NO822262L - Temperaturstabile borevaesker. - Google Patents

Temperaturstabile borevaesker.

Info

Publication number: NO822262L
Authority: NO; Norway
Prior art keywords: lignite; vinyl monomer; weight; polymerization; stated
Prior art date: 1981-07-27

Application number

NO822262A

Other languages

English (en)

Norwegian (no)

Inventor

David Frost

Original Assignee

Bw Mud Ltd

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.)

1981-07-27

Filing date

1982-06-30

Publication date

1983-01-28

1982-06-30 Application filed by Bw Mud Ltd filed Critical Bw Mud Ltd

1983-01-28 Publication of NO822262L publication Critical patent/NO822262L/no

Links

239000003077 lignite Substances 0.000 claims description 35
239000000178 monomer Substances 0.000 claims description 31
229920002554 vinyl polymer Polymers 0.000 claims description 29
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 28
238000006116 polymerization reaction Methods 0.000 claims description 20
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
238000005553 drilling Methods 0.000 claims description 13
QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 claims description 12
239000004021 humic acid Substances 0.000 claims description 11
239000007788 liquid Substances 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
229920000642 polymer Polymers 0.000 claims description 8
229920000578 graft copolymer Polymers 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
229920001577 copolymer Polymers 0.000 claims description 4
239000003999 initiator Substances 0.000 claims description 4
238000002156 mixing Methods 0.000 claims description 4
230000000379 polymerizing effect Effects 0.000 claims description 3
238000005549 size reduction Methods 0.000 claims description 3
239000010802 sludge Substances 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
239000000047 product Substances 0.000 description 17
238000006243 chemical reaction Methods 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 12
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 11
239000000203 mixture Substances 0.000 description 9
239000000243 solution Substances 0.000 description 7
238000003756 stirring Methods 0.000 description 7
239000002253 acid Substances 0.000 description 5
239000003513 alkali Substances 0.000 description 5
-1 alkali metal salts Chemical class 0.000 description 5
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
239000004927 clay Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
229920003169 water-soluble polymer Polymers 0.000 description 4
239000004160 Ammonium persulphate Substances 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
235000019395 ammonium persulphate Nutrition 0.000 description 3
230000007062 hydrolysis Effects 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
150000003573 thiols Chemical class 0.000 description 3
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
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 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
239000008186 active pharmaceutical agent Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000000605 extraction Methods 0.000 description 2
239000012263 liquid product Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 1
229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000011149 active material Substances 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
239000011362 coarse particle Substances 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
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
239000012933 diacyl peroxide Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000010559 graft polymerization reaction Methods 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
230000002794 monomerizing effect Effects 0.000 description 1
239000003129 oil well Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000010008 shearing Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
239000004289 sodium hydrogen sulphite Substances 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
SPDUKHLMYVCLOA-UHFFFAOYSA-M sodium;ethaneperoxoate Chemical compound [Na+].CC(=O)O[O-] SPDUKHLMYVCLOA-UHFFFAOYSA-M 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F289/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds not provided for in groups C08F251/00 - C08F287/00

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Graft Or Block Polymers (AREA)
Lubricants (AREA)
Compositions Of Macromolecular Compounds (AREA)
Drilling Tools (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)

NO822262A 1981-07-27 1982-06-30 Temperaturstabile borevaesker. NO822262L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB8123088		1981-07-27

Publications (1)

Publication Number	Publication Date
NO822262L true NO822262L (no)	1983-01-28

Family

ID=10523529

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO822262A NO822262L (no)	1981-07-27	1982-06-30	Temperaturstabile borevaesker.

Country Status (5)

Country	Link
EP (1)	EP0072445A3 (fr)
JP (1)	JPS5832614A (fr)
AU (1)	AU8642482A (fr)
DK (1)	DK333182A (fr)
NO (1)	NO822262L (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2131067A (en) *	1982-11-17	1984-06-13	Doverstrand Ltd	Improvements in drilling fluids
USRE33856E (en) *	1986-04-07	1992-03-24	Nalco Chemical Company	Terpolymer compositions for aqueous drilling fluids
USRE33855E (en) *	1986-04-07	1992-03-24	Nalco Chemical Company	Terpolymer composition for aqueous drilling fluids
DE19756172A1 (de) *	1997-12-17	1999-06-24	Stockhausen Chem Fab Gmbh	Verfahren zur Pfropfung von Lignin, danach hergestellte Polymerisate und deren Verwendung
JP2003082041A (ja) *	2001-09-12	2003-03-19	Tokyo Metropolis	吸水性材料、吸水性材料の製造方法、吸水材
US7576040B2 (en)	2007-01-11	2009-08-18	Halliburton Energy Services, Inc.	Cement compositions comprising humic acid grafted fluid loss control additives
US7523784B2 (en)	2007-01-11	2009-04-28	Halliburton Energy Services, Inc.	Method of using humic acid grafted fluid loss control additives in cementing operations
CA2674019C (fr)	2007-01-11	2012-01-03	Halliburton Energy Services, Inc.	Compositions de ciment comprenant des additifs regulateurs de perte de fluide greffes a l'acide humique et procedes d'utilisation

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SU724530A1 (ru) *	1973-12-03	1980-03-30	Львовский Ордена Ленина Политехнический Институт	Способ получени структуратора дл почв

1982
- 1982-06-30 NO NO822262A patent/NO822262L/no unknown
- 1982-07-17 EP EP82106452A patent/EP0072445A3/fr not_active Withdrawn
- 1982-07-26 DK DK333182A patent/DK333182A/da not_active Application Discontinuation
- 1982-07-26 JP JP57129095A patent/JPS5832614A/ja active Pending
- 1982-07-26 AU AU86424/82A patent/AU8642482A/en not_active Abandoned

Also Published As

Publication number	Publication date
EP0072445A3 (fr)	1983-09-21
DK333182A (da)	1983-01-28
AU8642482A (en)	1983-02-03
EP0072445A2 (fr)	1983-02-23
JPS5832614A (ja)	1983-02-25

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EP0216091B1 (fr)	1992-05-06	Emulsions inverses
US4172066A (en)	1979-10-23	Cross-linked, water-swellable polymer microgels
US10023782B2 (en)	2018-07-17	Salt-tolerant, thermally-stable rheology modifiers
US4059552A (en)	1977-11-22	Cross-linked water-swellable polymer particles
US4374738A (en)	1983-02-22	Drilling fluid composition
US3985659A (en)	1976-10-12	Drilling fluid composition
US8021516B2 (en)	2011-09-20	Use of water-soluble polymer complexes in aqueous systems
CA1168426A (fr)	1984-06-05	Fluide de forage au lignosulfonate avec additifs
EP0156030B1 (fr)	1987-06-10	Liquide aqueux de forage
US4131576A (en)	1978-12-26	Process for the preparation of graft copolymers of a water soluble monomer and polysaccharide employing a two-phase reaction system
US7956012B2 (en)	2011-06-07	Oil field treatment fluids with viscosified brines
US6169058B1 (en)	2001-01-02	Compositions and methods for hydraulic fracturing
WO2013138156A1 (fr)	2013-09-19	Synthèse et application d'additif à perte de fluide à haute pression et haute température, et stabilisant rhéologique
NO300643B1 (no)	1997-06-30	Vannopplöselig blandingspolymerisat og anvendelse derav, samt faststoffsuspensjon og vandig opplösning
WO2013162902A1 (fr)	2013-10-31	Combinaison synergique d'un additif de perte de circulation et d'un modificateur de rhéologie
DE2126171A1 (de)	1971-12-09	Tonmasse
NO310828B1 (no)	2001-09-03	Podepolymerer av keton-aldehyd-kondensasjons- eller -ko- kondensasjonsprodukter, fremgangsmåte for fremstilling oganvendelse av slike
US5132285A (en)	1992-07-21	Method for thickening or stabilizing aqueous media with polyamphoteric polysaccharides
JPH0657245A (ja)	1994-03-01	水性循環掘削流体
US4282340A (en)	1981-08-04	Polymerization process for preparation of acrylamide homopolymers with redox catalyst
WO2001005851A1 (fr)	2001-01-25	Composition polymere ampholyte et son procede d'utilisation
EP0072445A2 (fr)	1983-02-23	Fluides de forage stables à la chaleur
NO844203L (no)	1985-04-23	Vannopploeselige blandinspolymerisater og deres anvendelse som dispergatorer for faste stoffer
EP0339372B1 (fr)	1996-01-31	Méthode et composition pour l'épaississement et la stabilisation de milieux aqueux par l'utilisation de polysaccharides polyamphotères
US5132284A (en)	1992-07-21	Polyamphoteric polysaccharide graft copolymers neutrally charged