KR20020060985A - 소수성 회합이 가능한 중합체의 제조 방법, 사용 방법 및조성물 - Google Patents
소수성 회합이 가능한 중합체의 제조 방법, 사용 방법 및조성물 Download PDFInfo
- Publication number
- KR20020060985A KR20020060985A KR1020027007222A KR20027007222A KR20020060985A KR 20020060985 A KR20020060985 A KR 20020060985A KR 1020027007222 A KR1020027007222 A KR 1020027007222A KR 20027007222 A KR20027007222 A KR 20027007222A KR 20020060985 A KR20020060985 A KR 20020060985A
- Authority
- KR
- South Korea
- Prior art keywords
- monomer
- solution
- ethylenically unsaturated
- monomers
- hydrophobic
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 67
- 238000000034 method Methods 0.000 title claims abstract description 54
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 239000000178 monomer Substances 0.000 claims abstract description 169
- 239000000243 solution Substances 0.000 claims abstract description 58
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000006185 dispersion Substances 0.000 claims abstract description 48
- 150000003839 salts Chemical class 0.000 claims abstract description 36
- 239000004094 surface-active agent Substances 0.000 claims abstract description 35
- 125000000129 anionic group Chemical group 0.000 claims abstract description 33
- 239000012266 salt solution Substances 0.000 claims abstract description 28
- 238000002156 mixing Methods 0.000 claims abstract description 25
- 125000002091 cationic group Chemical group 0.000 claims abstract description 20
- 239000003999 initiator Substances 0.000 claims abstract description 19
- 239000011259 mixed solution Substances 0.000 claims abstract description 14
- 239000010802 sludge Substances 0.000 claims abstract description 4
- 238000004065 wastewater treatment Methods 0.000 claims abstract description 4
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims description 23
- 239000003381 stabilizer Substances 0.000 claims description 22
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 17
- 230000008569 process Effects 0.000 claims description 15
- 230000014759 maintenance of location Effects 0.000 claims description 12
- 150000003254 radicals Chemical class 0.000 claims description 6
- 230000003311 flocculating effect Effects 0.000 claims description 4
- 229920002907 Guar gum Polymers 0.000 claims description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000000665 guar gum Substances 0.000 claims description 3
- 229960002154 guar gum Drugs 0.000 claims description 3
- 235000010417 guar gum Nutrition 0.000 claims description 3
- 229920003169 water-soluble polymer Polymers 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 14
- 238000011084 recovery Methods 0.000 abstract description 11
- 239000003129 oil well Substances 0.000 abstract description 5
- 238000005553 drilling Methods 0.000 abstract description 4
- 239000012530 fluid Substances 0.000 abstract description 4
- 239000003973 paint Substances 0.000 abstract description 3
- 230000000379 polymerizing effect Effects 0.000 abstract description 3
- 238000009472 formulation Methods 0.000 abstract 3
- 238000006116 polymerization reaction Methods 0.000 description 21
- 229920001577 copolymer Polymers 0.000 description 19
- 238000012360 testing method Methods 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 12
- 239000000693 micelle Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000012267 brine Substances 0.000 description 10
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 10
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000010779 crude oil Substances 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- -1 lauryl methyl Chemical group 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 238000012674 dispersion polymerization Methods 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 7
- 229940001584 sodium metabisulfite Drugs 0.000 description 7
- 235000010262 sodium metabisulphite Nutrition 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- 229920002401 polyacrylamide Polymers 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000011121 hardwood Substances 0.000 description 4
- 239000011396 hydraulic cement Substances 0.000 description 4
- 125000001165 hydrophobic group Chemical group 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011122 softwood Substances 0.000 description 4
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical class CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
- 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 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 3
- 229920000591 gum Polymers 0.000 description 3
- 239000007970 homogeneous dispersion Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 238000005191 phase separation Methods 0.000 description 3
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- CSPHGSFZFWKVDL-UHFFFAOYSA-M (3-chloro-2-hydroxypropyl)-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)CCl CSPHGSFZFWKVDL-UHFFFAOYSA-M 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- 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
