1968
DOI: 10.1007/bf00903419
|View full text |Cite
|
Sign up to set email alerts
|

The pyrolysis of adamantane

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
4
0

Year Published

2010
2010
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 3 publications
0
4
0
Order By: Relevance
“…Experimentally, we know that adamantane molecules start to decompose at temperatures above 660 °C into liquid pyrolyzates including benzenes and alkylbenzenes as well as unsaturated gaseous components including ethylene by breaking and reconnecting CÀH and CÀC bonds. 23,36 We observed that adamantane turns into black shiny structures, possibly consisting of graphitized carbon, 37 and a yellow oily suspension under vacuum conditions. Within the confining volume of a nanotube, realized in our experiment, we may observe emergence of other carbon structures, including sp hybridized carbon chains, as the end product under vacuum conditions.…”
Section: Resultsmentioning
confidence: 90%
See 1 more Smart Citation
“…Experimentally, we know that adamantane molecules start to decompose at temperatures above 660 °C into liquid pyrolyzates including benzenes and alkylbenzenes as well as unsaturated gaseous components including ethylene by breaking and reconnecting CÀH and CÀC bonds. 23,36 We observed that adamantane turns into black shiny structures, possibly consisting of graphitized carbon, 37 and a yellow oily suspension under vacuum conditions. Within the confining volume of a nanotube, realized in our experiment, we may observe emergence of other carbon structures, including sp hybridized carbon chains, as the end product under vacuum conditions.…”
Section: Resultsmentioning
confidence: 90%
“…Our ab initio calculations indicate that the formation of carbon chains involves more than a single-step thermal conversion of adamantane to elemental carbon and hydrogen, since the reaction is a strongly endothermic process that requires a substantial amount of energy, Δ E = +20.8 eV per adamantane molecule. Experimentally, we know that adamantane molecules start to decompose at temperatures above 660 °C into liquid pyrolyzates including benzenes and alkylbenzenes as well as unsaturated gaseous components including ethylene by breaking and reconnecting C–H and C–C bonds. , We observed that adamantane turns into black shiny structures, possibly consisting of graphitized carbon, and a yellow oily suspension under vacuum conditions. Within the confining volume of a nanotube, realized in our experiment, we may observe emergence of other carbon structures, including sp hybridized carbon chains, as the end product under vacuum conditions.…”
Section: Resultsmentioning
confidence: 99%
“…Adamantane is most likely produced from either exo-THDCP or other compounds and it is likely decomposed to other compounds. However, it has been shown that adamantane decomposes at temperatures greater than 873 K. 21 Therefore, in the reaction conditions of this study, adamantane could be only produced from the decomposition of exo-THDCP. The composition of adamantane, which has an activation energy of 155 kcal/mol, increased by 0.035% at 623 K, 0.257% at 663 K, and 0.269% at 683 K. These results showed that the production of a compound with high activation energy was lower than those with low activation energy, although we only considered production of these compounds from exo-THDCP and not other compounds and did not considered decomposition of these compounds to other low-molecular-weight molecules.…”
Section: Comparison Between Experimental and Molecular Modelingmentioning
confidence: 76%
“…Adamantane is most likely produced from either exo -THDCP or other compounds and it is likely decomposed to other compounds. However, it has been shown that adamantane decomposes at temperatures greater than 873 K . Therefore, in the reaction conditions of this study, adamantane could be only produced from the decomposition of exo -THDCP.…”
Section: Comparison Between Experimental and Molecular Modelingmentioning
confidence: 81%