JPH06254319A - Electret filter - Google Patents
Electret filterInfo
- Publication number
- JPH06254319A JPH06254319A JP4527293A JP4527293A JPH06254319A JP H06254319 A JPH06254319 A JP H06254319A JP 4527293 A JP4527293 A JP 4527293A JP 4527293 A JP4527293 A JP 4527293A JP H06254319 A JPH06254319 A JP H06254319A
- Authority
- JP
- Japan
- Prior art keywords
- polyolefin
- electret
- filter
- work function
- metal
- 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
Landscapes
- Filtering Materials (AREA)
- Electrostatic Separation (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ビル空調用フィルタ
ー、掃除機用フィルター、空気清浄機用フィルター、エ
アコン用フィルター、OA機器用フィルターなどに用い
ることのできる、長期にわたって帯電レベルの高いエレ
クトレットフィルターに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electret filter which can be used for a building air conditioner filter, a vacuum cleaner filter, an air purifier filter, an air conditioner filter, an office automation equipment filter, etc. and has a high charge level for a long period of time. Regarding
【0002】[0002]
【従来の技術】ポリオレフィン系スプリット繊維を用い
たエレクトレットフィルターには、特公昭56−472
99公報、特公昭57−14467公報、特開昭62−
102809公報、特開平1−224020号公報など
がある。これらはいずれも高い表面電荷密度を有するエ
レクトレットフィルターとされているが、長期にわたっ
てフィルターを使用すること帯電量の減衰により粒子捕
集効率が経時的に低下し、捕集効率が回復しないという
問題があった。2. Description of the Related Art An electret filter using a polyolefin split fiber is disclosed in Japanese Examined Patent Publication No. 56-472.
99 gazette, Japanese Patent Publication No. 57-14467, Japanese Patent Laid-Open No. 62-
102809, Japanese Patent Laid-Open No. 1-224020, and the like. These are all electret filters having a high surface charge density, but using a filter for a long period of time reduces the particle collection efficiency due to the decay of the charge amount, and there is a problem that the collection efficiency does not recover. there were.
【0003】[0003]
【発明が解決しようとする課題】本発明はかかる問題点
を解決した、すなわち初期の粒子捕集効率が高く、また
帯電量の減衰を小さくすることにより長期にわたって帯
電レベルの高いエレクトレットフィルターを提供せんと
するものである。SUMMARY OF THE INVENTION The present invention has solved the above problems, that is, it does not provide an electret filter having a high charge level for a long period of time by having a high initial particle collection efficiency and reducing the attenuation of the charge amount. It is what
【0004】[0004]
【課題を解決するための手段】本発明は、かかる問題点
に鑑み鋭意検討した結果、本発明に到達したものであ
る。本発明は、炭素数が10以上の有機酸と、仕事関数
が4eV以上の金属のイオンとからなる有機酸金属塩を
含有したポリオレフィン系スプリット繊維からなるエレ
クトレットフィルターに関する。有機酸にはカルボン
酸、有機リン酸、有機スルホン酸などがあり、いずれの
場合も容易に金属イオンと塩を形勢する。炭素数が10
以上の有機酸は具体的には、ラウリン酸、リノレン酸、
t−ブチル安息香酸、ジ(t−ブチルフェニル)リン酸
などが挙げられ、好ましくはラウリン酸、ステアリン
酸、t−ブチル安息香酸である。炭素数が10以下の有
機酸の金属塩を使用した場合、その塩の親水性が増すた
め電荷減衰は大きくなり、本課題を解決できるレベルに
到達し得ない。また炭素数が小さい有機酸の金属塩で
は、ポリオレフィン樹脂に配合する際、およびこれら金
属塩を配合したポリオレフィン樹脂を成膜する際に熱分
解を起こすことがあり、生産性の点からも不敵当であ
る。また有機酸と塩を形勢する金属は多数あるが、その
うち仕事関数が4eV以上である金属は、例えばAl、
Fe、Ni、Co、Sn、Cu、Pb、Cdなどが挙げ
られる。これらのなかで安全性、成膜性、製造コストな
どを考慮するとAlが最も好ましい。したがって有機酸
金属塩の特に好ましい例としては、ラウリン酸アルミニ
ウム、ステアリン酸アルミニウル、t−ブチル安息香酸
アルミニウムである。このような、炭素数が10以上の
有機酸と仕事関数が4eV以上の金属のイオンとからな
る塩を含有したポリオレフィン系スプリット繊維より作
製したエレクトレットフィルターでは、高温下および高
湿下においても帯電量の減衰がきわめて小さいため、長
期にわたって帯電レベルが高く、粒子捕集効率の低下が
非常に小さい。逆に炭素数が10以下の有機酸、または
仕事関数が4eV未満の金属のイオンからなる有機酸金
属塩を含有した場合はその効果は小さく、特に炭素数が
10以下の有機酸と仕事関数の小さなアルカリ金属のイ
オンとからなる塩の場合では、帯電量の減衰がきわめて
大きくなり不敵当である。The present invention has arrived at the present invention as a result of extensive studies in view of such problems. The present invention relates to an electret filter composed of a polyolefin-based split fiber containing an organic acid metal salt composed of an organic acid having 10 or more carbon atoms and an ion of a metal having a work function of 4 eV or more. Organic acids include carboxylic acids, organic phosphoric acids, organic sulfonic acids and the like, and in any case, they readily form a salt with a metal ion. 10 carbon atoms
The above organic acids are specifically lauric acid, linolenic acid,
Examples thereof include t-butylbenzoic acid and di (t-butylphenyl) phosphoric acid, with lauric acid, stearic acid and t-butylbenzoic acid being preferred. When a metal salt of an organic acid having 10 or less carbon atoms is used, the hydrophilicity of the salt increases, so that charge attenuation becomes large, and it is impossible to reach a level at which this problem can be solved. In addition, metal salts of organic acids with a small number of carbon atoms may cause thermal decomposition during compounding with polyolefin resins and during film formation of polyolefin resins containing these metal salts, which is unfriendly from the viewpoint of productivity. It is right. In addition, there are many metals that form organic acids and salts, of which metals having a work function of 4 eV or more are, for example, Al,
Fe, Ni, Co, Sn, Cu, Pb, Cd, etc. are mentioned. Of these, Al is most preferable in consideration of safety, film forming property, manufacturing cost, and the like. Therefore, particularly preferable examples of the organic acid metal salt are aluminum laurate, aluminum stearate and aluminum t-butyl benzoate. In such an electret filter made from a polyolefin-based split fiber containing a salt composed of an organic acid having 10 or more carbon atoms and a metal ion having a work function of 4 eV or more, an electret amount is obtained even under high temperature and high humidity. Has a very small attenuation, the charge level is high for a long period of time, and the drop in particle collection efficiency is very small. Conversely, when an organic acid having 10 or less carbon atoms or an organic acid metal salt composed of metal ions having a work function of less than 4 eV is contained, the effect is small. In the case of a salt consisting of small alkali metal ions, the amount of charge is greatly attenuated, which is unfriendly.
【0005】本発明において上記の有機酸と仕事関数が
4eV以上の金属のイオンとからなる塩が、いかなる理
由でポリオレフィンの帯電量減衰を小さくするのかにつ
いては未だ不明確である。ポリオレフィンを適当な方法
で荷電するとポリオレフィン中に荷電(電子とホール)
が注入されエレクトレット体となる。ポリオレフィンエ
レクトレットにおける電荷のトップサイトとしては、ポ
リマーの構造欠陥やポリマー中の不純物自身が考えられ
ている。また不純物中の双極子が構造欠陥にトラップさ
れている電荷を安定化させるとの報告もある。また仕事
関数とは「固体内の電子1個をそのフェルミ準位から真
空準位にまで取り出すのに要する最小のエネルギー」と
定義されている。すなわち仕事関数の大きい金属ほど電
子が安定に存在し、イオン化しにくいことを意味してい
る。ポリオレフィン中に仕事関数の大きな金属を含有す
る場合、注入された電荷のうち電子がその金属自身ある
いは近傍いトラップされ安定化するため、電子の逃失お
よびホールとの結合による中和がおこりにくく、このよ
うな金属を含有しない場合に比べて帯電量の減衰が小さ
くなることが推定される。なおこれらの有機酸金属塩は
ポリオレフィン中の非晶相、結晶非晶界面相に存在する
ことが考えられる。In the present invention, it is still unclear as to why the salt composed of the above organic acid and a metal ion having a work function of 4 eV or more reduces the charge amount attenuation of the polyolefin. When polyolefin is charged by an appropriate method, it is charged in the polyolefin (electrons and holes)
Is injected into the electret body. Structural defects of the polymer and impurities themselves in the polymer are considered as the top charge sites in the polyolefin electret. It is also reported that the dipole in the impurity stabilizes the charges trapped in the structural defects. The work function is defined as "the minimum energy required to extract one electron in a solid from the Fermi level to the vacuum level". That is, it means that a metal having a higher work function has more stable electrons and is less likely to be ionized. When a metal having a large work function is contained in the polyolefin, electrons in the injected charge are trapped and stabilized in the metal itself or in the vicinity thereof, so that the escape of electrons and the neutralization due to the bonding with holes are less likely to occur. It is estimated that the attenuation of the charge amount is smaller than that in the case where no such metal is contained. Incidentally, it is considered that these organic acid metal salts exist in the amorphous phase or the crystalline amorphous interface phase in the polyolefin.
【0006】本発明において上記の有機酸金属塩の配合
量は、ポリオレフィンに大して0.1〜5.0重量%、
好ましくは0.5〜3.0重量%である。配合量がこれ
より少ないとその効果が充分ではなく、また配合量がこ
れより多くてもその効果は変わらない。In the present invention, the amount of the above-mentioned organic acid metal salt compounded is 0.1 to 5.0% by weight of the polyolefin.
It is preferably 0.5 to 3.0% by weight. If the compounding amount is less than this, the effect is not sufficient, and if the compounding amount is more than this, the effect does not change.
【0007】本発明における有機酸金属塩をポリオレフ
ィンに配合するのは、重合前、重合後のいずれでもよ
い。重合後に配合する場合には、ポリオレフィン樹脂の
粉末あるいはレジンに上記配合量の有機酸金属塩を混合
して均一に分散させた後、押出機、混練機などで溶融混
練する方法がある。The organic acid metal salt in the present invention may be blended with the polyolefin either before or after the polymerization. In the case of blending after polymerization, there is a method in which the above-mentioned blending amount of the organic acid metal salt is mixed with the powder or resin of the polyolefin resin and uniformly dispersed, and then melt-kneaded with an extruder, a kneader or the like.
【0008】一般にオリオレフィンでは熱劣化、酸化劣
化を防止するため酸化防止剤が配合される。本発明にお
いても上記の有機金属塩の他に酸化防止剤を配合するこ
とは不可欠であるが、これら酸化防止剤が上記の有機酸
金属塩退効果を阻害することはない。In general, an antioxidant is added to an ori-olefin in order to prevent thermal deterioration and oxidative deterioration. In the present invention, it is indispensable to add an antioxidant in addition to the above-mentioned organic metal salt, but these antioxidants do not inhibit the above-mentioned organic acid metal salt withdrawal effect.
【0009】本発明におけう、金属の仕事関数の測定方
法には、(1)高真空中で加熱して放出される電子1個
を計測する熱電子放出法、(2)高真空中で光を照射し
て放出される電子1個を計測する光電子放出法、(3)
強い電場を印加して放出される電子1個を計測する電場
電子放出法、(4)2つの物質の接触電位差を計測して
仕事関数を算出する血色電位差法があるが、この4つの
測定法のうちのいずれでもよい。(1)〜(3)の方法
ではそれぞれ放出電子による電流値から高地の関係式に
よって仕事関数が算出される。また(4)の方法では接
触電位差から高地の関係式によって仕事関数が算出され
る。In the present invention, the work function of a metal is measured by (1) a thermoelectron emission method for measuring one electron emitted by heating in a high vacuum, and (2) in a high vacuum. Photoelectron emission method for measuring one electron emitted by irradiating light, (3)
There are an electric field electron emission method that measures one electron emitted by applying a strong electric field, and (4) there is a blood color potential difference method that calculates the work function by measuring the contact potential difference between two substances. These four measurement methods Any of the above may be used. In the methods of (1) to (3), the work function is calculated from the current value of the emitted electrons by the relational expression of the altitude. Further, in the method of (4), the work function is calculated from the contact potential difference by the relational expression of high altitude.
【0010】本発明におけるポリオレフィンはポリプロ
ピレン、ポリエチレン、ポリスチレン、ポリ−4−メチ
ル−1−ペンテン、ポリ−3−メチル−1−ブテンなど
があるが、好ましくはポリプロピレンである。Polyolefin in the present invention includes polypropylene, polyethylene, polystyrene, poly-4-methyl-1-pentene, poly-3-methyl-1-butene, etc., among which polypropylene is preferred.
【0011】本発明においてスプリット繊維とは一軸熱
延伸フィルムを延伸方向に微細に割った繊維であり、連
続繊維であっても不連続繊維であっても構わない。また
スプリット繊維の幅は数μmから数100μmであり、
その分布は特に限定するものではないが、好ましい範囲
を例示すると20μm未満の繊維が20%以上、20〜
40μm未満の繊維が30%以下、40μm以上の繊維
が30%以下が挙げられる。ここで20μm未満の細い
繊維と40μm以上の太い繊維の含有率が特に重要であ
る。本発明においてスプリット繊維をつくる方法として
はヤスリ、針、刃を植え込んだロールを高速度で回転さ
せ、一軸熱延伸フィルムを傷つけ、あるいは切り目を入
れ微細に割る手法が挙げられる。In the present invention, split fibers are fibers obtained by finely splitting a uniaxially heat-stretched film in the stretching direction, and may be continuous fibers or discontinuous fibers. The width of the split fiber is several μm to several 100 μm,
The distribution is not particularly limited, but a preferable range is, for example, 20% or more of fibers having a size of less than 20 μm, 20 to 20.
30% or less of fibers of less than 40 μm and 30% or less of fibers of 40 μm or more. Here, the content of thin fibers of less than 20 μm and thick fibers of 40 μm or more is particularly important. In the present invention, as a method for producing split fibers, a method in which a file, a needle, or a roll in which a blade is implanted is rotated at a high speed to damage the uniaxially heat-stretched film or to make fine cuts is mentioned.
【0012】本発明において、繊維をエレクトレット化
する方法はスプリットする前でも後でもよく、具体的な
エレクトレット化の方法にはコロナ放電による荷電、電
子線照射による荷電、高電界下での荷電などが挙げられ
る。In the present invention, the method of electretizing the fibers may be before or after splitting. Specific electret methods include charging by corona discharge, charging by electron beam irradiation, charging under a high electric field and the like. Can be mentioned.
【0013】本発明において得られるエレクトレット化
ポリオレフィン系スプリット繊維はカーディング加工に
より不織布状にシート化され、次いでニードルパンチ加
工、熱エンボスカレンダー加工や超音波溶着加工によっ
てエレクトレットフィルターとなる。The electretized polyolefin-based split fiber obtained in the present invention is formed into a non-woven sheet by carding, and then needle punched, hot embossing calendering or ultrasonic welding is performed to obtain an electret filter.
【0014】本発明のエレクトレットフィルターは単一
材として用いることができるが、必要によってはニード
ルパンチ加工、超音波溶着加工や熱エンボスカレンダー
加工によってネット、不織布、織布などと貼り合わせて
用いることもできる。要によってはニードルパンチ加
工、超音波溶着加工や熱エンボスカレンダー加工によっ
てネット、不織布、織布などと貼り合わせて用いること
もできる。The electret filter of the present invention can be used as a single material, but if necessary, it can be used by laminating it with a net, a non-woven fabric, a woven fabric, etc. by needle punching, ultrasonic welding or hot embossing calendering. it can. If necessary, it can also be used by laminating with a net, a non-woven fabric, a woven fabric, etc. by needle punching, ultrasonic welding or hot embossing calendering.
【0015】[0015]
【各種測定法】エレクトレットフィルターの粒子捕集効
率は、0.3μmのNaCl粒子を用いてフィルター通
過風速10cm/秒において、フィルターの上、下流側
の粒子濃度をそれぞれレーザーパーティクルカウンター
(リオン製、KC−14)で測定し、上流側の粒子濃度
から下流側の粒子濃度を減じた値を上流側の粒子濃度で
除した値の百分率で示した。エレクトレットフィルター
の圧力損失はフィルターの上、下流の圧損差をマノスタ
ーゲージで測定した。図1に粒子捕集効率測定用の装置
を示す。電荷保持率の評価は、フィルターの初期の粒子
捕集効率(E0 )より求めた粒子透過率(100−
E0 )の自然対数値1n(100−E0 )に対する、6
0℃および100℃で24時間処理後の粒子捕集効率
(E1 )より求めた粒子透過率(100−E1 )の自然
対数値1n(100−E1 )から次式を用いて計算し
た。[Various measurement methods] The particle collection efficiency of the electret filter is 0.3 μm of NaCl particles, and the particle concentration on the upstream side and the downstream side of the filter is respectively measured with a laser particle counter (KC manufactured by Rion Co. The value obtained by subtracting the particle concentration on the downstream side from the particle concentration on the upstream side was divided by the particle concentration on the upstream side, and expressed as a percentage. The pressure loss of the electret filter was measured with a Manostar gauge. FIG. 1 shows an apparatus for measuring particle collection efficiency. The charge retention rate was evaluated by measuring the particle transmittance (100−) obtained from the initial particle collection efficiency (E 0 ) of the filter.
E 0) for the natural logarithm 1n of (100-E 0), 6
It was calculated from the natural logarithmic value 1n (100-E 1 ) of the particle transmittance (100-E 1 ) obtained from the particle collection efficiency (E 1 ) after treatment at 0 ° C. and 100 ° C. for 24 hours, using the following formula. .
【0016】[0016]
【数1】 [Equation 1]
【0017】[0017]
【実施例】以下に本発明を実施例でもって具体的に示
す。EXAMPLES The present invention will be specifically described below with reference to examples.
【0018】実施例1〜6 メルトフローインデックスが6、Mw/Mnが5で、酸
化防止剤のほかに表1に示した有機酸金属塩をそれぞれ
配合したアイソタクティックポリプロピレンを用いて幅
300mmで厚さ50μmのキャストフィルムをTダイ
で成膜し、次いでこのキャストフィルムを三段熱ロール
延伸方式で一段目、110℃で2.5倍延伸、二段目、
120℃で2倍延伸、三段目、135℃で1.3倍延伸
を連続的に行った。その後針電極により15kVの直流
高電圧を印加した後、針ロールでフィルムを割り、スプ
リット繊維を得た。次にこのスプリット繊維を75mm
にカットした後、カードに供給しカーディング加工し
て、ニードルパンチ加工を施して実施例1〜6のエレク
トレットフィルターを作製した。Examples 1 to 6 Isotactic polypropylene having a melt flow index of 6, Mw / Mn of 5 and an organic acid metal salt shown in Table 1 in addition to an antioxidant was used to obtain a width of 300 mm. A cast film having a thickness of 50 μm was formed by a T-die, and then this cast film was stretched at a first stage by a three-stage hot roll stretching method, stretched 2.5 times at 110 ° C., a second stage,
Two-fold stretching at 120 ° C., a third stage, and 1.3-fold stretching at 135 ° C. were continuously performed. After that, a high voltage of 15 kV was applied by a needle electrode, and then the film was split with a needle roll to obtain split fibers. Next, add this split fiber to 75 mm
After being cut into pieces, they were supplied to a card, carded and needle-punched to produce the electret filters of Examples 1 to 6.
【0019】比較例1〜3 比較のため、メルトフローインデックスとMw/Mnが
実施例と同じで、酸化防止剤と、表1に示したように炭
素数が10以上の有機酸と仕事関数が4eV未満の金属
のイオンとからなる塩を配合したアイソタクティックポ
リプロピレンを実施例と同様に成膜し、次いで全く同様
の条件で延伸、荷電、スプリット、不織布化により比較
例1〜3のエレクトレットフィルターを作製した。Comparative Examples 1 to 3 For comparison, the melt flow index and Mw / Mn are the same as those of the examples, and the antioxidant, the organic acid having 10 or more carbon atoms as shown in Table 1, and the work function are An electret polypropylene of Comparative Examples 1 to 3 was formed by forming a film of isotactic polypropylene mixed with a salt containing a metal ion of less than 4 eV in the same manner as in the example, and then stretching, charging, splitting, and forming a nonwoven fabric under exactly the same conditions. Was produced.
【0020】比較例4〜5 比較のため、メルトフローインデックスとMw/Mnが
実施例と同じで、酸化防止剤と、表1に示したように炭
素数が10以上の有機酸と仕事関数が4eV以上の金属
のイオンとからなる塩を配合したアイソタクティックポ
リプロピレンを実施例と同様に成膜し、次いで全く同様
の条件で延伸、荷電、スプリット、不織布化により比較
例4〜5のエレクトレットフィルターを作製した。Comparative Examples 4 to 5 For comparison, the melt flow index and Mw / Mn are the same as those of the examples, and the antioxidant, the organic acid having 10 or more carbon atoms as shown in Table 1 and the work function are Electret filters of Comparative Examples 4 to 5 were formed by forming an isotactic polypropylene film containing a salt composed of metal ions of 4 eV or more in the same manner as in the example, and then stretching, charging, splitting and forming a nonwoven fabric under exactly the same conditions. Was produced.
【0021】比較例6 比較のため、メルトフローインデックスとMw/Mnが
実施例と同じで、酸化防止剤のみを配合したアイソタク
ティックポリプロピレンを実施例と同様に成膜し、次い
で全く同様の条件で延伸、荷電、スプリット、不織布化
により比較例4〜5のエレクトレットフィルターを作製
した。Comparative Example 6 For comparison, an isotactic polypropylene having the same melt flow index and Mw / Mn as that of the example but containing only an antioxidant was formed in the same manner as in the example, and then under the same conditions. In, the electret filters of Comparative Examples 4 to 5 were produced by stretching, charging, splitting, and forming into a non-woven fabric.
【0022】表1にポリプロピレンに配合した有機酸金
属塩の種類、金属の仕事関数および配合量を示した。表
2にそれぞれのエレクトレットフィルターの初期性能、
60℃および100℃で24時間処理後の電荷保持率の
測定結果をまとめた。Table 1 shows the types of organic acid metal salts blended with polypropylene, the work function of the metal and the blending amount. Table 2 shows the initial performance of each electret filter.
The measurement results of the charge retention rate after treatment at 60 ° C. and 100 ° C. for 24 hours are summarized.
【0023】[0023]
【表1】 [Table 1]
【0024】[0024]
【表2】 [Table 2]
【0025】[0025]
【発明の効果】本発明は、上述のごとくポリオレフィン
中に、炭素数が10以上の有機酸と仕事関数が4eV以
上の金属のイオンとからなる有機酸金属塩を含有するこ
とにより、ポリオレフィンの帯電量の減衰を小さくする
ことで、エレクトレット化後の初期および長期の粒子捕
集効率が高いポリオレフィン系スプリット繊維からなる
エレクトレットフィルターを提供する。EFFECTS OF THE INVENTION The present invention contains the organic acid metal salt composed of an organic acid having 10 or more carbon atoms and an ion of a metal having a work function of 4 eV or more in the polyolefin as described above. Provided is an electret filter composed of a polyolefin-based split fiber having a high particle collection efficiency in the initial and long-term after electretization by reducing the amount of attenuation.
【図1】エレクトレットフィルターの粒子捕集効率の測
定方法を示す概略図である。FIG. 1 is a schematic view showing a method for measuring particle collection efficiency of an electret filter.
【符号の説明】 1:ダクト 2:上流側サンプリング管 3:下流側サンプリング管 4:差圧計 5:レーザーパーティクルカウンター 6:流量計 7:バルブ 8:ブロアー 9:エレクトレット繊維フィルター 10:NaCl粒子発生装置 11:アメリシウム中和器[Explanation of Codes] 1: Duct 2: Upstream sampling pipe 3: Downstream sampling pipe 4: Differential pressure gauge 5: Laser particle counter 6: Flow meter 7: Valve 8: Blower 9: Electret fiber filter 10: NaCl particle generator 11: Americium neutralizer
Claims (1)
化ポリオレフィン系スプリット繊維フィルターであっ
て、その有機酸金属塩が、炭素数が10以上の有機酸
と、仕事関数が4eV以上の金属のイオンとからなるこ
とを特徴とするエレクトレットフィルター。1. An electretized polyolefin-based split fiber filter containing an organic acid metal salt, wherein the organic acid metal salt is an organic acid having 10 or more carbon atoms and a metal ion having a work function of 4 eV or more. Electret filter characterized by being composed of.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4527293A JPH06254319A (en) | 1993-03-05 | 1993-03-05 | Electret filter |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4527293A JPH06254319A (en) | 1993-03-05 | 1993-03-05 | Electret filter |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06254319A true JPH06254319A (en) | 1994-09-13 |
Family
ID=12714684
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4527293A Pending JPH06254319A (en) | 1993-03-05 | 1993-03-05 | Electret filter |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06254319A (en) |
Cited By (13)
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---|---|---|---|---|
WO2014172308A2 (en) | 2013-04-19 | 2014-10-23 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
WO2015199972A1 (en) | 2014-06-23 | 2015-12-30 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
US9815068B2 (en) | 2012-12-28 | 2017-11-14 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
WO2018127831A1 (en) | 2017-01-05 | 2018-07-12 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
US10669481B2 (en) | 2015-07-07 | 2020-06-02 | 3M Innovative Properties Company | Substituted benzotriazole phenolate salts and antioxidant compositions formed therefrom |
US10919867B2 (en) | 2015-07-07 | 2021-02-16 | 3M Innovative Properties Company | Substituted benzotriazole phenols |
WO2021074863A1 (en) | 2019-10-16 | 2021-04-22 | 3M Innovative Properties Company | Dual-function melt additives |
WO2021111290A1 (en) | 2019-12-03 | 2021-06-10 | 3M Innovative Properties Company | Aromatic-heterocyclic ring melt additives |
WO2021111246A1 (en) | 2019-12-03 | 2021-06-10 | 3M Innovative Properties Company | Thiolate salt melt additives |
US11053373B2 (en) | 2015-07-07 | 2021-07-06 | 3M Innovative Properties Company | Polymeric matrices with ionic additives |
WO2021152422A1 (en) | 2020-01-27 | 2021-08-05 | 3M Innovative Properties Company | Substituted thiolate salt melt additives |
WO2021152426A1 (en) | 2020-01-27 | 2021-08-05 | 3M Innovative Properties Company | Substituted thiol melt additives |
EP4144901A2 (en) | 2020-12-02 | 2023-03-08 | Fiber Innovation Technology, Inc. | Splittable chargeable fiber, split multicomponent fiber, a split multicomponent fiber with a durable charge, nonwoven fabric, filter, and yarn containing the split fiber, and manufacturing processes therefor |
-
1993
- 1993-03-05 JP JP4527293A patent/JPH06254319A/en active Pending
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9815068B2 (en) | 2012-12-28 | 2017-11-14 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
US9815067B2 (en) | 2013-04-19 | 2017-11-14 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
WO2014172308A2 (en) | 2013-04-19 | 2014-10-23 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
WO2015199972A1 (en) | 2014-06-23 | 2015-12-30 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
US10240269B2 (en) | 2014-06-23 | 2019-03-26 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
US11053373B2 (en) | 2015-07-07 | 2021-07-06 | 3M Innovative Properties Company | Polymeric matrices with ionic additives |
US10669481B2 (en) | 2015-07-07 | 2020-06-02 | 3M Innovative Properties Company | Substituted benzotriazole phenolate salts and antioxidant compositions formed therefrom |
US10919867B2 (en) | 2015-07-07 | 2021-02-16 | 3M Innovative Properties Company | Substituted benzotriazole phenols |
US11078419B2 (en) | 2015-07-07 | 2021-08-03 | 3M Innovative Properties Company | Substituted benzotriazole phenolate salts and antioxidant compositions formed therefrom |
WO2018127831A1 (en) | 2017-01-05 | 2018-07-12 | 3M Innovative Properties Company | Electret webs with charge-enhancing additives |
WO2021074863A1 (en) | 2019-10-16 | 2021-04-22 | 3M Innovative Properties Company | Dual-function melt additives |
WO2021111246A1 (en) | 2019-12-03 | 2021-06-10 | 3M Innovative Properties Company | Thiolate salt melt additives |
WO2021111290A1 (en) | 2019-12-03 | 2021-06-10 | 3M Innovative Properties Company | Aromatic-heterocyclic ring melt additives |
WO2021152422A1 (en) | 2020-01-27 | 2021-08-05 | 3M Innovative Properties Company | Substituted thiolate salt melt additives |
WO2021152426A1 (en) | 2020-01-27 | 2021-08-05 | 3M Innovative Properties Company | Substituted thiol melt additives |
US11982031B2 (en) | 2020-01-27 | 2024-05-14 | 3M Innovative Properties Company | Substituted thiol melt additives |
EP4144901A2 (en) | 2020-12-02 | 2023-03-08 | Fiber Innovation Technology, Inc. | Splittable chargeable fiber, split multicomponent fiber, a split multicomponent fiber with a durable charge, nonwoven fabric, filter, and yarn containing the split fiber, and manufacturing processes therefor |
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