Irredie tion Time, mi&) 106. Table 3. PREPARATION OF 0,+BF4-a) Ratio F2:02 Irradiatedc) 02bF4- Produced, mg 15 1: 1 27 1.6 8.9 30 1: 1 53 3 8.8 60 1:l 96 6 7.9 60 2:l 129 12 11.0 60 3: 1 1% 16 10.6 60 5:1 127 2h 10.5 60 7:l 113 27 8.9 60 1:6 444 1.5 4.1 60e) 1: 1 45 2.7 14.9 120 3: 1 216 26 8.6 180 1:l 231 14 6.3 180 5: 1 248 47 6.9 12of 3: 1 21 2.6 0.2 a) 14 moles )f BF3 wes adde after irrai ition. b) Dose rate of 100 negarads/hour. c) d) Millimoles of oxygen used <strong>with</strong> F2:02 ratios was: 1:l = 14 moles; 2:l = 8.75 moles; 3:l = 7.0 moles; 5:1 = 4.4 moles; 7:1 = 3.5 moles; 1:6 = 21.9 moles. A second compound was formed vhich decomposed at 133% yielding about 3 moles of noncondensable gases. e) Dose rate of 25 megarads/hour. f) 10.5 moles of BF3 added to the reaction tube before irradiation. g) Molecules of product formed per 100 ev absorbed energy. ,
, 107. REFERENCES 1. 0. Ruff <strong>and</strong> M. Menzel, 2. Anorg. Chem. 211, 204 (1933). 2. A. D, Kirshenbaum <strong>and</strong> A. V. Grosse, J. Am. Chem. SOC. 8l, 1277 (1959). 3. A. V. Grosse, A. C. Streng, <strong>and</strong> A. D. Kirshenbaum, ibid. 5, 1004 (1961). 4. 5. 6. 7. 8. 9. 10. 11. 12. 13 - 14. A. G. Streng <strong>and</strong> A. V. Grosse, ibid. 88, 169 (1966). I. J. Solomon, Adv. Oxid. Research, U.S. Dept. Comm., AD 640405, (19661, Ill. Inst. of Tech. or Chem. Abst. 66, 820a6f, (1967). A. D. Kirshenbaum, A. V. Grosse, <strong>and</strong> J. G. Aston, ibid. &, 6398 (1959). A. D. Kirshenbaum <strong>and</strong> A. G. Streng, J. Chem. Phys. 2, 1440 (1961). A. C. Streng, Chem. Revs. 3, 607 (1963). T. J. Idalone <strong>and</strong> H. A. Mc Gee, Jr., J. Phys. Chem. 9, 4338 (1965). T. J. Malone <strong>and</strong> H. A. Mc Gee, Jr., ibid. 71, 3060 (1967). A. G. Streng <strong>and</strong> A. V. Grosse, Adv. in &em. Series, No. 36, Am. Chem. SOC., iu'ashington, D.C., 1962, pp. 159-164. M. S. Cohen, J. Inorg. Chem. 1, 972 (1962). A. G. Streng, J. Am. Chem. SOC. a, 1380 (1963). A. R. Young, 11, T. Hirata, <strong>and</strong> S. I. Marrow, ibid. 86, 20 (1964). 15. I. J. Solorran, R. I. Brabets, R. K. Uenishi, J. N. Kei+A, <strong>and</strong> J. M. Mc Donough, J. Inorg. Chem. 2, 457 (1964). 16. 17. 18. S. I. Xarrov <strong>and</strong> A. R. Young, 11, ibid. k, 759 (1965). C. D. agner <strong>and</strong> V. A. Campanile, Nucleonics 17, (7), 99 (1959). Quad 200 Quadrupole Mass Spectrometer, Electronic Associates Inc., Palo Alto, California. 19. I. J. Solonian, Illinois Institute of Technology, Research Institute, private communication, October 1967, in press. 20. 21. 22. N. N. Greenv~oOd, J. Chem. SOC., 3811 (1959). N. Barlett <strong>and</strong> D. Lohman, J. Chem. SOC., 5253 (1962). A. D. Kirshenbaum <strong>and</strong> A. V. Grosse, unpublished work under Air Force Contract No. AF04(611) -9555, Temple University, December 1965. 23. I. J. Soloman, et el, unpublished vork under Air Force Contract No. AF49(63) -1175, Illinois Institute of Technology, Research Institute, December 1962. ,
- Page 1 and 2:
Introduction 1. SECONDARY CELLS WIT
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I time curves at constant current d
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I 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11
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7. IV IV- Equivalent Weight, gr/ Eq
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1 3 9 SOYO FILLER,HQT PRESS Fig. 4.
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11. COAL PYROLYSIS USING LASER IRRA
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13. Macerals. Macerals from a singl
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i 1 I Photochemistry. A fundamental
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t P li. al ’ i ._ m LL
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' 19. PYROLYSIS OF COAL IN A MICROW
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I 21. In the third stage, the gas e
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.4 4 0 W 0 m .d m x .-( 0 x w M m s
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' 25. CONCLUSIONS The principal rea
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' .4 b s tract 28.
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30. the course of the experiment Ex
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d (Sulfur] dt m i trogenj dt 32. E
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34. Table 1, Properties of Feed Mat
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0 0 0 m 0 VI b N 0 c, VI N 0 v, N h
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- Literature Cited 38 1. Gordon, K
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40 z - B 30 w 6 20 yl w U 10 40. 10
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Z 0 In 80 CK W > 6 60- 0 I- 40- Z W
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44. 2.0 I 1.2 - 0 2 1.0- 0.8 i TIME
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- 2.81 1.NITROGEN 2. SULFUR 3. GASO
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48. The oil from the separator is v
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. 50 . Table I . Properties of Pitc
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52. Coke yield A - - - - 0 800 900
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FIGURE 8. 54. t 0.5 1 800 900 1,000
- Page 56 and 57: Introduction 56. FLUORODINITROETUNO
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- Page 64 and 65: 64. RECENT CHEMISTRY OF THE OXYGEN
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- Page 68 and 69: 68. In summary, two general methods
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- Page 72 and 73: vapor Pressure (psia) Figure 4. Vap
- Page 74 and 75: C H -0-C-NHF, - 2 5 II 0 74. H 9304
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- Page 94 and 95: 94. After condensation of oxidizer
- Page 96 and 97: Stirring Solenoid LHe 7. Cryostat 9
- Page 98 and 99: Introduction 98. RFACTIONS OF OxYcm
- Page 100 and 101: , Acknowledgement 100. This work wa
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