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EP1597307A2 - Mousses en polyurethanne d'ester hydrophile - Google Patents

Mousses en polyurethanne d'ester hydrophile

Info

Publication number
EP1597307A2
EP1597307A2 EP03814339A EP03814339A EP1597307A2 EP 1597307 A2 EP1597307 A2 EP 1597307A2 EP 03814339 A EP03814339 A EP 03814339A EP 03814339 A EP03814339 A EP 03814339A EP 1597307 A2 EP1597307 A2 EP 1597307A2
Authority
EP
European Patent Office
Prior art keywords
foam
parts
water
polyol
polyurethane foam
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.)
Withdrawn
Application number
EP03814339A
Other languages
German (de)
English (en)
Inventor
Sharon A. Free
Charles V. Rose
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.)
Foamex LP
Original Assignee
Foamex LP
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 Foamex LP filed Critical Foamex LP
Publication of EP1597307A2 publication Critical patent/EP1597307A2/fr
Withdrawn legal-status Critical Current

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
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36—After-treatment
    • C08J9/38—Destruction of cell membranes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34—Auxiliary operations
    • B29C44/56—After-treatment of articles, e.g. for altering the shape
    • B29C44/5627—After-treatment of articles, e.g. for altering the shape by mechanical deformation, e.g. crushing, embossing, stretching
    • B29C44/5636—After-treatment of articles, e.g. for altering the shape by mechanical deformation, e.g. crushing, embossing, stretching with the addition of heat
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
    • C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0008—Foam properties flexible
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0041—Foam properties having specified density
    • C08G2110/005—< 50kg/m3
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0083—Foam properties prepared using water as the sole blowing agent
    • 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
    • C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04—Polyurethanes

Definitions

  • This invention relates to certain ester polyurethane foams that have been chemically modified and then felted (compressed under heat and pressure), following which the foams have unexpectedly improved liquid absorption and wicking.
  • the foams may be incorporated into articles used to wipe and absorb liquids, such as household cleaning sponges and mop heads.
  • Polyurethane foams are generally prepared by the reaction of an active hydrogen-containing compound (i.e., a polyol) and a polyisocyanate, in the presence of a blowing agent such as water, and usually a reaction catalyst and foam stabilizer.
  • a blowing agent such as water
  • the cellular polymer structure of polyurethane foam has a skeletal framework of relatively heavy strands forming an outline for the cell structure.
  • the skeletal framework strands are connected by very thin membranes, often called windows, which form the cell walls. In open-celled foams, some of the windows are open or torn in each cell, thus forming an interconnecting network open to fluid flow (liquid or gas).
  • Household cleaning sponges and mop heads most commonly are formed from cellulose.
  • Paper pulp is the primary ingredient for cellulose sponges.
  • the pulp is reacted with carbon disulfide to form a soluble cellulose xanthate compound. This compound is dissolved into a honey-like liquid viscose and mixed with reinforcing fibers to add strength to the pulp mixture.
  • the cellulose is formed with a double cell structure to replicate natural sea sponges. Sodium sulfate crystals are added to the pulp, and this mixture is heated in a mold to melt the crystals. Heating regenerates the mix to pure cellulose and leaves the signature sponge holes where the crystals have melted away.
  • Bleaching chemicals and humectants maintain the moisture level and color purity of the cellulose sponge. While the cellulose has good water absorption and wicking, it has lower wet integrity than other materials. Moreover, upon drying, the cellulose becomes hard and brittle such that it must be pre-wet before using for wiping.
  • Open celled ester and ether polyurethane foams have greater softness and flexibility than cellulose, and retain flexibility upon drying without humectants. As compared to cellulose, foams have greater wet strength, better wet integrity and exhibit less swelling when wet. Foams also can be foamed to have a double cell structure to more resemble natural sea sponges. Generally, polyurethane foams can be produced more cheaply than cellulose. However, polyurethane foams are hydrophobic, lacking good liquid absorption and wicking characteristics, which makes them less suitable for household sponges and mop heads. Even after the polyurethane foams are post-treated with surfactants in an attempt to improve water absorption and wicking, they still do not match the performance of cellulose for these properties.
  • Reticulated polyurethane foams have been used as components of filters. Such foams also have been suggested for use as components of household sponges, particularly for the abrasive surface presented by a reticulated foam. See U.S. Patents
  • a hydrophilic ester polyurethane foam is made by first forming a cellular polyurethane foam that has a network of at least some strands and at least some cell windows by mixing together certain foam-forming components.
  • the recipes for polyurethane foams are expressed in terms of parts by weight per 100 parts polyol.
  • the foam formulation according to the invention includes: from 20.0 to 62.0 parts by weight of an isocyanate; from 1.5 to 5.0 parts of a blowing agent, such as water; from 0.5 to 2.0 parts of a blow catalyst; from 0 to 0.3 parts of a gel catalyst, and from 1.0 to 3.0 parts of a stabilizing surfactant, such as a silicone surfactant.
  • a blowing agent such as water
  • a blow catalyst such as a blow catalyst
  • 0 to 0.3 parts of a gel catalyst from 1.0 to 3.0 parts of a stabilizing surfactant, such as a silicone surfactant.
  • a stabilizing surfactant such as a silicone surfactant.
  • Other additives such as antimicrobial additives, double cell additives, dyes, pigments, colorants, crosslinking additives, fragrances, detergents and extenders may also be incorporated into the foam formulation.
  • the foam is permitted to rise and cure, preferably under atmospheric temperature and pressure.
  • the resulting foam has pore sizes preferably in the range of from 70 to 130 pores per linear inch (27.6 to 51.2 pores per cm), most preferably 70 to 90 pores per linear inch (27.6 to 35.4 pores per cm), but may also have a double cell or sea sponge-like structure.
  • the preferred double cell structure has a distribution of larger and medium sized cells scattered across a background of finer cells. The larger cells may range from 0.06 to 0.09 inches (1.52 to 2.29 mm) in diameter.
  • the cured foam is cut into slabs and then chemically treated by immersing the slab in a heated caustic bath for from three to fifteen minutes, preferably from six to ten minutes.
  • One preferred caustic bath is a sodium hydroxide solution (from 5.0 to 10.0 percent, preferably 7.5% NaOH) that is heated to from 70°F to 160°F (21 to 71°C), preferably from 120°F to 160°F (49 to 71°C).
  • the caustic solution etches away at least a portion of the cell windows within the foam cellular structure, leaving behind a hydrophilic ester polyurethane foam.
  • the treated foam is compressed between calendaring rolls, and then rinsed thoroughly and oven dried.
  • the foam is felted by compressing the foam to from one-half (1/2) to one-twentieth (1/20) of its initial thickness, preferably from one-third (1/3) to one- eighth (1/8) of its initial thickness, and heating the compressed foam at a temperature of from 340 to 380°F (171 to 193°C) for from 10 to 60 minutes.
  • the foam structure comprises a hydrophilic ester polyurethane foam with good wicking characteristics that will absorb water at a rate of at least about
  • the foam also has greater water holding capacity and wet strength than cellulose.
  • the felted hydrophilic ester polyurethane foam does not swell appreciably upon absorbing and retaining liquids and would make an ideal component of a household sponge or mop head.
  • Hydrophilic ester foams according to the invention are prepared preferably by mixing together the polyol component with the surfactants, catalysts, blowing agents and other additives, forming a polyol pre-mix. To the polyol pre-mix is added the isocyanate component. The foam mixture is then allowed to rise and cure, preferably under atmospheric conditions, to form the hydrophilic ester polyurethane foam. The foam-forming process may be carried out batch-wise, semi-continuously or continuously. Polyester polyurethane foams are more hydrophilic than polyether polyurethane foams due to the increased polarity of the carboxylic acid groups. Suitable polyester polyols for producing flexible polyester polyurethane foams are well known in the industry.
  • polyester polyols are those produced by reacting a dicarboxylic and/or monocarboxylic acid with an excess of a diol and/or polyhydroxy alcohol, for example, adipic acid, glutaric acid, succinic acid, phthalic acid or anhydride, and/or fatty acids (linolic acid, oleic acid and the like) with diethylene glycol, ethylene glycol, propylene glycol, dipropylene glycol, 1,4-butanediol, neopentyl glycol, trimethylolpropane, trimethylolethane, and/or pentaerythritol.
  • a dicarboxylic and/or monocarboxylic acid with an excess of a diol and/or polyhydroxy alcohol
  • a diol and/or polyhydroxy alcohol for example, adipic acid, glutaric acid, succinic acid, phthalic acid or anhydride, and/or fatty acids (linolic acid,
  • polyester polyols examples include LEXOREZ 1102-50 or LEXOREZ 1102-60 from Inolex Chemical Company or FOMREZ 50 or FOMREZ 60 from Crompton Corporation.
  • suitable polyester polyols can be prepared by reacting a lactone with an excess of a diol such as caprolactone with propylene glycol. See U.S. Pat. No. 4,331,555 for further discussion of suitable polyester polyols.
  • the polyester polyol is made by reacting adipic acid and ethylene glycol monomers with a glycerin initiator.
  • Hydrophilic ester polyols are typically reaction products of polyethylene glycol and adipic acid.
  • the polyol component of the foam-forming mixture of the invention comprises at least five (5) parts by weight, preferably ten (10) parts by weight, of a 50 hydroxyl hydrophilic ester polyol. 60 hydroxyl ester polyols and mixtures of 50 hydroxyl and 60 hydroxyl ester polyols and 50 hydroxyl hydrophilic ester polyols are also preferred.
  • hydroxyl number for a polyol is a measure of the amount of reactive hydroxyl groups available for reaction. The value is reported as the number of milligrams of potassium hydroxide equivalent to the hydroxyl groups found in one gram of the sample. "Functionality" of a polyol is defined as the average number of hydroxyl group sites per molecule.
  • the polyester polyols used to form the foams of the present invention have a hydroxyl number in the range of 20 to 150, more preferably in the range of 40 to 100, and most preferably in the range of 50 to 60.
  • polyisocyanate refers particularly to isocyanates that have previously been suggested for use in preparing polyurethane foams.
  • Polyisocyanates include di- and poly- isocyanates and prepolymers of polyols and polyisocyanates having excess isocyanate groups available to react with additional polyol.
  • index refers to the actual amount of isocyanate required for reaction with all of the active hydrogen- containing compounds present in the reaction mixture multiplied by 100.
  • the isocyanate index is in the range of between about 75 to 140.
  • the preferred isocyanate index is in the range of 90 to 110, most preferably 100 or below, with a particularly preferred range of 95 to 98.
  • polyester polyurethane foams are prepared using any suitable organic polyisocyanates well known in the art including, for example, hexamethylene dusocyanate, phenylene dusocyanate, toluene dusocyanate (TDI) and 4,4'- diphenylmethane dusocyanate (MDI).
  • suitable organic polyisocyanates well known in the art including, for example, hexamethylene dusocyanate, phenylene dusocyanate, toluene dusocyanate (TDI) and 4,4'- diphenylmethane dusocyanate (MDI).
  • methylene diisocyanates suitable for use are diphenyl methane dusocyanate and polymethylene polyphenyl isocyanate blends (sometimes referred to as "MDI" or "polymeric MDI").
  • the MDI blends can contain diphenylmethane 4, 4 'dusocyanate, as well as 2, 2' and 2, 4' isomers and higher molecular weight oligomers and have an isocyanate functionality of from about 2.1 to 2.7, preferably from about 2.1 to 2.5.
  • the isocyanate is selected from a commercial mixture of 2,4- and 2,6-toluene dusocyanate.
  • a well-known commercial toluene dusocyanate is TD80, a blend of 80% 2, 4 toluene dusocyanate and 20% 2, 6 toluene dusocyanate.
  • Polyisocyanates are typically used at a level of between 20 and
  • One or more surfactants are also employed in the foam-forming composition.
  • the surfactants lower the bulk surface tension, promote nucleation of bubbles, stabilize the rising cellular structure, emulsify incompatible ingredients, and may have some effect on the hydrophilicity of the resulting foam.
  • the surfactants typically used in polyurethane foam applications are polysiloxane-polyoxyalkylene copolymers, which are generally used at levels between about 0.5 and 3 parts by weight per 100 parts polyol. In the present invention, from 1.0 to 3.0 parts by weight per 100 parts polyol of surfactant is preferred.
  • Surfactants which may for example be organic or silicone based, such as FOMREZ M66-86A (Witco) and L532 (OSi Specialties) may be used to stabilize the cell structure, to act as emulsifiers and to assist in mixing.
  • the surfactant is a cell opening silicone surfactant in an amount from 1.5 to 2.5 parts by weight per 100 parts polyol.
  • Catalysts are used to control the relative rates of water-polyisocyanate (gas- forming or blowing) and polyol-polyisocyanate (gelling) reactions.
  • the catalyst may be a single component, or in most cases a mixture of two or more compounds.
  • Preferred catalysts for polyurethane foam production are organotin salts and tertiary amines.
  • the amine catalysts are known to have a greater effect on the water- polyisocyanate reaction, whereas the organotin catalysts are known to have a greater effect on the polyol-polyisocyanate reaction.
  • Total catalyst levels generally vary from 0 to 5.0 parts by weight per 100 parts polyol. The amount of catalyst used depends upon the formulation employed and the type of catalyst, as known to those skilled in the art.
  • amine catalyst from 0.5 to 2.0 parts, per 100 parts polyol
  • organotin catalyst from 0 to 0.7 parts, preferably from 0 to 0.3 parts, per 100 parts polyol.
  • Suitable urethane catalysts useful in the present invention are all those well known to the worker skilled in the art, including tertiary amines such as triethylenediamine, N-methylimidazole, 1,2-dimethylimidazole, N-methylmorpholine, N-ethylmorpholine, triethylamine, tributylamine, triethanolamine, dimethylethanolamine and bisdimethylaminodiethylether, and organotins such as stannous octoate, stannous acetate, stannous oleate, stannous laurate, dibutyltin dilaurate, and other such tin salts.
  • a double-cell structure may be created to replicate the appearance of natural sea sponges.
  • Materials used to create a double cell structure may be added to the foam forming mixture. These include: castor oil derivatives, stearic acid, acetic acid and low melting point waxes. These materials create voids larger than the prevailing pores within the resulting foam structure. If used, the double-cell additive preferably is added in an amount from 0.04 to 0.21 parts per 100 parts polyol.
  • a blowing agent may be included in the foam-forming composition.
  • the most typical blowing agent is water that may be added in amounts from 1.5 to 5.0 parts per 100 parts polyol.
  • Alternative blowing agents are liquid carbon dioxide, volatile organic compounds, such as pentane and acetone, and chlorinated compounds, such as methylene chloride, HFC's, HCFC's and CFC's.
  • additives may be incorporated into the foam-forming composition.
  • the optional additives include, but are not limited to, antimicrobial compounds, stabilizers, extenders, dyes, pigments, crosslinking additives, fragrances, detergents and anti-static agents.
  • antimicrobial compounds include, but are not limited to, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite
  • the hydrophilic ester polyurethane foam has cell sizes preferably ranging from 70 to 130 pores per linear inch (27.6 to 51 pores per cm), most preferably 70 to 90 pores per linear inch (27.6 to 35.4 pores per cm), but may also have a double cell or sea sponge-like structure.
  • the preferred double cell structure has a distribution of larger and medium sized cells scattered across a background of finer cells. The larger cells may range from 0.06 to 0.09 inches (1.5 to 2.3 mm) in diameter.
  • the foam is then chemically reticulated to remove cell windows by immersing the slab in a heated caustic bath for from three to fifteen minutes, preferably from six to ten minutes.
  • One preferred caustic bath is a sodium hydroxide solution (from 5.0 to 10.0 percent, preferably 7.5% NaOH) that is heated to from 70°F to 160°F (21 to 71°C), preferably from 120°F to 160°F (49 to 71°C).
  • the caustic solution etches away at least a portion of the cell windows within the foam cellular structure, leaving behind a hydrophilic ester polyurethane foam.
  • the treated foam is compressed between calendaring rolls, and then rinsed thoroughly and oven dried.
  • the foam is felted by compressing the foam to from One-half (1/2) to one-twentieth (1/20) of its initial thickness, preferably from one-third (1/3) to one- eighth (1/8) of its initial thickness, and heating the compressed foam at a temperature of from 340 to 380°F (171 to 193°C) for from 10 to 60 minutes.
  • the compression ratio is generally referred to as a firmness.
  • a foam compressed to one-third of its original thickness is a firmness 3 felt.
  • a foam compressed to one-fifth of its original thickness is a firmness 5 felt.
  • Cellulose sponges were obtained.
  • the cellulose sponges of Examples CI, C2 and C3 were from 3M, Nylonge and Spontex, respectively. Based on our testing, cellulose had a rate of water absorption of 29 to 35 lbs. water/ft ⁇ /minute (1.39 to 1.68 kPa/min) and an effective water absorption of over 40% (44%).
  • Polyurethane foams were prepared on a laboratory scale by mixing together the foam-forming ingredients and pouring them into a 15" x 15" (38.1 x 38.1 cm) cardboard box to form foam buns under atmospheric pressure (e.g., 1 atm.) and temperature (about 75°F (24°C)). The foam ingredients were mixed according to the proportions shown in Table 1.
  • Amounts are in kilograms and are based on parts by weight per hundred parts polyol.
  • the foams of Examples C4 to C6 are comparison foams not prepared according to the invention.
  • the foams of Examples 1 to 7 were prepared with formulations according to the invention, but were not felted.
  • Portions of the foam bun for each Example were cut into slabs and chemically treated or modified.
  • the slabs were immersed in a heated solution of 7.5% sodium hydroxide in water (heated to at least 120°F (49°C)) for eight minutes.
  • the slabs were then compressed between calendar rollers to squeeze out most of the caustic solution.
  • the slabs were then rinsed to remove the remaining caustic solution and then dried in an oven.
  • Example C4 was prepared as a standard ester polyurethane foam.
  • the foam of Example C5 was prepared with a hydrophilic polyol. Neither of the foams from
  • Example C6 is a thermally reticulated hydrophilic ester foam. Although the Example C6 foam had completely open cells, this foam had a very low liquid absorption rate.
  • LEXOREZ 1102-50A is an ester polyol with a hydroxyl number of 50 supplied by Inolex Chemical Company.
  • F45 is FOMREZ 45, a 50 hydroxyl hydrophilic ester polyol offered by Crompton.
  • TEGOSTAB B8301 is a cell opening silicone surfactant from Goldschmidt Chemical Corporation.
  • NIAX Silicone Y6353 is a cell opening silicone surfactant from OSi Specialties.
  • ULTRAFRESH DM50 is an antimicrobial additive supplied by Thomson Research.
  • the double cell additive (“DC additive”) is a castor oil derivative used to provide an optional sea sponge like structure to the foam.
  • KOSMOS K5N is a stannous octoate catalyst (tin catalyst) from Goldschmidt Chemical Corporation.
  • NEM is an amine catalyst, n-ethyl morpholine.
  • TD80 is a toluene dusocyanate mixture comprised of 80 percent 2,4- toluene dusocyanate and 20 percent 2,6- toluene dusocyanate.
  • the "index" is the isocyanate index.
  • the cellular structure of the foam can be uniform or have a distribution of different cell sizes. The uniform cell structure is described by the number of pores per linear inch. The number is derived from a visual comparison of the foam to a standard. Double-cell foams have cells of varying sizes. The pores of the larger cells are within the stated range.
  • the rate of liquid absorption was determined according to the following test method.
  • the weight and dimensions of a damp sponge sample are measured.
  • the sponge has a generally rectangular front and rear surface and a certain thickness.
  • the length and thickness of the sponge are measured to the nearest 0.01 inches (0.25 mm).
  • the sponge is wrung out and its wrung out weight is recorded.
  • a perforated plate is placed in the bottom of a solid tray. Water is added to a depth of 1/8 inch (3 mm) over the perforated plate.
  • the sponge is placed on the surface of the perforated plate and into the pool of water.
  • One side surface of the sponge is held within the pool such that the front and rear faces of the sponge are held pe ⁇ endicular to the surface of the water pool.
  • the sponge is removed after 5 seconds, and without losing water from the sponge, the sponge is weighed. The wet weight is recorded to the nearest 0.01 grams. The rate of water absorption is reported as pounds of water per square foot per minute. It is calculated as the wet weight minus the wrung out weight divided by the length times the thickness of the sponge. The percent effective abso ⁇ tion indicates the percent of water by volume a damp sponge will retain after saturation and draining for five minutes. The abso ⁇ tion is reported in cubic inches of water held by a cubic inch of sponge. The dimensions (length, width and thickness) of a damp sponge are measured to the nearest 0.01 inches (0.25 mm). The wet volume is calculated. Wring out the sponge and record the wrung out weight to the nearest 0.01 grams.
  • the sponge is then fully immersed in a pool of warm water, squeezed to remove trapped air and allowed to absorb water for one minute.
  • the sponge is removed with a hook and hung vertically for five minutes to allow water to drain therefrom. Thereafter, the sponge is reweighed to the nearest 0.01 grams - denominated the wet weight. The percent water retained by volume is calculated.
  • the percent effective abso ⁇ tion is the wet weight minus the wrung out weight divided by the wet volume.
  • the percent total abso ⁇ tion indicates the total amount of water a sponge can hold after draining for five minutes in a vertical position and is expressed as a percentage of its original dry weight.
  • the sponge is immersed in warm water and squeezed to remove trapped air.
  • the sponge is allowed to absorb water for one minute.
  • the sponge is then removed from the water with a hook and hung vertically to allow water to drain for five minutes. Thereafter, the sponge is weighed and the drained weight is recorded to the nearest 0.01 grams. Excess water is squeezed out of the sponge by hand. The sponge then is dried in an air-circulating oven for at least four hours at 220°F, cooled to room temperature and re- weighed. The dry weight of the sponge is recorded to the nearest 0.01 grams. The percent total abso ⁇ tion is 100 times the amount of water retained after draining (drained weight minus dry weight) divided by the dry weight of the sponge.
  • Wet out time measures the time duration required for a drop of water to be absorbed completely by a damp sponge sample.
  • the sponge sample is immersed in water and squeezed while in the water to remove trapped air. Upon removing from the water, the sponge is wrung out as completely as possible. A drop of water is placed on a facing surface of the damp sponge. The time for the drop to be absorbed by the damp sponge is recorded. The average wet out time was calculated after the test is repeated five times.
  • Wipe dry is evaluated by pouring 50 grams of water on a clean level surface. The sample sponge is weighed before the test and after each wiping pass across the water until no more water is absorbed. The sponge is not wrung out before or after weighing. The weight of the water picked up by the sponge after each pass is recorded.
  • Water holding capacity is measured by weighing a dry sponge, then immersing the sponge sample in water, squeezing to remove trapped air, soaking the sponge for five minutes, and weighing the saturated sponge.
  • the water holding capacity is the weight of water held per gram of sponge.
  • Example 1 foam had excellent abso ⁇ tion rates and performed comparable to cellulose sponges (Examples CI, C2 and C3).
  • the Example 1 foam was made from a low index conventional polyester formulation and was chemically modified in a caustic solution. The Example 1 foam wicked water and wiped similarly to the cellulose sponges, and had a greater water holding capacity.
  • the foam of Example 1 performed unexpectedly better than foams of equivalent composition that were not chemically modified (Example C4) and a hydrophilic ester foam (Example C5).
  • the combination of low index and chemical treating particularly where the foam is formed with a cell opening silicone surfactant, creates an unexpectedly superior hydrophilic ester polyurethane foam.
  • the foams of Examples 2 to 7 performed similarly to Example 1.
  • Example 2 shows that adding 10 parts per hundred of a hydrophilic polyol can increase the total abso ⁇ tion of the resulting foam.
  • the finer cell structure of Example 4 increased the effective and total abso ⁇ tion values of the foam and improved the wipe dry.
  • Examples 5 and 6 show the effect of increasing density.
  • Example 7 shows the effect of a different surfactant type on water absorbing properties.
  • Examples 8 to 13 are according to the invention, and Comparative Examples C5 to C9 represent prior art cellulose or ester polyurethane foams. Comparative Examples C5, C7 and C8 were not felted. Examples 8, 9 and 10 inco ⁇ orated the same ester polyurethane formulation with at least 5 parts by weight of a hydrophilic polyester polyol made from an adipic acid and a polyethylene glycol, but the foams of Examples 9 and 10 were felted. Table 4
  • ACQUELL is a registered trademark of Foamex L.P.
  • Felting the foams according to the invention achieved su ⁇ risingly higher rates of water abso ⁇ tion and effective water abso ⁇ tion.
  • the rates of water abso ⁇ tion for the felted foams of Examples 9 and 10 of the invention at various felting firmnesses exceeded the water abso ⁇ tion for other polyurethane foams and for cellulose.

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

Abstract

L'invention concerne la préparation d'une mousse en polyuréthanne d'ester reposant sur la réaction d'un mélange d'au moins un polyol de polyester avec au moins un isocyanate et au moins un agent de surface de silicone en présence d'un agent d'expansion, tel que l'eau, et d'autres additifs, tels que des catalyseurs. La mousse durcie est traitée chimiquement dans une solution caustique et, puis, elle est feutrée (comprimée sous l'effet de la chaleur et de la pression) pour former une mousse en polyuréthanne d'ester hydrophile possédant un taux d'absorption d'eau d'au moins 30 livres d'eau par pied carré par minute (1,44 kPa/min). La mousse présente également une capacité de rétention d'eau et une hydrorésistance meilleures que la cellulose.
EP03814339A 2002-12-23 2003-12-23 Mousses en polyurethanne d'ester hydrophile Withdrawn EP1597307A2 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US43527702P 2002-12-23 2002-12-23
US435277P 2002-12-23
PCT/US2003/041032 WO2004058864A2 (fr) 2002-12-23 2003-12-23 Mousses en polyurethanne d'ester hydrophile

Publications (1)

Publication Number Publication Date
EP1597307A2 true EP1597307A2 (fr) 2005-11-23

Family

ID=32682210

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03814339A Withdrawn EP1597307A2 (fr) 2002-12-23 2003-12-23 Mousses en polyurethanne d'ester hydrophile

Country Status (4)

Country Link
EP (1) EP1597307A2 (fr)
JP (1) JP4589730B2 (fr)
AU (1) AU2003300298A1 (fr)
WO (1) WO2004058864A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE112013005842T5 (de) * 2012-12-07 2015-08-20 Inoac Usa, Inc. Hydrophiler, thermisch retikulierter Polyurethan-Schaumstoff, der für die Herstellung eines Filters für geschmolzenes Metall verwendbar ist
KR102847198B1 (ko) * 2024-10-14 2025-08-18 김해룡 고흡수성 폴리우레탄 스펀지 및 그 제조방법

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GB789481A (en) * 1954-12-08 1958-01-22 Johann Bauer Process for the production of foam materials
GB858127A (en) * 1956-06-15 1961-01-04 Scott Paper Co Polymer foam modification
JP2702772B2 (ja) * 1989-04-28 1998-01-26 花王株式会社 吸水性ポリウレタンフォーム成形品の製造方法
JPH03239736A (ja) * 1990-02-19 1991-10-25 Kao Corp 吸水性ポリウレタンフォームの製造方法
JP2841011B2 (ja) * 1993-06-15 1998-12-24 三洋化成工業株式会社 熱成形用材料および熱成形方法
DE4341973A1 (de) * 1993-12-09 1995-06-14 Basf Ag Verfahren zur Herstellung von kompakten oder zelligen Polyurethanen, hierfür verwendbare Urethangruppen enthaltende Polyisocyanatzusammensetzungen und deren Verwendung
JP3733991B2 (ja) * 1996-07-10 2006-01-11 株式会社ブリヂストン 軟質ポリウレタンフォームの製造方法
US6045741A (en) * 1996-07-10 2000-04-04 Bridgestone Corporation Preparation of flexible polyurethane foam
JP2001504150A (ja) * 1996-11-08 2001-03-27 ハンツマン・アイシーアイ・ケミカルズ・エルエルシー 軟質ポリウレタン発泡体を製造するための方法
JP4053635B2 (ja) * 1997-11-17 2008-02-27 株式会社イノアックコーポレーション 抗菌性ポリウレタン樹脂及びその製造方法
JP2002012646A (ja) * 2000-06-29 2002-01-15 Bridgestone Corp 食品用シート材
US6756416B2 (en) * 2002-02-12 2004-06-29 Foamex L.P. Hydrophilic ester polyurethane foams

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See also references of WO2004058864A3 *

Also Published As

Publication number Publication date
WO2004058864A3 (fr) 2004-09-30
AU2003300298A8 (en) 2004-07-22
AU2003300298A1 (en) 2004-07-22
WO2004058864A2 (fr) 2004-07-15
JP4589730B2 (ja) 2010-12-01
JP2006511654A (ja) 2006-04-06

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