The Chemistry and Characteristics of Nitric Acid-Graphite Intercalation

1982 ◽  
Vol 20 ◽  
Author(s):  
Sophia R. Su ◽  
Daniel W. Oblas

ABSTRACTGas-phase intercalation of graphite by nitric acid is a one-step process. The weight uptake of the sample is a function of nitric acid vapor pressure. A pure second stage compound was formed when the HNO3 reservoir was maintained at 17°C. Only a fourth stage compound was formed when the acid was kept at 0°C. The product gases due to intercalation and gas species evolved during deintercalation were analyzed by mass spectrometry. NO2 and H2O were the major components detected from the intercalation product gases. A small amount of oxygen was also present. The existence of O2 is probably due to the photo-chemical decomposition of nitric acid. As such, the photodecomposition of nitric acid is not a contributory factor in the intercalation chemistry.

2014 ◽  
Vol 67 (5) ◽  
pp. 701 ◽  
Author(s):  
Michael G. Leeming ◽  
George N. Khairallah ◽  
Sandra Osburn ◽  
Krista Vikse ◽  
Richard A. J. O'Hair

Cobalt-mediated decarboxylative Glaser-like C–C bond coupling of carboxylates has been studied in the gas phase using collision-induced dissociation (CID) multistage mass spectrometry (MSn) experiments. Both the identity of the carboxylate RCO2– (R = Me, HC≡C, MeC≡C, and PhC≡C) and the nuclearity of the complex ([CoCl(O2CR)2]– versus [Co2Cl3(O2CR)2]–) play a role in the types of reactions observed and their relative activation energies. In the first stage of CID, the mononuclear complex [CoCl(O2CMe)2]– undergoes decarboxylation, while the dinuclear [Co2Cl3(O2CMe)2]– undergoes cluster fission to yield [CoCl3]–; all acetylenic carboxylate complexes [CoCl(O2CR)2]– and [Co2Cl3(O2CR)2]– undergo decarboxylation. Isolation of the decarboxylated products followed by a second stage of CID results in a second decarboxylation event for all systems except for [CoCl(Me)(O2CMe)]–, which undergoes bond homolysis. In the final stage of CID, all acetylenic complexes undergo Glaser coupling, forming reduced Co anions. Overall dinuclear cobalt clusters are superior to mononuclear complexes at promoting decarboxylation and reductive coupling. The order of reactivity among the acetylide ligands is PhC≡C > MeC≡C > HC≡C.


2015 ◽  
Vol 3 (7) ◽  
pp. 3266-3270 ◽  
Author(s):  
J. Linnemann ◽  
J. Giorgio ◽  
K. Wagner ◽  
G. Mathieson ◽  
G. G. Wallace ◽  
...  

This communication highlights a simple nitric acid treatment, which enhances the properties of titanium foil and improves the photovoltaic performance of dye sensitised solar cells.


2015 ◽  
Vol 19 (0) ◽  
pp. 55-58
Author(s):  
Zhen-xue Liu ◽  
◽  
Zhong-xue Gan ◽  
Jun-jie Gu ◽  
Qing-feng Song

1993 ◽  
Vol 22 (1) ◽  
pp. 70-80 ◽  
Author(s):  
G. E. Taylor ◽  
J. G. Owens ◽  
T. Grizzard ◽  
W. J. Selvidge

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