NO861099L - Preparat paa basis av titanforbindelser for anvendelse ved hydrauliskfrakturering av olje- og/eller gassfoerende formasjoner. - Google Patents

Preparat paa basis av titanforbindelser for anvendelse ved hydrauliskfrakturering av olje- og/eller gassfoerende formasjoner.

Info

Publication number: NO861099L
Authority: NO; Norway
Prior art keywords: cross; titanium; preparation according; acid; linking
Prior art date: 1985-03-21

Application number

NO861099A

Other languages

English (en)

Norwegian (no)

Inventor

Donald Edward Putzig

Kenneth Cleon Smeltz

Original Assignee

Du Pont

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.)

1985-03-21

Filing date

1986-03-20

Publication date

1986-09-22

1986-03-20 Application filed by Du Pont filed Critical Du Pont

1986-09-22 Publication of NO861099L publication Critical patent/NO861099L/no

Links

238000002360 preparation method Methods 0.000 title claims description 34
150000001875 compounds Chemical class 0.000 title claims description 6
238000004132 cross linking Methods 0.000 claims description 42
230000015572 biosynthetic process Effects 0.000 claims description 27
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 26
238000000034 method Methods 0.000 claims description 22
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 20
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 20
239000000600 sorbitol Substances 0.000 claims description 20
239000010936 titanium Substances 0.000 claims description 19
150000003609 titanium compounds Chemical class 0.000 claims description 19
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 15
239000003431 cross linking reagent Substances 0.000 claims description 15
229910052719 titanium Inorganic materials 0.000 claims description 15
239000012530 fluid Substances 0.000 claims description 14
229920005862 polyol Polymers 0.000 claims description 13
150000003077 polyols Chemical class 0.000 claims description 13
239000004310 lactic acid Substances 0.000 claims description 12
235000014655 lactic acid Nutrition 0.000 claims description 12
239000000463 material Substances 0.000 claims description 12
239000000243 solution Substances 0.000 claims description 10
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 9
239000001630 malic acid Substances 0.000 claims description 9
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 8
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 8
235000011090 malic acid Nutrition 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical group Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 7
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
229910003074 TiCl4 Inorganic materials 0.000 claims description 6
235000015165 citric acid Nutrition 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 4
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 4
150000007522 mineralic acids Chemical class 0.000 claims description 4
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
239000007795 chemical reaction product Substances 0.000 claims description 3
239000011975 tartaric acid Substances 0.000 claims description 3
235000002906 tartaric acid Nutrition 0.000 claims description 3
150000003608 titanium Chemical class 0.000 claims description 3
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 claims description 2
239000004386 Erythritol Substances 0.000 claims description 2
UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 2
229930195725 Mannitol Natural products 0.000 claims description 2
TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 2
UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 2
235000019414 erythritol Nutrition 0.000 claims description 2
229940009714 erythritol Drugs 0.000 claims description 2
FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 claims description 2
CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims description 2
229960000367 inositol Drugs 0.000 claims description 2
239000000594 mannitol Substances 0.000 claims description 2
235000010355 mannitol Nutrition 0.000 claims description 2
229920000642 polymer Polymers 0.000 claims description 2
CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims description 2
239000000811 xylitol Substances 0.000 claims description 2
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 2
235000010447 xylitol Nutrition 0.000 claims description 2
229960002675 xylitol Drugs 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims 1
239000000499 gel Substances 0.000 description 31
238000005755 formation reaction Methods 0.000 description 24
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
239000000203 mixture Substances 0.000 description 18
239000000047 product Substances 0.000 description 12
150000004676 glycans Chemical class 0.000 description 10
229920001282 polysaccharide Polymers 0.000 description 10
239000005017 polysaccharide Substances 0.000 description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
-1 hydroxypropyl Chemical group 0.000 description 8
244000303965 Cyamopsis psoralioides Species 0.000 description 7
229940099690 malic acid Drugs 0.000 description 6
239000003349 gelling agent Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
239000004971 Cross linker Substances 0.000 description 4
RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
239000013522 chelant Substances 0.000 description 4
229960004106 citric acid Drugs 0.000 description 4
230000018109 developmental process Effects 0.000 description 4
239000007789 gas Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
230000007423 decrease Effects 0.000 description 3
239000008367 deionised water Substances 0.000 description 3
229910021641 deionized water Inorganic materials 0.000 description 3
238000003756 stirring Methods 0.000 description 3
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 2
SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000000872 buffer Substances 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
239000001530 fumaric acid Substances 0.000 description 2
239000000174 gluconic acid Substances 0.000 description 2
235000012208 gluconic acid Nutrition 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
150000002763 monocarboxylic acids Chemical class 0.000 description 2
238000005086 pumping Methods 0.000 description 2
238000011084 recovery Methods 0.000 description 2
239000004576 sand Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
238000005303 weighing Methods 0.000 description 2
QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 description 1
RBNPOMFGQQGHHO-UHFFFAOYSA-N -2,3-Dihydroxypropanoic acid Natural products OCC(O)C(O)=O RBNPOMFGQQGHHO-UHFFFAOYSA-N 0.000 description 1
NAOLWIGVYRIGTP-UHFFFAOYSA-N 1,3,5-trihydroxyanthracene-9,10-dione Chemical compound C1=CC(O)=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1 NAOLWIGVYRIGTP-UHFFFAOYSA-N 0.000 description 1
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000002687 Caesalpinia echinata Nutrition 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
YASYEJJMZJALEJ-UHFFFAOYSA-N Citric acid monohydrate Chemical compound O.OC(=O)CC(O)(C(O)=O)CC(O)=O YASYEJJMZJALEJ-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-CUHNMECISA-N D-Cellobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-CUHNMECISA-N 0.000 description 1
RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 description 1
WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
229920000926 Galactomannan Polymers 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
229920002907 Guar gum Polymers 0.000 description 1
229920000569 Gum karaya Polymers 0.000 description 1
241001424361 Haematoxylum brasiletto Species 0.000 description 1
SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
229920000161 Locust bean gum Polymers 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
241000219100 Rhamnaceae Species 0.000 description 1
239000004133 Sodium thiosulphate Substances 0.000 description 1
241000934878 Sterculia Species 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
229910001570 bauxite Inorganic materials 0.000 description 1
SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229960002303 citric acid monohydrate Drugs 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
150000002016 disaccharides Chemical class 0.000 description 1
230000000694 effects Effects 0.000 description 1
229930182830 galactose Natural products 0.000 description 1
239000008103 glucose Substances 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
150000001261 hydroxy acids Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000000231 karaya gum Substances 0.000 description 1
235000010494 karaya gum Nutrition 0.000 description 1
229940039371 karaya gum Drugs 0.000 description 1
239000008101 lactose Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000711 locust bean gum Substances 0.000 description 1
235000010420 locust bean gum Nutrition 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
229960002510 mandelic acid Drugs 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
230000035699 permeability Effects 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000012453 solvate Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0091—Complexes with metal-heteroatom-bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/66—Compositions based on water or polar solvents
- C09K8/68—Compositions based on water or polar solvents containing organic compounds
- C09K8/685—Compositions based on water or polar solvents containing organic compounds containing cross-linking agents

