Solid reaction scale/experimental conditions

The apparatus s step change from ambient to desired reaction conditions eliminates transport effects between catalyst surface and gas phase reactants. Using catalytic reactors that are already used in industry enables easy transfer from the shock tube to a ffow reactor for practical performance evaluation and scale up. Moreover, it has capability to conduct temperature- and pressure-jump relaxation experiments, making this technique useful in studying reactions that operate near equilibrium. Currently there is no known experimental, gas-solid chemical kinetic method that can achieve this. 

In the preceding decade, solid-state NMR spectroscopy has provided important and novel information about the nature and properties of surface sites on working solid catalysts and the mechanisms of these surface reactions. This spectroscopic method offers the advantages of operation close to the conditions of industrial catalysis. A number of new techniques have been introduced and applied that allow investigations of surface reactions by solid-state NMR spectroscopy under both batch and flow conditions. Depending on the problems to be solved, both of these experimental approaches are useful for the investigation of calcined solid catalysts and surface compounds formed on these materials under reaction conditions. Problems with the time scale of NMR spectroscopy in comparison with the time scale of the catalytic reactions can be overcome by sophisticated experimental... 

This paper presents the first experimental results for the solid motion inside a pilot-scale rotary kiln. Such data are useful to enable efficient pyrolysis reactions inside a rotary kiln to be carried out, through the prediction of residence time and material hold-up, and the evaluation of different surfaces and temperature profiles according to the operating conditions. In the first part, the pilot-scale rotary kiln and the principle of the experiments will be described. An original dynamic solid motion model will be presented in the second part, this dynamic model is derived from the original static model of Seaman [1], The static and dynamic experimental results are finally compared with the simulated results. 

The following experimental procedures describe the solid-phase synthesis of peptides by means of Fmoc chemistry and TBTU activation (Scheme 8), as well as by HBTU-mediated coupling of Boc amino acid derivatives and in situ neutralization (Scheme 9). Segment condensations on solid phase with C-ternoinal glycine or proline residues can be easily achieved, even on a multigram scale (Scheme 10). Segment condensations involving the activation of other amino acids require the careful optimization of reaction conditions in order to suppress extensive epimerization (see Scheme 11 and Section 3.8.1.2). 

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