CA2031863C - Fiber-reinforced foamed material and method of producing it - Google Patents

Fiber-reinforced foamed material and method of producing it

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Publication number
CA2031863C
CA2031863C CA002031863A CA2031863A CA2031863C CA 2031863 C CA2031863 C CA 2031863C CA 002031863 A CA002031863 A CA 002031863A CA 2031863 A CA2031863 A CA 2031863A CA 2031863 C CA2031863 C CA 2031863C
Authority
CA
Canada
Prior art keywords
component
fiber
composite
foamed
reinforced
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 - Fee Related
Application number
CA002031863A
Other languages
French (fr)
Other versions
CA2031863A1 (en
Inventor
Setsuo Taguchi
Miyoshi Okamoto
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Publication of CA2031863A1 publication Critical patent/CA2031863A1/en
Application granted granted Critical
Publication of CA2031863C publication Critical patent/CA2031863C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • C08J9/0085Use of fibrous compounding ingredients
    • 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
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/302Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
    • 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
    • B32B27/42Layered products comprising a layer of synthetic resin comprising condensation resins of aldehydes, e.g. with phenols, ureas or melamines
    • 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
    • B32B5/02Layered 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 structural features of a fibrous or filamentary layer
    • B32B5/024Woven fabric
    • 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
    • B32B5/22Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
    • B32B5/24Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
    • B32B5/26Layered 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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
    • 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
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/227Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
    • D06M15/233Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated aromatic, e.g. styrene
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/41Phenol-aldehyde or phenol-ketone resins
    • 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
    • B32B2266/0221Vinyl resin
    • B32B2266/0228Aromatic vinyl resin, e.g. styrenic (co)polymers
    • 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
    • B32B2266/0285Condensation resins of aldehydes, e.g. with phenols, ureas, melamines
    • 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
    • B32B2307/738Thermoformability
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/902High modulus filament or fiber
    • 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
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/24994Fiber embedded in or on the surface of a polymeric matrix
    • 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.]
    • 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.]
    • Y10T428/249982With component specified as adhesive or bonding 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.]
    • Y10T428/249982With component specified as adhesive or bonding agent
    • Y10T428/249985Composition of adhesive or bonding component specified
    • 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.]
    • Y10T428/249986Void-containing component contains also a solid fiber or solid particle
    • 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
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2929Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
    • 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
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2929Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
    • Y10T428/2931Fibers or filaments nonconcentric [e.g., side-by-side or eccentric, etc.]
    • 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
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/2964Artificial fiber or filament
    • Y10T428/2967Synthetic resin or polymer
    • 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
    • Y10T428/30Self-sustaining carbon mass or layer with impregnant or other layer
    • 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
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/30Woven fabric [i.e., woven strand or strip material]
    • Y10T442/3146Strand material is composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
    • Y10T442/3154Sheath-core multicomponent strand material
    • 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
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/30Woven fabric [i.e., woven strand or strip material]
    • Y10T442/3325Including a foamed layer or component
    • Y10T442/3366Woven fabric is coated, impregnated, or autogenously bonded

Abstract

Disclosed is a fiber-reinforced foamed material compris-ing a foamed body of a resin having a flexural elasticity modulus not smaller than 150 kg/mm2, reinforcement fibers, and a bonding component through which the reinforcement fibers are integrated with the foamed body so as to reinforce the foamed body. At least a part of the reinforcement fibers are in the form of a composite fibrous material having a first component serving as the bonding component and a second component serving to reinforce the body. Also disclosed is a method for producing the fiber-reinforced foamed material which comprises the steps of: providing a foamable material and the composite fibrous material in the form of composite fibers and/or composite yarns each having the first component and the second component; and allowing the foamable material to foam together with the composite fibers or composite yarns at an appropriate tempera-ture, whereby the first component is thermally deformed or melted to serve as the bonding component, while the second component remains as the fibrous reinforcement component.

Description

FIBER-REINFORCED FOAM MATERIAL AND
METHOD OF PRODUCING IT

The present invention relates to a fiber-reinforced foamed material and a method of producing it. More particularly, the present invention relates to a fiber-reinforced foamed material which exhibits high resistance both to impact and flexing, as well as ~xcellent shape maintaining characteristics and which is produced by allowing a foamable material capable of forming a highly rigid foamed body to foam together with specific composite fibers and/or specific composite yarns as reinforcers.
Hitherto, foamed materials such as those of poly~y~ene and phenol resin, which generally exhibit small distortion against external force and, hence, superior shape maintaining characteristics and ~;~?n~ional stability, have been widely used as packaging materials for packaging various household electric appliances and precision instruments, materials of cooler boxes and heat-insulating architectural materials.
These known foamed materials, on the other hand, generally exhibit small resistance to stresses caused by application of an impact, bending or flexing. Thus, these foamed materials are liable to be cracked or bent even by a slight deformation, often resulting ln f--'~

2031~63 destruction of the structures made from such foamed materials. For these reasons, the known foamed materials have been considered as being unsuitable for use as materials which are expected to undergo strong impact or deforming forces caused by ben~;ng or torsion. Thus, the known foamed materials have a limited use despite the above-mentioned advantages.
For instance, foamed polystyrene, which is widely used for packaging household electric appliances cannot be used alone since the packaging material tends to be broken by an impact to allow damaging of the contents or to generate dust or fractions of the foamed material during transportation. In order to obviate such problems, it has been a common measure to use anothe~
material such as a corrugated board together with the foamed material such that the formed material is coated and reinforced by the other material, or to increase the thickness of the foamed material. All these countermeasures require laborious steps in the production process and raise costs for transportation and storage due to increase in the size and weight.
It has also been proposed to use a composite material in which a polystyrene foamed material is reinforced with another plastics material. Such a composite material, however, is generally too hard, heavy and expensive and, hence, is not preferred.

Methods have also been proposed in which a foamed material is reinforced with fibers mixed therein, as disclosed, for example, in JP-C-47-28097 and JP-A-48-100471. These methods, however, cannot provide a substantial reinforcement effect because of insufficient affinity or integration between the reinforcement fibers and the foamed material. Thus, these methods also are still unsatisfactory.
Referring now to foamed materials of a phenol resin, attempts have been made to apply this type of material to architectural materials, since this type of material exhibits high resistAnce~ to heat and fire, in additio~
to the ~r.P.l lent shape maint~;n;ng characteristics and ~;mensional stability mentioned before. Foamed materials of phenol resins, however, are generally fragile and easily collapsible, which make this type of material difficult to work and finish. In order to overcome this problem, measures have been taken such as laminating paper sheets on obverse and reverse sides of the foamed material or using a honeycomb structure with cells in which the resin foams. Such measures also are laborious and expensive. In addition, dropping of edges and fracturing into powder are liable to occur with this type of material during nail driving and cutting at the construction site. Thus, the aforesaid problems still remain unsolved.

Thus, attempts have been made to improve r~ch~nical performance or shape maint~;n; ng characteristics, as well as ~;~en~ional stability, by strengthening the foamed material with fibers. Unfortunately, however, these attempts could not provide satisfactory reinfo~ce"lent effect due to insufficient integration between the foamed material and the fibers after the foaming. This is attributable to the fact that the temperature at which the fibers can be thermally de~ormed or become molten is generally much higher than the temperature at which the resin is allowed to foam. It would be possible to use a fiber which is thermally deformed or molten at a t~mp~rature below the foaming temperature. Such a fiber, however, cannot make any contribution to the reinforcement because the fiber itself can no longer have strength after the foaming.
Low-rigidity polymers such as polyethylene and polypropylene exhibit high resist~nce~ to ben~ing and torsion by virtue of their excellent stretchability. A
composite material having improved strength and dirensional stability would be obt~in~hle by reinforcing such low-rigidity polymer with fibers. The low rigidity of the foamed material, however, allows an easy deformation of the foamed material. In such a composite material, the foamed resin is first deformed to leave stresses which are borne by the fibers. Such a composite material, therefore, cannot exhibit superior shape maintR;n;ng characteristics and fl;~e~cional stability, and no appreciable reinforcement effect is produced.
The behaviour of this type of material under a flexural stress will be described by way of example.
When a bPn~i ng force is applied to a material, tensile stress is generated in one side while compression stress is produced in the other side. A foamed material under a flexural stress, when the rigidity is low, is first buckled at the compressed side. Thus, the reinforcement effect of the fibers is developed only after such a buckling. It will be seen that the fibers cannot make any contribution.
Under such circumstances, we conducted investigations in an attempt to solve the abovementioned difficulties and, in particular, to provide a fiber-reinforced foamed material in which the fibers impart superior mechanical properties and excellent shape maintA;n;ng characteristics.
Surprisingly, we found that, by incorporating in the foamed material a special composite fibrous material, the abovementioned difficulties can be ~; n; m; sed or overcome without necessarily including additional materials for providing a unitary fiber-reinforced foamed material.
Thus, according to one aspect of the present invention, there is provided a fiber-reinforced foamed 6 20~1863 ~ ~ ~ 66623-191 material comprising (1) a foamed body of a resin having a 1exural elasticity modulus not smaller than 150 kg/mm2, (2) reinforcement fibers, and (3) a bonding component through which the reinforcement fibers are integrated with the foamed body so as to reinforce the foamed body, wherein at least some of the reinforcement fibers are provided by a composite fibrous material in the form of composite fibers and/or composite yarns, the composite fibrous material having a first component which has been thermally deformed or melted by heat applied during the foaming so as to serve as the bonding component and a second component which remains fibrous so as to reinforce the foamed body.
According to another aspect of the present invention, there is provided a method for producing a fiber-reinforced foamed material comprising the steps of: providing a foamable material and a composite fibrous material in the form of composite fibers and/or composite yarns each having a first component and a second component; and allowing the foamable material to foam together with the composite fibers or composite yarns at a temperature at least about 10C higher than the thermal deforma-tion temperature or melting temperature of the first component and at least about 20C lower than the thermal deformation temperature or melting temperature of the second component, whereby the first component is thermally deformed or melted to serve as a bonding component, while the second component remains as a fibrous reinforcement component, the fibrous reinforcement component being integrated with the foamed body through the bonding component so as to reinforce the foamed body.

20318~3 The method set forth above utilizes the reinforcement fibers in the form of composite fibers and/or composite yarns.
The composite yarns may be formed from different fibers, one being the first and another being the second component, or may be formed from the composite fibers.
The fibers or yarns may be randomly distributed within the foamed resin matrix, or may be aligned with one another.
However, preferably at least some of the reinforcement fibers may be formed from the composite fibrous material in the form of a cloth formed from such composite fibers or yarns. The composite fibers and/or composite yarns may be disposed on the surface of the foamed body and/or inside the foamed body, so as to reinforce it.
Preferably a fabric is provided at least at the surface of the fiber reinforced foamed material. The fabric may be, for example, a double knit construction in which the inner layer is knitted from the above-mentioned composite fibers or yarns so as to provide a strong bonding with the foamed body while the outer layer is knitted from fibers (not necessarily composite fibers as described above) and with a construction such that the outer layer provides the reinforced foam material with the desired properties, for example, waterproofing, decoration, etc.
Alternatively, the surface may be of a non-woven material, in which case, the outer surface of the fiber rein-forced foamed material may be shaped by pressing y~

