CA2921425A1 - Cement set activators for cement compositions and associated methods - Google Patents
Cement set activators for cement compositions and associated methods Download PDFInfo
- Publication number
- CA2921425A1 CA2921425A1 CA2921425A CA2921425A CA2921425A1 CA 2921425 A1 CA2921425 A1 CA 2921425A1 CA 2921425 A CA2921425 A CA 2921425A CA 2921425 A CA2921425 A CA 2921425A CA 2921425 A1 CA2921425 A1 CA 2921425A1
- Authority
- CA
- Canada
- Prior art keywords
- cement composition
- zeolite
- pozzolan
- cement
- delayed
- 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.)
- Granted
Links
- 239000004568 cement Substances 0.000 title claims abstract description 247
- 239000000203 mixture Substances 0.000 title claims abstract description 208
- 239000012190 activator Substances 0.000 title claims abstract description 55
- 238000000034 method Methods 0.000 title claims abstract description 39
- 239000010457 zeolite Substances 0.000 claims abstract description 99
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 83
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 82
- 239000000920 calcium hydroxide Substances 0.000 claims abstract description 38
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims abstract description 38
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims abstract description 37
- 235000011116 calcium hydroxide Nutrition 0.000 claims abstract description 37
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 33
- 238000011161 development Methods 0.000 claims abstract description 21
- 239000002270 dispersing agent Substances 0.000 claims description 42
- 239000008262 pumice Substances 0.000 claims description 23
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000010881 fly ash Substances 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 13
- 230000004913 activation Effects 0.000 claims description 11
- 150000001768 cations Chemical class 0.000 claims description 7
- 238000005086 pumping Methods 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 6
- 150000003007 phosphonic acid derivatives Chemical class 0.000 claims description 6
- -1 borate compound Chemical class 0.000 claims description 5
- 229910021487 silica fume Inorganic materials 0.000 claims description 4
- 229920001732 Lignosulfonate Polymers 0.000 claims description 3
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 abstract description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
- 239000012530 fluid Substances 0.000 description 23
- 239000000654 additive Substances 0.000 description 21
- 238000012360 testing method Methods 0.000 description 20
- 239000011734 sodium Substances 0.000 description 18
- 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 17
- 229910052708 sodium Inorganic materials 0.000 description 17
- 239000002245 particle Substances 0.000 description 16
- 230000008901 benefit Effects 0.000 description 10
- 238000003860 storage Methods 0.000 description 9
- 239000000377 silicon dioxide Substances 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 7
- 230000008719 thickening Effects 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000008186 active pharmaceutical agent Substances 0.000 description 6
- 239000010754 BS 2869 Class F Substances 0.000 description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 5
- 235000011941 Tilia x europaea Nutrition 0.000 description 5
- 230000001066 destructive effect Effects 0.000 description 5
- 230000001965 increasing effect Effects 0.000 description 5
- 239000004571 lime Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229920000388 Polyphosphate Polymers 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 230000003111 delayed effect Effects 0.000 description 4
- 239000001205 polyphosphate Substances 0.000 description 4
- 235000011176 polyphosphates Nutrition 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 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
- 238000009472 formulation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000000246 remedial effect Effects 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 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
- 239000011398 Portland cement Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000002585 base 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
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 229910002026 crystalline silica Inorganic materials 0.000 description 2
- 229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 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 2
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate 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
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 208000005156 Dehydration Diseases 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
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 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
- 239000003513 alkali Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 229910001579 aluminosilicate mineral Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000010428 baryte Substances 0.000 description 1
- 229910052601 baryte Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 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
- JLDKGEDPBONMDR-UHFFFAOYSA-N calcium;dioxido(oxo)silane;hydrate Chemical compound O.[Ca+2].[O-][Si]([O-])=O JLDKGEDPBONMDR-UHFFFAOYSA-N 0.000 description 1
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 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
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 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
- 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
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- YIBPLYRWHCQZEB-UHFFFAOYSA-N formaldehyde;propan-2-one Chemical compound O=C.CC(C)=O YIBPLYRWHCQZEB-UHFFFAOYSA-N 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 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
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- YDZQQRWRVYGNER-UHFFFAOYSA-N iron;titanium;trihydrate Chemical compound O.O.O.[Ti].[Fe] YDZQQRWRVYGNER-UHFFFAOYSA-N 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
- UPRXAOPZPSAYHF-UHFFFAOYSA-N lithium;cyclohexyl(propan-2-yl)azanide Chemical compound CC(C)N([Li])C1CCCCC1 UPRXAOPZPSAYHF-UHFFFAOYSA-N 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
- 230000014759 maintenance of location Effects 0.000 description 1
- ZWXOQTHCXRZUJP-UHFFFAOYSA-N manganese(2+);manganese(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Mn+2].[Mn+3].[Mn+3] ZWXOQTHCXRZUJP-UHFFFAOYSA-N 0.000 description 1
- 125000005341 metaphosphate group Chemical group 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 235000019691 monocalcium phosphate Nutrition 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 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
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001296 polysiloxane 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
- 239000000047 product Substances 0.000 description 1
- 238000004549 pulsed laser deposition Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 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
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 230000034655 secondary growth Effects 0.000 description 1
- 229910021646 siderite Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 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
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 description 1
- 210000003537 structural cell Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid 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
- 238000001771 vacuum deposition Methods 0.000 description 1
- 239000011800 void material 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
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B33/00—Sealing or packing boreholes or wells
- E21B33/10—Sealing or packing boreholes or wells in the borehole
- E21B33/13—Methods or devices for cementing, for plugging holes, crevices or the like
- E21B33/138—Plastering the borehole wall; Injecting into the formation
-
- 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
- C04B14/047—Zeolites
-
- 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
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/003—Phosphorus-containing compounds
-
- 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
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/16—Sulfur-containing compounds
- C04B24/20—Sulfonated aromatic compounds
- C04B24/22—Condensation or polymerisation products thereof
- C04B24/226—Sulfonated naphtalene-formaldehyde condensation products
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- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2605—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing polyether side chains
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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
- C04B28/02—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 hydraulic cements other than calcium sulfates
- C04B28/10—Lime cements or magnesium oxide cements
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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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- 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
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/06—Inhibiting the setting, e.g. mortars of the deferred action type containing water in breakable containers ; Inhibiting the action of active ingredients
- C04B40/0658—Retarder inhibited mortars activated by the addition of accelerators or retarder-neutralising agents
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- 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
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- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/0068—Ingredients with a function or property not provided for elsewhere in C04B2103/00
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Abstract
Disclosed herein are cement compositions and methods of using cement compositions in subterranean formations. An embodiment comprises a method of cementing in a subterranean formation comprising: providing a cement composition comprising water, a pozzolan, hydrated lime, and a zeolite activator; introducing the cement composition into a subterranean formation; and allowing the cement composition to set in the subterranean formation, wherein the zeolite activator accelerates compressive strength development of the cement composition.
Description
Attorney Docket No. 2011-1P-051250U1P4 PCT
CEMENT SET ACTWATORS FOR CEMENT COMPOSITIONS AND
ASSOCIATED METHODS
BACKGROUND
[000 I} The present 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.
CEMENT SET ACTWATORS FOR CEMENT COMPOSITIONS AND
ASSOCIATED METHODS
BACKGROUND
[000 I} The present 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 she-ath 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 prevents the migration of fluids in the annulus and protects the pipe string from corrosion.
Cement compositions may also be used in remedial cementing methods to seal cracks or holes in pipe strings or cement sheaths, to seal highly pemeable formation zones or fractures, or to place a cement plug and the like.
[00031 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., 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 activation and consequently develop reasonable compressive strengths. For example, a cement set activator may be added to a set-delayed cement composition to induce the composition to set into a hardened mass.
