JPS59124941A - Drug-containing resin composition and its molding - Google Patents

Drug-containing resin composition and its molding

Info

Publication number
JPS59124941A
JPS59124941A JP57233865A JP23386582A JPS59124941A JP S59124941 A JPS59124941 A JP S59124941A JP 57233865 A JP57233865 A JP 57233865A JP 23386582 A JP23386582 A JP 23386582A JP S59124941 A JPS59124941 A JP S59124941A
Authority
JP
Japan
Prior art keywords
drug
resin
thermoplastic resin
fragrance
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.)
Granted
Application number
JP57233865A
Other languages
Japanese (ja)
Other versions
JPH0421699B2 (en
Inventor
Hachiro Saito
八郎 斎藤
Motohide Okamoto
岡本 元秀
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.)
Eneos Corp
Original Assignee
Nippon Petrochemicals 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 Nippon Petrochemicals Co Ltd filed Critical Nippon Petrochemicals Co Ltd
Priority to JP57233865A priority Critical patent/JPS59124941A/en
Publication of JPS59124941A publication Critical patent/JPS59124941A/en
Publication of JPH0421699B2 publication Critical patent/JPH0421699B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled compsn. capable of retaining an invariable medicinal effect or fragrance over a long period of time, by melt-mixing a thermoplastic resin compsn. contg. a drug with a thermoplastic resin non-compatible with the drug. CONSTITUTION:A thermoplastic resin (a) e.g. ethylene/vinyl acetate copolymer) compatible with a drug (b), such as perfume, vaporizable rust inhibitor or insecticide, is impregnated with or melt-mixed with the reagent (b) to obtain a resin compsn. (A). Compsn. A is melt-mixed with other thermoplastic resin (B) (e.g. crystalline PP) compatible with component (a), but incompatible with component (b). EFFECT:The loss of the drug is reduced and the effect of the drug and its persistence can be controlled. USE:Food packaging, protection of fruit and clothing, packing material for machines, etc.

Description

【発明の詳細な説明】 本発明は、長期間にわたって一定の薬効または芳香を+
1わia L (’+jる薬剤含有樹脂組成物およびそ
の成形品に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides for
This invention relates to a drug-containing resin composition and a molded article thereof.

従来から、香料、防黴剤、防錆剤、防虫剤等・の気化性
の薬剤を、ポリエチレン、ポリプロピレン′9の通常の
薬剤非相溶性の熱可塑性樹脂に含浸し、または薬剤を4
1コ合し、押出成形や射出成形等によって、フィルムや
その他の成型品としたものが供されている。
Conventionally, vaporizable chemicals such as fragrances, fungicides, rust preventives, insect repellents, etc., have been impregnated into thermoplastic resins such as polyethylene and polypropylene '9 that are not compatible with ordinary chemicals.
They are combined into films and other molded products by extrusion molding, injection molding, etc.

(−がし、」、記の気化性薬剤は、一般的に揮発性や散
逸性か大きい物質であるため、非相溶性熱可、:l1l
i性樹脂に薬剤を含浸した樹脂組成物、または溶融した
非相溶性熱可塑性樹脂に薬剤を混合した樹脂組成物は、
成形時の薬剤の1Ilk逸が激しいので成形が困難であ
るばかりでなく、薬効の持続性も非1〜に短いものとな
る。
(-gashi), vaporizable agents are generally volatile and dissipative substances, so they are incompatible thermochemicals.
A resin composition in which an i-type resin is impregnated with a drug, or a resin composition in which a drug is mixed in a molten incompatible thermoplastic resin,
Since 1Ilk of the drug is severely lost during molding, not only is molding difficult, but the duration of the medicinal effect is also very short.

力、気化性薬剤と相溶性を有する熱可塑性樹脂は、薬剤
類を含浸したり、溶融混合することは比較的容易である
が、製膜性が劣り、かつ成形が困難である等、加工性に
問題を有している。
Thermoplastic resins that have compatibility with vaporizable drugs are relatively easy to impregnate or melt-mix with drugs, but they have poor processability, such as poor film-forming properties and difficulty in molding. I have a problem with this.

未発明は、−に記の問題点を解決すべく、鋭意検l:・
1を重ねた結果なされたものである。
In order to solve the problems described in -, the uninvented invention has been thoroughly investigated.
This is the result of stacking 1.

すなわち、本発明は、薬剤と相溶性をイIする熱呵・塑
性樹脂(A)に該薬剤を含浸した樹脂組成物および/ま
たは溶融した熱可塑性樹脂(A)に該薬剤を混合した樹
脂組成物を、該熱n(習性樹脂(A)と相溶性を有する
が該薬剤とは非相溶性である他の熱可塑性樹脂CB)に
溶融混合してなる薬剤含有樹脂組成物およびその成形品
に関するものである。
That is, the present invention provides a resin composition in which a thermoplastic resin (A) that is compatible with a drug is impregnated with the drug, and/or a resin composition in which the drug is mixed in a molten thermoplastic resin (A). The present invention relates to a drug-containing resin composition obtained by melt-mixing a substance into the thermoplastic resin (other thermoplastic resin CB which is compatible with the habit resin (A) but incompatible with the drug) and a molded article thereof. It is something.

