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JPH03109916A - Desiccant composition - Google Patents

Desiccant composition

Info

Publication number
JPH03109916A
JPH03109916A JP1254326A JP25432689A JPH03109916A JP H03109916 A JPH03109916 A JP H03109916A JP 1254326 A JP1254326 A JP 1254326A JP 25432689 A JP25432689 A JP 25432689A JP H03109916 A JPH03109916 A JP H03109916A
Authority
JP
Japan
Prior art keywords
desiccant
weight
parts
thermoplastic resin
compsn
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
JP1254326A
Other languages
Japanese (ja)
Other versions
JPH0753222B2 (en
Inventor
Hisao Mukai
向井 久雄
Katsumi Shigeta
繁田 勝巳
Yoshio Saida
斉田 好男
Eiji Isojima
礒嶌 英二
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.)
SASAKI KAGAKU YAKUHIN KK
TOMITA SEIYAKU KK
Tomita Pharmaceutical Co Ltd
Original Assignee
SASAKI KAGAKU YAKUHIN KK
TOMITA SEIYAKU KK
Tomita Pharmaceutical 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 SASAKI KAGAKU YAKUHIN KK, TOMITA SEIYAKU KK, Tomita Pharmaceutical Co Ltd filed Critical SASAKI KAGAKU YAKUHIN KK
Priority to EP90109700A priority Critical patent/EP0400460B1/en
Priority to DE69018312T priority patent/DE69018312T2/en
Priority to US07/526,817 priority patent/US5078909A/en
Publication of JPH03109916A publication Critical patent/JPH03109916A/en
Publication of JPH0753222B2 publication Critical patent/JPH0753222B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Packages (AREA)
  • Drying Of Gases (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

PURPOSE:To obtain a desiccant compsn. having high hygroscopicity, high water retentivity and superior moldability by kneading thermoplastic resin with a specified desiccant. CONSTITUTION:At least one kind of desiccant selected from among magnesium sulfate represented by formula MgSO4.nH2O (where 0<=n<=3), aluminum oxide, barium oxide, calcium oxide and silicon oxide is added to thermoplastic resin by 5-400 pts.wt. per 100 pts.wt. of the resin to give a desiccant compsn. This compsn. has high hygroscopicity and high water retentivity and can be molded into an arbitrary shape. When a blowing agent is added, a desiccant compsn. having higher hygroscopicity and giving a lightweight molded body can be obtd.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、乾燥剤組成物に関する。[Detailed description of the invention] Industrial applications The present invention relates to desiccant compositions.

従来の技術 従来、食品、医薬品、電子部品、精密機械等のあらゆる
分野において吸湿に起因する酸化等による商品等の品質
劣化を防ぐ目的で、シリカゲル、塩化カルシウム、生石
灰、ゼオライト等の乾燥剤が用いられている。これらの
乾燥剤は、上記用途において粒状あるいは粉末の形態で
紙、不織布等により包装されるか、もしくは、容器等に
封入された状態で、商品と共に包材へ投入されて用いら
れている。その為に、乾燥剤が本来有する優れた吸湿効
果及び吸湿速度が低下したり、乾燥剤の包装材破損によ
る商品への乾燥剤の付着、混入などの問題がしばしば発
生する。
Conventional technology Traditionally, desiccant agents such as silica gel, calcium chloride, quicklime, and zeolite have been used in all fields of food, medicine, electronic parts, precision machinery, etc. to prevent quality deterioration of products due to oxidation caused by moisture absorption. It is being In the above-mentioned applications, these desiccants are used in the form of granules or powder, packaged with paper, nonwoven fabric, etc., or sealed in a container, etc., and put into a packaging material together with the product. As a result, problems such as the desiccant's inherent excellent moisture absorption effect and moisture absorption rate are reduced, and the packaging material for the desiccant is damaged, resulting in the desiccant adhering to or contaminating the product, often occur.

また、塩化カルシウム等の潮解性乾燥剤の使用に際して
は、吸湿液化現象による弊害なども問題とされている。
Further, when using a deliquescent desiccant such as calcium chloride, there are problems such as adverse effects due to moisture absorption and liquefaction phenomenon.

特開昭61−227818号公報は、微多孔性熱可塑性
樹脂シートを乾燥剤の包装材料として用いることにより
、吸湿液化現象による液体漏洩防止を提案している。ま
た、不織布と複合乾燥剤とをサンドイッチ状に包含加工
し乾燥剤とする方法も実施されているが、これらはいず
れもコストアツブ等の欠点がある。
JP-A-61-227818 proposes preventing liquid leakage due to moisture absorption and liquefaction by using a microporous thermoplastic resin sheet as a packaging material for a desiccant. In addition, methods have been implemented in which a nonwoven fabric and a composite desiccant are incorporated into a sandwich to form a desiccant, but all of these methods have drawbacks such as high costs.

問題点を解決するための手段 本発明者は、上記問題点を解消若しくは著しく軽減すべ
く鋭意研究を重ねた結果、熱可塑性樹脂にある特定の乾
燥剤を混練することにより、高い吸湿力及び保水力を有
し、しかも飛散性、吸湿性、潮解性による液体漏洩等の
欠点を生じない乾燥剤組成物が得られることを見出し、
本発明を完成したものである。
Means for Solving the Problems As a result of extensive research in order to eliminate or significantly reduce the above problems, the present inventor has found that by kneading a specific desiccant into a thermoplastic resin, a thermoplastic resin with high hygroscopicity and retention can be obtained. It has been discovered that a desiccant composition can be obtained that has hydraulic power and does not have drawbacks such as liquid leakage due to scattering, hygroscopicity, and deliquescent properties,
This completes the present invention.

すなわち本発明は、熱可塑性樹脂100重量部に対し、
式MgSO4ΦnH20(但しO≦n≦3)で表される
硫酸マグネシウム、酸化アルミニウム、酸化バリウム、
酸化カルシウム及び酸化ケイ素の少なくとも一種5〜4
00重量部を含有する乾燥剤組成物に係るものである。
That is, in the present invention, for 100 parts by weight of thermoplastic resin,
Magnesium sulfate, aluminum oxide, barium oxide, represented by the formula MgSO4ΦnH20 (O≦n≦3),
At least one of calcium oxide and silicon oxide 5 to 4
00 parts by weight of the desiccant composition.

本発明の最大の特徴は、熱可塑性樹脂を乾燥剤と共に混
練して用いることにあり、それにより得られる乾燥剤組
成物は、フィルム状、シート状、プレート状、更には袋
状、ペレット状、容器状等用途に応じ任意の形状に容易
に加工成型することができる。こうして得られる成型品
は、それ自体乾燥剤であり、しかも包材となり得るもの
である。
The greatest feature of the present invention is that the thermoplastic resin is used by kneading it with a desiccant, and the desiccant composition obtained thereby can be in the form of a film, sheet, plate, bag, pellet, etc. It can be easily processed and molded into any shape depending on the purpose, such as a container shape. The molded product thus obtained is itself a desiccant and can also be used as a packaging material.

本発明における熱可塑性樹脂としては、特に限定されず
公知のものを使用できるが、例えばポリエチレン、ポリ
プロピレン、ポリカーボネート、ポリアミド、エチレン
−酢酸ビニル共重合体、エチレン−メタアクリレート共
重合体、ポリ塩化ビニル、ポリスチレン、ポリエステル
、ポリアクリル酸エステル、ポリ塩化ビニリデン等が挙
げられ、これらのうち一種又は二種以上を用いることが
できる。
The thermoplastic resin in the present invention is not particularly limited and any known one can be used, such as polyethylene, polypropylene, polycarbonate, polyamide, ethylene-vinyl acetate copolymer, ethylene-methacrylate copolymer, polyvinyl chloride, Examples include polystyrene, polyester, polyacrylic ester, polyvinylidene chloride, and one or more of these can be used.

また、熱可塑性樹脂とともに用いる乾燥剤としては、式
MgSO4・nH20(但しO≦n≦3)で表される硫
酸マグネシウム、酸化アルミニウム、酸化バリウム、酸
化カルシウム及び酸化ケイ素等が挙げられ、これら乾燥
剤の一種もしくは二種以上を用いることができ、特に前
記樹脂に対して卓越した分散性を有する硫酸マグネシウ
ムが好ましい。また上記乾燥剤は、使用に際して平均粒
子径50μm以下程度の粉末とするのが望ましい。必要
ならば、異なった粒子径のものを混合して用いてもよい
In addition, examples of the desiccant used with the thermoplastic resin include magnesium sulfate, aluminum oxide, barium oxide, calcium oxide, and silicon oxide represented by the formula MgSO4.nH20 (O≦n≦3). One or more of these can be used, with magnesium sulfate being particularly preferred as it has excellent dispersibility in the resin. Further, it is desirable that the desiccant is in the form of a powder with an average particle size of about 50 μm or less when used. If necessary, particles of different particle sizes may be mixed and used.

本発明において混練する原料の割合は、熱可塑性樹脂1
00重量部に対し、乾燥剤5〜400重量部程重量部門
であり、用途に応じ適宜選択される。乾燥剤の割合が上
記範囲の場合には、乾燥剤の樹脂中での分散性がよく高
い吸湿性及び保水性を有し、しかも成型適性に優れた乾
燥剤組成物を得ることができる。
In the present invention, the ratio of raw materials to be kneaded is 1 part thermoplastic resin, 1 part thermoplastic resin,
00 parts by weight, the desiccant is about 5 to 400 parts by weight, and is appropriately selected depending on the application. When the proportion of the desiccant is within the above range, it is possible to obtain a desiccant composition that has good dispersibility of the desiccant in the resin, has high hygroscopicity and water retention, and has excellent moldability.

本発明の乾燥剤組成物は、」−記熱可塑性樹脂及び乾燥
剤のほかに、発泡剤を原料として加えることもできる。
In addition to the thermoplastic resin and the desiccant, the desiccant composition of the present invention can also contain a foaming agent as a raw material.

発泡剤としては、特に限定されず公知のものを広く使用
することができ、例えばアゾイソブチルニトリル、アゾ
ジカルボンアミド、4゜4′−オキシベンゼンスルホニ
ルヒドラジッド等が挙げられ、その使用量は熱可塑性樹
脂100重量部に対し、0.2〜10重量部程度とする
のが好ましい。発泡剤の添加により得られる乾燥剤組成
物は、加工され発泡体に成型された場合に、軽量で、発
泡体内部にまで吸湿効果が及ぶために、更に高い吸湿力
をもたすものである。
The blowing agent is not particularly limited and a wide variety of known ones can be used, such as azoisobutylnitrile, azodicarbonamide, 4゜4'-oxybenzenesulfonyl hydrazide, etc., and the amount used is determined according to the thermoplastic The amount is preferably about 0.2 to 10 parts by weight per 100 parts by weight of the resin. When the desiccant composition obtained by adding a foaming agent is processed and molded into a foam, it is lightweight and has even higher hygroscopicity because the hygroscopic effect extends to the inside of the foam. .

また、このほか添加剤として公知の可塑剤、安定剤、滑
剤、着色剤等を必要に応じ、本発明の目的を阻害しない
程度に適宜加えてもかまわない。
In addition, known additives such as plasticizers, stabilizers, lubricants, colorants, etc. may be added as necessary to an extent that does not impede the object of the present invention.

本発明の乾燥剤組成物の製造方法としては、特に制限は
なく、通常次のような方法で製造することができる。
There are no particular restrictions on the method for producing the desiccant composition of the present invention, and the desiccant composition can generally be produced by the following method.

前記熱可塑性樹脂、乾燥剤及びその他の添加剤をミキシ
ングロール等を用い約100〜350℃のもと約5〜4
0分間混練すればよい。また、」二層のようにして得ら
れる本発明の組成物は、押出成型、共押出成型、射出成
型、中空成型、押出コ−ティング成型、架橋発泡成型等
により、任意の形状に加工成型することができ、更に他
の積層材を積層したラミネート体とすることもできる。
The thermoplastic resin, desiccant and other additives are mixed using a mixing roll or the like at about 100 to 350°C for about 5 to 40 minutes.
It is sufficient to knead for 0 minutes. Furthermore, the composition of the present invention obtained in a two-layered manner can be processed and molded into any shape by extrusion molding, coextrusion molding, injection molding, hollow molding, extrusion coating molding, crosslinking foam molding, etc. Furthermore, it is also possible to form a laminate body in which other laminate materials are laminated.

このようにして得られる本発明の乾燥剤組成物は、−船
釣な乾燥剤としての用途の他に、有機溶媒中の水分除去
用脱水剤としても利用できるものである。
The desiccant composition of the present invention thus obtained can be used not only as a desiccant for ships, but also as a dehydrating agent for removing moisture from organic solvents.

発明の効果 本発明の乾燥剤組成物は、加工が容易で、任意の形状に
成型できる。
Effects of the Invention The desiccant composition of the present invention is easy to process and can be molded into any shape.

本発明組成物の成型品は以下の特性を有するものである
The molded product of the composition of the present invention has the following characteristics.

1)高い吸湿力、保水力を有し、しかも腐食性、飛散性
、吸湿液化現象による液体漏洩もしくは水滴の発生など
を生じないために乾燥剤としての使用上の安全性、安定
性に優れている。
1) It has high hygroscopic and water-holding power, and is highly safe and stable when used as a desiccant because it is corrosive, scatters, and does not cause liquid leakage or water droplet generation due to moisture absorption and liquefaction phenomena. There is.

2)使用時に、従来の乾燥剤のように包装する必要がな
く、また袋状、容器状などの包材として成型されたもの
は、伝相自体が乾燥剤として働き、極めて合理的なもの
である。
2) When used, it does not need to be packaged like conventional desiccant agents, and when it is molded into packaging materials such as bags or containers, the denso itself acts as a desiccant agent, making it extremely rational. be.

3)吸湿効果が長時間持続する。3) Moisture absorption effect lasts for a long time.

4)製造及び加工が容易で、優れた工業生産性を有する
4) Easy to manufacture and process, and has excellent industrial productivity.

5)紫外線吸収に優れている(第1図参照)。5) Excellent ultraviolet absorption (see Figure 1).

以上のように本発明組成物の成型品は、従来の乾燥剤の
概念を変える画期的なもので食品、医薬品、化粧品、嗜
好品、精密機械、機械部品等の品質保護のための乾燥剤
又は吸湿性包材等として広範な用途を有するものである
As described above, the molded product of the composition of the present invention is an epoch-making product that changes the concept of conventional desiccants. Also, it has a wide range of uses as a hygroscopic packaging material.

実施例 以下実施例を示し、本発明の特徴とするところをより一
層明確にする。
EXAMPLES Examples will be shown below to further clarify the features of the present invention.

実施例1 ポリエチレン(密度0.92g/c弊)100重量部、
平均粒子径30μm程度の無水硫酸マグネシウム190
重量部及び滑剤としてステアリン酸1重量部を混合し、
実験用ミキシングロールにて130°Cで15分間加熱
混練して乾燥剤組成物を得た。この組成物を厚さ2m、
mのシートとし、打抜きカッターにて径10rnmのペ
レットを作製した。そして、これを試料とし吸水試験を
行った。
Example 1 100 parts by weight of polyethylene (density 0.92 g/c),
Anhydrous magnesium sulfate 190 with an average particle size of about 30 μm
parts by weight and 1 part by weight of stearic acid as a lubricant,
A desiccant composition was obtained by heating and kneading at 130° C. for 15 minutes using an experimental mixing roll. This composition was applied to a thickness of 2 m.
A sheet with a diameter of 10 nm was prepared using a punch cutter to produce pellets with a diameter of 10 nm. Then, a water absorption test was conducted using this as a sample.

その結果、吸水率が湿度90%では65%と高く、湿度
50%では33%、湿度20%では3%と低くなり、湿
度と吸水率がほぼ比例関係にあることがら調湿コントロ
ール性にも優れていることがわかり、この方面への応用
も可能である。
As a result, the water absorption rate is as high as 65% at 90% humidity, 33% at 50% humidity, and as low as 3% at 20% humidity.Since humidity and water absorption rate are almost proportional, it also improves humidity control. It was found to be excellent, and it is possible to apply it in this field.

実施例2 エチレン−酢酸ビニル共重合体(平均分子量31000
)100重量部、平均粒子径10.czm程度の無水硫
酸マグネシウム50重量部及び滑剤としてステアリン酸
1重量部を混合し、以下実施例1と同様にして乾燥剤組
成物を得、シートを試作後、プレスロールを用いポリエ
チレン(平均分子ff128000)とアルミニウム箔
でラミネートし、厚さ0.1mmのシートとし、加工し
て包装用袋を作製した。これを試料とし吸水試験を行っ
た。 また、この袋にネギ、ブロッコリー等の野菜を炭
酸ガスとともに封入し200Cで一週間放置したが、袋
内部には水滴、発汗等の現象は見られず、鮮度保持、吸
湿防止に効果があることが認められた。
Example 2 Ethylene-vinyl acetate copolymer (average molecular weight 31,000
) 100 parts by weight, average particle size 10. 50 parts by weight of anhydrous magnesium sulfate of about czm and 1 part by weight of stearic acid as a lubricant were mixed to obtain a desiccant composition in the same manner as in Example 1. After making a trial sheet, polyethylene (average molecular ff 128,000 ) and aluminum foil to form a sheet with a thickness of 0.1 mm, which was then processed to produce a packaging bag. A water absorption test was conducted using this as a sample. In addition, vegetables such as green onions and broccoli were sealed in this bag with carbon dioxide gas and left at 200C for a week, but no water droplets or sweating were observed inside the bag, indicating that it is effective in maintaining freshness and preventing moisture absorption. was recognized.

実施例3 エチレン−メチルメタクリレート(平均分子量3500
0)100重量部、平均粒子径6μm程度の硫酸マグネ
シウム3水塩・10重量部及び滑剤としてステアリン酸
1重量部を混合し、以下実施例1と同様にして乾燥剤組
成物を得、ベレットを作製後、押出機にて厚さ0.1.
mmのフィルムを作製し、これを試料として吸水試験を
行った。
Example 3 Ethylene-methyl methacrylate (average molecular weight 3500
0) Mix 100 parts by weight of magnesium sulfate trihydrate with an average particle size of about 6 μm and 1 part by weight of stearic acid as a lubricant to obtain a desiccant composition in the same manner as in Example 1. After production, the thickness is 0.1 mm using an extruder.
A film with a diameter of 1 mm was prepared and used as a sample for a water absorption test.

また、このフィルムに250〜500nmの波長の光を
照射し、透過率を求めた結果を第1図に示す。尚、図中
(A)はブランク、(B)は実施0 例3の試料の透過率曲線を表す。
Further, this film was irradiated with light having a wavelength of 250 to 500 nm, and the transmittance was determined. The results are shown in FIG. In the figure, (A) represents a blank, and (B) represents a transmittance curve of the sample of Example 3.

実施例4 ポリスチレン(平均分子量30000)100重量部、
平均粒子径3.5μmの硫酸マグネシウム1水塩(第2
図参照)5重量部及び発泡剤としてアゾイソブチルニト
リル0.5重量部を混合し、以下実施例1と同様に混練
して乾燥剤組成物を得た後、射出成型し発泡体を得た。
Example 4 100 parts by weight of polystyrene (average molecular weight 30,000),
Magnesium sulfate monohydrate (secondary
(see figure) and 0.5 parts by weight of azoisobutylnitrile as a blowing agent were mixed and kneaded in the same manner as in Example 1 to obtain a desiccant composition, which was then injection molded to obtain a foam.

これを試料として吸水試験を行った。A water absorption test was conducted using this as a sample.

実施例5 ポリ塩化ビニル(ペースト状、平均分子量1650)1
00重量部、平均粒子径10μmの無水硫酸マグネシウ
ム25重量部、可塑剤としてジオクチルフタレート80
重量部及び安定剤としてステアリン酸亜鉛2重量部を混
合し、実施例3と同様にして乾燥剤組成物を得、厚さ0
.1mmのフィルムを作製し、これを試料として吸水試
験を行った。
Example 5 Polyvinyl chloride (paste, average molecular weight 1650) 1
00 parts by weight, 25 parts by weight of anhydrous magnesium sulfate with an average particle size of 10 μm, and 80 parts by weight of dioctyl phthalate as a plasticizer.
parts by weight and 2 parts by weight of zinc stearate as a stabilizer to obtain a desiccant composition in the same manner as in Example 3.
.. A 1 mm film was prepared and used as a sample for a water absorption test.

比較例1及び2 実施例5における無水硫酸マグネシウムの代わりにシリ
カゲル(平均粒子径13μm)或いはゼオライト(平均
粒子径8μm)25重量部を用いて以下同様にフィルム
を作製し、これを試料として吸水試験を行った。
Comparative Examples 1 and 2 Films were prepared in the same manner using 25 parts by weight of silica gel (average particle size 13 μm) or zeolite (average particle size 8 μm) instead of anhydrous magnesium sulfate in Example 5, and water absorption tests were conducted using these as samples. I did it.

また、実施例5の場合の吸水率との比較を第3図に示す
。尚、図中(A)は実施例5、(B)は比較例2、(C
)は比較例1の試料を用いたものである。
Further, a comparison with the water absorption rate in the case of Example 5 is shown in FIG. In the figure, (A) is Example 5, (B) is Comparative Example 2, and (C
) uses the sample of Comparative Example 1.

[吸水試験] 」−記実施例1〜5、比較例1及び2で作製した試料を
それぞれ温度25℃、湿度90.50.20%の恒温槽
中に放置し、1.2.4.6.10.15.20日後の
吸水率を測定した。
[Water Absorption Test] - The samples prepared in Examples 1 to 5 and Comparative Examples 1 and 2 were left in a constant temperature bath at a temperature of 25°C and a humidity of 90.50.20%, and 1.2.4.6 .10.15.The water absorption rate was measured after 20 days.

吸水率は、試験前の試料自重に対する試験後の試料重量
の増加量を百分率で計算したものである。
The water absorption rate is calculated as the percentage increase in the weight of the sample after the test relative to the weight of the sample before the test.

その結果として、湿度90%のもののは第1表、■ ■ 湿度50%のものは第2表、 湿度20%のものは 第3表に示す。As a result, those with humidity of 90% are shown in Table 1, ■ ■ For those with humidity of 50%, see Table 2. 20% humidity It is shown in Table 3.

弗 表 3  Z 4 卯 3 表 実施例6 低密度ポリエチレン(LDPE:密度0.92g / 
ci、以下同様)100重量部及び平均粒子径4.59
μmの無水硫酸マグネシウム50重量部を混練押出成型
機を用いて、130℃で15分間ら 加熱混練してペレット状のものを得た。これをインフレ
ーション成型機により外層を高密度ポリエチレン(HD
PE:密度0.95g/cnf、以下同様)、内層をL
DPEとして共押出3層フィルム(IIDPE50μm
/ 50μm/ LDPE10μm)を作成した。
弗Table 3 Z 4 Rabbit 3 Table Example 6 Low density polyethylene (LDPE: density 0.92g /
ci, hereinafter the same) 100 parts by weight and average particle size 4.59
Pellets were obtained by heating and kneading 50 parts by weight of anhydrous magnesium sulfate having a particle diameter of 1.5 μm using a kneading extrusion molding machine at 130° C. for 15 minutes. The outer layer is made of high-density polyethylene (HD) using an inflation molding machine.
PE: Density 0.95g/cnf (same below), inner layer L
Coextruded three-layer film (IIDPE 50 μm
/50μm/LDPE10μm) was created.

この3層フィルム(50X50mm)を試料として温度
25℃、湿度75%の条件下で吸水試験を行った。その
結果を第4図中(A)に示す。
A water absorption test was conducted using this three-layer film (50 x 50 mm) as a sample under conditions of a temperature of 25° C. and a humidity of 75%. The results are shown in FIG. 4 (A).

実施例7 高重合度ポリアミド(ナイロン6、分子量16000)
:100重量部及び平均粒子径4.59μmの無水硫酸
マグネシウム50重量部を用い、以下実施例6と同様に
して3層フィルム(HDPE50μm150μm/LD
PEIOμm)を作成して吸水試験を行った。その結果
を第4図中(B)に示す。
Example 7 High polymerization degree polyamide (nylon 6, molecular weight 16000)
: 100 parts by weight and 50 parts by weight of anhydrous magnesium sulfate with an average particle size of 4.59 μm, a three-layer film (HDPE 50 μm 150 μm/LD
PEIOμm) was prepared and a water absorption test was conducted. The results are shown in FIG. 4 (B).

