WO2012010530A1 - Drilling fluid composition - Google Patents
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- WO2012010530A1 WO2012010530A1 PCT/EP2011/062186 EP2011062186W WO2012010530A1 WO 2012010530 A1 WO2012010530 A1 WO 2012010530A1 EP 2011062186 W EP2011062186 W EP 2011062186W WO 2012010530 A1 WO2012010530 A1 WO 2012010530A1
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- 238000005553 drilling Methods 0.000 title claims abstract description 74
- 239000012530 fluid Substances 0.000 title claims abstract description 66
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 23
- 239000010452 phosphate Substances 0.000 claims abstract description 23
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000004519 manufacturing process Methods 0.000 claims abstract description 5
- 150000002148 esters Chemical group 0.000 claims abstract description 4
- 239000002253 acid Substances 0.000 claims abstract description 3
- 150000001408 amides Chemical class 0.000 claims abstract description 3
- 150000003839 salts Chemical class 0.000 claims abstract description 3
- 239000012071 phase Substances 0.000 claims description 12
- 239000008346 aqueous phase Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 6
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical group [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 6
- 239000010428 baryte Substances 0.000 claims description 6
- 229910052601 baryte Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001033 ether group Chemical group 0.000 claims description 4
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- 125000005647 linker group Chemical group 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 26
- 239000010702 perfluoropolyether Substances 0.000 description 17
- 239000012267 brine Substances 0.000 description 7
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 6
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical group [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- 239000001110 calcium chloride Substances 0.000 description 4
- 229910001628 calcium chloride Inorganic materials 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000001595 flow curve Methods 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 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 description 2
- -1 calcium halides Chemical class 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000007539 photo-oxidation reaction Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000007669 thermal treatment Methods 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000006850 spacer group Chemical class 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/36—Water-in-oil emulsions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/04—Aqueous well-drilling compositions
- C09K8/26—Oil-in-water emulsions
- C09K8/28—Oil-in-water emulsions containing organic additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/34—Organic liquids
Definitions
- the present invention relates to a drilling fluid of optimized composition intended to solve problems encountered during operations such as drilling, completion or workover operations in a well, in particular for exploration and exploitation of deeply buried reservoirs.
- drilling fluid In drilling boreholes for exploring or exploiting oil and/or natural gas reservoirs, drilling fluid, otherwise known as drilling muds are used .
- the main functions of drilling fluids include: - providing hydrostatic pressure to prevent fluids coming from the reservoir from entering into the well bore; - lubricating and keeping the drill bit cool and clean during drilling; - carrying out drill cuttings, and - suspending the drill cuttings while drilling is paused and when the drilling assembly is brought in and out of the hole.
- the drilling fluid used for a particular job is selected to avoid damages to the geological formation hosting the reservoir and to limit corrosion.
- completion is all the preparation or outfitting operations required for bringing in a geologic formation from the wellbore. These completion operations use particular fluids called completion fluids.
- Workover fluids can be used in the producing well in circulation in a comparable manner to drilling fluids, or in form of a spacer fluid.
- HP/HT high pressure/high temperature
- mud compositions therein disclosed are not optimized in terms of viscosity profile, stability of the mud and thermal resistance.
- the invention thus pertains to a drilling fluid composition
- a drilling fluid composition comprising: - at least one (per)fluoropolyether oil comprising recurring units of formula -CF(CF 3 )CF 2 O- said oil having a kinematic viscosity of 30 to 80 cSt measured according to ASTM D455 standard at 20°C [oil (E)] and possessing a polydispersity index (PDI) of at least 1.15; and - at least one (per)fluoropolyether phosphate comprising at least one perfluoropolyoxyalkylenic chain and at least one phosphoric acid group, in its acid, amide, salt or ester form; [phosphate (P)].
- the Applicant has found that the particular combination of the oil (E) as above defined, having branched perfluoropolyether recurring units, possessing well defined kinematic viscosity and having a particular polydispersity index, and the phosphate (P) enables achieving outstanding performances in mud stability, even after long exposure to severe conditions (temperatures as high as 300°C) and rheological behaviour, which make the same suitable for operation in drilling boreholes in deeply-buried reservoirs.
- the oil (E) is preferably selected from the following classes: (1) B-O-[CF(CF 3 )CF 2 O] b1' (CFXO) b2' -B' wherein: - X is equal to -F or -CF 3 ; - B and B', equal to or different from each other, are selected from -CF 3 , -C 2 F 5 or -C 3 F 7 ; - b1' and b2', equal or different from each other, are independently integers ⁇ 0 selected such that the b1'/b2' ratio is comprised between 20 and 1,000 and b1’+b2’ is in the range 5 to 250; should b1’ and b2’ be both different from zero, the different recurring units are generally statistically distributed along the chain.
