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WO1996015180A1 - Materiau absorbant - Google Patents

Materiau absorbant Download PDF

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Publication number
WO1996015180A1
WO1996015180A1 PCT/US1995/014678 US9514678W WO9615180A1 WO 1996015180 A1 WO1996015180 A1 WO 1996015180A1 US 9514678 W US9514678 W US 9514678W WO 9615180 A1 WO9615180 A1 WO 9615180A1
Authority
WO
WIPO (PCT)
Prior art keywords
superabsorbent
functional groups
anionic
groups
superabsorbent material
Prior art date
Application number
PCT/US1995/014678
Other languages
English (en)
Inventor
Gianfranco Palumbo
Original Assignee
The Procter & Gamble Company
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to MX9703445A priority Critical patent/MX201287B/es
Priority to EP95940682A priority patent/EP0791031A4/fr
Priority to JP8516231A priority patent/JPH10509611A/ja
Priority to CA002204888A priority patent/CA2204888C/fr
Priority to KR1019970703134A priority patent/KR100372137B1/ko
Priority to US08/836,123 priority patent/US5804605A/en
Priority to BR9509651A priority patent/BR9509651A/pt
Priority to AU42350/96A priority patent/AU4235096A/en
Priority to CZ971406A priority patent/CZ140697A3/cs
Publication of WO1996015180A1 publication Critical patent/WO1996015180A1/fr

Links

Classifications

    • 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
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/02—Direct processing of dispersions, e.g. latex, to articles
    • 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
    • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
    • C08J3/075—Macromolecular gels

Definitions

  • the present invention relates to an absorbent material, more particularly a material of the type commonly referred to as a "superabsorbent".
  • superabsorbents are typically slightly cross-linked hydrophillic polymers.
  • the polymers may differ in their chemical nature but they share the property of being capable of absorbing and retaining even under moderate pressure amounts of aqueous fluids equivalent to many times their own weight.
  • superabsorbents can typically absorb up to 100 times their own weight or even more of distilled water.
  • Superabsorbents have been suggested for use in many different industrial applications where advantage can be taken of their water absorbing and/or retaining properties and examples include agriculture, the building industry, the production of alkaline batteries and filters.
  • the primary field of application for superabsorbents is in the production of hygienic and/or sanitary products such as disposable sanitary napkins and disposable diapers either for children or for incontinent adults.
  • superabsorbents are used, generally in combination with cellulose fibres, to absorb body fluids such as menses or urine.
  • body fluids such as menses or urine.
  • the absorbent capacity of superabsorbents for body fluids is dramatically lower than for deionised water. It is generally believed that this effect results from the electrolyte content of body fluids and the effect is often referred to as "salt poisoning".
  • the water absorption and water retention characteristics of superabsorbents are due to the presence in the polymer structure of ionisable functional groups. These groups are usually carboxyl groups, a high proportion of which are in the salt form when the polymer is dry but which undergo dissociation and solvation upon contact with water. In the dissociated state, the polymer chain will have a series of functional groups attached to it which groups have the same electric charge and thus repel one another. This leads to expansion of the polymer structure which, in turn, permits further absorption of water molecules although this expansion is subject to the constraints provided by the cross-links in the polymer structure which must be sufficient to prevent dissolution of the polymer. It is assumed that the presence of a significant concentration of electrolytes in the water interferes with dissociation of the functional groups and leads to the "salt poisoning" effect.
  • Japanese Patent Application- OPI No. 57-45,057 discloses an absorbent which comprises a mixture of a superabsorbent such as a cross-linked polyacrylate with an ion exchange resin in powder or granular form.
  • EP-A-0210756 relates to an absorbent structure comprising a superabsorbent and an anion exchanger, optionally together with a cation exchanger, wherein both ion exchangers are in fibrous form.
  • Combining a superabsorbent with an ion exchanger attempts to alleviate the salt poisoning effect by using the ion exchanger, generally as a combination of both an anion exchanger and a cation exchanger, to reduce the salt content of the liquid.
  • the ion exchanger has no direct effect on the performance of the superabsorbent and it may not be possible to reduce the salt content sufficiently to have the desired effect on the overall absorption capacity of the combination.
  • the ion exchanger has no absorbing effect itself and thus acts as a diluent to the superabsorbent.
  • An object of the present invention is to provide a superabsorbent with improved performance in the presence of electrolyte, for example in the case of menses or urine.
  • the present invention provides a superabsorbent material which comprises a combination of
  • the anionic superabsorbent preferably has from 50 to
  • the cationic superabsorbent preferably has from 50 to 100% and more preferably has substantially 100% in basic form.
  • anionic superabsorbents have to have functional groups in salt form before they act as superabsorbents.
  • Commercially available superabsorbents are usually available in salt form. It has now surprisingly been found according to the present invention that a combination of an anionic superabsorbent in free acid form with an anion exchanger in basic form is particularly effective as a superabsorbent in the case of electrolyte containing solutions, for example menses and urine.
  • anionic superabsorbent does not behave as an ion exchanger in the sense that contacting the material in acid form with an electrolyte containing solution does not result in conversion to the salt form.
  • the functional groups in anionic superabsorbents are typically carboxyl groups which act as a weak acid which does not dissociate when placed, for example, in a sodium chloride solution.
  • presence of the anion exchanger has the effect of attaching chloride ions from sodium chloride solution, thereby displacing the equilibrium in favour of conversion of the anionic superabsorbent into the salt form.
  • the anionic superabsorbent can be any material having superabsorbent properties in which the functional groups are anionic, namely sulphonic groups, sulphate groups, phosphate groups or carboxyl groups.
  • the functional groups are carboxyl groups.
  • the functional groups are attached to a slightly cross-linked acrylic base polymer.
  • the base polymer may be a polyacrylamide, polyvinyl alcohol, ethylene maleic anhydride copolymer, polyvinylether, polyvinyl sulphonic acid, polyacrylic acid, polyvinylpyrrolidone and polyvinylmorpholine. Copolymers of these monomers can also be used.
  • Starch and cellulose based polymers can also be used including hydroxypropyl cellulose, carboxymethyl cellulose and acrylic grafted starches.
  • Particular base polymers include cross-linked polyacrylates, hydrolysed acrylonitrile grafted starch, starch polyacrylates, and isobutylene maleic anhydride copolymers, Particularly preferred base polymers are starch polyacrylates and cross-linked polyacrylates.
  • the functional groups will generally be carboxyl groups.
  • DS of the derivative with the functional group is defined as the number of functional groups (generally carboxyl groups) per anhydroglucose units of cellulose.
  • the DS is generally from 0.1 to 1.5.
  • the DS for synthetic polymers may be defined as the number of functional groups per monomer or comonomer unit.
  • the DS is generally 1, for example 1 carboxyl group per monomer unit of polyacrylate.
  • anionic superabsorbents are available commercially, for example Favor 922 (Stockhausen) , Sanwet IM 1500 (Sanyo) , AQU D3236 (Aqualon Company (Hercules)) or DOW 2090. (DOW).
  • a particularly preferred anionic superabsorbent is FAVOR 922 (Stockhausen) .
  • Commercially available anionic superabsorbents are generally sold in salt form and need to be converted to the free acid form for use according to the invention, for example by the following method:
  • the sodium ion content may be determined by a potentometric method using a selective sodium sensitive electrode) .
  • Ion exchange is the reversible interchange of ions between a solid and liquid in which there is no permanent change in the structure of the solid, which is the ion- exchange material.
  • Ion exchange occurs in a variety of substances - e.g. silicates, phosphates, fluorides, humus, cellulose, wool, proteins, alumina, resins, lignin, cells, glass, barium sulphate, and silver chloride.
  • Ion exchange materials that depend on properties other than the interchange of ions between liquid and solid phases. Ion exchange has been used on an industrial basis since 1910 with the introduction of water softening using natural and, later, synthetic zeolites.
  • Inorganic ion exchange materials include both the naturally occurring materials such as the mineral zeolites (e.g. cliptonite) the green sands and clay (e.g. the montmorillonite group) , and synthetic products such as the gel zeolites, the hydrous oxides of polyvalent metals and the insoluble salts of polybaric acids with polyvalent metals.
  • the naturally occurring materials such as the mineral zeolites (e.g. cliptonite) the green sands and clay (e.g. the montmorillonite group)
  • synthetic products such as the gel zeolites, the hydrous oxides of polyvalent metals and the insoluble salts of polybaric acids with polyvalent metals.
  • Synthetic organic products include cation and anion ion exchange resins both of strong and weak type.
  • the ability of the weak base resins to sorb acids depends on their own basicity and the pH of the acid involved.
  • a variety of base strengths are obtained depending on the nature of the amine functionality.
  • Primary, secondary and tertiary amine functionality, or mixtures of them, can be put into various structures ranging from epichlorohydrin amine condensates and acrylic polymers, to styrene-devinyl benzene (DVB) copolymers.
  • Strong base, anion exchange resins especially those based on styrene-DVB copolymer are classed as type I and II.
  • Type I is a quaternarized amine product made by the reaction of trimethylamine with the copolymer after chloromethylation with chloromethyl methyl ether (CMME) .
  • CMME chloromethyl methyl ether
  • the type I functional group is the most strongly basic functional group available and has the greatest affinity for the weak acids that commonly are removing during a water demineralization process (e.g. silic acid and carbonic acid) .
  • Type II functionality is obtained by the reaction 'of the styrene-DVB copolymer with dimethylethanolamine. This quaternary amine has lower basicity than that of the type I resin, yet it is enough to remove the weak acid anions for most applications.
  • Quaternary amine functionality has been introduced into pyridinic and acrylate polymers with limited commercial application.
  • the anion exchanger is preferably an anion exchange resin containing functional groups in basic form.
  • Suitable functional groups include amine groups, i.e. primary, secondary and tertiary amine groups and quaternary ammonium groups.
  • Anion exchange resins which are commercially available and may be used in the present invention are:
  • Amberlite IRA 400 - This is a strong anion exchanger having quaternary ammonium functionality which is available in the chloride form. For use in the present invention it is necessary to convert it to OH " form, for example by NaOH treatment in a chromatographic column and washing with distilled water. The total exchange capacity is 3.8 meq/g of dry resin.
  • Amberlite IRA 68 This a weak basic anion exchanger having tertiary amine functionality which is available in the free base form.
  • the total exchange capacity is 5.6 meq (milliequivalents/g of dry resin) .
  • Amberlite ion exchangers are a trade mark of Rohn.
  • ION exchanger type III from Merck - This is a strong anion exchanger resin, the exchange capacity is about 5 meq/g.
  • ION exchanger type II form Merck - This is a weak anion exchange resin, the exchange capacity is about 5 meq/g.
  • Preferred anion exchange resins include Duolite A-102- OH, (Dia-prosim, France) which is a strong anionic exchange resin having quaternary ammonium functionality. The ion exchange capacity is 1.3 meq/ml. Other suitable anion exchange resins can be found in the product ranges of manufacturers such as Rohn and Merck.
  • the weight ratio of anionic superabsorbent to anionic exchanger is in the range 1:20 to 1:1 depending on molecular weight and ion exchange capacity, preferably the weight ratio is 1:2 to 1:4
  • the absorbent material according to the invention is particularly suitable for use in applications where it is desired to absorb electrolyte containing aqueous liquids.
  • liquids include in particular menses and urine and the absorbent material can be used as the filling in catamenials and diapers generally in admixture with a fibrous absorbent such as cellulose fluff.
  • the absorbent according to the invention can be present as granules or fibres.
  • the absorbent materials according to the invention show particularly good absorption of electrolyte containing aqueous liquids as is demonstrated below in the following examples by tests carried out using saline solution (1% NaCl) and synthetic urine.
  • the test was performed to show that, when in contact with an aqueous saline solution, an anion exchange resin in basic form together with an anionic superabsorbent in acid form act as an anion and cationic exchange mixture and thus deionization of the saline solution occurs.
  • the anionic superabsorbent is then converted to the salt form and thus has improved absorbency due to the low salt content of the solution.
  • 1% NaCl solution 150ml was placed in contact with the anion exchange resin A102 OH (3.9g), in a 250ml beaker for 2 hours under continuous stirring. This step allows the chloride ions from the solution to be replaced by the hydroxide ions from the resin.
  • the solution was then drawn up by a Pasteur pipette and transferred into another 2501 beaker containing 0.25g of Favor H being stirred. The addition of solution was stopped when the gel did not swell any further. Thereafter the gel was placed into a nonwover. tissue tea bag type envelope, which had one edge which was not sealed, and the absorbency after centrifugation at 60 x g for 10 minutes was measured as follows:
  • 1% NaCl represents a stringent test of the superabsorbent. Studies in the literature show that the salt content of urine varies depending on a number of factors but 1% by weight represents the maximum likely to the encountered in practice.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Manufacturing & Machinery (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

L'invention porte sur un matériau superabsorbant fait d'une combinaison (1) d'un superabsorbant anionique dans lequel 20 à 100 % des groupes fonctionnels se présentent sous forme d'acides libres, et (2) d'un échangeur d'anions dans lequel 20 à 100 % des groupes fonctionnels se présentent sous forme de bases. Ladite combinaison s'avère particulièrement efficace comme superabsorbant dans le cas de solutions contenant un électrolyte telles que le flux menstruel et l'urine.
PCT/US1995/014678 1994-11-10 1995-11-13 Materiau absorbant WO1996015180A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
MX9703445A MX201287B (es) 1994-11-10 1995-11-13 Material absorbente.
EP95940682A EP0791031A4 (fr) 1994-11-10 1995-11-13 Materiau absorbant
JP8516231A JPH10509611A (ja) 1994-11-10 1995-11-13 吸収性材料
CA002204888A CA2204888C (fr) 1994-11-10 1995-11-13 Materiau absorbant
KR1019970703134A KR100372137B1 (ko) 1994-11-10 1995-11-13 흡수물질
US08/836,123 US5804605A (en) 1994-11-10 1995-11-13 Absorbent material
BR9509651A BR9509651A (pt) 1994-11-10 1995-11-13 Material superabsorvente e utilização do mesmo
AU42350/96A AU4235096A (en) 1994-11-10 1995-11-13 Absorbent material
CZ971406A CZ140697A3 (en) 1994-11-10 1995-11-13 Superabsorptive material

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT94TO000889A IT1267494B1 (it) 1994-11-10 1994-11-10 Materiale assorbente, ad esempio di tipo superassorbente, e relativo uso.
ITTO94A000889 1994-11-10

Publications (1)

Publication Number Publication Date
WO1996015180A1 true WO1996015180A1 (fr) 1996-05-23

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ID=11412879

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1995/014678 WO1996015180A1 (fr) 1994-11-10 1995-11-13 Materiau absorbant

Country Status (12)

Country Link
EP (1) EP0791031A4 (fr)
JP (1) JPH10509611A (fr)
KR (1) KR100372137B1 (fr)
CN (1) CN1068888C (fr)
AU (1) AU4235096A (fr)
BR (1) BR9509651A (fr)
CA (1) CA2204888C (fr)
CZ (1) CZ140697A3 (fr)
HU (1) HUT77798A (fr)
IT (1) IT1267494B1 (fr)
MX (1) MX201287B (fr)
WO (1) WO1996015180A1 (fr)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998024832A1 (fr) * 1996-12-02 1998-06-11 Kimberly-Clark Worldwide, Inc. Composition absorbante
WO1999025745A1 (fr) * 1997-11-19 1999-05-27 Amcol International Corporation Gels superabsorbants a base de poly(vinylamine) et procede de fabrication
WO1999025748A1 (fr) * 1997-11-19 1999-05-27 Amcol International Corporation Gels extremement absorbants a base de poly(vinylguanidine)
WO1999025393A3 (fr) * 1997-11-19 1999-09-02 Amcol International Corp Particules multicomposant a gel superabsorbant
US5962578A (en) * 1997-11-19 1999-10-05 Amcol International Corporation Poly(dialkylaminoalkyl (meth)acrylamide)-based superabsorbent gels
US5981689A (en) * 1997-11-19 1999-11-09 Amcol International Corporation Poly(vinylamine)-based superabsorbent gels and method of manufacturing the same
WO2000009612A1 (fr) * 1998-08-13 2000-02-24 Nippon Shokubai Co., Ltd. Composition polymere reticulee gonflant dans l'eau et son procede de production
US6072101A (en) * 1997-11-19 2000-06-06 Amcol International Corporation Multicomponent superabsorbent gel particles
US6121509A (en) * 1998-01-07 2000-09-19 The Procter & Gamble Company Absorbent polymer compositions having high sorption capacities under an applied pressure and improved integrity when wet
US6232520B1 (en) 1997-02-19 2001-05-15 The Procter & Gamble Company Absorbent polymer compositions having high sorption capacities under an applied pressure
US6342298B1 (en) 1997-11-19 2002-01-29 Basf Aktiengesellschaft Multicomponent superabsorbent fibers
US6534554B1 (en) 1999-10-27 2003-03-18 Basf Aktiengesellschaft Multicomponent ion exchange resins
WO2003037392A1 (fr) * 2001-10-26 2003-05-08 Basf Aktiengesellschaft Particules superabsorbantes a constituants multiples susceptibles de former un gel
US6623576B2 (en) 1998-10-28 2003-09-23 Basf Aktiengesellschaft Continuous manufacture of superabsorbent/ion exchange sheet material
US6639120B1 (en) 1997-12-12 2003-10-28 Kimberly-Clark Worldwide, Inc. Structure having balanced pH profile
US6881792B2 (en) 1999-12-27 2005-04-19 Nippon Shokubai Co., Ltd. Production processes for basic water-absorbent resin and water-absorbing agent, and use thereof
EP1624002A1 (fr) * 2004-08-07 2006-02-08 The Procter & Gamble Company Particules de polymères du type superabsorbant avec les fonctionalisants, et un procédé pour leur préparation
US7012105B2 (en) 1997-12-12 2006-03-14 Kimberly-Clark Worldwide, Inc. Structure having balanced pH profile
US7285615B2 (en) 2003-09-02 2007-10-23 Nippon Shokubai Co., Ltd. Particulate water-absorbent resin composition

Families Citing this family (1)

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CN102775765B (zh) * 2012-08-13 2014-03-12 宜兴丹森科技有限公司 一种具有离子交换功能的亲水性聚氨酯软质泡沫材料及其应用

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US5466731A (en) * 1992-05-22 1995-11-14 Courtaulds Fibres (Holdings) Limited Fibre and film of a water-absorbent water-insoluble material having a matrix of a copolymer

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PH26954A (en) * 1985-05-15 1992-12-03 Procter & Gamble Disposable absorbent articles
US4818598A (en) * 1985-06-28 1989-04-04 The Procter & Gamble Company Absorbent structures

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US5466731A (en) * 1992-05-22 1995-11-14 Courtaulds Fibres (Holdings) Limited Fibre and film of a water-absorbent water-insoluble material having a matrix of a copolymer
US5461085A (en) * 1993-12-17 1995-10-24 Mitsui Toatsu Chemicals, Incorporated Superabsorbent polymer and process for producing same

Non-Patent Citations (1)

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Cited By (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6951895B1 (en) 1996-12-02 2005-10-04 Kimberly-Clark Worldwide, Inc. Absorbent composition
WO1998024832A1 (fr) * 1996-12-02 1998-06-11 Kimberly-Clark Worldwide, Inc. Composition absorbante
US6232520B1 (en) 1997-02-19 2001-05-15 The Procter & Gamble Company Absorbent polymer compositions having high sorption capacities under an applied pressure
US6159591A (en) * 1997-11-19 2000-12-12 Amcol International Corporation Multicomponent superabsorbent gel particles
US6222091B1 (en) 1997-11-19 2001-04-24 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US5981689A (en) * 1997-11-19 1999-11-09 Amcol International Corporation Poly(vinylamine)-based superabsorbent gels and method of manufacturing the same
WO1999025394A3 (fr) * 1997-11-19 1999-11-25 Amcol International Corp Gels superabsorbants a base de poly(dialkylaminoalkyle (meth)acrylamide)
EP2011462A1 (fr) 1997-11-19 2009-01-07 Basf Se Particules de gel superabsorbant multicomposants
US6072101A (en) * 1997-11-19 2000-06-06 Amcol International Corporation Multicomponent superabsorbent gel particles
US6087448A (en) * 1997-11-19 2000-07-11 Amcol International Corporation Solid superabsorbent material containing a poly(vinylguanidine) and an acidic water-absorbing resin
WO1999025393A3 (fr) * 1997-11-19 1999-09-02 Amcol International Corp Particules multicomposant a gel superabsorbant
US6121409A (en) * 1997-11-19 2000-09-19 Amcol International Corporation Poly(vinylamine)-based superabsorbent gels and method of manufacturing the same
US6596921B2 (en) 1997-11-19 2003-07-22 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US6194631B1 (en) 1997-11-19 2001-02-27 Amcol International Corporation Poly (vinylamine)-based superabsorbent gels and method of manufacturing the same
US5962578A (en) * 1997-11-19 1999-10-05 Amcol International Corporation Poly(dialkylaminoalkyl (meth)acrylamide)-based superabsorbent gels
WO1999025748A1 (fr) * 1997-11-19 1999-05-27 Amcol International Corporation Gels extremement absorbants a base de poly(vinylguanidine)
US6235965B1 (en) 1997-11-19 2001-05-22 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
WO1999025745A1 (fr) * 1997-11-19 1999-05-27 Amcol International Corporation Gels superabsorbants a base de poly(vinylamine) et procede de fabrication
US6342298B1 (en) 1997-11-19 2002-01-29 Basf Aktiengesellschaft Multicomponent superabsorbent fibers
US6376072B2 (en) 1997-11-19 2002-04-23 Basf Aktiengesellschaft Multicomponent superabsorbent fibers
US6392116B1 (en) 1997-11-19 2002-05-21 Basf Aktiengesellschaft Diapers having improved acquisition rates
US6509512B1 (en) 1997-11-19 2003-01-21 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US6603056B2 (en) 1997-11-19 2003-08-05 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US6555502B1 (en) 1997-11-19 2003-04-29 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US6596922B2 (en) 1997-11-19 2003-07-22 Basf Aktiengesellschaft Multicomponent superabsorbent gel particles
US6590137B2 (en) 1997-11-19 2003-07-08 Bask Aktiengesellschaft Multicomponent superabsorbent gel particles
US6639120B1 (en) 1997-12-12 2003-10-28 Kimberly-Clark Worldwide, Inc. Structure having balanced pH profile
US7012105B2 (en) 1997-12-12 2006-03-14 Kimberly-Clark Worldwide, Inc. Structure having balanced pH profile
US7317135B2 (en) 1997-12-12 2008-01-08 Kimberly-Clark Worldwide, Inc. Structure having balanced pH profile
US6121509A (en) * 1998-01-07 2000-09-19 The Procter & Gamble Company Absorbent polymer compositions having high sorption capacities under an applied pressure and improved integrity when wet
US6333109B1 (en) 1998-08-13 2001-12-25 Nippon Shokubai Co., Ltd. Water-swellable crosslinked polymer composition and production
WO2000009612A1 (fr) * 1998-08-13 2000-02-24 Nippon Shokubai Co., Ltd. Composition polymere reticulee gonflant dans l'eau et son procede de production
US6623576B2 (en) 1998-10-28 2003-09-23 Basf Aktiengesellschaft Continuous manufacture of superabsorbent/ion exchange sheet material
US6534554B1 (en) 1999-10-27 2003-03-18 Basf Aktiengesellschaft Multicomponent ion exchange resins
US6881792B2 (en) 1999-12-27 2005-04-19 Nippon Shokubai Co., Ltd. Production processes for basic water-absorbent resin and water-absorbing agent, and use thereof
WO2003037392A1 (fr) * 2001-10-26 2003-05-08 Basf Aktiengesellschaft Particules superabsorbantes a constituants multiples susceptibles de former un gel
US7285615B2 (en) 2003-09-02 2007-10-23 Nippon Shokubai Co., Ltd. Particulate water-absorbent resin composition
WO2006017716A3 (fr) * 2004-08-07 2006-05-26 Procter & Gamble Particules polymères superabsorbantes comprenant des fonctionnalisants et procédé de fabrication de celles-ci
EP1624002A1 (fr) * 2004-08-07 2006-02-08 The Procter & Gamble Company Particules de polymères du type superabsorbant avec les fonctionalisants, et un procédé pour leur préparation
US7655830B2 (en) 2004-08-07 2010-02-02 The Procter & Gamble Co. Superabsorbent polymer particles comprising functionalizers and method of making them

Also Published As

Publication number Publication date
MX9703445A (es) 1998-07-31
JPH10509611A (ja) 1998-09-22
CA2204888C (fr) 2001-01-30
KR100372137B1 (ko) 2003-03-15
IT1267494B1 (it) 1997-02-05
CZ140697A3 (en) 1997-10-15
KR970707218A (ko) 1997-12-01
MX201287B (es) 2001-04-10
AU4235096A (en) 1996-06-06
CN1171802A (zh) 1998-01-28
BR9509651A (pt) 1997-09-16
CN1068888C (zh) 2001-07-25
CA2204888A1 (fr) 1996-05-23
ITTO940889A1 (it) 1996-05-10
ITTO940889A0 (it) 1994-11-10
EP0791031A4 (fr) 2000-07-12
EP0791031A1 (fr) 1997-08-27
HUT77798A (hu) 1998-08-28

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