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JP7615718B2 - Wood base material, decorative material, and method for manufacturing wood base material - Google Patents
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JP7615718B2 - Wood base material, decorative material, and method for manufacturing wood base material - Google Patents

Wood base material, decorative material, and method for manufacturing wood base material Download PDF

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JP7615718B2
JP7615718B2 JP2021016970A JP2021016970A JP7615718B2 JP 7615718 B2 JP7615718 B2 JP 7615718B2 JP 2021016970 A JP2021016970 A JP 2021016970A JP 2021016970 A JP2021016970 A JP 2021016970A JP 7615718 B2 JP7615718 B2 JP 7615718B2
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大輔 村田
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Toppan Holdings Inc
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Description

本発明は、木質基材、化粧材及び木質基材の製造方法に関する。 The present invention relates to wood substrates, decorative materials, and methods for producing wood substrates.

木質基材は、木粉、木質チップ、木質繊維などの木質材料を接着剤と混合したものを加熱加圧成形して得られる基材である。この木質基材は、木質材料の種類などによりパーティクルボードや中密度繊維板などと称され、床や壁などの下地材、建具や家具など幅広い用途で使用されている。 Wood-based substrates are made by heating and pressurizing a mixture of wood materials such as wood flour, wood chips, and wood fibers with adhesive. These wood-based substrates are called particle boards or medium-density fiberboards depending on the type of wood material, and are used for a wide range of applications, such as undercoats for floors and walls, and for building materials and furniture.

木質基材の接着剤としては、従来、尿素樹脂系接着剤、メラミン樹脂系接着剤、またはフェノール樹脂系接着剤が、ホルムアルデヒドを含む硬化剤とともに用いられていた。ホルムアルデヒドは、シックハウス症候群の原因となる有害物質であるため、木質基材からの放散が問題となり、放散量低減のための各種施策が検討されている。しかしながら、従来技術では、ホルムアルデヒドの放散を完全に抑制することは困難であった。 Conventionally, urea resin adhesives, melamine resin adhesives, or phenol resin adhesives have been used as adhesives for wood substrates, along with hardeners containing formaldehyde. Formaldehyde is a harmful substance that causes sick house syndrome, so its emission from wood substrates has become a problem, and various measures to reduce the amount of emission have been considered. However, with conventional technology, it has been difficult to completely suppress the emission of formaldehyde.

これに対し、従来、ホルムアルデヒドを含まない接着剤として、粉体の糖類と粉体のポリカルボン酸とを主成分とする接着剤を用い、これを植物繊維と混合し加熱加圧成形することで繊維ボードを製造する方法が提案されていた(特許文献1の段落[0017]参照)。また、ホルムアルデヒドを含まない接着剤として、従来、ポリビニルアルコールと水とからなる接着剤を用いた木質基材を含む積層体の製造方法が提案されていた(特許文献2の段落[0017]、及び図1参照)。 In response to this, a method has been proposed in the past to use an adhesive containing powdered sugars and powdered polycarboxylic acids as its main components as a formaldehyde-free adhesive, mix this with plant fibers, and mold it under heat and pressure to produce a fiberboard (see paragraph [0017] of Patent Document 1). Also, a method has been proposed in the past to use an adhesive containing polyvinyl alcohol and water as a formaldehyde-free adhesive to produce a laminate containing a wood substrate (see paragraph [0017] and Figure 1 of Patent Document 2).

特開2016-55620号公報JP 2016-55620 A 特許第5553279号公報Patent No. 5553279

しかし、上記した従来の接着剤を用いた木質基材は、曲げ強度などの機械特性や耐水性、耐寒性、耐熱性が実用上十分なものではなかった。
そこで、本発明は、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制し、且つ実用的な耐水性を備えた木質基材、その木質基材を備えた化粧材及びその木質基材の製造方法を提供することを課題とする。
However, wood substrates using the above-mentioned conventional adhesives are not sufficient for practical use in terms of mechanical properties such as bending strength, water resistance, cold resistance, and heat resistance.
Therefore, an object of the present invention is to provide a wood base material that suppresses the emission of harmful substances such as formaldehyde that cause sick house syndrome and has practical water resistance, a decorative material that includes this wood base material, and a method for producing this wood base material.

本発明の一態様に係る木質基材は、粉体状及びチップ状の少なくとも一方の形状を有する木質材料と、熱可塑性樹脂組成物と、を含む木質基材であって、前記熱可塑性樹脂組成物が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、前記熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、前記酸含有樹脂の含有量が、前記熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内であることを特徴とする。 The wood substrate according to one aspect of the present invention is a wood substrate comprising a wood material having at least one of a powdered and chipped form and a thermoplastic resin composition, the thermoplastic resin composition comprising a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride, the thermoplastic resin being a polyolefin resin having a melting point in the range of 120°C to 140°C, and the content of the acid-containing resin being in the range of 5 parts by mass to 50 parts by mass per 100 parts by mass of the thermoplastic resin.

本発明の一態様に係る木質基材の熱可塑性樹脂は、密度が0.93g/cm以上のポリオレフィン樹脂であることを特徴とする。
本発明の一態様に係る木質基材の熱可塑性樹脂は、JIS K7210-1:2014に規定された方法において、温度190℃、荷重21.18Nの条件で、A法により測定したときに、1g/10分以上30g/10分以下の範囲内のメルトフローレートを有することを特徴とする。
The thermoplastic resin of the wood substrate according to one embodiment of the present invention is characterized in that it is a polyolefin resin having a density of 0.93 g/ cm3 or more.
The thermoplastic resin of the wood substrate according to one embodiment of the present invention is characterized in that it has a melt flow rate in the range of 1 g/10 min to 30 g/10 min when measured by Method A under conditions of a temperature of 190° C. and a load of 21.18 N in accordance with the method specified in JIS K7210-1:2014.

本発明の一態様に係る木質基材は、前記木質材料と、前記熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)が、95/5~70/30の範囲内であることを特徴とする。
本発明の一態様に係る木質基材は、前記酸含有樹脂が、無水マレイン酸変性ポリオレフィンであることを特徴とする。
The wood base material according to one embodiment of the present invention is characterized in that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) is within the range of 95/5 to 70/30.
In one aspect of the present invention, the acid-containing resin in the wood substrate is a maleic anhydride-modified polyolefin.

本発明の一態様に係る木質基材は、前記熱可塑性樹脂組成物が有機過酸化物をさらに含み、前記有機過酸化物の含有量が、前記熱可塑性樹脂100質量部に対し、0.01質量部以上3質量部以下の範囲内であることを特徴とする。
本発明の一態様に係る木質基材は、前記木質材料が、菌床を原料に含むことを特徴とする。
本発明の一態様に係る化粧材は、上述した木質基材に、意匠性基材が積層されてなることを特徴とする。
In one embodiment of the present invention, the wood substrate is characterized in that the thermoplastic resin composition further contains an organic peroxide, and the content of the organic peroxide is in the range of 0.01 parts by mass or more and 3 parts by mass or less per 100 parts by mass of the thermoplastic resin.
A wood base material according to one aspect of the present invention is characterized in that the wood material contains a mushroom bed as a raw material.
A decorative material according to one aspect of the present invention is characterized in that a decorative substrate is laminated onto the above-mentioned wood substrate.

本発明の一態様に係る木質基材の製造方法は、粉体状及びチップ状の少なくとも一方の形状を有する木質材料と、粉体状の熱可塑性樹脂組成物と、を含む原料混合物を加熱加圧して木質基材を形成する工程を有し、前記熱可塑性樹脂組成物が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、前記熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、前記酸含有樹脂の含有量が、前記熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内であることを特徴とする。 A method for producing a wood substrate according to one aspect of the present invention includes a step of forming a wood substrate by heating and pressurizing a raw material mixture containing a wood material having at least one of a powdered and chipped shape and a powdered thermoplastic resin composition, the thermoplastic resin composition containing a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride, the thermoplastic resin being a polyolefin resin having a melting point in the range of 120°C to 140°C, and the content of the acid-containing resin being in the range of 5 parts by mass to 50 parts by mass per 100 parts by mass of the thermoplastic resin.

本発明の一態様によれば、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制し、且つ実用的な耐水性を備えた木質基材、その木質基材を備えた化粧材及びその木質基材の製造方法を提供できる。 According to one aspect of the present invention, it is possible to provide a wood substrate that suppresses the emission of harmful substances such as formaldehyde that cause sick house syndrome and has practical water resistance, a decorative material that includes the wood substrate, and a method for manufacturing the wood substrate.

本発明の第1実施形態に係る木質基材の製造工程を説明するための模式図である。FIG. 2 is a schematic diagram illustrating a manufacturing process of a wood base material according to the first embodiment of the present invention. 本発明の第2実施形態に係る化粧材の構成を示す概略断面図である。4 is a schematic cross-sectional view showing the configuration of a decorative material according to a second embodiment of the present invention. FIG.

[第1実施形態]
図1には、本発明の第1実施形態に係る木質基材20が示されている。木質基材20は、木質材料11の種類などによりパーティクルボードや中密度繊維板などと称され、床や壁などの下地材、建具や家具など幅広い用途で使用されている。
木質基材20は、図1に示すように、粉体状及びチップ状の少なくとも一方の形状を有する木質材料11と、粉体状の熱可塑性樹脂組成物12とを含む原料混合物10を加熱加圧して形成される。なお、木質基材20には、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質は含まれていない。よって、木質基材20内部からのホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制することができる。
以下、木質基材20を構成する木質材料11と、熱可塑性樹脂組成物12とについて説明する。
[First embodiment]
1 shows a wood substrate 20 according to a first embodiment of the present invention. The wood substrate 20 is called a particle board, a medium density fiberboard, or the like depending on the type of wood material 11, and is used for a wide range of applications such as underlayment for floors and walls, fittings, and furniture.
As shown in Fig. 1, the wood substrate 20 is formed by heating and pressurizing a raw material mixture 10 containing a wood material 11 having at least one of a powdered and chipped shape and a powdered thermoplastic resin composition 12. The wood substrate 20 does not contain harmful substances such as formaldehyde that cause sick house syndrome. Therefore, it is possible to suppress the emission of harmful substances such as formaldehyde that cause sick house syndrome from inside the wood substrate 20.
The wood material 11 and the thermoplastic resin composition 12 that constitute the wood substrate 20 will be described below.

(木質材料11)
木質材料11は、粉体状及びチップ状の少なくとも一方の形状を有するものである。ここで、「粉体状」、「チップ状」には、サイズや形状の定義は一般に存在しない。本実施形態では、そのサイズ(平均粒径)が概ね数十ミクロン~数センチメートルの範囲にあるものをいう。本実施形態における木質材料11の平均粒径は、例えば、10μm以上10mm以下の範囲内である。
(Wood Materials 11)
The wood material 11 has at least one of a powder and chip shape. Here, there is generally no definition of size or shape for "powder" and "chip shape." In this embodiment, the size (average particle size) is generally in the range of several tens of microns to several centimeters. The average particle size of the wood material 11 in this embodiment is, for example, in the range of 10 μm to 10 mm.

木質材料11は、例えば、木粉、木質繊維、木材をチップ状に破砕したものが挙げられ、その原料としては、例えば、間伐材、オガ粉、廃木材などを用いることができる。
また、木質材料11は、木材以外でも、例えば、竹、麻、ヤシ繊維、クルミ殻など、木材と同様にセルロース成分を含むものであれば、その候補とすることができる。
Examples of the wood material 11 include wood powder, wood fiber, and wood crushed into chips, and examples of the raw material that can be used include thinned wood, sawdust, and waste wood.
Furthermore, materials other than wood may be used as the wood material 11, such as bamboo, hemp, coconut fiber, and walnut shells, as long as they contain cellulose components similar to wood.

木質材料11の原料としては、例えば、キノコ栽培時に大量に発生する使用済み菌床が好適である。菌床は、キノコ栽培に用いる培地であり、木材チップやオガ粉にフスマや米ぬかなどの栄養分を混ぜたものである。菌床は、キノコ栽培後の国内で年間30万トン前後が廃棄されていると推定されバイオマスとして有望であるが、リサイクルが進んでいないのが現状である。 As a raw material for the wood material 11, for example, used mushroom beds, which are generated in large quantities during mushroom cultivation, are suitable. The mushroom beds are a culture medium used in mushroom cultivation, and are made by mixing wood chips and sawdust with nutrients such as bran and rice bran. It is estimated that around 300,000 tons of mushroom beds are discarded annually in Japan after mushroom cultivation, making them a promising source of biomass, but recycling is currently not progressing well.

本実施形態において、菌床を木質材料11として使用する場合には、木質材料11全体の体積に占める菌床の割合は、1%以上100%以下の範囲内であればよく、好ましくは、50%以上100%以下の範囲内である。菌床の含有量が上記数値範囲内であれば、製造コストを通常の木質チップを用いた場合と比較して低減することができる。 In this embodiment, when a mushroom bed is used as the wood material 11, the ratio of the mushroom bed to the total volume of the wood material 11 may be within the range of 1% to 100%, and preferably within the range of 50% to 100%. If the mushroom bed content is within the above numerical range, the production cost can be reduced compared to when ordinary wood chips are used.

(木質材料11と熱可塑性樹脂組成物12との質量比)
木質材料11と熱可塑性樹脂組成物12との質量比(木質材料/熱可塑性樹脂組成物)は、95/5~70/30の範囲内であることが好ましい。
木質材料11の含有量が、上記した数値(95/5)より大きくなると、木質基材20に十分な機械強度を付与することができない。一方、木質材料11の含有量が、上記した数値(70/30)より小さくなると、加熱加圧時に木質基材20の変形が生じやすくなり好ましくない。
(Mass ratio of wood material 11 to thermoplastic resin composition 12)
The mass ratio of the wood material 11 to the thermoplastic resin composition 12 (wood material/thermoplastic resin composition) is preferably within the range of 95/5 to 70/30.
If the content of the wood material 11 is greater than the above-mentioned value (95/5), sufficient mechanical strength cannot be imparted to the wood base material 20. On the other hand, if the content of the wood material 11 is less than the above-mentioned value (70/30), the wood base material 20 is likely to deform when heated and pressed, which is not preferable.

(熱可塑性樹脂組成物12)
熱可塑性樹脂組成物12は、その形状が粉体状であり、且つ、熱可塑性樹脂と酸含有樹脂とを含有した組成物である。本実施形態における熱可塑性樹脂組成物12の平均粒径は、例えば、10μm以上1mm以下の範囲内である。
(Thermoplastic resin composition 12)
The thermoplastic resin composition 12 is in the form of powder and is a composition containing a thermoplastic resin and an acid-containing resin. The average particle size of the thermoplastic resin composition 12 in this embodiment is For example, the thickness is in the range of 10 μm to 1 mm.

(熱可塑性樹脂)
熱可塑性樹脂は、木質基材20に機械強度と耐熱性、さらには耐寒性を付与することができ、且つ加熱加圧時における変形が少ない点でポリオレフィン樹脂が好ましく、ポリプロピレン及びポリエチレンであればより好ましく、ポリエチレンであればさらに好ましい。熱可塑性樹脂は、密度が0.93g/cm以上、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂がより好ましく、密度が0.94g/cm以上、融点が125℃以上135℃以下の範囲内のポリオレフィン樹脂が更に好ましい。
(Thermoplastic resin)
The thermoplastic resin is preferably a polyolefin resin, more preferably polypropylene or polyethylene, and even more preferably polyethylene, because it can impart mechanical strength, heat resistance, and cold resistance to the wood substrate 20 and is less likely to deform when heated and pressurized. The thermoplastic resin is more preferably a polyolefin resin having a density of 0.93 g/ cm3 or more and a melting point in the range of 120°C to 140°C, and even more preferably a polyolefin resin having a density of 0.94 g/cm3 or more and a melting point in the range of 125°C to 135°C.

密度が0.93g/cm未満であると、木質基材20の耐熱性が低下する場合があるため好ましくない。
融点が120℃に満たないと、木質基材20に十分な耐熱性を得ることができず、機械強度が低下する場合が多いため好ましくない。また、融点が140℃を超えると、木質基材20に十分な耐寒性を得ることができず、加熱加圧時に変形を生じるため好ましくない。
If the density is less than 0.93 g/cm 3 , the heat resistance of the wood base material 20 may decrease, which is undesirable.
If the melting point is less than 120° C., the wood base material 20 cannot have sufficient heat resistance and the mechanical strength is often reduced, which is not preferable. On the other hand, if the melting point is more than 140° C., the wood base material 20 cannot have sufficient cold resistance and is likely to deform when heated and pressed, which is not preferable.

なお、本実施形態において、熱可塑性樹脂の密度の上限値は限定されるものではないが、1.00g/cm以下、好ましくは0.97g/cm以下である。これは、密度が1.00g/cmを超える熱可塑性樹脂は実質的に存在せず、仮に存在したとしてもその入手が極めて困難だからである。 In this embodiment, the upper limit of the density of the thermoplastic resin is not limited, but is 1.00 g/cm3 or less, and preferably 0.97 g/cm3 or less. This is because thermoplastic resins with a density exceeding 1.00 g/ cm3 do not substantially exist, and even if they exist, they are extremely difficult to obtain.

また、熱可塑性樹脂を備えた木質基材20であれば、熱可塑性樹脂が有する高い耐水性に起因して木質基材20全体に優れた耐水性を付与することができる。具体的には、耐水性に優れた熱可塑性樹脂が木質材料11の表面を覆うため、木質基材20全体の吸水膨張を抑制し木質基材20全体に優れた耐水性を付与することができる。 In addition, if the wood substrate 20 contains a thermoplastic resin, the high water resistance of the thermoplastic resin can impart excellent water resistance to the entire wood substrate 20. Specifically, since the thermoplastic resin with excellent water resistance covers the surface of the wood material 11, the water absorption and expansion of the entire wood substrate 20 can be suppressed, and excellent water resistance can be imparted to the entire wood substrate 20.

本実施形態において使用可能なポリオレフィン樹脂としては、上述したポリエチレンやポリプロピレン以外に、例えば、ポリメチルペンテン、ポリブテン、エチレン-プロピレン共重合体、エチレン-α-オレフィン共重合体、プロピレン-α-オレフィン共重合体等のポリオレフィン樹脂や、エチレン-酢酸ビニル共重合体、エチレン-ビニルアルコール共重合体、エチレン-(メタ)アクリル酸(エステル)共重合体、エチレン-不飽和カルボン酸共重合体金属中和物(アイオノマー)等のオレフィン系共重合体樹脂等のポリオレフィン系樹脂等、或いはこれらの2種以上の混合物、共重合体、複合体、積層体等が挙げられる。 In addition to the above-mentioned polyethylene and polypropylene, examples of polyolefin resins that can be used in this embodiment include polyolefin resins such as polymethylpentene, polybutene, ethylene-propylene copolymer, ethylene-α-olefin copolymer, and propylene-α-olefin copolymer, as well as polyolefin-based resins such as olefin-based copolymer resins such as ethylene-vinyl acetate copolymer, ethylene-vinyl alcohol copolymer, ethylene-(meth)acrylic acid (ester) copolymer, and ethylene-unsaturated carboxylic acid copolymer metal neutralized product (ionomer), or mixtures, copolymers, composites, laminates, and the like of two or more of these.

