JPS60110742A - Vinyl chloride resin composition for stretched film - Google Patents

Vinyl chloride resin composition for stretched film

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Publication number
JPS60110742A
JPS60110742A JP21866483A JP21866483A JPS60110742A JP S60110742 A JPS60110742 A JP S60110742A JP 21866483 A JP21866483 A JP 21866483A JP 21866483 A JP21866483 A JP 21866483A JP S60110742 A JPS60110742 A JP S60110742A
Authority
JP
Japan
Prior art keywords
vinyl chloride
plasticizer
chloride resin
film
parts
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
JP21866483A
Other languages
Japanese (ja)
Inventor
Morio Sano
佐野 守生
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo 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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP21866483A priority Critical patent/JPS60110742A/en
Publication of JPS60110742A publication Critical patent/JPS60110742A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a resin composition which exhibits excellent extrusion stability and film-forming properties and improved self-tack, and is free of hard spots, by incorporating a tackifying plasticizer and an epoxy plasticizer in specified proportions into a vinyl chloride resin. CONSTITUTION:15-40pts.wt. tackifying plasticizer (A), and an epoxy plasticizer (B) are incorporated into 100pts.wt. vinyl chloride resin, (A)+(B) being 30- 55pts.wt. in total. Preferably a vinyl chloride resin to be used is a homopolymer of vinyl chloride or a copolymer of vinyl chloride with copolymerizable monomers; a tackifying plasticizer is glyceryl monolauryl diacetate alone or glyceryl monolauryl diacetate together with an epoxidized linseed oil butyl ester; and an epoxy plasticizer is an epoxidized soybean oil or an epoxidized linseed oil.

Description

【発明の詳細な説明】 本発明は、塩化ビニル系樹脂の食品用を主体とした包装
用自己粘着性にすぐれたストレッチフィルム用塩化ビニ
ル系樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vinyl chloride resin composition for use in stretch films for packaging, mainly for food products, which has excellent self-adhesive properties.

従来より、プラスチックフィルムの弾性および自己粘者
性を利用した、いわゆるストレッチ包装は、精肉、;鮮
魚、−^′呆等をトレイと呼ばれる容器に入れて包装す
る食品の包装に多用されている。
Conventionally, so-called stretch packaging, which utilizes the elasticity and self-adhesive properties of plastic films, has been widely used for packaging foods such as meat, fresh fish, and other foods in containers called trays.

このストレッチ包装は、包装作采がm単である事、食品
の目減りや鮮度低下を防ぎかつ衛生的である事、更にフ
ィルムを緊張状態で包装するため、包装外観が美しく商
品価値を高め、一方包装コストが安い等の特徴を有する
This stretch packaging has a simple packaging style, prevents food loss and deterioration of freshness, and is hygienic.Furthermore, since the film is wrapped under tension, the packaging looks beautiful and increases product value. It has characteristics such as low packaging cost.

ところでこのストレッチ包装に用いられるフィルムには
、次の様な性質が請求される。
By the way, the following properties are required of the film used for this stretch packaging.

(1)透明性、光沢等光学的性質に優れている事。(1) Excellent optical properties such as transparency and gloss.

(2)防曇性、自己粘着性、ヒートシール性に優れてい
る事。
(2) Excellent anti-fog properties, self-adhesive properties, and heat-sealing properties.

(3)過度な未軟性、弾性、およびタテ/ヨコの強度バ
ランスを有し、また制い伸度を有する事。
(3) Excessive softness, elasticity, vertical/horizontal strength balance, and restrained elongation.

(4)耐寒性に優れている墨。(4) Sumi ink has excellent cold resistance.

(5) 適度の表面滑性を有し、自動包装機械過性に優
れている事。
(5) Appropriate surface smoothness and excellent resistance to automatic packaging machines.

(6)ば素、炭酸ガスが適度に透過し、水蒸気透過性が
小さい事。
(6) Appropriate permeability of barron and carbon dioxide gas, and low water vapor permeability.

上記の諸性質に後れ、従来から多用されているフィルム
は、軟賞ポリ塩化ビニル糸フィルム(以下Pvcフィル
ムと略す)であり、この他では、ポリオレフィン糸フィ
ルムやポリプタゾエン糸フイルムも上布されているが、
性能上Pvcフィルムに匹通するものは得られていない
The film that has been widely used in the past due to the above-mentioned properties is soft polyvinyl chloride yarn film (hereinafter abbreviated as PVC film), and in addition to this, polyolefin yarn film and polyptazoene yarn film are also used. There are, but
Nothing comparable to PVC film in terms of performance has yet been obtained.

ところで、Pvcフィルムの組成は、アゾピン酸系の可
塑剤を主可塑剤として補助的にエポキシ系可塑剤を加え
たものが一般的であるが、本来これらは塩化ビニル樹脂
用可塑剤としては、2次可塑剤といわれ塩化ビニル系樹
脂とは相溶性が十分でないものが多いため、可塑剤の総
量が60〜55車量部と多量に入っているにもかかわら
ず、溶融粘度が低い割には粉粒体状のコンパウンドのゲ
ル化速度がおそく、いいがえれば押出成型する場合YM
度と圧力を簡<寺成形条件を十分に考慮しないとブツ(
!l:呼ばれる未浴融物が発生したり、また押出量の時
間的変動が起り製膜安定性が十分でないという欠点があ
った。一方用途的にも自己粘着性を必要とするフィルム
であるため、この自己粘着性を可塑剤の総量を多くして
そのブリードで付与したり、また防倭剤と称する界面活
性剤で一部コントロールをしているが、oT塑削総量に
は限綻があり、また界面粘性剤では調整範囲がそれ程広
くなく、野菜等の株包装で水に藺れた状!甜では、特に
フィルム同志の粘着性が悪いという問題がある。
By the way, the composition of PVC film is generally composed of an azopic acid-based plasticizer as the main plasticizer and an epoxy-based plasticizer added as an auxiliary plasticizer. Many plasticizers are called secondary plasticizers and are not sufficiently compatible with vinyl chloride resins, so even though the total amount of plasticizers is as high as 60 to 55 parts by volume, the melt viscosity is low. The gelation rate of granular compounds is slow, and in other words, when extrusion molding, YM
It is difficult to easily adjust the degree and pressure if the molding conditions are not sufficiently considered (
! 1: There were disadvantages in that a so-called unbathed melt was generated, and the extrusion rate fluctuated over time, resulting in insufficient film formation stability. On the other hand, since the film requires self-adhesive properties for its intended use, this self-adhesive property is imparted by increasing the total amount of plasticizer and bleeding it, and it is also partially controlled using a surfactant called an anti-slip agent. However, there is a limit to the total amount of OT plastic processing, and the adjustment range for interfacial viscosity agents is not very wide, so it is like being stuck in water when packaging vegetables and other stocks! In the case of sweet, there is a problem in that the adhesion between the films is particularly poor.

上記の様な未ゲルの発生、押出量の変動、フィルムの粘
着性不足の問題を解決するため種々の検討を行った結果
、以下の結線に退した。
As a result of various studies to solve the above-mentioned problems of non-gelling, variation in extrusion rate, and insufficient film tackiness, we settled on the following connections.

本発明は、塩化ビニル系樹脂さ枯宥性付与可塑剤及びエ
ポキシ系可塑剤とを主成分さする組成物とすることによ
り、押出安定性、製膜性にすぐれ、ブツの発生がなくし
かも自己粘着性が向上するストレッチフィルム用塩化ビ
ニル系樹脂組成物を提供するものである。すなわち、本
発明は、塩化ビニル糸佃脂1oo恵曾部に対して、(A
)粘着性付与可塑剤15〜4o東電部、(B)エポキシ
系可塑剤6〜15重量部配合してなる樹脂以放物であっ
て、しかも(A) + (Blの会計が6o〜55重畑
部であるこ゛とを%激とする。
The present invention has excellent extrusion stability and film-forming properties, does not cause lumps, and is self-adhesive by using a composition containing a vinyl chloride resin, a plasticizer that imparts permanence properties, and an epoxy plasticizer as main components. The present invention provides a vinyl chloride resin composition for stretch films that has improved adhesiveness. That is, the present invention provides (A
) 15 to 4 parts by weight of a tackifying plasticizer, (B) 6 to 15 parts by weight of an epoxy plasticizer, and the accounting value of (A) + (Bl is 6 to 55 parts by weight) This is Hatabe and it is % intense.

