NO300643B1 - Vannopplöselig blandingspolymerisat og anvendelse derav, samt faststoffsuspensjon og vandig opplösning - Google Patents
Vannopplöselig blandingspolymerisat og anvendelse derav, samt faststoffsuspensjon og vandig opplösning Download PDFInfo
- Publication number
- NO300643B1 NO300643B1 NO914252A NO914252A NO300643B1 NO 300643 B1 NO300643 B1 NO 300643B1 NO 914252 A NO914252 A NO 914252A NO 914252 A NO914252 A NO 914252A NO 300643 B1 NO300643 B1 NO 300643B1
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- Norway
- Prior art keywords
- water
- polymerization
- formula
- mixed polymer
- groups
- Prior art date
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- 239000007787 solid Substances 0.000 title claims description 19
- 239000000725 suspension Substances 0.000 title claims description 18
- 239000007864 aqueous solution Substances 0.000 title claims description 16
- 239000000203 mixture Substances 0.000 title description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- 229920000642 polymer Polymers 0.000 claims description 45
- 239000004568 cement Substances 0.000 claims description 26
- 238000006116 polymerization reaction Methods 0.000 claims description 26
- 239000002002 slurry Substances 0.000 claims description 19
- 239000000654 additive Substances 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 238000012673 precipitation polymerization Methods 0.000 claims description 7
- 238000010528 free radical solution polymerization reaction Methods 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
- 239000012266 salt solution Substances 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- -1 alkali metal cation Chemical class 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 238000012688 inverse emulsion polymerization Methods 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 3
- 239000004570 mortar (masonry) Substances 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 239000011505 plaster Substances 0.000 claims description 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 238000010348 incorporation Methods 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 239000000243 solution Substances 0.000 description 24
- 239000000178 monomer Substances 0.000 description 16
- 239000003921 oil Substances 0.000 description 15
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 12
- 229920001577 copolymer Polymers 0.000 description 12
- 239000007789 gas Substances 0.000 description 12
- PNLUGRYDUHRLOF-UHFFFAOYSA-N n-ethenyl-n-methylacetamide Chemical compound C=CN(C)C(C)=O PNLUGRYDUHRLOF-UHFFFAOYSA-N 0.000 description 11
- 238000005553 drilling Methods 0.000 description 10
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 8
- 238000011010 flushing procedure Methods 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 239000011435 rock Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 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
- 239000012530 fluid Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000010440 gypsum Substances 0.000 description 4
- 229910052602 gypsum Inorganic materials 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000010802 sludge Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 235000010980 cellulose Nutrition 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 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 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-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
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- JEHKKBHWRAXMCH-UHFFFAOYSA-N benzenesulfinic acid Chemical compound O[S@@](=O)C1=CC=CC=C1 JEHKKBHWRAXMCH-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 235000011148 calcium chloride Nutrition 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 239000003651 drinking water Substances 0.000 description 2
- 235000020188 drinking water Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- DYBIGIADVHIODH-UHFFFAOYSA-N 2-nonylphenol;oxirane Chemical compound C1CO1.CCCCCCCCCC1=CC=CC=C1O DYBIGIADVHIODH-UHFFFAOYSA-N 0.000 description 1
- NHGFPFUWPYTLDM-UHFFFAOYSA-N 4-(prop-2-enoylamino)buta-1,3-diene-1-sulfonic acid Chemical compound OS(=O)(=O)C=CC=CNC(=O)C=C NHGFPFUWPYTLDM-UHFFFAOYSA-N 0.000 description 1
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 description 1
- 239000004160 Ammonium persulphate Substances 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
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 239000004117 Lignosulphonate Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 241001568665 Ocinebrellus inornatus Species 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920006329 Styropor Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
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- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910001622 calcium bromide Inorganic materials 0.000 description 1
- WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 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
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
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- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
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- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
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- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
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- 238000004062 sedimentation Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
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- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
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- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/16—Sulfur-containing compounds
- C04B24/161—Macromolecular compounds comprising sulfonate or sulfate groups
- C04B24/163—Macromolecular compounds comprising sulfonate or sulfate groups obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/16—Sulfur-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2652—Nitrogen containing polymers, e.g. polyacrylamides, polyacrylonitriles
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/58—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine
- C08F220/585—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS]
-
- 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
- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
- C08F226/04—Diallylamine
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/001—Pigment pastes, e.g. for mixing in paints in aqueous medium
-
- 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
- C09K8/04—Aqueous well-drilling compositions
- C09K8/14—Clay-containing compositions
- C09K8/18—Clay-containing compositions characterised by the organic compounds
- C09K8/22—Synthetic organic compounds
- C09K8/24—Polymers
-
- 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
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
-
- 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
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
- C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
- C09K8/487—Fluid loss control additives; Additives for reducing or preventing circulation loss
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Ceramic Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Wood Science & Technology (AREA)
- Dispersion Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4034642A DE4034642A1 (de) | 1990-10-31 | 1990-10-31 | Wasserloesliche mischpolymerisate und deren verwendung |
Publications (3)
Publication Number | Publication Date |
---|---|
NO914252D0 NO914252D0 (no) | 1991-10-30 |
NO914252L NO914252L (no) | 1992-05-04 |
NO300643B1 true NO300643B1 (no) | 1997-06-30 |
Family
ID=6417387
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO914252A NO300643B1 (no) | 1990-10-31 | 1991-10-30 | Vannopplöselig blandingspolymerisat og anvendelse derav, samt faststoffsuspensjon og vandig opplösning |
Country Status (9)
Country | Link |
---|---|
US (1) | US5510436A (es) |
EP (1) | EP0483638B1 (es) |
JP (1) | JPH05186537A (es) |
AR (1) | AR248034A1 (es) |
BR (1) | BR9104709A (es) |
CA (1) | CA2054518A1 (es) |
DE (2) | DE4034642A1 (es) |
MX (1) | MX9101832A (es) |
NO (1) | NO300643B1 (es) |
Families Citing this family (43)
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US5380705A (en) * | 1990-01-25 | 1995-01-10 | Phillips Petroleum Company | Drilling mud comprising tetrapolymer consisting of n-vinyl-2-pyrrolidone, acrylamidopropanesulfonicacid, acrylamide, and acrylic acid |
US5135909A (en) * | 1990-01-25 | 1992-08-04 | Phillips Petroleum Company | Drilling mud comprising tetrapolymer consisting of N-vinyl-2-pyrrolidone, acrylamidopropanesulfonic acid, acrylamide, and acrylic acid |
US5720888A (en) * | 1993-11-12 | 1998-02-24 | Betzdearborn Inc. | Water-soluble cationic copolymers and their use as flocculants |
US5700893A (en) * | 1993-11-12 | 1997-12-23 | Betzdearborn Inc. | Water-soluble cationic copolymers and their use as flocculants and drainage aids |
US5529699A (en) * | 1993-11-12 | 1996-06-25 | W. R. Grace & Co.-Conn. | Water-soluble cationic copolymers and their use as flocculants |
US5473033A (en) * | 1993-11-12 | 1995-12-05 | W. R. Grace & Co.-Conn. | Water-soluble cationic copolymers and their use as drainage retention aids in papermaking processes |
US5516852A (en) * | 1993-11-12 | 1996-05-14 | W. R. Grace & Co.-Conn. | Method of producing water-soluble cationic copolymers |
DE19508191A1 (de) * | 1995-03-09 | 1996-09-12 | Hoechst Ag | Anionische Polymermischungen mit reduzierter Schaumbildung in Wasser |
US6169058B1 (en) | 1997-06-05 | 2001-01-02 | Bj Services Company | Compositions and methods for hydraulic fracturing |
US6228812B1 (en) * | 1998-12-10 | 2001-05-08 | Bj Services Company | Compositions and methods for selective modification of subterranean formation permeability |
DE19909231C2 (de) | 1999-03-03 | 2001-04-19 | Clariant Gmbh | Wasserlösliche Copolymere auf AMPS-Basis und ihre Verwendung als Bohrhilfsmittel |
US6281172B1 (en) * | 1999-04-07 | 2001-08-28 | Akzo Nobel Nv | Quaternary nitrogen containing amphoteric water soluble polymers and their use in drilling fluids |
DE19926355A1 (de) * | 1999-06-10 | 2000-12-14 | Clariant Gmbh | Wasserlösliche Mischpolymere und ihre Verwendung für Exploration und Förderung von Erdöl und Erdgas |
DE19931218B4 (de) * | 1999-07-06 | 2005-06-02 | Clariant Gmbh | Verwendung von Polymeren als Anti-Nebel-Additiv in wasserbasierenden Kühlschmierstoffen |
DE19931219C2 (de) * | 1999-07-06 | 2001-06-07 | Clariant Gmbh | Verwendung von Polymeren als Anti-Nebel-Additiv in wasserbasierenden Kühlschmierstoffen |
DE19931220B4 (de) * | 1999-07-06 | 2005-03-10 | Clariant Gmbh | Verwendung von Polymeren als Anti-Nebel-Additiv in wasserbasierenden Kühlschmierstoffen |
AU6406000A (en) * | 1999-07-16 | 2001-02-05 | Calgon Corporation | Ampholyte polymer composition and method of use |
DE10000648A1 (de) | 2000-01-11 | 2001-07-12 | Clariant Gmbh | Wasserlösliche oder wasserquellbare vernetzte Copolymere |
EP1185579B1 (en) * | 2000-01-25 | 2009-09-09 | Cabot Corporation | Polymers containing modified pigments and methods of preparing the same |
US6465397B1 (en) * | 2000-02-11 | 2002-10-15 | Clariant Finance (Bvi) Limited | Synthetic crosslinked copolymer solutions and direct injection to subterranean oil and gas formations |
CN1118532C (zh) * | 2000-03-02 | 2003-08-20 | 王斌 | 高温高压高矿化度钻井液流变性稳定剂 |
DE10037629A1 (de) * | 2000-08-02 | 2002-02-14 | Skw Bauwerkstoffe Deutschland | Wasserlösliche oder wasserquellbare sulfogruppenhaltige assoziativverdickende Copolymere, Verfahren zu deren Herstellung und deren Verwendung |
DE10041392A1 (de) | 2000-08-23 | 2002-03-07 | Stockhausen Chem Fab Gmbh | Wasserlösliche Homo- und Copolymere mit verbesserter Umweltverträglichkeit |
DE10110336A1 (de) * | 2001-03-03 | 2002-09-12 | Clariant Gmbh | Tensidfreie kosmetische, dermatologische und pharmazeutische Mittel |
US7044170B2 (en) * | 2002-08-14 | 2006-05-16 | Construction Research & Technology Gmbh | Hydraulic cementitious composition with improved bleeding resistance |
DE10315182A1 (de) * | 2003-04-03 | 2004-10-14 | Clariant Gmbh | Verfahren zur Herstellung von stabilen Polymer-Konzentraten |
DE102004032304A1 (de) | 2004-07-03 | 2006-02-16 | Construction Research & Technology Gmbh | Wasserlösliche sulfogruppenhaltige Copolymere, Verfahren zu deren Herstellung und ihre Verwendung |
DE102006047091A1 (de) * | 2006-10-05 | 2008-04-10 | Basf Construction Polymers Gmbh | Neue Zusammensetzung auf Polyvinylalkohol-Basis |
US20110160336A1 (en) * | 2006-10-05 | 2011-06-30 | Roland Reichenbach-Klinke | Method of use of a polyvinyl alcohol-based composition |
DE102007037466A1 (de) | 2007-08-08 | 2009-02-12 | Basf Construction Polymers Gmbh | Pfropfpolymer-Mischung |
EP2075300A1 (en) | 2007-10-09 | 2009-07-01 | Bp Exploration Operating Company Limited | Wellbore fluid |
EP2075301A1 (en) | 2007-10-09 | 2009-07-01 | Bp Exploration Operating Company Limited | Technology useful in wellbore fluids |
US8685900B2 (en) * | 2009-04-03 | 2014-04-01 | Halliburton Energy Services, Inc. | Methods of using fluid loss additives comprising micro gels |
JP5434256B2 (ja) * | 2009-05-19 | 2014-03-05 | 東亞合成株式会社 | 掘削泥水用添加剤及びその製造方法並びにそれを用いた掘削泥水 |
WO2014005778A1 (en) | 2012-07-06 | 2014-01-09 | Basf Se | Biodegradable graft copolymer anti -accretion additive for water - based drilling fluids |
AU2013323888B2 (en) | 2012-09-28 | 2015-09-03 | Halliburton Energy Services, Inc. | Methods and compositions for treating a subterranean formation with salt-tolerant cement slurries |
JP6043591B2 (ja) * | 2012-10-31 | 2016-12-14 | 株式会社日本触媒 | セメント添加剤及びセメント組成物 |
US9315713B2 (en) | 2013-11-21 | 2016-04-19 | Halliburton Energy Services, Inc. | Amphoteric polymer suspending agent for use in calcium aluminate cement compositions |
CN104193897A (zh) * | 2014-08-28 | 2014-12-10 | 中国石油集团渤海钻探工程有限公司 | 一种耐高温抗盐油井水泥降失水剂及其制备方法 |
WO2016032494A1 (en) | 2014-08-28 | 2016-03-03 | Halliburton Energy Services, Inc. | Cement slurries with salt-tolerant fluid loss additives and methods relating thereto |
MX2017004209A (es) * | 2014-12-19 | 2017-06-06 | Halliburton Energy Services Inc | Composicion que incluye un polimero viscosificante y modificador de la viscosidad de poliamina para el tratamiento de formaciones subterraneas. |
US10113098B2 (en) | 2014-12-19 | 2018-10-30 | Halliburton Energy Servives, Inc. | Composition including viscosifier polymer and polyamine viscosity modifier for treatment of subterranean formations |
CN105237679B (zh) * | 2015-10-30 | 2017-12-19 | 卫辉市化工有限公司 | 一种油井水泥乳液聚合物降失水剂的制备方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US3629101A (en) * | 1968-03-02 | 1971-12-21 | Hoechst Ag | Water-base clayey drilling fluids |
DE2444108C2 (de) * | 1974-09-14 | 1978-01-19 | Hoechst Ag | Wasserbasische tonspuelung fuer tiefbohrungen und verwendung eines mischpolymerisats fuer solche spuelungen |
US3994852A (en) * | 1974-09-23 | 1976-11-30 | Calgon Corporation | Low fluid loss cementing compositions containing polyvinylpyrrolidone-polyacrylamide triblock polymers and their use |
US4015991A (en) * | 1975-08-08 | 1977-04-05 | Calgon Corporation | Low fluid loss cementing compositions containing hydrolyzed acrylamide/2-acrylamido-2-methylpropane sulfonic acid derivative copolymers and their use |
LU78170A1 (fr) * | 1977-09-23 | 1979-05-25 | Oreal | Nouvelles compositions cosmetiques pour les cheveux et la peau a base de polymeres amines comportant des motifs a structure cyclique |
US4176107A (en) * | 1978-01-20 | 1979-11-27 | Buckman Laboratories, Inc. | Water-soluble dispersions of high molecular water-soluble polymers containing a surfactant and a water-soluble organic carrier which is a hydroxy compound containing repeating alkylene oxide units |
DE2931897A1 (de) * | 1979-08-06 | 1981-02-26 | Cassella Ag | Wasserloesliches copolymerisat und seine herstellung |
DE3302168A1 (de) * | 1983-01-24 | 1984-07-26 | Hoechst Ag, 6230 Frankfurt | Zementschlaemme fuer tiefbohrungen mit einem gehalt an copolymerisaten zur verminderung des wasserverlustes |
US4619773A (en) * | 1983-05-02 | 1986-10-28 | Mobil Oil Corporation | High temperature stable aqueous brine fluids viscosified by water-soluble copolymers of acrylamidomethylpropanesulfonic acid salts |
US4555269A (en) * | 1984-03-23 | 1985-11-26 | Halliburton Company | Hydrolytically stable polymers for use in oil field cementing methods and compositions |
US4536292A (en) * | 1984-03-26 | 1985-08-20 | Calgon Corporation | Carboxylic/sulfonic/quaternary ammonium polymers for use as scale and corrosion inhibitors |
US4608425A (en) * | 1985-01-02 | 1986-08-26 | Exxon Research And Engineering Co. | High charge density polymeric complexes - viscosifiers for acid, base and salt (aqueous) solutions |
US4861499A (en) * | 1987-10-13 | 1989-08-29 | American Cyanamid Company | Water-dispersible hydrophobic thickening agent |
-
1990
- 1990-10-31 DE DE4034642A patent/DE4034642A1/de not_active Withdrawn
-
1991
- 1991-10-22 DE DE59107925T patent/DE59107925D1/de not_active Expired - Fee Related
- 1991-10-22 EP EP91117945A patent/EP0483638B1/de not_active Expired - Lifetime
- 1991-10-29 MX MX9101832A patent/MX9101832A/es not_active IP Right Cessation
- 1991-10-29 AR AR91321041A patent/AR248034A1/es active
- 1991-10-30 NO NO914252A patent/NO300643B1/no unknown
- 1991-10-30 BR BR919104709A patent/BR9104709A/pt not_active Application Discontinuation
- 1991-10-30 JP JP3285068A patent/JPH05186537A/ja active Pending
- 1991-10-30 CA CA002054518A patent/CA2054518A1/en not_active Abandoned
-
1994
- 1994-06-15 US US08/260,037 patent/US5510436A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0483638A1 (de) | 1992-05-06 |
EP0483638B1 (de) | 1996-06-12 |
NO914252L (no) | 1992-05-04 |
AR248034A1 (es) | 1995-05-31 |
CA2054518A1 (en) | 1992-05-01 |
DE4034642A1 (de) | 1992-05-07 |
DE59107925D1 (de) | 1996-07-18 |
JPH05186537A (ja) | 1993-07-27 |
NO914252D0 (no) | 1991-10-30 |
BR9104709A (pt) | 1992-06-16 |
MX9101832A (es) | 1992-06-05 |
US5510436A (en) | 1996-04-23 |
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