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Dolomite decomposition in a high temperature fluidised bed reactor

 

作者: Martin Hehl,   Harald Helmrich,   Karl Schugerl,  

 

期刊: Journal of Chemical Technology and Biotechnology. Chemical Technology  (WILEY Available online 1983)
卷期: Volume 33, issue 1  

页码: 12-24

 

ISSN:0264-3413

 

年代: 1983

 

DOI:10.1002/jctb.504330103

 

出版商: Wiley Subscription Services, Inc., A Wiley Company

 

关键词: Dolomite;Decomposition;fluidised bed

 

数据来源: WILEY

 

摘要:

AbstractThe decomposition of dolomite was investigated in a bench‐scale fluidised bed reactor (30 cm diameter) at temperatures between 600°C and 1000°C in batch and continuous operations. The composition of the solids was determined by X‐ray analysis, the gas composition by infrared (i.r.) spectroscopic analysis. The reaction kinetics were investigated in a small fluidised bed (2.6 cm diameter) as well as in the bench‐scale equipment and compared with kinetic data evaluated from differential thermal gravimetric (DTG) curves. The measurements were carried out by adding small amounts of dolomite into the isothermal fluidised bed. The resulting CO2concentration within the gas could then be very low, thus MgCO3and CaCO3decompose as parallel reactions (singlestage reaction). At somewhat higher CO2gas concentrations prevailing in technical operational conditions the decomposition mechanism changes into a two‐stage reaction where MgCO3decomposes first. The bed temperature, pressure drop, superficial gas velocity, solid conversion, and specific interfacial area of solids were determined as functions of time and/or reactor wall temperature with a constant temperature increase rate for batch runs. The distributions of the residence time of solids indicate that in the continuously operated fluidised bed well‐mixed conditions prevail. The concentrations of dolomite, CaCO3, MgO, CaO, and solid conversion as well as the specific surface area of particles were determined as functions of the mean residence time in the continuous reactor. By means of the CO2concentration in the gas phase and the mean residence time the conversions of the consecutive reactions can be

 

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