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The Formation Of CatiO3and Its Influence Of Electrolysis

Posted on:2013-02-24Degree:MasterType:Thesis
Country:ChinaCandidate:L Y RuFull Text:PDF
GTID:2231330362974750Subject:Chemistry
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Titanium is named the third metal after Ferrum and Aluminum,which has theadvantages of corrosion resistance, fatigue resistance, toughness, high specific strength,etal. In aerospace、civil、medicine industry, sailing and other fields, there are wide rangeof applications. In recent years, the demand of metal titanium increase gradually. Butthe metal titanium preparation process of industrialization—Kroll method, has somedisadvantages, making the use of metal titanium high cost, and limit the widespread useof metal titanium. FFC method is one of molten salt electrolysis and green technologyfor titanium,which is expected to replace the traditional process, domestic and foreignresearchers also do a lot of research work.Now, in the laboratory scope, this process hasbeen successful preparation of metal titanium, and widely used in other metal and alloypreparation.But FFC method has to improve electrolytic efficiency, and further study isneeded for improvement.Because titanium has a variety of valence, when FFC electrolysis method preparetitanium,the production is variety, reaction mechanism is complex. In the electrolyticprocess, middle products are easy to form, then influence the electrolysis, CaTiO3isamong them.In order to further research the formation of CaTiO3and how to influenceelectrolysis, this paper studied the following two aspects.The study of the formation of CaTiO3mainly include the research of CaO and Ca2+which play a dominant role of the formation of CaTiO3. Thermodynamics theorycalculate for the hydrolysis of CaCl2is done. Through the different temperature gibbsfree energy calculation analysis whether the hydrolysis of CaCl2is easy and form CaOfor CaTiO3in the range of experiment temperature; Through sample detection ofsintered samples including CaCl2in argon and in air atmosphere; CaO+TiO2(1:1);CaCl2+TiO2(1:1); untreated CaCl2; sintered TiO2+CaCl2in argon; unsintered TiO2+CaCl2in argon to confirm the effect of CaO and Ca2+to the formation of CaTiO3. Theresults show that in the temperature range CaCl2is not easy to hydrolysis producingCaO, CaO played a secondary role for the formation of CaTiO3, the main function ofCaCl2is providing Ca2+for CaTiO3, and Ca2+played a main role for the formation ofCaTiO3.Comparative study on the electrolysis difference of in situ CaTiO3and ex situCaTiO3under different time and different voltage is done, and the effect factors of in situ CaTiO3is studied.Study on the electrolysis results of in situ CaTiO3and ex situ CaTiO3underdifferent time is done through crystal structure, microstructure, pore structure analyzethe effect factors of in situ CaTiO3; Study on the electrolysis results of ex situ CaTiO3under different voltage for study on the effect of electrolytic driving force.The results show that crystal structure distortion of CaTiO3may promote theelectrolysis; large specific surface area may form more active-sites; pore structure ofCaTiO3may influence the migration of ions;in different electrolytic stages, there arebest electrolytic voltage for electrolysis, the existence of the side effects can affectelectrolytic driving force.
Keywords/Search Tags:CaTiO3, electrolysis, electrolytic time, electrolytic voltage
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