The present invention generally relates to the field of bitumen froth treatment operations and more particularly to enhanced processes with turndown functionality.
Bitumen froth treatment plants historically have been designed for a given froth feed flow despite the fact that the actual flow varies significantly in response to oil sand grade variation and upstream equipment availability. Variations in feed flow, composition and temperature can result in several challenges that affect recovery and unit reliability.
Conventional solutions to variable froth flow are to coordinate start up and shut down of froth treatment operations with upstream unit operations.
In addition to the significant coordination effort related to the displacement of oil sand to ore preparation sites as well as the logistics of supplying utilities for ore preparation, bitumen extraction and tailings disposal, there are significant time delays associated with obtaining stability for each unit operation. An upset in any one unit can directly impact the production chain.
Oil sand operations are characterized by oil sand grade variations. The grade variations of the oil sand ore often range between approximately 7 wt % and 15 wt % bitumen, which is typically blended in mine and preparation operations to a narrower range between approximately 10.5 wt % and 12 wt %. This blending is dependant on equipment availability.
For some previous naphthenic froth treatment operations, dilution centrifuges were provided in parallel, the on/off operation of which permitted a range of process turndown options to adjust to froth supply variations. However, in paraffinic froth treatment operations, the large separation vessels that are used are sensitive to feed variations and upsets can interrupt efficiency of the production chain.
There is a need for a technology that overcomes at least some of the disadvantages or inefficiencies of known techniques.
The present invention responds to the above need by providing a process for enhanced turndown in a bitumen froth treatment operation.
The invention provides a process for operating a bitumen froth treatment operation in turndown mode, comprising:
In one optional aspect, the step of separating is performed in a separation apparatus comprising:
In another optional aspect, the first and second stage separation vessels are gravity settlers.
In another optional aspect, the process includes returning a portion of the first stage underflow component into the first stage separation vessel.
In another optional aspect, the process includes returning a portion of the second stage underflow component into the second stage separation vessel.
In another optional aspect, the process includes recirculating a portion of the first stage overflow component into the bitumen froth.
In another optional aspect, the process includes recirculating a portion of the second stage overflow component into the first stage underflow.
In another optional aspect, the solvent containing stream added to the bitumen froth comprises at least a portion of the second stage overflow component.
In another optional aspect, the process includes heating the second stage overflow component prior to using as the solvent containing stream.
In another optional aspect, the process includes adding a second stage solvent containing stream to the first stage underflow component.
In another optional aspect, the second stage solvent containing stream consists essentially of solvent.
In another optional aspect, the process includes subjecting the first stage underflow component and the second stage solvent containing stream to mixing to produce a diluted first stage underflow for introduction into the second stage separation vessel.
In another optional aspect, the process includes subjecting the bitumen froth and the solvent containing stream to mixing to produce the diluted bitumen froth.
In another optional aspect, the process includes pre-heating the bitumen froth to produce heated bitumen froth prior to adding the solvent containing stream thereto.
In another optional aspect, the pre-heating is performed by direct steam injection into the bitumen froth.
In another optional aspect, the process includes recirculating a portion of the heated bitumen froth back into the bitumen froth upstream of the pre-heating.
In another optional aspect, the process includes tanking the heated bitumen froth prior to pumping the heated bitumen froth to the step adding of the solvent containing stream thereto.
In another optional aspect, the process includes regulating the flows of the recirculated dilbit component and the returned solvent diluted tailings component in response to the flow of the bitumen froth.
In another optional aspect, the step of separating is performed in a separation apparatus comprising:
a first stage separation vessel receiving the diluted bitumen froth and producing the diluted bitumen component and a first stage underflow component;
an addition line for adding make-up solvent to the first stage underflow component to produce a diluted first stage underflow component; and
In another optional aspect, sub-steps (a), (b), (c) and (d) are initiated sequentially.
In another optional aspect, in sub-step (a) the dilbit recirculation stream is provided with a flow corresponding to the reduction in the flow of the bitumen froth.
In another optional aspect, in sub-step (b) the first stage return stream is returned below an hydrocarbon-water interface within the first stage separation vessel.
In another optional aspect, in sub-step (b) the first stage return stream is returned to provide a velocity of the first stage underflow component sufficient to avoid solids settling and asphaltene mat formation.
In another optional aspect, in sub-step (c) the second stage recirculation stream is provided with a flow corresponding to the reduction in flow of the first stage underflow component due to the first stage return stream.
In another optional aspect, in sub-step (d) the second stage return stream is returned below an hydrocarbon-water interface within the second stage separation vessel.
In another optional aspect, in sub-step (d) the second stage return stream is returned to provide a velocity of the second stage underflow component sufficient to avoid solids settling and asphaltene mat formation.
In another optional aspect, sub-steps (a) and (c) are performed such that flows of the dilbit recirculation stream and the second stage recirculation stream are sufficient to avoid settling of solids in respective recirculation piping systems.
In another optional aspect, the process also includes sub-step (e) of recycling a portion of the bitumen froth back upstream.
In another optional aspect, step (e) is initiated in response to an additional reduction in the flow of the bitumen from below a given flow value.
In another optional aspect, the given flow value corresponds to a minimum pump requirement flow for pumping the bitumen froth.
In another optional aspect, the process also includes two parallel trains each comprising at least one of the separation apparatus.
In another optional aspect, the separation apparatus is sized and configured to allow full standby mode.
In another optional aspect, the bitumen froth treatment operation is a paraffinic froth treatment operation and the solvent is paraffinic solvent.
In another optional aspect, the bitumen froth treatment operation is a naphthenic froth treatment operation and the solvent is naphthenic solvent.
In another optional aspect, the process also includes following a control strategy comprising flow control of the bitumen froth, the diluted bitumen component, the first stage underflow component, the second stage overflow component and the solvent diluted tailings component and the make-up solvent to maintain material balance.
In another optional aspect, the control strategy comprises acquiring flow measurements of hydrocarbon-rich streams.
In another optional aspect, the control strategy comprises acquiring measurements of solvent, bitumen, water and/or mineral content in the solvent diluted froth or the diluted first stage underflow component.
In another optional aspect, the control strategy comprises solvent-to-bitumen ratio (S/B) control.
In another optional aspect, the S/B control comprises designating a master stream relative to a slave stream in terms of the S/B.
In another optional aspect, the S/B control comprises designating a master stream relative to a slave stream.
In another optional aspect, the control strategy comprises level control of bitumen froth in a froth tank, first stage separation vessel overflow, first stage separation vessel water-hydrocarbon interface, second stage separation vessel overflow and second stage separation vessel water-hydrocarbon interface.
In another optional aspect, the level control comprises adjusting pump speed, adjusting pump discharge valve or adjusting pump bypass recirculation valve or a combination thereof to maintain a stable level.
In another optional aspect, the process includes controlling the S/B ratio in the diluted froth stream.
