Compressor equipped emissions free dehydrator

Information

  • Patent Grant
  • 9527786
  • Patent Number
    9,527,786
  • Date Filed
    Friday, March 14, 2014
    10 years ago
  • Date Issued
    Tuesday, December 27, 2016
    7 years ago
Abstract
An emissions free dehydrator which can be used in conjunction with a compressor that compresses hydrocarbon vapors and gases. The dehydrator can capture virtually all hydrocarbon liquids and vapors produced by the process of removing water vapor from a flowing gas stream.
Description
BACKGROUND OF THE INVENTION

Field of the Invention (Technical Field)


An embodiment of the present invention relates to a compressor equipped emissions free dehydrator which can preferably capture at least substantially all hydrocarbon liquids and vapors produced by the process of removing water vapor from a flowing gas stream.


Description of Related Art


A conventional dehydrator contacts in a pressure vessel (absorber) the flowing gas stream. Normally, triethylene glycol is used as the contact medium. The triethylene glycol absorbs water vapor contained in the gas as well as some of the gas aromatics, (such as benzene, ethylbenzene, toluene, and xylenes commonly referred to as BTEX). The wet glycol (commonly called rich glycol) exits the absorber and is sent to a heated vessel (reboiler) where the glycol is heated to approximately 400 degrees F. Heating the glycol drives off the absorbed water as well as the absorbed BTEX (BTEX is a hazardous waste that has been proven to be carcinogenic). The heated stream of steam, BTEX, and other hydrocarbons exits the reboiler at approximately atmospheric pressure and 400 degrees F. To prevent atmospheric pollution, the heated stream must be processed to capture all the BTEX and any other hydrocarbon products the stream might contain.


Although BTEX is the major concern as a gas dehydration hazardous waste, there are other hazardous wastes such as methane gas (which may contain other hydrocarbon components) produced by the dehydration process. Most methane produced by gas dehydration is caused by glycol pumps, gas stripping of the rich glycol, and flashing as the rich glycol is released from high pressure to atmospheric pressure. There is thus a present need for a method, system, and apparatus which can capture the emissions and compress them to in excess of 200 pounds per square inch gauge pressure (“psig”).


Objects, advantages and novel features, and further scope of applicability of the present invention will be set forth in part in the detailed description to follow, taken in conjunction with the accompanying drawings, and in part will become apparent to those skilled in the art upon examination of the following, or may be learned by practice of the invention.


BRIEF SUMMARY OF EMBODIMENTS OF THE PRESENT INVENTION

An embodiment of the present invention relates to a method for dehydrating a hydrocarbon-containing gas which includes drying the hydrocarbon-containing gas in an absorber; directing the hydrocarbon-containing gas through a first heat exchanger after it has exited the absorber and before splitting a flow of the hydrocarbon-containing gas into a first portion of the hydrocarbon-containing gas and a second portion of the hydrocarbon-containing gas, wherein the second portion of the hydrocarbon-containing gas has its pressure reduced by a pressure regulator; directing the first portion of the hydrocarbon-containing gas to a second heat exchanger before directing the first portion of the hydrocarbon-containing gas to a stripping column, the second heat exchanger incorporated into a re-boiler; directing the first portion of the hydrocarbon-containing gas from the stripping column to the reboiler; and the first portion of the hydrocarbon-containing gas exiting a still column of the reboiler before directing the first portion of the hydrocarbon-containing gas to a condenser.


The method can also include first portion of the hydrocarbon-containing gas being cooled in the condenser at least in part by the second portion of the hydrocarbon-containing gas; passing the hydrocarbon-containing gas through an inlet separator before drying it in the absorber; and configuring the re-boiler to function as a glycol reconcentrator.


In one embodiment, after the second portion of the hydrocarbon-containing gas is directed through the condenser, it is directed to a gas sales line. Optionally, after exiting the condenser, the first portion of the hydrocarbon-containing gas is directed to a three-phase separator. In addition, gases exiting the three-phase separator can be directed to a compressor.


