JPS5820971B2 - Water absorbent resin composition - Google Patents

Water absorbent resin composition

Info

Publication number
JPS5820971B2
JPS5820971B2 JP1973880A JP1973880A JPS5820971B2 JP S5820971 B2 JPS5820971 B2 JP S5820971B2 JP 1973880 A JP1973880 A JP 1973880A JP 1973880 A JP1973880 A JP 1973880A JP S5820971 B2 JPS5820971 B2 JP S5820971B2
Authority
JP
Japan
Prior art keywords
water
resin composition
composition
polyvinylpyrrolidone
eva
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
Application number
JP1973880A
Other languages
Japanese (ja)
Other versions
JPS56116737A (en
Inventor
西崎克巳
鈴木祐二
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.)
Tosoh Corp
Original Assignee
Toyo Soda Manufacturing 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 Toyo Soda Manufacturing Co Ltd filed Critical Toyo Soda Manufacturing Co Ltd
Priority to JP1973880A priority Critical patent/JPS5820971B2/en
Publication of JPS56116737A publication Critical patent/JPS56116737A/en
Publication of JPS5820971B2 publication Critical patent/JPS5820971B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は、吸水性樹脂組成物に関し、さらに詳シくハ、
エチレン−酢酸ビニル共重合体けん化物(以下EVAけ
ん化物と略する)き水溶性高分子とからなる吸水性樹脂
組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a water-absorbing resin composition, and more specifically, c.
The present invention relates to a water-absorbing resin composition comprising a saponified ethylene-vinyl acetate copolymer (hereinafter abbreviated as saponified EVA) and a water-soluble polymer.

プラスチック材料の用途の多様化に伴い、もともと疎水
性であった熱可塑性樹脂に親水性、吸水性を付与するこ
とが要求されるようになってきた。
With the diversification of uses for plastic materials, it has become necessary to impart hydrophilicity and water absorption properties to thermoplastic resins, which were originally hydrophobic.

このような疎水性樹脂の改質は、通常、次の三方法によ
って行なうことができる。
Such modification of hydrophobic resins can usually be carried out by the following three methods.

1)高分子反応による親水基の導入 2)親水性化合物の混合 3)親水性高分子の混合 この内、■)の方法は、一般的に価格の上昇はさけられ
ず、また、親水性の多量の導入が困難なため、大巾な改
良は期待できないという欠点がある。
1) Introduction of hydrophilic groups by polymer reaction 2) Mixing of hydrophilic compounds 3) Mixing of hydrophilic polymers Among these methods, method The drawback is that large-scale improvements cannot be expected because it is difficult to introduce in large quantities.

2)の方法は、手軽に行なえ、しかも場合によっては安
価に行なえるので、親水性を少しでも改良したいときに
は有用である。
Method 2) is easy to carry out and can be carried out at low cost in some cases, so it is useful when it is desired to improve the hydrophilicity even slightly.

しかし、親水性化合物を熱可塑性樹脂に混合すると、一
般的には機械的性質が低下するなどの欠点があるため、
多量に混合することには問題がある。
However, mixing hydrophilic compounds with thermoplastic resins generally has drawbacks such as a decrease in mechanical properties.
There are problems with mixing large quantities.

3)の方法も2)の方法と同様な欠点を有する。Method 3) also has the same drawbacks as method 2).

そればかりか、親水性高分子は、通常、熱可塑性ではな
いため、これを熱塑性樹脂と共に混合すると分散が悪く
、熱可塑性樹脂の透明度を損うことも多い。
Moreover, since hydrophilic polymers are usually not thermoplastic, mixing them with thermoplastic resins results in poor dispersion and often impairs the transparency of the thermoplastic resin.

このように熱可塑性樹脂に、他の性質を損うことなく、
親水性、吸水性を付与することは容易な技術ではなかっ
た。
In this way, thermoplastic resins can be added without sacrificing other properties.
It was not an easy technique to impart hydrophilicity and water absorption properties.

