CA2716450C - Liquide isolant a base d'eau et methodes connexes - Google Patents

Liquide isolant a base d'eau et methodes connexes Download PDF

Info

Publication number: CA2716450C
Authority: CA; Canada
Prior art keywords: aqueous; based insulating; glycol; fluid; layered silicate
Prior art date: 2008-03-11
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.): Expired - Fee Related

Application number

CA2716450A

Other languages

English (en)

Other versions

CA2716450A1 (fr

Inventor

Ryan G. Ezell

Douglas J. Harrison

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Halliburton Energy Services Inc

Original Assignee

Halliburton Energy Services Inc

Priority date (The priority date 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 date listed.)

2008-03-11

Filing date

2009-03-05

Publication date

2013-02-19

2009-03-05 Application filed by Halliburton Energy Services Inc filed Critical Halliburton Energy Services Inc

2009-09-17 Publication of CA2716450A1 publication Critical patent/CA2716450A1/fr

2013-02-19 Application granted granted Critical

2013-02-19 Publication of CA2716450C publication Critical patent/CA2716450C/fr

Status Expired - Fee Related legal-status Critical Current

2029-03-05 Anticipated expiration legal-status Critical

Links

239000012530 fluid Substances 0.000 title claims abstract description 220
238000000034 method Methods 0.000 title claims abstract description 42
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 53
239000007788 liquid Substances 0.000 claims abstract description 36
229920000642 polymer Polymers 0.000 claims description 47
-1 poly(butyl acrylate) Polymers 0.000 claims description 32
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 24
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
229920005862 polyol Polymers 0.000 claims description 21
150000003077 polyols Chemical class 0.000 claims description 21
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 19
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 13
150000002009 diols Chemical class 0.000 claims description 9
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 8
229920001223 polyethylene glycol Polymers 0.000 claims description 8
229920001451 polypropylene glycol Polymers 0.000 claims description 8
239000005977 Ethylene Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
239000007795 chemical reaction product Substances 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
229920001577 copolymer Polymers 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 6
150000002148 esters Chemical class 0.000 claims description 6
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 6
150000005846 sugar alcohols Chemical class 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 5
239000012267 brine Substances 0.000 claims description 5
VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 claims description 5
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 5
229910052901 montmorillonite Inorganic materials 0.000 claims description 5
229920001059 synthetic polymer Polymers 0.000 claims description 5
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 5
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 4
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 4
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 4
KDKYADYSIPSCCQ-UHFFFAOYSA-N ethyl acetylene Natural products CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 claims description 4
229910000271 hectorite Inorganic materials 0.000 claims description 4
KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 claims description 4
239000003112 inhibitor Substances 0.000 claims description 4
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 4
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 4
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 claims description 4
229910000275 saponite Inorganic materials 0.000 claims description 4
229910021647 smectite Inorganic materials 0.000 claims description 4
229910052902 vermiculite Inorganic materials 0.000 claims description 4
239000010455 vermiculite Substances 0.000 claims description 4
235000019354 vermiculite Nutrition 0.000 claims description 4
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 3
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
239000004280 Sodium formate Substances 0.000 claims description 3
229910007935 ZrBr2 Inorganic materials 0.000 claims description 3
125000005396 acrylic acid ester group Chemical group 0.000 claims description 3
ATZQZZAXOPPAAQ-UHFFFAOYSA-M caesium formate Chemical compound [Cs+].[O-]C=O ATZQZZAXOPPAAQ-UHFFFAOYSA-M 0.000 claims description 3
229910001622 calcium bromide Inorganic materials 0.000 claims description 3
239000001110 calcium chloride Substances 0.000 claims description 3
229910001628 calcium chloride Inorganic materials 0.000 claims description 3
235000011148 calcium chloride Nutrition 0.000 claims description 3
WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 claims description 3
WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 claims description 3
229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
239000011780 sodium chloride Substances 0.000 claims description 3
HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 claims description 3
235000019254 sodium formate Nutrition 0.000 claims description 3
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 3
