JPS60258237A - Resin composition swelling with water - Google Patents

Resin composition swelling with water

Info

Publication number
JPS60258237A
JPS60258237A JP11407984A JP11407984A JPS60258237A JP S60258237 A JPS60258237 A JP S60258237A JP 11407984 A JP11407984 A JP 11407984A JP 11407984 A JP11407984 A JP 11407984A JP S60258237 A JPS60258237 A JP S60258237A
Authority
JP
Japan
Prior art keywords
water
elastomer
resin composition
added
resin
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.)
Pending
Application number
JP11407984A
Other languages
Japanese (ja)
Inventor
Akio Koyama
明夫 小山
Osamu Aoyanagi
青柳 收
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.)
PLUS TEKU KK
Original Assignee
PLUS TEKU KK
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 PLUS TEKU KK filed Critical PLUS TEKU KK
Priority to JP11407984A priority Critical patent/JPS60258237A/en
Publication of JPS60258237A publication Critical patent/JPS60258237A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:A composition that is obtained by adding a nonionic surfactant of ethylene oxide condensation product to a mixture of a high water-absorbing resin and an elastomer, thus giving moldings good in both water absorption and rapid expansion by extrusion. CONSTITUTION:100pts.wt. of a resin composition containing a high water-absorption resin and an elastomer, are added to 0.5-20pts.wt. of a nonionic surfactant of ethylene oxide polycondensation product. The weight ratio of the water-absorption polymer to the elastomer is 30/70-70/30. An example of the nonionic surfactant is water-soluble polyoxyethylene alkyl ether.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は工業用資材、農業用資材、土木建築用資材、玩
具、医療関連品などの広い用途に適し、すぐれた吸水力
を有するとともに吸収した水を放出する能力をもつ水膨
張性樹脂組成物に関するものである。
[Detailed Description of the Invention] Industrial Application Field The present invention is suitable for a wide range of applications such as industrial materials, agricultural materials, civil engineering and construction materials, toys, medical-related products, etc., and has excellent water absorption ability and absorbs water. This invention relates to a water-swellable resin composition that has the ability to release.

従来の技術 自重の数百倍以上の水を吸収する能力をもった高吸水性
樹脂はよく知られて居す、衛生材料、地質改良剤などの
用途に注目されている。
BACKGROUND OF THE INVENTION Superabsorbent resins, which have the ability to absorb several hundred times more water than their own weight, are well known and are attracting attention for their uses as sanitary materials and geological improvement agents.

また、高吸水性樹脂は一般に粉末状であり。Furthermore, superabsorbent resins are generally in powder form.

これをエラストマ即ち合成樹脂やゴム類に配合し更に可
塑剤、滑剤などを加えて成形品と用途が期待されている
It is expected to be used in molded products by blending it with elastomers, that is, synthetic resins and rubbers, and adding plasticizers, lubricants, etc.

しかしながら、高吸水性樹脂を単にエラストマに配合し
て押出または射出成形法によシ成形品としたものでは期
待した水吸収能力が得られないばかりか、水に接触した
とき速やかに吸収し急速に膨張するという高吸水性樹脂
の特性を発揮することができず、特にこの傾向は射出成
形法による成形品に著しい。
However, if a super absorbent resin is simply blended with an elastomer and molded into a molded product by extrusion or injection molding, not only will it not be possible to obtain the expected water absorption ability, but it will also quickly absorb water when it comes into contact with water. The property of superabsorbent resins, which is swelling, cannot be exhibited, and this tendency is particularly noticeable in molded products made by injection molding.

発明が解決しようとする問題点 本、発明は高吸水性樹脂を配合したエラストマを射出成
形法によシ成形品としたものがもつ水吸収能力、急速膨
張性に劣るという欠点を除去し、すぐれた水吸収性と@
、速膨張性とを具えた成形品を作ることができ、従って
広い分野で実用化が具体的に期待される水膨張性樹脂組
成物を提供するものである。
Problems to be Solved by the Invention The present invention eliminates the disadvantages of poor water absorption ability and poor rapid expansion properties of elastomers blended with super absorbent resin and molded by injection molding, and provides an excellent solution. Water absorption and @
The object of the present invention is to provide a water-swellable resin composition that can be used to produce molded articles with rapid expansion properties and is therefore expected to be put to practical use in a wide range of fields.

