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JPS6015137B2 - Electret - Google Patents
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JPS6015137B2 - Electret - Google Patents

Electret

Info

Publication number
JPS6015137B2
JPS6015137B2 JP12610778A JP12610778A JPS6015137B2 JP S6015137 B2 JPS6015137 B2 JP S6015137B2 JP 12610778 A JP12610778 A JP 12610778A JP 12610778 A JP12610778 A JP 12610778A JP S6015137 B2 JPS6015137 B2 JP S6015137B2
Authority
JP
Japan
Prior art keywords
electret
mol
methyl
copolymer
carbon atoms
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP12610778A
Other languages
Japanese (ja)
Other versions
JPS5553409A (en
Inventor
和之 山崎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsui Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP12610778A priority Critical patent/JPS6015137B2/en
Publication of JPS5553409A publication Critical patent/JPS5553409A/en
Publication of JPS6015137B2 publication Critical patent/JPS6015137B2/en
Expired legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は特定の4−メチル−1−ペンテン系重合体から
なるェレクトレツトに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electret comprising a specific 4-methyl-1-pentene polymer.

エレクトレツトはマイクロホン、スピーカー、カートリ
ッジなどの音響素子に用いられており、振動計、ひずみ
計などの計測素子、無接点スイッチ、防塵フィルターな
ど、メモリー素子などへの応用も試みられている。
Electrets are used in acoustic devices such as microphones, speakers, and cartridges, and attempts are being made to apply them to measurement devices such as vibration meters and strain meters, non-contact switches, dust filters, and other memory devices.

また近年ポリマーヱレクトレットフイルムが仮骨増殖に
試用されるなど医療分野への用途も拡がっている。従来
からェレクトレットの基材として、ポリエチレン、ポリ
プロピレンが検討されているが、その分極が比較的速や
かに減衰するため、その実用性は乏しい。
In addition, in recent years, polymer electret films have been used on a trial basis for callus growth, and their use in the medical field is also expanding. Polyethylene and polypropylene have been considered as base materials for electrets, but their polarization attenuates relatively quickly, making them impractical.

本発明者は、ェレクトレツトとして好適な基材を検討し
た結果、特定の4ーメチルー1−ペンテン系の重合体が
優れた性能を示すことを見出し、本発明に到達した。
As a result of examining substrates suitable for use as electrets, the present inventors discovered that a specific 4-methyl-1-pentene polymer exhibits excellent performance, and thus arrived at the present invention.

すなわち、本発明は4ーメチルー1ーベンテンと炭素数
6なし、し18のQーオレフィンとの共重合体からなる
ことを特徴とするェレクトレツトに関する。ここで炭素
数6ないし18のQ−オレフィンには1ーヘキセン、3
ーメチルー1ーベンテン、1−オクテン、1−デセン、
1ーテトラデセン、1ーオクタデセンなどがあり、これ
らの1種または2種以上が用いられる。
That is, the present invention relates to an electret characterized by comprising a copolymer of 4-methyl-1-bentene and a Q-olefin having 6 to 18 carbon atoms. Here, Q-olefins having 6 to 18 carbon atoms include 1-hexene, 3
-Methyl-1-bentene, 1-octene, 1-decene,
Examples include 1-tetradecene and 1-octadecene, and one or more of these may be used.

共重合体中における炭素数6ないし18のQーオレフィ
ンの平均含有量は0.3ないし20モル%、とくに約1
なし、し12モル%であることが望ましい。0.3モル
%未満とくには1モル%禾満では得られる共重合体の成
形性が劣り、ェレクトレット成形物も耐衝撃性に乏しい
The average content of Q-olefin having 6 to 18 carbon atoms in the copolymer is 0.3 to 20 mol%, especially about 1
It is desirable that the content be 12 mol%. If the content is less than 0.3 mol%, especially 1 mol%, the resulting copolymer will have poor moldability, and the electret molded product will also have poor impact resistance.

20モル%とくには12モル%を越えるとヱレクトレツ
ト性能が低下いまじめる。
If it exceeds 20 mol%, especially 12 mol%, the electret performance deteriorates seriously.

