JPS6169851A - Vinyl chloride resin composition for food packaging film - Google Patents

Vinyl chloride resin composition for food packaging film

Info

Publication number
JPS6169851A
JPS6169851A JP19135084A JP19135084A JPS6169851A JP S6169851 A JPS6169851 A JP S6169851A JP 19135084 A JP19135084 A JP 19135084A JP 19135084 A JP19135084 A JP 19135084A JP S6169851 A JPS6169851 A JP S6169851A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
plasticizer
acrylonitrile
resin composition
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
JP19135084A
Other languages
Japanese (ja)
Inventor
Hiroshi Yamaguchi
山口 容
Takaaki Nakano
中野 孝章
Masamitsu Hasegawa
長谷川 正光
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.)
Shin Etsu Polymer Co Ltd
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Polymer Co Ltd
Shin Etsu Chemical 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 Shin Etsu Polymer Co Ltd, Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Polymer Co Ltd
Priority to JP19135084A priority Critical patent/JPS6169851A/en
Publication of JPS6169851A publication Critical patent/JPS6169851A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled compsn. which has excellent resistance to oils and cold and little causes migration and bleeding of a plasticizer, consisting of a vinyl chloride resin, an acrylonitrile/butadiene copolymer and a plasticizer. CONSTITUTION:0.5-20pts.wt. acrylonitrile/butadiene copolymer having an acrylonitrile content of 20-50wt% and 20-60pts.wt. plasticizer selected from among diisononyl adipate, di-n-alkyl adipates derived from a 6-10C aliph. alcohol, tributyl acetylcitrate, epoxidized soybean oil and epoxidized linseed oil are blended with 100pts.wt. vinyl chloride resin having a degree of polymn. of 800-3,000, such as PVC.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は塩化ビニル系&脂組成物、特(二はn−へブタ
ンによる可塑剤などの抽出量が低減された、可塑剤など
の移行、溶出が少なく、かりは耐油性、耐寒性の向上さ
れた食品包装フィルム用として好適とされる塩化ビニル
系樹脂組成物に関するものである。
Detailed Description of the Invention (Industrial Field of Application) The present invention provides vinyl chloride and fat compositions, particularly (2) the transfer of plasticizers, etc., in which the extraction amount of plasticizers, etc. by n-hebutane is reduced; The present invention relates to a vinyl chloride resin composition suitable for use in food packaging films, which has little elution and improved oil resistance and cold resistance.

(従来の技術] 軟質塩化ビニル系フィルムは食品包装用、業務用ストレ
ッチフィルムとして業務用、家庭用に広く使用されてい
るが、これシニは微量ではあるが被包装物に可塑剤など
の移行または溶出することがあるため、厚生省告示C二
よってn−へブタンを二よる可塑剤などの抽出量を15
0 ppm以下とTることが規定されている。
(Prior art) Soft vinyl chloride film is widely used for food packaging, commercial stretch film, commercial use, and household use. Because they may elute, the amount of plasticizers extracted using n-hebutane should be reduced to 15% according to the Ministry of Health and Welfare notification C2.
It is specified that T is 0 ppm or less.

したがって一般市販の食品包装用塩化ビニル系フィルム
のn−ヘラダンg二よる可塑剤の抽出量は当然150p
pmJa下とされており、例えば可塑剤としてアジピン
酸ジイソノニル(以下DINAIと略記する)を含有す
る塩化ビニル系樹脂組成物から作られた厚さ10〜20
μmの食品包装用フィルムのそれは139ppm以下と
され、厚さが増加しても150ppmJ2L下となるよ
う(:されているが、これについてはより低い値とする
ことが望まれている。
Therefore, the amount of plasticizer extracted by n-heradane g2 from general commercially available vinyl chloride film for food packaging is naturally 150p.
pmJa and has a thickness of 10 to 20 mm and is made from a vinyl chloride resin composition containing diisononyl adipate (hereinafter abbreviated as DINAI) as a plasticizer, for example.
The value of μm food packaging film is set to be 139 ppm or less, and even if the thickness increases, it will be 150 ppm J2L or less (:), but it is desired that this value be lowered.

そのため、食品包装用フィルムを作るための塩化ビニル
系樹脂組成物i二ついては非移行性の可塑剤であるポリ
エステル系可塑剤を従来公知の可塑剤と併用するという
ことが検討されているが、このポリエステル系可塑剤は
使用量を高くしないと充分な効果が得られないので、こ
れに代るべき方法が望まれている。
Therefore, the use of polyester plasticizers, which are non-migratory plasticizers, in combination with conventionally known plasticizers is being considered in vinyl chloride resin compositions for making food packaging films. Since sufficient effects cannot be obtained from polyester plasticizers unless they are used in a large amount, an alternative method is desired.

