NO824042L - Bisalkyl-bis(trialkanolamin)zirkonater. - Google Patents

Bisalkyl-bis(trialkanolamin)zirkonater.

Info

Publication number: NO824042L
Authority: NO; Norway
Prior art keywords: zirconate; triethanolamine; bis; reaction product; approx
Prior art date: 1982-04-22

Application number

NO824042A

Other languages

English (en)

Norwegian (no)

Inventor

Gregory J Rummo

Robert Startup

Original Assignee

Key Fries 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.)

1982-04-22

Filing date

1982-12-02

Publication date

1983-10-24

1982-12-02 Application filed by Key Fries Inc filed Critical Key Fries Inc

1983-10-24 Publication of NO824042L publication Critical patent/NO824042L/no

Links

239000007788 liquid Substances 0.000 claims abstract description 10
239000002562 thickening agent Substances 0.000 claims abstract description 10
150000001412 amines Chemical class 0.000 claims abstract description 6
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 17
239000000047 product Substances 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 11
238000000034 method Methods 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
239000000203 mixture Substances 0.000 claims description 7
229910052845 zircon Inorganic materials 0.000 claims description 7
238000006243 chemical reaction Methods 0.000 claims description 6
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
150000004676 glycans Chemical class 0.000 claims description 4
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
229920001282 polysaccharide Polymers 0.000 claims description 4
239000005017 polysaccharide Substances 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims 7
239000012530 fluid Substances 0.000 abstract description 12
238000011084 recovery Methods 0.000 abstract description 6
230000015572 biosynthetic process Effects 0.000 abstract description 4
238000005553 drilling Methods 0.000 abstract description 4
238000007596 consolidation process Methods 0.000 abstract description 3
230000006641 stabilisation Effects 0.000 abstract description 3
238000011105 stabilization Methods 0.000 abstract description 3
238000003786 synthesis reaction Methods 0.000 abstract description 3
244000303965 Cyamopsis psoralioides Species 0.000 description 7
150000001414 amino alcohols Chemical class 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 6
-1 hydroxypropyl Chemical group 0.000 description 6
239000000243 solution Substances 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
239000011734 sodium Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
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 3
229920000926 Galactomannan Polymers 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
229920002907 Guar gum Polymers 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000000665 guar gum Substances 0.000 description 2
235000010417 guar gum Nutrition 0.000 description 2
229960002154 guar gum Drugs 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000012263 liquid product Substances 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
238000003756 stirring Methods 0.000 description 2
229910052719 titanium Inorganic materials 0.000 description 2
239000010936 titanium Substances 0.000 description 2
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
STVOGHJNKAEDJP-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]-2-ethylbutan-1-ol Chemical compound CCC(CC)(CO)N(CCO)CCO STVOGHJNKAEDJP-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
229920000569 Gum karaya Polymers 0.000 description 1
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 1
229920000161 Locust bean gum Polymers 0.000 description 1
241000276498 Pollachius virens Species 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
241000934878 Sterculia Species 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003349 gelling agent Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000008241 heterogeneous mixture Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 1
239000000711 locust bean gum Substances 0.000 description 1
235000010420 locust bean gum Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003129 oil well Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
150000002905 orthoesters Chemical class 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
BCWYYHBWCZYDNB-UHFFFAOYSA-N propan-2-ol;zirconium Chemical compound [Zr].CC(C)O.CC(C)O.CC(C)O.CC(C)O BCWYYHBWCZYDNB-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
235000015424 sodium Nutrition 0.000 description 1
239000012265 solid product Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000004753 textile Substances 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000001993 wax Substances 0.000 description 1
229910052726 zirconium Inorganic materials 0.000 description 1
150000003755 zirconium compounds Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—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
- 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
- C09K8/02—Well-drilling compositions
- C09K8/03—Specific additives for general use in well-drilling compositions
- C09K8/035—Organic additives
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/50—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
- C09K8/504—Compositions based on water or polar solvents
- C09K8/506—Compositions based on water or polar solvents containing organic compounds
- C09K8/508—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
- C09K8/512—Compositions based on water or polar solvents containing organic compounds macromolecular compounds containing cross-linking agents

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polyurethanes Or Polyureas (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Colloid Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

NO824042A 1982-04-22 1982-12-02 Bisalkyl-bis(trialkanolamin)zirkonater. NO824042L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US37102282A	1982-04-22	1982-04-22

Publications (1)

Publication Number	Publication Date
NO824042L true NO824042L (no)	1983-10-24

Family

ID=23462166

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO824042A NO824042L (no)	1982-04-22	1982-12-02	Bisalkyl-bis(trialkanolamin)zirkonater.

