AU2005332031A1 - Hydrophobic polymers and their use in preparing cellulosic fiber compositions - Google Patents
Hydrophobic polymers and their use in preparing cellulosic fiber compositions Download PDFInfo
- Publication number
- AU2005332031A1 AU2005332031A1 AU2005332031A AU2005332031A AU2005332031A1 AU 2005332031 A1 AU2005332031 A1 AU 2005332031A1 AU 2005332031 A AU2005332031 A AU 2005332031A AU 2005332031 A AU2005332031 A AU 2005332031A AU 2005332031 A1 AU2005332031 A1 AU 2005332031A1
- Authority
- AU
- Australia
- Prior art keywords
- acid
- hydrophobic
- polymer
- monomer
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229920001600 hydrophobic polymer Polymers 0.000 title claims description 34
- 239000000203 mixture Substances 0.000 title claims description 34
- 239000000835 fiber Substances 0.000 title claims description 17
- 239000000178 monomer Substances 0.000 claims description 79
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 79
- 229920000642 polymer Polymers 0.000 claims description 64
- 229920001577 copolymer Polymers 0.000 claims description 56
- 230000002209 hydrophobic effect Effects 0.000 claims description 55
- 238000000034 method Methods 0.000 claims description 55
- 239000000463 material Substances 0.000 claims description 54
- -1 diallyldimethylammonium halide Chemical class 0.000 claims description 39
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 38
- 230000014759 maintenance of location Effects 0.000 claims description 34
- 239000002002 slurry Substances 0.000 claims description 21
- 230000008569 process Effects 0.000 claims description 17
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
- 125000002091 cationic group Chemical group 0.000 claims description 15
- 239000000839 emulsion Substances 0.000 claims description 14
- 125000000129 anionic group Chemical group 0.000 claims description 13
- 239000000377 silicon dioxide Substances 0.000 claims description 13
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 239000008119 colloidal silica Substances 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 5
- 239000000499 gel Substances 0.000 claims description 5
- 230000006872 improvement Effects 0.000 claims description 5
- ZKYCLDTVJCJYIB-UHFFFAOYSA-N 2-methylidenedecanamide Chemical compound CCCCCCCCC(=C)C(N)=O ZKYCLDTVJCJYIB-UHFFFAOYSA-N 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims description 4
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 2
- NEYTXADIGVEHQD-UHFFFAOYSA-N 2-hydroxy-2-(prop-2-enoylamino)acetic acid Chemical compound OC(=O)C(O)NC(=O)C=C NEYTXADIGVEHQD-UHFFFAOYSA-N 0.000 claims description 2
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 claims description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- KWKOTMDQAMKXQF-UHFFFAOYSA-N [2-methyl-2-(prop-2-enoylamino)propyl]phosphonic acid Chemical compound OP(=O)(O)CC(C)(C)NC(=O)C=C KWKOTMDQAMKXQF-UHFFFAOYSA-N 0.000 claims description 2
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- OFESGEKAXKKFQT-UHFFFAOYSA-N n-ethenyl-n-methylformamide Chemical compound C=CN(C)C=O OFESGEKAXKKFQT-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 150000003673 urethanes Chemical class 0.000 claims description 2
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 claims description 2
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims description 2
- CLHYKAZPWIRRRD-UHFFFAOYSA-N 1-hydroxypropane-1-sulfonic acid Chemical compound CCC(O)S(O)(=O)=O CLHYKAZPWIRRRD-UHFFFAOYSA-N 0.000 claims 1
- 229920002313 fluoropolymer Polymers 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- RCLLINSDAJVOHP-UHFFFAOYSA-N n-ethyl-n',n'-dimethylprop-2-enehydrazide Chemical compound CCN(N(C)C)C(=O)C=C RCLLINSDAJVOHP-UHFFFAOYSA-N 0.000 claims 1
- 229920005615 natural polymer Polymers 0.000 claims 1
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 claims 1
- 239000000123 paper Substances 0.000 description 23
- 239000004094 surface-active agent Substances 0.000 description 22
- 238000012360 testing method Methods 0.000 description 18
- 125000000217 alkyl group Chemical group 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 150000002430 hydrocarbons Chemical group 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 229920003086 cellulose ether Polymers 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 125000001165 hydrophobic group Chemical group 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 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 6
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 6
- 239000000356 contaminant Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000011087 paperboard Substances 0.000 description 6
- 239000013055 pulp slurry Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 229920001131 Pulp (paper) Polymers 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000008394 flocculating agent Substances 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 239000011121 hardwood Substances 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000011122 softwood Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-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
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 229940037003 alum Drugs 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 229920000359 diblock copolymer Polymers 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000006266 etherification reaction Methods 0.000 description 3
- 229940117927 ethylene oxide Drugs 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000012065 filter cake Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000011859 microparticle Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
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- 239000012454 non-polar solvent Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 3
- 229920000428 triblock copolymer Polymers 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 229920003169 water-soluble polymer Polymers 0.000 description 3
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 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
- LAYAKLSFVAPMEL-UHFFFAOYSA-N 1-ethenoxydodecane Chemical compound CCCCCCCCCCCCOC=C LAYAKLSFVAPMEL-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
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 2
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- 102100031629 COP9 signalosome complex subunit 1 Human genes 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
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- 239000004606 Fillers/Extenders Substances 0.000 description 2
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Classifications
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/06—Paper forming aids
- D21H21/10—Retention agents or drainage improvers
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
- D21H17/375—Poly(meth)acrylamide
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
Landscapes
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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| US68481605P | 2005-05-26 | 2005-05-26 | |
| US60/684,816 | 2005-05-26 | ||
| US11/313,504 US20060266488A1 (en) | 2005-05-26 | 2005-12-21 | Hydrophobic polymers and their use in preparing cellulosic fiber compositions |
| US11/313,504 | 2005-12-21 | ||
| PCT/US2005/046946 WO2006127050A1 (en) | 2005-05-26 | 2005-12-23 | Hydrophobic polymers and their use in preparing cellulosic fiber compositions |
Publications (1)
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|---|---|
| AU2005332031A1 true AU2005332031A1 (en) | 2006-11-30 |
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| AU2005332031A Abandoned AU2005332031A1 (en) | 2005-05-26 | 2005-12-23 | Hydrophobic polymers and their use in preparing cellulosic fiber compositions |
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| EP (1) | EP1910617A1 (enExample) |
| JP (1) | JP2008545892A (enExample) |
| KR (1) | KR20080047510A (enExample) |
| AU (1) | AU2005332031A1 (enExample) |
| BR (1) | BRPI0520283A2 (enExample) |
| CA (1) | CA2609546A1 (enExample) |
| MX (1) | MX2007014703A (enExample) |
| TW (1) | TW200641203A (enExample) |
| WO (1) | WO2006127050A1 (enExample) |
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| US7671007B2 (en) * | 2006-05-04 | 2010-03-02 | Conopco, Inc. | Personal care compositions comprising hydrophobically modified cationic polymers |
| US7723453B2 (en) * | 2006-05-04 | 2010-05-25 | Conopco, Inc. | Hydrophobically modified cationic polymers |
| JP6204642B2 (ja) | 2008-10-21 | 2017-09-27 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 被着が増強されたセッケンベース液体洗浄配合物 |
| EP2319984B2 (en) * | 2009-11-04 | 2025-04-02 | Kemira Oyj | Process for production of paper |
| US8905135B2 (en) * | 2010-03-24 | 2014-12-09 | Halliburton Energy Services, Inc. | Zero shear viscosifying agent |
| EP2640891B1 (en) * | 2010-11-16 | 2016-03-30 | Basf Se | Manufacture of cellulosic pulp sheets |
| CN103422382A (zh) | 2012-05-21 | 2013-12-04 | 埃科莱布美国股份有限公司 | 在制浆和造纸过程中有机污染物去粘性的方法及组合物 |
| DE102014203744A1 (de) | 2014-02-28 | 2015-09-03 | Siemens Aktiengesellschaft | Leitfähiges Glimmschutzpapier, insbesondere für den Außenglimmschutz |
| DE102014203740A1 (de) | 2014-02-28 | 2015-09-03 | Siemens Aktiengesellschaft | Glimmschutzsystem, insbesondere Außenglimmschutzsystem für eine elektrische Maschine |
| WO2017003805A1 (en) | 2015-06-29 | 2017-01-05 | Ecolab Usa Inc. | Methods of making acrylamide-acrylic acid copolymers |
| WO2017003806A1 (en) | 2015-06-29 | 2017-01-05 | Ecolab Usa Inc. | Highly random acrylamide-acrylic acid copolymers |
| JP6532102B2 (ja) * | 2015-07-14 | 2019-06-19 | センカ株式会社 | 紙製造工程用汚れ防止剤組成物及び汚れ防止方法 |
| US9873982B2 (en) * | 2015-10-12 | 2018-01-23 | Solenis Technologies, L.P. | Method of increasing drainage performance of a pulp slurry during manufacture of paper products, and products therefrom |
| TW201739983A (zh) * | 2016-01-14 | 2017-11-16 | 亞齊羅馬Ｉｐ公司 | 丙烯酸酯共聚物之用途、使用其之具有纖維素纖維之基材之製造方法及其基板 |
| JP2019513194A (ja) * | 2016-03-18 | 2019-05-23 | ダウ グローバル テクノロジーズ エルエルシー | 紙コーティング組成物及びそれを作製するプロセス |
| JP6257700B2 (ja) * | 2016-05-30 | 2018-01-10 | ハリマ化成株式会社 | ピッチコントロール剤およびピッチコントロール方法 |
| CN112982029B (zh) * | 2021-02-04 | 2023-06-27 | 陕西鸿鑫耐斯环保科技有限公司 | 一种高密度溶剂油/水分离用ZrO2/滤纸的制备方法 |
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| US3284393A (en) * | 1959-11-04 | 1966-11-08 | Dow Chemical Co | Water-in-oil emulsion polymerization process for polymerizing watersoluble monomers |
| SE419236B (sv) * | 1979-06-01 | 1981-07-20 | Eka Ab | Ytmodifierat pigment av naturligt kaolinmaterial, samt for dess framstellning |
| US4431548A (en) * | 1979-10-15 | 1984-02-14 | Diamond Shamrock Chemicals Company | Use of an amphoteric water-in-oil self-inverting polymer emulsion as a flocculant |
| 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 |
| EP0172723B2 (en) * | 1984-08-15 | 1997-11-05 | Ciba Specialty Chemicals Water Treatments Limited | Water soluble polymers |
| GB8602121D0 (en) * | 1986-01-29 | 1986-03-05 | Allied Colloids Ltd | Paper & paper board |
| US5167766A (en) * | 1990-06-18 | 1992-12-01 | American Cyanamid Company | Charged organic polymer microbeads in paper making process |
| US5274055A (en) * | 1990-06-11 | 1993-12-28 | American Cyanamid Company | Charged organic polymer microbeads in paper-making process |
| CA2138314C (en) * | 1993-12-24 | 1999-09-21 | Hirotoshi Doki | Acrylamide polymers and use thereof |
| DE69507067T2 (de) * | 1994-04-14 | 1999-08-05 | Mitsui Chemicals, Inc., Tokio/Tokyo | Verfahren zur Herstellung von hochmolekularen Acrylamidpolymeren |
| US6020422A (en) * | 1996-11-15 | 2000-02-01 | Betzdearborn Inc. | Aqueous dispersion polymers |
| FR2767327B1 (fr) * | 1997-08-14 | 1999-10-29 | Atochem Elf Sa | Nouveaux polymeres associatifs et leur procede de preparation par emulsion inverse |
| US7306700B1 (en) * | 1998-04-27 | 2007-12-11 | Akzo Nobel Nv | Process for the production of paper |
| US6417268B1 (en) * | 1999-12-06 | 2002-07-09 | Hercules Incorporated | Method for making hydrophobically associative polymers, methods of use and compositions |
| AU1813801A (en) * | 1999-12-06 | 2001-06-12 | Hercules Incorporated | Method for using hydrophobically associative polymers in preparing cellulosic fiber compositions, and cellulosic fiber compositions incorporating the hydrophobically associative polymers |
| US6417236B1 (en) * | 2000-06-02 | 2002-07-09 | The United States Of America As Represented By The Secretary Of The Army | Active topical skin protectants using hybrid organic polysilsesquioxane materials |
| EP1319105A1 (en) * | 2000-09-20 | 2003-06-18 | Akzo Nobel N.V. | A process for the production of paper |
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| US6828014B2 (en) * | 2001-03-22 | 2004-12-07 | Kimberly-Clark Worldwide, Inc. | Water-dispersible, cationic polymers, a method of making same and items using same |
| MX247971B (es) * | 2001-12-07 | 2007-08-10 | Hercules Inc | Polimeros anioicos preparados en una matriz de emulsion inversa y su uso al preparar composiciones de fibra celulosica. |
| US7396874B2 (en) * | 2002-12-06 | 2008-07-08 | Hercules Incorporated | Cationic or amphoteric copolymers prepared in an inverse emulsion matrix and their use in preparing cellulosic fiber compositions |
-
2005
- 2005-12-21 US US11/313,504 patent/US20060266488A1/en not_active Abandoned
- 2005-12-23 EP EP05855496A patent/EP1910617A1/en not_active Withdrawn
- 2005-12-23 MX MX2007014703A patent/MX2007014703A/es unknown
- 2005-12-23 BR BRPI0520283-3A patent/BRPI0520283A2/pt not_active IP Right Cessation
- 2005-12-23 JP JP2008513448A patent/JP2008545892A/ja not_active Withdrawn
- 2005-12-23 AU AU2005332031A patent/AU2005332031A1/en not_active Abandoned
- 2005-12-23 KR KR1020077030060A patent/KR20080047510A/ko not_active Withdrawn
- 2005-12-23 WO PCT/US2005/046946 patent/WO2006127050A1/en not_active Ceased
- 2005-12-23 CA CA002609546A patent/CA2609546A1/en not_active Abandoned
- 2005-12-28 TW TW094147067A patent/TW200641203A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2008545892A (ja) | 2008-12-18 |
| BRPI0520283A2 (pt) | 2009-04-28 |
| WO2006127050A1 (en) | 2006-11-30 |
| TW200641203A (en) | 2006-12-01 |
| US20060266488A1 (en) | 2006-11-30 |
| CA2609546A1 (en) | 2006-11-30 |
| WO2006127050A8 (en) | 2008-01-31 |
| KR20080047510A (ko) | 2008-05-29 |
| MX2007014703A (es) | 2008-02-14 |
| EP1910617A1 (en) | 2008-04-16 |
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