JP2009101294A - Method for manufacturing molded body containing adsorbent and molded body containing adsorbent - Google Patents

Method for manufacturing molded body containing adsorbent and molded body containing adsorbent Download PDF

Info

Publication number
JP2009101294A
JP2009101294A JP2007275272A JP2007275272A JP2009101294A JP 2009101294 A JP2009101294 A JP 2009101294A JP 2007275272 A JP2007275272 A JP 2007275272A JP 2007275272 A JP2007275272 A JP 2007275272A JP 2009101294 A JP2009101294 A JP 2009101294A
Authority
JP
Japan
Prior art keywords
zeolite
adsorbent
weight
clay
molded body
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.)
Granted
Application number
JP2007275272A
Other languages
Japanese (ja)
Other versions
JP5016442B2 (en
Inventor
Yuriko Morinaka
祐理子 森中
Tatsuya Ogawa
達也 小川
Nagetsu Sakamoto
奈月 坂本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kyodo Printing Co Ltd
Original Assignee
Kyodo Printing Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kyodo Printing Co Ltd filed Critical Kyodo Printing Co Ltd
Priority to JP2007275272A priority Critical patent/JP5016442B2/en
Publication of JP2009101294A publication Critical patent/JP2009101294A/en
Application granted granted Critical
Publication of JP5016442B2 publication Critical patent/JP5016442B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

<P>PROBLEM TO BE SOLVED: To provide a molded body containing an adsorbent of a molded body highly containing zeolite, which contains zeolite of 95 wt.% or more so as to maintain adsorbing force, has high hardness and can mold a fine shape even without using a large scale apparatus, and to provide a molded body containing an adsorbent obtained by the above method. <P>SOLUTION: The molded body containing an adsorbent comprises the process of mixing a zeolite powder and an organic binder, the process of adding water to the above mixture and kneading it in a clay shape, the process of cutting the kneaded clay body, and the process of drying the cut clay body, wherein the organic binder is 15-30 wt parts to the zeolite powder of 100 wt parts, and the content ratio of zeolite in a final product is 95 wt.% or more. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、吸着剤含有成形体の製造方法及び吸着剤含有成形体に関し、詳しくは、ゼオライト高含有の吸着剤含有成形体の製造方法及び該製造方法により得られた吸着剤含有成形体に関する。   The present invention relates to a method for producing an adsorbent-containing molded article and an adsorbent-containing molded article, and more particularly to a method for producing an adsorbent-containing molded article having a high zeolite content and an adsorbent-containing molded article obtained by the production method.

従来、水分を含む気体成分を吸着させるためにゼオライトが使用されていたが、高湿度環境下では気体成分よりも水分を多く吸着する傾向にあるが、ゼオライトのマクロポアのサイズを特定の範囲にすることにより選択的にガスを分離したり、電子部品や電子製品内部で発生するアウトガスを吸着したり、冷蔵庫フロン冷媒の吸着、有機溶媒中の水分の除去、近年環境保護の観点からは発電所等の燃焼排気ガスからの二酸化炭素吸着分離の用途に広く用いられている。   Conventionally, zeolite has been used to adsorb gas components containing moisture, but it tends to adsorb more moisture than gas components in a high humidity environment, but the size of the macropores in the zeolite is in a specific range. To selectively separate gases, adsorb outgas generated inside electronic parts and electronic products, adsorb refrigerator refrigerants, remove moisture in organic solvents, power plants from the viewpoint of environmental protection in recent years It is widely used for the adsorption separation of carbon dioxide from combustion exhaust gas.

ゼオライト粉末と同等の吸着力を維持したままの成形体を作るにはゼオライト含有量を95重量%以上にする必要がある。しかしながら、ゼオライト粉末自身は集結性が無いため高含有させることが困難であった。また、ゼオライト90重量%ビーズが製造されているが(例えば、特許文献1参照)、粘土系材料をバインダーとして混練し造粒機で製造しているのでビーズ形状のみであった。そのビーズ形状は、電子部品に組み込む微細形状からするとサイズ精度は劣るものであった。   In order to produce a molded product that maintains the same adsorptive power as zeolite powder, the zeolite content needs to be 95% by weight or more. However, it is difficult to make the zeolite powder itself highly contained because it has no aggregation property. Moreover, although 90 wt% zeolite beads have been produced (see, for example, Patent Document 1), since the clay-based material is kneaded as a binder and produced by a granulator, it has only a bead shape. The bead shape was inferior in size accuracy from the fine shape incorporated in the electronic component.

また、引用文献2には、無機材料からなるミクロ多孔体と有機結合剤を混合し、加熱結晶化させゼオライト化させつつ、有機結合剤を焼失させて100%ゼオライト成形体を得ている。しかしながら、引用文献2は100t万能試験機な大型の装置を用いて成形品を高圧に押し出しているため、そのような大型の装置の使用はコストアップの要因ともなり、また電子部品に組み込む微細形状の成形は困難である。また、本発明者らが大型の装置を用いず同様にして追試したところ、高圧で押し出していないためか成形品の硬度が低い、又は成形品に固めることができなかった。   Further, in the cited document 2, a microporous body made of an inorganic material and an organic binder are mixed, heated and crystallized to be zeoliteized, and the organic binder is burned off to obtain a 100% zeolite molded body. However, since Cited Document 2 uses a large device such as a 100-ton universal testing machine to extrude the molded product to a high pressure, the use of such a large device increases the cost, and the fine shape incorporated into the electronic component. Is difficult to mold. In addition, when the inventors made a similar trial without using a large apparatus, the molded product had low hardness or could not be hardened into the molded product because it was not extruded at a high pressure.

そこで大型な装置を使用せず、ゼオライト含有量が95重量%以上の成形体を電子部品に組み込むことができるような微細形状を作れる製造方法が望まれていた。
特開平1−171554号公報 特開2000−327327号公報
Therefore, there has been a demand for a production method that can produce a fine shape that can incorporate a molded article having a zeolite content of 95% by weight or more into an electronic component without using a large apparatus.
JP-A-1-171554 JP 2000-327327 A

本発明の目的は、吸着力を維持することができるようにゼオライトを95重量%以上に高含有したゼオライト高含有成形体の吸着剤含有成形体の製造方法及び該製造方法により得られた吸着剤含有成形体を提供することである。   An object of the present invention is to provide a method for producing an adsorbent-containing molded article of a zeolite-rich molded article containing a high amount of zeolite at 95% by weight or more so that the adsorption power can be maintained, and an adsorbent obtained by the production method. It is to provide a containing molded body.

本発明の別の目的は、大型な装置を使用しなくても硬度が高く、微細形状を成形できる吸着剤含有成形体の製造方法を提供することである。   Another object of the present invention is to provide a method for producing an adsorbent-containing molded body having high hardness and capable of molding a fine shape without using a large apparatus.

本発明に従って、ゼオライト粉末及び有機系バインダーを混合する工程と、
該混合物に水を添加し、粘土状に混練する工程と、
該混練した粘土体を切断する工程と、
該切断した粘土体を乾燥させる工程と、
を有する吸着剤含有成形体の製造方法であって、
該ゼオライト粉末100重量部に対して有機系バインダーが15〜30重量部であり、
最終成形品のゼオライト含有率が95重量%以上である、
ことを特徴とする吸着剤含有成形体の製造方法が提供される。
Mixing the zeolite powder and the organic binder according to the present invention;
Adding water to the mixture and kneading into a clay;
Cutting the kneaded clay body;
Drying the cut clay body;
A method for producing an adsorbent-containing molded article having
The organic binder is 15 to 30 parts by weight with respect to 100 parts by weight of the zeolite powder,
The zeolite content of the final molded product is 95% by weight or more,
There is provided a method for producing an adsorbent-containing molded article characterized by the above.

また、本発明に従って、上記吸着剤含有成形体の製造方法により得られた吸着剤含有成形体が提供される。   Moreover, according to this invention, the adsorbent containing molded object obtained by the manufacturing method of the said adsorbent containing molded object is provided.

上述したように、本発明により、大型な装置を使用しなくてもゼオライトを95重量%以上に高含有した成形体は硬度が高く、微細形状を成形できる吸着剤含有成形体の製造方法及び該製造方法により得られた吸着剤含有成形体を提供することが可能となった。   As described above, according to the present invention, a molded body containing a high amount of zeolite to 95% by weight or more without using a large apparatus has high hardness, and a method for producing an adsorbent-containing molded body capable of molding a fine shape and the method It has become possible to provide an adsorbent-containing molded article obtained by the production method.

また、本発明ではゼオライトを使用しているので、得られた成形体は水分以外の有機ガスや臭気を高効率で吸着でき、様々な用途に応用可能である。   In addition, since zeolite is used in the present invention, the obtained molded body can adsorb organic gas and odor other than moisture with high efficiency and can be applied to various uses.

以下に、本発明の実施の形態について詳細に説明する。   Hereinafter, embodiments of the present invention will be described in detail.

本発明で用いるゼオライト粉末は、親水性ゼオライト、疎水性ゼオライトのどちらでも構わず、天然ゼオライト又は合成ゼオライトを出発原料として鉱酸等を用いた脱アルミニウム処理等によって調製する方法、或はシリカ源、アルミナ源、アルカリ源及び有機鉱化剤を混合し結晶化する直接合成法等により得られる。ゼオライトは、分子の大きさの違いによって物質を分離するのに用いられる多孔質の粒状物質であり、均一な細孔を有する構造であって、細孔の空洞に入る小さな分子を吸着して一種のふるいの作用を示すため、吸着可能な分子の種類はゼオライト種類によって決まる。有機成分等の気体成分を吸着する場合は、ゼオライトの細孔入口径が吸着される分子径よりも大きければよい。通常は、細孔入口が酸素8、10又は12員環のゼオライトであればよい。本発明では、特に水分より有機ガスや臭気成分を優先的に吸着するものが好ましい。   The zeolite powder used in the present invention may be either a hydrophilic zeolite or a hydrophobic zeolite, a method prepared by dealumination using a mineral acid or the like using a natural zeolite or a synthetic zeolite as a starting material, or a silica source, It can be obtained by a direct synthesis method in which an alumina source, an alkali source and an organic mineralizer are mixed and crystallized. Zeolite is a porous granular material used to separate substances according to the difference in molecular size, and has a structure with uniform pores. Therefore, the type of molecules that can be adsorbed depends on the type of zeolite. When adsorbing a gas component such as an organic component, the pore inlet diameter of the zeolite may be larger than the molecular diameter to be adsorbed. Usually, the pore inlet may be a zeolite having an oxygen 8, 10 or 12 membered ring. In the present invention, those that preferentially adsorb organic gas and odor components over moisture are preferred.

本発明においては、添加するゼオライト粉末として疎水性ゼオライトを使用することが好ましい。通常、ゼオライトとして広く用いられている親水性ゼオライトを添加すると溶媒の水分を吸着することにより添加直後に200℃付近まで発熱することがあり作業性や安全性等のハンドリングから、発熱しない疎水性ゼオライトが使用し易い。   In the present invention, it is preferable to use hydrophobic zeolite as the zeolite powder to be added. Usually, when hydrophilic zeolite widely used as zeolite is added, it may generate heat up to around 200 ° C immediately after the addition by adsorbing the water of the solvent, and hydrophobic zeolite that does not generate heat from handling such as workability and safety. Is easy to use.

本発明によって得られる成形体は、ゼオライト粉末と同等の吸着能力を維持したままの成形体を作るためゼオライトの含有量が95重量%以上であることが必要で、好ましくは100重量%である。本発明によるゼオライト含有率が高い、つまりバインダーが少ない又はバインダーを含有しないので硬さを保持した成形体を作るのは難しく、微細形状を作製する際にもろさがないようにする必要がある。   The molded product obtained by the present invention needs to have a zeolite content of 95% by weight or more, preferably 100% by weight, in order to produce a molded product that maintains the same adsorption capacity as the zeolite powder. The zeolite content according to the present invention is high, that is, the binder is small or does not contain a binder, so that it is difficult to produce a molded product that retains hardness, and it is necessary to make it brittle when producing a fine shape.

有機系バインダーの量は、ゼオライト粉末100重量部に対して、15〜30重量部であり、好ましくは15〜25重量部である。ゼオライト粉末100重量部に対して、15重量部未満であると、ゼオライト粉末を成形体に固めるのに結着力が不足して成形することができない。一方、30重量部を超えて添加されていると成形体の乾燥時の焼結で有機系バインダーが焼き飛ぶため、成型品に隙間が多くポーラスになり硬度が低下してしまう。   The amount of the organic binder is 15 to 30 parts by weight, preferably 15 to 25 parts by weight with respect to 100 parts by weight of the zeolite powder. When the amount is less than 15 parts by weight with respect to 100 parts by weight of the zeolite powder, the binding force is insufficient to harden the zeolite powder into a molded body, and thus molding cannot be performed. On the other hand, if it is added in an amount exceeding 30 parts by weight, the organic binder is burned off by sintering when the molded body is dried, so that there are many gaps in the molded product and the hardness is lowered.

成形品には、助剤として粘土鉱物を含有させることができ、ゼオライト粉末+有機系バインダー+粘土鉱物を添加した成形体は、有機系バインダー+粘土鉱物と同量の有機系バインダーのみを添加した成形体に比べ硬度が高くなる傾向がある。上記組成の場合、焼結させる高温でも消失しない粘土鉱物の含有量は、ゼオライト100重量部に対して、5重量部程度で十分な硬度が得られる。   The molded product can contain clay mineral as an auxiliary agent, and the molded body added with zeolite powder + organic binder + clay mineral has only organic binder + the same amount of organic binder as clay mineral added. There is a tendency for the hardness to be higher than that of the molded body. In the case of the above composition, sufficient hardness is obtained when the content of the clay mineral that does not disappear even at a high temperature to be sintered is about 5 parts by weight with respect to 100 parts by weight of the zeolite.