- Said products can be obtained by photooxidation of the hexafluoropropylene as described in CA 786877 MONTEDISON S.P.A. 19680406 , whose disclosures are herein incorporated by reference, and by subsequent conversion of the end groups as described in GB 1226566 MONTECATINI EDISON S.P.A. 19710331 whose disclosures are herein incorporated by reference ; (2) C 3 F 7 O-[CF(CF 3 )CF 2 O] o' -D wherein - D is equal to -C 2 F 5 or -C 3 F 7 ; - o' is an integer from 5 to 250.
- Said products can be prepared by ionic hexafluoropropylene epoxide oligomerization and subsequent treatment with fluorine as described in US 3242218 DU PONT 19660322 , whose disclosures are herein incorporated by reference; (3) ⁇ C 3 F 7 O-[CF(CF 3 )CF 2 O] dd’ -CF(CF 3 )- ⁇ 2 wherein - dd’ is an integer between 2 and 250.
- Said products can be obtained by ionic telomerization of the hexafluoropropylene epoxide and subsequent photochemical dimerization as reported in US 3214478 DU PONT 19651026 whose disclosures are herein incorporated by reference ; and (4) C’-O-[CF(CF 3 )CF 2 O] c1' (C 2 F 4 O) c2’ (CFX) c3’ -C” wherein - X is equal to -F or -CF 3 ; - C’ and C”, equal to or different from each other, are selected from -CF 3 , -C 2 F 5 or -C 3 F 7 ; - c1’, c2’ and c3’ equal or different from each other, are independently integers ⁇ 0, such that and c1’+c2’+c3’ is in the range 5 to 250; should at least two of c1’, c2’ and c3’ be different from zero, the different recurring units are
- Said products can be manufactured by photooxidation of a mixture of C 3 F 6 and C 2 F 4 and subsequent treatment with fluorine as described in US 3665041 MOTENDISON S.P.A. 19720523 , whose disclosures are herein incorporated by reference.
- the oil (E) possesses a polydispersity index (PDI) of at least 1.15; the polydispersity index (PDI) is hereby expressed as the ratio of weight average molecular weight (M w ) to number average molecular weight (M n ), as determined notably by GPC, wherein: - weight average molecular weight (M w ) is: - number average molecular weight (M n ) is:
- drilling fluids compositions otherwise complying with all above mentioned requirements, but failing to possess a PDI exceeding 1.15, do not possess adequate thermal stability to withstand operating conditions typically encountered in exploitation of deeply buried reservoirs; only those drilling fluids complying with this requirement maintain appropriate characteristics, including e.g. stable dispersion of solids and aqueous phase even after prolonged exposure to temperatures as high as 300°C.
- oils (E) will in certain embodiments be selected among those comprising less than 10 % wt, preferably less than 8 % wt, more preferably less than 5 % wt of fractions having molecular weight of less than 1000 Dalton.
- the oil (E) possesses a polydispersity index (PDI) of 1.15 to 2.0, preferably of 1.15 to 1.85, more preferably of 1.15 to 1.25.
- PDI polydispersity index
- the oil (E) possesses a kinematic viscosity of 30 to 80 cSt measured according to ASTM D455 standard at 20°C; kinematic viscosities values exceeding 80 cSt are not suited for this application; similarly oils (E) having kinematic viscosities of less than 30 cSt do not perform correctly when used in drilling fluids compositions.
- Oils which have been found to provide particularly good results within the drilling fluid compositions of the invention are those possessing a kinematic viscosity of 35 to 75 cSt, preferably of 40 to 65 cSt, when measured according to ASTM D455 standard at 20°C.
- the drilling mud composition of the invention generally comprises the phosphate (P) in an amount of 0.1 to 5 % by volume, with respect to the total volume of the fluid.
- phosphate (P) as above detailed is advantageously particularly effective for ensuring suitable stabilization of the drilling fluid and for retaining such stabilization efficiency even after prolonged operations at high temperatures.
- the (per)fluoropolyoxyalkylenic chains R P’ f and R P” f of formulae P-1, P-2, P-3 are preferably chains comprising recurring units (R 1 ), said recurring units having general formula: -(CF 2 ) k -CFZ f -O-, wherein k is an integer of from 0 to 3 and Z f is selected between a fluorine atom and a C 1 -C 6 perfluoro(oxy)alkyl group.
- Chain R P’ f more preferably complies with formula: R Fa -O-(CF 2 CF 2 O) a’ (CFYO) b’ (CF 2 CFY’O) c’ (CF 2 O) d’ (CF 2 (CF 2 ) z’ CF 2 O) e’ -, the recurring units being statistically distributed along the (per)fluoropolyoxyalkylene chain, wherein: - Y is -F or -CF 3 ; - Y’ is a C 1 -C 5 perfluoro(oxy)alkyl group; - z’ is 1 or 2; - a’, b’, c’, d’, e’ are integers ⁇ 0, - R Fa is a C 1 -C 3 ( per)fluoroalkyl group, possibly comprising halogens (Cl, Br in particular).
- Chain R P” f more preferably complies with formula: -(CF 2 CF 2 O) a” (CFYO) b” (CF 2 CFY”O) c” (CF 2 O) d” (CF 2 (CF 2 ) z” CF 2 O) e” -, the recurring units being statistically distributed along the (per)fluoropolyoxyalkylene chain, wherein: - Y” is a C 1 -C 5 perfluoro(oxy)alkyl group; - z” is 1 or 2; - a”, b”, c”, d”, e” are integers ⁇ 0.
- chain R P’ f complies with formula: R Fa -O-(CF 2 CF 2 O) a’ (CF 2 O) b’ (CF 2 (CF 2 ) z’ CF 2 O) c’ -, wherein: - z’ is 1 or 2; - a’, b’, c’ are integers ⁇ 0, - R Fa is a C 1 -C 3 ( per)fluoroalkyl group, possibly comprising halogens (Cl, Br in particular).
- chain R P” f complies with formula: -(CF 2 CF 2 O) a” (CF 2 O) b” (CF 2 (CF 2 ) z” CF 2 O) c” -, wherein: - z” is 1 or 2; - a”, b”, c” are integers ⁇ 0.
- groups L, L’, L are generally selected from linking groups of formula: -(CH 2 CH 2 O) k -, with average value for k being comprised between 1 and 5.
- a phosphate which has been found to yield particularly good result is a phosphate of formula: Z* 5 O-[(OZ* 4 )P(O)-(OCH 2 CH 2 ) k* -O-CH 2 CFY*-(CF 2 CF 2 O) a* (CF 2 O) b* (CF 2 (CF 2 ) z* CF 2 O) c* -CFY*CH 2 O-(CH 2 CH 2 O) k* ] v* -P(O)(OZ* 6 )(OZ* 7 ) wherein: - Y* is -F or -CF 3 ; - Z* 4, Z* 5, Z* 6 and Z* 7 , equal to or different from each other, are selected from H, alkaline or ammonium group; - k* is comprised between 1 and 3, preferably between 1 and 2; - z* is 1 or 2; - a*, b*, c* are integers ⁇ 0; -
- the drilling fluid composition of the invention generally comprises an aqueous phase.
- the drilling fluid composition advantageously is suited to withstand a massive brine inflow from the reservoir rock; to this aim is therefore advantageously formulated in form of a reverse water emulsion comprising a continuous phase comprising the oil (E) as main constituent.
- the drilling fluid composition comprises said oil (E) as main component of a continuous phase in admixture with an aqueous dispersed phase; phosphate (P) as above detailed advantageously enables appropriate stabilization of this aqueous dispersed phase in a continuous phase mainly consisting of oil (E).
- the aqueous phase generally comprises, preferably consists essentially of brines.
- the brines can be aqueous solutions of sodium, potassium and/or calcium halides (generally chlorides), sodium and/or potassium carbonates, alkaline formates and the like.
- a brine which has been found to provide particularly good result is a calcium chloride brine.
- the drilling fluid composition generally contains at least 1 %, sometimes at least 2 %, otherwise at least 3 % by volume (with respect to the total volume of the drilling fluid composition) of an aqueous phase, this latter generally dispersed in the oil (E) phase.
- the drilling fluid composition generally contains at most 80 %, sometimes at most 60 %, otherwise at most 50 % by volume (with respect to the total volume of the drilling fluid composition) of said aqueous phase, this latter generally dispersed in the oil (E) phase.
- drilling fluid compositions comprising 5 to 40% by volume (with respect to the total volume of the drilling fluid composition) of said aqueous phase, this latter generally dispersed in a phase comprising oil (E) as main component.
- the drilling fluid composition further advantageously comprises at least one weighting material; this weighting material is generally intended to ensure tuning of the density of the composition to target value.
- this weighting material is generally intended to ensure tuning of the density of the composition to target value.
- inorganic weighting materials are used.
- the choice of the weighting material is not critical, provided that it remains substantially inert in drilling fluid composition during its manufacture and use.
- weighting materials barite is preferred for its high density and inertness.
- Amount of weighting agent is generally selected as a function of the other ingredients; typically the composition will comprise from 5 and 25 % by volume of weighting agent, with respect to the total volume of the drilling fluid composition.
- the invention pertains also a method for manufacturing the drilling fluid composition as above detailed.
- the method generally comprises mixing the oil (E) and the phosphate (P) as above defined. Mixing can be performed in any appropriate equipment, including high speed homogenizers, stirred tanks, emulsifiers and the like.
- additional ingredients like notably the aqueous phase and the weighting material as above detailed can be additionally admixed with the oil (E) and the phosphate (P) to obtain the drilling fluid composition. It is nevertheless generally preferred to add these ingredients to a pre-mixed admixture of oil (E) and phosphate (P) as above detailed.
- the invention further pertains to the use of the drilling fluid composition in a drilling rig equipment.
- Figure 1 schematically depicts drilling rig equipment wherein the mud composition of the invention can be used.
- a drill pipe or string acts as a conduit for the drilling fluid; it is generally made of joints of hollow tubing connected together and stood in the derrick vertically.
- a drill bit (#7) device is attached to the end of the drill string; this bit breaks apart the rock being drilled. It also contains jets through which the drilling fluid exits.
- the rotary table (#6) or a top drive (not shown) rotates the drill string along with the attached tools and bit.
- a mechanical section or drawworks section (#13) contains the spool, whose main function is to reel in/out the drill line to raise/lower the travelling block.
- a mud pump (#11) is used to circulate drilling fluid through the system; the mud is suctioned from the mud tank or mud pit (#9) which provides a reserve store of drilling fluid.
- the mud flows through the conduit #14 and through the drill pipe (#5) down to the bit (#7). Loaded with drill cuttings it flows upwards in the borehole and is extracted through the conduit (#12) back to the mud pit.
- a shale shaker (#10) separates drill cuttings from the drilling fluid before it is pumped back down the borehole.
- the equipment can further comprise devices installed at the wellhead to prevent fluids and gases from unintentionally escaping from the borehole (not shown).
- Table 1 PFPE type PDI (M w /M n ) Density (g/ml) at 20°C Kinematic Viscosity (cSt) 20°C 40°C 100°C 2045X (1) 1.21 1.87 63 25 4.5 Y04 (2) 1.02 1.87 38 15 3.2
- FOMBLIN (R) 2045X is a (per)fluoropolyether oil having branched structure available from Solvay Solexis S.p.A.
- FOMBLIN (R) Y04 is a (per)fluoropolyether oil having branched structure commercially available from Solvay Solexis S.p.A., which was used for formulate a comparative mud composition.
- Both the FOMBLIN (R) 2045X PFPE and the FOMBLIN (R) Y04 PFPE belong to the family of branched PerFluoroPolyEthers, and have been manufactured by reaction of hexafluoropropene (HFP) and oxygen catalyzed by UV light.
- Branched PerFluoroPolyEthers have the following chemical structure: Branched PerFluoroPolyEthers (PFPE) are characterized by an outstanding thermal resistance (up to more than 300°C) and chemical resistance to very aggressive environments.
- the FOMBLIN ® 2045X PFPE and the FOMBLIN ® Y04 PFPE represent respectively a broader and narrower “cuts” of Molecular Weight Distribution (MWD) obtained by fractional distillation of the same matrix of branched PFPEs.
- MWD Molecular Weight Distribution
- a (per)fluoropolyether phosphate which is a mixture of mono- and diphosphoric PFPE esters, complying with formula: and commercially available from Solvay Solexis S.p.A. under trade name FLUOROLINK® F10 PFPE has been used. This compound was manufactured by reaction of diphosphorous pentoxide, orthophosphoric acid or pyrophosphoric acid with an ethoxylated perfluoroether diol.
- the ingredients were mixed using a homogenizer Ultra Turrax T25.
- the ingredients were introduced as follows: 1- introduction of PFPE oil (279.7g) 2- introduction of phosphate (P) (1.384 g) followed by stirring for 5 minutes; 3- introduction of CaCl 2 brine (at 300 g/l) (22.4 g) followed by stirring for 15 minutes; 4- introduction of barite (134.4 g) followed by stirring for 15 minutes.
- rotational speed of the homogenizer was set at 11 000 rpm at room temperature.
- the rheological characterization was carried out at different temperatures using the controlled stress rheometer Haake 150 with a 40 mm sanded plate geometry.
- the mud samples were introduced into sealed gold tubes placed inside an autoclave. This set up enabled to heat the samples at temperatures up to 300°C during 24 hours, with an external pressure of 100 bar.
- Fig. 2 and 3 show the flow curves of muds 1 and 2, respectively, before and after the thermal treatment at 250°C for 24 h.
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Abstract
Description
- providing hydrostatic pressure to prevent fluids coming from the reservoir from entering into the well bore;
- lubricating and keeping the drill bit cool and clean during drilling;
- carrying out drill cuttings, and
- suspending the drill cuttings while drilling is paused and when the drilling assembly is brought in and out of the hole.
- a well fluid density above 2000 kg/m3 is required in order to balance the bottomhole pressure at great well depths,
- the bottomhole static temperatures are often much higher than 200°C, and they can sometimes reach or even exceed 300°C.
- at least one (per)fluoropolyether oil comprising recurring units of formula -CF(CF3)CF2O-
said oil having a kinematic viscosity of 30 to 80 cSt measured according to ASTM D455 standard at 20°C [oil (E)] and possessing a polydispersity index (PDI) of at least 1.15; and
- at least one (per)fluoropolyether phosphate comprising at least one perfluoropolyoxyalkylenic chain and at least one phosphoric acid group, in its acid, amide, salt or ester form; [phosphate (P)].
(1) B-O-[CF(CF3)CF2O]b1'(CFXO)b2'-B'
wherein:
- X is equal to -F or -CF3;
- B and B', equal to or different from each other, are selected from -CF3, -C2F5 or -C3F7;
- b1' and b2', equal or different from each other, are independently integers ≥0 selected such that the b1'/b2' ratio is comprised between 20 and 1,000 and b1’+b2’ is in the
Said products can be obtained by photooxidation of the hexafluoropropylene as described in
(2) C3F7O-[CF(CF3)CF2O]o'-D
wherein
- D is equal to -C2F5 or -C3F7;
- o' is an integer from 5 to 250.
Said products can be prepared by ionic hexafluoropropylene epoxide oligomerization and subsequent treatment with fluorine as described in
(3) {C3F7O-[CF(CF3)CF2O]dd’-CF(CF3)-}2
wherein
- dd’ is an integer between 2 and 250.
Said products can be obtained by ionic telomerization of the hexafluoropropylene epoxide and subsequent photochemical dimerization as reported in
(4) C’-O-[CF(CF3)CF2O]c1'(C2F4O)c2’(CFX)c3’-C”
wherein
- X is equal to -F or -CF3;
- C’ and C”, equal to or different from each other, are selected from -CF3, -C2F5 or -C3F7;
- c1’, c2’ and c3’ equal or different from each other, are independently integers ≥0, such that and c1’+c2’+c3’ is in the
Said products can be manufactured by photooxidation of a mixture of C3F6 and C2F4 and subsequent treatment with fluorine as described in
- weight average molecular weight (Mw) is:
- number average molecular weight (Mn) is:
[RP’ f-CFYCH2-O-L]m-P(O)(OZ1)3-m (formula P-1)
RP” f-[CFYCH2-O-L’-P(O)(OZ2)(OZ3)]2 (formula P-2)
Z5O-[(OZ4)P(O)-L”-O-CH2CFY-RP” f-CFYCH2O-L’’]v-P(O)(OZ6)(OZ7) (formula P-3)
wherein:
- m = 1 to 3;
- Y is -F or -CF3;
- L, L’, L”, equal to or different from each other and at each occurrence, are a bond or a bivalent linking groups;
- v is an integer from 1 to 10, preferably from 1 to 5;
- Z1, Z2, Z3, Z4, Z5, Z6 and Z7, equal to or different from each other, are selected from H, alkaline or ammonium group, and RP f-CF2CH2-O-L- group;
- RP’ f is a monovalent (per)fluoropolyoxyalkylenic chain comprising fluorine and catenary ether atoms in the chain and terminated by a C1-C3 (per)fluoroalkyl group possibly comprising one or more halogens, in particular Cl, Br;
- RP” f is a divalent (per)fluoropolyoxyalkylenic chain comprising fluorine and catenary ether atoms in the chain.
RFa-O-(CF2CF2O)a’(CFYO)b’(CF2CFY’O)c’(CF2O)d’(CF2(CF2)z’CF2O)e’-,
the recurring units being statistically distributed along the (per)fluoropolyoxyalkylene chain, wherein:
- Y is -F or -CF3;
- Y’ is a C1-C5 perfluoro(oxy)alkyl group;
- z’ is 1 or 2;
- a’, b’, c’, d’, e’ are integers ≥ 0,
- RFa is a C1-C3 (per)fluoroalkyl group, possibly comprising halogens (Cl, Br in particular).
-(CF2CF2O)a”(CFYO)b”(CF2CFY”O)c”(CF2O)d”(CF2(CF2)z”CF2O)e”-,
the recurring units being statistically distributed along the (per)fluoropolyoxyalkylene chain, wherein:
- Y” is a C1-C5 perfluoro(oxy)alkyl group;
- z” is 1 or 2;
- a”, b”, c”, d”, e” are integers ≥ 0.
RFa-O-(CF2CF2O)a’(CF2O)b’(CF2(CF2)z’CF2O)c’-,
wherein:
- z’ is 1 or 2;
- a’, b’, c’ are integers ≥ 0,
- RFa is a C1-C3 (per)fluoroalkyl group, possibly comprising halogens (Cl, Br in particular).
-(CF2CF2O)a”(CF2O)b”(CF2(CF2)z”CF2O)c”-, wherein:
- z” is 1 or 2;
- a”, b”, c” are integers ≥ 0.
Z*5O-[(OZ*4)P(O)-(OCH2CH2)k*-O-CH2CFY*-(CF2CF2O)a*(CF2O)b*(CF2(CF2)z*CF2O)c*-CFY*CH2O-(CH2CH2O)k*]v*-P(O)(OZ*6)(OZ*7)
wherein:
- Y* is -F or -CF3;
- Z*4, Z*5, Z*6 and Z*7, equal to or different from each other, are selected from H, alkaline or ammonium group;
- k* is comprised between 1 and 3, preferably between 1 and 2;
- z* is 1 or 2;
- a*, b*, c* are integers ≥ 0;
- v* is an integer from 1 to 5, preferably from 1 to 3.
PFPE type | PDI (Mw/Mn) | Density (g/ml) at 20°C | Kinematic Viscosity (cSt) | ||
20°C | 40°C | 100°C | |||
2045X(1) | 1.21 | 1.87 | 63 | 25 | 4.5 |
Y04(2) | 1.02 | 1.87 | 38 | 15 | 3.2 |
(2) FOMBLIN(R) Y04 is a (per)fluoropolyether oil having branched structure commercially available from Solvay Solexis S.p.A., which was used for formulate a comparative mud composition.
Branched PerFluoroPolyEthers (PFPE) are characterized by an outstanding thermal resistance (up to more than 300°C) and chemical resistance to very aggressive environments.
The FOMBLIN® 2045X PFPE and the FOMBLIN® Y04 PFPE represent respectively a broader and narrower “cuts” of Molecular Weight Distribution (MWD) obtained by fractional distillation of the same matrix of branched PFPEs.
1- introduction of PFPE oil (279.7g)
2- introduction of phosphate (P) (1.384 g) followed by stirring for 5 minutes;
3- introduction of CaCl2 brine (at 300 g/l) (22.4 g) followed by stirring for 15 minutes;
4- introduction of barite (134.4 g) followed by stirring for 15 minutes.
During all the above steps, rotational speed of the homogenizer was set at 11 000 rpm at room temperature.
Mud | Composition | % by |
1 | Fomblin® 2045X PFPE | 73.6 |
Fluorolink® F10 PFPE | 0.4 | |
CaCl2 brine (300 g/l) | 10 | |
Barite | 16 | |
2 comparative | Fomblin® Y04 PFPE | 73.6 |
Fluorolink® F10 PFPE | 0.4 | |
CaCl2 brine (300g/l) | 10 | |
Barite | 16 |
Claims (16)
- A drilling fluid composition comprising:- at least one (per)fluoropolyether oil comprising recurring units of formula -CF(CF3)CF2O-said oil having a kinematic viscosity of 30 to 80 cSt measured according to ASTM D455 standard at 20°C [oil (E)] and possessing a polydispersity index (PDI) of at least 1.15; and- at least one (per)fluoropolyether phosphate comprising at least one perfluoropolyoxyalkylenic chain and at least one phosphoric acid group, in its acid, amide, salt or ester form [phosphate (P)].