Among other things, set-delayed cement compositions may be suitable for use in wellbore applications such as applications where it is desirable to prepare the cement composition in advance. This may allow the cement composition to be stored prior to use. In addition, this may allow the cement composition to be prepared at a convenient location before transportation to the job site. Accordingly, capital expenditures may be reduced due to a reduction in the need for on-SUBSTITUTE SHEET (RULE 26) 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. In addition, it may be problematic to activate some set-delayed cement compositions while maintaining acceptable thickening times and compressive strength development.
SUBSTITUTE SHEET (RULE 26) BRIEF DESCRIPTION OF THE DRAWINGS
1100051 These drawings illustrate certain aspects of some of the embodiments of the present methods and compositions, and should not be used to limit or define the methods or compositions.
100061 FIG. I illustrates a system for preparation and delivery of a cement composition to a wellbore in accordance with certain embodiments.
NOM FIG. 2A illustrates surface equipment that may be used in placement of a cement composition in a wellbore in accordance with certain embodiments.
(00081 FIG. 2B illustrates placement of a cement composition into a wellbore annulus in accordance with certain embodiments.
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 she-ath 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 prevents the migration of fluids in the annulus and protects the pipe string from corrosion.
Cement compositions may also be used in remedial cementing methods to seal cracks or holes in pipe strings or cement sheaths, to seal highly pemeable formation zones or fractures, or to place a cement plug and the like.
[00031 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., 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 activation and consequently develop reasonable compressive strengths. For example, a cement set activator may be added to a set-delayed cement composition to induce the composition to set into a hardened mass.
Among other things, set-delayed cement compositions may be suitable for use in wellbore applications such as applications where it is desirable to prepare the cement composition in advance. This may allow the cement composition to be stored prior to use. In addition, this may allow the cement composition to be prepared at a convenient location before transportation to the job site. Accordingly, capital expenditures may be reduced due to a reduction in the need for on-SUBSTITUTE SHEET (RULE 26) 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. In addition, it may be problematic to activate some set-delayed cement compositions while maintaining acceptable thickening times and compressive strength development.
SUBSTITUTE SHEET (RULE 26) BRIEF DESCRIPTION OF THE DRAWINGS
1100051 These drawings illustrate certain aspects of some of the embodiments of the present methods and compositions, and should not be used to limit or define the methods or compositions.
100061 FIG. I illustrates a system for preparation and delivery of a cement composition to a wellbore in accordance with certain embodiments.
NOM FIG. 2A illustrates surface equipment that may be used in placement of a cement composition in a wellbore in accordance with certain embodiments.
(00081 FIG. 2B illustrates placement of a cement composition into a wellbore annulus in accordance with certain embodiments.
3 SUBSTITUTE SHEET (RULE 26) DESCRIPTION OF PREFERRED EMBODIMENTS
[00091 The present 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. Particular embodiments provide improved cement set activators for the activation of cement compositions comprising pozzolan materials that have been retarded, have long set times, and/or have insufficient early strength.
[0010] Embodiments of the set-delayed cement compositions may generally comprise water, a pozzolan, and hydrated lime. Optionally, the cement compositions may further comprise a dispersant and/or a retarder. 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 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 bole static temperatures, e.g., temperatures less than about 200 F or ranging from about I 00 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.
[00113 The water used in embodiments 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 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 compositions in an amount in the range of from about 33%
to about 200% by weight of the pozzolan. In certain embodiments, the water may be present in the set-delayed cement compositions in an amount in the range of from about 35% to about 70% by weight of the pozzolan. With the benefit of this disclosure one of ordinary skill in the art will recognize the appropriate amount of water for a chosen application.
[0012] Embodiments of the set-delayed cement compositions may comprise a pozzolan. Any pozzolan is suitable for use in embodiments. Example embodiments
[00091 The present 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. Particular embodiments provide improved cement set activators for the activation of cement compositions comprising pozzolan materials that have been retarded, have long set times, and/or have insufficient early strength.
[0010] Embodiments of the set-delayed cement compositions may generally comprise water, a pozzolan, and hydrated lime. Optionally, the cement compositions may further comprise a dispersant and/or a retarder. 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 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 bole static temperatures, e.g., temperatures less than about 200 F or ranging from about I 00 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.
[00113 The water used in embodiments 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 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 compositions in an amount in the range of from about 33%
to about 200% by weight of the pozzolan. In certain embodiments, the water may be present in the set-delayed cement compositions in an amount in the range of from about 35% to about 70% by weight of the pozzolan. With the benefit of this disclosure one of ordinary skill in the art will recognize the appropriate amount of water for a chosen application.
[0012] Embodiments of the set-delayed cement compositions may comprise a pozzolan. Any pozzolan is suitable for use in embodiments. Example embodiments
4 SUBSTITUTE SHEET (RULE 26) comprising a pozzolan may comprise fly ash, silica fume, metakaolin, a natural pozzolan (e.g., pumice), or combinations thereof.
[0013] An example of a suitable pozzolan may comprise fly ash. A variety of fly ash may be suitable, including fly ash classified as Class C and Class F fly ash according to American Petroleum Institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Fifth Ed., July 1, 1990. Class C fly ash comprises both silica and lime, so it may set to form a hardened mass upon mixing with water. Class F fly ash generally does not contain a sufficient amount of lime to induce a cementitious reaction, therefore, an additional source of calcium ions is necessary for a set-delayed cement composition comprising Class F fly ash. In some embodiments, lime may be mixed with Class F fly ash in an amount in the range of about 0.1% to about 100% by weight of the fly ash. In some instances, the lime may be hydrated lime. Suitable examples of fly ash include, but are not limited to, POZ1v1IX1' A cement additive, commercially available from Halliburton Energy Services, Inc., Houston, Texas.
[0014] An example of a suitable pozzolan may comprise metakaolin. Generally, metakaolin is a white pozzolan that may be prepared by heating kaolin clay to temperatures in the range of about 600 to about 800 C.
[0015] An example of a suitable pozzolan may comprise a natural pozzolan.
Natural pozzolans are generally present on the Earth's surface and set and harden in the presence of hydrated lime and water. Embodiments comprising a natural pozzolan may comprise pumice, diatomaceous earth, volcanic ash, opaline shale, tuff, arid combinations thereof. The natural pozzolans may be ground or unground. Generally, the natural pozzolans may have any particle size distribution as desired for a particular application. In certain embodiments, the natural pozzolans may have a mean particle size in a range of from about I
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 natural pozzolans may have a mean particle size in a range of from about I micron to about 200 micron, from about 5 microns to about 100 microns, or from about 10 micron to about 50 microns. In one particular embodiment, the natural pozzolans may have a mean particle size of less than about 15 microns.
An example of a suitable commercial natural pozzolan is pumice available from Hess Pumice Products, Inc., Malad, Idaho, as DS-325 lightweight aggregate, which has 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 and may be less reactive due to their decreased surface area. One of ordinary skill in the art,
[0013] An example of a suitable pozzolan may comprise fly ash. A variety of fly ash may be suitable, including fly ash classified as Class C and Class F fly ash according to American Petroleum Institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Fifth Ed., July 1, 1990. Class C fly ash comprises both silica and lime, so it may set to form a hardened mass upon mixing with water. Class F fly ash generally does not contain a sufficient amount of lime to induce a cementitious reaction, therefore, an additional source of calcium ions is necessary for a set-delayed cement composition comprising Class F fly ash. In some embodiments, lime may be mixed with Class F fly ash in an amount in the range of about 0.1% to about 100% by weight of the fly ash. In some instances, the lime may be hydrated lime. Suitable examples of fly ash include, but are not limited to, POZ1v1IX1' A cement additive, commercially available from Halliburton Energy Services, Inc., Houston, Texas.
[0014] An example of a suitable pozzolan may comprise metakaolin. Generally, metakaolin is a white pozzolan that may be prepared by heating kaolin clay to temperatures in the range of about 600 to about 800 C.
