Thermodynamic Study on Mixed Electrolyte KCl and K2SO4 Aqueous Systems from EMF Measurements at 298.15 K.

ChemInform ◽  
2004 ◽  
Vol 35 (28) ◽  
Author(s):  
Jun Zhang ◽  
Shi-yang Gao ◽  
Shu-ping Xia
2017 ◽  
Vol 436 ◽  
pp. 1-12 ◽  
Author(s):  
Bahram Ghalami-Choobar ◽  
Mahmoud Azizpour ◽  
Hossein Ghanadzadeh Gilani ◽  
Naz Chaibakhsh

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Dunya Mahammad Babanly ◽  
Qorkhmaz Mansur Huseynov ◽  
Ziya Saxaveddin Aliev ◽  
Dilgam Babir Tagiyev ◽  
Mahammad Baba Babanly

The solid-phase diagram of the Tl-TlBr-S system was clarified and the fundamental thermodynamic properties of Tl6SBr4 compound were studied on the basis of electromotive force (EMF) measurements of concentration cells relative to a thallium electrode. The EMF results were used to calculate the relative partial thermodynamic functions of thallium in alloys and the standard integral thermodynamic functions (-ΔfG0, -ΔfH0, and S0298) of Tl6SBr4 compound. All data regarding thermodynamic properties of thallium chalcogen-halides are generalized and comparatively analyzed. Consequently, certain regularities between thermodynamic functions of thallium chalcogen-halides and their binary constituents as well as degree of ionization (DI) of chemical bonding were revealed.


1997 ◽  
Vol 101 (8) ◽  
pp. 1136-1145 ◽  
Author(s):  
Felipe Hernández-Luis ◽  
Luis Fernández-Mérida ◽  
Miguel A. Esteso ◽  
Héctor R. Galleguillos-Castro

2010 ◽  
Vol 638-642 ◽  
pp. 2950-2955
Author(s):  
Ervin Tal-Gutelmacher ◽  
Ryota Gemma ◽  
Eugen Nikitin ◽  
Astrid Pundt ◽  
Reiner Kirchheim

Titanium and its conventional alloys reveal a high affinity for hydrogen, being capable to absorb up to 60 at.% hydrogen at 600°C, and even higher contents can be alloyed with titanium at lower temperatures. Hydrogen exhibits a low solubility in the low-temperature hexagonal closed-packed (hcp) α phase and a very high solubility (up to 50 at.%) in the high temperature body-centered cubic (bcc) β phase. The presence of hydrogen in the amount exceeding 200 ppm leads to formation of hydrides in α and α + β titanium alloys. While the aforementioned hydrogen behavior within bulk titanium has been well-established and reviewed, this is not the case with titanium thin films. The interpretation of results in these nanosized systems is complicated because the exact determination of the hydrogen concentration is difficult. However, using electrochemical hydrogen loading technique under the proper conditions, the hydrogen concentration can be accurately determined via Faraday’s law. In this study the thermodynamics of the titanium films during hydrogen absorption were investigated by electromotive force (EMF) measurements. Titanium films of different thicknesses were prepared on sapphire substrates in an UHV chamber with a base pressure of 10-8 mbar, using ion beam sputter deposition under Ar-atmosphere at the pressure of 1,5ּ10-4 mbar. The crystal structure was investigated by means of X-Ray diffraction using a Co-Kα radiation. For electrochemical hydrogen loading, the films were covered by a 30 nm thick layer of Pd in order to prevent oxidation and facilitate hydrogen absorption. The samples were step-by-step loaded with hydrogen by electrochemical charging, which was carried out in a mixed electrolyte of phosphoric acid and glycerin (1:2 in volume). An Ag/AgCl (sat.) and Pt wires were used as the reference and the counter electrode, respectively. XRD measurements were performed before and after hydrogenation in order to investigate the effect of hydrogen loading on the films microstructure. The role of varying thicknesses on the main characteristics of hydrogen's absorption behavior, as well as hydrogen-induced microstructural changes in titanium thin films, are discussed in detail.


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