20318~3 against a wire net, for example by placing the wire net around the internal periphery of a mould, placing the non-woven fabric on the net and then allowing the foamed material to expand within the mould.
By the use of the composite fibrous material described above, it is possible to provide fiber-reinforced foam materials embodying the invention in which the fiber reinforcement can impart superior mechanical properties and excellent shape maint~ining characteristics to the foamed material without necessarily including other materials for improving bonding (though in fact, the material may still be particularly compatible with certain conventional adhesives where, for example, the fiber-reinforced foamed material is to be adhered to another material in a laminate structure).
Thus, we find that fiber-reinforced foamed materials embodying the invention are useful in fields in which impacts and other dynamic forces which could never be sust~ine~ by known materials are expected to be applied, such as architectural and civil engineering materials, e.g., soil retainers and other civil engineering materials, building materials in general, partitions (for example in offices), furniture, waterproof protecting plates, heat-insulating materials, especially for use in refrigerators and air conditioners, automotive interior - 2031863 . ~
g materials, packaging materials, and sports and general merch~n~i~e goods.
It is possible to obtain extremely lightweight materials which are especially ~ro~o~ical to manufacture and which can serve as an excellent repl~c~snt for wood in many of the above uses.
The fiber-reinforced foamed material according to the present invention exhibits a very high strength which widens the use of this material. For instance, the fiber-reinforced foamed member of the present invention can be used as the materials of various off-shore facilities such as airports, pontoon bridges, tennis courts, golf links and playgrounds.
Where, as mentioned above, at least some of the reinforcing fibers are used in the form of a cloth comprising the composite fibers and/or yarns, it i8 possible to effect a suitable decorative treatment on the surface of the foamed material. It is therefore possible to obtain products which are superior in all the aspects of appearance, m~ch~n;cal properties and waterproofing which could never be met simultaneously by known materials. Indeed, since the material may be provided with a highly waterproof surface they may find particular use as ~;n;ngs for refrigerators and air conditioners and as swimming aids, for example safety rings to be worn or grasped by a swimmer.

`~ 2031863 1~ .
A packaging material made of a fiber-reinforced foamed material of the present invention can be used directly for transportation of goods without any risk of damaging these goods and without the aid of any additional material such as corrugated board sheets. The elimination of other materials reduces the production cost. Transportation and storage costs also are reduced thanks to reduction in the size.
From the above, it can be seen that we have succeeded in m; ni ~; ~ing or overcoming the problems of conventional foamed, fiber-reinforced materials, i.e., insufficiency of the reinforcement effect produced by the fibers, by reinforcing a foamed material of a high-rigidity polymer with specific composite fibers or 2 cloth of the specific composite fibers.
Typically, a method embodying the present invention can be carried out by mi X; ng, in a specific high-rigidity polymer, a specific composite fiber and/or a cloth of such a composite fiber (referred to collectively as a composite fiber/cloth), with at least one component thereof being sufficiently drawn in the fiber axis direction so as to develop a high fiber strength, while at least one other component is sufficiently thermally deformable or meltable at the foaming temperature.
When a mixture of such foamable material and specific composite fiber/cloth is subjected to a foaming treatment, at least one component of the composite fiber/cloth is thermally deformed or be~- ?S molten so as to serve as a bond so that the composite fiber/cloth i8 integrally bonded to the foamed material by the energy produced during foaming. Meanwhile, at least one component of the composite fiber/cloth keeps the fibrous form so that any externally applied stress is shared by the foamed material and the composite fiber/cloth.
Using a method embodying the present invention it is possible to provide a fiber-reinforced foamed material having remarkably improved tensile strength, impact strength, flexural strength and torsional strength, while maint~;n;ng ex~ellent shape maint~;n;ng characteristics and dimensional stability, by virtue of the above-described reinforcing mPchanism.
The invention will now be described in more detailwith reference to the ~c~o~panying drawings in which Figs. 1 to 7 are schematic cross-sectional views of models of the composite fibers which can be used in a fiber-reinforced foamed material embodying the present invention. As will be explained later, the composite fibers 1 have core components 2, 2' and sheath components 3.
The fiber-reinforced foamed material of the present invention comprises, mainly, preferably at least two portions: namely, the foamed body and composite fibers which contribute to reinforcement. The composite fiber also has two portions: namely, a thermally-deformable or meltable portion (referred to hereinafter as a "first component") which exhibits a semi-fibrous or non-fibrous state after the foaming treatment and a fibrous portion (referred to hereinafter as a "second component") which re~; ns in the fibrous sta~e after the foaming treatment so as to contribute to the reinforcement.
The ratio between the foamed portion (P) and the composite fiber portion (F) is not limited. However, we have found that good results can be obtained when the ratio P/F in terms of weight ratio ranges between 99/1 and 30/70.
To achieve the objects of the invention, i.e., to attain high ~ech~n;cal properties and shape maint~; n; ng characteristics without impairing shape maintaining characteristic and dimensional stability, a polymer having a high rigidity is used as the foamable resin.
More specifically, the polymer suitably used has a flexural elasticity modulus which is at least about 150 kg/mm2, more preferably at least 200 kg/mm2. Thus, advantages of the present invention are not ~rromplished with low-rigidity polymers whose flexural elasticity modulus values are below 150 kg/mm2. In this specification, therefore, polymers having flexural rigidity of 150 kg/mm2 or higher will be referred to as high-rigidity polymers, while polymers of flexural elasticity modulus values below 150 kg/mm2 will be referred to as low-rigidity polymers. The values of the flexural elasticity modulus shown in this specification are those measured by a method specified in ASTM-D790.
Preferred examples of such high-rigidity polymers are polymers having at least one benzene ring in monomer units thereof, for example pol~ylene resin and phenol, especially phenol formalin, resins. Other examples of the high-rigidity polymers are thermoplastics or thermosetting foamable resins contA;n-ng, one, two or more of styrene-ethylene copolymers, acrylonitrile-styrene copolymers, acrylonitrile-butadiene-styrene (ABS ?
resins and phenol/urea formaline co-condensation resins.
The reason why a polymer having a benzene ring is preferably used in this invention is that this type of polymer generally exhibits high rigidity even $n amorphous or non-crystalline state and that the foamed product exhibits high shape maint~;n;ng characteristics and ~;men~ional stability. The high rigidity of the foamed material enables the tensile or compression stress to be borne simultaneously by the foamed material and the fibers, thus ensuring a high reinforcing effect.
Preferably, the second component of the composite fiber, which remains fibrous even after the foaming treatment, has been subjected to a drawing in the fiber ~031~63 axis direction at a sufficiently large drawing ratio to develop a high degree of orientation and strength. It is also preferred that this material exhibits an extremely small degradation in strength against heat applied during the foaming. More specifically, the second component alone should have a fiber strength which is at least about 2 g/d (about 2.2 dtex), more preferably at least 3 g/d (about 3.3 dtex). It is also preferred that the second component has a melting point which is not lower than 125C. More preferably, high-melt point polymers of 160~C or higher, especially 200C or higher, are used as the second co ~,oll~nt. Various spinnable polymers can suitably be used as the second component. Examples of such polymers are polyesters represented by polyethylene terephthalate and polyamides represented by nylon 6 and nylon 66, polyallylate, polypropylene, high density polypropylene, copolymeric denaturated compounds of these polymers and mixtures of these polymers with other compounds. One, two or more of the polymers mentioned above are selectively used in accordance with conditions such as the combination of the foamable material and the first ~o...pollent, foaming treatment temperature, use of the fiber-reinforced foamed material and so forth.
On the other hand, the first component serves as ~
bonAing component which ensures integration between the foamed material and the fibers. To this end, the first 2031~63 component must be thermally deformed or made molten by the application of heat during foaming. It is also preferred that the first component exhibits high bondability and compatibility with the foamed material.
This may be achieved by using, as the first component, a copolymer cont~ining a monsm~r unit present in the foamed material.
However, polymers which do not have the same ~onomPr unit as the foamed material can well achieve desired advantages of the invention provided that they can develop a large frictional force or anchoring effect between these polymers and the foamed material due to thermal deformation or melting so as to prevent dropping or slip of the fibers.
Preferably, the selection of the first and second components is conducted in a manner such as to meet the following conditions.
(1) (MD of ~irst component+10C) < foaming treatment temp.
(2) (foamin~ treatment temp.+50C) < MD of second component (3) (MD of first component+70C) < MD of second component ( 4 ) ( MD of foamed material+50C) < MD of second component In this specification, regarding the first component and the foamed material, the glass transition temperature as measured in accordance with ASTM-D3418 is recited as 2~31863 MD, and regarding the second ~omron~nt, MD means the melting point temperature as measured by the method specified in ASTM-D3418.
As will be seen from the conditions (1) to (4) shown above, the temperature difference between the first component MD and the foaming treatment temperature i8 preferably at least 10C, more preferably 20C or greater, in order that a sufficient bonding effect i8 developed by thermal deformation or melting of the first component as a result of the foaming treatment. It is also preferred that the temperature difference between the MD of the second component and the foaming treatment temperature is 20C or greater, more preferably 50C or greater, especially 80C or greater, in order to minim;ze reduction of the degree of orientation of the 8~CO~
~ol.,pollent, i.e, any reduction in the strength, caused by the heat applied during the foaming treatment. For the same reasons, the MD of the second component is preferably at least 70C, more preferably at least 90C, greater than the MD of the first component. The MD of the second component is preferably at least 50C, more preferably at least 70C, greater than the MD of the foamed material.
In order to obtain simultaneously both good formability of the foamed material and strong bo~Al~g power of the first component, it is preferred that the 2031~63 first component has a thermal deformation temperature or melting point which is at least 10C lower than the MD o$
the foamed material.
It is important that the combination of the polymers of the first and second components is determined to enhance the reinforcing effect by minimizing any reduction in the strength of the second component. Thi~
requires that the polymers of the first and secon~
~smpon~nts are selected to m~xl m; ze the difference in th~
thermal deformation temperature or the melting poin~
between both components. The polymers of both components may be of the same component system or of differen~

~y:j ~IIIS .
Thus, various polymers are selectable as the firs~
and ~-co~ ~o~,o,-ents provided that the above-mentione~
conditions are met.
When the first component is a polymer which contains the same ~onomer unit as the foamed material, two methods are available for lowering the MD of the first oo",~ol~ent down below the foaming treatment temperature: namely, a so-called internal plasticizing method in which a component capable of reducing the MD is formed by copolymerization and a so-called external plasticizing method in which a plasticizer is mixed with the first component.
The internal plasticizing method will be described with reference to the case where the foamed member is a styrene type polymer. A copolymer which reduces the MD
of the first component is obta1ne~ by copolymerizing the styrene type polymer with high-grade alcohol ester of acrylic acid and/or methacrylic acid. Examples of the styrene type polymer are poly~y~ene, styrene-ethylene copolymer and/or acrylonitrile-styrene copolymer. The alcohol component of the thus-obtained copolymer preferably has from 2 to 20, preferably 4 to 16, carbon atoms inclusively, considering the effect of reducing the MD and ease of fiber sp; nn~ ng. It is also preferred that the alcohol component has a side chain. The amount of (meth)acrylate, by weight of the total weight of the copolymer of (meth)acrylate and styrene type polymer is from 5 to 50 wt%, more preferably 10 to 30 wt% inclusive.
The external plasticizing method will also be explained with reference to a case where the foamed member is a styrene type polymer. Examples of plasticizer suitably used are arylenemethyl oligomer, butene oligomer, saturated high grade fatty acid ester, dibutylphthalate, diamylphthalate, dioctylphthalate, styrene oligomer, triphenylphosphate, tricresylphosphate, phenylstearylalcohol, diisoamylnaphthalene, trioctylbutanecarboxylate, methlydibutylbutane-tricarboxylate, triallylbutanetricarboxylate, and liquidparaffin. It is also possible to use 4,4'-~ 2031863 19dialkyldiphenylparaffins, 4-alkyldiphenylethanes, 4-n-butylphenylparaffins and ~ '-diphenylparaffins. One, two or more o the above-mentioned plasticizers are selectively used according to the purpose of use of the product. Considering the effects such as bondability to the foamed material and reduction in the MD, as well as ease of spinni~g of composite fibers, the amount of plasticizer to be added preferably ranges between 5 and wt%, more preferably between 10 and 30 wt%, inclusively, with respect to the poly-mer.
Needless to say, the invention does not exclude simultaneous use of the internal and external plasticizing methods.
As to the case where the polymer does not have the same monomer unit as the foamed material, we have found that a remarkable reinforcement effect by fibers can be obtained by using, when the fiber-reinforced foamed material comprises polys~y ene (optimum foaming treatment temperature 110C), a polyester thermally deformable at low temperature (acid component: terephthalic acid/isophthalic acid = 60/40 (mol ratio), glycol component: ethylene glycol, thermal deformation temperature: 75C) as the first componènt and polyethylene terephthalate (melting point: 265C) as the second component. A combination of a phenol resin (novolak type: optimum foaming treatment temperature 2~3~8~3 150C) as the foamed material, polyethylene as the first component and polyethylene terephthalate as the second component, as well as a combination of a phenol resin (resol type: optimum foaming treatment temperature 90C) as the foamed material, a poly~ylene copolymer as the first component and nylon 66 as the second component, can also be used suitably. These combinations remarkably improve the form maintaining characteristics of the product.
Various types of composite fibrous material are usable in methods embodying the invention, such as core/sheath type, bimetal type, multi-layer bonding type and radial multi-layered type composite fibrous structures, and composite fibers of these types are especially preferred. Among these types of composite fibers, a multi-core/sheath type composite fiber, having a multiplicity of core components in a sheath component, is used most preferably because this type of fiber exhibits a greater tP~en~y to integrate with the foamed material due to presence of bonding components among the multiplicity of cores.
Preferably, the first component of the composite fiber is arranged on the outer periphery or in the outer shell of the composite fiber. For instance, the first component is disposed in the sheath component in the cases of core/sheath type fibers shown in Figs. 1, 2 and 3. In composite fibers of bimetal type or multi-layer bo~Aln~ type as shown in Figs. 4, 5, 6 and 7, the first component may be disposed in either region, although it is preferably disposed in a portion where it has a large area exposed to the outside of the composite fiber.
There is no restriction in the size of the composite fiber, provided that the fiber can provide the re~uired reinforcement effect. In general, the diameter of the composite fiber preferably ranges from 0.1 to 1000 deniers inclusive (0.11 to llO0 dtêx). In the case of multi-core/sheath type fibers, the diameter of the core fiber preferably ranges between 1/3 and 1/1000 the diameter of the composite fiber. The number of cores in such a composite fiber preferably ranges from 3 to 10000 inclusive, more preferably from 10 to 1000 inclusive.
Figs. 2 and 3 show multi-core/sheath type composite fibers. In Figs. 2 and 3, numerals 2 and 2' denote core components, while 2 designates a sheath component.
Multi-core/sheath type composite fibers can produce an appreciable effect even when they have a multiplicity of core elements of the same type, though two or more types of core elements 2 and 2' are preferably used.
Various combinations of first type of core elements/second type of core elements/sheath elements are 2031~63 usable when a styrene type polymer is used as the foamed material. For instance, a combination of nylon/polyethylene terephthalate/styrene-2-ethylhexylacrylate copolymer, a combination of nylon 6/polybutylene/terephthalate/styrene-2-ethylhexylacrylate copolym e r, and a combination of nylon 6/polyallylate/styrene-stearylacrylate can be used according to the purpose or use. There is no limitation as to the numbers of the core elements of the first and second types, nor in the composition ratios. The core elements of the first and second types can have equal or different sizes. It is also possible to use different sizes of core elements in each type.
Although a composite fiber obtAine~ by composite sp; nn; ng has been specifically mentioned, it is possible to use mix-filament yarns or double and twist yarns formed from polymers which are mentioned before as materials of the core elements, sheath component or fibrous comronents. For instance, the reinforcer used in a material embodying the present invention may be a composite yarn formed from fibers or yarns of the first component material and fibers or yarns of the second component material.
It is not essential that the reinforcer be in the form of loose fibers or in the form of yarns. Thus, in a fiber-reinforced foamed material embodying the present invention, at least a part of the reinforcement may be provided by a cloth formed from the above-mentioned composite fibers and/or composite yarns arranged on the outer surface of, and/or inside, the foamed portion. In such a case, the foamed portion (P) and the cloth portion (H) may be laminated in various forms, such as P/H/P, H/P/H, P/H/P/H or P/H/P/H/P. In this laminate structure, when the cloth is disposed on one surface of the foamed material, the first component may provide a film or a plastics layer so as to provide a surface having a particular desired nature such as a smooth surface, decorative surface with patternized convexity and concavity and even a surface which permits clear printing of characters or patterns, unlike the conventional foamed material in which beads of the foam are exposed to provide a rough surface. The film or the plastics layer provided by the first component also offers a remarkable improvement in the waterproofing and resistance to wetness.
Obviously, the fiber-reinforced foam material of the present invention can simultaneously employ both fiberæ
or yarns and the cloth as reinforcers. The simultaneous use of the fibers or yarns and the cloth is preferred because such a combination provides a remarkable reinforcement effect. In such a case the cloth as a reinforcer can have various forms such as a woven cloth, a knitted fabric, a non-woven cloth or a network-like cloth. It is also possible to use a composite clot~
formed from two or more of these cloths, as well as a combination of these cloths.
When the reinforcer is used in the form of fibers or yarns, a multiplicity of such fibers or yarns may be dispersed in the foamed material. In contrast, when the reinforcer is used in the form of a cloth, one or more cloths in the form of sheets are present inside and/or o~
one or both surfaces of the foamed material. When fibers or yarns and cloths are used simultaneously as the reinforcers, the fiber-reinforced foamed material of the invention has as construction which is a combination o~
the above-described two types of structures.
The composite fiber used in a material in accordance with the present invention may be a long fibe~
(filament), a short fiber (staple) or a very short fibe~
(whisker). Which one of the filament, staple and whiske~
is used in the fiber-reinforced foamed material of the present invention may be a matter of great significance because the performance of the fiber-reinforced foamed material, in particular the strength as well as appearance and the production process, largely vary according to the type of the fiber.
The invention does not pose any restriction in the process for producing the fiber-reinforced foamed material and any suitable process can be employed. A
preferred example of the production process is as follows.
Polys~yLene granules or beads, prepared for example by suspension polymerisation (such beads are commercially available) are used as the foamable material, while multi-core/sheath type composite fibers, composed of core components of polyethylene terephthalate and a sheath component of styrene-acrylic acid ester copolymer, are used as the composite fibers. As the first step, steam is blown at the foamable poly~y r ene beads so as to cause a primary foaming. Then, the primarily foamed beads and the multi-core/sheath composite fibers are injected from different nozzles into a mold so as to be mixed in the mold. Subsequently, steam is blown into the mold so as to cause a ~Pco~ry fo~m;~g while allowing the sheath romr~n~nt of the composite fibers which is deformable at low temperature to be thermally deformed thereby integrating the sheath component with the foamed material, whereby a fiber-reinforced foamed material embodying the invention is obtained.
Alternatively, or additionally, to the fibres reinforcement within the foamed body, a fabric layer may be provided on one or more surfaces of the fibe~
reinforced material by placing a layer or layers o~
fabric within the mould and blowing the beads and any 2031~63 -further reinforcing fibers into the re~i n; ng space, Typically, opposite faces of the mould are covered with the fabric and the beads (and any further reinforcement) are blown into the space between the fabrics.
Another preferred process employs a foamable phenol resin (novolak type) as the foamed material and, as the fiber component, multi-core/sheath composite fibers composed of cores of polyethylene terephthalate and a sheath component of styrene-acrylic acid ester copolymer.
The fibers are cut into short pieces and are mixed with the phenol resin by a mixer. The mixture is charged into a forming mold in which it is then pressed and heated so as to allow it to foam, whereby a fiber-reinforced foamed material embodying the present invention is obtained.
Again, fabric surface layers may be provided in a ~nner similar to that described above.
The invention will be more fully understood from the following description of Examples. In the following description, the m;x; ng ratios are shown in terms of weight ratio.

Example l Commercially available foamable polystyrene beads (flexural rigidity in non-foamed state: 280 kg/mm2) were used as the foamable material. As the reinforcement fibers, polymeric oriented type filaments (36 core 203~863 elements cont~;ne~ in each filament, single fiber size:
4.0 denier i.e. 4.4 dtex) each composed of a sheath ~o~ o,~ent and a core r,~mpo~t was used. The sheath ~."~o-lent was made of 80 wt parts styrene-20 wt parts 2-ethylhexylacrylate (thermal deformation temperature:
57.6C). The core ~ol"yo.lent was made of polyethylene terephthalate (melting point: 261C). The polymeric oriented type filaments were cut into pieces of 51 mm long.
As the first step, steam was blown at the foamable poly~ylene beads so as to effect primary foaming. The primarily foamed beads and the cut pieces of the above-mentioned polymeric oriented type filaments emerged as respective jets from different ejectors into a forming mold opened at one side and exhibiting a substantially U-e~Ap~ cross-section, so as to fill the cavity in the mold. Subse~uently, steam was blown into the forming mold so as to allow s~on~y foaming of the primarily foamed beads (foaming treatment temperature: 105C), while integrating the foamed material and the polymeric oriented type filaments, whereby a fiber-reinforced foamed material of the invention was obt~ine~.
In the thus-obtained fiber-reinforced foamed material, the sheath component of the reinforcement fiber was efficiently changed into a bonding component so as to provide a high degree of integration between the foamed material and the reinforcement fibers. In addition, this fiber-reinforced foamed material exhibited superior resistA~ce~ to impact, bending and torsion, as well as - reduced tendency to crack. Containers for radio cassettes (radio unit with cassette tape player) were produced by using a pair of pieces of fiber-reinforced foamed material having a U-shaped cross-section, without using a corrugated board box. The containers were subjected to a transportation test with the radio cassette units encased therein. No damaging of the radio cassette units were found after the transportation.
For the purpose of comparison, fiber-reinforced foamed material was produced under the same conditions as Example 1 except that ordinary polyethylene terephthalate fibers (melting point: 261C, single filament size: 4.Q
denier (4.4 dtex), cut length: 51 mm) were used as the reinforcer, and contA;ne~s produced from this foamed material were subjected to the same test as Example 1.
After the test transportation, some of the radio cassette units showed peeling of the paint at corners of these units, as well as partial damaging of the units. The fiber-reinforced foamed material of this comparative Example showed insufficient integration between the foamed material and the polyethylene terephthalate fibers.

20318~3 .~

Example 2 A foamable powder of a novolak type phenol resin (flexural elasticity modulus: 350 kg/mm2) was used as the foamable material in combination with a reinfol~el--e~lt fiber which was a polymeric oriented type filament (36 core elements cont~in~.~ in each filament, single filament size 3.8 denier (4.2 dtex), cut length 10 mm) each composed of a core component of polyethylene terephthalate (melting point: 261C) and a sheath component of polystyrene (thermal deformation temperature: 84.4C). The foamable material and the cut pieces of reinforcement fiber were mixed by a mixer at such a ratio that the fiber content occupies 10 wt% of the mixture, and the mixture was charged into a formin~
mold. Heat and pressure were then applied to the forming mold by a heat press so as to allow the foamable material to form for 30 minutes at 140C, whereby a fiber-reinforced foamed material was obt~; n~ .
The thus-obt~ine~ fiber-reinforced foamed material showed remarkably improved form maintainin~
characteristics as compared with a conventional phenol type foamed material, and could be used conveniently as 2 heat-insulating architectural material without the assistance of any cardboard or honeycomb structure.

Example 3 A polymeric oriented type filament (16 core elements cont~;ne~ in each filament: single filament size: 3.8 denier i.e. 4.2 dtex) was cut into pieces of 10 mm length. The polymeric oriented type filament had a core component of polyethylene terephthalate (melting point:
261C) and a sheath component made of 80 wt% styrene-20 wt~ 2-ethylhexylacrylate copolymer (thermal deformation temperature: 57.6C). The cut pieces of filaments emerged as a jet from an ejector into a forming mold having a U-ch~ppA cross-section while air in the mold was removed by suction so that a layer of the polymeric oriented type fiber was formed on the inner surface of the mold. Then, commercially available poly~Lylene beads (flexural elastic modulus in non-foamed state: 280 kg/mm2) were heated for primary foaming, and the thus-obt~inPA primarily foamed poly~yLene beads were charged together with the polymeric oriented fibers into a forming mold. The charging was stopped when the cavity in the mold was completely filled, and the mold was closed. The mold was then heated by steam at 105C so as to thermally deform the sheath component of the polymeric oriented fibers, while allowing seconA~ry foaming of the primarily foamed beads.
Consequently, a fiber-reinforced foamed material was obtained in wlich a plastics sheet of polymeric oriented fibers with a thermally deformed sheath component was strongly bonded to the foamed material. The thus-obtained fiber-reinforced foamed material therefore exhibited lligh surface smoothness, and had high resist~n~ to impact, ben~i ng and torsion, as well as reduced cracking tenAPncy.
Cont~iners for radio cassette units were formed from this fiber-reinforced foamed material and were subjected to a test transportation without being packaged in corrugated board boxes. The radio cassette units could be safely transported without any damage.
The name of the contents and patterns were printed on the surface of this fiber-reinforced foamed material, The printing was conducted with a high degree of clearness which could never be obt~; ne~ when conventional poly~yLelle foamed materials were used.

Example 4 A sheet of cloth was woven from polymeric oriented type filaments (36 core elements contained in each filament, single filament size: 3.5 denier i.e. 3.9 dtex) each composed of a core component made of nylon 66 (melting point: 261C) and a sheath component made of styrene-2-ethylhexylacrylate copolymer (thermal deformation temperature: 57.6C). The cloth sheet was placed on an inner surface of a forming mold.
The mold cavity was then charged with primarily 2~31863 foamed foamable beads of polys~ylene (flexural elastic modulus in non-foamed state: 280 kg/mm2) and the beads were heated by steam so as to foam.
In consequence, a fiber-reinforced foamed material was obt~;nP~ with the surfaces covered by a cloth layer of the polymeric oriented type filaments composed of the sheath romronent changed into a plastics layer and the core çomponent, the cloth layer being strongly bonded to and united with the foamed material while possessing a woven structure. The thus-obtained fiber-reinforced foamed material showed high degree of surface smoothness, and exhibited high resist~nr-~ to impact, be~ ng and torsion, as well as reduced cracking tendency. Compact containers for frozen goods were formed from this material. These containers exhibited excellent cold-preservation effect, as well as ~X~ ent appearance and durability.

Example 5 A sheet of cloth was woven from polymeric oriented type filaments (36 core elements contained in each filament, single filament size: 3.5 denier i.e. 3.9 dtex) each composed of a core component made of polyethylene terephthalate (melting point: 261C) and a sheat~
component made of a low-melting point polyester (thermal deformation temperature: 75C). The cloth sheet was ~ .

placed on an inner surface of a forming mold.
The mold cavity was then charged with primarily foamed foamable beads of poly~ylene (flexural elastic modulus in non-foamed state: 280 kg/mm2) and the beads were heated by steam so as to foam.
In consequence, a fiber-reinforced foamed material was obtA; n~ with the surfaces covered by a cloth layer of the polymeric oriented type filaments composed of th~
sheath component changed into a plastics layer and the core component, the cloth layer being strongly bonded to and united with the foamed material while maintA;n;~g a woven structure. The thus-obtained fiber-reinforced foamed material showed high degree o surface smoothness, and exhibited high resis~Anc~ to impact, bP~; ng and torsion, as well as reduced cracking ten~ency.

Claims (27)

1. A fiber-reinforced foamed material comprising:
(1) a foamed body of a resin polymer, which resin polymer has a flexural elasticity modulus not smaller than 150 kg/mm2, (2) reinforcement fibers, and (3) a bonding component through which the reinforcement fibers are integrated with the foamed body so as to reinforce the foamed body, wherein at least some of the reinforcement fibers are provided by a composite fibrous material in the form of composite fibers and/or composite yarns, the composite fibrous material having a first component which has been thermally deformed or melted by heat applied during the foaming so as to serve as the bonding component and a second component which remains fibrous so as to reinforce the foamed body.
2. A fiber-reinforced foamed material according to claim 1, wherein at least some of the reinforcement fibers are present in the form of a cloth formed from the composite fibrous material.
3. A fiber-reinforced foamed material according to claim 2, wherein the reinforcement fibers formed from the composite fibrous material are provided additional to those forming the cloth.
4. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material is of a core/sheath type.
5. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material is of a bimetal type.
6. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material is of a multi-layer bonding type.
7. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material is of a radial multi-layer bonding type.
8. A fiber-reinforced foamed material according to claim 4, wherein the fibers of the composite fibrous material are core/-sheath type composite fibers having a multiplicity of core elements in the sheath.
9. A fiber-reinforced foamed material according to claim 8, wherein at least two types of core elements are present in the sheath.
10. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material comprises a composite yarn which is a mixed filament yarn composed of a plurality of yarn components.
11. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the composite fibrous material comprises a composite yarn which is a double and twist yarn composed of a plurality of yarn components.
12. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the first component of the composite fibrous material is a polymer having a thermal deformation temperature or a melting temperature which is at least 10°C
lower than the thermal deformation temperature or the melting temperature of the foamed body.
13. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the first component of the composite fibrous material is a polymer having a monomer unit also present in the foamed body.
14. A fiber-reinforced foamed material according to claim 14, wherein the first component of the composite fibrous material is a copolymer comprising the said monomer unit present in the foamed body and another monomer unit.
15. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the second component of the composite fibrous material is a polymer having a thermal deformation temperature or melting temperature which is not lower than 160°C.
16. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the second component of the composite fibrous material is a polymer having a thermal deformation temperature or melting temperature which is at least 50°C
higher than the thermal deformation temperature or the melting temperature of the foamed body.
17. A fiber-reinforced foamed material according to claim 16, wherein the second component of the composite fibrous material is a polymer having a thermal deformation temperature or melting temperature which is at least 70°C higher than the thermal deformation temperature or the melting temperature of the first component.
18. A fiber-reinforced foamed material according to any one of claims 1 to 3, wherein the foamed body is formed of a polymer having benzene rings.
19. A fiber-reinforced foamed material according to claim 18, wherein the foamed body is of polystyrene.
20. A fiber-reinforced foamed material according to claim 18, wherein the foamed body is of a phenol resin.
21. A fiber-reinforced foamed material according to claim 1, wherein:
the second component in the composite fibrous material has been subjected to a drawing in the fiber axis direction and has a fiber strength of at least 2 g/d and a thermal deformation or melting temperature which is (a) not lower than 125°C, (b) at least 50°C higher than the temperature at which the foaming is performed and (c) at least 50°C higher than the thermal deforma-tion or melting temperature of the foamed body, and the first component in the composite fibrous material has a thermal deformation or melting temperature which is (a) at least 10°C lower than the temperature at which the foaming is performed and (b) at least 70°C lower than the thermal deforma-tion or melting temperature of the second component.
22. A fiber-reinforced foamed material according to claim 21, wherein:
the resin polymer of which the foamed body is made is a member selected from the group consisting of polystyrene, phenol resin, styrene-ethylene copolymer, acrylonitrile-styrene copolymer, acrylonitrile-butadiene-styrene resin and phenol/urea formaldehyde co-condensation resin;
the second component is made of a polymer selected from the group consisting of polyesters, polyamides, polyallylate and polypropylene; and the first component is made of a polymer having a monomer unit also present in the resin polymer of the foamed body.
23. A method of producing a fiber-reinforced foamed material comprising the steps of:
providing a foamable material and a composite fibrous material in the form of composite fibers and/or composite yarns each having a first component and a second component; and allowing the foamable material to foam together with the composite fibrous material at a temperature at least 10°C higher than the thermal deformation temperature or melting temperature of the first component and at least 20°C lower than the thermal deformation temperature or melting temperature of the second component, whereby the first component is thermally deformed or melted to serve as a bonding component, while the second component remains as a fibrous reinforcement component, the fibrous reinforcement component being integrated with the foamed body through the bonding component so as to reinforce the foamed body.
24. A method according to claim 23, wherein the foamable material is allowed to foam at a temperature at least 50°C lower than the thermal deformation temperature or melting temperature of the second component.
25. A method according to claim 23, wherein at least some of the composite fibrous material is provided in the form of a cloth formed of the composite fibers and/or composite yarns.
26. A method according to claim 23, 24 or 25, wherein the foamed body is of a polystyrene resin.
27. A method according to claim 23, 24 or 25, wherein the foamed body is of a phenol resin.
CA002031863A 1989-12-11 1990-12-10 Fiber-reinforced foamed material and method of producing it Expired - Fee Related CA2031863C (en)

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US5200261A (en) 1993-04-06
EP0432997A3 (en) 1992-04-01
JPH07113068B2 (en) 1995-12-06
KR910011446A (en) 1991-08-07
EP0432997A2 (en) 1991-06-19
JPH03223343A (en) 1991-10-02
CA2031863A1 (en) 1991-06-12

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