scholarly journals In-situ determination of thickness and electrochemical properties of barrier oxide film on impure aluminium in aqueous solution

2018 ◽  
Vol 48 (6) ◽  
pp. 569-578 ◽  
Author(s):  
Nils-Håvard Giskeødegård ◽  
Ola Hunderi ◽  
Kemal Nisancioglu
2010 ◽  
Vol 663-665 ◽  
pp. 690-693 ◽  
Author(s):  
Kemawadee Udomphan ◽  
Atchana Wongchaisuwat ◽  
Ladda Meesuk

CdS, a bright yellow precipitate is well known for its optical, electrical, electro-optical and photochemical properties. CdS has also been prepared in the interlayer spaces of layered materials such as laponite and montmorillonite (bentonite). Several properties of intercalated CdS have been studied, but for the best of our knowledge there is no reports on its use. In this work, we applied CdS-intercalated bentonite / carbon composite as an electrode for determination of S2- ion in aqueous solution. CdS- intercalated bentonite was prepared by the in situ solid-solid reaction between Cd(II)-bentonite and Na2S. To construct a potentiometric electrode, CdS-intercalated bentonite was mixed with artificial graphite, polytetrafluoroethylene (PTFE) and carboxymethylcellulose (CMC) in an appropriate ratio. The electrode was used to determine S2- in aqueous solution, graphs of log [S2-] vs measured voltage (mv) gave linear relation up to 3 orders of ion concentrations. Apart from the reproducibility and good precision, the electrode is good for its selectivity, durability and low cost.


2008 ◽  
Vol 273-276 ◽  
pp. 283-293 ◽  
Author(s):  
Khaled Habib ◽  
K. Al-Muhanna ◽  
F. Al-Sabti ◽  
A. Al-Arbeed

In the present investigation, holographic interferometry was utilized for the first time to measure in situ the thickness of the oxide film, alternating current (A.C.) impedance, and double layer capacitance of aluminium samples during anodization processes in aqueous solution without any physical contact. The anodization process (oxidation) of the aluminium samples was carried out by the electrochemical impedance spectroscopy (EIS), in different concentrations of sulphuric acid (0.5-2.5 % H2SO4) at room temperature. In the mean time, the real-time holographic interferometric was used to measure the thickness of anodized (oxide) film of the aluminium samples in aqueous solutions. Also, mathematical models were applied to measure the alternating current (A.C.) impedance, and double layer capacitance of aluminium samples by holographic interferometry, during anodization processes in aqueous solution. Consequently, holographic interferometric is found very useful for surface finish industries especially for monitoring the early stage of anodization processes of metals, in which the thickness of the anodized film, the A.C. impedance, and the double layer capacitance of the aluminium samples in sulphuric acid (0.5-2.5 % H2SO4) can be determined in situ. Futhermore, a comparison was made between the electrochemical values obtained from the holographic interferometry measurements and from measurements of electrochemical impedance spectroscopy(EIS) on aluminium samples in sulphuric acid (0.5-2.5 % H2SO4). The comparison indicates that there is good agreement between the obtained electrochemical data from both techniques. However, there is a drastic difference between the measurement of the oxide film thickness by both techniques. The oxide film thickness of the aluminium samples in 0, 0.5, 1.0, 1.5, 2.0, 2.5% H2SO4 by the optical interferometry is in a micrometer scale. However, the oxide film thickness of the aluminium samples in 0, 0.5, 1.0, 1.5, 2.0, 2.5% H2SO4 by the E.I.Spectroscopy in a nanometer scale. This can be explained due to the fact that the E.I.Spectroscopy is useful technique to measure the electrochemical parameters and the thickness of the barrier (compact) oxide films. In contrast, the optical interferometry is found useful technique to characterize and measure the thickness of the porous oxide layer. Also, the optimum thickness of the oxide barrier film was detected to be equivalent to 0.612nm in sulphuric acid concentration of 2.5% H2SO4 by E.I. spectroscopy.


2011 ◽  
Vol 62 (1) ◽  
pp. 49-53 ◽  
Author(s):  
Vlastimil Řeháček ◽  
Ivan Hotový ◽  
Marian Vojs ◽  
Mário Kotlár ◽  
Thomas Kups ◽  
...  

Pyrolyzed Photoresist Film Electrodes for Application in Electroanalysis Pyrolyzed photoresist film (PPF) electrodes for application in electroanalysis were prepared on alumina substrates. These electrodes were characterized for their electrical, microstructural (by Raman spectroscopy) and electrochemical properties. As a support, the PPF electrodes were tested for simultaneous determination of Pb(II), Cd(II) and Zn(II) in an aqueous solution on in-situ formed bismuth film by square wave voltammetry (SWV). The dependence of the stripping responses on the concentration of target metals was linear in the range from 1 × 10-8 to 9 × 10-8 mol/L. The effect of activation of the PPF surface by argon plasma on analytical performance of bismuth film electrode (BiFE) on PPF support was also investigated.


1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


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