JPS58135121A - Manufacture of formed zeolite - Google Patents

Manufacture of formed zeolite

Info

Publication number
JPS58135121A
JPS58135121A JP57013752A JP1375282A JPS58135121A JP S58135121 A JPS58135121 A JP S58135121A JP 57013752 A JP57013752 A JP 57013752A JP 1375282 A JP1375282 A JP 1375282A JP S58135121 A JPS58135121 A JP S58135121A
Authority
JP
Japan
Prior art keywords
zeolite
water
powder
binder
amino acid
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
JP57013752A
Other languages
Japanese (ja)
Other versions
JPS6052088B2 (en
Inventor
Shingo Tokuda
徳田 晋吾
Toshiyuki Ikeda
俊幸 池田
Satoshi Matsumoto
敏 松本
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.)
Osaka Soda Co Ltd
Original Assignee
Osaka Soda 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 Osaka Soda Co Ltd filed Critical Osaka Soda Co Ltd
Priority to JP57013752A priority Critical patent/JPS6052088B2/en
Publication of JPS58135121A publication Critical patent/JPS58135121A/en
Publication of JPS6052088B2 publication Critical patent/JPS6052088B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

PURPOSE:To obtain a formed zeolite having excellent mechanical strength and high absorption capacity, by forming zeolite powder with a water-glass or clay binder in the presence of an amino acid. CONSTITUTION:Natural or synthetic zeolite powder is mixed with a water- glass binder such as sodium silicate or a clay binder such as kaolin and a water- soluble amino acid such as glycine, alanine, etc. the mixture is kneaded in the presence of water, formed, dried, and baked to obtain the objective formed zeolite. Since the strength of the formed zeolite is remarkably improved and the amount of the binder is reduced by the addition of amino acid, the decrease in the absorption capacity of the formed zeolite can be minimized.

Description

【発明の詳細な説明】 本発明はゼオライト成型体の製造法に関しその目的は特
殊な添加剤を加えてゼオライト粉末を成型1wA成する
ことにより機械的強度に優れ、かつ良好な吸着性能を有
するゼオライト成型体を得ることにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a zeolite molded body, and its purpose is to produce a zeolite having excellent mechanical strength and good adsorption performance by molding zeolite powder to 1 wA by adding special additives. The purpose is to obtain a molded body.

天然または合成のゼオライトは、その吸着性能を利用し
工業的に多くの分野において使用されているが、使用に
あたってはそのままの小塊粒または粉末等の状態で使用
されることは稀であり、多くの場合ゼオライトを適当な
粒状形態に成型し焼成して機械的強度を高めて使用して
いる。一般にゼオライト成型体を製造する際にカオリン
系粘土、ベントナイト系粘土等、無機系の粘土物質を加
え、あるいは添加助剤等を併用して成型している。しか
、しこの従来法では十分な強度を得るためには、結合剤
の添加量を増す故、焼成しても成型品中に残存しそのた
めにゼオライト本来の吸着能が近下し、逆に十分な吸着
能を保持するためには結合剤の添加量が不十分で機械的
強度が弱くなるという欠点があった。
Natural or synthetic zeolites are used in many industrial fields due to their adsorption properties, but they are rarely used in the form of small agglomerates or powders, and many In this case, zeolite is molded into a suitable granular form and fired to increase its mechanical strength. Generally, when producing a zeolite molded body, an inorganic clay material such as kaolin clay or bentonite clay is added, or additives and auxiliaries are used in combination. However, in this conventional method, in order to obtain sufficient strength, the amount of binder added increases, which remains in the molded product even after firing, which reduces the inherent adsorption capacity of zeolite, and conversely, it becomes insufficient. The problem was that the amount of binder added was insufficient to maintain sufficient adsorption ability, resulting in weak mechanical strength.

本発明者らはこのような欠点を無くすために種々検討を
行った結果アミノ酸の添加がゼオライトの成型に際し効
果的であることを見出しこれに基づいて本発明・を完成
したものである。           ・ 本発明はすなわちゼオライト粉末に水ガラス系もしくは
粘土系の結合剤および水溶性アミノ酸を加え水分の存在
下に混和、成型、乾燥。
The present inventors conducted various studies to eliminate such drawbacks, and as a result found that the addition of amino acids was effective in forming zeolite, and based on this, the present invention was completed. - The present invention involves adding a water glass-based or clay-based binder and a water-soluble amino acid to zeolite powder, mixing in the presence of water, molding, and drying.

焼成することを特徴とするゼオライト成型体の製造法で
ある。
This is a method for producing a zeolite molded body, which is characterized by firing.

本発明方法で素材として使用するゼオライトは天然品ま
たは合成品のいずれでも差支えなく通常粉状ないし粒状
で使用される。水ガラス系結合剤としてはケイ酸ナトリ
ウム、ケイ酸カリ、ケイ酸リチウムの様なものの水和溶
液が使用され、また粘土系結合剤としてはカオリン、ベ
ントナイト、Il性白土等が挙げられ、これらの添加量
はゼオライト粉末に対し30重量%以下が好ましい。水
溶性アミノ酸としてはたとえばグリシン、アラニン、ア
ミノ酪酸、バリン、ロイシン、セリン、フェニルアミン
、トリプトファン、メチオニン、グルタミン酸等が挙げ
られこれらを1種または2種以上予めalsに溶解し水
溶液として添加すれば分散が良好で混練時間の短縮が可
能である。アミノ酸の添加量はゼオライト粉末に対し0
.1〜゛20重量%、特に0.1〜10重量%が好まし
り0.1重量%未満−ではアミノ酸添加による成型品の
強度増加効果が充分でなくまた20重最%をこえると成
型品の吸着能が低下する。
The zeolite used as a raw material in the method of the present invention may be either a natural product or a synthetic product, and is usually used in powder or granule form. As water glass binders, hydrated solutions of sodium silicate, potassium silicate, lithium silicate, etc. are used, and as clay binders, kaolin, bentonite, Il clay, etc. are used. The amount added is preferably 30% by weight or less based on the zeolite powder. Examples of water-soluble amino acids include glycine, alanine, aminobutyric acid, valine, leucine, serine, phenylamine, tryptophan, methionine, glutamic acid, etc. If one or more of these are dissolved in als in advance and added as an aqueous solution, they will be dispersed. is good and the kneading time can be shortened. The amount of amino acids added is 0 to zeolite powder.
.. 1 to 20% by weight, particularly 0.1 to 10% by weight is preferred; if it is less than 0.1% by weight, the effect of increasing the strength of the molded product due to the addition of amino acids is not sufficient, and if it exceeds 20% by weight, the strength of the molded product will deteriorate. adsorption capacity decreases.

上記の結合剤およびアミノ酸のほかに要すれば分散剤、
押出助剤として活性炭酸カルシウム、シュウ酸ナトリウ
ム、ステアリン酸ナトリウム等を少量添加してもよい。
In addition to the above binders and amino acids, if necessary, a dispersing agent,
A small amount of activated calcium carbonate, sodium oxalate, sodium stearate, etc. may be added as an extrusion aid.

上記の混合物を水分の存在下で混線様により約0.5〜
3時閣混練することにより均一な混合物が得られる。水
分の添加量はアミノ酸および結合剤の添加量、ゼオライ
ト素材の種類等の要因で異なってくるが、通常ゼオライ
トに対し15〜45重量%程度に保持するのが均一な混
和物を得るために好ましい。
The above mixture is mixed in the presence of water by about 0.5~
A homogeneous mixture can be obtained by kneading for 3 minutes. The amount of water added varies depending on factors such as the amount of amino acids and binder added, the type of zeolite material, etc., but it is usually preferable to maintain it at about 15 to 45% by weight based on the zeolite in order to obtain a uniform mixture. .

得られた混和物を押出し成型後、通常100〜150℃
前後の予備乾燥を行って成型物中の付着水分を餘去し、
次いで最終的に350〜700℃で焼成してゼオライト
成型体製品とする。
After extrusion molding the obtained mixture, the temperature is usually 100 to 150°C.
Perform pre-drying before and after to remove moisture adhering to the molded product.
Then, it is finally calcined at 350 to 700°C to obtain a zeolite molded product.

焼成温度が700℃より高い場合はぜオライド自体の諸
性質を破壊するので、7(10’c以下の温度範囲が好
ましい。
If the calcination temperature is higher than 700°C, the properties of the zeolide itself will be destroyed, so a temperature range of 7 (10'C or lower) is preferable.

本発明法においては前記のようにアミノ酸の添加により
不添加の場合に比較して大巾に強度が向上するとともに
、併用する結合剤の使用曇を減少させることが可能とな
るのでゼオライト成型物の吸着能力の低下を僅少に止め
ることができる。また成型体の強度が増大するのでアミ
ノ酸不添加め場合よりも造粒が容易となり粒子表面も平
滑化されて相互接触による摩耗が減少する利点がある。
In the method of the present invention, as mentioned above, the strength of the zeolite molded product is greatly improved by adding amino acids compared to the case without addition, and it is also possible to reduce the clouding caused by the use of the binder used in combination. Decrease in adsorption capacity can be minimized. Furthermore, since the strength of the molded product is increased, granulation is easier than in the case where no amino acid is added, and the particle surfaces are smoothed, which has the advantage of reducing wear due to mutual contact.

実施例1 合成ゼオライト粉末(粒径200メツシユより細かい粉
末、4A型ゼオライト)の 120℃乾燥品2kgに、3号ナトリウム水ガラス(市
販品)200g、グリシン粉末64gを溶解させた水溶
液700■eを加え混練機を用いて30分間混線を行っ
た。混線後、上記混和物を成型機を用いて粒径的2mの
球状に成型し、次いで成型品を120℃で3時間乾燥し
、600℃で2WIl[ltR成して最終の球状成型体
を得た。
Example 1 To 2 kg of synthetic zeolite powder (powder with particle size finer than 200 mesh, type 4A zeolite) dried at 120°C, 700 μe of an aqueous solution in which 200 g of No. 3 sodium water glass (commercial product) and 64 g of glycine powder were dissolved was added. Mixing was performed for 30 minutes using an addition kneader. After cross-mixing, the above mixture was molded into a sphere with a particle diameter of 2 m using a molding machine, and then the molded product was dried at 120°C for 3 hours, and then subjected to 2WIl[ltR] at 600°C to obtain the final spherical molded body. Ta.

比較例1 グリシン粉末を添加しない以外は実施例1と同様の操作
を行い球状成型体を得た。
Comparative Example 1 A spherical molded body was obtained by carrying out the same operation as in Example 1 except that glycine powder was not added.

実施例2 実施例1における3号ナトリウム水ガラスの代りにベン
トナイト粉末400g !添加し次いでグリシン64g
を加えてミキサーにより混合し水700 mgを加えて
混練した以外は全〈実施例1と同様にして球状成型体を
得た。
Example 2 400g of bentonite powder was used instead of No. 3 sodium water glass in Example 1! Add then 64g of glycine
A spherical molded body was obtained in the same manner as in Example 1 except that 700 mg of water was added and kneaded.

比較例2 グリシン粉末を添加しない以外は実施例2と同様の操作
を行い球状成型体を得た。
Comparative Example 2 A spherical molded body was obtained by carrying out the same operation as in Example 2 except that glycine powder was not added.

実施例3 天然ゼオライト粉末(粒度200メツシユより細かい粉
末9モルデナイト型ゼオライト)の120℃乾燥品2−
にベントナイト粉末400gとアミノ酪酸粉末128g
とを添加しミキサーにより混合し水800 m&を加え
混練機を用いて40分間混線を行った。混線後、上記混
和物を成型機を用いて粒径的3wIの球状に成型し、次
いで成型品を150℃で2時間乾燥し550℃で2時開
焼成して最終の球状成型体を得た。
Example 3 120°C dry product 2- of natural zeolite powder (9 mordenite type zeolite powder with particle size finer than 200 mesh)
400g of bentonite powder and 128g of aminobutyric acid powder.
and mixed with a mixer, 800 ml of water was added, and mixed for 40 minutes using a kneader. After mixing, the above mixture was molded into a sphere with a particle size of 3 wI using a molding machine, and then the molded product was dried at 150°C for 2 hours and fired at 550°C for 2 hours to obtain a final spherical molded body. .

実施例4 アミノ醋酸粉末の代りにアラニン粉末 256gを添加した以外は実施例3と同様にして球状成
型体を得た。
Example 4 A spherical molded body was obtained in the same manner as in Example 3 except that 256 g of alanine powder was added instead of the aminoacetic acid powder.

実施例5(強度試験、吸着試験) 実施例1〜4.比較例1.2で得られた成型品試料に荷
重を加え、試料の破壊点における荷重を測定(100個
の試料についての値の代数平均値)し圧壊強度とした。
Example 5 (strength test, adsorption test) Examples 1 to 4. A load was applied to the molded product sample obtained in Comparative Example 1.2, and the load at the fracture point of the sample was measured (algebraic average value of the values for 100 samples) to determine the crushing strength.

また各試料について20℃、相対湿度65%における水
分吸着容量を測定した。その結果を第1表に示す。
Furthermore, the moisture adsorption capacity of each sample at 20° C. and 65% relative humidity was measured. The results are shown in Table 1.

第1表 第1表に示すように本発明方法により得た成型体は従来
法による成型体に比較し吸着能力の低下を来さず機械的
強度の改善されていることが判る。
As shown in Table 1, it can be seen that the molded bodies obtained by the method of the present invention have improved mechanical strength without a decrease in adsorption capacity compared to molded bodies obtained by the conventional method.

出願人  大阪曹達株式会社 代理人  弁理士 同条 透Applicant: Osaka Soda Co., Ltd. Agent: Patent attorney Toru Dojo

Claims (3)

【特許請求の範囲】[Claims] (1)ゼオライト粉末に水ガラス系もしくは粘土系の結
合剤および水溶性アミノ酸を加え水分の存在下に混和、
成型、乾燥、焼成することを特徴とするゼオライト成型
体の製造法。
(1) Add water glass-based or clay-based binder and water-soluble amino acids to zeolite powder and mix in the presence of water.
A method for producing a zeolite molded body, which is characterized by molding, drying, and firing.
(2)水溶性アミノ酸の添加量がゼオライト粉末に対し
0.1〜20重量%である特許請求の範囲第1項記載の
製造法。。
(2) The production method according to claim 1, wherein the amount of water-soluble amino acid added is 0.1 to 20% by weight based on the zeolite powder. .
(3)焼成温度が350〜700℃である特許請求の範
囲第1項もしくは第2項記載の製造法。
(3) The manufacturing method according to claim 1 or 2, wherein the firing temperature is 350 to 700°C.
JP57013752A 1982-01-30 1982-01-30 Manufacturing method of zeolite molded body Expired JPS6052088B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57013752A JPS6052088B2 (en) 1982-01-30 1982-01-30 Manufacturing method of zeolite molded body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57013752A JPS6052088B2 (en) 1982-01-30 1982-01-30 Manufacturing method of zeolite molded body

Publications (2)

Publication Number Publication Date
JPS58135121A true JPS58135121A (en) 1983-08-11
JPS6052088B2 JPS6052088B2 (en) 1985-11-18

Family

ID=11841978

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57013752A Expired JPS6052088B2 (en) 1982-01-30 1982-01-30 Manufacturing method of zeolite molded body

Country Status (1)

Country Link
JP (1) JPS6052088B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59199526A (en) * 1983-04-11 1984-11-12 デグツサ・アクチエンゲゼルシヤフト Granular zeolite bound with silicate and manufacture
CN104016364A (en) * 2014-06-01 2014-09-03 许盛英 Sodium modified chlorite
FR3045413A1 (en) * 2015-12-18 2017-06-23 Air Liquide ADSORBENT MONOLITHIC STRUCTURE AUTOSUPPORTE COMPRISING SODIUM SILICATE
JP2018111643A (en) * 2017-01-11 2018-07-19 東ソー株式会社 Method for producing heat-resistant zeolite molded body

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59199526A (en) * 1983-04-11 1984-11-12 デグツサ・アクチエンゲゼルシヤフト Granular zeolite bound with silicate and manufacture
CN104016364A (en) * 2014-06-01 2014-09-03 许盛英 Sodium modified chlorite
CN104016364B (en) * 2014-06-01 2016-07-06 重庆环德科技有限公司 Chlorite after sodium
FR3045413A1 (en) * 2015-12-18 2017-06-23 Air Liquide ADSORBENT MONOLITHIC STRUCTURE AUTOSUPPORTE COMPRISING SODIUM SILICATE
JP2018111643A (en) * 2017-01-11 2018-07-19 東ソー株式会社 Method for producing heat-resistant zeolite molded body

Also Published As

Publication number Publication date
JPS6052088B2 (en) 1985-11-18

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