粘土鉱物+有機系バインダーはゼオライト粉末100重量部に対して、20〜35重量部であることが好ましく、より好ましくは20〜25重量部である。20重量部未満であると成形品を固めることが困難である。一方、35重量部を超えて添加されていると、有機バインダーの含有が多くなり焼結後の成型品に隙間が多くポーラスになり硬度が低下してしまう。   The clay mineral + organic binder is preferably 20 to 35 parts by weight, more preferably 20 to 25 parts by weight with respect to 100 parts by weight of the zeolite powder. If it is less than 20 parts by weight, it is difficult to harden the molded product. On the other hand, when it is added in excess of 35 parts by weight, the content of the organic binder is increased, and there are many gaps in the sintered product after sintering, resulting in a decrease in hardness.

ゼオライト粉末に添加する水の量は、ゼオライト粉末100重量部に対して70重量部以上でないとゼオライト粉末を粘土状に混合混練することは難しく、好ましくは80〜200重量部である。ゼオライト粉末に親水性ゼオライトを用いるときは疎水性ゼオライトを用いる時に比べ多めに添加する必要がある。   If the amount of water added to the zeolite powder is not 70 parts by weight or more with respect to 100 parts by weight of the zeolite powder, it is difficult to mix and knead the zeolite powder in a clay state, preferably 80 to 200 parts by weight. When using hydrophilic zeolite for the zeolite powder, it is necessary to add more than when using hydrophobic zeolite.

有機系バインダーとしては、セルロース系が好ましく、例えばメチルセルロースが挙げられる。   As the organic binder, a cellulose type is preferable, and for example, methyl cellulose is used.

粘土鉱物としては、セピオライト系(セピオライト等)、カオリン系(カオリナイト、ナクライト、ディッカイト、ハロイサイト等)、アンティゴライト系(アンティゴライト、アメサイト、クロンステダイト等)、バイロフィライト系(バイロフィライト、滑石等)、雲母型系(イライト、海緑石、セラドナイト、セリサイト、白雲母等)、スメクタイト系(モンモリロナイト(ベントナイド)、バイデライト、ノントロナイト、サポナイト、ヘクトナイト等)、バームキュライト系(バームキュライト)、緑泥石系(緑泥石(クロライト)等)が挙げられる。   Clay minerals include sepiolite (sepiolite, etc.), kaolin (kaolinite, nacrite, dickite, halloysite, etc.), antigolite (antigolite, amesite, cronstedite, etc.), and bilophyllite (bilophyllite). Phyllite, talc, etc.), mica type (illite, sea green stone, ceradonite, sericite, muscovite, etc.), smectite (montmorillonite (bentonide), beidellite, nontronite, saponite, hectonite, etc.), balm cue Light system (balm curite), chlorite system (chlorite).

中でも、セピオライトが吸着能力から好ましい。セピオライトの吸着能力は、比表面積が230〜320m/gあり、ゼオライト(天然)の139〜169m/gに比べ大きい。水や湿気に対する吸水性能はセピオライトのほうが良好で、セピオライトはかなりの速さで吸水した水を放湿し始める傾向があり、一方ゼオライトは保水力がかなり強いので放湿性は劣る。本発明の用途において、電子部品内部に設置するには保水力の方が重視される傾向がある。 Among these, sepiolite is preferable because of its adsorption capacity. Adsorption capacity of sepiolite is located a specific surface area of 230~320m 2 / g, greater than the 139~169m 2 / g of zeolite (natural). Sepiolite has better water absorption performance against water and moisture, and sepiolite tends to begin to desorb the absorbed water at a fairly high speed, while zeolite has a rather strong water retention and is therefore less hygroscopic. In the application of the present invention, water retention tends to be more important for installation inside an electronic component.

本発明において、ゼオライト粉末及び有機系バインダーを混合後に水を添加させ、粘土状に混練し、粘土状になったものを3本ロール等の混練機で更に混練させ、その後該混練物を馴染ませるために冷蔵庫(0〜5℃)で8〜24時間養成する。次に、粘土状の混練物を所望する厚さに押出し、シート状の粘土体を得る。該シート状の粘土体をこの状態で切断又は型抜き成形すると刃物に張り付き微細形状に切断し難いので、含水率を低下させるために50〜70℃で予備乾燥を1〜10分させることが好ましい。予備乾燥後、粘土体を所望する形状に切断又は型抜き成形させ、成形体の有機系バインダーを消失させるために加熱処理をする。加熱処理は、一次乾燥と二次乾燥の段階的に別けて処理を行っている。一次乾燥においては、主に粘土体の水分を揮発させるため200℃〜400℃が好ましく、より好ましくは250℃〜350℃である。二次乾燥において、有機系バインダーを消失させるために好ましくは500℃〜800℃であり、更に好ましくは500℃〜700℃である。800℃を超えて加熱するとゼオライトの細孔構造が変化し、吸着性能が低下することがあるので注意すべきである。乾燥時間としてはそれぞれ1時間〜3時間が好ましい。   In the present invention, water is added after mixing the zeolite powder and the organic binder, and the mixture is kneaded into a clay, and the clay is further kneaded with a kneader such as a three-roller, and then the kneaded product is blended. Therefore, it trains for 8 to 24 hours in a refrigerator (0 to 5 ° C.). Next, the clay-like kneaded product is extruded to a desired thickness to obtain a sheet-like clay body. When the sheet-like clay body is cut or die-cut in this state, it is difficult to cut it into a fine shape by sticking to the blade, so it is preferable to perform pre-drying at 50 to 70 ° C. for 1 to 10 minutes in order to reduce the moisture content. . After preliminary drying, the clay body is cut or die-molded into a desired shape, and heat treatment is performed to eliminate the organic binder in the molded body. The heat treatment is performed in steps of primary drying and secondary drying. In primary drying, in order to volatilize the water | moisture content of a clay body mainly, 200 to 400 degreeC is preferable, More preferably, it is 250 to 350 degreeC. In secondary drying, the temperature is preferably 500 ° C. to 800 ° C., more preferably 500 ° C. to 700 ° C., in order to eliminate the organic binder. It should be noted that heating above 800 ° C. may change the pore structure of the zeolite and reduce the adsorption performance. The drying time is preferably 1 hour to 3 hours.

以下に、具体的な実施例を挙げて本発明をより詳細に説明するが、本発明はこれらの実施例により限定されるものではない。   Hereinafter, the present invention will be described in more detail with reference to specific examples, but the present invention is not limited to these examples.

(実施例1)
疎水性ゼオライト粉末 100g
(商品名:HiSiV3000、ユニオン昭和社製)
セルロース系バインダー 25g
(商品名:セランダー、主成分メチルセルロース、ユケン工業株式会社製)
上記の材料を室温(23℃)で混合した。次に、純水100gを添加し、混練する。粘土状になったものを3本ロールで混練し、混練物を冷蔵庫(3℃)で12時間養成する。
Example 1
Hydrophobic zeolite powder 100g
(Product name: HiSiV3000, manufactured by Union Showa)
Cellulose binder 25g
(Product name: Serander, main component methylcellulose, manufactured by Yuken Industry Co., Ltd.)
The above materials were mixed at room temperature (23 ° C.). Next, 100 g of pure water is added and kneaded. The clay-like material is kneaded with three rolls, and the kneaded product is trained in a refrigerator (3 ° C.) for 12 hours.

粘土体の混練物を押出機で押出し、厚さ2mmのシート状の粘土体を得た。その後、60℃で5分間予備乾燥させた。その後、粘土体を、直線状の長さ100mmの一枚の刃からなるカッターを用いてシート状の粘土体の端部から順に5mm×5mmに切断した。   The kneaded product of the clay body was extruded with an extruder to obtain a sheet-like clay body having a thickness of 2 mm. Then, it was pre-dried at 60 ° C. for 5 minutes. Thereafter, the clay body was cut into 5 mm × 5 mm in order from the end of the sheet-like clay body using a cutter composed of a single blade having a linear length of 100 mm.

次に、粘土体を電気炉により300℃で2時間一次乾燥、600℃で2時間二次乾燥させてセルロース系バインダーを消失させることにより、ゼオライト含有率100重量%の成形体が得られた。   Next, the clay body was primary dried at 300 ° C. for 2 hours and secondary dried at 600 ° C. for 2 hours in an electric furnace to eliminate the cellulosic binder, whereby a molded body having a zeolite content of 100% by weight was obtained.

得られたゼオライト成形体を下記の評価方法に従って評価を行った。結果を表1に示す。   The obtained zeolite compact was evaluated according to the following evaluation method. The results are shown in Table 1.

<評価>
「押出成形性」
上記の材料を押出機でシート状に押出すまでの成形性を観察した。
<Evaluation>
"Extrudability"
The moldability until the above material was extruded into a sheet with an extruder was observed.

「硬度」
5mm×5mm×2mmに得られた成形体を上部からデジタルファースゲージ(商品名:FGC−50、SHIMPO社製)を用いて荷重をかけヒビ割れた時点での値を測定し、5点測定した平均値を示す。実使用においては、電子部品内部に設置する際の取り扱いにあたり、成形品は10N以上の硬度があれば支障は生じなかった。
"hardness"
The molded body obtained to 5 mm × 5 mm × 2 mm was measured from the top using a digital first gauge (trade name: FGC-50, manufactured by SHIMPO), and the value at the time when the crack was cracked was measured. Average values are shown. In actual use, there was no problem if the molded product had a hardness of 10 N or more in handling when installed inside the electronic component.

(実施例2〜4)
実施例1において、セルロース系バインダーの量を表1に示すように変更した以外は、同様にして乾燥させ成形体を作製し、評価を行った。結果を表1に示す。
(Examples 2 to 4)
In Example 1, except that the amount of the cellulose-based binder was changed as shown in Table 1, it was dried in the same manner to produce a molded body and evaluated. The results are shown in Table 1.

(実施例5)
疎水性ゼオライト粉末 100g
セピオライト粉末 5g
(商品名:PANGEL、GROPO TOLSA(スペイン)社製)
セルロース系バインダー 20g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表1に示す。
(Example 5)
Hydrophobic zeolite powder 100g
Sepiolite powder 5g
(Product name: PANGEL, GROPO TOLSA (Spain))
Cellulose binder 20g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 1.

(実施例6〜8)
実施例5において、セルロース系バインダーの量を表1に示すように変更した以外は、同様にして乾燥させ成形体を作製し、評価を行った。結果を表1に示す。
(Examples 6 to 8)
In Example 5, except that the amount of the cellulose-based binder was changed as shown in Table 1, it was dried in the same manner to produce a molded body and evaluated. The results are shown in Table 1.

(実施例9)
親水性ゼオライト粉末(3A) 100g
セピオライト粉末 3g
セルロース系バインダー 18g
上記の材料を用い、純水150gとした以外は実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表1に示す。
Example 9
Hydrophilic zeolite powder (3A) 100g
Sepiolite powder 3g
Cellulose binder 18g
A clay body was produced in the same manner as in Example 1 except that 150 g of pure water was used. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 1.

(比較例1)
疎水性ゼオライト粉末 100g
セルロース系バインダー 35g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Example 1)
Hydrophobic zeolite powder 100g
Cellulose binder 35g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 2.

(比較例2〜3)
比較例1において、セルロース系バインダーの量を表2に示すように変更した以外は、同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Examples 2-3)
In Comparative Example 1, except that the amount of the cellulose-based binder was changed as shown in Table 2, it was dried in the same manner to produce a molded product, and evaluation was performed. The results are shown in Table 2.

(比較例4)
疎水性ゼオライト粉末 100g
セピオライト粉末 5g
セルロース系バインダー 35g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Example 4)
Hydrophobic zeolite powder 100g
Sepiolite powder 5g
Cellulose binder 35g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 2.

(比較例5〜6)
比較例4において、セルロース系バインダーの量を表2に示すように変更した以外は、同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Examples 5-6)
In Comparative Example 4, except that the amount of the cellulose-based binder was changed as shown in Table 2, it was dried in the same manner to produce a molded body and evaluated. The results are shown in Table 2.

(比較例7)
疎水性ゼオライト粉末 100g
セピオライト粉末 5g
セルロース系バインダー 10g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Example 7)
Hydrophobic zeolite powder 100g
Sepiolite powder 5g
Cellulosic binder 10g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 2.

(比較例8)
疎水性ゼオライト粉末 100g
セピオライト粉末 5g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Example 8)
Hydrophobic zeolite powder 100g
Sepiolite powder 5g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 2.

(比較例9)
疎水性ゼオライト粉末 100g
セピオライト粉末 40g
上記の材料を用いて実施例1と同様にして粘土体を作製した。その後、実施例1と同様にして乾燥させ成形体を作製し、評価を行った。結果を表2に示す。
(Comparative Example 9)
Hydrophobic zeolite powder 100g
Sepiolite powder 40g
A clay body was produced in the same manner as in Example 1 using the above materials. Then, it was made to dry like Example 1 and the molded object was produced, and evaluation was performed. The results are shown in Table 2.

Figure 2009101294
Figure 2009101294

Figure 2009101294
実施例1〜9は、本発明の範囲内であるので高硬度な成形体が得られた。実施例5〜8は、セルロース系バインダーを減量させた分セピオライトを増量させたところセルロース系バインダーのみに比べ硬度が向上した成形体が得られた。実施例9は、ゼオライト粉末として親水性ゼオライトを用いたもので疎水性ゼオライトと同様に高硬度な成形体が得られたが、水の添加時に発熱するので冷却時間が追加されるため生産性の若干の低下が見られた。
Figure 2009101294
Since Examples 1 to 9 were within the scope of the present invention, a molded product having high hardness was obtained. In Examples 5 to 8, when the amount of sepiolite was increased by reducing the amount of the cellulose binder, a molded article having improved hardness as compared with the cellulose binder alone was obtained. In Example 9, a hydrophilic zeolite was used as the zeolite powder, and a molded article having a high hardness was obtained as in the case of the hydrophobic zeolite. However, since heat is generated when water is added, the cooling time is added, resulting in an increase in productivity. A slight decrease was observed.

比較例1〜6は有機系バインダーが多過ぎたため、焼結後の成形体に隙間が多く硬度が低かった。比較例4〜6はセピオライトを含有しているため比較例1〜3に比べ硬度が上がっているが実使用するには硬度が不足している。比較例7は有機系バインダーが少ないためゼオライト粉末を成形体として固めることが不可能であった。比較例8は有機系バインダーを含有していないため、水を添加してもボソボソ・パサパサの粉末状からは変化せず、成形体として固めることが不可能であった。比較例9は粘土鉱物のセピオライトが多い分硬度が高いため、シート状にならず、割れ等が発生し成形性に劣るものであり、ゼオライト含有量が少なく吸着能力が低いものであった。   Since Comparative Examples 1-6 had too many organic binders, there were many gaps in the sintered compact and the hardness was low. Since Comparative Examples 4 to 6 contain sepiolite, the hardness is higher than Comparative Examples 1 to 3, but the hardness is insufficient for actual use. In Comparative Example 7, since the organic binder was small, it was impossible to harden the zeolite powder as a compact. Since Comparative Example 8 did not contain an organic binder, even if water was added, it did not change from the powdered form of Bosobosapasa and could not be hardened as a molded body. In Comparative Example 9, since the amount of the clay mineral sepiolite is large, the hardness is high, so it does not form a sheet, cracks and the like are inferior in moldability, and has a low zeolite content and a low adsorption capacity.

実施例1〜8及び比較例1〜7における、硬度を縦軸、ゼオライト100重量部に対してセルロース含有量を横軸にとったグラフを図1に示す。図1からも判るように、本発明の範囲において高硬度な吸着剤含有成形体を得ることができる。   In Examples 1 to 8 and Comparative Examples 1 to 7, a graph in which the hardness is on the vertical axis and the cellulose content is on the horizontal axis with respect to 100 parts by weight of zeolite is shown in FIG. As can be seen from FIG. 1, an adsorbent-containing molded body having a high hardness can be obtained within the scope of the present invention.

本発明の製造方法によって、大型な装置を使用しなくてもゼオライトを95重量%以上に高含有した成形体は硬度が高く、微細形状を成形でき、吸着分野に広く用いることが可能である。   According to the production method of the present invention, a compact containing 95% by weight or more of zeolite has a high hardness without using a large apparatus, can form a fine shape, and can be widely used in the adsorption field.

本発明で特定した範囲における吸着剤含有成形体の硬度を示す図である。It is a figure which shows the hardness of the adsorption body containing molded object in the range specified by this invention.

Claims (5)

ゼオライト粉末及び有機系バインダーを混合する工程と、
該混合物に水を添加し、粘土状に混練する工程と、
該混練した粘土体を切断する工程と、
該切断した粘土体を乾燥させる工程と、
を有する吸着剤含有成形体の製造方法であって、
該ゼオライト粉末100重量部に対して有機系バインダーが15〜30重量部であり、
最終成形品のゼオライト含有率が95重量%以上である、
ことを特徴とする吸着剤含有成形体の製造方法。
Mixing the zeolite powder and the organic binder;
Adding water to the mixture and kneading into a clay;
Cutting the kneaded clay body;
Drying the cut clay body;
A method for producing an adsorbent-containing molded article having
The organic binder is 15 to 30 parts by weight with respect to 100 parts by weight of the zeolite powder,
The zeolite content of the final molded product is 95% by weight or more,
A method for producing an adsorbent-containing molded article characterized by the above.
前記ゼオライト粉末及び有機系バインダーを混合する工程において、更に粘土鉱物を混合する請求項1に記載の吸着剤含有成形体の製造方法。   The method for producing an adsorbent-containing shaped article according to claim 1, wherein a clay mineral is further mixed in the step of mixing the zeolite powder and the organic binder. 前記粘土鉱物の混合量が、ゼオライト粉末100重量部に対して5重量部以下であり、かつ粘土鉱物+有機系バインダーがゼオライト粉末100重量部に対して20〜35重量部である請求項1又は2に記載の吸着剤含有成形体の製造方法。   The mixing amount of the clay mineral is 5 parts by weight or less with respect to 100 parts by weight of the zeolite powder, and the clay mineral + organic binder is 20 to 35 parts by weight with respect to 100 parts by weight of the zeolite powder. 2. A method for producing an adsorbent-containing molded article according to 2. 前記粘土鉱物がセピオライトである請求項1〜3のいずれかに記載の吸着剤含有成形体の製造方法。   The method for producing an adsorbent-containing molded article according to any one of claims 1 to 3, wherein the clay mineral is sepiolite. 請求項1〜4のいずれかに記載の吸着剤含有成形体の製造方法によって得られたことを特徴とする吸着剤含有成形体。   An adsorbent-containing molded article obtained by the method for producing an adsorbent-containing molded article according to any one of claims 1 to 4.
JP2007275272A 2007-10-23 2007-10-23 Method for producing adsorbent-containing molded body and adsorbent-containing molded body Expired - Fee Related JP5016442B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007275272A JP5016442B2 (en) 2007-10-23 2007-10-23 Method for producing adsorbent-containing molded body and adsorbent-containing molded body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007275272A JP5016442B2 (en) 2007-10-23 2007-10-23 Method for producing adsorbent-containing molded body and adsorbent-containing molded body

