JPH046898Y2 - - Google Patents
Info
- Publication number
- JPH046898Y2 JPH046898Y2 JP15406185U JP15406185U JPH046898Y2 JP H046898 Y2 JPH046898 Y2 JP H046898Y2 JP 15406185 U JP15406185 U JP 15406185U JP 15406185 U JP15406185 U JP 15406185U JP H046898 Y2 JPH046898 Y2 JP H046898Y2
- Authority
- JP
- Japan
- Prior art keywords
- base material
- activated carbon
- acf
- layer
- adhesive layer
- 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
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 61
- 239000000463 material Substances 0.000 claims description 42
- 239000010410 layer Substances 0.000 claims description 25
- 239000012790 adhesive layer Substances 0.000 claims description 20
- 238000001179 sorption measurement Methods 0.000 claims description 18
- 239000003463 adsorbent Substances 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 12
- 239000004745 nonwoven fabric Substances 0.000 claims description 6
- -1 felt Substances 0.000 claims description 4
- 239000002759 woven fabric Substances 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 12
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 229920006282 Phenolic fiber Polymers 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
Landscapes
- Separation Of Gases By Adsorption (AREA)
- Laminated Bodies (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Description
【考案の詳細な説明】
本考案は、繊維状活性炭(以下、単にACFと
記載することがある)または粉末活性炭(以下、
単にACと記載することがある)が本来の吸着性、
表面積を保持し、かつ、良好な機械的物性、導電
性を兼備した2次元状の吸着材料に関する。[Detailed description of the invention] The present invention is based on fibrous activated carbon (hereinafter sometimes simply referred to as ACF) or powdered activated carbon (hereinafter referred to simply as ACF).
(sometimes simply written as AC) is the original adsorption property,
The present invention relates to a two-dimensional adsorbent material that maintains surface area and has good mechanical properties and conductivity.
ACFおよびACは高度な吸着性、きわめて大な
る表面積および良好な導電性を有し、これら特性
を利用し、静電、有害物質除去、ガス分離等の吸
着材料他の用途に対し、広く使用されている。こ
れら用途に対する適用性を広げるためACFおよ
びACを2次元の面、膜等の構造体とする必要が
あり、過去種々の試みが検討、実施されている。 ACF and AC have a high degree of adsorption, extremely large surface area, and good electrical conductivity. Taking advantage of these properties, they are widely used as adsorbent materials and other applications such as electrostatics, hazardous substance removal, and gas separation. ing. In order to expand their applicability to these uses, it is necessary to make ACF and AC into structures such as two-dimensional surfaces and films, and various attempts have been made and implemented in the past.
現状の2次元構造体としては、ACFにおいて
はポリノジツク・レーヨン、フエノール系等で代
表される有機繊維を紡績・製編織したのち、炭
化・賦活し、AGFのクロス状の2次元状構造体
としたり、ACFを生産したのち、これを用いて
不織布とし、同様の構造体を得る方法が一般的に
実施されている。一方、ACにおいては、ウレタ
ン、アクリル系等の樹脂液中にACを添加し、必
要により、発泡処理を伴う成型加工により2次元
状構造体を得たり、あるいは布帛、不織布等の基
材へこの樹脂液を塗布する構造が提案されてい
る。 Current two-dimensional structures include ACF, which spins, knits, and weaves organic fibers such as polynosic rayon and phenolic fibers, then carbonizes and activates them to create AGF cross-shaped two-dimensional structures. A commonly practiced method is to produce ACF and then use it to make a nonwoven fabric to obtain a similar structure. On the other hand, in AC, AC is added to a resin liquid such as urethane or acrylic, and if necessary, a two-dimensional structure is obtained by molding with foaming treatment, or it is applied to a base material such as fabric or non-woven fabric. A structure in which a resin liquid is applied has been proposed.
しかし、これらの2次元構造体には多くの欠陥
があり、実用面において、その使用に制約が必要
であつたり、あるいは吸着性能等の基本性能の犠
牲を伴なつたりして、やむを得ず実用に供されて
いるのが現状である。すなわち、前記ACFのク
ロス、不織布においては、ACFの基本性能を損
わない点では好ましいが、ACF自体きわめて脆
弱であるため得られる構造体は当然脆弱でわずか
の屈曲等の応力によりその構造破壊が生じ、実用
面で大きな制約を受ける結果となる。一方、AC
に関しては、その表面に樹脂液が付着するため吸
着性能とくに吸着速度を著しく低下させ、また導
電性の低下が発生する問題がある。 However, these two-dimensional structures have many defects, and in practical terms, their use may require restrictions, or may involve sacrificing basic performance such as adsorption performance, making it unavoidable to put them into practical use. The current situation is that In other words, the aforementioned ACF cloth and nonwoven fabric are preferable in that they do not impair the basic performance of ACF, but since ACF itself is extremely fragile, the resulting structure is naturally fragile and its structure can be destroyed by stress such as slight bending. This results in significant practical limitations. On the other hand, AC
However, since the resin liquid adheres to the surface, there is a problem in that the adsorption performance, especially the adsorption speed, is significantly reduced, and the conductivity is also reduced.
本考案者らはかかる不都合に関し、発想の転換
を計り、鋭意努力した結果、実用に充分耐えうる
強度を有する導電性基材層に対し、導電性の接着
層を介し、ACF短繊維またはAC粒子をこれらそ
れぞれの表面のごく一部分のみをこの接着層で固
着・一体化することより、前記問題がなく、活性
炭の有する高吸着、大表面積、良好な導電性を保
持し、かつ、これらの欠点である機械的物性が改
善された吸着材料の構造を見出し、本考案を完成
させた。 The inventors of the present invention tried to change their way of thinking in order to solve this problem, and as a result of their earnest efforts, they applied ACF short fibers or AC particles to a conductive base material layer having sufficient strength for practical use through a conductive adhesive layer. By fixing and integrating only a small portion of each of these surfaces with this adhesive layer, it does not have the above problems, maintains the high adsorption, large surface area, and good conductivity of activated carbon, and also eliminates these drawbacks. The present invention was completed by discovering the structure of an adsorbent material with improved mechanical properties.
すなわち本考案は、導電性を有する製編織され
た布帛、不織布、フエルト、紙等よりなる単位断
面積当りの引張強度が1Kg/cm2以上の基材層に対
し、その片面または両面に導電性接着層を介し、
ACFまたはAC層を配した構造である吸着材料で
ある。ここで基材層および接着層の体積固有電気
抵抗は105cm・Ω以下が好ましく、また使用する
ACFの繊維長は0.1mmないし20mmの範囲でかつ、
その単位重量当りの表面積は500m2/gないし
4500m2/gが好ましい。一方、ACにおいてはそ
の平均粒度(直径)が1μmないし500μmの範囲
が好ましい。また接着層を介して配するACFは
基材層に対しほぼ垂直とする構造がより好まし
い。 In other words, the present invention provides a base material layer made of conductive knitted fabric, non-woven fabric, felt, paper, etc., with a tensile strength per unit cross-sectional area of 1 kg/cm 2 or more, which is conductive on one or both sides. Through the adhesive layer,
It is an adsorption material that has a structure with an ACF or AC layer. Here, the volume specific electrical resistance of the base material layer and the adhesive layer is preferably 10 5 cm・Ω or less, and the
The fiber length of ACF is in the range of 0.1 mm to 20 mm, and
Its surface area per unit weight is 500m 2 /g or
4500m 2 /g is preferred. On the other hand, the average particle size (diameter) of AC is preferably in the range of 1 μm to 500 μm. Further, it is more preferable that the ACF disposed via the adhesive layer be substantially perpendicular to the base material layer.
ここで使用する基材は導電性と機械的物性を考
慮しておく必要があり、通気性、通液性は用途面
よりの要求により適宜選択すればよい。これらの
点より使用し得る素材としては、例えば金属メッ
キ繊維、金属繊維、炭素繊維、導電性微粉末混合
防糸繊維、導電性樹脂被覆有機繊維金属容射した
布、不織布、フエルト、紙等が可能である。な
お、基材の引張強度を1Kg/cm2以上に限定した理
由は基材の機械的物性により、本考案の吸着材料
の機械的物性を左右するためで1Kg/cm2以下で
は、実用上の支障があり、本考案の有用性を損な
うためである。 The conductivity and mechanical properties of the base material used here must be taken into consideration, and the air permeability and liquid permeability may be appropriately selected depending on the requirements of the application. From these points, materials that can be used include, for example, metal-plated fibers, metal fibers, carbon fibers, conductive fine powder mixed yarn-proof fibers, conductive resin-coated organic fibers, metal-coated cloth, non-woven fabrics, felt, paper, etc. It is possible. The reason why the tensile strength of the base material was limited to 1 Kg/cm 2 or more is that the mechanical properties of the base material affect the mechanical properties of the adsorbent material of the present invention. This is because it is a hindrance and impairs the usefulness of the present invention.
基材層と接着層の体積固有電気抵抗を105Ω・
cm以下としたのはこれ以上の場合、充分な導電性
が得られず静電除去性他の電気特性を低下させる
等のためである。 The volume specific electrical resistance of the base material layer and adhesive layer is set to 10 5 Ω・
The reason why the thickness is set to be less than cm is that if it is more than this, sufficient conductivity cannot be obtained and the electrostatic removal property and other electrical properties are deteriorated.
前述したように、本考案の吸着材において、基
材層と接着層は共に導電性を有している必要があ
り、これにより本考案の吸着材を空気フイルター
や引火性薬剤ガスの吸着材として用いた場合、帯
電防止、静電防止および除電性の付与が可能とな
り、その結果粉じん爆発、引火爆発、目づまり等
を回避することができる。 As mentioned above, in the adsorbent of the present invention, both the base layer and the adhesive layer must have conductivity, which makes the adsorbent of the present invention suitable for use as an air filter or as an adsorbent for flammable drug gases. When used, it becomes possible to provide antistatic, antistatic, and static neutralizing properties, and as a result, dust explosions, flammable explosions, clogging, etc. can be avoided.
ACFの平均繊維長が0.1mmないし20mmとした理
由は、0.1mm以下では生産性に問題あり、高価格
となり、また接着層に埋没される率が高くなり、
吸着性の低下を生じるためであり、20mm以上で
は、ACFの脆弱な性質を本考案でさえも押え得
ず、機械的 力が加わつた際ACFの切断、脱落
の危険性が高まる理由による。また、この単位重
量当りの表面積を500m2/gないし、4500m2/g
の範囲を好ましいとした理由は、500m2/g以下
では吸着性能が低くすぎ、逆に4500m2/g以上の
場合は、あまりにもACFが脆弱すぎ、本考案で
も対応不可となるためである。一方、ACの平均
直径を1μmないし500μmとした理由は、1μm以
下では充填密度が低くなりACの面密度(目付)
が低くなりすぎるためであり、500μm以上では
本考案の場合ACのごく一部しか接着層に保持さ
れず機械的応力が加わつた場合、脱落の危険性が
増大するためである。 The reason why the average fiber length of ACF is set to 0.1 mm to 20 mm is that if it is less than 0.1 mm, there will be problems with productivity, the price will be high, and the rate of being buried in the adhesive layer will be high.
This is because the adsorption property decreases, and if the diameter is 20 mm or more, even the present invention cannot suppress the fragile nature of the ACF, increasing the risk of the ACF breaking or falling off when mechanical force is applied. Also, the surface area per unit weight is between 500m 2 /g and 4500m 2 /g.
The reason why this range is preferable is that the adsorption performance is too low if it is less than 500 m 2 /g, and conversely, if it is more than 4500 m 2 /g, the ACF is too fragile and cannot be handled by the present invention. On the other hand, the reason why the average diameter of AC is set to 1 μm to 500 μm is that if it is less than 1 μm, the packing density will be low, and the areal density (fabric weight) of AC
This is because the AC becomes too low, and in the case of the present invention, only a small portion of the AC is retained by the adhesive layer, increasing the risk of it falling off when mechanical stress is applied.
また、基材層に対し、接着層を介し、ACFを
配するに当り、基材層にほぼ垂直に配するのが好
ましいとした理由はACFが接着層に埋没する率
がきわめて低くなり、本考案の特長をより発揮し
やすいためであり、具体的には電気植毛法がとく
に有効な手段である。 In addition, when disposing ACF on the base material layer via the adhesive layer, the reason why it is preferable to arrange it almost perpendicularly to the base material layer is that the rate of ACF being buried in the adhesive layer is extremely low, and the reason is that This is because it is easier to demonstrate the features of the invention, and specifically, electric flocking is a particularly effective method.
ここで使用しうる接着剤としては、例えばエポ
キシ系、アクリル系、フエノール系等が可能で、
これらに対し、導電性カーボン、金属微粉末を添
加する等のいかなる方法により導電性を付与して
もよい、またACの素材は、特に制約する必要は
なく、一般的に使用されているやし殻活性炭の粉
砕品等が可能である。 Examples of adhesives that can be used here include epoxy, acrylic, and phenol adhesives.
Conductivity may be imparted to these by any method such as adding conductive carbon or fine metal powder, and the material of the AC does not need to be particularly restricted; commonly used palm Pulverized shell activated carbon etc. are possible.
なお、本考案は、吸着材料を想定しているが、
他の用途をあえて、避ける必要はなく、例えば大
表面積、導電性能を活かし、種々の電気材料等に
も応用可能である。 Although this invention assumes adsorption materials,
There is no need to avoid other uses; for example, by taking advantage of its large surface area and conductive properties, it can be applied to various electrical materials.
以下に図面および実施例により、本考案を説明
する。 The invention will be explained below with reference to the drawings and examples.
実施例 1
ニツケルメツキされたポリビニルアルコール系
繊維よりなる単位断面積当りの強度200Kg/cm2の
布帛を基材層とし、この片面にカーボンとニツケ
ル微粉末添加のアクリル酸エステル系接着剤を
10μmコーテイングしたのち、0.5mm繊維長、単位
重量当りの表面積が1500m2/gであるフエノール
系ACFを電気植毛法により加工し、ACF目付50
g/m2の本考案の吸着材料を得た。基材層および
接着層の体積固有電気抵抗値は共に105Ω・cm以
下である。Example 1 A fabric made of nickel-plated polyvinyl alcohol fiber with a strength per unit cross-sectional area of 200 kg/cm 2 was used as the base material layer, and an acrylic ester adhesive containing carbon and fine nickel powder was applied to one side of the fabric.
After coating with a thickness of 10 μm, phenolic ACF with a fiber length of 0.5 mm and a surface area per unit weight of 1500 m 2 /g was processed using the electro-flocking method to obtain an ACF fabric weight of 50.
g/m 2 of the adsorbent material of the present invention was obtained. Both the base material layer and the adhesive layer have a volume specific electrical resistance value of 10 5 Ω·cm or less.
一方比較例として、フエノール系繊維を紡績・
製織・炭化・賦活し、ACF目付50g/m2のクロ
スを用いた。 On the other hand, as a comparative example, phenolic fiber was spun and
A cloth that had been woven, carbonized, and activated and had an ACF area weight of 50 g/m 2 was used.
この両者について、吸着性、帯電防止性、機械
的物性を評価した。吸着性は、JISK−1474の方
法により、ベンゼン蒸気を用いて測定したところ
利用者とも25g/m2の吸着量を示し、静電防止性
はJISM7102に準じナイロン布を敷布とし、22℃
×30%RHの条件で帯電電密度を測定したところ
両者とも0.1μc/m2以下の良好な性能を示した。
一方、機械的物性を評価するため両者を軽く手み
をしたところ、本考案のものはなんらの損傷もな
かつたが、比較例のものは、大巾な損傷を受け、
その形体の保持さえも不可であつた。 Both were evaluated for adsorption, antistatic properties, and mechanical properties. The adsorption properties were measured using benzene vapor according to the JISK-1474 method, and both users showed an adsorption amount of 25 g/ m2 , and the antistatic properties were measured using nylon cloth according to JISM7102 at 22°C.
When the charge density was measured under the conditions of ×30% RH, both exhibited good performance of 0.1 μc/m 2 or less.
On the other hand, when both were lightly touched to evaluate their mechanical properties, the one of the present invention had no damage, but the one of the comparative example suffered extensive damage.
It was impossible to even maintain its shape.
実施例 2
実施例1と同じく基材層および接着剤を用い平
均径260μmのやし殻活性炭(AC)を電気植毛法
によりACの目付120g/m2の本考案品を加工し
た。Example 2 Using the same base material layer and adhesive as in Example 1, coconut shell activated carbon (AC) with an average diameter of 260 μm was processed into a product of the present invention with a basis weight of 120 g/m 2 by electro-flocking.
対照例とし、本考案と同じ基材および接着剤を
使用し、接着剤中に前記と同一のACを添加し、
基材にナイフ・コーテイングにより、AC目付120
g/m2の加工布を得た。 As a control example, the same base material and adhesive as in the present invention were used, and the same AC as above was added to the adhesive.
AC basis weight 120 due to knife coating on the base material
A processed fabric of g/m 2 was obtained.
25℃においてベンゼン飽和蒸気圧下に前記2種
を入れ、30分后の吸着量を測定したところ本考案
のものは40g/m2の吸着量を示したのに対し、比
較例は15g/m2しかなく、本考案が優れているこ
とが立証された。 When the above two types were placed under benzene saturated vapor pressure at 25°C and the adsorption amount was measured after 30 minutes, the adsorption amount of the present invention was 40 g/m 2 , while the comparative example was 15 g/m 2 This proves that the present invention is superior.
実施例 3
ステンレス製金属繊維を製織した布帛(引張り
強度1Kg/cm2以上)に対し、カーボン微粉末を添
加したフエノール系接着剤を片面に10μmコーテ
ングしたのち、実施例1のACFを電気植毛法に
より、ACF目付45g/m2の吸着材料を得た。基
材層および接着層の体積固有電気抵抗値は共に
105Ω・cm以上である。Example 3 A fabric woven from stainless steel metal fibers (tensile strength of 1 Kg/cm 2 or more) was coated with 10 μm of phenolic adhesive containing fine carbon powder on one side, and then the ACF of Example 1 was applied by electro-flocking method. As a result, an adsorbent material with an ACF area weight of 45 g/m 2 was obtained. Both the volume specific electrical resistance values of the base material layer and adhesive layer are
10 5 Ω・cm or more.
この吸着材料は、吸着性、帯電防止性、機械的
物性は実施例1と同様に優れ、また、高度の耐熱
性を有する吸着材料であることを判明した。 It was found that this adsorbent material had excellent adsorption properties, antistatic properties, and mechanical properties as in Example 1, and also had a high degree of heat resistance.
第1図は、基材層の片面に対し、接着剤層を介
し、ACFを配した例で、1は基材層、2は接着
層、3はACF層を示す。第2図は、基材層の両
面に対し、接着剤層を介し、ACFを配した例で
1〜3の内容は第1図と同様である。第3図は基
材層の片面に対し、接着剤層を介し、ACを配し
たもので、1は基材層、2は接着層、3はAC層
を示す。
FIG. 1 shows an example in which ACF is arranged on one side of a base material layer via an adhesive layer, where 1 is the base material layer, 2 is the adhesive layer, and 3 is the ACF layer. FIG. 2 shows an example in which ACF is disposed on both sides of the base material layer via an adhesive layer, and the contents of 1 to 3 are the same as in FIG. 1. In FIG. 3, AC is arranged on one side of a base material layer via an adhesive layer, where 1 is the base material layer, 2 is the adhesive layer, and 3 is the AC layer.
Claims (1)
ト、紙等よりなる単位断面積当りの引張強度が
1Kg/cm2以上の基材層に対し、その片面または
両面に導電性接着層を介し、繊維状活性炭層あ
るいは粉末状活性炭層を配した吸着材料。 2 基材層および接着層の体積固有電気抵抗が
105Ω・cm以下である実用新案登録請求の範囲
第1項記載の吸着材料。 3 繊維状活性炭の平均繊維長が0.1mmないし20
mmの範囲で、かつ、その単位重量当りの表面積
が500m2/gないし4500m2/gの範囲である実
用新案登録請求の範囲第1項記載の吸着材料。 4 粉末活性炭の平均直径が1μmないし500μm
の範囲である実用新案登録請求の範囲第1項記
載の吸着材料。 5 繊維状活性炭が基材層に対しほぼ垂直に配列
されている実用新案登録請求の範囲第1項記載
の吸着材料。[Scope of Claim for Utility Model Registration] 1. A base material layer made of conductive knitted woven fabric, non-woven fabric, felt, paper, etc. and having a tensile strength per unit cross-sectional area of 1 Kg/cm 2 or more, on one or both sides thereof. An adsorption material with a fibrous activated carbon layer or powdered activated carbon layer interposed between a conductive adhesive layer. 2 The volume specific electrical resistance of the base material layer and adhesive layer is
The adsorbent material according to claim 1 of the utility model registration claim, which has a resistance of 10 5 Ω·cm or less. 3 The average fiber length of the fibrous activated carbon is 0.1 mm to 20
The adsorbent material according to claim 1, which is registered as a utility model and has a surface area of 500 m 2 /g to 4500 m 2 /g. 4 The average diameter of powdered activated carbon is 1 μm to 500 μm
The adsorbent material according to claim 1 of the utility model registration claim, which is within the scope of. 5. The adsorption material according to claim 1, wherein the fibrous activated carbon is arranged substantially perpendicularly to the base material layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15406185U JPH046898Y2 (en) | 1985-10-07 | 1985-10-07 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15406185U JPH046898Y2 (en) | 1985-10-07 | 1985-10-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6260327U JPS6260327U (en) | 1987-04-14 |
| JPH046898Y2 true JPH046898Y2 (en) | 1992-02-25 |
Family
ID=31073514
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15406185U Expired JPH046898Y2 (en) | 1985-10-07 | 1985-10-07 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH046898Y2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20170098511A (en) * | 2016-02-22 | 2017-08-30 | 현대자동차주식회사 | Air filter for fuel cell vehicle |
-
1985
- 1985-10-07 JP JP15406185U patent/JPH046898Y2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6260327U (en) | 1987-04-14 |
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