The present disclosure relates to processes for the separation of carbon dioxide from other gases, and more particularly to processes for the separation of carbon dioxide from methane-containing gas mixtures.
Adsorptive separation systems are known for use in separation of gas streams comprising multiple gas components. Pressure swing, temperature swing, and partial pressure swing or displacement purge adsorption are exemplary processes known in the art for performing such separations of multi-component gas mixtures. In the exemplary case of separation of methane-containing gas mixtures, existing adsorption based separation processes do not provide for desirably efficient separation of methane from other gas components. Existing adsorptive methane separation processes typically include sequential pressure or temperature swing adsorption systems requiring multiple adsorption steps and corresponding multiple adsorption systems or subsystems, and typically result in the delivery of product methane gas streams at relatively low pressure, commonly as a component of desorption exhaust. Existing processes may also result in delivery of methane product gas at relatively low purity and/or recovery due to the lack of efficiency in adsorptively separating methane from other common gas mixture components. Such other common gas mixture components may for example comprise carbon dioxide, nitrogen and oxygen in impure methane-containing feed gas streams. Examples of such impure methane-containing gas streams may include biogas, landfill gas, impure natural gas or other methane-containing commercial gas streams. In applications where such impure methane streams are desired to be stored and used as compressed or liquified gas fuels, the relatively low purity of the methane product streams typically produced by some existing adsorptive separation processes may result in inefficiencies and/or impracticalities in the compression and/or liquifaction processes used to store such fuel gases.
Disclosed herein are inventive adsorptive gas separation processes that addresses some shortcomings of the prior art. In one embodiment, an adsorptive gas separation process is provided capable of producing a purified methane product gas as a light non-adsorbed product gas (as opposed to a heavy desorbed exhaust gas component) from a feed gas mixture comprising at least methane, and carbon dioxide. In an exemplary embodiment, the feed gas mixture may comprise at least about 10% carbon dioxide, and the purified methane product gas may be desirably purified to contain less than about 5000 ppm carbon dioxide. In another exemplary embodiment, the feed gas mixture may comprise at least about 20% carbon dioxide, and the purified methane product gas may be desirably purified to contain less than about 5000 ppm carbon dioxide. In yet a further exemplary embodiment, the feed gas mixture may comprise at least about 50% carbon dioxide, and the purified methane product gas may be desirably purified to contain less than about 5000 ppm carbon dioxide. In any of the preceding exemplary embodiments, the purified methane product gas may be more desirably purified to contain less than about 1000 ppm carbon dioxide, and most desirably less than 100 ppm carbon dioxide.
In another embodiment, an adsorptive gas separation process is provided capable of producing a purified methane product gas at a recovery of at least about 50% in a single adsorption step with a single adsorption device, from a feed gas mixture comprising at least methane and carbon dioxide. In an exemplary embodiment, the feed gas mixture may comprise at least about 10% carbon dioxide, and the purified methane product gas may be desirably purified to contain less than about 5000 ppm carbon dioxide. In another exemplary embodiment, the feed gas mixture may comprise at least about 20% carbon dioxide, and in yet another exemplary embodiment, may comprise at least about 50% carbon dioxide. In any of the preceding exemplary embodiments, the purified methane product gas may be more desirably purified to contain less than about 1000 ppm carbon dioxide, and most desirably less than 100 ppm carbon dioxide.
In a further embodiment, an adsorptive gas separation process is provided capable of producing purified methane product gas from a feed gas mixture comprising at least methane and carbon dioxide, by adsorption of the feed gas mixture in an adsorber in contact with at least a first adsorbent material suited for adsorbing at least a majority of the carbon dioxide in the feed gas stream, and a second adsorbent material suited for substantially removing remaining amounts of carbon dioxide while substantially excluding methane from adsorption. In an exemplary embodiment, the feed gas mixture may comprise at least about 10% carbon dioxide, and the purified methane product gas may be desirably purified to contain less than about 5000 ppm carbon dioxide. In a further exemplary embodiment, the feed gas mixture may comprise at least about 20% carbon dioxide, and in yet another exemplary embodiment, may comprise at least about 50% carbon dioxide. In any of the preceding exemplary embodiments, the purified methane product gas may be more desirably purified to contain less than about 1000 ppm carbon dioxide, and most desirably less than 100 ppm carbon dioxide.
In a further embodiment, an adsorptive gas separation process is provided capable of providing enriched methane product gas from a feed gas mixture comprising at least methane and carbon dioxide, by adsorption of at least a majority of the carbon dioxide on an alumina-based adsorbent material to produce the enriched methane product gas. In an exemplary embodiment, the feed gas stream may comprise at least about 15% carbon dioxide, and the enriched methane product gas stream may desirably comprise less than about 5% carbon dioxide. In a further exemplary embodiment, the feed gas stream may comprise at least about 25% carbon dioxide, and the enriched methane product gas stream may desirably comprise less than about 5% carbon dioxide. In yet a further exemplary embodiment, the feed gas stream may comprise at least about 50% carbon dioxide.
In an above-mentioned embodiment, the inventive process may be used to produce a relatively purified methane product gas stream by adsorption from an impure methane containing feed gas additionally comprising at least about 10% carbon dioxide, where the purified methane product is produced as the light, non-adsorbed product gas, and delivered at the pressure of the adsorption process. In another exemplary embodiment, the feed gas may comprise at least about 20% carbon dioxide. The purified methane product gas may desirably be purified to comprise less than about 5000 ppm of carbon dioxide, more desirably to comprise less than about 1000 ppm carbon dioxide, and in particular may be purified to comprise less than about 100 ppm carbon dioxide, such as is desirable for use in some commercial applications such as the liquifaction of methane gas for storage as a liquified gas fuel. In an exemplary embodiment, the inventive adsorption process may comprise a pressure swing adsorption (PSA) process wherein the feed gas mixture may be passed over an adsorbent material to produce a non-adsorbed product gas delivered at a higher pressure, and a desorbed exhaust gas delivered at a lower pressure of the process, wherein the purified methane product gas (comprising desirably less than about 5000 ppm carbon dioxide, or more desirably less than about 1000 ppm carbon dioxide, or particularly less than about 100 ppm carbon dioxide) may be delivered as the non-adsorbed product gas.
Common impure methane feed gas mixtures may additionally comprise gas components other than methane and carbon dioxide, which may include for example, and without limitation, nitrogen and oxygen. In addition to the removal of carbon dioxide from the purified methane product gas, the present inventive process may also be used to desirably purify the methane product gas by substantially reducing the concentration of oxygen in the methane product gas relative to the feed gas mixture, such as is desirable to reduce oxygen concentration in the purified methane product gas in applications where oxygen levels may become a safety concern in downstream uses of the methane product gas. This may be the case in liquifaction applications where oxygen in the methane product may become concentrated during the liquifaction process to produce a liquified methane fuel.
In a further embodiment, as summarized above, the inventive process may be used to produce a purified methane product gas from a feed gas mixture comprising at least methane and carbon dioxide by adsorption of at least a portion of the carbon dioxide component in a single pass through the adsorption process, in a single adsorption device, wherein the methane product gas is purified to contain less than about 5000 ppm carbon dioxide while recovering at least about 50% of the methane in the feed gas. In one example, a purified methane product gas may be obtained with a gas flow path through a single adsorption process unit represented by a single adsorber element (which may or may not include a single adsorbent bed provided the multiple beds are contiguous with each other along the gas flow path). In other words, a purified methane product gas may be obtained without having to introduce a feed gas into a first adsorbent element to obtain an intermediate product that is subsequently introduced into a second adsorber element In an exemplary such embodiment, the feed gas mixture may comprise at least about 10% carbon dioxide, and the purified methane product gas may desirably be further purified to contain less than about 1000 ppm carbon dioxide, and particularly less than about 100 ppm carbon dioxide, such as is desirable for liquifaction of the purified methane product gas for storage as a liquified methane fuel gas. In a further exemplary embodiment, the feed gas mixture may comprise at least about 20% carbon dioxide, and in a yet further exemplary embodiment, the feed gas mixture may comprise at least about 50% carbon dioxide. Additionally, the present inventive adsorptive separation process may be used to desirably produce a purified methane product gas containing less than about 5000 ppm carbon dioxide at a recovery of at least about 65% and particularly at a recovery of at least 75% of the methane in the feed gas mixture.
In a further embodiment of the present inventive adsorptive gas separation processes, multiple adsorbent materials in a single adsorber unit or element may be used to produce the desired purified methane product gas from the feed gas mixture comprising at least methane and carbon dioxide by means of adsorptive separation. In an exemplary embodiment, a first adsorbent material may be used to adsorb at least a majority of the carbon dioxide from the feed gas mixture. Such first adsorbent material may be selected from suitable adsorbent materials either known in the art, or developed in the future, such suitable adsorbent materials having both desirably high adsorptive capacities for adsorption of carbon dioxide, and relatively low adsorptive capacity for methane, resulting in a distinct selectivity for adsorption of carbon dioxide in preference to methane. Such suitable adsorbent materials may comprise for example, and without limitation, aluminas, silicas, hydrophobic zeolites (such as zeolite Y or ZSM-5 for example), activated carbon, and combinations thereof. In particular, activated alumina and silica gel, or a combination thereof may desirably be applied to the inventive process as a suitable first adsorbent material, as they both demonstrate desirably high adsorptive carbon dioxide capacity and relatively low adsorptive methane capacity, and are therefore selective for the adsorption of carbon dioxide over methane. In a further exemplary embodiment, silica gel followed in the adsorption path by activated alumina may be used as a first adsorbent material in the inventive processes. A second adsorbent material may be used in the present inventive adsorptive gas separation processes to adsorb any remaining portion of carbon dioxide in the process gas stream following adsorption of at least a majority of the carbon dioxide from the feed gas mixture by the first adsorbent material. In order to substantially adsorb the remaining portion of carbon dioxide, the second adsorbent material may be selected from any suitable adsorbent materials known in the art, or subsequently developed, such suitable adsorbent materials having a desirably high adsorptive selectivity for carbon dioxide relative to methane. In particular, adsorbent materials with very high adsorptive selectivities for carbon dioxide over methane to the point of substantially excluding methane from adsorption on the adsorbent material may be preferably selected for use as the second adsorbent material in the inventive processes. Such suitable second adsorbent materials may comprise for example, and without limitation, zeolite 3A, carbon molecular sieves, titanosilicate molecular sieve materials (also known as mixed tetrahedral/octahedral molecular sieve materials) and combinations thereof. More desirably, such suitable second adsorbent materials may comprise carbon molecular sieves, titanosilicate molecular sieves materials (such as ETS-4 for example), and combinations thereof, wherein such more desirable second adsorbent materials may be prepared to substantially exclude methane from adsorption while actively adsorbing carbon dioxide. In all cases, suitable adsorbent materials for application in any of the embodiments may be formed into any suitable shape or form for adsorption of gas components in a suitable adsorption apparatus, such forms which may comprise for example, and without limitation, powders, pellets, beads, sheets and particularly thin sheets, cloths, fabrics or combinations thereof, such as are known in the art or hereafter developed for use in adsorption processes.
In embodiments of the present inventive gas separation processes adapted to pressure swing adsorption (PSA) techniques, a maximum, or higher pressure for the PSA process may be selected that desirably provides for both bulk adsorption of at least a majority of the carbon monoxide on the first adsorbent material in the PSA adsorbers, and adsorption of substantially any remaining amounts of carbon dioxide on the second adsorbent material in the PSA adsorbers. In an exemplary embodiment of the inventive processes adapted for PSA, such suitable maximum PSA pressure may be desirably chosen to be between about 100-250 psig and more desirably between about 130-230 psig. In further embodiments adapted for PSA, a minimum, or lower PSA pressure may be chosen that desirably provides for the desorption of adsorbed gas components from the adsorbent material(s) during regeneration of the PSA adsorbers between adsorption cycles. Such minimum PSA pressure may be chosen as ambient pressure, or in an exemplary embodiment comprising vacuum assisted desorption of the PSA adsorbers, such minimum pressure may be desirably chosen to be below ambient pressure.
An exemplary, and non-limiting PSA adsorber pressure profile suitable for adaptation of the present inventive adsorptive separation processes to a 6-adsorber PSA device for the purification of a methane product gas by PSA from a feed gas mixture comprising at least methane and carbon dioxide components is illustrated in
In view of the many possible embodiments to which the principles of this disclosure may be applied, it should be recognized that the illustrated embodiments are only preferred examples and should not be taken as limiting the scope of the invention.
This is the U.S. National Stage of International Application No. PCT/US2005/040375, filed Nov. 5, 2004, which was published in English under PCT Article 21(2), which in turn claims the benefit of U.S. Provisional Application No. 60/625,202, filed Nov. 5, 2004, which are incorporated herein in their entirety.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2005/040375 | 11/7/2005 | WO | 00 | 5/3/2007 |
Publishing Document | Publishing Date | Country | Kind |
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WO2006/052937 | 5/18/2006 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3094569 | Thomas | Jun 1963 | A |
3204388 | Asker | Sep 1965 | A |
3430418 | Wagner | Mar 1969 | A |
3513631 | Siebert et al. | May 1970 | A |
3564816 | Batta | Feb 1971 | A |
3594984 | Toyama et al. | Jul 1971 | A |
3751878 | Collins | Aug 1973 | A |
3847672 | Trocciola et al. | Nov 1974 | A |
3865924 | Gidaspow et al. | Feb 1975 | A |
4019879 | Rabo et al. | Apr 1977 | A |
4077779 | Sircar et al. | Mar 1978 | A |
4144037 | Armond et al. | Mar 1979 | A |
4153434 | Settlemyer | May 1979 | A |
4200682 | Sederquist | Apr 1980 | A |
4272265 | Snyder | Jun 1981 | A |
4322394 | Mezey et al. | Mar 1982 | A |
4354859 | Keller, II et al. | Oct 1982 | A |
4406675 | Dangieri et al. | Sep 1983 | A |
4452612 | Mattia | Jun 1984 | A |
4530705 | Firey | Jul 1985 | A |
4532192 | Baker et al. | Jul 1985 | A |
4553981 | Fuderer | Nov 1985 | A |
4555453 | Appleby | Nov 1985 | A |
4578214 | Jungerhans | Mar 1986 | A |
4587114 | Hirai et al. | May 1986 | A |
4595642 | Nakanishi et al. | Jun 1986 | A |
4696682 | Hirai et al. | Sep 1987 | A |
4702903 | Keefer | Oct 1987 | A |
4726816 | Fuderer | Feb 1988 | A |
4743276 | Nishida et al. | May 1988 | A |
4758253 | Davidson et al. | Jul 1988 | A |
4759997 | Ohyauchi et al. | Jul 1988 | A |
4781735 | Tagawa et al. | Nov 1988 | A |
4783433 | Tajima et al. | Nov 1988 | A |
4790858 | Sircar | Dec 1988 | A |
4801308 | Keefer | Jan 1989 | A |
4816121 | Keefer | Mar 1989 | A |
4857083 | DiMartino | Aug 1989 | A |
4914076 | Tsuji et al. | Apr 1990 | A |
4915771 | O'Brien et al. | Apr 1990 | A |
4917711 | Xie et al. | Apr 1990 | A |
4963339 | Krishnamurthy et al. | Oct 1990 | A |
4968329 | Keefer | Nov 1990 | A |
4969935 | Hay | Nov 1990 | A |
4988580 | Ohsaki et al. | Jan 1991 | A |
4994331 | Cohen | Feb 1991 | A |
5068159 | Konoshita | Nov 1991 | A |
5079103 | Schramm | Jan 1992 | A |
5082473 | Keefer | Jan 1992 | A |
5096469 | Keefer | Mar 1992 | A |
5096470 | Krishnamurthy | Mar 1992 | A |
5126310 | Golden et al. | Jun 1992 | A |
5133784 | Boudet et al. | Jul 1992 | A |
5147735 | Ippommatsu et al. | Sep 1992 | A |
5175061 | Hildebrandt et al. | Dec 1992 | A |
5227598 | Woodmansee et al. | Jul 1993 | A |
5245110 | Van Dijk et al. | Sep 1993 | A |
5246676 | Hay | Sep 1993 | A |
5248325 | Kagimoto et al. | Sep 1993 | A |
5256172 | Keefer | Oct 1993 | A |
5256174 | Kai et al. | Oct 1993 | A |
5258571 | Golden et al. | Nov 1993 | A |
5271916 | Vanderborgh et al. | Dec 1993 | A |
5282886 | Kobayashi et al. | Feb 1994 | A |
5328503 | Kumar et al. | Jul 1994 | A |
5360679 | Buswell et al. | Nov 1994 | A |
5366818 | Wilkinson et al. | Nov 1994 | A |
5393326 | Engler et al. | Feb 1995 | A |
5411578 | Watson et al. | May 1995 | A |
5411721 | Doshi et al. | May 1995 | A |
5415748 | Emiliani et al. | May 1995 | A |
5429665 | Botich | Jul 1995 | A |
5431716 | Ebbeson | Jul 1995 | A |
5434016 | Benz et al. | Jul 1995 | A |
5441559 | Petit et al. | Aug 1995 | A |
5487775 | LaCava et al. | Jan 1996 | A |
5509956 | Opperman et al. | Apr 1996 | A |
5523326 | Dandekar et al. | Jun 1996 | A |
5529763 | Peng et al. | Jun 1996 | A |
5529970 | Peng | Jun 1996 | A |
5531809 | Golden et al. | Jul 1996 | A |
5543238 | Strasser | Aug 1996 | A |
5579610 | Jackson | Dec 1996 | A |
5593478 | Hill et al. | Jan 1997 | A |
5604047 | Bellows et al. | Feb 1997 | A |
5632807 | Tomita et al. | May 1997 | A |
5645950 | Benz et al. | Jul 1997 | A |
5646305 | Wagner et al. | Jul 1997 | A |
5656067 | Watson et al. | Aug 1997 | A |
5658370 | Vigor et al. | Aug 1997 | A |
5711926 | Knaebel | Jan 1998 | A |
5714276 | Okamoto | Feb 1998 | A |
5766311 | Ackley et al. | Jun 1998 | A |
5810909 | Notaro et al. | Sep 1998 | A |
5811201 | Skowronski | Sep 1998 | A |
5827358 | Kulish et al. | Oct 1998 | A |
5840099 | Kratz et al. | Nov 1998 | A |
5876486 | Steinwandel et al. | Mar 1999 | A |
5891217 | Lemcoff et al. | Apr 1999 | A |
5900329 | Reiter et al. | May 1999 | A |
5917136 | Gaffney et al. | Jun 1999 | A |
5925322 | Werth | Jul 1999 | A |
5938819 | Seery | Aug 1999 | A |
5955039 | Dowdy | Sep 1999 | A |
5958109 | Fuderer | Sep 1999 | A |
5968680 | Wolfe et al. | Oct 1999 | A |
5980857 | Kapoor et al. | Nov 1999 | A |
5981096 | Hornburg et al. | Nov 1999 | A |
5998056 | Divisek et al. | Dec 1999 | A |
6022399 | Ertl et al. | Feb 2000 | A |
6045933 | Okamoto | Apr 2000 | A |
6051050 | Keefer et al. | Apr 2000 | A |
6056804 | Keefer et al. | May 2000 | A |
6060032 | Hable et al. | May 2000 | A |
6063161 | Keefer et al. | May 2000 | A |
6077620 | Pettit | Jun 2000 | A |
6090312 | Ziaka et al. | Jul 2000 | A |
6143057 | Bülow et al. | Nov 2000 | A |
6162558 | Borup et al. | Dec 2000 | A |
6176897 | Keefer | Jan 2001 | B1 |
6190623 | Sanger et al. | Feb 2001 | B1 |
6190791 | Hornburg | Feb 2001 | B1 |
6200365 | Eimer et al. | Mar 2001 | B1 |
6210822 | Abersfelder et al. | Apr 2001 | B1 |
6231644 | Jain et al. | May 2001 | B1 |
6255010 | George et al. | Jul 2001 | B1 |
6283723 | Milburn et al. | Sep 2001 | B1 |
6293998 | Dolan et al. | Sep 2001 | B1 |
6296823 | Ertl et al. | Oct 2001 | B1 |
6312843 | Kimbara et al. | Nov 2001 | B1 |
6358300 | Fornof et al. | Mar 2002 | B1 |
6358302 | Deng et al. | Mar 2002 | B1 |
6398853 | Keefer et al. | Jun 2002 | B1 |
6406523 | Connor et al. | Jun 2002 | B1 |
6428915 | Ban et al. | Aug 2002 | B1 |
6471748 | Ackley | Oct 2002 | B1 |
6607854 | Rehg et al. | Aug 2003 | B1 |
6610124 | Dolan et al. | Aug 2003 | B1 |
6667128 | Edlund | Dec 2003 | B2 |
6692545 | Gittleman et al. | Feb 2004 | B2 |
6902602 | Keefer et al. | Jun 2005 | B2 |
6921597 | Keefer et al. | Jul 2005 | B2 |
7041272 | Keefer et al. | May 2006 | B2 |
7087331 | Keefer et al. | Aug 2006 | B2 |
7097925 | Keefer | Aug 2006 | B2 |
20010047824 | Hill et al. | Dec 2001 | A1 |
20020004157 | Keefer et al. | Jan 2002 | A1 |
20020098394 | Keefer et al. | Jul 2002 | A1 |
20020104518 | Keefer et al. | Aug 2002 | A1 |
20020110503 | Gittleman et al. | Aug 2002 | A1 |
20020110504 | Gittleman et al. | Aug 2002 | A1 |
20020112479 | Keefer et al. | Aug 2002 | A1 |
20020127442 | Connor et al. | Sep 2002 | A1 |
20020142198 | Towler et al. | Oct 2002 | A1 |
20020142208 | Keefer et al. | Oct 2002 | A1 |
20030143448 | Keefer et al. | Jul 2003 | A1 |
20030157390 | Keefer et al. | Aug 2003 | A1 |
20040005492 | Keefer et al. | Jan 2004 | A1 |
20040131912 | Keefer et al. | Jul 2004 | A1 |
20040197612 | Keefer et al. | Oct 2004 | A1 |
20050284291 | Alizadeh-Khiavi | Dec 2005 | A1 |
20070068386 | Mitariten | Mar 2007 | A1 |
Number | Date | Country |
---|---|---|
1256038 | Jun 1989 | CA |
2016045 | Aug 1994 | CA |
2109055 | Apr 1995 | CA |
2087972 | Jan 2000 | CA |
2087973 | Jan 2001 | CA |
2325072 | Apr 2002 | CA |
3913581 | Oct 1990 | DE |
0 143 537 | Jun 1985 | EP |
0 341 189 | Nov 1989 | EP |
0 345 908 | Dec 1989 | EP |
0 143 537 | Mar 1990 | EP |
0 681 860 | Nov 1995 | EP |
0 691 701 | Jan 1996 | EP |
0 737 648 | Oct 1996 | EP |
0 750 361 | Dec 1996 | EP |
0 751 045 | Jan 1997 | EP |
0 853 967 | Jul 1998 | EP |
1 070 531 | Jan 2001 | EP |
1 095 689 | May 2001 | EP |
1 172 772 | Jan 2002 | EP |
2 042 365 | Sep 1980 | GB |
59075574 | Apr 1984 | JP |
62274561 | Nov 1987 | JP |
62278770 | Dec 1987 | JP |
63034862 | Feb 1988 | JP |
63166137 | Jul 1988 | JP |
63228572 | Sep 1988 | JP |
04206161 | Jul 1992 | JP |
05166528 | Jul 1993 | JP |
07094200 | Jul 1995 | JP |
8045526 | Feb 1996 | JP |
10027621 | Jan 1998 | JP |
10325360 | Dec 1998 | JP |
11214021 | Aug 1999 | JP |
2002 358972 | Dec 2002 | JP |
WO 9404249 | Mar 1994 | WO |
WO 9613871 | May 1996 | WO |
WO 9829182 | Jul 1998 | WO |
WO 9901202 | Jan 1999 | WO |
WO 9916249 | Apr 1999 | WO |
WO 9928013 | Jun 1999 | WO |
WO 9946032 | Sep 1999 | WO |
WO 0016425 | Mar 2000 | WO |
WO 0016880 | Mar 2000 | WO |
WO 0076628 | Dec 2000 | WO |
WO 0076630 | Dec 2000 | WO |
WO 0147050 | Jun 2001 | WO |
WO 0224309 | Mar 2002 | WO |
WO 0235623 | May 2002 | WO |
WO 0237590 | May 2002 | WO |
WO 0245821 | Jun 2002 | WO |
WO 0247797 | Jun 2002 | WO |
WO 02056400 | Jul 2002 | WO |
WO 03020674 | Mar 2003 | WO |
WO 03077339 | Sep 2003 | WO |
WO 2004030130 | Apr 2004 | WO |
Number | Date | Country | |
---|---|---|---|
20070261551 A1 | Nov 2007 | US |
Number | Date | Country | |
---|---|---|---|
60625202 | Nov 2004 | US |