JPS63110716A - Manufacture of electrette film - Google Patents
Manufacture of electrette filmInfo
- Publication number
- JPS63110716A JPS63110716A JP25779486A JP25779486A JPS63110716A JP S63110716 A JPS63110716 A JP S63110716A JP 25779486 A JP25779486 A JP 25779486A JP 25779486 A JP25779486 A JP 25779486A JP S63110716 A JPS63110716 A JP S63110716A
- Authority
- JP
- Japan
- Prior art keywords
- film
- magnesium
- electret
- charge
- water content
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- -1 fatty acid magnesium salt Chemical class 0.000 claims description 4
- 159000000003 magnesium salts Chemical class 0.000 claims description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
- 238000000034 method Methods 0.000 description 9
- 238000005259 measurement Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 235000019359 magnesium stearate Nutrition 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000002861 polymer material Substances 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 235000010933 magnesium salts of fatty acid Nutrition 0.000 description 3
- 239000001778 magnesium salts of fatty acids Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- NYKBOLCRGNSBBC-UHFFFAOYSA-L magnesium;heptanoate Chemical compound [Mg+2].CCCCCCC([O-])=O.CCCCCCC([O-])=O NYKBOLCRGNSBBC-UHFFFAOYSA-L 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229940063002 magnesium palmitate Drugs 0.000 description 1
- 229940057948 magnesium stearate Drugs 0.000 description 1
- GMIMAWFYOOIAQD-GNNYBVKZSA-L magnesium;(z,12r)-12-hydroxyoctadec-9-enoate Chemical compound [Mg+2].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O GMIMAWFYOOIAQD-GNNYBVKZSA-L 0.000 description 1
- BJZBHTNKDCBDNQ-UHFFFAOYSA-L magnesium;dodecanoate Chemical compound [Mg+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O BJZBHTNKDCBDNQ-UHFFFAOYSA-L 0.000 description 1
- ABSWXCXMXIZDSN-UHFFFAOYSA-L magnesium;hexadecanoate Chemical compound [Mg+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O ABSWXCXMXIZDSN-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920006113 non-polar polymer Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 230000007847 structural defect Effects 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
「産業上の利用分野」
本発明は高性能フィルタとして広く利用されているエレ
クトレットフィルタ等をつくるのに用いられるエレクト
レットフィルムの製造法に関する。DETAILED DESCRIPTION OF THE INVENTION "Field of Industrial Application" The present invention relates to a method for producing an electret film used for producing electret filters and the like that are widely used as high-performance filters.
「従来の技術」
エレクトレットフィルタは、0.1〜0.5μm程度の
タバコの煙のような微粒子をクーロン力および誘起起電
力によって効率的に捕集するので、病院の特殊室、エレ
クトロニクス産業のクリンルーム等の空調システムの除
塵フィルタ、作業用防塵マスク、電気掃除機等に組込ま
れるフィルタ、或いは超高性能HE P Aフィルタの
前処理フィルタ等として広く利用されている。``Prior art'' Electret filters efficiently collect fine particles such as cigarette smoke with a size of about 0.1 to 0.5 μm using Coulomb force and induced electromotive force, so they are used in special rooms in hospitals and in cleanliness in the electronics industry. It is widely used as a dust removal filter for air conditioning systems in rooms, etc., a dust mask for work, a filter incorporated in vacuum cleaners, etc., or a pre-treatment filter for ultra-high performance HEPA filters.
従来、上記エレクトレットフィルタの製法には、■無極
性高分子物質をフィルタ成形した後コロナ荷電するか、
或いはフィルムを加熱延伸時または加熱延伸後にコロナ
荷電したエレクトレットフィル12を用いる方法(特公
昭56−47299号公報)、■絶縁性高分子物質に脂
肪酸金属塩を配合し、フィルム成形した後延伸および摩
凛処理を施したフィルムを用いる方法(特開昭60−1
96921号公報)等が知られている。Conventionally, the manufacturing method for the above-mentioned electret filters includes: (1) corona charging after molding a non-polar polymer substance into a filter;
Alternatively, a method using corona-charged electret fill 12 during or after heating the film (Japanese Patent Publication No. 56-47299); Method using Rin-treated film (JP-A-60-1
96921) and the like are known.
[発明が解決しようとする問題点」
エレクトレットフィルムを用いてフィルタをつくるには
、通常、フィルムを小解繊した後、不織布加工等によっ
てフィルタとしている。[Problems to be Solved by the Invention] To make a filter using an electret film, the film is usually defibrated into small pieces and then processed into a filter by non-woven fabric processing or the like.
この場合荷電量の経時的減衰は避けられない問題である
が、フィルタか限りなく初陣荷電に近い残存荷電を有し
ていることが極めて重要である。In this case, attenuation of the amount of charge over time is an unavoidable problem, but it is extremely important that the filter has a residual charge as close as possible to the initial charge.
ところで、前記■の方法はフィルムがコロナ放電によっ
てピンホールが発生しない最高電圧を与えて荷電しても
、初期荷電量には限界があり、その経時的減衰も比較的
大きい。一方、前記■の方法は、荷1ffiが小さく、
また摩擦荷電のため負のFi電のみで、さらに安定した
荷711mが得られず製品にむらを生ずる不都合があっ
た。By the way, in the method (2) above, even if the film is charged at the maximum voltage at which pinholes do not occur due to corona discharge, there is a limit to the amount of initial charge, and its attenuation over time is relatively large. On the other hand, in the method (■) above, the load 1ffi is small,
Further, due to frictional charging, only a negative Fi charge was generated, and a more stable load 711m could not be obtained, resulting in unevenness in the product.
本発明者等は、初期荷電量が大きく、しかもトラップさ
れた荷電量の減衰の小さいエレクトレットフィルムを得
るべく鋭意研究をした結果、エレクトレットフィルムの
荷riffiおよび減衰速度がポリマーの構造欠陥、不
純物等の化学構造によって異なること、コロナ荷電が安
定して大きな荷?11tffiが得られることを知見し
た。The present inventors have conducted intensive research to obtain an electret film with a large initial charge amount and a small attenuation of the trapped charge amount, and have found that the charge riffi and decay rate of the electret film are due to polymer structural defects, impurities, etc. Does it differ depending on the chemical structure, and is the corona charge a stable and large charge? It was found that 11tffi could be obtained.
本発明は上記の知見に基づいて開発されたもので、荷電
量が大きく、その減衰速度の小さいエレクトレットフィ
ルムの製造法を提供することを目的とする。The present invention was developed based on the above findings, and an object of the present invention is to provide a method for producing an electret film that has a large charge amount and a low decay rate.
「問題点を解決するための手段」
本発明は上記の目的を達成ずべ(なされたしので、その
要旨は、絶縁性高分子物質に、水分臼(1里が4wt%
以下の脂肪酸マグネシラノ、塩またはオキシ脂肪酸マグ
ネシウム塩を混和してフィルムを成形した後、このフィ
ルムを加熱延伸すると同時にコロナ荷電するか、または
加熱延伸した後コロナ荷電することを特徴とするエレク
トレットフィルムの製造法にある。``Means for Solving the Problems'' The present invention has achieved the above-mentioned objects, so the gist of the present invention is to add water to an insulating polymer material (1 ri = 4 wt%).
Production of an electret film characterized by mixing the following fatty acid magnesylano, salt or oxyfatty acid magnesium salt to form a film, and then heating and stretching the film and corona charging it at the same time, or heating and stretching and then corona charging the film. It's in the law.
「発明の具体的構成および作用」 以下本発明の詳細な説明する。"Specific structure and operation of the invention" The present invention will be explained in detail below.
本発明に用いられる絶縁性高分子物質としては体積固有
抵抗値がl□tsΩ・cm以上、好ましくは1015Ω
・cm以上であり、そのフィルムが解繊可能であればい
ずれでもよく、例えばポリプロピレン、ポリエチレン、
ポリエステル、塩化ビニル系樹脂、フッ素樹脂等があげ
られる。The insulating polymer material used in the present invention has a volume resistivity of 1□tsΩ・cm or more, preferably 1015Ω.
・Any film can be used as long as it is larger than cm and the film can be defibrated, such as polypropylene, polyethylene,
Examples include polyester, vinyl chloride resin, and fluororesin.
また、絶縁性高分子物質に配合される脂肪酸またはオキ
シ脂肪酸のマグネシウム塩としては、水分含有量が4w
L%以下であることが必要である。Furthermore, magnesium salts of fatty acids or oxyfatty acids blended into insulating polymeric substances have a water content of 4w.
It is necessary that it is L% or less.
脂肪酸またはオキシ脂肪酸のマグネシウム塩としては、
例えばエナント酸マグネシウム、ラウリン酸マグネシウ
ム、パルミチン酸マグネシウム、ステアリン酸マグネシ
ウム、リシノール酸マグネシウム、オキシステアリン酸
マグネシウム、ラッパルミチン酸マグネシウム等があげ
られる。Magnesium salts of fatty acids or oxyfatty acids include:
Examples include magnesium enanthate, magnesium laurate, magnesium palmitate, magnesium stearate, magnesium ricinoleate, magnesium oxystearate, magnesium lappalmitate, and the like.
