The present invention relates to a process for recovering heavy oil and, more particularly, to a process for solidifying inorganic and organic constituents contained in produced water that is a by-product from recovering heavy oil.
The present invention relates to a process for concentrating produced water with a high concentration of inorganics and organics which are a byproduct of an oil recovery process. The process includes evaporation of the produced water in a crystallizer which is designed to evaporate virtually all free water from the produced water leaving solid crystals suspended in an organic melt. The organic melt from oil operations is a fluid at temperatures above 100° C. Upon cooling the organics freeze to form a solid. The frozen organic solid traps the suspended solid crystals. The organic solid can be cast in place in a landfill.
In one particular embodiment, the present invention entails a method of recovering oil from a SAGD (steam assist gravity drainage) oil well and treating the resulting produced water. The terms “oil” and “heavy oil” includes bitumen. This method or process entails recovering an oil-water mixture from an oil well and separating from the oil-water mixture to yield produced water. The produced water is directed to an evaporator that produces a distillate that is directed to a steam generator that produces steam that is injected into an injection well. The evaporator produces a blowdown stream that is directed to a crystallizer. In the crystallizer, the blowdown is concentrated as water is evaporated from the blowdown. The concentration of the blowdown causes inorganic and organic solids to precipitate from the blowdown and to form an organic melt. The organic melt is cooled to form a solidified structure which is suitable for disposal in a landfill.
The other objects and advantages of the present invention will become apparent and obvious from a study of the following description and the accompanying drawings which are merely illustrative of such an invention.
Conventional oil recovery involves drilling a well and pumping a mixture of oil and water from the well. Oil is separated from the water, and the water is usually injected into a sub-surface formation. Conventional recovery works well for low viscosity oil. However, conventional oil recovery processes do not work well for higher viscosity, or heavy oil.
Enhanced Oil Recovery processes employ thermal methods to improve the recovery of heavy oils from sub-surface reservoirs. The injection of steam into heavy oil bearing formations is a widely practiced enhanced oil recovery method. Typically, several tons of steam are required for each ton of oil recovered. Steam heats the oil in the reservoir, which reduces the viscosity of the oil and allows the oil to flow to a collection well. Steam condenses and mixes with the oil, the condensed steam being called produced water. The mixture of oil and produced water that flows to the collection well is pumped to the surface. Oil is separated from the produced water by conventional processes employed in conventional oil recovery operations.
For economic and environmental reasons it is desirable to recycle the produced water used in steam injection enhanced oil recovery. This is accomplished by treating the produced water, producing a feedwater, and directing the treated feedwater to a steam generator or boiler which produces steam. The complete water cycle includes the steps of:
There are various methods for treating the produced water to form feedwater for steam generation. One approach is to chemically treat the produced water using various physical/chemical processes. Another approach is to subject the produced water to an evaporation process to produce distillate which is suitable for steam generation feedwater. However, the produced water typically contains significant amounts of silica-based compounds, dissolved organics, sparingly soluble salts, and soluble chloride based salts. These silica-based compounds, dissolved organics, and sparingly soluble salts will tend to foul process surfaces by deposition of silica on the surfaces, hardness scaling, or organic fouling. These scales and fouling layers reduce the thermal conductivity of heat transfer elements in the evaporator equipment and thus reduce the efficiency of heat exchange and steam generation. The chloride based soluble salts will corrode equipment if allowed to accumulate in the system. To prevent or retard scaling, fouling, and corrosion, many water treatment processes remove silica-based compounds, dissolved organics, sparing soluble salts, and soluble chloride based salts in the form of sludge or concentrated wastewater streams. These concentrated wastewater streams are difficult to dispose of in an environmentally safe manner.
The present invention entails a Zero Liquid Discharge (ZLD) process using a ultra high solids crystallizer 10 for heavy oil wastewater treatment wherein inorganic and organic constituents of produced water are converted into a solid for disposal in a landfill. Crystallizer 10 concentrates wastewater with a high fraction of organic solids to a point where virtually all of the free water is removed leaving only solid crystals, such as salt crystals, suspended in an organic melt. Upon cooling the melt solidifies into a material which is suitable for landfill disposal. Fly ash can be added to vary the material handling properties of the melt. Calcium chloride can be added to vary the curing time of the melt.
As discussed above, heavy oil recovery utilizes the heat released from condensing steam to release oil from oil-bearing deposits. The resulting oil-water mixture is collected and pumped to the surface where the oil is separated from the mixture leaving what is called produced water. Produced water is water from underground formations that is brought to the surface during oil production. Herein the term produced water also means waste streams that are derived from produced water during the course of treating produced water. Produced water includes dissolved inorganic solids, dissolved organic compounds, suspended inorganic and organic solids, and dissolved gases. Two examples of SAGD produced water chemistries are shown in Table 1. These produced water compositions are for illustration and not all constituents are listed. In these examples, sodium chloride is the dominant single inorganic constituent. These chemistries have a significant level of Total Organic Carbon (TOC).
Table 2 shows that the organic matter in these SAGD produced water examples is between 26% and 54% (by weight) of the total solids. In addition to dissolved solids, produced water from heavy oil recovery processes typically includes several hundred ppms of suspended solids. All of the treatment processes which recycle produced water and generate steam produce concentrated wastewater stream(s). All or a portion of these streams must be purged from the system to prevent accumulation of the dissolved organic and inorganic solids in the system. The present invention is directed, then, at methods of treating the wastewater using a crystallizer, preferably an ultra high solids crystallizer, to produce an organic melt with suspended solid crystals such as salt crystals which will solidify upon cooling into a solid which can be disposed in a landfill.
Organic matter is typically long chain hydrocarbon molecules derived from bitumen and dissolved in water. The organics are complex and interact with water in different ways depending on their concentration and temperature. For example, when SAGD produced water is concentrated by evaporation of water to a total solids concentration (defined as the sum of dissolved and suspended organic and inorganic solids) of 50% (by weight) at a temperature of approximately 110° C. the liquid portion of the mixture has water like properties. When the mixture is cooled to a temperature of 20° C., the suspended solids settle and the remaining liquid has water like properties. When a SAGD produced water is concentrated by evaporation of water to a total solids concentration (defined as the sum of dissolved and suspended organic and inorganic solids) of 75% to 85% (by weight) at a temperature of approximately 120° C., the liquid portion of the mixture has properties similar to a viscous, asphalt like, semi-solid melt. When the mixture is cooled to a temperature of 20° C. the liquid becomes a semi-solid and there is no apparent free water. The semi-solid becomes a solid with a compressive strength of approximately 3,500 kg/m2 or higher after a period of time which can be several days to several weeks after cooling. In the case of a SAGD produced water waste, the inorganic solids will substantially precipitate after the water is evaporated. The precipitates become suspended in the hydrocarbon semi-solid melt and upon cooling the precipitates are encapsulated in the solidified material. The approximate composition of the solidified melt is shown in Table 3.
Free water is defined as water which is present in liquid form upon cooling of the melt. Expressed in another way, free water means that when the water cools, it becomes a solid. It should be noted, however, that there is approximately 15-25% water still present in the solidified material. Also it should be noted that free water is water which is easily separated from the melt or for example, would pass through a paint filter if a sample of the solidified melt was set on the filter.
Turning now to the general process according to the present invention, the process is depicted schematically in
The basic elements of a forced circulation crystallizer 10 are shown in
Steam is utilized to heat the liquid flowing through the heat exchanger 16. In particular, as viewed in
Water in the recirculating fluid boils off from the fluid in the vapor body 14. These vapors exit the vapor body 14 via a vapor outlet 14A and flow to a condenser in the case of a boiler steam heated system or to a compressor in the case of a mechanical vapor compression system. A portion of the recirculating fluid is discharged via a product outlet 18 as organic melt. Fresh wastewater is introduced via inlet 20 into the recirculating fluid to replace the organic melt which has been discharged and the fluid that has been vaporized. Typically there is virtually no free water in the recirculating fluid. Free water is defined as water which is present in liquid form upon cooling of the melt. The organic melt is a viscous liquid which can be pumped from the crystallizer to a location where it cools into a solid.
Fly ash can be blended into the melt so that the blend has properties which make it suitable for solids handling equipment. Blending can be performed using a pug mill, which converts the melt into a semi-solid state. The blend can be discharged from the pug mill onto a conveyer belt for transport to the landfill or discharged into a truck for transport to a landfill. The blend can also be extruded into impermeable casings to prevent contact with water. The ratio of fly ash added to the organic melt is typically in a ratio of 1 to 2 or 1 to 1. The time required for the solidified melt to cure from a semi-solid to a solid can be accelerated by the addition of between 0.5% to 4.0% (by weight) calcium chloride. The concentration of total solids in the crystallizer to reach the no free water condition is typically at least 70% by weight. After solidification, the material can be encapsulated in various materials or coated with various materials to prevent leaching if the material comes into contact with water.
First, with respect to
In the process shown in
In the process depicted in
In the above specification, from time to time percentage compositions are given. If not particularly set forth, the percentage compositions are always by weight.
The present invention may, of course, be carried out in other specific ways than those herein set forth without departing from the scope and the essential characteristics of the invention. The present embodiments are therefore to be construed in all aspects as illustrative and not restrictive and all changes coming within the meaning and equivalency range of the appended claims are intended to be embraced therein.
The present application claims priority from provisional U.S. Patent Application Ser. No. 61/391,205 filed Oct. 8, 2010, the content of which is expressly incorporated herein by reference.
Number | Date | Country | |
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61391205 | Oct 2010 | US |