ZA200700147B - Surface cross-linked superabsorbent polymer particles and methods of making them - Google Patents
Surface cross-linked superabsorbent polymer particles and methods of making them Download PDFInfo
- Publication number
- ZA200700147B ZA200700147B ZA200700147A ZA200700147A ZA200700147B ZA 200700147 B ZA200700147 B ZA 200700147B ZA 200700147 A ZA200700147 A ZA 200700147A ZA 200700147 A ZA200700147 A ZA 200700147A ZA 200700147 B ZA200700147 B ZA 200700147B
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- ZA
- South Africa
- Prior art keywords
- cross
- linking
- polymer particles
- molecules
- superabsorbent polymer
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 60
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- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229940106135 cellulose Drugs 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- SBHCLVQMTBWHCD-UHFFFAOYSA-N icosa-2,4,6,8,10-pentaenoic acid Chemical compound CCCCCCCCCC=CC=CC=CC=CC=CC(O)=O SBHCLVQMTBWHCD-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006193 liquid solution Substances 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical group 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- VCQYDZJGTXAFRL-UHFFFAOYSA-N s-phenyl benzenecarbothioate Chemical class C=1C=CC=CC=1C(=O)SC1=CC=CC=C1 VCQYDZJGTXAFRL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- SQAIGLXMIMWFEQ-UHFFFAOYSA-N tetrakis(prop-2-enyl) silicate Chemical compound C=CCO[Si](OCC=C)(OCC=C)OCC=C SQAIGLXMIMWFEQ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- PLCFYBDYBCOLSP-UHFFFAOYSA-N tris(prop-2-enyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound C=CCOC(=O)CC(O)(CC(=O)OCC=C)C(=O)OCC=C PLCFYBDYBCOLSP-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
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/53—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium
- A61F13/534—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium having an inhomogeneous composition through the thickness of the pad
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/28—Treatment by wave energy or particle radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/60—Liquid-swellable gel-forming materials, e.g. super-absorbents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/53—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium
- A61F2013/530481—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium having superabsorbent materials, i.e. highly absorbent polymer gel materials
- A61F2013/530708—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium having superabsorbent materials, i.e. highly absorbent polymer gel materials characterized by the absorbency properties
- A61F2013/530737—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium having superabsorbent materials, i.e. highly absorbent polymer gel materials characterized by the absorbency properties by the absorbent capacity
- A61F2013/530766—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the absorbing medium having superabsorbent materials, i.e. highly absorbent polymer gel materials characterized by the absorbency properties by the absorbent capacity by the cross-link factor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Dispersion Chemistry (AREA)
