JP2024060542A - Stampable sheet and molded article thereof - Google Patents

Abstract

To provide a stampable sheet that is superior in both flame shielding and heat insulation.SOLUTION: A stampable sheet contains a thermoplastic resin composition (X) and inorganic fiber (Y). The thermoplastic resin composition (X) contains a thermoplastic resin and a phosphorous flame retardant. The stampable sheet has an expansion ratio of 300% or more when heated at 1200°C for 5 minutes.SELECTED DRAWING: None

Description

The present invention relates to a stampable sheet and a molded body using the same.

In recent years, research and development of electric and hybrid vehicles has been promoted as part of environmental measures, and the development of high-energy density batteries and weight reduction are being actively promoted in order to improve the driving range. Such high-energy density batteries are at risk of catching fire in the event of an accident, so as a safety measure for passengers, the housing material must have high flame retardancy, and therefore, in many cases, metal materials such as iron are used in combination with fire-resistant materials.
However, metal materials have the drawback of being heavy, and when fire-resistant materials are used in combination, issues arise regarding workability and increased costs due to the increased number of parts. Therefore, attempts are being made to use resins, which have the potential to achieve both weight reduction and flame resistance. Currently, in order to create a sustainable society, emphasis is being placed on reducing carbon dioxide emissions and recyclability. Many thermosetting materials have high flame retardancy and are common as composite materials, but in terms of recyclability, thermoplastic resin materials are advantageous.

In addition, China has announced a safety standard called GB 38031-2020 "Safety Requirements for Electric Vehicle Power Batteries," which requires that a warning be issued five minutes before the battery experiences thermal runaway. It is believed that this can be achieved by using housing materials that provide flame protection for at least five minutes after the battery ignites.

To address these issues, for example, Patent Document 1 proposes adding a brominated flame retardant or an antimony oxide compound to a carbon fiber reinforced polypropylene resin, but the additives used therein have a problem in terms of their persistence in living organisms.
In response to this, Patent Document 2 proposes a flame-retardant polyolefin-based composition in which a polyolefin-based resin contains a (poly)phosphate compound, as a technology for making polypropylene-based resin flame-retardant while taking into consideration bioretention.
Moreover, Patent Document 3 proposes a flame-retardant resin composition comprising a polypropylene resin, long glass fibers, and a phosphate compound.

JP 2014-62189 A JP 2013-119575 A JP 2011-88970 A

Conventional fiber-reinforced composite material technology, which has the potential to achieve both lightweight and flame-resistant properties in high-energy density batteries, has many shortcomings. Specifically, stampable sheets, which are the raw material for fiber-reinforced composite materials, are required to have high flame-resistant properties and further improved insulation properties.

The present invention was made to solve the above problems, and aims to provide a stampable sheet that combines high flame-proofing and heat-insulating properties.

As a result of intensive research to solve the above problems, the present inventors have found that a stampable sheet containing a thermoplastic resin composition (X) and inorganic fibers (Y), in which the thermoplastic resin composition (X) contains a thermoplastic resin and a phosphorus-based flame retardant, and having an expansion ratio of 300% or more when heated under specific conditions, can solve the above problems, and have completed the present invention based on these findings.
That is, the present invention provides the following [1] to [10].
[1] A stampable sheet comprising a thermoplastic resin composition (X) and inorganic fibers (Y), wherein the thermoplastic resin composition (X) comprises a thermoplastic resin and a phosphorus-based flame retardant, and has an expansion ratio of 300% or more when heated at 1200°C for 5 minutes.
[2] The stampable sheet according to the above [1], wherein the inorganic fibers (Y) are inorganic fiber nonwoven fabric.
[3] The stampable sheet according to [2] above, wherein the needle penetration depth of the inorganic fiber nonwoven fabric is 15 mm or more.
[4] The stampable sheet according to any one of [1] to [3] above, wherein the thermoplastic resin constituting the thermoplastic resin composition (X) is a polyolefin resin.
[5] The stampable sheet according to any one of the above [1] to [4], wherein the thermoplastic resin composition (X) further contains a dispersant.
[6] The stampable sheet according to the above [5], wherein the dispersant is a copolymer of an α-olefin and an unsaturated carboxylic acid.
[7] The stampable sheet according to [5] or [6] above, wherein the content of the dispersant per 100 parts by mass of the phosphorus-based flame retardant is more than 0 and not more than 25 parts by mass.
[8] The stampable sheet according to any one of the above [1] to [7], wherein the inorganic fiber (Y) is at least one selected from glass fibers, ceramic fibers, metal fibers, and metal oxide fibers.
[9] The stampable sheet according to any one of [1] to [8] above, wherein the content of the phosphorus-based flame retardant is 1 to 30 mass% based on the total weight.
[10] A molded product obtained by stamping the stampable sheet according to any one of [1] to [9] above.

The present invention provides a stampable sheet that combines high flame-proofing and heat-insulating properties.

1 is a schematic diagram showing the configuration and manufacturing method of the stampable sheet of the present invention. 1 is a schematic diagram showing the configuration and manufacturing method of the stampable sheet of the present invention.

The following describes in detail the embodiments of the present invention, but the following description is merely an example of an embodiment of the present invention, and the present invention is not limited to these contents in any way.

[Stampable sheet]
The stampable sheet of the present invention contains a thermoplastic resin composition (X) and inorganic fibers (Y), and the thermoplastic resin composition (X) contains a thermoplastic resin and a phosphorus-based flame retardant. It is also characterized in that the expansion ratio (hereinafter, simply referred to as "expansion ratio") when heated at 1200 ° C for 5 minutes is 300% or more. Because the expansion ratio is high, char is easily formed by the phosphorus-based flame retardant contained in the thermoplastic resin composition (X) in the gap space of the inorganic fiber Y generated by expansion. On the other hand, the formed char is fixed in the gap of the inorganic fiber, so that the formation of dense char is promoted. This provides high flame-proofing and heat-insulating effects. The stampable sheet of the present invention has an expansion ratio of 300% or more, so that the stampable sheet has excellent flame-proofing and heat-insulating properties.
The stampable sheet of the present invention may have an expansion ratio of 300% or more, but from the viewpoint of exhibiting a higher level of flame-proofing and heat-insulating properties, the expansion ratio is preferably 310% or more, and more preferably 320% or more. On the other hand, from the viewpoint of ensuring sufficient strength, the expansion ratio is preferably 1000% or less, and more preferably 800% or less.

A specific embodiment is, for example, a stampable sheet having a layer in which the thermoplastic resin composition (X) and an inorganic fiber nonwoven fabric are integrated.
An example of a suitable embodiment is a stampable sheet having a needle depth of 15 mm or more of the inorganic fiber nonwoven fabric. If the needle depth is 15 mm or more, the stampable sheet will expand due to springback when heated, and the flame-proofing and heat-insulating properties of the stampable sheet can be improved. From the same viewpoint, the needle depth of the inorganic fiber nonwoven fabric is preferably 15 mm or more. On the other hand, from the viewpoint of productivity, it is preferably 20 mm or less, more preferably 18 mm or less.

Another example of a suitable embodiment is a stampable sheet having a layer in which the thermoplastic resin composition (X) and three or more inorganic fiber nonwoven fabrics are integrated. When there are three or more inorganic fiber nonwoven fabrics, the stampable sheet undergoes greater expansion due to springback when heated, improving the flame-proofing and heat-insulating properties of the stampable sheet. From the same viewpoint, the number of inorganic fiber nonwoven fabrics can be four or more, or five or more. On the other hand, from the viewpoint of productivity, ten or fewer sheets are preferable, and eight or fewer sheets are more preferable.

[Thermoplastic resin composition (X)]
The thermoplastic resin composition (X) according to the present invention contains at least (a) a thermoplastic resin and (b) a phosphorus-based flame retardant. Hereinafter, (a) the thermoplastic resin and (b) the phosphorus-based flame retardant will be described in detail.

<(a) Thermoplastic resin>
The thermoplastic resin used in the stampable sheet of the present invention is not particularly limited, but may be polyolefin resin, polycarbonate resin, polyester resin, acrylonitrile styrene resin, ABS resin, polyamide resin, modified polyphenylene oxide, etc. may be used. These may be used alone or in combination of two or more. For example, the thermoplastic resin (a) may be a composite resin of two or more of the above thermoplastic resins.

The polyolefin resin is not particularly limited, and examples thereof include the resins described below. The polyester resin is not particularly limited, and examples thereof include polybutylene terephthalate. The polyamide resin is not particularly limited, and examples thereof include nylon 66 and nylon 6.
Among them, the present invention is particularly useful when the thermoplastic resin (a) contains at least a polyolefin resin. In the present invention, the term "polyolefin resin" refers to a resin in which the proportion of olefin units or cycloolefin units is 90 mol % or more relative to 100 mol % of all structural units constituting the resin.
The proportion of olefin units or cycloolefin units relative to 100 mol % of all structural units constituting the polyolefin resin is preferably 95 mol % or more, and particularly preferably 98 mol % or more.

Examples of polyolefin resins include α-olefin polymers such as polyethylene, polypropylene, polybutene, poly(3-methyl-1-butene), poly(3-methyl-1-pentene), and poly(4-methyl-1-pentene); α-olefin copolymers such as ethylene-propylene block or random copolymers, α-olefin-propylene block or random copolymers having 4 or more carbon atoms, ethylene-methyl methacrylate copolymers, and ethylene-vinyl acetate copolymers; and cycloolefin polymers such as polycyclohexene and polycyclopentene. Examples of polyethylene include low-density polyethylene, linear low-density polyethylene, and high-density polyethylene. Examples of polypropylene include isotactic polypropylene, syndiotactic polypropylene, hemiisotactic polypropylene, and stereoblock polypropylene. In the α-olefin-propylene block or random copolymers having 4 or more carbon atoms, examples of the α-olefins having 4 or more carbon atoms include butene, 3-methyl-1-butene, 3-methyl-1-pentene, and 4-methyl-1-pentene. These polyolefin resins may be used alone or in combination of two or more.
Of the above olefin resins, polypropylene resin (hereinafter sometimes referred to as "PP resin") is particularly preferred.

(Melt Flow Rate (MFR))
The melt flow rate (hereinafter sometimes abbreviated as MFR) (230°C, 2.16 kg load) of the thermoplastic resin (a) used in the present invention is preferably 40 to 500 g/10 min. If the MFR is 40 g/10 min or more, no defects will occur during stamping molding of the stampable sheet, and the processability will not decrease. Furthermore, if it is 500 g/10 min or less, no burrs will occur during the production of the stampable sheet. From the above viewpoints, the MFR is preferably 50 to 400 g/10 min, more preferably 60 to 400 g/10 min, and more preferably 70 to 300 g/10 min.
The MFR of the (a) thermoplastic resin can be adjusted, for example, by controlling the hydrogen concentration during polymerization.
The MFR is a value measured in accordance with JIS K7210.

((a) Thermoplastic Resin Content)
The content of the (a) thermoplastic resin in the stampable sheet of the present invention is not particularly limited, but is preferably 15 to 80% by mass. When the content of the thermoplastic resin is 15% by mass or more, the molding processability is particularly good, and the stampable sheet can be easily molded. On the other hand, when the content of the thermoplastic resin is 80% by mass or less, sufficient amounts of flame retardant, dispersant, and inorganic fiber can be contained, and good flame resistance can be obtained. From the above viewpoints, the content of the thermoplastic resin in the stampable sheet is preferably 35 to 70% by mass, and more preferably 40 to 60% by mass.

<(a-1) Polypropylene Resin>
The thermoplastic resin (a) used in the stampable sheet of the present invention preferably contains a polypropylene-based resin. Examples of the polypropylene-based resin include a propylene homopolymer and a propylene-α-olefin copolymer. Here, the propylene-α-olefin copolymer may be either a random copolymer or a block copolymer.

(α-Olefin)
Examples of the α-olefin constituting the copolymer include ethylene, 1-butene, 2-methyl-1-propene, 1-pentene, 2-methyl-1-butene, 3-methyl-1-butene, 1-hexene, 2-ethyl-1-butene, 2,3-dimethyl-1-butene, 2-methyl-1-pentene, 3-methyl-1-pentene, 4-methyl-1-pentene, 3,3-dimethyl-1-butene, 1-heptene, methyl-1-hexene, dimethyl-1-pentene, ethyl-1-pentene, trimethyl-1-butene, and 1-octene. One of these may be copolymerized with propylene, or two or more may be copolymerized with propylene. Among these, from the viewpoint of improving the impact strength of the stampable sheet, ethylene or 1-butene, which have a large effect, are preferred, and ethylene is the most preferred.

(Propylene-ethylene random copolymer)
In the case of a random copolymer of propylene and ethylene, it preferably contains 90 to 99.5% by mass, more preferably 92 to 99% by mass, of propylene units and preferably 0.5 to 10% by mass, more preferably 1 to 8% by mass of ethylene units. When the ethylene units are equal to or more than the lower limit, the stampable sheet can have sufficient impact strength, and when the ethylene units are equal to or less than the upper limit, sufficient rigidity can be maintained.
The contents of propylene units and ethylene units in the random copolymer of propylene and ethylene can be adjusted by controlling the composition ratio of propylene and ethylene during polymerization of the random copolymer of propylene and ethylene.
The propylene content of the random copolymer of propylene and ethylene is a value measured using a cross fractionation device, FT-IR, or the like, and the measurement conditions and the like may be, for example, those described in JP-A-2008-189893.

(Melt Flow Rate (MFR))
The melt flow rate (hereinafter sometimes abbreviated as MFR) (230°C, 2.16 kg load) of the polypropylene resin (a-1) used in the present invention is preferably 40 to 500 g/10 min. If the MFR is 40 g/10 min or more, no defects will occur during stamping molding of the stampable sheet, and the processability will not decrease. Furthermore, if it is 500 g/10 min or less, no burrs will occur during the production of the stampable sheet. From the above viewpoints, the MFR is preferably 50 to 400 g/10 min, more preferably 60 to 400 g/10 min, and more preferably 70 to 300 g/10 min.
The MFR of the polypropylene resin (propylene homopolymer) (A-1) can be adjusted by controlling the hydrogen concentration during polymerization.
The MFR is a value measured in accordance with JIS K7210.

((a-1) Content of polypropylene resin)
The content of the polypropylene resin (a-1) in the stampable sheet of the present invention is not particularly limited, but is preferably 15 to 80% by mass. If the content of the polypropylene resin is 15% by mass or more, the molding processability is sufficient, and the stampable sheet can be easily molded. On the other hand, if the content is 80% by mass or less, the content of the flame retardant, dispersant, and inorganic fiber becomes insufficient, and sufficient flame resistance is obtained. From the above viewpoints, the content of the polypropylene resin in the stampable sheet is more preferably 35 to 70% by mass, and even more preferably 40 to 60% by mass.

<Modified polyolefin resin>
The stampable sheet of the present invention may further contain a modified polyolefin resin in addition to the polypropylene resin. Specific examples of the modified polyolefin resin include acid-modified polyolefin resin and hydroxy-modified polyolefin resin, and these may be used alone or in combination.
The types of acid-modified polyolefin resins and hydroxy-modified polyolefin resins used as the modified polyolefin resins are not particularly limited, and may be any of the conventionally known resins.

(Acid-modified polyolefin resin)
Examples of acid-modified polyolefin resins include those obtained by graft copolymerizing polyolefins such as polyethylene, polypropylene, ethylene-α-olefin copolymers, ethylene-α-olefin-non-conjugated diene compound copolymers (such as EPDM), and ethylene-aromatic monovinyl compound-conjugated diene compound copolymer elastomers with unsaturated carboxylic acids such as maleic acid or maleic anhydride, thereby chemically modifying the polyolefins.
The graft copolymerization is carried out, for example, by reacting the polyolefin with an unsaturated carboxylic acid in a suitable solvent using a radical generator such as benzoyl peroxide. The unsaturated carboxylic acid or its derivative component can also be introduced into the polymer chain by random or block copolymerization with a polyolefin monomer.

Examples of unsaturated carboxylic acids used for modification include compounds having a carboxyl group, such as maleic acid, fumaric acid, itaconic acid, acrylic acid, and methacrylic acid, and a polymerizable double bond into which a functional group, such as a hydroxyl group or an amino group, has been introduced as necessary.
Derivatives of unsaturated carboxylic acids include their acid anhydrides, esters, amides, imides, metal salts, etc., and specific examples thereof include maleic anhydride, itaconic anhydride, methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, etc. Of these, maleic anhydride is preferred.

Preferred acid-modified polyolefin resins include those modified by graft polymerization of maleic anhydride to an olefin polymer having ethylene and/or propylene as the main polymer unit, and those modified by copolymerization of an olefin mainly consisting of ethylene and/or propylene with maleic anhydride. Specific examples include a combination of polyethylene/maleic anhydride grafted ethylene-butene-1 copolymer, or a combination of polypropylene/maleic anhydride grafted polypropylene.

(Hydroxy-modified polyolefin resin)
The hydroxy-modified polyolefin resin is a modified polyolefin resin containing a hydroxyl group. The hydroxy-modified polyolefin resin may have a hydroxyl group at an appropriate site, for example, at the end of the main chain or on a side chain.
Examples of the olefin resin constituting the hydroxy-modified polyolefin resin include homopolymers or copolymers of α-olefins such as ethylene, propylene, butene, 4-methylpentene-1, hexene, octene, nonene, decene, and dodecene, and copolymers of the above-mentioned α-olefins with copolymerizable monomers.
Examples of preferred hydroxy-modified polyolefin resins include hydroxy-modified polyethylene resins such as low-, medium- or high-density polyethylene, linear low-density polyethylene, ultra-high molecular weight polyethylene, ethylene-(meth)acrylic acid ester copolymers, and ethylene-vinyl acetate copolymers; and hydroxy-modified polypropylene resins such as polypropylene homopolymers such as isotactic polypropylene, random copolymers of propylene and α-olefins (e.g., ethylene, butene, hexane, etc.), propylene-α-olefin block copolymers, and hydroxy-modified poly(4-methylpentene-1).

<(b) Phosphorus-based flame retardant>
The fiber-reinforced resin composite material of the present invention contains (b) a phosphorus-based flame retardant. Phosphorus-based flame retardants are preferred from the viewpoint of improving flame-resistance, not remaining in the body, and having excellent flame retardancy. In the present invention, the phosphorus-based flame retardant is essential, but other flame retardants may be used in combination, specifically, bromine-based flame retardants, antimony-based flame retardants, etc. In addition, in terms of classification focusing on the action mechanism of the flame retardant, it is preferred from the viewpoint of improving flame-resistance that (b) the flame retardant is an intumescent flame retardant.

The phosphorus-based flame retardant is a phosphorus compound, i.e., a compound containing a phosphorus atom in the molecule, and exerts a flame retardant effect by forming char when the resin composition is burned.
The phosphorus-based flame retardant may be a known one, and examples thereof include (poly)phosphates, (poly)phosphate esters, etc. Here, "(poly)phosphates" refers to phosphates or polyphosphates, and "(poly)phosphate esters" refers to phosphate esters or polyphosphate esters.
The phosphorus-based flame retardant is preferably solid at 80°C.

As the phosphorus-based flame retardant, a (poly)phosphate is preferred from the standpoint of flame retardancy.
Examples of (poly)phosphates include ammonium polyphosphate, melamine polyphosphate, piperazine polyphosphate, piperazine orthophosphate, melamine pyrophosphate, piperazine pyrophosphate, melamine polyphosphate, melamine orthophosphate, calcium phosphate, and magnesium phosphate.
In addition, in the above examples, compounds in which melamine or piperazine is replaced with other nitrogen compounds can be used in the same manner. Examples of other nitrogen compounds include N,N,N',N'-tetramethyldiaminomethane, ethylenediamine, N,N'-dimethylethylenediamine, N,N'-diethylethylenediamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, N,N,N',N'-tetramethylethylenediamine, N,N,N',N'-diethylethylenediamine, 1,2-propanediamine, 1,3-propanediamine, tetramethyl Diamine, pentamethylenediamine, hexamethylenediamine, 1,7-diaminoheptane, 1,8-diaminooctane, 1,9-diaminononane, 1,10-diaminodecane, trans-2,5-dimethylpiperazine, 1,4-bis(2-aminoethyl)piperazine, 1,4-bis(3-aminopropyl)piperazine, acetoguanamine, benzoguanamine, acrylguanamine, 2,4-diamino-6-nonyl-1,3,5-triamine 2,4-diamino-6-hydroxy-1,3,5-triazine, 2-amino-4,6-dihydroxy-1,3,5-triazine, 2,4-diamino-6-methoxy-1,3,5-triazine, 2,4-diamino-6-ethoxy-1,3,5-triazine, 2,4-diamino-6-propoxy-1,3,5-triazine, 2,4-diamino-6-isopropoxy-1,3,5-triazine, 2,4-diamino-6-mercapto-1, Examples of such (poly)phosphates include 3,5-triazine, 2-amino-4,6-dimercapto-1,3,5-triazine, ammeline, benzguanamine, acetoguanamine, phthalodiguanamine, melamine cyanurate, melamine pyrophosphate, butylenediguanamine, norbornenediguanamine, methylenediguanamine, ethylenedimelamine, trimethylenedimelamine, tetramethylenedimelamine, hexamethylenedimelamine, 1,3-hexylenedimelamine, etc. These (poly)phosphates may be used alone or in combination of two or more.

Among the above phosphorus-based flame retardants, a salt of (poly)phosphoric acid and a nitrogen compound (hereinafter also referred to as "compound (b1)") is preferred. Compound (b1) is an intumescent flame retardant, and forms a surface expansion layer (intemescent) which is a foamed char when the resin composition is burned. The formation of the surface expansion layer suppresses the diffusion and heat transfer of decomposition products, and excellent flame retardancy is exhibited.
Examples of the nitrogen compound in the compound (b1) include ammonia, melamine, piperazine, and the other nitrogen compounds described above.

Commercially available phosphorus-based flame retardants include Adeka STAB FP-2100J, FP-2200, and FP-2500S (manufactured by ADEKA Corporation).

(Brominated flame retardants)
Examples of bromine-based flame retardants include decabromodiphenyl ether, tetrabromobisphenol A, tetrabromobisphenol S, 1,2-bis(2',3',4',5',6'-pentabromophenyl)ethane, 1,2-bis(2,4,6-tribromophenoxy)ethane, 2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine, 2,6-dibromophenol, 2,4-dibromophenol, Examples of the polybrominated polystyrene include brominated polystyrene, ethylene bistetrabromophthalimide, hexabromocyclododecane, hexabromobenzene, pentabromobenzyl acrylate, 2,2-bis[4'(2'',3''-dibromopropoxy)-3',5'-dibromophenyl]-propane, bis[3,5-dibromo-4-(2,3-dibromopropoxy)phenyl]sulfone, and tris(2,3-dibromopropyl)isocyanurate.

(Antimony-based flame retardant)
Examples of antimony-based flame retardants include antimony trioxide, antimony tetroxide, antimony pentoxide, sodium pyroantimonate, antimony trichloride, antimony trisulfide, antimony oxychloride, antimony perchloropentane dichloride, and potassium antimonate, with antimony trioxide and antimony pentoxide being particularly preferred.

(Intumescent flame retardant)
Intumescent flame retardants are flame retardants that suppress the combustion of materials by forming a surface expansion layer (intumescent) that prevents the diffusion of radiant heat from the combustion source and combustion gases and smoke from the burning material to the outside. Examples of intumescent flame retardants include salts of (poly)phosphoric acid and nitrogen compounds. Specific examples include ammonium salts and amine salts of (poly)phosphoric acid, such as ammonium polyphosphate, melamine polyphosphate, piperazine polyphosphate, ammonium pyrophosphate, melamine pyrophosphate, and piperazine pyrophosphate.

Among the above flame retardants, halogen-free flame retardants are preferred from the viewpoint of environmental friendliness, and intumescent flame retardants are preferred from the viewpoint of improving the flame-proofing properties of the resulting stampable sheet.
The flame retardants may be used alone or in combination of two or more.

(b) Content of phosphorus-based flame retardant
The content of the phosphorus-based flame retardant in the stampable sheet of the present invention is not particularly limited, but is preferably in the range of 1 to 30% by mass as the content in the thermoplastic resin composition (X). When the content is 1% by mass or more, good flame retardancy can be imparted to the stampable sheet, and good flame shielding properties can be obtained. On the other hand, when the flame retardant is 30% by mass or less, the thermoplastic resin can be contained in a sufficient content ratio, so that the molding processability becomes better. From the above viewpoints, the content of the flame retardant in the thermoplastic resin composition (X) is more preferably in the range of 1 to 25% by mass, and even more preferably in the range of 3 to 20% by mass.

<(c) Dispersant>
The (c) dispersant is not particularly limited as long as it can disperse the (b) phosphorus-based flame retardant in the (a) thermoplastic resin, but a polymer dispersant can be suitably used in terms of compatibility with the (a) thermoplastic resin. Preferably, a polymer dispersant capable of dispersing the (b) phosphorus-based flame retardant in the (a-1) polypropylene resin can be suitably used. As the polymer dispersant, a polymer dispersant having a functional group is preferred, and from the standpoint of dispersion stability, a polymer dispersant having a functional group such as a carboxyl group, a phosphoric acid group, a sulfonic acid group, a primary, secondary or tertiary amino group, a quaternary ammonium base, a group derived from a nitrogen-containing heterocycle such as pyridine, pyrimidine or pyrazine is preferred.
In the present invention, a polymer dispersant having a carboxyl group is preferred, and in particular, when a phosphorus-based flame retardant suitable as a flame retardant is used, a copolymer of an α-olefin and an unsaturated carboxylic acid is preferred. By using such a dispersant, the dispersibility of the phosphorus-based flame retardant can be improved, and the content of the flame retardant can be reduced.

(Copolymer of α-olefin and unsaturated carboxylic acid)
In the "copolymer of α-olefin and unsaturated carboxylic acid" according to the present invention (hereinafter referred to as "copolymer (c1)"), the proportion of α-olefin units in the total of 100 mol % of α-olefin units and unsaturated carboxylic acid units is preferably 20 mol % or more and 80 mol % or less.
In the copolymer (c1), the ratio of the α-olefin units to the total amount of the α-olefin units and the unsaturated carboxylic acid units is more preferably 30 mol % or more, and more preferably 70 mol % or less. If the ratio of the α-olefins is equal to or more than the lower limit, (a) the compatibility with the polyolefin resin is better, and if it is equal to or less than the upper limit, (b) the compatibility with the phosphorus-based flame retardant is better.

In the copolymer (c1), the α-olefin is preferably an α-olefin having 5 or more carbon atoms, and more preferably an α-olefin having 10 to 80 carbon atoms. If the α-olefin has 5 or more carbon atoms, it tends to have better compatibility with the thermoplastic resin (a), and if it has 80 or less carbon atoms, it is advantageous in terms of raw material costs. From the above viewpoints, it is even more preferable that the α-olefin has 12 to 70 carbon atoms, and particularly preferably 18 to 60 carbon atoms.

In the copolymer (c1), examples of the unsaturated carboxylic acid include (meth)acrylic acid, maleic acid, methylmaleic acid, fumaric acid, methylfumaric acid, tetrahydrophthalic acid, itaconic acid, citraconic acid, crotonic acid, isocrotonic acid, glutaconic acid, norbornane-5-ene-2,3-dicarboxylic acid, and esters, anhydrides, imides, etc. of these unsaturated carboxylic acids. Note that "(meth)acrylic acid" refers to acrylic acid or methacrylic acid.
Specific examples of the ester, anhydride or imide of an unsaturated carboxylic acid include (meth)acrylic acid esters such as methyl (meth)acrylate, ethyl (meth)acrylate, butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, and glycidyl (meth)acrylate; dicarboxylic acid anhydrides such as maleic anhydride, itaconic anhydride, citraconic anhydride, and 5-norbornene-2,3-dicarboxylic acid anhydride; maleimide compounds such as maleimide, N-ethylmaleimide, and N-phenylmaleimide. These may be used alone or in combination of two or more.
Among the above, esters and dicarboxylic anhydrides are preferred from the viewpoint of copolymerization reactivity, and among these, dicarboxylic anhydrides are preferred, with maleic anhydride being particularly preferred, from the viewpoint of compatibility with phosphorus-based flame retardants that are suitable as flame retardants.

The weight average molecular weight of the copolymer (c1) is preferably 2,000 or more, more preferably 3,000 or more, and is preferably 50,000 or less, more preferably 30,000 or less. When the weight average molecular weight of the copolymer (c1) is within the above range, the dispersibility of the flame retardant (b) is more excellent.
The weight average molecular weight of the copolymer (c1) is a value calculated as standard polystyrene by dissolving the copolymer (c1) in tetrahydrofuran (THF) and measuring the result by gel permeation chromatography.

Commercially available copolymers (c1) include Ricorb CE2 (Clariant Japan Co., Ltd.) and Diacalna 30M (Mitsubishi Chemical Co., Ltd.).

The content of the dispersant (c) in this stampable sheet relative to 100 parts by mass of the phosphorus-based flame retardant (b) is in the range of more than 0 and not more than 25 parts by mass, and preferably in the range of 0.01 to 10 parts by mass.
According to the study by the inventors, the flame retardant is uniformly dispersed in the inorganic fibers constituting the stampable sheet with a thermoplastic resin as a matrix resin, and the flame-proofing property of the stampable sheet can be significantly improved. Although the detailed mechanism is unclear, the inventors speculate as follows. That is, when the flame retardant is uniformly dispersed in the resin between the inorganic fibers, the char formed by the phosphorus-based flame retardant coming into contact with flame is fixed in the gaps between the inorganic fibers. Furthermore, the size of the char formed by expansion upon contact with flame is restricted by the gaps between the inorganic fibers, and the size of the char formed becomes uniform. It is believed that the combination of the fixing effect of the char by the inorganic fibers and the uniformity of the char size results in the formation of a dense char, and the flame-proofing property of the stampable sheet is significantly improved. Based on these findings, the inventors have found that by setting the ratio of the content of the dispersant to the flame retardant to a specific range, the flame retardant can be controlled to be uniformly present in the resin between the inorganic fibers, and the flame-proofing property of the stampable sheet can be significantly improved.
For the above reasons, if the content of (c) dispersant is more than 0, the dispersibility of (b) phosphorus-based flame retardant is sufficient, and sufficient flame-proofing properties cannot be imparted to the stampable sheet. On the other hand, if the content is 25 parts by mass or less, the physical properties of the stampable sheet are sufficient. From the same viewpoint, the content of (c) dispersant is preferably 0.01 parts by mass or more, more preferably 0.1 parts by mass or more, even more preferably 1 part by mass or more, and particularly preferably 2 parts by mass or more. On the other hand, the upper limit is more preferably 20 parts by mass or less, even more preferably 15 parts by mass or less, even more preferably 10 parts by mass or less, even more preferably 5 parts by mass or less, and particularly preferably 3 parts by mass or less.

In addition, the ratio of the (c) dispersant to the total of 100 parts by mass of the (a) thermoplastic resin and the (b) phosphorus-based flame retardant is preferably 0.01 parts by mass or more, more preferably 0.05 parts by mass or more, and even more preferably 0.1 parts by mass or more. On the other hand, it is preferably 10 parts by mass or less, more preferably 5.0 parts by mass or less, even more preferably 2.0 parts by mass or less, more preferably 1.5 parts by mass or less, and even more preferably 1.0 parts by mass or less. If the ratio of the (c) dispersant is equal to or greater than the lower limit, the (b) phosphorus-based flame retardant is better dispersed, and the flame retardancy and physical properties of the stampable sheet obtained and the appearance of the molded product obtained are better. If the ratio of the (c) dispersant is equal to or less than the upper limit, the effect of the (c) dispersant on the flame retardancy of the stampable sheet can be further suppressed. In particular, the ratio of the dispersant (c) to the total of 100 parts by mass of the polyolefin resin and the phosphorus-based flame retardant (b) is preferably 0.01 parts by mass or more, more preferably 0.05 parts by mass or more, and even more preferably 0.1 parts by mass or more. On the other hand, it is preferably 10 parts by mass or less, more preferably 5.0 parts by mass or less, even more preferably 2.0 parts by mass or less, more preferably 1.5 parts by mass or less, and even more preferably 1.0 parts by mass or less.

For the (Y) inorganic fibers described in detail below, the ratio of the (c) dispersant to 100 parts by mass of the (Y) inorganic fibers is preferably 0.01 parts by mass or more, more preferably 0.05 parts by mass or more, and even more preferably 0.1 parts by mass or more. On the other hand, it is preferably 10 parts by mass or less, more preferably 5.0 parts by mass or less, and even more preferably 2.0 parts by mass or less. If the ratio of the (c) dispersant is equal to or greater than the lower limit, the flame retardancy and physical properties of the stampable sheet obtained and the appearance of the molded product obtained are improved. If the ratio of the (c) dispersant is equal to or less than the upper limit, the effect of the (c) dispersant on the flame retardancy of the stampable sheet can be further suppressed.

<(Y) Inorganic Fiber>
The stampable sheet of the present invention contains (Y) inorganic fiber. As (Y) inorganic fiber, various fibers can be used, for example, glass fiber, rock wool, alumina fiber, silica alumina fiber and other metal oxide fibers, potassium titanate fiber, calcium silicate (wollastonite) fiber, ceramic fiber such as ceramic fiber, carbon fiber, metal fiber, etc. These inorganic fibers may be used alone or in combination of two or more.
Of the above inorganic fibers, at least one selected from glass fibers and alumina fibers is preferred from the viewpoints of flame resistance and processability.
The (Y) inorganic fiber may contain two or more inorganic fibers having different melting temperatures. As a combination of two or more inorganic fibers having different melting temperatures, at least one of the fibers is preferably glass fiber, and the other one or more is preferably one or more inorganic fibers selected from the group consisting of alumina fiber, silica fiber, alkaline earth silicate fiber (biosoluble), and carbon fiber. By containing two or more inorganic fibers having different melting temperatures, it is possible to effectively prevent the deterioration of the flame-shielding function.
The inorganic fibers used in the present invention may be used in combination with a sizing agent or a surface treatment agent, such as compounds having a functional group, such as epoxy compounds, silane compounds, and titanate compounds.

The average fiber diameter of the inorganic fibers is preferably 3 to 25 μm.
The fiber diameter can be measured using a scanning electron microscope or the like, and the average fiber diameter can be obtained, for example, by measuring the fiber diameters of 10 randomly selected fibers and calculating the average value.

The average fiber length is preferably 30 mm or more, more preferably 40 mm or more, and even more preferably 50 mm or more. When the average fiber length is 30 mm or more, the resin component is easily bound by the continuous long fibers, and dense char is easily formed. Therefore, the stampable sheet of the present invention can obtain excellent flame-proofing properties.
The fiber length can be measured using a ruler, calipers, or the like from an image enlarged by a microscope or the like as necessary, and the average fiber length can be obtained, for example, by measuring the fiber lengths of 10 randomly selected fibers and calculating the average value.

The inorganic fiber content in the stampable sheet of the present invention is 1 to 80% by mass as a whole. When the inorganic fiber content is 1% by mass or more, the strength, rigidity, and impact resistance of the stampable sheet are sufficient, and when it is 80% by mass or less, it is preferable in terms of manufacturing and processing the stampable sheet. In addition, when the inorganic fiber content is 80% by mass or less, the specific gravity of the stampable sheet is light, and the weight reduction effect as a metal substitute is remarkable.
From the above viewpoints, the content of the (Y) inorganic fibers in the stampable sheet is more preferably 3 to 60 mass %, further preferably 10 to 50 mass %, and particularly preferably 30 to 45 mass %.

(Glass fiber)
One of the inorganic fibers (Y) suitable for the stampable sheet of the present invention is glass fiber. The glass fiber may be, for example, a long fiber having an average fiber length of 30 mm or more, or a fiber having a short average fiber length (chopped strand), but it is preferable to use a glass fiber having a long average fiber length from the viewpoint of flame retardancy, rigidity, impact resistance, etc.

The average fiber diameter of the glass fibers is preferably in the range of 9 to 25 μm. When the average fiber diameter is 9 μm or more, the stampable sheet has sufficient rigidity and impact resistance, while when the average fiber diameter is 25 μm or less, the stampable sheet has good strength. From the above viewpoints, the average fiber diameter of the glass fibers is more preferably in the range of 10 to 15 μm.
The average fiber diameter and average fiber length of the glass fibers can be measured by the above-mentioned method.

There are no particular limitations on the material of the glass fiber used in the present invention, and it may be any of alkali-free glass, low-alkali glass, and alkali-containing glass, and any of the various compositions that have been used conventionally as glass fibers can be used.

(Alumina fiber)
One of the inorganic fibers (D) suitable for the stampable sheet of the present invention is alumina fiber. Alumina fiber is usually a fiber made of alumina and silica, and in the stampable sheet of the present invention, the alumina/silica composition ratio (mass ratio) of the alumina fiber is preferably in the range called a mullite composition of 65/35 to 98/2 or a high alumina composition, more preferably in the range of 70/30 to 95/5, and particularly preferably in the range of 70/30 to 74/26.

The average fiber diameter of the alumina fibers is preferably in the range of 3 to 25 μm, and it is preferable that the alumina fibers are substantially free of fibers with a fiber diameter of 3 μm or less. Here, "substantially free of fibers with a fiber diameter of 3 μm or less" means that the amount of fibers with a fiber diameter of 3 μm or less is 0.1 mass % or less of the total inorganic fiber mass.
The average fiber diameter of the alumina fibers is more preferably 5 to 8 μm. If the average fiber diameter of the inorganic fibers is too large, the repulsive force and toughness of the mat-like inorganic fiber assembly layer will decrease, while if the average fiber diameter is too small, the amount of dust suspended in the air will increase, and the probability of containing inorganic fibers having a fiber diameter of 3 μm or less will increase.

(Carbon fiber)
The suitable range for carbon fiber is similar to that for glass fiber.

<Optionally Added Ingredients>
In addition to the above-mentioned components, the stampable sheet of the present invention may contain any additive components for the purpose of further improving the effects of the invention or imparting other effects, within a range that does not significantly impair the effects of the present invention.
Specific examples of the additives include colorants such as pigments, light stabilizers such as hindered amines, ultraviolet absorbers such as benzotriazoles, nucleating agents such as sorbitols, antioxidants such as phenols and phosphorus, antistatic agents such as nonionic surfactants, neutralizing agents such as inorganic compounds, antibacterial and antifungal agents such as thiazoles, flame retardants and flame retardant assistants such as halogen compounds and lignophenols, plasticizers, dispersants such as organic metal salts, lubricants such as fatty acid amides, metal deactivators such as nitrogen compounds, polyolefin resins other than the polypropylene resins, thermoplastic resins such as polyamide resins and polyester resins, and elastomers (rubber components) such as olefin elastomers and styrene elastomers.
These optional components may be used in combination of two or more kinds.

Colorants such as inorganic or organic pigments are effective in imparting or improving the colored appearance, appearance, texture, commercial value, weather resistance, durability, etc. of polypropylene resin compositions and molded articles thereof.
Specific examples of inorganic pigments include carbon black such as furnace carbon and ketjen carbon; titanium oxide; iron oxide (e.g., red iron oxide); chromic acid (e.g., yellow lead); molybdic acid; selenide sulfide; and ferrocyanide. Specific examples of organic pigments include azo pigments such as sparingly soluble azo lake, soluble azo lake, insoluble azo chelate, condensed azo chelate, and other azo chelates; phthalocyanine pigments such as phthalocyanine blue and phthalocyanine green; threne pigments such as anthraquinone, perinone, perylene, and thioindigo; dye lake; quinacridone; dioxazine; and isoindolinone. In order to achieve a metallic or pearlescent look, aluminum flakes and pearl pigments can be added. Dyes can also be added.

Light stabilizers and ultraviolet absorbers, for example, hindered amine compounds, benzotriazoles, benzophenones, and salicylates, are effective in imparting or improving the weather resistance, durability, and the like of polypropylene resin compositions and molded articles thereof, and are effective in further improving weather discoloration resistance.
Specific examples of the hindered amine compound include a condensation product of dimethyl succinate and 1-(2-hydroxyethyl)-4-hydroxy-2,2,6,6-tetramethylpiperidine; poly[[6-(1,1,3,3-tetramethylbutyl)imino-1,3,5-triazine-2,4-diyl][(2,2,6,6-tetramethyl-4-piperidyl)imino]hexamethylene[(2,2,6,6-tetramethyl-4-piperidyl)imino]]; tetrakis(2,2,6,6-tetramethyl-4-piperidyl)1,2,3,4-butane tetracarboxylate; tetrakis(1,2,2,6,6-pentamethyl-4-piperidyl)1,2,3,4-butane tetracarboxylate; bis(1,2,2,6,6-pentamethoxy) 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole;2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole;2-hydroxy-4-methoxybenzophenone;2-hydroxy-4-n-octoxybenzophenone; and the like. Examples of the salicylate-based compounds include 4-t-butylphenyl salicylate; 2,4-di-t-butylphenyl 3',5'-di-t-butyl-4'-hydroxybenzoate; and the like.
Here, the method of using the light stabilizer and the ultraviolet absorber in combination is preferable because it has a large effect of improving weather resistance, durability, weather discoloration resistance, and the like.

As the antioxidant, for example, a phenol-based, phosphorus-based or sulfur-based antioxidant is effective in imparting or improving heat resistance, processing stability, heat aging resistance, etc. to a polypropylene resin composition and a molded article thereof.
Furthermore, antistatic agents such as nonionic and cationic antistatic agents are effective in imparting and improving antistatic properties to polypropylene resin compositions and molded articles thereof.

Examples of olefin-based elastomers include ethylene-α-olefin copolymer elastomers such as ethylene-propylene copolymer elastomer (EPR), ethylene-butene copolymer elastomer (EBR), ethylene-hexene copolymer elastomer (EHR), and ethylene-octene copolymer elastomer (EOR); ethylene-α-olefin-diene terpolymer elastomers such as ethylene-propylene-ethylidenenorbornene copolymer, ethylene-propylene-butadiene copolymer, and ethylene-propylene-isoprene copolymer; and styrene-butadiene-styrene triblock copolymer elastomer (SBS).
Examples of the styrene-based elastomer include styrene-based elastomers such as styrene-isoprene-styrene triblock copolymer elastomer (SIS), styrene-ethylene-butylene copolymer elastomer (SEB), styrene-ethylene-propylene copolymer elastomer (SEP), styrene-ethylene-butylene-styrene copolymer elastomer (SEBS), styrene-ethylene-butylene-ethylene copolymer elastomer (SEBC), hydrogenated styrene-butadiene elastomer (HSBR), styrene-ethylene-propylene-styrene copolymer elastomer (SEPS), styrene-ethylene-ethylene-propylene-styrene copolymer elastomer (SEEPS), styrene-butadiene-butylene-styrene copolymer elastomer (SBBS), partially hydrogenated styrene-isoprene-styrene copolymer elastomer, and partially hydrogenated styrene-isoprene-butadiene-styrene copolymer elastomer, as well as hydrogenated polymer-based elastomers such as ethylene-ethylene-butylene-ethylene copolymer elastomer (CEBC).
Among these, the use of an ethylene-octene copolymer elastomer (EOR) and/or an ethylene-butene copolymer elastomer (EBR) is preferred in that it is easy to impart appropriate flexibility to the polypropylene resin composition of the present invention and its molded article, and they tend to have excellent impact resistance.

<Method for producing thermoplastic resin composition (X)>
As described above, the thermoplastic resin composition (X) according to the present invention contains (a) a thermoplastic resin, a modified polyolefin resin added as needed, (b) a phosphorus-based flame retardant, and (c) a dispersant added as needed. In addition, optional additive components may be further blended. In the thermoplastic resin composition (X) described above, when the thermoplastic resin (a) is a polypropylene resin (a-1), it may be particularly called a polypropylene resin composition (hereinafter, sometimes referred to as a "PP composition").
The thermoplastic resin composition (X) or the PP composition can be produced by a conventionally known method, and can be produced by blending, mixing, and melt-kneading the above-mentioned components.
The mixing is carried out using a mixer such as a tumbler, a V blender, or a ribbon blender, and the melt kneading is carried out using equipment such as a single-screw extruder, a twin-screw extruder, a Banbury mixer, a roll mixer, a Brabender plastograph, or a kneader, and the materials are melt kneaded and granulated.

<Method for manufacturing stampable sheet>
The stampable sheet of the present invention is not particularly limited in its manufacturing method, but is preferably manufactured by impregnating a mat made of inorganic fibers (Y) (hereinafter sometimes referred to as "inorganic fiber mat (Y)") with the thermoplastic resin composition (X) or the PP composition. The impregnation method includes a method of applying the thermoplastic composition or the PP composition to the inorganic fiber mat (Y), a method of preparing a sheet of the thermoplastic resin composition or the PP composition (hereinafter sometimes referred to as "thermoplastic resin sheet" or "PP sheet"), laminating the thermoplastic resin sheet or the PP sheet on the inorganic fiber mat, and heating and melting the sheet to impregnate the inorganic fiber mat, and the like.
In the present invention, from the viewpoint of impregnation of the resin of the stampable sheet into the fibers, a method of laminating a thermoplastic resin sheet or a PP sheet on an inorganic fiber mat and heating and melting it is preferable. In particular, the inorganic fiber mat is laminated between two thermoplastic resin sheets or PP sheets, and then the laminate is heated and pressed, and then cooled and solidified.
The thickness of the thermoplastic resin sheet or PP sheet is not particularly limited as long as it allows good impregnation of the fiber mat.

(Inorganic fiber mat)
The form of the inorganic fibers used in the method for producing a stampable sheet is not particularly limited, and various forms can be used, but those formed in a mat or sheet form are preferred.
More specifically, a mat formed from glass fibers (hereinafter referred to as a "glass fiber mat") and a mat formed from metal oxide fibers such as alumina fibers (hereinafter referred to as a "metal oxide mat") are preferred.

The basis weight (mass per unit area) of the inorganic fiber mat is not particularly limited and is appropriately determined depending on the application, but is preferably 300 g/m ² or more, more preferably more than 800 g/m ² , and more preferably more than 1500 g/m ^2. The basis weight of the inorganic fiber mat is not particularly limited, but is preferably 5000 g/m ² or less, more preferably 4500 g/m ² or less, even more preferably 4000 g/m ² or less, and particularly preferably 3500 g/m ² or less.

The basis weight per unit area of the inorganic fiber mat can be set within the above range by adjusting the amount of fiber per unit area when the inorganic fiber aggregates that make up the inorganic fiber mat are stacked using a folding device. The inorganic fiber mat of the present invention may be composed of multiple inorganic fiber mats bonded together or may be composed of a single material, but is preferably composed of a single material in terms of handling properties and peel strength at the adhesive interface.

(fiberglass mat)
The form of the glass fiber mat used in the present invention includes felt and blanket processed with short fiber glass wool, chopped strand mat processed with continuous glass fiber, swirl (spiral) mat of continuous glass fiber, unidirectionally aligned mat, etc. Among these, the use of a glass fiber mat obtained by needle punching a swirl (spiral) mat of continuous glass fiber is particularly preferable because the stampable sheet has excellent strength and impact resistance.

(Metal oxide fiber mat)
The metal oxide fiber mat according to the present invention is a mat that is made of metal oxide fibers such as alumina fibers and that has been subjected to a needling treatment.

In the method of laminating a thermoplastic resin sheet or a PP sheet on an inorganic fiber mat and heating and melting the sheet, the heating temperature is preferably 170 to 300° C. If the heating temperature is 170° C. or higher, the flowability of the polypropylene resin is sufficient, and the inorganic fiber mat can be sufficiently impregnated with the PP composition, thereby obtaining a suitable stampable sheet. On the other hand, if the heating temperature is 300° C. or lower, the thermoplastic resin composition or the PP composition does not deteriorate.
Furthermore, the pressure applied is preferably 0.1 to 1 MPa. If the pressure applied is 0.1 MPa or more, the thermoplastic resin composition or the PP composition can be sufficiently impregnated into the inorganic fiber mat, and a suitable stampable sheet can be obtained. On the other hand, if the pressure applied is 1 MPa or less, the thermoplastic resin composition or the PP composition flows, and no burrs are generated.
The cooling temperature is not particularly limited as long as it is equal to or lower than the freezing point of the thermoplastic resin in the thermoplastic resin composition or the PP composition, but if the cooling temperature is equal to or lower than 80° C., the stampable sheet obtained will not deform when it is taken out. From the above viewpoints, the cooling temperature is preferably from room temperature to 80° C.

Methods for obtaining a stampable sheet by heating and pressurizing the above laminate and cooling it include press-molding the laminate in a mold equipped with a heating device, and lamination processing in which the laminate is heated and pressurized by passing it between two pairs of rollers equipped with a heating device. In particular, lamination processing is preferred for its high productivity, as it allows for continuous production.

<Thickness of stampable sheet>
The thickness of the stampable sheet of the present invention is usually 1 to 10 mm, preferably 2 to 5 mm. When the thickness of the stampable sheet is 1 mm or more, the stampable sheet is easy to produce, while when the thickness of the stampable sheet is 10 mm or less, long-term preheating is not required when processing the stampable sheet by stamping molding or the like, and good molding processability is obtained.

<Molded body>
The stampable sheet of the present invention can be molded into a desired shape by stamping in a conventional manner to obtain a molded article made of the stampable sheet.

(Application)
Examples of applications of the stampable sheet of the present invention include various parts in the industrial field, such as automobile parts and electrical and electronic equipment parts. In particular, since it has excellent strength, rigidity, and conductivity, and is also excellent in processability, it can be suitably used for applications that require a good balance of these performances, such as various housings and cases such as battery cases.

<Textiles>
The fibers in the fiber-reinforced resin according to the present invention may be organic or inorganic fibers, but inorganic fibers are preferred from the viewpoint of heat resistance, and examples thereof include glass fibers, rock wool, basalt fibers, alumina fibers, silica alumina fibers, potassium titanate fibers, calcium silicate (wollastonite) fibers, alkaline earth silicate fibers (biosoluble), silica fibers, carbon fibers, etc. These inorganic fibers may be used alone or in combination of two or more.

[Structure]
The structure of the present invention includes a battery housing and a battery cell. The battery housing of the present invention is as described in detail above.
The structure in the present invention is preferably a battery, and the battery is not particularly limited. Examples of the battery include secondary batteries such as lithium ion batteries, nickel-hydrogen batteries, lithium-sulfur batteries, nickel-cadmium batteries, nickel-iron batteries, nickel-zinc batteries, sodium-sulfur batteries, lead-acid batteries, and air batteries. Among these, lithium ion batteries are preferred, and the battery housing of the present invention is particularly suitable for use in suppressing thermal runaway of lithium ion batteries. That is, the battery housing of the present invention is preferably a battery housing for a lithium ion battery.

[Electric Mobility]
In the present invention, electric mobility refers to transportation equipment such as vehicles, ships, and airplanes that run on electricity as an energy source. Note that vehicles include hybrid cars in addition to electric vehicles (EVs).
The above-described battery housing and battery structures having battery cells of the present invention are highly safe and extremely useful for electric mobility using battery modules with high energy density to extend driving distance.

The first aspect of the present invention will be described in detail below using examples, but the present invention is not limited to these examples.
(Evaluation method)
1. Evaluation of flame barrier properties For the sheets prepared in each Example and Comparative Example, a flame from a burner at 1300°C was applied from one surface, and after 15 minutes, it was evaluated whether the flame penetrated. The distance from the burner nozzle to the sample was 160 mm. The flame surface was set to 1200°C. The flame surface temperature was confirmed with a thermocouple thermometer.

2. Evaluation of heat insulation In the flame-shielding evaluation described in 1 above, the temperature of the surface (back surface) opposite to the surface exposed to the burner flame of the test piece was measured with a non-contact radiation thermometer (FT-H50K manufactured by Keyence Corporation). The measurement area was φ35 mm. The center of the measurement area was visually set to be immediately above the position of the burner flame. Table 1 shows the maximum temperature (°C) reached on the back surface within 120 seconds.

(Materials used)
1. Polypropylene resin (component a)
"Novatec PP SA06GA" (melt flow rate: 60 g/10 min) manufactured by Japan Polypropylene Corporation was used.

2. Flame retardant (component b)
Phosphorus-based flame retardant composition (ADEKA CORPORATION, Adeka STAB FP-2500S, containing 50 to 60 mass% piperazine pyrophosphate, 35 to 45 mass% melamine pyrophosphate, and 3 to 6 mass% zinc oxide based on the total mass of the phosphorus-based flame retardant composition)

3. Dispersant (component c)
α-Olefin/maleic anhydride copolymer (Mitsubishi Chemical Corporation, Diacalna 30M, weight average molecular weight 7,800).

5. Glass fiber mat (Y component)
(1) Glass fiber mat A
A long-fiber glass fiber mat was used, which was prepared by needle-punching a swirl mat (basis weight 880 g/m ² ) made from continuous glass fibers (fiber diameter 23 μm) of a roving with a needle punch depth set to 16.0 mm.
(1) Glass fiber mat B
A long-fiber glass fiber mat was used, which was prepared by needle-punching a swirl mat (basis weight 880 g/m ² ) made from continuous glass fibers (fiber diameter 23 μm) of roving with a needle punch depth set to 14.6 mm.

Preparation Example 1 (Preparation of PP Composition)
The above component a (68% by mass), component b (30% by mass), and component c (2% by mass) were melt-kneaded (230° C.) to prepare pellets of a polypropylene resin composition (PP composition).

Comparative Preparation Example 1
Pellets of a polypropylene resin composition (PP composition) were prepared in the same manner as in Preparation Example 1, except that the components b and c were not used.

Example 1
The following description will be given with reference to FIG.
The pellets of the PP composition granulated in Preparation Example 1 were placed in an extruder, melted, and extruded into a sheet, and a glass fiber mat A (12 in FIG. 1) was sandwiched from both sides of the extruded sheet-like thermoplastic resin composition (X) (hereinafter referred to as "sheet X"; 11 in FIG. 1) to obtain a laminate. The glass fiber mat A used here has a needle penetration depth of 16.0 mm.
Next, sheet X (13 in FIG. 1) was laminated on both surfaces of the laminate, and the laminate was heated and pressed at 230° C. for 4 minutes while applying a pressure of 0.3 MPa using a laminator, and then cooled and solidified to obtain a stampable sheet (thickness: 2.5 mm). In the stampable sheet, the thermoplastic resin composition component in sheet X was impregnated into glass fiber mat A to form a layer in which the glass fiber mat and the resin composition were integrated.
The layer structure and composition of Example 1 are shown in Table 1. The results of evaluation by the above method are shown in Table 2. Table 2 shows the results of evaluation performed with the outermost layer on the sheet X side as the flame-contact surface.

Example 2
The following description will be given with reference to FIG.
The pellets of the PP composition granulated in Preparation Example 1 were put into an extruder, melted, and then extruded into a sheet shape, and the extruded sheet-shaped thermoplastic resin composition (X) (sheet X, 21 in FIG. 2) was laminated so as to be sandwiched between both sides of the glass fiber mat B (22 in FIG. 2) to obtain a laminate. Next, glass fiber mat B (22' in FIG. 2) was laminated on both surfaces of the laminate. Sheet X was further laminated on both surfaces so that the outermost layer was sheet X (21'' in FIG. 2). Thereafter, the laminate was heated and pressed at 230° C. for 4 minutes while applying a pressure of 0.3 MPa using a laminator, and then cooled and solidified to obtain a stampable sheet (thickness: 2.5 mm). In the stampable sheet, the thermoplastic resin composition component in sheet X was impregnated into three sheets of glass fiber mat B to form a layer in which the glass fiber mat and the resin composition were integrated.
The layer structure and composition of Example 3 are shown in Table 1. The results of evaluation by the above-mentioned methods are shown in Table 2.

Comparative Example 1
A stampable sheet (thickness: 2.5 mm) was obtained in the same manner as in Example 1, except that the glass fiber mat B was used instead of the glass fiber mat A in Example 1, and the pellets obtained in Comparative Preparation Example 1 were used. The layer structure and composition of Comparative Example 1 are shown in Table 1. The evaluation results are shown in Table 2.

As shown in Examples 1 and 2, the stampable sheet of the present invention has excellent flame-proofing properties, and the flame was blocked even after 15 minutes. In addition, the maximum temperature reached up to 120 seconds (2 minutes) was suppressed, and the sheet had excellent heat insulation properties.
In contrast, the flame penetrated to the back surface in about 140 seconds in Comparative Example 1. Also, the maximum temperature reached up to 120 seconds (2 minutes) was significantly higher than in Examples 1 and 2.

The stampable sheet of the present invention has high flame-proofing and heat-insulating properties, and is therefore useful as a material for various industrial parts that require high safety, such as aircraft, ships, automobile parts, electrical and electronic equipment parts, building materials, etc. In particular, it can be suitably used for various battery housings and cases that have traditionally been made of metal, and is expected to contribute to the safety of automobiles as well as improve energy efficiency and reduce _CO2 emissions by reducing weight.

10 stampable sheet 11 sheet X (thermoplastic resin sheet)
12 Glass fiber mat A
13 Sheet X (thermoplastic resin sheet)
20 stampable sheet 21 sheet X (thermoplastic resin sheet)
21 'Sheet X (thermoplastic resin sheet)
22 Glass fiber mat B
22' Glass fiber mat B

Claims (10)

A stampable sheet comprising a thermoplastic resin composition (X) and inorganic fibers (Y),
The thermoplastic resin composition (X) contains a thermoplastic resin and a phosphorus-based flame retardant,
A stampable sheet having an expansion ratio of 300% or more when heated at 1200°C for 5 minutes. The stampable sheet according to claim 1, wherein the inorganic fibers (Y) are inorganic fiber nonwoven fabric. The stampable sheet according to claim 2, wherein the needle depth of the inorganic fiber nonwoven fabric is 15 mm or more. The stampable sheet according to claim 1, wherein the thermoplastic resin constituting the thermoplastic resin composition (X) is a polyolefin resin. The stampable sheet according to claim 1, wherein the thermoplastic resin composition (X) further contains a dispersant. The stampable sheet according to claim 5, wherein the dispersant is a copolymer of an α-olefin and an unsaturated carboxylic acid. The stampable sheet according to claim 5, wherein the content of the dispersant per 100 parts by mass of the phosphorus-based flame retardant is more than 0 and not more than 25 parts by mass. The stampable sheet according to claim 1, wherein the inorganic fibers (Y) are at least one selected from glass fibers, ceramic fibers, metal fibers, and metal oxide fibers. The stampable sheet according to claim 1, wherein the content of the phosphorus-based flame retardant is 1 to 30 mass % based on the total weight. A molded product obtained by stamping the stampable sheet according to claim 1.