本発明者らは、上記薬剤と相溶性を有する熱可塑性樹脂
(A)に薬剤を充分に含浸させても、該樹脂表面から薬
剤が脱着揮散し難く、十分な芳香または薬効を発揮し得
す、製膜または成形も困難であるか、該薬剤含有組成物
を薬剤と非相溶性でかつ熱可塑性樹脂(A)と相溶性を
有する熱可塑性樹脂(B)に溶融混合させると、前記芳
香性または薬効性の効果が発揮され、かつ、その芳香お
よび薬効の持続性をコントロールでき、その−11、製
11りまたは成形し易いという知見を得て、本発明を完
成するに至ったものである。
The present inventors have discovered that even if the thermoplastic resin (A) that is compatible with the above-mentioned drug is sufficiently impregnated with the drug, the drug is difficult to desorb and volatilize from the resin surface, and sufficient aroma or medicinal efficacy can be exerted. , film formation or molding is difficult, or when the drug-containing composition is melt-mixed with a thermoplastic resin (B) that is incompatible with the drug and compatible with the thermoplastic resin (A), the aromatic The present invention was completed based on the knowledge that it exhibits medicinal effects, can control the fragrance and persistence of its medicinal effects, and is easy to manufacture or mold. .

本発明において使用する熱可塑性樹脂(A)としては、
石油樹脂、未加硫ゴム、ポリブテン、ポリ1.i化ビニ
ル樹脂、カルボキシル基含有エチレンへ張合体′へがあ
るが、特にエチレン−酢酸ビニルj1、中合体(EVA
)、エチレン−アクリル耐エチル共1千合体(EEA)
 1のカルボキシル基含有エチレン共小合体は、薬剤お
よび後述の熱可塑性樹脂CB)と、11常に良好な相溶
性を有する点で好ましい。
As the thermoplastic resin (A) used in the present invention,
Petroleum resin, unvulcanized rubber, polybutene, poly 1. I-vinyl resin, carboxyl group-containing ethylene polymer, but especially ethylene-vinyl acetate j1, intermediate polymer (EVA)
), 1,000 ethylene-acrylic ethyl resistant combination (EEA)
The carboxyl group-containing ethylene copolymer of No. 1 is preferable because it always has good compatibility with the drug and the thermoplastic resin CB described below.

とりわけ、エチレン−酢酸ビニル共重合体が好ましい。Particularly preferred is ethylene-vinyl acetate copolymer.

・力、熱i(塑性樹脂(B)とは−高、中、低密度のエ
チレンtjり抄型合体、あるいぼ、エチレン−プロピレ
ン共重合体、エチレン−ブテン−1共重合体、エチレン
−ヘキセン−1共重合体、エチし・ソー4−メfルヘン
テンー1共重合体、エチレンーオ’7rン利共重合体等
のエチレンを主成分とするα−オレフィンとのノI−重
合体、またはポリプロピレン、プロピレンを主成分とす
る他のα−オレフィンとの共重合体、ポリブテン−1、
ポリ−4−メチルペンテン−14N 、+7)ポリオレ
フィン系樹脂、およびそれらのマレイン化物、ナイロン
−6、ナイロン−8,13、ナイロン−12等のボリア
l−系樹脂、ポリヒニルアルコール系樹脂、ポリエステ
ル系樹脂、エチレン−酢酸ビニル共重合体のケン化物お
よびそれらの混合物などであり、比較的高い結晶性を有
し、かつ製11り性等の加工性が良好な樹脂か用いられ
る。
・Force, heat (What is plastic resin (B)? High, medium, and low density ethylene tj paper type amalgamation, warts, ethylene-propylene copolymer, ethylene-butene-1 copolymer, ethylene-hexene Polymers with α-olefins containing ethylene as a main component, such as -1 copolymers, ethyl-4-methylene-1 copolymers, and ethylene-on-7r copolymers; or polypropylene; Copolymer of propylene with other α-olefins, polybutene-1,
Poly-4-methylpentene-14N, +7) polyolefin resins and maleated products thereof, boria l-based resins such as nylon-6, nylon-8, 13, and nylon-12, polyhinyl alcohol-based resins, polyesters resins, saponified products of ethylene-vinyl acetate copolymers, and mixtures thereof.Resins that have relatively high crystallinity and good processability such as ease of manufacture are used.

これらの樹脂のうち、汎用性を有し、かつ安価で加工性
も良なfである等の点てポリオレフィン系樹脂が好まし
い。
Among these resins, polyolefin resins are preferred because they are versatile, inexpensive, and have good processability.

本発明の樹脂組成物およびその成形品の成分たる薬剤は
、香料、防錆剤、防(散剤、防腐剤、防虫剤、防鼠剤、
消臭剤、殺山剤、害虫忌避剤、防汚剤等である。
The drugs that are components of the resin composition and molded products of the present invention include fragrances, rust preventives, preventatives (powders, preservatives, insect repellents, rodent repellents,
These include deodorants, foresticides, pest repellents, and antifouling agents.

」ユ記薬剤の代表的な例を以下に列挙する。Typical examples of drugs listed below are listed below.

香料には、天然香料と人造香料とがあり、天然香料とし
ては、ジャコラ、シヘット(レイビョウ香)、カスドル
(カイリ香)およびアンバーグリス(リュウゼン香)等
の動物性香料、ラベンダー油、ハツカ油、レモン油、オ
レンジ油、ローズ油ショウノウ油、ビヤクダン油、ヒノ
キ油等の植物精油からなる植物性香料がある。
Fragrances include natural fragrances and artificial fragrances, and natural fragrances include animal fragrances such as jacola, shihet (raybyou incense), kasdol (kairi incense), and ambergris (ambergris), lavender oil, mustard oil, There are botanical fragrances made from plant essential oils such as lemon oil, orange oil, rose oil, camphor oil, sandalwood oil, and cypress oil.

また、人造香料としては、テルペン化合物、または刀香
族化合物等からなる合成香料、あるいは精油からにとし
て分留によって成分を分けた単離香料、その他各種の単
N+香斜、合成香才゛1、天然香料などを4昆合して実
用に適するように調製した調合香料などを包含する。
In addition, artificial fragrances include synthetic fragrances made of terpene compounds or aromatic compounds, isolated fragrances whose components are separated by fractional distillation from essential oils, and various other types of single N+ incense and synthetic fragrances. It includes mixed fragrances prepared by combining four natural fragrances and other natural fragrances to make them suitable for practical use.

気化fノl防錆剤としては、ジシクロ−・キシルアンモ
−ラム−’ll!4r m 塩、シクロヘキシルアンモ
ニウム炭酸J工4、イソプロピルアンモニウム安息香耐
塩、ジイソプロピルアンモニウムコハク酸塩等のような
有機アミンの無機および有機耐塩、安息香酸やナラI・
−ル酎のような芳香族酸、カプリル酩、ペラルゴン酸、
カプリン酪のよシな炭素数 6から10の脂肋醇、ベン
ゾトリアゾール、メチルベンゾトリアゾールのような複
素環式アミン、m−ジニトロベンゼン、ニトロナフタレ
ンのようなニトロ置換)′J査族化合物、ヘキサメチレ
ンテトラミンおよびその誘導体なとが挙げられ、これら
の1種または2種以」−の47コ合物が使用される。
As a vaporized rust preventive agent, dicyclo-xylammorum-'ll! 4r m salts, inorganic and organic salts of organic amines such as cyclohexylammonium carbonate J4, isopropylammonium benzoate, diisopropylammonium succinate, etc., benzoic acid and oak I.
- Aromatic acids such as alcoholic acid, caprylic acid, pelargonic acid,
Capric acid has 6 to 10 carbon atoms, heterocyclic amines such as benzotriazole, methylbenzotriazole, nitro-substituted compounds such as m-dinitrobenzene, nitronaphthalene, Examples include methylenetetramine and its derivatives, and 47 compounds of one or more of these are used.

また前記のその他の薬剤の具体例としては、ンルビン酸
、テヒ)〜口酢酸などの食品用の防腐剤、あるいは、サ
イアベンダソール、/\イナシン、α−ソロムシンナム
アルデヒド(BCA)等のUi ijl 剤、DDT剤
、 BHC剤、ドl) 7剤、パラチオン剤、DIlV
P剤、PGP剤等の防虫、殺虫剤、ホルマリン、サリチ
ル酸、フレオン−1・、フェノール、二トロフラソノ、
ニトロフリルアクリル酊アミF等の殺菌剤、酢酸フェニ
ル水銀、オレイン酸フェニル水銀、ナフテン耐錆、オレ
イン酸銅等の防汚剤、あるいはナラマイシン(商品名、
田辺製薬社製)、ラムタリン(商品名、松下電工社製)
、コトマイシン(商品名、大阪化成社製)等の防鼠剤な
どが挙げられ、これらの薬剤は、目的、用途等により2
種類以」二を4昆合して使用しても良い。
Further, specific examples of the other drugs mentioned above include food preservatives such as nruvic acid, tehi) to oral acetic acid, and Ui such as thiabendasole, /\inacin, and α-solomucinnamaldehyde (BCA). ijl agent, DDT agent, BHC agent, Dol) 7 agent, parathion agent, DIlV
Insect repellents such as P agents and PGP agents, insecticides, formalin, salicylic acid, freon-1, phenol, nitrofurasono,
Disinfectants such as nitrofuryl acrylic amine F, phenylmercury acetate, phenylmercury oleate, antifouling agents such as naphthene rust-resistant, copper oleate, or naramycin (trade name,
Tanabe Pharmaceutical Co., Ltd.), Ramtalin (trade name, Matsushita Electric Works Co., Ltd.)
, cotomycin (trade name, manufactured by Osaka Kasei Co., Ltd.) and other rodent repellents.
You may use a combination of 2 and 4 types.

本発明の組成物は、前記薬剤を、相溶性熱可塑性樹脂(
A)にあらかじめ含浸し、または溶融した熱可塑性樹脂
(A)に混合した後に、薬剤と非相溶性の熱?if塑性
樹脂(B)に配合して溶融混合した組成物であるが、薬
剤が香料等のような液体の場合には、熱可塑性樹脂(A
)に浸漬含浸させるか、あるいは防鯖剤、防虫剤、防黴
剤等のような固体の場合においては、適当な溶剤に溶解
して含浸させても良いが、直接所定量の樹脂(A)と薬
剤とを、11f1例の混練機または押出機内で溶融混合
することが好ましい。
The composition of the present invention combines the drug with a compatible thermoplastic resin (
Heat that is incompatible with the drug after pre-impregnating with A) or mixing with the molten thermoplastic resin (A)? If the composition is blended with plastic resin (B) and melt-mixed, but if the drug is a liquid such as perfume, thermoplastic resin (A
), or in the case of solids such as mackerel repellents, insect repellents, mold repellents, etc., they may be dissolved in a suitable solvent and impregnated; and the drug are preferably melt-mixed in a kneader or extruder, such as 11f1.

」記薬剤の含有量は、[]的、用途等により、薬剤のイ
Φ類および熱可塑性樹脂(A)および(B)の4φ類に
従って定めればよい。例えば、薬剤として香料を使用1
7、樹脂(A)をエチレン−酢酸ビニルバ屯合体(以下
、中に“EVA’“と言う)とした場合においては、香
料の含有量はEVAの酢酸ビニル(vA)含イ1量にほ
ぼ比例し、VA含有量が30重量%てあれば、香料もほ
ぼ30爪量%程度が含浸可能となる。しかし、芳香の強
さは、含イ1石料の量と共に強くなるが、最終製品中に
は0.01〜1重量%程度で充分であるから、香料含浸
EVAを10から100倍jl(に希釈する場合には、
EVA中には 1〜10重量%程度の香料を含浸させれ
ば充分である。
The content of the drug may be determined according to Class A of the drug and Class 4 of the thermoplastic resins (A) and (B) depending on the purpose, use, etc. For example, using fragrance as a medicine1
7. When the resin (A) is an ethylene-vinyl acetate composite (hereinafter referred to as "EVA'"), the fragrance content is approximately proportional to the vinyl acetate (vA) content of EVA. However, if the VA content is 30% by weight, approximately 30% of fragrance can be impregnated. However, the strength of the fragrance increases with the amount of the fragrance-containing stone, but 0.01 to 1% by weight is sufficient in the final product, so the fragrance-impregnated EVA is diluted 10 to 100 times. If you do,
It is sufficient to impregnate EVA with about 1 to 10% by weight of fragrance.

一方、芳香等の薬剤効力の持続性は、VA含有量および
前記薬剤含有樹脂(A)と熱可塑性樹脂(B)との混合
比率に依存する。例えは、木発明者らの実験によれば、
前記の香料を10重量%含浸したEVA (VAI5重
量%)に対して、熱可塑性樹脂(B)として低雀度ポリ
エチレンを用い、■から10倍量に昂ゝ釈、した場合に
は、0.5〜1年の芳香性をハ゛続し、lOから100
倍量に希釈した場合には約0.1〜0.5年の芳香性を
持続している。これらの持続性も、薬剤の種類、樹脂(
A)の種類やカルボキシル基の含有量、樹脂(B)の種
類等によって異なるか、他の薬剤についても同様な傾向
にあり、1」的、用途等に応じて適宜選択される。
On the other hand, the sustainability of drug efficacy such as aroma depends on the VA content and the mixing ratio of the drug-containing resin (A) and the thermoplastic resin (B). For example, according to the experiments of the inventors of wood,
When EVA (VAI 5% by weight) impregnated with 10% by weight of the above-mentioned fragrance is diluted from ■ to 10 times the amount by using low-strength polyethylene as the thermoplastic resin (B), 0. Continues aroma for 5 to 1 year, from lO to 100
When diluted to double the amount, it maintains its fragrance for about 0.1 to 0.5 years. The durability of these substances also depends on the type of drug, resin (
It varies depending on the type of A), the content of carboxyl groups, the type of resin (B), etc., and the same tendency applies to other drugs, and it is selected as appropriate depending on the purpose, use, etc.

本発明の組成物においては、タルク、炭酸カルシウム、
クレイ、シリカ、アルミナ、木粉、紙片等の充填剤、顔
料、紫外線吸収剤、酸化防市剤、可塑剤等の通常使用さ
れる添加剤を添加しても差支えない。また、香料含有熱
可塑性樹脂(A’)と、あらかじめ充填剤を含有させた
他の熱可塑性樹脂(B)とを混合する方法は、熱り塑性
樹脂(A)。
In the composition of the present invention, talc, calcium carbonate,
There is no problem in adding commonly used additives such as fillers such as clay, silica, alumina, wood powder, and paper chips, pigments, ultraviolet absorbers, oxidation inhibitors, and plasticizers. Further, a method of mixing the fragrance-containing thermoplastic resin (A') and another thermoplastic resin (B) containing a filler in advance is the thermoplastic resin (A).

熱可塑性樹脂(B)、充填剤および香料を直接Hg合、
溶融、成形する方法よりも、充填剤への香料の吸収がJ
l常に少なく効率的である一0本発明に使用される配合
機または混合機は、通例のもので良く、例えば、ヘンシ
ェルミキサー、ダルトンミキサー、ニーグー、バンバリ
ーミキサ−1熱ロールミル、あるいは押出機等を使用す
ることができる。
Thermoplastic resin (B), filler and fragrance are directly combined with Hg,
J
The compounding machine or mixer used in the present invention may be any conventional one, such as a Henschel mixer, a Dalton mixer, a Nigu, a Banbury mixer, a hot roll mill, or an extruder. can be used.

本願に含まれる他の発明は、香料をEVAに含浸した樹
脂組成物および/または溶融したEVAに香料を混合し
た樹脂組成物と、結晶性ポリオレフィン樹脂とからなる
ことを特徴とする香料含有成形品に関するものである。
Another invention included in the present application is a fragrance-containing molded article comprising a resin composition in which EVA is impregnated with a fragrance and/or a resin composition in which a fragrance is mixed in molten EVA, and a crystalline polyolefin resin. It is related to.

香料を直接結晶性ポリオレフィン樹脂に含浸する場合、
液体である香料が結晶性ポリオレフィン樹脂には含浸せ
ずに単なる樹脂表面への付着のみにとどまったり、また
、固体香料が低融点のために、成形機のシリンダー中で
融解して液体となり混合し難いので、香料含有、′トが
低く、効力の持続性に乏しいばかりでなく、混線時のロ
スが大きい。
When directly impregnating fragrance into crystalline polyolefin resin,
Liquid fragrances do not impregnate the crystalline polyolefin resin and simply stick to the resin surface, and solid fragrances have a low melting point, so they melt and become liquid in the cylinder of the molding machine and mix. Because it is difficult to use, it contains fragrance, has low heat content, and not only has poor long-lasting efficacy, but also has large losses when mixed.

これに比較して、本発明の成形品は、以下の特徴を有す
る。すなわち、 (1)高濃度の香料含有量のフィルムまたは成形品を造
ることが可能である; (2)芳香の強弱および持続性をコントロールすること
ができる; (3)成形加工条件が穏和で、香料の変質が殆どない; (4)加工時の揮発、散逸が少ないのでロスが殆どなく
、香料を有効に含有せしめlj)るので非常に経済的で
ある; (5)製膜性等の加工性が良好である;および(6)香
料含有樹脂組成物と結晶性ポリオレフィン樹脂とを直接
押出機内で混練成形することができるなどの多くの利点
を有している。
In comparison, the molded article of the present invention has the following characteristics. That is, (1) it is possible to make a film or molded product with a high concentration of fragrance; (2) it is possible to control the intensity and persistence of the fragrance; (3) the molding conditions are mild; There is almost no deterioration of the fragrance; (4) There is little volatilization and dissipation during processing, so there is almost no loss, and the fragrance is effectively contained, so it is very economical; (5) Processing such as film forming properties and (6) the fragrance-containing resin composition and the crystalline polyolefin resin can be kneaded and molded directly in an extruder.

なお、上記の結晶性ポリオレフィン樹脂とは、前記の熱
可塑性樹脂CB)中のポリオレフィン系樹脂で結晶性5
0%以上を有するものである。ポリオレフィン系樹脂の
結晶性が50%未満の場合には酸1模フィルムのブロッ
キングが著しいものとなり好ましくない。
The above-mentioned crystalline polyolefin resin is a polyolefin-based resin in the above-mentioned thermoplastic resin CB) and has crystallinity 5.
0% or more. If the crystallinity of the polyolefin resin is less than 50%, the blocking of the acid 1 film becomes significant, which is not preferable.

に記のように本発明の組成物および成形品は薬効の持続
性や成形性に優れ、かつ安価に製造できる′、9・の種
々の利点を有しており、押出成形、射出成形、中空成形
等の種々の成形法によって、フィルム、シート、パイプ
、造花、人形、容器等の包装材料や成形品に供せられ、
成形品がフィルムの場合には、例えば、インフレーショ
ン法、Tダイ法等の通例の方法が適用できる。
As mentioned above, the compositions and molded articles of the present invention have various advantages such as long-lasting medicinal effects, excellent moldability, and can be manufactured at low cost. It is applied to packaging materials and molded products such as films, sheets, pipes, artificial flowers, dolls, and containers by various forming methods such as molding.
When the molded article is a film, conventional methods such as an inflation method and a T-die method can be applied.

また、賦香フィルムまたは賦香製品の一例としては、食
品の包装、定期券等のラミネート材1台所のごみ袋、あ
るいは化粧室、I・イレ、洗面所、物置、地下室、食堂
、船舶、自動η1、鉄道車輌等の室内などあらゆる場所
で使用される。一方、防i敵剤、防虫剤等を含有する製
品は、果樹、果実。
In addition, examples of scented films or scented products include food packaging, laminate materials for commuter passes, garbage bags for kitchens, restrooms, bathrooms, washrooms, storerooms, basements, cafeterias, ships, automobiles, etc. η1, used everywhere, including indoors of railway vehicles. On the other hand, products containing i.p. repellents, insect repellents, etc. are for fruit trees and fruits.

穀物、衣類、皮革製品等の保護等に有用であり、防錆剤
含有製品は鋼管、機械の梱包資材等として用いられる等
、本発明の組成物およびその成形品は広範な用途を有す
る。
The composition of the present invention and its molded products have a wide range of uses, such as being useful for protecting grains, clothing, leather products, etc., and products containing rust inhibitors being used as packaging materials for steel pipes, machinery, etc.

以下に、本発明を実施例により、更に具体的に詳述する
Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例1 エチレン−酢酸ビニル共重合体(日木石油化学株式会社
製、商品名=日石レクスロンV 270 )にローズ系
調合香ネ゛1を含浸させたところ、17重量%が含浸さ
れた。上記香料含有エチレン−酢酸ビニル共重合体10
重量部を低密度ポリエチレン(以下” L D P E
”と言う、日本石油化学株式会社製、商品名:1石しク
スロンF 22) 100重量部と溶融41ル合してペ
レ・ント化し、そのベレットを常温で大気中に放置して
置いたが、6ケ月以上経ても芳香は失なわれていなかっ
た。
Example 1 When an ethylene-vinyl acetate copolymer (manufactured by Nichiki Petrochemical Co., Ltd., trade name: Nisseki Rexron V 270) was impregnated with rose-based fragrance blend 1, 17% by weight of the copolymer was impregnated. The above fragrance-containing ethylene-vinyl acetate copolymer 10
The weight part is low density polyethylene (hereinafter referred to as “LDPE”)
", manufactured by Nippon Petrochemical Co., Ltd., trade name: 1 stone Xuron F 22) was combined with 100 parts by weight of molten 41 kg to form a pellet, and the pellet was left in the atmosphere at room temperature. The fragrance had not been lost even after more than 6 months had passed.

比較例1 実施例1の低密度ポリエチレンペレントに、実施例1と
同じローズ系調合香料を含浸させたところ、約3重量%
しか含浸しなかった。この香料含有ペレットを常温で大
気中に放置して置いたところ、3週間程度で殆ど芳香が
失われた。
Comparative Example 1 When the low-density polyethylene pellet of Example 1 was impregnated with the same rose-based blended fragrance as in Example 1, the amount was about 3% by weight.
Only impregnated. When these fragrance-containing pellets were left in the air at room temperature, most of the fragrance was lost in about 3 weeks.

実施例2 実施例1で使用したEVAに市販のリラ系調合香料を含
浸させたところ15重量%が含浸された。上記の香料含
有EVA 35重量部と実施例1のLDPE Ei5屯
1一部とを混合した後、押出機にて製膜したところ、香
料な 5重量%含有したブロッキングの無い良好なイン
フレーションフィルムを製造することができた。
Example 2 When the EVA used in Example 1 was impregnated with a commercially available Lyra-based perfume, 15% by weight was impregnated. After mixing 35 parts by weight of the above fragrance-containing EVA and 1 part of 5 tons of LDPE Ei of Example 1, a film was formed using an extruder, and a good blown film without blocking containing 5% by weight of fragrance was produced. We were able to.

実施例3 実施例2において使用したリラ系調合香料をレモン系香
料に代えた他は、実施例2と同様に試験を行なったとこ
ろ、同様の良好な結果を得た。
Example 3 A test was carried out in the same manner as in Example 2, except that the lira-based blended fragrance used in Example 2 was replaced with a lemon-based fragrance, and the same good results were obtained.

比較例2 上記の実施例2で得られた香料含有EVA 35重M部
と実施例1のEVA”’85重量部とを混合した後、実
施例2と同様にして製膜したところ、ブロッキングが著
しく、良好なインフレーションフィルムにはならなかっ
た。
Comparative Example 2 After mixing 35 parts by weight of the fragrance-containing EVA obtained in Example 2 and 85 parts by weight of the EVA of Example 1, a film was formed in the same manner as in Example 2, and blocking was observed. Remarkably, it did not result in a good blown film.

比較例3 実施例1で用いたLDPEに、直接市販□のリラ系調合
香料を含浸したところ、香料は約0.5重量%しか含有
させることができなかった。
Comparative Example 3 When the LDPE used in Example 1 was directly impregnated with a commercially available □ Lila-based perfume, only about 0.5% by weight of the perfume could be contained.

上記の香ネ:■含有LDPEを使用して、実施例2と同
様ニインフレーションフィルムを成形したところ香料を
0.3重量%含有したフィルムしか得ることができなか
った。
When a 2-inflation film was formed in the same manner as in Example 2 using the above-mentioned LDPE containing perfume, only a film containing 0.3% by weight of perfume could be obtained.

特許出願人  日本石油化学株式会社Patent applicant: Japan Petrochemical Co., Ltd.

Claims (1)

【特許請求の範囲】 (])薬剤と相溶性を有する熱可塑性樹脂(A 、)に
該薬剤を含浸した樹脂組成物および/また。tよ溶融1
〜た熱可塑性樹脂(A)に該薬剤を混合した樹脂M」成
物を、該熱可塑性樹脂(A)と相溶性を有するが該薬剤
とは非相溶性である他の熱可塑性樹脂(B)に溶融混合
してなる薬剤含有樹脂組成物。 (2)前記熱可塑性樹脂(A)がカルボキシル基を有す
るエチレン共重合体である、特許請求の範囲第1項に記
載の薬剤含有樹脂組成物。 (3)前記カルボキシル基を有するエチレン共重合体が
エチレン−酢酸ビニル共重合体である、特許請求の範囲
第1項または第2項に記載の薬剤含有樹脂組成物。 (4)前記熱可塑性樹脂(B)がポリオレフィン樹脂で
ある、特許請求の範囲第1項から第3項のいずれかに記
載の薬剤含有樹脂組成物。 (5)前記ポリオレフィン樹脂がポ1、)エチレン、ポ
リプロピレンまたはそれらの混合物である、特許請求の
範囲第1項から第4項のいずれかに記載の薬剤含有樹脂
組成物。 (6)前記薬剤が気化性薬剤である、特1)1請求の範
囲第1項から第5項のいずれかに記載の薬剤含有樹脂組
成物。 (,7)前記気化性薬剤が香料、防徴剤′、防錆剤、防
虫剤、忌避剤の群から選ばれた少なくとも1種の薬剤で
ある、特許請求の範囲第6項に記載の薬剤含有樹脂組成
物。 (8)結晶性ポリオレフィン樹脂と、エチレン−酢酸ビ
ニル共重合体に香料を含浸した樹脂組成物および/また
は溶融したエチレン−酢酸ビニル共重合体に香料を混合
した樹脂組成物とを溶融混合してなることを特徴とする
香料含有成形品。 (9)前記成形品がフィルムである、特許請求の範囲第
8項に記載の香料含有成形品。
[Claims] (]) A resin composition and/or a thermoplastic resin (A) that is compatible with a drug and impregnated with the drug. t yo melt 1
The composition "Resin M" in which the drug is mixed with the thermoplastic resin (A) containing the thermoplastic resin (A) is mixed with another thermoplastic resin (B) which is compatible with the thermoplastic resin (A) but incompatible with the drug. ) A drug-containing resin composition formed by melt-mixing. (2) The drug-containing resin composition according to claim 1, wherein the thermoplastic resin (A) is an ethylene copolymer having a carboxyl group. (3) The drug-containing resin composition according to claim 1 or 2, wherein the ethylene copolymer having a carboxyl group is an ethylene-vinyl acetate copolymer. (4) The drug-containing resin composition according to any one of claims 1 to 3, wherein the thermoplastic resin (B) is a polyolefin resin. (5) The drug-containing resin composition according to any one of claims 1 to 4, wherein the polyolefin resin is polyethylene, polypropylene, or a mixture thereof. (6) The drug-containing resin composition according to any one of claims 1 to 5, wherein the drug is a vaporizable drug. (,7) The drug according to claim 6, wherein the vaporizable drug is at least one drug selected from the group of fragrances, preventive agents, rust preventives, insect repellents, and repellents. Containing resin composition. (8) By melt-mixing a crystalline polyolefin resin and a resin composition in which an ethylene-vinyl acetate copolymer is impregnated with a fragrance and/or a resin composition in which a fragrance is mixed into a molten ethylene-vinyl acetate copolymer. A fragrance-containing molded product characterized by: (9) The fragrance-containing molded article according to claim 8, wherein the molded article is a film.
JP57233865A 1982-12-29 1982-12-29 Drug-containing resin composition and its molding Granted JPS59124941A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57233865A JPS59124941A (en) 1982-12-29 1982-12-29 Drug-containing resin composition and its molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57233865A JPS59124941A (en) 1982-12-29 1982-12-29 Drug-containing resin composition and its molding

Publications (2)

Publication Number Publication Date
JPS59124941A true JPS59124941A (en) 1984-07-19
JPH0421699B2 JPH0421699B2 (en) 1992-04-13

Family

ID=16961775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57233865A Granted JPS59124941A (en) 1982-12-29 1982-12-29 Drug-containing resin composition and its molding

Country Status (1)

Country Link
JP (1) JPS59124941A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61137804A (en) * 1984-12-11 1986-06-25 Nippon Ekishiyou Kk Production of tool for plant growth having insecticidal effect
WO1991000744A1 (en) * 1989-07-06 1991-01-24 Delphic Manor Pty. Ltd. Fragranced articles
WO1998030621A1 (en) * 1997-01-10 1998-07-16 Antonio Campagnoli Scented plastics
US6969552B2 (en) 1995-05-17 2005-11-29 Tetra Laval Holdings & Finance, S.A. Resin composition containing a reducing agent to be used in a multi-layer laminate for storing liquid foods
JP2006256997A (en) * 2005-03-16 2006-09-28 Sumika Life Tech Co Ltd Insect pest-controller and mosquito-controller

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5620055A (en) * 1979-07-28 1981-02-25 Sanwa Denko:Kk Premaster batch for production of molded product, containing perfume, pharmaceutical, etc.

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5620055A (en) * 1979-07-28 1981-02-25 Sanwa Denko:Kk Premaster batch for production of molded product, containing perfume, pharmaceutical, etc.

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61137804A (en) * 1984-12-11 1986-06-25 Nippon Ekishiyou Kk Production of tool for plant growth having insecticidal effect
WO1991000744A1 (en) * 1989-07-06 1991-01-24 Delphic Manor Pty. Ltd. Fragranced articles
US6969552B2 (en) 1995-05-17 2005-11-29 Tetra Laval Holdings & Finance, S.A. Resin composition containing a reducing agent to be used in a multi-layer laminate for storing liquid foods
WO1998030621A1 (en) * 1997-01-10 1998-07-16 Antonio Campagnoli Scented plastics
JP2006256997A (en) * 2005-03-16 2006-09-28 Sumika Life Tech Co Ltd Insect pest-controller and mosquito-controller

Also Published As

Publication number Publication date
JPH0421699B2 (en) 1992-04-13

Similar Documents

Publication Publication Date Title
CA1261736A (en) Active agent-containing laminated material and method for producing the same
CA1247269A (en) Synthetic resin product containing compound included in cyclodextrin and process for the production of the same
US6921581B2 (en) Plastic films containing a fragrance and an odor barrier material within and a method for their production
US9512339B2 (en) Polymeric compositions for sustained release of volatile materials
JPH0418846Y2 (en)
US20050272878A1 (en) Polymeric compositions for sustained release of volatile materials
EP0217275A2 (en) Method for producing laminated material
JPH08302080A (en) Sustainable insect-proofing olefin resin composition and molded form therefrom
JPS59124941A (en) Drug-containing resin composition and its molding
JPH05504348A (en) Animal repellent LLDPE
US20020165297A1 (en) Polymeric resins impregnated with insect repellants
JPH02252462A (en) Method and apparatus for dissipating volatile chemical
JPH065880Y2 (en) Drug-containing adhesive laminate
JP2000136272A (en) Low malodorous polyolefin resin composition and low malodorous polyolefin resin molded product using the same
JPH0379264B2 (en)
JPH0525880Y2 (en)
JPH043987Y2 (en)
JPH0231422Y2 (en)
JP7209342B2 (en) ANTIMICROBIAL RESIN COMPOSITION AND RESIN MOLDED PRODUCT USING THE SAME
JPH0579099B2 (en)
US20040031861A1 (en) Essential oils in additive concentrates
JPS62158041A (en) Manufacture of laminated paper containing chemical
JPH07207165A (en) Antibacterial insecticidal thermoplastic resin composition and its molded article
JPS62230702A (en) Film containing rodenticide
JP4443111B2 (en) Coating film forming composition