- The drilling fluid composition of claim 1, wherein the oil (E) is selected from the following classes:selected from the following classes:(1) B-O-[CF(CF3)CF2O]b1'(CFXO)b2'-B'wherein:- X is equal to -F or -CF3;- B and B', equal to or different from each other, are selected from -CF3, -C2F5 or -C3F7;- b1' and b2', equal or different from each other, are independently integers ≥0 selected such that the b1'/b2' ratio is comprised between 20 and 1,000 and b1’+b2’ is in the range 5 to 250; should b1’ and b2’ be both different from zero, the different recurring units are generally statistically distributed along the chain.(2) C3F7O-[CF(CF3)CF2O]o'-Dwherein- D is equal to -C2F5 or -C3F7;- o' is an integer from 5 to 250.(3) {C3F7O-[CF(CF3)CF2O]dd’-CF(CF3)-}2wherein- dd’ is an integer between 2 and 250.(4) C’-O-[CF(CF3)CF2O]c1'(C2F4O)c2’(CFX)c3’-C”wherein- X is equal to -F or -CF3;- C’ and C”, equal to or different from each other, are selected from -CF3, -C2F5 or -C3F7;- c1’, c2’ and c3’ equal or different from each other, are independently integers ≥0, such that and c1’+c2’+c3’ is in the range 5 to 250; should at least two of c1’, c2’ and c3’ be different from zero, the different recurring units are generally statistically distributed along the chain.
- The drilling fluid composition of anyone of the preceding claims, wherein the oil (E) possesses a polydispersity index (PDI) of 1.15 to 2.0, preferably of 1.15 to 1.85, more preferably of 1.15 to 1.25.
- The drilling fluid composition of anyone of the preceding claims, wherein the oil (E) possesses a kinematic viscosity of 40 to 60 cSt, measured according to ASTM D455 standard at 20°C.
- The drilling fluid composition of anyone of the preceding claims, wherein phosphate (P) is selected from the group consisting of compounds complying with any of formulae P-1, P-2 and P-3:[RP’ f-CFYCH2-O-L]m-P(O)(OZ1)3-m (formula P-1)RP” f-[CFYCH2-O-L’-P(O)(OZ2)(OZ3)]2 (formula P-2)Z5O-[(OZ4)P(O)-L”-O-CH2CFY-RP” f-CFYCH2O-L’’]v-P(O)(OZ6)(OZ7) (formula P-3)wherein:- m = 1 to 3;- Y is -F or -CF3;- L, L’, L”, equal to or different from each other and at each occurrence, are a bond or a bivalent linking groups;- v is an integer from 1 to 10, preferably from 1 to 5;- Z1, Z2, Z3, Z4, Z5, Z6 and Z7, equal to or different from each other, are selected from H, alkaline or ammonium group, and RP f-CF2CH2-O-L- group;- RP’ f is a monovalent (per)fluoropolyoxyalkylenic chain comprising fluorine and catenary ether atoms in the chain and terminated by a C1-C3 (per)fluoroalkyl group possibly comprising one or more halogens, in particular Cl, Br;- RP” f is a divalent (per)fluoropolyoxyalkylenic chain comprising fluorine and catenary ether atoms in the chain.
- The drilling fluid composition of claim 5, wherein the phosphate (P) complies with formula: Z*5O-[(OZ*4)P(O)-(OCH2CH2)k*-O-CH2CFY*-(CF2CF2O)a*(CF2O)b*(CF2(CF2)z*CF2O)c*-CFY*CH2O-(CH2CH2O)k*]v*-P(O)(OZ*6)(OZ*7)wherein:- Y* is -F or -CF3;- Z*4, Z*5, Z*6 and Z*7, equal to or different from each other, are selected from H, alkaline or ammonium group;- k* is comprised between 1 and 3, preferably between 1 and 2;- z* is 1 or 2;- a*, b*, c* are integers ≥ 0;- v* is an integer from 1 to 5, preferably from 1 to 3.
- The drilling fluid composition of anyone of the preceding claims, said composition comprising an aqueous phase.
- The drilling fluid composition of claim 7, said composition being formulated in the form of a reverse water emulsion comprising a continuous phase comprising the oil (E) as main constituent.
- The drilling fluid composition of claim 8, said composition comprising said oil (E) as main component of a continuous phase in admixture with an aqueous dispersed phase comprising one or more than one brines.
- The drilling fluid compositions according to anyone of the claims 7 to 9, said composition comprising 5 to 40% by volume of said aqueous phase, with respect to the total volume of the drilling fluid composition.
- The drilling fluid composition according to anyone of the preceding claims, said composition further comprising at least one weighting material.
- The drilling fluid composition of claim 11, wherein said weighting agent is barite.
- The drilling fluid composition according to anyone of claims 11 to 12, comprising from 5 to 25 % by volume of weighting agent, with respect to the total volume of the drilling fluid composition.
- A method for manufacturing the drilling fluid composition according to anyone of the preceding claims, said method comprising mixing the oil (E) and the phosphate (P).
- Use of the drilling fluid composition according to anyone of claims 1 to 13 in a drilling rig equipment.
- Use according to claim 15, wherein in said drilling rig equipment a drill pipe or string (#5) acts as a conduit for said drilling fluid composition, a drill bit (#7) device is attached to the end of the drill string, said bit containing jets through which said drilling fluid composition exits.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11732476.4A EP2596074A1 (en) | 2010-07-22 | 2011-07-18 | Drilling fluid composition |
CN2011800381489A CN103097487A (en) | 2010-07-22 | 2011-07-18 | Drilling fluid composition |
US13/810,754 US20130248257A1 (en) | 2010-07-22 | 2011-07-18 | Drilling Fluid Composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP10305809 | 2010-07-22 | ||
EP10305809.5 | 2010-07-22 |
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WO2012010530A1 true WO2012010530A1 (en) | 2012-01-26 |
Family
ID=43216961
Family Applications (1)
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PCT/EP2011/062186 WO2012010530A1 (en) | 2010-07-22 | 2011-07-18 | Drilling fluid composition |
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US (1) | US20130248257A1 (en) |
EP (1) | EP2596074A1 (en) |
CN (1) | CN103097487A (en) |
AR (1) | AR082315A1 (en) |
WO (1) | WO2012010530A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2890759A4 (en) * | 2012-08-31 | 2016-03-23 | Halliburton Energy Services Inc | Fluorous additives for use in a fluorous-based treatment fluid |
AU2015218434B2 (en) * | 2012-08-31 | 2016-11-17 | Halliburton Energy Services, Inc. | Fluorous additives for use in a fluorous-based treatment fluid |
CN112111033A (en) * | 2019-06-21 | 2020-12-22 | 中国石油天然气集团有限公司 | Carbon dioxide viscosity-increasing and fluid loss-reducing copolymer and preparation method and application thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9543619B2 (en) | 2015-02-03 | 2017-01-10 | Blue Current, Inc. | Functionalized phosphorus containing fluoropolymers and electrolyte compositions |
US10308587B2 (en) | 2015-02-03 | 2019-06-04 | Blue Current, Inc. | Functionalized fluoropolymers and electrolyte compositions |
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- 2011-07-18 US US13/810,754 patent/US20130248257A1/en not_active Abandoned
- 2011-07-18 EP EP11732476.4A patent/EP2596074A1/en not_active Withdrawn
- 2011-07-18 CN CN2011800381489A patent/CN103097487A/en active Pending
- 2011-07-18 WO PCT/EP2011/062186 patent/WO2012010530A1/en active Application Filing
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Publication number | Priority date | Publication date | Assignee | Title |
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EP2890759A4 (en) * | 2012-08-31 | 2016-03-23 | Halliburton Energy Services Inc | Fluorous additives for use in a fluorous-based treatment fluid |
AU2015218434B2 (en) * | 2012-08-31 | 2016-11-17 | Halliburton Energy Services, Inc. | Fluorous additives for use in a fluorous-based treatment fluid |
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CN112111033A (en) * | 2019-06-21 | 2020-12-22 | 中国石油天然气集团有限公司 | Carbon dioxide viscosity-increasing and fluid loss-reducing copolymer and preparation method and application thereof |
CN112111033B (en) * | 2019-06-21 | 2022-08-05 | 中国石油天然气集团有限公司 | Carbon dioxide viscosity-increasing and fluid loss-reducing copolymer and preparation method and application thereof |
Also Published As
Publication number | Publication date |
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AR082315A1 (en) | 2012-11-28 |
EP2596074A1 (en) | 2013-05-29 |
CN103097487A (en) | 2013-05-08 |
US20130248257A1 (en) | 2013-09-26 |
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