CA2928213C - Use of synthetic smectite in set-delayed cement compositions comprising pumice - Google Patents
Use of synthetic smectite in set-delayed cement compositions comprising pumice Download PDFInfo
- Publication number
- CA2928213C CA2928213C CA2928213A CA2928213A CA2928213C CA 2928213 C CA2928213 C CA 2928213C CA 2928213 A CA2928213 A CA 2928213A CA 2928213 A CA2928213 A CA 2928213A CA 2928213 C CA2928213 C CA 2928213C
- Authority
- CA
- Canada
- Prior art keywords
- delayed cement
- cement composition
- delayed
- pumice
- composition
- 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.)
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- 239000004568 cement Substances 0.000 title claims abstract description 283
- 239000000203 mixture Substances 0.000 title claims abstract description 267
- 229910021647 smectite Inorganic materials 0.000 title claims abstract description 61
- 239000008262 pumice Substances 0.000 title claims abstract description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000000920 calcium hydroxide Substances 0.000 claims abstract description 30
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims abstract description 30
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims abstract description 29
- 235000011116 calcium hydroxide Nutrition 0.000 claims abstract description 29
- 239000000654 additive Substances 0.000 claims description 82
- 230000000996 additive effect Effects 0.000 claims description 63
- 239000002270 dispersing agent Substances 0.000 claims description 46
- 239000007788 liquid Substances 0.000 claims description 33
- 239000012530 fluid Substances 0.000 claims description 26
- 239000012190 activator Substances 0.000 claims description 21
- 239000002245 particle Substances 0.000 claims description 20
- 238000002156 mixing Methods 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 9
- 229920002873 Polyethylenimine Polymers 0.000 claims description 9
- 239000004917 carbon fiber Substances 0.000 claims description 9
- 238000005086 pumping Methods 0.000 claims description 8
- 230000002708 enhancing effect Effects 0.000 claims description 4
- 230000003213 activating effect Effects 0.000 claims description 3
- -1 borate compound Chemical class 0.000 claims description 3
- 150000003007 phosphonic acid derivatives Chemical class 0.000 claims description 3
- 229920001732 Lignosulfonate Polymers 0.000 claims description 2
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 abstract description 35
- 239000002002 slurry Substances 0.000 description 34
- 239000000523 sample Substances 0.000 description 19
- 208000005156 Dehydration Diseases 0.000 description 17
- 239000008186 active pharmaceutical agent Substances 0.000 description 14
- 230000008901 benefit Effects 0.000 description 14
- 238000012360 testing method Methods 0.000 description 14
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 10
- 235000011941 Tilia x europaea Nutrition 0.000 description 10
- 239000004571 lime Substances 0.000 description 10
- 230000004913 activation Effects 0.000 description 9
- 239000004927 clay Substances 0.000 description 9
- 230000001066 destructive effect Effects 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- 239000000835 fiber Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- 229940094522 laponite Drugs 0.000 description 6
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical group [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000008719 thickening Effects 0.000 description 6
- 239000013068 control sample Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000007088 Archimedes method Methods 0.000 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 description 4
- 229920000388 Polyphosphate Polymers 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- OSBMVGFXROCQIZ-UHFFFAOYSA-I pentasodium;[bis(phosphonatomethyl)amino]methyl-hydroxyphosphinate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].OP([O-])(=O)CN(CP([O-])([O-])=O)CP([O-])([O-])=O OSBMVGFXROCQIZ-UHFFFAOYSA-I 0.000 description 4
- 239000001205 polyphosphate Substances 0.000 description 4
- 235000011176 polyphosphates Nutrition 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 4
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 230000000246 remedial effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000007832 Na2SO4 Substances 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 235000011148 calcium chloride Nutrition 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- 235000012255 calcium oxide Nutrition 0.000 description 2
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 description 2
- 229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 125000005341 metaphosphate group Chemical group 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- RNIHAPSVIGPAFF-UHFFFAOYSA-N Acrylamide-acrylic acid resin Chemical compound NC(=O)C=C.OC(=O)C=C RNIHAPSVIGPAFF-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- PGNYGWRFIFYBKV-UHFFFAOYSA-N [Mg].[Li].[Na] Chemical compound [Mg].[Li].[Na] PGNYGWRFIFYBKV-UHFFFAOYSA-N 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-L calcium bis(dihydrogenphosphate) Chemical compound [Ca+2].OP(O)([O-])=O.OP(O)([O-])=O YYRMJZQKEFZXMX-UHFFFAOYSA-L 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 1
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 210000003722 extracellular fluid Anatomy 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- YIBPLYRWHCQZEB-UHFFFAOYSA-N formaldehyde;propan-2-one Chemical class O=C.CC(C)=O YIBPLYRWHCQZEB-UHFFFAOYSA-N 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 229940046892 lead acetate Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000019691 monocalcium phosphate Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- PYUBPZNJWXUSID-UHFFFAOYSA-N pentadecapotassium;pentaborate Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] PYUBPZNJWXUSID-UHFFFAOYSA-N 0.000 description 1
- 239000011301 petroleum pitch Substances 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical group [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- UGTZMIPZNRIWHX-UHFFFAOYSA-K sodium trimetaphosphate Chemical compound [Na+].[Na+].[Na+].[O-]P1(=O)OP([O-])(=O)OP([O-])(=O)O1 UGTZMIPZNRIWHX-UHFFFAOYSA-K 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- UDEJEOLNSNYQSX-UHFFFAOYSA-J tetrasodium;2,4,6,8-tetraoxido-1,3,5,7,2$l^{5},4$l^{5},6$l^{5},8$l^{5}-tetraoxatetraphosphocane 2,4,6,8-tetraoxide Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P1(=O)OP([O-])(=O)OP([O-])(=O)OP([O-])(=O)O1 UDEJEOLNSNYQSX-UHFFFAOYSA-J 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 229910000375 tin(II) sulfate Inorganic materials 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
- C04B14/04—Silica-rich materials; Silicates
- C04B14/14—Minerals of vulcanic origin
- C04B14/16—Minerals of vulcanic origin porous, e.g. pumice
-
- 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
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
- C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
- C04B14/04—Silica-rich materials; Silicates
- C04B14/10—Clay
- C04B14/106—Kaolin
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/18—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
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- General Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Civil Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
Disclosed herein are cement compositions and methods of using set-delayed cement compositions in subterranean formations. In one embodiment a method of cementing in a subterranean formation is described. The method comprises providing a set-delayed cement composition comprising pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water; introducing the set-delayed cement composition into a subterranean formation; and allowing the set-delayed cement composition to set in the subterranean formation.
Description
USE OF SYNTHETIC SMECTITE IN SET-DELAYED CEMENT
COMPOSITIONS COMPRISING PUMICE
BACKGROUND
[0001] Embodiments relate to subterranean cementing operations and, in certain embodiments, to set-delayed cement compositions and methods of using set-delayed cement compositions in subterranean formations.
COMPOSITIONS COMPRISING PUMICE
BACKGROUND
[0001] Embodiments relate to subterranean cementing operations and, in certain embodiments, to set-delayed cement compositions and methods of using set-delayed cement compositions in subterranean formations.
[0002] Cement compositions may be used in a variety of subterranean operations. For example, in subterranean well construction, a pipe string (e.g., casing, liners, expandable tubulars, etc.) may be run into a wellbore and cemented in place. The process of cementing the pipe string in place is commonly referred to as "primary cementing." In a typical primary cementing method, a cement composition may be pumped into an annulus between the walls of the wellbore and the exterior surface of the pipe string disposed therein.
The cement composition may set in the annular space, thereby forming an annular sheath of hardened, substantially impermeable cement (i.e., a cement sheath) that may support and position the pipe string in the wellbore and may bond the exterior surface of the pipe string to the subterranean formation. Among other things, the cement sheath surrounding the pipe string functions to prevent the migration of fluids in the annulus, as well as protecting the pipe string from corrosion. Cement compositions also may be used in remedial cementing methods, for example, to seal cracks or holes in pipe strings or cement sheaths, to seal highly permeable formation zones or fractures, to place a cement plug, and the like.
The cement composition may set in the annular space, thereby forming an annular sheath of hardened, substantially impermeable cement (i.e., a cement sheath) that may support and position the pipe string in the wellbore and may bond the exterior surface of the pipe string to the subterranean formation. Among other things, the cement sheath surrounding the pipe string functions to prevent the migration of fluids in the annulus, as well as protecting the pipe string from corrosion. Cement compositions also may be used in remedial cementing methods, for example, to seal cracks or holes in pipe strings or cement sheaths, to seal highly permeable formation zones or fractures, to place a cement plug, and the like.
[0003] A broad variety of cement compositions have been used in subterranean cementing operations. In some instances, set-delayed cement compositions have been used.
Set-delayed cement compositions are characterized by remaining in a pumpable fluid state for at least about one day (e.g., at least about 7 days, about 2 weeks, about 2 years or more) at room temperature (e.g., about 80 F) in quiescent storage. When desired for use, the set-delayed cement compositions should be capable of being activated whereby reasonable compressive strengths are developed. For example, a cement set activator may be added to a set-delayed cement composition whereby the composition sets into a hardened mass. Among other things, the set-delayed cement composition may be suitable for use in wellbore applications, for example, where it is desired to prepare the cement composition in advance.
This may allow, for example, the cement composition to be stored prior to its use. In addition, this may allow, for example, the cement composition to be prepared at a convenient location and then transported to the job site. Accordingly, capital expenditures may be reduced due to a reduction in the need for on-site bulk storage and mixing equipment. This may be particularly useful for offshore cementing operations where space onboard the vessels may be limited.
Set-delayed cement compositions are characterized by remaining in a pumpable fluid state for at least about one day (e.g., at least about 7 days, about 2 weeks, about 2 years or more) at room temperature (e.g., about 80 F) in quiescent storage. When desired for use, the set-delayed cement compositions should be capable of being activated whereby reasonable compressive strengths are developed. For example, a cement set activator may be added to a set-delayed cement composition whereby the composition sets into a hardened mass. Among other things, the set-delayed cement composition may be suitable for use in wellbore applications, for example, where it is desired to prepare the cement composition in advance.
This may allow, for example, the cement composition to be stored prior to its use. In addition, this may allow, for example, the cement composition to be prepared at a convenient location and then transported to the job site. Accordingly, capital expenditures may be reduced due to a reduction in the need for on-site bulk storage and mixing equipment. This may be particularly useful for offshore cementing operations where space onboard the vessels may be limited.