ここでいう水分含有量とは、脂肪酸またはオキシ脂肪酸
のマグネシウム塩の水分をカールフィッシ、ヤー試薬に
よって測定した値であり、この値が4wt%を越えたも
のを使用したフィルムは、例外なく荷電減衰速度が大き
く不適当である。The water content here refers to the water content of magnesium salts of fatty acids or oxyfatty acids measured using Karl Fissi and Yar reagents, and films using materials with this value exceeding 4 wt% will have charge decay without exception. The speed is too high and inappropriate.
上記水分含有量が4wt%以下の脂肪酸またはオキシ脂
肪酸のマグネシウム塩の絶縁性高分子物質にたいする配
合量は0.1〜2.0wt%、特に0.5〜2.0wt
%が好ましい。配合量がO、l wt%未満ては効果が
なく、2.0wt%を越えてら効果が変らず不経済であ
る。The amount of the magnesium salt of fatty acid or oxyfatty acid having a water content of 4 wt% or less based on the insulating polymer material is 0.1 to 2.0 wt%, particularly 0.5 to 2.0 wt%.
% is preferred. If the amount is less than 0.1 wt%, there is no effect, and if it exceeds 2.0 wt%, the effect will not change and it will be uneconomical.
上記絶縁性高分子物質に脂肪酸またオキシ脂肪酸のマグ
ネシウム塩を混和してフィルムを成形した後、加熱延伸
すると同時にコロナ荷電するか、または加熱延伸した後
コロナ荷電することにより優れたエレクトレットフィル
ムが得られる。An excellent electret film can be obtained by mixing a magnesium salt of a fatty acid or oxyfatty acid with the above insulating polymeric substance and forming a film, and then heating and stretching and corona charging at the same time, or heating and stretching and then corona charging. .
フィルムの延伸は、熱ロール、ホットプレートなどいず
れの延伸方法を用いてもよい。延伸温度および延伸倍率
は特に制限はなく、フィルムの種類、形状等により最適
条件に設定すればよい。The film may be stretched using any stretching method such as a hot roll or a hot plate. The stretching temperature and stretching ratio are not particularly limited and may be set to optimal conditions depending on the type, shape, etc. of the film.
延伸温度と延伸倍率の好ましい例を示すと、例えばポリ
プロピレンフィルムを熱ロールで延伸する場合、延伸温
度は110−140℃、延伸倍率は4〜lO倍の範囲内
であることが好ましい。To give a preferable example of the stretching temperature and stretching ratio, for example, when a polypropylene film is stretched with a hot roll, the stretching temperature is preferably 110 to 140°C, and the stretching ratio is preferably within the range of 4 to 10 times.
上記コロナ荷電は、フィルムにピン71;−ルが発生し
ない範囲で高い電圧を用いることが荷電量を高めるため
好ましく、使用する絶縁性高分子物質の種類によって異
なるが、通常5〜20 K Vで行なわれる。For the above-mentioned corona charging, it is preferable to use a high voltage within a range that does not generate pins on the film in order to increase the amount of charge, and it is usually 5 to 20 KV, although it varies depending on the type of insulating polymer material used. It is done.
「実施例」 次に実施例、比較例を示して本発明の詳細な説明する。"Example" Next, the present invention will be explained in detail by showing Examples and Comparative Examples.
実施例1
体積固有抵抗が1QI5Ω・cmのボリブロピレンに水
分含有量が3.4wt%のステアリン酸マグネシウムを
0.5wt%、昆和して、厚み40μmのフィルムを成
形した。このフィルムを120°Cの熱ロールで延伸倍
率5倍に延伸しながらl0KVでコロナ荷電を与え、厚
み20μmのエレクトレットフィルムを作成し、荷電直
後の荷7[を量および60日間放置後の荷電量を測定し
た。Example 1 0.5 wt % of magnesium stearate having a water content of 3.4 wt % was added to polybropyrene having a volume resistivity of 1QI5 Ω·cm to form a film with a thickness of 40 μm. This film was stretched with a heated roll at 120°C to a stretching ratio of 5 times and corona charged at 10 KV to create an electret film with a thickness of 20 μm. was measured.