In another optional aspect, the process also includes following a control strategy comprising flow control of the bitumen froth, the diluted bitumen component, the solvent diluted tailings component, and the solvent, to maintain material balance.
In another embodiment, the invention provides method for turndown of a froth separation vessel for treating a bitumen froth with addition of a paraffinic solvent to produce a solvent diluted bitumen froth with a solvent-to-bitumen ratio, the froth separation vessel separating the solvent diluted bitumen froth provided at a feed flow into a diluted bitumen component and a solvent diluted tailings underflow component, wherein in response to a reduction in flow of the bitumen froth, the method comprises:
In an optional aspect, step (i) comprises recirculating a portion of the diluted bitumen component back into the bitumen froth.
In another optional aspect, step (ii) comprises reducing the amount of the solvent added to the bitumen froth.
In another optional aspect, step (ii) comprises recirculating a portion of the diluted bitumen component back into the bitumen froth.
In another optional aspect, step (iii) comprises returning a portion of the solvent diluted tailings back into the froth separation vessel below a hydrocarbon-water interface.
In another optional aspect, the froth separation vessel comprises:
In another optional aspect, the method includes sub-step (e) of recycling a portion of the bitumen froth back upstream.
In another optional aspect, step (e) is initiated in response to an additional reduction in the flow of the bitumen from below a given flow value.
In another optional aspect, the given flow value corresponds to a minimum pump requirement flow for pumping the bitumen froth.
In another optional aspect, the method includes two parallel trains each comprising at least one of the froth separation vessel.
In another optional aspect, the separation apparatus is sized and configured to allow full standby mode.
In another optional aspect, the method includes following a control strategy comprising flow control of the bitumen froth, the diluted bitumen component, the solvent diluted tailings component and the solvent, to maintain material balance.
In another embodiment, the invention provides a process for operating a bitumen froth treatment operation, comprising:
In one aspect, this process may be associated or have steps or features of the previously described method or process.
The invention also provides a use of diluted bitumen derived from a paraffinic froth treatment comprising adding a solvent containing stream to bitumen froth to produce diluted bitumen froth and separating the diluted bitumen froth into the diluted bitumen and a solvent diluted tailings component, as a viscosity modifying agent of the bitumen froth.
In one aspect, the diluted bitumen is at saturation with respect to asphaltenes. A portion of the diluted bitumen may be recycled into the bitumen froth upstream of mixing of the bitumen froth and the solvent containing stream. The diluted bitumen may preferably avoid increasing asphaltene precipitation from the bitumen froth. The diluted bitumen may reduce solvent-to-bitumen ratio in the diluted bitumen froth to promote solubility stability.
According to embodiments of the present invention, a froth separation apparatus is able to turn down to a recirculation mode in response to variations in froth feed supply. The process allows the ability to respond to froth feed supply variation, to commission and shut down froth treatment processing equipment independent of froth supply and design smaller and more cost efficient froth treatment equipment such as separation vessels.
Referring to
Referring still to
The heated bitumen froth may be held in a froth tank 20 a bottom outlet 22 of which is coupled to a froth pump 24. The froth pump 24 supplies the heated froth 16 under pressure.
A solvent containing stream 26 is added to the heated bitumen froth 14. There may be a mixer 28 provided immediately downstream or as part of the addition point of the solvent containing stream 26. The mixer may include one or more mixers in parallel and/or series to help produce a diluted bitumen froth 30. The mixer may be designed, constructed, configured and operated as described in Canadian patent application No. 2,733,862. As will be described in greater detailed herein-below, the solvent containing stream is preferably an overflow stream from a downstream separation vessel, but it could also at least partially consist of fresh or make-up solvent.
Still referring to
A second solvent containing stream 38, which may be referred to as make-up solvent, is then added to the first stage underflow 36. There is a second stage mixer 40 provided immediately downstream or as part of the addition point of the second solvent containing stream 38. Thus the second solvent 38 can be added immediately upstream or concurrent with the mixer. Preferably, the second solvent containing stream 38 consists essentially of solvent, which has been recovered in a solvent recovery unit and a tailings solvent recovery unit from the dilbit and the solvent diluted tailings respectively. The mixer facilitates production of a diluted first stage underflow 42.
The diluted first stage underflow 42 is then fed to a second stage separation vessel 44 which produces a second stage underflow which is solvent diluted tailings 46 which is pumped by a second stage underflow pump 47 and a second stage overflow 48 which his pumped by a second stage overflow pump 49. The second stage overflow 48 preferably contains sufficiently high content of solvent that it is used as the solvent containing stream 26 for addition into the heated bitumen froth 16. In one aspect, the second stage overflow 48 is heated in a second stage heater 50, also referred to as a “trim heater” receiving steam S and producing condensate C, prior to addition into the heated bitumen froth 16. The temperature of the bitumen froth feed 30 may be controlled via a heating controller 51 coupled to the second stage heater 50.
Still referring to
The recirculated bitumen froth component 60 may also be referred to as “froth recirc”, the recirculated dilbit component 52 may also be referred to as “1st stage O/F recirc”, the returned first stage underflow component 56 may also be referred to as “1st stage U/F recirc”, the recirculated second stage overflow component 58 may also be referred to as “2nd stage O/F recirc”, and the returned second stage underflow component 54 may also be referred to as “2nd stage underflow recirc”.
In standard operating mode of the froth treatment unit, the recirculation and return lines illustrated bold in
In one preferred aspect of the present invention, in the standard operating mode of the froth treatment unit, flow control either by direct flow measurement or inferred by calculation methods represents the primary control of key process variables (PV) which include the flow of bitumen froth 16, 1st stage O/F 34, 1st stage U/F 36, make-up solvent 38, 2nd stage O/F 48 and 2nd stage U/F 46, to maintain the process material balance. Preferably, the flow measurement selected by the control system reflects measurement reliability. For example, flow measurement of hydrocarbon or hydrocarbon-rich streams such as settler O/F is considered relatively reliable when compared to flow metering on streams such as froth or U/F. This measurement reliability combined with inline measurements of solvent, bitumen, water and mineral in diluted froth or diluted underflow streams can either allow inference or correction of erroneous froth or underflow measurements used by the control system. It is also noted that the relative volumes of the froth tank 20, the 1st stage O/F 22, and the 2nd stage O/F cause analytical measurements of bitumen, solvent, water and mineral to respond relatively slowly when compared to flow sensors which quickly sense step changes from a process turn down. The analytical measurements can be online or routine samples for off line analysis.
In addition to the key flow process variables, flow controls coupled with inline analytical measurements permit the derivation and control of key process ratios such as S/B. Designating one stream as the master stream, relative to another stream as a slave (SP) allows maintaining key process ratios to the master stream that will be illustrated in an example and permits stable turndown of operation to a froth feed interruption. By quickly adjusting flows to maintain key ratios, analytical measurement delays are mitigated and are not critical. In one preferred aspect, the flow is adjusted and the analytical measurements are used as confirmations or time averaged updates or the like.
