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JPH0710346B2 - Adsorption material - Google Patents
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JPH0710346B2 - Adsorption material - Google Patents

Adsorption material

Info

Publication number
JPH0710346B2
JPH0710346B2 JP62091749A JP9174987A JPH0710346B2 JP H0710346 B2 JPH0710346 B2 JP H0710346B2 JP 62091749 A JP62091749 A JP 62091749A JP 9174987 A JP9174987 A JP 9174987A JP H0710346 B2 JPH0710346 B2 JP H0710346B2
Authority
JP
Japan
Prior art keywords
adsorbent
zeolite
adsorbent material
film
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP62091749A
Other languages
Japanese (ja)
Other versions
JPS63256133A (en
Inventor
薫 赤埴
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.)
Hagihara Industries Inc
Original Assignee
Hagihara Industries Inc
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 Hagihara Industries Inc filed Critical Hagihara Industries Inc
Priority to JP62091749A priority Critical patent/JPH0710346B2/en
Publication of JPS63256133A publication Critical patent/JPS63256133A/en
Publication of JPH0710346B2 publication Critical patent/JPH0710346B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Separation Of Gases By Adsorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はゼオライト系吸着剤を1−50重量%配合した樹
脂合成をフイルム状に押出したのち、延伸割繊すること
を特徴とする吸着能の高い吸着材料の製造方法および吸
着剤材料に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial field of application) The present invention is characterized in that a resin composition containing a zeolite adsorbent in an amount of 1 to 50% by weight is extruded into a film, and then stretched and split. TECHNICAL FIELD The present invention relates to a method for producing an adsorbent material having high efficiency and an adsorbent material.

(従来の技術) 吸着剤の代表的なものとして活性炭・活性白土などがあ
り、脱臭・脱色などの用途に用いられ、吸着効果の点か
ら気体や液体との接触をよくするため、形態としては粉
状・粒状・顆粒状・塊状で使用されることが多い。
(Prior art) Typical examples of adsorbents include activated carbon and activated clay, which are used for deodorization and decolorization, etc., and in terms of adsorption effect, improve contact with gas or liquid. Often used in powder, granular, granular, or lump form.

(発明が解決しようとする問題点) しかしながらこれらの形態のままでは飛散・流失などの
問題があり、取扱ううえで不便なことが多く用途が限定
される欠点を有している。とくに吸着能のすぐれている
活性炭は黒色であり汚染の問題が生じる。
(Problems to be Solved by the Invention) However, these forms still have problems such as scattering and runoff, and they are often inconvenient to handle, and have a drawback that their applications are limited. In particular, activated carbon, which has excellent adsorption ability, is black and causes a problem of contamination.

(問題を解決するための手段) 本発明者らは吸着剤の吸着能をできるだけ低下させず
に、吸着剤を保持する有用な形態の吸着材料を開発すべ
く鋭意努力した結果、ゼオライト系吸着剤を合成樹脂に
配合し、これをフイルム状に押し出したのち延伸割繊す
ることにより得られることを見い出した。
(Means for Solving the Problem) The present inventors have made diligent efforts to develop a useful adsorbent material that retains the adsorbent without reducing the adsorbability of the adsorbent as much as possible. It was found that the compound was obtained by blending the above with a synthetic resin, extruding this into a film, and then stretching and splitting.

以下本発明の吸着材料の製造方法および吸着材料につい
て詳述する。
The method for producing an adsorbent material and the adsorbent material of the present invention will be described in detail below.

(作用) ゼオライトはアルカリ金属、アルカリ土金属を含有する
立体網状構造を呈するアルミノケイ酸塩で結晶内に脱着
自由な水分を含有し、気体・液体を吸着する性質があ
り、またイオン交換能も呈することから吸着剤として活
性炭についで有用なものである。本発明はこのゼオライ
トを主成分として利用するものである。本発明における
ゼオライト系吸着剤はゼオライトとして天然ゼオライト
と合成ゼオライトがある。天然ゼオライトは安価で利用
しやすく有用である。なお天然ゼオライトを焼成処理あ
るいは硫酸処理により吸着能を向上させることも出来
る。さらにゼオライトの吸着能を一層改良したものとし
て、ゼオライトに水酸化第二鉄および水酸化カルシウム
を添加したものはより効果がある。
(Function) Zeolite is an aluminosilicate having a three-dimensional network structure containing an alkali metal and an alkaline earth metal, contains water that can be freely desorbed in the crystal, has the property of adsorbing gas and liquid, and also exhibits ion exchange capacity. Therefore, it is a useful adsorbent after activated carbon. The present invention uses this zeolite as a main component. The zeolite-based adsorbent in the present invention includes natural zeolite and synthetic zeolite as zeolite. Natural zeolite is inexpensive, easy to use, and useful. It is also possible to improve the adsorption capacity of natural zeolite by calcination or sulfuric acid treatment. Further, zeolite having ferric hydroxide and calcium hydroxide added thereto is more effective as one having further improved adsorption capacity of zeolite.

