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GB858127A - Polymer foam modification - Google Patents

Polymer foam modification

Info

Publication number
GB858127A
GB858127A GB18164/57A GB1816457A GB858127A GB 858127 A GB858127 A GB 858127A GB 18164/57 A GB18164/57 A GB 18164/57A GB 1816457 A GB1816457 A GB 1816457A GB 858127 A GB858127 A GB 858127A
Authority
GB
United Kingdom
Prior art keywords
cell
groups
treatment
foamed
hydrolysis
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.)
Expired
Application number
GB18164/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kimberly Clark Tissue Co
Original Assignee
Scott Paper Co
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 Scott Paper Co filed Critical Scott Paper Co
Publication of GB858127A publication Critical patent/GB858127A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36After-treatment
    • C08J9/38Destruction of cell membranes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cell Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

A foamed, open-cell, cellular polymeric polyurethane material in the form of an integrally formed 3-dimensionally reticulated structure comprises a network of strands defining the outlines of a plurality of polygons making up a plurality of polyhedrons, at least a plurality of the faces of the polyhedrons being open, and at least a portion of the linking groups in the polymer chain are selected from =C.CO.-, -O-CO.N=, =C-CO-N= and =N.CO.N= groups, the polymer being partially hydrolysed. Such material is produced by subjecting a foamed open cell polyurethane containing the specified groups to the action of a hydrolyzing agent under hydrolyzing conditions until the physical characteristics of the material are altered. Substantially all or only part of the cell faces may be removed, depending on the hydrolysis conditions. The products are believed to contain carboxyl and hydroxyl groups. The material subjected to hydrolysis may be one formed by reacting under foam-forming conditions (usually the presence of water and amine catalyst) a polyisocyanate and a polyester (which may be styrene- or oil-modified), polyether (which may contain amine residues or have been modified by reaction with an epoxide), polyesteramide or alcohol-modified urea-formaldehyde resin. Oil, wetting agent or silicone may be added. In the hydrolysis steam or hot water may be used alone or with a catalyst. Specified are enzymes such as lipase and pepsin; alkalis such as alkali metal or ammonium hydroxide, quaternary bases, amines and alkaline salts such as as trisodium phosphate; acids such as hydrochloric, sulphuric, phosphoric, toluene sulphonic and acetic acids. Figures are given which depict on an enlarged scale a typical cell before and after treatment. In a typical example a reaction product of toluene -2, 4- and -2, 6-diisocyanates and a polyester resin is converted to a foamed product by treatment with water, diethylethanolamine and polyoxyethylated vegetable oil dispersing agent. The foam is kneaded with sodium hydroxide solution at 50 DEG C. and washed and dried. A Table shows loss in weight, density, hydrophilicity and softness after various times of treatment. The products are useful as filtering devices, gas-liquid contacting devices, catalyst carriers, rug anchors, door mats, drain pads, scouring pads, sponges, insulating pads, tire liners, spacing devices, flexible partitions, draperies, upholstery padding, mattresses and pillows. Reference has been directed by the Comptroller to Specification 789,481.ALSO:A foamed, open-cell, cellular polymeric polyurethane material in the form of an integrally formed 3-dimensionally reticulated structure comprises a network of strands defining the outlines of a plurality of polygons making up a plurality of polyhedrons, at least a plurality of the faces of the polyhedrons being open, and at least a portion of the linking groups in the polymer chain are selected from =C,CO,-, -O-CO,N=, =C-CO-N= and =N,CO,N= groups, the polymer being partially hydrolysed. Such material is produced by subjecting a foamed open cell polyurethane containing the specified groups to the action of a hydrolyzing agent under hydrolysing conditions until the physical characteristics of the material are altered. Substantially all or only part of the cell faces may be removed, depending on the hydrolysis conditions. The products are believed to contain carboxyl and hydroxyl groups. The material subjected to hydrolysis may be one formed by reacting under foam-forming conditions (usually the presence of water and a minecatalyst) a polyisocyanate and a polyester (which may be styrene- or oil-modified), polyether (which may contain amine residues or have been modified by reaction with an epoxide), polyesteramide or alcohol-modified urea-formaldehyde resin. Oil, wetting agent or silicone may be added. In the hydrolysis steam or hot water may be used alone or with a catalyst. Specified are enzymes such as lipase and pepsin; alkalis such as alkali metal or ammonium hydroxide, quaternary bases, amines and alkaline salts such as trisodium phosphate; acids such as hydrochloric, sulphuric, phosphoric, toluene sulphonic and acetic acids. Drawings are given which depict on an enlarged scale a typical cell before and after treatment. In a typical example a reaction product of toluene -2,4- and -2,6- diisocyanates and a polyester resin is converted to a foamed product by treatment with water, diethylethanolamine and polyoxyethylated vegetable oil dispersing agent. The foam is kneaded with sodium hydroxide solution at 50 DEG C. and washed and dried. A Table shows loss in weight, density, hydrophilicity and softness after various times of treatment. The products are useful as filtering devices, gas-liquid contacting devices, catalyst carriers, rug anchors, door mats, drain pads, scouring pads, sponges, insulating pads, tire liners, spacing devices, flexible partitions, draperies, upholstery padding, mattresses and pillows. Reference has been directed by the Comptroller to Specification 789,481.
GB18164/57A 1956-06-15 1957-06-07 Polymer foam modification Expired GB858127A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US858127XA 1956-06-15 1956-06-15

Publications (1)

Publication Number Publication Date
GB858127A true GB858127A (en) 1961-01-04

Family

ID=22194113

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18164/57A Expired GB858127A (en) 1956-06-15 1957-06-07 Polymer foam modification

Country Status (1)

Country Link
GB (1) GB858127A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3228527A (en) * 1961-05-17 1966-01-11 Maremont Corp Water separating fuel filter
US3293174A (en) * 1962-03-08 1966-12-20 Ici Ltd Plant and processes for the treatment of effluent and sewage
US3306454A (en) * 1962-09-24 1967-02-28 Edmond F Webb Fluid container with contaminantcollecting means
US3360131A (en) * 1964-06-15 1967-12-26 Henry J Witkowski Filter with polyurethane foam element
US3395086A (en) * 1963-09-11 1968-07-30 Res Dev Co Removal of moisture from organic liquid solvent
US3410057A (en) * 1964-01-09 1968-11-12 Bernard J. Lerner Method for gas-liquid disentrainment operations
US3957017A (en) * 1974-11-04 1976-05-18 Syntex (U.S.A.) Inc. Contaminant filter in a closed-loop aquaculture system
US4072614A (en) * 1975-02-21 1978-02-07 Harris Frank N Oil and water separators
US4594366A (en) * 1983-06-29 1986-06-10 Union Carbide Corporation Connected branched polyols and polyurethanes based thereon
WO1999033641A1 (en) * 1997-12-24 1999-07-08 Molecular Geodesics, Inc. Foam scaffold materials
WO2003068839A1 (en) * 2002-02-12 2003-08-21 Foamex L.P. Hydrophilic ester polyurethane foams
WO2004058864A2 (en) * 2002-12-23 2004-07-15 Foamex L.P. Hydrophilic ester polyurethane foams
US6841586B2 (en) 2002-02-12 2005-01-11 Foamex, L.P. Felted hydrophilic ester polyurethane foams
US8202262B2 (en) 1994-08-22 2012-06-19 Kci Licensing, Inc. Wound therapy device and related methods
US8247466B2 (en) 2008-04-21 2012-08-21 Fxi, Inc. Variable felted polyurethane foams for sponges and wipes
CN116874710A (en) * 2022-08-29 2023-10-13 江苏长顺高分子材料研究院有限公司 Flame-retardant polyurethane rigid foam, preparation method and application thereof

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3228527A (en) * 1961-05-17 1966-01-11 Maremont Corp Water separating fuel filter
US3293174A (en) * 1962-03-08 1966-12-20 Ici Ltd Plant and processes for the treatment of effluent and sewage
US3306454A (en) * 1962-09-24 1967-02-28 Edmond F Webb Fluid container with contaminantcollecting means
US3395086A (en) * 1963-09-11 1968-07-30 Res Dev Co Removal of moisture from organic liquid solvent
US3410057A (en) * 1964-01-09 1968-11-12 Bernard J. Lerner Method for gas-liquid disentrainment operations
US3360131A (en) * 1964-06-15 1967-12-26 Henry J Witkowski Filter with polyurethane foam element
US3957017A (en) * 1974-11-04 1976-05-18 Syntex (U.S.A.) Inc. Contaminant filter in a closed-loop aquaculture system
US4072614A (en) * 1975-02-21 1978-02-07 Harris Frank N Oil and water separators
US4594366A (en) * 1983-06-29 1986-06-10 Union Carbide Corporation Connected branched polyols and polyurethanes based thereon
US8202262B2 (en) 1994-08-22 2012-06-19 Kci Licensing, Inc. Wound therapy device and related methods
WO1999033641A1 (en) * 1997-12-24 1999-07-08 Molecular Geodesics, Inc. Foam scaffold materials
WO2003068839A1 (en) * 2002-02-12 2003-08-21 Foamex L.P. Hydrophilic ester polyurethane foams
US6756416B2 (en) 2002-02-12 2004-06-29 Foamex L.P. Hydrophilic ester polyurethane foams
US6841586B2 (en) 2002-02-12 2005-01-11 Foamex, L.P. Felted hydrophilic ester polyurethane foams
WO2004058864A2 (en) * 2002-12-23 2004-07-15 Foamex L.P. Hydrophilic ester polyurethane foams
WO2004058864A3 (en) * 2002-12-23 2004-09-30 Foamex Lp Hydrophilic ester polyurethane foams
US8247466B2 (en) 2008-04-21 2012-08-21 Fxi, Inc. Variable felted polyurethane foams for sponges and wipes
CN116874710A (en) * 2022-08-29 2023-10-13 江苏长顺高分子材料研究院有限公司 Flame-retardant polyurethane rigid foam, preparation method and application thereof

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