問題点を解決するための手段 本発明にあっては、高吸水性樹脂をエラストマに配合し
た樹脂組成物において、酸化エチレン縮金物系の非イオ
ン界面活性剤を添加したことによシ前述の問題点を解決
した。
Means for Solving the Problems In the present invention, the above-mentioned problems are solved by adding an ethylene oxide metal condensate-based nonionic surfactant to a resin composition in which a super absorbent resin is blended with an elastomer. Resolved the point.

囲ち、従来の樹脂組成物で作られた成形品は表面にエラ
ストマの被膜が作られやすく。
However, molded products made from conventional resin compositions tend to have an elastomer coating formed on their surfaces.

これが水の浸透を妨げているものであることが観察の結
果判った。干して1本発明は、成形性を阻害しないとと
もに表面の被膜に水とのすぐれた親和性を与える添加剤
として酸化エチレン縮合物系の非イオン界面活性剤が有
効であることを見出して完成したものである。
As a result of observation, it was found that this was what was preventing water from penetrating. The present invention was completed based on the discovery that an ethylene oxide condensate-based nonionic surfactant is effective as an additive that does not inhibit moldability and gives the surface coating an excellent affinity for water. It is something.

実施態様 1 本発明の水膨張性樹脂組成物を構成する高吸水性樹脂と
しては、デンプン系、セルロース系2合成ポリマ系に大
別される既知のものを用いることができる。これらはい
ずれも水溶性樹脂の分子の一部を架橋して親水性と高い
浸透圧とをもたせたものであシ、デンプン系およびセル
ロース系のものはデンプン、セルロースとアルリルニト
リル、メチルメタクリレート、アクリル酸、アクリルア
ミド、酢酸ビニルなどとのクラフト重合物1合成ポリマ
系のものは変性ポリビニルアルコール、架橋ポリアクリ
ル酸、アクリル酸−多官能モノマー疎水性モノマの共重
合物、ビニルアルコール−アクリル酸エステルのブロッ
ク共重合物が例示される。
Embodiment 1 As the superabsorbent resin constituting the water-swellable resin composition of the present invention, known resins broadly classified into starch type, cellulose type, and synthetic polymer type can be used. All of these are made by cross-linking a part of the molecules of water-soluble resins to give them hydrophilicity and high osmotic pressure. Craft polymers with acrylic acid, acrylamide, vinyl acetate, etc.1 Synthetic polymers include modified polyvinyl alcohol, crosslinked polyacrylic acid, copolymers of acrylic acid with polyfunctional monomers and hydrophobic monomers, and copolymers of vinyl alcohol with acrylic acid esters. An example is a block copolymer.

また、前記の高吸水性樹脂が配合されるエラストマとし
ては、塩化ビニル樹脂、ウレタン樹脂、エチレン・酢酸
ビニル共重合体、エチレン・プロピレン共重合体などの
熱可塑性合成樹脂および天然ゴム、クロロピレン。
Elastomers to which the superabsorbent resin is blended include thermoplastic synthetic resins such as vinyl chloride resin, urethane resin, ethylene/vinyl acetate copolymer, ethylene/propylene copolymer, natural rubber, and chloropyrene.

FPDMなどのゴムが例示される。Rubber such as FPDM is exemplified.

尚、高吸水性樹脂の配合割合を大きくすれば膨張性が向
上することは自明であるが、配合割合を極度に大きくす
ると成形性が低下するので、膨張性と成形性とを考慮し
て高吸水性樹脂とエラストマとの配合割合を重量比で3
o : 70乃至70 : 30好ましくは50 : 
so乃至6o:4o程度の範囲とする。
It is obvious that increasing the blending ratio of super absorbent resin will improve the expandability, but if the blending ratio is extremely increased, the moldability will decrease, so take into consideration the expandability and moldability. The blending ratio of water absorbent resin and elastomer is 3 by weight.
o: 70 to 70: 30 preferably 50:
The range is from so to about 6:4o.