本発明で云う塩化ビニル系41111J#とは、塩化ビ
ニルの単独重合体および共東合用能な七ツマ−すなわち
静間ビニル、エチレン、プロピレン等、α−オレフィン
との共度汗体寺が上げられる。
The vinyl chloride-based 41111J# used in the present invention includes homopolymers of vinyl chloride and polymers that can be used in combination with vinyl, ethylene, propylene, and α-olefins.

次に、塩化ビニル糸佃脂に配合される可塑剤としては、 (N 帖層性付与可塑剤としては、(1)グリセリルモ
ノラウリルジアセテート単独、(II)グリセリルモノ
ラウリルジアセテートとエポキシ化アマニ油ブチルエス
テル(以下11LOBという) 、(+li+グリセリ
ルモノラウリルジアセテートとELOB及びアゾピン酸
シイソノニル(以下DiNAという)又は炭素数が6.
8,100直鎖アルキル基を冶スるアジピン酸ゾ(n−
ヘキシル、n−オクチル、n−デシル)(以下Dn 6
−8−1 OAという) 、(iv)グリセリルモノラ
ウリルジアセテートとDiNA及び/又はLln 6−
8−1 OA(B) エポキシ系可塑剤としては、エポ
キシ化大豆油(以下ESBOという)及び/又はエポキ
シ化アマニ油(以下ELOという)のfAJ群+tBJ
群から選択されたものである。
Next, the plasticizers to be added to the vinyl chloride thread tsukudashi include (N) The plasticizers that impart layering properties include (1) glyceryl monolauryl diacetate alone, (II) glyceryl monolauryl diacetate and epoxidized linseed. oil butyl ester (hereinafter referred to as 11LOB), (+li+glyceryl monolauryl diacetate and ELOB and siisononyl azopic acid (hereinafter referred to as DiNA) or carbon number 6.
Adipic acid (n-
hexyl, n-octyl, n-decyl) (hereinafter referred to as Dn 6
-8-1 OA), (iv) glyceryl monolauryl diacetate and DiNA and/or Lln 6-
8-1 OA (B) As an epoxy plasticizer, fAJ group + tBJ of epoxidized soybean oil (hereinafter referred to as ESBO) and/or epoxidized linseed oil (hereinafter referred to as ELO)
selected from the group.

また、選択された可re AIJを併用するに際しては
、塩化ビニル樹脂に対して、(N#に属する粘着性付与
剤15〜40粛杖都とtBJ群に属するエポキシ系可塑
剤6〜15厭殻部であって、かつ(A)+(B)との合
計が60〜55服吋都とする。(At 十(BJの合計
量が304 置部未満では、フィルム柔軟性と自己粘着
性が不足し、また(A) + (Blの行計lが55重
量部8越えると、未軟性及び自己粘庸性共過剰となる。
In addition, when using the selected AIJ together, it is necessary to use a tackifying agent of 15 to 40 ml of a tackifier belonging to the N# group and a 6 to 15 ml of an epoxy plasticizer belonging to the tBJ group to the vinyl chloride resin. If the total amount of BJ is less than 304 parts, the film flexibility and self-adhesiveness are insufficient. However, if the total amount of (A) + (Bl) exceeds 55 parts by weight, 8 parts by weight, both non-softening and self-viscosity properties become excessive.