プロピレンを主成分とする単独又は共重合体であるポリプロピレン系樹脂としては、例えば、ホモポリプロピレン樹脂、ランダムポリプロピレン樹脂、ブロックポリプロピレン樹脂等を単独又は適宜配合した樹脂、またはそれらに更にアタクチックポリプロピレンを適宜配合した樹脂等を使用することができる。また、プロピレン以外のオレフィン系単量体を含む共重合体であってもよく、例えば、ポリプロピレン結晶部を有し、且つプロピレン以外の炭素数2~20のα-オレフィン、好ましくはエチレン、ブテン-1、4-メチルペンテン-1、ヘキセン-1又はオクテン-1のコモノマーの1種又は2種以上を15モル%以上含有するプロピレン-α-オレフィン共重合体等を例示できる。また、通常ポリプロピレン系樹脂の柔軟化に用いられている低密度ポリエチレン、エチレン-α-オレフィン共重合体、エチレン-プロピレン共重合ゴム、エチレン-プロピレン-非共役ジエン共重合ゴム、スチレン-ブタジエン共重合体又はその水素添加物等の改質剤を適宜添加できる。ここで、上記「主成分」とは、ポリプロピレン系樹脂全体の質量の50質量%以上をプロピレン成分が占めている状態をいう。
なお、上記した材料の中でも特に、密度及び融点の観点から高密度ポリエチレン(HDPE)が本実施形態のポリオレフィン樹脂として好ましい。
Examples of polypropylene-based resins that are homopolymers or copolymers mainly composed of propylene include homopolypropylene resins, random polypropylene resins, block polypropylene resins, etc., or resins obtained by appropriately blending these resins with atactic polypropylene. Copolymers containing olefin monomers other than propylene are also acceptable, and examples thereof include propylene-α-olefin copolymers having polypropylene crystal parts and containing 15 mol% or more of one or more comonomers of α-olefins having 2 to 20 carbon atoms other than propylene, preferably ethylene, butene-1, 4-methylpentene-1, hexene-1, or octene-1. Modifiers such as low-density polyethylene, ethylene-α-olefin copolymers, ethylene-propylene copolymer rubber, ethylene-propylene-non-conjugated diene copolymer rubber, styrene-butadiene copolymers, or hydrogenated products thereof, which are usually used to soften polypropylene-based resins, can be appropriately added. Here, the above-mentioned "main component" refers to a state in which the propylene component accounts for 50 mass % or more of the total mass of the polypropylene-based resin.
Among the above-mentioned materials, high density polyethylene (HDPE) is particularly preferable as the polyolefin resin of this embodiment in terms of density and melting point.

また、熱可塑性樹脂のメルトフローレートは、JIS K7210-1:2014に規定された方法において、温度190℃、荷重21.18Nの条件で、A法により測定したときに、1g/10分以上30g/10分以下の範囲内であることが好ましい。
メルトフローレートが1g/10分に満たないと、木質基材等に馴染みにくいため好ましくない。また、メルトフローレートが30g/10分を超えると、加熱加圧による成形が困難となるため好ましくない。
In addition, the melt flow rate of the thermoplastic resin is preferably in the range of 1 g/10 min to 30 g/10 min when measured by Method A under conditions of a temperature of 190° C. and a load of 21.18 N in the method specified in JIS K7210-1:2014.
If the melt flow rate is less than 1 g/10 min, it is not preferable because it is difficult to blend with wood substrates, etc. If the melt flow rate exceeds 30 g/10 min, it is not preferable because it becomes difficult to mold the composition by applying heat and pressure.

(酸含有樹脂)
酸含有樹脂は、木質材料11と熱可塑性樹脂との接着性を向上させるため、カルボン酸及びカルボン酸無水物の少なくとも一つを含む樹脂が用いられる。
酸含有樹脂としては、例えば、無水マレイン酸変性ポリエチレンや無水マレイン酸ポリプロレンなど無水マレイン酸変性ポリオレフィン、エチレン(メタ)アクリル酸共重合体、または無水イタコン酸変性ポリエチレンなどを用いることができるが、セルロースを含む木質材料11との馴染み易さ(接着性の観点)から、無水マレイン酸変性ポリオレフィンが好ましく、無水マレイン酸変性ポリエチレンがさらに好ましい。
(Acid-containing resin)
The acid-containing resin used is a resin containing at least one of a carboxylic acid and a carboxylic acid anhydride in order to improve the adhesiveness between the wood material 11 and the thermoplastic resin.
Examples of the acid-containing resin that can be used include maleic anhydride-modified polyolefins such as maleic anhydride-modified polyethylene and maleic anhydride polypropylene, ethylene (meth)acrylic acid copolymers, and itaconic anhydride-modified polyethylene. From the viewpoint of compatibility with the wood material 11 containing cellulose (in terms of adhesiveness), maleic anhydride-modified polyolefins are preferred, and maleic anhydride-modified polyethylene is even more preferred.

(酸含有樹脂の添加量)
酸含有樹脂の添加量は、熱可塑性樹脂100質量部に対して5質量部以上50質量部以下の範囲内が好ましく、10質量部以上40質量部以下の範囲内がさらに好ましい。
酸含有樹脂の添加量が5質量部に満たないと、木質材料11と熱可塑性樹脂との接着性が不足するため、木質基材20に十分な強度を付与することができない。また、酸含有樹脂の添加量が50質量部を超えると木質基材20の強度が低下する場合が多いため好ましくない。
(Amount of Acid-Containing Resin Added)
The amount of the acid-containing resin added is preferably in the range of 5 parts by mass to 50 parts by mass, and more preferably in the range of 10 parts by mass to 40 parts by mass, per 100 parts by mass of the thermoplastic resin.
If the amount of the acid-containing resin added is less than 5 parts by mass, the adhesion between the wood material 11 and the thermoplastic resin will be insufficient, making it impossible to impart sufficient strength to the wood substrate 20. If the amount of the acid-containing resin added is more than 50 parts by mass, the strength of the wood substrate 20 will often decrease, which is not preferable.

なお、木質材料11と熱可塑性樹脂との接着性が不足した状態では、木質材料11を構成する木質チップ等の表面全体を熱可塑性樹脂で覆うことができていないため、木質材料11内に侵入した水分によって木質基材20全体が吸水膨張し、木質基材20全体の耐水性が低下する。 When the adhesion between the wood material 11 and the thermoplastic resin is insufficient, the entire surface of the wood chips and other components that make up the wood material 11 cannot be covered with thermoplastic resin, and moisture that has penetrated into the wood material 11 causes the entire wood base material 20 to absorb water and expand, reducing the water resistance of the entire wood base material 20.

(有機過酸化物)
熱可塑性樹脂組成物12は、有機過酸化物をさらに含んでいてもよい。
有機過酸化物は、原料混合物10の加熱加圧工程において、熱可塑性樹脂同士をラジカル架橋するために用いてもよい。また、酸含有樹脂にラジカル架橋性を有する材料を用いれば、熱可塑性樹脂組成物12に有機過酸化物を添加することで、酸含有樹脂と熱可塑性樹脂とに架橋を生じさせることができる。熱可塑性樹脂同士、または酸含有樹脂と熱可塑性樹脂との間にラジカル架橋が形成されると、その架橋構造により、木質基材20全体の機械強度が向上する。
(Organic peroxides)
The thermoplastic resin composition 12 may further contain an organic peroxide.
The organic peroxide may be used for radical crosslinking between thermoplastic resins in the heating and pressurizing step of the raw material mixture 10. In addition, if a material having radical crosslinking properties is used for the acid-containing resin, crosslinking can be caused between the acid-containing resin and the thermoplastic resin by adding an organic peroxide to the thermoplastic resin composition 12. When radical crosslinking is formed between thermoplastic resins or between the acid-containing resin and the thermoplastic resin, the mechanical strength of the entire wood substrate 20 is improved due to the crosslinked structure.

有機過酸化物は、特に限定されるものではなく、例えば、パーオキシケタール、ジアルキルパーオキサイド、ジアシルパーオキサイド、パーオキシエステルなどの既存材料から、反応性や安定性を考慮し適宜選択して用いられる。
また、有機過酸化物は、ラジカル架橋剤の一種であり、例えば、ヒドロペルオキシド類、ジアシルペルオキシド類、ペルオキシジカルボナート類、ペルオキシエステル類、ペルオキシカルボナート類、ジアルキルペルオキシド類、ケトンペルオキシド類等がある。
The organic peroxide is not particularly limited, and may be appropriately selected from existing materials such as peroxyketals, dialkyl peroxides, diacyl peroxides, and peroxyesters, taking into consideration their reactivity and stability.
The organic peroxide is a type of radical crosslinking agent, and examples thereof include hydroperoxides, diacyl peroxides, peroxydicarbonates, peroxyesters, peroxycarbonates, dialkyl peroxides, and ketone peroxides.

(有機過酸化物の添加量)
有機過酸化物の添加量は、熱可塑性樹脂100質量部に対して0.01質量部以上3質量部以下の範囲内が望ましい。
有機過酸化物の添加量が0.01質量部に満たないと、原料混合物の加熱加圧時の反応性が不足するため、木質基材の強度向上に寄与しない。また、有機過酸化物の添加量が3質量部を超えると反応時の分解生成物が多くなり、木質基材の変形の原因になる場合があるため好ましくない。
(Amount of organic peroxide added)
The amount of the organic peroxide added is desirably within the range of 0.01 parts by mass to 3 parts by mass relative to 100 parts by mass of the thermoplastic resin.
If the amount of organic peroxide added is less than 0.01 parts by mass, the reactivity of the raw material mixture when heated and pressurized is insufficient, and therefore the strength of the wood substrate is not improved. If the amount of organic peroxide added is more than 3 parts by mass, the amount of decomposition products during the reaction increases, which may cause deformation of the wood substrate, and is therefore undesirable.

