Separation of carbon dioxide from other gases

Information

  • Patent Grant
  • 7828877
  • Patent Number
    7,828,877
  • Date Filed
    Monday, November 7, 2005
    19 years ago
  • Date Issued
    Tuesday, November 9, 2010
    14 years ago
Abstract
An inventive 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 embodiment of the invention, 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 embodiment of the invention, 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.
Description
FIELD

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.


BACKGROUND

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.


SUMMARY

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.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 shows a purely exemplary 6 bed pressure swing adsorption (PSA) cycle comprising a single common adsorber pressure profile (i.e., relative pressure vs. phase angle) suitable for implementing an embodiment of the presently disclosed adsorption processes using PSA techniques. As is known in the art, the “phase angle” of a PSA cycle is employed to divide the progress of a one complete cycle into 360° to be able to determine the implementation of each individual step during the cycle.





DETAILED DESCRIPTION OF SEVERAL EMBODIMENTS

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 FIG. 1. The relative pressure levels of various stages of the exemplary PSA cycle for a single PSA adsorber vessel are shown against the progressive phase of the cycle, wherein the progressive phase of the 6-adsorber PSA cycle are represented as 12 half-steps. The disclosed pressure cycle comprises three depressurization steps, and three re-pressurization steps, and both a supply purge stream and a product purge stream in order to desirably increase the recovery of methane in the purified methane product gas, relative to some simpler PSA cycles, such as are known in the art, which may employ product purge alone to regenerate the adsorbent materials.


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.

Claims
  • 1. An adsorptive gas separation process for producing a purified methane product gas from a feed gas mixture comprising at least methane and carbon dioxide, wherein the feed gas mixture comprises at least about 10% carbon dioxide, and the purified methane product gas is produced 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 subsequently a second adsorbent material suited for substantially removing remaining amounts of carbon dioxide while substantially excluding methane from adsorption, and wherein the purified methane product gas contains less than about 5000 ppm carbon dioxide, wherein the first adsorbent material is selected from the group consisting of aluminas, silicas, silica gel, hydrophohic zeolites, activated carbon and combinations thereof and the second adsorbent material is selected from the group consisting of zeolite 3A, carbon molecular sieves, titanosilicate molecular sieve materials and combinations thereof, and the separation process further includes vacuum assisted desorption of the adsorber during regeneration of the adsorber.
  • 2. The adsorptive gas separation process according to claim 1 wherein the feed gas mixture comprises at least about 20% carbon dioxide.
  • 3. The adsorptive gas separation process according to claim 1 wherein the feed gas mixture comprises at least about 50% carbon dioxide.
  • 4. The adsorptive gas separation process according to claim 1 wherein the purified methane product gas contains less than about 1000 ppm of carbon dioxide.
  • 5. The adsorptive gas separation process according to claim 1 wherein the purified methane product gas contains less than about 100 ppm of carbon dioxide.
  • 6. The adsorptive gas separation process according to claim 1 wherein the adsorptive gas separation process comprises a pressure swing adsorption process.
  • 7. The adsorptive gas separation process according to claim 6 wherein the pressure swing adsorption process defines a higher pressure and a lower pressure, and wherein the higher pressure is between about 100-250 psig.
  • 8. The adsorptive gas separation process according to claim 6 wherein the pressure swing adsorption process defines a higher pressure and a lower pressure, and wherein the higher pressure is between about 130-230 psig.
  • 9. An adsorptive gas separation process for producing a purified methane product gas from a feed gas mixture comprising methane and carbon dioxide, the process comprising the sequential steps of: contacting the feed gas mixture with a first adsorbent material suited for adsorbing a majority of the carbon dioxide in the feed gas stream, wherein the first adsorbent material is selected from the group consisting of aluminas, silicas, silica gel, hydrophohic zeolites, activated carbon and combinations thereof; andcontacting the gas mixture with a second adsorbent material suited for substantially removing remaining amounts of carbon dioxide while substantially excluding methane from adsorption, wherein the second adsorbent material is selected from the group consisting of zeolite 3A, carbon molecular sieves, titanosilicate molecular sieve materials and combinations thereof; andwherein the process further includes vacuum assisted desorption of the first adsorbent material and the second adsorbent material during regeneration.
  • 10. The process of claim 9 wherein the process is a pressure swing adsorption process.
  • 11. The process of claim 9 wherein the first adsorbent material comprises activated alumina.
  • 12. The process of claim 11 wherein the first adsorbent material additionally comprises silica gel.
  • 13. The process of claim 9 wherein the first adsorbent material is activated alumina and the second adsorbent material is a carbon molecular sieve.
  • 14. The process of claim 9 wherein the feed gas mixture comprises at least about 10% carbon dioxide.
  • 15. The process of claim 9 wherein the purified methane product gas comprises less than about 5000 ppm carbon dioxide.
  • 16. The adsorptive gas separation process according to claim 9 wherein the feed gas mixture comprises at least about 20% carbon dioxide.
  • 17. The adsorptive gas separation process according to claim 9 wherein the feed gas mixture comprises at least about 50% carbon dioxide.
  • 18. The adsorptive gas separation process according to claim 9 wherein the purified methane product gas contains less than about 1000 ppm of carbon dioxide.
  • 19. The adsorptive gas separation process according to claim 9 wherein the purified methane product gas contains less than about 100 ppm of carbon dioxide.
  • 20. The adsorptive gas separation process according to claim 10 wherein the pressure swing adsorption process defines a higher pressure and a lower pressure, and wherein the higher pressure is between about 100-250 psig.
  • 21. The adsorptive gas separation process according to claim 10 wherein the pressure swing adsorption process defines a higher pressure and a lower pressure, and wherein the higher pressure is between about 130-230 psig.
CROSS REFERENCE TO RELATED APPLICATIONS

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.

PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/US2005/040375 11/7/2005 WO 00 5/3/2007
Publishing Document Publishing Date Country Kind
WO2006/052937 5/18/2006 WO A
US Referenced Citations (162)
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
Foreign Referenced Citations (56)
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
Related Publications (1)
Number Date Country
20070261551 A1 Nov 2007 US
Provisional Applications (1)
Number Date Country
60625202 Nov 2004 US