JP2005111331A - Catalyst carrier and catalyst filter - Google Patents
Catalyst carrier and catalyst filter Download PDFInfo
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- JP2005111331A JP2005111331A JP2003346825A JP2003346825A JP2005111331A JP 2005111331 A JP2005111331 A JP 2005111331A JP 2003346825 A JP2003346825 A JP 2003346825A JP 2003346825 A JP2003346825 A JP 2003346825A JP 2005111331 A JP2005111331 A JP 2005111331A
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- 239000003054 catalyst Substances 0.000 title claims abstract description 96
- 239000011230 binding agent Substances 0.000 claims abstract description 44
- 239000000835 fiber Substances 0.000 claims abstract description 23
- 239000006185 dispersion Substances 0.000 claims abstract description 20
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 13
- 239000011256 inorganic filler Substances 0.000 claims abstract description 13
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 13
- 239000011800 void material Substances 0.000 claims abstract 4
- 239000003463 adsorbent Substances 0.000 claims description 18
- 239000007788 liquid Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 12
- 229910052623 talc Inorganic materials 0.000 claims description 11
- 239000000454 talc Substances 0.000 claims description 10
- 238000000354 decomposition reaction Methods 0.000 claims description 9
- 239000007791 liquid phase Substances 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 8
- 239000012071 phase Substances 0.000 claims description 7
- 238000002336 sorption--desorption measurement Methods 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- -1 magnesium silicate compound Chemical class 0.000 claims description 6
- 230000000274 adsorptive effect Effects 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000391 magnesium silicate Substances 0.000 claims description 3
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 3
- 235000019792 magnesium silicate Nutrition 0.000 claims description 3
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 150000002894 organic compounds Chemical class 0.000 claims 2
- 239000002131 composite material Substances 0.000 claims 1
- 230000001143 conditioned effect Effects 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000010030 laminating Methods 0.000 abstract description 4
- 239000002002 slurry Substances 0.000 abstract description 2
- 239000000919 ceramic Substances 0.000 description 26
- 238000010304 firing Methods 0.000 description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 17
- 239000008119 colloidal silica Substances 0.000 description 14
- 239000002245 particle Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 8
- 238000001179 sorption measurement Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 238000009423 ventilation Methods 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 238000005470 impregnation Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004115 Sodium Silicate Substances 0.000 description 4
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 4
- 229910052912 lithium silicate Inorganic materials 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- 239000004113 Sepiolite Substances 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 238000002407 reforming Methods 0.000 description 3
- 229910052624 sepiolite Inorganic materials 0.000 description 3
- 235000019355 sepiolite Nutrition 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000004887 air purification Methods 0.000 description 2
- 239000007809 chemical reaction catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003230 hygroscopic agent Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- VCNTUJWBXWAWEJ-UHFFFAOYSA-J aluminum;sodium;dicarbonate Chemical compound [Na+].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O VCNTUJWBXWAWEJ-UHFFFAOYSA-J 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910001647 dawsonite Inorganic materials 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- FSBVERYRVPGNGG-UHFFFAOYSA-N dimagnesium dioxido-bis[[oxido(oxo)silyl]oxy]silane hydrate Chemical compound O.[Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O FSBVERYRVPGNGG-UHFFFAOYSA-N 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical class [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000008279 sol Substances 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Images
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- Removal Of Specific Substances (AREA)
- Physical Water Treatments (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
- Drying Of Gases (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Water Treatment By Sorption (AREA)
- Catalysts (AREA)
- Exhaust Gas After Treatment (AREA)
- Central Air Conditioning (AREA)
- Separation Of Gases By Adsorption (AREA)
Abstract
Description
本発明は、触媒もしくは吸湿剤の担持体かつ、触媒、吸湿剤を担持したフィルタに関する発明である。 The present invention relates to a support for a catalyst or a hygroscopic agent and a filter carrying the catalyst and the hygroscopic agent.
従来、この種のハニカム状担持体は、成分としてセラミック繊維もしくはガラス繊維と有機繊維、さらに山皮(セピオライト)などの鉱物を基材紙として漉いた紙をハニカム状に加工し、このハニカム体を焼成することで無機質のハニカム状担体がされたものが知られている(例えば、特許文献1参照)。 Conventionally, this type of honeycomb-shaped carrier is obtained by processing a paper made of ceramic fibers or glass fibers and organic fibers as components and minerals such as mountain bark (sepiolite) as a base paper into a honeycomb shape. A material in which an inorganic honeycomb carrier is formed by firing is known (see, for example, Patent Document 1).
以下、そのハニカム状触媒担体について図1および図2を参照しながら説明する。 Hereinafter, the honeycomb-shaped catalyst carrier will be described with reference to FIG. 1 and FIG.
図1に示すように、セラミック紙101は、セラミック繊維、パルプ、山皮、有機および無機バインダからなり、それを波状に加工したセラミック紙102と有機系と無機系の混合接着剤によって接着した片波成形体を形成する。図2に示すように図1の片波成形体を積層し、ハニカム状積層体を得られる。それを焼成することで、ハニカム状触媒担体が得られる。
As shown in FIG. 1,
また、この種のハニカム状担持体には成分としてセラミック繊維、パルプ、有機質または無機質のバインダよりなるシートをハニカム状に成形し、これにコロイダルシリカもしくはエチルシリケートを含浸させたあとこのケイ素化合物をシリカゲルに変換し、ついで焼成することでシート中の有機質を燃焼除去した結果、触媒担体が得られることが知られている(例えば、特許文献2参照)。 Further, in this type of honeycomb-shaped support, a sheet made of ceramic fiber, pulp, organic or inorganic binder is formed as a component into a honeycomb shape, impregnated with colloidal silica or ethyl silicate, and then the silicon compound is mixed with silica gel. It is known that a catalyst carrier can be obtained as a result of burning and removing organic matter in the sheet by converting to sinter and then firing (see, for example, Patent Document 2).
図1に示すセラミック紙101にはセラミック繊維、有機繊維、有機結合体から構成されたもので、この紙を波上に加工したセラミック紙102と接着した片波成形体を、図2に示したハニカム状積層体に加工する。これをコロイダルシリカ、もしくはエチルシリケートの液に含浸し、加熱処理することで、ハニカム状積層体を硬化させる。
本来、片波構造を形成するためには紙中に有機質のパルプを必要とし、触媒の担体として利用するためには、最終的には焼成によって有機質を焼き飛ばす必要がある。しかし、このような従来のハニカム状触媒担体では、やきとばされた部分は空洞となり、強度が弱くなってしまうため有機パルプの分量をできる限り減らして加工していた。しかし有機のパルプ分が少ないと片波加工は困難になり、大量に速くは製造しづらいという課題があった。また十分な強度を出すためコロイダルシリカ等に含浸するとその粒径が小さいことから、繊維の奥まで粒子が入り込み、触媒を担持するための空間が得にくいという課題もあった。そのため、このような片波ハニカム状の触媒担体では紙を漉いた状態で有機質が多くても焼成後の強度が十分に保たれ、空隙率の高い構造体であることが要求されている。 Originally, organic pulp is required in the paper in order to form a one-wave structure, and in order to use it as a catalyst carrier, it is necessary to eventually burn off the organic matter by firing. However, in such a conventional honeycomb-shaped catalyst carrier, the burned-out portion becomes a cavity and the strength is weakened, so that the amount of the organic pulp is reduced as much as possible. However, if the organic pulp content is small, single-wave processing becomes difficult, and there is a problem that it is difficult to produce a large amount quickly. Further, when colloidal silica or the like is impregnated in order to obtain sufficient strength, the particle size is small, so that there is a problem that the particles enter into the back of the fiber and it is difficult to obtain a space for supporting the catalyst. For this reason, such a single-wave honeycomb catalyst carrier is required to have a structure having a high porosity with sufficient strength after firing even if there is a large amount of organic matter in a state where paper is rolled up.
本発明は、このような従来の課題を解決するものであり、パルプを多く含んでいても、焼成後の強度を確保することができ、また空隙率も40%以上である触媒担体を提供することを目的としている。 The present invention solves such a conventional problem, and provides a catalyst carrier that can ensure strength after firing even if it contains a large amount of pulp, and has a porosity of 40% or more. The purpose is that.
また、ハニカム状に加工された触媒担体を触媒粒子、または吸着体粒子、または吸着体と触媒の混合材料の分散媒に含浸することで、触媒フィルタ、吸着フィルタ、吸着触媒フィルタを得ることを目的としている。 Another object of the present invention is to obtain a catalyst filter, an adsorption filter, and an adsorption catalyst filter by impregnating a catalyst carrier processed into a honeycomb shape into a dispersion medium of catalyst particles, adsorbent particles, or a mixed material of an adsorbent and a catalyst. It is said.
本発明の触媒担体は上記目的を達成するために、有機パルプ分を多くふくむセラミック繊維混抄紙であっても、コロイダルシリカとタルクをはじめとするフィラーとの分散液に含浸し、焼成することで、焼成後も強度を保ち、かつ空隙率の高い触媒担体を得ることを可能としたものである。 In order to achieve the above object, the catalyst carrier of the present invention is impregnated with a dispersion of colloidal silica and a filler such as talc and fired, even if it is a ceramic fiber mixed paper containing a large amount of organic pulp. Thus, it is possible to obtain a catalyst carrier having a high porosity even after firing.
この手段により比較的少ないコロイダルシリカ量で、片波ハニカム状構造体の焼成後の強度を向上させることができ、また、空隙率が高い構造体が得られる。 By this means, the strength after firing of the single-wave honeycomb structure can be improved with a relatively small amount of colloidal silica, and a structure having a high porosity can be obtained.
また、この手法で得られた触媒担体に、触媒もしくは吸着体を担持することによって、気相、液相で用いることができる触媒反応フィルタや、ガス、水分を吸脱着できる吸着フィルタが得られる。 Further, by supporting a catalyst or adsorbent on the catalyst carrier obtained by this method, a catalytic reaction filter that can be used in a gas phase or a liquid phase and an adsorption filter that can adsorb and desorb gas and moisture can be obtained.
本発明によれば軽い重量で強度のあるという効果のある触媒担体を提供できる。 According to the present invention, it is possible to provide a catalyst carrier having an effect of being light and strong.
また、前記触媒担体を作成し、これに触媒、もしくは吸着剤を担持することで、空気浄化フィルタ、空気改質フィルタなどを提供できる。 Moreover, an air purification filter, an air reforming filter, etc. can be provided by producing the catalyst carrier and supporting the catalyst or adsorbent on the catalyst carrier.
また、有機パルプを多く含むセラミック紙のため、焼成後の空隙率が高く、触媒や吸着剤の付着量が多い。 Moreover, since the ceramic paper contains a large amount of organic pulp, the porosity after firing is high, and the amount of catalyst and adsorbent attached is large.
本発明は、無機質繊維40〜80重量%、好ましくはセラミック繊維0〜80重量%とガラス繊維0〜80重量%とその他無機鉱物系の繊維状物質0〜20重量%で合計の無機質繊維60〜80重量%で構成されたものと、有機パルプ5〜30重量%で、低い組成では紙の加工が難しく、高すぎる組成では焼成後の構造体の空隙が大きすぎで構造体の強度が保ちにくいため好ましくは10〜25重量%と、有機バインダと無機バインダのいずれか一方もしくは両方を主原料として漉かれた無機繊維紙を、無機バインダ、好ましくはコロイダルシリカ、と無機フィラー、好ましくは滑石、セピオライトなどの珪酸マグネシウム、の分散液に含浸し、それを乾燥後、400℃以上、紙の形状が変化しない場合に限り好ましくは800℃以上で焼成し、前記有機繊維と、有機バインダを含む紙の場合は有機バインダを焼き飛ばすことによって得られる、触媒担体とその製造法を示したものであり、有機成分を紙に多く含ませて、加工性を向上させた紙であっても、その焼成後の強度は無機フィラーとそれを結合する無機バインダーにより保たれるという特徴を有する。
In the present invention, 40 to 80% by weight of inorganic fibers, preferably 0 to 80% by weight of ceramic fibers, 0 to 80% by weight of glass fibers, and 0 to 20% by weight of other inorganic mineral-based fibrous substances, the total amount of
なお、本発明では前記の無機繊維紙を片波成形体に成形し、前記片波成形体を積層してハニカム状のブロック体を形成し、かつハニカム状ブロック体を前記無機フィラーと無機バインダの分散液につけて乾燥したハニカム構造物を前記温度で焼成することで開口面積がひろくて圧力損失が低く、かつ接触面積の広い触媒担体フィルタが得られる。積層の方法としては、片波を一枚づつ重ねる方法や、長い片波成形体を巻き取る円形の積層体を得る方法がある。 In the present invention, the inorganic fiber paper is formed into a single wave molded body, the single wave molded bodies are laminated to form a honeycomb block body, and the honeycomb block body is formed of the inorganic filler and the inorganic binder. By firing the honeycomb structure dried on the dispersion at the above temperature, a catalyst carrier filter having a wide opening area, a low pressure loss, and a wide contact area can be obtained. As a laminating method, there are a method of superimposing single waves one by one, and a method of obtaining a circular laminate that winds up a long single-wave molded body.
なお、上記の触媒担体フィルタを、触媒材料と無機バインダを分散した分散液に含浸して、触媒を前記ハニカム構造物の紙内部の空隙部および表面に担持することで気相もしくは液相反応用触媒フィルタが得られる。 The catalyst carrier filter described above is impregnated with a dispersion liquid in which a catalyst material and an inorganic binder are dispersed, and the catalyst is supported on the voids and the surface inside the paper of the honeycomb structure so as to be used for a gas phase or liquid phase reaction. A catalytic filter is obtained.
また、前記の無機繊維紙を片波成形体に成形し、前記片波成形体を積層してハニカム状のブロック体を形成し、かつハニカム状ブロックを前記無機フィラーと無機バインダの分散液につけて乾燥したあと、ハニカム構造物を前記温度で焼成する前に、触媒材料と無機バインダを分散した分散液に含浸して、触媒をハニカム構造物の紙内部の空隙部および表面に担持して、その後で、前記温度で焼成することでも、同様にハニカム構造の気相もしくは液相反応用触媒フィルタを得ることができる。 Further, the inorganic fiber paper is formed into a single-wave molded body, the single-wave molded bodies are laminated to form a honeycomb-shaped block body, and the honeycomb-shaped block is attached to a dispersion of the inorganic filler and the inorganic binder. After drying, before firing the honeycomb structure at the above temperature, impregnated with a dispersion liquid in which the catalyst material and the inorganic binder are dispersed, and the catalyst is supported in the voids and the surface inside the paper of the honeycomb structure, and thereafter Thus, a honeycomb-structured gas phase or liquid phase reaction catalyst filter can also be obtained by firing at the above temperature.
なお、前記手法の製造法を用いて得られた気相反応用触媒フィルタは、空気清浄機等に用いることができ、空気浄化、改質に利用できる。 The gas phase reaction catalyst filter obtained by using the production method described above can be used in an air purifier or the like, and can be used for air purification and reforming.
なお、前記手法の製造法を用いて得られた液相反応用触媒フィルタは、河川や排水の浄化機として利用できる。 In addition, the catalyst filter for liquid phase reaction obtained using the manufacturing method of the said method can be utilized as a purifier of a river or waste water.
なお、前記の触媒の代わりに吸着剤を用いることで、空気中の有機ガス、水分を吸脱着する吸脱着フィルタが得られる。また吸着剤に吸着した物質はヒーター等熱エネルギーによって、吸着体から放出されるため、吸着と放出の系を分けることで、調湿やガスの濃縮等に利用できる。 By using an adsorbent instead of the catalyst, an adsorption / desorption filter that adsorbs / desorbs organic gas and moisture in the air can be obtained. In addition, since the substance adsorbed on the adsorbent is released from the adsorbent by thermal energy such as a heater, it can be used for humidity control or gas concentration by separating the adsorption and release systems.
なお、水分の吸脱着フィルタは除湿機、調湿機等に利用できる。 The moisture absorption / desorption filter can be used in a dehumidifier, a humidity controller, and the like.
さらには、前記ハニカム構造体に触媒と吸着剤を同時に、もしくは吸着剤表面に触媒粒子を担持した吸着触媒粒子を担持することで、有機ガス等を吸着によって濃縮し、別部分でヒーター等の熱源や、光線によるエネルギーによって触媒と吸着した物質を反応させ、分解を行う吸着分解フィルタを得ることができる。 Furthermore, by supporting the catalyst and adsorbent on the honeycomb structure at the same time or adsorbing catalyst particles carrying catalyst particles on the adsorbent surface, the organic gas or the like is concentrated by adsorption, and a heat source such as a heater in another part. Alternatively, it is possible to obtain an adsorptive decomposition filter that causes decomposition by reacting a substance adsorbed with a catalyst by energy of light.
吸着分解フィルタは、脱臭機や、液相では環境ホルモンをはじめとする、低濃度化学物質の分解装置等に応用できる。 The adsorptive decomposition filter can be applied to a deodorizer, a decomposition apparatus for low-concentration chemical substances including environmental hormones in the liquid phase, and the like.
以下、本発明の実施例について図面を参照しながら説明する。 Embodiments of the present invention will be described below with reference to the drawings.
なお、従来と同一部品については同一番号を付与し、その説明は省略する。 In addition, the same number is attached | subjected about the same component as the past, and the description is abbreviate | omitted.
