Tricyclodecane
Appearance
| |||
Names | |||
---|---|---|---|
IUPAC name
tricyclo[5.2.1.02,6]decane
| |||
Other names
Tetrahydrodicyclopentadiene
| |||
Identifiers | |||
3D model (JSmol)
|
|||
ChemSpider | |||
EC Number |
| ||
PubChem CID
|
|||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C10H16 | |||
Molar mass | 136.238 g·mol−1 | ||
Hazards | |||
GHS labelling:[1] | |||
![]() ![]() ![]() | |||
Danger | |||
H226, H302, H304, H315, H319, H335 | |||
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P330, P331, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, P501 | |||
Related compounds | |||
Related compounds
|
Twistane | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Tricyclodecane (TCD) is an organic compound with the formula C10H16. It is classed as a hydrocarbon. It has two main stereoisomers–the endo and exo forms.[2] Its primary use in the exo form is as a component of jet fuel.[3] It is used here primarily because of its high energy density. The exo isomer also has a low freezing point.[4][5] Because of this, its properties have been studied extensively.[6][7][8][9][10] It is often called tetrahydrodicyclopentadiene.
Reactions
Its reactions with other materials has been studied,[11][12] as have various production methods.[13][14] The two isomers can interconvert in the presence of aluminum chloride[verification needed] as catalyst, with preference for forming the exo as the major product.[15]
References
- ^ "Tetrahydrodicyclopentadiene". pubchem.ncbi.nlm.nih.gov.
- ^ "Exo-tricyclo[5.2.1.0(2.6)]decane". webbook.nist.gov. Retrieved 2023-10-03.
- ^ Hudzik, Jason M.; Asatryan, Rubik; Bozzelli, Joseph W. (2010-09-09). "Thermochemical Properties of exo -Tricyclo[5.2.1.0 2,6 ]decane (JP-10 Jet Fuel) and Derived Tricyclodecyl Radicals". The Journal of Physical Chemistry A. 114 (35): 9545–9553. Bibcode:2010JPCA..114.9545H. doi:10.1021/jp1049556. ISSN 1089-5639. PMID 20712369.
- ^ Herbinet, Olivier; Sirjean, Baptiste; Bounaceur, Roda; Fournet, René; Battin-Leclerc, Frédérique; Scacchi, Gérard; Marquaire, Paul-Marie (2006-10-01). "Primary Mechanism of the Thermal Decomposition of Tricyclodecane". The Journal of Physical Chemistry A. 110 (39): 11298–11314. Bibcode:2006JPCA..11011298H. doi:10.1021/jp0623802. ISSN 1089-5639. PMID 17004739.
- ^ Wu, Junjun; Gao, Lu Gem; Ning, Hongbo; Ren, Wei; Truhlar, Donald G. (2020-06-01). "Direct dynamics of a large complex hydrocarbon reaction system: The reaction of OH with exo-tricyclodecane (the main component of Jet Propellant-10)". Combustion and Flame. 216: 82–91. doi:10.1016/j.combustflame.2020.02.019. ISSN 0010-2180. S2CID 216384271.
- ^ "Exo-tricyclo[5.2.1.0(2.6)]decane". Cheméo. Retrieved 2023-10-03.
- ^ Seiser, R.; Niemann, U.; Seshadri, K. (2011-01-01). "Experimental study of combustion of n-decane and JP-10 in non-premixed flows". Proceedings of the Combustion Institute. 33 (1): 1045–1052. doi:10.1016/j.proci.2010.06.078. ISSN 1540-7489.
- ^ Tao, Yujie; Xu, Rui; Wang, Kun; Shao, Jiankun; Johnson, Sarah E.; Movaghar, Ashkan; Han, Xu; Park, Ji-Woong; Lu, Tianfeng; Brezinsky, Kenneth; Egolfopoulos, Fokion N.; Davidson, David F.; Hanson, Ronald K.; Bowman, Craig T.; Wang, Hai (2018-12-01). "A Physics based approach to modeling real fuel combustion chemistry III Reaction kinetic model of JP10". Combustion and Flame. 198: 466–476. doi:10.1016/j.combustflame.2018.08.022. ISSN 0010-2180. S2CID 104745782.
- ^ Li, Heng; Liu, Guozhu; Jiang, Rongpei; Wang, Li; Zhang, Xiangwen (2015-05-01). "Experimental and kinetic modeling study of exo-TCD pyrolysis under low pressure". Combustion and Flame. 162 (5): 2177–2190. doi:10.1016/j.combustflame.2015.01.015. ISSN 0010-2180.
- ^ Goh, K. H. H.; Geipel, P.; Hampp, F.; Lindstedt, R. P. (2013-01-01). "Regime transition from premixed to flameless oxidation in turbulent JP-10 flames". Proceedings of the Combustion Institute. 34 (2): 3311–3318. doi:10.1016/j.proci.2012.06.173. ISSN 1540-7489.
- ^ "STTR Navy FY09A - Characterization of the High Temperature Decomposition Products of JP-10". www.navysbir.com. Retrieved 2023-10-03.
- ^ Wu, Junjun; Gao, Lu Gem; Ning, Hongbo; Ren, Wei; Truhlar, Donald G. (2020-06-01). "Direct dynamics of a large complex hydrocarbon reaction system: The reaction of OH with exo-tricyclodecane (the main component of Jet Propellant-10)". Combustion and Flame. 216: 82–91. doi:10.1016/j.combustflame.2020.02.019. ISSN 0010-2180. S2CID 216384271.
- ^ US2766301A, Karl, Buchner; Otto, Roelen & Josef, Meis, "Production of tricyclodecane", issued 1956-10-09
- ^ Baptiste, Sirjean. "Theoretical Study of the Thermal Decomposition of a Jet Fuel Surrogate".
- ^ Lili, Q. I.; Min*, J. I.; Xinkui, Wang; Min, H. E.; Tianxi, C. a. I. (2010-04-25). "AlCl3/MCM-41 as a Catalyst for Isomerization of Endo-tricyclodecane". Chinese Journal of Catalysis. 31 (4): 383. ISSN 0253-9837.