Country Status (5)

Country	Link
EP (1)	EP0092755B1 (de)
AT (1)	ATE20667T1 (de)
DE (1)	DE3364422D1 (de)
DK (1)	DK175083A (de)
NO (1)	NO824042L (de)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4477360A (en) *	1983-06-13	1984-10-16	Halliburton Company	Method and compositions for fracturing subterranean formations
JPH02504645A (ja) *	1986-10-02	1990-12-27	ザ　ルブリゾル　コーポレーション	チタン錯体およびジルコニウム錯体，および燃料組成物
US4801389A (en) *	1987-08-03	1989-01-31	Dowell Schlumberger Incorporated	High temperature guar-based fracturing fluid
US4799550A (en) *	1988-04-18	1989-01-24	Halliburton Company	Subterranean formation treating with delayed crosslinking gel fluids
EP0437416A3 (en) *	1990-01-11	1991-12-18	Ciba-Geigy Ag	Compositions containing a 2,2',2"-nitrilotriethanol-cyclometallate
IL100669A0 (en)	1991-05-13	1992-09-06	Lubrizol Corp	Low-sulfur diesel fuel containing organometallic complexes
US5376154A (en)	1991-05-13	1994-12-27	The Lubrizol Corporation	Low-sulfur diesel fuels containing organometallic complexes
US5344467A (en)	1991-05-13	1994-09-06	The Lubrizol Corporation	Organometallic complex-antioxidant combinations, and concentrates and diesel fuels containing same
US5360459A (en)	1991-05-13	1994-11-01	The Lubrizol Corporation	Copper-containing organometallic complexes and concentrates and diesel fuels containing same
TW230781B (de)	1991-05-13	1994-09-21	Lubysu Co
WO1996033966A1 (en) *	1995-04-25	1996-10-31	Bj Services Company	Gelation additive for hydraulic fracturing fluids
US8697610B2 (en)	2007-05-11	2014-04-15	Schlumberger Technology Corporation	Well treatment with complexed metal crosslinkers
US7754660B2 (en) *	2007-12-18	2010-07-13	E.I. Du Pont De Nemours And Company	Process to prepare zirconium-based cross-linker compositions and their use in oil field applications
US8853135B2 (en)	2008-05-07	2014-10-07	Schlumberger Technology Corporation	Method for treating wellbore in a subterranean formation with high density brines and complexed metal crosslinkers
US8636066B2 (en)	2010-03-12	2014-01-28	Baker Hughes Incorporated	Method of enhancing productivity of a formation with unhydrated borated galactomannan gum
RU2682833C2 (ru)	2014-01-27	2019-03-21	Бейкер Хьюз Инкорпорейтед	Способ проведения повторного гидравлического разрыва пласта с использованием борированной галактоманнановой камеди
US11585196B2 (en)	2019-10-23	2023-02-21	Baker Hughes Oilfield Operations Llc	Methods of using energized well treating fluids

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3028297A (en) *	1956-06-15	1962-04-03	Linden Lab Inc	Orthotitanic compound used in method for improving wet strength of paper and resulting paper
US2894966A (en) *	1956-07-10	1959-07-14	Nat Lead Co	Process for the preparation of stabilized organotitanium compounds
US2978347A (en) *	1956-12-21	1961-04-04	Union Carbide Corp	Organo-zirconium derivatives

1982
- 1982-12-02 NO NO824042A patent/NO824042L/no unknown
1983
- 1983-04-16 AT AT83103706T patent/ATE20667T1/de not_active IP Right Cessation
- 1983-04-16 EP EP83103706A patent/EP0092755B1/de not_active Expired
- 1983-04-16 DE DE8383103706T patent/DE3364422D1/de not_active Expired
- 1983-04-21 DK DK175083A patent/DK175083A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
EP0092755B1 (de)	1986-07-09
DK175083A (da)	1983-10-23
DE3364422D1 (de)	1986-08-14
ATE20667T1 (de)	1986-07-15
DK175083D0 (da)	1983-04-21
EP0092755A1 (de)	1983-11-02

Publication	Publication Date	Title
EP0092755B1 (de)	1986-07-09	Dialkyl-bis(trialkanolamine)zirkonate
US7754660B2 (en)	2010-07-13	Process to prepare zirconium-based cross-linker compositions and their use in oil field applications
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US4578488A (en)	1986-03-25	Bisalkyl bis(trialkanol amine)zirconates and use of same as thickening agents for aqueous polysaccharide solutions
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US4369124A (en)	1983-01-18	High viscosity complexed aqueous gels and methods and additives for forming such gels
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US20090166041A1 (en)	2009-07-02	Zirconium-hydroxy alkylated amine-hydroxy carboxylic acid cross-linking composition for use with high pH polymer solutions
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US4958038A (en)	1990-09-18	Organotitanium compositions useful for cross-linking
US5021171A (en)	1991-06-04	Organotitanium compositions useful for cross-linking
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