scholarly journals Lithium Hydroxide Assisted Endo ‐Selective [4+4]‐Photocycloaddition of Pyran‐2‐ones

Author(s):  
Lei Li ◽  
William L. Turnbull ◽  
Robert McDonald ◽  
F. G. West
Keyword(s):  
2009 ◽  
Author(s):  
Ulrich Jordis ◽  
Jaywant Phopase ◽  
A. Khan Farhan

CORROSION ◽  
1971 ◽  
Vol 27 (8) ◽  
pp. 353-359 ◽  
Author(s):  
R. L. JONES ◽  
E. W. STEINKULLER
Keyword(s):  

2012 ◽  
Vol 81 ◽  
pp. 224-226 ◽  
Author(s):  
Ziyan Zhang ◽  
Wen Chen ◽  
Erfu Ni ◽  
Kanghua Chen

2000 ◽  
Author(s):  
Jeong-Ju Cho ◽  
M. Urquidi-Macdonald

Abstract New gel electrolytes composed of silica powder and organic electrolytes for the application of lithium/seawater batteries were tested with a porous separator. The maximum current density was ∼25mA/cm2. The discharging current was decreased suddenly because of two reasons. One reason is that the porous separator became clogged with lithium hydroxide and the other is because of the deposition of lithiumsilicate on the lithium surface, which was confirmed using SEM, XPS and hydroxide ion flux measurements. The efficiency (5 ∼ 27%) of the lithium oxidation was also obtained by measuring the hydrogen volume. The efficiency is strongly dependent on the ambient temperature. The effect of additives and other gel systems was also investigated.


2006 ◽  
Vol 320 ◽  
pp. 271-274 ◽  
Author(s):  
Minakshi Manickam ◽  
Pritam Singh ◽  
Touma B. Issa ◽  
Stephen Thurgate ◽  
Kathryn Prince

The electrochemistry of olivine-type iron phosphate (FePO4) as a battery cathode material, in aqueous lithium hydroxide (LiOH), has been investigated. The material forms intercalated LiFePO4 reversibly on electroreduction/oxidation. The formation of Fe3O4 phase, in addition to the regeneration of FePO4 during reverse oxidation of LiFePO4, also occurs. In this regard, the mechanism of FePO4 discharge/charge in aqueous LiOH differs from that in non-aqueous solvents.


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