(発明の構成) 本発明はこのような不利を解決したn−へブタンによる
可塑剤抽出量の低減された食品包装フィルム用の塩化ビ
ニル系樹脂組酸物に関するものであり、これは1)塩化
ビニル系樹AM10011童部、2)アクリロニトリル
・ブタジェン共重合体0.5〜211!i部、3)可塑
剤20〜60富量部とからなることを特徴とするもので
ある。
(Structure of the Invention) The present invention relates to a vinyl chloride-based resin composite acid for food packaging films that solves these disadvantages and has a reduced amount of plasticizer extracted by n-hebutane. Vinyl tree AM10011 Dobe, 2) Acrylonitrile-butadiene copolymer 0.5-211! i part, 3) 20 to 60 parts rich in plasticizer.

これを説明すると、本発明者らは可塑剤の移行、溶出の
少ない塩化ビニル系樹脂組成物について種々検討した結
果、可塑剤を含有する塩化ビニル系樹脂組成物にアクリ
ロニトリル・ブタジェン共重合体く以下NBRと略記す
る)を添加すると、この組成物から作られたフィルムの
n−へブタンによる可塑剤の抽出量を大巾に減少させる
ことができることを見出すと共C二、これによればフィ
ルムの耐油性、耐寒性、食品包装用のポリスチレン製の
トレーに可塑剤が移行してクラックを発生させるP8非
移行性も同上されるので、このフィルムには油を使った
惣菜などの包装への適応性が与えられるほか、この橋の
フィルムを使用した食品包装用トレーの劣化性が軽減さ
れることを確認し、このNBRの種類、添加量などC二
ついての研究を進めて本発明を完成させた。
To explain this, the present inventors have conducted various studies on vinyl chloride resin compositions with little plasticizer migration and elution. It has been found that the amount of plasticizer extracted by n-hebutane in films made from this composition can be greatly reduced by adding NBR (abbreviated as NBR). Oil resistance, cold resistance, and P8 non-migration, which causes plasticizers to migrate to polystyrene trays used for food packaging and cause cracks, are also mentioned above, so this film is suitable for packaging foods that use oil. It was confirmed that the deterioration of food packaging trays using this bridge film was reduced, and the present invention was completed by conducting research on the type and amount of NBR added. Ta.

本発明の塩化ビニル系樹脂組成物を構成する1)成分と
しての塩化ビニル樹脂は一般に市販されている公知のも
のでよく、これは塩化ビニルの単独重合体でもこれと共
1合し得る他のビニル系単量体、例えば酢酸ビニル、エ
チレン、プロピレンなどのオレフィンとの共重合体であ
ってもよい。しかし、このものは包装用フィルム、特C
二食品包装用フィルムを作るための原材料とされるもの
であることから、亀今度が800〜3.000特C:は
1.000〜1,500程度のものとすることがよい。
The vinyl chloride resin as the component 1) constituting the vinyl chloride resin composition of the present invention may be a publicly available commercially available one, and may be a homopolymer of vinyl chloride or other polymers that can be copolymerized with the vinyl chloride resin. It may also be a copolymer with a vinyl monomer, such as vinyl acetate, or an olefin such as ethylene or propylene. However, this product is a packaging film, special C
2.Since it is used as a raw material for making food packaging films, it is preferable that the tortoise diameter is about 800 to 3,000 and the special C: is about 1,000 to 1,500.

また、この2)成分としてのNBRはアクリロニトリル
とブタジェンとを乳化重合して得られる公知のものでよ
いが、上記したl)成分としての塩化ビニル系樹脂との
混合を容易に行なうため(:粉末状のものとすることが
よい。このNBRが塩化ビニル樹脂と広範囲の相溶性を
有するもので、塩化ビニル樹ItliIC対し揮発、移
行、抽出を全く起さない一種の高分子量可塑剤として作
動するものであるということは公知とされるところであ
るが、他の一般公知の可塑剤と併用されたときにその可
塑剤のn−ヘプタン1:よる抽出量を減少させるという
効果を有するということは新しい知見である。
NBR as component 2) may be a known NBR obtained by emulsion polymerization of acrylonitrile and butadiene, but in order to easily mix it with the vinyl chloride resin as component 1) described above (: powder This NBR has a wide range of compatibility with the vinyl chloride resin, and acts as a type of high molecular weight plasticizer that does not cause any volatilization, migration, or extraction from the vinyl chloride resin ItliIC. However, it is a new finding that when used in combination with other commonly known plasticizers, the plasticizer has the effect of reducing the amount of n-heptane extracted. It is.