次に、酸化エチレン縮金物系の非イオン界面活性剤とし
ては、ポリオキシエチレンアルキルエーテル、ポリオキ
シエチレンアルキルフェノールエーテル、ポリオキシエ
チレンソルビタン脂肪酸エステル、ポリオキシェチレ7
脂肪酸エステル、オキシエチレン・オキシプロピレンプ
ロツ、クポリマ、ポリオキシエチレンアルキルアミンな
どが例示される。
Next, examples of nonionic surfactants based on ethylene oxide condensates include polyoxyethylene alkyl ether, polyoxyethylene alkylphenol ether, polyoxyethylene sorbitan fatty acid ester, and polyoxyethylene 7
Examples include fatty acid esters, oxyethylene/oxypropylene proteases, cupolymers, and polyoxyethylene alkylamines.

ここで、界面活性剤を利用する場合の指標としてその分
子に含まれている親水性部と親油性部とのバランスを数
値化し、界面活性の度合いや溶解度などの指標としたも
のが便宜的に受入れられている。この指標はHLB(H
ydrophile Lipophile Ba1an
ce )と称され。
Here, as an index when using a surfactant, it is convenient to quantify the balance between the hydrophilic part and lipophilic part contained in the molecule, and use it as an index of the degree of surface activity and solubility. It is accepted. This indicator is HLB (H
hydrophile Lipophile Ba1an
ce).

非イオン界面活性剤のうちでHLB=1θ〜2oのもの
は水溶性、 HLB = 5〜9のものは水分散性、 
HLB = 1〜4のものは油溶性であp、従って本発
明に適する界面活性剤はHLB =10〜20のもので
あって、これを添加した樹脂組成物は水に接触したとき
HLBが小さいものと比較して急速に膨張することが容
易に理解される。
Among nonionic surfactants, those with HLB = 1θ to 2o are water-soluble, those with HLB = 5 to 9 are water-dispersible,
Surfactants with HLB = 1 to 4 are oil-soluble and therefore, surfactants suitable for the present invention are those with HLB = 10 to 20, and the resin composition to which this is added has a small HLB when in contact with water. It is easily understood that it expands rapidly compared to other materials.

尚、このような界面活性剤は、高吸水性樹脂とエラスト
マとからなる樹脂組成物100(重量部)に対して0.
5乃至20.好ましくは1乃至15の割合で添加するも
ので、0.5よシも少量のときは膨張性向上に寄与せず
、20よシも大量のときは膨張速度が飽和に達しそれ以
上添加しても不経済である。
Incidentally, such a surfactant is used in an amount of 0.00% based on 100 parts by weight of the resin composition consisting of a superabsorbent resin and an elastomer.
5 to 20. Preferably, it is added at a ratio of 1 to 15. If the amount is less than 0.5, it will not contribute to improving expansion properties, and if the amount is more than 20, the expansion rate will reach saturation and no more should be added. It is also uneconomical.

更に、成形助剤として可塑剤、安定剤、充填剤など一般
の成形に用いられている助剤を添加し、また用途によっ
ては顔料や発泡剤を添加することもある。
Furthermore, auxiliaries used in general molding such as plasticizers, stabilizers, and fillers are added as molding aids, and pigments and blowing agents may also be added depending on the purpose.

次に本発明の試験結果を述べる。Next, test results of the present invention will be described.

全試料は8インチ径ロールを用いロール温度120±5
℃で先ずエラストマを2分間混練 1・ □した後に高
吸水性樹脂その他を加えて更に5分間混線し、これを日
精樹脂製射出成形機(Ts−200型)を用いシリンダ
の前部温度150℃、後部温度160℃、ノズル温度1
60℃、射出圧力フ5〜80”Q 、射出時間5〜7秒
、冷却時間20秒の条件で120 X 15 X 4 
(U)の大きさに成形し、長さ50111に切断して製
造した。
All samples were made using 8-inch diameter rolls at a roll temperature of 120±5.
First, the elastomer was kneaded for 2 minutes at 1. □, then the super absorbent resin and others were added and kneaded for another 5 minutes, and then the temperature at the front of the cylinder was 150°C using a Nissei Plastics injection molding machine (Model Ts-200). , rear temperature 160℃, nozzle temperature 1
120 x 15 x 4 under the conditions of 60°C, injection pressure 5-80"Q, injection time 5-7 seconds, and cooling time 20 seconds.
It was manufactured by molding it into a size (U) and cutting it into a length of 50111 mm.

膨張性は室温で水に浸漬し1重量変化を時間的に追跡し
重量倍率で示した。
The swelling property was measured by immersing the sample in water at room temperature and tracking the change in weight over time, and expressing it as a weight magnification.

fた。成形性をロール混練性と金型からの離型性とによ
って評価した。ロール混線性は混線時にロール表面l\
の耐着性に乏しくバンクとしてまとまりにくいものを×
とし、ロール表面で自由に切シ返し混線操作ができバン
クとしてまとめやすいものを○とし、特に良好なものを
◎とした。金型からの離型性は成形品が金型から離れに
くく且つ剥離後に金型面に粉状物質が残存しているもの
をXとし。
It was. The moldability was evaluated by roll kneading property and mold releasability from the mold. Roll crosstalk is caused by the roll surface l\
Items that have poor adhesion resistance and are difficult to organize as banks
Those that can be freely cut and crossed on the roll surface and are easy to organize into banks are marked as ○, and those that are particularly good are marked as ◎. The releasability from the mold is defined as X if the molded product is difficult to separate from the mold and powdery substances remain on the mold surface after peeling.

離れやすく且つ金型面が清浄なものを○とし。Mark as ○ if it is easy to separate and the mold surface is clean.

特に良好なものを◎とした。Particularly good ones were marked as ◎.

更に試験1,4では参考として硬度(JISA 0秒)
、引張伸び(匍を測定した。
Furthermore, in tests 1 and 4, hardness (JISA 0 seconds) was used as a reference.
, tensile elongation (sample) was measured.

先ず試験1,2の試料は高吸水性樹脂としてビニルアル
コール−アクリル酸エステル共重合体(住友化学工業製
、商品名スミカゲル5p−s′2o)、エラストマとし
てエチレン・プロピレン共重合体(住友化学工業製、商
品名エスプーレン512B )を選び、Jcの各100
(重量部)ずつと流動パラフィン30.アジピン酸ジオ
クチルIQ、ステアリン酸1(重量部)とによって樹脂
組成物を構成した。
First, the samples for Tests 1 and 2 were a vinyl alcohol-acrylic acid ester copolymer (Sumitomo Chemical Co., Ltd., trade name Sumikagel 5p-s'2o) as a super absorbent resin, and an ethylene-propylene copolymer (Sumitomo Chemical Co., Ltd., product name Sumikagel 5p-s'2o) as an elastomer. (product name: S-Puren 512B), and 100 each of Jc.
(parts by weight) and liquid paraffin 30. A resin composition was composed of dioctyl adipate IQ and stearic acid 1 (parts by weight).

(試験1) 界面活性剤としてポリオキシエチレンソルビタンモノス
テアレート(HLB=14.9) 。
(Test 1) Polyoxyethylene sorbitan monostearate (HLB=14.9) was used as a surfactant.

ポリオキンエチレンソルビタンモノオレエート(HLR
=15.0) 、ポリエチレングリコールモノステアレ
ート(HLB=13.4) 、ポリオキシエチレンラウ
リルエーテル(HLB=10.5)を前記樹脂組成物に
5(重量部)ずつそれぞれ添加した本発明の実施例A、
B、C,Dと。
Polyquine ethylene sorbitan monooleate (HLR
Implementation of the present invention in which 5 (parts by weight) of polyethylene glycol monostearate (HLB = 15.0), polyethylene glycol monostearate (HLB = 13.4), and polyoxyethylene lauryl ether (HLB = 10.5) were each added to the resin composition. Example A,
B, C, D.

界面活性剤を添加しない比較例aおよびソルビタンモノ
ステアレート(HLB=4.7)、ソルビタンモノオレ
エート(HLB=4.3)、ステアリン酸モ/グリセラ
イド(HLB=2.8) を前記樹脂組成物に5(重量
部)−r、つそれぞれ添加した比較例す、c、a 1更
にグリセリン。
Comparative Example a in which no surfactant was added and sorbitan monostearate (HLB = 4.7), sorbitan monooleate (HLB = 4.3), and stearic acid mo/glyceride (HLB = 2.8) were used in the resin composition. Comparative Examples A, C, A, and A were each added with 5 (parts by weight) of glycerin.

ポリエチレングリコールを前記樹脂組成物に10(重量
部)ずつそれぞれ添加した比較例e r fどの水浸漬
時間による膨張性を重量測定した結果を次表および第1
図に示す(数値は重量倍)。
Comparative example in which 10 (parts by weight) of polyethylene glycol was added to the resin composition.
Shown in the figure (values are multiplied by weight).

(試験2) 試験1の結果膨張性の最もすぐれているポリオキシエチ
レンソルビタンモノオレエ−トの配合比を変え、それぞ
れ0,2,5゜15(重量部)ずつ前記樹脂組成物に添
加した本発明の実施例E、F、G、Hの水浸漬時間によ
る膨張性を重量測定した結果を次表および第2図に示す
(Test 2) The blending ratio of polyoxyethylene sorbitan monooleate, which had the best expandability as a result of Test 1, was varied, and 0, 2, and 5°15 (parts by weight) of each were added to the resin composition. The following table and FIG. 2 show the results of weighing the swelling properties of Examples E, F, G, and H of the present invention depending on the water immersion time.

(試験3) 前記と同じ高吸水性樹脂およびエラストマとしてエチレ
ン−酢酸ビニル共重合体(犬日本インキ化学工業製、商
品名エバスレン4]Op)を選び、その各100(重量
部)ずつとジオクチルフタレート20.ポリエチレング
リコール30.ポリエチレンワックス2゜ステアリン酸
3(重量部)とによって構成した樹脂組成物にポリオキ
シエチレンンルビタンモノステアレートを5(重量部)
添加した本発明の実施例Iと添加しない比較例2との水
浸漬時間による膨張性を重量測定した結果を次表および
第3図に示す。
(Test 3) Ethylene-vinyl acetate copolymer (manufactured by Inu Nippon Ink Chemical Industry Co., Ltd., trade name Evasurene 4] Op) was selected as the same superabsorbent resin and elastomer as above, and 100 (parts by weight) of each of them and dioctyl phthalate were added. 20. Polyethylene glycol 30. 5 (parts by weight) of polyoxyethylene rubitan monostearate was added to a resin composition composed of 2° polyethylene wax and 3 (parts by weight) stearic acid.
The following table and FIG. 3 show the results of gravimetric measurements of the swelling properties of Example I of the present invention, in which the additive was added, and Comparative Example 2, in which the additive was not added, depending on the water immersion time.

(試験4) 前述と同じ高吸水性樹脂とエラストマとの6c合割合を
変えた本発明の実施例J、K。
(Test 4) Examples J and K of the present invention in which the 6c ratio of the superabsorbent resin and elastomer was changed as described above.

L、M、Nの水浸漬時間による膨張性を重量測定した結
果を次表および第4図に示す。
The following table and FIG. 4 show the results of weighing the expansibility of L, M, and N depending on the water immersion time.

但し、いずれもアジピン酸ジオクチル10゜流動パラフ
ィン30.ヌテアリン酸1およびポリオキシエチレンソ
ルビタンモノステアレート5(重量部)を添加した。
However, in both cases, dioctyl adipate is 10° and liquid paraffin is 30°. 1 part of nutearic acid and 5 parts by weight of polyoxyethylene sorbitan monostearate were added.

実施態様に述べた試験結果から判るように。As can be seen from the test results described in the embodiments.

)− 高吸水性樹脂をエラストマに配合した樹脂組成物に酸化
エチンン縮金物糸の非イオン界面活性剤を添加した本発
明の水膨張性樹脂組成物は、成形加工性に支障を与えな
いとともに射出成形法で成形しても水とのすぐれた親和
性を有する表面被膜が作られるのである。従って、工業
用、農業用、建築用の資材のほかに玩具、医療関連品な
ど用途に適した形状の成形品を容易に提供できるととも
に、すぐれた水数[IV、性と急速膨張性とを示すとい
う高吸水性樹脂の特性を発揮させることができるもので
ある。
) - The water-swellable resin composition of the present invention, which is made by adding a nonionic surfactant such as ethyne oxide and metal thread to a resin composition in which a highly water-absorbent resin is blended with an elastomer, does not impede moldability and is easy to inject. Even when molded using a molding method, a surface coating with excellent affinity for water is created. Therefore, in addition to industrial, agricultural, and construction materials, it is possible to easily provide molded products with shapes suitable for uses such as toys and medical-related products. It is possible to exhibit the characteristics of a super absorbent resin.

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

第]図、第2図、第3図、第4図(ま・水浸漬時間と膨
張性との関係を示す試験結果のグラフである。 sl の (イ8) * ;3ヒー q、a4 1’fl(B)メ(浸 」I
]へ 1fl(日) メ(」失 )責 萌 出 (日)
Figures 1, 2, 3, and 4 are graphs of test results showing the relationship between water immersion time and expandability. 'fl(B)me(immersion' I)
] to 1fl (Sun) Me (' し ) responsibility Moe (Sun)

Claims (3)

【特許請求の範囲】[Claims] (1)高吸水性樹脂をエラストマに配合した樹脂組成物
において、酸化エチレン縮合物系の非イオン界面活性剤
が添加されていることを特徴とする水膨張性樹脂組成物
(1) A water-swellable resin composition comprising a highly water-absorbent resin mixed with an elastomer and containing an ethylene oxide condensate-based nonionic surfactant.
(2)高吸水性樹脂とエラストマとの配合割合は重量比
で30ニア0乃至70 ; aoであり、非イオン界面
活性剤はこの樹脂組成物100(重量部)に対してO0
5乃至200割合で添加されている特許請求の範囲(1
)に記載の水膨張性樹脂組成物。
(2) The blending ratio of the super absorbent resin and the elastomer is 30 nia 0 to 70;
Claims (1) added at a ratio of 5 to 200
) The water-swellable resin composition described in (1).
(3)非イオン界面活性剤は水溶性である特許端(3) Nonionic surfactant is water-soluble patented edge
JP11407984A 1984-06-04 1984-06-04 Resin composition swelling with water Pending JPS60258237A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11407984A JPS60258237A (en) 1984-06-04 1984-06-04 Resin composition swelling with water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11407984A JPS60258237A (en) 1984-06-04 1984-06-04 Resin composition swelling with water

Publications (1)

Publication Number Publication Date
JPS60258237A true JPS60258237A (en) 1985-12-20

Family

ID=14628529

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11407984A Pending JPS60258237A (en) 1984-06-04 1984-06-04 Resin composition swelling with water

Country Status (1)

Country Link
JP (1) JPS60258237A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004504446A (en) * 2000-07-24 2004-02-12 ダウ グローバル テクノロジーズ インコーポレイティド Thermoplastic superabsorbent polymer blend composition and preparation of the composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57190065A (en) * 1981-04-07 1982-11-22 Sanyo Chem Ind Ltd Rubber composition for water-swelling sealing material
JPS60210645A (en) * 1984-04-04 1985-10-23 Sumitomo Electric Ind Ltd Rubbery elastomer composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57190065A (en) * 1981-04-07 1982-11-22 Sanyo Chem Ind Ltd Rubber composition for water-swelling sealing material
JPS60210645A (en) * 1984-04-04 1985-10-23 Sumitomo Electric Ind Ltd Rubbery elastomer composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004504446A (en) * 2000-07-24 2004-02-12 ダウ グローバル テクノロジーズ インコーポレイティド Thermoplastic superabsorbent polymer blend composition and preparation of the composition

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