JP2009260063A - Electret composes of polyphenylene ether system foam - Google Patents

Electret composes of polyphenylene ether system foam Download PDF

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JP2009260063A
JP2009260063A JP2008107810A JP2008107810A JP2009260063A JP 2009260063 A JP2009260063 A JP 2009260063A JP 2008107810 A JP2008107810 A JP 2008107810A JP 2008107810 A JP2008107810 A JP 2008107810A JP 2009260063 A JP2009260063 A JP 2009260063A
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polyphenylene ether
electret
thickness direction
modified polyphenylene
resin foam
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Naruhiro Yasumoto
考広 安本
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Kaneka Corp
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Kaneka Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a resin foam electret which can convert electric energy into mechanical energy, or convert the mechanical energy into the electric energy, is excellent in charge retention nature at high temperature, and can easily be manufactured. <P>SOLUTION: The electret is obtained by charging denatured polyphenylene ether system resin foam, and preferably, by charging denatured polyphenylene ether system resin foam of which the ratio A/B between average cell diameter A in the thickness direction and average cell diameter B of a plane perpendicular to the thickness direction is ≤1, and the number of cells in the thickness direction is ≥2. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、変性ポリフェニレンエーテル系樹脂発泡体を帯電させることにより得られるエレクトレットに関する。   The present invention relates to an electret obtained by charging a modified polyphenylene ether resin foam.

電気的なエネルギーを機械的なエネルギーに、または機械的なエネルギーを電気的なエネルギーに変換するものとして、エレクトレットが知られている。エレクトレットは、スピーカーやマイクロフォンなどの音響機器や、圧力センサーなどに利用されている。   An electret is known as one that converts electrical energy into mechanical energy or mechanical energy into electrical energy. Electrets are used for acoustic devices such as speakers and microphones, pressure sensors, and the like.

従来、有機系材料によるエレクトレットとして、帯電させたポリフッ化ビニリデンのフィルムが利用されてきた。しかし、圧電性が低いという問題があった。近年、ポリプロピレン発泡フィルムを帯電させたものが高い圧電性を示すことが見出されたが、高温での電荷保持性が十分でないため60℃で圧電性能が低下するという問題点があった(非特許文献1)。高温下でも電荷保持性に優れている発泡体としては、ポリテトラフルオロエチレンやテトラフルオロエチレン−ヘキサフルオロエチレン共重合体などフッ素系樹脂発泡体が知られている(特許文献1)。しかし、フッ素系樹脂発泡体では、高温での電荷保持性が優れているが、発泡体の製造が容易ではないという問題があった。
特開2007−231077号公報 Ferroelectrics, 2006年, 331巻, 189−199項
Conventionally, a charged polyvinylidene fluoride film has been used as an electret made of an organic material. However, there is a problem that the piezoelectricity is low. In recent years, it has been found that a charged polypropylene foam film exhibits high piezoelectricity, but there is a problem that the piezoelectric performance deteriorates at 60 ° C. due to insufficient charge retention at high temperatures (non- Patent Document 1). Fluoropolymer foams such as polytetrafluoroethylene and tetrafluoroethylene-hexafluoroethylene copolymer are known as foams excellent in charge retention even at high temperatures (Patent Document 1). However, the fluororesin foam has excellent charge retention at high temperatures, but has a problem that the foam is not easy to produce.
JP 2007-231077 A Ferroelectrics, 2006, 331, 189-199

本発明の目的は、高温での電荷保持性に優れ、容易に製造可能な樹脂発泡体エレクトレットを提供することにある。   An object of the present invention is to provide a resin foam electret that is excellent in charge retention at high temperatures and can be easily manufactured.

本発明者らは上記課題を解決するために鋭意研究を重ねた結果、容易に製造可能な変性ポリフェニレンエーテル系樹脂発泡体を帯電させたものが良好な圧電性を示し、高温下での電荷保持性が優れていることを見出し、本発明を完成するに至った。   As a result of intensive research to solve the above-mentioned problems, the inventors of the present invention have shown that a charged product of a modified polyphenylene ether-based resin foam that can be easily produced exhibits good piezoelectricity and retains charge at high temperatures. As a result, the present invention has been completed.