これらの4ーメチルー1ーベンテン共重合体には、必要
に応じて不飽和カルボン酸およびその誘導体から選ばれ
た少なくとも1種以上のモノマーを配合して、あるいは
さらに加熱などによって4ーメチル−1−ペンテン共重
合体にグラフト共重合して、変性することや同グラフト
物をベースポリマーにブレンドすることも行われる。
These 4-methyl-1-pentene copolymers may be blended with at least one monomer selected from unsaturated carboxylic acids and derivatives thereof, or further heated to form 4-methyl-1-pentene copolymers. It is also possible to graft-copolymerize a polymer and modify it, or to blend the grafted material into a base polymer.

4ーメチル−1ーベンテン共重合体には、必要に応じて
ポリアミド、ポリエステル、ポリカーボネート、アィオ
ノマー樹脂、ポリ酢酸ピニル、ポリスチレン、ABS樹
脂、アクリル樹脂、塩化ビニル樹脂、石油樹脂、ロジン
、天然ゴム、フッ素樹脂等が含まれていてもよい。
For the 4-methyl-1-bentene copolymer, polyamide, polyester, polycarbonate, ionomer resin, polypynylacetate, polystyrene, ABS resin, acrylic resin, vinyl chloride resin, petroleum resin, rosin, natural rubber, fluororesin can be used as necessary. etc. may be included.

また変性ポリオレフィンの特性を害さない限り、必要に
応じて他の添加物、たとえばプロセス油、可塑剤、有機
または無機充填剤、染料、顔料、造核剤、離型剤、難燃
剤、電圧安定剤、酸化防止剤、紫外線吸収剤などが配合
される。これらの例としては酸化マグネシウム、水酸化
マグネシウム、タルク、硫酸バリウム、石コゥ、炭酸カ
ルシウム、炭酸マグネシウム、クレイ、シリ力、ハイド
ロタルサイト、チタニア、雲母、ガラス粉、ガラス繊維
、木粉、ビニロン繊維、合成木材繊維などがある。ェレ
クトレツト化には従来公知の種々の方法、たとえば熱ヱ
レクトレット法、ェレクトロェレクトレット法、ラジオ
ェレクトレット法、メカノェZレクトレツト法などの方
法が採用される。
In addition, other additives may be added as necessary, such as process oils, plasticizers, organic or inorganic fillers, dyes, pigments, nucleating agents, mold release agents, flame retardants, voltage stabilizers, as long as they do not impair the properties of the modified polyolefin. , antioxidants, ultraviolet absorbers, etc. Examples of these are magnesium oxide, magnesium hydroxide, talc, barium sulfate, gypsum, calcium carbonate, magnesium carbonate, clay, silicate, hydrotalcite, titania, mica, glass powder, glass fiber, wood flour, vinylon fiber. , synthetic wood fibers, etc. Various conventionally known methods, such as a thermal electret method, an electroelectret method, a radioelectret method, and a mechanical Z-electret method, can be used for the electret formation.

本発明のェレクトレットは、繊維状、フィルム状、チュ
ーブ状、細管状、多孔質状などの形状に成形して、ある
いはさらに織布、不織布として、また他の樹脂と積層あ
るいは被覆層として用いるZことができる。
The electret of the present invention can be formed into a fibrous, film, tube, capillary, porous, etc. shape, or used as a woven fabric, nonwoven fabric, laminated with other resins, or as a coating layer. Can be done.

ェレクトレット化はこれら成形の各段階と同時に、また
目的に応じてその前後に行われる。本発明のェレクトレ
ットは電荷の長期保存性が改良されているため、マイク
ロホンなどの音響素2子をはじめ、計測素子、各種フィ
ルター、記憶素子、さらに医療分野など広い用途に使用
される。
Electretization is performed simultaneously with each of these molding steps, or before or after each step depending on the purpose. Since the electret of the present invention has improved long-term charge storage, it can be used in a wide range of applications, including acoustic device pairs such as microphones, measurement devices, various filters, memory devices, and the medical field.