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
General Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Colloid Chemistry (AREA)
Lubricants (AREA)
Conductive Materials (AREA)
Inorganic Compounds Of Heavy Metals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO861099A 1985-03-21 1986-03-20 Preparat paa basis av titanforbindelser for anvendelse ved hydrauliskfrakturering av olje- og/eller gassfoerende formasjoner. NO861099L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US71451385A	1985-03-21	1985-03-21

Publications (1)

Publication Number	Publication Date
NO861099L true NO861099L (no)	1986-09-22

Family

ID=24870342

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO861099A NO861099L (no)	1985-03-21	1986-03-20	Preparat paa basis av titanforbindelser for anvendelse ved hydrauliskfrakturering av olje- og/eller gassfoerende formasjoner.

Country Status (6)

Country	Link
EP (1)	EP0195531A3 (fr)
JP (1)	JPS61216730A (fr)
AU (1)	AU579457B2 (fr)
CA (1)	CA1257861A (fr)
NO (1)	NO861099L (fr)
NZ (1)	NZ215539A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ222812A (en) *	1986-12-08	1989-08-29	Du Pont	Organic titanium compositions and their use as cross-linking agents in a hydraulic fracturing process
US4958038A (en) *	1987-12-21	1990-09-18	E. I. Du Pont De Nemours And Company	Organotitanium compositions useful for cross-linking
GB2226024B (en) *	1988-12-16	1992-06-10	Tioxide Group Plc	Organo-metallic compounds
CN117164625A (zh) *	2023-09-05	2023-12-05	东营施普瑞石油工程技术有限公司	一种压裂液低聚交联剂及其制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2898356A (en) *	1955-09-06	1959-08-04	Nat Lead Co	Organotitanium compounds and process of preparation
CA1134258A (fr) *	1981-09-28	1982-10-26	Ronald S. Bullen	Methode de fracturation a l'aide de dioxyde de carbone
AU576475B2 (en) *	1982-09-27	1988-09-01	Halliburton Company	Method and composition for fracturing subterranean formations
US4464270A (en) *	1982-09-27	1984-08-07	Halliburton Company	Method and compositions for fracturing subterranean formations
US4462917A (en) *	1982-09-27	1984-07-31	Halliburton Company	Method and compositions for fracturing subterranean formations
US4553601A (en) *	1984-09-26	1985-11-19	Halliburton Company	Method for fracturing subterranean formations

