This application is related to U.S. patent application Ser. No. 09/643,420, filed Aug. 23, 2001, for APPARATUS AND PROCESS FOR THE REFRIGERATION, LIQUEFACTION AND SEPARATION OF GASES WITH VARYING LEVELS OF PURITY, now U.S. Pat. No. 6,425,263, issued Jul. 30, 2002, which is a continuation of U.S. patent application Ser. No. 09/212,490, filed Dec. 16, 1998, for APPARATUS AND PROCESS FOR THE REFRIGERATION, LIQUEFACTION AND SEPARATION OF GASES WITH VARYING LEVELS OF PURITY, now U.S. Pat. No. 6,105,390, issued Aug. 22, 2000, which claims the benefit of U.S. Provisional Patent Application Ser. No. 60/069,698 filed Dec. 16, 1997. This application is also related to U.S. patent application Ser. No. 11/381,904, filed May 5, 2006, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 7,594,414, issued Sep. 29, 2009; U.S. patent application Ser. No. 11/383,411, filed May 15, 2006, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 7,591,150, issued Sep. 22, 2009; U.S. patent application Ser. No. 11/560,682, filed Nov. 16, 2006, for APPARATUS FOR THE LIQUEFACTION OF GAS AND METHODS RELATING TO SAME; U.S. patent application Ser. No. 11/536,477, filed Sep. 28, 2006, for APPARATUS FOR THE LIQUEFACTION OF A GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 7,637,122, issued Dec. 29, 2009; U.S. patent application Ser. No. 11/674,984, filed Feb. 14, 2007, for SYSTEMS AND METHODS FOR DELIVERING HYDROGEN AND SEPARATION OF HYDROGEN FROM A CARRIER MEDIUM, now abandoned, which is a continuation-in-part of U.S. patent application Ser. No. 11/124,589, filed May 5, 2005, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 7,219,512, issued May 22, 2007, which is a continuation of U.S. patent application Ser. No. 10/414,991, filed Apr. 14, 2003, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 6,962,061, issued Nov. 8, 2005, and U.S. patent application Ser. No. 10/414,883, filed Apr. 14, 2003, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 6,886,362, issued May 3, 2005, which is a divisional of U.S. patent application Ser. No. 10/086,066, filed Feb. 27, 2002, for APPARATUS FOR THE LIQUEFACTION OF NATURAL GAS AND METHODS RELATED TO SAME, now U.S. Pat. No. 6,581,409, issued Jun. 24, 2003, and which claims the benefit of U.S. Provisional Patent Application Ser. No. 60/288,985, filed May 4, 2001, for SMALL SCALE NATURAL GAS LIQUEFACTION PLANT. This application is also related to U.S. patent application Ser. No. 11/855,071, filed Sep. 13, 2007, for HEAT EXCHANGER AND ASSOCIATED METHODS, now U.S. Pat. No. 8,061,413, issued Nov. 22, 2011; U.S. patent application Ser. No. 12/603,948, filed Oct. 22, 2009, for COMPLETE LIQUEFACTION METHODS AND APPARATUS, now U.S. Pat. 8,555,672, issued Oct. 15, 2013; and U.S. patent application Ser. No. 12/604,139, filed Oct. 22, 2009, for NATURAL GAS LIQUEFACTION CORE MODULES, PLANTS INCLUDING SAME AND RELATED METHODS. The disclosure of each of the foregoing documents is incorporated by reference herein in its entirety. This application is also related to U.S. patent application Ser. No. 12/648,659, filed Dec. 29, 2009, for METHODS AND APPARATUS FOR FORMING AND SEPARATING A SLURRY OF LNG AND SOLID CARBON DIOXIDE, which is a continuation of U.S. patent application Ser. No. 11/536,477, filed Sep. 28, 2006, for APPARATUS FOR THE LIQUEFACTION OF A GAS AND METHODS RELATING TO SAME, now U.S. Pat. No. 7,637,122, issued Dec. 29, 2009; U.S. patent application Ser. No. 12/938,761, filed Nov. 3, 2010, for VAPORIZATION CHAMBERS AND ASSOCIATED METHODS; U.S. patent application Ser. No. 12/938,826, filed Nov. 3, 2010, for HEAT EXCHANGER AND RELATED METHODS; U.S. patent application Ser. No. 12/938,967, filed Nov. 3, 2010, for SUBLIMATION SYSTEMS AND ASSOCIATED METHODS; U.S. patent application Ser. No. 13/284,737, filed Oct. 28, 2011, for METHODS OF CONVEYING FLUIDS AND METHODS OF SUBLIMATING SOLID PARTICLES, now U.S. Pat. No. 8,544,295, issued Oct. 1, 2013, which is a divisional of U.S. patent application Ser. No. 11/855,071, filed Sep. 13, 2007, for HEAT EXCHANGERS COMPRISING AT LEAST ONE POROUS MEMBER POSITIONED WITHIN A CASING, now U.S. Pat. No. 8,061,413, issued Nov. 22, 2011; and U.S. patent application Ser. No. 13/528,246, filed Jun. 20, 2012, for NATURAL GAS LIQUEFACTION EMPLOYING INDEPENDENT REFRIGERANT PATH.
The present invention relates generally to the compression and liquefaction of gases and, more particularly, to methods and apparatus for the partial liquefaction of a gas, such as natural gas, by utilizing a combined refrigerant and expansion process with multiple tail gas streams.
Natural gas is a known alternative to combustion fuels such as gasoline and diesel. Much effort has gone into the development of natural gas as an alternative combustion fuel in order to combat various drawbacks of gasoline and diesel including production costs and the subsequent emissions created by the use thereof. As is known in the art, natural gas is a cleaner burning fuel than other combustion fuels. Additionally, natural gas is considered to be safer than gasoline or diesel as natural gas will rise in the air and dissipate, rather than settling.
To be used as an alternative combustion fuel, natural gas (also termed “feed gas” herein) is conventionally converted into compressed natural gas (CNG) or liquified (or liquid) natural gas (LNG) for purposes of storing and transporting the fuel prior to its use. Conventionally, two of the known basic cycles for the liquefaction of natural gases are referred to as the “cascade cycle” and the “expansion cycle.”
Briefly, the cascade cycle consists of a series of heat exchanges with the feed gas, each exchange being at successively lower temperatures until liquefaction is accomplished. The levels of refrigeration are obtained with different refrigerants or with the same refrigerant at different evaporating pressures. The cascade cycle is considered to be very efficient at producing LNG as operating costs are relatively low. However, the efficiency in operation is often seen to be offset by the relatively high investment costs associated with the expensive heat exchange and the compression equipment associated with the refrigerant system. Additionally, a liquefaction plant incorporating such a system may be impractical where physical space is limited, as the physical components used in cascading systems are relatively large.
In an expansion cycle, gas is conventionally compressed to a selected pressure, cooled, and then allowed to expand through an expansion turbine, thereby producing work as well as reducing the temperature of the feed gas. The low temperature feed gas is then heat exchanged to effect liquefaction of the feed gas. Conventionally, such a cycle has been seen as being impracticable in the liquefaction of natural gas since there is no provision for handling some of the components present in natural gas, which freeze at the temperatures encountered in the heat exchangers, for example, water and carbon dioxide.
Additionally, to make the operation of conventional systems cost effective, such systems are conventionally built on a large scale to handle large volumes of natural gas. As a result, fewer facilities are built, making it more difficult to provide the raw gas to the liquefaction plant or facility as well as making distribution of the liquefied product an issue. Another major problem with large-scale facilities is the capital and operating expenses associated therewith. For example, a conventional large-scale liquefaction plant, i.e., producing on the order of 70,000 gallons of LNG per day, may cost $16.3 million to $24.5 million, or more, in capital expenses.
An additional problem with large facilities is the cost associated with storing large amounts of fuel in anticipation of future use and/or transportation. Not only is there a cost associated with building large storage facilities, but there is also an efficiency issue related therewith as stored LNG will tend to warm and vaporize over time creating a loss of the LNG fuel product. Further, safety may become an issue when larger amounts of LNG fuel product are stored.
In confronting the foregoing issues, various systems have been devised that attempt to produce LNG or CNG from feed gas on a smaller scale, in an effort to eliminate long-term storage issues and to reduce the capital and operating expenses associated with the liquefaction and/or compression of natural gas.
For example, small scale LNG plants have been devised to produce LNG at a pressure letdown station, wherein gas from a relatively high pressure transmission line is utilized to produce LNG and tail gases from the liquefaction process are directed into a single lower pressure downstream transmission line. However, such plants may only be suitable for pressure let down stations having a relatively high pressure difference between upstream and downstream transmission lines, or may be inefficient at pressure let down stations having relatively low pressure drops. In view of this, the production of LNG at certain existing let down stations may be impractical using existing LNG plants.
Additionally, since many sources of natural gas, such as residential or industrial service gas, are considered to be relatively “dirty,” the requirement of providing “clean” or “pre-purified” gas is actually a requirement of implementing expensive and often complex filtration and purification systems prior to the liquefaction process. This requirement simply adds expense and complexity to the construction and operation of such liquefaction plants or facilities.
In view of the foregoing, it would be advantageous to provide a method, and a plant for carrying out such a method, which is flexible and has improved efficiency in producing liquefied natural gas. Additionally, it would be advantageous to provide a more efficient method for producing liquefied natural gas from a source of relatively “dirty” or “unpurified” natural gas without the need for “pre-purification.”
It would be desirable to develop new liquefaction methods and plants that take advantage of pressure let down locations that may have multiple transmission lines carrying natural gas at varied pressures, and pressure let down stations having relatively low pressure drops. Additionally, it would be desirable to develop new liquefaction methods and plants that enable more efficient use of various tail gases generated during liquefaction. The flexibility of such a design would also make it applicable to be used as a modular design for optimal implementation of small scale liquefaction plants in a variety of different locations.
It would be additionally advantageous to provide a plant for the liquefaction of natural gas which is relatively inexpensive to build and operate, and which desirably requires little or no operator oversight.
It would be additionally advantageous to provide such a plant which is relatively easily transportable and which may be located and operated at existing sources of natural gas which are within or near populated communities, thus providing easy access for consumers of LNG fuel.
In one embodiment, a method of natural gas liquefaction may include directing a gaseous natural gas (NG) process stream and a cooling stream into a plant, cooling the gaseous NG process stream by transferring heat from the gaseous NG process stream to the cooling stream, and expanding the cooled gaseous NG process stream to form a liquid NG process stream and a first tail stream comprising a gaseous NG. The method may further include directing the first tail gas stream out of the plant at a first pressure, separating a secondary liquid NG stream from the liquid NG process stream and vaporizing at the secondary liquid NG stream with a heat exchanger to form a tail stream comprising gaseous NG. Additionally, the second tail gas stream may be directed out of the plant at a second pressure, the second pressure different than the first pressure of the first tail gas stream.
In another embodiment, a method of natural gas liquefaction may include directing a gaseous natural gas (NG) process stream comprising gaseous carbon dioxide (CO2) into a plant, cooling the gaseous NG process stream within a heat exchanger, and expanding the cooled gaseous NG process stream to form a liquid NG process stream comprising solid CO2. The method may further include directing a substantially pure liquid NG into a storage tank. Additionally, the method may include separating the CO2 from the liquid NG process stream and processing the CO2 to provide a CO2 product stream.
In an additional embodiment, a method of natural gas liquefaction may include directing a marginal gaseous natural gas (NG) process stream comprising at least one impurity into a plant and combining the marginal gaseous NG process stream with a secondary substantially pure NG stream to provide an improved gaseous NG process stream. The method may further include cooling the improved gaseous NG process stream within a heat exchanger, expanding the cooled improved gaseous NG process stream to form a liquid natural gas (LNG) process stream, and separating the at least one impurity from the LNG process stream to provide a substantially pure LNG process stream. Additionally, the method may include providing the secondary substantially pure NG stream from the substantially pure LNG process stream.
In a further embodiment, a natural gas liquefaction plant may include a gaseous natural gas process stream inlet, a multi-pass heat exchanger comprising a first channel configured to cool a gaseous natural gas process stream and an expander valve configured to cool at least a portion of the gaseous natural gas process stream to a liquid state. The natural gas liquefaction plant may further include a liquid natural gas outlet, a first tail gas outlet, and at least a second tail gas outlet, the at least a second tail gas outlet separate from the first tail gas outlet.
The foregoing and other advantages of the invention will become apparent upon reading the following detailed description and upon reference to the drawings.
Illustrated in
As further shown in
A first tail gas stream 30 may include a combination of streams from the plant 10. For example, as shown in
Finally, as shown in
In operation, the cooling stream 14 may be directed into the plant 10 in a gaseous phase through the cooling fluid inlet 54 and then directed into the turbo compressor 56 to be compressed. The compressed cooling stream 14 may then exit the turbo compressor 56 and be directed into the ambient heat exchanger 58, which may transfer heat from the cooling stream 14 to ambient air. Additionally, the cooling stream 14 may be directed through a first channel of the primary heat exchanger 34, where it may be further cooled.
In some embodiments, the primary heat exchanger 34 may comprise a high performance aluminum multi-pass plate and fin type heat exchanger, such as may be purchased from Chart Industries Inc., 1 Infinity Corporate Centre Drive, Suite 300, Garfield, Heights, Ohio 44125, or other well-known manufacturers of such equipment.
After passing through the primary heat exchanger 34, the cooling stream 14 may be expanded and cooled in the turbo expander 60. For example, the turbo expander 60 may comprise a turbo expander having a specific design for a mass flow rate, pressure level of gas, and temperature of gas to the inlet, such as may be purchased from GE Oil and Gas, 1333 West Loop South, Houston, Tex. 77027-9116, USA, or other well-known manufacturers of such equipment. Additionally, the energy required to drive the turbo compressor 56 may be provided by the turbo expander 60, such as by the turbo expander 60 being directly connected to the turbo compressor 56 or by the turbo expander 60 driving an electrical generator (not shown) to produce electrical energy to drive an electrical motor (not shown) that may be connected to the turbo compressor 56. The cooled cooling stream 14 may then be directed through a second channel of the primary heat exchanger 34 and then exit the plant 10 via the cooling fluid outlet 62.
Meanwhile, a gaseous NG may be directed into the NG inlet 32 to provide the process stream 12 to the plant 10 and the process stream 12 may then be directed through a third channel of the primary heat exchanger 34. Heat from the process stream 12 may be transferred to the cooling stream 14 within the primary heat exchanger 34 and the process stream 12 may exit the primary heat exchanger 34 in a cooled gaseous state. The process stream 12 may then be directed through the expansion valve 36, such as a Joule-Thomson expansion valve, wherein the process stream 12 may be expanded and cooled to form a liquid natural gas (LNG) portion and a gaseous NG portion. Additionally, carbon dioxide (CO2) that may be contained within the process stream 12 may become solidified and suspended within the LNG portion, as carbon dioxide has a higher freezing temperature than methane (CH4), which is the primary component of NG. The LNG portion and the gaseous portion may be directed into the gas-liquid separation tank 38, and the LNG portion may be directed out of the separation tank 38 as a LNG process stream 12, which may then be directed into the transfer tank 40. A transfer motive gas stream 16, such as a gaseous NG, may then be directed into the plant 10 through the transfer motive gas inlet 64 through the valve 66, which may be utilized to regulate the pressure of the transfer motive gas stream 16 prior to being directed into the transfer tank 40. The transfer motive gas stream 16 may facilitate the transfer of the liquid NG process stream 12 through the hydrocyclone 42, such as may be available, for example, from Krebs Engineering of Tucson, Ariz., wherein the solid CO2 may be separated from the liquid NG process stream 12. For example, the transfer motive gas stream 16 may be utilized to pressurize the liquid of the process stream 12 to move the process stream 12 through the hydrocyclone 42.
Optionally, a separate transfer tank 40 may not be used and instead a portion of the separation tank 38 may be utilized as a transfer tank or a pump may be utilized to transfer the process stream 12 into the hydrocyclone 42. In additional embodiments, a pump may be utilized to transfer the process stream from the separation tank 38 into the hydrocyclone. A pump may provide certain advantages, as it may provide a constant system flow, when compared to a batch process utilizing a transfer tank. However, a transfer tank configuration, such as shown in
In the hydrocyclone 42, a slurry including the solid CO2 from the LNG process stream 12 may be directed through an underflow outlet 82 and the LNG process stream 12 may be directed through an overflow outlet 84. The LNG process stream 12 may then be directed through the filter 44, which may remove any remaining CO2 or other impurities, which may be removed from the system through a filter outlet 86, such as during a cleaning process. In some embodiments, the filter 44 may comprise one screen filter or a plurality of screen filters that are placed in parallel. A substantially pure LNG process stream 12, such as substantially pure liquid CH4, may then exit the filter 44 and be directed into a LNG process stream 12 and a secondary LNG stream that may form the second tail gas stream 26. The LNG process stream 12 may be directed through the valve 48 and into the storage tank 50, wherein it may be withdrawn for use through the LNG outlet 52, such as to a vehicle which is powered by LNG or into a transport vehicle.
Additionally, the CO2 slurry in the hydrocyclone 42 may be directed through the underflow outlet 82 to form the CO2 management stream 22 and be directed to the CO2 sublimation chamber 70 to sublimate the solid CO2 for removal from the plant 10. Additionally, the separation chamber vent stream 18, the transfer tank vent stream 20 and the storage tank vent stream 24 may be combined in the mixer 74 to provide a gas stream 28 that may be used to sublimate the CO2 management stream 22. The gas stream 28 may be relatively cool upon exiting the mixer 74 and may be directed through a fourth channel of the primary heat exchanger 34 to extract heat from the process stream 12 in the third channel of the primary heat exchanger 34. The gas stream 28 may then be directed through the compressor 76 to further pressurize and warm the gas stream 28 prior to directing the gas stream 28 into the CO2 sublimation chamber 70 to sublimate the CO2 of the CO2 management stream 22 from the underflow outlet 82 of the hydrocyclone 42. In some embodiments, a heat exchanger, such as described in application Ser. No. 11/855,071, filed Sep. 13, 2007, titled Heat Exchanger and Associated Method, owned by the assignee of the present invention, the disclosure thereof which is previously incorporated by reference in its entirely herein, may be utilized as the sublimation chamber 70. In further embodiments, a portion of the gas stream 28, such as an excess flow portion, may be directed out of the plant 10 through a tee (not shown) prior to being directed into the CO2 sublimation chamber 70 and may provide an additional tail stream (not shown).
The combined gaseous CO2 from the CO2 management stream 22 and the gases from the stream 28 may then exit the sublimation chamber 70 as the first tail gas stream 30, which may be relatively cool. For example, the first tail gas stream 30 may be just above the CO2 sublimation temperature upon exiting the sublimation chamber 70. The first tail gas stream 30 may then be directed through a fifth channel of the primary heat exchanger 34 to extract heat from the process stream 12 in the third channel prior to exiting the plant 10 through the first tail gas outlet 72 at a first pressure.
Finally, the second tail gas stream 26, which may initially comprise a secondary substantially pure LNG stream from the splitter 46, may be directed through the pump 78. In additional embodiments, the pump 78 may not be required and may not be included in the plant 10. For example, sufficient pressure may be imparted to the process stream 12 within the transfer tank 40 by the transfer motive gas stream 16 such that the pump 78 may not be required and may not be included in the plant 10. The second tail gas stream 26 may then be directed through a sixth channel of the primary heat exchanger 34, where it may extract heat from the process stream 12 in the third channel, and may become vaporized to form gaseous NG. The second tail stream 26 may then be directed out of the plant 10 via the second tail gas outlet 80 at a second pressure, the second pressure different than the first pressure of the first tail gas stream 30 exiting the first tail gas outlet 72.
In some embodiments, as the process stream 12 progresses through the primary heat exchanger 34, the process stream 12 may be cooled first by the cooling stream 14, which may extract about two-thirds (⅔) of the heat to be removed from the process stream 12 within the heat exchanger 34. Remaining cooling of the process stream 12 within the primary heat exchanger 34 may then be accomplished by the transfer of heat from the process stream 12 to the second tail gas stream 26. In view of this, the amount of flow that is directed into the second tail gas stream 26 may be regulated to achieve a particular amount of heat extraction from the process stream 12 within the heat exchanger 34.
In view of the foregoing, and as further described herein, the plant 10 may be utilized to liquefy natural gas in a wide variety of locations having a wide variety of supply of gas configurations. Ideal locations for natural gas liquefaction may have a high incoming gas pressure level and low downstream tail gas pipeline pressure levels having significant flow rate capacities for gas therein. However, many locations where gas liquefaction is needed do not conform to such ideal conditions of a high incoming gas pressure level and a low downstream tail gas pressure levels having significant flow rate levels of gas therein. In view of this, the invention described herein offers flexibility in the process and apparatus to take advantage of the pressure levels and flow rates of gas in pipelines at a particular location. Such may be accomplished by separating the various gas flow streams in the plant 10, as shown in
In some embodiments, the plant 10 may be utilized at a NG distribution pressure letdown location 100, as shown in
Optionally, the cooling stream outlet 62 may be coupled to the cooling stream inlet 54 to provide a closed cooling stream loop, and any suitable relatively high pressure gas may be used, such as nitrogen or another gas.
The first tail gas outlet 72 may be coupled to one of the intermediate pressure pipeline 104 and the relatively low pressure pipeline 106 and, as the first tail gas outlet 72 and second tail gas outlet 80 are separate and may configured to provide tail gas streams 26, 30 at different pressures, the second tail gas outlet 80 may be coupled to one of the intermediate pressure pipeline 104 and the relatively low pressure pipeline 106, independent of the first tail gas outlet 72. In view of this, the first tail gas outlet 72 may be coupled to the relatively low pressure pipeline 10 while the second tail gas outlet is coupled to the intermediate pressure pipeline 104, or the first tail gas outlet may be coupled to the relatively low pressure pipeline 10 while the second tail gas outlet is coupled to the intermediate pressure pipeline 104. Each tail gas stream 14, 26, 30 may be directed into an available pipeline 102, 104, 106 at different pressures, and can be configured to release each tail gas stream 14, 26, 30 at a pressure that is economical and efficient for the specific letdown station 100 and plant 10.
The first tail gas stream 30 may contain a substantial amount of CO2, and, in some embodiments, may be coupled to a CO2 processing plant (not shown) as a product stream to provide a purified CO2 product. For example, a CO2 processing plant may be utilized to process the CO2 separated from the liquid NG process stream, and may provide a substantially pure CO2 as a product. In view of this, a byproduct that would normally be removed as waste could be utilized as a product stream that could be used or sold.
Furthermore, the second tail gas stream 26 may consist of substantially pure NG and may be combusted upon exit from the plant 10. In some embodiments, the second tail gas stream 26 may be combusted in a flare (not shown). In other embodiments, the second tail gas stream 26 may be combusted in an engine (not shown) to provide power to the plant 10. For example, if it would require significant energy to compress the second tail stream to a pressure of an available pipeline for removal, or if such a pipeline was unavailable, it may be economical to combust the second tail gas stream 26 in a flare. In another example, the second tail gas stream could be provided to an engine that may produce power that may be utilized to power components of the plant 10, such as one or more of the compressors 56, 76.
In additional embodiments, a portion, or all, of the second tail gas stream 26 may be redirected into the process stream 12. In some embodiments, the second tail gas stream 26 may be utilized to dilute a marginal process stream 12, which may include one or more impurities, to provide a process stream 12 with a lower percentage of impurities that may be more efficiently processed. For example, a CO2 rich process stream 12 may be diluted with substantially pure NG from the second tail gas stream 26 to provide a process stream 12 composition that has a lower CO2 percentage.
Similarly, the ability of the plant 10 to accommodate multiple independent input streams may also provide for greater flexibility and efficiency of the plant 10. For example, the process stream 12, cooling stream 14 and transfer motive gas stream 16 may all be fed into the plant 10 from different sources at different pressures and flows. It may be advantageous in some cases to provide the process stream 12 at a relatively high pressure, such as about 800 psia. However, it may not be particularly advantageous to provide such high pressures for other input streams, such as the transfer motive gas stream 16. For example, where a higher process stream 12 pressure may result in an improved process stream 12 efficiency, systems that utilize a single input stream necessarily require a higher input pressure for all of the input streams. However, the plant 10 may allow methods wherein only the pressure of the process stream 12 may be increased, while the other input streams 14, 16 may be input into the plant 10 at a lower pressure, reducing the amount of gas input into the plant 10 that must be compressed, thus resulting in a reduced energy requirement for the plant 10.
Optionally, the inlet streams may be additionally processed prior to being directed into the plant 10. For example, the inlet streams may be compressed or expanded to provide the input streams at a particular pressure and temperature that is different than the source pressure and temperature. For another example, one or more external dehydrators (not shown) may be used to remove water from one or more of: the gaseous NG prior to being directed into the NG inlet 32, the cooling stream 14 prior to being directed into the cooling fluid inlet 54, and the transfer motive gas stream 16 prior to being directed into the transfer fluid inlet 64.
By maintaining separate input gas streams inlets 32, 54, 64 and separate tail gas stream outlets 62, 72, 80, the plant 10 may be flexible. In other words, a single plant design may accommodate, and be relatively efficient at, a variety of source gas locations.
Another example of the flexibility of the disclosed plant 10 may be found in the arrangement of the cooling stream 14. The cooling gas for the cooling stream 14 comes into the plant through the cooling fluid inlet 54 and may then be directed through the turbo compressor 56 to increase the pressure of the cooling stream 14. The cooling stream may then be cooled, such as by the ambient heat exchanger 58 and the primary heat exchanger 34, prior to entering the turbo expander 60, where it may be expanded and cooled prior to being redirected through the primary heat exchanger 34. As previously discussed, the energy from expanding the gas in the turbo expander 60 may be utilized to power the turbo compressor 56, which may provide a power savings for the plant 10. Additionally, there is a relationship between the amount of pressure generated by the turbo compressor 56 and the amount of heat that may be withdrawn from the cooling stream 14 prior to the cooling stream 14 being directed into the turbo expander 60, and the pressure and temperature of the cooling stream 14 upon exiting the turbo expander 60. Embodiments of the present invention may exploit this relationship to provide improved efficiency, due to the ability to change the cooling stream outlet pressure to match the needed pipeline capacity of a pipeline that may be used to carry the cooling stream tail gas away from the plant 10.
As a non-limiting example, the cooling stream tail gas outlet 62 may direct the tail gas from the cooling stream 14 out of the plant 10 into an intermediate pressure pipeline 104 that requires gas at a pressure of about 200 psia and a temperature of about 50° F. When gaseous NG is utilized to provide the cooling stream 14, the temperature and pressure of the cooling stream 14 may be limited by the CO2 concentration that is contained in the NG, as temperatures below a critical temperature at a particular pressure will result in a phase change of the CO2. A separate cooling stream tail gas outlet 62 allows flows and pressures to be adjusted in the primary heat exchanger 34 to balance the process needs with the available cooling provided by the expander 60.
Significant energy savings may be realized by matching the turbo expander 60 outlet pressure with available tail gas pressure requirements. When a tail gas pipeline, such as the intermediate pressure tail gas pipeline 104 or the relatively low pressure tail gas pipeline 106, is not available the tail gases 62, 72, 80 from the plant 10 may need to be recompressed. In such a case, the ability to limit the pressure drop from the turbo expander 60 may be very valuable, as this may reduce the compression ratio required between the cooling stream tail gas outlet 62 and a relatively high pressure inlet, such as the relatively high pressure pipeline 102, and reduce the energy required to compress the cooling stream 14 tail gas.
Additionally, cooling for the plant 10 may come from sources other than the turbo expander 60 of the cooling stream 14, which may allow flexibility and control of the cooling stream input 54 and output 62 pressures. For example, cooling may come from the ambient heat exchanger 58, as well as from cooled streams from other areas of the plant, such as from the CO2 sublimation chamber 70 and from the second tail stream 26. In additional embodiments, cooling may be obtained by including a chiller or an active refrigeration system.
In some embodiments, the plant 10 may be configured as a “small-scale” natural gas liquefaction plant 10 which is coupled to a source of natural gas such as a pipeline 102, although other sources, such as a well head, are contemplated as being equally suitable. The term “small-scale” is used to differentiate from a larger-scale plant having the capacity of producing, for example 70,000 gallons of LNG or more per day. In comparison, the presently disclosed liquefaction plant may have a capacity of producing, for example, approximately 30,000 gallons of LNG a day but may be scaled for a different output as needed and is not limited to small-scale operations or plants. Additionally, the liquefaction plant 10 of the present invention may be considerably smaller in size than a large-scale plant and may be transported from one site to another. However, the plant 10 may also be configured as a large-scale plant if desired. The plant 10 may also be relatively inexpensive to build and operate, and may be configured to require little or no operator oversight.
Furthermore, the plant 10 may be configured as a portable plant that may be moved, such as by truck, and may be configured to couple to any number of letdown stations or other NG sources.
The plant 10 and methods illustrated and described herein may include the use of any conventional apparatus and methods to remove carbon dioxide, nitrogen, oxygen, ethane, etc. from the natural gas supply before entry into the plant 10. Additionally, if the source of natural gas has little carbon dioxide, nitrogen, oxygen, ethane, etc., the use of hydrocyclones and carbon dioxide sublimation in the liquefaction process and apparatus may not be needed and, therefore, need not be included.
While the invention may be susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and have been described in detail herein. However, it should be understood that the invention is not intended to be limited to the particular forms disclosed. Rather, the invention includes all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the following appended claims.
This invention was made with government support under Contract Number DE-AC07-05ID14517 awarded by the United States Department of Energy. The government has certain rights in the invention.
Number | Name | Date | Kind |
---|---|---|---|
1222801 | Rosenbaum | Apr 1917 | A |
2037679 | Dana | Apr 1936 | A |
2037714 | Gaines, Jr. | Apr 1936 | A |
2040059 | Mesinger | May 1936 | A |
2093805 | de Baufre | Sep 1937 | A |
2157103 | Zenner | May 1939 | A |
2209534 | Moore | Jul 1940 | A |
2494120 | Ferro, Jr. | Oct 1950 | A |
2669941 | Stafford | Feb 1954 | A |
2701641 | Krijgsman | Feb 1955 | A |
2858020 | Bek | Oct 1958 | A |
2900797 | Kurata et al. | Aug 1959 | A |
2937503 | Swearingen et al. | May 1960 | A |
3132016 | Kurata | May 1964 | A |
3168136 | Ammon | Feb 1965 | A |
3182461 | Johanson | May 1965 | A |
3193468 | Sprague | Jul 1965 | A |
3213631 | Kniel | Oct 1965 | A |
3218816 | Grenier | Nov 1965 | A |
3236057 | Hashemi-Tafreshi | Feb 1966 | A |
3254496 | Roche et al. | Jun 1966 | A |
3289756 | Jaeger | Dec 1966 | A |
3292380 | Bucklin | Dec 1966 | A |
3312073 | Jackson et al. | Apr 1967 | A |
3315475 | Harmens | Apr 1967 | A |
3323315 | Carr | Jun 1967 | A |
3326453 | Kun | Jun 1967 | A |
3349020 | Crownover et al. | Oct 1967 | A |
3362173 | Kneil | Jan 1968 | A |
3376709 | Dickey et al. | Apr 1968 | A |
3406496 | Betteridge et al. | Oct 1968 | A |
3407052 | Huntress et al. | Oct 1968 | A |
3416324 | Swearingen | Dec 1968 | A |
3422887 | Berkeley | Jan 1969 | A |
3448587 | Goard et al. | Jun 1969 | A |
3487652 | McKay | Jan 1970 | A |
3503220 | Desai | Mar 1970 | A |
3516262 | Bernstein | Jun 1970 | A |
3548606 | Kuerston | Dec 1970 | A |
3596473 | Streich | Aug 1971 | A |
3608323 | Salama | Sep 1971 | A |
3616652 | Engel | Nov 1971 | A |
3628340 | Meisler et al. | Dec 1971 | A |
3677019 | Olszewski | Jul 1972 | A |
3690114 | Swearingen et al. | Sep 1972 | A |
3724225 | Mancini et al. | Apr 1973 | A |
3724226 | Pachaly | Apr 1973 | A |
3735600 | Dowdell et al. | May 1973 | A |
3846993 | Bates | Nov 1974 | A |
3886885 | Becker et al. | Jun 1975 | A |
3897226 | Doherty | Jul 1975 | A |
4001116 | Selcukoglu | Jan 1977 | A |
4004430 | Solomon et al. | Jan 1977 | A |
4007601 | Webbon | Feb 1977 | A |
4022597 | Bacon | May 1977 | A |
4025315 | Mazelli | May 1977 | A |
4032337 | Boyer | Jun 1977 | A |
4120911 | Davidson | Oct 1978 | A |
4128410 | Bacon | Dec 1978 | A |
4148723 | Mozley | Apr 1979 | A |
4161107 | Korsakov-Bogatkov et al. | Jul 1979 | A |
4183369 | Thomas | Jan 1980 | A |
4187689 | Selcukoglu et al. | Feb 1980 | A |
4224902 | Binder et al. | Sep 1980 | A |
4294274 | LeRoy | Oct 1981 | A |
4318723 | Holmes et al. | Mar 1982 | A |
4334902 | Paradowski | Jun 1982 | A |
4359871 | Strass | Nov 1982 | A |
4370150 | Fenstermaker | Jan 1983 | A |
4453956 | Fabbri et al. | Jun 1984 | A |
4479533 | Persson et al. | Oct 1984 | A |
4479536 | Lameris | Oct 1984 | A |
4522636 | Markbreiter et al. | Jun 1985 | A |
4528006 | Vitovec et al. | Jul 1985 | A |
4561496 | Kehrer | Dec 1985 | A |
4609390 | Wilson | Sep 1986 | A |
4611655 | Molignoni | Sep 1986 | A |
4645522 | Dobrotwir | Feb 1987 | A |
4654522 | Gornick et al. | Mar 1987 | A |
4783272 | Patterson | Nov 1988 | A |
4798242 | Kito et al. | Jan 1989 | A |
4822393 | Markbreiter et al. | Apr 1989 | A |
4846862 | Cook | Jul 1989 | A |
4869313 | Fredley | Sep 1989 | A |
4970867 | Herron et al. | Nov 1990 | A |
4993485 | Gorman | Feb 1991 | A |
4994097 | Brouwers | Feb 1991 | A |
5003782 | Kucerija | Apr 1991 | A |
5032143 | Ritakallio | Jul 1991 | A |
5036671 | Nelson et al. | Aug 1991 | A |
5062270 | Haut et al. | Nov 1991 | A |
5074758 | McIntyre | Dec 1991 | A |
5174796 | Davis et al. | Dec 1992 | A |
5218832 | Woolley | Jun 1993 | A |
5252613 | Chang et al. | Oct 1993 | A |
5291736 | Paradowski | Mar 1994 | A |
5325673 | Durr et al. | Jul 1994 | A |
5327730 | Myers et al. | Jul 1994 | A |
5375422 | Butts | Dec 1994 | A |
5379832 | Dempsey | Jan 1995 | A |
5386699 | Myers et al. | Feb 1995 | A |
5390499 | Rhoades et al. | Feb 1995 | A |
5419392 | Maruyama | May 1995 | A |
5450728 | Vora et al. | Sep 1995 | A |
5473900 | Low | Dec 1995 | A |
5489725 | Minkkinen et al. | Feb 1996 | A |
5505048 | Ha et al. | Apr 1996 | A |
5505232 | Barclay | Apr 1996 | A |
5511382 | Denis et al. | Apr 1996 | A |
5537827 | Low et al. | Jul 1996 | A |
5551256 | Schmidt | Sep 1996 | A |
5600969 | Low | Feb 1997 | A |
5615561 | Houshmand et al. | Apr 1997 | A |
5615738 | Cameron et al. | Apr 1997 | A |
5655388 | Bonaquist et al. | Aug 1997 | A |
5669234 | Houser et al. | Sep 1997 | A |
5704227 | Krabbendam | Jan 1998 | A |
5718126 | Capron et al. | Feb 1998 | A |
5755114 | Foglietta | May 1998 | A |
5755280 | Da Costa et al. | May 1998 | A |
5799505 | Bonaquist et al. | Sep 1998 | A |
5819555 | Engdahl | Oct 1998 | A |
5836173 | Lynch et al. | Nov 1998 | A |
5916260 | Dubar | Jun 1999 | A |
5950453 | Bowen et al. | Sep 1999 | A |
5956971 | Cole et al. | Sep 1999 | A |
5983665 | Howard et al. | Nov 1999 | A |
6023944 | Blundell | Feb 2000 | A |
6041620 | Olszewski et al. | Mar 2000 | A |
6085546 | Johnston | Jul 2000 | A |
6085547 | Johnston | Jul 2000 | A |
6105390 | Bingham et al. | Aug 2000 | A |
6131395 | Greene et al. | Oct 2000 | A |
6131407 | Wissolik | Oct 2000 | A |
6138473 | Boyer-Vidal | Oct 2000 | A |
6138746 | Livolsi et al. | Oct 2000 | A |
6196021 | Wissolik | Mar 2001 | B1 |
6200536 | Tonkovich et al. | Mar 2001 | B1 |
6212891 | Minta et al. | Apr 2001 | B1 |
6220052 | Tate, Jr. et al. | Apr 2001 | B1 |
6220053 | Hass et al. | Apr 2001 | B1 |
6250244 | Dubar et al. | Jun 2001 | B1 |
6301927 | Reddy | Oct 2001 | B1 |
6354105 | Lee et al. | Mar 2002 | B1 |
6367286 | Price | Apr 2002 | B1 |
6370910 | Grootjans et al. | Apr 2002 | B1 |
6372019 | Alferov et al. | Apr 2002 | B1 |
6375906 | Edlund et al. | Apr 2002 | B1 |
6378330 | Minta et al. | Apr 2002 | B1 |
6382310 | Smith | May 2002 | B1 |
6389844 | Klein Nagel Voort | May 2002 | B1 |
6390114 | Haandrikman et al. | May 2002 | B1 |
6397936 | Crowley et al. | Jun 2002 | B1 |
6400896 | Longardner | Jun 2002 | B1 |
6410087 | Wilde et al. | Jun 2002 | B1 |
6412302 | Foglietta | Jul 2002 | B1 |
6425263 | Bingham et al. | Jul 2002 | B1 |
6427464 | Beaverson et al. | Aug 2002 | B1 |
6442969 | Rojey et al. | Sep 2002 | B1 |
6484533 | Allam et al. | Nov 2002 | B1 |
6581409 | Wilding et al. | Jun 2003 | B2 |
6581510 | Koch et al. | Jun 2003 | B2 |
6694774 | Rashad et al. | Feb 2004 | B1 |
6722399 | Cano | Apr 2004 | B1 |
6742358 | Wilkinson et al. | Jun 2004 | B2 |
6767388 | Lecomte et al. | Jul 2004 | B2 |
6962061 | Wilding et al. | Nov 2005 | B2 |
7219512 | Wilding et al. | May 2007 | B1 |
7228714 | Howard | Jun 2007 | B2 |
7325415 | Amin et al. | Feb 2008 | B2 |
7469556 | Howard | Dec 2008 | B2 |
7575624 | Cartwright et al. | Aug 2009 | B2 |
7591150 | Turner et al. | Sep 2009 | B2 |
7594414 | Wilding et al. | Sep 2009 | B2 |
7765920 | Keller | Aug 2010 | B2 |
20030196452 | Wilding et al. | Oct 2003 | A1 |
20040083888 | Qualls | May 2004 | A1 |
20040105812 | Tonkovich et al. | Jun 2004 | A1 |
20040148962 | Rashad et al. | Aug 2004 | A1 |
20040177646 | Wilkinson et al. | Sep 2004 | A1 |
20050144979 | Zollinger et al. | Jul 2005 | A1 |
20050183452 | Hahn et al. | Aug 2005 | A1 |
20050220704 | Morrow et al. | Oct 2005 | A1 |
20050279132 | Eaton et al. | Dec 2005 | A1 |
20060053806 | Tassel | Mar 2006 | A1 |
20060213222 | Whitesell | Sep 2006 | A1 |
20060213223 | Wilding et al. | Sep 2006 | A1 |
20070017250 | Turner et al. | Jan 2007 | A1 |
20070107465 | Turner et al. | May 2007 | A1 |
20070137246 | McKellar et al. | Jun 2007 | A1 |
20070193303 | Hawrysz et al. | Aug 2007 | A1 |
20080148770 | Migliore et al. | Jun 2008 | A1 |
20080156035 | Aspelund et al. | Jul 2008 | A1 |
20090071634 | Turner et al. | Mar 2009 | A1 |
20090277217 | Ransbarger et al. | Nov 2009 | A1 |
20100018248 | Fieler et al. | Jan 2010 | A1 |
20100088920 | LaRou | Apr 2010 | A1 |
20100186446 | Turner et al. | Jul 2010 | A1 |
20100223950 | Malsam | Sep 2010 | A1 |
20100313597 | Bridgwood | Dec 2010 | A1 |
20100326533 | Mooney et al. | Dec 2010 | A1 |
20120103012 | Turner et al. | May 2012 | A1 |
20120103428 | Turner et al. | May 2012 | A1 |
20120103561 | Turner et al. | May 2012 | A1 |
Number | Date | Country |
---|---|---|
0 676 599 | Oct 1995 | EP |
1 205 721 | May 2002 | EP |
58-159830 | Sep 1983 | JP |
11200817 | Jul 1999 | JP |
2002071861 | Mar 2002 | JP |
8800936 | Feb 1988 | WO |
9859206 | Dec 1998 | WO |
03062725 | Jul 2003 | WO |
2010023238 | Mar 2010 | WO |
Entry |
---|
Bodner Research Web, “Phase Diagrams,” http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/phase.php. |
Search Report for PCT/US2006/041039 dated Aug. 8, 2007. |
Search Report for PCT/US2007/084677 dated Jul. 1, 2008. |
International Preliminary Report for PCT/US08/68938 dated Mar. 16, 2010. |
Search Report for PCT/US20101045340 dated Oct. 13, 2010. |
Search Report for PCT/US20101045332 dated Oct. 18, 2010. |
Search Report for PCT/US2008/051012 dated May 20, 2008. |
Search Report for PCT/US2010/045321 dated Oct. 1, 2010. |
International Preliminary Examination Report for PCT/US2002/20924 dated Jun. 17, 2003. |
Search Report for PCT/US1998/027232, dated Jul. 7, 1999. |
U.S. Appl. No. 12/603,948, filed Oct. 22, 2009, titled, “Complete Liquefaction Methods and Apparatus,” by Turner et al. |
U.S. Appl. No. 12/604,139, filed Oct. 22, 2009, titled, “Natural Gas Liquefaction Core Modules, Plants Including Same and Related Methods,” by Wilding et al. |
PCT International Preliminary Report on Patentability and Written Opinion for PCT/US2010/045321 dated Oct. 1, 2010, 6 pages. |
“A National Vision of America's Transition to a Hydrogen Economy—To 2030 and Beyond,” Based on the results of the National Hydrogen Vision Meeting Washington, DC Nov. 15-16, 2001, United States Department of Energy. |
Curtin University of Technology, LNG Microcell Progress Update, May 2002, Curtin/Corelab. |
“Generation of Hydrogen and Transportation and Transmission of Energy Generated on the U.S. Outer Continental Shelf to Onshore,” (Minerals Management Service), May 2006. |
Holmes et al., “Ryan/Holmes Cryogenic Acid Gas/Hydrocarbon Separations Provide Economic Benefits for LNG Production,” 7th International Conference on Liquefied Natural Gas; Jakarta, Indonesia; May 1983; Institute of Gas Technology, Session II, vol. 1, pp. 1-15. |
“Hydrogen as an Energy Carrier and its Production by Nuclear Power,” IAEA-TECDOC-1085, International Atomic Energy Agency, May 1999. |
“Hydrogen Infrastructure Delivery, Reliability R&D Needs,” Science Applications International Corporation, Prepared for U.S. Department of Energy, NETL Natural Gas & Infrastructure Reliability Program <www.netl.doe.gov/technologies/oil-gas/publications/td/Final%20White%20Paper%20072604.pdf>. |
International Search Report dated Sep. 17, 2002 (4 pages). |
Mott Corporation, “Porous metal solutions,” Jun. 2007, 16 pages. |
“Porous Metal Design Guidebook,” Metal Powder Industries Federation, Princeton, NJ, <<http://www.mpif.org/designcenter/porous.pdf >>, Jun. 2007, 25 pages. |
“The Hydrogen Economy: Opportunities, Costs, Barriers, and R&D Needs,” National Academy of Engineering and Board on Energy and Environmental Systems, 2004, The National Academies Press, <http://books.nap.edu/books/0309091632/html/index.html>. |
“The Hydrogen Initiative, Panel on Public Affairs,” American Physical Society, Mar. 2004, <http://www.aps.org/public—affairs/popa/reports/index.cfm>. |
PCT International Preliminary Report on Patentability and Written Opinion for PCT/US2006/041039 dated Apr. 9, 2009, 7 pages. |
PCT International Preliminary Report on Patentability and Written Opinion for PCT/US2007/084677 dated May 28, 2009, 7 pages. |
PCT International Search Report and Written Opinion for PCT/US08/68938 dated Oct. 10, 2008, 8 pages. |
PCT International Preliminary Report on Patentability and Written Opinion for PCT/US2008/051012 dated Aug. 27, 2009, 7 pages. |
PCT International Preliminary Report on Patentability and Written Opinion for PCT/US2010/045332 dated Oct. 18, 2010, 11 pages. |
U.S. Appl. No. 13/528,246, filed Jun. 20, 2012, titled “Natural Gas Liquefaction Employing Independent Refrigerant Path,” by Turner et al. |
Number | Date | Country | |
---|---|---|---|
20110094263 A1 | Apr 2011 | US |