An embodiment of the present invention also relates to a dehydrator having an absorber with an outlet in fluid communication with a first heat exchanger, an outlet of the first heat exchanger in fluid communication with a pressure regulator, the pressure regulator in fluid communication with a second heat exchanger, the second heat exchanger disposed at least partially in a re-boiler, the reboiler comprising a stripping column; and the stripping column comprising an inlet in fluid communication with an outlet of the second heat exchanger and the stripping column comprising an outlet in fluid communication with an inlet of the re-boiler. An outlet of a still column of said re-boiler is in fluid communication with a first entrance of a condenser. The condenser can include a second entrance in fluid communication with the first heat exchanger. Optionally, an outlet of an inlet separator can be in fluid communication with the absorber. The first outlet of the condenser can be in fluid communication with a gas sales line. A second outlet of the condenser can be in fluid communication with an inlet of a three-phase separator. A gas outlet of the three-phase separator can be in fluid communication with an inlet of a compressor.


Objects, advantages and novel features, and further scope of applicability of the present invention will be set forth in part in the detailed description to follow, taken in conjunction with the accompanying drawing, and in part will become apparent to those skilled in the art upon examination of the following, or may be learned by practice of the invention. The objects and advantages of the invention may be realized and attained by means of the instrumentalities and combinations particularly pointed out in the appended claims.





BRIEF DESCRIPTION OF THE DRAWING

The accompanying drawing, which is incorporated into and forms a part of the specification, illustrates one or more embodiments of the present invention and, together with the description, serves to explain the principles of the invention. The drawing is only for the purpose of illustrating one or more preferred embodiments of the invention and is not to be construed as limiting the invention.



FIG. 1 is a flow diagram illustrating an embodiment of the present invention.





DETAILED DESCRIPTION OF THE INVENTION

Regardless of the source, a compressor equipped emissions free dehydrator according to an embodiment of the present invention can preferably capture the emissions and compress them to in excess of 200 psig. Although a user can optionally choose to direct them to a different location, in one embodiment, after compression, the captured emissions are preferably introduced into the inlet scrubber of another compressor to be compressed into the sales line and sold with the other gas.


After compression, the captured emissions are generally introduced into the inlet scrubber of another compressor to be compressed into the sales line and sold with the other gas.


The major equipment added to a standard dehydrator to capture the emissions are a condenser to receive the effluent from the reboiler still column, a three-phased separator to receive and send to storage or disposal the condensed liquids (water and hydrocarbons) condensed from the effluent exiting the still column of the reboiler, and a compressor (screw or reciprocating) to compress the uncondensed portion of the effluent from the still column and the methane produced by the dehydration process from ounces psig to pounds psig.


Referring to FIG. 1, the components of a standard dehydrator are illustrated, as well as the components necessary to convert it to an emissions free unit in accordance with an embodiment of the present invention. As illustrated therein, gas to be dehydrated at an elevated pressure in excess of 100 psig preferably enters inlet separator 2 at inlet 1. The gas preferably exits inlet separator 2 and flows through line 3 to inlet 4 of absorber 5. While flowing through absorber 5, the gas preferably contacts a dehydrating agent, which can optionally include dry triethlene glycol, the drying agent, preferably absorbs water vapor and aromatic hydrocarbons (BTEX) from the gas.


In one embodiment, the gas exits absorber 5 and flows through line 6 into heat exchanger 7, which can be a gas to glycol heat exchanger. The gas then preferably exits gas to glycol heat exchanger 7 and flows through line 8 to point 9. At point 9, the gas line preferably splits into lines 10 and 11. From point 9, some of the dehydrated gas preferably flows through line 10 to pressure regulator 12. Pressure regulator 12 preferably reduces the gas pressure to approximately 3 psig. The pressure setting of regulator 12 can be user-determined and can optionally be determined based upon the pressure needed to establish the volume of gas required for gas stripping of the glycol.


The volume of gas being used for gas stripping of the glycol is preferably indicated, optionally via a meter (not shown). From regulator 12, the gas preferably flows through line 13 to inlet 19 of gas to glycol heat exchanger 14. Gas to glycol heat exchanger 14 is preferably immersed, at least partially, in the hot glycol contained in reboiler 18. The gas preferably flows through heat exchanger 14 to be heated before exiting at outlet 20. As further illustrated in FIG. 1, the gas then flows through line 15 to the inlet 21 of stripping column 16.