- Hematology (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04017071A EP1629854B1 (fr) | 2004-07-20 | 2004-07-20 | Particules polymériques superabsorbantes réticulées en surface et leurs procédés de fabrication |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200700147B true ZA200700147B (en) | 2008-05-28 |
Family
ID=34925825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200700147A ZA200700147B (en) | 2004-07-20 | 2007-01-04 | Surface cross-linked superabsorbent polymer particles and methods of making them |
Country Status (14)
Country | Link |
---|---|
US (2) | US7588777B2 (fr) |
EP (1) | EP1629854B1 (fr) |
JP (1) | JP2008506528A (fr) |
KR (1) | KR20070039050A (fr) |
CN (1) | CN101076358A (fr) |
AR (1) | AR054672A1 (fr) |
AT (1) | ATE484298T1 (fr) |
AU (1) | AU2005274865A1 (fr) |
BR (1) | BRPI0513537A (fr) |
CA (1) | CA2573442A1 (fr) |
DE (1) | DE602004029569D1 (fr) |
IN (1) | IN2006DE07971A (fr) |
WO (1) | WO2006020161A2 (fr) |
ZA (1) | ZA200700147B (fr) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8080705B2 (en) * | 2004-07-28 | 2011-12-20 | The Procter & Gamble Company | Superabsorbent polymers comprising direct covalent bonds between polymer chain segments and method of making them |
TW200621868A (en) * | 2004-12-10 | 2006-07-01 | Nippon Catalytic Chem Ind | Method for surface-treatment of water absorbent resin |
EP1757645A1 (fr) * | 2005-08-23 | 2007-02-28 | Nippon Shokubai Co.,Ltd. | Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet |
EP1757648A1 (fr) | 2005-08-23 | 2007-02-28 | Nippon Shokubai Co.,Ltd. | Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet en présence d'acides de Bronsted |
EP1757643A1 (fr) * | 2005-08-23 | 2007-02-28 | Nippon Shokubai Co.,Ltd. | Procédé pour la réticulation de la surface de particules polymères ultra-absorbantes par rayonnement ultraviolet sous vide |
WO2008102322A2 (fr) * | 2007-02-22 | 2008-08-28 | The Procter & Gamble Company | Procédé de traitement de surface d'un matériau particulaire au moyen d'un rayonnement électromagnétique |
US7935860B2 (en) * | 2007-03-23 | 2011-05-03 | Kimberly-Clark Worldwide, Inc. | Absorbent articles comprising high permeability superabsorbent polymer compositions |
CN101925623B (zh) * | 2008-01-29 | 2013-11-06 | 巴斯夫欧洲公司 | 生产吸水性聚合物颗粒的方法 |
US8453354B2 (en) | 2009-10-01 | 2013-06-04 | Nike, Inc. | Rigid cantilevered stud |
DE102010004478A1 (de) | 2010-01-12 | 2011-07-14 | Riesinger, Birgit, 48346 | Neue Technologien zur Verwendung in Wundauflagen mit superabsorbierenden Polymeren |
EP2447286A1 (fr) * | 2010-11-01 | 2012-05-02 | The Procter & Gamble Company | Procédé utilisant un milieu supercritique pour produire des polymères |
KR101290740B1 (ko) * | 2010-11-22 | 2013-07-29 | 주식회사 엘지화학 | 고흡수성 수지의 제조 방법 |
KR101495779B1 (ko) * | 2010-11-30 | 2015-02-25 | 주식회사 엘지화학 | 고흡수성 수지의 제조 방법 |
EP2740449B1 (fr) * | 2012-12-10 | 2019-01-23 | The Procter & Gamble Company | Article absorbant à haute teneur en matériau absorbant |
KR101604272B1 (ko) | 2013-05-09 | 2016-03-25 | 주식회사 엘지화학 | 고흡수성 수지의 제조방법 |
WO2014182128A1 (fr) * | 2013-05-09 | 2014-11-13 | 주식회사 엘지화학 | Procede de preparation pour une resine superabsorbante |
EP2944376B1 (fr) * | 2014-05-13 | 2019-11-13 | The Procter and Gamble Company | Particules de polymère superabsorbant agglomérées |
CN109311286B (zh) * | 2016-05-31 | 2021-06-25 | 花王株式会社 | 吸收性物品 |
AU2018221352B2 (en) | 2017-02-16 | 2022-02-17 | Nutrition & Biosciences USA 4, Inc. | Crosslinked dextran and crosslinked dextran-poly alpha-1,3-glucan graft copolymers |
JP2020533498A (ja) | 2017-09-13 | 2020-11-19 | デュポン・インダストリアル・バイオサイエンシーズ・ユーエスエイ・エルエルシー | 多糖を含む不織ウェブ |
KR102600854B1 (ko) * | 2017-12-28 | 2023-11-10 | 롯데정밀화학 주식회사 | 셀룰로오스 유도체 입자의 제조방법, 상기 방법에 의해 제조된 셀룰로오스 유도체 입자 및 이를 포함하는 흡수성 물품 |
KR20200132929A (ko) | 2018-03-13 | 2020-11-25 | 엠제이제이 테크놀로지스 인코포레이티드 | 고흡수성 폴리머 및 이를 제조 및 사용하는 방법 |
KR102452566B1 (ko) * | 2018-04-27 | 2022-10-06 | 주식회사 엘지화학 | 고흡수성 수지 조성물 |
Family Cites Families (100)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3661875A (en) * | 1970-01-27 | 1972-05-09 | Du Pont | 1-(1-alkenyl)bicyclo(1.1.0)butanes and their polymers |
US3959569A (en) * | 1970-07-27 | 1976-05-25 | The Dow Chemical Company | Preparation of water-absorbent articles |
US3860003B2 (en) * | 1973-11-21 | 1990-06-19 | Contractable side portions for disposable diaper | |
US3935099A (en) * | 1974-04-03 | 1976-01-27 | The United States Of America As Represented By The Secretary Of Agriculture | Method of reducing water content of emulsions, suspensions, and dispersions with highly absorbent starch-containing polymeric compositions |
JPS51125468A (en) * | 1975-03-27 | 1976-11-01 | Sanyo Chem Ind Ltd | Method of preparing resins of high water absorbency |
JPS5265597A (en) * | 1975-11-27 | 1977-05-31 | Sumitomo Chem Co Ltd | Preparation of high polimeric materials with improved water absorption |
JPS5346389A (en) * | 1976-10-07 | 1978-04-25 | Kao Corp | Preparation of self-crosslinking polymer of acrylic alkali metal salt |
US4062817A (en) * | 1977-04-04 | 1977-12-13 | The B.F. Goodrich Company | Water absorbent polymers comprising unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, and another acrylic ester containing alkyl group 2-8 carbon atoms |
US4286082A (en) * | 1979-04-06 | 1981-08-25 | Nippon Shokubai Kagaku Kogyo & Co., Ltd. | Absorbent resin composition and process for producing same |
JPS6056724B2 (ja) * | 1980-10-22 | 1985-12-11 | 株式会社クラレ | 吸水性樹脂の製造方法 |
GB2088392B (en) * | 1980-12-03 | 1984-05-02 | Sumitomo Chemical Co | Production of hydrogels |
JPS57158209A (en) * | 1981-03-25 | 1982-09-30 | Kao Corp | Production of bead-form highly water-absorbing polymer |
US4985518A (en) * | 1981-10-26 | 1991-01-15 | American Colloid Company | Process for preparing water-absorbing resins |
JPS58180233A (ja) * | 1982-04-19 | 1983-10-21 | Nippon Shokubai Kagaku Kogyo Co Ltd | 吸収剤 |
US4610678A (en) * | 1983-06-24 | 1986-09-09 | Weisman Paul T | High-density absorbent structures |
US4734478A (en) * | 1984-07-02 | 1988-03-29 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Water absorbing agent |
US4625001A (en) * | 1984-09-25 | 1986-11-25 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Method for continuous production of cross-linked polymer |
JPS6187702A (ja) * | 1984-10-05 | 1986-05-06 | Seitetsu Kagaku Co Ltd | 吸水性樹脂の製造方法 |
US4748076A (en) * | 1985-02-16 | 1988-05-31 | Hayashikane Shipbuilding & Engineering Co., Ltd. | Water absorbent fibrous product and a method of producing the same |
JPS61275355A (ja) * | 1985-05-29 | 1986-12-05 | Kao Corp | 吸収性物品 |
US4654039A (en) * | 1985-06-18 | 1987-03-31 | The Proctor & Gamble Company | Hydrogel-forming polymer compositions for use in absorbent structures |
DE3668553D1 (de) * | 1985-06-22 | 1990-03-08 | Taiyo Fishery Co Ltd | Waessrige zusammensetzung, verfahren zur herstellung eines wasserabsorbierenden polymers und eines damit ueberzogenen gegenstandes. |
US4690996A (en) * | 1985-08-28 | 1987-09-01 | National Starch And Chemical Corporation | Inverse emulsions |
DE3537276A1 (de) * | 1985-10-19 | 1987-04-23 | Basf Ag | Verfahren zur kontinuierlichen herstellung von vernetzten feinteiligen gelfoermigen polymerisaten |
DE3609545A1 (de) * | 1986-03-21 | 1987-09-24 | Basf Ag | Verfahren zur diskontinuierlichen herstellung von vernetzten, feinteiligen polymerisaten |
US4737559A (en) | 1986-05-19 | 1988-04-12 | Minnesota Mining And Manufacturing Co. | Pressure-sensitive adhesive crosslinked by copolymerizable aromatic ketone monomers |
US4783510A (en) * | 1986-06-04 | 1988-11-08 | Taiyo Fishery Co., Ltd. | Process for improving a water absorbent polyacrylic acid polymer and an improved polymer produced by said process |
JPH0647626B2 (ja) * | 1986-07-01 | 1994-06-22 | 三菱油化株式会社 | 吸水性複合材料の製造法 |
US4834735A (en) * | 1986-07-18 | 1989-05-30 | The Proctor & Gamble Company | High density absorbent members having lower density and lower basis weight acquisition zones |
JPH0192226A (ja) | 1987-04-01 | 1989-04-11 | Taiyo Fishery Co Ltd | 吸水性ポリマ− |
JPS63260907A (ja) | 1987-04-17 | 1988-10-27 | Mitsubishi Petrochem Co Ltd | 高吸水性ポリマ−の製造法 |
US4940464A (en) * | 1987-12-16 | 1990-07-10 | Kimberly-Clark Corporation | Disposable incontinence garment or training pant |
JPH01292103A (ja) * | 1988-05-19 | 1989-11-24 | Mitsubishi Rayon Co Ltd | 吸収材の製造方法 |
CA1333439C (fr) * | 1988-05-23 | 1994-12-06 | Akito Yano | Methode pour la production de polymere hydrophile |
US5264533A (en) * | 1988-06-16 | 1993-11-23 | Basf Aktiengesellschaft | Benzophenone derivatives and their preparation |
KR930007272B1 (ko) * | 1988-06-28 | 1993-08-04 | 닙본 쇼쿠바이 가브시기 가이샤 | 흡수성 수지 및 그 제법 |
US5244735A (en) * | 1988-06-28 | 1993-09-14 | Nippon Shokubai Kagaku Kabushiki Kaisha | Water-absorbent resin and production process |
US4950692A (en) * | 1988-12-19 | 1990-08-21 | Nalco Chemical Company | Method for reconstituting superabsorbent polymer fines |
DE3844445A1 (de) * | 1988-12-31 | 1990-07-19 | Basf Ag | Uv-vernetzbare massen auf basis von (meth)-acrylesterpolymerisaten |
US5248805A (en) * | 1988-12-31 | 1993-09-28 | Basf Aktiengesellschaft | Radiation-senstive, ethylenically unsaturated, copolymerizable compounds and their preparation |
US5145906A (en) * | 1989-09-28 | 1992-09-08 | Hoechst Celanese Corporation | Super-absorbent polymer having improved absorbency properties |
US5137537A (en) * | 1989-11-07 | 1992-08-11 | The Procter & Gamble Cellulose Company | Absorbent structure containing individualized, polycarboxylic acid crosslinked wood pulp cellulose fibers |
EP0454497B1 (fr) * | 1990-04-27 | 1997-02-26 | Nippon Shokubai Co., Ltd. | Méthode de préparation de résines absorbantes résistant aux sels |
US5241009A (en) | 1990-05-07 | 1993-08-31 | Kimberly-Clark Corporation | Polymeric composition containing carboxy nueutralized with lithium or potassium |
ES2070369T3 (es) * | 1990-07-17 | 1995-06-01 | Sanyo Chemical Ind Ltd | Procedimiento para la fabricacion de resinas absorbentes de agua. |
DE4037079A1 (de) * | 1990-11-22 | 1992-05-27 | Basf Ag | Ungesaettigte phenonderivate und ihre verwendung als haftklebstoffe |
US5478879A (en) * | 1991-01-22 | 1995-12-26 | Nippon Shokubai Co., Ltd. | Method for production of absorbent resin |
TW241279B (fr) * | 1991-02-01 | 1995-02-21 | Catalyst co ltd | |
US5151092A (en) * | 1991-06-13 | 1992-09-29 | The Procter & Gamble Company | Absorbent article with dynamic elastic waist feature having a predisposed resilient flexural hinge |
US5250640A (en) * | 1991-04-10 | 1993-10-05 | Nippon Shokubai Co., Ltd. | Method for production of particulate hydrogel polymer and absorbent resin |
US5075344A (en) | 1991-05-20 | 1991-12-24 | The Dow Chemical Company | Process for producing a superabsorbent polymer |
US5147345A (en) * | 1991-08-12 | 1992-09-15 | The Procter & Gamble Company | High efficiency absorbent articles for incontinence management |
US5260345A (en) * | 1991-08-12 | 1993-11-09 | The Procter & Gamble Company | Absorbent foam materials for aqueous body fluids and absorbent articles containing such materials |
US5387207A (en) * | 1991-08-12 | 1995-02-07 | The Procter & Gamble Company | Thin-unit-wet absorbent foam materials for aqueous body fluids and process for making same |
US5135209A (en) * | 1991-11-12 | 1992-08-04 | Penny Thomas H | Pipe clamp apparatus |
EP0625998B1 (fr) * | 1992-02-10 | 1996-06-05 | Minnesota Mining And Manufacturing Company | Elastomeres reticules par rayonnement |
JP2675729B2 (ja) * | 1992-12-16 | 1997-11-12 | 株式会社日本触媒 | 吸水性樹脂の製造方法 |
US5342338A (en) * | 1993-06-11 | 1994-08-30 | The Procter & Gamble Company | Disposable absorbent article for low-viscosity fecal material |
US5397316A (en) * | 1993-06-25 | 1995-03-14 | The Procter & Gamble Company | Slitted absorbent members for aqueous body fluids formed of expandable absorbent materials |
JPH07142627A (ja) * | 1993-11-18 | 1995-06-02 | Fujitsu Ltd | 半導体装置及びその製造方法 |
SG72621A1 (en) * | 1993-11-19 | 2000-05-23 | Procter & Gamble | Absorbent article with multi-directional extensible side panels |
US5554145A (en) * | 1994-02-28 | 1996-09-10 | The Procter & Gamble Company | Absorbent article with multiple zone structural elastic-like film web extensible waist feature |
CN1150218C (zh) * | 1994-04-11 | 2004-05-19 | 赫希斯特人造丝公司 | 超吸收性聚合物及其制品 |
US5569234A (en) * | 1995-04-03 | 1996-10-29 | The Procter & Gamble Company | Disposable pull-on pant |
US6194531B1 (en) | 1996-06-05 | 2001-02-27 | Nippon Shokubai Co., Ltd. | Method for production of cross-linked polymer |
DE69731597T2 (de) | 1996-11-20 | 2005-12-01 | Sanyo Chemical Industries, Ltd. | Wasserabsorbierendes Mittel und Verfahren zu seiner Herstellung |
US6228930B1 (en) * | 1997-06-18 | 2001-05-08 | Nippon Shokubai Co., Ltd. | Water-absorbent resin granule-containing composition and production process for water-absorbent resin granule |
TW473485B (en) | 1997-12-10 | 2002-01-21 | Nippon Catalytic Chem Ind | The production process of a water-absorbent resin |
US6007833A (en) * | 1998-03-19 | 1999-12-28 | Surmodics, Inc. | Crosslinkable macromers bearing initiator groups |
KR100476170B1 (ko) | 1998-04-28 | 2005-03-10 | 니폰 쇼쿠바이 컴파니 리미티드 | 흡수성수지 함수겔상물의 제조방법 |
EP1169379B1 (fr) * | 1999-03-12 | 2004-09-22 | Basf Aktiengesellschaft | Composition polymerique superabsorbente de couleur stable |
US6803107B2 (en) * | 1999-09-07 | 2004-10-12 | Basf Aktiengesellschaft | Surface-treated superabsorbent polymer particles |
US6417425B1 (en) * | 2000-02-01 | 2002-07-09 | Basf Corporation | Absorbent article and process for preparing an absorbent article |
US6906159B2 (en) | 2000-08-03 | 2005-06-14 | Nippon Shokubai Co., Ltd. | Water-absorbent resin, hydropolymer, process for producing them, and uses of them |
WO2002094328A2 (fr) * | 2001-05-23 | 2002-11-28 | Basf Aktiengesellschaft | Article absorbant |
DE60233494D1 (de) * | 2001-06-08 | 2009-10-08 | Basf Se | Wasserlösliche strahlungsaktivierbare polymerharze |
WO2003043670A1 (fr) | 2001-11-21 | 2003-05-30 | Basf Aktiengesellschaft | Hydrogels superabsorbants a revetement polyamine reticule |
JP2003156961A (ja) | 2001-11-22 | 2003-05-30 | Fuji Xerox Co Ltd | 定着用回転体、加圧用回転体、転写用回転体、帯電用回転体、転写同時定着用回転体 |
AU2002349359A1 (en) * | 2001-12-20 | 2003-07-09 | Basf Aktiengesellschaft | Absorbent article |
EP1516009A1 (fr) * | 2002-06-11 | 2005-03-23 | Basf Aktiengesellschaft | Esters (meth)acryliques de trimethylolpropane polyalcoxyle |
PL374441A1 (en) * | 2002-06-11 | 2005-10-17 | Basf Aktiengesellschaft | (meth)acrylic esters of polyalkoxylated trimethylolpropane |
US20030233082A1 (en) * | 2002-06-13 | 2003-12-18 | The Procter & Gamble Company | Highly flexible and low deformation fastening device |
US20040143030A1 (en) * | 2002-09-11 | 2004-07-22 | Fumiyoshi Ikkai | Method of producing synthetic polymer gel and said gel |
WO2004031253A1 (fr) * | 2002-10-02 | 2004-04-15 | Coloplast A/S | Hydrogel |
EP1913912B2 (fr) * | 2003-02-12 | 2020-03-18 | The Procter and Gamble Company | Partie centrale absorbante pour un article absorbant |
DE10358372A1 (de) * | 2003-04-03 | 2004-10-14 | Basf Ag | Gemische von Verbindungen mit mindestens zwei Doppelbindungen und deren Verwendung |
MXPA05010333A (es) * | 2003-04-03 | 2005-11-17 | Basf Ag | Mezclas de (met) acrilatos de trimetilolpropano polialcoxilado. |
US7405321B2 (en) * | 2003-06-06 | 2008-07-29 | Basf Aktiengesellschaft | (Meth)acrylic ester of alkenylene glycols and the use thereof |
DE10334271B4 (de) * | 2003-07-25 | 2006-02-23 | Stockhausen Gmbh | Verfahren zur Agglomeration von Superabsorberfeinteilchen, daraus erhältliche Superabsorberpartikel, deren Verwendung sowie diese beinhaltende Verbunde |
EP1506788A1 (fr) * | 2003-08-06 | 2005-02-16 | The Procter & Gamble Company | Polymères superabsorbants contenant des agents de réticulation de surface activables par rayonnement et leur procédé de fabrication |
EP1504772A1 (fr) * | 2003-08-06 | 2005-02-09 | The Procter & Gamble Company | Polymères superabsorbants contenant des agents de réticulation de surface activables par rayonnement et leur procédé de fabrication |
EP1510229B1 (fr) * | 2003-08-27 | 2010-07-14 | Nippon Shokubai Co., Ltd. | Procédé de production de particules de résine absorbant l'eau traitées en surface |
EP1516884B2 (fr) | 2003-09-19 | 2023-02-22 | Nippon Shokubai Co., Ltd. | Résine absorbant l'eau avec des couches traitées et procédé de préparation |
CN100429273C (zh) | 2003-11-07 | 2008-10-29 | 株式会社日本触媒 | 粒状吸水树脂组合物及其生产方法 |
JP4866733B2 (ja) | 2004-03-31 | 2012-02-01 | 株式会社日本触媒 | 水性液吸収剤の製造方法 |
US7794441B2 (en) * | 2004-04-14 | 2010-09-14 | The Procter & Gamble Company | Dual cuff for a unitary disposable absorbent article being spaced away from backsheet |
EP1624002B1 (fr) | 2004-08-07 | 2019-04-03 | The Procter & Gamble Company | Particules de polymères du type superabsorbant avec les fonctionalisants, et un procédé pour leur préparation. |
EP1757646A1 (fr) | 2005-08-23 | 2007-02-28 | The Procter and Gamble Company | Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet |
CA2620653A1 (fr) * | 2005-08-23 | 2007-03-01 | The Procter & Gamble Company | Articles absorbants comprenant des particules polymeriques superabsorbantes reticulees de surface produites selon un procede dans lequel est utilise un rayonnement ultraviolet extreme |
WO2007024926A1 (fr) * | 2005-08-23 | 2007-03-01 | The Procter & Gamble Company | Articles absorbants comprenant des particules polymeriques superabsorbantes reticulees de surface produites selon un procede dans lequel est utilise un rayonnement ultraviolet extreme |
-
2004
- 2004-07-20 EP EP04017071A patent/EP1629854B1/fr not_active Expired - Lifetime
- 2004-07-20 AT AT04017071T patent/ATE484298T1/de not_active IP Right Cessation
- 2004-07-20 DE DE602004029569T patent/DE602004029569D1/de not_active Expired - Lifetime
-
2005
- 2005-07-15 JP JP2007522607A patent/JP2008506528A/ja not_active Withdrawn
- 2005-07-15 CN CNA2005800214777A patent/CN101076358A/zh active Pending
- 2005-07-15 CA CA002573442A patent/CA2573442A1/fr not_active Abandoned
- 2005-07-15 KR KR1020077001267A patent/KR20070039050A/ko not_active Application Discontinuation
- 2005-07-15 WO PCT/US2005/025343 patent/WO2006020161A2/fr active Application Filing
- 2005-07-15 BR BRPI0513537-0A patent/BRPI0513537A/pt not_active Application Discontinuation
- 2005-07-15 AU AU2005274865A patent/AU2005274865A1/en not_active Abandoned
- 2005-07-18 US US11/183,356 patent/US7588777B2/en not_active Expired - Fee Related
- 2005-07-19 AR ARP050102982A patent/AR054672A1/es not_active Application Discontinuation
-
2006
- 2006-12-28 IN IN7971DE2006 patent/IN2006DE07971A/en unknown
-
2007
- 2007-01-04 ZA ZA200700147A patent/ZA200700147B/en unknown
-
2009
- 2009-08-07 US US12/537,585 patent/US7871640B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US7871640B2 (en) | 2011-01-18 |
ATE484298T1 (de) | 2010-10-15 |
JP2008506528A (ja) | 2008-03-06 |
CA2573442A1 (fr) | 2006-02-23 |
WO2006020161A2 (fr) | 2006-02-23 |
IN2006DE07971A (fr) | 2007-04-27 |
WO2006020161A3 (fr) | 2006-06-01 |
US20060020053A1 (en) | 2006-01-26 |
EP1629854A1 (fr) | 2006-03-01 |
US20090299315A1 (en) | 2009-12-03 |
CN101076358A (zh) | 2007-11-21 |
AR054672A1 (es) | 2007-07-11 |
BRPI0513537A (pt) | 2008-05-06 |
DE602004029569D1 (de) | 2010-11-25 |
AU2005274865A1 (en) | 2006-02-23 |
EP1629854B1 (fr) | 2010-10-13 |
KR20070039050A (ko) | 2007-04-11 |
US7588777B2 (en) | 2009-09-15 |
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