Referring to
In addition, it should be noted as illustrated in
In turndown operating mode of the froth treatment unit, the recirculation and return lines are opened as illustrated in
In one preferred aspect, the system is configured and process operated to respond to a step change in froth flow. In response to a step change, the recirculation system opens line 52, 56, 58 and 54 in a sequential order, as will be further understood from the description herein-below. In addition, the recirculation system is preferably managed and controlled in accordance with a desired S/B ratio for the given temperature and pressure conditions of the FSU and a consistent flow to each of the first and second stage mixers and separation vessels 32, 44. From a high-level operating standpoint, the process is operated so that a reduction of bitumen froth 12 flow results in a corresponding reduction in produced dilbit 61, produced solvent diluted tailings 63 and fresh solvent 38, while generally maintaining the flow of the streams that remain within the system. The process may include the following recirculation methodologies:
First, in response to a step change reduction in bitumen froth 12 flow, the dilbit recirculation 52 is initiated. The dilbit recirculation 52 may be provided, managed or controlled to essentially compensate for the difference in reduced froth flow to maintain the efficiency of the mixer 28 and separation in the first stage separation vessel 32. The froth pump 24 would continue to provide a flow of heated froth which is mixed with the 2nd stage O/F 26 and the dilbit recirculation 52 would maintain a generally constant flow of diluted bitumen froth 30 to the first stage separation vessel 32, and circulate a generally constant flow of high diluted bitumen 34 to the 1st stage O/F pump 39.
If froth 12 flow supplied to the FSU is reduced below the minimum froth pump requirement, an additional turndown strategy may be adopted. More particularly, the pump can continue to operate at its minimum flow requirement, but a portion of the pumped froth is recycled by opening the froth recirculation line 60. This will therefore reduce the amount of froth being provided to the mixer 28 and separation vessel 32 and, consequently, the dilbit recirculation 52 flow is preferably increased to compensate for this additional reduction is froth flow, again to maintain a consistent fluid flow through the mixer 28 to the separation vessel 32.
Increasing the dilbit recirculation 52 flow allows consistent first stage mixing and separation performance and also causes some changes within the first stage separation vessel 32. The amount of water and mineral in the incoming diluted froth stream 30 decreases and thus the hydrocarbon-water interface 62 within the settler 32 moves downward. The lower water/minerals phase is reduced and replaced by a larger upper hydrocarbon phase. It is desirable to keep the velocity of the water/minerals phase within the vessel 32 and its underflow outlet sufficiently high so as to avoid various settling and plugging issues. For instance, mineral solids can settle out of the phase if the velocities fall below a critical settling value. In addition, in the case of paraffinic froth treatment (PFT), in which asphaltenes are precipitated out with the water/mineral bottom phase, it is also desirable to keep the lower phase and underflow at a velocity sufficient to avoid formation and deposition of asphaltene mats which are difficult to break-up, clean and remove. Consequently, the first stage underflow recirculation 56 may be engaged in response to an underflow velocity set point and/or a hydrocarbon-water interface 62 level in the settler 32. The underflow recirculation may also be dependent on or controlled by the minimum flow requirement of the underflow pump 37. This 1st stage U/F recirculation maintains water/minerals and asphaltenes in the lower section of the settler 32 avoiding solids packing and plugging settler underflow outlets which risk occurring at low flow rates. The 1st stage U/F recirculation also facilitates maintaining the first underflow pump 37 above minimum flow rate and avoiding of settling in the settler 32 at low flows.
Initiating the first stage underflow recirculation 56, in turn, causes a reduction in the second stage feed flow. In response to the reduced first stage underflow flow provided to the second stage, the second stage overflow recirculation 58 may be engaged. Preferably and similarly to the first stage overflow recirculation 52, the second stage overflow recirculation 58 is provided to compensate for the reduction of first stage underflow 36 lost to its own recirculation 56.
The second stage overflow recirculation 58 contains a high concentration of solvent and thus the fresh solvent 38 flow may be decreased. It is also noted that a reduction in bitumen froth 12 leads to a corresponding reduction in solvent 38 demands.
By increasing the second stage overflow recirculation 58, the more solvent and bitumen is contained in the second stage feed stream 42 and, in turn, the relative proportions of hydrocarbon and water/minerals phases will change in the second stage separation vessel 44. A second stage hydrocarbon-water interface 64 separating the phase moves down as more hydrocarbons are present in the vessel 44. Similarly to the first stage, the second stage underflow recycle 54 is engaged to ensure that the lower water/minerals phase, which may also contain significant amounts of asphaltenes in certain embodiments, maintain a velocity to avoid clogging, plugging and asphaltene mat formation issues.
Once the transition to turndown mode is complete, the FSU may operate smoothly with constant stream flows until ready to transition back to standard operating mode.
In turndown mode, portions of the first and second stage overflow streams recirculate back as respective first and second stage feed supplies. This maintains stable feed flows to each of the froth separation vessels while facilitating unit turndown mode by replacing feed from upstream operation. The 1st and 2nd stage O/F recirculation further facilitates maintaining feed to respective FSVs at velocities at or above minimum velocities to avoid settling of solids in the respective pipe systems.
In turndown mode, portions of the first and second stage underflows are recycled back into the lower section of the respective first and second stage froth separation vessels (FSVs).
A control system 66 facilitates the recirculation controllers to automatically transition the unit operation and minimize operator intervention and associated risk of error.
According to an embodiment of the present invention, the recirculation system of the froth separation unit process streams facilitates commissioning a froth treatment unit independent of upstream operations and allows unit turndown to match variations in bitumen supply.
More particularly, a portion of the 1st stage O/F is preferably recycled back into the bitumen froth upstream of the 1st stage mixer 28. At its temperature and pressure conditions, the 1st stage O/F is saturated with asphaltenes and thus the first stage recirculation 52 replaces froth with 1st stage O/F acting generally as a diluent. In other words, the dilbit contains its maximum concentration of asphaltenes and cannot receive additional asphaltenes when mixed with the heated froth 16 and first solvent containing stream 26. By way of example, in a paraffinic froth treatment process, the dilbit may contain about ⅓ bitumen with 10% of the bitumen being asphaltenes and about ⅔ of solvent. In a naphthenic process, the dilbit contains about ⅓ naphthenic solvent. In addition, with essentially a clean hydrocarbon stream, little valve erosion ensures reliable operation in this mode.
In paraffinic froth treatment (PFT), recycling 1st stage O/F at its saturation point with respect to asphaltenes for blending with froth prior to the mixer may be performed to act as a viscosity modifying agent chemical additive that does not increase asphaltene precipitation. As 1st stage O/F is saturated with asphaltenes, reducing the S/B ratio with froth promotes solubility stability while diluting bitumen viscosity.
In one aspect, the 1st stage U/F is recycled back to the bottom of the FSV below the hydrocarbon-water interface.
In another aspect, the 2nd stage O/F is recycled back into the 1st stage U/F stream upstream of the 2nd stage mixer. As 2nd stage O/F is partially saturated by asphaltenes, replacing 1st stage U/F with 2nd stage O/F effectively dilutes the stream. The low bitumen content of 1st stage U/F mitigates asphaltene precipitation in the mixer. It is also noted that the 2nd stage O/F may be recirculated into the 2nd stage solvent feed stream prior to addition to the 1st stage U/F stream or into a combination of solvent feed and 1st stage U/F.
In another preferred aspect, the 2nd stage U/F recirc is returned back to the bottom of the second stage FSV below the hydrocarbon-water interface.
In another preferred aspect, both O/F recirc streams and both U/F return streams operate near the operating pressure of the FSU system which minimizes differential pressure across flow control valves which reduces both power and erosion in the recirc operating mode. In addition, the froth and U/F low flow transition may occur when froth and U/F pumps are at or below minimum flow requirements for the pumps and the valves redirecting the recirculation stream may only operate in an on/off mode.
In another aspect, the froth pumps 24 pressurize froth from near atmospheric pressure to FSU process pressure. The 1st stage O/F recirc could “back off” the froth pumps, in the case of variable speed control pumps, until minimum flow provisions on the pump discharge occur at which time the minimum flow would divert froth back to the froth heater.
In transitioning to turndown mode, the process may employ a number of control strategies and operating schedules. In one embodiment, the transition to turndown mode includes, for instance in response to a bitumen froth supply reduction, increasing the 1st stage O/F recirc flow rate. Maintaining a constant froth feed supply to the mixer, the variable speed froth pump reduces the flow rate of froth supplied from the froth tank. The froth pump flow reduction continues until the pump reaches a minimum flow requirement, according to equipment specifications. In order to further increase the proportion of 1st stage O/F recirc provided as feed relative to untreated heated froth, the froth recirc valve may be switched to an open position thus allowing flow through the froth recirc line.
In one optional aspect, the supplied bitumen froth is deaerated prior to heating to produce the heated froth which is pumped and blended with 2nd stage O/F, which may be referred to as “a first solvent containing stream”. To maintain a constant feed to the 1st stage FSV with froth feed variations, 1st stage O/F is recycled to froth feed which by pressure balance or similar control causes froth pumps to turn down. For paraffinic froth treatment (PFT), as 1st stage O/F is at its saturation point with respect to asphaltenes, blending with froth prior to the mixer does not increase asphaltene precipitation, however due to the volumetric flow critical line velocities above critical setting velocities are maintained while froth flow reduces. In event the froth flow is less than the minimum flow required for stable pump operation, froth is diverted back to the froth heater and an interlock valve is closed to prevent solvent flowing to the froth tank and causing a safety or environmental issue due to solvent flashing in the froth tank.
1st stage U/F is pumped and blended with feed solvent. To maintain a constant feed to the 2nd stage FSV with 1st stage U/F variations resulting from froth feed variations, 2nd stage O/F is recycled to either the 1st stage U/F as shown in the figure which by pressure balance or similar control causes 1st stage U/F pumps to turn down. As 2nd stage O/F is partially saturated with asphaltenes and the bitumen content of 1st stage U/F is limited, blending with 1st stage U/F prior to the mixer does not notably increase asphaltene precipitation, however the volumetric flow maintains critical line velocities above critical setting velocities while 1st stage U/F flow reduces. The control scheme provides maintaining the 1st stage U/F flow the minimum flow required for stable pump operation by diverting 1st stage U/F back to the FSV via an interlock valve to prevent reverse flow of solvent to the FSV and leading to safety or environmental issues.
Activation of either the froth interlock valve or the 1st stage U/F interlock valve for minimum flow protection would cause other valves noted in
The recirculation of 1st or 2nd stage O/F back to the respective FSVs via feed systems ensures the O/F pumps operate above minimum flow rates for stable operation.
In a preferred aspect, a control scheme responds to a step change in froth flows and as a master control strategy reduces risk of operator error in timing the appropriate control response required in the current operating strategy.
In another optional aspect, the recirculation strategy for the FSU is coupled with recirculation controls in the solvent recovery unit (SRU) and tailings solvent recovery unit (TSRU) to maintain stable froth treatment plant operations over with ranges of froth feed rates and qualities.
It is also noted that the FSU can be put on standby mode with full internal recirculation and where the effective flows for the froth, produced dilbit, produced solvent diluted tailings and fresh solvent are brought to zero.
The following legend outlines the elements in
It is noted that minimum flow requirement for a pump is specific to the given selected pump and results in certain limitations to the FSV turndown possibilities. To achieve the minimum desired turndown, careful selection of pumps is preferred. Alternately, where FSU multiple trains operate in parallel, each train for example including a system as illustrated in
It is also noted that analogous control strategies may be used in connection with SRUs and/or TSRUs.
A HYSYS™ dynamic simulation model was built and run to test the froth separation unit control and recirculation system. The results of the model test were that the control system was able to handle and control a step change drop of about 50% in feed flow from the froth tank to the 1st stage settler. The recirculation loops were able to bring flows back to the minimum flows as specified in the model. The solvent to bitumen ratio (S/B) controller was able to bring the ratio back after the initial spike due to the drop in fresh feed flow.
More particularly, the model was a dynamic simulation built in HYSYS™ v7.1. The component slate was simplified and selected to give a vapour and two liquid phases, and have the ability to measure an S/B ratio. All the unit operations were included and modeled as best fit within HYSYS™. Pumps were all modelled as standard HYSYS™ centrifugal pumps with performance curves, settlers were modelled as vertical 3-phase vessels with internal weir enabled—the overflow side of the weir is used to simulate the overflow vessels on the settlers. All proposed controllers were included with generic tuning parameters, which control the system process variable (PV) to match a set point (SP). The control algorithm incorporated master PV controllers such as S/B ratio to relate froth and solvent flows and maintain relative material balance relationship between the process streams involved. In this specific simulation, the solvent flows were assigned a slave relationship relative to the bitumen flow; that is, the solvent controller SP was reset based on the bitumen froth flow and the master S/B ratio.
With the recirculation loops incorporated into the dynamic HYSYS™ model, the simulation model was allowed to run 5 minutes to permit PVs to line out to the controller SP prior to introducing about a 50% step change in the froth feed flow. The simulation was then run for an additional 55 minutes and the added control system response as illustrated on
Step change in froth flow illustrated in
As a result of the inventory in the 1st stage separation vessel, the step change in froth flow as illustrated in
As illustrated in
The added control system was able to respond to the feed step change. The recirculation controllers worked as designed and were able to bring flows back to stable flows. The S/B controller had a spike in S/B ratio from 1.6 to 2.15, but was able to respond and bring the ratio back to 1.6. Tuning of the S/B master controller and slave flow controller resulted in a faster response in S/B ratio.
In terms of model limitations, it is noted that the model used a simplified component slate. Vessels (used for froth tank and settlers) assume perfect mixing in the phases. The process lags or dead time in the model reflect inventories within process vessels without allowing for the limited piping volumes and associated inventories in paraffinic froth treatment process. Hence, the control loop responses illustrated in
The control methodology concepts may be adapted and structured to auto-control other potential process supply limitations such as solvent.
In reference to
Finally, the present invention should not be limited to the particular examples, figures, aspects and embodiments described herein.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/CA2012/050247 | 4/19/2012 | WO | 00 | 10/28/2013 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2012/149648 | 11/8/2012 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
181668 | Gregg et al. | Aug 1876 | A |
654965 | Franke | Jul 1900 | A |
1085135 | Kelly, Jr. | Jan 1914 | A |
1147356 | Allen | Jul 1915 | A |
1159044 | Kelly, Jr. | Nov 1915 | A |
1201558 | Cobb | Oct 1916 | A |
1254562 | Allen | Jan 1918 | A |
1261671 | Zachert | Apr 1918 | A |
1494375 | Reilly | May 1924 | A |
1754119 | Pink | Apr 1930 | A |
1777535 | Stratford | Oct 1930 | A |
2010008 | Bray | Aug 1935 | A |
2047989 | William | Jul 1936 | A |
2091078 | McKittrick et al. | Aug 1937 | A |
2111717 | Young | Mar 1938 | A |
2188013 | Pilat et al. | Jan 1940 | A |
2240008 | Atwell | Apr 1941 | A |
2410483 | Dons et al. | Nov 1946 | A |
2853426 | Peet | Sep 1958 | A |
2868714 | Gilmore | Jan 1959 | A |
3081823 | Constantikes | Mar 1963 | A |
3220193 | Sttohmeyer, Jr. | Nov 1965 | A |
3271293 | Clark | Sep 1966 | A |
3278415 | Doberenz et al. | Oct 1966 | A |
3291569 | Rossi | Dec 1966 | A |
3575842 | Simpson | Apr 1971 | A |
3705491 | Foster-Pegg | Dec 1972 | A |
3779902 | Mitchell et al. | Dec 1973 | A |
3808120 | Smith | Apr 1974 | A |
3901791 | Baillie | Aug 1975 | A |
3929625 | Lucas | Dec 1975 | A |
3954414 | Samson, Jr. et al. | May 1976 | A |
3957655 | Barefoot | May 1976 | A |
4013542 | Gudelis et al. | Mar 1977 | A |
4035282 | Stuchberry et al. | Jul 1977 | A |
4115241 | Harrison et al. | Sep 1978 | A |
4116809 | Kizior | Sep 1978 | A |
4120775 | Murray et al. | Oct 1978 | A |
4140620 | Paulett | Feb 1979 | A |
4209422 | Zimmerman et al. | Jun 1980 | A |
4210820 | Wittig | Jul 1980 | A |
4230467 | Buchwald | Oct 1980 | A |
4251627 | Calamur | Feb 1981 | A |
4284242 | Randell | Aug 1981 | A |
4314974 | Libby et al. | Feb 1982 | A |
4315815 | Gearhart | Feb 1982 | A |
4321147 | McCoy et al. | Mar 1982 | A |
4324652 | Hack | Apr 1982 | A |
4342657 | Blair | Aug 1982 | A |
4346560 | Rapier | Aug 1982 | A |
4395330 | Auboir et al. | Jul 1983 | A |
4410417 | Miller et al. | Oct 1983 | A |
4425227 | Smith | Jan 1984 | A |
4461696 | Bock et al. | Jul 1984 | A |
4470899 | Miller et al. | Sep 1984 | A |
4495057 | Amirijafari et al. | Jan 1985 | A |
4514305 | Filby | Apr 1985 | A |
4518479 | Schweigharett et al. | May 1985 | A |
4532024 | Haschke et al. | Jul 1985 | A |
4539093 | Friedman et al. | Sep 1985 | A |
4545892 | Cymbalisty et al. | Oct 1985 | A |
4572781 | Krasuk et al. | Feb 1986 | A |
4584087 | Peck | Apr 1986 | A |
4609455 | Weimer et al. | Sep 1986 | A |
4634520 | Angelov et al. | Jan 1987 | A |
4640767 | Zajic et al. | Feb 1987 | A |
4644974 | Zingg | Feb 1987 | A |
4648964 | Leto et al. | Mar 1987 | A |
4678558 | Belluteau et al. | Jul 1987 | A |
4722782 | Graham et al. | Feb 1988 | A |
4726759 | Wegnwe | Feb 1988 | A |
4781819 | Chirinos et al. | Nov 1988 | A |
4802975 | Mehlberg | Feb 1989 | A |
4822481 | Taylor | Apr 1989 | A |
4828688 | Corti et al. | May 1989 | A |
4859317 | Shelfantook et al. | Aug 1989 | A |
4888108 | Farnand | Dec 1989 | A |
4906355 | Lechnick et al. | Mar 1990 | A |
4929341 | Thirumalachar et al. | May 1990 | A |
4931072 | Striedieck | Jun 1990 | A |
4950363 | Silvey | Aug 1990 | A |
4966685 | Hall et al. | Oct 1990 | A |
4968413 | Datta et al. | Nov 1990 | A |
5022983 | Myers et al. | Jun 1991 | A |
5039227 | Leung et al. | Aug 1991 | A |
5133837 | Elmore | Jul 1992 | A |
5143598 | Graham et al. | Sep 1992 | A |
5186820 | Schultz et al. | Feb 1993 | A |
5223148 | Tipman et al. | Jun 1993 | A |
5236577 | Tipman | Aug 1993 | A |
5264118 | Cymerman et al. | Nov 1993 | A |
5282984 | Ashrawi | Feb 1994 | A |
5298167 | Arnold | Mar 1994 | A |
5443046 | White | Aug 1995 | A |
5558768 | Ikura et al. | Sep 1996 | A |
5645714 | Strand et al. | Jul 1997 | A |
5690811 | Davis et al. | Nov 1997 | A |
5817398 | Hollander | Oct 1998 | A |
5871634 | Wiehe et al. | Feb 1999 | A |
5876592 | Tipman et al. | Mar 1999 | A |
5879540 | Zinke et al. | Mar 1999 | A |
5914010 | Hood et al. | Jun 1999 | A |
5937817 | Schanz et al. | Aug 1999 | A |
5948241 | Owen | Sep 1999 | A |
5954277 | Maciejewski et al. | Sep 1999 | A |
5968349 | Duyvesteyn et al. | Oct 1999 | A |
5985138 | Humphreys | Nov 1999 | A |
5988198 | Neiman et al. | Nov 1999 | A |
5997723 | Wiehe et al. | Dec 1999 | A |
6004455 | Rendall | Dec 1999 | A |
6007708 | Allcock et al. | Dec 1999 | A |
6007709 | Duyvesteyn et al. | Dec 1999 | A |
6019888 | Mishra et al. | Feb 2000 | A |
6036748 | Wallace et al. | Mar 2000 | A |
6076753 | Maciejewski et al. | Jun 2000 | A |
6110359 | Davis et al. | Aug 2000 | A |
6120678 | Stephenson et al. | Sep 2000 | A |
6159442 | Thumm et al. | Dec 2000 | A |
6214213 | Tipman et al. | Apr 2001 | B1 |
6355159 | Myers et al. | Mar 2002 | B1 |
6358403 | Brown et al. | Mar 2002 | B1 |
6361025 | Cincotta et al. | Mar 2002 | B1 |
6391190 | Spence et al. | May 2002 | B1 |
6482250 | Williams et al. | Nov 2002 | B1 |
6497813 | Ackerson et al. | Dec 2002 | B2 |
6523573 | Robison et al. | Feb 2003 | B2 |
6566410 | Zaki et al. | May 2003 | B1 |
6746599 | Cymerman et al. | Jun 2004 | B2 |
6800116 | Stevens et al. | Oct 2004 | B2 |
7152851 | Cincotta | Dec 2006 | B2 |
7357857 | Hart et al. | Apr 2008 | B2 |
7569137 | Hyndman | Aug 2009 | B2 |
7690445 | Perez-Cordova | Apr 2010 | B2 |
7749378 | Iqbal et al. | Jul 2010 | B2 |
7820031 | D'Alessandro et al. | Oct 2010 | B2 |
7909989 | Duyvesteyn et al. | Mar 2011 | B2 |
7934549 | Cimolai | May 2011 | B2 |
8133316 | Poncelet et al. | Mar 2012 | B2 |
8141636 | Speirs et al. | Mar 2012 | B2 |
8147682 | Lahaie et al. | Apr 2012 | B2 |
8157003 | Hackett et al. | Apr 2012 | B2 |
8252107 | Esmaeili et al. | Aug 2012 | B2 |
8261831 | Lockhart et al. | Sep 2012 | B2 |
8262865 | Sharma et al. | Sep 2012 | B2 |
8312928 | Lockhart et al. | Nov 2012 | B2 |
8343337 | Moffett et al. | Jan 2013 | B2 |
8354020 | Sharma et al. | Jan 2013 | B2 |
8357291 | Sury et al. | Jan 2013 | B2 |
8382976 | Moran et al. | Feb 2013 | B2 |
8394180 | Diaz et al. | Mar 2013 | B2 |
8449764 | Chakrabarty et al. | May 2013 | B2 |
8454821 | Chakrabarty et al. | Jun 2013 | B2 |
8455405 | Chakrabarty | Jun 2013 | B2 |
8550258 | Bara et al. | Oct 2013 | B2 |
8585891 | Lourenco et al. | Nov 2013 | B2 |
20020043579 | Scheybeler | Apr 2002 | A1 |
20030089636 | Marchionna et al. | May 2003 | A1 |
20040074845 | Hagino et al. | Apr 2004 | A1 |
20040256325 | Frankiewicz | Dec 2004 | A1 |
20050150816 | Gaston | Jul 2005 | A1 |
20050150844 | Hyndman | Jul 2005 | A1 |
20060065869 | Chipman et al. | Mar 2006 | A1 |
20060138055 | Garner et al. | Jun 2006 | A1 |
20060196812 | Beetge et al. | Sep 2006 | A1 |
20070125719 | Yarbrough | Jun 2007 | A1 |
20070180741 | Bjornson et al. | Aug 2007 | A1 |
20070284283 | Duyvesteyn | Dec 2007 | A1 |
20080000810 | Garner et al. | Jan 2008 | A1 |
20080185350 | Remesat et al. | Aug 2008 | A1 |
20080210602 | Duyvesteyn | Sep 2008 | A1 |
20090134059 | Myers et al. | May 2009 | A1 |
20090200210 | Hommema | Aug 2009 | A1 |
20090200688 | Cincotta | Aug 2009 | A1 |
20090294328 | Iqbal | Dec 2009 | A1 |
20090321322 | Sharma | Dec 2009 | A1 |
20090321324 | Sharma | Dec 2009 | A1 |
20100006474 | Gaston et al. | Jan 2010 | A1 |
20100076236 | Van Heuzen et al. | Mar 2010 | A1 |
20100078306 | Alhazmy | Apr 2010 | A1 |
20100089800 | MacDonald et al. | Apr 2010 | A1 |
20100096297 | Stevens et al. | Apr 2010 | A1 |
20100126395 | Gauthier | May 2010 | A1 |
20100126906 | Sury | May 2010 | A1 |
20100133149 | O'Connor et al. | Jun 2010 | A1 |
20100147516 | Betzer-Zilevitch | Jun 2010 | A1 |
20100155293 | Verstraete et al. | Jun 2010 | A1 |
20100155304 | Ding et al. | Jun 2010 | A1 |
20100206772 | Keppers | Aug 2010 | A1 |
20100243534 | Ng et al. | Sep 2010 | A1 |
20100258477 | Kukkonen et al. | Oct 2010 | A1 |
20100258478 | Moran et al. | Oct 2010 | A1 |
20100264068 | Ikebe et al. | Oct 2010 | A1 |
20100276341 | Speirs et al. | Nov 2010 | A1 |
20100276983 | Dunn et al. | Nov 2010 | A1 |
20100282642 | Kan | Nov 2010 | A1 |
20100298173 | Smith et al. | Nov 2010 | A1 |
20100320133 | Page et al. | Dec 2010 | A1 |
20110005750 | Boerseth et al. | Jan 2011 | A1 |
20110011769 | Sutton et al. | Jan 2011 | A1 |
20110061610 | Speirs et al. | Mar 2011 | A1 |
20110062090 | Bara | Mar 2011 | A1 |
20110089013 | Sakurai et al. | Apr 2011 | A1 |
20110100931 | Lake et al. | May 2011 | A1 |
20110127197 | Blackbourn et al. | Jun 2011 | A1 |
20110146164 | Haney et al. | Jun 2011 | A1 |
20110174683 | Cui et al. | Jul 2011 | A1 |
20110219680 | Wilkomirsky Fuica | Sep 2011 | A1 |
20110233115 | Moran et al. | Sep 2011 | A1 |
20110265558 | Feimer et al. | Nov 2011 | A1 |
20110284428 | Adeyinka et al. | Nov 2011 | A1 |
20120000830 | Monaghan et al. | Jan 2012 | A1 |
20120000831 | Moran et al. | Jan 2012 | A1 |
20120029259 | McFarlane et al. | Feb 2012 | A1 |
20120043178 | Kan | Feb 2012 | A1 |
20120074044 | McFarlane | Mar 2012 | A1 |
20120074045 | Stauffer et al. | Mar 2012 | A1 |
20120145604 | Wen | Jun 2012 | A1 |
20120175315 | Revington et al. | Jul 2012 | A1 |
20120217187 | Sharma et al. | Aug 2012 | A1 |
20120288419 | Esmaeili et al. | Nov 2012 | A1 |
20130043165 | Revington et al. | Feb 2013 | A1 |
20130081298 | Bugg et al. | Apr 2013 | A1 |
20130140249 | Sury et al. | Jun 2013 | A1 |
20130168294 | Chakrabarty et al. | Jul 2013 | A1 |
20130313886 | Van Der Merwe et al. | Nov 2013 | A1 |
20130345485 | Duerr et al. | Dec 2013 | A1 |
20140001101 | Van Der Merwe et al. | Jan 2014 | A1 |
20140011147 | Van Der Merwe | Jan 2014 | A1 |
20140048408 | Van Der Merwe et al. | Feb 2014 | A1 |
20140076785 | Penner et al. | Mar 2014 | A1 |
20140083911 | Van Der Merwe et al. | Mar 2014 | A1 |
Number | Date | Country |
---|---|---|
1027501 | Mar 1978 | CA |
1055868 | Jun 1979 | CA |
1059052 | Jul 1979 | CA |
1072474 | Feb 1980 | CA |
1081641 | Jul 1980 | CA |
1165712 | Apr 1984 | CA |
1247550 | Dec 1988 | CA |
1249414 | Jan 1989 | CA |
2075108 | Jan 1994 | CA |
2123076 | Nov 1995 | CA |
2165865 | Jun 1997 | CA |
2174801 | Oct 1997 | CA |
2232929 | Sep 1998 | CA |
2217300 | Mar 1999 | CA |
2272045 | Nov 2000 | CA |
2350001 | Dec 2002 | CA |
2353109 | Jan 2003 | CA |
2387257 | Nov 2003 | CA |
2527058 | Mar 2004 | CA |
2425840 | Oct 2004 | CA |
2454942 | Jul 2005 | CA |
2455011 | Jul 2005 | CA |
2751587 | Jul 2005 | CA |
2751773 | Jul 2005 | CA |
2520943 | Apr 2006 | CA |
2490734 | Jun 2006 | CA |
2502329 | Sep 2006 | CA |
2521248 | Mar 2007 | CA |
2524110 | Apr 2007 | CA |
2526336 | May 2007 | CA |
2567185 | Apr 2008 | CA |
2610122 | May 2008 | CA |
2610124 | May 2008 | CA |
2573633 | Jul 2008 | CA |
2673961 | Jul 2008 | CA |
2582059 | Sep 2008 | CA |
2588043 | Nov 2008 | CA |
2606312 | Apr 2009 | CA |
2610052 | May 2009 | CA |
2616036 | Jun 2009 | CA |
2630392 | Nov 2009 | CA |
2669059 | Dec 2009 | CA |
2638120 | Jan 2010 | CA |
2652355 | Aug 2010 | CA |
2657360 | Sep 2010 | CA |
2678818 | Mar 2011 | CA |
2701317 | Mar 2011 | CA |
2729457 | Jul 2011 | CA |
2733862 | Jul 2011 | CA |
2705055 | Nov 2011 | CA |
2768852 | Nov 2011 | CA |
2748477 | Mar 2012 | CA |
2752558 | Mar 2012 | CA |
2735311 | Sep 2012 | CA |
587798 | May 1947 | GB |
Entry |
---|
Andrews et al. “Great Canadian Oil Sands Experience in Commercial Processing of Athabasca Tar Sands” American Chemical Society San Francisco Meeting Apr. 2-5, 1968, p. F5-F18. |
Mitchell et al. “The solubility of asphaltenes in hydrocarbon solvents” Fuel, 1973, N. 02, vol. 52, p. 149-152. |
Kemp, “Pinch Analysis and Process Integration, A User Guide on Process Integration for the Efficient Use of Energy”, Second edition, Elsevier 2007. |
Svreck et al “Successfully Specify Three-Phase Separators” Chemical Engineering Progress, Sep. 1994, p. 29-40. |
Svreck et al. “Design Two-Phase Separators within the Right Limits” Chemical Engineering Progress, Oct. 1993, p. 53-60. |
Fu et al.“New technique for determination of diffusivities of volatile hydrocarbons in semi-solid bitumen”, Fuel, 1979, vol. 58, August, pp. 557-560. |
Kamoun et al.“High Speed Shadowgraphy Investigations of Superheated Liquid Jet Atomization”, ILASS-Americas 22nd Annual Conference on Liquid Atomization and Spray Systems, Cincinnati Ohio, May 2010. |
Duan et al.'s “Numerical Analyses of Flashing Jet Structure and Droplet Size Characteristics” Journal of Nuclear Science and Technology, 2006, vol. 43, No. 3, p. 285-294. |
Sou et al., “Effects of Cavitation in a Nozzle on liquid Jet atomization” International Journal of Heat and Mass Transfer; vol. 50, p. 3575-3582, 2007. |
Ransom et al., “The relaps choke flow model and application to a large scale flow test”, The American Society of Mechanical Engineers, Heat Transfer Division, 1980, Saratoga, New York. |
Power,“Froth Treatment: Past, Present &Future” Oil Sand Symposium, University of Alberta, May 3-5, 2004. |
Rahmani, “Shear-Induced Growth of Asphaltene Aggregates” Oil Sand Symposium, University of Alberta, May 4, 2004. |
Paul et al. “Handbook of Industrial Mixing: Science and Practice” Wiley Interscience 2004, p. 391-477. |
Blevins “Applied fluid dynamics handbook”, Van Nostrand Reinhold Company 1984, p. 80-83. |
Wu et al., “Experimental study on steam plume and temperature distribution for sonic jet” J. Phys.: Conf.Ser. 147 2009, 012079. |
Yeon et al., “An Experimental Investigation of Direct Condensation of Steam Jet in Subcooled Water” Journal of Korean Nuclear Society vol. 29, No. 1, pp. 45-57, Feb. 1997. |
Long et al., “Structure of water/solids/asphaltenes aggregates and effect of mixing temperature on settling rate in solvent-diluted bitumen” Fuel 2004, vol. 83, p. 823-832. |
Rahimi et al., “Partial Upgrading of Athabasca Bitumen Froth by Asphaltene Removal”, Unitar International Conference on Heavy Crude and Tar Sande, No. 1998.074, p. 1-8. |
Hoehenberger, “Water Treatment, Cycle Chemistry, Boiler Operation and Related Problems/Failures on Steam Generator Systems > 30 bar”, TÜSÜD Industry Services, 2006, p. 1-14. |
Schroyer, “Understand the Basics of Steam Injection Heating”, Chemical Engineering Progress, Hydro-Thermal Corporation, May 1997, p. 1-4. |
Prosonix, “PSX Steam Jet Diffuser . . . Technology That Makes a Difference”, PSX Jet Diffuser 20110209. |
Prosonix, “ProSonix Technical Bulletin”, TB-4 Liquid & Steam Pressure Relationship. |
Prosonix, “PSX Technical Bulletin”, TB-7 Internally Modulated Steam Control 0210. |
Prosonix, “Sparging Efficiency vs. Direct Steam Injection”, TB-6 Sparging Efficiency & Performance 20101210. |
Siemens, “Pictures of the Future”, Spring 2006, Power Plants—Siemens Global Website, http://www.siemens.com/innovation/en/publikationen/publications—pof/pof—spring—2006/infrastructures—articles/power—plants.htm. |
George, “Mining for Oil”, Scientific American, Mar. 1998, p. 84-85. |
Speight, “Deasphalting and Dewaxing Processes”, The Chemistry and Technology of Petroleum, Fourth Edition, Chapter 19, CRC Press 2006. |
Jeribi et al., “Adsorption Kinetics of Asphaltenes at Liquid Interfaces”, Journal of Colloid and Interface Science, vol. 256, Issue 2, Dec. 15, 2002, pp. 268-272. |
Branan, “Pocket Guide to Chemical Engineering” Elsevier Science & Technology Books, Nov. 1999. |
Perry, “Perry's Chemical Engineers' Handbook” (7th Ed.), 1997. |
Clarke et al., “Asphaltenes precipitation from Cold Lake and Athabasca bitumens”, Petroleum Science and Technology, 1998, 16:3-4, p. 287-305. |
Al-Atar, “Effect of Oil Compatibility and Resins/Asphaltenes Ratio on Heat Exchanger Fouling of Mixtures Containing Heavy Oil”, Master Degree Thesis report, The University of British Columbia, Feb. 2000. |
Gearhart, “Rose® process offers energy savings for solvent extraction”, Proceedings from the Fifth Industrial Energy Technology Conference vol. II, Houston, TX, Apr. 17-20, 1983, p. 823-835. |
Clarke et al., “Asphaltene precipitation: detection using heat transfer analysis, and inhibition using chemical additives” Fuel, vol. 76, Issue 7, May 1997, p. 607-614. |
Shell Canada Limited, Application for Approval of the Jackpine Mine—Phase 1, ERCB application No. 1271285, May 2002. |
Imperial Oil Ressources Ventures Limited, Application for the Imperial Oil Resources Ventures Limited (Imperial Oil) and ExxonMobil Canada Properties (ExxonMobil Canada) Kearl Oil Sands Project—Mine Development (Kearl Project), ERCB Application No. 1408771, Jul. 12, 2005. |
Shell Canada Limited, Application for the Approval of Muskeg River Mine Project, ERCB Application No. 970588, Dec. 19, 1997. |
Beckman Coulter, Particle Size and Size Distribution Analysis, Coulter Counter.com, pp. 1-3. |
Outokumpu Technology, Slurry particle size analyzer, PSI 200 TM, 2006, pp. 1-8. |
Johnson, Particle size distribution in clays, Clays and Clay Minerals, pp. 89-91. |
Buckley et al., Solubility of the Least-Soluble Asphaltenes, Asphaltenes, Heavy Oils, and Petroleomics, Springer, 2007, Chapter 16, pp. 401-437. |
Gerson et al., The Relation of Surfactant Properties to the Extraction of Bitumen from Athabasca Tar Sand by a Solvent-Aqueous-Surfactant Process, Chemistry for Energy, American Chemical Society, 1979, Chapter 6, pp. 66-79. |
Nour et al., Characterization and Demulsification of Water-in-crude Oil Emulsions, Journal of Applied Sciences, vol. 7, issue 10, 2007, pp. 1437-1441. |
Malcolmson et al., In-Line Particle Size Measurements for Cement and Other Abrasive Process Environments, for Presentation at the IEEE/PCA 40th Cement Industry Technical Conference, 1998, pp. 1-13. |
International Search Report and Written Opinion for PCT/PCT/CA2012/050247 dated Jul. 10, 2010. |
William L. Luyben, “Heat-Exchanger Bypass Control”, Ind. Eng. Chem. Res. 2011, 50, 965-973. |
Dutta-B, “Principles of Mass Transfer and Separation Processes”, p. 344, 2009. |
Schaschke, Carl. (2014). Dictionary of Chemical Engineering. Oxford University Press. p. 67. Online version available at:http://app.knovel.com/hotlink/toc/id:kpDCE00021/dictionary-chemical-engineering/dictionary-chemical-engineering. |
Imran Ali, “Process Heating by Direct Steam Injection”, Pharmaceutical Guide; Dec. 2010. |
Choung, J. et al., “Effect of Temperature on the Stability of Froth Formed in the Recycle Process Water of Oil Sands Extraction”, The Canadian Journal of Chemical Engineering, vol. 82, Aug. 2004, pp. 801-806. |
Wiwchar, K. et al., “Column flotation in an oilsand application”, Proceedings 36th Annual Meeting of the Canadian Mineral Processors, Ottawa, Ontario, Canada, Jan. 20-22, 2004. |
Cleyle, P. et al., “Column Flotation Testing at Suncor Energy Inc.”, Oilsand 2006 Conference, CD, University of Alberta, Feb. 22-24, 2006. |
Finch, J. et al. “Column Flotation”, 1st ed. Pergamon Press, 1990, pp. 1-7, 75-79, 82-89, 148-149, 152-159. |
Baczek, “Paste Thickening Design Evolving to Higher Capacities and Efficiencies”, International Minimizing Supplement to Paste Tailing Management, Mar. 2007. 16 pages. |
Versteeg et al., “An Introduction to Computational Fluid Dynamics: the Finite Volume Method”, 2nd Edition, Pearson Prentice Hall, First published 1995 and 2nd Edition published 2007, pp. 9, 33-77, 88-97, 78-87, 98-114, 115, 131-133, 156-164, 186-196, 256-264. |
Ferziger et al., “Computational Methods for Fluid Dynamics”, 3rd Edition, Springer, 2002, pp. 142-151, 188-206, 226-245, 265-307, 324-328. |
Hobbs, D.M., “Optimization of a static mixer using dynamical systems techniques”, published 1998, Elsevier Science, Chemical Engineering, vol. 53, No. 18, pp. 3199-3213. |
Godard, et al., “A Review of Suncor Energy's Millennium Extraction Process”, Proceedings 36th Annual Meeting of the Canadian Mineral Processors, pp. 141-152 (2004). |
Mankowski et al., “Syncrude's Low Energy Extraction Process: Commercial Implementation”, Proceedings 31st Annual Meeting of the Canadian Mineral Processors, pp. 154-181 (1999). |
“Choked Flow of Gases”, O'Keefe Controls Co., pp. 38, 16-18 (2000). |
Number | Date | Country | |
---|---|---|---|
20140048450 A1 | Feb 2014 | US |