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The dynamics of the platinum catalyzed interconversion of methylcyclohexane, toluene, and hydrogen near equilibrium were investigated in a closed reactor system by a frequency response method at temperatures in the range of 433 to 473 K and at total pressures in the vicinity of 80 to 110 Torr. The gas phase in contact with the platinum catalyst was always hydrogen-rich, with hydrogen to hydrocarbon mole ratios maintained in the range of 3.2 to 4.6. The frequency response method utilized small perturbations (lower than 1%) of the volume of the system, with measurements of the total pressure being used to determine the response of the system. The range of perturbation frequencies investigated was approximately 0.002 to 3 Hz (0.013 to 19 rad s(-1)). The experiments revealed two characteristic relaxation frequencies that are associated with the dynamics of the interconversion. The dynamics of the system are interpreted in terms of a simple two-step interconversion sequence with the aid of a phenomenological frequency response theory formulated in terms of relaxation frequencies of the steps and equilibrium properties of the system. It is concluded that one of the steps, a toluene adsorption-desorption step, is much slower than the other, a step involving the interconversion of the gas-phase methylcyclohexane and chemisorbed toluene that releases or consumes hydrogen in the process. 相似文献
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Energy spectra for decaying 2D turbulence in a bounded domain 总被引:1,自引:0,他引:1
We use results derived in the framework of the replica approach to study the liquid-glass thermodynamic transition. The main results are derived without using replicas and applied to the study of the Lennard-Jones binary mixture introduced by Kob and Andersen. We find that there is a phase transition due to the entropy crisis. We compute both analytically and numerically the value of the phase transition point T(K) and the specific heat in the low temperature phase. 相似文献
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Mora JF Van Berkel GJ Enke CG Cole RB Martinez-Sanchez M Fenn JB 《Journal of mass spectrometry : JMS》2000,35(8):939-952
Editorial Comment Last month we presented, as a Special Feature, a set of five articles that constituted a Commentary on the fundamentals and mechanism of electrospray ionization (ESI). These articles produced some lively discussion among the authors on the role of electrochemistry in ESI. Six authors participated in a detailed exchange of views on this topic, the final results of which constitute this month's Special Feature. We particularly hope that younger scientists will find value in this month's Special Feature, not only for the science that it teaches but also what it reveals about the processes by which scientific conclusions are drawn. To a degree, the contributions part the curtains on these processes and show science in action. We sincerely thank the contributors to this discussion. The give and take of intellectual debate is not always easy, and to a remarkable extent this set of authors has maintained good humor and friendships, even when disagreeing strongly on substance. Graham Cooks and Richard Caprioli Copyright 2000 John Wiley & Sons, Ltd. 相似文献
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Van Berkel GJ Quirke JM Adams CL 《Rapid communications in mass spectrometry : RCM》2000,14(10):849-858
A survey of derivatization strategies and prospective derivatization reactions for conversion of simple alkenes and alkynes to 'electrospray-active' species is presented. General synthetic strategies are discussed and illustrative examples of prospective derivatives prepared from model compounds are presented along with their electrospray ionization (ES) mass spectra. The identified derivatives of these neutral, nonpolar analytes are either ionic or are ionizable in solution through Bronsted acid/base chemistry, by Lewis acid/base chemistry, or by chemical or electrochemical electron-transfer chemistry. Once ionized, the derivatives are expected to be amenable to detection by electrospray ionization-mass spectrometry. Derivatives are identified for positive and negative ion analysis of both alkenes and alkynes. Copyright 2000 John Wiley & Sons, Ltd. 相似文献
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