Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20186| Title: | Decomposition of 2,2,3,3-Tetramethylbutane in the Presence of Oxygen |
| Authors: | Atri, Gulshan M. Baldwin, Roy R. Evans, Geoffrey A. Walker, Raymond W. |
| Keywords: | Journal of the Chemical Society : Faraday Transaction - I Chemistry Tetramethylbutane Oxygen |
| Issue Date: | 1978 |
| Publisher: | Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (02) |
| Abstract: | The oxidation of 2,2,3,3-tetramethylbutane in KCl-coated vessels has been studied between 440 and 54O°C, and over the pressure range 60-500 Torr. The results are consistent with a simple mechanism comprising reactions (l)-(3) (CH3)3C— C(CH3)3 -> 2t-C4H9 t-C4H9 + O2 —> i-C4H8 + HO2 surface HO2-> tH2O+iO2. (1) (2) (3) After allowance for a small (<20 %) contribution from a chain process, accurate Arrhenius parameters Ai = 6.0x 1016 s-1, Ei = 290.4 kJ mol-1 have been obtained by combination with Tsang’s results. From the thermochemistry of reaction (1) and literature values for k-i, values of AfJ7298 (t-Bu) = 44.0 + 4.0 kJ mob* and 5298(t-Bu) = 304.2±4.0 J K-1 mol-1 are recommended. Analysis of the products shows that ~1 % of the t-butyl radicals give isobutene oxide and over the temperature range 470-542°C, Az/Au = 13.8 and £13 — E2 = 13.0 kJ mol-1 where reaction (13) is the overall process, t-C4H9 + O2 — C4H8O+OH. (13) Reaction (13) is discussed in terms of the peroxy radical isomerisation and decomposition theory and Arrhenius parameters are suggested for the (1, 4/>) H atom transfer reaction (17) in t-butylperoxy radicals (CH3)3CO2 -> (CH3)2C(OOH)CH2. (17) |
| URI: | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20186 |
| Appears in Collections: | Journal Articles (before-1995) |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 0366-0379.pdf Restricted Access | 1.04 MB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.