このNBRの配合量はl)成分としての塩化ビニル系樹
脂100奮竜部C二対し0.5電量部以下では可塑剤の
n−へブタンC二よる抽出前低減の効果がほとんどなく
、20部以上添加してもその効果は特に増大しないので
、0.5〜20tt部の範囲とすればよく、特C:は1
〜10!を部の範囲とすることがよい。
If the blending amount of NBR is 0.5 parts by coul or less per 100 parts of vinyl chloride resin as component l), there is almost no effect of reduction before extraction by the plasticizer n-hebutane C, and 20 parts. Since the effect does not particularly increase even if the addition exceeds 0.5 to 20 tt parts, the special C: is 1
~10! It is recommended that the range be within the range of

なお、このNBRImついてはこれC二含まれるアクリ
ロニトリル量によってアクリロニトリルが36〜41%
の高ニトリル、31〜35%の中高ニトリル、25〜3
0%の中低ニドIJル、18〜24%の低ニトリルのも
のがあるが、本発明の目的(二おいては塩化ビニルとの
相溶性と可塑剤溶出防止効果のバランスということから
アクリロニトリルが20〜50を量%、特には30〜4
0重量%、ブタシェフ80〜50重竜%、特C二は70
〜bo軍1%のものとすることがよい。
In addition, for this NBRIm, acrylonitrile is 36 to 41% depending on the amount of acrylonitrile contained in C2.
high nitrile, 31-35% medium-high nitrile, 25-3
There are 0% medium-low nitrile ones and 18-24% low nitrile ones, but for the purpose of the present invention (2), acrylonitrile is used because of the balance between compatibility with vinyl chloride and plasticizer elution prevention effect. 20-50% by weight, especially 30-4
0% by weight, butashev 80-50 heavy dragon%, special C2 is 70%
It is preferable to set it to 1% of the ~bo army.

っぎf二本発明の組成物を構成する3)成分としての可
塑剤は塩化ビニル系樹脂シー通常使用されているもので
よく、これにはフタル酸ジオクチル、フタル酸ジブチル
などのフタル酸エステル類、アジピン酸ジオクチル、ア
ゼライン酸ジオクチルなどの直鎖二塩基酸エステル類、
トリクレジルホスフェート、トリキシレニルホスフェー
トなどのリン酸エステル類、アセチルクエン酸トリエチ
ル、アセチルクエン酸トリブチルなどのヒドロキシ多価
カルボン酸エステル、メチルアセチルレンル−トなどの
ヒマシ油誘導体、大豆油、アマニ油などをエポキシ化し
たエポキシ化植物油、○、〜01゜のロー肪酸のエチレ
ングリコールエステルなどのようなエチレングリコール
誘導体、さらにはポリエステル系可塑剤などが例示され
るが、本発明の組成物が食品包装用フィルムとされるも
のであることからはアジピン酸ジイソノニル、アジピン
#ジーn−フルキル(炭異数6〜10の1旨肪族アルコ
ールから作られたもの)、アセチルクエン酸トリブチル
、エボ車シ化大豆油、エポキシ化アマニ油から選ばれた
ものとすることが好ましい。なお、この可塑剤の配合t
はその種類によって相違するけれども、これは1)成分
としての塩化ビニル系樹脂100tt部C:対し20重
量部以下では軟質フィルムを形成させるための可塑化効
果が不足し、60部以上とするとフィルムの伸びおよび
自己粘着性が過剰となるので、これは20〜60享1i
部の範囲と丁ればよい。
The plasticizer as component 3) constituting the composition of the present invention may be one commonly used in vinyl chloride resins, including phthalate esters such as dioctyl phthalate and dibutyl phthalate. , linear dibasic acid esters such as dioctyl adipate and dioctyl azelaate,
Phosphate esters such as tricresyl phosphate and tricylenyl phosphate, hydroxy polycarboxylic acid esters such as triethyl acetyl citrate and tributyl acetyl citrate, castor oil derivatives such as methyl acetylene root, soybean oil, linseed oil Examples include epoxidized vegetable oils such as epoxidized vegetable oils, ethylene glycol derivatives such as ethylene glycol esters of low fatty acids of ○, ~01°, and polyester plasticizers. Since it is considered to be a packaging film, it includes diisononyl adipate, adipic acid n-furkyl (made from a monovalent aliphatic alcohol with a carbon atom number of 6 to 10), acetyl tributyl citrate, and Evo car film. Preferably, the oil is selected from epoxidized soybean oil and epoxidized linseed oil. In addition, this plasticizer formulation t
Although it differs depending on the type, this is as follows: 1) 100 tt parts of vinyl chloride resin as a component C: On the other hand, if it is less than 20 parts by weight, the plasticizing effect for forming a soft film is insufficient, and if it is more than 60 parts, the plasticizing effect for forming a soft film is insufficient. This may result in excessive elongation and self-adhesion.
Just match the range of the department.

つぎシ一本発明の実施例をあげるが、例中の部は重量部
を示したものである。
Next, examples of the present invention will be given, and parts in the examples indicate parts by weight.

実施例1 塩化ビニル樹脂・TK1300(信越化学工業(株)製
画品名〕100部と可塑剤−DINA30部、エポキシ
化大豆油10部、0a−Zn系安定剤(昭島化学社製)
1部との配合物に、第1表C二表示した量のNBR・ケ
ミガム(グツドイヤー社製商品名)をヘンシェルミキサ
ー中で混合して塩化ビニル樹脂組成物を作り、これをT
−ダイ押出成形で厚さ16μmのフィルムとし、これに
ついてのn−ヘプタンC;よる”1ffi剤の押出量な
しらべたところ、第1表に併記したとおりの結果が得ら
れた。
Example 1 100 parts of vinyl chloride resin TK1300 (product name manufactured by Shin-Etsu Chemical Co., Ltd.), 30 parts of plasticizer-DINA, 10 parts of epoxidized soybean oil, 0a-Zn stabilizer (manufactured by Akishima Chemical Co., Ltd.)
A vinyl chloride resin composition was prepared by mixing 1 part of NBR/chemigum (product name manufactured by Gutdeyer Co., Ltd.) in the amount shown in Table 1 C2 in a Henschel mixer.
- A film with a thickness of 16 μm was formed by die extrusion molding, and the extrusion amount of the 1ffi agent based on n-heptane C was compared, and the results shown in Table 1 were obtained.

III表 実施例2 塩化ビニル樹脂・TK−1300(信越化学工業(株1
製商品名)100部C:可塑剤としてDINA30部と
エポキシ化大豆油10部、0a−Zn系複合安定剤(昭
島化学社製)1部および182表【:表示した量のNB
R・ケミガム(グツドイヤー社製商品名ンを添加し、ヘ
ンシェルミキサー中で混合して塩化ビニル樹脂組成物を
作った。
Table III Example 2 Vinyl chloride resin TK-1300 (Shin-Etsu Chemical Co., Ltd. 1
Product name) 100 parts C: 30 parts of DINA as a plasticizer, 10 parts of epoxidized soybean oil, 1 part of Oa-Zn composite stabilizer (manufactured by Akishima Chemical Co., Ltd.) and Table 182 [: Displayed amount of NB
R. Chemi Gum (trade name, manufactured by Gutdeyer) was added and mixed in a Henschel mixer to prepare a vinyl chloride resin composition.

つぎC二、この組成物からT−ダイ押出成形で厚さ16
μmのフィルムを作り、このフィルムについてn−へブ
タンC二よる可塑剤の抽出量を測定すると共に、JIS
  K−7216m規定された脆化温度とクラツシュベ
ルグ柔軟温度測定器による柔軟温度を測定してその耐寒
性をしらべたところ、第2表(;併記したとおりの結果
が得られた。
Next, C2, from this composition, a thickness of 16 mm was formed by T-die extrusion molding.
A μm film was made, and the amount of plasticizer extracted by n-hebutane C2 was measured on this film.
When the cold resistance was examined by measuring the embrittlement temperature specified by K-7216m and the softness temperature using a Kratschberg softness temperature measuring device, the results shown in Table 2 were obtained.

また、このフィルムCニハイインパクトポリスチvンv
 −) 0.33mmt(帝国化成(株ン製、HIPS
シートと略記する〕と二軸延伸ポリスチレンシート0.
251[三菱モンナント(株)製、opsシートと略記
する]とをiね、プレス機で20KP/(Xの圧力で3
時間常温プレスしたのち、このトレーC:ついての引張
り強度と伸びを測定したところ、”fi3−71FC示
したとおりの結果が得られた。
In addition, this film C Ni-high impact polystyrene v
-) 0.33mmt (manufactured by Teikoku Kasei Co., Ltd., HIPS
sheet] and biaxially oriented polystyrene sheet 0.
251 [manufactured by Mitsubishi Monnant Co., Ltd., abbreviated as ops sheet] was heated with a press machine at a pressure of 20 KP/(X).
After pressing at room temperature for an hour, the tensile strength and elongation of this tray C were measured, and the results as shown in "fi3-71FC" were obtained.

第   2   表Table 2

Claims (1)

【特許請求の範囲】 1、1)塩化ビニル系樹脂100重量部 2)アクリロニトリル・ ブタジエン共重合体0.5〜20重量部 3)可塑剤20〜60重量部 とからなることを特徴とする食品包装フィルム用塩化ビ
ニル系樹脂組成物。 2、アクリロニトリル・ブタジエン共重合体がアクリロ
ニトリル20〜50重量%、ブタジエン50〜80重量
%のものである特許請求の範囲第1項記載の食品包装フ
ィルム用塩化ビニル系樹脂組成物。 3、可塑剤がアジピン酸ジイソノニル、アジピン酸ジ−
n−アルキル、アセチルクエン酸トリブチル、エポキシ
化大豆油およびエポキシ化アマニ油から選ばれたもので
ある特許請求の範囲第1項記載の食品包装フィルム用塩
化ビニル系樹脂組成物。
[Scope of Claims] 1. A food product comprising: 1) 100 parts by weight of a vinyl chloride resin; 2) 0.5 to 20 parts by weight of an acrylonitrile-butadiene copolymer; and 3) 20 to 60 parts by weight of a plasticizer. Vinyl chloride resin composition for packaging films. 2. The vinyl chloride resin composition for food packaging films according to claim 1, wherein the acrylonitrile-butadiene copolymer contains 20 to 50% by weight of acrylonitrile and 50 to 80% by weight of butadiene. 3. Plasticizer is diisononyl adipate, di-adipate
The vinyl chloride resin composition for food packaging films according to claim 1, which is selected from n-alkyl, acetyl tributyl citrate, epoxidized soybean oil, and epoxidized linseed oil.
JP19135084A 1984-09-12 1984-09-12 Vinyl chloride resin composition for food packaging film Pending JPS6169851A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19135084A JPS6169851A (en) 1984-09-12 1984-09-12 Vinyl chloride resin composition for food packaging film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19135084A JPS6169851A (en) 1984-09-12 1984-09-12 Vinyl chloride resin composition for food packaging film

Publications (1)

Publication Number Publication Date
JPS6169851A true JPS6169851A (en) 1986-04-10

Family

ID=16273109

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19135084A Pending JPS6169851A (en) 1984-09-12 1984-09-12 Vinyl chloride resin composition for food packaging film

Country Status (1)

Country Link
JP (1) JPS6169851A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03146538A (en) * 1989-10-31 1991-06-21 Toyoda Gosei Co Ltd Nitrile rubber-polyvinyl chloride polyblend rubber formulation
JP2007197605A (en) * 2006-01-27 2007-08-09 Mitsubishi Plastics Ind Ltd Polyvinyl chloride resin composition and stretch film
JP2007224205A (en) * 2006-02-24 2007-09-06 Mitsubishi Plastics Ind Ltd Vinylchloride-based resin composition and stretch film
JP2007231055A (en) * 2006-02-28 2007-09-13 Mitsubishi Plastics Ind Ltd Vinyl chloride-based resin composition for food packaging and stretch film
JP2008006605A (en) * 2006-06-27 2008-01-17 Mitsubishi Plastics Ind Ltd Vinyl chloride type laminated/stretched film and its manufacturing method
CN102604269A (en) * 2012-03-20 2012-07-25 绍兴宏润消防器材有限公司 Low-temperature anti-vapour food preservative film
KR20120085270A (en) * 2009-09-30 2012-07-31 다우 글로벌 테크놀로지스 엘엘씨 Acetylated derivatives of castor oil and their blends with epoxidized fatty acid esters

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4920934A (en) * 1972-06-17 1974-02-23
JPS53112947A (en) * 1977-03-14 1978-10-02 Sanyo Trading Co Vinyl chloride resin composition and articles made thereof
JPS5730749A (en) * 1980-07-31 1982-02-19 Dainippon Ink & Chem Inc Vinyl chloride type resin composition for food and medical treatment

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4920934A (en) * 1972-06-17 1974-02-23
JPS53112947A (en) * 1977-03-14 1978-10-02 Sanyo Trading Co Vinyl chloride resin composition and articles made thereof
JPS5730749A (en) * 1980-07-31 1982-02-19 Dainippon Ink & Chem Inc Vinyl chloride type resin composition for food and medical treatment

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03146538A (en) * 1989-10-31 1991-06-21 Toyoda Gosei Co Ltd Nitrile rubber-polyvinyl chloride polyblend rubber formulation
JP2007197605A (en) * 2006-01-27 2007-08-09 Mitsubishi Plastics Ind Ltd Polyvinyl chloride resin composition and stretch film
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