本発明者らは、先にEVAけん化物と水溶性高分子との
ブレンドを研究していたところ、偶然、ある種のEVA
けん化物とある種の水溶性高分子をブレンドすると、も
とのEVAけん化物の性質を損うことなく、均一にまじ
りあい、しかも、水溶性高分子を多量にブレンドするこ
ともできることを見出した。
The present inventors had previously researched blends of saponified EVA and water-soluble polymers, and happened to discover that a certain type of EVA
We discovered that when a saponified material is blended with a certain type of water-soluble polymer, they are mixed uniformly without impairing the properties of the original saponified EVA material, and it is also possible to blend a large amount of the water-soluble polymer. .

すなわち、EVAけん化物と水溶性高分子とのブレンド
により、吸水性のある樹脂組成物が容易に得られたので
ある。
That is, a water-absorbing resin composition was easily obtained by blending the saponified EVA and the water-soluble polymer.

そればかりか、該樹脂組成物は、金属とか、他の高分子
材料のための良好な接着剤成分ともなり得ることがわか
った。
Moreover, it has been found that the resin composition can also be a good adhesive component for metals and other polymeric materials.

こうして該樹脂組成物は、吸水性および接着性をあわせ
もつ組成物として、フィルム、成形品、発泡体、接着剤
などとして使用されつつあるが、水にふれたり、水中で
使用したりすると、含まれている水溶性高分子が水によ
り徐々に抽出され、該組成物の性能が時間とともに変化
することがあることがわかってきた。
In this way, the resin composition is being used as a composition having both water absorption and adhesive properties in films, molded products, foams, adhesives, etc. However, if it comes into contact with water or is used in water, it may contain moisture. It has been found that the water-soluble polymer contained in the composition may be gradually extracted by water, and the performance of the composition may change over time.

本発明者らは、このような問題点を解決するために、鋭
意研究を行なった結果、水溶性高分子として、ポリアク
リル酸とポリビニルピロリドンを組合せて用いれば、吸
水性、接着性が良好で、しかも、水によって抽出される
こともないことを見出した。
In order to solve these problems, the present inventors conducted extensive research and found that using a combination of polyacrylic acid and polyvinylpyrrolidone as water-soluble polymers has good water absorption and adhesive properties. Moreover, they found that it was not extracted by water.

すなわち、本発明は、EVAけん化物、ポリアクリル酸
およびポリビニルピロリドンを必須の構成成分とする新
規な組成物に関する。
That is, the present invention relates to a novel composition containing saponified EVA, polyacrylic acid, and polyvinylpyrrolidone as essential components.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明にていうEVAけん化物は、80〜98モル係の
エチレンを含有するEVAを、酸またはアルカリ触媒を
用いる公知の方法で、けん化することによって得られる
The saponified EVA according to the present invention is obtained by saponifying EVA containing 80 to 98 moles of ethylene by a known method using an acid or alkali catalyst.

けん化度は20チ以上であることが好ましい。The degree of saponification is preferably 20 degrees or more.

けん化度が低くヒドロキシル基の含量が少なすぎると水
溶性高分子と均一に混合できなくなり、透明性とか、機
械的性質の低下を引き起こす。
If the degree of saponification is low and the content of hydroxyl groups is too small, it will not be possible to mix uniformly with the water-soluble polymer, resulting in a decrease in transparency and mechanical properties.

EVAけん化物とともに用いられるポリアクリル酸とポ
リビニルピロリドンに必要な性状は、水に可溶であると
いうことだけである。
The only property required for the polyacrylic acid and polyvinylpyrrolidone used with EVA saponification is that they are soluble in water.

分子量は室温で水アメ状を示す1000程度のもの以上
であれば、本発明の効果を十分に発揮することができる
The effects of the present invention can be fully exhibited as long as the molecular weight is about 1000 or more and exhibits a starch syrup-like appearance at room temperature.

