DE102013014866A1 - Process and plant for the production of hydrocarbon products - Google Patents

Abstract

The invention relates to a process for producing hydrocarbon products comprising providing a hydrocarbon stream (C4) comprising predominantly branched and unbranched hydrocarbons each having four carbon atoms. From this, a first and a second partial stream (i-C4, n-C4) are obtained, wherein the first partial stream (i-C4) predominantly branched hydrocarbons having four carbon atoms and the second partial stream (n-C4) predominantly unbranched hydrocarbons having four carbon atoms having. The method further comprises steam splitting at least a portion of the first substream (i-C4) at a first, higher splitter sharpness and at least a portion of the second substream (n-C4) at a second, lower splitter sharpness. A corresponding system is also the subject of the invention.

Description

The invention relates to a method and a plant for the production of hydrocarbon products according to the preambles of the independent claims.

State of the art

Methods and apparatus for steam cracking of hydrocarbons are known and, for example, in the article "Ethylene" in Ullmann's Encyclopedia of Industrial Chemistry, online since April 15, 2007, DOI 10.1002 / 14356007.a10_045.pub2 , described.

In recent processes and devices for steam cracking increasingly mild cleavage conditions are used (see below), because in this particular so-called value products, such as propylene and butadiene, win with improved yield, as explained below. At the same time, however, the reaction of the furnace insert also decreases with mild cleavage conditions, so that compounds contained in it are found in a comparatively large amount in the cleavage gas and lead to a "dilution" of the desired products.

Object of the present invention is to remedy this situation and while maintaining the advantages of mild cleavage conditions to avoid their disadvantages. In particular, by reducing the mentioned dilution effect, the concentration and amount of the desired products, in particular 1,3-butadiene, should be increased.

Disclosure of the invention

This object is achieved by a method and a plant for the production of hydrocarbon products with the features of the independent claims. Preferred embodiments are subject of the dependent claims and the following description.

Before explaining the features and advantages of the present invention, its principles and the terms used will be explained.

Steam-cracking processes are carried out on a commercial scale almost exclusively in tubular reactors in which individual reaction tubes (in the form of coils, so-called coils) or groups of corresponding reaction tubes can also be operated under different clearance conditions. Reaction tubes or groups of reaction tubes operated under identical or comparable fission conditions, if appropriate, but also operated under uniform fission conditions, are referred to below as "cracking furnaces". A cracking furnace in the language used here is thus a structural unit used for the vapor cracking, which equates to a furnace insert or exposes it to comparable cracking conditions. A steam cracking plant may have one or more such cracking furnaces.

The term "furnace insert" here refers to one or more liquid and / or gaseous streams which are fed to one or more cracking furnaces. Also, streams obtained by a corresponding steam cracking process, as explained below, may be recycled to one or more cracking furnaces and reused as furnace feed. As a furnace insert is a variety of hydrocarbons and hydrocarbon mixtures of ethane to gas oil up to a boiling point of typically 600 ° C.

A furnace insert can consist of a so-called "fresh use", ie an insert which is provided externally and obtained, for example, from one or more petroleum fractions, natural gas components having two to four carbon atoms and / or natural gas condensates. A furnace insert can also consist of one or more so-called "recycle streams", ie streams that are generated in the plant itself and returned to a corresponding cracking furnace. A furnace insert may also consist of a mixture of one or more fresh feeds with one or more recycle streams.

The furnace insert is at least partially reacted in the respective cracking furnace and leaves the cracking furnace as a so-called "raw gas", which, as described below with reference to the 1A and 1B can be subjected to a series of post-treatment steps. Such post-treatment steps comprise first a treatment of the raw gas, for example by quenching, cooling and drying, whereby a so-called "cracking gas" is obtained. Sometimes, the raw gas is already referred to as cracking gas.

In particular, current processes include the separation of the split gas into a series of fractions based on the different boiling points of the components contained. In the art, abbreviations are used which indicate the carbon number of the predominantly or exclusively contained hydrocarbons. Thus, a "C1 fraction" is a fraction which contains predominantly or exclusively methane (but conventionally also hydrogen under certain circumstances, then also called "C1minus fraction"). By contrast, a "C2 fraction" contains predominantly or exclusively ethane, ethylene and / or Acetylene. A "C3 fraction" contains predominantly propane, propylene, methyl acetylene and / or propadiene. A "C4 fraction" contains predominantly or exclusively butane, butene, butadiene and / or butyne, it being possible for the respective isomers to be present in different proportions, depending on the source of the C4 fraction. The same applies to a "C5 fraction" and the higher fractions. Several such fractions can also be summarized in terms of process and / or notation. For example, a "C2plus fraction" contains predominantly or exclusively hydrocarbons having two or more and a "C2minus fraction" predominantly or exclusively hydrocarbons having one or two carbon atoms.