すなわち本発明は、変性ポリフェニレンエーテル系樹脂発泡体を帯電させることにより得られるエレクトレットに関する。   That is, the present invention relates to an electret obtained by charging a modified polyphenylene ether resin foam.

好ましい態様としては、前記変性ポリフェニレンエーテル系樹脂発泡体の厚み方向の平均セル径Aと厚み方向に垂直な面の平均セル径Bの比A/Bが1以下であることを特徴とする前記記載のエレクトレットに関し、より好ましい態様としては、前記変性ポリフェニレンエーテル系樹脂発泡体の厚み方向のセル数が2以上であることを特徴とする前記記載のエレクトレットに関する。   As a preferred embodiment, the ratio A / B between the average cell diameter A in the thickness direction of the modified polyphenylene ether-based resin foam and the average cell diameter B in the plane perpendicular to the thickness direction is 1 or less. As a more preferred embodiment, the above-mentioned electret is characterized in that the number of cells in the thickness direction of the modified polyphenylene ether resin foam is 2 or more.

発泡体として変性ポリフェニレンエーテル系樹脂発泡体を利用し、帯電させることにより、耐久性に優れ、良好な圧電性を示し、高温下での電荷保持性が優れたエレクトレットを容易に得ることができる。   By using a modified polyphenylene ether resin foam as a foam and charging it, an electret having excellent durability, good piezoelectricity, and excellent charge retention at high temperatures can be easily obtained.

本発明における変性ポリフェニレンエーテル系樹脂発泡体の機材樹脂である変性ポリフェニレンエーテル系樹脂としては、ポリフェニレンエーテル系樹脂へのスチレン系単量体を重合させたスチレン・フェニレンエーテル共重合体、ポリフェニレンエーテル系樹脂とポリスチレン系樹脂を混合してなる樹脂、等があげられる。   The modified polyphenylene ether resin, which is a material resin of the modified polyphenylene ether resin foam in the present invention, includes a styrene / phenylene ether copolymer obtained by polymerizing a styrene monomer to a polyphenylene ether resin, and a polyphenylene ether resin. And a resin obtained by mixing a polystyrene resin and the like.

これら変性ポリフェニレンエーテル系樹脂のなかでは、低コストであり、その混合比を変化させることにより、簡単に耐熱性、剛性等の品質に優れ、加工性を変化させたものを得ることができる点から、ポリフェニレンエーテル系樹脂とポリスチレン系樹脂を混合してなる樹脂であることが好ましい。   Among these modified polyphenylene ether resins, it is low-cost, and by changing the mixing ratio, it is possible to easily obtain a product with excellent quality such as heat resistance and rigidity, and with changed workability. A resin obtained by mixing a polyphenylene ether resin and a polystyrene resin is preferable.

前記変性ポリフェニレンエーテル系樹脂は、変性ポリフェニレンエーテル系樹脂中ポリフェニレンエーテル系樹脂10重量%以上70重量%以下とポリスチレン系樹脂30重量%以上90重量%以下からなることが好ましく、より好ましくは、ポリフェニレンエーテル系樹脂30重量%以上60重量%以下とポリスチレン系樹脂40重量%以上70重量%以下である。   The modified polyphenylene ether resin preferably comprises 10% by weight to 70% by weight of the polyphenylene ether resin and 30% by weight to 90% by weight of the polystyrene resin in the modified polyphenylene ether resin, more preferably polyphenylene ether. 30% by weight or more and 60% by weight or less of the resin and 40% by weight or more and 70% by weight or less of the polystyrene resin.

前記ポリフェニレンエーテル系樹脂の具体例としては、例えば、ポリ(2,6−ジメチルフェニレン−1,4−エーテル)、ポリ(2−メチル−6−エチルフェニレン−4−エーテル)、ポリ(2,6−ジエチルフェニレン−1,4−エーテル)、ポリ(2,6−ジエチルフェニレン−1,4−エーテル)、ポリ(2−メチル−6−n−プロピルフェニレン−1,4−エーテル)、ポリ(2−メチル−6−n−ブチルフェニレン−1,4−エーテル)、ポリ(2−メチル−6−クロルフェニレン−1,4−エーテル)、ポリ(2−メチル−6−ブロムフェニレン−1,4−エーテル)、ポリ(2−エチル−6−クロルフェニレン−1,4−エーテル)などがあげられ、これらは単独で用いてもよいし、2種以上を組み合わせて用いもよい。   Specific examples of the polyphenylene ether resin include poly (2,6-dimethylphenylene-1,4-ether), poly (2-methyl-6-ethylphenylene-4-ether), and poly (2,6 -Diethylphenylene-1,4-ether), poly (2,6-diethylphenylene-1,4-ether), poly (2-methyl-6-n-propylphenylene-1,4-ether), poly (2 -Methyl-6-n-butylphenylene-1,4-ether), poly (2-methyl-6-chlorophenylene-1,4-ether), poly (2-methyl-6-bromophenylene-1,4-ether) Ether) and poly (2-ethyl-6-chlorophenylene-1,4-ether). These may be used alone or in combination of two or more.

また、ポリフェニレンエーテル系樹脂に重合、好ましくはグラフト重合させるスチレン系単量体の具体例としては、例えば、スチレン、α−メチルスチレン、2,4−ジメチルスチレン、モノクロルスチレン、ジクロルスチレン、p−メチルスチレン、エチルスチレンなどがあげられる。これらは単独で用いてもよく、2種以上組み合わせてもよい。なかでも、汎用性およびコストの点で、スチレンが好ましい。   Specific examples of the styrene monomer that is polymerized to polyphenylene ether resin, preferably graft polymerized, include, for example, styrene, α-methylstyrene, 2,4-dimethylstyrene, monochlorostyrene, dichlorostyrene, p- Examples include methyl styrene and ethyl styrene. These may be used alone or in combination of two or more. Of these, styrene is preferable in terms of versatility and cost.

ポリスチレン系樹脂の具体例としては、前記スチレン系単量体を主成分とする樹脂があげられる。ポリスチレン系樹脂は、スチレンまたはスチレン誘導体だけからなる単独重合体に限らず、他の単量体と共重合することによって作られた共重合体であってもよい。   Specific examples of the polystyrene-based resin include resins having the styrene-based monomer as a main component. The polystyrene resin is not limited to a homopolymer composed of only styrene or a styrene derivative, but may be a copolymer made by copolymerizing with another monomer.

本発明における変性ポリフェニレンエーテル系樹脂発泡体は、例えば、150〜300℃の押出機内で前記変性ポリフェニレンエーテル系樹脂および発泡剤を溶融混練後、押出機内において130〜200℃の発泡温度に調節し、環状のリップを有するサーキュラーダイスを用い、そのダイスのリップから大気圧中に押し出して円筒状の発泡体を得、次いで、その円筒状発泡体を引き取りながら、冷却筒(マンドレル)による成形加工によって冷却後、切り開く方法によって製造することができる。またサーキュラーダイスの代わりにTダイを用いてフィルム状に発泡体を得、ロールなどで引き取る方法によっても製造される。また得られた、発泡体をスライス等切削加工してもよい。   The modified polyphenylene ether-based resin foam in the present invention is, for example, after melt-kneading the modified polyphenylene ether-based resin and the foaming agent in an extruder at 150 to 300 ° C., and adjusted to a foaming temperature of 130 to 200 ° C. in the extruder, Using a circular die having an annular lip, extrusion is performed from the lip of the die into atmospheric pressure to obtain a cylindrical foam, and then cooled by molding with a cooling cylinder (mandrel) while taking the cylindrical foam. Thereafter, it can be produced by a slitting method. Further, it is also produced by a method in which a foam is obtained in the form of a film using a T die instead of a circular die and taken up with a roll or the like. Further, the obtained foam may be cut by cutting or the like.