さらに、(A)群と(131群との比率としては、(N
tJ+の可塑剤が15重ht部未満では、(BI Jf
’の可塑剤を15屯触部としてもフィルムの柔軟性と自
己帖焉性が不足する。次に(AJ#の可塑剤が40重量
部を越えると、自己粘着性が過剰となり、フィルム巻出
し時の抵抗か大きくなり過ぎる、また(B)群の可塑剤
が6M犠部未満では、熱安定性が慈く、押出加工性が低
下する、さらに15厘置部を越えると、押出加工時にダ
イに目ヤニ等の発生がj貝者となり、」早出υ1」エト
トが低下する。
Furthermore, the ratio between group (A) and group (131) is (N
If the plasticizer in tJ+ is less than 15 parts by weight, (BI Jf
Even if 15 tons of plasticizer was added to the film, the film would still lack flexibility and self-stretching properties. Next, if the plasticizer of group (B) exceeds 40 parts by weight, the self-adhesiveness will be excessive and the resistance during film unwinding will become too large. Stability is poor, extrusion processability decreases, and if the extrusion process exceeds 15 mm, stains and the like will occur on the die during extrusion, resulting in a decrease in "early output υ1".

本発明の(N!pF粘看性付与1丁塑薊の賛は、15〜
40jX挺部であるが、mLI記(1すの場合は、グリ
セリルモノラウリルシアセテコト12〜2 S m i
it部とELOB 3〜15重量部で、合計が15〜4
0屯財部であるこきが好しい。すなわち、ELOBが、
15車量部を越えるとグリセリルモノラウリルジアセテ
ート単独に比べ、自己粘着性が過剰となり、フィルム巻
出し抵抗が大きくなりすぎる。
The value of (N!pF viscosity-imparting plastic) of the present invention is 15~
40j
It part and ELOB 3-15 parts by weight, total 15-4
I like Koki who is a 0ton treasurer. That is, ELOB is
If it exceeds 15 parts by weight, the self-adhesiveness will be excessive compared to glyceryl monolauryl diacetate alone, and the film unwinding resistance will become too large.

また(川)のノM8−は、グリセリルモノラウリルゾア
セテート9〜28重賛部、+r;LoB3〜15事微部
及びDiNA又はDn6−8−1’OA3〜9重置部で
、合計が15〜40塩量部であり、(lv)の場合は1
.グリセリルモノラウリルゾアセテート9〜67軍量部
、DiNA及び/又はDn 6−8−1 OA夫々6〜
9服量部で、合計が15〜40屯策部であることが好ま
しい。
In addition, (river) no M8- has glyceryl monolaurylzoacetate 9-28 overlapped part, +r;LoB3-15 part and DiNA or Dn6-8-1'OA3-9 overlapped part, total 15 ~40 parts of salt, (lv) 1
.. Glyceryl monolaurylzoacetate 9-67 parts, DiNA and/or Dn 6-8-1 OA each 6-67 parts
Preferably, the dosage is 9 portions, for a total of 15 to 40 portions.

なお本発明においては、上記のoJ TjlJ剤群の他
に必−要に応じて、安定剤、キレータ−1滑削、界1田
活性剤、漸色剤、酸化防止剤、紫外脚吸収剤等を亦加す
る墨もてきる。
In addition, in the present invention, in addition to the above-mentioned oJ TjlJ agents, stabilizers, chelator-1 lubrication agents, Kaiichiden activators, color retardants, antioxidants, ultraviolet leg absorbers, etc. may be used as necessary. I also have ink to add.

本発明の塩化ビニル系樹脂組成物は、埴化ビニル系樹力
「に対して、上記特定の可塑をりと必要に応じたその他
の添加剤をヘンシェル、リボンブレンダー咎の混合機を
用いて促来公知の方法で混合して得られる。茨たこの側
脂組成物は、公知の装膜手段すなわちTダイ法、インフ
レーション法により10〜20μ程厩の厚みをゼするフ
ィルムに製膜される。
The vinyl chloride resin composition of the present invention is produced by adding the above-mentioned specific plasticizing agent and other additives as necessary to the vinyl chloride resin composition using a mixer such as a Henschel or a ribbon blender. It is obtained by mixing according to a conventionally known method.The briar octopus side fat composition is formed into a film having a thickness of about 10 to 20 microns by a known film forming method, ie, a T-die method or an inflation method.

以下実施例により本発明を詳Jiltに説明する。The present invention will be explained in detail below with reference to Examples.

実施例1〜9 塩化ビニル桐館(鬼気化学工業(4’l 4!! %商
品名デンカビニル88−11O−8)100東it部と
表に示す可塑剤の夫々の絵加量及びカルシウム−q1!
鉛系安定剤1.0重量部、ソルビタン糸界面1占性A+
J1.0取量部、グリセリン系界自活性剤肌5亀叶部、
高級アルコールEO付加物系界面性剤0.5mjf部を
ジャケット付ヘンシェルミキサーで加熱、混合し、夫々
のコンパウンドを作成した。
Examples 1 to 9 Vinyl chloride Kiritate (Kiki Kagaku Kogyo (4'l 4!!% trade name Denkabinyl 88-11O-8) 100 parts and the respective painting weights and calcium-q1 of the plasticizers shown in the table !
1.0 parts by weight of lead-based stabilizer, sorbitan yarn interface 1-occupancy A+
J1.0 amount part, glycerin-based world self-activating agent skin 5 turtle part,
Each compound was prepared by heating and mixing 0.5 mjf part of a higher alcohol EO adduct surfactant in a jacketed Henschel mixer.

次にこのコンパウンドを65 ml/m押出様で200
〜205°Cで押出し、+x 500 m/m肉厚約1
7μのフィルムを得た。押出性、フィルム内のブツ、自
己粘扁力共すぐれていた。結果を辰に示す。
Next, this compound was extruded at 65 ml/m for 200
Extruded at ~205°C, +x 500 m/m wall thickness approx. 1
A 7μ film was obtained. It had excellent extrudability, lumps in the film, and self-adhesive force. Show the results to Tatsu.

比較例1〜5 可塑剤の冷加財を表に示す通りとした以外は、実施例♂
同様の操作を行った。押出性、フィルム内プツ、自己粘
庸力のいずれかが劣った。結果を表に示す。
Comparative Examples 1 to 5 Example ♂ except that the plasticizer chilled material was as shown in the table.
A similar operation was performed. Extrudability, in-film adhesiveness, and self-viscosity were poor. The results are shown in the table.

物性測定方法は、次の1lJ1っであった。The physical properties were measured using the following method.

1)押出量:1分間ごとの押出h4を10回測定し、押
出(資)の平均値(X)及び範囲(R)をめた。
1) Extrusion amount: The extrusion h4 per minute was measured 10 times, and the average value (X) and range (R) of the extrusion (value) were determined.

2) フッ: 2 Q ctlt×2Q cntの1枚
のフィルム中に0.5m+πφ以上の未#−物が伺個存
在するか、10枚のフィルムの平均値とした。
2) Fu: 2Q ctlt x 2Q cnt The average value of 10 films was determined to determine whether there were unnumbered particles of 0.5m+πφ or more in one film.

6)自己粘着カニ巻ロールから厚さ約1ytyis約2
 [1cm X 20 cutのシートを切り出す。次
にこのシートから正確に10C/ft×15Cr/Lを
切り出し、フィルム間に空気が入らないように2 & 
1 !+1とする。この2枚のフィルムの10 cm 
+隅の一方の端部を一部剥がし、10cIIL幅の端部
に幅1ぼ×長さ12αの板紙をセロ/’%ンテーノで止
める。
6) Thickness from self-adhesive crab roll is about 1ytyis about 2
[Cut out a 1cm x 20 cut sheet. Next, cut out a piece of 10C/ft x 15Cr/L accurately from this sheet, and make sure that there is no air between the films.
1! +1. 10 cm of these two films
One end of the + corner is partially peeled off, and a paperboard measuring 1 cm wide x 12 α long is fastened to the 10 cIIL wide end using cello/'% nteno.

次のこの板紙の部分を引張り試験<aのチャックでつか
み引張りスピード200 tan 7分でフィルムを剥
がし、剥′離抗力を測定し、サンプル10回の平均値が
、55〜80 jj / cmを実用的自己枯漕力の範
囲とした。
Next, hold this paperboard part with a chuck with a tensile test < a and peel off the film at a tensile speed of 200 tan for 7 minutes and measure the peel resistance.The average value of 10 samples was 55 to 80 jj/cm. It was defined as the range of self-destruction.

なお表の可塑剤は次の通りである。The plasticizers in the table are as follows.

1)グリセリルモノラウリルジアセテート:埋研ビタミ
ン(I陶製、商品名PL−012J2) ELOB :
エポキシ化アマニ油ブチルエステル、[アデカアーがス
(印製、商品名L)−178J3)DiNA:アゾピン
酸ジイソノニル「三部化工((1目も商品名DiNA 
J 4) Dn 6−8−10 A :アゾピン酸ゾ(n−
ヘキシル、n−オクチル、n−デシルリン[大日本イン
キ化学(印製、間品名Dn610AJ5) ESBO:
エポキシ化大豆油、[アデカアーガス(會M装、1糊品
名o150PJ 6) ELO:エポキシ化アマニ油[アデカアーがス(
陶製、商品名0180AJ
1) Glyceryl monolauryl diacetate: Buken Vitamin (manufactured by I Tou, trade name PL-012J2) ELOB:
Epoxidized linseed oil butyl ester, [ADEKA ARGASU Co., Ltd., trade name L-178J3] DiNA: Diisononyl azopic acid "Sanbe Kako ((1st item also trade name DiNA)
J 4) Dn 6-8-10 A: Azopic acid zo(n-
Hexyl, n-octyl, n-decyl phosphorus [Dainippon Ink Chemical Co., Ltd., product name Dn610AJ5] ESBO:
Epoxidized soybean oil, [ADEKA ARGUS (M-SOU, 1 glue product name o150PJ 6) ELO: Epoxidized linseed oil [ADEKA ARGUS (
Ceramic, product name 0180AJ

Claims (1)

【特許請求の範囲】[Claims] 塩化ビニル樹脂100直it部に対して囚 粘漸性付与
可塑剤15〜40重量部(B) エポキシ系可塑剤6〜
157を酸部配合してなる樹脂組成物であって、しかも
(A)+(B)の合計が60〜55重量部であることを
特徴とするストレッチフィルム用塩化ビニル系樹脂組成
物。
15 to 40 parts by weight of viscosity-imparting plasticizer per 100 parts of vinyl chloride resin (B) 6 to 40 parts by weight of epoxy plasticizer
1. A vinyl chloride resin composition for a stretch film, characterized in that the total amount of (A) + (B) is 60 to 55 parts by weight.
JP21866483A 1983-11-22 1983-11-22 Vinyl chloride resin composition for stretched film Pending JPS60110742A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21866483A JPS60110742A (en) 1983-11-22 1983-11-22 Vinyl chloride resin composition for stretched film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21866483A JPS60110742A (en) 1983-11-22 1983-11-22 Vinyl chloride resin composition for stretched film

Publications (1)

Publication Number Publication Date
JPS60110742A true JPS60110742A (en) 1985-06-17

Family

ID=16723484

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21866483A Pending JPS60110742A (en) 1983-11-22 1983-11-22 Vinyl chloride resin composition for stretched film

Country Status (1)

Country Link
JP (1) JPS60110742A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010100681A (en) * 2008-10-21 2010-05-06 Okamoto Ind Inc Vinyl chloride resin stretch film

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010100681A (en) * 2008-10-21 2010-05-06 Okamoto Ind Inc Vinyl chloride resin stretch film

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