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 229940050176 methyl chloride Drugs 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000006254 rheological additive Substances 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- LAYAKLSFVAPMEL-UHFFFAOYSA-N 1-ethenoxydodecane Chemical compound CCCCCCCCCCCCOC=C LAYAKLSFVAPMEL-UHFFFAOYSA-N 0.000 description 1
- UKDKWYQGLUUPBF-UHFFFAOYSA-N 1-ethenoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOC=C UKDKWYQGLUUPBF-UHFFFAOYSA-N 0.000 description 1
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical class CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 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
- PABGQABTFFNYFH-UHFFFAOYSA-N 2-methyl-n-octadecylprop-2-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C(C)=C PABGQABTFFNYFH-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 208000023445 Congenital pulmonary airway malformation Diseases 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-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
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- AMVQGJHFDJVOOB-UHFFFAOYSA-H aluminium sulfate octadecahydrate Chemical group O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O AMVQGJHFDJVOOB-UHFFFAOYSA-H 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- CSMFSDCPJHNZRY-UHFFFAOYSA-M decyl sulfate Chemical class CCCCCCCCCCOS([O-])(=O)=O CSMFSDCPJHNZRY-UHFFFAOYSA-M 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- OGTRTCPRIPAVGZ-UHFFFAOYSA-N dodecyl prop-2-enoate;sodium Chemical compound [Na].CCCCCCCCCCCCOC(=O)C=C OGTRTCPRIPAVGZ-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000015784 hyperosmotic salinity response Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- JRUSUOGPILMFBM-UHFFFAOYSA-N n,n-dioctylprop-2-enamide Chemical compound CCCCCCCCN(C(=O)C=C)CCCCCCCC JRUSUOGPILMFBM-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- WDQKICIMIPUDBL-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]prop-2-enamide Chemical compound CN(C)CCNC(=O)C=C WDQKICIMIPUDBL-UHFFFAOYSA-N 0.000 description 1
- PNLUGRYDUHRLOF-UHFFFAOYSA-N n-ethenyl-n-methylacetamide Chemical compound C=CN(C)C(C)=O PNLUGRYDUHRLOF-UHFFFAOYSA-N 0.000 description 1
- OFESGEKAXKKFQT-UHFFFAOYSA-N n-ethenyl-n-methylformamide Chemical compound C=CN(C)C=O OFESGEKAXKKFQT-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- DPDUMCDONQYFCT-UHFFFAOYSA-N n-ethenyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC=C DPDUMCDONQYFCT-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- CNWVYEGPPMQTKA-UHFFFAOYSA-N n-octadecylprop-2-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C=C CNWVYEGPPMQTKA-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- URLJMZWTXZTZRR-UHFFFAOYSA-N sodium myristyl sulfate Chemical class CCCCCCCCCCCCCCOS(O)(=O)=O URLJMZWTXZTZRR-UHFFFAOYSA-N 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 229960000776 sodium tetradecyl sulfate Drugs 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- CSMFSDCPJHNZRY-UHFFFAOYSA-N sulfuric acid monodecyl ester Natural products CCCCCCCCCCOS(O)(=O)=O CSMFSDCPJHNZRY-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- ATZHWSYYKQKSSY-UHFFFAOYSA-N tetradecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)=C ATZHWSYYKQKSSY-UHFFFAOYSA-N 0.000 description 1
- XZHNPVKXBNDGJD-UHFFFAOYSA-N tetradecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C=C XZHNPVKXBNDGJD-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical group FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 description 1
- XOALFFJGWSCQEO-UHFFFAOYSA-N tridecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C=C XOALFFJGWSCQEO-UHFFFAOYSA-N 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 239000004711 α-olefin 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treatment Of Sludge (AREA)
- Paper (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
- Polyesters Or Polycarbonates (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
Description
중합체 | 단량체 | 공급비 (몰%) |
I | AA/AM | 45/55 |
II | AA/AM/LA | 45/54/1 |
중합체 | 단량체 | 공급비 (몰%) |
III | AA/AM | 50/50 |
IV | AA/AM/LA | 50/49.25/0.75 |
Claims (17)
- 계면활성제, 1종 이상의 소수성 에틸렌계 불포화 단량체, 비이온성 에틸렌계 단량체, 양이온성 에틸렌계 불포화 단량체, 음이온성 에틸렌계 불포화 단량체 또는 그의 혼합물로부터 선택된 1종 이상의 친수성 단량체, 및 물을 포함하는 단량체 용액을 형성시키고;다가 염, 안정화제 및 물을 함유하는 염 용액을 형성시키고;단량체 용액과 염 용액을 혼합하여 혼합 용액을 형성시키고;혼합 용액에 개시제를 첨가하여 단량체를 중합시켜 소수성 회합이 가능한 중합체를 형성시키는것을 포함하는 소수성 회합이 가능한 중합체의 제조 방법.
- 제1항에 있어서, 단량체 용액은1종 이상의 친수성 단량체와 물을 혼합하여 단량체 용액을 형성시키고;1종 이상의 소수성 에틸렌계 불포화 단량체 및 계면활성제를 그 단량체 용액에 첨가하고;균질할 때까지 혼합함으로써 형성되는 방법.
- 제1항에 있어서, 안정화제가 염 용액의 10 중량% 이하의 양으로 존재하는 방법.
- 제3항에 있어서, 안정화제가 화학적으로 개질된 구아 검인 방법.
- 제3항에 있어서, 안정화제가 염 용액의 약 0.05 내지 약 2 중량%의 양으로 존재하는 방법.
- 제3항에 있어서, 안정화제가 염 용액의 약 0.1 내지 약 0.5 중량%의 양으로 존재하는 방법.
- 제1항에 있어서, 계면활성제가 단량체 용액의 약 10 중량% 이하의 양으로 존재하는 방법.
- 제7항에 있어서, 계면활성제가 소듐 도데실 설페이트인 방법.
- 제1항에 있어서, 단량체 용액 중의 단량체가 아크릴산, 아크릴아미드 및 라우릴 아크릴레이트인 방법.
- 제1항에 있어서, 염이 염 용액의 약 50 중량% 이하의 양으로 존재하는 방법.
- 제1항에 있어서, 염 용액 중의 염이 약 10 내지 약 30 중량%의 양으로 존재하고, 자유 라디칼 개시제가 총 단량체 100 g 당 약 0.01 내지 약 0.5 g의 양으로 존재하는 방법.
- 제1항의 방법에 의해 제조되는 소수성 회합이 가능한 수용성 중합체를 포함하는 수성 분산액.
