JP5082292B2 - Adsorbent sheet - Google Patents

Adsorbent sheet Download PDF

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JP5082292B2
JP5082292B2 JP2006129300A JP2006129300A JP5082292B2 JP 5082292 B2 JP5082292 B2 JP 5082292B2 JP 2006129300 A JP2006129300 A JP 2006129300A JP 2006129300 A JP2006129300 A JP 2006129300A JP 5082292 B2 JP5082292 B2 JP 5082292B2
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sheet
adsorbent
nonwoven fabric
base material
fiber
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JP2007301434A (en
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慎一 峯村
豊太 関
禎仁 後藤
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Toyobo Co Ltd
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Description

本発明は、除塵機能と脱臭機能を有した空気浄化用濾材に関するものである。   The present invention relates to a filter medium for air purification having a dust removing function and a deodorizing function.

近年、自動車用、家庭用フィルター等の分野において、濾材の高機能化・多様化の要請が急激に高まっており、除塵機能と脱臭機能を兼備する空気浄化用濾材の検討が多くなされている。そして、これら空気浄化用濾材として、粒子状または繊維状の吸着剤と接着剤を用いてシート化する方法が多く採用されており、例えば、基材間に粒状吸着剤と粒状接着剤の混合物を散布し、これを加熱接着してなる吸着濾材が開示されている(例えば特許文献1参照)。かかる吸着濾材は低コストで通気性に優れる吸着性シートが得られるが、吸着剤層と基材層との接着が弱いため剥離が生じやすく、プリーツ加工等で外力がかかる場合、あるいはフィルタを高風量下に曝した場合では吸着剤の脱落が大きい等実用上の問題を有していた。かかる問題を解決するため、例えば接着シートを用いて吸着剤層と基材を接着した吸着性シートが開示されている(例えば特許文献2参照)。しかしながら、かかる吸着性シートは、接着シートが通気性を阻害して通気抵抗が高くなり、更には接着面で粉塵が目詰まりしやすい、あるいは吸着性能を阻害するという問題を有していた。
特開平11−5058号公報 特開2002−273123号公報
In recent years, in the fields of automobiles, household filters, and the like, there has been a rapid increase in the demand for higher functionality and diversification of filter media, and many studies have been made on air purification filter media having both a dust removal function and a deodorization function. And as these air purification filter media, a method of forming a sheet using a particulate or fibrous adsorbent and an adhesive is often employed. For example, a mixture of a granular adsorbent and a granular adhesive between substrates is used. An adsorptive filter medium formed by spraying and heat-bonding this is disclosed (for example, see Patent Document 1). Such adsorptive filter media can provide an adsorbent sheet that is low in cost and excellent in air permeability. However, since the adhesion between the adsorbent layer and the base material layer is weak, peeling easily occurs, and when external force is applied by pleating or the like, or the filter is increased. When exposed to air flow, there were practical problems such as a large dropout of the adsorbent. In order to solve such a problem, for example, an adsorbent sheet in which an adsorbent layer and a substrate are bonded using an adhesive sheet is disclosed (for example, see Patent Document 2). However, such an adsorbent sheet has a problem that the adhesive sheet impairs the air permeability and increases the air resistance, and further, the adhering surface tends to clog the dust or impedes the adsorbing performance.
Japanese Patent Laid-Open No. 11-5058 JP 2002-273123 A

本発明は、上記従来技術の課題を背景になされたもので、充分な基材層と吸着層との接着性を有し、プリーツ加工性にも優れ、低通気抵抗、かつ高脱臭性能を有する吸着性シートを提供しようとするものである。 The present invention has been made against the background of the above-described prior art, has sufficient adhesion between the base material layer and the adsorbing layer, has excellent pleatability, has low ventilation resistance, and high deodorization performance. An attempt is made to provide an adsorbent sheet.

本発明者らは上記課題を解決するため、鋭意研究した結果、遂に本発明を完成するに至った。即ち、本発明は、(1)基材層間に吸着剤及び熱可塑性樹脂を含む吸着シートであって、該基材層の少なくとも片面がニードルパンチ加工及び/又は水流交絡加工が施された不織布であることを特徴とする吸着性シート、(2) (1)に記載の不織布がバインダー成分を含まない不織布である、(3) (1)乃至(2)に記載の不織布がエレクトレット不織布である(1)〜(3)のいずれかに記載の吸着性シートである。 As a result of intensive studies to solve the above problems, the present inventors have finally completed the present invention. That is, the present invention is (1) an adsorbent sheet containing an adsorbent and a thermoplastic resin between base material layers, wherein at least one surface of the base material layer is a nonwoven fabric subjected to needle punching and / or hydroentanglement processing. (2) The non-woven fabric according to (1) or (2) is an electret non-woven fabric, wherein the non-woven fabric according to (2) (1) is a non-woven fabric that does not contain a binder component. The adsorbent sheet according to any one of 1) to (3).

本発明による吸着性シートは、基材層と吸着層間の強い接着性を有し、低通気抵抗かつ脱臭性能も良好な吸着性シートを提供できるという利点がある。 The adsorbent sheet according to the present invention has an advantage that it can provide an adsorbent sheet having strong adhesion between the base material layer and the adsorbing layer, and having low ventilation resistance and good deodorization performance.

以下、本発明を詳細に説明する。
本発明の吸着性シートは、基材層間に吸着剤及び熱可塑性樹脂を含む吸着性シートであって、該基材層の少なくとも片面がニードルパンチ加工及び/又は水流交絡加工が施された不織布であることが好ましい。本願発明者等が知る限り、ニードルパンチ加工、水流交絡加工がなされた不織布は、毛羽が多く、表面平滑性が低いため、フィルター等に用いる吸着性シートには用いられていなかった。しかし、特に基材層間に吸着剤及び熱可塑性樹脂を含むシートに用いれば、シート全体として使用する接着剤を劇的に低減することができるという特異な効果を本願発明者等は見出した。すなわち、従来の基材シートでは、実用に耐える接着強力を得るために接着シートを使用する、あるいは吸着性シート全体への熱プレス負荷を大きくする等の処理がなされており、結果として、高通気抵抗化、脱臭性能の低下等の悪影響を招来していた。一方、本発明のニードルパンチ加工及び/又は水流交絡加工が施された不織布は毛羽が発生するが、かかる毛羽が吸着層に入り込んでアンカーとなり、吸着剤を固定するために用いる吸着層内の接着剤が吸着層と基材層を接着する機能も発揮し、シート全体として使用する接着剤を劇的に低減することが可能となり、柔軟且つ低通気抵抗の吸着性シートを得ることができる。
Hereinafter, the present invention will be described in detail.
The adsorbent sheet of the present invention is an adsorbent sheet containing an adsorbent and a thermoplastic resin between base material layers, and at least one surface of the base material layer is a nonwoven fabric on which needle punch processing and / or hydroentanglement processing is performed. Preferably there is. As far as the inventors of the present application are aware, nonwoven fabrics that have been subjected to needle punching and hydroentanglement have many fuzz and low surface smoothness, so they have not been used in adsorbent sheets used for filters and the like. However, the present inventors have found a unique effect that the adhesive used as the entire sheet can be drastically reduced, particularly when used for a sheet containing an adsorbent and a thermoplastic resin between the base material layers. That is, in the conventional base material sheet, processing such as using an adhesive sheet to increase the adhesive strength to withstand practical use or increasing the heat press load on the entire adsorbent sheet has been performed. Adverse effects such as resistance and reduced deodorization performance were caused. On the other hand, the nonwoven fabric subjected to the needle punch processing and / or hydroentanglement processing of the present invention generates fluff, but the fluff enters the adsorption layer and becomes an anchor, and adhesion in the adsorption layer used for fixing the adsorbent The agent also exhibits the function of adhering the adsorbing layer and the base material layer, and it is possible to dramatically reduce the adhesive used as the entire sheet, thereby obtaining an adsorbent sheet that is flexible and has low ventilation resistance.

なお、本発明の吸着性シートに用いる基材不織布は水流交絡法、ニードルパンチ製法により不織布とされたものであるが、これらの処理は別法により不織布とされた後に実施してもよい。たとえば、一担、加熱圧着等により長繊維不織布を形成した後、前述した交絡法を施してもよい。このような基材不織布は繊維末端が多数存在し、かかる繊維末端が吸着剤層の中に深く入り込み、吸着層と基材層の接合を強固にする。   In addition, although the base nonwoven fabric used for the adsorptive sheet of this invention is made into the nonwoven fabric by the hydroentanglement method and the needle punch manufacturing method, you may implement after these processing is made into the nonwoven fabric by another method. For example, the entanglement method described above may be performed after a long-fiber nonwoven fabric is formed by heating or pressure bonding. Such a base nonwoven fabric has a large number of fiber ends, and the fiber ends penetrate deeply into the adsorbent layer, thereby strengthening the bonding between the adsorption layer and the base material layer.

本発明の基材不織布は、繊維径が3〜100μmが好ましい範囲である。かかる範囲であれば、柔軟性を保持しつつ、吸着層と基材層をつなぎ止める役割を十分に果たすことができるからである。より好ましくは5〜80μm、更に好ましくは10〜60μmである。   The base nonwoven fabric of the present invention preferably has a fiber diameter of 3 to 100 μm. This is because, within such a range, the role of holding the adsorbing layer and the base material layer can be sufficiently achieved while maintaining flexibility. More preferably, it is 5-80 micrometers, More preferably, it is 10-60 micrometers.

本発明の基材不織布は、繊維長20〜200mmであることが好ましい。かかる範囲であれば、基材の強度を保持しつつ、適度な数の繊維末端が存在するからである。より好ましくは、30mm〜150mm、更に好ましくは40mm〜100mmである。   The base nonwoven fabric of the present invention preferably has a fiber length of 20 to 200 mm. This is because within this range, an appropriate number of fiber ends are present while maintaining the strength of the substrate. More preferably, they are 30 mm-150 mm, More preferably, they are 40 mm-100 mm.

本発明の基材層を構成する基材不織布の充填密度は0.15g/cc以下、であることが好ましい。なぜなら、後に述べる粉粒状吸着剤と熱可塑性粉末樹脂の混合粉粒体をこの基材不織布上に散布後、熱プレスし吸着性シートを得ようとするとある程度基材不織布の充填密度が低い方が低通気抵抗化を実現でき、かつ接着性も向上し、一体構造化できるからである。より好ましくは0.10g/cc以下である。   The filling density of the base nonwoven fabric constituting the base layer of the present invention is preferably 0.15 g / cc or less. This is because, after spraying the mixed granular material of granular adsorbent and thermoplastic powder resin, which will be described later, on this base nonwoven fabric, it is better to lower the packing density of the base nonwoven fabric to some extent when trying to obtain an adsorptive sheet by hot pressing This is because low ventilation resistance can be realized, adhesion can be improved, and an integrated structure can be achieved. More preferably, it is 0.10 g / cc or less.

本発明の基材不織布は、厚みは0.1mm以上1.0mm以下が好ましい。0.1mm以下であれば目付斑も考慮すると粉粒状吸着剤の抜け、脱落の懸念が生じ、また1.0mm以上であればシート全体の厚みが厚すぎるため、プリーツ状ユニットとした場合に構造抵抗が大きくなり、結果としてユニット全体での圧損が高くなり過ぎ実用上問題がある。目付量としては5〜100g/m2であることが好ましい。5g/m2未満であれば粉粒状吸着剤、及び熱可塑性粉末樹脂の抜けが多くなり実用上問題となる。100g/m2以上であれば、シート厚みが厚くなるためプリーツ状ユニットとした場合の構造抵抗が大きくなり実用上問題となる。 The base nonwoven fabric of the present invention preferably has a thickness of 0.1 mm to 1.0 mm. If it is 0.1 mm or less, there is a concern that the granular adsorbent may come off or fall off when considering the spot weight, and if it is 1.0 mm or more, the entire sheet is too thick. The resistance increases, and as a result, the pressure loss in the entire unit becomes too high, which causes a practical problem. The basis weight is preferably 5 to 100 g / m 2 . If it is less than 5 g / m 2 , the powdery adsorbent and the thermoplastic powder resin are more likely to come off, resulting in a practical problem. If it is 100 g / m 2 or more, the sheet thickness is increased, so that the structural resistance in the case of a pleated unit is increased, which is a practical problem.

本発明の基材不織布を構成する繊維材質はポリオレフィン系、レーヨン系、ポリエステル系、ポリアミド系、ポリウレタン系、アクリル系、ポリビニルアルコール系、ポリカーボネート等特に規定はなく、芯鞘繊維を使用しても種々の混合繊維であっても当然構わない。また、タバコ煙粒子、カーボン粒子、海塩粒子をはじめとするサブミクロン粒子に対する除去効果も増大することができる帯電した不織布、いわゆるエレクトレットシートを基材に使用することもできる。エレクトレットシートを基材とすることにより、ダスト等が吸着層に侵入して吸着層内の細孔が閉塞することを防止し、フィルター寿命を延長することができるからである。   The fiber material constituting the base nonwoven fabric of the present invention is not particularly specified, such as polyolefin, rayon, polyester, polyamide, polyurethane, acrylic, polyvinyl alcohol, polycarbonate, etc. Of course, it may be a mixed fiber. In addition, a charged non-woven fabric, so-called electret sheet, which can increase the effect of removing submicron particles such as tobacco smoke particles, carbon particles, and sea salt particles can also be used as a substrate. This is because by using the electret sheet as a base material, it is possible to prevent dust and the like from entering the adsorption layer and block pores in the adsorption layer, thereby extending the filter life.

また、繊維同士の接着は繊維成分自体の融着、あるいは一般に後加工で付与するようなバインダー成分を含まないことが好ましい。これら樹脂成分により低通気抵抗性が損なわれるだけでなく、粉粒状吸着剤と熱可塑性粉末樹脂混合品と熱処理により一体化しても、繊維同士の接着性が強固となるため、結果として粉粒状吸着剤層と基材不織布の接着性は見かけ上小さくなりがちになり、層間剥離等が発生しやすくなり品質上問題が生じやすくなる。すなわち、吸着性シートにプリーツ加工等で何らかの外力が加えられた場合、基材層を構成する繊維が接着剤で強固に接合されていると、吸着層と基材層間の接合点で破壊が起こるのに対し、基材層がニードルパンチ加工及び/又は水流交絡法のみでなれば、変形時に基材層内の繊維間でスリップして変形を吸収し、吸着層と基材層の接合点の破壊を防止できるからである。このような問題を避けるために低融点成分、あるいは低ガラス転移温度を有するバインダーを使用しても接着力はアップするが同時に粉粒状吸着剤の表面被覆率が高くなるため吸着特性の低下等のデメリットが生じる。いずれにしても、基材層内の繊維同士の接着はあまり強固にならないことが好ましい。   Further, it is preferable that the adhesion between the fibers does not include a binder component that is given by fusion of the fiber components themselves or generally by post-processing. These resin components not only impair the low ventilation resistance, but even if they are integrated by heat treatment with a granular adsorbent and a thermoplastic powder resin mixture, the adhesion between fibers becomes strong, resulting in granular adsorption. The adhesiveness between the agent layer and the base non-woven fabric tends to be apparently reduced, and delamination or the like is liable to occur, resulting in a quality problem. That is, when some external force is applied to the adsorbent sheet by pleating or the like, if the fibers constituting the base material layer are firmly joined with an adhesive, the adhesive layer and the base material layer are broken at the joining point. On the other hand, if the base material layer is formed only by needle punching and / or hydroentanglement, the deformation slips between fibers in the base material layer during deformation to absorb the deformation. This is because destruction can be prevented. In order to avoid such a problem, even if a binder having a low melting point component or a low glass transition temperature is used, the adhesion force is improved, but at the same time, the surface coverage of the granular adsorbent is increased, so that the adsorption characteristics are reduced. Disadvantages arise. In any case, it is preferable that the adhesion between the fibers in the base material layer is not so strong.

本発明の吸着性シートに用いる基材層は、融点又は分解温度が、吸着層を構成する熱可塑性樹脂の融点より高い材料からなることが好ましい。基材層を構成する材料の融点又は分解温度が熱可塑性樹脂の融点より高ければ、吸着層を加熱接着する際、上述のような問題を生じ難いからである。具体的には10℃以上熱可塑性樹脂の融点より高いことが好ましく、より好ましくは20℃以上、更に好ましくは30℃以上である。上限は特に問題とならないが、200℃を超えても、効果は変わらず、一般的にコストパフォーマンスが低下する。   The base material layer used in the adsorbent sheet of the present invention is preferably made of a material having a melting point or decomposition temperature higher than the melting point of the thermoplastic resin constituting the adsorbing layer. This is because if the melting point or decomposition temperature of the material constituting the base material layer is higher than the melting point of the thermoplastic resin, the above-described problems are hardly caused when the adsorption layer is heat-bonded. Specifically, it is preferably 10 ° C. or higher and higher than the melting point of the thermoplastic resin, more preferably 20 ° C. or higher, and further preferably 30 ° C. or higher. The upper limit is not particularly problematic, but even if it exceeds 200 ° C., the effect is not changed, and the cost performance is generally lowered.

本発明の基材不織布の繊維配向はランダム状、クロス状、パラレル状いずれでも構わない。また、ニードルパンチ加工を行う場合、ぺネ数5〜120本/cm2であることが好ましい。かかる範囲であれば、粒子状接着剤が基材層内に一部侵入して圧力損失が高くなることを防止しつつ、吸着層と基材層との接合が強くなるからである。より好ましくは10〜100本/cm2、更に好ましくは15〜80本/cm2である。 The fiber orientation of the substrate nonwoven fabric of the present invention may be random, cloth or parallel. Moreover, when performing a needle punch process, it is preferable that the number of penetrations is 5-120 pieces / cm < 2 >. This is because, within this range, the bonding between the adsorption layer and the base material layer is strengthened while preventing the particulate adhesive from partially entering the base material layer and increasing the pressure loss. More preferably, it is 10-100 pieces / cm < 2 >, More preferably, it is 15-80 pieces / cm < 2 >.

本発明で用いる接着剤は、熱可塑性粉末樹脂であることが好ましい。粉末樹脂であれば、吸着剤及び基材不織布の毛羽部分に均一に分散することができるからである。 The adhesive used in the present invention is preferably a thermoplastic powder resin. This is because the powder resin can be uniformly dispersed in the fluff portion of the adsorbent and the base nonwoven fabric.

熱可塑性粉末樹脂として種類はポリオレフィン系、ポリアミド系、ポリウレタン系、ポリエステル系、エチレンーアクリル共重合体、ポリアクリレート、ポリアーレン、ポリアクリル、ポリジエン、エチレンー酢酸ビニル、PVC、PS等があげられる。   Examples of the thermoplastic powder resin include polyolefin-based, polyamide-based, polyurethane-based, polyester-based, ethylene-acrylic copolymer, polyacrylate, polyarene, polyacrylic, polydiene, ethylene-vinyl acetate, PVC, PS, and the like.

熱可塑性粉末樹脂の大きさは平均で1〜40μmが好ましい。より好ましくは5〜30μmである。更に好ましくは1〜40μmの範囲に95重量%以上が含まれることである。かかる範囲の粒子径であれば、熱可塑性樹脂が、粉粒状吸着剤の表面細孔を塞ぐことを低減できる一方、吸着剤との混合時にファンデルワールス力や静電気力による粉粒状吸着剤への予備接着が有効になされ、均一に分散することができ、吸着剤層と基材層の部分的剥離を効果的に防止することができるからである。   The average size of the thermoplastic powder resin is preferably 1 to 40 μm. More preferably, it is 5-30 micrometers. More preferably, 95% by weight or more is contained in the range of 1 to 40 μm. If the particle size is within this range, the thermoplastic resin can reduce blocking of the surface pores of the granular adsorbent, while at the time of mixing with the adsorbent, the van der Waals force or electrostatic force to the granular adsorbent. This is because the preliminary adhesion is effectively performed and can be uniformly dispersed, and the partial peeling between the adsorbent layer and the base material layer can be effectively prevented.

熱可塑性粉末樹脂の形状は特に規定はないが、球状、破砕状等があげられる。当然ながら、2種以上の熱可塑性粉末樹脂を併用もできる。更には、薬品担持した粉粒状吸着剤あるいは薬品担持した基材不織布を使用した場合でもこの処方であれば、粉粒状吸着剤表面に熱可塑性粉末樹脂がドライ状態の混合時から仮接着した状態になるため仮に該薬品が相異なる性質のものであっても後のシート化工程でも互いに干渉することを避けることができるので充分な効果が発揮される。   The shape of the thermoplastic powder resin is not particularly limited, but examples thereof include a spherical shape and a crushed shape. Of course, two or more thermoplastic powder resins can be used in combination. Furthermore, even when using a powder-supported granular adsorbent or a substrate-supported non-woven fabric with chemicals, if this formulation is used, the thermoplastic powder resin is temporarily bonded to the surface of the powder-shaped adsorbent from the time of mixing in the dry state. Therefore, even if the chemicals have different properties, they can be prevented from interfering with each other in the subsequent sheet forming step, so that a sufficient effect is exhibited.

熱可塑性粉末樹脂の融点は、移動車両等の室内の環境温度等考慮すると80℃以上がよい。より好ましくは100℃以上がよい。   The melting point of the thermoplastic powder resin is preferably 80 ° C. or higher in consideration of the environmental temperature in the room of a moving vehicle or the like. More preferably, it is 100 ° C. or higher.

熱可塑性粉末樹脂の溶融時の流動性はJIS K 7210記載のMI値でみれば1〜80g/10minがよい。より好ましくは3〜30g/10minである。かかる範囲であれば、吸着剤の表面の閉塞を防止しつつ、吸着層と基材層を強固に接着することができる。   The fluidity at the time of melting of the thermoplastic powder resin is preferably 1 to 80 g / 10 min in terms of the MI value described in JIS K 7210. More preferably, it is 3-30 g / 10min. Within such a range, the adsorption layer and the base material layer can be firmly bonded while preventing the surface of the adsorbent from being blocked.

熱可塑性粉末樹脂の使用量は粉粒状吸着剤に対して1〜40重量%使用するのが好ましい。より好ましくは5〜30重量%である。かかる範囲内であれば、基材層との接着力、通気抵抗、脱臭性能に優れる吸着シートが得られるからである。   The amount of the thermoplastic powder resin used is preferably 1 to 40% by weight based on the particulate adsorbent. More preferably, it is 5 to 30% by weight. This is because, within such a range, an adsorption sheet excellent in adhesive strength with the base material layer, ventilation resistance, and deodorizing performance can be obtained.

熱可塑性粉末樹脂の粒径調整法は、機械粉砕、冷凍粉砕、化学調整法等があげられる。また最終的に篩にかけ一定粒径を得ることができるが、一定の粒径を確保できる方法であれば特に限定されない。   Examples of the method for adjusting the particle size of the thermoplastic powder resin include mechanical pulverization, freeze pulverization, and chemical adjustment. Moreover, although it can finally screen and obtain a fixed particle size, if it is a method which can ensure a fixed particle size, it will not specifically limit.

構成単位としては基材不織布と粉粒状吸着剤及び熱可塑性粉末樹脂の混合粉粒体であるが、更に取り扱い性を良好にするために粉粒状吸着剤剥き出し側、つまり基材不織布との対抗面に通気性の良好な基材層(以下通気性シート)を積層することができる。通気性シートは粉粒状吸着剤表面に熱可塑性粉末樹脂が付着しているため、この熱可塑性粉末樹脂を有効利用し接着できる。通気性シートは基材不織布と同様のものが使用可能であるが、吸着性シートをプリーツ形状、波状形状等の空気浄化用フィルターユニットとして使用する場合、シート厚みが薄い方が、折り山ピッチを小さくし、吸着性シート面積を大きくし、通気抵抗低減、脱臭性能を向上させることが可能となるため通気性シートも薄いものを使用する方が好ましい。おおよそ全体厚みとして0.3〜2.5mmが好ましい。   As a structural unit, it is a mixed granular material of a base nonwoven fabric, a granular adsorbent and a thermoplastic powder resin, but in order to further improve the handleability, the exposed side of the granular adsorbent, that is, the facing surface of the base nonwoven fabric A base material layer having good air permeability (hereinafter referred to as an air permeable sheet) can be laminated. Since the breathable sheet has a thermoplastic powder resin adhering to the surface of the granular adsorbent, the thermoplastic powder resin can be effectively used and bonded. The breathable sheet can be the same as the base nonwoven fabric, but when using the adsorbent sheet as an air purification filter unit such as a pleated or wavy shape, the thinner the sheet thickness, the smaller the fold pitch. It is preferable to use a thin breathable sheet because it can be reduced, the adsorbent sheet area can be increased, the airflow resistance can be reduced, and the deodorizing performance can be improved. The overall thickness is preferably 0.3 to 2.5 mm.

本発明の吸着性シートに用いられる吸着剤の平均粒子径は、通気性、吸着材の脱落、シート加工性等を考慮して、JIS標準ふるい(JIS Z8801)による値で平均60〜800μmであることが好ましく、100〜600μmであればより好ましい。平均粒子径が60μm未満の場合には、一定の高吸着容量を得るのに通気抵抗が大きくなりすぎ、また、同時にシート充填密度が高くなりやすく、粉塵供給時に早期の通気抵抗上昇を引き起こす原因にもなる。平均粒子径が800μmを越える場合には、脱落が生じやすくなり、またワンパスでの初期吸着性能が極端に低くなり、更にはプリーツ形状及び波状等の空気浄化用フィルターユニットとしたときの折り曲げ、及び波状加工時の加工性が悪くなる。なお、上記の粒状粉粒状吸着剤は、通常の分級機を使用して所定の粒度調整をすることにより、得ることが可能である。   The average particle diameter of the adsorbent used in the adsorbent sheet of the present invention is an average of 60 to 800 μm in terms of JIS standard sieve (JIS Z8801) in consideration of air permeability, adsorbent dropout, sheet processability and the like. It is preferable that the thickness is 100 to 600 μm. When the average particle size is less than 60 μm, the airflow resistance becomes too large to obtain a certain high adsorption capacity, and at the same time, the sheet filling density tends to be high, which causes an early increase in airflow resistance when supplying dust. Also become. If the average particle diameter exceeds 800 μm, it will be easy to drop off, the initial adsorption performance in one pass will be extremely low, and it will be folded when it is used as a filter unit for air purification such as a pleated shape and a wave shape, and Workability at the time of corrugated processing deteriorates. In addition, said granular powder granular adsorbent can be obtained by carrying out predetermined particle size adjustment using a normal classifier.

本発明の吸着性シートに用いられる粉粒状吸着剤は粉末状、粒状、破砕状、造粒状、ビーズ状があげられるが幅広く種々のガスを吸着できる活性炭系が好ましい。例えば、ヤシガラ系、木質系、石炭系、ピッチ系等の活性炭が好適に用いられる。表面観察によって見られる内部への導入孔いわゆるマクロ孔数は多い方がよい。活性炭と熱可塑性粉末樹脂から混合粉粒体をつくった際に、熱可塑性粉末樹脂が活性炭表面を被覆しても熱プレス加工時に細孔内部からのガス脱着により、吸着可能な細孔を開放することができる。また、活性炭表面はある程度粗い方が溶融した樹脂の流動性も悪くなり、吸着性能低下を抑えることができる。   Examples of the granular adsorbent used in the adsorbent sheet of the present invention include powder, granule, crushed, granulated, and bead-like, but an activated carbon system that can adsorb a wide variety of gases is preferable. For example, activated carbon such as coconut shell, wood, coal, and pitch is preferably used. It is better that the number of so-called macropores introduced into the interior as seen by surface observation is large. When a mixed powder is made from activated carbon and thermoplastic powder resin, the adsorbable pores are released by gas desorption from the inside of the pores during hot pressing even if the thermoplastic powder resin covers the activated carbon surface. be able to. In addition, if the surface of the activated carbon is rough to some extent, the fluidity of the melted resin also deteriorates, and a decrease in adsorption performance can be suppressed.

本発明の吸着性シートに用いられる粉粒状吸着剤のJIS K1474に準拠して測定したときのトルエン吸着量は、20重量%以上が好ましい。悪臭ガス等の無極性のガス状及び液状物質に対して高い吸着性能を必要とするためである。   The amount of toluene adsorbed when measured in accordance with JIS K1474 of the granular adsorbent used in the adsorbent sheet of the present invention is preferably 20% by weight or more. This is because high adsorption performance is required for nonpolar gaseous and liquid substances such as malodorous gases.

本発明の吸着性シートに用いられる吸着剤は、極性物質やアルデヒド類の吸着性能を向上することを目的として、薬品処理を施して用いてもよい。 The adsorbent used in the adsorbent sheet of the present invention may be used after chemical treatment for the purpose of improving the adsorption performance of polar substances and aldehydes.

ガス薬品処理に用いられる薬品としては、アルデヒド系ガスやNOx等の窒素化合物、SOx等の硫黄化合物、酢酸等の酸性の極性物質に対しては、例えばエタノールアミン、ポリエチレンイミン、アニリン、P―アニシジン、スルファニル酸等のアミン系薬剤や水酸化ナトリウム、水酸化カリウム、炭酸グアニジン、リン酸グアニジン、アミノグアニジン硫酸塩、5.5―ジメチルヒダントイン、ベンゾグアナミン、2.2―イミノジエタノール、2.2.2―ニトロトリエタノール、エタノールアミン塩酸塩、2−アミノエタノール、2.2−イミノジエタノール塩酸塩、P―アミノ安息香酸、スルファニル酸ナトリウム、L―アルギニン、メチルアミン塩酸塩、セミカルバジド塩酸塩、ヒドラジン、ヒドロキノン、硫酸ヒドロキシルアミン、過マンガン酸塩、炭酸カリウム、炭酸水素カリウム等が好適に用いられ、アンモニア、メチルアミン、トリメチルアミン、ピリジン等の塩基性の極性物質に対しては、例えば、リン酸、クエン酸、リンゴ酸、アスコルビン酸、酒石酸等が好適に用いられる。なお、薬品処理は、例えば、活性炭に薬品を担持させたり、添着することにより行う。また、活性炭に直接薬品を処理する以外に、シート面表面付近に通常のコーティング法等で添着加工する方法やシート全体に含浸添着することも可能である。この際、アルギン酸ソーダやポリエチレンオキサイド等の増粘剤を混入した薬品水溶液をつくり、これを担持、添着を実施する方法もできる。この方法では水への溶解度が低い薬品を担持、添着し、更に薬品の脱落を抑制するのにも有効である。 Examples of chemicals used for gas chemical treatment include aldehyde gases, nitrogen compounds such as NOx, sulfur compounds such as SOx, and acidic polar substances such as acetic acid such as ethanolamine, polyethyleneimine, aniline, and P-anisidine. , Amine drugs such as sulfanilic acid, sodium hydroxide, potassium hydroxide, guanidine carbonate, guanidine phosphate, aminoguanidine sulfate, 5.5-dimethylhydantoin, benzoguanamine, 2.2-iminodiethanol, 2.2.2 Nitrotriethanol, ethanolamine hydrochloride, 2-aminoethanol, 2.2-iminodiethanol hydrochloride, P-aminobenzoic acid, sodium sulfanilate, L-arginine, methylamine hydrochloride, semicarbazide hydrochloride, hydrazine, hydroquinone , Hydroxylamine sulfate Permanganate, potassium carbonate, potassium hydrogen carbonate and the like are preferably used. For basic polar substances such as ammonia, methylamine, trimethylamine and pyridine, for example, phosphoric acid, citric acid, malic acid, ascorbine Acid, tartaric acid and the like are preferably used. The chemical treatment is performed by, for example, supporting or attaching a chemical to activated carbon. In addition to directly treating the activated carbon with chemicals, it is possible to impregnate the entire sheet or impregnate the entire sheet by a method such as an ordinary coating method in the vicinity of the sheet surface. At this time, a chemical aqueous solution in which a thickener such as sodium alginate or polyethylene oxide is mixed can be prepared, supported, and attached. This method is effective in supporting and attaching a chemical having low solubility in water and further suppressing the chemical from falling off.

本発明の吸着性シートは、抗菌剤、抗かび剤、抗ウイルス剤、難燃剤等の付随的機能を有する成分等を含めて構成してもよい。これらの成分は繊維類や不織布、織物中に練り込んでも、後加工で添着、及び担持して付与してもよい。例えば、難燃剤を含めて構成することにより、FMVSS.302で規定されている遅燃性の基準やUL難燃規格に合致した吸着性シートを製造することが可能である。   The adsorptive sheet of the present invention may be configured to include components having incidental functions such as antibacterial agents, antifungal agents, antiviral agents, and flame retardants. These components may be kneaded into fibers, non-woven fabrics, or woven fabrics, or may be attached and supported by post-processing. For example, by including a flame retardant, FMVSS. It is possible to manufacture an adsorbent sheet that meets the standards for retarding flame retardancy defined in 302 and UL flame retardant standards.

上記の付随的機能を有する成分は、粉粒状吸着剤等へ添着又は担持してもよい。但し、この際には、粉粒状吸着剤本来の吸着機能を損なわないよう留意する必要がある。また、基材不織布や通気性シート等の繊維に吸着性能を有する機能を付与、例えば、酸やアルカリの薬剤を添着したりイオン交換繊維等を用いることにより、脱臭機能を強化することも可能である。   The component having the incidental function may be attached or supported on the particulate adsorbent or the like. However, in this case, care must be taken not to impair the original adsorption function of the granular adsorbent. Moreover, it is possible to enhance the deodorizing function by adding a function having adsorption performance to fibers such as non-woven fabric and breathable sheet, for example, by attaching an acid or alkali chemical or using ion exchange fibers. is there.

吸着性シートの基本的な製法について説明する。まず、粉粒状吸着剤と熱可塑性粉末樹脂を所定の重量秤量し、シェーカー(撹拌器)に入れ、約10分間回転速度30rpmで撹拌する。この際の水分率は混合物重量の15%以内が好ましい。この時点で熱可塑性粉末樹脂が粉粒状吸着剤表面に仮接着された混合物となっている。次に、この混合粉粒体を基材不織布の上に散布し、熱プレス処理を実施する。熱プレスの際のシート表面温度は熱可塑性粉末樹脂融点の3〜30℃、好ましくは5〜20℃高い程度が好ましい。この際、通気性シートを更に積層すれば、より取り扱い性に優れた吸着性シートが得られる。   The basic manufacturing method of the adsorptive sheet will be described. First, the granular adsorbent and the thermoplastic powder resin are weighed to a predetermined weight, placed in a shaker (stirrer), and stirred at a rotational speed of 30 rpm for about 10 minutes. The moisture content at this time is preferably within 15% of the weight of the mixture. At this point, the thermoplastic powder resin is a mixture temporarily bonded to the surface of the granular adsorbent. Next, this mixed granular material is sprayed on a base nonwoven fabric, and a hot press process is implemented. The sheet surface temperature during hot pressing is preferably about 3 to 30 ° C, preferably 5 to 20 ° C higher than the melting point of the thermoplastic powder resin. Under the present circumstances, if an air permeable sheet is further laminated | stacked, the adsorptive sheet excellent in the handleability will be obtained.

また、熱処理する前に赤外線等で予め予備加熱し、仮接着しておけば、プレス時におこりがちな混合粉粒体の不規則な流動も生じず、より分散性が良好な吸着性シートが製造できる。赤外線による熱処理は、気流などを起こさず、混合粉粒体を静置した状態で加熱することができ、混合粉粒体の飛散などを防止することができる。   In addition, if pre-heated and pre-bonded with infrared rays or the like before heat treatment, mixed powder particles that tend to occur at the time of pressing will not be generated, and an adsorbent sheet with better dispersibility is produced. it can. The heat treatment using infrared rays does not cause an air current and the like, can be heated in a state where the mixed powder particles are allowed to stand, and scattering of the mixed powder particles can be prevented.

最終的に熱プレスしシート製造するにはよく使用されるロール間熱プレス法、あるいは上下ともフラットな熱ベルトコンベヤー間にはさみこむフラットベッドラミネート法等があげられる。より均一な厚み、接着状態をつくりだすには後者の方がより好ましい。また、本特許で記載する基材不織布と上記製法の特徴の組み合わせにより、粉粒状吸着剤同志の過度の結着を抑制することができると同時に、基材不織布との実用上充分な接着強力を得ることができる。   In order to produce a sheet by finally hot pressing, a hot press method between rolls or a flat bed laminating method in which the upper and lower parts are sandwiched between flat heat belt conveyors can be used. The latter is more preferable for producing a more uniform thickness and adhesion. In addition, the combination of the base nonwoven fabric described in this patent and the characteristics of the above production method can suppress excessive binding between the particulate adsorbents, and at the same time has practically sufficient adhesive strength with the base nonwoven fabric. Can be obtained.

当然ながら前述した構成単位を複数層重ね合わせることもできる。該処方の詳細は実施例中で述べる。   Of course, a plurality of the structural units described above can be overlapped. Details of the formulation are given in the examples.

本発明の濾材を使用したプリーツ状フィルタユニットの厚みは、10〜400mmが好ましい。カーエアコンに内蔵装着をはじめとする車載用途や家庭用空気清浄機であれば、通常の内部スペースの関係から、10〜60mm程度、ビル空調用途へよく設置される大型のフィルターユニットであれば40〜400mm程度が収納スペースから考えると好ましい。   The thickness of the pleated filter unit using the filter medium of the present invention is preferably 10 to 400 mm. For in-vehicle applications such as built-in car air conditioners and home air purifiers, 40 to approximately 10 to 60 mm, a large filter unit that is often installed for building air conditioning applications, due to the normal internal space. About ~ 400 mm is preferable considering the storage space.

本発明のフィルタユニットのひだ山頂点間隔は2〜30mmが好ましい。2mm以下ではひだ山間が密着しすぎでデッドスペースが多く、効率的にシートを活用できなくなる。一方、30mm以上ではシート展開面積が小さくなるためフィルター厚みに応じた除去効果を得ることができなくなる。   The pleat peak apex distance of the filter unit of the present invention is preferably 2 to 30 mm. If it is 2 mm or less, the ridges are too close together and there is a lot of dead space, making it impossible to use the sheet efficiently. On the other hand, if it is 30 mm or more, the sheet development area becomes small, so that it is impossible to obtain a removal effect corresponding to the filter thickness.

本発明のフィルターユニットは、いずれの面を上流側に使用しても構わないが、嵩高いシート面を上流に使用する方が粉塵保持量も大きくなり好ましい。 In the filter unit of the present invention, any surface may be used on the upstream side, but it is preferable to use a bulky sheet surface upstream because the dust holding amount is increased.

以下本発明を実施例によって更に詳細に説明するが、下記実施例は本発明を限定する性質のものではなく、前・後記の趣旨に沿って設計変更することはいずれも本発明の技術的範囲に含まれるものである。   Hereinafter, the present invention will be described in more detail with reference to examples. However, the following examples are not intended to limit the present invention, and any design changes in accordance with the gist of the preceding and following descriptions are all within the technical scope of the present invention. Is included.

尚、実施例中の数値は以下のような方法で測定した値である。   In addition, the numerical value in an Example is the value measured by the following methods.

(1)厚み
荷重7gf/cm2の圧力を加えた時の値
(1) Thickness Value when a pressure of 7 gf / cm 2 is applied

(2)ASHRAEダスト粉塵保持量
(線速30cm/s、供給濃度0.5g/m3の条件下で測定)
粉塵に対する目詰まり度の代用特性。初期通気抵抗から150Pa上昇したときを寿命と判断し、該時点において濾材に堆積した粉塵量を天秤で秤量した値である。サンプルサイズは15cm×15cmで測定実施した。本実施例中では基材シート(粉粒状吸着剤散布側)を上流にして負荷試験を実施。
(2) ASHRAE dust retention (measured under the conditions of a linear speed of 30 cm / s and a supply concentration of 0.5 g / m 3 )
Substitution characteristic of clogging degree against dust. When the initial ventilation resistance is increased by 150 Pa, the lifetime is determined, and the amount of dust deposited on the filter medium at that time is measured with a balance. The sample size was measured at 15 cm × 15 cm. In this example, the load test was conducted with the base sheet (powder adsorbent spraying side) upstream.

(3)通気抵抗は線速30cm/sの条件下での値。測定は70φに切り取ったサンプルで実施。 (3) Ventilation resistance is a value under a linear speed of 30 cm / s. Measurement was performed on a sample cut to 70φ.

(4)脱臭性能
トルエンガスを用いて線速16cm/sにおいてフィルターの上下流の濃度 をそれぞれガステック製検知管で測定し、上流側のガス濃度から下流側のガス 濃度を減じた値を上流側のガス濃度で除した値の百分率で示した。測定は6c m×6cmに切り取ったサンプルで実施。なお、本特許では上流側濃度は80 ppmとし、測定開始から1分後の除去率のデータを実施例に記載した。
(4) Deodorizing performance Using toluene gas, the upstream and downstream concentrations of the filter were measured with a gas-tech detector tube at a linear speed of 16 cm / s, and the value obtained by subtracting the downstream gas concentration from the upstream gas concentration was measured upstream. It was expressed as a percentage of the value divided by the gas concentration on the side. Measurement was carried out on a sample cut to 6cm x 6cm. In this patent, the upstream concentration was 80 ppm, and the removal rate data one minute after the start of measurement was described in the examples.

(5)剥離強度
基材シートと粉粒状吸着剤層の平均剥離強度を測定。試験片の大きさは幅50mm、長さ200mmとして、引張速度100mm/minとして実施。
(5) Peel strength Measure the average peel strength of the substrate sheet and the granular adsorbent layer. The test piece is 50 mm wide and 200 mm long, with a tensile speed of 100 mm / min.

以下、実施例で詳細説明する。   Hereinafter, the embodiment will be described in detail.

シートA:融点163℃のポリプロピレン繊維2.2dtex×51mmをカードにかけウェッブを作製後、ウォーターパンチ法にてシート化し、目付35g/m2、厚み0.5mm、通気抵抗6Paのスパンレース不織布を製造した。その後、このシートをコロナ荷電法により帯電させた。 Sheet A: Polypropylene fiber with a melting point of 163 ° C. of 2.2 dtex × 51 mm is carded to produce a web, and then formed into a sheet by the water punch method to produce a spunlace nonwoven fabric having a basis weight of 35 g / m 2 , a thickness of 0.5 mm, and a ventilation resistance of 6 Pa. did. Thereafter, the sheet was charged by a corona charging method.

シートB:融点165℃のポリプロピレン繊維5dの繊度で、目付50g/m2のウェッブをスパンボンド法で作製し、その後、ニードルパンチを施し、繊維を絡ませながら厚み0.7mm、通気抵抗4Paシートを製造した。その後、このシートをコロナ荷電法により帯電させた。 Sheet B: A web with a fineness of polypropylene fiber 5d having a melting point of 165 ° C. and a basis weight of 50 g / m 2 is prepared by a spunbond method, and then a needle punch is applied to form a sheet having a thickness of 0.7 mm and a ventilation resistance of 4 Pa while entwining the fibers. Manufactured. Thereafter, the sheet was charged by a corona charging method.

シートC:2.2dtex×51mm、融点163℃のポリプロピレン繊維及び1.7dtex×44mm、融点260℃のポリエステル繊維を重量比1:1で混合したシートを、ニードルパンチによりシート化及び繊維同士を摩擦させ目付25g/m2の帯電された不織布を作製した。 Sheet C: A sheet in which a polypropylene fiber having a 2.2 dtex × 51 mm and a melting point of 163 ° C. and a polyester fiber having a melting point of 1.7 dtex × 44 mm and a melting point of 260 ° C. are mixed at a weight ratio of 1: 1. A charged nonwoven fabric having a basis weight of 25 g / m 2 was produced.

シートD:融点163℃のポリプロピレン製フィルムをコロナ荷電実施することにより帯電させた。このフィルムをスプリット後、カードにかけウェッブを作製し、更にポリプロピレン製の目付15g/m2のスパンボンド不織布とニードルパンチにて一体加工し、総目付40g/m2、通気抵抗4Paの帯電不織布を作製した。 Sheet D: A polypropylene film having a melting point of 163 ° C. was charged by corona charging. After splitting this film, it is applied to a card to produce a web, and further processed integrally with a spunbond nonwoven fabric made of polypropylene with a weight per unit of 15 g / m 2 with a needle punch to produce a charged nonwoven fabric with a total basis weight of 40 g / m 2 and a ventilation resistance of 4 Pa. did.

シートE:ポリエステル芯鞘繊維4.4dtex×51mm、15重量%(芯部融点265℃、鞘部融点150℃)、ポリエステル芯鞘繊維22dtex×51mm、70重量%(芯部融点265℃、鞘部融点190℃)、及び非芯鞘繊維17dtex×51mm、15重量%(融点265℃)の繊維をカードにより混合後ウェッブ化し、その後、プレス加工実施することにより目付65g/m2、厚み0.3mm、通気抵抗4.0Paの不織布をサーマルボンド法にて作製した。 Sheet E: Polyester core / sheath fiber 4.4 dtex × 51 mm, 15% by weight (core melting point 265 ° C., sheath melting point 150 ° C.), polyester core / sheath fiber 22 dtex × 51 mm, 70% by weight (core melting point 265 ° C., sheath) (Melting point 190 ° C.) and non-core sheath fiber 17 dtex × 51 mm, 15% by weight (melting point 265 ° C.) fiber was mixed with a card and then made into a web, and then pressed to give a basis weight of 65 g / m 2 and a thickness of 0.3 mm. A nonwoven fabric having a ventilation resistance of 4.0 Pa was prepared by a thermal bond method.

シートF:スパンボンド法により融点265℃のポリエステル長繊維不織布2.2dtex、目付20g/m2、厚み0.18mm、通気抵抗5Paの不織布を作製した(東洋紡製エクーレ6201A)。 Sheet F: A non-woven fabric having a polyester long fiber nonwoven fabric of 2.2 dtex having a melting point of 265 ° C., a basis weight of 20 g / m 2 , a thickness of 0.18 mm, and a ventilation resistance of 5 Pa was produced by a spunbond method (Toyobo Ecule 6201A).

シートG:シートFにアクリル系エマルジョンバインダー(ガラス転移点0℃)を10g/m2塗布し目付30g/m2、厚み0.20mm、通気抵抗7Paの不織布を作製した。 Sheet G: sheet F an acrylic emulsion binder (glass transition point 0 ℃) 10g / m 2 coated on basis weight 30 g / m 2, to prepare a thickness 0.20 mm, airflow resistance 7Pa nonwoven.

参考例1)平均粒径300μm、JIS K 1474法によって測定したトルエン吸着能が47重量%である石炭系粒状活性炭を1kg、熱可塑性粉末樹脂として住友精化製フロービーズEA209(エチレンーアクリル酸共重合、平均粒径10μm、MI9g/10min、融点105℃)を0.1kg重量部秤量し、約10分間撹拌混合した。この混合粉粒体をシートAの上に220g/mになるように散布し、更にシートEを上から重ね合わせテフロン(登録商標)/ガラス製のベルト間に挟み込み、このベルト間隔を0.9mm、圧力10N/cmに設定し120℃、30秒間熱プレス加工実施した。その後冷却し所望の吸着性シートを得た。
( Reference Example 1 ) 1 kg of coal-based granular activated carbon having an average particle size of 300 μm and a toluene adsorption capacity measured by JIS K 1474 method of 47% by weight as a thermoplastic powder resin, flow beads EA209 (ethylene-acrylic acid) 0.1 kg by weight of copolymer, average particle size 10 μm, MI 9 g / 10 min, melting point 105 ° C.) was weighed and mixed for about 10 minutes. The mixed powder is spread on the sheet A so as to be 220 g / m 2 , and the sheet E is overlapped from above and sandwiched between Teflon (registered trademark) / glass belts. It was set to 9 mm and a pressure of 10 N / cm 2 , and hot pressing was performed at 120 ° C. for 30 seconds. Thereafter, it was cooled to obtain a desired adsorbent sheet.

参考例2参考例1同様の材料、方法で粒状活性炭/熱可塑性粉末樹脂混合物を作製し、この混合粉粒体をシートBの上に220g/mになるように散布し、更にシートEを上から重ね合わせ、参考例1同様の方法で熱プレス、冷却を実施し所望の吸着性シートを得た。
( Reference Example 2 ) A granular activated carbon / thermoplastic powder resin mixture is prepared by the same material and method as in Reference Example 1 , and this mixed powder is spread on the sheet B so as to be 220 g / m 2. E was overlapped from above and hot pressing and cooling were performed in the same manner as in Reference Example 1 to obtain a desired adsorbent sheet.

(実施例参考例1同様の材料、方法で粒状活性炭/熱可塑性粉末樹脂混合物を作製し、この混合粉粒体をシートCの上に220g/mになるように散布し、更にシートEを上から重ね合わせ、参考例1同様の方法で熱プレス、冷却を実施し所望の吸着性シートを得た。
(Example 1 ) A granular activated carbon / thermoplastic powder resin mixture is prepared by the same material and method as in Reference Example 1 , and this mixed powder is spread on sheet C to 220 g / m 2 , and further a sheet. E was overlapped from above and hot pressing and cooling were performed in the same manner as in Reference Example 1 to obtain a desired adsorbent sheet.

(比較例1)実施例1同様の材料、方法で粒状活性炭/熱可塑性粉末樹脂混合物を作製し、この混合粉粒体をシートFの上に220g/m2になるように散布し、更にシートEを上から重ね合わせ、実施例1同様の方法で熱プレス、冷却を実施し所望の吸着性シートを得た。 (Comparative Example 1) A granular activated carbon / thermoplastic powder resin mixture was prepared by the same material and method as in Example 1, and this mixed powder was dispersed on the sheet F so as to be 220 g / m 2. E was superposed from above and hot pressing and cooling were performed in the same manner as in Example 1 to obtain a desired adsorbent sheet.

(比較例2)実施例1同様の材料、方法で粒状活性炭/熱可塑性粉末樹脂混合物を作製し、この混合粉粒体をシートGの上に220g/m2になるように散布し、更にシートEを上から重ね合わせ、実施例1同様の方法で熱プレス、冷却を実施し所望の吸着性シートを得た。
表1に主なデータ等をまとめた。
(Comparative Example 2) A granular activated carbon / thermoplastic powder resin mixture was prepared by the same material and method as in Example 1, and this mixed powder was dispersed on the sheet G so as to be 220 g / m 2. E was superposed from above and hot pressing and cooling were performed in the same manner as in Example 1 to obtain a desired adsorbent sheet.
Table 1 summarizes the main data.

参考例3参考例1同様の材料、方法で粒状活性炭/熱可塑性粉末樹脂混合物を作製し、この混合粉粒体をシートDの上に220g/mになるように散布し、更にシートEを上から重ね合わせ、参考例1同様の方法で熱プレス、冷却を実施し所望の吸着性シートを得た。
( Reference Example 3 ) A granular activated carbon / thermoplastic powder resin mixture is produced by the same material and method as in Reference Example 1 , and this mixed powder is spread on sheet D to 220 g / m 2 , and further the sheet. E was overlapped from above and hot pressing and cooling were performed in the same manner as in Reference Example 1 to obtain a desired adsorbent sheet.

以上述べた如く、本発明の吸着性シートは、粒子状吸着材、熱可塑性粉末樹脂及び基材に使用する不織布を選定することにより、低圧力損失、高脱臭性能、高粉塵保持量を充分な接着性を維持した中で実現することができ、産業界に貢献することが大である。   As described above, the adsorptive sheet of the present invention has sufficient low pressure loss, high deodorization performance, and high dust holding capacity by selecting the particulate adsorbent, the thermoplastic powder resin, and the nonwoven fabric used for the base material. It can be realized while maintaining adhesiveness, and contributes greatly to the industry.

本発明の吸着性シートの模式図Schematic diagram of the adsorbent sheet of the present invention

符号の説明Explanation of symbols

1 吸着性シート
2 基材シート
3 粉粒状吸着剤
4 通気性シート
DESCRIPTION OF SYMBOLS 1 Adsorbent sheet 2 Base material sheet 3 Granular adsorbent 4 Breathable sheet

Claims (4)

基材層間に吸着剤及び熱可塑性樹脂を含む吸着シートであって、該基材層の少なくとも片面がニードルパンチ加工が施された短繊維不織布であることを特徴とする吸着性シート。 An adsorbent sheet comprising an adsorbent and a thermoplastic resin between base material layers, wherein at least one surface of the base material layer is a short fiber nonwoven fabric subjected to needle punching. 前記短繊維不織布に使用される繊維の繊維長が20〜200mmである請求項1記載の吸着シート。The adsorption sheet according to claim 1 whose fiber length of the fiber used for said short fiber nonwoven fabric is 20-200 mm. 前記短繊維不織布がバインダー成分を含まない不織布である請求項1または2記載の吸着性シート。 Absorptive sheet of the short-fiber nonwoven fabric Ru nonwoven der contains no binder component according to claim 1 or 2 wherein. 前記短繊維不織布がエレクトレット不織布である請求項1〜3のいずれかに記載の吸着シート。
The adsorption sheet according to any one of claims 1 to 3 short-fiber nonwoven fabric Ru electret nonwoven der.
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JP2013220375A (en) * 2012-04-16 2013-10-28 Toyobo Co Ltd Filter medium
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WO2014196564A1 (en) 2013-06-07 2014-12-11 東洋紡株式会社 Filtering medium for deodorizing filter
JP6323670B2 (en) * 2013-06-07 2018-05-16 東洋紡株式会社 Filter medium for deodorizing filter
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