実施例2
水分含有量が3.4wt%のステアリン酸マグネシウム
の代りに、水分含有量が3.6wt%のオキシステアリ
ン酸マグネシウムを用いた他は、実施例1と同じにして
測定を行なった。Example 2 Measurements were carried out in the same manner as in Example 1, except that magnesium oxystearate having a water content of 3.6 wt% was used instead of magnesium stearate having a water content of 3.4 wt%.
実施例3
ステアリン酸マグネシウムの代りに水分含有量が3wt
%のエナント酸マグネシウムを用いた他は実施例1を同
じにして測定を行なった。Example 3 Moisture content is 3wt instead of magnesium stearate
The measurements were carried out in the same manner as in Example 1 except that % magnesium enanthate was used.
比較例1
水分含有量が4,7wt%のステアリン酸マグネシウム
を用いた他は実施例1と同じにして測定を行なった。Comparative Example 1 Measurements were carried out in the same manner as in Example 1, except that magnesium stearate with a water content of 4.7 wt% was used.
比較例2
ステアリン酸マグネシウムを用いなかった他は実施例1
と同じにして測定を行なった。Comparative Example 2 Example 1 except that magnesium stearate was not used
Measurements were carried out in the same manner.
比較例3
コロナ荷電の代りに摩凛荷電を行なった他は、実施例1
と同じにして測定を行なった。Comparative Example 3 Example 1 except that Marin charging was performed instead of corona charging.
Measurements were carried out in the same manner.
比較例4
水分含有量が3.2wt%のステアリン酸亜鉛を用いた
他は実施例1と同じにして測定を行なった。Comparative Example 4 Measurement was carried out in the same manner as in Example 1 except that zinc stearate having a water content of 3.2 wt% was used.
実施例1〜3、比較例1〜4の測定結果を第1表に示す
。The measurement results of Examples 1 to 3 and Comparative Examples 1 to 4 are shown in Table 1.
以 下 余 白
第 1 表
第1表より明らかなように本発明の方法によってつくら
れたエレクトレットフィルムは初期荷電墳が大きく、ま
た減衰1も少ないことがわかる。As is clear from Table 1, the electret film produced by the method of the present invention has a large initial charge mound and a small attenuation 1.
上記本発明の方法で製造したエレクトレットフィルムを
ストリップ繊維化した後、不織布加工したフィルタは、
除塵効果の極めて優れたしのであった。After converting the electret film produced by the method of the present invention into strip fibers, the filter is processed into a nonwoven fabric.
It was extremely effective in removing dust.
「発明の効果」
辺上述べたように本発明の方法は、初期荷電1が大きく
、しかも荷電量の減衰の小さいエレクトレットフィルム
が得られる優れた方法である。"Effects of the Invention" As mentioned above, the method of the present invention is an excellent method for obtaining an electret film with a large initial charge 1 and a small attenuation of the amount of charge.
Claims (1)
肪酸マグネシウム塩またはオキシ脂肪酸マグネシウム塩
を混和してフィルムを成形した後、このフィルムを加熱
延伸すると同時にコロナ荷電するか、または加熱延伸し
た後コロナ荷電することを特徴とするエレクトレットフ
ィルムの製造法。After forming a film by mixing a fatty acid magnesium salt or an oxyfatty acid magnesium salt with a water content of 4 wt% or less into an insulating polymeric substance, the film is heated and stretched and corona charged at the same time, or after the film is heated and stretched. A method for producing an electret film characterized by corona charging.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25779486A JPS63110716A (en) | 1986-10-29 | 1986-10-29 | Manufacture of electrette film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25779486A JPS63110716A (en) | 1986-10-29 | 1986-10-29 | Manufacture of electrette film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63110716A true JPS63110716A (en) | 1988-05-16 |
Family
ID=17311198
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25779486A Pending JPS63110716A (en) | 1986-10-29 | 1986-10-29 | Manufacture of electrette film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63110716A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0615007A1 (en) * | 1993-03-09 | 1994-09-14 | Hoechst Aktiengesellschaft | Electret fibers with improved charge stabilisation, process for their production and textile material containing these electret fibers |
JP2002001023A (en) * | 2000-06-19 | 2002-01-08 | Toyobo Co Ltd | Factory air-conditioning filter system and factory air- conditioning method |
-
1986
- 1986-10-29 JP JP25779486A patent/JPS63110716A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0615007A1 (en) * | 1993-03-09 | 1994-09-14 | Hoechst Aktiengesellschaft | Electret fibers with improved charge stabilisation, process for their production and textile material containing these electret fibers |
JP2002001023A (en) * | 2000-06-19 | 2002-01-08 | Toyobo Co Ltd | Factory air-conditioning filter system and factory air- conditioning method |
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