(実施例1)
無機質繊維としてセラミック繊維70重量%とガラス繊維8重量%と有機質繊維としてパルプ10重量%と有機バインダ10重量%と無機バインダ2重量%の組成よりなり、厚さ0.2mm、坪量52g/m2の抄造したセラミック紙を101用いて、これを無機フィラーとして滑石(たとえば日本タルク株式会社L−1)と、無機バインダとしてコロイダルシリカ(たとえば日産化学株式会社スノーテックスC)と、抑泡剤(たとえばサンノプコ株式会社SNデフォーマー380)と水を表1のA、B、Cに示すような配合スラリー中にて、マグネチックスターラーを用いて十分に撹拌し、前記セラミック紙101を含浸させた。その後550℃で2時間焼成して有機物を除去した。
(Example 1)
It consists of 70% ceramic fiber and 8% glass fiber as inorganic fiber, 10% pulp as organic fiber, 10% organic binder and 2% inorganic binder, 0.2mm thickness and 52g / m basis weight. Using the paper-made ceramic paper of No. 2 as 101, talc (for example, Nippon Talc Co., Ltd. L-1) as an inorganic filler, colloidal silica (for example, Nissan Chemical Co., Ltd. Snowtex C) as an inorganic binder, and a foam inhibitor ( For example, Sannoco Co., Ltd. SN deformer 380) and water were sufficiently stirred using a magnetic stirrer in a blending slurry as shown in A, B, and C of Table 1, and impregnated with the
(実施例2)
セラミック繊維60重量%と無機質繊維9重量%とパルプ17重量%と有機バインダ12重量%と無機バインダ2重量%の組成よりなり、厚さ0.17mm、坪量53g/m2の抄造したセラミック紙101を用いて、前記の表1のD、E、Fに示すように実施例1と同様の配合の液に含浸し、その後550℃で2時間焼成して有機物を除去した。
(Example 2)
Ceramic paper made of 60% by weight ceramic fiber, 9% by weight inorganic fiber, 17% by weight pulp, 12% by weight organic binder, and 2% by weight inorganic binder, with a thickness of 0.17 mm and a basis weight of 53 g /
(比較例)
実施例1および実施例2で用いたセラミック紙101を前記の表1の比較例−G〜Lに示すようなコロイダルシリカ(たとえば日産化学株式会社スノーテックスC、スノーテックス40)に1回もしくは2回含浸して乾燥後、実施例1および実施例2と同様に550℃で2時間焼成して有機物を除去した。
(Comparative example)
The
実施例1および実施例2に示したセラミック紙101の含浸液中の固形分の割合としては滑石1〜10重量部に対してコロイダルシリカ20〜18重量部で、1重量部程度の滑石の量の添加では無添加のものと大きな変化は見られない。その一方で、多く添加しすぎても強度は向上せず、紙の重量を重くしてしまい、無駄が生じる。好ましくは滑石3〜10重量部に対し、19.5〜17重量部であると良い。
The solid content in the impregnation liquid of the
なお、含浸液の固形分濃度としては、高濃度では沈降が進んだり、粘度の著しい上昇が起こるため30重量%以下が望ましい。一方で、10重量%以下の希薄な液では一度の含浸による固形分の担持が少なく、望むほどの焼成後の強度を得るためには複数回以上の含浸が必要になるため、10重量%以上30重量%未満の固形分濃度が望ましい。 The solid content concentration of the impregnating liquid is preferably 30% by weight or less because sedimentation proceeds at a high concentration or a significant increase in viscosity occurs. On the other hand, in a dilute liquid of 10% by weight or less, there is little loading of solid content by one impregnation, and in order to obtain the desired strength after firing, impregnation more than once is necessary. A solids concentration of less than 30% by weight is desirable.
なお、以上の実施例1および実施例2では、含浸液中の無機フィラーとして、滑石を扱ったが、これは板状の粒子で、1μm以下の粒径のものであることが望ましく、5μmより大きい粒子では分散液中でフィラーが沈降してしまい取り扱いが難しくなるため好ましくない。また、粒子径が大きいとセラミック紙101の繊維間の隙間に粒子が入りにくくなり、無機バインダと無機質繊維とが結合しにくくなり、焼成後の強度が得にくいことからも、粒子径が1μm程度のものが望ましいといえる。
In Example 1 and Example 2 above, talc was used as the inorganic filler in the impregnating liquid, but this is a plate-like particle, preferably having a particle size of 1 μm or less, from 5 μm. Larger particles are not preferred because the filler settles in the dispersion and is difficult to handle. Also, if the particle size is large, it is difficult for the particles to enter the gaps between the fibers of the
なお、実施例1および実施例2の滑石の代わりに、無機フィラーとしてセピオライト、ゾノトライト、ウオラストナイト、石膏繊維、ドーソナイトなどの繊維状フィラーや、炭化ケイ素ウィスカー、窒化ケイ素ウィスカー、チタン酸カリウムウィスカーなどのウィスカー結晶物、その他ゾノトライト、ゼオライトなどであっても良い。 In addition, instead of the talc of Example 1 and Example 2, fibrous fillers such as sepiolite, zonotolite, wollastonite, gypsum fiber, and dawsonite as inorganic fillers, silicon carbide whiskers, silicon nitride whiskers, potassium titanate whiskers, and the like Whisker crystals, other zonotlites, zeolites and the like may be used.
なお、実施例1および実施例2では無機バインダとしてコロイダルシリカを用いたが、アルミナゾル、珪酸ソーダ、有機溶媒に分散したシリカゾル、珪酸リチウムなどであっても良い。 In Example 1 and Example 2, colloidal silica was used as the inorganic binder, but alumina sol, sodium silicate, silica sol dispersed in an organic solvent, lithium silicate, or the like may be used.
なお、紙として従来、パルプ繊維が数重量%のものが望ましいをされていたが、ハニカム形状をはじめとした加工性の面では有機分が多いことが望ましく、表1で示したとおり、有機成分が合計20重量%以上であっても、その強度は滑石と無機バインダを加えることで十分な強度が得られる。 Conventionally, paper having a pulp fiber content of several weight% has been desirable. However, in view of processability including a honeycomb shape, it is desirable that the organic content is large. Is 20% by weight or more in total, sufficient strength can be obtained by adding talc and an inorganic binder.
(実施例3)
実施例1でもちいたセラミック紙101を用いて、波長2.6mm、波高1.5mmの波形紙101となし、固形分でアクリル酸エステル24%、エチレン酢酸ビニル36重量%、コロイダルシリカ40重量%よりなる接着剤をもちいて平面紙102と接着して図1に示す片波成形体となし、該片波成形体を前記と同様の接着剤をもちいて積層し、図2に示すハニカム状積層体を得る。このハニカム状積層体を、前記の表1に示す実施例1−Bの含浸液に含浸したのち乾燥し、表2に示すようなパターンを用いて焼成した。
(Example 3)
The
焼成時の最高温度は表2に示すようにハニカム構造体の圧縮強度が向上することから800℃以上が望ましい。 As shown in Table 2, the maximum temperature during firing is preferably 800 ° C. or higher because the compressive strength of the honeycomb structure is improved.
実施例3では800℃が最高焼成温度であったが、ハニカム状積層体が変形したり、材料が溶融することによる空隙率の低下しない温度であればそれ以上の高温であっても良い。 In Example 3, the maximum firing temperature was 800 ° C., but may be a higher temperature as long as the porosity does not decrease due to deformation of the honeycomb-shaped laminate or melting of the material.
(実施例4)
実施例3−Cのように前記の表1の実施例1−Bの含浸液に含浸したのち800℃以上の温度で焼成して得られたハニカム状積層触媒担体を、たとえば白金系触媒、マンガン系触媒、パラジウム系触媒、スズ系触媒、チタン系触媒等の触媒粒子と、たとえばコロイダルシリカ、珪酸リチウム、珪酸ナトリウム等の分散液に含浸して、加熱乾燥処理を行って触媒担持フィルタが得られる。
Example 4
As in Example 3-C, a honeycomb-shaped laminated catalyst carrier obtained by impregnating the impregnating solution of Example 1-B in Table 1 and calcining at a temperature of 800 ° C. or higher is obtained by using, for example, a platinum catalyst, manganese A catalyst-carrying filter is obtained by impregnating a catalyst particle such as a palladium catalyst, a palladium catalyst, a tin catalyst, or a titanium catalyst with a dispersion of, for example, colloidal silica, lithium silicate, or sodium silicate, followed by heat drying. .
(実施例5)
実施例3−Cのように前記の表1の実施例1−Bの含浸液に含浸したのち800℃以上の温度で焼成して得られたハニカム状積層触媒担体を、たとえばゼオライトやシリカゲル等の吸着剤と、たとえばコロイダルシリカ、珪酸リチウム、珪酸ナトリウム等の分散液に含浸して、加熱乾燥処理を行って吸脱着フィルタが得られる。
(Example 5)
As in Example 3-C, a honeycomb-shaped laminated catalyst carrier obtained by impregnating the impregnating liquid of Example 1-B in Table 1 and calcining at a temperature of 800 ° C. or higher is obtained by using, for example, zeolite or silica gel. An adsorption / desorption filter is obtained by impregnating an adsorbent and a dispersion such as colloidal silica, lithium silicate, sodium silicate and the like, followed by heat drying.
(実施例6)
実施例3−Cのように前記の表1の実施例1−Bの含浸液に含浸したのち800℃以上の温度で焼成して得られたハニカム状積層触媒担体を、たとえば親水性ゼオライトや疎水性ゼオライト、シリカゲル等の吸着剤と、たとえば白金系触媒、マンガン系触媒、パラジウム系触媒、スズ系触媒、チタン系触媒等の触媒粒子と、たとえばコロイダルシリカ、珪酸リチウム、珪酸ナトリウム等の分散液に含浸して、加熱乾燥処理を行って触媒による吸着物の分解を目的とした吸着分解フィルタが得られる。
(Example 6)
The honeycomb-shaped laminated catalyst carrier obtained by impregnating the impregnating liquid of Example 1-B in Table 1 as described in Example 3-C and calcining at a temperature of 800 ° C. or higher is obtained by, for example, hydrophilic zeolite or hydrophobic Adsorbents such as water-soluble zeolite and silica gel, and catalyst particles such as platinum-based catalysts, manganese-based catalysts, palladium-based catalysts, tin-based catalysts, and titanium-based catalysts, and dispersions such as colloidal silica, lithium silicate, and sodium silicate. An adsorptive decomposition filter for the purpose of decomposing the adsorbate by the catalyst is obtained by impregnation and heat drying.
(実施例7)
実施例4乃至6のいずれかによって得られたフィルタにおいて特に、ハニカム積層体を図5に示すように円形形状に成形し、フィルタ回転動力部105により円形形状のフィルタを回転させることにより、回転式の連続再生型の触媒フィルタ、吸脱着フィルタ、吸着分解フィルタが得られる。特に吸脱着フィルタの場合、得られたフィルタの通風穴に対して通気部103と、加熱処理部104を設けることで、通気部103にて気体中の有機ガスや湿気を吸着して、加熱処理部104にては有機ガス、湿気の脱着をして、再度フィルタが通気部103にてガスや湿気を吸着できる状態に再生することができ、連続的な使用が可能となる。また、吸着分解フィルタの場合、加熱処理部104または加熱処理部104の代わりに光源を設けることで、通気部にて気体中の有機ガスを吸着して、加熱処理部もしくは光照射部(図示せず)でその熱エネルギーもしくは光エネルギーによって触媒と有機ガスの反応を起こして、有機ガスの分解を行い、再度フィルタが通気部103にて有機ガスを吸着できる状態に再生することができ、連続的な使用が可能となる。また触媒フィルタにおいては、通気部103の後ろ部分にも加熱処理部、もしくは光源を置くことで、連続的な有機ガスの分解が可能である装置を得ることができる。
(Example 7)
In particular, in the filter obtained by any one of Examples 4 to 6, the honeycomb laminated body is formed into a circular shape as shown in FIG. 5, and the circular filter is rotated by the filter
(実施例8)
実施例4乃至6のいずれかにおいて、前記の表1の実施例1−Bの含浸液に含浸したのちに、実施例4乃至6のいずれかに記載されている触媒分散液、もしくは吸着剤分散液、もしくは吸着剤と触媒の混合分散液に含浸し、乾燥処理した後、材料が変質しない温度範囲で有機成分を焼き飛ばすことによっても、触媒フィルタ、もしくは吸脱着フィルタ、もしくは吸着分解フィルタが得られ、実施例7のような回転式のフィルタを得ることもできる。
(Example 8)
In any of Examples 4 to 6, after impregnating the impregnation liquid of Example 1-B in Table 1 above, the catalyst dispersion or adsorbent dispersion described in any of Examples 4 to 6 The catalyst filter, adsorption / desorption filter, or adsorptive decomposition filter can also be obtained by impregnating the liquid or a mixed dispersion of adsorbent and catalyst, drying, and then burning off the organic components in a temperature range where the material does not deteriorate. Thus, a rotary filter as in the seventh embodiment can be obtained.
本発明の触媒担体および触媒フィルタは、セラミック紙を片波加工、さらに積層加工するため従来の触媒担体にあった押し出し成形などと比べ薄い壁面を持った触媒担体が得られ、また従来のセラミック繊維と有機パルプの混抄紙よりもセラミック紙中のパルプ量が多くなったことにより、セラミック紙の加工性が向上する特徴が得られ、これにより従来の触媒担体よりも生産性の向上が期待される。また、特殊紙を加工する特別な設備や技術がなくても、紙の加工性が向上したことから、比較的容易に硬度をもつ触媒担体が得られる。 The catalyst carrier and the catalyst filter of the present invention provide a catalyst carrier having a thin wall surface compared to the extrusion molding or the like in the conventional catalyst carrier because the ceramic paper is subjected to one-wave processing and further laminating processing, and the conventional ceramic fiber The amount of pulp in the ceramic paper is larger than that of the mixed paper of the organic pulp and the characteristics of improving the processability of the ceramic paper are obtained, which is expected to improve the productivity compared to the conventional catalyst carrier . Further, even if there is no special equipment or technique for processing special paper, since the paper processability is improved, a catalyst carrier having hardness can be obtained relatively easily.
また、触媒や吸着剤を担持したフィルタは、気相、液相の浄化、改質を目的とした機器に組み込んで利用できる。 Further, a filter carrying a catalyst or an adsorbent can be used by being incorporated in a device for purifying and reforming the gas phase and liquid phase.
101 セラミック紙(平紙)
102 セラミック紙(波紙)
103 通風部(吸着部)
104 加熱処理部(再生部)
105 フィルタ回転動力部
101 Ceramic paper (flat paper)
102 Ceramic paper (wave paper)
103 Ventilation part (adsorption part)
104 Heat treatment unit (reproduction unit)
105 Filter rotation power section
Claims (14)
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Cited By (7)
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JP2007014880A (en) * | 2005-07-07 | 2007-01-25 | Toyobo Co Ltd | Adsorbing sheet, adsorbing element and production method thereof |
KR100801165B1 (en) | 2005-12-13 | 2008-02-11 | 주식회사 엘지화학 | A ceramic paper which reduces an organic fiber content, and Ceramic filter and Preparation method thereof using the same |
JP2011092825A (en) * | 2009-10-28 | 2011-05-12 | F C C:Kk | Paper catalyst and method of manufacturing the same |
KR101158248B1 (en) * | 2011-01-11 | 2012-08-06 | 주식회사 동호 | Ecological unit and ecological system in river including the same |
KR101210922B1 (en) * | 2012-09-27 | 2012-12-11 | 유한회사 코쿤 | Waste water treatment method |
WO2015099114A1 (en) * | 2013-12-27 | 2015-07-02 | 株式会社エフ・シ-・シ- | Method for producing catalyst structure, and catalyst structure |
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JP2007014880A (en) * | 2005-07-07 | 2007-01-25 | Toyobo Co Ltd | Adsorbing sheet, adsorbing element and production method thereof |
JP4635751B2 (en) * | 2005-07-07 | 2011-02-23 | 東洋紡績株式会社 | Adsorption element manufacturing method |
KR100801165B1 (en) | 2005-12-13 | 2008-02-11 | 주식회사 엘지화학 | A ceramic paper which reduces an organic fiber content, and Ceramic filter and Preparation method thereof using the same |
JP2011092825A (en) * | 2009-10-28 | 2011-05-12 | F C C:Kk | Paper catalyst and method of manufacturing the same |
KR101158248B1 (en) * | 2011-01-11 | 2012-08-06 | 주식회사 동호 | Ecological unit and ecological system in river including the same |
KR101210922B1 (en) * | 2012-09-27 | 2012-12-11 | 유한회사 코쿤 | Waste water treatment method |
WO2015099114A1 (en) * | 2013-12-27 | 2015-07-02 | 株式会社エフ・シ-・シ- | Method for producing catalyst structure, and catalyst structure |
JP2015123426A (en) * | 2013-12-27 | 2015-07-06 | 株式会社エフ・シー・シー | Method for manufacturing catalyst structure, and catalyst structure |
CN112138727A (en) * | 2020-09-24 | 2020-12-29 | 江西博鑫精陶环保科技有限公司 | Inorganic fiber honeycomb carrier and preparation method thereof |
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