1986
- 1986-02-21 EP EP86301274A patent/EP0195531A3/fr not_active Ceased
- 1986-03-13 CA CA000504071A patent/CA1257861A/fr not_active Expired
- 1986-03-18 AU AU54909/86A patent/AU579457B2/en not_active Ceased
- 1986-03-20 JP JP61061052A patent/JPS61216730A/ja active Pending
- 1986-03-20 NZ NZ215539A patent/NZ215539A/xx unknown
- 1986-03-20 NO NO861099A patent/NO861099L/no unknown

Also Published As

Publication number	Publication date
EP0195531A3 (fr)	1987-12-02
JPS61216730A (ja)	1986-09-26
CA1257861A (fr)	1989-07-25
EP0195531A2 (fr)	1986-09-24
NZ215539A (en)	1988-11-29
AU579457B2 (en)	1988-11-24
AU5490986A (en)	1986-09-25

Publication	Publication Date	Title
US4462917A (en)	1984-07-31	Method and compositions for fracturing subterranean formations
US4686052A (en)	1987-08-11	Stabilized fracture fluid and crosslinker therefor
US4502967A (en)	1985-03-05	Method and compositions for fracturing subterranean formations
US6983801B2 (en)	2006-01-10	Well treatment fluid compositions and methods for their use
EP0233660B1 (fr)	1991-10-02	Composition de réticulation retardée
US8252731B2 (en)	2012-08-28	Solid zirconium-based cross-linking agent and use in oil field applications
US6908886B2 (en)	2005-06-21	Annular fluids and method of emplacing the same
CA2576157C (fr)	2010-03-16	Stabilisation de guars polymeres reticules et de derives de guars modifies
US3922173A (en)	1975-11-25	Temperature-stable aqueous gels
CN101675062B (zh)	2013-06-12	锆基交联剂组合物及其在高pH值油田应用中的用途
US8518861B2 (en)	2013-08-27	Solid zirconium-based cross-linking agent and use in oil field applications
NO173522B (no)	1993-09-13	Vandig gel og fremgangsmaate for behandling av underjordiske formasjoner
US7851417B2 (en)	2010-12-14	Process to prepare borozirconate solution and use as cross-linker in hydraulic fracturing fluids
US7347265B2 (en)	2008-03-25	Method of forming temporary blocking gel containing guar derivative
WO2009079535A1 (fr)	2009-06-25	Procédé de préparation de compositions réticulantes à base de zirconium et leur utilisation dans des applications pétrolifères
CA2704542A1 (fr)	2009-05-07	Liquide de fracturation aqueux au zirconium de haute temperature et son utilisation
CN101605801A (zh)	2009-12-16	稳定锆-三乙醇胺络合物的方法以及在油田应用中的用途
US4657080A (en)	1987-04-14	Method of fracturing a subterranean formation using delayed crosslinker compositions containing organic titanium complexes
US4861500A (en)	1989-08-29	Delayed crosslinker composition containing organic titanium complexes and hydroxycarboxylic acids
CA2678783C (fr)	2016-10-18	Compositions d'agent de reticulation a base de zirconium et leur utilisation dans des applications de champ petrolifere a ph eleve
EP0104927B1 (fr)	1987-12-16	Méthode et compositions pour la fracturation de formations souterraines
US4953621A (en)	1990-09-04	Organic titanium compositions useful as cross-linkers
US7732384B2 (en)	2010-06-08	Solid borozirconate and borotitanate cross-linkers
NO861099L (no)	1986-09-22	Preparat paa basis av titanforbindelser for anvendelse ved hydrauliskfrakturering av olje- og/eller gassfoerende formasjoner.
US4749040A (en)	1988-06-07	Method of fracturing a subterranean formation using delayed crosslinker compositions containing organic titanium complexes