MLchartDataset catalogue

Patent · US6503979B1 · B1 · US

Method for cross-linking hydrogels with bis- and poly-2-oxazolidinones

(11) Publication number
US6503979B1
(21) Application number
US-62285300-A
(22) Filing date
1998-02-24
(30) Priority date
1998-02-26
(43) Publication date
2003-01-07
(45) Date of grant
2003-01-07
(52) CPC
  • C08J Working-up; general processes of compounding; after-treatment not covered by subclasses C08B, C08C, C08F, C08G or C08H: 3/245, 2300/14
  • 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: 15/60
  • C08F Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds: 120/06, 8/30
  • C08G Macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds: 73/06
  • Y10S Technical subjects covered by former uspc cross-reference art collections [xracs] and digests: 524/916
(73) Assignee
BASF AG
(54) Title
Method for cross-linking hydrogels with bis- and poly-2-oxazolidinones
(57) Abstract

The invention contains a process for the surface postcrosslinking of water-absorbing polymers in which the polymers are treated with a surface postcrosslinking solution and during or after the treatment are postcrosslinked by means of an increase in temperature and are dried, wherein the crossiinker comprises a bis-2-oxazolidinone or a poly-2-oxazolidinone comprising structural units of the formula in which R 1 is branched or unbranched C 1 -C 18 -alkylene, branched or unbranched C 2 -C 18 -alkenylene, C 5 -C 18 -cycloalkylene, phenylene, naphthylene, anthracenylene, hydrocarbon-substituted phenylene, naphthylene or anthracenylene or another substituted or unsubstituted C 6 -C 18 -arylene radical, R 2 is branched or unbranched C 1 -C 18 -alkylene and n is an integer from 1 to 50 or a mixture of bis-2-oxazolidinones and poly-2-oxazolidinones dissolved in an inert solvent.

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Claims (15)

  1. A process for the surface post-crosslinking of a water-absorbing polymer in which the polymer is treated with a surface postcrosslinking solution comprising a crosslinker and during or after the treatment are postcrosslinked by means of an increase in temperature and are dried, wherein the crosslinker comprises a bis-2-oxazolidinone or a poly-2-oxazolidinone comprising structural units of the formula in which R 1 is branched or unbranched C 1 -C 18 -alkylene, branched or unbranched C 2 -C 18 -alkylene, phenylene, naphthylene, anthracenylene, hydrocarbon-substituted phenylene, naphtlylene or anthracenylene or another substituted or unsubstituted C 6 -C 16 -arylene radical, R 2 is branched or unbranched C 1 -C 16 -alkylene and n is an integer from 1 to 50 or a mixture of bis-2-oxazolidinones and polyoxazolidinones dissolved in an inert solvent, wherein the bis-2-oxazolidinone or poly-2-oxazolidinone crosslinker is endgroup-capped by a radical, wherein said radical is selected from the group consisting of hydrogen, branched C 1 -C 18 -alkyl, unbranched C 1 -C 18 -alkyl, branched C 2 -C 18 -alkenyl, unbranched C 2 -C 18 -alkenyl, substituted C 6 -C 18 aryl, or unsubstituted C 6 -C 18 aryl.
  2. The process as claimed in claim 1, wherein the water-absorbing polymer is a polymeric acrylic acid or a polyacrylate.
  3. The process as claimed in claim 1, further comprising a catalyst for crosslinking, wherein the catalyst used for crosslinking is selected from the group consisting of an inorganic acid, an inorganic anhydride, a polymeric inorganic acid, an inorganic acid salt, an organic acid, an organic acid anhydride, and an organic acid salt.
  4. The process as claimed in claim 3, wherein the catalyst is boric acid, sulfuric acid, phosphoric acid, or a polymer, anhydride or salt thereof, or hydriodic acid or salt thereof.
  5. The process as claimed in claim 1, wherein the inert solvent is water, a mixture of water with an organic solvent of unlimited miscibility with water, or a mixture of water with a simple or polyfunctional alcohol.
  6. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 10-90% by weight.
  7. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol is methanol, ethanol, isopropanol, ethylene glycol, 1,2-propanediol or 1,3-propanediol.
  8. The process as claimed in claim 1, wherein the surface postcrosslinking solution is employed in a proportion of 1-20% by weight, based on the mass of the polymer.
  9. A liquid-absorbing polymer prepared by the process as claimed in claim 1.
  10. The process as claimed in claim 1, wherein the water-absorbing polymer is a polymeric acrylic acid or a polyacrylate obtained by means of free-radical addition polymerization using a polyfunctional ethylenically unsaturated free-radical crosslinker which may in addition carry one or more free hydroxyl groups.
  11. The process as claim in claim 1, wherein the surface postcrosslinking solution is employed in a proportion of 2.5-15% by weight, based on the mass of the polymer.
  12. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 30-70% by weight.
  13. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 40-60% by weight.
  14. A hygiene article, packaging material or nonwoven comprising a water-absorbing hydrogel, wherein said water-absorbing hydrogel comprises a polymer produced by the process as claimed in claim 1.
  15. The process as claimed in claim 3, wherein the catalyst is tartaric acid, acetic acid, toluenesulfonic acid, or an anhydride or salt thereof.

Citations (12)

  • EP0083022A2
  • EP0349935A2
  • EP0372981A2
  • EP0530438A1
  • EP0543303A1
  • US2001025093A1
  • US2002061978A1
  • US5019606A
  • US5331059A
  • US5385983A
  • US5840822A
  • US6140388A
Record as JSON
{
  "publication_number": "US6503979B1",
  "country": "US",
  "kind": "B1",
  "title": "Method for cross-linking hydrogels with bis- and poly-2-oxazolidinones",
  "abstract": "The invention contains a process for the surface postcrosslinking of water-absorbing polymers in which the polymers are treated with a surface postcrosslinking solution and during or after the treatment are postcrosslinked by means of an increase in temperature and are dried, wherein the crossiinker comprises a bis-2-oxazolidinone or a poly-2-oxazolidinone comprising structural units of the formula in which R 1 is branched or unbranched C 1 -C 18 -alkylene, branched or unbranched C 2 -C 18 -alkenylene, C 5 -C 18 -cycloalkylene, phenylene, naphthylene, anthracenylene, hydrocarbon-substituted phenylene, naphthylene or anthracenylene or another substituted or unsubstituted C 6 -C 18 -arylene radical, R 2 is branched or unbranched C 1 -C 18 -alkylene and n is an integer from 1 to 50 or a mixture of bis-2-oxazolidinones and poly-2-oxazolidinones dissolved in an inert solvent.",
  "claims": [
    "1. A process for the surface post-crosslinking of a water-absorbing polymer in which the polymer is treated with a surface postcrosslinking solution comprising a crosslinker and during or after the treatment are postcrosslinked by means of an increase in temperature and are dried, wherein the crosslinker comprises a bis-2-oxazolidinone or a poly-2-oxazolidinone comprising structural units of the formula in which R 1 is branched or unbranched C 1 -C 18 -alkylene, branched or unbranched C 2 -C 18 -alkylene, phenylene, naphthylene, anthracenylene, hydrocarbon-substituted phenylene, naphtlylene or anthracenylene or another substituted or unsubstituted C 6 -C 16 -arylene radical, R 2 is branched or unbranched C 1 -C 16 -alkylene and n is an integer from 1 to 50 or a mixture of bis-2-oxazolidinones and polyoxazolidinones dissolved in an inert solvent, wherein the bis-2-oxazolidinone or poly-2-oxazolidinone crosslinker is endgroup-capped by a radical, wherein said radical is selected from the group consisting of hydrogen, branched C 1 -C 18 -alkyl, unbranched C 1 -C 18 -alkyl, branched C 2 -C 18 -alkenyl, unbranched C 2 -C 18 -alkenyl, substituted C 6 -C 18 aryl, or unsubstituted C 6 -C 18 aryl.",
    "2. The process as claimed in claim 1, wherein the water-absorbing polymer is a polymeric acrylic acid or a polyacrylate.",
    "3. The process as claimed in claim 1, further comprising a catalyst for crosslinking, wherein the catalyst used for crosslinking is selected from the group consisting of an inorganic acid, an inorganic anhydride, a polymeric inorganic acid, an inorganic acid salt, an organic acid, an organic acid anhydride, and an organic acid salt.",
    "4. The process as claimed in claim 3, wherein the catalyst is boric acid, sulfuric acid, phosphoric acid, or a polymer, anhydride or salt thereof, or hydriodic acid or salt thereof.",
    "5. The process as claimed in claim 1, wherein the inert solvent is water, a mixture of water with an organic solvent of unlimited miscibility with water, or a mixture of water with a simple or polyfunctional alcohol.",
    "6. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 10-90% by weight.",
    "7. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol is methanol, ethanol, isopropanol, ethylene glycol, 1,2-propanediol or 1,3-propanediol.",
    "8. The process as claimed in claim 1, wherein the surface postcrosslinking solution is employed in a proportion of 1-20% by weight, based on the mass of the polymer.",
    "9. A liquid-absorbing polymer prepared by the process as claimed in claim 1.",
    "10. The process as claimed in claim 1, wherein the water-absorbing polymer is a polymeric acrylic acid or a polyacrylate obtained by means of free-radical addition polymerization using a polyfunctional ethylenically unsaturated free-radical crosslinker which may in addition carry one or more free hydroxyl groups.",
    "11. The process as claim in claim 1, wherein the surface postcrosslinking solution is employed in a proportion of 2.5-15% by weight, based on the mass of the polymer.",
    "12. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 30-70% by weight.",
    "13. The process as claimed in claim 5, wherein the simple or polyfunctional alcohol in said mixture of water with said simple or polyfunctional alcohol is 40-60% by weight.",
    "14. A hygiene article, packaging material or nonwoven comprising a water-absorbing hydrogel, wherein said water-absorbing hydrogel comprises a polymer produced by the process as claimed in claim 1.",
    "15. The process as claimed in claim 3, wherein the catalyst is tartaric acid, acetic acid, toluenesulfonic acid, or an anhydride or salt thereof."
  ],
  "cpc": [
    "C08J 3/245",
    "A61L 15/60",
    "C08F 120/06",
    "C08F 8/30",
    "C08G 73/06",
    "C08J 2300/14",
    "Y10S 524/916"
  ],
  "assignees": [
    "BASF AG"
  ],
  "filing_date": "1998-02-24",
  "publication_date": "2003-01-07",
  "grant_date": "2003-01-07",
  "priority_date": "1998-02-26",
  "application_number": "US-62285300-A",
  "family_id": "7858919",
  "citations": [
    "EP0083022A2",
    "EP0349935A2",
    "EP0372981A2",
    "EP0530438A1",
    "EP0543303A1",
    "US2001025093A1",
    "US2002061978A1",
    "US5019606A",
    "US5331059A",
    "US5385983A",
    "US5840822A",
    "US6140388A"
  ]
}

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