current densities to a specimen. In this paper we describe an electrode to provide long-lived stable current in field emission sources.The source geometry was based upon the results of extensive computer modeling. The design attempted to maximize the total current available at a specimen.


Author(s):  
R. Sharma ◽  
B.L. Ramakrishna ◽  
N.N. Thadhani ◽  
D. Hianes ◽  
Z. Iqbal

After materials with superconducting temperatures higher than liquid nitrogen have been prepared, more emphasis has been on increasing the current densities (Jc) of high Tc superconductors than finding new materials with higher transition temperatures. Different processing techniques i.e thin films, shock wave processing, neutron radiation etc. have been applied in order to increase Jc. Microstructural studies of compounds thus prepared have shown either a decrease in gram boundaries that act as weak-links or increase in defect structure that act as flux-pinning centers. We have studied shock wave synthesized Tl-Ba-Cu-O and shock wave processed Y-123 superconductors with somewhat different properties compared to those prepared by solid-state reaction. Here we report the defect structures observed in the shock-processed Y-124 superconductors.


Author(s):  
T. F. Kelly ◽  
P. J. Lee ◽  
E. E. Hellstrom ◽  
D. C. Larbalestier

Recently there has been much excitement over a new class of high Tc (>30 K) ceramic superconductors of the form A1-xBxCuO4-x, where A is a rare earth and B is from Group II. Unfortunately these materials have only been able to support small transport current densities 1-10 A/cm2. It is very desirable to increase these values by 2 to 3 orders of magnitude for useful high field applications. The reason for these small transport currents is as yet unknown. Evidence has, however, been presented for superconducting clusters on a 50-100 nm scale and on a 1-3 μm scale. We therefore planned a detailed TEM and STEM microanalysis study in order to see whether any evidence for the clusters could be seen.A La1.8Sr0.2Cu04 pellet was cut into 1 mm thick slices from which 3 mm discs were cut. The discs were subsequently mechanically ground to 100 μm total thickness and dimpled to 20 μm thickness at the center.


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