In one embodiment, while flowing through stripping column 16 the hot, dehydrated gas preferably contacts the hot regenerated glycol exiting reboiler 18, further removing water from the regenerated glycol and super concentrating the glycol. The stripping gas preferably exits the stripping column at outlet 22 and flows through line 17 to enter reboiler 18 at point 23. In this embodiment, the stripping gas flows through reboiler 18, mixing with the water vapor and hydrocarbons being released from the rich glycol by heating in reboiler 18. The heated mixture of steam and hydrocarbons (hereinafter referred to as effluent) exits reboiler 18 at still column outlet 24. The effluent then preferably flows through line 25 to enter effluent condenser 27 at inlet 26. The effluent flows through effluent condenser 27, where it is cooled by the dehydrated gas flowing from point 9, through line 11, effluent condenser 27 and line 28 to sales.


In one embodiment, instead of using the sales gas, effluent condenser 27 can also optionally be cooled by circulating through the condenser glycol that has been air or gas cooled. Cooling of the effluent results in a quantity of the water and hydrocarbon vapors, in the effluent, condensing from the vapor to the liquid phase. A stream of water, liquid hydrocarbons, and uncondensed vapors can preferably exit condenser 27 at outlet 85. The uncondensed vapors and condensed liquids flow through line 29 to three-way safety valve 30. Three-way valve 30 preferably provides pressure relief for reboiler 18 and other components of the low pressure system in case of a mechanical or electric failure. Any vapors released by three-way safety valve 30 can be routed to a flare (not shown). From three-way safety valve 30, the condensed liquids and uncondensed vapors flow through line 31 to point 33. Point 33 can also receive gas from gas to glycol separator 49.


Referring again to FIG. 1, the sources of methane and other hydrocarbon components created by the dehydration process will be described. In reboiler 18, the rich glycol is preferably heated by fire tube 42. In one embodiment, the temperature to which they are heated can be in excess of 300 degrees F., and can most preferably be to a temperature of approximately 400 degrees F. in order to drive off the absorbed water and hydrocarbon aromatics from the flowing gas stream as well as any entrained hydrocarbons. After regeneration, the dried glycol is referred to as lean glycol. The lean glycol preferably exits reboiler 18 through line 43 and flows downward through packing in gas stripping column 16 where, as previously described, it is further dried by the stripping gas flowing upward through the packing. The lean glycol exits gas stripping column 16 through line 44 and flows to glycol to glycol heat exchanger 45 where it is cooled by the rich glycol (the source of the rich glycol will be explained later). The cooled lean glycol exits glycol to glycol heat exchanger 45 through line 46 and flows into glycol storage 47. The lean glycol then preferably exits glycol storage 47 through line 48 and flows to suction port 50 of glycol pump 51.


In one embodiment, the gas that was used to partially drive glycol pump 51 is a major source of the methane and it is thus most preferably captured. In one embodiment, where electricity is available, an electrically-powered pump can optionally be used instead of glycol pump 51. From discharge port 52 of glycol pump 51, the lean glycol is preferably pumped through line 53 into gas to glycol heat exchanger 7. The dehydrated gas flowing through glycol to gas heat exchanger 7 further cools the lean glycol before it enters absorber 5 through line 54.


In one embodiment, the lean glycol flows downward in absorber 5, preferably contacting the flowing gas stream and absorbing water vapor and BTEX from the gas. The water and hydrocarbon-rich glycol, at high pressure, exit absorber 5 through line 55 and flows to particulate filter 56. The high pressure rich glycol preferably flows through filter 56, which can be a particulate filter, and exits through line 57. The high pressure rich glycol then preferably flows through line 57 to inlet port 58 of the hydraulic motor that drives the pumping mechanism of pump 51.


In one embodiment, the approximately 75% of the power required to drive the hydraulic motor on pump 51 can be provided by the high pressure glycol exiting absorber 5. In this embodiment, the balance of power, approximately 25%, is preferably supplied by gas entrained in the rich glycol flowing from absorber 5, which can optionally be formed primarily from methane. Of course other power percentages and ratios can be used depending upon a particular application.


The rich low pressure glycol preferably exits the hydraulic motor of pump 51 at outlet port 59 and flows through line 60 to glycol to gas separator 49. Glycol to gas separator 49 can separate the rich glycol from the entrained gas (mainly methane). As previously described, the rich glycol exits glycol to gas separator 49 and flows through line 86 to glycol to glycol heat exchanger 45. While flowing through glycol to glycol heat exchanger 45, the rich glycol can be heated by the lean glycol exiting gas stripping column 16 through line 44. The heated rich glycol exits glycol to glycol heat exchanger 45 and flows through line 61 into inlet 63 of still column on reboiler 18. As previously described, the effluent from the rich glycol preferably exits reboiler 18 at point 24 and flows through line 25 into effluent condenser 27.


As further illustrated in FIG. 1, gas, which can optionally be primarily methane, released from the rich glycol, preferably exits gas to glycol separator 49 through line 64 and flows to point 65. From point 65, the gas can either flow through line 66 to fuel gas regulator 67 or line 70 to backpressure regulator 71. Backpressure regulator 71 preferably maintains the operating pressure, which in one embodiment can generally be from about 25 to about 50 psig, on gas to glycol separator 49.


The fuel required to fire reboiler 18 can optionally come from two sources—either gas to glycol separator 49, or point 72 on sales gas line 28. The fuel gas connection at point 72 can preferably supply fuel gas only during start-up or an upset condition of the dehydrator. Under normal operating conditions, all of the gas required to fire reboiler 18 can come from gas to glycol separator 49. Under upset conditions or while starting the dehydrator, fuel gas can optionally be caused to flow from point 72 through line 73 to fuel gas regulator 74. Fuel gas regulator 74 is preferably set to supply fuel gas at a lower set pressure than the set pressure of fuel gas regulator 67. From point 69, fuel gas from either of fuel gas regulators 67 or 74, preferably flows through line 76 to burner 77.


As further illustrated in FIG. 1, gas from gas to glycol separator 49, which is not required to fire reboiler 18, preferably flows from back pressure regulator 71 through line 78 to point 33. At point 33, the waste methane and other hydrocarbon components created by the dehydration process preferably combines with the uncondensed vapors and condensed liquids and flows through line 32 to enter three-phased separator 34. Three-phased separator 34 preferably operates at approximately 4 ounces of pressure and separates the total stream into its condensed liquids and uncondensed vapor components. In one embodiment, the condensed liquids are further separated into hydrocarbon and water components. The hydrocarbon components are preferably pumped, by pump 35, to storage. In this embodiment, the water components are preferably pumped by pump 36 to a disposal location or storage location. The uncondensed vapors preferably exit three-phased separator 34 at outlet 37 and flow through line 38 to inlet 39 of compressor 40. Compressor 40 preferably compresses the uncondensed vapors and recovered gases from a suction pressure of about 1 ounce to about 12 ounces and most preferably from a suction pressure of about 4 ounces, to a discharge pressure of about 15 psig to in excess of 200 psig. From outlet 41 of compressor 40, the uncondensed vapors and recovered gas preferably flow through line 178 to point 79 and from point 79 can optionally be discharged through line 80. From point 79, when required to maintain a suction pressure on compressor 40, gas can flow through line 81, pressure regulator 82, and line 83 to point 84.


Although the foregoing discussion refers to the term “glycol” any other liquid drying agent can be used in place thereof. Although various glycol pumps can be used and will provide desirable results. In one embodiment, the glycol pump used is preferably a KIMRAY® or other similar glycol pump.


Although the invention has been described in detail with particular reference to these preferred embodiments, other embodiments can achieve the same results. Variations and modifications of the present invention will be obvious to those skilled in the art and it is intended to cover in the appended claims all such modifications and equivalents. The entire disclosures of all references, applications, patents, and publications cited above are hereby incorporated by reference.

Claims
  • 1. A dehydrator comprising: an absorber having an outlet in fluid communication with a first heat exchanger;an outlet of said first heat exchanger in fluid communication with a pressure regulator;said pressure regulator in fluid communication with a second heat exchanger;said second heat exchanger disposed at least partially in a re-boiler, said reboiler comprising a still column; anda stripping column comprising an inlet in fluid communication with an outlet of the second heat exchanger and said stripping column comprising an outlet in fluid communication with an inlet of said re-boiler.
  • 2. The dehydrator of claim 1 wherein an outlet of said still column of said re-boiler is in fluid communication with a first entrance of a condenser.
  • 3. The dehydrator of claim 2 wherein said condenser comprises a second entrance in fluid communication with said first heat exchanger.
  • 4. The dehydrator of claim 1 further comprising an outlet of an inlet separator in fluid communication with said absorber.
  • 5. The dehydrator of claim 1 wherein said re-boiler comprises a glycol reconcentrator.
  • 6. The dehydrator of claim 2 wherein a first outlet of said condenser is in fluid communication with a gas sales line.
  • 7. The dehydrator of claim 2 wherein a second outlet of said condenser is in fluid communication with an inlet of a three-phase separator.
  • 8. The dehydrator system of claim 7 wherein a gas outlet of said three-phase separator is in fluid communication with an inlet of a compressor.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to and the benefit of the filing of U.S. Provisional Patent Application Ser. No. 61/793,149, entitled “Compressor Equipped Emissions Free Dehydrator”, filed on Mar. 15, 2013, and the specification thereof is incorporated herein by reference.

US Referenced Citations (227)
Number Name Date Kind
844694 Smith Feb 1907 A
1903481 Schweisthal Apr 1933 A
2225959 Miller Dec 1940 A
2726729 Williams Dec 1955 A
2738026 Glasgow et al. Mar 1956 A
2765872 Hartman et al. Oct 1956 A
2786543 Hayes et al. Mar 1957 A
2812827 Worley et al. Nov 1957 A
2815901 Hale Dec 1957 A
2853149 Gosselin Sep 1958 A
2937140 Stinson May 1960 A
2970107 Gilmore Jan 1961 A
2984360 Smith May 1961 A
3018640 Heller et al. Jan 1962 A
3025928 Heath Mar 1962 A
3027651 Nerge Apr 1962 A
3094574 Glasgow et al. Jun 1963 A
3105855 Meyers Oct 1963 A
3119674 Glasgow et al. Jan 1964 A
3152753 Adams Oct 1964 A
3182434 Fryar May 1965 A
3232027 Lorenz et al. Feb 1966 A
3237847 Wilson Mar 1966 A
3254473 Fryar et al. Jun 1966 A
3255573 Cox, Jr. et al. Jun 1966 A
3288448 Patterson et al. Nov 1966 A
3321890 Barnhart May 1967 A
3347019 Barnhart Oct 1967 A
3360127 Wood, Jr. Dec 1967 A
3396512 McMinn et al. Aug 1968 A
3398723 Smalling Aug 1968 A
3407052 Huntress et al. Oct 1968 A
3528758 Perkins Sep 1970 A
3540821 Siegmund Nov 1970 A
3541763 Heath et al. Nov 1970 A
3589984 Reid Jun 1971 A
3616598 Floral, Jr. Nov 1971 A
3648434 Gravis, III et al. Mar 1972 A
3659401 Giammarco May 1972 A
3662017 Woerner et al. May 1972 A
3672127 Mayse et al. Jun 1972 A
3736725 Alleman et al. Jun 1973 A
3817687 Cavallero et al. Jun 1974 A
3829521 Green Aug 1974 A
3855337 Foral, Jr. et al. Dec 1974 A
3872682 Shook Mar 1975 A
3949749 Stewart Apr 1976 A
3989487 Peterson Nov 1976 A
4009985 Hirt Mar 1977 A
4010009 Moyer Mar 1977 A
4010065 Alleman Mar 1977 A
4058147 Stary et al. Nov 1977 A
4098303 Gammell Jul 1978 A
4108618 Schneider Aug 1978 A
4118170 Hirt Oct 1978 A
4134271 Datis Jan 1979 A
4139596 Vaseen Feb 1979 A
4162145 Alleman Jul 1979 A
4165618 Tyree, Jr. Aug 1979 A
4198214 Heath et al. Apr 1980 A
4270938 Schmidt et al. Jun 1981 A
4286929 Heath et al. Sep 1981 A
4305895 Heath et al. Dec 1981 A
4322265 Wood Mar 1982 A
4332643 Reid Jun 1982 A
4342572 Heath Aug 1982 A
4362462 Blotenberg Dec 1982 A
4369049 Heath Jan 1983 A
4396371 Lorenz et al. Aug 1983 A
4402652 Gerlach et al. Sep 1983 A
4421062 Padilla, Sr. Dec 1983 A
4431433 Gerlach et al. Feb 1984 A
4435196 Pielkenrood Mar 1984 A
4459098 Turek et al. Jul 1984 A
4462813 May et al. Jul 1984 A
4474549 Capone Oct 1984 A
4474550 Heath et al. Oct 1984 A
4493770 Moilliet Jan 1985 A
4501253 Gerstmann et al. Feb 1985 A
4505333 Ricks Mar 1985 A
4511374 Heath Apr 1985 A
4539023 Boley Sep 1985 A
4568268 Gerlach et al. Feb 1986 A
4579565 Heath Apr 1986 A
4583998 Reid et al. Apr 1986 A
4588372 Torborg May 1986 A
4588424 Heath et al. May 1986 A
4597733 Dean et al. Jul 1986 A
4615673 Heath et al. Oct 1986 A
4617030 Heath Oct 1986 A
4659344 Gerlach et al. Apr 1987 A
4674446 Padilla, Sr. Jun 1987 A
4676806 Dean et al. Jun 1987 A
4689053 Heath Aug 1987 A
4701188 Mims Oct 1987 A
4715808 Heath et al. Dec 1987 A
4737168 Heath Apr 1988 A
4778443 Sands et al. Oct 1988 A
4780115 Ranke Oct 1988 A
4824447 Goldsberry Apr 1989 A
4830580 Hata et al. May 1989 A
4919777 Bull Apr 1990 A
4948393 Hodson et al. Aug 1990 A
4949544 Hines Aug 1990 A
4978291 Nakai Dec 1990 A
4983364 Buck et al. Jan 1991 A
5016447 Lane et al. May 1991 A
5080802 Cairo, Jr. et al. Jan 1992 A
5084074 Beer et al. Jan 1992 A
5129925 Marsala et al. Jul 1992 A
5130078 Dillman Jul 1992 A
5132011 Ferris Jul 1992 A
5163981 Choi Nov 1992 A
5167675 Rhodes Dec 1992 A
5191990 Fritts Mar 1993 A
5195587 Webb Mar 1993 A
5209762 Lowell May 1993 A
5249739 Bartels et al. Oct 1993 A
5269886 Brigham Dec 1993 A
5346537 Lowell Sep 1994 A
5377723 Hilliard Jan 1995 A
5419299 Fukasawa et al. May 1995 A
5453114 Ebeling Sep 1995 A
5476126 Hilliard et al. Dec 1995 A
5490873 Behrens et al. Feb 1996 A
5501253 Weiss Mar 1996 A
5513680 Hilliard et al. May 1996 A
5536303 Ebeling Jul 1996 A
5571310 Nanaji Nov 1996 A
5579740 Cotton et al. Dec 1996 A
5626027 Dormer et al. May 1997 A
5664144 Yanai et al. Sep 1997 A
5665144 Hill et al. Sep 1997 A
5678411 Matsumura et al. Oct 1997 A
5755854 Nanaji May 1998 A
5766313 Heath Jun 1998 A
5826433 Dube Oct 1998 A
5857616 Karnoff et al. Jan 1999 A
5878725 Osterbrink Mar 1999 A
5882486 Moore Mar 1999 A
5885060 Cunkelman et al. Mar 1999 A
5988232 Koch et al. Nov 1999 A
6004380 Landreau et al. Dec 1999 A
6010674 Miles et al. Jan 2000 A
6023003 Dunning et al. Feb 2000 A
6027311 Hill et al. Feb 2000 A
6095793 Greeb Aug 2000 A
6142191 Sutton et al. Nov 2000 A
6183540 Thonsgaard Feb 2001 B1
6193500 Bradt et al. Feb 2001 B1
6223789 Koch May 2001 B1
6224369 Moneyhun May 2001 B1
6238461 Heath May 2001 B1
6251166 Anderson Jun 2001 B1
6273937 Schucker Aug 2001 B1
6299671 Christensen Oct 2001 B1
6314981 Mayzou et al. Nov 2001 B1
6332408 Howlett Dec 2001 B2
6363744 Finn et al. Apr 2002 B2
6364933 Heath Apr 2002 B1
6425942 Forster Jul 2002 B1
6461413 Landreau et al. Oct 2002 B1
6478576 Bradt et al. Nov 2002 B1
6499476 Reddy Dec 2002 B1
6532999 Pope et al. Mar 2003 B2
6533574 Pechoux Mar 2003 B1
6537349 Choi et al. Mar 2003 B2
6537458 Polderman Mar 2003 B1
6551379 Heath Apr 2003 B2
6604558 Sauer Aug 2003 B2
6616731 Hillstrom Sep 2003 B1
6719824 Bowser Apr 2004 B1
6745576 Granger Jun 2004 B1
6931919 Weldon Aug 2005 B2
6984257 Heath et al. Jan 2006 B2
7005057 Kalnes Feb 2006 B1
7025084 Perry et al. Apr 2006 B2
7131265 Lechner Nov 2006 B2
RE39944 Heath Dec 2007 E
7350581 Wynn Apr 2008 B2
7481237 Jones et al. Jan 2009 B2
7497180 Karlsson et al. Mar 2009 B2
7531030 Heath et al. May 2009 B2
7575672 Gilmore Aug 2009 B1
7791882 Chu et al. Sep 2010 B2
7905722 Heath et al. Mar 2011 B1
8529215 Heath et al. Sep 2013 B2
8840703 Heath et al. Sep 2014 B1
8864887 Heath et al. Oct 2014 B2
8900343 Heath et al. Dec 2014 B1
9291409 Heath et al. Mar 2016 B1
20010008073 Finn et al. Jul 2001 A1
20020073843 Heath Jun 2002 A1
20020081213 Takahashi et al. Jun 2002 A1
20020178918 Lecomte et al. Dec 2002 A1
20020185006 Lecomte et al. Dec 2002 A1
20030005823 Le Blanc et al. Jan 2003 A1
20030167690 Edlund et al. Sep 2003 A1
20040031389 Heath et al. Feb 2004 A1
20040186630 Shier et al. Sep 2004 A1
20040211192 Lechner Oct 2004 A1
20050115248 Koehler et al. Jun 2005 A1
20050266362 Stone et al. Dec 2005 A1
20060144080 Heath et al. Jul 2006 A1
20060156744 Cusiter et al. Jul 2006 A1
20060156758 An et al. Jul 2006 A1
20060218900 Lechner Oct 2006 A1
20060254777 Wynn Nov 2006 A1
20060260468 Amin Nov 2006 A1
20070051114 Mahlanen Mar 2007 A1
20070084341 Heath et al. Apr 2007 A1
20070151292 Heath et al. Jul 2007 A1
20070175226 Karlsson et al. Aug 2007 A1
20070186770 Heath et al. Aug 2007 A1
20070199696 Walford Aug 2007 A1
20080008602 Pozivil et al. Jan 2008 A1
20080120993 An et al. May 2008 A1
20090133578 Brasa et al. May 2009 A1
20090223246 Heath et al. Sep 2009 A1
20100040989 Heath et al. Feb 2010 A1
20100083678 Lifson et al. Apr 2010 A1
20100083691 Immink et al. Apr 2010 A1
20100263393 Chen et al. Oct 2010 A1
20100313586 Yakumaru et al. Dec 2010 A1
20120079851 Heath et al. Apr 2012 A1
20120261092 Heath et al. Oct 2012 A1
20130319844 Heath et al. Dec 2013 A1
Foreign Referenced Citations (21)
Number Date Country
011862 Sep 2000 AR
024366 Oct 2002 AR
2281610 Sep 1998 CA
2426071 Oct 2003 CA
2224389 Feb 2008 CA
2311440 Jun 2011 CA
2563747 May 2013 CA
2523110 Aug 2014 CA
2541606 Oct 2014 CA
2809118 Feb 2015 CA
2573514 Sep 2015 CA
2542039 Sep 1984 FR
370591 Apr 1932 GB
573819 Dec 1945 GB
58185990 Oct 1983 JP
1801092 Mar 1993 RU
2159913 Nov 2000 RU
1021809 Jun 1983 SU
2005068847 Jul 2005 WO
2010080040 Jul 2010 WO
2013170190 Nov 2013 WO
Non-Patent Literature Citations (4)
Entry
“Environmental Technology Verification Report”, Greenhouse Gas Technology Center Southern Research Institute.
“Natural Gas Dehydration”, The Environmental Technology Verification Program, Sep. 2003.
Archer, “TEG Regenerator Vapor Recovery in Amoco's Northwestern Business Unit”, Amoco Northwestern Business Unit, Aug. 1992.
Reid, “Coldfinger an Exhauster for Removing Trace Quantities of Water from Glycol Solutions Used for Gas Dehydration”, Ball-Reid Engineers, Inc., Oklahoma City, Oklahoma, 1975, 592-602.
Provisional Applications (1)
Number Date Country
61793149 Mar 2013 US