これらの水溶性高分子の使用量は、EVAけん化物10
0重量部に対し、それぞれ2〜200重量部の範囲が好
ましい。
The amount of these water-soluble polymers used is 10% of the EVA saponification product.
The range of 2 to 200 parts by weight is preferable for 0 parts by weight.

ポリアクリル酸とポリビニルピロリドンの比率は、1対
10から10対1の範囲であれば、その目的に応じて変
えることができる。
The ratio of polyacrylic acid to polyvinylpyrrolidone can be varied depending on the purpose as long as it is in the range of 1:10 to 10:1.

EVAけん化物と水溶性高分子との混線は、加熱ロール
、バンバリーなどの公知の混線装置を用いて行なわれる
The EVA saponification product and the water-soluble polymer are mixed using a known mixing device such as a heating roll or a Banbury.

この際、高分子量の水溶性高分子は水溶液の状態で混練
装置に供給するのが均一に混線できるので好ましい。
At this time, it is preferable to supply the high molecular weight water-soluble polymer to the kneading device in the form of an aqueous solution, since uniform mixing can be achieved.

また、混練に際し、酸化防止剤、熱安定剤、帯電防止剤
、滑剤、加工助剤等の公知の添加剤を加えることが好ま
しい。
Further, during kneading, it is preferable to add known additives such as antioxidants, heat stabilizers, antistatic agents, lubricants, and processing aids.

EVAけん化物と水溶性高分子とを、上記のように混練
することによって得られた組成物は、各種の公知の成形
加工機械を用いて、フィルム状とかモールド状で使用す
ることができる。
The composition obtained by kneading the saponified EVA and the water-soluble polymer as described above can be used in the form of a film or a mold using various known molding machines.

その場合には、周囲の湿度に応じて吸湿したり、乾燥し
たりするが、発汗は観察されない。
In that case, the skin absorbs moisture or dries depending on the surrounding humidity, but no sweating is observed.

また、本発明の組成分は他の熱可塑性樹脂とブレンドし
たり、積層したりして、それらを改質する目的で使用す
ることもできる。
Further, the composition of the present invention can be blended or laminated with other thermoplastic resins and used for the purpose of modifying them.

以上述べてきたように、本発明は、水溶性高分子との混
練によって吸水性の組成物を得ることに関する。
As described above, the present invention relates to obtaining a water-absorbing composition by kneading with a water-soluble polymer.

しかしながら、本発明の組成物による効果は、吸水性の
付与のみならず、以下に記すように、EvAけん化物の
接着性の改良をももたらす。
However, the effect of the composition of the present invention is not only to provide water absorption, but also to improve the adhesion of saponified EvA as described below.

すなわち、EVAけん化物のセルロース系物質や金属に
対する接着性は、従来より知られているが、ポリアクリ
ル酸とかポリビニルピロリドンとのブレンドにより、セ
ルロース系物質や金属に対;する接着性がより向上する
のである。
In other words, the adhesion of saponified EVA to cellulosic substances and metals has been known for a long time, but by blending it with polyacrylic acid or polyvinylpyrrolidone, the adhesion to cellulosic substances and metals is further improved. It is.

このように本発明は、吸水性に富む組成物を手軽に提供
することから、合成樹脂の用途を更に拡大することがで
き、極めて重要であると考えられる。
As described above, the present invention can further expand the applications of synthetic resins because it easily provides a composition with high water absorption properties, and is therefore considered to be extremely important.

以下本発明の実施例について説明する。Examples of the present invention will be described below.

実施例 1 エチレン含量が88.6モル係でメルトインデックス(
MI )が18.!7/10分のエチレン−酢酸ビニル
共重合体6kg、メタノール18kg、水酸化ナトリウ
ム700gを507反応器に仕込み、攪拌しながら70
°Cで3時聞けん化反応を行った。
Example 1 Melt index (
MI ) is 18. ! 6 kg of 7/10 ethylene-vinyl acetate copolymer, 18 kg of methanol, and 700 g of sodium hydroxide were charged into a 507 reactor, and the 70
The saponification reaction was carried out at °C for 3 hours.