- 제1항에 있어서, 단량체 용액이 비이온성 에틸렌계 단량체, 양이온성 에틸렌계 불포화 단량체, 음이온성 에틸렌계 불포화 단량체 또는 그의 혼합물로부터 선택된 1종 이상의 친수성 단량체와 물을 혼합하고 1종 이상의 소수성 에틸렌계 불포화 단량체 및 계면활성제를 첨가하고 균질할 때까지 혼합함으로써 형성되는 방법.
- 제1항에 있어서, 단량체 용액이 아크릴산, 아크릴아미드, 라우릴 아크릴레이트, 음이온성 계면활성제 및 물을 포함하는 방법.
- 제1항, 13항 또는 14항의 수성 분산액 유효량을 보류 및 배수 촉진제로서 첨가하는 것을 포함하는, 펄프 퍼니쉬로부터 종이를 제조하는 개선된 제지법.
- 제1항, 13항 또는 14항의 수성 분산액 유효량의 존재를 하나 이상의 응집 보조제로서 포함하는, 하나 이상의 응집 보조제를 함유하는 개선된 폐수 처리 시스템.
- 제1항, 13항 또는 14항의 수성 분산액 유효량의 존재를 하나 이상의 응집 보조제로서 포함하는, 하나 이상의 응집 보조제를 함유하는 개선된 탈수 슬러지 시스템.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/455,024 | 1999-12-06 | ||
US09/455,024 US6417268B1 (en) | 1999-12-06 | 1999-12-06 | Method for making hydrophobically associative polymers, methods of use and compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20020060985A true KR20020060985A (ko) | 2002-07-19 |
KR100668023B1 KR100668023B1 (ko) | 2007-01-15 |
Family
ID=23807059
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020027007222A KR100668023B1 (ko) | 1999-12-06 | 2000-12-05 | 소수성 회합이 가능한 중합체의 제조 방법, 사용 방법 및조성물 |
Country Status (19)
Country | Link |
---|---|
US (1) | US6417268B1 (ko) |
EP (1) | EP1250360B1 (ko) |
JP (1) | JP2003515624A (ko) |
KR (1) | KR100668023B1 (ko) |
CN (1) | CN1152888C (ko) |
AT (1) | ATE277086T1 (ko) |
AU (1) | AU2063101A (ko) |
BR (1) | BR0016152B1 (ko) |
CA (1) | CA2392430C (ko) |
DE (1) | DE60014172T2 (ko) |
ES (1) | ES2223627T3 (ko) |
MX (1) | MXPA02005315A (ko) |
NZ (1) | NZ519147A (ko) |
PL (1) | PL199372B1 (ko) |
PT (1) | PT1250360E (ko) |
RU (1) | RU2263683C2 (ko) |
TW (1) | TW581774B (ko) |
WO (1) | WO2001040318A2 (ko) |
ZA (1) | ZA200205442B (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100811212B1 (ko) * | 2005-12-16 | 2008-03-07 | 주식회사 그린테크놀로지 | 수용성 음이온성 고분자 분산액 및 그 제조방법 |
Families Citing this family (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6581684B2 (en) | 2000-04-24 | 2003-06-24 | Shell Oil Company | In Situ thermal processing of a hydrocarbon containing formation to produce sulfur containing formation fluids |
US7004251B2 (en) | 2001-04-24 | 2006-02-28 | Shell Oil Company | In situ thermal processing and remediation of an oil shale formation |
US7063145B2 (en) | 2001-10-24 | 2006-06-20 | Shell Oil Company | Methods and systems for heating a hydrocarbon containing formation in situ with an opening contacting the earth's surface at two locations |
US8273693B2 (en) | 2001-12-12 | 2012-09-25 | Clearwater International Llc | Polymeric gel system and methods for making and using same in hydrocarbon recovery |
WO2004009904A1 (ja) * | 2002-07-19 | 2004-01-29 | Kao Corporation | 紙質向上剤 |
DE60202869T2 (de) * | 2002-09-11 | 2006-04-27 | Gkss-Forschungszentrum Geesthacht Gmbh | Polymermasse, Materialien hieraus und deren Anwendungen |
FR2859993B1 (fr) * | 2003-09-24 | 2006-01-21 | Inst Francais Du Petrole | Laitier de cimentation de puits petrolier |
FR2868783B1 (fr) | 2004-04-07 | 2006-06-16 | Snf Sas Soc Par Actions Simpli | Nouveaux polymeres amphoteres associatifs de haut poids moleculaire et leurs applications |
US20060142431A1 (en) * | 2004-12-29 | 2006-06-29 | Sutman Frank J | Retention and drainage in the manufacture of paper |
US20060137843A1 (en) * | 2004-12-29 | 2006-06-29 | Sutman Frank J | Retention and drainage in the manufacture of paper |
US20060142429A1 (en) * | 2004-12-29 | 2006-06-29 | Gelman Robert A | Retention and drainage in the manufacture of paper |
US20060142430A1 (en) * | 2004-12-29 | 2006-06-29 | Harrington John C | Retention and drainage in the manufacture of paper |
US20060142432A1 (en) * | 2004-12-29 | 2006-06-29 | Harrington John C | Retention and drainage in the manufacture of paper |
US8308902B2 (en) | 2004-12-29 | 2012-11-13 | Hercules Incorporated | Retention and drainage in the manufacture of paper |
EP1835808B1 (en) * | 2004-12-30 | 2013-11-06 | Rhodia Chimie | Herbicidal composition comprising a glyphosate salt and a betaine |
US20060260509A1 (en) * | 2005-04-22 | 2006-11-23 | Evers Glenn R | Compositions for enhanced paper brightness and whiteness |
US20060266488A1 (en) * | 2005-05-26 | 2006-11-30 | Doherty Erin A S | Hydrophobic polymers and their use in preparing cellulosic fiber compositions |
US8206553B2 (en) * | 2005-06-24 | 2012-06-26 | Hercules Incorporated | Retention and drainage in the manufacture of paper |
