CA2378850A1 - Water soluble anionic or nonionic dispersion polymer - Google Patents
Water soluble anionic or nonionic dispersion polymer Download PDFInfo
- Publication number
- CA2378850A1 CA2378850A1 CA002378850A CA2378850A CA2378850A1 CA 2378850 A1 CA2378850 A1 CA 2378850A1 CA 002378850 A CA002378850 A CA 002378850A CA 2378850 A CA2378850 A CA 2378850A CA 2378850 A1 CA2378850 A1 CA 2378850A1
- Authority
- CA
- Canada
- Prior art keywords
- acid
- acrylamido
- dispersion
- methyl
- stabilizer
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- 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
- C08F2/20—Aqueous medium with the aid of macromolecular dispersing agents
-
- 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
- C08F220/56—Acrylamide; Methacrylamide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- 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
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
Abstract
A high molecular-weight water-soluble polymer dispersion, having a bulk Brookfield viscosity of from about 10 to about 25,000 cps at 25 degrees Celsius, comprising from about 5 to about 50 weight percent of a water-soluble polymer prepared by polymerizing, under free-radical forming conditions in an aqueous medium of a water-soluble salt in the presence of a stabilizer at a pH greater than 5, 0-30 mole percent of acrylic acid and 0-100 mole percent of acrylamide; wherein the stabilizer is an anionic water-soluble polymer having an intrinsic viscosity in 1M NaNO3 of from about 0.1-10 and comprises from about 0.1 to about 5 weight percent; and wherein the water-soluble salt is selected from the group consisting of ammonium, alkali metal and alkali earth metal halides, sulfates, and phosphates and comprises 5 to about 40 weight percent of the total weight of the dispersion.
Claims (12)
1. ~A high molecular weight water-soluble dispersion polymer having a bulk Brookfield viscosity of from about 10 to about 25,000 cps at 25°C
comprising from about to about 50 weight percent of a water soluble polymer prepared by polymerizing under free radical forming conditions in an aqueous solution of a water-soluble salt in the presence of a stabilizer at a pH greater than 5:
0-30 mole percent of at least one anionic monomer, and, ii. 100-70 mole percent of at least one non-ionic monomer;
wherein the stabilizer is an anionic water soluble polymer having an intrinsic viscosity in 1M NaNO3 of from about 0.1-10 and comprises from about 0.1 to about 5 weight percent based on the total weight of the dispersion, and the water soluble salt is selected from the group consisting of ammonium, alkali metal and alkaline earth metal halides, sulfates, and phosphates and comprises from about 5 to about 40 weight percent based on the weight of the dispersion.
comprising from about to about 50 weight percent of a water soluble polymer prepared by polymerizing under free radical forming conditions in an aqueous solution of a water-soluble salt in the presence of a stabilizer at a pH greater than 5:
0-30 mole percent of at least one anionic monomer, and, ii. 100-70 mole percent of at least one non-ionic monomer;
wherein the stabilizer is an anionic water soluble polymer having an intrinsic viscosity in 1M NaNO3 of from about 0.1-10 and comprises from about 0.1 to about 5 weight percent based on the total weight of the dispersion, and the water soluble salt is selected from the group consisting of ammonium, alkali metal and alkaline earth metal halides, sulfates, and phosphates and comprises from about 5 to about 40 weight percent based on the weight of the dispersion.
2. ~The dispersion polymer of claim 1 wherein the anionic monomer is selected from the group consisting of acrylic acid, methacrylic acid, 2-acrylamido-2-methyl-propanesulfonic acid, acrylamidomethylbutanoic acid, maleic acid, fumaric acid, itaconic acid, vinyl sulfonic acid, styrene sulfonic acid, vinyl phosphonic acid, allyl sulfonic acid, allyl phosphonic acid, sulfomethylated acrylamide, phosphonomethylated acrylamide and the water soluble alkali metal, alkaline earth metal, and ammonium salts thereof and the nonionic monomer is selected from the group consisting of acrylamide, methacrylamide, N-isopropylacrylamide, N-t-butyl acrylamide, and N-methylolacrylamide.
3. The dispersion polymer of claim 2 wherein the anionic monomer is acrylic acid or a water soluble alkali metal, alkaline earth metal, or ammonium salt thereof and the nonionic monomer is acrylamide.
4. The dispersion polymer of claim 3 wherein the stabilizer is an anionic polymer selected from polyacrylic acid, poly(meth)acrylic acid, poly(2-acrylamido-2-methyl-1-propanesulfonic acid); poly(2-acrylamido-2-methyl-1-propanesulfonic acid/acrylic acid) and poly(2-acrylamido-2-methyl-1-propanesulfonic acid/methacrylic acid).
