Classifications

• • 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
  • B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
  • B29C41/003—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor characterised by the choice of material
• • 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
  • B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
  • B29C41/02—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
  • B29C41/18—Slush casting, i.e. pouring moulding material into a hollow mould with excess material being poured off
• • 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
  • C08G18/48—Polyethers
  • C08G18/4866—Polyethers having a low unsaturation value
• • 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
  • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
  • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
  • C08G18/6666—Compounds of group C08G18/48 or C08G18/52
  • C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
  • C08G18/6674—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
  • C08L75/04—Polyurethanes
  • C08L75/08—Polyurethanes from polyethers
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B60—VEHICLES IN GENERAL
  • B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
  • B60R13/00—Elements for body-finishing, identifying, or decorating; Arrangements or adaptations for advertising purposes
  • B60R13/02—Internal Trim mouldings ; Internal Ledges; Wall liners for passenger compartments; Roof liners
  • B60R13/0256—Dashboard liners
• • 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
  • C08G2140/00—Compositions for moulding powders
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/249921—Web or sheet containing structurally defined element or component
  • Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
  • Y10T428/24994—Fiber embedded in or on the surface of a polymeric matrix
  • Y10T428/24995—Two or more layers
  • Y10T428/249952—At least one thermosetting synthetic polymeric material layer
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/249921—Web or sheet containing structurally defined element or component
  • Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
  • Y10T428/249987—With nonvoid component of specified composition
  • Y10T428/249991—Synthetic resin or natural rubbers
  • Y10T428/249992—Linear or thermoplastic
  • Y10T428/249993—Hydrocarbon polymer
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
  • Y10T428/269—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension including synthetic resin or polymer layer or component

Definitions

• the present invention relates to resins that are useful for making instrument panel skins used in automobile interiors.
• Vacuum formed instrument panels have a hard "hand” and do not perform cleanly (no shredding or sharding) during -30°C airbag deployment at -30°C Moreover, long term weathering has shown that these products become brittle.
• Spray urethane (aliphatic with inherent light stability and aromatic where a coating is required for weatherability) have less desirable "hand.” Although the spray urethane exhibits property retention after aging and weathering, these materials also exhibit shredding and sharding during -30° seamless airbag deployment.
• Slush molding can utilize PVC and TPU elastomers. Although certain modified PVCs have acceptable unpainted "hand" for instrument panels, the same materials tend to exhibit the same shredding and sharding issues during -30°C seamless airbag deployments.
• the present invention solves one or more problems of the prior art by providing in at least one embodiment an instrument panel skin suitable for automobile interior applications.
• the instrument panel skin comprises residues of a thermoplastic urethane elastomer and a propylene-ethylene copolymer.
• the thermoplastic urethane elastomer includes a polyol, a chain extender, an organic diisocyanate, and a hindered amine light stabilizer and a benzotriazole ultraviolet stabilizing agent.
• the instrument panels of the present invention exhibit both improved touch characteristics while exhibiting acceptable low temperature airbag deployment characteristics.
• a method for forming the instrument panel skin set forth above includes a step of introducing a urethane-based resin composition and a propylene-ethylene copolymer into a mold tool.
• these compositions are in the form of a powder.
• the urethane based resin includes residues of a composition having polyol, a chain extender, an organic diisocyanate, and a hindered amine light stabilizer and a benzotriazole ultraviolet stabilizing agent.
• the urethane based resin composition is heated to a sufficient temperature to form a layer over at least a portion of the mold tool. Excess powder is poured from the mold tool and heating continued if necessary.
• the instrument panel skin is removed from the mold tool.
• FIGURES IA and IB area pictorial flowchart depicting an embodiment for forming an instrument panel skin
• FIGURE 2 is a pictorial flowchart depicting the application of a support structure to an instrument panel skin.
• a pictorial flowchart depicting a slush molding method for forming an instrument panel skin comprises introducing urethane-based resin composition 10 into mold tool 12. At least a portion of mold tool 12 is made from a metal such as stainless steel or nickel.
• Urethane-based resin composition 10 comprises a thermoplastic urethane elastomer composition and a propylene-ethylene copolymer.
• thermoplastic urethane elastomer composition Suitable compositions for the thermoplastic urethane elastomer composition are the light stable aliphatic thermoplastic urethane elastomers set forth in U.S. Patent Nos.
• the thermoplastic urethane elastomer includes residues of a composition having a polyol and an organic diisocyanate.
• the thermoplastic urethane elastomer includes a chain extender.
• the urethane base resin further includes a hindered amine light stabilizer and/or a benzotriazole ultraviolet stabilizing agent.
• urethane based resin composition 10 is heated to a sufficient temperature to form layer 14 over at least a portion of mold tool 12. In one refinement, urethane based resin composition 10 is heated to a temperature between about 170° C and 250° C.
• step c) powder is poured out from mold tool 12. Mold is further heated if necessary so that all the powder melts.
• instrument panel skin 20 is removed from mold tool 12 is step e). Typically, instrument panel skin 20 has a thickness from about 0.5 mm to about 2 mm.
• Urethane-based resin composition 10 optionally includes one or more pigments.
• the pigments are present in an amount from about 0.2 to about 10 weight percent of the total weight of the urethane-based resin composition.
• mold tool 12 has a texture surface that contacts urethane-based composition 10 to impart a texture surface onto instrument panel skin 20.
• a flowchart showing the application of a backing to instrument panel skin 20 is provided.
• structural component 22 is applied to instrument panel skin 20.
• Such structural components are applied by any number of methods known to those skilled in the art.
• structural component 22 has a thickness from about 2 mm to about 20 mm.
• foam resins such as Dow Specflex NM815 are utilized.
• skin 22 may be placed in a mold that provides a predetermined shape and a urethane backing sprayed over the back of instrument panel skin 20.
• structural component 22 can be molded onto instrument panel skin 20. In such circumstances thermoplastic resins may be used.
• instrument panel skin 20 comprises the residues of urethane -based resin composition that includes thermoplastic urethane elastomer composition and a propylene-ethylene copolymer.
• the propylene-ethylene copolymer used in the present embodiment is characterized by a number of physical characteristics.
• the propylene-ethylene copolymer has a total crystallinity less than about 20 %.
• the propylene-ethylene copolymer has a flexural modulus (1% secant) from about 1500 psi to about 2500 psi and a Shore A hardness from about 40 to about 80 (ISO 898 ASTM D2240 ).
• propylene-ethylene copolymers examples include, but are not limited to the VersifyTM line or elastomers commercially available from The Dow Chemical Company. VersifyTM 2400 is found to be particularly useful.
• the propylene-ethylene copolymer is present in an amount from about 1 to 25 weight percent of the urethane-based composition.
• the propylene-ethylene copolymer is present in an amount from about 5 to 20 weight percent of the urethane-based composition.
• the propylene-ethylene copolymer is present in an amount of about 20 % weight percent of the urethane-based composition.
• the instrument panel skins of the present invention are found to have significant heat stability.
• the elongation properties are found to vary by less than 10% after 500 hours aging at 120° C.
• the instrument panel skins maintain sufficient elongation to pass a -30°C seamless airbag deployment test before and after heat aging 400 hours at 107°C.
• the instrument panel skins have a combination of low glass transition temperature and retained elongation greater than about 100% after aging for 500 hours at 120° C .