[0015] An example of a suitable pozzolan may comprise a natural pozzolan.
Natural pozzolans are generally present on the Earth's surface and set and harden in the presence of hydrated lime and water. Embodiments comprising a natural pozzolan may comprise pumice, diatomaceous earth, volcanic ash, opaline shale, tuff, arid combinations thereof. The natural pozzolans may be ground or unground. Generally, the natural pozzolans may have any particle size distribution as desired for a particular application. In certain embodiments, the natural pozzolans may have a mean particle size in a range of from about I
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 natural pozzolans may have a mean particle size in a range of from about I micron to about 200 micron, from about 5 microns to about 100 microns, or from about 10 micron to about 50 microns. In one particular embodiment, the natural pozzolans may have a mean particle size of less than about 15 microns.
An example of a suitable commercial natural pozzolan is pumice available from Hess Pumice Products, Inc., Malad, Idaho, as DS-325 lightweight aggregate, which has 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 and may be less reactive due to their decreased surface area. One of ordinary skill in the art,
5 SUBSTITUTE SHEET (RULE 26)
6 with the benefit of this disclosure, should be able to select a particle size for the natural pozzolans suitable for use for a chosen application.
[00161 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 forrn the hydrated lime. The hydrated lime may be included in embodiments of the cement compositions. for example, to form a hydraulic composition with the pozzolan. For example, the hydrated lime may be included in a pozzolan-to-hydrated-lime weight ratio of about Ithl to about 1: i or a ratio of about 3:1 to about 5:1. Where present, the hydrated lime may be included in die set-delayed cement compositions in an amount in the range of from about 10% to about 100% by weight of the pozzolan, 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 pozzolan. In some embodiments, the cementitious components present in the set-delayed cement composition may consist essentially of the pozzolan and the hydrated lime. For example, the cementitious components may primarily comprise the pozzolan and the hydrated lime without any additional cementitious components (e.g., Portland 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 hydrated lime to include for a chosen application.
[0017j 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 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-finictionalized 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 SUBSTITUTE SHEET (RULE 26) 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 10%
by weight of the pozzolan. In specific embodiments, the set retarder may be present in an amotmt ranging between any of and/or including any of about 0.01%, about 0.1%, about 1%, about 2%, about 4%, about 6%, about 8%, or about 10% by weight of the pozzolan. 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-forrnaldehyde-based dispersants (e.g., suifonated acetone formaldehyde condensate), examples of which may include Daxadg 19 dispersant available from Geo Specialty Chemicals, Ambler, Pennsylvania. Other suitable dispersants may be polycarboxylated ether dispersants such as Liquimentg 558IF and Liquimentg 514L
dispersants available from BASF Corporation Houston, Texas; or Ethacryrd G
dispersant available from Coatex, Genay, France. An additional example of a suitable commercially available dispersant is CFRT"-3 dispersant, available from Halliburton Energy Services, Inc, Houston, Texas. The Liquimentg 5I4L 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 pozzolan and hydrated lime in the composition for an extended period of time.
[00191 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 pozzolan. In specific embodiments, the dispersant may be present in an amount ranging between any of ancVor 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 pozzolan. 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] Some embodiments of the set-delayed cement compositions may comprise silica sources in addition to the pozzolan; for example, crystalline silica and/or amorphous silica. Crystalline silica is a powder that may be included in embodiments of the set-delayed
[00161 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 forrn the hydrated lime. The hydrated lime may be included in embodiments of the cement compositions. for example, to form a hydraulic composition with the pozzolan. For example, the hydrated lime may be included in a pozzolan-to-hydrated-lime weight ratio of about Ithl to about 1: i or a ratio of about 3:1 to about 5:1. Where present, the hydrated lime may be included in die set-delayed cement compositions in an amount in the range of from about 10% to about 100% by weight of the pozzolan, 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 pozzolan. In some embodiments, the cementitious components present in the set-delayed cement composition may consist essentially of the pozzolan and the hydrated lime. For example, the cementitious components may primarily comprise the pozzolan and the hydrated lime without any additional cementitious components (e.g., Portland 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 hydrated lime to include for a chosen application.
[0017j 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 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-finictionalized 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 SUBSTITUTE SHEET (RULE 26) 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 10%
by weight of the pozzolan. In specific embodiments, the set retarder may be present in an amotmt ranging between any of and/or including any of about 0.01%, about 0.1%, about 1%, about 2%, about 4%, about 6%, about 8%, or about 10% by weight of the pozzolan. 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-forrnaldehyde-based dispersants (e.g., suifonated acetone formaldehyde condensate), examples of which may include Daxadg 19 dispersant available from Geo Specialty Chemicals, Ambler, Pennsylvania. Other suitable dispersants may be polycarboxylated ether dispersants such as Liquimentg 558IF and Liquimentg 514L
dispersants available from BASF Corporation Houston, Texas; or Ethacryrd G
dispersant available from Coatex, Genay, France. An additional example of a suitable commercially available dispersant is CFRT"-3 dispersant, available from Halliburton Energy Services, Inc, Houston, Texas. The Liquimentg 5I4L 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 pozzolan and hydrated lime in the composition for an extended period of time.
[00191 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 pozzolan. In specific embodiments, the dispersant may be present in an amount ranging between any of ancVor 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 pozzolan. 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] Some embodiments of the set-delayed cement compositions may comprise silica sources in addition to the pozzolan; for example, crystalline silica and/or amorphous silica. Crystalline silica is a powder that may be included in embodiments of the set-delayed
7 SUBSTITUTE SHEET (RULE 26) cement compositions, for example, to prevent cement compressive strength retrogression.
Amorphous silica is a powder that may be included in embodiments of the set-delayed cement compositions as a lightweight filler and/or to increase cement compressive strength.
Amorphous silica is generally a byproduct of a ferrosilicon production process, wherein the amorphous silica may be formed by oxidation and condensation of gaseous silicon suboxide, SiO, which is formed as an intermediate during the process. An example of a suitable source of amorphous silica is Silicone cement addifive available from Halliburton Energy Services, Inc., Houston, Texas. Embodiments comprising additional silica sources may utilize the additional silica source as needed to enhance compressive strength or set times.
[0021] 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, 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 art, with the benefit of this disclosure, should readily be able to determine the type and amount of additive usefttl for a particular application and desired result.
[0022] 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 cement compositions may have a density in the range of from about 4 pounds per gallon ("lb/p1") to about 20 Ibigal. In certain embodiments, the cement compositions may have a density in the range =of from about 8 lb/pi to about 17 lb/gal. Embodiments of the set-delayed cement compositions may be foamed or tmfoamed 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 storage, but prior to placement in a subterranean formation.
In embodiments, weighting additives may be used 10 increase the density of the set-delayed cement compositions. Examples of suitable weighting additives may include barite, hematite, hausmannite, calcium carbonate, siderite, ilmenite, or combinations thereof.
In particular embodiments, the weighting additives may have a specific gravity of 3 or greater. Those of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density for a particular application.
Amorphous silica is a powder that may be included in embodiments of the set-delayed cement compositions as a lightweight filler and/or to increase cement compressive strength.
Amorphous silica is generally a byproduct of a ferrosilicon production process, wherein the amorphous silica may be formed by oxidation and condensation of gaseous silicon suboxide, SiO, which is formed as an intermediate during the process. An example of a suitable source of amorphous silica is Silicone cement addifive available from Halliburton Energy Services, Inc., Houston, Texas. Embodiments comprising additional silica sources may utilize the additional silica source as needed to enhance compressive strength or set times.
[0021] 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, 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 art, with the benefit of this disclosure, should readily be able to determine the type and amount of additive usefttl for a particular application and desired result.
