None
Embodiments of the invention relate to processes for removal of mercury from crude oil.
Presence of mercury in crude oil can cause problems with downstream processing units as well as health and environmental issues. Such concerns provide incentives to remove the mercury from the crude oil. Therefore, there exists a need for improved processes of removing mercury from crude oil before downstream processing into products.
In one embodiment, a process of removing mercury from crude oil includes separating a crude oil stream into a gaseous hydrocarbon stream and a liquid hydrocarbon stream and removing mercury from the gaseous hydrocarbon stream to provide a treated gas stream. Contacting the treated gas stream with the liquid hydrocarbon stream transfers mercury from the liquid hydrocarbon stream to the treated gas stream and thereby forms a treated liquid stream and a mercury rich gas stream. The method further includes removing mercury from the mercury rich gas stream.
According to one embodiment, a process includes transferring mercury from a liquid hydrocarbon stream to a natural gas stream. The transferring occurs by contacting the liquid hydrocarbon stream with the natural gas stream to thereby form a treated liquid stream and a mercury rich gas stream. In addition, the method includes removing mercury from the mercury rich gas stream.
For one embodiment, a process includes separating a crude oil stream into a gaseous hydrocarbon stream and a liquid hydrocarbon stream, removing mercury from the gaseous hydrocarbon stream to provide a treated gas stream, and introducing the treated gas stream into contact with the liquid hydrocarbon stream to transfer mercury from the liquid hydrocarbon stream to the treated gas stream and thereby form a treated liquid stream and a mercury rich gas stream. Separating the treated gas stream to remove propane and butane from the treated gas stream occurs prior to contacting the treated gas stream with the liquid hydrocarbon stream. Introducing a pentane-plus vapor stream separated from the treated gas stream into contact with the treated liquid stream enables absorbing the pentane-plus vapor stream into the treated liquid stream. Removing mercury from the mercury rich gas stream provides recycled gas that provides part of the treated gas stream.
The invention, together with further advantages thereof, may best be understood by reference to the following description taken in conjunction with the accompanying drawings.
Embodiments of the invention relate to removal of mercury from crude oil. Such removal relies on transferring mercury from a liquid hydrocarbon stream to a natural gas stream upon contacting the liquid hydrocarbon stream with the natural gas stream. Processing of the natural gas stream after used to strip the mercury from the liquid hydrocarbon stream removes the mercury from the natural gas stream. The removal of the mercury from the crude oil provides marketable products and can be performed onsite at well locations, such as offshore platforms with limited space and facilities, prior to transport to refineries. For example, initial production may contain concentrations of mercury above acceptable thresholds or penalty levels for the refineries such that the removal of the mercury reduces or eliminates penalties and otherwise makes the products marketable.
For some embodiments, the contactor 114 includes multiple (e.g., 2, 4, 6 or more) theoretical stages 122 (depicted by “X” within the contactor 114) of separation between vapor and liquid phases. Either trays or packing material in a flow path of fluids described herein passing through the contactor 114 may form the theoretical stages 122. For example, the packing material disposed inside of the contactor 114 to define the stages 122 may include random oriented objects or a shaped structure and may be made of metallic or ceramic solid material. In some embodiments, amount of the packing material utilized depends on a desired number of the stages 122 provided by the packing material.
The dryer 652 removes water vapor from the gasses that pass through the MRU 608, or are introduced into the MRU 608 for embodiments with the dryer located ahead of the MRU 608, prior to the gasses being introduced into the gas separating unit 654. The gas separating unit 654 separates the gasses treated in the MRU 608 into: 1) a propane stream denoted as C3, 2) a butanes stream depicted as C4, 3) a product gas stream 616 that includes methane and ethane (C1-C2), and 4) a pentane-plus gas stream that feeds into the condenser 656 and includes hydrocarbons having at least five carbon atoms per molecule. A portion of the product gas stream 616 enters into a stripping zone 613 of the contactor 614 to achieve the removal of mercury from liquids passing through the contactor 614. In some embodiments, any portion or all of the product gas stream 616 introduced into the stripping zone 613 may bypass separation (i.e., removal of propane, butane and/or pentane-plus) and still achieve mercury and/or propane and butane stripping from the liquids passing through the stripping zone 613 of the contactor 614 as described herein.
The pentane-plus gas stream introduced into the condenser 656 condenses and is separated into vapors that include pentanes and higher molecular weight hydrocarbons output from the condenser 656 as a blend component stream 657 and liquids (identified as C5+) including hydrocarbons having at least five carbon atoms per molecule. At least a portion of the blend component stream 657 enters into an absorption zone 615 contained in the contactor 614 for transfer of at least a portion of the vapors within the blend component stream 657 to a treated liquid hydrocarbon stream from the stripping zone 613, thereby forming an enriched treated liquid hydrocarbon stream. The absorption zone 615 provides contact surface area, mixing and residence time sufficient (e.g., via packing material and/or trays shown in
Since propane and butane are stripped from the crude oil stream in the stripping zone 613 of the contactor 614, blending back in contents of the blend component stream 657 in the absorption zone 615 of contactor 614 can occur without exceeding a threshold for vapor pressure in the crude product. Further, utilizing the absorption zone 615 enables limiting amount of the blend component stream 657 that is combined with the mercury rich gas stream 618 entering the recovery unit 650 since the compressor 651 may have limited capacity. Sufficient quantities of the product gas stream 616 can thus pass through the contactor 614 and exit as the mercury rich gas stream 618 to achieve desired reductions in the mercury content within the crude product without overwhelming the capacity of the compressor 651 that receives the mercury rich gas stream 618.
The crude oil stream in some embodiments comprises, consists of, or consists essentially of a broad range crude oil. For example, the crude oil stream may include hydrocarbons containing at least one carbon atom per molecule. The gaseous hydrocarbon stream comprises, consists of, or consists essentially of hydrocarbons containing from about 1 to about 6 carbon atoms per molecule.
In some embodiments, the temperature at which the crude oil stream is separated into the gaseous hydrocarbon stream and the liquid hydrocarbon stream is at least about 50° C. or at least about 60° C. The pressure at which the crude oil stream is separated into the gaseous hydrocarbon stream and the liquid hydrocarbon stream is at least about 0.5 Bars or at least about 1 Bars, for some embodiments.
The mercury removal unit has a fixed bed comprising any mercury sorbent material capable of removing mercury from gases. In some embodiments, the treated gas stream comprises less than about 20 wt. % of the mercury contained in the mercury-containing gas feed or less than about 10 wt. % of the mercury contained in the mercury-containing gas feed. The treated liquid hydrocarbon stream may comprise less than about 50 wt. % of the elemental mercury contained in the liquid hydrocarbon stream or less than about 20 wt. % of the elemental mercury contained in the liquid hydrocarbon stream. The liquid hydrocarbon stream for some embodiments comprises at least about 10 ppb elemental mercury or comprises at least about 200 ppb elemental mercury.
The recycle gas stream is contacted with the liquid hydrocarbon stream at a temperature in the range of from about 70° C. to about 300° C. or from about 150° C. to about 200° C.; a pressure in the range of from about 0.5 Bars to about 15 Bars, from about 1 Bar to about 10 Bars, or from about 2 Bars to about 7 Bars; and a gas to liquid ratio in the range of from about 50 to about 300 standard cubic feet of gas/bbl of liquid (SCF/bbl) or from about 100 to about 200 SCF/bbl.
The following examples are provided to further illustrate this invention and are not to be considered as limiting the scope of this invention.
A simulation of the liquid/gas contactor was constructed using an equation of state thermodynamic prediction model for mercury partitioning between gas and liquid using data for elemental mercury in a naturally obtained crude oil blend. Results of the calculation are shown in
Common pressure of a Low Pressure Coalescer/Separator present at the well site (which is redeployed as set forth herein as a gas/oil contactor) ranges from about <1 to ˜3 Bars. In typical applications, reservoir temperature of high mercury crude oils is greater than about 150° C. This simulation thus shows that 90% mercury removal is achievable at the temperature and pressure conditions often present at the crude oil well site.
An experiment was run to test the removal of elemental mercury (Hg) from a hydrocarbon by sparging with a lighter hydrocarbon. The elemental mercury was dissolved in decane at about 1,300 ppbw.
A third experiment (Run 3) was performed wherein, prior to adding the elemental mercury, the decane was water washed and passed over a silica gel column to remove trace levels of chloride, oxide or sulfur compounds that could, at the conditions of the experiment, oxidize the mercury and cause it to form non-spargable mercury compounds. Also shown in
A simulation was run in order to evaluate affect of the number of theoretical stages (e.g., as indicated by reference number 122 in
The preferred embodiment of the present invention has been disclosed and illustrated. However, the invention is intended to be as broad as defined in the claims below. Those skilled in the art may be able to study the preferred embodiments and identify other ways to practice the invention that are not exactly as described herein. It is the intent of the inventors that variations and equivalents of the invention are within the scope of the claims below and the description, abstract and drawings are not to be used to limit the scope of the invention.
This application is a continuation-in-part of U.S. patent application Ser. No. 12/174,816, filed Aug. 11, 2008, which is herein incorporated by reference.
Number | Name | Date | Kind |
---|---|---|---|
4599177 | Hayashi et al. | Jul 1986 | A |
4693731 | Tarakad et al. | Sep 1987 | A |
4962276 | Yan | Oct 1990 | A |
4966684 | Audeh | Oct 1990 | A |
4981577 | Audeh et al. | Jan 1991 | A |
4983277 | Audeh et al. | Jan 1991 | A |
4985137 | Audeh | Jan 1991 | A |
6350372 | Degnan et al. | Feb 2002 | B1 |
6475451 | Leppin et al. | Nov 2002 | B1 |
6537443 | Frankiewicz et al. | Mar 2003 | B1 |
6770119 | Harada et al. | Aug 2004 | B2 |
7416582 | Hakka et al. | Aug 2008 | B2 |
7563360 | Yamaguchi et al. | Jul 2009 | B2 |
20030075484 | Sakai et al. | Apr 2003 | A1 |
20050167335 | Yamaguchi | Aug 2005 | A1 |
20070278086 | Vermeulen | Dec 2007 | A1 |
Number | Date | Country |
---|---|---|
WO2006090597 | Aug 2006 | WO |
Number | Date | Country | |
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20100032345 A1 | Feb 2010 | US |
Number | Date | Country | |
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Parent | 12174816 | Aug 2008 | US |
Child | 12538606 | US |