US20060289139A1 (en) * | 2005-06-24 | 2006-12-28 | Fushan Zhang | Retention and drainage in the manufacture of paper |
US20060289136A1 (en) * | 2005-06-24 | 2006-12-28 | Doherty Erin A S | Retention and drainage in the manufacture of paper |
CN100389136C (zh) * | 2005-07-01 | 2008-05-21 | 中国科学院化学研究所 | 一种疏水缔合聚丙烯酰胺及其制备方法 |
CA2629862C (en) | 2005-11-14 | 2014-03-18 | Rhodia Inc. | Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
US7597147B2 (en) | 2006-04-21 | 2009-10-06 | Shell Oil Company | Temperature limited heaters using phase transformation of ferromagnetic material |
US20100029483A1 (en) | 2006-10-16 | 2010-02-04 | Rhodia Inc. | Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
US7730945B2 (en) | 2006-10-20 | 2010-06-08 | Shell Oil Company | Using geothermal energy to heat a portion of a formation for an in situ heat treatment process |
KR100868298B1 (ko) * | 2006-12-26 | 2008-11-11 | 제일모직주식회사 | 내변색성 및 투과율이 우수한 메타크릴계 수지 조성물 및그 제조 방법 |
JP4840995B2 (ja) * | 2007-01-17 | 2011-12-21 | ハイモ株式会社 | 油中水型分散液の希釈液、その調製方法及びその使用方法 |
FR2913350B1 (fr) * | 2007-03-08 | 2010-05-21 | Rhodia Recherches & Tech | Utilisation d'une betaine a titre d'agent moussant et d'agent de reduction du drainage de la mousse |
FR2914647B1 (fr) | 2007-04-05 | 2011-10-21 | Rhodia Recherches Et Tech | Copolymere comprenant des unites betainiques et des unites hydrophobes et/ou amphiphiles,procede de preparation,et utilisations. |
WO2008131180A1 (en) | 2007-04-20 | 2008-10-30 | Shell Oil Company | Varying properties of in situ heat treatment of a tar sands formation based on assessed viscosities |
US8099997B2 (en) | 2007-06-22 | 2012-01-24 | Weatherford/Lamb, Inc. | Potassium formate gel designed for the prevention of water ingress and dewatering of pipelines or flowlines |
US8065905B2 (en) | 2007-06-22 | 2011-11-29 | Clearwater International, Llc | Composition and method for pipeline conditioning and freezing point suppression |
US20090200290A1 (en) | 2007-10-19 | 2009-08-13 | Paul Gregory Cardinal | Variable voltage load tap changing transformer |
WO2009060026A2 (en) * | 2007-11-07 | 2009-05-14 | Rhodia Operations | Herbicidal composition comprising an aminophosphate or aminophosphonate salt and a viscosity reducing agent |
RU2536470C2 (ru) * | 2009-02-12 | 2014-12-27 | Геркулес Инкорпорейтед | Состав на водной основе для применения в целях личной гигиены, в быту и в организациях |
EP2453751B1 (en) * | 2009-07-14 | 2017-06-28 | Rhodia Opérations | Agricultural adjuvant compositions, pesticide compositions, and methods for using such compositions |
US8905135B2 (en) * | 2010-03-24 | 2014-12-09 | Halliburton Energy Services, Inc. | Zero shear viscosifying agent |
US8701768B2 (en) | 2010-04-09 | 2014-04-22 | Shell Oil Company | Methods for treating hydrocarbon formations |
US8557125B2 (en) * | 2010-06-07 | 2013-10-15 | General Electric Company | Treatment additives, methods for making and methods for clarifying aqueous media |
EP2603075B1 (en) | 2010-08-10 | 2017-07-12 | Rhodia Operations | Agricultural pesticide compositions |
FI125418B (fi) | 2010-10-15 | 2015-10-15 | Kemira Oyj | Anioninen dispersiopolymerointimenetelmä |
US20120125231A1 (en) * | 2010-11-15 | 2012-05-24 | Penford Products Co. | Coating Formulation |
JP2014502602A (ja) * | 2010-12-16 | 2014-02-03 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップ | 粘弾性界面活性剤及び疎水性修飾ポリマーの水性組成物を含むパーソナルケア組成物 |
BR112014007230A2 (pt) * | 2011-09-29 | 2017-04-04 | Dow Global Technologies Llc | composição aquosa de cimentação e método para cimentar um tubo de revestimento de perfuração de um poço |
US9751781B2 (en) | 2012-03-20 | 2017-09-05 | The Research Foundation For The State University Of New York | Method to separate lignin-rich solid phase from acidic biomass suspension at an acidic pH |
CN103865512A (zh) * | 2012-12-12 | 2014-06-18 | 成都顺达利聚合物有限公司 | 一种缔合型两性离子聚合物稠化剂和增稠辅剂组成的清洁压裂液 |
US9228123B2 (en) | 2013-03-12 | 2016-01-05 | Ecolab Usa Inc. | Temperature sensitive viscoelastic well-treatment fluids |
CN104692564B (zh) * | 2013-12-06 | 2016-12-07 | 中国石油天然气股份有限公司 | 一种压裂返排液重复利用方法及处理装置 |
CN106611274A (zh) * | 2016-04-27 | 2017-05-03 | 四川用联信息技术有限公司 | 一种疏水缔合聚合物表面活性剂的合成方法 |
CA3055286C (en) | 2017-04-21 | 2021-09-07 | Halliburton Energy Services, Inc. | Associative polymer fluid with clay nanoparticles for proppant suspension |