229920002125 Sokalan® Polymers 0.000 claims description 2
150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
239000011324 bead Substances 0.000 claims description 2
239000003139 biocide Substances 0.000 claims description 2
239000000872 buffer Substances 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
230000007797 corrosion Effects 0.000 claims description 2
238000005260 corrosion Methods 0.000 claims description 2
239000011521 glass Substances 0.000 claims description 2
239000004005 microsphere Substances 0.000 claims description 2
239000003002 pH adjusting agent Substances 0.000 claims description 2
229920001485 poly(butyl acrylate) polymer Polymers 0.000 claims description 2
229920001490 poly(butyl methacrylate) polymer Polymers 0.000 claims description 2
239000006254 rheological additive Substances 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
239000002202 Polyethylene glycol Substances 0.000 claims 6
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims 4
ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 claims 3
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims 3
230000036571 hydration Effects 0.000 claims 3
238000006703 hydration reaction Methods 0.000 claims 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
229920002126 Acrylic acid copolymer Polymers 0.000 claims 1
230000000996 additive effect Effects 0.000 claims 1
230000003115 biocidal effect Effects 0.000 claims 1
239000012044 organic layer Substances 0.000 claims 1
239000000700 radioactive tracer Substances 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 41
239000003431 cross linking reagent Substances 0.000 description 22
238000009472 formulation Methods 0.000 description 20
230000008901 benefit Effects 0.000 description 12
239000000499 gel Substances 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
238000004519 manufacturing process Methods 0.000 description 7
230000003068 static effect Effects 0.000 description 7
238000012360 testing method Methods 0.000 description 7
230000032683 aging Effects 0.000 description 6
239000000463 material Substances 0.000 description 6
238000005259 measurement Methods 0.000 description 6
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
229920002401 polyacrylamide Polymers 0.000 description 6
238000012546 transfer Methods 0.000 description 6
229920002873 Polyethylenimine Polymers 0.000 description 5
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 5
229920001519 homopolymer Polymers 0.000 description 5
239000003921 oil Substances 0.000 description 5
235000013824 polyphenols Nutrition 0.000 description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
239000002243 precursor Substances 0.000 description 4
235000013772 propylene glycol Nutrition 0.000 description 4
230000009467 reduction Effects 0.000 description 4
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
239000004971 Cross linker Substances 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000001994 activation Methods 0.000 description 3
230000004913 activation Effects 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
239000004927 clay Substances 0.000 description 3
XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
238000001879 gelation Methods 0.000 description 3
239000003349 gelling agent Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
150000004760 silicates Chemical class 0.000 description 3
230000001988 toxicity Effects 0.000 description 3
231100000419 toxicity Toxicity 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
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IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 2
229960001138 acetylsalicylic acid Drugs 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
229960004050 aminobenzoic acid Drugs 0.000 description 2
230000009286 beneficial effect Effects 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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238000004132 cross linking Methods 0.000 description 2
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
229940049953 phenylacetate Drugs 0.000 description 2
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
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150000003839 salts Chemical class 0.000 description 2
229920001897 terpolymer Polymers 0.000 description 2
238000007725 thermal activation Methods 0.000 description 2
AZJYLVAUMGUUBL-UHFFFAOYSA-A u1qj22mc8e Chemical compound [F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 AZJYLVAUMGUUBL-UHFFFAOYSA-A 0.000 description 2
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XYOMMVNZIAGSMW-UHFFFAOYSA-N (prop-2-enoylamino)methyl propane-1-sulfonate Chemical compound CCCS(=O)(=O)OCNC(=O)C=C XYOMMVNZIAGSMW-UHFFFAOYSA-N 0.000 description 1
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
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QNIRRHUUOQAEPB-UHFFFAOYSA-N 2-(prop-2-enoylamino)butane-2-sulfonic acid Chemical class CCC(C)(S(O)(=O)=O)NC(=O)C=C QNIRRHUUOQAEPB-UHFFFAOYSA-N 0.000 description 1
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XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002028 premature Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000005086 pumping Methods 0.000 description 1
229960000581 salicylamide Drugs 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
230000035882 stress Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1