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2012130546A Division JP5366277B2 (en) 2012-06-08 2012-06-08 Adsorbent-containing molded product

Publications (2)

Publication Number Publication Date
JP2009101294A true JP2009101294A (en) 2009-05-14
JP5016442B2 JP5016442B2 (en) 2012-09-05

Family

ID=40703635

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007275272A Expired - Fee Related JP5016442B2 (en) 2007-10-23 2007-10-23 Method for producing adsorbent-containing molded body and adsorbent-containing molded body

Country Status (1)

Country Link
JP (1) JP5016442B2 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62283812A (en) * 1986-06-03 1987-12-09 Nippon Chem Ind Co Ltd:The Zeolite molded body and its production
JPH02160616A (en) * 1988-12-15 1990-06-20 Tosoh Corp Production of formed article of type-a zeolite
JPH04160014A (en) * 1990-03-17 1992-06-03 Takeda Chem Ind Ltd Zeolite kneaded composition for molding and zeolite molded body
JPH1087322A (en) * 1996-09-13 1998-04-07 Tosoh Corp High strength and low wear zeolite granule, its production and adsorption separation method using same
JP2000128524A (en) * 1998-10-19 2000-05-09 Mitsubishi Chemicals Corp Zeolite composition for molding, molded material thereof and molding
JP2003002636A (en) * 2001-06-19 2003-01-08 Tosoh Corp Binder-less zeolite bead molding, manufacturing method for the same, and adsorbing and removing method using the same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62283812A (en) * 1986-06-03 1987-12-09 Nippon Chem Ind Co Ltd:The Zeolite molded body and its production
JPH02160616A (en) * 1988-12-15 1990-06-20 Tosoh Corp Production of formed article of type-a zeolite
JPH04160014A (en) * 1990-03-17 1992-06-03 Takeda Chem Ind Ltd Zeolite kneaded composition for molding and zeolite molded body
JPH1087322A (en) * 1996-09-13 1998-04-07 Tosoh Corp High strength and low wear zeolite granule, its production and adsorption separation method using same
JP2000128524A (en) * 1998-10-19 2000-05-09 Mitsubishi Chemicals Corp Zeolite composition for molding, molded material thereof and molding
JP2003002636A (en) * 2001-06-19 2003-01-08 Tosoh Corp Binder-less zeolite bead molding, manufacturing method for the same, and adsorbing and removing method using the same

Also Published As

Publication number Publication date
JP5016442B2 (en) 2012-09-05

Similar Documents

Publication Publication Date Title
US5376609A (en) Activated carbon bodies having bentonite and cellulose fibers
AU762465B2 (en) Shaped body of zeolite, a process for its production and its use
JPH07207119A (en) Carbon particle body and its preparation
CN101987294A (en) Method for preparing honeycomb ceramic adsorbent material by utilizing attapulgite clay
JPH09173828A (en) Production of activated carbon article and use thereof
JP5366277B2 (en) Adsorbent-containing molded product
KR101314532B1 (en) Granular mesoporous silica including inorganic binder and fabrication method thereof
JP5016442B2 (en) Method for producing adsorbent-containing molded body and adsorbent-containing molded body
KR101778412B1 (en) Adsorbent for selective adsorption of carbon monoxide and method for preparation thereof
CN110407574B (en) Calcium zirconate-calcium hexaluminate composite porous ceramic and preparation method thereof
KR100392701B1 (en) A mesoporus zeolite honeycomb and a method for producing thereof
KR20150056101A (en) Adsorbents using alum sludges and method of manufacturing the same
RU2706077C2 (en) Extrudable ceramic composition and method of producing
JP2007063085A (en) Calcium carbonate composition
KR20180072892A (en) Flame retardant adsorbent for exhaust gas removal odor and VOCs and its manufacturing method
JP5368176B2 (en) Adsorbent and method for producing adsorbent
JPH08155295A (en) Carbon body and preparation thereof
KR20120093797A (en) Porous ceramic media for microbes by sawdust and method of manufacturing the same
JP5260894B2 (en) Method for producing adsorbent-containing molded body and adsorbent-containing molded body
JP2004168629A (en) Porous sintered compact, and production method therefor
JP6618342B2 (en) Zeolite kneaded product using kumbai powder, method for producing the same, and method for producing zeolite extrudate using the zeolite kneaded material
KR101111642B1 (en) Manufacturing method of spherical form activated carbon
CN1307541A (en) Extrusion product based on hydrated lime
KR101421267B1 (en) Method of Manufacturing Cordierite Honeycomb Using Agalmatolite
JP2001181070A (en) Method for producing baked material and the resultant baked material

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20101001

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20110714

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110817

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20111017

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20111107

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120106

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20120510

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20120608

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20150615

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees