JPH0420571A - Sheet or film for packaging food - Google Patents

Sheet or film for packaging food

Info

Publication number
JPH0420571A
JPH0420571A JP2125895A JP12589590A JPH0420571A JP H0420571 A JPH0420571 A JP H0420571A JP 2125895 A JP2125895 A JP 2125895A JP 12589590 A JP12589590 A JP 12589590A JP H0420571 A JPH0420571 A JP H0420571A
Authority
JP
Japan
Prior art keywords
film
acid monoglyceride
antibacterial
sheet
properties
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
JP2125895A
Other languages
Japanese (ja)
Other versions
JP2830371B2 (en
Inventor
Kimio Suzuki
公雄 鈴木
Tamotsu Kawai
川合 保
Katsuhiko Hayashi
克彦 林
Takeshi Shimofusachi
剛 下房地
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.)
Osaka Kasei Co Ltd
Mitsubishi Kasei Corp
Original Assignee
Osaka Kasei Co Ltd
Mitsubishi Kasei Corp
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 Osaka Kasei Co Ltd, Mitsubishi Kasei Corp filed Critical Osaka Kasei Co Ltd
Priority to JP2125895A priority Critical patent/JP2830371B2/en
Publication of JPH0420571A publication Critical patent/JPH0420571A/en
Application granted granted Critical
Publication of JP2830371B2 publication Critical patent/JP2830371B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the title sheet or film which has antibacterial, anti-fogging and antistatic properties and is safe even when in contact with foods by fabricating a thermoplastic resin having a small amount of a specified fatty acid monoglyceride mixture incorporated therein. CONSTITUTION:0.01-5wt.% mixture of octanoic acid monoglyceride and/or decanoic acid monoglyceride and lauric acid monoglyceride is incorporated into a thermoplastic resin (preferably a polyolefin, PVC or polyamide resin) to produce a sheet or film. This sheet or film is quite safe even when in contact with the human body and foods and has persistent antibacterial, anti-fogging and antistatic properties.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は抗菌性、防曇性、帯電防止性を合せ持つ食品包
装用シートまたはフィルムに関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a food packaging sheet or film that has antibacterial, antifogging, and antistatic properties.

さらに詳しくは、食品に触れた場合でも、安全性の高い
抗菌性、防曇性、帯電防止性を有するシートまたはフィ
ルムに関する。
More specifically, the present invention relates to a sheet or film that has antibacterial, antifogging, and antistatic properties and is highly safe even when it comes into contact with food.

〔従来の技術〕[Conventional technology]

食品包装には従来塵埃や細菌による汚染を防ぎ、清潔に
保つために、ハトロン紙や合成樹脂フィルムで包装され
るが、さらに効果を上げるために、この包装材料に抗菌
剤処理をすることが提案されている。
Traditionally, food is packaged with Hatron paper or synthetic resin film to prevent contamination from dust and bacteria and to keep it clean, but it is proposed that this packaging material be treated with an antibacterial agent to further increase its effectiveness. has been done.

例えば、フェノール系や、安息香酸系の殺菌剤を含浸さ
せた紙や、有機ハロゲン系や、ヘンズイミダゾール系の
殺菌剤を練り込んだフィルム等が製造されているが安全
性や効力の面で欠点があった。
For example, paper impregnated with phenol-based or benzoic acid-based fungicides, and films impregnated with organic halogen-based or henzimidazole-based fungicides are manufactured, but they have drawbacks in terms of safety and efficacy. was there.

また銀、銅1亜鉛等の金属イオンが抗菌性を有すること
に着目し、金属の微粉末を高分子化合物に接着または添
加する方法あるいは金属の化合物を高分子化合物に含有
させる方法が知られている。
In addition, focusing on the fact that metal ions such as silver, copper and zinc have antibacterial properties, there are known methods of adhering or adding fine metal powders to polymer compounds, or methods of incorporating metal compounds into polymer compounds. There is.

その一方法としてイオン交換能又は、錯体形成能を有す
る官能基を高分子に含有させ、この官能基に金属イオン
を保持させる方法があるが、この方法では官能基と高分
子との相互作用等によって高分子が著しく物性変化を起
し易く、用い得る高分子の種類及び官能基の種類と量と
に、極めて制限され易いものとならざるを得なかった。
One method is to make a polymer contain a functional group that has ion-exchange ability or a complex-forming ability, and have this functional group hold metal ions, but in this method, the interaction between the functional group and the polymer As a result, the physical properties of the polymer tend to change significantly, and the types of polymers that can be used and the types and amounts of functional groups that can be used are extremely limited.

それに対して抗菌作用を有する金属イオンをイオン交換
能を有する無機系固体粒子に保持させて、これを高分子
体に付与させる方法があるが(特開平1−186804
)、固体粒子の凝集や偏在等により抗菌力にバラツキが
生じたり、柔軟性や、透明度など高分子体の物性を損う
場合がある。また通常は包埋等により多量(2〜3%以
上)の練込みを要していた。また、特に食品包装用フィ
ルムではこうした抗菌性と共に見ばえを良くし、商品性
を高め、かつ菌の培地となりやすい水滴をつくらない為
に防曇性、はこり等の耐着を防く為に帯電防止性が求め
られており、防曇性、帯電防止性と共に抗菌性も同時に
合わせ持つ食品包装用シートまたはフィルム出現が切望
されていた。
On the other hand, there is a method in which metal ions with antibacterial effects are held in inorganic solid particles with ion-exchange ability, and these are added to a polymer (Japanese Patent Application Laid-Open No. 1-186804).
), agglomeration or uneven distribution of solid particles may cause variations in antibacterial activity, and may impair the physical properties of the polymer, such as flexibility and transparency. Further, a large amount (2 to 3% or more) of kneading is usually required for embedding or the like. In addition, especially for food packaging films, in addition to these antibacterial properties, it also improves the appearance and marketability, and also has anti-fog properties to prevent the formation of water droplets that can easily become a culture medium for bacteria, and to prevent adhesion such as flaking. Antistatic properties are required for food products, and there has been a strong desire for food packaging sheets or films that have both antifogging and antistatic properties as well as antibacterial properties.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

本発明は、従来の技術で不充分な点を改善し、安全で長
期間有効な抗菌力を持ち、同時に防曇性、帯電防止性を
合わせ持ち、用途に通した物性を維持したフィルム・シ
ート、シートから加工される容器などの食品包装用品を
提供することを目的とする。
The present invention improves the inadequacies of conventional technology, and provides films and sheets that have safe and long-lasting antibacterial activity, as well as anti-fog and antistatic properties, and maintain physical properties suitable for various uses. The purpose of the Company is to provide food packaging supplies such as containers processed from sheets.

[課題を解決するための手段] 本発明はオクタン酸モノグリセリド、デカン酸モノグリ
セリド及びラウリン酸モノグリセリド(以下それぞれC
s、CIoおよびCI2と略称する。)の混合物を含有
させたシート、フィルムが優れた抗菌性、防曇性、帯電
防止性を合せ持っていることを見い出し本発明に到達し
たものである。
[Means for Solving the Problems] The present invention provides octanoic acid monoglyceride, decanoic acid monoglyceride, and lauric acid monoglyceride (hereinafter each C
abbreviated as s, CIo and CI2. The present invention was achieved based on the discovery that sheets and films containing a mixture of (1) have excellent antibacterial, antifogging, and antistatic properties.

食用油脂から製造した脂肪酸モノグリセリドは食品添加
物として、使用食品、使用量に規制が設けられていない
程安全な化合物である。その中の一部のものが抗菌力が
あることは知られているが、熱可塑性樹脂に溶融、混合
した場合の抗菌特性については全く知られていなかった
Fatty acid monoglycerides produced from edible fats and oils are such safe compounds that there are no restrictions on the foods in which they can be used or the amounts used as food additives. It is known that some of them have antibacterial properties, but nothing was known about their antibacterial properties when melted and mixed with thermoplastic resins.

本発明に用いる脂肪酸モノグリセリドは、C8と01゜
の何れか一方又は両方と01□との混合物である。
The fatty acid monoglyceride used in the present invention is a mixture of either or both of C8 and 01° and 01□.

使用量は熱可塑性樹脂に対して該混合物を0.01〜5
重量%好ましくは0.1〜3重量%特に好ましくは0.
3〜2重量%である。下限値以下では、抗菌効力、防曇
効力共不充分である。上限値以上加えることは、実用上
の抗菌効力として不必要である上べたつきが大きくなり
、シート及びフィルムの物性変化が大きくなる等好まし
くない。
The amount used is 0.01-5% of the mixture based on the thermoplastic resin.
% by weight, preferably 0.1-3% by weight, particularly preferably 0.
It is 3 to 2% by weight. Below the lower limit, both antibacterial and antifogging effects are insufficient. Adding more than the upper limit is not preferable because it increases stickiness, which is unnecessary for practical antibacterial efficacy, and increases changes in physical properties of sheets and films.

脂肪酸モノグリセリドC,,C,。およびCI2の混合
割合は特に限定されないがC6またはCIOまたはC8
+C,。の重量とC1□の重量比はC,、C,。または
Cm +C+o: C+□=3.3〜0.2:1で優れ
た抗菌性を発揮し好ましい。
Fatty acid monoglyceride C,,C,. The mixing ratio of CI2 is not particularly limited, but C6 or CIO or C8
+C,. The weight ratio of C1□ to C1□ is C,,C,. Or Cm + C + o: C + □ = 3.3 to 0.2:1, which exhibits excellent antibacterial properties and is preferred.

防曇性は室温付近の環境と冷蔵庫の中の様な低温環境と
で最適な混合比が異なる。10°C以上の環境ではC8
およびCIOは親水性が高いため、溶出しやすく、比較
的短時間で防曇性を失うため、Cs、CIoまたはCs
 +clo: C+z=5〜0.3 : 1の範囲内が
好ましい。10’C未満の低温では疎水性が強調されC
8の溶出は押えられる方向だが、Cs、CooまたはC
a +Coo 二C+z= 10〜0.3 :lの混合
比で混合するのが好ましい。特にはC。
The optimal mixing ratio for antifogging properties differs depending on the environment near room temperature and the low temperature environment such as inside a refrigerator. C8 in environments above 10°C
and CIO are highly hydrophilic, so they are easily eluted and lose their antifogging properties in a relatively short period of time, so Cs, CIo or Cs
+clo: C+z=5 to 0.3:1 is preferred. At low temperatures below 10'C, hydrophobicity is emphasized and C
The elution of 8 is in the suppressed direction, but Cs, Coo or C
It is preferable to mix at a mixing ratio of a+Coo2C+z=10 to 0.3:l. Especially C.

CIOまたはCs 十C+o: CIz=5〜0.3 
: 1の混合比では通常使用される広い温度範囲にわた
って長期的な防曇性を発揮する。
CIO or Cs 10C+o: CIz=5~0.3
: A mixture ratio of 1 exhibits long-term antifogging properties over a wide temperature range commonly used.

本発明の混合物は、シート フィルムなどに溶融成形す
る以前の工程で周知の方法により溶融混合することによ
り調整することができる。
The mixture of the present invention can be prepared by melt-mixing by a well-known method prior to melt-forming into a sheet, film, or the like.

本発明に通用される熱可塑性樹脂は、ポリエチレン、ポ
リプロピレン、エチレン−酢酸ビニル共重合体、エチレ
ン−αオレフィン共重合体の何れか、単独又は、これら
の中の混合物から成るポリオレフィン系樹脂、(ここで
エチレン−αオレフィン共重合体のαオレフィンとして
は、炭素数4〜10でブテン−1,ペンテン−1,イソ
ブチン。
The thermoplastic resin that can be used in the present invention is a polyolefin resin consisting of any one of polyethylene, polypropylene, ethylene-vinyl acetate copolymer, and ethylene-α-olefin copolymer, either alone or in a mixture thereof. The α-olefin of the ethylene-α-olefin copolymer has 4 to 10 carbon atoms and includes 1-butene, 1-pentene, and isobutyne.

3−メチル−ブテン−1,ヘキセン−1,4−メチル−
ペンテン−1,ヘプテン−1,オクテン1、デセン−1
等が挙げられる)ナイロン6、すイロン12などのポリ
アミド樹脂、ポリスチレン、ABS樹脂などのポリスチ
レン樹脂、ポリ塩化ビニル、ポリ酢酸ビニル、ポリメタ
クリル酸メチルなどのビニル樹脂、ポレエチレンテレフ
タレートポリブチレンテレフタレート、ポリカーボネー
ト。
3-methyl-butene-1,hexene-1,4-methyl-
Pentene-1, Heptene-1, Octene-1, Decene-1
etc.) Polyamide resins such as nylon 6 and Suilon 12, polystyrene resins such as polystyrene and ABS resins, vinyl resins such as polyvinyl chloride, polyvinyl acetate, and polymethyl methacrylate, polyethylene terephthalate, polybutylene terephthalate, and polycarbonate. .

ポリアセタール、ポリフェニレンオキシドのようなポリ
エーテル樹脂、ポリウレタン樹脂などがある。中でもポ
リオレフィン系樹脂、ポリ塩化ビニル ポリアミド樹脂
が好ましい。
Examples include polyacetal, polyether resins such as polyphenylene oxide, and polyurethane resins. Among these, polyolefin resins and polyvinyl chloride polyamide resins are preferred.

シート、フィルムに成形加工する方法としては、公知の
方法が利用できる。予め、バンバリー型ミキサー −軸
あるいは多軸混練機等で前記熱可塑性樹脂に均一に混練
し、インフレーション法、Tダイ法、カレンダー法等通
常の成形加工方法で加工し、他の機能を附与するために
共押出し法や他のシート、フィルムとのラミネーション
による多層化もできる。又、チューブラ−二軸延伸、テ
ンター二軸延伸を施すことも好ましい。通常用いられる
厚みは0.01〜21!ll11であり、好ましくは0
.03〜1,5■である。
Any known method can be used to form the material into a sheet or film. In advance, the thermoplastic resin is uniformly kneaded using a Banbury-type mixer-shaft or multi-shaft kneading machine, etc., and processed by a normal molding method such as an inflation method, a T-die method, or a calendar method to impart other functions. Therefore, it can be multilayered by coextrusion or lamination with other sheets or films. Further, it is also preferable to perform tubular biaxial stretching or tenter biaxial stretching. The thickness usually used is 0.01~21! ll11, preferably 0
.. It is 03 to 1,5 ■.

尚、樹脂に通常添加される可塑剤、熱安定剤酸化防止剤
、充填剤、滑剤、アンチブロンキング剤、紫外線吸収剤
9着色剤、改質材等は必要に応じて使用することはさし
つかえない。
In addition, plasticizers, heat stabilizers, antioxidants, fillers, lubricants, anti-bronching agents, ultraviolet absorbers, colorants, modifiers, etc. that are normally added to resins may be used as necessary. .

(作用〕 Cs、C1゜およびCI□各単独の抗菌力は菌の種類に
よって相違するが、概してC1l≧C3゜〉C72の順
に小になる。しかしそれぞれを樹脂に混練するとおよそ
CIl≦01゜〈C1□の順になる。
(Effect) The antibacterial activity of Cs, C1゜, and CI□ alone differs depending on the type of bacteria, but generally decreases in the order of C1l≧C3゜〉C72.However, when each is kneaded into resin, approximately CIl≦01゜〈 The order is C1□.

この理由はC8およびC4゜は比較的高沸点の物質であ
るが、それでも樹脂に混練する際の加熱処理による蒸発
揮散損失がかなり多いためと考えられる。
The reason for this is thought to be that although C8 and C4° are substances with relatively high boiling points, they still suffer considerable evaporation loss due to heat treatment when kneading into resin.

そこでC8,C,。それぞれ単独またはC8,C,。So C8, C,. Each alone or C8, C,.

の混合物にCI2を加えることによってC8またはC1
゜の揮散を引止め損失を大幅に少くすることができ、さ
らにCe、C+oおよびCI□のそれぞれの抗菌スペク
トルが相剰的に働き抗菌効力も増強されるものである。
C8 or C1 by adding CI2 to the mixture of
It is possible to suppress the volatilization of ゜ and significantly reduce the loss, and furthermore, the antibacterial spectra of Ce, C+o and CI□ work together in a mutually beneficial manner, thereby enhancing the antibacterial efficacy.

またC8およびCIOは親水性が比較的高いため樹脂の
表面部分に存在するCa、C+。は付着水滴によって溶
出され易く、そのため防曇作用が低下するが、親水性が
より少ないCI□を混合することで溶出を抑制し防曇効
果を高めるとともに有効期間を延長することができる。
In addition, C8 and CIO have relatively high hydrophilicity, so Ca and C+ exist on the surface of the resin. is easily eluted by adhering water droplets, which reduces the antifogging effect; however, by mixing CI□, which has less hydrophilicity, elution can be suppressed, the antifogging effect can be enhanced, and the effective period can be extended.

帯電防止効果は脂肪酸モノグリセリドのもつ適度の界面
活性効果によるものである。
The antistatic effect is due to the moderate surfactant effect of fatty acid monoglycerides.

〔実施例] 次に実施例を挙げて本発明を説明するが、本発明は、こ
れらの実施例に限定されるものではない。
[Examples] Next, the present invention will be explained with reference to Examples, but the present invention is not limited to these Examples.

試料調整 実施例に用いた試料は次の方法で調整した。Sample preparation The samples used in the examples were prepared by the following method.

(本発明の試料) 低密度ポリエチレン(三菱化成社製 三菱ポリエチF1
31  MFR=1.3  ρ−0,924)のペレッ
ト粉砕品に08と01□をそれぞれ1:21:3.3:
1の重量比で混合した組成物、C1゜とC1□をそれぞ
れ1:3.3:1の重量比で混合した組成物、およびC
8と01゜を等重量づつ混合したものとC+zを3:1
の重量比で混合した組成物をそれぞれ均一に混合し、二
軸スクリュータイプ混練機を用いて溶融混練し、5重量
%マスターハツチを作成した。このマスターハツチをF
131ペレットで、0.1%、0.3%、0.5%含有
まで希釈し、厚さ50μmのフィルムをインフレーショ
ン法で得た。
(Sample of the present invention) Low density polyethylene (Mitsubishi Polyethylene F1 manufactured by Mitsubishi Chemical Corporation)
31 MFR = 1.3 ρ-0,924) 08 and 01□ were added to the crushed pellets at 1:21:3.3, respectively.
A composition in which C1° and C1□ were mixed in a weight ratio of 1:3.3:1, respectively;
A mixture of equal weights of 8 and 01° and C+z at 3:1
The compositions were mixed uniformly at a weight ratio of , and melt-kneaded using a twin-screw type kneader to prepare a 5% by weight master hatch. F this master hatch
131 pellets to contain 0.1%, 0.3%, and 0.5%, and a film with a thickness of 50 μm was obtained by an inflation method.

(比較の試料) モノグリセリドとしてC,、C,、またはC1□をそれ
ぞれ単独に用いた以外は上記と全く同し方法で厚さ50
μmのフィルムを得た。
(Comparative sample) A sample with a thickness of 50 mm was prepared in exactly the same manner as above except that C, C, or C1□ was used alone as the monoglyceride.
A μm film was obtained.

またモノグリセリドの代りにゼオライト銀(Xと略する
)、パラオキシ安息香酸ブチルエステル(Yと略する)
を用いた以外は上記と全く同し方法で厚さ50μmのフ
ィルムを得た。
Also, instead of monoglyceride, zeolite silver (abbreviated as X), paraoxybenzoic acid butyl ester (abbreviated as Y)
A film with a thickness of 50 μm was obtained in exactly the same manner as above except that .

(無添加の試料) F131ベレットを用いてインフレーション法で厚さ5
0μmのフィルムを得た。
(Sample without additives) Using an F131 pellet, the thickness was 5 mm using the inflation method.
A film of 0 μm was obtained.

実施例−1 前記のフィルム試料を用いて、次の方法で抗菌効力試験
を実施した。
Example-1 Using the above film sample, an antibacterial efficacy test was carried out in the following manner.

抗菌効力試験方法 5taphylococcus aureus  F 
D A” 209P(黄色ブドウ球菌) Bacillus cereus     (セレウス
菌)Escherichia coli  T F O
3301(大腸菌)を供試して、AATCC−90改法
により抗菌試験を実施した。すなわち、各細菌を直径8
5IIIIIIプラスチツク製シヤーレ中に菌数が約2
〜5X10’個となるように調整して5dの普通寒天培
地で均一に分散、固化させた。
Antibacterial efficacy test method 5 taphylococcus aureus F
D A” 209P (Staphylococcus aureus) Bacillus cereus (Bacillus cereus) Escherichia coli T F O
3301 (Escherichia coli) was used, and an antibacterial test was conducted according to the revised AATCC-90 method. That is, each bacterium has a diameter of 8
5IIIIII The number of bacteria in a plastic tray is approximately 2.
The particles were adjusted to 5 x 10' pieces and uniformly dispersed and solidified on a 5 d ordinary agar medium.

本寒天培地の表面に各フィルム試料25X25胴裁片を
貼付して、37°Cで24時間培養後、阻止円の有無を
調査した。
A 25×25 body piece of each film sample was attached to the surface of this agar medium, and after culturing at 37° C. for 24 hours, the presence or absence of an inhibition circle was examined.

結果を表−1に示す。The results are shown in Table-1.

比較例に較べて、格段に有効なことが示されている。ま
た本結果はフィルム接触面だけでなく、非接触範囲にも
効果の及ぶことが分かる。
It has been shown that this method is much more effective than the comparative example. Furthermore, it can be seen that this result is effective not only on the film contact surface but also on the non-contact area.

実施例−2 前記のフィルム試料および菌株を供試して、繊維衛生協
議会の菌数測定方法に準じて試験をした。
Example 2 The film samples and bacterial strains described above were used and tested in accordance with the bacterial count measurement method of the Textile Hygiene Council.

フィルム試料を非滅菌および121°C920分のオー
トクレーブ滅菌の2法について実施した結果を表−2に
示す。
Table 2 shows the results of sterilizing film samples using two methods: non-sterilization and autoclave sterilization at 121° C. for 920 minutes.

比較例に較べて、本発明の各例が優れており、静菌性で
な(殺菌性があることが分る。
It can be seen that each example of the present invention is superior to the comparative example and has bacteriostatic (sterilizing) properties.

実施例−3 前記で作成したフィルム試料について防曇試験を行った
Example 3 An anti-fog test was conducted on the film sample prepared above.

高温試験については、カップに水を入れ50±1°Cに
調整する。この上に実施例−1のフィルムを覆い密封し
23°C150%RHの環境に放置した際の各経過時間
ごとのフィルムの曇っていない面積を百分率で示す。
For high temperature tests, fill a cup with water and adjust to 50±1°C. The film of Example 1 was covered and sealed on top of this, and the non-cloudy area of the film was expressed as a percentage for each elapsed time when the film was left in an environment of 23° C. and 150% RH.

低温状Qはカップに水を入れ18°C±1°Cに調整し
この上に実施例−1のフィルムを覆い密封し5°Cの冷
蔵庫内に放置した際の各経過時間ごとの曇っていない面
積を百分率で示す。
The low-temperature state Q was measured by filling a cup with water, adjusting it to 18°C ± 1°C, covering it with the film of Example 1, sealing it, and leaving it in a refrigerator at 5°C. The area without area is expressed as a percentage.

実施した結果を表−3に示す。C8,C,。にCI□を
混合することでCB 、  CIO,CI2それぞれ単
独よりも防曇性が向上することが分る。
The results are shown in Table 3. C8, C,. It can be seen that by mixing CI□ with CB, the antifogging property is improved more than when each of CB, CIO, and CI2 is used alone.

実施例−4 帯電防止効力試験 前記のフィルム試料を用いて23”C,50%RH環境
下で表面固有抵抗を測定した。
Example 4 Antistatic Efficacy Test Using the above film sample, the surface resistivity was measured in an environment of 23"C and 50% RH.

実施結果を表−4に示す。何れも良好な帯電防止性を示
した。
The implementation results are shown in Table-4. All exhibited good antistatic properties.

裏−1 抗菌効力試験(ハロー試(社) 表−2 抗菌効力試験−数測之 *培剤律礁囲町巻数 表−3 防 曇 試 ・験 〔発明の効果] 本発明により、人体や食品に接触しても極めて、安全で
長時間効力を発揮する抗菌性、防曇性、帯電防止性を合
せ持つ食品包装用シートまたはフィルムを提供すること
ができる。
Back - 1 Antibacterial efficacy test (Hello Test Co., Ltd.) Table 2 Antibacterial efficacy test - Number measurement *Culture agent Ritsho Ikimachi volume table - 3 Anti-fogging test/test [Effect of the invention] The present invention has been shown to be effective against the human body and food. It is possible to provide a sheet or film for food packaging that has antibacterial, antifogging, and antistatic properties that are extremely safe even when in contact and exhibit long-lasting effects.

Claims (3)

【特許請求の範囲】[Claims] (1)オクタン酸モノグリセリドおよび/またはデカン
酸モノグリセリドとラウリン酸モノグリセリドとを0.
01〜5重量%含有する熱可塑性樹脂からなることを特
徴とする食品包装用シートまたはフィルム。
(1) Octanoic acid monoglyceride and/or decanoic acid monoglyceride and lauric acid monoglyceride are mixed at 0.0%.
1. A food packaging sheet or film comprising a thermoplastic resin containing 0.01 to 5% by weight.
(2)熱可塑性樹脂がポリオレフィン系樹脂、ポリ塩化
ビニール樹脂またはポリアミド樹脂の何れかである請求
項1記載の食品包装用シートまたはフィルム。
(2) The food packaging sheet or film according to claim 1, wherein the thermoplastic resin is a polyolefin resin, a polyvinyl chloride resin, or a polyamide resin.
(3)オクタン酸モノグリセリドおよび/またはデカン
酸モノグリセリドと、ラウリン酸モノグリセリドとの重
量比が(10〜0.3):1である請求項1記載の食品
包装用シートまたはフィルム。
(3) The food packaging sheet or film according to claim 1, wherein the weight ratio of octanoic acid monoglyceride and/or decanoic acid monoglyceride to lauric acid monoglyceride is (10 to 0.3):1.
JP2125895A 1990-05-16 1990-05-16 Food packaging sheet or film Expired - Lifetime JP2830371B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2125895A JP2830371B2 (en) 1990-05-16 1990-05-16 Food packaging sheet or film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2125895A JP2830371B2 (en) 1990-05-16 1990-05-16 Food packaging sheet or film

Publications (2)

Publication Number Publication Date
JPH0420571A true JPH0420571A (en) 1992-01-24
JP2830371B2 JP2830371B2 (en) 1998-12-02

Family

ID=14921566

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2125895A Expired - Lifetime JP2830371B2 (en) 1990-05-16 1990-05-16 Food packaging sheet or film

Country Status (1)

Country Link
JP (1) JP2830371B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011012221A (en) * 2009-07-06 2011-01-20 Taiyo Kagaku Co Ltd Antibacterial resin composition
US9777407B2 (en) 2009-03-27 2017-10-03 3M Innovative Properties Company Hydrophilic polyproylene melt additives

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6762339B1 (en) 1999-05-21 2004-07-13 3M Innovative Properties Company Hydrophilic polypropylene fibers having antimicrobial activity

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9777407B2 (en) 2009-03-27 2017-10-03 3M Innovative Properties Company Hydrophilic polyproylene melt additives
JP2011012221A (en) * 2009-07-06 2011-01-20 Taiyo Kagaku Co Ltd Antibacterial resin composition

Also Published As

Publication number Publication date
JP2830371B2 (en) 1998-12-02

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