Classifications

- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L59/00—Thermal insulation in general
- F16L59/14—Arrangements for the insulation of pipes or pipe systems
- F16L59/143—Pre-insulated pipes
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
- 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
- E21B36/00—Heating, cooling or insulating arrangements for boreholes or wells, e.g. for use in permafrost zones
- E21B36/003—Insulating arrangements
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
- C10M2207/0225—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups used as base material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/0406—Ethers; Acetals; Ortho-esters; Ortho-carbonates used as base material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
- C10M2209/1045—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only used as base material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
- C10M2209/1055—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only used as base material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
- C10M2209/1085—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified used as base material

Landscapes

Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Geology (AREA)
General Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Mining & Mineral Resources (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Environmental & Geological Engineering (AREA)
General Life Sciences & Earth Sciences (AREA)
Geochemistry & Mineralogy (AREA)
Physics & Mathematics (AREA)
Mechanical Engineering (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Fluid Mechanics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Thermal Insulation (AREA)
Lubricants (AREA)
Laminated Bodies (AREA)
Silicates, Zeolites, And Molecular Sieves (AREA)
Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
Rigid Pipes And Flexible Pipes (AREA)
Organic Insulating Materials (AREA)

CA2716450A 2008-03-11 2009-03-05 Liquide isolant a base d'eau et methodes connexes Expired - Fee Related CA2716450C (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US12/046,086 US20080224087A1 (en)	2007-03-14	2008-03-11	Aqueous-Based Insulating Fluids and Related Methods
US12/046,086		2008-03-11
PCT/GB2009/000609 WO2009112808A2 (fr)	2008-03-11	2009-03-05	Fluides isolants à base d'eau améliorés et procédés apparentés

Publications (2)

Publication Number	Publication Date
CA2716450A1 CA2716450A1 (fr)	2009-09-17
CA2716450C true CA2716450C (fr)	2013-02-19

Family

ID=40999887

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA2716450A Expired - Fee Related CA2716450C (fr)	2008-03-11	2009-03-05	Liquide isolant a base d'eau et methodes connexes

Country Status (10)

Country	Link
US (1)	US20080224087A1 (fr)
EP (1)	EP2271735A2 (fr)
JP (1)	JP2011513677A (fr)
CN (1)	CN102037110A (fr)
AU (1)	AU2009223980A1 (fr)
BR (1)	BRPI0909062A2 (fr)
CA (1)	CA2716450C (fr)
MX (1)	MX2010009988A (fr)
RU (1)	RU2475624C2 (fr)
WO (1)	WO2009112808A2 (fr)

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2008
- 2008-03-11 US US12/046,086 patent/US20080224087A1/en not_active Abandoned
2009
- 2009-03-05 MX MX2010009988A patent/MX2010009988A/es unknown
- 2009-03-05 AU AU2009223980A patent/AU2009223980A1/en not_active Abandoned
- 2009-03-05 EP EP09721009A patent/EP2271735A2/fr not_active Withdrawn
- 2009-03-05 JP JP2010550250A patent/JP2011513677A/ja active Pending
- 2009-03-05 CA CA2716450A patent/CA2716450C/fr not_active Expired - Fee Related
- 2009-03-05 CN CN2009801082932A patent/CN102037110A/zh active Pending
- 2009-03-05 WO PCT/GB2009/000609 patent/WO2009112808A2/fr active Application Filing
- 2009-03-05 BR BRPI0909062-2A patent/BRPI0909062A2/pt not_active IP Right Cessation
- 2009-03-05 RU RU2010141547/03A patent/RU2475624C2/ru not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP2271735A2 (fr)	2011-01-12
RU2475624C2 (ru)	2013-02-20
CN102037110A (zh)	2011-04-27
WO2009112808A2 (fr)	2009-09-17
JP2011513677A (ja)	2011-04-28
US20080224087A1 (en)	2008-09-18
BRPI0909062A2 (pt)	2015-08-25
MX2010009988A (es)	2010-09-30
AU2009223980A1 (en)	2009-09-17
WO2009112808A3 (fr)	2009-11-26
CA2716450A1 (fr)	2009-09-17
RU2010141547A (ru)	2012-04-20

Legal Events

Date	Code	Title	Description
2010-08-26	EEER	Examination request
2015-04-16	MKLA	Lapsed	Effective date: 20150305

Publication	Publication Date	Title
AU2008224687B2 (en)	2011-12-01	Improved aqueous-based insulating fluids and related methods
CA2716450C (fr)	2013-02-19	Liquide isolant a base d'eau et methodes connexes
RU2503704C2 (ru)	2014-01-10	Базовые жидкости, безвредные для окружающей среды, и способы их приготовления и использования
US7306039B2 (en)	2007-12-11	Methods of using crosslinkable compositions
US20070167332A1 (en)	2007-07-19	Quaternary ammonium salts as thickening agents for aqueous systems
NO20150791A1 (en)	2015-06-17	Novel Weighted Elastomer Systems For Use In Cement, Spacer And Drilling Fluids
BR112017019466B1 (pt)	2022-11-22	Composição para o tratamento de óleo e gás compreendendo hidroxietil celulose e polivinilpirrolidona reticulada
CA2529396A1 (fr)	2006-06-17	Methodes et compositions pour isolants thermiques
US20150166875A1 (en)	2015-06-18	Hydratable polymer system based on a chia derived gelling agent and methods for making and using same
US20140069643A1 (en)	2014-03-13	Electron-poor orthoester for generating acid in a well fluid
EP3710553A1 (fr)	2020-09-23	Fluide isolant pour isolation thermique
US20130213656A1 (en)	2013-08-22	Aqueous-Based Insulating Fluids and Related Methods
US7923414B2 (en)	2011-04-12	Rheology modifier comprising a tetrakis(hydroxyalkyl) phosphonium salt for polymer fluids
CA2898888C (fr)	2019-04-02	Fluides d'isolation a base aqueuse et procedes associes
EP2909285A1 (fr)	2015-08-26	Agents gélifiants et leurs procédés d'utilisation
CN110168044B (zh)	2022-02-01	高性能盐水增粘剂