[0022] 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 cement compositions may have a density in the range of from about 4 pounds per gallon ("lb/p1") to about 20 Ibigal. In certain embodiments, the cement compositions may have a density in the range =of from about 8 lb/pi to about 17 lb/gal. Embodiments of the set-delayed cement compositions may be foamed or tmfoamed 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 storage, but prior to placement in a subterranean formation.
In embodiments, weighting additives may be used 10 increase the density of the set-delayed cement compositions. Examples of suitable weighting additives may include barite, hematite, hausmannite, calcium carbonate, siderite, ilmenite, or combinations thereof.
In particular embodiments, the weighting additives may have a specific gravity of 3 or greater. Those of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density for a particular application.
8 SUBSTITUTE SHEET (RULE 26) [00231 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 elle day (e.gõ at least about 1 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 I 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 10B-2, Recommended Practice for Testing Well Cements, First Edition, July 2005.
[0024) 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.
[0025) 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-forte per square inch (psi). Non-destructive methods may employ a 'MAIN ultrasonic cement analyzer, available from Fann Instrument Company, Houston, TX. Compressive strength
[0024) 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.
[0025) 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-forte per square inch (psi). Non-destructive methods may employ a 'MAIN ultrasonic cement analyzer, available from Fann Instrument Company, Houston, TX. Compressive strength
9 SUBSTITUTE SHEET (RULE 26) values may be determined in accordance with API RP 1013-2, Recommended Practice Jiff Testing Well Cements, First Edition, July 2005.
[0026] 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.
[0027] 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 Be and may be reported as the time to reach 70 Be. 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.
[0028] 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 cornbinations 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 metapbosphate SUBSTITUTE SHEET (RULE 26) salts that may be used include sodium hexametaphosphate, sodium trimetaphosphate, sodium tetrametaphosphate, sodium pentametaphosphate, sodium heptatnetaphosphate, 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, [0029] As discussed above, zcolites may be included as activators in embodiments of the set-delayed cement compositions. Zeolites are generally porous alumino-silicate minerals that may be either natural or synthetic. Synthetic zeolites are based on the same type of structural cell as natural zeolites and may comprise aluminosilicate hydrates. As used herein, the term "zeolite" refers to all natural and synthetic forms of zeolite. An example of a suitable source of zeolite is Valfor-100 zeolite or AcIvere 401 zeolite available from the PQ Corporation, Malvern, Pennsylvania.
[0030] Embodiments of the set-delayed cement compositions may comprise a cement set activator comprising a zeolite, a combination of zeolites, a combination of zeolite and a non-zeolite activator, a combination of zeolites and a non-zeolite activator, a combination of zeolites and a combination of non-zeolite activators, or combinations thereof.
Embodiments comprising zeolite may comprise any zeolite. Examples of zeolites include mordenite, zsm-5, zeolite x, zeolite y, zeolite a, etc. Furthermore, embodiments comprising zeolite may comprise zeolite in combination with a cation such as Ne,K, Ca.
Mg2+, etc.
Zeolites comprising cations such as sodium may also provide additional cation sources to the set-delayed cement composition as the zeolites dissolve. An example of a zeolite comprising a cation (e.g., Na) is the afore-mentioned Valfoi"' 100 zeolite. Without being limited by theory, it is believed that zeolites increase the surface area of the pozzolan without increasing their particles size. Increased surface areas for the pozzolan may allow for a faster dissolution rate of silica, the free silica is able to react with calcium species, such as those from hydrated lime, to form calcium-silicate-hydrate gels. Increasing the surface area without altering the particle size is advantageous because it allows for greater reactivity without affecting other properties such as viscosity or pumpability. Sodium zeolites may also exchange sodium for calcium in solution thereby increasing the pH and increasing the rate of dissolution of silica in the slurry.
[0031] Zeolites may be added to the set-delayed cement compositions in a number of ways. One embodiment comprises a method wherein the zeolites are added directly to the set-delayed cement compositions in an amount sufficient to activate or accelerate the setting SUBSTITUTE SHEET (RULE 26) of the cement composition. An alternative embodiment is to induce the growth of the zeolite crystals directly on the pozzolan. The pozzolan may be a nutrient source for zeolite crystals and be induced to grow zeolite crystals either as a film or as an integral part of the particle if the pozzolanic particles were placed under zeolite synthesis conditions.
Various seeding methods such as pulsed laser deposition. secondary growth, vacuum deposition, etc. may be used to produce a variety of zeolites (e.g., zsm-5, zeolite x, etc.) on the pozzolan. The synthesized zeolites may form crystals, film, and/or integrate directly into the pozzolan. The pozzolan with the zeolite disposed thereon may be provided and used in preparation of a set-delayed cement composition.
[0032] The cement set activator should be added to embodiments of the set-delayed cement composition in an amount sufficient to induce the set-delayed composition to set into a hardened mass. In certain embodiments, the cement set activator may be added to the cement composition in an amount in the range of about 0.1% to about 20% by weight of the pozzolan. 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
[0026] 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.
[0027] 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 Be and may be reported as the time to reach 70 Be. 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.
[0028] 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 cornbinations 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 metapbosphate SUBSTITUTE SHEET (RULE 26) salts that may be used include sodium hexametaphosphate, sodium trimetaphosphate, sodium tetrametaphosphate, sodium pentametaphosphate, sodium heptatnetaphosphate, 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, [0029] As discussed above, zcolites may be included as activators in embodiments of the set-delayed cement compositions. Zeolites are generally porous alumino-silicate minerals that may be either natural or synthetic. Synthetic zeolites are based on the same type of structural cell as natural zeolites and may comprise aluminosilicate hydrates. As used herein, the term "zeolite" refers to all natural and synthetic forms of zeolite. An example of a suitable source of zeolite is Valfor-100 zeolite or AcIvere 401 zeolite available from the PQ Corporation, Malvern, Pennsylvania.
[0030] Embodiments of the set-delayed cement compositions may comprise a cement set activator comprising a zeolite, a combination of zeolites, a combination of zeolite and a non-zeolite activator, a combination of zeolites and a non-zeolite activator, a combination of zeolites and a combination of non-zeolite activators, or combinations thereof.
Embodiments comprising zeolite may comprise any zeolite. Examples of zeolites include mordenite, zsm-5, zeolite x, zeolite y, zeolite a, etc. Furthermore, embodiments comprising zeolite may comprise zeolite in combination with a cation such as Ne,K, Ca.
Mg2+, etc.
Zeolites comprising cations such as sodium may also provide additional cation sources to the set-delayed cement composition as the zeolites dissolve. An example of a zeolite comprising a cation (e.g., Na) is the afore-mentioned Valfoi"' 100 zeolite. Without being limited by theory, it is believed that zeolites increase the surface area of the pozzolan without increasing their particles size. Increased surface areas for the pozzolan may allow for a faster dissolution rate of silica, the free silica is able to react with calcium species, such as those from hydrated lime, to form calcium-silicate-hydrate gels. Increasing the surface area without altering the particle size is advantageous because it allows for greater reactivity without affecting other properties such as viscosity or pumpability. Sodium zeolites may also exchange sodium for calcium in solution thereby increasing the pH and increasing the rate of dissolution of silica in the slurry.
[0031] Zeolites may be added to the set-delayed cement compositions in a number of ways. One embodiment comprises a method wherein the zeolites are added directly to the set-delayed cement compositions in an amount sufficient to activate or accelerate the setting SUBSTITUTE SHEET (RULE 26) of the cement composition. An alternative embodiment is to induce the growth of the zeolite crystals directly on the pozzolan. The pozzolan may be a nutrient source for zeolite crystals and be induced to grow zeolite crystals either as a film or as an integral part of the particle if the pozzolanic particles were placed under zeolite synthesis conditions.
Various seeding methods such as pulsed laser deposition. secondary growth, vacuum deposition, etc. may be used to produce a variety of zeolites (e.g., zsm-5, zeolite x, etc.) on the pozzolan. The synthesized zeolites may form crystals, film, and/or integrate directly into the pozzolan. The pozzolan with the zeolite disposed thereon may be provided and used in preparation of a set-delayed cement composition.