本発明におけるゼオライト系吸着剤の吸着能をできるだ
け低下させずに吸着剤を保持する有用な形態について検
討を加えたところ、ゼオライト系吸着剤を1−50重量%
合成樹脂に配合し、これをフイルム状に押し出したのち
延伸割繊することにより、吸着能の低下の少ない吸着材
料が得られた。本発明における吸着材料は繊維状の形態
であり、取扱いにおいてもまた用途応用においても非常
に有用である。
When a study was made on a useful form of retaining the adsorbent without reducing the adsorption capacity of the zeolite-based adsorbent in the present invention as much as possible, 1-50 wt% of the zeolite-based adsorbent
By admixing it with a synthetic resin, extruding this into a film, and then stretching and splitting it, an adsorbent material with a small decrease in adsorptive capacity was obtained. The adsorbent material in the present invention is in a fibrous form and is very useful in handling and application.

本発明における合成樹脂はポリオレフィン、ポリアミ
ド、ポリエステルなどの延伸可能な結晶性ポリマーであ
り、特に延伸割繊性のすぐれるポリプロピレンまたは/
およびポリエチレンのポリオレフィンがもっとも適して
いる。
The synthetic resin in the present invention is a stretchable crystalline polymer such as polyolefin, polyamide, polyester, etc., and particularly polypropylene or / or polypropylene having excellent stretch splitting property.
And polyethylene polyolefins are most suitable.

合成樹脂に配合するゼオライト系吸着剤は1−50重量
%、好ましくは3−30重量%である。すなはち1重量%
以下では吸着能が小さく、50重量%以上では成膜、延
伸、割繊が困難である。
Zeolite-based adsorbent compounded in the synthetic resin is 1-50% by weight, preferably 3-30% by weight. Sunahachi 1% by weight
If it is less than 50% by weight, the adsorption ability is small, and if it is 50% by weight or more, film formation, stretching and splitting are difficult.

ゼオライト系吸着剤を配合した合成樹脂の成膜、延伸、
割繊はフイルム成膜装置で合成樹脂フイルムを押出した
のち、フイルムを3−10倍に延伸し、ロールカッターな
どで割繊してフィブリル化することにより、吸着能の非
常にすぐれた吸着材料を得る。
Film formation, stretching of synthetic resin containing zeolite adsorbent,
Split fibers are made by extruding a synthetic resin film with a film forming device, stretching the film 3 to 10 times, and splitting it with a roll cutter or the like to fibrillate it to obtain an adsorbent material with excellent adsorption ability. obtain.

(実施例) 実施例を以下に示す。(Example) An example is shown below.

実施例1 MI値1.0のポリプロピレン90部とMI値1.0の高密度ポリエ
チレン10部に、天然ゼオライト、水酸化第二鉄、水酸化
カルシウムの重量比80:17:3の混合物を250℃で焼成処理
して微粉化したものを30重量%混合したのち、押出機に
て230℃で混練押出ペレット化する。このペレットをイ
ンフレーションフイルム成膜装置にて220℃でフイルム
としたのち、50mm巾のものにスリット調整し、これを15
0℃にて10倍延伸したあと、ロータリーカッターに通し
て割繊して、巻取り12万デニールの繊維状吸着材料を得
た。
Example 1 90 parts of polypropylene having an MI value of 1.0 and 10 parts of high-density polyethylene having an MI value of 1.0 were fired at 250 ° C. with a mixture of natural zeolite, ferric hydroxide and calcium hydroxide in a weight ratio of 80: 17: 3. Then, 30% by weight of the pulverized product is mixed, and then kneaded and extruded into pellets at 230 ° C. by an extruder. These pellets were made into a film at 220 ° C with an inflation film forming device, and then slit adjusted to have a width of 50 mm.
After being stretched 10 times at 0 ° C., it was split into fibers through a rotary cutter to obtain a fibrous adsorbent material with a winding of 120,000 denier.

吸着材料のアンモニアおよび硫化水素に対する吸着能を
測定した結果を第1表に示す。
Table 1 shows the results of measuring the adsorption ability of the adsorbent material with respect to ammonia and hydrogen sulfide.

実施例2 MI値1.0のポリプロピレンに325メッシュの天然ゼオライ
ト粉末で250℃で焼成処理したものを15重量%混合した
のち、実施例1と同様にペレット化、成膜、延伸、割繊
して繊維状吸着材料を得た。
Example 2 A polypropylene having an MI value of 1.0 was mixed with 15 wt% of 325-mesh natural zeolite powder that had been calcined at 250 ° C., and then pelletized, film-formed, drawn and split into fibers in the same manner as in Example 1. The adsorbent material was obtained.

実施例3 相対粘度3.1のナイロン6に天然ゼオライトを5重量%
混合したのち、Tダイス押出機にてフイルムを270℃で
成膜し、200℃にて3倍延伸したのちロータリーカッタ
ーにて割繊して繊維状吸着材料を得た。
Example 3 Nylon 6 having a relative viscosity of 3.1 and 5% by weight of natural zeolite
After mixing, a film was formed on the film at 270 ° C. by a T-die extruder, stretched 3 times at 200 ° C., and then split by a rotary cutter to obtain a fibrous adsorption material.

比較例1 実施例1におけるペレットを比較例として測定した吸着
能の結果を表2に示す。
Comparative Example 1 Table 2 shows the results of the adsorption capacities measured using the pellets of Example 1 as a comparative example.

比較例2 実施例1における割繊前の延伸フイルムを比較例とし
た。
Comparative Example 2 The stretched film before splitting in Example 1 was used as a comparative example.

比較例3 実施例2において吸着剤を使用しないポリプロピレンの
繊維状材料を比較例とした。
Comparative Example 3 A polypropylene fibrous material which does not use an adsorbent in Example 2 was used as a comparative example.

参考例1 実施例1における吸着剤を参考例として測定した吸着能
の結果を表3に示す。
Reference Example 1 Table 3 shows the results of the adsorption ability measured by using the adsorbent in Example 1 as a reference example.

参考例2 実施例2における吸着剤を比較例とした。Reference Example 2 The adsorbent in Example 2 was used as a comparative example.

なお吸着能の測定はガスバリヤー性の良いフイルム袋内
に、試料1gと約900ppmに調整したアンモニアガス、ある
いは約300ppmに調整した硫化水素ガスを600ml封入し、
封入直後と3時間後に各々のガス検知管にて濃度測定を
行った。
To measure the adsorption capacity, 600 g of 1 g of sample and ammonia gas adjusted to about 900 ppm or hydrogen sulfide gas adjusted to about 300 ppm was enclosed in a film bag with a good gas barrier property,
Immediately after encapsulation and after 3 hours, the concentration was measured with each gas detector tube.

(発明の効果) 本発明によれば吸着能の低下が少なく、繊維状形態を保
っているため吸着剤の飛散・流失などの問題がなく、取
扱いが便利であり多方面の用途展開が可能となる。
(Advantages of the Invention) According to the present invention, there is little decrease in adsorption capacity, and since the fibrous form is maintained, there are no problems such as scattering and runoff of adsorbent, convenient handling, and possible development of various applications. Become.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】ゼオライト系吸着剤を1−50重量%配合し
た合成樹脂をフイルム状に押出したのち延伸割繊するこ
とを特徴とする吸着材料の製造方法および吸着材料。
1. A method for producing an adsorbent material and an adsorbent material, comprising the steps of extruding a synthetic resin containing 1 to 50% by weight of a zeolite adsorbent into a film and then stretching and splitting the resin.
【請求項2】ゼオライト系吸着剤のゼオライトが天然ゼ
オライトである特許請求の範囲第一項記載の吸着材料。
2. The adsorbent material according to claim 1, wherein the zeolite of the zeolite-based adsorbent is a natural zeolite.
【請求項3】ゼオライト系吸着剤が天然ゼオライト、水
酸化第二鉄および水酸化カルシウムからなる特許請求の
範囲第一項記載の吸着材料。
3. The adsorbent material according to claim 1, wherein the zeolitic adsorbent comprises natural zeolite, ferric hydroxide and calcium hydroxide.
【請求項4】合成樹脂がポリプロピレンおよび/または
ポリエチレンのポリオレフインである特許請求の範囲第
一項記載の吸着材料。
4. The adsorbent material according to claim 1, wherein the synthetic resin is polypropylene and / or polyethylene polyolefin.
JP62091749A 1987-04-14 1987-04-14 Adsorption material Expired - Lifetime JPH0710346B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62091749A JPH0710346B2 (en) 1987-04-14 1987-04-14 Adsorption material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62091749A JPH0710346B2 (en) 1987-04-14 1987-04-14 Adsorption material

Publications (2)

Publication Number Publication Date
JPS63256133A JPS63256133A (en) 1988-10-24
JPH0710346B2 true JPH0710346B2 (en) 1995-02-08

Family

ID=14035181

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62091749A Expired - Lifetime JPH0710346B2 (en) 1987-04-14 1987-04-14 Adsorption material

Country Status (1)

Country Link
JP (1) JPH0710346B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012032786A1 (en) 2010-09-09 2012-03-15 パナソニック株式会社 Sheet-shaped gas adsorbent and insulating body using same
JP5873963B2 (en) 2011-04-12 2016-03-01 パナソニックIpマネジメント株式会社 Acoustic speaker device
US11092809B2 (en) 2018-05-03 2021-08-17 Apple Inc. Display system with optical module having pressure-relieving feature
JP7813093B2 (en) * 2020-03-31 2026-02-12 大日本印刷株式会社 Odor-absorbing stretch film

Also Published As

Publication number Publication date
JPS63256133A (en) 1988-10-24

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