5. The dispersion polymer of claim 4 wherein the stabilizer has a concentration of from about 0.25 to about 2 weight percent based on the total weight of the dispersion and an intrinsic viscosity in 1 M NaNO3 of from about 0.75 to about 7.0 dl/g.
6. The dispersion polymer of claim 5 wherein the stabilizer is poly(2-acrylamido-2-methyl-1-propanesulfonic acid/acrylic acid) comprising from about 3 to about 80 mole percent 2-acrylamido-2-methyl-1-propanesulfonic acid and from about 97 to about 20 mole percent acrylic acid.
7. The dispersion polymer of claim 5 wherein the stabilizer is poly(2-acrylamido-2-methyl-1-propanesulfonic acid/methacrylic acid) comprising from about 5 to about 90 mole percent 2-acrylamido-2-methyl-1-propanesulfonic acid and from about 95 to about mole percent methacrylic acid.
8. The dispersion polymer of claim 5 wherein the water-soluble polymer is poly(acrylic acid/acrylamide having a mole ratio of about 7:93 for acrylic acid to acrylamide.
9. The dispersion polymer of claim 8 wherein the stabilizer is poly(2-acrylamido-2-methyl-1-propanesulfonic acid/acrylic acid) having a mole ratio of about 7:93 for 2-acrylamido-2-methyl-1-propanesulfonic acid to acrylic acid.
10. The dispersion polymer of claim 8 wherein the stabilizer is poly(2-acrylamido-2-methyl-1-propanesulfonic acid/methacrylic acid) comprising from about 20 to about 30 mole percent 2-acrylamido-2-methyl-1-propanesulfonic acid and from about 80 to about 70 mole percent methacrylic acid.
11. The dispersion polymer of claim 5 wherein the water-soluble polymer is polyacrylamide.
12. A method of preparing a high molecular weight dispersion polymer having a bulk Brookfield viscosity of from about 10 to about 25,000 cps at 25°C
comprising a) adding a free-radical initiator to an aqueous mixture comprising:
i. from about 5 to about 50 weight percent of a mixture comprising 0-30 mole percent of at least one anionic monomer and 100-70 mole percent of at least one non-ionic vinyl monomer;
ii. from about 0.1 to about 5 weight percent based on the total weight of the dispersion of a stabilizer, wherein the stabilizer is an anionic water soluble polymer having an intrinsic viscosity in 1M NaNO3 of from about 0.1-10 and iii. from about 5 to about 40 weight percent based on the weight of the dispersion of a water soluble salt selected from the group consisting of ammonium, alkali metal and alkaline earth metal halides, sulfates, and phosphates; and b) polymerizing the monomers.
comprising a) adding a free-radical initiator to an aqueous mixture comprising:
i. from about 5 to about 50 weight percent of a mixture comprising 0-30 mole percent of at least one anionic monomer and 100-70 mole percent of at least one non-ionic vinyl monomer;
ii. from about 0.1 to about 5 weight percent based on the total weight of the dispersion of a stabilizer, wherein the stabilizer is an anionic water soluble polymer having an intrinsic viscosity in 1M NaNO3 of from about 0.1-10 and iii. from about 5 to about 40 weight percent based on the weight of the dispersion of a water soluble salt selected from the group consisting of ammonium, alkali metal and alkaline earth metal halides, sulfates, and phosphates; and b) polymerizing the monomers.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/392,673 | 1999-09-08 | ||
US09/392,673 US6265477B1 (en) | 1999-09-08 | 1999-09-08 | Aqueous dispersion of a particulate high molecular weight anionic or nonionic polymer |
PCT/US2000/040721 WO2001018064A1 (en) | 1999-09-08 | 2000-08-22 | Water soluble anionic or nonionic dispersion polymer |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2378850A1 true CA2378850A1 (en) | 2001-03-15 |
CA2378850C CA2378850C (en) | 2009-11-10 |
Family
ID=23551546
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002378850A Expired - Lifetime CA2378850C (en) | 1999-09-08 | 2000-08-22 | Water soluble anionic or nonionic dispersion polymer |
Country Status (16)
Country | Link |
---|---|
US (1) | US6265477B1 (en) |
EP (1) | EP1218415B1 (en) |
JP (1) | JP4689122B2 (en) |
KR (1) | KR100658101B1 (en) |
AR (1) | AR025588A1 (en) |
AU (1) | AU782319B2 (en) |
BR (1) | BR0013855A (en) |
CA (1) | CA2378850C (en) |
DK (1) | DK1218415T3 (en) |
ES (1) | ES2447415T3 (en) |
MX (1) | MXPA02001707A (en) |
NO (1) | NO339153B1 (en) |
NZ (1) | NZ517020A (en) |
TW (1) | TW593353B (en) |
WO (1) | WO2001018064A1 (en) |
ZA (1) | ZA200200433B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8721896B2 (en) | 2012-01-25 | 2014-05-13 | Sortwell & Co. | Method for dispersing and aggregating components of mineral slurries and low molecular weight multivalent polymers for mineral aggregation |
US9150442B2 (en) | 2010-07-26 | 2015-10-06 | Sortwell & Co. | Method for dispersing and aggregating components of mineral slurries and high-molecular weight multivalent polymers for clay aggregation |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6331229B1 (en) | 1999-09-08 | 2001-12-18 | Nalco Chemical Company | Method of increasing retention and drainage in papermaking using high molecular weight water-soluble anionic or monionic dispersion polymers |
US7060273B2 (en) * | 2001-04-06 | 2006-06-13 | Progenics Pharmaceuticals, Inc. | Methods for inhibiting HIV-1 infection |
US6696067B2 (en) * | 2001-04-12 | 2004-02-24 | Ondeo Nalco Company | Cosmetic compositions containing dispersion polymers |
DE10208361A1 (en) * | 2002-02-27 | 2003-09-04 | Basf Ag | Process for the preparation of an aqueous thermally curable polymer dispersion |
US6787506B2 (en) | 2002-04-03 | 2004-09-07 | Nalco Energy Services, L.P. | Use of dispersion polymers as friction reducers in aqueous fracturing fluids |
US7566469B2 (en) * | 2003-10-13 | 2009-07-28 | Nalco Company | Method of dewatering grain stillage solids |
DE10351004A1 (en) | 2003-10-30 | 2005-05-25 | Basf Ag | Aqueous nanodispersion-forming formulations of active agents, especially plant protectants such as fungicides, comprise random copolymer of unsaturated sulfonic acid(s) |
DE102004013750A1 (en) * | 2004-03-18 | 2005-11-03 | Stockhausen Gmbh | Anionic water-in-water polymer dispersions, process for their preparation and their use |
ZA200709250B (en) * | 2005-05-20 | 2009-02-25 | Akzo Nobel Nv | Process for preparing a polymer dispersion and a polymer dispersion |
US8039550B2 (en) | 2005-05-20 | 2011-10-18 | Akzo Nobel N.V. | Process for preparing a polymer dispersion and a polymer dispersion |
US8900641B2 (en) * | 2006-12-28 | 2014-12-02 | Nalco Company | Antimicrobial composition |
US20090220446A1 (en) * | 2008-03-03 | 2009-09-03 | Hessefort Yin Z | Method for treating hair |
RU2495053C2 (en) * | 2008-08-22 | 2013-10-10 | Акцо Нобель Н.В. | Polymer dispersion |
US8865632B1 (en) | 2008-11-10 | 2014-10-21 | Cesi Chemical, Inc. | Drag-reducing copolymer compositions |
US20100187181A1 (en) * | 2009-01-29 | 2010-07-29 | Sortwell Edwin T | Method for Dispersing and Aggregating Components of Mineral Slurries |
CN101875706B (en) * | 2009-04-30 | 2012-05-30 | 中国海洋石油总公司 | Method for preparing aqueous emulsion of polyacrylic acid |
PL2470570T3 (en) * | 2009-08-24 | 2014-05-30 | Solenis Technologies Cayman Lp | Anionic cross-linked polymers in water-in-water polymer dispersions |
FI125418B (en) | 2010-10-15 | 2015-10-15 | Kemira Oyj | Anionic dispersion polymerization process |
US9776105B2 (en) | 2010-11-19 | 2017-10-03 | Nalco Company | Method for conditioning and processing whole or thin stillage to aid in the separation and recovery of protein and oil fractions |
CN102336995B (en) * | 2011-07-08 | 2013-07-10 | 西安交通大学 | Preparation method of novel luminous high molecular aquagel |
US10066107B2 (en) | 2012-09-19 | 2018-09-04 | Solenis Technologies, L.P. | Process for improving the rheological properties of an aqueous dispersion |
US9329159B2 (en) | 2013-03-08 | 2016-05-03 | Ecolab Usa Inc. | Methods and systems for analyzing a liquid medium |
US10005982B2 (en) | 2015-07-18 | 2018-06-26 | Ecolab Usa Inc. | Chemical additives to improve oil separation in stillage process operations |
AR106581A1 (en) | 2015-11-04 | 2018-01-31 | Ecolab Usa Inc | FRICTION REDUCING COMPOSITIONS FORMULATED WITH HIGH CONCENTRATION SALMUERA |
US10442732B2 (en) | 2016-05-20 | 2019-10-15 | United States Gypsum Company | Gypsum slurries with linear polycarboxylate dispersants |
EP3679076B1 (en) * | 2017-09-08 | 2024-01-24 | Solenis Technologies Cayman, L.P. | Composition comprising cross-linked anionic, organic polymeric microparticles, its preparation and use in paper and paperboard making processes |
WO2022235623A1 (en) | 2021-05-06 | 2022-11-10 | Ecolab Usa Inc. | Systems and processes for injecting gas-infused additives |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3898037A (en) * | 1972-06-01 | 1975-08-05 | Betz Laboratories | Acrylamido-sulfonic acid polymers and their use |
CA1267483A (en) | 1984-11-19 | 1990-04-03 | Hisao Takeda | Process for the production of a water-soluble polymer dispersion |
JPH0672170B2 (en) * | 1985-07-18 | 1994-09-14 | ハイモ株式会社 | Method for producing water-soluble polymer dispersion |
US5837776A (en) * | 1996-03-20 | 1998-11-17 | Nalco Chemical Company | Process for producing water soluble anionic dispersion polymers |
US5605970A (en) | 1996-03-20 | 1997-02-25 | Nalco Chemical Company | Synthesis of high molecular weight anionic dispersion polymers |
US5985992A (en) * | 1997-12-10 | 1999-11-16 | Cytec Technology Corp. | Anionic polymer products and processes |
-
1999
- 1999-09-08 US US09/392,673 patent/US6265477B1/en not_active Expired - Lifetime
-
2000
- 2000-08-22 KR KR1020027002140A patent/KR100658101B1/en active IP Right Grant
- 2000-08-22 BR BR0013855-0A patent/BR0013855A/en not_active Application Discontinuation
- 2000-08-22 EP EP00969026.4A patent/EP1218415B1/en not_active Expired - Lifetime
- 2000-08-22 ES ES00969026.4T patent/ES2447415T3/en not_active Expired - Lifetime
- 2000-08-22 MX MXPA02001707A patent/MXPA02001707A/en active IP Right Grant
- 2000-08-22 DK DK00969026.4T patent/DK1218415T3/en active
- 2000-08-22 JP JP2001522286A patent/JP4689122B2/en not_active Expired - Lifetime
- 2000-08-22 AU AU78856/00A patent/AU782319B2/en not_active Expired
- 2000-08-22 CA CA002378850A patent/CA2378850C/en not_active Expired - Lifetime
- 2000-08-22 WO PCT/US2000/040721 patent/WO2001018064A1/en active IP Right Grant
- 2000-08-22 NZ NZ51702000A patent/NZ517020A/en unknown
- 2000-09-07 TW TW089118343A patent/TW593353B/en not_active IP Right Cessation
- 2000-09-07 AR ARP000104680A patent/AR025588A1/en unknown
-
2002
- 2002-01-17 ZA ZA200200433A patent/ZA200200433B/en unknown
- 2002-03-07 NO NO20021131A patent/NO339153B1/en not_active IP Right Cessation
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9150442B2 (en) | 2010-07-26 | 2015-10-06 | Sortwell & Co. | Method for dispersing and aggregating components of mineral slurries and high-molecular weight multivalent polymers for clay aggregation |
US9540469B2 (en) | 2010-07-26 | 2017-01-10 | Basf Se | Multivalent polymers for clay aggregation |
US8721896B2 (en) | 2012-01-25 | 2014-05-13 | Sortwell & Co. | Method for dispersing and aggregating components of mineral slurries and low molecular weight multivalent polymers for mineral aggregation |
US9090726B2 (en) | 2012-01-25 | 2015-07-28 | Sortwell & Co. | Low molecular weight multivalent cation-containing acrylate polymers |
US9487610B2 (en) | 2012-01-25 | 2016-11-08 | Basf Se | Low molecular weight multivalent cation-containing acrylate polymers |
Also Published As
Publication number | Publication date |
---|---|
NO20021131D0 (en) | 2002-03-07 |
TW593353B (en) | 2004-06-21 |
NO20021131L (en) | 2002-05-08 |
AU7885600A (en) | 2001-04-10 |
DK1218415T3 (en) | 2014-01-20 |
KR100658101B1 (en) | 2006-12-15 |
NO339153B1 (en) | 2016-11-14 |
JP4689122B2 (en) | 2011-05-25 |
MXPA02001707A (en) | 2002-08-06 |
ES2447415T3 (en) | 2014-03-12 |
BR0013855A (en) | 2002-07-16 |
WO2001018064A1 (en) | 2001-03-15 |
CA2378850C (en) | 2009-11-10 |
EP1218415B1 (en) | 2013-11-20 |
EP1218415A1 (en) | 2002-07-03 |
AR025588A1 (en) | 2002-12-04 |
EP1218415A4 (en) | 2004-03-31 |
JP2003508598A (en) | 2003-03-04 |
AU782319B2 (en) | 2005-07-21 |
ZA200200433B (en) | 2003-05-28 |
NZ517020A (en) | 2004-12-24 |
US6265477B1 (en) | 2001-07-24 |
KR20020053803A (en) | 2002-07-05 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKEX | Expiry |
Effective date: 20200824 |