Liquid and gaseous streams may be rich or poor in one or more components as used herein, with "rich" for a content of at least 90%, 95%, 99%, 99.5%, 99.9%, 99.99 % or 99.999% and "poor" for a content of at most 10%, 5%, 1%, 0.1%, 0.01% or 0.001% on a molar, weight or volume basis. The term "predominantly" refers to a content of at least 50%, 60%, 70%, 80% or 90% or corresponds to the term "rich". Liquid and gaseous streams may also be enriched or enriched in one or more components as used herein, which terms refer to a corresponding level in a starting mixture from which the liquid or gaseous stream was obtained. The liquid or gaseous stream is "enriched" if it is at least 1.1 times, 1.5 times, 2 times, 5 times, 10 times, 100 times or 1000 times, "depleted" if it contains not more than 0,9 times, 0,5 times, 0,1 times, 0,01 times or 0,001 times the content of a corresponding component, relative to the starting mixture. A current "derived" from a respective output current may be formed, for example, by tapping off or disconnecting from the output current or by combining with at least one further current.

The mentioned "cracking conditions" in a cracking furnace include, inter alia, the partial pressure of the furnace insert, which can be influenced by the addition of different amounts of steam and the set pressure in the cracking furnace, the residence time in the cracking furnace and the temperatures and temperature profiles used therein. The furnace geometry and furnace design also plays a role. To produce ethylene, a cracking furnace is operated, for example, at an oven inlet temperature of 500 to 680 ° C. and at a furnace outlet temperature of 775 to 875 ° C. Here, the "furnace inlet temperature" is the temperature of a gas stream at the beginning of a reaction tube and the "furnace outlet temperature" is the temperature of a gas stream at the end of a reaction tube. Typically, the latter is the maximum temperature to which the corresponding gas stream is heated. The furnace insert is at a, also measured at the furnace outlet pressure of 165 to 225 kPa steam in a ratio of typically 0.25 to 0.85 kg / kg added. The specific values used depend on the particular furnace used and the desired fission products.

Since the values mentioned influence each other at least partially on each other, the term "cracking severity" has been used to characterize the fission conditions. For liquid furnace inserts, the gap resolution can be described by the ratio of propylene to ethylene (P / E) or by the ratio of methane to propylene (M / P) in the cracked gas on a weight basis (kg / kg). The P / E and M / P ratios are directly dependent on the temperature, but, in contrast to the real temperature in or at the exit of a cracking furnace, they can be measured much more accurately and used, for example, as a controlled variable in a corresponding control method. However, the P / E ratio is only conditionally suitable for characterizing the resolution of gaseous furnace inserts or compounds having two to four carbon atoms.

For gaseous furnace inserts, the conversion or conversion of a respective considered component of the furnace insert can be specified as a measure of the gap resolution. The term conversion or conversion (English Conversion) is here as commonly used in the art (see, for example, the aforementioned article "Ethylene" in Ullmann's Encyclopedia of Industrial Chemistry). In particular, for the C4 fractions or C4 substreams used in the present case, a description of the resolution of the gap via the reaction of key components such as n-butane and isobutane is well suited.

The splitting or cleavage conditions are "sharp" when more than 92% of n-butane is reacted in a corresponding fraction. At even sharper cleavage conditions, n-butane may also be converted to greater than 93%, 94% or 95%. A conversion of n-butane to 100% typically does not occur. The upper limit of the "sharp" splitting or cleavage conditions is therefore for example 99%, 98%, 97% or 96% conversion of n-butane. On the other hand, the splitting or cleavage conditions are "mild" when n-butane is converted to less than 92%. With less than 91%, less than 90%, less than 89%, less than 88% or less than 87% conversion of n-butane, increasingly milder splitting or cleavage conditions are present. With less than 86% conversion of n-butane, the gap sharpening or Cleavage conditions here referred to as "very mild". Very mild splitting or fission conditions also include, for example, a conversion of n-butane to less than 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%. , 70% or 65% and more than 50% or 60%.

The gap sharpening or the gap conditions are also "sharp" even if iso-butane is converted in a corresponding fraction to more than 91%. If the fissuring conditions are even sharper, iso-butane may also be converted to more than 92%, 93% or 94%. A conversion of iso-butane to 100% is typically not. The upper limit of the "sharp" splitting or cleavage conditions is therefore, for example, 99%, 98%, 97% or 96% conversion of isobutane. On the other hand, the gap sharpening or the cleavage conditions are "mild" when iso-butane is converted to less than 91%. With less than 90%, less than 89%, less than 88%, less than 87% or less than 86% conversion of iso-butane, increasingly milder splitting or cleavage conditions are present. With less than 83% conversion of iso-butane, the gap-sharpening or cleavage conditions are referred to herein as "very mild". Very mild splitting or fission conditions also include, for example, a conversion of iso-butane to less than 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75% or 70% and to more than 45%. or 50%.

The mentioned gap sharpening or cleavage conditions depend in particular on the above-explained furnace outlet temperature at the end of the reaction tube or slit furnaces used in each case. The higher this is, the "sharper", the lower, the "milder" the gap sharpening or gap conditions.

It is further understood that the reaction of other components need not be identical to that of n- and isobutane. For example, when 1- and 2-butene are cleaved together with n-butane, they are typically reacted to a greater extent than the n-butane. Conversely, iso-butene is converted to a lesser extent than iso-butane when cleaved with it. With a percentage conversion of a key component, here n-butane or iso-butane, therefore, in each case one furnace outlet temperature and the respective percentage conversions of the other components in use are linked. This furnace outlet temperature is in turn dependent, among other things, on the cracking furnace. The offset between the respective percentage conversions depends on a number of other factors.

Advantages of the invention

The present invention starts from a process for producing hydrocarbon products which provides a hydrocarbon stream comprising predominantly branched and unbranched hydrocarbons having four carbon atoms (hereinafter also referred to as C4 fraction or C4 stream, abbreviated C4). In that regard, the process of the invention corresponds, for example, to known processes for the production of hydrocarbon products by steam cracking, in which such a C4 fraction is separated from a cracking gas which has possibly been treated accordingly. This can be done in known systems in a so-called Debutanizer (but also separates all other hydrocarbons with four carbon atoms from a corresponding hydrocarbon stream). Details of this are shown in the referenced article "Ethylene" in Ullmann's Encyclopedia of Industrial Chemistry, and with reference to the 1A and 1B illustrated.

However, the invention is not limited to the use of C4 streams provided by steam columns and downstream process steps, but is equally suitable for C4 streams which are at least partially produced by other processes, for example by refinery processes. For example, the invention can be used with C4 streams that have not previously been steam split and then fed to a corresponding steam cracking process. These may be, for example, petroleum fractions, natural gas components having two to four carbon atoms, natural gas condensates and the like.

The invention now provides, from the mentioned hydrocarbon stream having predominantly branched and unbranched hydrocarbons having four carbon atoms, a first and a second partial stream to win, wherein the first partial stream predominantly branched hydrocarbons having four carbon atoms and the second partial stream predominantly unbranched hydrocarbons with four Has carbon atoms. The first partial stream is hereinafter also referred to as iso-C4 fraction or iso-C4 stream (abbreviated to iso-C4), the second sub-stream also as n-C4 fraction or n-C4 stream (n-C4).

The invention further contemplates splitting at least a portion of the first sub-stream or a stream derived therefrom at a first, higher splitter sharpness and at least a portion of the second sub-stream or a stream derived therefrom at a second, lower splitter sharpness. The "columns" includes, the corresponding Partial flow (or a corresponding proportion) alone or together with other streams, possibly also after previous combination to a collecting stream to feed into a cracking furnace according to the definition made at the outset and remove the cracking furnace, a cracked gas.

The terms "higher" and "lower" used to characterize the gap sharpening relate to each other. In other words, at least a portion of the first partial flow is split at a first gap sharpness and at least a portion of the second partial flow at a second gap sharpness, wherein the first gap sharpness is higher than the second and the second is less than the first.

The steam splitting of C4 fractions of different origin is state of the art. A reliable prediction of the split result is possible with the existing tools. As a rule, these are mixtures of branched and unbranched C4 compounds. In the previously mentioned refining operations, these predominantly include paraffinic compounds, in recycle streams of steam cracking processes or in products of other processing methods (eg from refineries) predominantly olefinic compounds.

In particular, in the case of naphtha cleavage under mild cleavage conditions or a high proportion of C4 fresh inserts, the fraction of the C4 fraction obtained from the corresponding cleavage gas is also large and, in particular, relatively weakly concentrated at 1,3-butadiene and optionally at other value products derived from C4 Fraction should be extracted. As a result, the recovery of 1,3-butadiene is uneconomical.

In particular, in the steam cracking of hydrocarbons at unusually mild cleavage conditions, it is therefore, as mentioned, to a significant increase in the amount of some product fractions and an associated reduction in the concentration of added value products (dilution effect). The recovery of the value products is made more difficult or more expensive.

The invention is based on the finding that branched C4 compounds in the cracking furnace contribute to the formation of 1,3-butadiene to a limited extent owing to their structure. Relatively high methane formation from such compounds is unavoidable, especially when the branched C4 compounds are recycled to completion. Thus, when C4 mixtures are split under mild or even very mild conditions, C4 fractions result in relatively high mass flows with a simultaneously low concentration of 1,3-butadiene.

This effect is counteracted according to the invention by separating the C4 fraction prior to steam splitting, for example by distillation, into iso and n-C4 substreams (the first and second substreams mentioned) and cleaving them under different conditions. The (first) iso-C4 substream is split sharper than the (second) n-C4 substream, the (first) iso-C4 substream in particular very sharp, the (second) n-C4 substream particularly particularly mild is split.

By maintaining the advantages of the invention, the disadvantages of the mild cleavage are reduced or completely avoided, ie. H. the amount of C4 fraction is reduced, thereby increasing the concentration of the target product, here in particular 1,3-butadiene. The specific extraction effort is reduced.

The essence of the invention thus consists in minimizing the C4 fraction as a whole by deliberately increasing the structural conversion of iso-C4 compounds by sharp cleavage conditions after prior separation of n-C4 compounds. As a result, the selective application of mild, in particular very mild gap conditions on the n-C4 compounds is made possible, so that the achievable by these high selectivities, eg. B. in the direction of 1,3-butadiene can be achieved.

Particular advantages are obtained if the first partial stream, that is to say that which has predominantly branched hydrocarbons with four carbon atoms, is at least partially subjected to a hydrogenation process before the steam cracking at the first, higher atomic resolution. Here, the iso-butene (olefinic) is at least partially converted to iso-butane (paraffinic). In the context of the present invention, it has been found that the isobutane in the subsequent cleavage process, d. H. at the first, higher slit sharpness, easier or more usable products can be implemented. This allows a further reduction in the amount of C4 fraction and thereby a concentration of the target products, as mentioned above.

For the hydrogenation of olefins or olefin-containing hydrocarbon mixtures, numerous catalytic processes are known from the prior art, which can also be used in the context of the present invention. Hydrogenation catalysts have as hydrogenation-active component one or more elements of the 6th, 7th or 8th subgroup of the periodic table in elemental or bound form. They may be doped with various additives to affect certain catalyst properties, such as lifetime, resistance to certain catalyst poisons, selectivity, or regenerability. The hydrogenation catalysts contain the hydrogenation-active Component many on carriers, such as mordenites, zeolites, Al2O3 modifications, SiO2 modifications and others. For the substantial hydrogenation of the olefins reaction temperatures of 150 to 250 ° C are generally used.

The method variants explained above may comprise at least partially forming the mentioned hydrocarbon stream from which the first and the second substream are obtained from at least one split gas stream which is generated together with fresh feed in the steam splitting of the first and second substreams according to the invention or corresponding proportions thereof.

However, the hydrocarbon stream may also be formed, at least in part, from a cracking gas obtained by steam cracking a fresh feed, or from an uncleaved fresh feed. These variants allow a very flexible adjustment of the respective desired contents of the hydrocarbon stream with respect to the individual C4 compounds.

Advantageously, the first, higher splitting sharpness, which is used for the iso-C4 compounds results in a conversion of the isobutane contained to at least 91% or more, as explained above for the concept of slit-sharpness. For the iso-C4 compounds, therefore, sharp or very sharp gap sharpening or gap conditions are used. These may also correspond, for example, more than 92%, 93% or 94% and up to 99% conversion of iso-butane. The second, lower resolution, which is used for the n-C4 compounds, however, advantageously results in a conversion of the n-butane contained to at most 92% or less, as also explained above. For the n-C4 compounds, therefore, mild or very mild gap sharpening or cleavage conditions are used. For example, they may also be less than 90%, 88%, 86%, 84%, 82%, 80%, 78%, 76%, 74%, 72%, 70% or 65%, but more than 50% or 60, for example % Conversion of n-butane. With increasingly mild cleavage conditions arise in relation to the fresh use more desirable products such as butadiene and propylene, so that the yield increases and improves the product range.

The gap sharpening differences are normalized to a common underlying value, for example a conversion of n-butane or isobutane or both, by 1 to 20%, in particular by 2 to 20%.

Corresponding methods advantageously include the use of a vapor quantity of 0.4 kg / kg, in particular from 0.2 to 0.7 kg / kg, for example from 0.3 to 0.5 kg / kg at the first, higher splitting acuity and the use a vapor amount of 0.4 kg / kg, in particular from 0.2 to 0.7 kg / kg, for example from 0.3 to 0.5 kg / kg at the second, lower resolution. The values used in each case may be the same or different and, in particular, adapted to further split inserts.

The method according to the invention proves to be particularly advantageous if the steam splitting in the first, higher splitting sharpness and / or the steam splitting in the second, lower splitting sharpness is in each case carried out in at least one cracking furnace to which at least one further furnace insert is supplied. For example, it is possible to use a cracking furnace designed for a corresponding throughput, which is operated at the second, lower gap sharpness and in which not only the second part-stream with the n-C4 compounds but also a "regular" fresh use is mildly split. The iso-C4 compounds can be cleaved alone in a cleavage oven. However, in certain cases, for example when similar cracking furnaces are used for cost reasons, it may be more appropriate to sharply split the iso-C4 compounds together with a fresh feed.

As mentioned, the present invention has the particular purpose of improving a process in which 1,3-butadiene is separated from the hydrocarbon stream. All known processes for the extraction of 1,3-butadiene are suitable here.

Further advantages may be obtained if isobutene present in the hydrocarbon stream is at least partially converted to a tert-butyl ether after the separation of the 1,3-butadiene and this is also extracted. The preparation of methyl tert-butyl ether (2-methoxy-2-methylpropane, MTBE) is basically known. MTBE is produced industrially acid catalyzed from isobutene and methanol, which is added to the hydrocarbon stream. MTBE is mainly used as an anti-knock agent but is also finding increasing use as a solvent and extractant in organic chemistry. Ethanol gives ethyl tert-butyl ether. Other alcohols can be used.

Also advantageous is a process in which 1-butene present in the hydrocarbon stream is at least partially hydroisomerized to 2-butene after the at least partial conversion of the isobutene. The resulting 2-butene can be converted particularly selectively to the desired butadiene in the subsequent mild cleavage. Corresponding hydroisomerization processes are also known. For example, this can also be a Removal of remaining traces of butadiene done.

It may also be advantageous for the C4 hydrocarbon stream, which comprises predominantly branched and unbranched hydrocarbons each having four carbon atoms, before or after hydroisomerization or another process, at least one further stream, in particular a butene (C4-acetylene) and / or Feed hydrocarbons containing five carbon atoms. For example, co-extracted C5 compounds may be used in a butadiene extraction and fed to meaningful use.

The plant according to the invention for the production of hydrocarbon products benefits from the advantages explained above, to which reference is expressly made. It has means adapted to provide a hydrocarbon stream comprising predominantly branched and unbranched hydrocarbons each having four carbon atoms.

Furthermore, at least one separation device is provided, which is adapted to recover a first and a second partial stream from the hydrocarbon stream, wherein the first partial stream predominantly branched hydrocarbons having four carbon atoms and the second partial stream predominantly unbranched hydrocarbons having four carbon atoms.

The system additionally comprises at least one vapor-splitting device which is set up to split at least a part of the first sub-stream at a first, higher gap sharpness and at least a part of the second sub-stream at a second, lower gap sharpness.

The system according to the invention is advantageously set up for carrying out a method, as explained above.

The at least one separating device advantageously comprises at least one separating column, and the steam-splitting device advantageously comprises at least one cracking furnace, which is set up for operation at the first, higher splitting power, and at least one cracking furnace, which is set up for operation at the second, lower splitting power.

The invention is explained below with reference to the accompanying figures over the prior art.

Brief description of the drawings

1A schematically illustrates the process of a method for producing hydrocarbons according to the prior art.

1B schematically illustrates the process of a method for producing hydrocarbons according to the prior art.

2 schematically illustrates the flow of a method for producing hydrocarbons according to an embodiment of the invention.

In the figures, corresponding elements are provided with identical reference numerals and will not be explained repeatedly for the sake of clarity.

Detailed description of the drawings

In 1A the sequence of a process for the production of hydrocarbons according to the prior art is shown in the form of a schematic flow chart. The core of the process is a steam cracking process 10 using one or more cracking furnaces 11 to 13 can be carried out. The following is only the operation of the cracking furnace 11 explains the other cracking furnaces 12 and 13 can work in the same way.

The cracking furnace 11 is charged with a stream A as a furnace insert, which may be at least partially a so-called fresh use, which is provided from external sources, and partly to a so-called recycle stream, which is obtained in the process itself, as below explained. Also the other cracking furnaces 12 and 13 can be charged with appropriate currents. Different streams can also be used in different cracking furnaces 11 to 13 can be fed, a stream can be divided into several cracking furnaces or multiple streams can be combined to form a collection stream, for example, as stream A one of the cracking furnaces 11 to 13 is supplied.

By steam cracks in the steam cracking process 10 a crude gas stream B is obtained, which is sometimes referred to at this point as a gap gas stream. The raw gas stream B is in a series of unillustrated treatment stages of a treatment process 20 treated, for example, subjected to a so-called oil quench, pre-fractionated, compressed, further cooled and dried.

The correspondingly treated stream B, the actual cracked gas C, is subsequently subjected to a separation process 30 subjected. In this will be obtained a number of fractions, which are referred to here, as explained above, according to the carbon number of the predominantly contained hydrocarbons. The Indian 1A illustrated separation process 30 works on the principle "Demethanizer First", a separation process according to the principle "Deethanizer First" is in 1B shown.

In the separation process 30 is from the cracked gas C first in a first separation unit 31 (the so-called demethanizer) a C1 or C1minus fraction (denoted by the reference C1) separated gaseous, which, if not previously removed, may also contain hydrogen. It is typically used as fuel gas. There remains a liquid C2plus fraction (reference C2 +), which in a second separation unit 32 (the so-called deethanizer) is transferred.

In the second separation unit 32 From the C2plus fraction a C2 fraction (C2) is separated in gaseous form and, for example, a hydrotreatment process 41 subjected to convert contained acetylene to ethylene. Subsequently, the C2 fraction is in a C2 separation unit 35 in ethylene (reference C2H4) and ethane (C2H6). The latter can be used as recycle stream D in one or more cracking furnaces 11 to 13 again the steam cracking process 10 be subjected. In the example shown, the recycle streams D and E are added to stream A. The recycle streams D and E and the stream A can also be in different cracking furnaces 11 to 13 be guided.

In the second separation unit 32 remains a liquid C3plus fraction (reference C3 +), which in a third separation unit 33 (the so-called depopanizer) is transferred. In the third separation unit 33 From the C3plus fraction a C3 fraction (reference C3) is separated and another hydrotreatment process 42 to convert propylene contained in the C3 fraction to propene. Subsequently, the C3 fraction is in a C3 separation unit 36 in propene (reference C3H6) and propane (reference C3H8) separated. The latter can be used as recycle stream E in one or more cracking furnaces 11 to 13 , separately or with other streams, again the steam cracking process 10 be subjected.

In the third separation unit 33 Accordingly, a liquid C4plus fraction (reference C4 +), which is in a fourth separation unit remains 34 (the so-called Debutanizer) is transferred. In the fourth separation unit 34 is separated from the C4plus fraction a C4 fraction (reference C4). There remains a liquid C5plus fraction (reference C5 +).

It is understood that all of the fractions shown can also be subjected to suitable post-treatment steps. For example, as shown below, 1,3-butadiene can be separated from the C4 fraction. It is also possible to use additional recycle streams, which are analogous to the recycle streams D and E, the steam splitting process 10 can be subjected.

In 1B the flow of an alternative method for producing hydrocarbons by steam cracking according to the prior art is shown in the form of a schematic flow chart. Again, the core of the process is a steam cracking process 10 using one or more cracking furnaces 11 to 13 can expire. Unlike the in 1A illustrated method here is the cracking gas C an alternative separation process 30 subjected to the principle of "Deethanizer First".

In the separation process 30 is from the cracked gas C first in a first separation unit 37 a C2-minus fraction (reference C2-) separated gaseous, which may contain predominantly methane, ethane, ethylene and acetylene and, if not previously removed, even hydrogen. The C2minus fraction becomes a total hydrotreatment process 43 subjected to reacting acetylene to ethylene. Subsequently, from the C2minus fraction in a C2minus separation unit 38 a C1 fraction is separated and used as above. There remains a C2 fraction that is in a C2 separation unit 35 as separated above in ethylene and ethane. The latter can also be used here as recycle stream D in one or more cracking furnaces 11 to 13 again the steam cracking process 10 be subjected. In the first separation unit 37 remains a liquid C3plus fraction, which in the separation units 33 to 36 and the hydrotreatment unit 42 , how to 1 explained, treated.

The skilled worker is, for example, from the aforementioned article "Ethylene" in Ullmann's Encyclopedia of Industrial Chemistry, several other alternative methods known, which differ in particular in the preparation of the cracking gas C and / or the separation process used.

The C4 fraction may also be partially recycled as a corresponding recycle stream in one or more of the cracking furnaces 11 to 13 again the steam cracking process 10 be subjected. However, especially when mild cleavage conditions are used, branched C4 compounds (iso-C4 compounds) contained in the C4 fraction can be converted to a lesser extent than n-C4 compounds and are therefore found to be a large part again in the split gas stream C again. The iso-C4 compounds are therefore circulated several times through a corresponding system. The consequence of such a mild vapor cracking is thus a significant increase in the quantity of some product fractions, here the iso-C4 compounds, and a concomitant reduction in the concentration of value-added products, here for example 1,3-butadiene, by dilution effects. The recovery of the value products is made more difficult or more expensive. In other words, the iso-C4 compounds are structurally virtually unaffected by 1,3-butadiene formation. The formation of a relatively high amount of largely worthless methane is unavoidable, especially if the iso-C4 compounds are recycled to completion.

If, therefore, C4 fractions are cleaved with iso-C4 compounds, regardless of their origin, under mild or very mild conditions, this in turn results in C4 product fractions of relatively high mass flows with a simultaneously low 1,3-butadiene concentration.

In 2 the sequence of a process for the production of hydrocarbons by steam cracking according to an embodiment of the invention is shown in the form of a schematic flow chart. Again, the core of the process is a steam cracking process 10 that using pitching ovens 11 to 13 can expire. To illustrate the universal applicability of the method shown here, the recovery of a C4plus fraction from the cracking gas C is not shown, but this can, as in the 1A and 1B or in any other manner known in the art. The C4plus fraction becomes a separation unit in the example shown here 34 supplied, which operates as described above. However, if no or only a few C5plus hydrocarbons are formed in a steam cracking process, the use of this separation unit could 34 also be waived. However, a C4 fraction can also be from external equipment, z. From a refinery.

One example from the separation unit 34 C4 fraction obtained can be a 1,3-butadiene recovery unit 50 in which 1,3-butadiene, here referred to as BD, is extracted. 1,3-butadiene is one of the desired products of value here, the remaining portions of the C4 fraction C4 are to a predominant proportion of lesser economic value and "dilute" the desired 1,3-butadiene, which makes its extraction difficult.

The invention provides according to the illustrated embodiment, in a separation unit 39 Iso-C4 and n-C4 compounds (here referred to as i-C4 and n-C4), ie branched and unbranched C4 compounds, to separate from each other and to obtain corresponding partial flows. The substream, which contains predominantly the iso-C4 compounds, is referred to herein as the "first substream". This can be recycled as recycle stream H and either again the steam cracking process 10 or one separately from the steam cracking process 10 implemented further steam splitting process. Preferably, the first partial stream with the iso-C4 compounds is subjected to severe cleavage conditions, for which purpose the cracking furnace 12 is set up. Previously, hydrogenation of iso-butene can be done, as with block 44 illustrated. A the cracking furnace 12 removed stream G can for example be added to the cracking gas C, possibly after this also previously the treatment process 20 was subjected.

The partial stream, which contains predominantly the n-C4 compounds, can be recycled as recycle stream F and here again either the steam cracking process 10 or even separately to the steam cracking process 10 implemented further steam splitting process. The n-C4 compounds are preferably subjected to mild to very mild cleavage conditions, for which purpose the cracking furnace 13 is set up. A the cracking furnace 13 taken stream I can be added, for example, to the cracking gas C, possibly after this before the treatment process 20 was subjected.

Although not shown, it is understood that the cracking furnaces 11 to 13 even more recycle streams or fresh inserts can be supplied.

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited non-patent literature

• "Ethylene" in Ullmann's Encyclopedia of Industrial Chemistry, online since April 15, 2007, DOI 10.1002 / 14356007.a10_045.pub2 [0002]

Claims (15)

Process for producing hydrocarbon products comprising: a) providing a hydrocarbon stream (C4) which comprises predominantly branched and unbranched hydrocarbons each having four carbon atoms, marked by b) obtaining a first and a second substream (i-C4, n-C4) from the hydrocarbon stream (C4), wherein the first substream (i-C4) predominantly branched hydrocarbons having four carbon atoms and the second substream (n-C4) predominantly having unbranched hydrocarbons having four carbon atoms, and c) vapor gaps of at least part of the first partial flow (i-C4) or of a current derived therefrom at a first, higher gap resolution and at least part of the second partial flow (n-C4) or a current derived therefrom at a second, lower gap sharpness. The method of claim 1, wherein the first partial stream (i-C4) is at least partially subjected to a hydrogenation process before the vapor cracking at the first, higher gap sharpness. Process according to Claim 1 or 2, in which the hydrocarbon stream (C4) provided according to a) is generated at least partly from at least one cracked gas (C) obtained by steam cracking according to c). Process according to one of the preceding claims, in which the hydrocarbon stream (C4) provided according to a) is generated, at least partially, from a cracked gas (C) which comprises steam splitting a fresh feed (A), in particular one or more petroleum fractions, natural gas components having two to four Carbon atoms and / or natural gas condensates is formed. Process according to one of the preceding claims, in which the hydrocarbon stream (C4) provided according to a) is at least partially formed from an uncleaved fresh feed (A), in particular from one or more petroleum fractions, natural gas natural gas components having two to four carbon atoms and / or natural gas condensates. Method according to one of the preceding claims, wherein the first, higher resolution in a ratio of iso-butane in the first partial stream of more than 91%, in particular more than 92%, 93% or 94% and up to 99%, and the second, lower splitting sharpness in a conversion of n-butane in the second partial stream of less than 92%, in particular less than 90%, 88%, 86%, 84%, 82%, 80%, 78%, 76%, 74%, 72%, 70% or 65% and more than 50% or 60%. Method according to one of the preceding claims, in which the first, higher splitting sharpness is higher by 1 to 30%, in particular by 2 to 20%, than the second, lower splitting sharpness. A method according to any one of the preceding claims, wherein the steam splitting at the first, higher splitting power is effected using a steam amount of 0.4 kg / kg, in particular from 0.2 to 0.7 kg / kg, and the steam splitting at the second, lower Disk sharpness using a steam amount of 0.4 kg / kg, in particular from 0.2 to 0.7 kg / kg, is performed. Method according to one of the preceding claims, in which the steam splitting at the first, higher splitting sharpness and / or at the second, lower splitter sharpness in each case in at least one cracking furnace ( 12 . 13 ), to which at least one additional furnace insert (A) is supplied in the form of at least one recycle stream and / or at least one fresh feed. A process according to any one of the preceding claims, wherein 1,3-butadiene (BD) is separated from the hydrocarbon stream (C4) prior to recovering the first and second substreams (i-C4, n-C4) of b). Process according to Claim 10, in which isobutene present in the hydrocarbon stream (C4) is at least partly converted to a tert-butyl ether after the separation of the 1,3-butadiene (BD) and the tert-butyl ether is likewise separated off from the hydrocarbon stream (C4). The process of claim 11, wherein 1-butene contained in the hydrocarbon stream (C4) is at least partially hydroisomerized to 2-butene. Plant for the production of hydrocarbon products, comprising: a) means adapted to provide a hydrocarbon stream (C4) comprising predominantly branched and unbranched hydrocarbons of four carbon atoms each, characterized by b) at least one separator adapted to to recover a first and a second partial stream (i-C4, n-C4) from the hydrocarbon stream (C4), the first substream (i-C4) predominantly branched hydrocarbons having four carbon atoms and the second partial stream (n-C4) predominantly unbranched Having hydrocarbons having four carbon atoms, and c) at least one vapor-splitting device which is set up to split at least a part of the first sub-stream (i-C4) at a first, higher splitter sharpness and at least a part of the second sub-stream (n-C4) at a second, lower splitter sharpness. Installation according to Claim 13, which is set up to carry out a method according to one of Claims 1 to 12. Plant according to Claim 13 or 14, in which the steam-splitting device comprises at least one cracking furnace ( 12 ), which is set up for operation in the first, higher splitting sharpness, and at least one cracking furnace ( 13 ), which is set up for operation at the second, lower gap sharpness.

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