EP3802725A1 (en) * | 2018-06-06 | 2021-04-14 | Basf Se | Associative copolymers with hydrophobic quaternized (meth)acrylamide and (meth)acrylic acid derivatives |
EP3802726A1 (en) * | 2018-06-06 | 2021-04-14 | Basf Se | Associative copolymers with hydrophobic quaternized (meth)acrylamide and (meth)acrylic acid derivatives |
US11332563B2 (en) | 2018-07-30 | 2022-05-17 | Ecolab Usa Inc. | Fast dissolving, water soluble, hydrophobically-modified polyelectrolytes |
CA3108176A1 (en) | 2018-07-30 | 2020-02-06 | Championx Usa, Inc. | Salt-tolerant, fast-dissolving, water-soluble rheology modifiers |
CN109096439B (zh) * | 2018-09-07 | 2020-06-30 | 石家庄华莱鼎盛科技有限公司 | 钻井液用增粘剂仿生天然凝胶及其制备方法 |
FR3093514A1 (fr) * | 2019-03-05 | 2020-09-11 | Rhodia Operations | Suspension de polymères associatifs pour le traitement de formations souterraines |
RU2692770C1 (ru) * | 2019-03-25 | 2019-06-27 | федеральное государственное бюджетное образовательное учреждение высшего образования "Нижегородский государственный технический университет им. Р.Е. Алексеева" (НГТУ) | Способ получения N-[(дибутиламино)метил]метакриламида |
GB2597008B (en) * | 2019-06-06 | 2023-05-10 | Halliburton Energy Services Inc | Methods and compositions including associative polymers |
Family Cites Families (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3091542A (en) | 1960-09-20 | 1963-05-28 | Dow Chemical Co | Insolubilization of water-soluble cellulose ethers |
US3272640A (en) | 1960-12-22 | 1966-09-13 | Hercules Powder Co Ltd | Water insolubilizing and insensitizing process |
US3435027A (en) | 1965-12-13 | 1969-03-25 | Hercules Inc | Cellulose ether-esters and process |
US4066495A (en) | 1974-06-26 | 1978-01-03 | Anheuser-Busch, Incorporated | Method of making paper containing cationic starch and an anionic retention aid |
DE2538281B2 (de) | 1975-08-28 | 1980-07-17 | Basf Ag, 6700 Ludwigshafen | Retentions- und Flockungsmittel auf Basis von Polyacrylamiden |
US4228277A (en) | 1979-02-12 | 1980-10-14 | Hercules Incorporated | Modified nonionic cellulose ethers |
SE419236B (sv) | 1979-06-01 | 1981-07-20 | Eka Ab | Ytmodifierat pigment av naturligt kaolinmaterial, samt for dess framstellning |
US4243802A (en) | 1979-06-06 | 1981-01-06 | Hercules Incorporated | Surfactant-soluble cellulose derivatives |
SE432951B (sv) | 1980-05-28 | 1984-04-30 | Eka Ab | Pappersprodukt innehallande cellulosafibrer och ett bindemedelssystem som omfattar kolloidal kiselsyra och katjonisk sterkelse samt forfarande for framstellning av pappersprodukten |
US4305860A (en) | 1980-08-21 | 1981-12-15 | National Starch And Chemical Corporation | Stable, pumpable, solvent-free colloidal polyampholyte latices, their preparation and use in paper |
US4814096A (en) | 1981-02-06 | 1989-03-21 | The Dow Chemical Company | Enhanced oil recovery process using a hydrophobic associative composition containing a hydrophilic/hydrophobic polymer |
US4432881A (en) | 1981-02-06 | 1984-02-21 | The Dow Chemical Company | Water-dispersible hydrophobic thickening agent |
US4395524A (en) | 1981-04-10 | 1983-07-26 | Rohm And Haas Company | Acrylamide copolymer thickener for aqueous systems |
US4443589A (en) | 1981-08-28 | 1984-04-17 | Mobil Oil Corporation | Acrylic modified anionic water dispersible cellulose esters |
US4521580A (en) | 1982-12-29 | 1985-06-04 | Exxon Research & Engineering Co. | Microemulsion process for producing acrylamide-alkyl acrylamide copolymers |
EP0115703B1 (en) | 1982-12-29 | 1987-08-12 | Exxon Research And Engineering Company | A micellar process for the formation of acrylamide-alkyl acrylamide copolymers |
US4528348A (en) | 1982-12-29 | 1985-07-09 | Exxon Research & Engineering Company | Micellar process for the production of acrylamide-alkyl acrylamide copolymers |
DE3327600A1 (de) | 1983-07-30 | 1985-02-14 | Sandoz-Patent-GmbH, 7850 Lörrach | Copolymerisat- und tensidhaltige praeparate, deren herstellung und verwendung |
US4577013A (en) | 1983-12-22 | 1986-03-18 | Ciba-Geigy Corporation | Ionically modified cellulose material, its preparation and its use |
US4921902A (en) | 1984-02-02 | 1990-05-01 | The Dow Chemical Company | Hydrophobie associative composition containing a polymer of a water-soluble monomer and an amphiphilic monomer |
US4524175A (en) | 1984-04-16 | 1985-06-18 | The Dow Chemical Company | Water-in-oil emulsions of hydrophobe association polymers |