[0032] The cement set activator should be added to embodiments of the set-delayed cement composition in an amount sufficient to induce the set-delayed composition to set into a hardened mass. In certain embodiments, the cement set activator may be added to the cement composition in an amount in the range of about 0.1% to about 20% by weight of the pozzolan. 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 pozzolan. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the cement set activator to include for a chosen application.
[00333 While the preceding may describe the use of zeolites as activators in set-delayed cement compositions, it is to be understood that zeolites may be used in other cement systems comprising a pozzolan to accelerate the set time of the cement composition and to enhance the development of early compressive strength. In some embodiments, a zeolite may be used in a cement composition comprising a pozzolan and water.
In other embodiments, the cement composition may further comprise hydrated lime and other optional additives, such as those described above. The disclosure of the zeolite used herein is not to be limited to set-delayed pozzolan cement compositions but may be used for any pozzolan cement composition regardless of whether the cement composition may be categorized as "set-delayed."
[0034] As will be appreciated by those of ordinary skill in the art, embodiments t-,if the set-delayed cetrieht compositions may be used in a variety of subterranean operations, including primary and remedial cementing. In some embodiments, a set-delayed cement cotnposition may he provided that comprises water, a pozzolan, hydrated lime, a set retarder, and optionally a dispersant. 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 SUBSTITUTE SHEET (RULE 26) 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.
[0035} In some embodiments, a set-delayed cement composition may be provided that comprises water, a pozzolan, hydrated time, a set retarder, and optionally a dispersant.
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 I 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.
[0036) 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.
[0037] 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).
[0038] An embodiment con-tprises a method of cementing in a subterranean formation comprising: providing a cement cotnposition comprising water, a pozzolan, hydrated lime, and a zeolite activator; introducing the cement composition into a subterranean formation; and allowing the cement composition to set in the subterranean SUBSTITUTE SHEET (RULE 26) formation, wherein the zeolite activator accelerates compressive strength development of the cement composition [0039] An embodiment comprises an activated set-delayed cement composition comprising: water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator.
[00401 An embodiment comprises a cementing system comprising: a set-delayed cement composition comprising water, a pozzolan, hydrated lime, and a set retarder, a zeolite activator for activation of the set-delayed cement composition; mixing equipment for mixing the set-delayed cement composition and the zeolite activator to form an activated cement composition; and pumping equipment for delivering the activated cement composition into a wellbore.
[0041] Referring now to FIG, 1, preparation of a cement composition (which may be set delayed or non-set delayed) in accordance with example embodiments will now be described. FIG. 1 illustrates a system 2 for preparation of a cement composition and delivery to a wellbore in accordance with certain embodiments. As shown, the 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.
[0042] An example technique for placing a cement composition into a subterranean formation will now be described with reference to FIGS. 2A and 213. FIG. 2A
illustrates surface equipment 10 that may be used in placement of a 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 tbe 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 cement composition 14 through a feed pipe 16 and to a cementing head 1$ which conveys the cement composition 14 downhole.
SUBSTITUTE SHEET (RULE 26) [00431 Turning now to FIG 2B, the set-delayed or non-set-delayed pozzolanic 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 subterianean 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 eentralin the casing 30 in the wellbore 22 prior to and during the cementing operation.
[0044] With continued reference to FIG. 28, the cement composition 14 may be pumped down the interior of the casing 30. The 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 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 pozzolanic cement composition 14, By way of example, reverse circulation techniques may be used that include introducing the cement composition 14 into the subterranean formation 20 by way of the wellbore annulus 32 instead of through the casing 30.
[00451 As it is introduced, the 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 cement composition 14, for example, to separate the 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 pozzolanic cement composition 14 through the bottom plug 44. In FM. 2B, the= bottom plug 44 is shown on the SUBSTITUTE SHEET (RULE 26) landing collar 46. In the illustrated embodiment. a top plug 48 may be introduced into the wellbore 22 behind the cement composition 14. The top plug 48 may separate the cement composition 14 from a displacement fluid 50 and also push the cement composition 14 through the bottom plug 44.
[00461 The exemplary 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 cement compositions. For example, the disclosed 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 exemplary cement compositions. The disclosed cement compositions may also directly or indirectly affect any transport or delivery equipment used to convey the 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 cement compositions from one location to another, any pumps, compressors, or motors (e.g., topside or downhole) used to drive the cement compositions into motion, any valves or related joints used to regulate the pressure or flow rate of the cement compositions, and any sensors (i.e.. pressure and temperature), gauges, and/or combinations thereof, and the like. The disclosed cement compositions may also directly or indirectly affect the various downhole equipment and tools that may come into contact with the 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, hydromechanical 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.
SUBSTITUTE SHEET (RULE 26) f0047] To facilitate a better understanding of the 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 disclosure.
EXAMPLES
Example 1 [0048] Four samples were prepared to test the effectiveness of sodium zeolite A as an activator of lime-pozzolan cement compositions. The sodium zeolite A used for the experiment was Val for 100 zeolite from the l'Q Corporation, Malvern, Pennsylvania.
Valfor 100 zeolite has a median particle size of 5 microns and a high surface area (i.e., 71.4 m2/g). Two lime-pozzolan cement formulations were prepared with and without sodium zeolite A. The formulation with sodium zeolite A had a density of 14.0 lb/gal and was comprised of 304 grams of pumice (DS-325 lightweight aggregate), 45 grams of hydrated lime, 25 grams of sodium zeolite A (Valfor 100), 1.9 grams of dispersant (Liquiment 5581F dispersant), and 158.5 grams of water. The formulation without sodium zeolite A had a density of 14.0 lb/pi and was comprised of 304 grams of pumice (DS-325 lightweight aggregate), 45 grams of hydrated lime, 1.9 grams of dispersant (Liquiment 5581F), and 145.5 grams of water. The strength development of the samples was monitored via a Fann UCAT" ultrasonic cement analyzer at test temperatures of 80 F and 100 F. The UCAT" was used to determine the compressive strengths of the samples after twenty-four hours as well as the time for the samples to develop compressive strengths of 50 psi and 500 psi. The UCAT" determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table 1 below.
SUBSTITUTE SHEET (RULE 26) Table 1 Comparison of Lime-Pox/Ann Cement with and without a Zeolite Activator Test Zeolite (% by Time to 50 psi Time to 500 24-Hour Temperature weight of (hr:min) psi Compressive pumice + (hr:min) Strength (psi) hydrated lime) 80 F 7.20% 4:23 17:10 688 80 F = 0.00% 20:03 69 100 F 7.20% 2:41 8:30 1562 100 F 0.00% 7:22 29:30 374 Example 2 [0049] A sample of pumice was treated with sodium hydroxide and sodium chloride to produce zeolite on the pumice. The zeolite synthesis was carried out by mixing 300 grams of pumice (DS-325 lightweight aggregate) with 1.25 liters of 30% NaCI solution that contained 25 grams of Na011. After mixing was completed, the sample was placed in a sealed plastic container and heated at 85 C for 17 hours. After treatment, the solids were filtered and washed several times with deionized water and then dried. The solids were used to form a Ihne-pozzolan set-delayed cement composition comprising 250 grams of zeolitized pumice, 50 grams of hydrated lime, 349 grams of dispersant (Liquiment 5141., dispersant), 3.13 grams of set retarder (Micro Matrix* cement retarder), and 207.4 grams of water. As a control, a lime-pozzolan set-delayed cement composition was prepared that did not comprise the zeolitized pumice. The control composition comprised 250 grams pumice (DS-lightweight aggregate), 50 grams of hydrated lime, 3.49 grarns of dispersant (Liquiment*
5141, dispersant), 3.13 grams of set retarder (Micro Matrix cement retarder), and 154.9 grams of water, The strength development of the samples was monitored via UCA
at a test temperature of 100 F. The UCA'M was used to determine the compressive strengths of the experimental sample and the control after seventy-two hours as well as the time for the experimental sample and the control to develop compressive strengths of 50 psi and 100 psi.
The UCATM determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the SUBSTITUTE SHEET (RULE 26) onset of the strength development) of the compressive strength versus time graph, The results of these tests are set forth in Table 2 below.
Table 2 Comparison of Lime-Pozzolan Cement with and without a Zeolitized Pumice Activator Test Pozzolan Time to 50 psi Time to 100 psi 72-Hour Temperature (hr:min) (hr:min) Compressive Strength (psi) 100 F Zeol itized 58:45 62:24 331 pumice 100 F pumice --*
* After 78 hours the slurry had not set.
Example 3 [0050} Several samples of set-delayed cement compositions were prepared. The samples comprised pumice (DS-325 lightweight aggregate), 20% hydrated lime, and 60%
water. The density of each sample was 13.5 lb/gal. In addition to the base composition, a varying amount of dispersant (Liquiment* 5581F dispersant), cement retarder (Micro Matrix* cement retarder), and activator (activator type varied by sample) were added to individual samples. The activator types chosen were sodium zeolite A (Valfoe 100 zeolite), hydrated sodium zeolite A (Advera 401 zeolite), divalent salt (CaCl2), and cement (API
Class A). The dispersant was added as a percentage by weight a the pumice (bwoP). The cement retarder was added in units of gallons per 46 lb. sack of pumice (galisk). Each activator comprised 10% of the samples by weight of the pumice and the hydrated lime (bwoP HL). The strength development and initial set times of the samples were monitored via UCATh at a test temperature of 80 F. The UCe was used to determine the compressive strengths of the experimental sample and the control after twenty-four hours.
The UCAlm determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table .3 below.
SUBSTITUTE SHEET (RULE 26) Table 3 Comparison of Different Types of Activators UCAnr Data Cement Activator Dispersant 24-Hour Retarder (10%
(% bwop) Initial Set Compressive (gal/sk) bwoP+HL) (hr:min) Strength (psi) 524 (316)*; tested 0.575 0.015 Zeolite NaA 12:09 same day as mixed 778 (343)*; tested one day after 0.625 0.015 Zeolite NaA 7:03 mixing Hydrated 0.625 0.015 Zeolite NaA 7:56 603 0.725 0.015 CaC12 53:52 0.725 0.015 Cement 15:33 71 0.50 0.020 Zeolite NaA 11:46 580 (230)*
250 psi at 30:30 0,55 0.025 Zeolite NaA 24:43 500 psi at 36:05 0.55 0.025 Zeolite NaA (100 F) 11:20 965 (678)*
* Values in parentheses are crush values for UCAT" samples.
Example 4 [0051} Two set-delayed cement composition samples were prepared. The samples comprised pumice (DS-325 lightweight aggregate), 20% hydrated lime, 65% water, 2%
weight additive (Micromax weight additive), 0.6% dispersant (Liquiment* 5581F
dispersant), and 0.04 galisk cement retarder (Micro Matrix* cement retarder).
Additionally, one experimental sample comprised 10% bwoPIIIL sodium zeolite A activator (Valfor 100 zeolite). The density of each sample was 13.5 lb/gal. The strength development of the samples was monitored via UCA at a test temperature of I 00 F. The UCArm was used to determine the time to 50 psi and the time to 500 psi of the experimental sample and the control. The LICA determines the compressive strength rate as a ftmction of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these= tests are set forth in Table 4 below.
SUBSTITUTE SHEET (RULE 26) Table 4 Comparison of Lime-P=01AR Cement with and without a Zeolite Activator Activator UCAT" Data (10% Time to 50 psi Time to 500 psi bwoP+HL) (hr: min) (hr:min) 50:00+*
Zeolite NaA 38:25 56:65 * Had not set by 50 hours.
Example 5 [00521 Seven experimental samples of set-delayed cement compositions were prepared. The samples comprised 609 grams fly ash (Magnablend Class F fly ash, available from Magnablend inc.. Waxahachie, Texas), 21 grams silica fume, 3.5 grams cement friction reducer (CFR-3'" cement friction reducer, available from Halliburton Energy Services inc., Houston, Texas), and 317 grams water. In addition to the base composition, a varying amount of hydrated sodium zeolite A activator (Advere 401 zeolite) was added to each experimental sample. The strength development of the samples was monitored via UCAr" at a test temperature of 150 F. The UCATu was used to determine the compressive strengths of the experimental samples after twenty-four hours. The UCArm determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table 5 below.
SUBSTITUTE SHEET (RULE 26) Table 5 Zeolite Concentration versus Compressive Strength Zeolite Activator (grams) 24-Hour Compressive Strength at 150 F
(Psi) [00531 Additionally the strength development of the zeolite sample comprising grams from Table 5 above, was additionally measured by the UCAI'l at test temperatures of 100 F and 120 F. The results of these tests are set forth in Table 6 below.
Table 6 Zeolite concentration versus Compressive Strength at 100 F, 120 F, and 150 F
Zeolite Activator 24 Hour Comp. 24-hour Comp. 24-Hour Comp.
(grams) Strength at 100 F Strength at 120 F Strength at 150 F
(Psi) (psi) (psi) 49 620 770 1220*
0 Did Not Set 60 1010 *Permeability 0.013 md 00541 lt 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.
SUBSTITUTE SHEET (RULE 26) [00551 For the sake of brevity, only certain ranges are explicitly disclosed herein.
However, ranges from any lower lirnit 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-h") 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.
[00561 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, and they 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 all those embodiments are 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 those embodiments. 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 that may be incorporated herein by reference. the definitions that are consistent with this specification should be adopted.
SUBSTITUTE SHEET (RULE 26)
[00333 While the preceding may describe the use of zeolites as activators in set-delayed cement compositions, it is to be understood that zeolites may be used in other cement systems comprising a pozzolan to accelerate the set time of the cement composition and to enhance the development of early compressive strength. In some embodiments, a zeolite may be used in a cement composition comprising a pozzolan and water.
In other embodiments, the cement composition may further comprise hydrated lime and other optional additives, such as those described above. The disclosure of the zeolite used herein is not to be limited to set-delayed pozzolan cement compositions but may be used for any pozzolan cement composition regardless of whether the cement composition may be categorized as "set-delayed."
[0034] As will be appreciated by those of ordinary skill in the art, embodiments t-,if the set-delayed cetrieht compositions may be used in a variety of subterranean operations, including primary and remedial cementing. In some embodiments, a set-delayed cement cotnposition may he provided that comprises water, a pozzolan, hydrated lime, a set retarder, and optionally a dispersant. 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 SUBSTITUTE SHEET (RULE 26) 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.
[0035} In some embodiments, a set-delayed cement composition may be provided that comprises water, a pozzolan, hydrated time, a set retarder, and optionally a dispersant.
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 I 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.
[0036) 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.
[0037] 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).
[0038] An embodiment con-tprises a method of cementing in a subterranean formation comprising: providing a cement cotnposition comprising water, a pozzolan, hydrated lime, and a zeolite activator; introducing the cement composition into a subterranean formation; and allowing the cement composition to set in the subterranean SUBSTITUTE SHEET (RULE 26) formation, wherein the zeolite activator accelerates compressive strength development of the cement composition [0039] An embodiment comprises an activated set-delayed cement composition comprising: water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator.
[00401 An embodiment comprises a cementing system comprising: a set-delayed cement composition comprising water, a pozzolan, hydrated lime, and a set retarder, a zeolite activator for activation of the set-delayed cement composition; mixing equipment for mixing the set-delayed cement composition and the zeolite activator to form an activated cement composition; and pumping equipment for delivering the activated cement composition into a wellbore.
[0041] Referring now to FIG, 1, preparation of a cement composition (which may be set delayed or non-set delayed) in accordance with example embodiments will now be described. FIG. 1 illustrates a system 2 for preparation of a cement composition and delivery to a wellbore in accordance with certain embodiments. As shown, the 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.
[0042] An example technique for placing a cement composition into a subterranean formation will now be described with reference to FIGS. 2A and 213. FIG. 2A
illustrates surface equipment 10 that may be used in placement of a 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 tbe 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 cement composition 14 through a feed pipe 16 and to a cementing head 1$ which conveys the cement composition 14 downhole.
SUBSTITUTE SHEET (RULE 26) [00431 Turning now to FIG 2B, the set-delayed or non-set-delayed pozzolanic 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 subterianean 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 eentralin the casing 30 in the wellbore 22 prior to and during the cementing operation.
[0044] With continued reference to FIG. 28, the cement composition 14 may be pumped down the interior of the casing 30. The 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 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 pozzolanic cement composition 14, By way of example, reverse circulation techniques may be used that include introducing the cement composition 14 into the subterranean formation 20 by way of the wellbore annulus 32 instead of through the casing 30.
[00451 As it is introduced, the 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 cement composition 14, for example, to separate the 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 pozzolanic cement composition 14 through the bottom plug 44. In FM. 2B, the= bottom plug 44 is shown on the SUBSTITUTE SHEET (RULE 26) landing collar 46. In the illustrated embodiment. a top plug 48 may be introduced into the wellbore 22 behind the cement composition 14. The top plug 48 may separate the cement composition 14 from a displacement fluid 50 and also push the cement composition 14 through the bottom plug 44.
[00461 The exemplary 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 cement compositions. For example, the disclosed 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 exemplary cement compositions. The disclosed cement compositions may also directly or indirectly affect any transport or delivery equipment used to convey the 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 cement compositions from one location to another, any pumps, compressors, or motors (e.g., topside or downhole) used to drive the cement compositions into motion, any valves or related joints used to regulate the pressure or flow rate of the cement compositions, and any sensors (i.e.. pressure and temperature), gauges, and/or combinations thereof, and the like. The disclosed cement compositions may also directly or indirectly affect the various downhole equipment and tools that may come into contact with the 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, hydromechanical 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.
SUBSTITUTE SHEET (RULE 26) f0047] To facilitate a better understanding of the 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 disclosure.
EXAMPLES
Example 1 [0048] Four samples were prepared to test the effectiveness of sodium zeolite A as an activator of lime-pozzolan cement compositions. The sodium zeolite A used for the experiment was Val for 100 zeolite from the l'Q Corporation, Malvern, Pennsylvania.
Valfor 100 zeolite has a median particle size of 5 microns and a high surface area (i.e., 71.4 m2/g). Two lime-pozzolan cement formulations were prepared with and without sodium zeolite A. The formulation with sodium zeolite A had a density of 14.0 lb/gal and was comprised of 304 grams of pumice (DS-325 lightweight aggregate), 45 grams of hydrated lime, 25 grams of sodium zeolite A (Valfor 100), 1.9 grams of dispersant (Liquiment 5581F dispersant), and 158.5 grams of water. The formulation without sodium zeolite A had a density of 14.0 lb/pi and was comprised of 304 grams of pumice (DS-325 lightweight aggregate), 45 grams of hydrated lime, 1.9 grams of dispersant (Liquiment 5581F), and 145.5 grams of water. The strength development of the samples was monitored via a Fann UCAT" ultrasonic cement analyzer at test temperatures of 80 F and 100 F. The UCAT" was used to determine the compressive strengths of the samples after twenty-four hours as well as the time for the samples to develop compressive strengths of 50 psi and 500 psi. The UCAT" determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table 1 below.
SUBSTITUTE SHEET (RULE 26) Table 1 Comparison of Lime-Pox/Ann Cement with and without a Zeolite Activator Test Zeolite (% by Time to 50 psi Time to 500 24-Hour Temperature weight of (hr:min) psi Compressive pumice + (hr:min) Strength (psi) hydrated lime) 80 F 7.20% 4:23 17:10 688 80 F = 0.00% 20:03 69 100 F 7.20% 2:41 8:30 1562 100 F 0.00% 7:22 29:30 374 Example 2 [0049] A sample of pumice was treated with sodium hydroxide and sodium chloride to produce zeolite on the pumice. The zeolite synthesis was carried out by mixing 300 grams of pumice (DS-325 lightweight aggregate) with 1.25 liters of 30% NaCI solution that contained 25 grams of Na011. After mixing was completed, the sample was placed in a sealed plastic container and heated at 85 C for 17 hours. After treatment, the solids were filtered and washed several times with deionized water and then dried. The solids were used to form a Ihne-pozzolan set-delayed cement composition comprising 250 grams of zeolitized pumice, 50 grams of hydrated lime, 349 grams of dispersant (Liquiment 5141., dispersant), 3.13 grams of set retarder (Micro Matrix* cement retarder), and 207.4 grams of water. As a control, a lime-pozzolan set-delayed cement composition was prepared that did not comprise the zeolitized pumice. The control composition comprised 250 grams pumice (DS-lightweight aggregate), 50 grams of hydrated lime, 3.49 grarns of dispersant (Liquiment*
5141, dispersant), 3.13 grams of set retarder (Micro Matrix cement retarder), and 154.9 grams of water, The strength development of the samples was monitored via UCA
at a test temperature of 100 F. The UCA'M was used to determine the compressive strengths of the experimental sample and the control after seventy-two hours as well as the time for the experimental sample and the control to develop compressive strengths of 50 psi and 100 psi.
The UCATM determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the SUBSTITUTE SHEET (RULE 26) onset of the strength development) of the compressive strength versus time graph, The results of these tests are set forth in Table 2 below.
Table 2 Comparison of Lime-Pozzolan Cement with and without a Zeolitized Pumice Activator Test Pozzolan Time to 50 psi Time to 100 psi 72-Hour Temperature (hr:min) (hr:min) Compressive Strength (psi) 100 F Zeol itized 58:45 62:24 331 pumice 100 F pumice --*
* After 78 hours the slurry had not set.
Example 3 [0050} Several samples of set-delayed cement compositions were prepared. The samples comprised pumice (DS-325 lightweight aggregate), 20% hydrated lime, and 60%
water. The density of each sample was 13.5 lb/gal. In addition to the base composition, a varying amount of dispersant (Liquiment* 5581F dispersant), cement retarder (Micro Matrix* cement retarder), and activator (activator type varied by sample) were added to individual samples. The activator types chosen were sodium zeolite A (Valfoe 100 zeolite), hydrated sodium zeolite A (Advera 401 zeolite), divalent salt (CaCl2), and cement (API
Class A). The dispersant was added as a percentage by weight a the pumice (bwoP). The cement retarder was added in units of gallons per 46 lb. sack of pumice (galisk). Each activator comprised 10% of the samples by weight of the pumice and the hydrated lime (bwoP HL). The strength development and initial set times of the samples were monitored via UCATh at a test temperature of 80 F. The UCe was used to determine the compressive strengths of the experimental sample and the control after twenty-four hours.
The UCAlm determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table .3 below.
SUBSTITUTE SHEET (RULE 26) Table 3 Comparison of Different Types of Activators UCAnr Data Cement Activator Dispersant 24-Hour Retarder (10%
(% bwop) Initial Set Compressive (gal/sk) bwoP+HL) (hr:min) Strength (psi) 524 (316)*; tested 0.575 0.015 Zeolite NaA 12:09 same day as mixed 778 (343)*; tested one day after 0.625 0.015 Zeolite NaA 7:03 mixing Hydrated 0.625 0.015 Zeolite NaA 7:56 603 0.725 0.015 CaC12 53:52 0.725 0.015 Cement 15:33 71 0.50 0.020 Zeolite NaA 11:46 580 (230)*
250 psi at 30:30 0,55 0.025 Zeolite NaA 24:43 500 psi at 36:05 0.55 0.025 Zeolite NaA (100 F) 11:20 965 (678)*
* Values in parentheses are crush values for UCAT" samples.
Example 4 [0051} Two set-delayed cement composition samples were prepared. The samples comprised pumice (DS-325 lightweight aggregate), 20% hydrated lime, 65% water, 2%
weight additive (Micromax weight additive), 0.6% dispersant (Liquiment* 5581F
dispersant), and 0.04 galisk cement retarder (Micro Matrix* cement retarder).
Additionally, one experimental sample comprised 10% bwoPIIIL sodium zeolite A activator (Valfor 100 zeolite). The density of each sample was 13.5 lb/gal. The strength development of the samples was monitored via UCA at a test temperature of I 00 F. The UCArm was used to determine the time to 50 psi and the time to 500 psi of the experimental sample and the control. The LICA determines the compressive strength rate as a ftmction of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these= tests are set forth in Table 4 below.
SUBSTITUTE SHEET (RULE 26) Table 4 Comparison of Lime-P=01AR Cement with and without a Zeolite Activator Activator UCAT" Data (10% Time to 50 psi Time to 500 psi bwoP+HL) (hr: min) (hr:min) 50:00+*
Zeolite NaA 38:25 56:65 * Had not set by 50 hours.
Example 5 [00521 Seven experimental samples of set-delayed cement compositions were prepared. The samples comprised 609 grams fly ash (Magnablend Class F fly ash, available from Magnablend inc.. Waxahachie, Texas), 21 grams silica fume, 3.5 grams cement friction reducer (CFR-3'" cement friction reducer, available from Halliburton Energy Services inc., Houston, Texas), and 317 grams water. In addition to the base composition, a varying amount of hydrated sodium zeolite A activator (Advere 401 zeolite) was added to each experimental sample. The strength development of the samples was monitored via UCAr" at a test temperature of 150 F. The UCATu was used to determine the compressive strengths of the experimental samples after twenty-four hours. The UCArm determines the compressive strength rate as a function of time. The rate of strength development was calculated as the slope of the initial linear part (starting from the onset of the strength development) of the compressive strength versus time graph. The results of these tests are set forth in Table 5 below.
SUBSTITUTE SHEET (RULE 26) Table 5 Zeolite Concentration versus Compressive Strength Zeolite Activator (grams) 24-Hour Compressive Strength at 150 F
(Psi) [00531 Additionally the strength development of the zeolite sample comprising grams from Table 5 above, was additionally measured by the UCAI'l at test temperatures of 100 F and 120 F. The results of these tests are set forth in Table 6 below.
Table 6 Zeolite concentration versus Compressive Strength at 100 F, 120 F, and 150 F
Zeolite Activator 24 Hour Comp. 24-hour Comp. 24-Hour Comp.
(grams) Strength at 100 F Strength at 120 F Strength at 150 F
(Psi) (psi) (psi) 49 620 770 1220*
0 Did Not Set 60 1010 *Permeability 0.013 md 00541 lt 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.
SUBSTITUTE SHEET (RULE 26) [00551 For the sake of brevity, only certain ranges are explicitly disclosed herein.
However, ranges from any lower lirnit 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-h") 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.
[00561 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, and they 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 all those embodiments are 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 those embodiments. 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 that may be incorporated herein by reference. the definitions that are consistent with this specification should be adopted.
SUBSTITUTE SHEET (RULE 26)
Claims (20)
1. A method of cementing in a subterranean formation comprising:
providing a cement composition comprising water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator;
introducing the cement composition into a subterranean formation; and allowing the cement composition to set in the subterranean formation, wherein the zeolite activator accelerates compressive strength development of the cement composition.
providing a cement composition comprising water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator;
introducing the cement composition into a subterranean formation; and allowing the cement composition to set in the subterranean formation, wherein the zeolite activator accelerates compressive strength development of the cement composition.
2. A method according to claim 1 further comprising the steps of providing a set-delayed cement composition comprising the water, the pozzolan, the hydrated lime, and a set retarder; and adding the zeolite activator to the set-delayed cement composition to produce the cement composition.
3. A method according to claim 2 further comprising storing the set-delayed cement composition for at least about 7 days prior to adding the zeolite activator.
4. A method according to any of claims 1 to 3 wherein the pozzolan is selected from the group consisting of: fly ash, silica fume, metakaolin, pumice, and any combination thereof.
5. A method according to any of claims 1 to 4 wherein the zeolite activator comprises a zeolite in combination with a cation.
6. A method according to any of claims 1 to 5 wherein the zeolite activator comprises a zeolite present on a surface of the pozzolan.
7. A method according to any of claims 1 to 6 wherein the zeolite activator is present in an amount in the range of about 0.1% to about 20% by weight of the pozzolan.
8. A method according to any of claims 1 to 7 wherein the 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 cellulose derivate, a synthetic co- or ter-polymer comprising sulfonate and carboxylic acid groups, a borate compound, and any combination thereof.
9. A method according to any of claims 1 to 8 wherein the cement composition further comprises a dispersant.
10. A method according to claim 9 wherein the dispersant comprises at least one dispersant selected from the group consisting of a sulfonated-formaldehyde-based dispersant, a polycarboxylated ether dispersant, and a combination thereof.
11. A method according to any of claims 1 to 10 wherein the cement composition further comprises a phosphonic acid derivative cement set retarder and a polycarboxylated ether dispersant.
12. A method according to any of claims 1 to 11 wherein the cement composition is introduced into the subterranean formation by a process comprising pumping the set-delayed cement composition through a conduit, through a casing shoe, and into a wellbore annulus.
13. An activated set-delayed cement composition comprising:
water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator.
water, a pozzolan, hydrated lime, a set retarder, and a zeolite activator.
14. An activated set-delayed cement composition according to claim 13 comprising one or more of the features defined in any one of claims 4 to 11.
15. A cementing system comprising:
a set-delayed cement composition comprising water, a pozzolan, hydrated lime, and a set retarder;
a zeolite activator for activation of the set-delayed cement composition;
mixing equipment for mixing the set-delayed cement composition and the zeolite activator to form an activated cement composition; and pumping equipment for delivering the activated cement composition into a wellbore.
a set-delayed cement composition comprising water, a pozzolan, hydrated lime, and a set retarder;
a zeolite activator for activation of the set-delayed cement composition;
mixing equipment for mixing the set-delayed cement composition and the zeolite activator to form an activated cement composition; and pumping equipment for delivering the activated cement composition into a wellbore.
16. A system according to claim 15 wherein the pozzolan is selected from the group consisting of: fly ash, silica fume, metakaolin, pumice, and any combination thereof.
17. A system according to claim 14 or 16 wherein the zeolite comprises zeolite in combination with a cation.
18. A system according to any of claims 14 to 17 wherein the set retarder comprises a phosphonic acid derivative, and wherein the set-delayed cement composition further comprises a polycarboxylated ether dispersant.
19. A system according to any of claims 14 to 18 wherein the zeolite activator comprises a zeolite present on a surface of the pozzolan.
20. A system according to any of claims 14 to 19 wherein the 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 cellulose derivate, a synthetic co- or ter-polymer comprising sulfonate and carboxylic acid groups, a borate compound, and any combination thereof.
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PCT/US2014/054791 WO2015035386A1 (en) | 2013-09-09 | 2014-09-09 | Cement set activators for cement compositions and associated methods |
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US6964302B2 (en) * | 2002-12-10 | 2005-11-15 | Halliburton Energy Services, Inc. | Zeolite-containing cement composition |
US7442248B2 (en) * | 2003-11-18 | 2008-10-28 | Research Incubator, Ltd. | Cementitious composition |
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