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Gonzalez, G.1
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9
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37049143633
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For studies on THN autoxidation, see
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(a) For studies on THN autoxidation, see: Robertson, A. Waters, W. A. J. Chem. Soc. 1948, 1574-1590;
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Tian, G.1
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0000391384
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For studies of the high-temperature reactions of 1,2-dihydronapthalene and
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(b) For studies of the high-temperature reactions of 1,2-dihydronapthalene and THN, see: Franz, J. A.; Camaioni, D. M.; Beishline, R. R.; Dalling, D. K. J. Org. Chem. 1984, 49, 3563-3570;
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see, T.H.N.1
Franz, J.A.2
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Bounsceur, R.; Scacchi, G.; Marquaire, P.-M. Ind. Eng. Chem. Res. 2000, 39, 4152-4165.
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(a) Strohm, J. J.; Berkhous, S. K.; Schobert, H. H.; Song, C. Prepr. Pap.-Am. Chem. Soc. Pet. Chem. 2004, 49 (4), 453-456.
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Strohm, J.J.1
Berkhous, S.K.2
Schobert, H.H.3
Song, C.4
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16
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44949273781
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The formation of 1,4-napthoquinone from THNone oxidation has also been reported; see: Zarrabi, K.; Durfee, S. L.; Daniel, S. R.; Voorhees, K. J. J. Anal. Appl. Pyrolysis 1991, 21, 1-14.
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(b) The formation of 1,4-napthoquinone from THNone oxidation has also been reported; see: Zarrabi, K.; Durfee, S. L.; Daniel, S. R.; Voorhees, K. J. J. Anal. Appl. Pyrolysis 1991, 21, 1-14.
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23344448029
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Beaver, B. D.; Gao, L.; Burgess-Clifford, C.; Sobkowiak, M. Energy Fuels 2005, 19, 1574-1579.
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Sobkowiak, M.4
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33845992579
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See also
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(b) See also: Balster, L. M.; Zabarnick, S.; Striebich, R. C.; Shafer, L. M.; West, Z. J. Energy Fuels 2006, 20, 2564-2571.
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Balster, L.M.1
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Beaver, B. J. Chem. Ed. 1999, 76 (8), 1108-1112.
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Beaver, B.1
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0031546372
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The benzylic C-H bond strength in THN is estimated to be 83 kcal/ mol; see: Laarhoven, L. J. J.; Mulder, P. J. Phys. Chem. B 1997, 101, 73-77.
-
(a) The benzylic C-H bond strength in THN is estimated to be 83 kcal/ mol; see: Laarhoven, L. J. J.; Mulder, P. J. Phys. Chem. B 1997, 101, 73-77.
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-
-
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23
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34247094166
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The O-H bond strength in BHT is estimated to be 82 kcal/mol; see: Wayner, D. D. M.; Lusztyk, E.; Ingold, K. U. J. Org. Chem. 1996, 61, 6430-6433.
-
(b) The O-H bond strength in BHT is estimated to be 82 kcal/mol; see: Wayner, D. D. M.; Lusztyk, E.; Ingold, K. U. J. Org. Chem. 1996, 61, 6430-6433.
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-
-
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24
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34247093207
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This hypothesis can account for the differing extents of THN oxidation in previously published model tubing bomb experiments and similar experiments reported in this work
-
(a) This hypothesis can account for the differing extents of THN oxidation in previously published model tubing bomb experiments and similar experiments reported in this work.
-
-
-
-
25
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33746896973
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See Part I of this series: Beaver, B. D.; Burgess Clifford, C.; Fedak, M. E.; Gao, L.; Iyer, P.; Sobkowiak, M. Energy Fuels 2006, 20 (4), 1639-1646.
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(b) See Part I of this series: Beaver, B. D.; Burgess Clifford, C.; Fedak, M. E.; Gao, L.; Iyer, P.; Sobkowiak, M. Energy Fuels 2006, 20 (4), 1639-1646.
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26
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34247109907
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The rate law for inhibited peroxyl radical chain mechanisms can be summarixed as -d[RH]dt = k[RH]/[AH], where [RH] and [AH] represent the molar concentration of hydrocarbon (THN) and antioxidant (BHT), respectively, with κ being an assortment of various rate constants. For details, see: Tudos, F.; Fodor, Z.; Iring, M. In Oxidation Inhibition in Organic Materials, II; Pospisil, J., Klemchuk, P. P., Eds.; CRC Press: Boca Raton, FL, 1990; p 234.
-
The rate law for inhibited peroxyl radical chain mechanisms can be summarixed as -d[RH]dt = k[RH]/[AH], where [RH] and [AH] represent the molar concentration of hydrocarbon (THN) and antioxidant (BHT), respectively, with κ being an assortment of various rate constants. For details, see: Tudos, F.; Fodor, Z.; Iring, M. In Oxidation Inhibition in Organic Materials, Vol. II; Pospisil, J., Klemchuk, P. P., Eds.; CRC Press: Boca Raton, FL, 1990; p 234.
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27
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0141964682
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Strohm, J. J.; Andrésen, J. M.; Song, C. Prepr. Pap.-Am. Chem. Soc. Pet. Chem. 2002, 47 (3), 189-191.
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Strohm, J.J.1
Andrésen, J.M.2
Song, C.3
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