US4694058A (en) | 1985-11-25 | 1987-09-15 | Exxon Research And Engineering Company | High molecular weight terpolymers of acrylamide, acrylic acid salts and alkylacrylamide |
US4694046A (en) | 1985-11-25 | 1987-09-15 | Exxon Research And Engineering Company | Hydrophobically associating terpolymers of acrylamide, salts of acrylic acid and alkyl acrylamide |
GB8602121D0 (en) | 1986-01-29 | 1986-03-05 | Allied Colloids Ltd | Paper & paper board |
US5089578A (en) | 1986-03-28 | 1992-02-18 | Exxon Research And Engineering Company | Hydrophobically associating terpolymers containing sulfonate functionality |
US5100953A (en) | 1986-03-28 | 1992-03-31 | Exxon Research And Engineering Company | Solutions of hydrophobically associating terpolymers containing sulfonate functionality |
US4730028A (en) | 1986-03-28 | 1988-03-08 | Exxon Research And Engineering Company | Process for preparing hydrophobically associating terpolymers containing sulfonate functionality |
US4684704A (en) | 1986-06-19 | 1987-08-04 | Hercules Incorporated | Hydrophobically modified hydroxyethyl cellulose in aqueous polymerization dispersions |
US4831092A (en) | 1986-09-08 | 1989-05-16 | Exxon Research And Engineering Company | Micellar process for preparing hydrophobically functionalized cationic polymers (C-2114) |
US4835234A (en) | 1986-09-08 | 1989-05-30 | Exxon Research And Engineering Company | Hydrophobically functionalized cationic polymers |
US5362827A (en) | 1986-09-08 | 1994-11-08 | Exxon Research & Engineering Co. | Solution process for preparation hydrophobically functionalized cationic polymers (C-2691) |
US4709759A (en) | 1986-12-29 | 1987-12-01 | Exxon Research And Engineering Company | Enhanced oil recovery with hydrophobically associating polymers containing N-vinyl-pyrrolidone functionality |
US4883850A (en) | 1987-06-22 | 1989-11-28 | Aqualon Company | Process for preparation of polymers by suspension polymerization of vinyl monomer in the presence of hydrophobically modified watersoluble, nonionic cellulose ether polymer in combination with electrolyte |
US4861499A (en) | 1987-10-13 | 1989-08-29 | American Cyanamid Company | Water-dispersible hydrophobic thickening agent |
US4892589A (en) | 1987-10-30 | 1990-01-09 | Aqualon Company | Composition comprising water-soluble, nonionic hydrophobically modified hydroxyethyl cellulose and water-soluble, nonionic hydroxyethyl cellulose |
US4792593A (en) | 1987-11-05 | 1988-12-20 | Exxon Research And Engineering Company | Novel acrylamide acrylate copolymers |
DE3743040A1 (de) | 1987-12-18 | 1989-07-13 | Basf Ag | Verfahren zur herstellung von waessrigen polymerdispersionen |
US4853447A (en) | 1987-12-21 | 1989-08-01 | Exxon Research And Engineering Company | Polymerization of cationic N,N-dimethylalkylamine type monomers |
US4847342A (en) | 1987-12-21 | 1989-07-11 | Exxon Research And Engineering Company | Cationic-hydrogen bonding type hydrophobically associating copolymers |
US4798653A (en) | 1988-03-08 | 1989-01-17 | Procomp, Inc. | Retention and drainage aid for papermaking |
EP0333499B1 (en) | 1988-03-18 | 1994-10-05 | Ciba Specialty Chemicals Water Treatments Limited | Polymerisation processes and products obtained from these |
US4845175A (en) | 1988-03-24 | 1989-07-04 | Union Carbide Corporation | Preparation of aqueous polymer emulsions in the presence of hydrophobically modified hydroxyethylcellulose |
FR2630117B1 (fr) | 1988-04-13 | 1990-08-24 | Hoechst France | Dispersions aqueuses de polymeres thermoreticulables a base de (meth)acrylate d'alkyle, leur procede de preparation et leur application notamment comme liants et/ou agents d'impregnation |
US5021526A (en) | 1988-07-05 | 1991-06-04 | The Standard Oil Company | Anionic polymeric stabilizers for oil-in-water emulsions |
US5340865A (en) | 1988-12-19 | 1994-08-23 | Cytec Technology Corp. | Cross-linked cationic polyermic microparticles |
US4963632A (en) | 1988-12-29 | 1990-10-16 | Exxon Research And Engineering Company | Mixed micellar process for preparing hydrophobically associating polymers |
US5116923A (en) | 1988-12-29 | 1992-05-26 | Exxon Research And Engineering Company | Hydrophobically associating polymers containing dimethyl acrylamide functionality |
US4981935A (en) | 1988-12-29 | 1991-01-01 | Exxon Research And Engineering Company | Hydrophobically associating polymers containing dimethyl acrylamide functionality |