本発明における変性ポリフェニレンエーテル系樹脂発泡体の製造に使用される発泡剤としては、例えば、プロパン、ノルマルブタン、イソブタン、ノルマルペンタン、イソペンタン、などの脂肪族炭化水素類、シクロブタン、シクロペンタン、シクロヘキサンなどの脂環式炭化水素類、窒素、炭酸ガス、空気などの無機ガスがあげられる。これらは単独または2種以上混合して使用してよい。   Examples of the foaming agent used in the production of the modified polyphenylene ether-based resin foam in the present invention include aliphatic hydrocarbons such as propane, normal butane, isobutane, normal pentane, and isopentane, cyclobutane, cyclopentane, and cyclohexane. Inorganic gases such as alicyclic hydrocarbons, nitrogen, carbon dioxide and air. You may use these individually or in mixture of 2 or more types.

前記発泡剤量は、発泡剤の種類および目標密度により異なるが、変性ポリフェニレンエーテル系樹脂100重量部に対して、1重量部以上5重量部以下であることが好ましい。   The amount of the foaming agent varies depending on the type of foaming agent and the target density, but is preferably 1 part by weight or more and 5 parts by weight or less with respect to 100 parts by weight of the modified polyphenylene ether resin.

本発明においては、変性ポリフェニレンエーテル系樹脂発泡体の厚み方向のセル数を前記範囲にコントロールするために、必要に応じて、タルクなどの造核剤を併用してもよい。必要に応じて用いられる該造核剤の添加量は、特に制限はないが、通常、変性ポリフェニレンエーテル系樹脂100重量部に対して、0.01重量部以上10重量部以下であることが好ましい。   In the present invention, in order to control the number of cells in the thickness direction of the modified polyphenylene ether-based resin foam within the above range, a nucleating agent such as talc may be used in combination as necessary. The addition amount of the nucleating agent used as necessary is not particularly limited, but is usually preferably 0.01 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the modified polyphenylene ether resin. .

さらに本発明においては、変性ポリフェニレンエーテル系樹脂発泡体の製造において、変性ポリフェニレンエーテル系樹脂の発泡性を損なわない範囲で、熱可塑性樹脂や、酸化防止剤、金属不活性剤、燐系加工安定剤、紫外線吸収剤、紫外線安定剤、蛍光増白剤、金属石鹸、制酸吸着剤などの安定剤、または架橋剤、連鎖移動剤、造核剤、滑剤、可塑剤、充填材、強化材、顔料、染料、難燃剤などの添加剤を添加してもよい。   Furthermore, in the present invention, in the production of the modified polyphenylene ether resin foam, a thermoplastic resin, an antioxidant, a metal deactivator, and a phosphorus processing stabilizer are within the range that does not impair the foamability of the modified polyphenylene ether resin. , UV absorbers, UV stabilizers, fluorescent brighteners, metal soaps, antacid adsorbent stabilizers, or crosslinking agents, chain transfer agents, nucleating agents, lubricants, plasticizers, fillers, reinforcing materials, pigments Additives such as dyes and flame retardants may be added.

本発明における変性ポリフェニレンエーテル系樹脂発泡体はこの様にして得ることができる。   The modified polyphenylene ether resin foam in the present invention can be obtained in this manner.

本発明における変性ポリフェニレンエーテル系樹脂発泡体の厚み方向の平均セル径Aと厚み方向に垂直な面の平均セル径Bの比A/Bが1以下であることが好ましく、より好ましくは0.5以下である。ここで、変性ポリフェニレンエーテル系樹脂発泡体の厚みとは、エレクトレット化において高電圧を印加する方向と平行な方向をいう。   The ratio A / B of the average cell diameter A in the thickness direction of the modified polyphenylene ether-based resin foam in the present invention to the average cell diameter B in the plane perpendicular to the thickness direction is preferably 1 or less, more preferably 0.5. It is as follows. Here, the thickness of the modified polyphenylene ether-based resin foam refers to a direction parallel to a direction in which a high voltage is applied in electretization.

また、本発明における変性ポリフェニレンエーテル系樹脂発泡体の厚み方向の平均セル径Aは、変性ポリフェニレンエーテル系樹脂発泡体の厚みを超えなければ特に限定は無いが、厚み方向のセル数が2以上であることが好ましい。厚み方向のセル数は、断面を顕微鏡にて150倍に拡大して観察することにより読み取る。   The average cell diameter A in the thickness direction of the modified polyphenylene ether resin foam in the present invention is not particularly limited as long as it does not exceed the thickness of the modified polyphenylene ether resin foam, but the number of cells in the thickness direction is 2 or more. Preferably there is. The number of cells in the thickness direction is read by observing the cross-section magnified 150 times with a microscope.

なお、本発明における変性ポリフェニレンエーテル系樹脂発泡体の厚み方向の平均セル径Aと厚み方向に垂直な面の平均セル径Bは、変性ポリフェニレンエーテル系樹脂発泡体の厚み方向に平行な2つの直交する断面を顕微鏡にて150倍に拡大し、顕微鏡に付属のスケールを用い、それぞれ20個のセルについて厚み方向及び厚み方向に対し垂直方向
のセル径を読み取り、算術平均により算出する。垂直方向のセル径は長径と短径を読み取る。
The average cell diameter A in the thickness direction of the modified polyphenylene ether resin foam in the present invention and the average cell diameter B in the plane perpendicular to the thickness direction are two orthogonal directions parallel to the thickness direction of the modified polyphenylene ether resin foam. The cross section to be enlarged is magnified 150 times with a microscope, and the cell diameter in the direction perpendicular to the thickness direction and the thickness direction is read for each of 20 cells using a scale attached to the microscope, and is calculated by arithmetic average. Read the major and minor diameters of the cell diameter in the vertical direction.

本発明における変性ポリフェニレンエーテル系樹脂発泡体の厚みは、特に限定されないが、通常0.05〜2mmである。この範囲であれば、エレクトレットとしての性能を示すことができる。   The thickness of the modified polyphenylene ether resin foam in the present invention is not particularly limited, but is usually 0.05 to 2 mm. If it is this range, the performance as an electret can be shown.

上記の方法で得られた変性ポリフェニレンエーテル系樹脂発泡体に高電圧を印加し帯電させることによりエレクトレットを得ることができる。高電圧を印加する方法としては、コロナ放電装置を用いる方法や発泡体に電極を取り付け高圧電源に接続する方法がある。電極を取り付ける必要がないため、コロナ放電装置により高電圧を印加し帯電させる方法が好ましい。印加する電圧が低すぎると、帯電が不十分となるため0.5kV以上の電圧を印加することが好ましい。   An electret can be obtained by applying a high voltage to the modified polyphenylene ether-based resin foam obtained by the above method and charging it. As a method of applying a high voltage, there are a method using a corona discharge device and a method of attaching an electrode to a foam and connecting it to a high voltage power source. Since it is not necessary to attach an electrode, a method in which a high voltage is applied and charged by a corona discharge device is preferable. If the applied voltage is too low, charging becomes insufficient, and it is preferable to apply a voltage of 0.5 kV or more.

以下に実施例を示し、本発明をより具体的に説明するが、本発明はこれらの実施例に何ら限定されるものではない。なお、実施例において「部」や「%」は質量基準である。   EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to these examples. In the examples, “parts” and “%” are based on mass.

〔電荷の熱安定性評価〕
エレクトレットを60℃のオーブンで処理し、表面電荷を表面電位計により5点測定し平均した。
[Evaluation of thermal stability of electric charge]
The electret was processed in an oven at 60 ° C., and the surface charge was measured and averaged at five points using a surface potentiometer.

〔圧電性評価〕
エレクトレットの厚み方向に対し垂直な面の両面全体にアルミ箔を密着させ、アルミ箔と電圧測定装置を接続した。これに100gのSUS板(125mm×50mm)をアルミ箔上に1cmの高さより落下させ、発生する電圧を測定した。
[Piezoelectric evaluation]
An aluminum foil was adhered to both sides of the surface perpendicular to the thickness direction of the electret, and the aluminum foil and the voltage measuring device were connected. A 100 g SUS plate (125 mm × 50 mm) was dropped onto the aluminum foil from a height of 1 cm, and the generated voltage was measured.

(実施例1)
ポリフェニレンエーテル樹脂40重量%およびポリスチレン樹脂60重量%となるように、ポリフェニレンエーテル樹脂(日本GE社製、EFN−4230:ポリフェニレンエーテル成分/ポリスチレン成分=70/30)57.1重量部およびポリスチレン樹脂(PSジャパン社製、G8102:PS成分=100)42.9重量部を混合した変性ポリフェニレンエーテル樹脂100重量部、タルク(林化成(株)社製、タルカンパウダーPK)0.34重量部、ステアリン酸マグネシウム(堺化学工業(株)社製、SM−1000)0.08重量部、およびポリブテン(日石ポリブテン製、LV−50)0.05重量部をリボンブレンダーで撹拌混合した。得られた配合物を、115mmφ押出機(第1段押出機)と152mmφ押出機(第2段押出機)が直列に連結されたタンデム押出機に供給し、樹脂温度が約280℃になるように、第1段押出機中で溶融混練させた後、発泡剤として炭化水素系発泡剤(iso−ブタン/n−ブタン=85/15)を変性ポリフェニレンエーテル樹脂100重量部に対して3.9重量部圧入混合した。その後、第2段押出機のシリンダ−温度を135〜145℃に冷却した後、サーキュラーダイより大気圧下に150kg/時間の速度にて押出した。得られた円筒状発泡体を、マンドレル(外径445mmであり、循環水により40℃に温調)を用いて成形しながら10.0m/minで引き取りつつ、これをカッターで切り開くことにより、シート状態とし、長さ200mを直径260mmの巻き芯材を用いて、円筒ロールになるように巻き取った。得られた発泡シ−トは、発泡倍率15倍、独立気泡率90%、目付150g/m、シ−ト幅1400mmおよびシート厚み2.3mmであった。
(Example 1)
57.1 parts by weight of a polyphenylene ether resin (manufactured by GE Japan, EFN-4230: polyphenylene ether component / polystyrene component = 70/30) and polystyrene resin (40% by weight of polyphenylene ether resin and 60% by weight of polystyrene resin) PS Japan, G8102: PS component = 100) 42.9 parts by weight of modified polyphenylene ether resin mixed, talc (manufactured by Hayashi Kasei Co., Ltd., Talcan powder PK) 0.34 parts by weight, stearic acid 0.08 part by weight of magnesium (manufactured by Sakai Chemical Industry Co., Ltd., SM-1000) and 0.05 part by weight of polybutene (manufactured by Nisseki Polybutene, LV-50) were stirred and mixed with a ribbon blender. The obtained blend is supplied to a tandem extruder in which a 115 mmφ extruder (first stage extruder) and a 152 mmφ extruder (second stage extruder) are connected in series so that the resin temperature becomes about 280 ° C. Then, after melt-kneading in the first-stage extruder, a hydrocarbon-based blowing agent (iso-butane / n-butane = 85/15) as a blowing agent is 3.9 with respect to 100 parts by weight of the modified polyphenylene ether resin. Part by weight was press-fitted and mixed. Thereafter, the cylinder temperature of the second stage extruder was cooled to 135 to 145 ° C. and then extruded from a circular die at a rate of 150 kg / hour under atmospheric pressure. While the obtained cylindrical foam is formed using a mandrel (outer diameter of 445 mm, temperature-controlled at 40 ° C. with circulating water) while being taken off at 10.0 m / min, the sheet is cut by a cutter to obtain a sheet. In a state, a length of 200 m was wound using a winding core material having a diameter of 260 mm so as to form a cylindrical roll. The obtained foamed sheet had an expansion ratio of 15 times, a closed cell ratio of 90%, a basis weight of 150 g / m 2 , a sheet width of 1400 mm, and a sheet thickness of 2.3 mm.

得られた発泡シートをスライスし、厚み0.3mmの変性ポリフェニレンエーテル樹脂発泡体を得た。得られた変性ポリフェニレンエーテル樹脂発泡体の厚み方向の平均セル径は0.05mm、厚み方向と垂直な面の平均セル径は0.12mm×0.20mmであった。   The obtained foamed sheet was sliced to obtain a modified polyphenylene ether resin foam having a thickness of 0.3 mm. The average cell diameter in the thickness direction of the obtained modified polyphenylene ether resin foam was 0.05 mm, and the average cell diameter in the plane perpendicular to the thickness direction was 0.12 mm × 0.20 mm.

変性ポリフェニレンエーテル樹脂発泡体(50mm×50mm×0.3mm)に、コロナ放電で15kVの電圧を3分間印加しエレクトレットを得た。電荷の熱安定性評価及び圧電性の評価を行った。   A 15 kV voltage was applied to the modified polyphenylene ether resin foam (50 mm × 50 mm × 0.3 mm) by corona discharge for 3 minutes to obtain an electret. The thermal stability of the electric charge and the piezoelectricity were evaluated.

(比較例1)
ポリプロピレン発泡シート(50mm×50mm×1.7mm、発泡倍率6.2倍、独立気泡率80%、目付量240g/m、厚み方向平均セル径0.18mm、厚み方向と垂直な面の平均セル径は0.37mm×0.46mm)にコロナ放電で15kVの電圧を3分間印加しエレクトレットを得た。電荷の熱安定性評価及び圧電性の評価を行った。
(Comparative Example 1)
Polypropylene foam sheet (50 mm × 50 mm × 1.7 mm, expansion ratio 6.2 times, closed cell ratio 80%, basis weight 240 g / m 2 , thickness direction average cell diameter 0.18 mm, average cell in plane perpendicular to thickness direction The diameter was 0.37 mm × 0.46 mm), and a voltage of 15 kV was applied for 3 minutes by corona discharge to obtain an electret. The thermal stability of the electric charge and the piezoelectricity were evaluated.

Figure 2009260063
Figure 2009260063

実施例1と比較例1の電荷の熱安定性評価の結果を示したグラフである。4 is a graph showing the results of evaluation of thermal stability of charges in Example 1 and Comparative Example 1.

Claims (3)

変性ポリフェニレンエーテル系樹脂発泡体を帯電させることにより得られるエレクトレット。   An electret obtained by charging a modified polyphenylene ether resin foam. 前記変性ポリフェニレンエーテル系樹脂発泡体の厚み方向の平均セル径Aと厚み方向に垂直な面の平均セル径Bの比A/Bが1以下であることを特徴とする請求項1記載のエレクトレット。   The electret according to claim 1, wherein a ratio A / B between an average cell diameter A in the thickness direction of the modified polyphenylene ether-based resin foam and an average cell diameter B in a plane perpendicular to the thickness direction is 1 or less. 前記変性ポリフェニレンエーテル系樹脂発泡体の厚み方向のセル数が2以上であることを特徴とする請求項1または2に記載のエレクトレット。   The electret according to claim 1 or 2, wherein the number of cells in the thickness direction of the modified polyphenylene ether-based resin foam is 2 or more.
JP2008107810A 2008-04-17 2008-04-17 Electret composes of polyphenylene ether system foam Pending JP2009260063A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012197374A (en) * 2011-03-22 2012-10-18 Sekisui Plastics Co Ltd Polystyrene-based resin expanded sheet, container, and method for producing polystyrene-based resin expanded sheet
WO2015137251A1 (en) * 2014-03-10 2015-09-17 積水化学工業株式会社 Piezoelectric sensor
CN105036063A (en) * 2015-07-02 2015-11-11 北京理工大学 MEMS technology preparation method of piezoelectret matrix

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012197374A (en) * 2011-03-22 2012-10-18 Sekisui Plastics Co Ltd Polystyrene-based resin expanded sheet, container, and method for producing polystyrene-based resin expanded sheet
WO2015137251A1 (en) * 2014-03-10 2015-09-17 積水化学工業株式会社 Piezoelectric sensor
JPWO2015137251A1 (en) * 2014-03-10 2017-04-06 積水化学工業株式会社 Piezoelectric sensor
JP2019056710A (en) * 2014-03-10 2019-04-11 積水化学工業株式会社 Piezoelectric sensor
CN105036063A (en) * 2015-07-02 2015-11-11 北京理工大学 MEMS technology preparation method of piezoelectret matrix
CN105036063B (en) * 2015-07-02 2016-06-29 北京理工大学 A kind of MEMS technology preparation method of piezo-electric electret matrix

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