The invention relates to a process for the hydrogenation of material flows containing olefins and sulphur as commonly occurring in crude oil refineries. By the process according to the invention the sulphur compounds contained in these flows are hydrogenated in a reactor to achieve a complete or partly conversion into hydrogen sulphide and the olefins contained in these flows are hydrogenated to achieve a complete or partly conversion into alkanes. The process and especially the temperature distribution in the reactor are controlled by adjusting the olefin content in the feed streams supplied to the reactor. The invention also relates to a contrivance which serves to carry out the process and is suited to implement the mentioned process steps.
DE 102007059243 A1 describes a process for the hydrogenation of olefin-containing material flows which incorporate organic sulphur compounds and are converted into hydrogen sulphide by hydrogenation. The hydrogenation serves to eliminate the sulphur compounds from the introduced material flow by removing the hydrogen sulphide from the product gas as obtained material mixture in a gas scrubbing process subsequent to the hydrogenation.
The feed streams are passed through the reactor, which is provided in gas flow direction with several successive catalyst beds serving to perform a consecutive hydrogenation. The feed streams typically consist in a gas or an evaporated liquid. Downstream of each catalyst bed there is a feed device for a further feed stream by which further feed stream can be introduced into the reactor gas flow. As the catalyst beds and the reactor gas flow heat up after each hydrogenation step, it is possible to control the temperature distribution inside the reactor via the distribution of the feed stream downstream of the individual catalyst beds. By adding fresh feed stream downstream of the respective catalyst bed, the feed stream will cool down again.
In this way it is possible to carry out the hydrogenation in a continually optimum temperature range. The catalyst can thus be kept at a temperature which ensures optimum range of application. This procedure will produce several material flows downstream of the individual catalyst beds. This may lead to different pressure conditions inside the reactor, which may pose a problem depending on the respective process type. It is therefore the aim to control the addition of the olefin downstream of the individual catalyst beds such that this addition is not performed via the flow rate control.
The invention achieves this aim by adding feed streams of precisely controlled olefin content. As the gas flow and the catalyst bed in the reactor are only heated by the reaction heat of the olefin hydrogenation reaction, the temperature distribution in the reactor can be controlled by adding feed streams of different olefin contents. Here, a feed stream always signifies a gaseous material flow.
Especially claimed is a process for the hydrodesulphurisation of olefin-containing feedstocks with the aid of a feed stream containing hydrogen, in which
and which is characterised in that
Part of the total olefin amount is supplied via the head of the reactor. The temperature at the reactor head is usually approx. 300° C., which is well suited to carry out the hydrogenation reaction. The content of olefins in the first olefin-containing feed stream can advantageously be controlled by adding a dilution stream lean in or free of olefins or both dilution streams to the first feed stream. In this way an olefin-containing feed stream is produced.
The olefin-lean and the olefin-free feed stream may be added in a mixture with the option to either add them separately in two individually controlled streams or in premixed condition. By adding these two material mixtures as dilution streams it is possible to adjust the desired content of olefins in the feed stream and also to control the temperature in the reactor. Depending on the desired process mode it is also possible to introduce another material flow containing a gas lean in or free of olefins. Thus it is possible to further dilute the feed stream. It is also possible to increase the content of olefins in the first feed stream by separate addition of a material flow rich in olefins into the first feed stream. In principle, the first feed stream introduced contains olefins already.
According to an embodiment of the invention a material flow which is lean in olefins and a material flow which is free of olefins are added as dilution streams to the first feed stream. In this way it is possible to control the hydrogenation via the olefin content in this flow such that it produces a precisely defined amount of heat. This serves to adjust the temperature downstream of the first catalyst bed such that mixing it with the second feed stream will produce exactly the temperature that is required for the passage through the second catalyst bed.
If it seems to be necessary, it is possible to add an olefin-rich material flow to the feed stream in order to increase the olefin content in the first feed stream. This may be done on a temporary or a permanent basis. The olefin-rich material flow can be added separately or in premixed condition with another material flow. Finally it is possible to add an olefin-free, olefin-lean and olefin-rich material flow separately to the first feed stream so to control the olefin content in the first feed stream. Although the addition is preferably performed separately, it is also possible to add these material flows in premixed condition. The pre-mixture can be implemented in any mixing combination and ratio desired.
The reactor may be provided with more than two catalyst beds. In another embodiment of the invention the material flow obtained from the reaction is passed through a third catalyst bed, which will heat the bed and the passing gas flow. This means that downstream of the second catalyst bed a third feed stream is supplied into the reactor laterally downstream of the second catalyst bed to the material flow which has been heated by the second hydrogenation and that the gas flow for hydrogenation first passes the second catalyst bed and then the third catalyst bed.
An embodiment of the invention provides in an exemplary fashion that downstream of the second catalyst bed a third feed stream is fed into the reactor laterally downstream of the second catalyst bed to the material flow heated by the second hydrogenation, and the material flow to be hydrogenated passes the second catalyst bed first and then a third catalyst bed. It is possible to pass the material flow, which has been sent through the third partial amount of the hydrodesulphurisation catalyst, through one or several additional partial amounts of a hydrodesulphurisation catalyst and to introduce a further feed stream into the reactor laterally downstream of the catalyst beds.
To control the temperature distribution also in this third catalyst bed, a material flow lean in olefins and a material flow free of olefins are analogously fed into the supply line for the second feed stream downstream of the first catalyst bed. By the amounts of individual material flows admixed it is possible to also adjust the olefin content in this second feed stream. This makes it possible in turn to control the temperature of the third catalyst bed. Likewise it is possible according to an embodiment of the invention to additionally introduce a material flow rich in olefins into the reactor.
At last it is also possible to pass the gas flow through as many catalyst beds as desired. Downstream of each catalyst bed, a further material flow may be introduced laterally, being of an olefin content which allows to adjust the temperature of the subsequent hydrogenation in an optimum way. This means that after the material flow has been sent through the third partial amount of the hydrodesulphurisation catalyst it is passed through one or several additional partial amounts of a hydrodesulphurisation catalyst and a further feed stream is introduced into the reactor laterally downstream of the catalyst beds. It is possible to also supply a material flow lean in olefins or free of olefins to the respective feed stream to deplete the latter of olefins if this is required. In this way it is possible to adjust the olefin content of the respective feed stream by adding a material flow. The addition can be performed in the form of separate material flows which are lean in or free of olefins or in the form of premixed flows.
It is finally possible to increase the olefin content by adding an olefin-containing material flow. Such addition may optionally take place downstream of every catalyst bed desired. In general, however, this is not required. The addition of the mentioned material flows as dilution streams can be implemented in any mixing combination and ratio desired.
The olefin-free gas is preferably hydrogen, methane or a mixture of these substances. The olefin-lean gas is also preferably a gas which contains hydrogen or methane as main component or both. It is also possible, however, to add a different gas to the material flows supplied. This may, for instance, be alkanes or carbon dioxide. The olefin-rich, olefin-lean or the olefin-free material flow material may eventually be mixed in any form desired. Advantageously they also do not contain any undesired foreign gases.
The feed stream is preferably supplied via the head of the hydrogenation reaction reactor. The proportion of the gas supplied at the head is basically optional, preferably, however, it ranges between 1 and 99 percent by mass. Ideally the material flow of the gas supplied at the head ranges between 5 and 15 percent by mass. By the overall hydrogenation reaction it is possible to produce a feed stream which has a content of organic sulphur compounds of below 100 ppb. In a subsequent gas scrubbing process it is possible to remove the hydrogen sulphide so that a gas is obtained which is basically free of sulphur.
The feed stream as feed stream for the hydrodesulphurisation preferably contains light olefins which are in gaseous form at the operating temperature. These are preferably in the C-number range from 2 to 6. It is also possible, however, to use higher olefins which are in liquid form at the operating temperature or heavier hydrocarbons. These may also be in the higher C-number range. As feed stream it is basically possible to use all olefins that allow desulphurisation by hydrogenation and scrubbing.
The hydrogenation reaction is preferably carried out at a temperature of 150 to 500° C. Optimum temperatures range between 250 and 400° C. The feed stream is therefore preferably introduced into the reactor at a temperature of 200 to 400° C. With particularly suitable reaction parameters the feed stream is introduced into the reactor at a temperature of 250° C. to 350° C. The respective temperature in the reactor will then emerge from the prevailing reaction parameters. The introduction of an olefin-leaner feed stream in a suited place will cool down the reaction mixture. By controlling the reaction parameters via the olefin content of the feed streams it is much easier to control the pressure inside the reactor. In a favourable type of configuration the latter ranges between 0.1 and 10 MPa.
Heating of the feed stream up to the temperature required for the reaction may be done in any way desired. For this purpose, burners or steam heaters, for example, may be used. Heating of the feed stream will, however, preferably be implemented via heat exchangers in any place desired. As a heating agent the heated material flow in the reactor may be used. The heat exchangers may be used for heating in any place desired as, for example, on the individual feed streams. Heating may also be done on the material flows which are introduced into the feed streams. It may also be done on the feed stream which is introduced at the reactor head.
In an embodiment of the inventive process, the process for hydrodesulphurisation is followed by a gas scrubbing process or a separation of hydrogen sulphide, which may be of any type and at any point of the process desired. The process for hydrodesulphurisation may be followed, for example, by an adsorption process using a chemical adsorbent.
The invention also claims a contrivance which serves to run the process according to the invention. Especially claimed is a contrivance which is characterised in that
These are feed lines which allow introducing an olefin-rich material flow into the respective feed stream. In such case, the olefin content in the feed stream increases and the temperature in the subsequent catalyst bed increases accordingly. These may also be feed lines for an olefin-lean or olefin-free material flow to reduce the olefin content in the feed streams accordingly. The feed lines for material flows may be installed at any point of the reactor or the feed lines for the feed streams. These may also be used in any combination desired.
This serves to ensure accurate dosage of the olefin amount in the feed streams. In addition, it is thus possible to control the temperature in the reactor precisely. For splitting the gas flow, a device for splitting the feed stream is installed directly in the feed line for the fresh feed stream. The inventive device also comprises valves by which the supply of gas to the individual spray or injection devices in the reactor can be controlled precisely. Depending on the heating extent of the gas in the individual catalyst beds, the amount of material feed is dosed. In this way it is possible to maintain the temperature inside the reactor within the specified temperature limits.
If the feed stream is passed through more than two catalyst beds, the reactor is fitted with additional catalyst beds. Also included are the required additional feed devices for the feed streams and material flows. In such case a contrivance is claimed, in which
The feed rate and the composition of the feed stream into the reactor are preferably controlled via the temperature as parameter. Hence temperature sensors or thermometers can be installed in any place inside the reactor. Likewise there may be heating or cooling devices in any place of the inventive contrivance, which allow for additional temperature control. It goes without saying that the inventive contrivance also comprises the required control devices, no matter if these are of electric, electronic or mechanical nature. It is also possible, however, to control the feed rate and the composition of the supplied material flow via other signals as, for example, the sulphur or olefin content of the gas or of a combination of these measured values. For this purpose, there may be measuring sensors in any place of the feed lines or inside the reactor.
The contrivance according to the invention is shown in principle in patent DE 102008059243 A1. The latter differs from the present contrivance especially by the additional pipelines for olefin-containing feed streams.
The contrivance according to the invention may further comprise other devices in any place which are required to maintain optimum operation. These may be, for example, valves, pumps, gas manifolds or gas conveying devices. These may likewise be sensors, thermometers, flow meters or analysis instruments. These may be installed in any place of the inventive contrivance.
The inventive process and the inventive contrivance allow carrying out the hydrodesulphurisation of olefin-containing gases with minor equipment and without extensive cooling or heating devices. The desulphurisation is effective so that the sulphur content of the feed stream in the subsequent gas scrubbing process can be reduced to the ppb range (ppb: parts per billion, 10−7 mole percent). The process provides for reliable and safe temperature control and handling of the process. The inventive process yields a product gas which basically still only contains hydrogen sulphide in the form of a sulphur compound.
The contrivance according to the invention is illustrated in more detail by means of a drawing, the embodiment not being limited to this drawing.
Number | Date | Country | Kind |
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10 2009 032 802.5 | Jul 2009 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2010/004092 | 7/7/2010 | WO | 00 | 6/27/2012 |