A thermogravimetric analysis/mass spectroscopy study of the thermal and chemical stability of carbon in the Pt/C catalytic system

Carbon ◽  
2010 ◽  
Vol 48 (8) ◽  
pp. 2244-2254 ◽  
Author(s):  
Rémy Sellin ◽  
Jean-Marc Clacens ◽  
Christophe Coutanceau
1976 ◽  
Vol 29 (11) ◽  
pp. 2369 ◽  
Author(s):  
S Dilli ◽  
E Patsalides

The complexes of vanadium(111) and oxovanadium(1V) with pentane-2,4-dione; l,l,l-trifluoropentane-2,4-dione; 1,1,1,5,5,5-hexafluoropentane-2,4-dione; l,l,l-trifluoro-5-methylhexane-2,4-dione; l,l,l-trifluoro-5,5-dimethylhexane-2,4-dine 1,1,1,2,2-pentafluoro-6,6-dimethylheptane-3,5-dione and 1,1,1,2,2,3,3-heptafluoro-7,7-dimethyloctane-4,6-dione have been prepared. The volatility, thermal and chemical stability of the chelates have been examined by simultaneous differential thermal and thermogravimetric analysis in dynamic atmospheres of nitrogen, air and water-saturated nitrogen and air, in addition to heating under vacuum to temperatures approaching 360�C. The vanadium(111) chelates of the fluorinated β-diketones volatilized with little evidence of decomposition even in air and were stable in the absence of air to 280-320�C. In contrast, the oxovanadium(1V)chelates partly decomposed during volatilization at temperatures as low as 150�C, and completelydecomposed over the temperature range 180-240�C.


Author(s):  
TaeGyeong Lim ◽  
Ba Trung Ho ◽  
Ji Won Suk

Highly porous activated graphene coated on CVD-graphene/Cu wires enables high-performance wire supercapacitors with enhanced thermal and chemical stability.


2021 ◽  
Author(s):  
Taksande Kiran ◽  
Effrosyni Gkaniatsou ◽  
Corine Simonnet-Jégat ◽  
Carine Livage ◽  
Guillaume Maurin ◽  
...  

A highly performing proton conducting composite was prepared through the impregnation of EMIMCl ionic liquid in the mesoporous MIL-101(Cr)-SO3H MOF. The resulting EMIMCl@MIL-101(Cr)-SO3H composite displays high thermal and chemical stability,...


2016 ◽  
Vol 8 (1) ◽  
pp. 188 ◽  
Author(s):  
Laila M. Break

<p>Fluorinated nucleosides very important in increased biological and chemical stability of organ fluorine compounds. Synthesis of two 5-(Trifluoromethyl)-<em>1H</em>-benzimidazole derivatives (3) and (4).</p><p>Ribosylation of each compound (3) and (4) with 1-<em>O</em>-acetyl-2,3,5-tri-<em>O</em>-benzoyl-<em>β</em>-D-ribofuranose (6) afforded mixture <em>b</em>- and <em>a</em>- anomeric of the benzoylated nucleoside derivatives (8), (9) and <em>b</em>- anomeric (12), respectively. Debenzoylation of the protected nucleosides by reaction with sodium metal in dry methanol yielded the corresponding free N-nucleosides (10), (11) and (13) respectively. The new synthesized compounds were characterized using the well-known spectroscopic tools (IR, <sup>1</sup>HNMR, <sup>13</sup>CNMR and mass spectroscopy).</p>


1975 ◽  
Vol 6 (22) ◽  
pp. no-no
Author(s):  
F. GOTTO ◽  
M. MASOERO ◽  
R. SANTI ◽  
G. GALLUZZI ◽  
D. H. R. BARTON

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