US5003000A (en) | 1988-12-29 | 1991-03-26 | Exxon Research & Engineering Company | Hydrophobically associating polymers containing dimethyl acrylamide functionality |
US5120838A (en) | 1989-10-30 | 1992-06-09 | Aqualon Company | Alkylaryl hydrophobically modified cellulose ethers |
US4994112A (en) | 1989-10-30 | 1991-02-19 | Aqualon Company | Hydrophobically modified cellulosic thickeners for paper coating |
US5274055A (en) | 1990-06-11 | 1993-12-28 | American Cyanamid Company | Charged organic polymer microbeads in paper-making process |
US5167766A (en) | 1990-06-18 | 1992-12-01 | American Cyanamid Company | Charged organic polymer microbeads in paper making process |
DE4028746A1 (de) | 1990-09-11 | 1992-03-12 | Hoechst Ag | Modifizierte celluloseether und ihre verwendung in dispersionsfarben |
FR2671088B1 (fr) | 1990-12-27 | 1994-04-15 | Oreal | Nouveaux copolymeres a base de n-alkyl acrylamide, leur preparation et leur utilisation comme agents epaississants, notamment dans des compositions de shampooing. |
US5415740A (en) | 1991-04-25 | 1995-05-16 | Betz Paperchem, Inc. | Method for improving retention and drainage characteristics in alkaline papermaking |
US5211854A (en) | 1991-04-25 | 1993-05-18 | Betz Laboratories, Inc. | Water soluble graft copolymers and methods of use thereof |
US5171803A (en) | 1991-05-24 | 1992-12-15 | Hoechst Celanese Corp. | Copolymer with side chains exhibiting nonlinear optical response |
US5314581A (en) | 1991-12-10 | 1994-05-24 | Betz Paperchem, Inc. | Apparatus for simulating processing parameters and predicting variables in a papermaking operation including sequential pulsation, gravity and vacuum drainage, fines retention and paper formation |
EP0630909B1 (en) | 1993-06-04 | 1998-10-14 | Nalco Chemical Company | Dispersion polymerization process |
US5597858A (en) | 1993-06-10 | 1997-01-28 | Nalco Chemical Company | Hydrophobically associating dispersants used in forming polymer dispersions |
US5431783A (en) | 1993-07-19 | 1995-07-11 | Cytec Technology Corp. | Compositions and methods for improving performance during separation of solids from liquid particulate dispersions |
FR2716928B1 (fr) | 1994-03-03 | 1996-05-03 | Inst Francais Du Petrole | Procédé et fluide à base d'eau utilisant des dérivés cellulosiques modifiées hydrophobiquement comme réducteur de filtrat. |
US5482595A (en) | 1994-03-22 | 1996-01-09 | Betz Paperchem, Inc. | Method for improving retention and drainage characteristics in alkaline papermaking |
US5605970A (en) | 1996-03-20 | 1997-02-25 | Nalco Chemical Company | Synthesis of high molecular weight anionic dispersion polymers |
US5837776A (en) | 1996-03-20 | 1998-11-17 | Nalco Chemical Company | Process for producing water soluble anionic dispersion polymers |
US5614602A (en) | 1996-07-09 | 1997-03-25 | Betzdearborn Inc. | Process for the preparation of aqueous dispersion polymers |
US5889097A (en) | 1996-10-03 | 1999-03-30 | Cytec Technology Corp. | Anionic water-soluble polymer precipitation in salt solution |
US5725779A (en) | 1996-10-03 | 1998-03-10 | Cytec Technology Corp. | Anionic water-soluble polymer precipitation in salt solution |
DK0950138T3 (da) | 1996-12-31 | 2002-07-01 | Ciba Spec Chem Water Treat Ltd | Fremgangsmåder og materialer til fremstilling af papir |
US5969011A (en) | 1997-02-05 | 1999-10-19 | Akzo Nobel Nv | Sizing of paper |
US6093217A (en) | 1997-02-05 | 2000-07-25 | Akzo Nobel N.V. | Sizing of paper |
AU8401998A (en) | 1997-07-15 | 1999-02-10 | Rhodia Chimie | Method for producing polymers using micellar polymerization |
FR2767327B1 (fr) | 1997-08-14 | 1999-10-29 | Atochem Elf Sa | Nouveaux polymeres associatifs et leur procede de preparation par emulsion inverse |
US5985992A (en) | 1997-12-10 | 1999-11-16 | Cytec Technology Corp. | Anionic polymer products and processes |
CN1300306A (zh) | 1998-03-13 | 2001-06-20 | 宝洁公司 | 耐磨的聚合物泡沫体和用其制备的污物接收器 |
EP0953680A1 (en) | 1998-04-27 | 1999-11-03 | Akzo Nobel N.V. | A process for the production of paper |
-
1999
- 1999-12-06 US US09/455,024 patent/US6417268B1/en not_active Expired - Lifetime
-
2000
- 2000-12-05 WO PCT/US2000/033046 patent/WO2001040318A2/en active IP Right Grant
- 2000-12-05 MX MXPA02005315A patent/MXPA02005315A/es active IP Right Grant
- 2000-12-05 CN CNB008167869A patent/CN1152888C/zh not_active Expired - Fee Related
- 2000-12-05 AT AT00983941T patent/ATE277086T1/de active
- 2000-12-05 BR BRPI0016152-7A patent/BR0016152B1/pt not_active IP Right Cessation
- 2000-12-05 PL PL355312A patent/PL199372B1/pl not_active IP Right Cessation
- 2000-12-05 JP JP2001541072A patent/JP2003515624A/ja active Pending
- 2000-12-05 AU AU20631/01A patent/AU2063101A/en not_active Abandoned
- 2000-12-05 ES ES00983941T patent/ES2223627T3/es not_active Expired - Lifetime
- 2000-12-05 DE DE60014172T patent/DE60014172T2/de not_active Expired - Lifetime
- 2000-12-05 NZ NZ519147A patent/NZ519147A/xx unknown
- 2000-12-05 KR KR1020027007222A patent/KR100668023B1/ko not_active IP Right Cessation
- 2000-12-05 EP EP00983941A patent/EP1250360B1/en not_active Expired - Lifetime
- 2000-12-05 RU RU2002117312/04A patent/RU2263683C2/ru not_active IP Right Cessation
- 2000-12-05 CA CA002392430A patent/CA2392430C/en not_active Expired - Fee Related
- 2000-12-05 PT PT00983941T patent/PT1250360E/pt unknown
- 2000-12-27 TW TW089127964A patent/TW581774B/zh not_active IP Right Cessation
-
2002
- 2002-07-08 ZA ZA200205442A patent/ZA200205442B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100811212B1 (ko) * | 2005-12-16 | 2008-03-07 | 주식회사 그린테크놀로지 | 수용성 음이온성 고분자 분산액 및 그 제조방법 |
Also Published As
Publication number | Publication date |
---|---|
MXPA02005315A (es) | 2002-12-11 |
BR0016152A (pt) | 2002-08-20 |
KR100668023B1 (ko) | 2007-01-15 |
ATE277086T1 (de) | 2004-10-15 |
DE60014172D1 (de) | 2004-10-28 |
NZ519147A (en) | 2003-02-28 |
BR0016152B1 (pt) | 2011-11-01 |
ES2223627T3 (es) | 2005-03-01 |
ZA200205442B (en) | 2003-12-31 |
CN1407994A (zh) | 2003-04-02 |
PT1250360E (pt) | 2005-01-31 |
PL355312A1 (en) | 2004-04-19 |
WO2001040318A2 (en) | 2001-06-07 |
EP1250360A2 (en) | 2002-10-23 |
CA2392430C (en) | 2007-01-30 |
JP2003515624A (ja) | 2003-05-07 |
AU2063101A (en) | 2001-06-12 |
WO2001040318A3 (en) | 2002-01-31 |
CN1152888C (zh) | 2004-06-09 |
US6417268B1 (en) | 2002-07-09 |
CA2392430A1 (en) | 2001-06-07 |
TW581774B (en) | 2004-04-01 |
DE60014172T2 (de) | 2005-10-06 |
RU2263683C2 (ru) | 2005-11-10 |
EP1250360B1 (en) | 2004-09-22 |
PL199372B1 (pl) | 2008-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100668023B1 (ko) | 소수성 회합이 가능한 중합체의 제조 방법, 사용 방법 및조성물 | |
EP1683817B1 (en) | Anionic copolymers prepared in an inverse emulsion matrix and their use in preparing cellulosic fiber compositions | |
US4690996A (en) | Inverse emulsions | |
EP0172723B1 (en) | Water soluble polymers | |
CN100334149C (zh) | 高分子量两性离子聚合物 | |
EP0262577B1 (en) | Manufacture of high molecular weight poly (vinylamines) | |
WO2013138156A1 (en) | Synthesis and application of high pressure high temperature fluid loss additive and rheology stabilizer | |
AU2008315917B2 (en) | Inverse emulsion polymers containing a polymeric coagulant | |
US4525496A (en) | Self-inverting water-in-oil emulsions of water-soluble polymers | |
US4952656A (en) | Manufacture of high molecular weight poly(vinylamines) | |
JP2003517104A (ja) | セルロース系繊維組成物製造における疎水的会合性ポリマーの使用方法と、疎水的会合性ポリマー組み込みセルロース系繊維組成物 | |
WO2013162902A1 (en) | Synergistic combination of a fluid loss additive and rheology modifier | |
EP0264649B1 (en) | Manufacture of high molecular weight poly(n-vinylamides) and poly(vinylamines) by inverse emulsion polymerization | |
MX2007014703A (es) | Polimeros hidrofobicos y su uso en la preparacion de composiciones de fibras celulosicas. | |
TWI400382B (zh) | 改良紙類製造中之保留性及濾水性 | |
JP2008525665A (ja) | 紙製造における改善された歩留まりおよび濾水 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0105 | International application |
Patent event date: 20020605 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20050718 Comment text: Request for Examination of Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20060626 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20061120 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20070105 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20070108 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20091224 Start annual number: 4 End annual number: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20101224 Start annual number: 5 End annual number: 5 |
|
FPAY | Annual fee payment |
Payment date: 20111226 Year of fee payment: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20111226 Start annual number: 6 End annual number: 6 |
|
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |