WO2006034640A1 - A polyurethane composite, its preparation and use - Google Patents

A polyurethane composite, its preparation and use Download PDF

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Publication number
WO2006034640A1
WO2006034640A1 PCT/CN2005/001571 CN2005001571W WO2006034640A1 WO 2006034640 A1 WO2006034640 A1 WO 2006034640A1 CN 2005001571 W CN2005001571 W CN 2005001571W WO 2006034640 A1 WO2006034640 A1 WO 2006034640A1
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WO
WIPO (PCT)
Prior art keywords
polyurethane
diisocyanate
polyol
foam
mold
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.)
Ceased
Application number
PCT/CN2005/001571
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English (en)
French (fr)
Chinese (zh)
Inventor
Chenxi Zhang
Jen-Chieh Lin
Chi-Kwong Chow
Xiang Wang
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.)
Bayer China Ltd
Covestro Deutschland AG
Original Assignee
Bayer China Ltd
Bayer MaterialScience AG
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Filing date
Publication date
Application filed by Bayer China Ltd, Bayer MaterialScience AG filed Critical Bayer China Ltd
Priority to US11/663,815 priority Critical patent/US8017229B2/en
Priority to EP20050791954 priority patent/EP1818347B1/en
Priority to JP2007533854A priority patent/JP4977029B2/ja
Publication of WO2006034640A1 publication Critical patent/WO2006034640A1/zh
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • B29C44/04Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles consisting of at least two parts of chemically or physically different materials, e.g. having different densities
    • B29C44/0461Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles consisting of at least two parts of chemically or physically different materials, e.g. having different densities by having different chemical compositions in different places, e.g. having different concentrations of foaming agent, feeding one composition after the other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C67/00Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
    • B29C67/24Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00 characterised by the choice of material
    • B29C67/246Moulding high reactive monomers or prepolymers, e.g. by reaction injection moulding [RIM], liquid injection moulding [LIM]
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/065Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/40Layered products comprising a layer of synthetic resin comprising polyurethanes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/18Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
    • B32B5/20Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material foamed in situ
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02Physical, chemical or physicochemical properties
    • B32B7/022Mechanical properties
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4804Two or more polyethers of different physical or chemical nature
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2075/00Use of PU, i.e. polyureas or polyurethanes or derivatives thereof, as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/04Condition, form or state of moulded material or of the material to be shaped cellular or porous
    • B29K2105/043Skinned foam
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/02Organic
    • B32B2266/0214Materials belonging to B32B27/00
    • B32B2266/0278Polyurethane
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/08Closed cell foam
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/72Density
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0008Foam properties flexible
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0025Foam properties rigid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0033Foam properties having integral skins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • C08G2110/0058≥50 and <150kg/m3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • C08G2110/0066≥ 150kg/m3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0083Foam properties prepared using water as the sole blowing agent
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249976Voids specified as closed
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249976Voids specified as closed
    • Y10T428/249977Specified thickness of void-containing component [absolute or relative], numerical cell dimension or density
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249987With nonvoid component of specified composition
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249987With nonvoid component of specified composition
    • Y10T428/249991Synthetic resin or natural rubbers

Definitions

  • the present invention relates to polyurethane composites, methods of making the composites and their use, for example, in bicycle saddles, upholstery materials. Background technique
  • Polypropylene liners are used to provide support and impact resistance, while polyurethane outer layers are used to provide soft comfort and abrasion resistance.
  • the polypropylene and the polyurethane are generally separately formed into the desired corresponding shapes, and then the two are bonded together by an adhesive.
  • the object of the present invention is to solve the above-mentioned shortcomings in the field for a long time, to replace the polypropylene-containing composite material with a polyurethane composite material, to simplify the production process, to improve the production efficiency and the product qualification rate, to avoid the use of the binder, and to reduce the binder.
  • the present invention provides a polyurethane composite comprising a layer of rigid polyurethane as an inner liner and a layer of veneer (surface closed cell) polyurethane foam directly foamed on the rigid polyurethane inner liner
  • the rigid polyurethane is a reaction product of a polyisocyanate with a polyether polyol or a polyester polyol and a chain extender, and has a density of 600 to 1200 kg/m 3 and a Shore D hardness of 40 to 80.
  • the tensile strength is 10-60 MPa
  • the flexural strength is 20-60 MPa
  • the elastic flexural modulus is 800-2500 MPa
  • the elongation at break is 10-25%
  • the whole skin (surface closed cell) or HR polyurethane flexible foam It is a reaction product of a di/polyisocyanate and a polyol formed by the action of water as a foaming agent, and has a density of 60-180 kg/m 3 , a tensile strength of 60-250 kPa, and an elongation at break of 70-180.
  • tear strength is 130-220N/m
  • ball rebound value is 40-70%
  • IFD 25% is 200-600 N
  • IFD 65% is 600-1800 N.
  • Another aspect of the present invention provides a method of manufacturing the polyurethane composite, comprising the steps of:
  • One aspect of the present invention provides a polyurethane composite comprising a layer of a rigid polyurethane as an inner liner and a layer of a polyurethane flexible foam directly foamed on the rigid polyurethane inner liner.
  • the rigid polyurethane used to constitute the polyurethane composite of the present invention is a reaction product of a polyisocyanate with a polyether polyol or/and a polyester polyol and a chain extender.
  • the polyisocyanate is a conventional polyisocyanate, non-limiting examples of which are toluene diisocyanate, such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, diphenylmethane diisocyanate, for example, 4, 4' Phenylmethane diisocyanate, a modified product of diphenylmethane diisocyanate having an NCO% content of between 18 and 33.6.
  • toluene diisocyanate such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, diphenylmethane diisocyanate, for example, 4, 4' Phenylmethane diisocyanate, a modified product of diphenylmethane diisocyanate having an NCO% content of between 18 and 33.6.
  • Polyisocyanate materials useful as rigid polyurethane liners of the present invention are commercially available, non-limiting Examples are for example:
  • PAPI M227, ISONATE M 143 purchased from Dow;
  • Non-limiting examples of polyether polyols suitable for use in the present invention are propylene glycol, ethylene glycol, glycerol, trimethylolpropane, pentaerythritol, sucrose, sorbitol, ethylenediamine, toluenediamine, and the like.
  • the starting agent forms a polyether polyol having a functionality of from 2 to 8, preferably from 2 to 6, and a hydroxyl number of from 20 to 800.
  • the polyether polyol preferably has a hydroxyl value of from 100 to 700.
  • Non-limiting examples of polyester polyols are adipic acid or/and phthalic anhydride with ethylene glycol, propylene glycol, glycerol, trimethylolpropane, 1, 4-butanediol, 1, 6 hexanediol, pentanediol and other polycondensation reaction products, the functionality is 2-4, the hydroxyl value is 50-500.
  • Polyols suitable for use in the present invention are also commercially available. Non-limiting examples thereof are, for example, Baydur CSP EF 0801-1, Baydur TPPU 601 K20B and Baydur PU 85 BD04 available from Bayer.
  • Chain extenders suitable for use in the present invention include glycols, triols and diamines; non-limiting examples of which are ethylene glycol, butylene glycol, glycerol, trimethylolpropane, diethylene glycol
  • the dipropylene glycol and the diamine include an aromatic diamine or an aliphatic diamine such as ethylenediamine, toluenediamine and the like.
  • the molar ratio of the polyisocyanate to the polyol is from 100 to 130:100, preferably from 105 to 120:100, more preferably from 108 to 115:100.
  • the rigid polyurethane product used to constitute the polyurethane composite of the present invention has a density of 600 to 1200 kg/m 3 , preferably 1000 to 1200 kg/m 3 ; Shore A hardness of 90 to 99, preferably 95 to 98. ; Shore D (Shore
  • D) hardness is 40-80, preferably 65-75; product tensile strength is 10-60 MPa, preferably 35-45 MPa
  • the elongation at break is 10-25%, preferably 12-20%.
  • a flame retardant such as tris(2-chloroethyl) phosphate (TCEP) and tris(1,3-dichloro-2) phosphate may be added to the rigid polyurethane of the composite material of the present invention as needed.
  • TCEP tris(2-chloroethyl) phosphate
  • DMPP dimethylpropyl phosphate
  • the polyurethane composite of the present invention also includes a whole skin (surface closed cell) polyurethane soft foam.
  • the polyurethane soft foam is a reaction product of a diisocyanate and a glycol formed by the action of water as a blowing agent.
  • the diisocyanate is a conventional diisocyanate, non-limiting examples of which are, for example, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, hexamethylene diisocyanate, tetramethylene diisocyanate, naphthalene diisocyanate, Dibenzoyl diisocyanate, preferably diphenylmethane diisocyanate (MDI) and a modified product having a NCO% content of 24-33 (preferably 18-30); or a mixture of diphenylmethane diisocyanate (MDI) and toluene diisocyanate (TDI) having a NCO% content of 26 to 42.
  • MDI diphenylmethane diisocyanate
  • TDI toluene diisocyanate
  • the polyol has a functionality of from 2 to 4 and a hydroxyl number of from 18 to 60, preferably from 20 to 50.
  • Non-limiting examples of mixed graft polyols are polyols having a functionality of 2-4, a hydroxyl number of 18-25, and a solids content of 20-46% (polystyrene PS, polyacrylonitrile PA, polyurea). .
  • Polyols for forming polyurethane flexible foams are commercially available. Non-limiting examples thereof are, for example, Bayfit 2856-LY, Bayfit HM 1124 and Bayfit 2873-LY available from Bayer.
  • the polyol system for forming the whole skin (surface closed cell) polyurethane soft foam of the present invention contains 0.4 to 1.0% by weight, preferably 0.6 to 0.8% by weight, based on the weight of the polyol system. During the polymerization, the water contained therein acts as a blowing agent.
  • the present invention is a density integral skin (surface closed-cell) or HR flexible polyurethane foam product 60- 180kg / m 3, preferably of 70-150kg / m 3; the present invention is stretched integral skin (surface closed-cell) flexible polyurethane foam
  • the strength is 60-250 kPa, preferably 80-200 kPa; the elongation at break is 70-180%, preferably 87-160%; the tear strength is 130-220 N/m, preferably 150-200 N/ m, the rebounding rebound value is 40-70%, preferably 50-65%; IFD25% is 200-600N, preferably 300-500N; IFD 65% is 600-1800N, preferably 900-1100N.
  • An ultraviolet light stabilizer may also be added to the composite flexible polyurethane foam of the present invention.
  • the ultraviolet light stabilizer is not particularly limited and it may be a conventional ultraviolet light stabilizer.
  • Non-limiting examples thereof are, for example, Irganox 565 (2-(4-hydroxy-3, 5-di-tert-butylanilino)-4,6-bis(n-octylthio) 1, 3, available from Ciba-Geigy, 5-triazine) and the like.
  • additives such as flame retardants such as tris(2-chloroethyl) phosphate (TCEP) and phosphoric acid (1, 3) may be added to the hard and flexible polyurethane foam of the composite of the present invention as needed.
  • flame retardants such as tris(2-chloroethyl) phosphate (TCEP) and phosphoric acid (1, 3)
  • TCEP tris(2-chloroethyl) phosphate
  • DMPP dimethylpropyl phosphate
  • foam stabilizer and the like.
  • Another aspect of the present invention provides a method of manufacturing the polyurethane composite, comprising the steps of:
  • a polyisocyanate and polyol combination system for forming the rigid polyurethane inner liner is added to the upper mold of a composite mold; after 2 to 6 minutes, the mold is opened to form a rigid polyurethane inner liner.
  • the term "composite mold” means a mold having an upper mold and a lower mold, the upper mold being capable of independently molding a shaped article, usually a rigid polyurethane liner having a shape
  • the lower mold can place the reaction system of the polyurethane soft foam, so that after the mold is closed, the polyurethane soft foam can be directly formed on the formed rigid polyurethane inner liner.
  • the shape of the upper mold of the composite mold depends on the specific use. In the case where the composite material of the present invention is used in a bicycle saddle, the shape of the upper mold of the composite mold corresponds to the shape of the bicycle saddle, so that the upper and lower molds of the mold are closed and the polyurethane soft foam is located in the lower mold of the mold.
  • the shape of the upper mold of the composite mold corresponds to the column Partially curved shape.
  • the upper and lower mold mounting positions are interchangeable during use.
  • a diisocyanate and polyol combination system for forming the whole skin (surface closed cell) polyurethane flexible foam is added to the lower mold of the composite mold.
  • the polyurethane composite of the present invention is composed of a rigid polyurethane which can withstand heavy pressure and impact and a veneer (surface closed cell) polyurethane foam which is directly foamed on the rigid polyurethane.
  • the rigid polyurethane provides impact and pressure resistance
  • the skin (surface closed cell) polyurethane soft foam surface layer provides comfort and wear resistance.
  • This polyurethane composite eliminates the prior art manual surface treatment of hard support materials, increasing productivity and yield.
  • the material is composed entirely of homogenous polyurethane, it is not necessary to peel off the sorting process during recycling, which saves labor costs and is suitable for large-scale industrial production.
  • the surface soft foam layer of the composite material of the present invention not only provides a soft hand but also has a sound absorbing effect, thereby replacing the fabric decoration and achieving fire prevention and reduction. Cost and other effects.
  • Hydroxyl value is about 370 mg KOH/g
  • Viscosity approx. 1,700 mPa - s 100 parts by weight, Baydur CSP EF0801-1 B component polyether compound and
  • component A SBUJ243 reaction index 110
  • Desmodur 44P01 modified MDI-modified polyphenylmethane diisocyanate purchased from Bayer China (limited) company
  • Baydur TP.PU 60IK20 purchased from Bayer China (limited) company Unit hydroxyl value 515 ⁇ 25 mg KOH / g
  • Desmodur PU1511L modified MDI purchased from Bayer China (limited) company
  • NCO% is about 31%
  • Bayfit 2856-LY 100 parts by weight, Bayfit 2856-LY, B component polyether compound with 35 parts by weight, A SBU
  • Bayfit HM 1124 purchased from Bayer China (limited)
  • the product has the following properties:
  • Example 8 In an upper mold for preparing a composite mold for a bicycle saddle, a rigid polyurethane was prepared as described in Example 1, but was not demolded, even if it remained in the upper mold; The reaction system described in Example 4, after closing the mold for 10 minutes, was demolded to obtain a bicycle saddle made of the composite material of the present invention. The bicycle saddle combines the properties of the rigid polyurethane and polyurethane soft foam of the present invention.
  • the composite material of the present invention was prepared as described in Example 7 in a circular arc mold, but the rigid polyurethane described in Example 2 and the polyurethane soft foam described in Example 6 were used. A curved composite sheet material is obtained after demolding.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Laminated Bodies (AREA)
PCT/CN2005/001571 2004-09-28 2005-09-26 A polyurethane composite, its preparation and use Ceased WO2006034640A1 (en)

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US11/663,815 US8017229B2 (en) 2004-09-28 2005-09-26 Polyurethane composite, its preparation and use
EP20050791954 EP1818347B1 (en) 2004-09-28 2005-09-26 A polyurethane composite, its preparation and use
JP2007533854A JP4977029B2 (ja) 2004-09-28 2005-09-26 ポリウレタン複合体、その製造方法及びその用途

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CN200410066715.3 2004-09-28
CN200410066715A CN1754914B (zh) 2004-09-28 2004-09-28 聚氨酯复合材料、其制备方法和用途

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WO (1) WO2006034640A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113785024A (zh) * 2019-06-07 2021-12-10 Swimc有限公司 用于薄涂层的聚合物组合物
IT202300006786A1 (it) 2023-04-06 2024-10-06 Maclart S R L Metodo per la realizzazione di selle per biciclette e sella per bicilette così realizzata

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2718561A1 (en) * 2008-04-04 2009-10-08 Bayer Materialscience Ag Photovoltaic solar module
IT1401474B1 (it) * 2010-07-20 2013-07-26 Eni Spa Metodo di monitoraggio e di analisi delle condizioni di una condotta
CN103509170A (zh) * 2012-06-28 2014-01-15 广州静尔音环保科技有限公司 一种新型透明吸音膜材料及其制备工艺
CN103866961A (zh) * 2012-12-13 2014-06-18 飞虎(厦门)聚氨酯制品有限公司 复合材料聚氨酯硬泡装饰罗马柱
JP6179289B2 (ja) * 2013-09-10 2017-08-16 住友電気工業株式会社 ケーブル
TWI697510B (zh) * 2015-09-01 2020-07-01 日商三井化學股份有限公司 緩衝材、塗裝用自動運動裝置用緩衝材、附緩衝材之自動運動裝置及附緩衝材之塗裝用自動運動裝置
CN107099017B (zh) * 2017-05-09 2020-02-04 东莞市普力达光学材料科技有限公司 高密度聚氨酯泡棉及其制备方法、以及泡棉胶带
CN107914357A (zh) * 2017-11-17 2018-04-17 广东东箭汽车科技股份有限公司 一种汽车保险杠的制备方法
CN109180905B (zh) * 2018-07-05 2021-02-05 山东一诺威聚氨酯股份有限公司 低压缩形变高弹性聚氨酯鞋垫组合料及其制备方法
CA3143005A1 (en) 2019-06-26 2020-12-30 Huntsman International Llc Process for making a flexible polyurethane foam having a hardness gradient
CN115651148B (zh) * 2022-11-02 2024-07-02 佳化化学科技发展(上海)有限公司 一种低密度全水发泡聚氨酯硬质泡沫
CN117659334B (zh) * 2023-12-09 2024-05-28 无锡市伟友汽摩配件有限公司 一种聚醚酯型聚氨酯高强度抗撕裂靠背及其制备方法

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1299242A (en) * 1969-04-02 1972-12-13 Universal Oil Prod Co Method of making a polyurethane article having a resilient mass bonded to a rigid structure
JPS6066712A (ja) * 1983-09-21 1985-04-16 日本発条株式会社 クツシヨン体とその発泡成形方法
JPH02257909A (ja) * 1989-03-30 1990-10-18 Aisin Seiki Co Ltd シートのクッション
JPH02286308A (ja) * 1989-04-28 1990-11-26 Araco Corp 異硬度シートパッドの成形方法
JPH03175009A (ja) * 1989-12-05 1991-07-30 Toyo Rubber Chem Ind Co Ltd 車輌用クッション体の製造方法
US5288442A (en) * 1991-07-31 1994-02-22 Skis Rossignol S.A. Process for the manufacture of a complex moulded structure, and especially of a ski
JPH06218738A (ja) * 1993-01-27 1994-08-09 Toyo Tire & Rubber Co Ltd 一体発泡成型品及びその製造方法
US5395580A (en) * 1990-03-14 1995-03-07 Kasai Kogyo Co. Method for fabricating automotive interior components
US5530989A (en) * 1994-12-20 1996-07-02 The Dow Chemical Company Dual durometer handles
JP2001342284A (ja) * 2000-05-30 2001-12-11 Bridgestone Corp エネルギー吸収材及びその製造方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58174701A (ja) 1982-04-07 1983-10-13 Diesel Kiki Co Ltd 油圧アクチユエ−タ装置
GB8825520D0 (en) 1988-11-01 1988-12-07 Powell H D Saddles
JPH0557735A (ja) * 1991-09-04 1993-03-09 Nippon Plast Co Ltd エアバツクカバー及びその製造方法
ITVI980007A1 (it) 1998-01-21 1998-04-21 Selle Royal Spa Selle Royal Sp Metodo per il costampaggio di materie plastiche pemetodo per il costampaggio di materie plastiche per la realizzazione di supporti elastici integralir la realizzazione di supporti elastici integrali, nonche' supporti ottenuti con tale me , nonche' supporti ottenuti con tale me
DE19957397C1 (de) 1999-11-29 2001-07-19 Technogel Gmbh & Co Kg Formkörper aus Polyurethan und Verfahren zu seiner Herstellung
IT1315498B1 (it) * 2000-08-04 2003-02-18 Selle Royal Spa Sella in materiale composito, in particolare per bicicletta e metodoper la sua realizzazione
US6450572B1 (en) 2001-05-04 2002-09-17 Raymond J. Kuipers Total comfort bicycle saddle
JP2003211612A (ja) * 2002-01-23 2003-07-29 Okamoto Ind Inc ウレタン樹脂系表皮材
US6863953B2 (en) 2001-09-13 2005-03-08 Okamoto Industries, Inc. Surface material of urethane resin and a method for preparation thereof
DE10247789A1 (de) 2002-10-14 2004-04-22 Bayer Ag Zellige Polyurethanelastomere, Verfahren zu ihrer Herstellung und ihre Verwendung

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1299242A (en) * 1969-04-02 1972-12-13 Universal Oil Prod Co Method of making a polyurethane article having a resilient mass bonded to a rigid structure
JPS6066712A (ja) * 1983-09-21 1985-04-16 日本発条株式会社 クツシヨン体とその発泡成形方法
JPH02257909A (ja) * 1989-03-30 1990-10-18 Aisin Seiki Co Ltd シートのクッション
JPH02286308A (ja) * 1989-04-28 1990-11-26 Araco Corp 異硬度シートパッドの成形方法
JPH03175009A (ja) * 1989-12-05 1991-07-30 Toyo Rubber Chem Ind Co Ltd 車輌用クッション体の製造方法
US5395580A (en) * 1990-03-14 1995-03-07 Kasai Kogyo Co. Method for fabricating automotive interior components
US5288442A (en) * 1991-07-31 1994-02-22 Skis Rossignol S.A. Process for the manufacture of a complex moulded structure, and especially of a ski
JPH06218738A (ja) * 1993-01-27 1994-08-09 Toyo Tire & Rubber Co Ltd 一体発泡成型品及びその製造方法
US5530989A (en) * 1994-12-20 1996-07-02 The Dow Chemical Company Dual durometer handles
JP2001342284A (ja) * 2000-05-30 2001-12-11 Bridgestone Corp エネルギー吸収材及びその製造方法

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113785024A (zh) * 2019-06-07 2021-12-10 Swimc有限公司 用于薄涂层的聚合物组合物
CN113785024B (zh) * 2019-06-07 2023-08-15 Swimc有限公司 用于薄涂层的聚合物组合物
US12252624B2 (en) 2019-06-07 2025-03-18 Swimc Llc Polymer composition for thin coatings
IT202300006786A1 (it) 2023-04-06 2024-10-06 Maclart S R L Metodo per la realizzazione di selle per biciclette e sella per bicilette così realizzata

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JP2008514460A (ja) 2008-05-08
EP1818347A4 (en) 2011-05-11
EP1818347B1 (en) 2013-07-10
CN1754914B (zh) 2010-05-26
EP1818347A1 (en) 2007-08-15
JP4977029B2 (ja) 2012-07-18
US20080261022A1 (en) 2008-10-23
US8017229B2 (en) 2011-09-13
CN1754914A (zh) 2006-04-05

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