以下実施例を示す。比較例 1 メルトフローィンデックス(MI)0.9、密度20.
954夕/のの高密度ポリエチレン(HDPE)を用い
て厚さ50仏のT−ダィフィルムを成形した。
Examples are shown below. Comparative Example 1 Melt flow index (MI) 0.9, density 20.
A T-die film with a thickness of 50 mm was molded using high-density polyethylene (HDPE) of 954 mm/mm.

このフィルムを一対の電極間に介在させ、直流電圧61
0KVを印カロした後、室温から120ooに加熱し、
2分後加熱を止め、室温に強制冷却した後、3直流電圧
の印加を止めェレクトレットを製作した。このヱレクト
レットの表面電位は製造直後−1800Vであり、これ
を更に2500、60〜70%RHの雰囲気に7日間放
置した後にはほとんど零になつ3てし、た。
This film is interposed between a pair of electrodes, and a DC voltage of 61
After impressing 0KV, heat from room temperature to 120oo,
After 2 minutes, the heating was stopped, and after forced cooling to room temperature, the application of the 3 DC voltage was stopped, and an electret was produced. The surface potential of this electret was -1800 V immediately after production, and after being left in an atmosphere of 2500 V and 60 to 70% RH for 7 days, it became almost zero.

ただし表面電位は回転センター型表面電圧計で測定した
However, the surface potential was measured with a rotating center type surface voltmeter.

比較例 2 M17、密度0.91多/地のアィソタクチックポリプ
ロピレン(PP)を厚さ50仏のT−ダィフィルムに成
形した。
Comparative Example 2 Isotactic polypropylene (PP) of M17 and a density of 0.91 polypropylene was molded into a T-die film with a thickness of 50 mm.

このフィルムを比較例1と同機にェレクトレット化して
、その表面電位を測定した。
This film was made into an electret using the same machine as Comparative Example 1, and its surface potential was measured.

結果を第1表に示す。実施例 1 1−デセンを2.5モル%含有する4ーメチル−1ーベ
ンテン共重合体(4一M−1−P共重合体)を厚さ50
仏のTーダィフィルムに成形し、比較例1と同機にェレ
クトレット化して、その表面電位を測定した。
The results are shown in Table 1. Example 1 A 4-methyl-1-bentene copolymer (4-M-1-P copolymer) containing 2.5 mol% of 1-decene was deposited to a thickness of 50 mol %.
It was molded into a French T-die film and made into an electret using the same machine as Comparative Example 1, and its surface potential was measured.

結果を第1表に示す。TPXェレクトレットの静電圧は
、7日後はその値で安定した。その他同様に行った結果
を第1表に示す。
The results are shown in Table 1. The electrostatic voltage of the TPX electret stabilized at that value after 7 days. Other similar results are shown in Table 1.

第1表 .Table 1.

Claims (1)

【特許請求の範囲】 1 4−メチル−1−ペンテンと炭素数6ないし18の
α−オレフインとの共重合体からなることを特徴とする
エレクトレツト。 2 炭素数6ないし18のα−オレフインの平均含有量
が0.3ないし20モル%であることを特徴とする特許
請求の範囲第1項記載のエレクトレツト。
[Scope of Claims] 1. An electret comprising a copolymer of 4-methyl-1-pentene and an α-olefin having 6 to 18 carbon atoms. 2. The electret according to claim 1, wherein the average content of α-olefin having 6 to 18 carbon atoms is 0.3 to 20 mol%.
JP12610778A 1978-10-16 1978-10-16 Electret Expired JPS6015137B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12610778A JPS6015137B2 (en) 1978-10-16 1978-10-16 Electret

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12610778A JPS6015137B2 (en) 1978-10-16 1978-10-16 Electret

Publications (2)

Publication Number Publication Date
JPS5553409A JPS5553409A (en) 1980-04-18
JPS6015137B2 true JPS6015137B2 (en) 1985-04-17

Family

ID=14926785

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12610778A Expired JPS6015137B2 (en) 1978-10-16 1978-10-16 Electret

Country Status (1)

Country Link
JP (1) JPS6015137B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH043530U (en) * 1990-04-27 1992-01-13

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH043530U (en) * 1990-04-27 1992-01-13

Also Published As

Publication number Publication date
JPS5553409A (en) 1980-04-18

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