反応終了後生成分を濾過、乾燥し、エチレン88.6モ
ル係、酢酸ビニル1.0モル係、ビニルアルコール10
.4モル係からなるEVAけん化物4.9kgを得た。
After the reaction was completed, the product was filtered and dried to give 88.6 moles of ethylene, 1.0 moles of vinyl acetate, and 10 moles of vinyl alcohol.
.. 4.9 kg of saponified EVA consisting of 4 moles was obtained.

このEVAけん化物30.9とポリアクリル酸の30係
水溶液(和光紬薬製)160gとポリビニルピロリドン
22gを170℃で25分間ロール混練を行ない、冷却
後粉砕機で粉末とした。
This saponified EVA 30.9, 160 g of a 30% aqueous solution of polyacrylic acid (manufactured by Wako Tsumugi Pharmaceutical Co., Ltd.), and 22 g of polyvinylpyrrolidone were roll-kneaded at 170° C. for 25 minutes, and after cooling, the mixture was powdered using a pulverizer.

〈吸水性の測定〉 該粉末を一定量精秤し、水を底部に入れたデシケータ−
中に室温で一日放置し、増加した重量(支)で吸水性を
表わした。
<Measurement of water absorption> Precisely weigh a certain amount of the powder and place it in a desiccator with water in the bottom.
The water absorbency was expressed by the increased weight (weight) after being left at room temperature for one day.

く水溶性ポリマーの抽出率の測定〉 該粉末約5gを精秤し、10m1の水とともに室温で一
日放置し、濾過、水洗後50℃で48時間真空乾燥を行
ない秤量する。
Measurement of Extraction Rate of Water-Soluble Polymer> Approximately 5 g of the powder is accurately weighed, left for one day at room temperature with 10 ml of water, filtered, washed with water, dried under vacuum at 50° C. for 48 hours, and weighed.

減少した重量は水によって抽出された水溶性ポリマーに
相当するので、抽出前の粉末中の水溶性ポリマーの重量
に対する百分率を計算し、抽出率とした。
Since the reduced weight corresponds to the water-soluble polymer extracted by water, the percentage with respect to the weight of the water-soluble polymer in the powder before extraction was calculated and taken as the extraction rate.

上述のようにして測定した吸水性は16.3%で水によ
る抽出率は0.6%であった。
The water absorption measured as described above was 16.3%, and the extraction rate with water was 0.6%.

比較例 1 実施例1において、ポリビニルピロリドンを用いないで
、同様にロール混線を行ない、粉砕して粉末を作った。
Comparative Example 1 In Example 1, a roll cross-wire was carried out in the same manner as in Example 1 without using polyvinylpyrrolidone, and the material was pulverized to form a powder.

この粉末の吸水性と抽出率を実施例1と同様にして測定
したところ、吸水性が10.2饅で、抽出率は33.5
%であった。
When the water absorption and extraction rate of this powder were measured in the same manner as in Example 1, the water absorption was 10.2 m and the extraction rate was 33.5.
%Met.

組成物に含まれていたポリアクリル酸のうち、約1/3
が水によってとかし出されてしまうことがわかる。
Approximately 1/3 of the polyacrylic acid contained in the composition
You can see that it is washed out by water.

実施例 2 実施例1で用いたEVAけん化物の代りに、エチレン8
8.6モル係、酢酸ビニル8.0モル宏ビニルアルコー
ル3.4モル係を含み、MIが25g/10分のEVA
けん化物50gを用い、ポリアクリル酸の30%水溶液
83.9とポリビニルピロリドン25gとともに170
℃で25分間ロール混線を行なった。
Example 2 Instead of the saponified EVA used in Example 1, ethylene 8
EVA containing 8.6 moles of vinyl acetate, 8.0 moles of vinyl acetate and 3.4 moles of vinyl alcohol, and an MI of 25 g/10 min.
Using 50 g of saponified material, 170 g of 30% aqueous solution of polyacrylic acid and 25 g of polyvinylpyrrolidone were added.
Roll crossing was carried out at ℃ for 25 minutes.

実施例1と同様に粉末化し、吸水性と水による抽出率を
測定したところ、11.3%と1.2%という値が得ら
れた。
When it was powdered in the same manner as in Example 1 and the water absorption and water extraction rate were measured, values of 11.3% and 1.2% were obtained.

比較のために、ポリビニルピロリドンを用いないで同様
にロール混練を行ない、粉末の吸水性と抽出率を測定し
たところ、3.4%と10.8%であった。
For comparison, roll kneading was carried out in the same manner without using polyvinylpyrrolidone, and the water absorption and extraction rate of the powder were measured and found to be 3.4% and 10.8%.

Claims (1)

【特許請求の範囲】 1 エチレン−酢酸ビニル共重合体けん化物とポリアク
リル酸とポリビニルピロリドンとからなる吸水性樹脂組
成物。 2 エチレン含量が80〜98モル係の範囲内にあり、
酢酸基の20%以上を水酸基に変換したエチレン−酢酸
ビニル共重合体けん化物を用いる、特許請求の範囲第1
項の組成物。 3 エチレン−酢酸ビニル共重合体けん化物100重量
部に対し、ポリアクリル酸を2〜200重量部ト重量ヒ
トポリビニルピロリドン00重量部用いる、特許請求の
範囲第1または2項の組成物。
[Scope of Claims] 1. A water-absorbing resin composition comprising a saponified ethylene-vinyl acetate copolymer, polyacrylic acid, and polyvinylpyrrolidone. 2. The ethylene content is within the range of 80 to 98 moles,
Claim 1, which uses a saponified ethylene-vinyl acetate copolymer in which 20% or more of the acetate groups are converted to hydroxyl groups.
composition of the term. 3. The composition according to claim 1 or 2, wherein 2 to 200 parts by weight of polyacrylic acid and 00 parts by weight of human polyvinylpyrrolidone are used per 100 parts by weight of saponified ethylene-vinyl acetate copolymer.
JP1973880A 1980-02-21 1980-02-21 Water absorbent resin composition Expired JPS5820971B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1973880A JPS5820971B2 (en) 1980-02-21 1980-02-21 Water absorbent resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1973880A JPS5820971B2 (en) 1980-02-21 1980-02-21 Water absorbent resin composition

Publications (2)

Publication Number Publication Date
JPS56116737A JPS56116737A (en) 1981-09-12
JPS5820971B2 true JPS5820971B2 (en) 1983-04-26

Family

ID=12007668

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1973880A Expired JPS5820971B2 (en) 1980-02-21 1980-02-21 Water absorbent resin composition

Country Status (1)

Country Link
JP (1) JPS5820971B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6146770A (en) * 1984-08-14 1986-03-07 Fuji Heavy Ind Ltd Side rail round structure in automobile
JPS6230977U (en) * 1985-08-09 1987-02-24
JPS6320606Y2 (en) * 1981-12-09 1988-06-08
JPH0534275Y2 (en) * 1986-12-26 1993-08-31
JPH0534276Y2 (en) * 1986-12-26 1993-08-31

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6320606Y2 (en) * 1981-12-09 1988-06-08
JPS6146770A (en) * 1984-08-14 1986-03-07 Fuji Heavy Ind Ltd Side rail round structure in automobile
JPS6230977U (en) * 1985-08-09 1987-02-24
JPH0534275Y2 (en) * 1986-12-26 1993-08-31
JPH0534276Y2 (en) * 1986-12-26 1993-08-31

Also Published As

Publication number Publication date
JPS56116737A (en) 1981-09-12

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