• the operation of the present invention is not limited to any particularly theory, it is believed that the use of the propylene-ethylene copolymer at least partially responsible for these properties.
• the thermoplastic skin of the present invention includes the residues of a polyol.
• Suitable polyols are disclosed in U.S. Patent Nos. 5,824,738 and 6,187,859. Specific examples, include, but are not limit to polyether polyols.
• the polyol is formed in a process utilizing an organometallic catalyst that results in a polyol having a low level of terminal unsaturation.
• the polyol has a level of terminal unsaturation less than about 0.04 meq/g. In another refinement, the polyol has a level of terminal unsaturation less than about 0.02 meq/g.
• polyol is Poly L 255-28 (sold by Olin corporation, Stamford, Connecticut).
• Poly L 255-28 is a ethylene oxide capped poly (propylene oxide) polyol with an approximate molecular weight of 4000 and a hydroxyl number of 28.
• the polyol component can be present in amounts ranging from approximately 40% to 70% of the total weight of the thermoplastic urethane elastomer composition, in a refinement, the polyol is present in an amount between 40% and 60% of the total weight of the thermoplastic urethane elastomer composition. The amount of polyol is adjusted in this range to vary the hardness of the elastomer produced.
• the thermoplastic urethane elastomer composition includes a chain extending agent.
• Suitable chain extending agents include aromatic secondary or aliphatic primary or secondary diamines, ethylene glycol, diethylene glycol, propylene glycol, pentane diol, 3-methylpentane-l,5-diol, hexane diol, HQEE [hydroquinone bis(2-hydroxyethyl) ether], CHDM (1,4-cyclohexanedimethanol), and HBPA (hydrogenated bisphenol A).
• a particularly useful chain extender is 1,4-butanediol.
• such chain extenders are present in concentrations varying from 6 weight % to 15 weight % of the total weight of the thermoplastic urethane elastomer composition. In another refinement, the chain extenders are present in an amount from 7% to 13% of the total weight of the thermoplastic urethane elastomer composition.
• the thermoplastic urethane elastomer composition used in the present embodiment includes one or more isocyanates.
• Suitable isocyanates include aliphatic organic diisocyanates, or mixture of diisocyanates.
• organic isocyanates include, but are not limited to, (TMXDI) meta-tetramethylxylene diisocyanate and paratetramethylxylene diisocyanate, isophorone diisocyanate (IPDI), dibenzyl diisocyanate, xylene diisocyanate (XDI), 3, 3'-bis toluene-4,4-diisocyanate, hexamethylene diisocyanate (HDI), hydrogenated MDI, hydrogenated XDI, cyclohexane diisocyanate, paraphenylene diisocyanate, mixtures and derivatives thereof and the like.
• TXDI meta-tetramethylxylene diisocyanate and paratetramethylxylene diiso
• the organic diisocyanates are present in an amount from 20 weight % to 50 weight % of the total weight of the thermoplastic urethane elastomer composition. In another refinement, the organic diisocyanates are present in an amount from 25 weight % to 40 weight % of the total weight of the thermoplastic urethane elastomer composition.
• the thermoplastic urethane elastomer composition may include an ultraviolet stabilizing agent.
• Suitable ultraviolet stabilizing agents may include a combination of a hindered amine light stabilizers (HALS) and a benzotriazole.
• HALS include, but are not limited to, bis(l,2,2,6,6-pentamethyl-l-4-piperidinyl) sebacate (Chemical Abstract Number 41556-26-7, also known as Tinuvin 292 or 765 Ciba-Geigy Corp., Hawthorne, NY).
• benxotriazoles examples include hydroxyphenyl benzotriazoles such as a benzotriazole mixture of poly (oxy-l,2-ethanediyl), alpha- [3-[3- (2H-benzotriazol -2-yl)-5 -( 1 , 1 -dimethylethyl)-4-hydroxyphenyl] - 1 -oxopropyl] -omega-hydroxy- and p o l y ( o x y - l , 2 - e t h an e d i yl ) , a l p h a - [ 3 - [ 3 - ( 2 H - benzotriazol-2-yl)-5-(l,l-dimethylethyl)-4-hydroxyphenyl]- l-oxopropyl)-omega-[3-[(2H-benzotriazol-2-yl)-5-(l,
• the combination of ultraviolet stabilizing agent are present in a ratio in a range of approximately 1 : 1 to 2:1 by weight.
• the total concentration of ultraviolet stabilizing agents are present in an amount from about 0.5 to 2.0 weight %, of the total weight of the urethane elastomer composition.
• the urethane elastomer composition includes an antioxidant.
• an antioxidant any suitable antioxidant, or mixture of antioxidants, may be used in the practice of the present invention.
• Representative examples include, but are not limited to, Irganox 1010 [tetrakis (methylene(3,5-di-tert-butyl-4-hydroxycinnamate)] methane from Ciba-Geigy; Irganox 1076 [Octodecyl 3,5 di-tert-butyl-4-hydroxyhydrocinnamate] from Ciba-Geigy; I r g a n o x 2 4 5 [ E t h y l e n e b i s ( o x y e t h y l e n ) bis-(3-tert-butyl-4-hydroxy-5-methylhydrocinnamate)] from Ciba-Geigy; and Vanox
• the antioxidants may be present at a total concentration in a range of approximately 0.10 weight % to 1.0 weight % of the total weight of the urethane elastomer composition. In another refinement, the antioxidants may be present at a total concentration in a range of approximately 0.25 weight % to 0.75 weight % of the total weight of the urethane elastomer composition.
• Table 1 provides the compositions of several test samples that were used to form skin layers via a slush molding process as set forth above. The components are blended together in a Leistritz twin screw extruder. The resulting pellets are cyrogenically ground into a powder, dried, and molded into test panels using a Ford random square grain tool. Table 2 provides the properties of skins made from the test compositions. The aacct Elongation at break is after 500 hrs at 120 C. Table 1. Sample compositions

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Mechanical Engineering (AREA)
• Polyurethanes Or Polyureas (AREA)
• Moulding By Coating Moulds (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Instrument Panels (AREA)
• Laminated Bodies (AREA)
• Air Bags (AREA)

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• 2008
  • 2008-04-15 US US12/103,526 patent/US7833623B2/en active Active
• 2009
  • 2009-02-06 CA CA 2721436 patent/CA2721436C/en not_active Expired - Fee Related
  • 2009-02-06 WO PCT/US2009/033396 patent/WO2009128975A1/en not_active Ceased
  • 2009-02-06 CN CN200980113314XA patent/CN102083911A/zh active Pending
  • 2009-02-06 EP EP20090731621 patent/EP2274380A1/en not_active Withdrawn
  • 2009-02-06 MX MX2010011214A patent/MX2010011214A/es active IP Right Grant
  • 2009-02-06 JP JP2011505044A patent/JP5666426B2/ja not_active Expired - Fee Related
  • 2009-02-06 KR KR1020107025438A patent/KR101243179B1/ko not_active Expired - Fee Related

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