• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The invention relates to an apparatus for separating substantially unpressurised gas mixtures using membrane gas permeation comprising at least two separation stages which may be connected in parallel or in series, a compressor for pressurizing the gas mixture supplied in a feed line, optionally a second compressor for supplying a permeate a separation stage with pressure, as well as at least one recirculation line for at least one retentate and / or permeate of a separation stage, characterized by two pairs of separation stages (a1, a2; b1, b2), each via a conduit (Ra1; Rb1) for transferring the retentate from the two compressors (c1, c2) for applying the pressure to the respective first separating stage (a1; b1) of a pair with pressure; a line (Pa1. b1) of a pair; ) for forwarding the permeate of the first separation stage (a1) of a first pair (a1, a2) to the d the second separating stage pair (b1, b2) with pressurizing compressor (c2), one line each (Ra2; Rb2) for withdrawing the retentate of the respective second separation step (a2; b2) of the pairs; one line (Pa2: Pb2) for recycling the permeate of the respective second separation step (a2; b2) of the pairs; anda conduit (Pb1) for withdrawing the permeate of the first separation stage (b1) of the second separation stage pair (b1, b2).
    公开号:AT513644A1
    申请号:T1248/2012
    申请日:2012-11-27
    公开日:2014-06-15
    发明作者:Aleksander Makaruk；Michael Harasek
    申请人:Tech Universität Wien；
    IPC主号:
    专利说明:

    •·················································································
    The present invention relates to a method and a Permeatorsystem for the separation of gas mixtures, in particular for the separation of mixtures of methane and carbon dioxide, as obtained in the biomass fermentation in biogas plants.
    The fermentation of biomass has become increasingly important in recent years, as it can produce renewable methane, which is used as a substitute for the dwindling natural gas resource. In these processes are typically mixtures, which - in addition to components of air, hydrogen sulfide and gaseous organic compounds - mainly consist of methane (CH4) and carbon dioxide (CO2), from which the methane is obtained by gas separation in the purest possible form. For this purpose, the separation process used is primarily membrane gas permeation, mostly using polymer film membranes, with various combinations of different numbers of compressors and permeators, i. Membranes are used.
    Some such permeator systems are described in detail in the literature. Thus, references [1] to [5] all describe a one-step embodiment with only one separation membrane or separation step. Of course, this embodiment requires the least investment, but involves very high methane losses. Consequently, multi-permeation systems for the separation of CH4 and CO2 have also been extensively studied, but mainly in terms of natural gas production. Bhide and Stern [6] found that for a wide range of CO 2 concentrations in natural gas, the most economical configuration would be a three-stage permeator system with two compressors. Similarly, Spillman [7] and Qi and Henson [8] have noted, however, to reduce the cost of natural gas, they recommend a simpler two-stage configuration. Datta and Sen [9], however, have found that it is difficult to develop an optimal system for large concentration ranges of CO2 in natural gas, and Xu and Agrawal [10], [11] have suggested that optimal configuration may be due to minimal energy losses due to characterized by mixing. -1 - 2/37 Λ * • · · · ·······································································
    However, only a few researchers have dealt specifically with the evaluation of pemeator systems for biogas processing or the preparation of gas mixtures from biomass gasification processes. For example, Schell and Houston [3] have investigated not only the single-stage embodiment but also two-stage systems with one or two compressors and, optionally, permeate or retentate recycle. However, their conclusions are only of limited significance, especially as few concrete conceptual details are compared.
    In general, a major difference between natural gas and biogas is that the crude product gas produced in biomass fermentation in biogas plants is generally almost depressurized, while natural gas is typically under a high pressure of 30 to 150 bar, which has completely different requirements Interpretation of the separation systems provides.
    Several configurations K1 to K8 of multistage permeator systems according to the prior art are shown schematically in FIGS. 1 to 3 using the example of the separation of a gas mixture containing CH 4 and CO 2. K1 of FIG. 1 is described in references [1], [3] and [13] with reference to biogas and references [6], [9] and [12] relating to natural gas and comprises two separation stages a1 and a2 recycling the permeate from the second to the feed of the first stage. Ref. [13] shows that at average values for the area ratio Aa2 / Aai of the two membranes of a1 and a2, the methane yield can be increased almost without increasing the energy requirement. However, K1 generally requires enormous amounts of energy as the methane yield approaches 100% since large amounts of permeate must be recycled from a2. K2 from FIG. 1 comprises two separation stages a1 and b1, each with a compressor, wherein in b1 the permeate is separated from a1 and the resultant stream obtained as retentate is likewise obtained. K2 is described in Refs. [6] and [12] for natural gas. K3 from FIG. 1 is similar to K2, but here the retentate from b1 is recycled into the feed of a1. This configuration has been discussed in terms of both natural gas and biogas; see references [1], [6], [7], [9] and [12]. While Refs. [1] and [7] describe them as too expensive, the high costs in Ref. [9] are considered to be reasonable under certain circumstances. K4 of FIG. 1 is a three-stage combination of a single separation stage a1 with the configuration K1, shown here with two separation stages b1 and b2, wherein the permeate from a1 represents the feed of the separation stage b1. Their retentate is further separated in the permeator b2, whose retentate is obtained together with the retentate from a1, while the permeate of b2 is recycled into the feed of b1. C02-rich gas is extracted only in the form of the permeate from b1. This configuration has hardly been described so far; see ref. [9]. K5 and K6 of Fig. 2 are also three-stage embodiments, which can be regarded as a combination of K1 with the separation stages a1 and a2 and another permeator b1 with its own compressor. In both cases, the feed in the two stages a1 and a2 is purified to a CFL-rich stream, with the third stage retentate b1 being recycled either into the feed to a1 (K5) or to a2 (K6). Such configurations have also rarely been described; see, e.g. [8] and [9] as well as in the patent literature US 6,168,649 B1 (K5 shown in Fig. 2) and WO 2012/000727 A1 (K5 shown in Fig. 8). FIGS. 5 and 6 of WO 2012/000727 A1 show two further embodiments of three-stage permeator systems, in which - in contrast to K5 - in each case the permeate from stage a2 (instead of that from a1) is further purified, for which sometimes a third compressor is used. K7 of FIG. 3 herein is shown in FIG. 11 of WO 2012/000727 A1 (as a system according to the invention there) and represents another K5 similar system with three separation membranes, but does not include a separate (second) compressor in front of the permeator z1. However, as can also be deduced from the search report for WO 2012/000727 A1, such a system K7 was already known from US Pat. No. 6,565,626 B1. ································································································································ In both cases, in any case, the permeate from the first separation stage a1 is supplied to the permeator z1 without any further pressurization, while the retentate of the separation stage a1 is in turn further purified in the stage a2. Its retentate is finally recovered as CH4-rich gas, while its (nearly pressureless) permeate is recycled, combined with the feed to a1 and fed to the first compressor.
    Such purification of the permeate of one separation stage without pressurization by another membrane is also referred to as " intermediate expansion step " denotes that the already at a relatively low pressure permeant gas stream is allowed to expand through another separation membrane through. Since significantly lower pressure ratios between the feed / retentate side and the permeate side are achieved in the intermediate expansion stages as compared to a compressor pressurized permeator, significantly larger membrane areas are required to pass the desired amount of gas, i. to separate. Furthermore, by introducing an intermediate expansion stage into a permeator system, a visible effect, i. E. To achieve a higher gas purity in the permeate, it is usually necessary to use membranes with higher selectivities. However, these are less permeable / permeable, resulting in an even greater need for membrane area. For this reason, it has become common in the art not to regard such intermediate expansion stages as separate separation stages, which is also expressed herein for clarity by the different designation of the membrane ("z" instead of "a"). For the purposes herein, therefore, only those membranes are referred to and counted as a separation stage, which have a directly upstream compressor or fed exclusively with the retentate of a preceding separation stage, which is in relation to the corresponding permeate at a significantly higher pressure. Typical ratios between retentate and permeatseitigem pressure are between about 5: 1 and 50: 1. -4- 5/37
    K8 of Figure 3 is another separation system known from US 6,565,626 B1 with an intermediate expansion step where the permeate from separation stage a1 is allowed to pass through another separation membrane z1 without pressurization by an additional compressor. Its retentate is in turn recycled and mixed with the feed to the compressor preceding the first separation stage a1, while its permeate is further purified in a permeator b1 which is fed by a second compressor. Its permeate accumulates as C02-rich gas, while the retentate is recycled and forms the feed for membrane z1 together with the permeate of a1.
    This feed is therefore composed of a relatively pressureless permeate stream and a relatively high pressure retentate stream. Thus, the membrane z1 is not considered " true " in accordance with the current and previously discussed definition. own separation stage, but only to be regarded as an intermediate expansion stage. It turns out that for systems with three or more separation membranes and one, two or more compressors, there are various possibilities for the separation of gas mixtures, especially if additional intermediate expansion stages are also used.
    Of course, the known permeator systems K1 to K8 all have the disadvantage that the energy consumption increases almost exponentially if methane yields of more than 95% or even close to 100% are to be achieved. Moreover, there is no evidence in the literature for K5 and K6 that valuable (i.e., CH4) concentrations of < 1% (v / v) can be achieved in the permeate to be discarded, but this would be necessary in order to deliver the gas stream as exhaust gas ("offgas") to the environment without having to clean it consuming. For system K7, which comprises only a single compressor for two real separation stages and an intermediate expansion stage, WO 2012/000727 A1 describes separations of CH4 and CO 2 in the calculation examples in which methane contents in the CO 2 -rich gas of 0.5% (v / v) or less. However, membranes with a selectivity of 45 are used for this, and it is mentioned in the description that the selectivity is best even between 45 and -5-. Should be located. Specific information on energy consumption is missing completely. The same permeator system K7 is used as a comparative example, but using membranes with a selectivity of only 20, which verifiably yields a significantly worse result.
    With regard to system K8, in the numerous exemplary embodiments of US Pat. No. 6,565,626 B1, essentially methane / carbon dioxide separations (if appropriate in the presence of further gases, especially nitrogen) are calculated, but in all cases of a desired purity of the valuable substance CH4 of only around 96% is assumed and membranes with a selectivity of CO2 / CH4 of 20 are expected. In the CO 2 -rich gas, between 12.6% (Example 41, System K7: two-stage + intermediate expansion) and 20.0% (Example 13, System K8: three-stage + intermediate expansion) and 62.7% (Example 1; System K1: two-stage) methane again. The methane yields are at best 92% (in Example 13) relatively low, and the improvement of Example 13 over Example 10, which also uses System K8, but even containing 35% methane in the CC2-rich gas, is, as stated in Example 13, by an increase in the membrane area by about 23% and an increase in compressor power by more than 50% bought expensive. The system K8 would thus be unsuitable for current requirements for gas purity and economy.
    It was therefore the object of the present invention to overcome the above disadvantages of the known permeator systems, in particular to reduce energy consumption while at the same time achieving high separation efficiency.
    DISCLOSURE OF THE INVENTION
    This object is achieved by the invention by providing a permeator system in the form of a device for separating substantially unpressurised gas mixtures using membrane gas permeation, comprising at least two separation stages, which may be connected in parallel or in series, a compressor for supplying the fed in a feed line Gas mixture with pressure, if necessary a second compressor for supplying a permeate from a gas phase -6- 7/37 ························································································· ··
    • t «I # * · ·« · II • I ··· «Il |
    Separation stage with pressure, as well as at least one return line for at least one retentate and / or permeate a separation stage, wherein the inventive device is characterized by: two pairs of separation stages, each via a line for forwarding the retentate from the respective first separation stage of a pair in the second are connected in series; two compressors for feeding the first stage of separation of a pair with pressure; a conduit for forwarding the permeate of the first separation stage of a first pair to the compressor which pressurizes the second separation stage pair; one line each for withdrawing the retentate of the respective second separation stage of the pairs; one line each to recycle the permeate of the respective second separation stage of the pairs; and a conduit for drawing off the permeate of the first separation stage of the second stage pair.
    By means of such an arrangement of two pairs of separation stages whose retentates are each enriched in one component of the gas mixture-herein generally referred to as gas 1, it is not only possible with a suitable choice of the membranes and membrane surfaces to use this component of the mixture, but also a second component. herein referred to as gas 2 - to obtain in substantially pure form, which is contained in the permeate of the first separation stage of the second pair. If the gas mixture to be separated, for example, a roughly prepurified biomass raw gas, with methane as gas 1 and carbon dioxide as gas 2, of which, of course, especially methane as recyclable material to be cleaned, the so-called "methane slip, so the methane content in the as "; offgas " carbon dioxide-rich gas 2, are greatly reduced, i. to values below 1% (v / v) and even below 0.5% (v / v). This allows, among other things, a simple discharge of the off-gas into the environment, and without costly cleaning. -7- 8/37 • · «· * ··· · · · • ♦ · · · ···« ··································
    This is made possible by the fact that the retentate of the first separation stage of the first pair of another and its permeate even two further separation stages are fed, wherein two permeates of these separation stages are recycled (and the third is discharged as gas 2). In this way, a very low proportion of gas 1, namely consistently below 1% (v / v) and sometimes even below 0.5% (v / v), is found in gas 2, while gas 1 continues to be essentially in pure form can be obtained. In comparison to systems according to the prior art, the energy consumption of the compressors is significantly reduced, as the later examples prove.
    In general, a further degree of freedom is added to the permeator system by virtue of the genuine fourth separation stage, which is additionally provided in comparison to the prior art, by means of which the separation process can be optimized more simply with regard to energy consumption. Essential here, of course, continues to be the appropriate selection of the membranes and especially the membrane surfaces and the area ratios and the selectivity of the membranes for the gases to be separated. This will be explained in more detail in the later examples.
    Below " substantially depressurized " herein is an outlet pressure of the gas mixture to be separated of typically atmospheric pressure, i. 0 bar (g), to understand how it prevails, for example, in biomass fermentation in biogas plants. In special cases, e.g. in biomass gasification processes, the gas mixture can be produced with pressures of up to a maximum of 3-5 bar (g). Especially compared to natural gas, which is typically under a pressure of about 30 to 150 bar, the latter (bi) gas mixtures, seen from a process engineering point of view, to be described as (nearly) depressurized.
    In preferred embodiments of the apparatus, the line for recycling the permeate of the second separation stage of the first pair returns to the first pair of pressurizing compressor, so that the gases contained in this permeate can go through the complete separation process again. -8- 9/37 ψ • (··· »♦ · · · · · · · · · · · · · ·····································
    In this case, the line for recycling the permeate of the second separation stage of the first pair preferably opens in front of the compressor pressurizing the first pair in the feed line for the non-pressurized gas mixture to be separated. That is, the feed and the recycled permeate, both of which are substantially depressurized, are pressurized together and introduced into the first separation stage of the first pair, for which only one compressor is required. Alternatively, the recycled permeate can also be pressurized by means of an additional compressor and mixed with the already pressurized feed, which is advantageous if the feed of the gas mixture to be separated is already produced under a pressure, albeit a low one, eg in biomass gasification processes, and this pressure should not be lowered by mixing with the virtually unpressurized recyclate. In these cases, feed and recycled material can be separately pressurized and then mixed. Of course, the pressures and flow rates are coordinated so that the mixture has the pressure required for the first separation stage.
    The line for recycling the permeate of the second separation stage of the second pair, according to the present invention, leads either to the compressor pressurizing the second pair, i. to the first separation stage of the second pair, or to which the first pair of pressurizing compressor, i. to the first separation stage of the first pair, or can also be divided in a certain ratio and returned to both separation stages. This allows a flexible choice of membranes and area ratios since this second stage permeate of the second pair will re-pass, depending on the ratio between gas 1 and gas 2 therein, the entire permeator system, or only the second stage pair, or both proportionally ,
    Again, the recycle lines of the recycled permeate are preferably combined before the respective compressors with the feed lines to the first stages of the pairs. In special cases, however, additional compressors may be provided for the recycled permeate to pressurize them to the required pressure before they are mixed with the already pressurized feed of the first separation stage of the respective pair ,
    In a second aspect, the invention relates to a corresponding method for the separation of substantially pressureless gas mixtures by means of membrane gas permeation using a device according to the first aspect of the invention as described above, the method comprising - in analogy to the embodiments of the device according to the invention - the following : passing the gas mixture through two pairs of separation stages, of which in each case the first separation stage is pressurized by a respective compressor and the retentates of these first separation stages are forwarded to the respective second separation stage; wherein the permeate of the first separation stage of the first pair is introduced into or represents the feed of the first separation stage of the second pair; recycling the permeates of the respective second separation stages of the pairs; the removal of the enriched in a component of the gas mixture retentates of the respective second separation stages; and withdrawing the enriched in another component of the gas mixture permeate the first separation stage of the second pair. The advantages are the same as described above for the device according to the invention, in particular a particularly high purity of the separated streams of gases 1 and 2 with significantly lower energy consumption.
    The permeate of the second separation stage of the first pair is preferably recycled to the first separation stage of the first pair, wherein it is particularly preferably mixed with the to be separated, substantially pressureless gas mixture before the mixture thus obtained is pressurized, which requires only a compressor. The permeate of the second separation stage of the second pair can in turn be recycled either to the first separation stage of the second pair or to the first separation stage of the first pair or both, so as to optimize the process depending on the nature of the gas to be separated and equipment conditions of the system. -10- 11/37 »·················································································································································································································
    The membranes of the individual separation stages are preferably selected from polymer film and ceramic membranes, since these provide the best results in the field of gas separation. For example, dense polymer layers are typically more permeable to CO 2 than to CH 4 and are therefore often used to separate these two gases. For the separation of corrosive gas mixtures, however, more resistant ceramic membranes are often used in this regard.
    The fields of application of the device and method of the invention are of course not particularly limited. Preferred examples include biomass gasification, optionally with methanation, anaerobic digestion, and combinations of water electrolysis and methanation.
    An essential criterion is the selectivity of the membranes for the gases to be separated therewith. This is expressed by the ratio of the rates of passage of two different gases and is typically between 10 and 50, usually about 20, to provide useful results in terms of separation efficiency and energy requirements without overly increasing energy consumption and costs. The later examples consider membranes with different selectivities.
    BRIEF DESCRIPTION OF THE DRAWINGS
    The invention will be described in more detail below with reference to the accompanying drawings, in which the following is shown.
    Figures 1-3 show, as previously mentioned, prior art permeator systems with two or three stages of separation, the permeator systems of Figure 3 additionally comprising an intermediate expansion stage.
    Fig. 4 shows a comparison of several membranes of different selectivities in a simple Permeatorsystem according to the prior art. -11 - 12/37 • · · · · · · · · · · · · · · · · · · · ······················································
    FIGS. 5 and 6 show two embodiments of the permeate system according to the invention with four separation stages.
    Figures 7 to 12 show comparisons of inventive permeator systems of Examples 1 to 3 with prior art systems.
    It should be noted that FIGS. 5 and 6, which show embodiments of the device according to the invention and thus simultaneously illustrate the method according to the invention, denote " P " and " R " Both the lines in which the respective permeates or retentates are guided, and the gas streams themselves are called.
    DETAILED DESCRIPTION OF THE INVENTION
    1 to 3, as described above, various prior art permeator systems are shown with 2 or 3 separation stages and optionally an intermediate expansion stage, assuming a separation of CH 4 and CO 2 as is conventional in the art, How to do it in a biogas treatment, for example, to extract methane as pure as possible product gas. For purposes of comparison with the present invention, prior to entering the first separation stage, compressors are provided for these known configurations to process a non-pressurized feed. However, as also mentioned at the beginning, not all of these permeator systems have been described with reference to biogas or other non-pressurized gas feeds.
    The most obvious difference between the permeator systems of the present invention, as illustrated in Figures 5 and 6, is the additional fourth stage of separation, which, as defined above and in contrast to the known system K8, has a " true " Forming fourth stage, since it is fed exclusively with standing under a relatively high pressure retentate or by a directly upstream compressor. Formally, the embodiment according to the invention from FIG. 5 could be regarded as a combination of two known systems K1, in which the permeate of the first separation stage of a first system K1 is set up in another such system - 12/37 • f ······· . By contrast, it is not possible to combine that from FIG. 6 from the two-stage and three-stage permeator systems illustrated in FIGS. 1 to 3, since none of these systems provides recycling of the permeate of a third or fourth separation stage back to the very first. Also, both embodiments of the invention can not be operated as a mere combination of known systems K1, since with the true fourth separation stage compared to three-stage solutions, an additional degree of freedom is introduced into the system. On the one hand, this allows for better optimization and the preservation of purer product gas streams with simultaneously lower energy consumption, but on the other hand also requires a more precise fine-tuning of the pressure and membrane surface conditions in order to justify the additional apparatus and process-related expense. As the following examples show, the performance of both shown in the drawings embodiments of the invention Permeatorsystems is many times better than those of the known system K1.
    Comparative Example 1
    In Fig. 4, results obtained by validated computer modeling are plotted for the known permeator system K1 of Fig. 1 using four different membrane pairs with different selectivities for the separation of CH4 and CO2 (see reference [13] of the present inventors ). On the x-axis, the methane yield is plotted as a percentage of the methane contained in the gas mixture to be separated. On the y-axis on the left side is the specific compression energy in kWh / m3 of gas and on the right the content of " methane in permeate ", i. in C02-rich offgas, expressed in% (v / v), which changes along the diagonals drawn.
    The goal of any such separation is a high methane yield with low energy consumption and low methane content in the offgas, preferably a maximum methane content of 1% (v / v) to drain the offgas possible without subsequent purification in the environment. This desired result is indicated by the vertical " finish line " which cuts the methane content diagonal at 1% (v / v), which in the present case would correspond to a 99.5% methane yield. -13- 14/37 • »· · · · · · · · · · · · · · · · · · · · · ···· · ···
    The curves in Fig. 4 show the values for the permeator system K1 with different selectivities of the membrane pairs of 10, 20, 35 and 50. These values mean that carbon dioxide 10, 20, 35 or 50 times faster Membrane happens as methane. Two identical membranes were used for the model calculation and 10 for the pressure generated by the single compressor. The size and area ratios of the membranes were varied in the calculation, resulting in different ratios of the retentate and permeate. This means that different amounts of gas are recycled depending on the membrane data, which translates into energy consumption. Of course, to achieve higher yields and purities, it is necessary to recycle and re-purify larger quantities of gas, increasing energy consumption.
    It can be seen that in this comparative example with the permeator system K1 from FIG. 1, the desired values can be achieved, starting with a membrane selectivity of 20 with reasonably realistic energy consumption, but for which an energy of approximately 1.7 kWh / m 3 of gas is required because very large amounts of permeate must be recycled. Even using membranes with selectivities of 35 and 50, 0.7 and 0.5 kWh / m3 are still required. These values are approximately 6 times, 3 times and 2.5 times, respectively, those energy consumption values that are necessary for each 95% extraction of methane, which is given by the starting points of the curves on the y-axis. Under these initial conditions of membrane selectivity of 20, however, almost 9% (v / v) of methane would still be contained in the offgas, so that in practice a great deal of energy would be required for the subsequent purification thereof.
    It will thus be appreciated that in this K1 system, at least selectivity 35, better 50, selectivity membranes must be used to provide reasonably acceptable overall energy consumption, i. with recycling of relatively low gas volumes, to be able to achieve a methane yield of 99% or more. -14- 15/37 ······························································································
    Example 1 & Comparative Examples 2 to 4
    A first modeling of a permeator system according to the invention using two pairs of separation stages as shown in FIG. 5 (Example 1, B1) and three comparisons with the conventional permeator systems K1 (Comparative Example 2, V2), K3 (V3) and K4 (V4) Fig. 1 was carried out with the following parameters:
    Membrane selectivity: 20; Compressor pressure: 10 bar (a); Raw gas pressure, permeate-side pressure: 1 bar (a)
    The target was again a maximum of 1% (v / v) of methane in the offgas, which in this case corresponds to a methane yield of just under 99.4%.
    In Fig. 7, the computer calculated results are graphed in the same manner as in Fig. 4. Starting with a virtually the same energy consumption of about 0.24 kWh / m3 for all four Permeatorsysteme for a methane yield of 95%, the energy required for the system K1 in Comparative Example 2 increases again quickly and reaches a value of about 1 at the desired yield kWh / m3.
    Although the system K3 also consists of only two separation stages, it does not purify the retentate of the first stage a1, but rather its permeate in the second stage b1, for which a second compressor is required. The retentate of the second stage b1 is returned to the feed of a1 and thus passes through the system again. Methane is recovered in this case only as a retentate of a1. K4 represents a three-stage system in which a first separation stage a1 serves to recover the methane in the retentate, while the permeate of a1 is purified in a two-stage system. K4 is a system K1, so to speak, preceded by a separation stage. Methane is recovered here in the retentate of the first and the third separation stage. Of course, in this case, a second compressor is required.
    From Fig. 7 it can be seen that there are hardly any differences between K3 and K4, i. Comparative Examples 3 and 4 show, as compared with Comparative Example 2, a he - 15-16/37 • ·········································································· Significantly better separation performance with approximately the same energy consumption, which remains almost constant up to about 97% methane yield and at the desired just under 99.4% compared to the initial values not quintupled as in V2, but only about doubled. Above all, it is surprising that the difference between V3 and V4 is only about 10%, although system K4 comprises an additional, third separation stage.
    The permeator system of Example 1 according to the invention shows starting at about 97.5% methane yield a noticeably lower energy consumption than the comparative examples 3 and 4 and from about 98-98.5% a much lower. At the target point, energy demand has only increased by about one-sixth from 0.24 to about 0.28 kWh / m3 compared to baseline. The permeator systems of the two comparative examples 3 and 4 are higher here by about one-third, namely at about 0.44 or just under 0.40 kWh / m3, which means that in example 1 at least 30% of the energy is saved compared to V2 and V3 can.
    This result is surprising in view of the small difference between V3 and V4, since it was not to be expected that a much greater improvement can be achieved by providing a fourth separation stage than with the transition from two to three separation stages.
    FIG. 8 shows the case that with constant modeling data of this first example group, the target of 1% (v / v) methane in the permeate is changed to 99% methane yield. The vertical " finish line " shifts relative to FIG. by the corresponding amount to the left. As can be seen from the position of the point of intersection with the diagonal, this specification corresponds to a residual content of about 1.4% (v / v) of methane in the permeate. The differences from the three prior art systems (as well as those between systems K3 and K4) are somewhat smaller but still significant: even with these " reduced " Yield and purity requirements can be saved compared to V3 and V4 about 20% of energy. -16-
    FIG. 9 shows the inverse of FIG. 8, namely slightly " tightened " Targets, i. a methane yield of 99.5%, which corresponds to a methane content in the permeate of just under 0.8% (v / v). This goal can not be achieved with system K1 in V2 or only with an exorbitant energy consumption with recycling of most of the gas feed. Although the systems K3 and K4 of Comparative Examples 3 and 4 achieve the specification, they require energies of approximately 0.55 and 0.50 kWh / m3 of gas respectively, while the system according to the invention from FIG. 5 has just under 0.3 kWh / m3 gets along. This represents a Energieerspamis of 45% and 40% over the prior art.
    Example 2 & Comparative Examples 5 to 7
    Analogously to example 1, a separation using the prior art permeator systems K1, K3 and K4 as V5, V6 and V7 and the system according to the invention from figure 5 (B2) was computer modeled, but membranes with a selectivity of 50 instead of 20 were used and the target concentration of methane in the offgas was set at 0.5% (v / v). The results are shown graphically in FIG.
    In this example set, the system starts from V5, i. Permeator system K1, on the y-axis (at 95% methane yield) with a slightly lower energy consumption than the other three systems. At about 98%, all four systems are on par, but above that the energy demand of V5 increases again and is at the target point about 3.5 times the initial value.
    Example 2 and Comparative Examples 6 and 7 are the same starting from the starting point to about 99.2% methane yield, but there are again noticeable benefits to the permeator system of the invention, resulting in an end point energy savings of about 15-20% over V6 and V7 , Again, there are hardly any differences between these two state-of-the-art permeate systems, ie the systems K3 and K4, in this case even only about 5% difference in energy consumption. -17- 18/37 • φ i a φφφ · φ φ φ φ · · φ φ φ φ φ φ φφ φφφ φφ φφ φφφ φφ
    If one increases the targets in analogy to Example 1, i. move the vertical " finish line " towards higher methane yields and residuals to the right, the benefits of the invention will become even more apparent.
    Example 3 & Comparative Examples 8 to 10
    The modeling of Example 1 with membranes of selectivity 20 and a target concentration of not more than 1% (v / v) methane in the offgas, which in turn corresponds to almost 99.4% methane yield, was repeated, in which case not the energy consumption but the membrane area the measurand was of interest. The results are shown graphically in FIG. 11.
    The graph logically resembles that in Figure 7 and again shows the inadequacy of system K1 in V8 for the set goals. However, in this example group, the difference between the permeator systems K3 and K4 in V9 and V10 occurs a little more clearly than before in energy consumption. Nevertheless, the improvement over K3 and K4 achievable by the apparatus and method of the present invention in Example 3 can still be clearly seen. Thus, in the present Example 3, a permeator system of the present invention as shown in Fig. 4 requires about 500 and 700 m 2 smaller membrane areas than Comparative Examples 9 and 10, again representing a savings of about 15-20% over systems K3 and K4 ,
    Finally, Fig. 12 shows the case where, for the systems of Example 3 and Comparative Examples 8 to 10, the target is 99.5% methane yield, i. a residual methane content in the offgas of about 0.7% (v / v) was set. The membrane area required for the inventive system of Example 3 barely changes, namely only from about 2550 to about 2600 m2, the saving compared to K4, however, increases from about 500 to about 700 m2 and compared to K3 even from about 700 to just 1100 m2. The two systems of Comparative Examples 9 and 10 thus require for the same separation performance as the inventive system of FIG. 5 by 42% and 27% larger membrane areas. -18- 19/37 • · * * ···· »· · • # ··· ·················································
    Example 4
    The results of several comparisons of the two embodiments of the permeator system according to the invention according to FIG. 5 and FIG. 6 showed that these systems produced hardly any different simulation data in simulations performed analogously to the above. The differences were actually so small that they can not be graphically represented in similar diagrams as described above. Apparently, the additional degree of freedom introduced by the fourth separation stage and the resulting increased separation efficiency means that it does not play a significant role whether the permeate of the fourth separation stage b2 only passes through the second or the first pair of separation stages again.
    In summary, the present invention thus provides a permeator system and a method to be carried out therewith for the separation of substantially unpressurised gas mixtures which, compared with the prior art, produce much lower energy consumption and require significantly smaller membrane areas or selectivities. -19- 20/37, 0 • · ι * · «···« «·
    • · t · · · I ·· ··· · 4 ·· ··· ··
    LITERATURE REFERENCES
    [1] W.J. Schell, C.D. Houston, " Use of Membranes for Biogas Treatment ", Energy Progress 3, 96-100 (1983).
    [2] R. Rautenbach, W. Dahm, " Oxygen and methane enrichment - a comparison of module arrangements in gas permeation ", Chemical Engineering & Technology 10 (1), 256-261 (1987).
    [3] R. Rautenbach, K. Welsch, 'Treatment of landfill gas by gas permeation - pilot plant results and comparison to alternative', Desalination 90 (1-3), 193-207 (1993), ISSN 0011-9164.
    [4] SA Stern, B. Krishnakumar, SG Charati, WS Amato, AA Friedman, DJ Fuess, "Performance of a bench-scale membrane pilot plans for the upgrading of biogas in a wastewater treatment plant," Journal of Membrane Science 151 (1), 63-74 (1998), ISSN 0376-7388.
    [5] M. Miltner, A. Makaruk, H. Bala, M. Harasek, " Biogas Upgrading for Transportation Purposes -Operational Experiences with Austria's First Bio-CNG Filling Station, ", Chemical Engineering Transactions 18, 617-622 (2009) ,
    [6] B.D. Bhide, S.A. Stern, " Membrane processes for the removal of acid gases from natural gas. II. Effects of operating conditions, economic parameters, and membrane properties ", Journal of Membrane Science 81 (3), 239-252 (1993), ISSN 0376-7388.
    [7] R.W. Spillman, "Economics of gas separation membranes", Chemical Engineering Progress 85, 41-62 (1989).
    [8] R. Qi, Μ. A. Henson, "Optimization-based design of spiral and membrane systems for C02 / CH4 separations", Separation and Purification Technology 13 (3), 209-225 (1998), ISSN 1383-5866.
    [9] A.K. Datta, P.K. Sen, "Optimization of membrane unit for natural gas", Journal of Membrane Science 283 (1-2), 291-300 (2006), ISSN 0376-7388.
    [10] J. Xu, R. Agrawal, " Gas Separation membrane cascades. I. One-compressor cascades with minimal exergy losses due to mixing ", Journal of Membrane Science 112, 115-128 (1996), ISSN 0376-7388.
    [11] R. Agrawal, J. Xu, " Gas Separation Membrane Cascades. II. Two-compressor cascades, Journal of Membrane Science 112 (2), 129-146 (1996), ISSN 0376-7388.
    [12] B.D. Bhide, S.A. Stern, " Membrane processes for the removal of acid gases from natural gas. I. Process configurations and optimization of operating conditions ", Journal of Membrane Science 81 (3), 209-237 (1993), ISSN 0376-7388.
    [13] A. Makaruk, M. Miltner, M. Harasek, " Membrane biogas upgrading processes for the production of natural gas substitute ", Separation and Purification Technology 74 (1), 83-92 (2010), ISSN 1383-5866 , 20-21 / 37
    权利要求:
    Claims (9)
    [1]
    1. A device for separating substantially pressureless gas mixtures using membrane gas permeation comprising at least two separation stages, the may be connected in parallel or in series, a compressor for pressurizing the fed in a feed line gas mixture, optionally a second compressor for pressurizing a permeate from a separation stage with pressure, and at least one return line for at least one retentate and / or permeate a separation stage, characterized by two pairs of separation stages (a1, a2; b1, b2) which are each connected via a line (Rai; Rbi) for the transfer of the retentate from the respective first separation stage (a1; b1) of one pair into the second (a2; b2) connected in series; two compressors (c1, c2) for feeding the respective first separation stage (a1; b1) of a pair with pressure; a line (Pai) for forwarding the permeate of the first separation stage (a1) of a first pair (a1, a2) to the compressor (c2) pressurizing the second stage pair (b1, b2); one respective line (Ra2; Rb2) for subtracting the retentate of the respective second separation stage (a2; b2) of the pairs; one line each (Pa2; Pb2) for recycling the permeate of the respective second separation stage (a2; b2) of the pairs; and a pipe (Pbi) for drawing off the permeate of the first separation stage (b1) of the second separation stage pair (b1, b2).
    [2]
    2. Apparatus according to claim 1, characterized in that the line (Pa2) for recycling the permeate of the second separation stage (a2) of the first pair to the said first pair (a1, a2) pressurizing compressor (c1) returns.
    [3]
    3. Apparatus according to claim 2, characterized in that the line (Pa2) for recycling the permeate of the second separation stage (a2) of the first pair before -22- 22/37 ·· • • t% · • ·· i · • · The first pair (a1, a2) with pressure acting compressor (c1) opens into the feed line of the gas mixture to be separated.
    [4]
    4. Device according to one of claims 1 to 3, characterized in that the line (Pb2) for recycling the permeate of the second separation stage (b2) of the second pair to the said second pair (b1, b2) pressurizing compressor (c2) and / or to which the first pair (a1, a2) is pressurized compressor (c1) returns.
    [5]
    5. A method of separating substantially unpressurised gas mixtures by membrane gas permeation using an apparatus according to any one of claims 1 to 4, comprising: passing the gas mixture through two pairs of separation stages (a1, a2, b1, b2), respectively the first separation stage (a1; b1) is pressurized by a respective compressor (c1; c2) and the retentates of these first separation stages (a1; b1) are forwarded to the respective second separation stage (a2; b2); wherein the permeate of the first separation stage (a1) of the first pair (a1, a2) is introduced into or represents the feed of the first separation stage (b1) of the second pair (b1, b2); recycling the permeates (Pa2, Pb2) of the respective second separation stages (a2, b2) of the pairs; the removal of the enriched in a component of the gas mixture retentates (Ra2, Rb2) of the respective second separation stages (a2, b2); and withdrawing the enriched in another component of the gas mixture permeate (Pbi) of the first separation stage (b1) of the second pair (b1, b2).
    [6]
    6. The method according to claim 5, characterized in that the permeate (Pa2) of the second separation stage (a2) of the first pair (a1, a2) to the first separation stage (a1) of the first pair is recycled.
    [7]
    7. The method according to claim 6, characterized in that the permeate (Pa2) of the second separation stage (a2) of the first pair (a1, a2) with the to be separated, in the -23- 23/37 ··· ··· ♦ • The mixture is mixed with essentially unpressurized gas, after which the resulting mixture is pressurized.
    [8]
    8. The method according to any one of claims 5 to 7, characterized in that the permeate (Pb2) of the second separation stage (b2) of the second pair (b1, b2) to the first separation stage (b1) of the second pair (b1, b2) is recycled and / or to the first separation stage (a1) of the first pair (a1, a2) is recycled.
    [9]
    9. Device according to one of claims 1 to 4 or method according to one of claims 5 to 8, characterized in that the membranes of the individual separation stages of polymer film and ceramic membranes are selected. Vienna, 27 November 2012 Vienna University of Technology

    jiupl & Ellmeyer KG -24- 24/37

    类似技术:
    公开号 | 公开日 | 专利标题
    AT513644B1|2014-09-15|Permeator system for the separation of gas mixtures
    EP2588217B1|2017-02-22|Process for separation of gases
    DE69529759T2|2004-02-19|MULTI-STAGE SEPARATION PROCESS WITH SEMIPERMEABLED MEMBRANES
    EP0019105B1|1983-06-22|Pressure swing adsorption process and its use for the production of organic acids
    EP3338876B1|2020-07-01|Method for separating gases by membranes
    EP2562237B1|2018-08-22|Method for providing a gas with very high methane content and assembly for same
    EP2714243B1|2016-09-14|System and method for treating natural gas that contains methane
    EP3498668A1|2019-06-19|Method and assembly for recovering pure helium
    DE202008016134U1|2009-04-16|Device for enriching the fuel gas components in lean gases
    AT514614B1|2015-05-15|Method and system for storing energy
    WO2017137581A1|2017-08-17|Method for the synthesis of methanol
    EP2440312B1|2016-04-13|Device and method for separating a gas mixture
    DE2847310A1|1979-05-03|PROCESS FOR SEPARATING GASES
    EP3513863A1|2019-07-24|Method and assembly for recovering pure helium
    DE102019203065A1|2020-09-10|Process for the production of methanol or methane
    AT521106B1|2020-03-15|Process for the separation and compression of hydrogen from gas mixtures
    EP3020696B1|2019-07-03|Method for the production of one or more reaction products
    DE102014000507A1|2015-07-16|Process and apparatus for producing dimethyl ether
    AT513061B1|2014-03-15|Apparatus and method for controlling the concentration of product gas in an offgas
    DE102010006103A1|2011-08-18|Process for producing export steam in an industrial plant
    DE4434101C1|1995-08-31|Pressure-swing adsorption process to purify or analyse a gas stream
    EP2481705A1|2012-08-01|Method and device for material and/or energy recovery of biogenic residual materials
    DE102019113003A1|2020-11-19|Process and plant for the synthesis of methanol
    DE102006015088A1|2007-10-04|Procedure for treatment of gaseous fuel from natural gas/gaseous petroleum byproduct by an arrangement, comprises compressing and recooling incoming gas mixture, and removing the resulting condensate from gas stream in gas/liquid-separator
    DE102016204331A1|2017-08-10|Process for the production of ammonia from crude gas
    同族专利:
    公开号 | 公开日
    AT513644B1|2014-09-15|
    EP2735355A1|2014-05-28|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE102008032864A1|2008-07-14|2010-01-21|Erdgas Südwest GmbH|Method and device for enriching the fuel gas components in lean gases|
    AT507891A4|2009-06-10|2010-09-15|Axiom Angewandte Prozesstechni|DEVICE AND METHOD FOR SEPARATING A GAS MIXTURE|
    US6168649B1|1998-12-09|2001-01-02|Mg Generon, Inc.|Membrane for separation of xenon from oxygen and nitrogen and method of using same|
    US6565626B1|2001-12-28|2003-05-20|Membrane Technology And Research, Inc.|Natural gas separation using nitrogen-selective membranes|
    US20040000513A1|2002-06-27|2004-01-01|Colling Craig W.|Apparatus using solid perm-selective membranes in multiple groups for simultaneous recovery of specified products from a fluid mixture|
    US7537641B2|2005-12-02|2009-05-26|Membrane Technology And Research, Inc.|Natural gas treatment process for stimulated well|
    WO2009087156A1|2008-01-08|2009-07-16|Shell Internationale Research Maatschappij B.V.|Multi - stage membrane separation process|
    MX2012014777A|2010-07-01|2013-04-29|Evonik Fibres Gmbh|Process for separation of gases.|EA034642B1|2014-12-29|2020-03-02|Эвоник Фибрес Гмбх|Process for separation of gases with reduced maintenance costs|
    JP6511912B2|2015-03-30|2019-05-15|宇部興産株式会社|Gas separation system and method for producing enriched gas|
    JP6464881B2|2015-03-30|2019-02-06|宇部興産株式会社|Gas separation system and method for producing enriched gas|
    FR3063437B1|2017-03-02|2019-03-29|L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude|APPARATUS AND METHOD FOR MEMBRANE PERMEATION TREATMENT OF A GAS SUPPLY FLOW COMPRISING METHANE AND CARBON DIOXIDE|
    FR3084841B1|2018-08-08|2020-07-24|Air Liquide|TREATMENT BY MEMBRANE PERMEATION WITH ADJUSTMENT OF THE PRESSURE OF THE SUPPLY GAS FLOW ACCORDING TO THE CH4 CONCENTRATION IN THE SECOND RETENTAT|
    FR3084840B1|2018-08-08|2020-07-31|Air Liquide|TREATMENT BY MEMBRANE PERMEATION WITH ADJUSTMENT OF THE TEMPERATURE OF THE FIRST RETENTAT DEPENDING ON THE CH4 CONCENTRATION IN THE THIRD AND / OR FOURTH PERMEAT|
    FR3084842B1|2018-08-08|2020-07-24|Air Liquide|TREATMENT BY MEMBRANE PERMEATION WITH ADJUSTMENT OF THE NUMBER OF MEMBRANES IMPLEMENTED DEPENDING ON THE PRESSURE OF THE GAS FLOW SUPPLY|
    FR3089821B1|2018-12-14|2021-06-18|Air Liquide|Installation and method of treatment by membrane permeation of a gas stream with adjustment of the suction pressure of the third permeate|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    ATA1248/2012A|AT513644B1|2012-11-27|2012-11-27|Permeator system for the separation of gas mixtures|ATA1248/2012A| AT513644B1|2012-11-27|2012-11-27|Permeator system for the separation of gas mixtures|
    EP13194642.8A| EP2735355A1|2012-11-27|2013-11-27|Permeator system for separating gas mixtures|
    [返回顶部]