The invention relates to a process for the dehydrogenation of alkanes with constant product composition by passing an alkane over a suitable catalyst, a gas stream being formed which contains an alkene, hydrogen and a non-converted alkane. As the dehydrogenation of alkanes belongs to the group of reversible equilibrium reactions, the chemical equilibrium is reached during the reaction after a specific residence time under ideal catalyst conditions. Consistency in the product composition, i.e. a constant content of alkene, alkane and hydrogen in the product gas is achieved by shifting the chemical equilibrium to the desired direction by modifying the process parameters.
The dehydrogenation of alkanes takes place on a suitable catalyst. The activity of the catalyst gradually decreases while the reaction conditions remain the same, thus causing permanent changes of the product composition at the reactor outlet during a production cycle provided the process parameters remain unchanged. Failures in the downstream plant sections may occur on account of the permanently changing product composition. The rectification columns, for example, are susceptible to variations in the concentration of the feedstock stream.
U.S. Pat. No. 5,243,122 A describes a process for the dehydrogenation of light alkanes in an allothermal reformer, the temperature of the catalyst bed being controlled and slightly increased during the reaction such that the composition of the reactor effluent remains constant during the reaction. This measure delays the decrease in the catalyst activity such that the composition of the product stream and particularly the alkene/alkane ratio contained therein remain constant during operation. Thermal reaction control is provided by a special valve control system for fuel gas supply. However, the reformers are arranged in parallel, other influencing factors except for the temperature have not been considered.
Normally, after some time during the reaction, carbon-bearing deposits occur on the catalyst, drastically reducing the alkane conversion rate. For this reason the reaction is carried out in cycles. After a specific reaction time the reaction is stopped and an oxygen-containing gas which may also contain water vapour is passed over the catalyst. The carbon-bearing deposits are oxidised by this gas such that the catalyst is no longer covered and the reaction can start again.
The objective of the invention is therefore to develop an alkane dehydrogenation process which ensures constant product composition at the reactor outlet throughout the entire operating period.
The objective is achieved by passing a gaseous alkane-containing material stream in continuous operating mode through a catalyst bed in several reactors of adiabatic, allothermal or isothermal type or combinations thereof, a gas stream being produced which contains an alkene, hydrogen and a non-converted alkane, and by
At one or several points of a reactor measured values of temperature, pressure or steam/hydrocarbon ratio can be taken, then the process parameters can be controlled and influenced selectively by means of controllers such that the composition of the product gas at the end of the reactor system remains constant throughout the operating period.
In embodiments of the invention it is envisaged that two to ten identical or different reactor types are operated as an interlinked system. However, two to four reactors are preferred for economical reasons. The reactors may be of the allothermal, adiabatic or isothermal types. Of course, the reactors may also be combined with different types to achieve a corresponding effectiveness and economic efficiency. To achieve a constant product composition, the process parameters of temperature, pressure and steam/hydrocarbon ratio may be influenced selectively. The temperature can be controlled in at least one of the reactors by the fuel gas/oxygen supply and a suitable temperature sensor. In the same way the pressure in the reactor can be controlled by means of a control valve in the product gas discharge. The steam/hydrocarbon ratio in the reactor is determined by the supplied amounts of steam and gaseous hydrocarbon, this action being preferred to take place in the first of the reactors.
In further embodiments of the invention an analyser for measuring the composition of the product gas is deployed. The analyser may be, for example, a gas chromatograph. With the specified target value of temperature, pressure or steam/hydrocarbon ratio the composition of the product gas is determined with the aid of the analyser. As a result, both individual and combined process parameters can be influenced such that the desired constant product composition can be achieved. The same can also be achieved by specifying a time-variable function, as for example, a ramp function, by means of a process control system.
In further embodiments of the invention the use of the inventive process for the production of alkenes from alkanes is also claimed, particularly the use of the process for the dehydrogenation of propane to propene, of n-butane to n-butenes and butadiene, of isobutane to isobutene, or mixtures thereof and for the dehydrocyclisation of alkanes to aromatic hydrocarbons. However, any alkane or any hydrocarbon can be dehydrogenated that is dehydrogenable by a state-of-the-art dehydrogenation process.
The invention is illustrated by some examples, an allothermal reactor being considered as embodiment for the dehydrogenation of propane to propene in order to present the inventive process. The reactor is operated with the following process parameters: inlet temperature: 510° C., temperature difference ΔT between inlet and outlet: 75K, outlet pressure p: 6.0 bar, molar steam/hydrocarbon ratio STHC: 3.5.
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Table 1 summarises the examples which show the obvious effects of the influence of the process parameters on the product gas composition.
1)STHC: molar steam/hydrocarbon ratio
The invention is explained in the following on the basis of the drawings.
Number | Date | Country | Kind |
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10 2009 034 464.0 | Jul 2009 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP10/04348 | 7/16/2010 | WO | 00 | 3/5/2012 |