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、実施例3におけるフィルムの光透過1 八 率の曲線である。 第2図は、実施例4で用いた硫酸マグネシウムの粒度分
布測定結果を表す図である。 第3図は、実施例5、比較例1及び2の吸水試験におけ
る経過日数−吸水率曲線図である。 第4図は、実施例6及び7の吸水試験における経過日数
−吸水率曲線図である。 (以 上) 7 昔 く肝 ペ q呆斗 胃45目 惰ト ペ
FIG. 1 is a curve of light transmittance of the film in Example 3. FIG. 2 is a diagram showing the particle size distribution measurement results of magnesium sulfate used in Example 4. FIG. 3 is a graph of elapsed days-water absorption rate curve in the water absorption test of Example 5 and Comparative Examples 1 and 2. FIG. 4 is a graph of elapsed days versus water absorption rate curve in the water absorption test of Examples 6 and 7. (That's all) 7. A long time ago.

Claims (1)

【特許請求の範囲】 [1]熱可塑性樹脂100重量部に対し、式MgSO_
4・nH_2O(但し0≦n≦3)で表される硫酸マグ
ネシウム、酸化アルミニウム、酸化バリウム、酸化カル
シウム及び酸化ケイ素の少なくとも一種5〜400重量
部を含有する乾燥剤組成物。 [2]組成物が発泡剤を含有する請求項[1]に記載の
乾燥剤組成物。
[Claims] [1] For 100 parts by weight of thermoplastic resin, the formula MgSO_
A desiccant composition containing 5 to 400 parts by weight of at least one of magnesium sulfate, aluminum oxide, barium oxide, calcium oxide, and silicon oxide represented by 4.nH_2O (0≦n≦3). [2] The desiccant composition according to claim [1], wherein the composition contains a foaming agent.
JP1254326A 1989-05-23 1989-09-28 Desiccant composition Expired - Fee Related JPH0753222B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP90109700A EP0400460B1 (en) 1989-05-23 1990-05-22 Moisture-absorbent compositions
DE69018312T DE69018312T2 (en) 1989-05-23 1990-05-22 Moisture absorbent compositions.
US07/526,817 US5078909A (en) 1989-05-23 1990-05-22 Moisture-absorbent compositions and molded items

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP13043189 1989-05-23
JP1-130431 1989-05-23
JP1259429A JPH0796092B2 (en) 1989-05-23 1989-10-03 Desiccant molding

Publications (2)

Publication Number Publication Date
JPH03109916A true JPH03109916A (en) 1991-05-09
JPH0753222B2 JPH0753222B2 (en) 1995-06-07

Family

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JP1259429A Expired - Lifetime JPH0796092B2 (en) 1989-05-23 1989-10-03 Desiccant molding

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP1259429A Expired - Lifetime JPH0796092B2 (en) 1989-05-23 1989-10-03 Desiccant molding

Country Status (1)

Country Link
JP (2) JPH0753222B2 (en)

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JPH03109917A (en) * 1989-05-23 1991-05-09 Tomita Seiyaku Kk Formed desiccant
JPH0595871U (en) * 1992-06-09 1993-12-27 佐々木化学薬品株式会社 Hygroscopic packaging material
WO2003090905A1 (en) * 2002-04-26 2003-11-06 Japan Gore-Tex Inc. Molded adsorbent and adsorbent unit
JP2010517880A (en) * 2007-02-02 2010-05-27 アルカン グローバル ファーマシューティカル パッケージング インコーポレイテッド Container for moisture sensitive products
JP2010527308A (en) * 2007-03-29 2010-08-12 マルチソーブ テクノロジーズ インコーポレイティド Adsorbent composite barrier selection method for packaging applications.
WO2011052433A1 (en) * 2009-10-26 2011-05-05 日本クラウンコルク株式会社 Moisture-absorbing resin composition and molded products thereof
WO2013011941A1 (en) * 2011-07-15 2013-01-24 富田製薬株式会社 Magnesium sulfate desiccant and method for producing same
JP2014091782A (en) * 2012-11-02 2014-05-19 Hitachi Chemical Co Ltd Prepreg preservation method, laminate, and laminate packaging material
US8853124B2 (en) 2005-01-21 2014-10-07 Multisorb Technologies, Inc. Resin bonded sorbent
US10793696B2 (en) 2015-01-23 2020-10-06 Tomita Pharmaceutical Co., Ltd. Polyolefin composition containing hygroscopic inorganic filler, and molded body using said polyolefin composition

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JP3474295B2 (en) * 1995-02-15 2003-12-08 富士写真フイルム株式会社 Humidity control / gas absorbing molded product
CZ331597A3 (en) * 1995-04-19 1999-07-14 Capitol Vial Inc. Dessicant inserted in an enclosed container
JP2001009985A (en) 1999-07-02 2001-01-16 Hisamitsu Pharmaceut Co Inc Packaging bag for sticking agent and packaged sticking agent
JP2002347714A (en) * 2001-05-28 2002-12-04 Asahi Kasei Corp Method for packaging hygroscopic film
EP1323468A1 (en) * 2001-12-31 2003-07-02 Grace GmbH &amp; Co. KG Adsorbing material comprised of porous functional solid incorporated in a polymer matrix
JP3979542B1 (en) 2006-08-30 2007-09-19 佐々木化学薬品株式会社 Desiccant composition, desiccant molded product, equilibrium humidity control method thereof, and control method of equilibrium humidity maintenance time
JP5288934B2 (en) 2008-08-08 2013-09-11 三菱鉛筆株式会社 Liquid applicator
JP5388006B2 (en) * 2009-02-27 2014-01-15 共同印刷株式会社 Desiccant-containing multilayer film and electronic device provided with the film
JP2011067809A (en) * 2009-08-31 2011-04-07 Shinten Kogyo Kk Oil absorbent and method of preserving the same
US8785183B2 (en) * 2010-09-21 2014-07-22 Biogaia Ab Active plastic material in oil

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JPH0753222B2 (en) * 1989-05-23 1995-06-07 富田製薬株式会社 Desiccant composition

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JPS6168119A (en) * 1984-09-11 1986-04-08 Shinryo Air Conditioning Co Ltd Dehumidifier and dehumidifying method using said dehumidifier
JPS61120638A (en) * 1984-11-16 1986-06-07 Marutani Kakoki Kk Adsorbing body for charging package

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03109917A (en) * 1989-05-23 1991-05-09 Tomita Seiyaku Kk Formed desiccant
JPH0595871U (en) * 1992-06-09 1993-12-27 佐々木化学薬品株式会社 Hygroscopic packaging material
WO2003090905A1 (en) * 2002-04-26 2003-11-06 Japan Gore-Tex Inc. Molded adsorbent and adsorbent unit
US7300500B2 (en) 2002-04-26 2007-11-27 Japan Gore-Tex, Inc. Adsorbent-formed object and an adsorbent unit
US8853124B2 (en) 2005-01-21 2014-10-07 Multisorb Technologies, Inc. Resin bonded sorbent
JP2010517880A (en) * 2007-02-02 2010-05-27 アルカン グローバル ファーマシューティカル パッケージング インコーポレイテッド Container for moisture sensitive products
US8524115B2 (en) 2007-03-29 2013-09-03 Multisorb Technologies, Inc. Adsorptive composite barriers for packaging applications
JP2010527308A (en) * 2007-03-29 2010-08-12 マルチソーブ テクノロジーズ インコーポレイティド Adsorbent composite barrier selection method for packaging applications.
WO2011052433A1 (en) * 2009-10-26 2011-05-05 日本クラウンコルク株式会社 Moisture-absorbing resin composition and molded products thereof
US9205960B2 (en) 2009-10-26 2015-12-08 Dainichiseika Color & Chemicals Mfg. Co., Ltd. Moisture-absorbing resin composition and molded product thereof
WO2013011941A1 (en) * 2011-07-15 2013-01-24 富田製薬株式会社 Magnesium sulfate desiccant and method for producing same
JP5272260B1 (en) * 2011-07-15 2013-08-28 富田製薬株式会社 Magnesium sulfate desiccant and method for producing the same
JP2014091782A (en) * 2012-11-02 2014-05-19 Hitachi Chemical Co Ltd Prepreg preservation method, laminate, and laminate packaging material
US10793696B2 (en) 2015-01-23 2020-10-06 Tomita Pharmaceutical Co., Ltd. Polyolefin composition containing hygroscopic inorganic filler, and molded body using said polyolefin composition

Also Published As

Publication number Publication date
JPH03109917A (en) 1991-05-09
JPH0753222B2 (en) 1995-06-07
JPH0796092B2 (en) 1991-05-09

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