GB2447941A - A process for treating slop mud - Google Patents
A process for treating slop mud Download PDFInfo
- Publication number
- GB2447941A GB2447941A GB0706007A GB0706007A GB2447941A GB 2447941 A GB2447941 A GB 2447941A GB 0706007 A GB0706007 A GB 0706007A GB 0706007 A GB0706007 A GB 0706007A GB 2447941 A GB2447941 A GB 2447941A
- Authority
- GB
- United Kingdom
- Prior art keywords
- continuous phase
- water
- mud
- oil
- slop
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 54
- 230000008569 process Effects 0.000 title claims abstract description 52
- 241000446313 Lamella Species 0.000 claims abstract description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 44
- 238000005553 drilling Methods 0.000 claims abstract description 28
- 239000012530 fluid Substances 0.000 claims abstract description 27
- 238000002156 mixing Methods 0.000 claims abstract description 17
- 230000005484 gravity Effects 0.000 claims abstract description 12
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims description 22
- 239000013530 defoamer Substances 0.000 claims description 10
- 229930195733 hydrocarbon Natural products 0.000 claims description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims description 10
- ULDAPNVYSDTSFM-VDWCLKJHSA-N (2r,3s,4s,5r)-2-(hydroxymethyl)-6-undecoxyoxane-3,4,5-triol Chemical compound CCCCCCCCCCCOC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O ULDAPNVYSDTSFM-VDWCLKJHSA-N 0.000 claims description 9
- -1 1,3 dimethylbutyl Chemical group 0.000 claims description 9
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 230000003068 static effect Effects 0.000 abstract description 5
- 239000012071 phase Substances 0.000 description 85
- 238000012360 testing method Methods 0.000 description 24
- 238000000926 separation method Methods 0.000 description 22
- 239000003921 oil Substances 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 10
- 238000005191 phase separation Methods 0.000 description 8
- 239000002699 waste material Substances 0.000 description 7
- 238000010923 batch production Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 239000008394 flocculating agent Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 230000033228 biological regulation Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000013505 freshwater Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 239000001164 aluminium sulphate Substances 0.000 description 2
- 235000011128 aluminium sulphate Nutrition 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- 238000009300 dissolved air flotation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000008398 formation water Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B21/00—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor
- E21B21/06—Arrangements for treating drilling fluids outside the borehole
- E21B21/062—Arrangements for treating drilling fluids outside the borehole by mixing components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/04—Breaking emulsions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/0208—Separation of non-miscible liquids by sedimentation
- B01D17/0211—Separation of non-miscible liquids by sedimentation with baffles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/0208—Separation of non-miscible liquids by sedimentation
- B01D17/0214—Separation of non-miscible liquids by sedimentation with removal of one of the phases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/04—Breaking emulsions
- B01D17/047—Breaking emulsions with separation aids
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B21/00—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor
- E21B21/06—Arrangements for treating drilling fluids outside the borehole
- E21B21/063—Arrangements for treating drilling fluids outside the borehole by separating components
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/34—Arrangements for separating materials produced by the well
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/10—Nature of the water, waste water, sewage or sludge to be treated from quarries or from mining activities
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Geology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Thermal Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Environmental & Geological Engineering (AREA)
- Mechanical Engineering (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
A process for treating slop mud comprises the steps of: mixing a demulsifier into a flow of slop mud, flowing the mixed slop mud and demulsifier into a flow channel in which the slop mud gravity stratifies into a flow of a water-continuous phase and a flow of an oil-continuous phase, and removing the water-continuous phase from the stratified slop mud. Preferably movement of the slop mud may be sufficient to cause mixing 31 or the mixing step may be carried out with a static shear mixer. The process may include a further step of heating the slop mud before it flows into the flow channel which preferably is an inclined conduit 41. Advantageously the process allows for a faster and more efficient means for separating excess water from slop mud and allows for re-use as a drilling fluid. A separate invention for a lamella separator 4 is also disclosed.
Description
PROCESS FOR SEPARATION OF WATER FROM SLOP MUD
Field of the Invention
The present invention relates to the separation of slop mud into an oil-continuous phase and a water-continuous phase.
Background of the Invention
As a result of rigorous environmental regulations shifting towards zero-discharge, drilling wastes are the focus of attention in the oil and gas exploration industry. Drilling with oil-based mud (OBM) or synthetic-based mud (SBM) generates waste streams often referred to as "slop mud" or "slop water". Slop mud is produced when an oil/synthetic/diesel-based drilling fluid becomes contaminated with water. Slop muds may be generated during the drilling process itself if significant quantities of formation water invade the drilling fluid. Alternatively these waste streams may be by-products of cleaning the drill floor, shaker room, pump room and other areas where spillage and interfaces during displacement occur. Contamination can also take place during boat cleaning operations, pit cleaning and other similar operations.
Oil-based drilling fluids are generally used in the form of invert emulsion muds, consisting of an oleaginous phase, a non-oleaginous phase and finely divided particles. Also typically included are emulsifiers and emulsifier systems, weighting agents, fluid loss additives, viscosity regulators and the like, for stabilizing the system as a whole and for establishing the desired performance properties. Typically, the oil-water ratio (OWR) of a drilling fluid may be in the range 60/40 to 90/10.
After contamination, the slop mud may contain 50% to 90% loosely emulsified water and 10% to 50% non-aqueous drilling fluid. The lowering of the oil-water ratio (OWR) increases viscosity, decreases emulsion stability and ultimately renders the fluid unusable as a drilling fluid. However, hydrocarbon contamination renders the slop mud ineligible for, e.g. discharge at sea. Thus the slop mud is typically sent for disposal or reconditioning. For operators, these volumes add up to high disposal expenses and represent a potentially serious environmental issue.
In addition to good fluid design and solids-control equipment to help reduce the amount of waste generated, separation processes exist to treat slop mud waste streams. These function by breaking the weakly emulsified water phase and recovering the OBM/SBM so that mud can be reused without substantial reconditioning. At the same time, the amount of waste generated can be reduced. The primary goal of this form of slop separation is to break only the weakly emulsified water phase and recover the oil/synthetic/diesel-based drilling fluid.
Batch processes have been developed for separating water from slop mud, for example as described in US 2004/0094483 Al and US 2006/0186056 Al.
In a batch process, siop mud is pumped into large stirred treatment tanks to which demulsifying chemicals are added which cause the water droplets to coalesce. The mixing of the demulsifier with the slop mud is inefficient in batch processes due to the volume ratio or "dead spaces" which remain unstirred. Once sufficiently mixed, the stirring is stopped and the slop mud is allowed to separate under gravity.
Typically, a water-continuous layer floats to the-surface; the oil-continuous layer is denser than water because it contains a significant quantity of dispersed, dense particulate solids that remain oil-wet. Water droplets that have coalesced may have to travel distances of the order of a metre through the relatively viscous oil-continuous layer in order to reach the interface between the two layers. Consequently, the separation process can last several hours and batches are often left to separate overnight. In addition to the time required to mix in the demulsifier and to allow the layers to separate, a significant proportion of the process time is taken up by the filling and emptying of the tanks themselves.
In order to reduce the time taken for the separation to occur, high doses of demulsifying chemicals may be used. Typically, the demulsifier treatment concentration ranges from 1 to 4% by volume.
Once separation has occurred, the separated constituents (drilling fluid and water) are transferred to separate holding/treatment vessels.
Continuous processes based on centrifuge technology exist for treating an aqueous phase polluted by oil, chemicals and particles in emulsified form, for example slop oil, bilge water and drain water. However, centrifuging results in either two-phase separation of the solids from the liquid phase (oil and water) or three-phase separation of the solids, oils and water. Centrifuging is therefore not adapted to the separation of slop mud, by which it is intended to recover an oil-based or synthetic-based drilling mud which is an oil-continuous phase containing emulsified water and a significant proportion of finely divided particles.
Summary of the Invention
Faster and more efficient processes for separating excess water from slop mud, to facilitate the recovery and re-use of the drilling fluid and the safe discharge or re-use of the water, would be desirable.
In a first aspect, the present invention provides a process for treating siop mud, comprising the steps of: mixing a demulsifier into a flow of said slop mud, flowing the mixed slop mud and demulsifier into a flow channel in which the slop mud gravity stratifies into a flow of a water-continuous phase and a flow of an oil-continuous phase, and removing the water-continuous phase from the stratified slop mud.
By maintaining flows of the stratified water-continuous and oil-continuous phases in the flow channel, the process can avoid the long separation times of conventional batch processes. In particular, long travel distances for water droplets through the mud can be avoided.
Typically, the oil-continuous phase is denser than the water-continuous phase. For example, the oil-continuous phase may contain substantially all of the solids content (such as weighting agent) of the siop mud. Thus, the drilling mud can be recovered from the slop mud using this process. This provides an advantage over centrifuge methods of treating waste streams, which separate the solids from the liquid phase(s) Preferably, the mixed slop mud and demulsifier flow into the flow channel in a continuous stream. This can reduce the space required for storing the slop mud prior to treatment.
Preferably, the water-continuous phase and/or the oil-continuous phase are removed in a continuous stream. An advantage of treating slop mud in a continuous process rather than in a batch process is that the apparatus required can be compact, as large settling tanks are not needed. This is particularly advantageous in off-shore applications.
Preferably, the process may include the further step of heating the slop mud before it flows into the flow channel.
An advantage of heating the slop mud is that the rate of separation of the oil-continuous phase and the water-continuous phase may be increased by reducing the viscosity of the fluids. This increases the overall rate at which slop mud can be treated, and may reduce the concentration of demulsifier required. Reducing the concentration of demulsifier lowers the concentration of contaminants in the recovered water and eases the downstream polishing of the water to meet discharge criteria.
The process may include the further step of mixing a defoamer into the slop mud before the siop mud stratifies. The defoamer may reduce foaming of the separated water-continuous phase caused by, for example, the demulsifier.
Preferably, the flow channel is inclined. In this way, the flows of the water-continuous and oil-continuous phases in the channel can be maintained by gravity. Advantageously, the flow channel is adapted to maintain laminar and stratified flows of the water-continuous and the oil-continuous phases and thereby prevent the separated phases from remixing. Thus, preferably the channel is adapted to maintain a Reynolds number of 2000 or less in the flows of both the water-continuous and oil-continuous phases. Furthermore, the channel may be adapted to maintain a Froude number of 1 or less in the flows of both the water-continuous and oil-continuous layers.
The process may include the further step of holding the stratified slop mud in a holding vessel, the water continuous phase and the oil-continuous phase being removed from the holding vessel in two separate flow streams. Preferably, the position of the interface between the oil-continuous phase and the water-continuous phase in the holding vessel is controlled by controlling the rate of flow of one or both of the separate flow streams. The holding vessel may have a sloped side down which the stratified slop mud flows into the vessel. This reduces remixing of the stratified phases.
The mixed slop mud and demulsifier may be flowed through a plurality of flow channels. For example, the plurality of flow channels may be formed by the plates of a lamella separator. Such a separator may also function as a holding vessel for the separated phases. The holding vessel may include a level sensor to determine the position of the interface between the oil-continuous phase and the water-continuous phase.
The demulsifier may contain, for example, an alkyl ethoxylate, alkyl glucoside, branched alkyl suiphosucciriate, octyl or decyl polyglucoside, alkane suiphonate or alkane sulphate.
Preferably, the demulsifier contains sodium di(l,3 dimethylbutyl) suiphosuccinate, 2-ethyl hexanol ethoxylate, octyl monoglucoside, or undecyl glucoside. More preferably, undecyl glucoside is used, because this demulsifier has been found to reduce the separation time of the slop mud.
The process may include the further step of reconditioning the oil-continuous phase to produce an oil-based mud or synthetic-based mud suitable for reuse as a drilling fluid. The step of reconditioning the oil-continuous phase may include adding an emulsifying agent and/or further OBM or SBM to the oil-continuous phase.
The water-continuous phase may be removed to a holding tank.
The process may comprise the further step of treating the water-continuous phase to remove residual hydrocarbons and/or solids from the water-continuous phase. The further step of treating the water-continuous phase may include adding a defoamer to the water-continuous phase. The further step of treating the water-continuous phase may include centrifuging and/or filtering the water-continuous phase to remove residual hydrocarbons and/or solids. The further step of treating the water-continuous phase may include, for example, the addition of de-oiling polymer, coagulant or flocculant, pH control, and/or dissolved air flotation. Suitable flocculant includes inorganic flocculant based on bentonite, aluminium sulphate and/or calcium hydroxide, organic flocculant based on a cationic polymer (e.g. polyacrylamide), a deoiling polymer based on e.g. polyaluminium hydroxychioride, or a combination of any one or more of the above. The water-continuous phase may be heated before the further step of treating the water-continuous phase (e.g. by centrifuging), preferably to a temperature between 40 C and 50 C.
A further aspect of the invention provides an apparatus for treating slop mud, comprising: supplies of a slop mud and a demulsifier, a mixer operatively connected to the supplies for mixing the slop mud and demulsifier, a lamella separator arranged to receive the mixed slop mud and demulsifier, an outlet (e.g. overflow) from the lamella separator for a water-continuous phase separated from the mixed slop mud and demulsifier, and an outlet (e.g. underfiow) from the lamella separator for an oil-continuous phase separated from the mixed slop mud and demulsifier. Preferably, the apparatus further comprises a reconditioning unit for reconditioning the oil- continuous phase to produce an oil-based mud or synthetic-based mud suitable for reuse as a drilling fluid. Preferably, the apparatus further comprises a treatment unit for treating the water-continuous phase to remove residual hydrocarbons and/or solids from the water-continuous phase.
A further aspect of the invention is the use of a lamella separator to separate a mixture of slop mud and a demulsifier into a denser oil-continuous phase and a less-dense water-continuous phase.
Brief Description of the Drawings
Embodiments of the invention will now be described by way of example with reference to the accompanying drawings in which: Figure 1 shows a schematic representation of a process according to a first implementation; and Figure 2 shows a schematic representation of a process according to a second implementation.
Detailed Description
A first implementation of the invention will be described with reference to Figure 1. The slop mud enters the system through an inlet 11. The slop mud may be pumped into the system, or it may flow under gravity alone. It then passes through an in-line mixer 31, in which it is mixed with a quantity of demulsifier. The mixer may be a simple static mixer (e.g. a static shear mixer manufactured by Komax or Westfall), or it may be a dynamic one. Alternatively, the action of e.g. a centrifugal pump used to move the slop may be sufficient to mix the demulsifier and slop mud.
In Figure 1, the demulsifier is introduced into the slop mud flow through an inlet 21 prior to entering the mixer 31.
Alternatively, the demulsifier may be introduced directly into the mixer.
As a result of the action of the demulsifier, the fluid exiting the mixer will begin to separate. The mixed slop mud and demulsifier flow along an inclined conduit 41, during which the slop mud stratifies due to gravity. The denser oil-continuous phase, which contains substantially all of the solids content of the slop mud, settles towards the bottom of the conduit 41. The less dense, water-continuous phase floats to the surface.
The demulsified slop mud separates rapidly into layers provided that the distance travelled by coalesced water droplets to the interface between the layers is kept relatively small. Therefore the depth of the channel or the diameter of the pipe is preferably not too large, in order to minimise the distance that coalesced drops need to travel in order to reach the water-continuous layer. The length of conduit 41 is preferably sufficient to ensure good separation of the phases.
The conduit 41 may be inclined gently downwards in order to facilitate the flow by gravity. The shear forces between the channel and the flowing slop mud facilitate the separation of the oil-continuous and water-continuous phases by causing gentle mixing. The velocity of the flow must be low enough to allow coalesced droplets to migrate out of the oil-continuous layer and into the water-continuous layer without substantial remixing of the layers. Thus, in each layer, the Reynolds number of the flow is preferably less than 2000 and the Froude number is preferably less than 1 to maintain laminar and stratified flow. These dimensionless numbers are defined as follows: Reynolds number = pv1/ Froude number (v2/gl)112 with p=fluid density, v=fluid velocity, q=fluid viscosity, l=layer thickness and g=acceleration due to gravity.
In Figure 1, the stratified flow exits the conduit 41 into a holding vessel 42. To maintain a clean separation of the flowing layers, one side of this vessel is sloped; the layers flow down this slope into the vessel preventing substantial rernixing. Exit ports 44, 45 are located near the bottom and top of the vessel respectively. Alternatively, a plurality of exit ports may be provided at various heights. Asuitable sensor 43 for detecting the interface between the two fluids is located in the vessel, which may be, for example, a simple float device, conductivity probe or guided wave radar probe.
A control loop maintains the position of this interface in the centre of the vessel by adjusting the flow rates of each layer out of the exit ports.
The outflow 51 of the oil-continuous layer contains substantially all of the solids content of the slop mud and can have an oil-water ratio (OWR) suitable for reuse as a drilling fluid. The oil-continuous phase may therefore be sent directly for re-use as a drilling fluid, or for suitable re-conditioning if necessary. For example, emulsifiers or fresh drilling mud may be added to the recovered oil-continuous phase to reduce the demulsifier concentration and thereby improve the stability of the emulsion.
The water-continuous layer may contain residual hydrocarbons, solids or other contaminants which must be either removed or reduced to acceptably low concentrations for discharge. These remaining contaminants are generally such small droplets or particles that gravity is not sufficiently strong to remove them. Therefore, the outflow 61 from the water-continuous layer may be sent for further treatment in order that the water meets the regulation standards for discharge. The outflow 61 may be fed or pumped into a holding tank ready for further treatment. Further treatment of the water-continuous phase may include, for example, centrifuging (in e.g. a disk stack centrifuge), the addition of de-olling polymers, coagulants or flocculants, pH control, dissolved air flotation, or filtration. Suitable flocculants include inorganic flocculants based on bentonite, aluminium sulphate and calcium hydroxide, organic flocculants based on low and high molecular weight cationic polymers (e.g. polyacrylamide), or deoiling polymers based on polyaluminium hydroxychloride, or combinations of the above. The water-continuous layer may be heated, e.g. before centrifuging, to aid separation by reducing viscosity. A temperature of about 45 C is preferred, to prevent scaling.
The process can separate slop mud emulsions using simple demulsifiers such as alkyl ethoxylates, alkyl glucosides and branched alkyl sulfosuccinates. Preferred demulsifying surfactants include sodium di(l,3 dimethylbutyl) suiphosuccinate, 2-ethyl hexanol ethoxylate, octyl rnonoglucoside, and undecyl glucoside. More preferably, the demulsifier is undecyl glucoside. However, this list of demulsifiers is not exhaustive and other suitable demulsifiers may also be used, for example combinations with alkyl polyglycosides (e.g. octyl and decyl polyglucosides), alkane sulphonates and alkane sulfates. An important factor in determining the choice of demulsifier is the rate of separation of the oil-continuous and water-continuous phases.
In order to operate the process continuously, it is preferable that the demulsifier rapidly separates the oil-continuous and water-continuous phases. Preferably, the demulsifier is oil-insoluble to reduce the carry-over of demulsifier into the recovered oil-continuous phase. Of the chemicals listed above, all are oil-insoluble except for 2-ethyl hexanol ethoxylate, which is dispersible in oil.
The inventors have discovered that, provided that vigorous mixing conditions are used, addition of a suitable demulsifying surfactant causes rapid destabilisation of the slop mud emulsion and coalescence of the water droplets within it. Such mixing conditions may lead to the continual break-up and reformation of droplets, but they do not cause re-emulsification. Thus the need for gentle mixing conditions is eliminated and a high-energy mixer can be used.
When using undecyl glucoside (Simulsol SL11WTM, obtained from Seppic), the inventors found that the rate of separation of the oil-continuous and water-continuous phases increases with temperature. Therefore, it is preferable to heat the slop mud before mixing with the demulsifier. The demulsifier may also be heated. It may be necessary to increase the proportion of demulsifier added to the slop mud, inversely with temperature, in order to obtain a satisfactory phase separation at relatively low temperatures.
Some demulsifiers, for example undecyl glucoside, cause the separated water-continuous phase to froth. A defoarner may be introduced to the slop mud before it flows into the conduit 41, or before it is mixed with the demulsifier, to reduce this effect. Alternatively, a defoamer may be added to the water-continuous phase after removal from the holding vessel 42, to reduce its frothiness before e.g. centrifuging. Suitable defoamers include silicon-based defoamers (e.g. Defoam X EHTM from I4-I SWACO, which is an aqueous emulsion of diethylpolysiloxane) and fatty-acid-based defoamers (e.g. Defomex 1O8NTM from Lamberti) A second implementation of the invention will be described with reference to Figure 2. The slop mud enters the system through an inlet 1. The slop mud may be pumped into the system, or it may flow under gravity alone. It then passes through an inline mixer 3, in which it is mixed with a quantity of demulsifier. Alternatively, the demulsifier may be introduced into the slop mud before it enters the mixer.
The demulsifier may be introduced into the slop mud from a demulsifier dosing system 2. As in the first implementation, various types of mixer may be used.
Preferred demulsifiers have been discussed above with respect to the first implementation.
The mixed slop mud and demulsifier then flow into a lamella separator 4. Lamella separators are commercially available (e.g. Pan America Environmental slant plate clarifier systems, or Leiblein GmbH lamella separators) and comprise a stack of plates inclined at an angle. Typically this angle ranges from 450 to 600 to the horizontal. The spacing between the plates is typically 50 to 75 mm (2 to 3 inches) . The spaces between the plates provide a plurality of inclined flow channels, which greatly increase the separation rate compared to a single flow channel. In some lamella separator arrangements, the influent is fed into the lamella separator so that it enters each inclined channel at the bottom of each channel. A disadvantage of such arrangements, however, is that the influent meets a counterfiow of emerging oil-continuous phase at the bottom of the channel. In other lamella separator arrangements, however, the influent enters each inclined channel a distance above the bottom the channel. For example, the influent may enter each channel a distance from the bottom of the channel which is equal to about 1/3 of the overall length of the channel.
As the slop mud emulsion separates, the denser oil-continuous phase, including substantially all the solids content of the drilling fluid, settles towards the lower plate of each channel and then flows down to the base of the separator. The less dense, water-continuous layer moves in the opposite direction, beneath the ceiling of each channel towards the top of the separator. Preferably, the flow rate into the lamella separator is such that the flow is laminar and the stratified layers do not remix in the flow channels. Preferably, for both the water-continuous and the oil-continuous phases, the Reynolds number is 2000 or less and the Froude number is 1 or less. The demulsified slop mud separates rapidly into oil-continuous and water-continuous layers because the distance travelled by coalesced water droplets to the interface between the layers within each flow channel is relatively small.
The underfiow 5 of the lamella separator 4 is the oil-continuous phase, which can be removed from an outlet at the bottom of the separator. A pump may be used to remove the underfiow. The overflow 6 of the lamella separator 4 is the water-continuous phase, which can be removed from the top of the separator. The lamella separator 4 may include a level sensor to determine the position of the interface between the oil-continuous phase and the water-continuous phase. The position of the interface can then be controlled by controlling the rates of removal of the overflow and/or the underfiow of the lamella separator.
The recovered oil-continuous phase contains substantially all of the solids content of the slop mud and can have an oil-water ratio (OWR) suitable for reuse as a drilling fluid. It may be reconditioned if necessary, as discussed above with respect to the first implementation.
In Figure 2, the overflow 6 is fed or pumped into a holding tank 7 ready for further treatment. As explained above, the water-continuous phase may contain residual hydrocarbons, solids or other contaminants and may therefore require further treatment to meet the regulation standards for discharge.
This further treatment may include centrifuging the water-continuous phase in a disk-stack centrifuge 8, resulting in three-phase separation of the water, oil and solids, which can each be removed from separate outlets. The water-continuous layer may be heated before centrifuging in the disk stack, to aid separation by reducing viscosity. A temperature of about 45 C is preferred, to prevent scaling.
As also discussed above, it may be desirable to introduce a defoamer, either to the slop mud flow or to the separated water- continuous phase, to reduce frothing.
An advantage of the process is that it may be operated continuously and separation times reduced. This means that the apparatus required for the process can be relatively compact. The efficiency of the process is increased by using, for example, in-line mixers, suitable demulsifiers to obtain a high slop mud separation rate, and a lamella separator with its high separation surface area. In contrast, existing batch methods require the slop mud to settle in tanks for some hours.
Examples:
Tests were performed using an apparatus as shown in Figure 2.
Table 1 shows the results of Tests 1 to 4 which are described below.
For each test described below, the demulsifier used was undecyl glucoside (Simulsol SL11WTM from Seppic) A slop mud was prepared in a slop mud preparation tank by mixing 50% volume of M-I VERSAVERTTM oil-based drilling mud (the base mud) and 50% volume of fresh water. A shear mixer was used to prepare the slop so as to achieve a stable and homogeneous emulsion. The siop was continually agitated using submersed agitators and thoroughly mixed each day to ensure phase separation did not take place in the preparation tank.
Chemical and physical tests (to API standards) were carried out on the base mud and the slop mud and the slop mud temperature was monitored throughout the trial.
The slop mud was next fed into the system of Figure 2 using a Moyno pump. The demulsifier was injected into the slop feed stream downstream of the Moyno pump through a 2" Westfall static shear mixer. The demulsifier dosing system consisted of a gear pump. Two further 2" Komax static shear mixers were used in-line to achieve the mixing energy required for homogeneous dispersion of the demulsifier into the siop mud, although these extra mixers may not be required.
The mixed slop mud and demulsifier were fed into a lamella separator (a "10m3/hr" model from Tipp timwelt) . A Moyno pump was used to remove the underfiow (oil-continuous layer) from the lamella separator prevent build up of the recovered drilling fluid phase in the lamellas and to prevent short-circuiting of the feed.
A flow meter was used to measure the feed flow rate of the slop mud and demulsifier mix. The temperature of the slop mud, the surfactant dosage and the flow rates of the underfiow and overflow from the lamella separator were recorded.
Test 1 The demulsifier was added to the slop mud at a concentration of 1% vol. The slop mud and demulsifier mix was fed to the lamella separator at a flow rate of 5 m3/hr and at a temperature of 37 C. The recovered mud was pumped out from time to time as the underfiow of the lamella separator.
The base mud was prepared with an OWR of 73/27. After addition of the fresh water to the base mud in a 50/50 ratio, the OWR of the resulting slop mud was reduced to 37/63. The recovered mud from the lamella underfiow was found to have an OWR of 75/25 which is comparable to the OWR of the base mud.
Similarly, the specific gravity (SG), plastic viscosity (PV) and yield point (YP) of the recovered mud were comparable to the base mud properties. The electrical stability (ES) of the recovered mud decreased to 180V from the base mud ES of BOOV. This is because some demulsifier is carried over into the
oil-continuous phase and tends to lower the stability of the emulsion. Although the demulsifiers used are preferably oil-insoluble, the oil-continuous phase contains some water, and therefore some demulsifier since the demulsifier will generally distribute throughout all the water present in the slop mud. It is also possible that oil-soluble emulsifiers present in the original drilling mud cause movement of the demulsifier from the water-continuous phase to the oil-continuous phase. Emulsifiers or fresh mud can be added to the recovered mud to reduce the dernulsifier concentration and increase the emulsion stability.
The overflow from the lamella separator was analysed using a hot spin centrifuge and found to be >99% water, with trace amounts of oil and solids.
Test 2 The properties of the base mud and slop mud used in Test 2 were the same as in Test 1. The demulsifier was added to the slop mud at a concentration of 1% vol. The slop mud and dernulsifier mix was fed to the lamella separator at a flow rate of 10 m3/hr and at a temperature of 37 C.
The underfiow of the lamella separator was pumped out continuously at a rate of approximately 4.5m3/hr. This rate is is close to that predicted for continuous operation if the process yields 90% water recovery from a slop mud comprising a 50/50 mix of mud and fresh water.
The properties of the recovered mud from the lamella separator underfiow were acceptably close to those of the base mud. The OWR of the recovered mud was identical to that of the base mud. Again, the ES of the recovered mud decreased from the base mud ES of 800V, to 240V.
The overflow from the lamella separator was analysed using a hot spin centrifuge and found to be >99% water, with trace amounts of oil and solids.
This test demonstrates that the process according to the second implementation of the invention can continuously separate slop mud into an oil-continuous phase and a water- continuous phase at a rate of at least 10 m3/hr. The oil-continuous phase has properties very close to those required for reuse as a drilling mud, and therefore requires very little further conditioning.
Test 3 The properties of the base mud and slop mud used in Test 3 were the same as in Test 1. The slop mud and demulsifier mix was fed to the lamella separator at a flow rate of lOrn3/hr and at a lower temperature of 21 C to investigate the effect of slop mud temperature on the process.
In Test 2, with 1% demulsifier (by volume) at 37 C and a feed flow rate of 10 m3/hr, phase separation of the slop mud was observed to occur as the slop entered the feed chamber of the lamella separator. However, on reducing the temperature to 21 C, a decrease in the phase separation was observed. The demulsifier dose was therefore increased to 1.3% vol. to obtain phase separation as the slop entered the feed chamber.
The underfiow of the lamella separator was pumped out continuously at a rate of approximately 7.2m3/hr.
The properties of the recovered mud (the lamella separator underfiow) were found to be close to those of the base mud and acceptable. The OWR of the recovered mud was 71/29.
Test 4 The properties of the base mud and slop mud used in Test 4 were the same as in Test 1. The demulsifier was added to the slop mud at a lower concentration of 0.5% vol. The slop mud and demulsifier mix was fed to the lamella separator at a flow rate of 10 m3/hr and at a temperature of 37 C.
The underflow of the lamella separator was pumped out continuously at a rate of approximately 4.5m3/hr.
The OWR of the recovered mud was 56/44, which was substantially higher than that of the slop mud, 37/63.
However, this value was lower than that of the original base mud 73/27.
The overflow from the lamelia separator was analysed using a hot spin centrifuge and found to contain 92% water, with 5% oil and 3% solids.
These results show that the conditions of Test 4 are not optimum, although a useful quantity of water was removed from the siop mud.
Further Treatment of the Water-Continuous Phase A further test was carried out using a slop mud feed rate of 10m3/hr, demulsifier Simulsol SL11W1TM at 1.3% concentration by volume, and pumping out the underflow from the lamella separator at 5-6m3/hr. Once the process was optimised and steady state conditions were achieved for 30 minutes, the overflow stream from the lamella separator was collected in the holding tank ready for processing it through a disk stack centrifuge. The presence of the undecyl glucoside demulsifier caused significant foaming of water-continuous phase. The defoamer Defoarn X EH (an aqueous solution of diethyl polysiloxane) was therefore added before disk stack operation.
Tests of the disk stack centrifuge were carried out using a feed flow rate from the holding tank of 0.5 m3/hr and 3 m3/hr.
Water samples taken upstream and downstream of the disk stack during the operation were analysed.
The overflow stream of the lamella separator (i.e. upstream of the disk stack) had a total petroleum hydrocarbons (TPH) value of 53 mg/i. The addition of the defoamer at a concentration of 167 ppm increased this value further, to within the range 190-255 mg/i. The disk stack treatment resulted in a steady 68%-77% reduction of the TPH value, and the water recovered downstream of the disk stack had a TPH value of 17 mg/i and 51-79 mg/i, with and without defoamer addition respectively.
The water recovered from the disk stack can be further treated, for example, by filtration, to meet the discharge criteria of <15 mg/i TPH.
Test 1 Test 2 Test 3 Test 4 -o -o 0 0 o o o I41 4-4 4-4 4-1 U 1-1 4-I 4-4 9-1 U) 0 U U (1) 41) c 0 0 0 0 rate (m3/hr) 5 5 10 10 10 10 10 10 % vol. 1 1 1 1 1.3 1.3 0.5 0.5 demulsifier Slop mud 37 C 37 C 37 C 37 C 21 C 21 C 37 C 37 C temperature Underfiow On-off On-off 4.5 4.5 7.2 7.2 4.5 4.5 pump-out rate pump pump SG 1.25 1.12 1.23 1.2 1.22 1.17 PV 49 98 31 30 32 37 YP 18 76 16 12 15 17 Solids % v/v 16 10 Trace 15 Trace 15 15 3 14 Oil % v/v 61 33 Trace 64 Trace 62 60 5 48 Water % v/v 23 57 >99 21 >99 23 25 92 38 OWR 73/27 37/63 75/25 73/27 71/29 56/44 ES 800 160 n/a 180 n/a 240 260 n/a 140 Table 1: Test results While the invention has been described in conjunction with the exemplary embodiments described above, many equivalent modifications and variations will be apparent to those skilled in the art when given this disclosure. Accordingly, the exemplary embodiments of the invention set forth above are considered to be illustrative and not limiting. Various changes to the described embodiments may be made without departing from the spirit and scope of the invention.
All the references cited herein are incorporated by reference in their entirety.
Claims (30)
1. A process for treating slop mud, comprising the steps of: mixing a demulsifier into a flow of said slop mud, flowing the mixed slop mud and demulsifier into a flow channel in which the slop mud gravity stratifies into a flow of a water-continuous phase and a flow of an oil-continuous phase, and removing the water-continuous phase from the stratified slop mud.
2. The process according to claim 1, wherein the oil-continuous phase is denser than the water-continuous phase.
3. The process according to any one of claims 1 to 2, wherein the mixed slop mud and demulsifier flow into the flow channel in a continuous stream.
4. The process according to any one of claims 1 to 3, wherein the water-continuous phase and/or the oil-continuous phase is removed from the stratified slop mud in a continuous stream.
5. The process according to any one of claims 1 to 4, including a further step of heating the slop mud before it flows into the flow channel.
6. The process according to any one of claims 1 to 5, wherein the flow channel is inclined.
7 The process according to any one of claims 1 to 6, wherein the flow channel is adapted to maintain laminar and stratified flows of the water-continuous phase and the oil-continuous phase.
8. The process according to claim 7, wherein the channel is adapted to maintain a Reynolds number of 2000 or less in the flow of the water-continuous phase and the flow of the oil-continuous phase.
9. The process according to claim 7, wherein the channel is adapted to maintain a F'roude number of 1 or less in the flow of the water-continuous phase and the flow of the oil-continuous phase.
10. The process according to any one of claims 1 to 9, comprising the further step of: holding the stratified slop mud in a holding vessel, the water continuous phase and the oil-continuous phase being removed from the holding vessel in separate flow streams.
11. The process according to claim 10, in which the position of the interface between the oil-continuous phase and the water-continuous phase in the holding vessel is controlled by controlling the rate of flow of one or both of the separate flow streams.
12. The process according to claim 10 or claim 11, wherein the holding vessel has a sloped side down which the stratified slop mud flows into the vessel.
13. The process according to any one of claims 1 to 12, wherein the mixed slop mud and demulsifier are flowed though a plurality of flow channels.
14. The process according to claim 13, wherein the plurality of flow channels is formed by the plates of a lamella separator.
15. The process according to claim 14, wherein the plates of the lamella separator are inclined at an angle of between 45 and 60 to the horizontal.
16. The process according to any one of claims ito 15, in which the demulsifier contains sodium di(1,3 dimethylbutyl) suiphosuccinate, 2-ethyl hexanol ethoxylate, octyl monoglucoside, undecyl glucoside.
17. The process according to any one of claims 1 to 16, comprising the further step of reconditioning the oil-continuous phase to produce an oil-based mud (OBM) or synthetic-based mud (SBM) suitable for reuse as a drilling fluid.
18. The process according to claim 17, wherein the step of reconditioning of the oil-continuous phase includes adding an emulsifying agent and/or further OBM or SBM to the oil-continuous phase.
19. The process according to any one of claims 1 to 18, wherein the water-continuous phase is removed to a holding tank.
20. The process according to any one of claims 1 to 19, comprising the further step of treating the water-continuous phase after removal from the stratified slop mud to remove residual hydrocarbons and/or solids from the water-continuous phase.
21. The process according to claim 20, in which the further step of treating the water-continuous phase includes centrifuging and/or filtering the water-continuous phase to remove residual hydrocarbons and/or solids.
22. The process according to claim 20, in which the water-continuous phase is heated before the further step of treating the water-continuous phase.
23. The process according to claim 22, in which the water-continuous phase is heated to a temperature between 40 C and 50 C.
24. The process according to any one of claims 1 to 23, including the further step of mixing a defoamer into the slop mud before the mud stratifies.
25. The process according to any one of claims 20-23, in which the further step of treating the water-continuous phase includes adding a defoamer to the water-continuous phase.
26. An apparatus for treating slop mud, comprising: supplies of a slop mud and a demulsifier, a mixer operatively connected to the supplies for mixing the siop mud and dernulsifier, a lamella separator arranged to receive the mixed slop mud and demulsifier, an outlet from the lamella separator for a water-continuous phase separated from the mixed slop mud and demulsifier, and an outlet from the lamella separator for an oil-continuous phase separated from the mixed slop mud and demulsifier.
27. The apparatus of claim 26, further comprising a reconditioning unit for reconditioning the oil-continuous phase to produce an oil-based mud or synthetic-based mud suitable for reuse as a drilling fluid.
28. The apparatus of claim 26 or claim 27, further comprising a treatment unit for treating the water-continuous phase to remove residual hydrocarbons and/or solids from the water-continuous phase.
29. The use of a lamella separator to separate a mixture of a slop mud and a demulsifier into a denser oil-continuous phase and a less-dense water-continuous phase.
30. An apparatus as any one herein described with reference to and as shown in the accompanying drawings.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0706007A GB2447941A (en) | 2007-03-28 | 2007-03-28 | A process for treating slop mud |
PCT/GB2008/000175 WO2008117005A1 (en) | 2007-03-28 | 2008-01-18 | Process for separation of water from slop mud |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0706007A GB2447941A (en) | 2007-03-28 | 2007-03-28 | A process for treating slop mud |
Publications (2)
Publication Number | Publication Date |
---|---|
GB0706007D0 GB0706007D0 (en) | 2007-05-09 |
GB2447941A true GB2447941A (en) | 2008-10-01 |
Family
ID=38050373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB0706007A Withdrawn GB2447941A (en) | 2007-03-28 | 2007-03-28 | A process for treating slop mud |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB2447941A (en) |
WO (1) | WO2008117005A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013091032A1 (en) * | 2011-12-22 | 2013-06-27 | Tomov Petko Ivanov | Method for processing of oil sludge and oil sediments |
CN110510841A (en) * | 2019-08-23 | 2019-11-29 | 曹振 | A kind of dregs silt release agent and its application method |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8784545B2 (en) | 2011-04-12 | 2014-07-22 | Mathena, Inc. | Shale-gas separating and cleanout system |
US9353586B2 (en) | 2012-05-11 | 2016-05-31 | Mathena, Inc. | Control panel, and digital display units and sensors therefor |
US8981174B2 (en) | 2013-04-30 | 2015-03-17 | Pall Corporation | Methods and systems for processing crude oil using cross-flow filtration |
USD763414S1 (en) | 2013-12-10 | 2016-08-09 | Mathena, Inc. | Fluid line drive-over |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5762149A (en) * | 1995-03-27 | 1998-06-09 | Baker Hughes Incorporated | Method and apparatus for well bore construction |
WO2006050786A1 (en) * | 2004-11-15 | 2006-05-18 | Schlumberger Holdings Limited | In-line flow separation of fluids in a pipe separator |
US20060186056A1 (en) * | 2005-02-07 | 2006-08-24 | Catalin Ivan | Apparatus for separation of water from oil-based drilling fluid and advanced water treatment |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4551239A (en) * | 1983-04-11 | 1985-11-05 | Exxon Research & Engineering Co. | Water based demulsifier formulation and process for its use in dewatering and desalting crude hydrocarbon oils |
US4507208A (en) * | 1983-06-30 | 1985-03-26 | Drilling Waste, Incorporated | Process for handling waste from oil well operations |
US4836302A (en) * | 1986-12-03 | 1989-06-06 | Heilhecker Joe K | Apparatus and method for removing and recovering oil and/or other oil-based drilling mud additives from drill cuttings |
CA2184535C (en) * | 1996-08-30 | 2000-04-18 | H. Craig Willis | Apparatus and method for separation of solids from liquid |
US6391195B1 (en) * | 2000-12-26 | 2002-05-21 | Kenneth R. Layton | Apparatus for cleaning clearwater drilling muds |
US6881349B2 (en) * | 2002-11-15 | 2005-04-19 | M-I Llc | Method for recycling of oil based drilling fluid contaminated with water and water contaminated with oil based drilling fluid |
BE1014852A7 (en) * | 2002-05-29 | 2004-05-04 | Cb Consult | Hydro decanter slats separator. |
-
2007
- 2007-03-28 GB GB0706007A patent/GB2447941A/en not_active Withdrawn
-
2008
- 2008-01-18 WO PCT/GB2008/000175 patent/WO2008117005A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5762149A (en) * | 1995-03-27 | 1998-06-09 | Baker Hughes Incorporated | Method and apparatus for well bore construction |
WO2006050786A1 (en) * | 2004-11-15 | 2006-05-18 | Schlumberger Holdings Limited | In-line flow separation of fluids in a pipe separator |
US20060186056A1 (en) * | 2005-02-07 | 2006-08-24 | Catalin Ivan | Apparatus for separation of water from oil-based drilling fluid and advanced water treatment |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013091032A1 (en) * | 2011-12-22 | 2013-06-27 | Tomov Petko Ivanov | Method for processing of oil sludge and oil sediments |
CN110510841A (en) * | 2019-08-23 | 2019-11-29 | 曹振 | A kind of dregs silt release agent and its application method |
Also Published As
Publication number | Publication date |
---|---|
WO2008117005A1 (en) | 2008-10-02 |
GB0706007D0 (en) | 2007-05-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Piccioli et al. | Gas flotation of petroleum produced water: a review on status, fundamental aspects, and perspectives | |
US7497954B2 (en) | Apparatus for separation of water from oil-based drilling fluid and advanced water treatment | |
Deng et al. | Produced water from polymer flooding process in crude oil extraction: characterization and treatment by a novel crossflow oil–water separator | |
Santander et al. | Modified jet flotation in oil (petroleum) emulsion/water separations | |
KR101217363B1 (en) | A method and device for converting horizontal tanks into gas flotation separators | |
US10913013B2 (en) | System and method to process effluent brine and interface rag from an oil dehydration/desalting system | |
US6132630A (en) | Methods for wastewater treatment | |
NO176170B (en) | Method of Removing Water-Soluble Organic Materials from Oil Process Water | |
GB2447941A (en) | A process for treating slop mud | |
EP2355913B1 (en) | Separation method for immiscible fluids | |
WO2017117352A1 (en) | Underwater gas/liquid-liquid method and separation system and use of deoling membrane | |
WO2019067674A1 (en) | Conserving fresh wash water usage in desalting crude oil | |
Kajitvichyanukul et al. | Oil water separation | |
KR102217671B1 (en) | Oil-water separator flotation treatment apparatus and the system comprising thereof | |
WO1992019347A1 (en) | Oil and water separation system | |
Osamor et al. | Oil/water Separation: State-of-the-art | |
JP2892604B2 (en) | Method and apparatus for dissolved air flotation and similar gas-liquid contact operations | |
CN214936479U (en) | Novel atmospheric and vacuum electro-desalting sewage deep oil-water separation equipment | |
RU2695732C2 (en) | Method for preparation of hydrocarbon phase of waste invert-emulsion drilling mud as base for preparation of process fluids used in drilling and development of wells | |
McCosh et al. | Continuous improvement in slop-mud treatment technology | |
Krebs et al. | Emulsion separation | |
US20240286942A1 (en) | Method and System for Processing a Fluid | |
Das et al. | Separation of oil-water mixture in tank | |
Kajitvichyanukul et al. | and Lawrence K. Wang | |
Alhammo | Comparison between Four Chamber Flotation Unit and Dissolved Flotation Unit for the Treatment of Back-Produced Polymer Water |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |