The Corrosion Behavior of Titanium in Hydrogen Peroxide Solution with Various Additives

2007 ◽  
Vol 330-332 ◽  
pp. 1285-1288 ◽  
Author(s):  
Lei Xie ◽  
Xiao Xiang Wang ◽  
Jian Li

The corrosion behavior of titanium in hydrogen peroxide solutions was studied by measuring the titanium ions concentration using spectrophotometer. The influence of additives (K+ , Ca2+ ,Na+ ,Mg2+ ,Cl- ,HPO4 2-, H2PO4 - ) on the corrosion behavior of titanium was examined. The results indicated that Ca2+ exhibited the highest inhibition to the titanium corrosion in hydrogen peroxide solutions, while HPO4 2- behaved as an accelerator to the corrosion. It was suggested that the Ca2+ was absorbed on the titanium surface to form a thin film of CaTiO3 or CaO2, and consequently, inhibited the corrosion of titanium. The acceleration of the titanium corrosion in the present of HPO4 2- was caused probably by the increased defect of surface oxide films after absorption of HPO4 2- ions.

2010 ◽  
Vol 62 (4) ◽  
pp. 320-325 ◽  
Author(s):  
M. Wang ◽  
W. Wang ◽  
B. L. He ◽  
M. L. Sun ◽  
Y. S. Bao ◽  
...  

2009 ◽  
Vol 59 (12) ◽  
pp. 1400-1404
Author(s):  
Marius Tudorascu ◽  
Spiridon Oprea ◽  
Afrodita Doina Marculescu ◽  
Stefania Tudorascu

The mechanism of the enzymatic iodination process of diethylmaleate and diethylfumarate (which present no miscibility with water) in the presence of lactoperoxidase, both in diluted hydrogen peroxide solution and in a generating system of hydrogen peroxide using ammonium and calcium iodides as halide sources in disperse system (after an ultrasonic pretreatment) was studied. The obtained sole product (diethyl-2, 3-diiodosuccinate) after the enzymatic iodination process was directly hydrolyzed to a tartaric acid present in an optically inactive form. The mechanism of obtaining the intermediate and final products and respectively, the existence of both D, L-tartaric acid and meso-tartaric acids (as lithium bitartrates) were also investigated.


1963 ◽  
Vol 110 (6) ◽  
pp. 680 ◽  
Author(s):  
H. S. Isaacs ◽  
J. S. Llewelyn Leach
Keyword(s):  

2014 ◽  
Vol 602-603 ◽  
pp. 871-875
Author(s):  
Yen Pei Fu ◽  
Jian Jhih Chen

In this study, ZnO films, prepared by Chemical Bath Deposition (CBD), are applied as the conductive layers for thin film solar cells. Zinc acetate is used as a source of zinc, and different proportions of ammonia solution are added and well mixed. The growth of zinc oxide films in reaction solutions is taken place at 80°C and then heated to 500°C for one hour. In this study, the different ammonia concentrations and deposition times is controlled. The thin film structure is Hexagonal structure, which is determined by X-ray diffraction spectrometer (XRD) analysis. Scanning electron microscopy (SEM) is used as the observation of surface morphology, the bottom of the film is the interface where the heterogeneous nucleation happens. With the increase of deposition time, there were a few attached zinc oxide particles, which is formed by homogeneous nucleation. According to UV / visible light (UV / Vis) absorption spectrometer transmittance measurements and the relationship between/among the incident wavelength, it can be converted to the energy gaps (Eg), which are about 3.0 to 3.2eV, by using fluorescence spectroscopy analysis. The emission of zinc oxide films has two wavelengths which are located on 510nm and 570nm. According to Based on the all analytic results, the ammonia concentration at 0.05M, and the deposition time is 120 minutes, would obtain the conditions of ZnO films which is more suitable for applications of conductive layer material in thin film solar cell.


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