さらに、熱可塑性樹脂組成物12に有機過酸化物を添加することで、熱可塑性樹脂と、酸含有樹脂と、木質材料11との間にラジカル架橋による3次元ネットワーク(結合)を形成することが可能となる。これにより、木質基材20全体の機械強度が向上する。 Furthermore, by adding an organic peroxide to the thermoplastic resin composition 12, it becomes possible to form a three-dimensional network (bonds) by radical crosslinking between the thermoplastic resin, the acid-containing resin, and the wood material 11. This improves the mechanical strength of the entire wood substrate 20.

(熱可塑性樹脂組成物12の作成方法)
有機過酸化物と酸含有樹脂とを含む熱可塑性樹脂組成物12は、各種公知の方法で作製することが可能である。例えば、一軸混錬機やバッチ式混錬機を用いて熱可塑性樹脂とともに酸含有樹脂と有機過酸化物とを加熱混錬後、機械的粉砕や凍結粉砕などの方法で粉体化することができる。
(Method of Preparing Thermoplastic Resin Composition 12)
The thermoplastic resin composition 12 containing an organic peroxide and an acid-containing resin can be produced by various known methods. For example, the acid-containing resin and the organic peroxide can be heated and kneaded together with the thermoplastic resin using a single-axis kneader or a batch kneader, and then powdered by a method such as mechanical crushing or freeze crushing.

(原料混合物10の加熱加圧による製造方法)
原料混合物10の加熱加圧は各種公知の方法を用いることができるが、枠型を用いたプレス成型が好適である。
加熱温度は通常は、120℃以上250℃以下の範囲内であり、熱可塑性樹脂の融点以上であることが必要であるが、加熱温度が250℃を超えると木質材料11の熱劣化が顕著に生じ場合がある。加圧圧力は、通常は10kgf/cm以上400kgf/cm以下の範囲内であり、所望する木質基材の密度により適宜した値を用いる。
(Production method by heating and pressurizing raw material mixture 10)
The raw material mixture 10 can be heated and pressurized by various known methods, but press molding using a mold is preferred.
The heating temperature is usually within the range of 120° C. to 250° C. and must be equal to or higher than the melting point of the thermoplastic resin, but if the heating temperature exceeds 250° C., significant thermal degradation of the wood material 11 may occur. The pressing pressure is usually within the range of 10 kgf/ cm2 to 400 kgf/ cm2 , and an appropriate value is used depending on the desired density of the wood base material.

上記で得られる木質基材20の密度や形状は用途に応じて適宜決定されるが、密度については0.5g/cm以上1.2g/cm以下の範囲内が好ましく、0.6g/cm以上1.1g/cm以下の範囲内がさらに好ましい。木質基材20の密度が上記数値の範囲内であれば、木質基材20全体の機械強度がさらに向上する。さらに、木質基材20の密度が上記数値の範囲内であれば、木質基材20全体に含まれる細孔容量が少なくなるため、耐熱性や耐寒性も向上する。 The density and shape of the wood substrate 20 obtained as described above are appropriately determined depending on the application, but the density is preferably in the range of 0.5 g/ cm3 to 1.2 g/ cm3 , and more preferably in the range of 0.6 g/ cm3 to 1.1 g/ cm2 . If the density of the wood substrate 20 is within the above numerical range, the mechanical strength of the entire wood substrate 20 is further improved. Furthermore, if the density of the wood substrate 20 is within the above numerical range, the pore volume contained in the entire wood substrate 20 is reduced, and therefore the heat resistance and cold resistance are also improved.

[第2実施形態]
図2を用いて第2実施形態について説明する。
第2実施形態は、先に図1を用いて説明した第1実施形態に係る木質基材20に、意匠性を有する意匠性基材31を積層した化粧材30である。
本実施形態によれば、木質基材20に意匠性基材31を積層することで、意匠性を付与することができる。
[Second embodiment]
The second embodiment will be described with reference to FIG.
The second embodiment is a decorative material 30 in which a decorative substrate 31 having a design is laminated on the wood substrate 20 according to the first embodiment described above with reference to FIG.
According to this embodiment, by laminating the decorative substrate 31 on the wood substrate 20, a decorative feature can be imparted.

すなわち、木質基材20は、基材単独でも化粧材として実用に供することができるが、木質基材20にさらに優れた意匠性を付与するため、図2に示すように絵柄などの意匠が付与された紙やフィルムなどの意匠性基材31を木質基材20に積層して化粧材30としてもよい。 That is, the wood base material 20 can be used as a decorative material by itself, but in order to impart even more excellent design to the wood base material 20, a decorative base material 31 such as paper or film with a design such as a picture may be laminated onto the wood base material 20 as shown in FIG. 2 to form the decorative material 30.

[本実施形態の効果]
本実施形態に係る木質基材20は、粉体状及びチップ状の少なくとも一方の形状を有する木質材料11と、熱可塑性樹脂組成物12と、を含み、熱可塑性樹脂組成物12が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、酸含有樹脂の含有量が、熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内である。
[Effects of this embodiment]
The wood substrate 20 of this embodiment comprises a wood material 11 having at least one of a powder and chip form, and a thermoplastic resin composition 12. The thermoplastic resin composition 12 contains a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride. The thermoplastic resin is a polyolefin resin having a melting point in the range of 120°C or more and 140°C or less, and the content of the acid-containing resin is in the range of 5 parts by mass or more and 50 parts by mass or less per 100 parts by mass of the thermoplastic resin.

このような構成であれば、木質基材20は、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質を含有していないため、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制することができる。また、木質基材20は熱可塑性樹脂を含んでいるため、その熱可塑性樹脂が有する高い耐水性に起因して木質基材20に優れた耐水性を付与することができる。 With this configuration, the wood base material 20 does not contain harmful substances that cause sick house syndrome, such as formaldehyde, and therefore the emission of harmful substances that cause sick house syndrome, such as formaldehyde, can be suppressed. In addition, since the wood base material 20 contains a thermoplastic resin, the high water resistance of the thermoplastic resin can impart excellent water resistance to the wood base material 20.

また、本実施形態の熱可塑性樹脂は、その密度が0.93g/cm以上のポリオレフィン樹脂であってもよい。
このような構成であれば、木質基材20の耐熱性をさらに向上させることができる。
The thermoplastic resin of the present embodiment may be a polyolefin resin having a density of 0.93 g/cm 3 or more.
With this configuration, the heat resistance of the wood base material 20 can be further improved.

また、本実施形態の熱可塑性樹脂は、JIS K7210-1:2014に規定された方法において、温度190℃、荷重21.18Nの条件で、A法により測定したときに、1g/10分以上30g/10分以下の範囲内のメルトフローレートを有していてもよい。
このような構成であれば、熱可塑性樹脂が木質基材等に馴染みに易く、加熱加圧による成形が容易となる。
In addition, the thermoplastic resin of this embodiment has a melt flow rate in the range of 1 g/10 min or more and 30 g/10 min or less when measured by Method A under conditions of a temperature of 190 ° C. and a load of 21.18 N in the method specified in JIS K7210-1:2014. It may have a melt flow rate of 1 g/10 min or more and 30 g/10 min or less.
With such a structure, the thermoplastic resin easily blends with the wood substrate and the like, facilitating molding by heating and pressurization.

また、本実施形態の木質材料11と熱可塑性樹脂組成物12との質量比(木質材料/熱可塑性樹脂組成物)は、95/5~70/30の範囲内であってもよい。
このような構成であれば、木質基材20に十分な機械強度を付与しつつ、加熱加圧時における木質基材20の変形を低減することができる。
The mass ratio of the wood material 11 to the thermoplastic resin composition 12 in this embodiment (wood material/thermoplastic resin composition) may be within a range of 95/5 to 70/30.
With this configuration, it is possible to impart sufficient mechanical strength to the wood base material 20 while reducing deformation of the wood base material 20 when heated and pressurized.

また、本実施形態の酸含有樹脂は、無水マレイン酸変性ポリオレフィンであってもよい。
このような構成であれば、木質材料11と熱可塑性樹脂との接着性をさらに向上させることができる。
The acid-containing resin of the present embodiment may be a maleic anhydride-modified polyolefin.
With this configuration, the adhesion between the wood material 11 and the thermoplastic resin can be further improved.

また、本実施形態の熱可塑性樹脂組成物12は、有機過酸化物をさらに含み、その有機過酸化物の含有量は、熱可塑性樹脂100質量部に対し、0.01質量部以上3質量部以下の範囲内であってもよい。
このような構成であれば、木質基材20の強度が向上し、且つ木質基材20の変形を低減することができる。さらに、このような構成であれば、熱可塑性樹脂と、酸含有樹脂と、木質材料11との間にラジカル架橋による3次元ネットワーク(結合)を形成することが可能となり、木質基材20の機械強度を向上させることができる。
In addition, the thermoplastic resin composition 12 of this embodiment further contains an organic peroxide, and the content of the organic peroxide may be in the range of 0.01 parts by mass or more and 3 parts by mass or less per 100 parts by mass of the thermoplastic resin.
Such a configuration improves the strength of the wood substrate 20 and reduces deformation of the wood substrate 20. Furthermore, such a configuration makes it possible to form a three-dimensional network (bonds) by radical crosslinking between the thermoplastic resin, the acid-containing resin, and the wood material 11, thereby improving the mechanical strength of the wood substrate 20.

また、本実施形態の木質材料11は、菌床を原料に含んでいてもよい。
このような構成であれば、環境に配慮した木質材料11を製造することができる。
Furthermore, the wood material 11 of this embodiment may contain a mushroom bed as a raw material.
With this configuration, the wood material 11 can be manufactured in an environmentally friendly manner.

また、本実施形態の化粧材30は、木質基材20に意匠性基材31を積層させたものであってもよい。
このような構成であれば、木質基材20の意匠性を高めることができる。
The decorative material 30 of this embodiment may be formed by laminating a decorative substrate 31 onto a wood substrate 20 .
With this configuration, the design of the wood base material 20 can be improved.

また、本実施形態の木質基材20の製造方法は、粉体状及びチップ状の少なくとも一方の形状を有する木質材料11と、粉体状の熱可塑性樹脂組成物12と、を含む原料混合物10を加熱加圧して木質基材20を形成する工程を有し、熱可塑性樹脂組成物12が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、酸含有樹脂の含有量は、熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内である。 The manufacturing method of the wood substrate 20 of this embodiment includes a step of forming the wood substrate 20 by heating and pressurizing a raw material mixture 10 containing a wood material 11 having at least one of a powdered and chipped shape and a powdered thermoplastic resin composition 12, the thermoplastic resin composition 12 containing a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride, the thermoplastic resin being a polyolefin resin having a melting point in the range of 120°C to 140°C, and the content of the acid-containing resin being in the range of 5 parts by mass to 50 parts by mass per 100 parts by mass of the thermoplastic resin.

このような構成であれば、製造された木質基材20は、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質を含有していないため、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制することができる。また、製造された木質基材20は熱可塑性樹脂を含んでいるため、その熱可塑性樹脂が有する高い耐水性に起因して木質基材20に優れた耐水性を付与することができる。 With this configuration, the manufactured wood base material 20 does not contain harmful substances such as formaldehyde that cause sick house syndrome, and therefore the emission of harmful substances such as formaldehyde that cause sick house syndrome can be suppressed. In addition, since the manufactured wood base material 20 contains a thermoplastic resin, the high water resistance of the thermoplastic resin can impart excellent water resistance to the wood base material 20.

[実施例]
以下に、本発明の第1実施形態に係る木質基材の実施例1~28及び比較例1~4について説明する。なお、本発明は、下記の実施例1~28に限定されるものではない。
[Example]
Below, examples 1 to 28 of wood base materials according to the first embodiment of the present invention and comparative examples 1 to 4 will be described. Note that the present invention is not limited to the following examples 1 to 28.

(実施例1)
実施例1の熱可塑性樹脂組成物の成分、質量は、次の通りである。
(1)高密度ポリエチレン樹脂 100質量部
(融点129℃、密度0.952g/cm、MFR(190℃、2.16kg荷重下)21g/10min)
(2)無水マレイン酸変性ポリエチレン 25質量部
(3)有機過酸化物(パーオキシケタール): 1質量部
上記(1)~(3)をバッチ式混錬装置で加熱混錬後、機械粉砕することで、粉体状の熱可塑性樹脂組成物を得た。
Example 1
The components and masses of the thermoplastic resin composition of Example 1 are as follows.
(1) High density polyethylene resin 100 parts by mass (melting point 129°C, density 0.952 g/ cm3 , MFR (190°C, under a load of 2.16 kg) 21 g/10 min)
(2) Maleic anhydride modified polyethylene: 25 parts by weight (3) Organic peroxide (peroxyketal): 1 part by weight The above (1) to (3) were heated and kneaded in a batch kneader, and then mechanically pulverized to obtain a powdered thermoplastic resin composition.

木質材料には、キノコ収穫後の菌床(平均粒径2mm)を洗浄、乾燥した材料を用いた。
木質材料と熱可塑性樹脂組成物とを、質量比(木質材料/熱可塑性樹脂組成物)「85/15」で乾式混合することで、木質基材の原料混合物を得た。
この原料混合物をアルミ製の型枠に導入し、熱プレス装置で加熱加圧することで本実施例の木質基材を得た(プレス条件:40kgf/cm、200℃10分、基材材厚:10mm、基材密度:0.8g/cm)。
The wood material used was a washed and dried mushroom bed (average particle size: 2 mm) after harvesting.
The wood material and the thermoplastic resin composition were dry mixed in a mass ratio (wood material/thermoplastic resin composition) of "85/15" to obtain a raw material mixture for the wood base material.
This raw material mixture was introduced into an aluminum mold and heated and pressed in a hot press to obtain the wood substrate of this example (pressing conditions: 40 kgf/cm 2 , 200° C. for 10 minutes, substrate thickness: 10 mm, substrate density: 0.8 g/cm 3 ).

以上のように、本実施例の木質基材は、その製造工程において、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質を使用していない。よって、本実施例の木質基材であれば、ホルムアルデヒド等のシックハウス症候群の原因となる有害物質の放散を抑制することができる。 As described above, the manufacturing process of the wood base material of this embodiment does not use harmful substances such as formaldehyde that cause sick house syndrome. Therefore, the wood base material of this embodiment can suppress the emission of harmful substances such as formaldehyde that cause sick house syndrome.

(実施例2)
実施例2では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「70/30」に変更し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 2
In Example 2, the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "70/30," and otherwise a wood base material was obtained in the same manner as in Example 1.

(実施例3)
実施例3では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「95/5」に変更し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 3
In Example 3, the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "95/5," and otherwise a wood base material was obtained in the same manner as in Example 1.

(実施例4)
実施例4では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「60/40」に変更し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 4
In Example 4, the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "60/40," and otherwise a wood base material was obtained in the same manner as in Example 1.

(実施例5)
実施例5では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「97/3」に変更し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 5
In Example 5, the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "97/3," and otherwise a wood base material was obtained in the same manner as in Example 1.

(実施例6)
実施例6では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点124℃、密度0.940g/cm、MFR(190℃、2.16kg荷重下)20g/10minの直鎖系低密度ポリエチレンに変更し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 6
In Example 6, the (1) high-density polyethylene in the thermoplastic resin composition was changed to a linear low-density polyethylene having a melting point of 124°C, a density of 0.940 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 20 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 1.

(実施例7)
実施例7では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点120℃、密度0.919g/cm、MFR(190℃、2.16kg荷重下)20g/10minの直鎖系低密度ポリエチレンに変更し、それ以外は実施例1と同様の方法で木質基材を得た。
(Example 7)
In Example 7, the (1) high-density polyethylene in the thermoplastic resin composition was changed to a linear low-density polyethylene having a melting point of 120°C, a density of 0.919 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 20 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 1.

(実施例8)
実施例8では、熱可塑性樹脂組成物中の(2)酸含有樹脂の配合量を5部とし、それ以外は実施例1と同様の方法で木質基材を得た。
(実施例9)
実施例9では、熱可塑性樹脂組成物中の(2)酸含有樹脂の配合量を50部とし、それ以外は実施例1と同様の方法で木質基材を得た。
(Example 8)
In Example 8, a wood base material was obtained in the same manner as in Example 1, except that the amount of (2) the acid-containing resin in the thermoplastic resin composition was changed to 5 parts.
(Example 9)
In Example 9, a wood base material was obtained in the same manner as in Example 1, except that the amount of (2) the acid-containing resin in the thermoplastic resin composition was changed to 50 parts.

(実施例10)
実施例7では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点130℃、密度0.960g/cm、MFR(190℃、2.16kg荷重下)13g/10minの高密度ポリエチレンとし、それ以外は実施例1と同様の方法で木質基材を得た。
(Example 10)
In Example 7, a wood base material was obtained in the same manner as in Example 1, except that (1) the high-density polyethylene in the thermoplastic resin composition was changed to a high-density polyethylene having a melting point of 130°C, a density of 0.960 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 13 g/10 min.

(実施例11)
実施例11では、熱可塑性樹脂組成物中の(3)有機過酸化物を配合しなかった以外は実施例1と同様の方法で木質基材を得た。
(実施例12)
実施例12では、熱可塑性樹脂組成物中の(3)有機過酸化物を5部配合し、それ以外は実施例1と同様の方法で木質基材を得た。
Example 11
In Example 11, a wood base material was obtained in the same manner as in Example 1, except that the (3) organic peroxide in the thermoplastic resin composition was not blended.
Example 12
In Example 12, a wood base material was obtained in the same manner as in Example 1, except that 5 parts of (3) an organic peroxide was added to the thermoplastic resin composition.

(実施例13)
実施例13では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点130℃、密度0.945g/cm、MFR(190℃、2.16kg荷重下)0.05g/10minの高密度ポリエチレンとし、それ以外は実施例1と同様の方法で木質基材を得た。
Example 13
In Example 13, a wood substrate was obtained in the same manner as in Example 1, except that (1) the high-density polyethylene in the thermoplastic resin composition was changed to a high-density polyethylene having a melting point of 130°C, a density of 0.945 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 0.05 g/10 min.

(実施例14)
実施例14では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点133℃、密度0.960g/cm、MFR(190℃、2.16kg荷重下)40g/10minの高密度ポリエチレンとし、それ以外は実施例1と同様の方法で木質基材を得た。
(Example 14)
In Example 14, a wood base material was obtained in the same manner as in Example 1, except that (1) the high-density polyethylene in the thermoplastic resin composition was changed to a high-density polyethylene having a melting point of 133°C, a density of 0.960 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 40 g/10 min.

(実施例15)
実施例15では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点122℃、密度0.922g/cm、MFR(190℃、2.16kg荷重下)0.6g/10minの低密度ポリエチレンに変更し、(2)酸含有樹脂を「無水マレイン酸ポリプロレン」に変更し、且つその配合量を5部とし、(3)有機過酸化物を配合せず、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を「60/40」とし、木質材料を「木質チップ(平均粒径2mm)」に変更し、それ以外は実施例1と同様の方法で木質基材を得た。
(Example 15)
In Example 15, (1) the high-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene with a melting point of 122°C, a density of 0.922 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 0.6 g/10 min, (2) the acid-containing resin was changed to "maleic anhydride polypropylene" and its amount was set to 5 parts, (3) no organic peroxide was added, the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was set to "60/40", and the wood material was changed to "wood chips (average particle size 2 mm)", and otherwise a wood base material was obtained in the same manner as in Example 1.

(実施例16)
実施例16では、熱可塑性樹脂組成物中の(1)低密度ポリエチレンを、融点122℃の低密度ポリエチレンに変更し、(2)酸含有樹脂の配合量を50部とし、それ以外は実施例15と同様の方法で木質基材を得た。
(Example 16)
In Example 16, a wood base material was obtained in the same manner as in Example 15, except that (1) the low-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene having a melting point of 122°C and (2) the amount of the acid-containing resin was changed to 50 parts.

(実施例17)
実施例17では、熱可塑性樹脂組成物中の(1)低密度ポリエチレンを、融点131℃、密度0.949g/cm、MFR(190℃、2.16kg荷重下)0.05g/10minの低密度ポリエチレンに変更し、それ以外は実施例15と同様の方法で木質基材を得た。
(Example 17)
In Example 17, the (1) low-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene having a melting point of 131°C, a density of 0.949 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 0.05 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 15.

(実施例18)
実施例18では、熱可塑性樹脂組成物中の(1)低密度ポリエチレンを、融点131℃、密度0.949g/cm、MFR(190℃、2.16kg荷重下)0.05g/10minの低密度ポリエチレンに変更し、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 18)
In Example 18, the (1) low-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene having a melting point of 131°C, a density of 0.949 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 0.05 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 16.

(実施例19)
実施例19では、熱可塑性樹脂組成物中の(1)低密度ポリエチレンを、密度0.923g/cm、MFR(190℃、2.16kg荷重下)1.00g/10minの低密度ポリエチレンに変更し、それ以外は実施例15と同様の方法で木質基材を得た。
(Example 19)
In Example 19, the (1) low-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene having a density of 0.923 g/cm 3 and an MFR (190°C, under a load of 2.16 kg) of 1.00 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 15.

(実施例20)
実施例20では、熱可塑性樹脂組成物中の(1)低密度ポリエチレンを、融点123℃、密度0.923g/cm、MFR(190℃、2.16kg荷重下)30.00g/10minの低密度ポリエチレンに変更し、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 20)
In Example 20, the (1) low-density polyethylene in the thermoplastic resin composition was changed to a low-density polyethylene having a melting point of 123°C, a density of 0.923 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 30.00 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 16.

(実施例21)
実施例21では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を「95/5」とし、それ以外は実施例15と同様の方法で木質基材を得た。
(実施例22)
実施例22では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を「70/30」とし、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 21)
In Example 21, a wood base material was obtained in the same manner as in Example 15, except that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was 95/5.
(Example 22)
In Example 22, a wood base material was obtained in the same manner as in Example 16, except that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was set to "70/30."

(実施例23)
実施例23では、熱可塑性樹脂組成物中の(2)酸含有樹脂を「無水マレイン酸変性ポリエチレン」に変更し、それ以外は実施例15と同様の方法で木質基材を得た。
(実施例24)
実施例24では、熱可塑性樹脂組成物中の(2)酸含有樹脂を「無水マレイン酸変性ポリエチレン」に変更し、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 23)
In Example 23, a wood base material was obtained in the same manner as in Example 15, except that (2) the acid-containing resin in the thermoplastic resin composition was changed to “maleic anhydride-modified polyethylene.”
(Example 24)
In Example 24, a wood base material was obtained in the same manner as in Example 16, except that (2) the acid-containing resin in the thermoplastic resin composition was changed to “maleic anhydride-modified polyethylene.”

(実施例25)
実施例25では、熱可塑性樹脂組成物中の(2)有機過酸化物(パーオキシケタール)の配合量を0.01部とし、それ以外は実施例15と同様の方法で木質基材を得た。
(実施例26)
実施例26では、熱可塑性樹脂組成物中の(2)有機過酸化物(パーオキシケタール)の配合量を3.00部とし、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 25)
In Example 25, a wood base material was obtained in the same manner as in Example 15, except that the amount of (2) organic peroxide (peroxyketal) in the thermoplastic resin composition was 0.01 part.
(Example 26)
In Example 26, a wood base material was obtained in the same manner as in Example 16, except that the amount of (2) organic peroxide (peroxyketal) in the thermoplastic resin composition was 3.00 parts.

(実施例27)
実施例27では、木質材料を「キノコ収穫後の菌床(平均粒径2mm)」に変更し、それ以外は実施例15と同様の方法で木質基材を得た。
(実施例28)
実施例28では、木質材料を「キノコ収穫後の菌床(平均粒径2mm)」に変更し、それ以外は実施例16と同様の方法で木質基材を得た。
(Example 27)
In Example 27, a wood base material was obtained in the same manner as in Example 15, except that the wood material was changed to a "harvested mushroom bed (average particle size 2 mm)".
(Example 28)
In Example 28, a wood base material was obtained in the same manner as in Example 16, except that the wood material was changed to a "harvested mushroom bed (average particle size 2 mm)".

(比較例1)
比較例1では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点163℃、密度0.910g/cmのホモポリプロピレンとし、それ以外は実施例1と同様の方法で木質基材を得た。
(Comparative Example 1)
In Comparative Example 1, a wood base material was obtained in the same manner as in Example 1, except that (1) the high density polyethylene in the thermoplastic resin composition was replaced with homopolypropylene having a melting point of 163° C. and a density of 0.910 g/cm 3 .

(比較例2)
比較例2では、熱可塑性樹脂組成物中の(1)高密度ポリエチレンを、融点106℃、密度0.918g/cm、MFR(190℃、2.16kg荷重下)7g/10minの低密度ポリエチレンとし、それ以外は実施例1と同様の方法で木質基材を得た。
(Comparative Example 2)
In Comparative Example 2, the (1) high-density polyethylene in the thermoplastic resin composition was replaced with a low-density polyethylene having a melting point of 106°C, a density of 0.918 g/ cm3 , and an MFR (190°C, under a load of 2.16 kg) of 7 g/10 min, and the rest of the wood base material was obtained in the same manner as in Example 1.

(比較例3)
比較例3では、熱可塑性樹脂組成物中の(2)酸含有樹脂の配合量を60部とし、それ以外は実施例1と同様の方法で木質基材を得た。
(比較例4)
比較例4では、熱可塑性樹脂組成物中の(2)酸含有樹脂の配合量を3部とし、それ以外は実施例1と同様の方法で木質基材を得た。
(Comparative Example 3)
In Comparative Example 3, a wood base material was obtained in the same manner as in Example 1, except that the amount of (2) the acid-containing resin in the thermoplastic resin composition was 60 parts.
(Comparative Example 4)
In Comparative Example 4, a wood base material was obtained in the same manner as in Example 1, except that the amount of (2) the acid-containing resin in the thermoplastic resin composition was 3 parts.

(木質基材の評価)
木質基材の物性評価は、次の(1)機械強度、(2)耐水性、(3)基材変形、(4)耐寒性、(5)耐熱性、の5点で評価した。
(機械強度)
機械強度は、JISA5908に準拠する方法で曲げ強度を測定した。測定値(単位:N/mm)に対する機械強度の評価基準は当該JISの規格値を踏まえ、以下とした。
機械強度の評価基準は、次の通り、「○」、「△」、「×」の3段階で評価し、「○」及び「△」を合格とし、「×」を不合格とした。
○:13以上(合格)
△:8以上13未満(合格)
×:8未満(不合格)
(Evaluation of wood-based materials)
The physical properties of the wood base material were evaluated based on the following five points: (1) mechanical strength, (2) water resistance, (3) substrate deformation, (4) cold resistance, and (5) heat resistance.
(Mechanical strength)
The mechanical strength was measured as bending strength by a method conforming to JIS A 5908. The evaluation criteria for mechanical strength with respect to the measured values (unit: N/mm 2 ) were set as follows, based on the standard values of the JIS.
The mechanical strength was evaluated according to the following three-level scale of "good", "defective", and "bad", with "good" and "defective" being acceptable and "bad" being unacceptable.
○: 13 or more (pass)
△: 8 or more but less than 13 (pass)
×: Less than 8 (failed)

(耐水性)
耐水性は、JISA5908に準拠する方法で吸水厚さ膨潤率を測定した。測定値(単位:%)に対する耐水性の評価基準は当該JISの規格値を踏まえ、以下とした。
耐水性の評価基準は、次の通り、「○」、「△」、「×」の3段階で評価し、「○」及び「△」を合格とし、「×」を不合格とした。
○:8未満(合格)
△:8以上12未満(合格)
×:12以上(不合格)
(water resistance)
The water resistance was measured by measuring the water absorption thickness swelling rate according to a method in accordance with JIS A 5908. The evaluation criteria for water resistance for the measured value (unit: %) were set as follows, based on the standard values of the JIS.
The water resistance was evaluated according to the following three-level scale of "good", "defective" and "bad", with "good" and "defective" representing pass and "bad" representing fail.
○: Less than 8 (pass)
△: 8 or more but less than 12 (pass)
×: 12 or more (fail)

(基材変形)
基材変形とは、基材表面が部分的に膨れた状態であり、主にプレス中に基材内部で発生するガスの滞留により発生する。基材変形は基材端部の状態により如実に反映されるため、基材端部の外観を目視評価した。
基材変形の評価基準は、次の通り、「○」、「△」、「×」の3段階で評価し、「○」及び「△」を合格とし、「×」を不合格とした。
○:空隙なし(合格)
△:痕跡程度の空隙あり(合格)
×:空隙あり(不合格)
(Substrate deformation)
The substrate deformation is a state in which the substrate surface is partially swollen, and is mainly caused by the retention of gas generated inside the substrate during pressing. Since the substrate deformation is clearly reflected by the state of the substrate edge, the appearance of the substrate edge was visually evaluated.
The evaluation criteria for the substrate deformation were as follows: 3-level evaluation of "good", "defective", and "bad", with "good" and "defective" representing pass and "bad" representing fail.
○: No voids (passed)
△: Traces of voids (passed)
×: Voids present (failed)

(耐寒性)
耐寒性とは、5℃環境下に1時間置き、その後JISA5908に準拠する方法で曲げ強度を測定した。測定値(単位:N/mm)に対する機械強度の評価基準は当該JISの規格値を踏まえ、以下とした。
機械強度の評価基準は、次の通り、「○」、「△」、「×」の3段階で評価し、「○」及び「△」を合格とし、「×」を不合格とした。
○:13以上(合格)
△:8以上13未満(合格)
×:8未満(不合格)
(Cold resistance)
For cold resistance, the specimen was placed in a 5° C. environment for 1 hour, and then the bending strength was measured by a method conforming to JIS A 5908. The evaluation criteria for mechanical strength with respect to the measured value (unit: N/mm 2 ) were set as follows, based on the standard values of the JIS.
The mechanical strength was evaluated according to the following three-level scale of "good", "defective", and "bad", with "good" and "defective" being acceptable and "bad" being unacceptable.
○: 13 or more (pass)
△: 8 or more but less than 13 (pass)
×: Less than 8 (failed)

(耐熱性)
耐熱性とは、70℃環境下に1時間置き、その後JISA5908に準拠する方法で曲げ強度を測定した。測定値(単位:N/mm)に対する機械強度の評価基準は当該JISの規格値を踏まえ、以下とした。
機械強度の評価基準は、次の通り、「○」、「△」、「×」の3段階で評価し、「○」及び「△」を合格とし、「×」を不合格とした。
○:8以上(合格)
△:3以上8未満(合格)
×:3未満(不合格)
(Heat resistance)
Heat resistance was measured by placing the sample in a 70° C. environment for 1 hour, and then measuring the bending strength by a method conforming to JIS A 5908. The evaluation criteria for mechanical strength with respect to the measured value (unit: N/mm 2 ) were set as follows, based on the standard values of the JIS.
The mechanical strength was evaluated according to the following three-level scale of "good", "defective", and "bad", with "good" and "defective" being acceptable and "bad" being unacceptable.
○: 8 or more (pass)
△: 3 or more but less than 8 (pass)
×: Less than 3 (failed)

(評価結果)木質基材の評価結果は、次の表1の通りである。
なお、表中の「酸含有樹脂配合量」及び「有機過酸化物配合量」は、それぞれ熱可塑性樹脂100質量部に対する各成分の配合量を示し、「配合比」は「木質材料/熱可塑性樹脂組成物」を示し、「MFR」はJIS K7210:2014, 190℃, 2.16kgの条件で測定された値を示す。
(Evaluation Results) The evaluation results of the wood base materials are as shown in Table 1 below.
In the table, "Amount of acid-containing resin" and "Amount of organic peroxide" respectively indicate the amount of each component per 100 parts by mass of thermoplastic resin, "Blending ratio" indicates "wood material/thermoplastic resin composition," and "MFR" indicates the value measured under the conditions of JIS K7210:2014, 190°C, 2.16 kg.

Figure 0007615718000001
Figure 0007615718000001

5点の物性評価のすべてが「合格」なのは、実施例1~28であり、比較例1~4は1個以上の不合格を含んでいた。 Examples 1 to 28 were "passed" in all five physical property evaluations, while Comparative Examples 1 to 4 included one or more failures.

(機械強度の評価結果)
機械強度が不合格なものは、比較例2、比較例3及び比較例4の3件であった。
比較例2では、熱可塑性樹脂として低密度ポリエチレンを用いており、又、比較例3では「酸含有樹脂」の添加量が多すぎ、又、比較例4では「酸含有樹脂」の添加量が少なすぎることが原因と推測できる。すなわち、「熱可塑性樹脂」の種類と「酸含有樹脂」の過量、少量により、機械強度が低下することが推測できる。
(Mechanical strength evaluation results)
The three comparative examples, Comparative Example 2, Comparative Example 3 and Comparative Example 4, failed in terms of mechanical strength.
It is presumed that the cause is that low-density polyethylene was used as the thermoplastic resin in Comparative Example 2, that the amount of "acid-containing resin" added was too large in Comparative Example 3, and that the amount of "acid-containing resin" added was too small in Comparative Example 4. In other words, it is presumed that the mechanical strength decreases depending on the type of "thermoplastic resin" and whether the "acid-containing resin" is used in an excessive or small amount.

(耐水性の評価結果)
耐水性が不合格なものはなかったが、実施例8、実施例11、実施例15~25、27、28、比較例4は、合格の中でも比較的耐水性に劣るものであった。
実施例8、実施例15、実施例17、実施例19、実施例21、実施例23、実施例25、実施例27、比較例4では、「酸含有樹脂」の量が少量であったことにより、耐水性が低下することが推測できる。又、実施例11、実施例16、実施例18、実施例20、実施例22、実施例24、実施例28では「有機過酸化物」を使用しないことが原因と推測できる。
(Water resistance evaluation results)
Although there were no samples that failed the water resistance test, Examples 8, 11, 15 to 25, 27, and 28, and Comparative Example 4 were relatively poor in water resistance even among the samples that passed the test.
It is presumed that the water resistance is reduced due to the small amount of "acid-containing resin" in Examples 8, 15, 17, 19, 21, 23, 25, 27, and Comparative Example 4. It is presumed that the water resistance is reduced due to the small amount of "acid-containing resin" in Examples 11, 16, 18, 20, 22, 24, and 28 because "organic peroxide" is not used.

(基材変形の評価結果)
基材変形が不合格なものは、比較例1の1件だけであった。
比較例1では、「熱可塑性樹脂」の融点が140℃以上のポリオレフィン樹脂であったことが原因と推測できる。
(Evaluation results of substrate deformation)
Only one example, Comparative Example 1, failed in terms of substrate deformation.
It is presumed that this is because in Comparative Example 1, the "thermoplastic resin" was a polyolefin resin with a melting point of 140°C or higher.

(耐寒性)
耐寒性が不合格なものは、比較例1の1件だけであった。
比較例1では、「熱可塑性樹脂」の融点が140℃以上のポリオレフィン樹脂であったことが原因と推測できる。
(Cold resistance)
Only one sample, Comparative Example 1, failed the cold resistance test.
It is presumed that this is because in Comparative Example 1, the "thermoplastic resin" was a polyolefin resin with a melting point of 140°C or higher.

(耐熱性)
耐熱性が不合格なものは、比較例2の1件だけであった。
比較例2では、「熱可塑性樹脂」の融点が120℃以下のポリオレフィン樹脂であったことが原因と推測できる。
(Heat resistance)
Only one example, Comparative Example 2, failed in terms of heat resistance.
It is presumed that this is because in Comparative Example 2, the "thermoplastic resin" was a polyolefin resin with a melting point of 120°C or lower.

(実施例1~28の評価結果)
実施例1~28の評価結果は、5点の物性評価のすべてが「合格」である。
機械強度の評価結果に「△」を含むのは、実施例5、実施例8、実施例9及び実施例14~28の18件である。
実施例5では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「97/3」に変更したことが原因と推測できる。実施例8、実施例15、実施例17、実施例19、実施例21、実施例23、実施例25、実施例27では、酸含有樹脂の配合量を、実施例1の25質量部から5質量部に減じたことが原因と推測できる。実施例9、実施例16、実施例18、実施例20、実施例22、実施例24、実施例26、実施例28では、酸含有樹脂の配合量を、実施例1の25質量部から50質量部に増したことが原因と推測できる。実施例14ではMFRが高いことが原因と推測できる。
(Evaluation Results of Examples 1 to 28)
The evaluation results for Examples 1 to 28 were "pass" for all five physical property evaluations.
The evaluation results for mechanical strength including "Δ" were given to 18 examples, namely, Examples 5, 8, 9, and 14 to 28.
In Example 5, it is presumed that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "97/3". In Examples 8, 15, 17, 19, 21, 23, 25, and 27, it is presumed that the amount of the acid-containing resin was reduced from 25 parts by mass in Example 1 to 5 parts by mass. In Examples 9, 16, 18, 20, 22, 24, 26, and 28, it is presumed that the amount of the acid-containing resin was increased from 25 parts by mass in Example 1 to 50 parts by mass. In Example 14, it is presumed that the MFR is high.

耐水性の評価結果に「△」を含むのは、実施例8及び実施例11、実施例15~25、27、28の15件である。
実施例8、実施例15、実施例17、実施例19、実施例21、実施例23、実施例25、実施例27では、酸含有樹脂の配合量を、実施例1の25質量部から5質量部に減じたことが原因と推測できる。実施例11、実施例16、実施例18、実施例20、実施例22、実施例24、実施例28では、有機過酸化物の配合量を、実施例1の1質量部から0質量部に減じたことが原因と推測できる。
Fifteen examples, namely, Examples 8, 11, 15 to 25, 27, and 28, had a water resistance evaluation result of "△".
In Examples 8, 15, 17, 19, 21, 23, 25, and 27, it is presumed that the cause is that the amount of the acid-containing resin was reduced from 25 parts by mass in Example 1 to 5 parts by mass. In Examples 11, 16, 18, 20, 22, 24, and 28, it is presumed that the cause is that the amount of the organic peroxide was reduced from 1 part by mass in Example 1 to 0 part by mass.

基材変形の評価結果に「△」を含むのは、実施例4、実施例12、実施例13、実施例15~28の17件である。
実施例4、実施例15~20、実施例23~28では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「60/40」に変更したことが原因と推測できる。実施例22では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「70/30」に変更したことが原因と推測できる。実施例12では、有機過酸化物の配合量を、実施例1の1質量部から5質量部に増加したことが原因と推測できる。実施例13では、熱可塑性樹脂のMFRを、実施例1の21g/10minから0.05g/10minに変更したことが原因と推測できる。実施例21では、木質材料と熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)を、実施例1の「85/15」から「95/5」に変更したことが原因と推測できる。つまり、実施例21では、熱可塑性樹脂組成物の含有量が少なく、基材の変形が生じたと考えられる。
Seventeen examples, namely, Examples 4, 12, 13, and 15 to 28, include a grade of "△" in the evaluation results for substrate deformation.
In Examples 4, 15 to 20, and 23 to 28, it is presumed that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "60/40". In Example 22, it is presumed that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "70/30". In Example 12, it is presumed that the amount of organic peroxide was increased from 1 part by mass in Example 1 to 5 parts by mass. In Example 13, it is presumed that the MFR of the thermoplastic resin was changed from 21 g/10 min in Example 1 to 0.05 g/10 min. In Example 21, it is presumed that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) was changed from "85/15" in Example 1 to "95/5". That is, it is considered that in Example 21, the content of the thermoplastic resin composition was small, which caused deformation of the substrate.

(総合的な評価結果)
総合的な評価結果としては、実施例1~28は、5点の物性評価のすべてが「合格」であり、表1から明らかなように、本発明の木質基材は優れた機械強度と耐水性、耐寒性、耐熱性を有し、基材変形も問題ないことが示された。
(Overall evaluation results)
As a comprehensive evaluation result, all five physical property evaluations for Examples 1 to 28 were "passed." As is clear from Table 1, it was shown that the wood base material of the present invention has excellent mechanical strength, water resistance, cold resistance, and heat resistance, and there is no problem with substrate deformation.

10 原料混合物
11 木質材料
12 熱可塑性樹脂組成物
20 木質基材
30 化粧材
31 意匠性基材
10 Raw material mixture 11 Wood material 12 Thermoplastic resin composition 20 Wood substrate 30 Decorative material 31 Design substrate

Claims (15)

粉体状及びチップ状の少なくとも一方の形状を有する木質材料と、熱可塑性樹脂組成物と、を含む木質基材であって、
前記熱可塑性樹脂組成物が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、
前記熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、
前記酸含有樹脂の含有量が、前記熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内であることを特徴とする木質基材。
A wood substrate comprising a wood material having at least one of a powder form and a chip form and a thermoplastic resin composition,
The thermoplastic resin composition contains a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride,
The thermoplastic resin is a polyolefin resin having a melting point in the range of 120° C. or more and 140° C. or less,
A wood substrate comprising the acid-containing resin in an amount ranging from 5 parts by mass to 50 parts by mass relative to 100 parts by mass of the thermoplastic resin.
前記熱可塑性樹脂は、密度が0.93g/cm以上のポリオレフィン樹脂であることを特徴とする請求項1に記載の木質基材。 2. The wood base material according to claim 1, wherein the thermoplastic resin is a polyolefin resin having a density of 0.93 g/ cm3 or more. 前記熱可塑性樹脂が、JIS K7210-1:2014に規定された方法において、温度190℃、荷重21.18Nの条件で、A法により測定したときに、1g/10分以上30g/10分以下の範囲内のメルトフローレートを有することを特徴とする請求項1または2に記載の木質基材。 The wood substrate according to claim 1 or 2, characterized in that the thermoplastic resin has a melt flow rate in the range of 1 g/10 min to 30 g/10 min when measured by Method A under conditions of a temperature of 190°C and a load of 21.18 N in accordance with the method specified in JIS K7210-1:2014. 前記木質材料と、前記熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)が、95/5~70/30の範囲内であることを特徴とする請求項1~3のいずれか1項に記載の木質基材。 The wood substrate according to any one of claims 1 to 3, characterized in that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) is within the range of 95/5 to 70/30. 前記木質材料と、前記熱可塑性樹脂組成物との質量比(木質材料/熱可塑性樹脂組成物)が、97/3~85/15の範囲内であることを特徴とする請求項1~3のいずれか1項に記載の木質基材。The wood base material according to any one of claims 1 to 3, characterized in that the mass ratio of the wood material to the thermoplastic resin composition (wood material/thermoplastic resin composition) is within a range of 97/3 to 85/15. 前記酸含有樹脂が、無水マレイン酸変性ポリオレフィンであることを特徴とする請求項1~のいずれか1項に記載の木質基材。 The wood substrate according to any one of claims 1 to 5 , wherein the acid-containing resin is a maleic anhydride-modified polyolefin. 前記酸含有樹脂が、エチレン(メタ)アクリル酸共重合体であることを特徴とする請求項1~5のいずれか1項に記載の木質基材。6. The wood base material according to claim 1, wherein the acid-containing resin is an ethylene (meth)acrylic acid copolymer. 前記熱可塑性樹脂組成物が有機過酸化物をさらに含み、
前記有機過酸化物の含有量が、前記熱可塑性樹脂100質量部に対し、0.01質量部以上3質量部以下の範囲内であることを特徴とする請求項1~のいずれか1項に記載の木質基材。
The thermoplastic resin composition further comprises an organic peroxide,
The wood substrate according to any one of claims 1 to 7 , characterized in that the content of the organic peroxide is in the range of 0.01 parts by mass or more and 3 parts by mass or less per 100 parts by mass of the thermoplastic resin.
前記熱可塑性樹脂組成物が有機過酸化物をさらに含み、The thermoplastic resin composition further comprises an organic peroxide,
前記熱可塑性樹脂組成物は、前記有機過酸化物として、パーオキシケタール、ジアシルパーオキサイド、またはパーオキシエステルを含むことを特徴とする請求項1~8のいずれか1項に記載の木質基材。The wood substrate according to any one of claims 1 to 8, characterized in that the thermoplastic resin composition contains a peroxyketal, a diacyl peroxide, or a peroxyester as the organic peroxide.
前記木質材料が、菌床を原料に含むことを特徴とする請求項1~のいずれか1項に記載の木質基材。 The wood substrate according to any one of claims 1 to 9 , characterized in that the wood material contains a mushroom bed as a raw material. 前記熱可塑性樹脂は、前記ポリオレフィン樹脂として、ポリエチレン樹脂のみを含むことを特徴とする請求項1~10のいずれか1項に記載の木質基材。The wood base material according to any one of claims 1 to 10, characterized in that the thermoplastic resin contains only a polyethylene resin as the polyolefin resin. 前記酸含有樹脂の含有量が、前記熱可塑性樹脂100質量部に対し、25質量部以上であることを特徴とする請求項1~11のいずれか1項に記載の木質基材。12. The wood base material according to claim 1, wherein the content of the acid-containing resin is 25 parts by mass or more per 100 parts by mass of the thermoplastic resin. 前記熱可塑性樹脂組成物は、フェノール樹脂を含まないことを特徴とする請求項1~12のいずれか1項に記載の木質基材。The wood substrate according to any one of claims 1 to 12, characterized in that the thermoplastic resin composition does not contain a phenolic resin. 請求項1~13のいずれか1項に記載の木質基材に、意匠性基材が積層されてなることを特徴とする化粧材。 A decorative material comprising the wood substrate according to any one of claims 1 to 13 and a decorative substrate laminated thereon. 請求項1~13のいずれか1項に記載の木質基材の製造方法であって、
粉体状及びチップ状の少なくとも一方の形状を有する木質材料と、粉体状の熱可塑性樹脂組成物と、を含む原料混合物を加熱加圧して木質基材を形成する工程を有し、
前記熱可塑性樹脂組成物が、熱可塑性樹脂と、カルボン酸及びカルボン酸無水物の少なくとも一つを含む酸含有樹脂と、を含有し、
前記熱可塑性樹脂は、融点が120℃以上140℃以下の範囲内のポリオレフィン樹脂であり、
前記酸含有樹脂の含有量が、前記熱可塑性樹脂100質量部に対し、5質量部以上50質量部以下の範囲内であることを特徴とする木質基材の製造方法。
A method for producing a wood substrate according to any one of claims 1 to 13,
The method includes a step of heating and pressurizing a raw material mixture containing a wood material having at least one of a powdered and chipped form and a powdered thermoplastic resin composition to form a wood substrate,
The thermoplastic resin composition contains a thermoplastic resin and an acid-containing resin containing at least one of a carboxylic acid and a carboxylic acid anhydride,
The thermoplastic resin is a polyolefin resin having a melting point in the range of 120° C. or more and 140° C. or less,
A method for producing a wood substrate, wherein the content of the acid-containing resin is within a range of 5 parts by mass or more and 50 parts by mass or less per 100 parts by mass of the thermoplastic resin.
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