[0004] While set-delayed cement compositions have been developed heretofore, challenges exist with their successful use in subterranean cementing operations. For example, set-delayed cement compositions prepared with Portland cement may have undesired gelation issues which can limit their use and effectiveness in cementing operations.
Other set-delayed compositions that have been developed, for example, those comprising hydrated lime and quartz, may be effective in some operations but may have limited use at lower temperatures as they may not develop sufficient compressive strength when used in subterranean formations having lower bottom hole static temperatures.
Other set-delayed compositions that have been developed, for example, those comprising hydrated lime and quartz, may be effective in some operations but may have limited use at lower temperatures as they may not develop sufficient compressive strength when used in subterranean formations having lower bottom hole static temperatures.
[0005] A broad variety of cement densities may be required for an operation depending upon on the well conditions at the site. Set-delayed cement compositions may require unique solutions to adjust the density of the composition while maintaining a stable composition that can be stored until needed. As such, some chemical solutions may destabilize the slurry. Other solutions such as glass beads may dissolve over time providing only a temporary benefit.
BRIEF DESCRIPTION OF THE DRAWINGS
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] These drawings illustrate certain aspects of some of the embodiments of the present method, and should not be used to limit or define the method.
[0007] FIG. I illustrates a system for the preparation and delivery of a set-delayed Scement composition to a wellbore in accordance with certain embodiments.
[0008] FIG. 2A illustrates surface equipment that may be used in the placement of a set-delayed cement composition in a wellbore in accordance with certain embodiments.
[0009] FIG. 28 illustrates the placement of a set-delayed cement composition into a wellbore annulus in accordance with certain embodiments.
DESCRIPTION OF PREFERRED EMBODIMENTS
DESCRIPTION OF PREFERRED EMBODIMENTS
[0010] Embodiments relate to subterranean cementing operations and, in certain embodiments, to set-delayed cement compositions and methods of using set-delayed cement compositions in subterranean formations. Embodiments comprise lightweight stabilized set-delayed cement compositions for use in subterranean formations. Embodiments may comprise use synthetic smectites to stabilize the set-delayed cement compositions. The term set-delayed is used herein to refer to the composition before and after activation so long as the composition prior to activation was characterized by remaining in a pumpable fluid state for at least about one day (e.g., at least about 7 days, about 2 weeks, about 2 years or more) at room temperature (e.g., about 80 F) in quiescent storage.
[0011] Embodiments of the set-delayed cement compositions may generally comprise water, pumice, hydrated lime, synthetic smectites, and a set retarder.
Optionally, the set-delayed cement compositions may further comprise a dispersant. Embodiments of the set-delayed cement compositions may be foamed. Advantageously, embodiments of the set-delayed cement compositions may be capable of remaining in a pumpable fluid state for an extended period of time. For example, the set-delayed cement compositions may remain in a pumpable fluid state for at least about I day, about 2 weeks, about 2 years, or longer.
Advantageously, the set-delayed cement compositions may develop reasonable compressive strengths after activation at relatively low temperatures. While the set-delayed cement compositions may be suitable for a number of subterranean cementing operations, they may be particularly suitable for use in subterranean formations having relatively low bottom hole static temperatures, e.g., temperatures less than about 200 F or ranging from about 100 F to about 200 F. In alternative embodiments, the set-delayed cement compositions may be used in subterranean formations having bottom hole static temperatures up to 450 F
or higher.
Optionally, the set-delayed cement compositions may further comprise a dispersant. Embodiments of the set-delayed cement compositions may be foamed. Advantageously, embodiments of the set-delayed cement compositions may be capable of remaining in a pumpable fluid state for an extended period of time. For example, the set-delayed cement compositions may remain in a pumpable fluid state for at least about I day, about 2 weeks, about 2 years, or longer.
Advantageously, the set-delayed cement compositions may develop reasonable compressive strengths after activation at relatively low temperatures. While the set-delayed cement compositions may be suitable for a number of subterranean cementing operations, they may be particularly suitable for use in subterranean formations having relatively low bottom hole static temperatures, e.g., temperatures less than about 200 F or ranging from about 100 F to about 200 F. In alternative embodiments, the set-delayed cement compositions may be used in subterranean formations having bottom hole static temperatures up to 450 F
or higher.
[0012] The water used in embodiments of the set-delayed cement compositions may be from any source provided that it does not contain an excess of compounds that may undesirably affect other components in the set-delayed cement compositions.
For example, a set-delayed cement composition may comprise fresh water or salt water. Salt water generally may include one or more dissolved salts therein and may be saturated or unsaturated as desired for a particular application. Seawater or brines may be suitable for use in embodiments.
Further, the water may be present in an amount sufficient to form a pumpable slurry. In certain embodiments, the water may be present in the set-delayed cement composition in an amount in the range of from about 33% to about 200% by weight of the pumice. In certain embodiments, the water may be present in the set-delayed cement compositions in an amount in thc range of from about 35% to about 70% by weight of the pumice. One of ordinary skill in the art with the benefit of this disclosure will recognize the appropriate amount of water for a chosen application.
For example, a set-delayed cement composition may comprise fresh water or salt water. Salt water generally may include one or more dissolved salts therein and may be saturated or unsaturated as desired for a particular application. Seawater or brines may be suitable for use in embodiments.
Further, the water may be present in an amount sufficient to form a pumpable slurry. In certain embodiments, the water may be present in the set-delayed cement composition in an amount in the range of from about 33% to about 200% by weight of the pumice. In certain embodiments, the water may be present in the set-delayed cement compositions in an amount in thc range of from about 35% to about 70% by weight of the pumice. One of ordinary skill in the art with the benefit of this disclosure will recognize the appropriate amount of water for a chosen application.
[0013] Embodiments of the set-delayed cement compositions may comprise pumice.
Generally, pumice is a volcanic rock that can exhibit cementitious properties in that it may set and harden in the presence of hydrated lime and water. The pumice may also be ground.
Generally, the pumice may have any particle size distribution as desired for a particular application.
In certain embodiments, the pumice may have a mean particle size in a range of from about 1 micron to about 200 microns. The mean particle size corresponds to d50 values as measured by particle size analyzers such as those manufactured by Malvern Instruments, Worcestershire, United Kingdom. In specific embodiments, the pumice may have a mean particle size in a range of from about 1 micron to about 200 microns, from about 5 microns to about 100 microns, or from about 10 microns to about 25 microns. In one particular embodiment, the pumice may have a mean particle size of less than about 15 microns. An example of a suitable pumice is available from Hess Pumice Products, Inc., Malad, Idaho, as DS325TM lightweight aggregate, having a particle size of less than about 15 microns. It should be appreciated that particle sizes too small may have mixability problems while particle sizes too large may not be effectively suspended in the compositions. One of ordinary skill in the art, with the benefit of this disclosure, should be able to select a particle size for the pumice suitable for a chosen application.
Generally, pumice is a volcanic rock that can exhibit cementitious properties in that it may set and harden in the presence of hydrated lime and water. The pumice may also be ground.
Generally, the pumice may have any particle size distribution as desired for a particular application.
In certain embodiments, the pumice may have a mean particle size in a range of from about 1 micron to about 200 microns. The mean particle size corresponds to d50 values as measured by particle size analyzers such as those manufactured by Malvern Instruments, Worcestershire, United Kingdom. In specific embodiments, the pumice may have a mean particle size in a range of from about 1 micron to about 200 microns, from about 5 microns to about 100 microns, or from about 10 microns to about 25 microns. In one particular embodiment, the pumice may have a mean particle size of less than about 15 microns. An example of a suitable pumice is available from Hess Pumice Products, Inc., Malad, Idaho, as DS325TM lightweight aggregate, having a particle size of less than about 15 microns. It should be appreciated that particle sizes too small may have mixability problems while particle sizes too large may not be effectively suspended in the compositions. One of ordinary skill in the art, with the benefit of this disclosure, should be able to select a particle size for the pumice suitable for a chosen application.
[0014] Embodiments of the set-delayed cement compositions may comprise hydrated lime. As used herein, the term "hydrated lime" will be understood to mean calcium hydroxide. In some embodiments, the hydrated lime may be provided as quicklime (calcium oxide) which hydrates when mixed with water to form the hydrated lime. The hydrated lime may be included in embodiments of the set-delayed cement compositions, for example, to form a hydraulic composition with the pumice. For example, the hydrated lime may be included in a pumice-to-hydrated-lime weight ratio of about 10:1 to about 1:1 or 3:1 to about 5:1. Where present, the hydrated lime may be included in the set-delayed cement compositions in an amount in the range of from about 10% to about 100%
by weight of the pumice, for example. In some embodiments, the hydrated lime may be present in an amount ranging between any of and/or including any of about 10%, about 20%, about 40%, about 60%, about 80%, or about 100% by weight of the pumice. In some embodiments, the cementitious components present in the set-delayed cement composition may consist essentially of the pumice and the hydrated lime. For example, the cementitious components may primarily comprise the pumice and the hydrated lime without any additional components (e.g., Portland cement, fly ash, slag cement) that hydraulically set in the presence of water. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the hydrated lime to include for a chosen application.
by weight of the pumice, for example. In some embodiments, the hydrated lime may be present in an amount ranging between any of and/or including any of about 10%, about 20%, about 40%, about 60%, about 80%, or about 100% by weight of the pumice. In some embodiments, the cementitious components present in the set-delayed cement composition may consist essentially of the pumice and the hydrated lime. For example, the cementitious components may primarily comprise the pumice and the hydrated lime without any additional components (e.g., Portland cement, fly ash, slag cement) that hydraulically set in the presence of water. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the hydrated lime to include for a chosen application.
[0015] Embodiments of the set-delayed cement compositions may comprise a synthetic smectite. Among other reasons, a synthetic smectite may be added to aid in stabilization of the set-delayed cement composition, for example, when the set-delayed cement composition is lightweight. Synthetic smectites may be aqueous mixtures of water and synthetic trioctahedral smectites which are similar to the natural clay hectorite. In embodiments, some synthetic smectites are layered hydrous sodium lithium magnesium silicates, further, some may be modified with tetrasodiumpyrophosphate. An example of a commercially available synthetic smectite is Laponite available from Southern Clay Products, Gonzales, Texas. Synthetic smectite may be a platelet-like clay particle with a thickness of less than about 100 nm and lateral dimensions of in a range of about I to about 100 nm. Without being limited by theory, synthetic smectite clay particles may swell in water and may produce gels with water at concentrations greater than 0.5%. When water is added to a synthetic smectite, it is believed that the synthetic smectite platelets become ionized and the rising osmotic pressure in the interstitial fluid may be the cause of the particle swelling. When at equilibrium in water, the faces of typical synthetic smectites are negatively charged while the edges of the synthetic smectite particles are positively charged. The polarity of the particles may be the cause of the rheological alterations in the set-delayed cement composition. In embodiments, a synthetic smectite may be added to the set-delayed cement composition as a liquid additive or as a dry powder. The synthetic smectite may be added to the set-delayed cement compositions as a dry blend or to the set-delayed cement slurry. In embodiments, the synthetic smectite may comprise a synthetic smectite with a surface modification. For example, pyrophosphate may be used to bind the edges of the synthetic smectite.
[0016] The synthetic smectite may be included in embodiments of the set-delayed cement compositions, for example, to stabilize the set-delayed cement composition as additional water is added to create a lightweight set-delayed cement composition. Where present, the synthetic smectite may be included in the set-delayed cement compositions in an amount in the range of from about 0.01% to about 5% by weight of the water, for example. In some embodiments, the synthetic smectite may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, about 1%, about 2%, or about 5% by weight of the water.
[0017] Embodiments of the set-delayed cement compositions may comprise a set retarder. A broad variety of set retarders may be suitable for use in the set-delayed cement compositions. For example, the set retarder may comprise phosphonic acids, such as amino tris(methylene phosphonic acid), ethylenediamine tetra(methylene phosphonic acid), diethylenetriamine penta(methylene phosphonic acid), etc.; lignosulfonates, such as sodium lignosulfonate, calcium lignosulfonate, etc.; salts such as stannous sulfate, lead acetate, monobasic calcium phosphate, organic acids, such as citric acid, tartaric acid, etc.; cellulose derivatives such as hydroxyl ethyl cellulose (HEC) and carboxymethyl hydroxyethyl cellulose (CMHEC); synthetic co- or ter-polymers comprising sulfonate and carboxylic acid groups such as sulfonate-functionalized acrylamide-acrylic acid co-polymers; borate compounds such as alkali borates, sodium metaborate, sodium tetraborate, potassium pentaborate; derivatives thereof, or mixtures thereof. Examples of suitable set retarders include, among others, phosphonic acid derivatives. One example of a suitable set retarder is Micro Matrix cement retarder, available from Halliburton Energy Services, Inc. Generally, the set retarder may be present in the set-delayed cement compositions in an amount sufficient to delay the setting for a desired time. In some embodiments, the set retarder may be present in the set-delayed cement compositions in an amount in the range of from about 0.01% to about 5% by weight of the water. In specific embodiments, the set retarder may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, about 1%, about 2%, about 4%, or about 5%, by weight of the water. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the set retarder to include for a chosen application.
[0018] As previously mentioned, embodiments of the set-delayed cement compositions may optionally comprise a dispersant. Examples of suitable dispersants include, without limitation, sulfonated-formaldehyde-based dispersants (e.g., sulfonated acetone formaldehyde condensate), examples of which may include Daxad 19 dispersant available from Geo Specialty Chemicals, Ambler, Pennsylvania. Other suitable dispersants may be polycarboxylated ether dispersants such as Liquiment 5581F and Liquiment dispersants available from BASF Corporation Houston, Texas; or Ethacryl" G
dispersant available from Coatex, Genay, France. An additional example of a suitable commercially available dispersant is CFe-3 dispersant, available from Halliburton Energy Services, Inc, Houston, Texas. The Liquiment 514L dispersant may comprise 36% by weight of the polycarboxylated ether in water. While a variety of dispersants may be used in accordance with embodiments, polycarboxylated ether dispersants may be particularly suitable for use in some embodiments. Without being limited by theory, it is believed that polycarboxylated ether dispersants may synergistically interact with other components of the set-delayed cement composition. For example, it is believed that the polycarboxylated ether dispersants may react with certain set retarders (e.g., phosphonic acid derivatives) resulting in formation of a gel that suspends the pumice and hydrated lime in the composition for an extended period of time.
dispersant available from Coatex, Genay, France. An additional example of a suitable commercially available dispersant is CFe-3 dispersant, available from Halliburton Energy Services, Inc, Houston, Texas. The Liquiment 514L dispersant may comprise 36% by weight of the polycarboxylated ether in water. While a variety of dispersants may be used in accordance with embodiments, polycarboxylated ether dispersants may be particularly suitable for use in some embodiments. Without being limited by theory, it is believed that polycarboxylated ether dispersants may synergistically interact with other components of the set-delayed cement composition. For example, it is believed that the polycarboxylated ether dispersants may react with certain set retarders (e.g., phosphonic acid derivatives) resulting in formation of a gel that suspends the pumice and hydrated lime in the composition for an extended period of time.
[0019] In some embodiments, the dispersant may be included in the set-delayed cement compositions in an amount in the range of from about 0.01% to about 5%
by weight of the pumice. In specific embodiments, the dispersant may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, about 0.5%, about 1%, about 2%, about 3%, about 4%, or about 5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the dispersant to include for a chosen application.
by weight of the pumice. In specific embodiments, the dispersant may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, about 0.5%, about 1%, about 2%, about 3%, about 4%, or about 5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the dispersant to include for a chosen application.
[0020] In some embodiments, a viscosifier may be included in the set-delayed cement compositions. The viscosifier may be included to optimize fluid rheology and to stabilize the suspension. Without limitation, examples of viscosifiers include biopolymers.
An example of a commercially available viscosifier is SA-101r available from Halliburton Energy Services, Inc., Houston, TX. The viscosifier may be included in the set-delayed cement compositions in an amount in the range of from about 0.01% to about 0.5% by weight of the pumice. In specific embodiments, the viscosifier may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.05%, about 0.1%, about 0.2%, about 0.3%, about 0.4%, or about 0.5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of viscosifier to include for a chosen application.
An example of a commercially available viscosifier is SA-101r available from Halliburton Energy Services, Inc., Houston, TX. The viscosifier may be included in the set-delayed cement compositions in an amount in the range of from about 0.01% to about 0.5% by weight of the pumice. In specific embodiments, the viscosifier may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.05%, about 0.1%, about 0.2%, about 0.3%, about 0.4%, or about 0.5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of viscosifier to include for a chosen application.
[0021] Embodiments of the set-delayed cement compositions may comprise a mechanical property enhancing additive. Mechanical-property-enhancing additives may be included in embodiments of the set-delayed compositions to, for example, ensure adequate compressive strength and long-term structural integrity. These properties can be affected by the strains, stresses, temperature, pressure, and impact effects from a subterranean environment. Examples of mechanical property enhancing additives include fibers, such as graphitic carbon fibers, glass fibers, steel fibers, mineral fibers, silica fibers, polyester fibers, ground rubber tires, polyamide fibers, and polyolefin fibers, among others.
Specific examples of graphitic carbon fibers include fibers derived from polyacrylonitrile, rayon, and petroleum pitch. A commercial example of a mechanical-property-enhancing additive is Welll,ife 684 additive available from Halliburton Energy Services, Inc. Houston, Texas.
Where used, the mechanical-property-enhancing additives may be present in an amount from about 0.01% to about 5% by weight of the pumice. In specific embodiments, the mechanical-property-enhancing additives may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, 0.5%, about 1%, about 2%, about 3%, about 4%, or about 5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the mechanical-property-enhancing additives to include for a chosen application.
Specific examples of graphitic carbon fibers include fibers derived from polyacrylonitrile, rayon, and petroleum pitch. A commercial example of a mechanical-property-enhancing additive is Welll,ife 684 additive available from Halliburton Energy Services, Inc. Houston, Texas.
Where used, the mechanical-property-enhancing additives may be present in an amount from about 0.01% to about 5% by weight of the pumice. In specific embodiments, the mechanical-property-enhancing additives may be present in an amount ranging between any of and/or including any of about 0.01%, about 0.1%, 0.5%, about 1%, about 2%, about 3%, about 4%, or about 5% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the mechanical-property-enhancing additives to include for a chosen application.
[0022] Other additives suitable for use in subterranean cementing operations also may be included in embodiments of the set-delayed cement compositions. Examples of such additives include, but are not limited to: weighting agents, lightweight additives, gas-generating additives, mechanical-property-enhancing additives, lost-circulation materials, filtration-control additives, fluid-loss-control additives, defoaming agents, foaming agents, thixotropic additives, mechanical-property-enhancing additives, polyimines, and combinations thereof. In embodiments, one or more of these additives may be added to the set-delayed cement compositions after storing but prior to the placement of a set-delayed cement composition into a subterranean formation. A person having ordinary skill in the an, with the benefit of this disclosure, should readily be able to determine the type and amount of additive useful for a particular application and desired result.
[0023] Those of ordinary skill in the art will appreciate that embodiments of the set-delayed cement compositions generally should have a density suitable for a particular application. By way of example, the set-delayed cement compositions may have a density in the range of from about 4 pounds per gallon ("lb/gal") to about 20 lb/gal. In certain embodiments, the set-delayed cement compositions may have a density in the range of from about 8 lb/gal to about 17 lb/gal. In some embodiments, the set-delayed cement compositions may be lightweight. The set-delayed cement composition may be considered lightweight if it has a density of about 13 lb/gal or less. In particular embodiments, the set-delayed cement composition may have a density from about 8 lb/gal to about 13 lb/gal.
Embodiments of the set-delayed cement compositions may be foamed or unfoamed or may comprise other means to reduce their densities, such as hollow microspheres, low-density elastic beads, or other density-reducing additives known in the art. In embodiments, the density may be reduced after storing the composition, but prior to placement in a subterranean formation.
Those of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density for a particular application.
Embodiments of the set-delayed cement compositions may be foamed or unfoamed or may comprise other means to reduce their densities, such as hollow microspheres, low-density elastic beads, or other density-reducing additives known in the art. In embodiments, the density may be reduced after storing the composition, but prior to placement in a subterranean formation.
Those of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density for a particular application.
[0024] The density of the set-delayed cement compositions may be altered before injection into the wellbore. Embodiments of the set-delayed cement compositions may comprise a synthetic smectite and water to provide a lightweight composition that does not exert excessive force on formations penetrated by the wellbore. Water may be added to the slurry in addition to the water already present in the slurry in order to lower the density of the slurry further. Alternatively, enough initial water may be added to a dry blend of a set-delayed cement composition to achieve a targeted density while producing the slurry.
Amongst other reasons, a synthetic smectite may be added to the set-delayed cement compositions to stabilize the set-delayed cement compositions should large amounts of water be required in order to produce a slurry with a specific density. In particular embodiments, the synthetic smectite may be added as a dry powder and/or as a liquid additive (i.e. mixed with additional water) at the well site or in the manufacture of the set-delayed cement composition. As such, the synthetic smectite, as a dry powder and/or a liquid additive, may be added to the set-delayed cement compositions when the set-delayed cement compositions are a dry blend or when the set-delayed cement compositions are a slurry. By way of example, a set-delayed cement slurry may have a synthetic smectite added immediately prior to use (e.g., as a dry powder or as a liquid additive). The amount of synthetic smectite to add to the set-delayed cement compositions is dependent upon the amount of additional water needed to achieve a specific density. In embodiments, the synthetic smectite may be added to the set-delayed cement compositions before, after, or in combination with an activator. Moreover, additional additives may be added to the set-delayed cement compositions in combination with the synthetic smectite. For example, polyethyleneimine and/or mechanical-property-enhancing additives such as carbon fibers may be mixed or blended with the synthetic smectite liquid additive or the synthetic smectite dry powder and the resulting combination added to the set-delayed cement compositions (i.e. added to either the set-delayed cement composition dry blend or to the set-delayed cement slurry). With the benefit of this disclosure, one having ordinary skill in the art will be able to choose an amount of a synthetic smectite and water to add for a specific application.
Amongst other reasons, a synthetic smectite may be added to the set-delayed cement compositions to stabilize the set-delayed cement compositions should large amounts of water be required in order to produce a slurry with a specific density. In particular embodiments, the synthetic smectite may be added as a dry powder and/or as a liquid additive (i.e. mixed with additional water) at the well site or in the manufacture of the set-delayed cement composition. As such, the synthetic smectite, as a dry powder and/or a liquid additive, may be added to the set-delayed cement compositions when the set-delayed cement compositions are a dry blend or when the set-delayed cement compositions are a slurry. By way of example, a set-delayed cement slurry may have a synthetic smectite added immediately prior to use (e.g., as a dry powder or as a liquid additive). The amount of synthetic smectite to add to the set-delayed cement compositions is dependent upon the amount of additional water needed to achieve a specific density. In embodiments, the synthetic smectite may be added to the set-delayed cement compositions before, after, or in combination with an activator. Moreover, additional additives may be added to the set-delayed cement compositions in combination with the synthetic smectite. For example, polyethyleneimine and/or mechanical-property-enhancing additives such as carbon fibers may be mixed or blended with the synthetic smectite liquid additive or the synthetic smectite dry powder and the resulting combination added to the set-delayed cement compositions (i.e. added to either the set-delayed cement composition dry blend or to the set-delayed cement slurry). With the benefit of this disclosure, one having ordinary skill in the art will be able to choose an amount of a synthetic smectite and water to add for a specific application.
[0025] In some embodiments, a liquid additive comprising water and a synthetic smectite may be added to a set-delayed cement composition to lower the density of the set-delayed cement composition. The set-delayed cement composition may comprise water, pumice, hydrated lime, and a set retarder. Other additives described herein may also be included in the set-delayed cement composition. The set-delayed cement composition may have an initial density of from about 13 lb/gal to about 20 lb/gal. By addition of the liquid additive, the density of the set-delayed cement composition may be lowered. By way of example, a sufficient amount of the liquid additive may be added to lower the density by about 1 lb/gal or more. In some embodiments, the liquid additive may be used to lower the density to about 8 lb/gal to about 13 lb/gal. The synthetic smectite may be included in the liquid additive in amount of about 0.01% to about 2% percent by weight.
[0026] As previously mentioned, the set-delayed cement compositions may have a delayed set in that they remain in a pumpable fluid state for at least one day (e.g., at least about I day, about 2 weeks, about 2 years or more) at room temperature (e.g., about 80 F) in quiescent storage. For example, the set-delayed cement compositions may remain in a pumpable fluid state for a period of time from about 1 day to about 7 days or more. In some embodiments, the set-delayed cement compositions may remain in a pumpable fluid state for at least about 1 day, about 7 days, about 10 days, about 20 days, about 30 days, about 40 days, about 50 days, about 60 days, or longer. A fluid is considered to be in a pumpable fluid state where the fluid has a consistency of less than 70 Bearden units of consistency ("Bc"), as measured on a pressurized consistometer in accordance with the procedure for determining cement thickening times set forth in API RP Practice 103-2, Recommended Practice for Testing Well Cements, First Edition, July 2005.
[0027] When desired for use, embodiments of the set-delayed cement compositions may be activated (e.g., by combination with an activator) to set into a hardened mass. The term "cement set activator" or "activator", as used herein, refers to an additive that activates a set-delayed or heavily retarded cement composition and may also accelerate the setting of the set-delayed, heavily retarded, or other cement composition. By way of example, embodiments of the set-delayed cement compositions may be activated to form a hardened mass in a time period in the range of from about 1 hour to about 12 hours. For example, embodiments of the set-delayed cement compositions may set to form a hardened mass in a time period ranging between any of and/or including any of about 1 day, about 2 days, about 4 days, about 6 days, about 8 days, about 10 days, or about 12 days.
[0028] In some embodiments, the set-delayed cement compositions may set to have a desirable compressive strength after activation. Compressive strength is generally the capacity of a material or structure to withstand axially directed pushing forces. The compressive strength may be measured at a specified time after the set-delayed cement composition has been activated and the resultant composition is maintained under specified temperature and pressure conditions. Compressive strength can be measured by either destructive or non-destructive methods. The destructive method physically tests the strength of treatment fluid samples at various points in time by crushing the samples in a compression-testing machine.
The compressive strength is calculated from the failure load divided by the cross-sectional area resisting the load and is reported in units of pound-force per square inch (psi). Non-destructive methods may employ a UCAT" ultrasonic cement analyzer, available from Farm Instrument Company, Houston, TX. Compressive strength values may be determined in accordance with API RP 10B-2, Recommended Practice for Testing Well Cements, First Edition, July 2005.
The compressive strength is calculated from the failure load divided by the cross-sectional area resisting the load and is reported in units of pound-force per square inch (psi). Non-destructive methods may employ a UCAT" ultrasonic cement analyzer, available from Farm Instrument Company, Houston, TX. Compressive strength values may be determined in accordance with API RP 10B-2, Recommended Practice for Testing Well Cements, First Edition, July 2005.
[0029] By way of example, the set-delayed cement compositions may develop a 24-hour compressive strength in the range of from about 50 psi to about 5000 psi, alternatively, from about 100 psi to about 4500 psi, or alternatively from about 500 psi to about 4000 psi. In some embodiments, the set-delayed cement compositions may develop a compressive strength in 24 hours of at least about 50 psi, at least about 100 psi, at least about 500 psi, or more. In some embodiments, the compressive strength values may be determined using destructive or non-destructive methods at a temperature ranging from 100 F to 200 F.
[0030] In some embodiments, the set-delayed cement compositions may have desirable thickening times after activation. Thickening time typically refers to the time a fluid, such as a set-delayed cement composition, remains in a fluid state capable of being pumped.
A number of different laboratory techniques may be used to measure thickening time. A
pressurized consistometer, operated in accordance with the procedure set forth in the aforementioned API RP Practice 10B-2, may be used to measure whether a fluid is in a pumpable fluid state. The thickening time may be the time for the treatment fluid to reach 70 Bc and may be reported as the time to reach 70 Bc. In some embodiments, the cement compositions may have a thickening time of greater than about 1 hour, alternatively, greater than about 2 hours, alternatively greater than about 5 hours at 3,000 psi and temperatures in a range of from about 50 F to about 400 F, alternatively, in a range of from about 80 F to about 250 F, and alternatively at a temperature of about 140 F.
A number of different laboratory techniques may be used to measure thickening time. A
pressurized consistometer, operated in accordance with the procedure set forth in the aforementioned API RP Practice 10B-2, may be used to measure whether a fluid is in a pumpable fluid state. The thickening time may be the time for the treatment fluid to reach 70 Bc and may be reported as the time to reach 70 Bc. In some embodiments, the cement compositions may have a thickening time of greater than about 1 hour, alternatively, greater than about 2 hours, alternatively greater than about 5 hours at 3,000 psi and temperatures in a range of from about 50 F to about 400 F, alternatively, in a range of from about 80 F to about 250 F, and alternatively at a temperature of about 140 F.
[0031] Embodiments may include the addition of a cement set activator to the set-delayed cement compositions. Examples of suitable cement set activators include, but are not limited to: zeolites, amines such as triethanolamine, diethanolamine;
silicates such as sodium silicate; zinc formate; calcium acetate; Groups IA and 11A hydroxides such as sodium hydroxide, magnesium hydroxide, and calcium hydroxide; monovalent salts such as sodium chloride; divalent salts such as calcium chloride; nanosilica (i.e., silica having a particle size of less than or equal to about 100 nanometers); polyphosphates; and combinations thereof. In some embodiments, a combination of the polyphosphate and a monovalent salt may be used for activation. The monovalent salt may be any salt that dissociates to form a monovalent cation, such as sodium and potassium salts. Specific examples of suitable monovalent salts include potassium sulfate, and sodium sulfate. A variety of different polyphosphates may be used in combination with the monovalent salt for activation of the set-delayed cement compositions, including polymeric metaphosphate salts, phosphate salts, and combinations thereof. Specific examples of polymeric metaphosphate salts that may be used include sodium hexametaphosphate, sodium trimetaphosphate, sodium tetrametaphosphate, sodium pentametaphosphate, sodium heptametaphosphate, sodium octametaphosphate, and =
combinations thereof. A specific example of a suitable cement set activator comprises a combination of sodium sulfate and sodium hexametaphosphate. In particular embodiments, the activator may be provided and added to the set-delayed cement composition as a liquid additive, for example, a liquid additive comprising a monovalent salt, a polyphosphate, and optionally a dispersant.
silicates such as sodium silicate; zinc formate; calcium acetate; Groups IA and 11A hydroxides such as sodium hydroxide, magnesium hydroxide, and calcium hydroxide; monovalent salts such as sodium chloride; divalent salts such as calcium chloride; nanosilica (i.e., silica having a particle size of less than or equal to about 100 nanometers); polyphosphates; and combinations thereof. In some embodiments, a combination of the polyphosphate and a monovalent salt may be used for activation. The monovalent salt may be any salt that dissociates to form a monovalent cation, such as sodium and potassium salts. Specific examples of suitable monovalent salts include potassium sulfate, and sodium sulfate. A variety of different polyphosphates may be used in combination with the monovalent salt for activation of the set-delayed cement compositions, including polymeric metaphosphate salts, phosphate salts, and combinations thereof. Specific examples of polymeric metaphosphate salts that may be used include sodium hexametaphosphate, sodium trimetaphosphate, sodium tetrametaphosphate, sodium pentametaphosphate, sodium heptametaphosphate, sodium octametaphosphate, and =
combinations thereof. A specific example of a suitable cement set activator comprises a combination of sodium sulfate and sodium hexametaphosphate. In particular embodiments, the activator may be provided and added to the set-delayed cement composition as a liquid additive, for example, a liquid additive comprising a monovalent salt, a polyphosphate, and optionally a dispersant.
[0032] The cement set activator may be added to embodiments of the set-delayed cement composition in an amount sufficient to induce the set-delayed cement composition to set into a hardened mass. In certain embodiments, the cement set activator may be added to the set-delayed cement composition in an amount in the range of about 0.1% to about 20% by weight of the pumice. In specific embodiments, the cement set activator may be present in an amount ranging between any of and/or including any of about 0.1%, about 1%, about 5%, about 10%, about 15%, or about 20% by weight of the pumice. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of cement set activator to include for a chosen application.
[0033] As will be appreciated by those of ordinary skill in the art, embodiments of the set-delayed cement compositions may be used in a variety of subterranean operations, including primary and remedial cementing. In some embodiments, a set-delayed cement composition may be provided that comprises water, pumice, hydrated lime, a synthetic smectite, a set retarder, and optionally a dispersant, a mechanical-property-enhancing additive, or polyethyleneimine. The set-delayed cement composition may be introduced into a subterranean formation and allowed to set therein. As used herein, introducing the set-delayed cement composition into a subterranean formation includes introduction into any portion of the subterranean formation, including, without limitation, into a wellbore drilled into the subterranean formation, into a near wellbore region surrounding the wellbore, or into both.
Embodiments may further include activation of the set-delayed cement composition. The activation of the set-delayed cement composition may comprise, for example, the addition of a cement set activator to the set-delayed cement composition.
Embodiments may further include activation of the set-delayed cement composition. The activation of the set-delayed cement composition may comprise, for example, the addition of a cement set activator to the set-delayed cement composition.
[0034] In some embodiments, a set-delayed cement composition may be provided that comprises water, pumice, hydrated lime, a synthetic smectite, a set retarder, and optionally a dispersant, a mechanical-property-enhancing additive, or polyethyleneimine.
The set-delayed cement composition may be stored, for example, in a vessel or other suitable container. The set-delayed cement composition may be permitted to remain in storage for a desired time period. For example, the set-delayed cement composition may remain in storage for a time period of about 1 day or longer. For example, the set-delayed cement composition may remain in storage for a time period of about 1 day, about 2 days, about 5 days, about 7 days, about 10 days, about 20 days, about 30 days, about 40 days, about 50 days, about 60 days, or longer. In some embodiments, the set-delayed cement composition may remain in storage for a time period in a range of from about 1 day to about 7 days or longer. Thereafter, the set-delayed cement composition may be activated, for example, by addition of a cement set activator, introduced into a subterranean formation, and allowed to set therein.
The set-delayed cement composition may be stored, for example, in a vessel or other suitable container. The set-delayed cement composition may be permitted to remain in storage for a desired time period. For example, the set-delayed cement composition may remain in storage for a time period of about 1 day or longer. For example, the set-delayed cement composition may remain in storage for a time period of about 1 day, about 2 days, about 5 days, about 7 days, about 10 days, about 20 days, about 30 days, about 40 days, about 50 days, about 60 days, or longer. In some embodiments, the set-delayed cement composition may remain in storage for a time period in a range of from about 1 day to about 7 days or longer. Thereafter, the set-delayed cement composition may be activated, for example, by addition of a cement set activator, introduced into a subterranean formation, and allowed to set therein.
[0035] In primary cementing embodiments, for example, embodiments of the set-delayed cement composition may be introduced into an annular space between a conduit located in a wellbore and the walls of a wellbore (and/or a larger conduit in the wellbore), wherein the wellbore penetrates the subterranean formation. The set-delayed cement composition may be allowed to set in the annular space to form an annular sheath of hardened cement. The set-delayed cement composition may form a barrier that prevents the migration of fluids in the wellbore. The set-delayed cement composition may also, for example, support the conduit in the wellbore.
[0036] In remedial cementing embodiments, a set-delayed cement composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs.
By way of example, the set-delayed composition may be placed in a wellbore to plug an opening (e.g., a void or crack) in the formation, in a gravel pack, in the conduit, in the cement sheath, and/or between the cement sheath and the conduit (e.g., a microannulus).
By way of example, the set-delayed composition may be placed in a wellbore to plug an opening (e.g., a void or crack) in the formation, in a gravel pack, in the conduit, in the cement sheath, and/or between the cement sheath and the conduit (e.g., a microannulus).
[0037] An embodiment comprises a method of cementing in a subterranean formation comprising: providing a set-delayed cement composition comprising pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water; introducing the set-delayed cement composition into a subterranean formation; and allowing the set-delayed cement composition to set in the subterranean formation.
[0038] An embodiment comprises a set-delayed cement composition for cementing in a subterranean formation comprising: pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water.
[0039] An embodiment comprises a set-delayed cementing system for cementing in a subterranean formation comprising: a set-delayed cement composition comprising: water, pumice, hydrated lime, a synthetic smectite, and a cement set retarder; a cement set activator for activating the set-delayed cement composition; mixing equipment for mixing the set-delayed cement composition and the cement set activator to produce an activated set-delayed cement composition; and pumping equipment for pumping the activated set-delayed cement composition into the subterranean formation.
[0040] Referring now to FIG. 1, the preparation of a set-delayed cement composition in accordance with example embodiments will now be described. FIG. 1 illustrates a system 2 = CA 02928213 2016-04-20 for the preparation of a set-delayed cement composition and subsequent delivery of the composition to a wellbore in accordance with certain embodiments. As shown, the set-delayed cement composition may be mixed in mixing equipment 4, such as a jet mixer, re-circulating mixer, or a batch mixer, for example, and then pumped via pumping equipment 6 to the wellbore. In some embodiments, the mixing equipment 4 and the pumping equipment 6 may be disposed on one or more cement trucks as will be apparent to those of ordinary skill in the art. In some embodiments, a jet mixer may be used, for example, to continuously mix the lime/settable material with the water as it is being pumped to the wellbore.
In set-delayed embodiments, a re-circulating mixer and/or a batch mixer may be used to mix the set-delayed cement composition, and the activator may be added to the mixer as a powder prior to pumping the cement composition downhole. In lightweight set-delayed cement compositions, a synthetic smectite may be added as a liquid additive mixture with water. This liquid additive may be added to the set-delayed cement composition as it is mixed in mixing equipment 4.
In set-delayed embodiments, a re-circulating mixer and/or a batch mixer may be used to mix the set-delayed cement composition, and the activator may be added to the mixer as a powder prior to pumping the cement composition downhole. In lightweight set-delayed cement compositions, a synthetic smectite may be added as a liquid additive mixture with water. This liquid additive may be added to the set-delayed cement composition as it is mixed in mixing equipment 4.
[0041] An example technique for placing a set-delayed cement composition into a subterranean formation will now be described with reference to FIGS. 2A and 2B. FIG. 2A
illustrates surface equipment 10 that may be used in placement of a set-delayed cement composition in accordance with certain embodiments. It should be noted that while FIG. 2A
generally depicts a land-based operation, those skilled in the art will readily recognize that the principles described herein are equally applicable to subsea operations that employ floating or sea-based platforms and rigs, without departing from the scope of the disclosure. As illustrated by FIG. 2A, the surface equipment 10 may include a cementing unit 12, which may include one or more cement trucks. The cementing unit 12 may include mixing equipment 4 and pumping equipment 6 (e.g., FIG. 1) as will be apparent to those of ordinary skill in the art. The cementing unit 12 may pump a set-delayed cement composition 14 through a feed pipe 16 and to a cementing head 18 which conveys the set-delayed cement composition 14 downhole.
illustrates surface equipment 10 that may be used in placement of a set-delayed cement composition in accordance with certain embodiments. It should be noted that while FIG. 2A
generally depicts a land-based operation, those skilled in the art will readily recognize that the principles described herein are equally applicable to subsea operations that employ floating or sea-based platforms and rigs, without departing from the scope of the disclosure. As illustrated by FIG. 2A, the surface equipment 10 may include a cementing unit 12, which may include one or more cement trucks. The cementing unit 12 may include mixing equipment 4 and pumping equipment 6 (e.g., FIG. 1) as will be apparent to those of ordinary skill in the art. The cementing unit 12 may pump a set-delayed cement composition 14 through a feed pipe 16 and to a cementing head 18 which conveys the set-delayed cement composition 14 downhole.
[0042] Turning now to FIG. 2B, the set-delayed cement composition 14 may be placed into a subterranean formation 20 in accordance with example embodiments. As illustrated, a wellbore 22 may be drilled into the subterranean formation 20.
While wellbore 22 is shown extending generally vertically into the subterranean formation 20, the principles described herein are also applicable to wellbores that extend at an angle through the subterranean formation 20, such as horizontal and slanted wellbores. As illustrated, the wellbore 22 comprises walls 24. In the illustrated embodiment, a surface casing 26 has been inserted into the wellbore 22. The surface casing 26 may be cemented to the walls 24 of the wellbore 22 by cement sheath 28. In the illustrated embodiment, one or more additional conduits (e.g., intermediate casing, production casing, liners, etc.), shown here as casing 30 may also be disposed in the wellbore 22. As illustrated, there is a wellbore annulus 32 formed between the casing 30 and the walls 24 of the wellbore 22 and/or the surface casing 26. One or more centralizers 34 may be attached to the casing 30, for example, to centralize the casing 30 in the wellbore 22 prior to and during the cementing operation.
While wellbore 22 is shown extending generally vertically into the subterranean formation 20, the principles described herein are also applicable to wellbores that extend at an angle through the subterranean formation 20, such as horizontal and slanted wellbores. As illustrated, the wellbore 22 comprises walls 24. In the illustrated embodiment, a surface casing 26 has been inserted into the wellbore 22. The surface casing 26 may be cemented to the walls 24 of the wellbore 22 by cement sheath 28. In the illustrated embodiment, one or more additional conduits (e.g., intermediate casing, production casing, liners, etc.), shown here as casing 30 may also be disposed in the wellbore 22. As illustrated, there is a wellbore annulus 32 formed between the casing 30 and the walls 24 of the wellbore 22 and/or the surface casing 26. One or more centralizers 34 may be attached to the casing 30, for example, to centralize the casing 30 in the wellbore 22 prior to and during the cementing operation.
[0043] With continued reference to FIG. 2B, the set-delayed cement composition may be pumped down the interior of the casing 30. The set-delayed cement composition 14 may be allowed to flow down the interior of the casing 30 through the casing shoe 42 at the bottom of the casing 30 and up around the casing 30 into the wellbore annulus 32. The set-delayed cement composition 14 may be allowed to set in the wellbore annulus 32, for example, to form a cement sheath that supports and positions the casing 30 in the wellbore 22. While not illustrated, other techniques may also be utilized for introduction of the set-delayed cement composition 14. By way of example, reverse circulation techniques may be used that include introducing the set-delayed cement composition 14 into the subterranean formation 20 by way of the wellbore annulus 32 instead of through the casing 30.
[0044] As it is introduced, the set-delayed cement composition 14 may displace other fluids 36, such as drilling fluids and/or spacer fluids that may be present in the interior of the casing 30 and/or the wellbore annulus 32. At least a portion of the displaced fluids 36 may exit the wellbore annulus 32 via a flow line 38 and be deposited, for example, in one or more retention pits 40 (e.g., a mud pit), as shown on FIG. 2A. Referring again to FIG. 2B, a bottom plug 44 may be introduced into the wellbore 22 ahead of the set-delayed cement composition 14, for example, to separate the set-delayed cement composition 14 from the fluids 36 that may be inside the casing 30 prior to cementing. After the bottom plug 44 reaches the landing collar 46, a diaphragm or other suitable device should rupture to allow the set-delayed cement composition 14 through the bottom plug 44. In FIG. 2B, the bottom plug 44 is shown on the landing collar 46. In the illustrated embodiment, a top plug 48 may be introduced into the wellbore 22 behind the set-delayed cement composition 14. The top plug 48 may separate the set-delayed cement composition 14 from a displacement fluid 50 and also push the set-delayed cement composition 14 through the bottom plug 44.
[0045] The exemplary set-delayed cement compositions disclosed herein may directly or indirectly affect one or more components or pieces of equipment associated with the preparation, delivery, recapture, recycling, reuse, and/or disposal of the disclosed set-delayed cement compositions. For example, the disclosed set-delayed cement compositions may directly or indirectly affect one or more mixers, related mixing equipment, mud pits, storage facilities or units, composition separators, heat exchangers, sensors, gauges, pumps, compressors, and the like used generate, store, monitor, regulate, and/or recondition the = = CA 02928213 2016-04-20 exemplary set-delayed cement compositions. The disclosed set-delayed cement compositions may also directly or indirectly affect any transport or delivery equipment used to convey the set-delayed cement compositions to a well site or downhole such as, for example, any transport vessels, conduits, pipelines, trucks, tubulars, and/or pipes used to compositionally move the set-delayed cement compositions from one location to another, any pumps, compressors, or motors (e.g., topside or downhole) used to drive the set-delayed cement compositions into motion, any valves or related joints used to regulate the pressure or flow rate of the set-delayed cement compositions, and any sensors (i.e., pressure and temperature), gauges, and/or combinations thereof, and the like. The disclosed set-delayed cement compositions may also directly or indirectly affect the various downhole equipment and tools that may come into contact with the set-delayed cement compositions such as, but not limited to, wellbore casing, wellbore liner, completion string, insert strings, drill string, coiled tubing, slickline, wireline, drill pipe, drill collars, mud motors, downhole motors and/or pumps, cement pumps, surface-mounted motors and/or pumps, centralizers, turbolizers, scratchers, floats (e.g., shoes, collars, valves, etc.), logging tools and related telemetry equipment, actuators (e.g., electromechanical devices, hydrornechanical devices, etc.), sliding sleeves, production sleeves, plugs, screens, filters, flow control devices (e.g., inflow control devices, autonomous inflow control devices, outflow control devices, etc.), couplings (e.g., electro-hydraulic wet connect, dry connect, inductive coupler, etc.), control lines (e.g., electrical, fiber optic, hydraulic, etc.), surveillance lines, drill bits and reamers, sensors or distributed sensors, downhole heat exchangers, valves and corresponding actuation devices, tool seals, packers, cement plugs, bridge plugs, and other wellbore isolation devices, or components, and the like.
[0046] To fticilitate a better understanding of the present embodiments, the following examples of certain aspects of some embodiments are given. In no way should the following examples be read to limit, or define, the entire scope of the embodiments.
EXAMPLES
Example 1
EXAMPLES
Example 1
[0047] The following example describes a set-delayed cement composition comprising the following components:
Table 1 Compositional Makeup Component Amount Pumice 250g Lime 50g Fluid Loss Control Additive 3 g Synthetic Smectite 3 g Dispersant 7.1 g Retarder 6.4 g Water 301 g
Table 1 Compositional Makeup Component Amount Pumice 250g Lime 50g Fluid Loss Control Additive 3 g Synthetic Smectite 3 g Dispersant 7.1 g Retarder 6.4 g Water 301 g
[0048] The synthetic smectite was blended in 301 grams of water at 1000 rpm in a Waring Blender for 1 minute. Following this blending step, the dispersant and the retarder were added to the synthetic smectite mixture. The mixture was then blended for another minute at 1000 rpm. Following this blending step, the pumice, lime, and fluid loss control additive were added and blended with the mixture according to API Recommended Practice for Testing Well Cements, API Recommended Practice 10B-2. The fluid loss control additive was HALAD -344 fluid loss additive available from Halliburton Energy Services, Inc., Houston, Texas. The synthetic smectite was Laponite RD available from Southern Clay Products, Inc., Gonzales, Texas. The dispersant was Coatex Ethacryl G dispersant available from Coatex, Chester, South Carolina. The cement retarder was Dequest 2006 available from ltalmatch Chemicals, Red Bank, New Jersey.
[0049] After preparation, the rheological properties of the sample were measured using a Model 35A Fann Viscometer and a No. 2 spring with a Fann Yield Stress Adapter (FYSA), in accordance with the procedure set forth in API RP Practice 10B-2, Recommended Practice for Testing Well Cements. The results are presented in Table 2 below.
Table 2 Rheological Profile FYSA Readings (Centipoise) Up Reading 7 10 32 50 69 Down Reading 3 4 29 48
Table 2 Rheological Profile FYSA Readings (Centipoise) Up Reading 7 10 32 50 69 Down Reading 3 4 29 48
[0050] The slurry remained stable for more than 2 weeks and displayed no free water or solids settling. The slurry was activated with 4.0 grams of Na2SO4 and 4.0 grams of sodium hexametaphosphate. The destructive compressive strength was measured by allowing the sample to cure for 24 hours in a 2" by 4" plastic cylinder that was placed in a water bath at 140 F to form a set cylinder. Immediately after removal from the water bath, destructive compressive strengths were determined using a mechanical press in accordance with API RP
10B-2, Recommended Practice for Testing Well Cements. The sample had a 24 hour =
compressive strength of 121 psi. The reported compressive strengths are an average for two cylinders of each sample. The Archimedes Method was used to measure the slurry density of the sample in top, middle, and bottom portions. The density was uniform for all three sections and was 11.15 pounds per gallon.
Example 2
10B-2, Recommended Practice for Testing Well Cements. The sample had a 24 hour =
compressive strength of 121 psi. The reported compressive strengths are an average for two cylinders of each sample. The Archimedes Method was used to measure the slurry density of the sample in top, middle, and bottom portions. The density was uniform for all three sections and was 11.15 pounds per gallon.
Example 2
[0051] The following example describes a set-delayed cement composition comprising the following components:
Table 3 Compositional Makeup Component Amount Pumice 125g Lime 25 g Fluid Loss Control Additive 3 g Synthetic Smectite 3 g Dispersant 2.7g Retarder 6.4g Water 301 g
Table 3 Compositional Makeup Component Amount Pumice 125g Lime 25 g Fluid Loss Control Additive 3 g Synthetic Smectite 3 g Dispersant 2.7g Retarder 6.4g Water 301 g
[0052] The synthetic smectite was blended in 301 grams of water at 1000 rpm in a Waring Blender for I minute. Following this blending step, the dispersant and the retarder were added to the synthetic smectite mixture. The mixture was then blended for another minute at 1000 rpm. Following this blending step, the pumice, lime, and fluid loss control additive were added and blended with the mixture in accordance with API RP 10B-2, Recommended Practice for Testing Well Cements. The fluid loss control additive was HALAID -344 fluid loss additive available from Halliburton Energy Services, Inc., Houston, Texas. The synthetic smectite was Laponite RD available from Southern Clay Products, Inc., Gonzales, Texas. The dispersant was Coatex Ethacryl G dispersant available from Coatex, Chester, South Carolina.
The cement retarder was Dequest 2006 available from Italmatch Chemicals, Red Bank, New Jersey.
The cement retarder was Dequest 2006 available from Italmatch Chemicals, Red Bank, New Jersey.
[0053] After preparation, the rheological properties of the sample were measured using a Model 35A Fann Viscometer and a No. 2 spring with a Fann Yield Stress Adapter (FYSA), in accordance with the procedure set forth in API RP Practice 10B-2, Recommended Practice for Testing Well Cements. The results are presented in Table 4 below.
Table 4 Rheologieal Profile FYSA Readings (Centipoise) Up Reading 4 6 14 22 30 Down Reading 2 3 11 19
Table 4 Rheologieal Profile FYSA Readings (Centipoise) Up Reading 4 6 14 22 30 Down Reading 2 3 11 19
[0054] The slurry remained stable for more than 2 weeks and displayed no free water or solids settling. The Archimedes Method was used to measure the slurry density of the sample in top, middle, and bottom portions. The density was uniform for all three sections and was 9.45 pounds per gallon.
Example 3
Example 3
[0055] The following example describes a set-delayed cement composition comprising the following components:
Table 5 Compositional Makeup Component Amount Pumice 500 g Lime 100 g Fluid Loss Control Additive 3 g Dispersant 9.2 g Retarder 6.4 g Water 301 g
Table 5 Compositional Makeup Component Amount Pumice 500 g Lime 100 g Fluid Loss Control Additive 3 g Dispersant 9.2 g Retarder 6.4 g Water 301 g
[0056] The dispersant and the retarder were added to 301 g of water. The mixture was then blended for a minute at 1000 rpm in a Waring* Blender. Following this blending step, the pumice, lime, and fluid loss control additive were added and blended with the mixture according to API RP 10B-2, Recommended Practice for Testing Well Cements. The fluid loss control additive was HALADe-344 fluid loss additive available from Halliburton Energy Services, Inc., Houston, Texas. The dispersant was Coatex Ethacryl G
dispersant available from Coatex, Chester, South Carolina. The cement retarder was Dequest 2006 available from Italmatch Chemicals, Red Bank, New Jersey. The slurry had a density of 13. 2 pounds per gallon.
dispersant available from Coatex, Chester, South Carolina. The cement retarder was Dequest 2006 available from Italmatch Chemicals, Red Bank, New Jersey. The slurry had a density of 13. 2 pounds per gallon.
[0057] A liquid additive was prepared separate from the slurry comprising 300 g of water and 7 g of synthetic smectite. The synthetic smectite was Laponite RD
available from Southern Clay Products, Inc., Gonzales, Texas. The liquid additive was blended at 1000 rpm in a Waring Blender for one minute. 200 mL of the 13.2 PPG cement slurry was added to the liquid additive. The final density of the slurry was 10.3 PPG.
available from Southern Clay Products, Inc., Gonzales, Texas. The liquid additive was blended at 1000 rpm in a Waring Blender for one minute. 200 mL of the 13.2 PPG cement slurry was added to the liquid additive. The final density of the slurry was 10.3 PPG.
[0058] After preparation, the rheological properties of the sample were measured using a Model 35A Fann Viscometer and a No. 2 spring with a Fann Yield Stress Adapter (FYSA), in accordance with the procedure set forth in API RP Practice 10B-2, Recommended Practice for Testing Well Cements. The results are presented in Table 6 below.
Table 6 Rheological Profile FYSA Readings (Centipoise) Up Reading 8 9 11 12 13 Down Reading 6 6 8 10
Table 6 Rheological Profile FYSA Readings (Centipoise) Up Reading 8 9 11 12 13 Down Reading 6 6 8 10
[0059] The slurry remained stable for more than 2 weeks and displayed some free water but no solids settling.
Example 4
Example 4
[0060] The following example describes a set-delayed cement composition comprising the following components:
Table 7 Compositional Makeup Component Amount Pumice 500 g Lime 100 g Fluid Loss Control Additive 3 g Dispersant 11.8 g Retarder 4.2 g Water 300 g
Table 7 Compositional Makeup Component Amount Pumice 500 g Lime 100 g Fluid Loss Control Additive 3 g Dispersant 11.8 g Retarder 4.2 g Water 300 g
[0061] The dispersant and the retarder were added to 300 g of water.
The mixture was then blended for a minute at 1000 rpm in a Waring Blender. Following this blending step, the pumice, lime, and fluid loss control additive were added and blended with the mixture according to API RP 10B-2, Recommended Practice for Testing Well Cements. The slurry was left to sit for 24 hours. It displayed no solids settling and was flowable. The fluid loss control additive was HALAD -344 fluid loss additive available from Halliburton Energy Services, Inc., Houston, Texas. The dispersant was Coatex XPl7O2TM dispersant available from Coatex, = CA 02928213 2016-04-20 Chester, South Carolina. The cement retarder was Dequest 2006 available from ltalmatch Chemicals, Red Bank, New Jersey.
The mixture was then blended for a minute at 1000 rpm in a Waring Blender. Following this blending step, the pumice, lime, and fluid loss control additive were added and blended with the mixture according to API RP 10B-2, Recommended Practice for Testing Well Cements. The slurry was left to sit for 24 hours. It displayed no solids settling and was flowable. The fluid loss control additive was HALAD -344 fluid loss additive available from Halliburton Energy Services, Inc., Houston, Texas. The dispersant was Coatex XPl7O2TM dispersant available from Coatex, = CA 02928213 2016-04-20 Chester, South Carolina. The cement retarder was Dequest 2006 available from ltalmatch Chemicals, Red Bank, New Jersey.
[0062] Three individual samples of 300 g each were taken from the cement slurry and each sample was mixed with a different liquid additive comprising synthetic smectite and water. The liquid additive compositions are described in Table 8 below.
Table 8 Liquid Additive Makeup Liquid Additive Mixture Liquid Additive Mixture 1 Liquid Additive Mixture 2 Component Amount Component Amount Component Amount Water 100 g Water 100 g Water 100 g Synthetic Synthetic Smectite 1 g Synthetic Smectite 1 g 1 g Smectite Polyethyleneimine 1g Polyethyleneimine I g Viscosifier 0.25 g Carbon Fibers 3.33 g Carbon Fibers 3.33 g
Table 8 Liquid Additive Makeup Liquid Additive Mixture Liquid Additive Mixture 1 Liquid Additive Mixture 2 Component Amount Component Amount Component Amount Water 100 g Water 100 g Water 100 g Synthetic Synthetic Smectite 1 g Synthetic Smectite 1 g 1 g Smectite Polyethyleneimine 1g Polyethyleneimine I g Viscosifier 0.25 g Carbon Fibers 3.33 g Carbon Fibers 3.33 g
[0063] The synthetic smectite was Laponite RD available from Southern Clay Products, Inc., Gonzales, Texas. The carbon fibers were WellLife 684 additive available from Halliburton Energy Services, Inc. Houston, Texas. The viscosifier was SA-1015"
available from Halliburton Energy Services, Inc., Houston, TX. The polyethyleneimine is a linear poly(ethyleneimine) with an average molecular weight of 60,000 daltons, it is available commercially from Sigma-Aldrich, St. Louis, Missouri. Each liquid additive mixture was blended at 1000 rpm in a Waring Blender for one minute.
available from Halliburton Energy Services, Inc., Houston, TX. The polyethyleneimine is a linear poly(ethyleneimine) with an average molecular weight of 60,000 daltons, it is available commercially from Sigma-Aldrich, St. Louis, Missouri. Each liquid additive mixture was blended at 1000 rpm in a Waring Blender for one minute.
[0064] Each slurry was allowed to sit for 24 hours. No solids settling or free water were observed in any sample. The slurry was activated with 4.0 grams of Na2SO4 (1.3% by weight of the pumice) and 4.0 grams of sodium hexametaphosphate (1.3% by weight of the pumice). The destructive compressive strength was measured by allowing each sample to cure for 24 hours in a 2" by 4" plastic cylinder that was placed in a water bath at 140 F to form a set cylinder. Immediately after removal from the water bath, destructive compressive strengths were determined using a mechanical press in accordance with API RP 10B-2, Recommended Practice for Testing Well Cements. The reported compressive strengths are an average for two cylinders of each sample. The Archimedes Method was used to measure the slurry density of the sample in top, middle, and bottom portions. The density was uniform for all three slurries and was 11.2 pounds per gallon. Compressive strength data is displayed in Table 9 below.
= CA 02928213 2016-04-20 Table 9 Compressive Strength Profile Liquid Additive Mixture 1 Liquid Additive Mixture 2 Liquid Additive Mixture 3 366 13 psi 430 psi 398 6 psi 17% increase 9% increase
= CA 02928213 2016-04-20 Table 9 Compressive Strength Profile Liquid Additive Mixture 1 Liquid Additive Mixture 2 Liquid Additive Mixture 3 366 13 psi 430 psi 398 6 psi 17% increase 9% increase
[0065] As illustrated in the table above, the liquid additive mixtures with the carbon fibers provided an 11.2 ppg set-delayed cement composition and a 9-17%
increase in 24 hour compressive strength.
Example 5
increase in 24 hour compressive strength.
Example 5
[0066] The following example describes a set-delayed cement composition comprising the following components:
Table 10 Compositional Makeup Component Amount Unit Pumice 100 %bwoP
Lime 19.8 %bwoP
Weighting Agent 2.06 %bwoP
Dispersant 1.8 %bwoP
Primary Retarder 0.06 Gal/sk Secondary Retarder 0.516 %bwoP
Water 64.1 %bwoP
%bwoP = percent by weight of the pumice; Gal/sk = gallons per 46 lb. sack of pumice
Table 10 Compositional Makeup Component Amount Unit Pumice 100 %bwoP
Lime 19.8 %bwoP
Weighting Agent 2.06 %bwoP
Dispersant 1.8 %bwoP
Primary Retarder 0.06 Gal/sk Secondary Retarder 0.516 %bwoP
Water 64.1 %bwoP
%bwoP = percent by weight of the pumice; Gal/sk = gallons per 46 lb. sack of pumice
[0067] The mixture was then blended for one minute at 1000 rpm Waring Blender for 1 minute according to API RP 10B-2, Recommended Practice for Testing Well Cements.
The weighting agent was MICROMAX weight additive available from Halliburton Energy Services, Inc., Houston, Texas. The dispersant was Coatex Ethaeryl G
dispersant available from Coatex, Chester, South Carolina. The primary cement retarder was Micro Matrix Cement Retarder available from Halliburton Energy Services, Inc., Houston, Texas. The secondary cement retarder was HR 5 retarder available from Halliburton Energy Services, Inc., Houston, Texas.
The weighting agent was MICROMAX weight additive available from Halliburton Energy Services, Inc., Houston, Texas. The dispersant was Coatex Ethaeryl G
dispersant available from Coatex, Chester, South Carolina. The primary cement retarder was Micro Matrix Cement Retarder available from Halliburton Energy Services, Inc., Houston, Texas. The secondary cement retarder was HR 5 retarder available from Halliburton Energy Services, Inc., Houston, Texas.
[0068] After preparation, an experimental sample comprising a liquid additive was prepared. The liquid additive comprised synthetic smectite (i.e. Laponite RD
available from Southern Clay Products, Inc., Gonzales, Texas) and water. 250 g a 1% (by weight of water) aqueous synthetic smectite liquid additive was added to 600 g of the cement slurry described =
in Table 10 above. 16.6 g (5.2% by weight of the pumice) of CaC12 was then added to this resulting mixture to activate the slurry. The slurry was then blended for 30 seconds at 4000 rpm in a Waring Blender.
available from Southern Clay Products, Inc., Gonzales, Texas) and water. 250 g a 1% (by weight of water) aqueous synthetic smectite liquid additive was added to 600 g of the cement slurry described =
in Table 10 above. 16.6 g (5.2% by weight of the pumice) of CaC12 was then added to this resulting mixture to activate the slurry. The slurry was then blended for 30 seconds at 4000 rpm in a Waring Blender.
[0069] A control sample was then prepared that comprised 600 of the cement slurry described in Table 10 above and an additional 250 g of water. No synthetic smectite was present in the control sample. 16.6 g (5.2% by weight of the pumice) of CaCl2 was then added to this resulting mixture to activate the slurry. The slurry was then blended for 30 seconds at 4000 rpm in a Waring e Blender.
[0070] The experimental sample and the control sample were then placed into 2"
by 4" plastic cylinders that were placed in a water bath at 140 F for one week to form a set cylinder. The Archimedes Method was used to measure the slurry density of each sample in top, middle, and bottom portions. The densities are described in Table 11 below.
Table 11 Sample Densities Experimental Sample Control Sample Top 10.810 Top 9.9086 Middle 10.946 Middle 9.9395 Bottom 10.987 Bottom 10.253
by 4" plastic cylinders that were placed in a water bath at 140 F for one week to form a set cylinder. The Archimedes Method was used to measure the slurry density of each sample in top, middle, and bottom portions. The densities are described in Table 11 below.
Table 11 Sample Densities Experimental Sample Control Sample Top 10.810 Top 9.9086 Middle 10.946 Middle 9.9395 Bottom 10.987 Bottom 10.253
[0071] The control sample had free water and solids settling. The experimental sample had no free water and only minimal solids settling was observed.
[0072] It should be understood that the compositions and methods are described in terms of "comprising," "containing," or "including" various components or steps, the compositions and methods can also "consist essentially of' or "consist of' the various components and steps. Moreover, the indefinite articles "a" or "an," as used in the claims, are defined herein to mean one or more than one of the element that it introduces.
[0073] For the sake of brevity, only certain ranges are explicitly disclosed herein.
However, ranges from any lower limit may be combined with any upper limit to recite a range not explicitly recited, as well as, ranges from any lower limit may be combined with any other lower limit to recite a range not explicitly recited, in the same way, ranges from any upper limit may be combined with any other upper limit to recite a range not explicitly recited.
Additionally, whenever a numerical range with a lower limit and an upper limit is disclosed, any number and any included range falling within the range are specifically disclosed. In particular, every range of values (of the form, "from about a to about b," or, equivalently, "from approximately a to b," or, equivalently, "from approximately a-b") disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values even if not explicitly recited. Thus, every point or individual value may serve as its own lower or upper limit combined with any other point or individual value or any other lower or upper limit, to recite a range not explicitly recited.
However, ranges from any lower limit may be combined with any upper limit to recite a range not explicitly recited, as well as, ranges from any lower limit may be combined with any other lower limit to recite a range not explicitly recited, in the same way, ranges from any upper limit may be combined with any other upper limit to recite a range not explicitly recited.
Additionally, whenever a numerical range with a lower limit and an upper limit is disclosed, any number and any included range falling within the range are specifically disclosed. In particular, every range of values (of the form, "from about a to about b," or, equivalently, "from approximately a to b," or, equivalently, "from approximately a-b") disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values even if not explicitly recited. Thus, every point or individual value may serve as its own lower or upper limit combined with any other point or individual value or any other lower or upper limit, to recite a range not explicitly recited.
[0074]
Therefore, the present embodiments are well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. The particular embodiments disclosed above are illustrative only, as the present embodiments may be modified and practiced in different but equivalent manners apparent to those skilled in the art having the benefit of the teachings herein. Although individual embodiments are discussed, all combinations of each embodiment are contemplated and covered by the disclosure. Furthermore, no limitations are intended to the details of construction or design herein shown, other than as described in the claims below. Also, the terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee. It is therefore evident that the particular illustrative embodiments disclosed above may be altered or modified and all such variations are considered within the scope and spirit of the present disclosure. If there is any conflict in the usages of a word or term in this specification and one or more patent(s) or other documents, the definitions that are consistent with this specification should be adopted.
Therefore, the present embodiments are well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. The particular embodiments disclosed above are illustrative only, as the present embodiments may be modified and practiced in different but equivalent manners apparent to those skilled in the art having the benefit of the teachings herein. Although individual embodiments are discussed, all combinations of each embodiment are contemplated and covered by the disclosure. Furthermore, no limitations are intended to the details of construction or design herein shown, other than as described in the claims below. Also, the terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee. It is therefore evident that the particular illustrative embodiments disclosed above may be altered or modified and all such variations are considered within the scope and spirit of the present disclosure. If there is any conflict in the usages of a word or term in this specification and one or more patent(s) or other documents, the definitions that are consistent with this specification should be adopted.
Claims (20)
1. A method of cementing in a subterranean formation comprising:
providing a set-delayed cement composition comprising pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns;
introducing the set-delayed cement composition into a subterranean formation;
and allowing the set-delayed cement composition to set in the subterranean formation.
providing a set-delayed cement composition comprising pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns;
introducing the set-delayed cement composition into a subterranean formation;
and allowing the set-delayed cement composition to set in the subterranean formation.
2. A method according to claim 1 further comprising preparing the set-delayed cement composition wherein preparing the set-delayed cement composition comprises adding the synthetic smectite to a heavier set-delayed cement composition as a liquid additive comprising the synthetic smectite and water.
3. A method according to claim 2 wherein the liquid additive is added to the heavier set-delayed cement composition to reduce the density of the heavier set-delayed cement composition to a range of 4 pounds per gallon to 12 pounds per gallon.
4. A method according to any one of claims 1 to 3 wherein the set-delayed cement composition comprises a mechanical-property-enhancing additive.
5. A method according to claim 4 wherein the mechanical-property enhancing additive comprises carbon fibers.
6. A method according to any one of claims 1 to 5 wherein the set-delayed cement composition comprises polyethyleneimine.
7. A method according to either one of claims 1 or 2 wherein the set-delayed cement composition has a density in a range of 8 pounds per gallon to 12 pounds per gallon.
8. A method according to any one of claims 1 to 7 wherein the pumice has a mean particle size in a range of 10 micron to 25 microns.
9. A method according to any one of claims 1 to 8 wherein the pumice and the hydrated lime are present in a weight ratio of pumice to hydrated lime of 10:1 to 1:1.
10. A method according to any one of claims 1 to 9 wherein the cement set retarder comprises at least one retarder selected from the group consisting of a phosphonic acid, a phosphonic acid derivative, a lignosulfonate, a salt, an organic acid, a carboxymethylated hydroxyethylated cellulose, a synthetic co- or ter-polymer comprising sulfonate and carboxylic acid groups, a borate compound, and any mixture thereof.
11. A method according to any one of claims 1 to 10 wherein the set-delayed cement composition further comprises a dispersant and wherein the dispersant comprises at least one dispersant selected from the group consisting of a sulfonated-formaldehyde-based dispersant, a polycarboxylated ether dispersant, and any combination thereof.
12. A method according to any one of claims 1 to 11 wherein the set-delayed cement composition remains in a pumpable fluid state for a time period of at least 7 days prior to the activating.
13. A method according to any one of claims 1 to 12 further comprising adding a cement set activator to the set-delayed cement composition.
14. A set-delayed cement composition for cementing in a subterranean formation comprising:
pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns.
pumice, hydrated lime, a cement set retarder, a synthetic smectite, and water, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns.
15. A composition according to claim 14 wherein the set-delayed cement composition further comprises a mechanical-property-enhancing additive.
16. A composition according to claim 15 wherein the mechanical-property enhancing additive comprises carbon fibers.
17. A composition according to any one of claims 14 to 16 wherein the set-delayed cement composition further comprises polyethyleneimine.
18. A composition according to any one of claims 14 to 17 wherein the set-delayed cement composition has a density in a range of 8 pounds per gallon to 14 pounds per gallon.
19. A set-delayed cementing system for cementing in a subterranean formation comprising:
a set-delayed cement composition comprising:
water, pumice, hydrated lime a synthetic smectite, and a cement set retarder, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns;
a cement set activator for activating the set-delayed cement composition;
mixing equipment for mixing the set-delayed cement composition and the cement set activator to produce an activated set-delayed cement composition; and pumping equipment for pumping the activated set-delayed cement composition into the subterranean formation.
a set-delayed cement composition comprising:
water, pumice, hydrated lime a synthetic smectite, and a cement set retarder, wherein the pumice has a mean particle size in a range of 1 micron to 200 microns;
a cement set activator for activating the set-delayed cement composition;
mixing equipment for mixing the set-delayed cement composition and the cement set activator to produce an activated set-delayed cement composition; and pumping equipment for pumping the activated set-delayed cement composition into the subterranean formation.
20. A system according to claim 19 wherein the set-delayed cement composition further comprises a mechanical-property-enhancing additive and/or polyethyleimine.
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US14/098,198 US9580638B2 (en) | 2012-03-09 | 2013-12-05 | Use of synthetic smectite in set-delayed cement compositions |
US14/098,198 | 2013-12-05 | ||
PCT/US2014/068804 WO2015085177A1 (en) | 2013-12-05 | 2014-12-05 | Use of synthetic smectite in set-delayed cement compositions comprising pumice |
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