JP3033428B2 - Method of manufacturing multilayer plastic container - Google Patents
Method of manufacturing multilayer plastic containerInfo
- Publication number
- JP3033428B2 JP3033428B2 JP6057730A JP5773094A JP3033428B2 JP 3033428 B2 JP3033428 B2 JP 3033428B2 JP 6057730 A JP6057730 A JP 6057730A JP 5773094 A JP5773094 A JP 5773094A JP 3033428 B2 JP3033428 B2 JP 3033428B2
- Authority
- JP
- Japan
- Prior art keywords
- antibacterial
- container
- layer
- fungicide
- plastic container
- 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.)
- Expired - Fee Related
Links
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- Laminated Bodies (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、熱可塑性樹脂を溶融し
一定形状に冷却固化して成る多層プラスチック容器に関
し、より詳細には容器表面及び内容物等の接触物に菌、
黴等の発生を抑制する性能を有する多層プラスチック容
器の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a multilayer plastic container obtained by melting a thermoplastic resin and cooling and solidifying the same into a predetermined shape, and more particularly to a contact object such as a container surface and contents. Fungus,
Multi-layer plastic container that has the ability to suppress the generation of mold and the like
The present invention relates to a method for manufacturing a vessel .
【0002】[0002]
【従来の技術】熱可塑性樹脂に抗菌防黴剤を溶融混練
し、容器を製作することは、従来より行われている。し
かし、容器に十分な抗菌防黴性能を持たせる為の薬剤を
添加した場合、添加した薬剤が容器表面にブリードアウ
トし、この薬剤が膜状となって、印刷適性等の後加工適
性が低下するという問題が従来より指摘されており、こ
のような後加工を必要がある容器においては、十分な抗
菌性を付与することが困難であった。Antibacterial antifungal agent by melt-kneading of the Related Art Thermoplastic resins, to fabricate the container has been done conventionally. However, when a drug is added to the container to provide sufficient antibacterial and antifungal properties, the added drug bleeds out to the surface of the container , and the drug becomes a film, which deteriorates post-processing suitability such as printability. and it has been pointed out conventionally problem that, in the container it is necessary to post-processing such, it is difficult to impart sufficient antimicrobial.
【0003】[0003]
【発明が解決しようとする課題】本発明は、前記の状況
に鑑みてなされたものであり、熱可塑性樹脂を溶融し、
一定形状に冷却固化して成る多層プラスチック容器にお
いて、十分な抗菌防黴効果並びに良好な印刷適性を付与
した容器の製造方法を提供するものである。DISCLOSURE OF THE INVENTION The present invention has been made in view of the above circumstances, and has been made by melting a thermoplastic resin,
An object of the present invention is to provide a method for producing a container having a sufficient antibacterial and antifungal effect and good printability in a multilayer plastic container which is cooled and solidified into a predetermined shape.
【0004】[0004]
【課題を解決するための手段】本発明は、熱可塑性樹脂
に抗菌防黴剤を添加し製造した容器において、構成を多
層化し、各層における抗菌防黴剤の添加量を異なるもの
とし、印刷等の後加工適性、持続性を向上したことを特
徴とする多層プラスチック容器の製造方法に関する。す
なわち、本発明の多層プラスチック容器の製造方法にお
いて、最外層は印刷後加工工程に支障をきたさない程度
の抗菌防黴剤添加量とし、その内側に設けた層の抗菌防
黴剤添加量を前記最外層となる層よりも高濃度とし、経
時等により薬剤の層間移行を容器内部において最外層に
向かって起こさせ、印刷後加工処理が終了した後、所望
の抗菌防黴性能を容器にもたせることにより前記諸問題
を解決したものである。Means for Solving the Problems The present invention, in containers with an added antimicrobial antifungal agent to the thermoplastic resin produced, and multi-layered structure, and the addition amount of the antibacterial antifungal agents different in each layer, printing The present invention relates to a method for producing a multilayer plastic container, characterized by having improved post-processing suitability and durability. That is, have you <br/> to a method for manufacturing a multilayer plastic container of the present invention, the outermost layer is the antibacterial antifungal agent addition amount to the extent that does not disturb the post printing processing step, the antimicrobial layer provided on the inner side wherein the antifungal agent addition amount is higher concentration than the layer serving as the outermost layer, the interlayer migration of the drug to cause toward the outermost layer inside the container with time or the like, after the post-printing processing has been completed, the desired antibacterial These problems have been solved by imparting antifungal properties to the container.
【0005】以下さらに詳細に説明する。現在、一般的
に用いられているプラスチック容器で、抗菌防黴剤を溶
融混練し製品化されたものは従来より存在する。しか
し、これらの容器においては、後加工において直接容器
の表面に印刷等の表面処理が行えず、用途が限定れてし
まうという問題がある。A more detailed description will be given below. At present, there is a conventionally used plastic container obtained by melting and kneading an antibacterial and antifungal agent into a commercial product. However, in these containers, can not be carried out a surface treatment such as printing directly to the surface of the container <br/> In post-processing, there is a problem that the application will be limited.
【0006】本発明は、抗菌防黴剤を溶融混練し製品化
するにあたり、実用上十分な抗菌防黴性能を付与し、且
つ十分な印刷加工適性を持たせる為に成されたもので、
外側となる層の薬剤濃度を低く、その内側となる層の薬
剤濃度を高くし、また各層に用いる薬剤を有機系の抗菌
防黴剤とした多層プラスチック容器である。 [0006] The present invention is intended to impart practically sufficient antibacterial and fungicidal properties and to provide sufficient printing process suitability when a kneading and kneading of an antibacterial and fungicide is completed.
This is a multilayer plastic container in which the drug concentration in the outer layer is low , the drug concentration in the inner layer is high, and the drug used for each layer is an organic antibacterial and fungicide .
【0007】プラスチック容器において、溶融混練した
抗菌防黴剤がその効果を発揮するメカニズム等について
は、各種文献等により様々な内容で報じられている。こ
れらによれば、菌、黴に対して細胞の呼吸系、電子伝達
系等の基本代謝系の酸素阻害、細胞膜内の物質移動阻害
をせしめ、細胞の発育を阻止するという報告がある。ま
た、有機系、無機系の薬剤の比較では、有機系薬剤は無
機系薬剤に比べ、ブリードアウト即ち容器よりの遊離量
が多く、遊離速度が速い。また、薬剤成分が膜状を形成
し易い為、少量の添加で、効果を付与出来るが、この分
持続性に問題を残す。また、前記の薬剤成分が膜状を形
成し易い問題点により印刷に代表される表面装飾等の後
加工が施しにくいという問題点が生じる。これに対し、
無機系の薬剤は遊離し難く容器表面に膜を形成し難い
為、効果の持続性は半永久的であるが、薬剤添加量が多
く必要である。この為、溶融混練によって得たプラスチ
ック容器の表面は荒れ易く、薬剤の添加量が多い分製品
の価格も高くなるという問題が生じる。[0007] Various mechanisms have been reported in various literatures on the mechanism of the effect of the melt- kneaded antibacterial and antifungal agent in plastic containers . According to these reports, it has been reported that bacteria and fungi inhibit oxygen in the basic metabolic system such as the respiratory system and electron transfer system of cells, and inhibit mass transfer in cell membranes, thereby inhibiting cell growth. In comparison between organic and inorganic drugs, organic drugs have a greater amount of bleed-out, that is, release from the container , and a faster release rate than inorganic drugs. In addition, since the drug component easily forms a film, an effect can be imparted by adding a small amount of the drug component, but this leaves a problem in sustainability. Further, there is a problem that it is difficult to perform post-processing such as surface decoration typified by printing due to the problem that the above-mentioned drug component easily forms a film. In contrast,
Inorganic drugs are hardly released and hard to form a film on the surface of the container , so the effect lasts semipermanently, but a large amount of drug is required. For this reason, the surface of the plastic container obtained by melt- kneading tends to be rough, and there is a problem in that the price of the product increases due to the large amount of the drug added.
【0008】本発明においては、プラスチック容器を多
層化し抗菌防黴剤に濃度勾配を設け、即ち最外層となる
層の薬剤添加量は容器製造時においては最低限に抑え、
外側層に比べその内側に配される層の薬剤添加量を高濃
度とし、薬剤の層間移行並び容器よりのブリードアウト
により印刷に代表される表面装飾後加工適性、効果の持
続性等を高めるものであるが、この点については薬剤を
溶融混練する際のベースとなるプラスチック材料で、分
子間の間隙がある程度広いものであれば良く、例えば、
ポリオレフィン樹脂等の熱可塑性樹脂であって良い。In the present invention, the plastic container is multi-layered to provide a concentration gradient to the antibacterial and antifungal agent, that is, the amount of drug added to the outermost layer is minimized during the production of the container .
Drug addition amount of the layer that is disposed on the inner side than the outer layer and high density, surface decoration after processing suitability by bleedout from layer shifting arrangement containers of drugs represented by print, increase durability, etc. Effect However, in this regard, a plastic material that serves as a base when melt- kneading a drug may be used as long as the gap between molecules is wide to some extent.
It may be a thermoplastic resin such as a polyolefin resin.
【0009】本発明の多層プラスチック容器の層構成と
しては、抗菌防黴剤添加量が高い層の少なくとも外側
に、高い層より抗菌防黴剤の添加量が50%以下の低い
層を設け、層間で抗菌防黴剤の添加量に濃度勾配をつ
け、外側の低い層の表面をフレーム処理し、印刷を施す
ものである。 [0009] The layer constitution of the multilayer plastic container of the present invention comprises at least the outer side of the layer having a high antimicrobial and fungicide addition amount
In addition, the amount of the antibacterial and fungicide added is 50% or less lower than that of the higher layer.
Layers, and add a concentration gradient between the
Frame and print the surface of the outer lower layer
Things.
【0010】本発明の多層プラスチック容器の製造方法
としては、多層共押し出しにより連続して形成された筒
状のパリソンを金型内に導入した後、前記パリソン内に
圧縮エアーを吹き込んで成形を行うダイレクトブロー成
形、多層射出成形により試験管状のパリソンを成形し、
これを吹き込み金型内に導入した後、前記パリソン内に
圧縮エアーを吹き込んで成形を行うインジェクションブ
ロー成形、多層射出成形により試験管状に成形されたパ
リソンを金型内に導入した後、前記パリソンを延伸ロッ
ドにより容器の縦方向に延伸し、同時に圧縮エアーを吹
き込んで成形を行う2軸延伸ブロー成形、押し出しによ
り成形されたプラスチックシートより圧空成形及び真空
成形によって容器を成形する方法を用いることが出来
る。In the method for manufacturing a multilayer plastic container of the present invention, a cylindrical parison formed continuously by multilayer coextrusion is introduced into a mold, and then compressed air is blown into the parison to perform molding. Test tube parison is formed by direct blow molding and multilayer injection molding,
After introducing this into the blow mold, injection blow molding in which compressed air is blown into the parison to perform molding, a parison molded into a test tube by multilayer injection molding is introduced into the mold, and then the parison is removed. the stretching rod was stretched in the longitudinal direction of the container, biaxial stretch blow molding forming is carried out by blowing compressed air at the same time, it is possible to use a method of molding a container by pressure forming and vacuum forming of a plastic sheet formed by extrusion .
【0011】本多層プラスチック容器に溶融混練するこ
との出来る抗菌防黴剤としては、有機系薬剤では有機塩
素化合物、有機銅化合物、有機錫化合物4級アンモニュ
ム塩類、例えば10.10’オキシビスフェノキシアル
シンに代表される有機ヒ素化合物が挙げられるがその他
の薬剤であっても良い。また、無機系薬剤としては錫等
の金属イオン系のものが適しているが、その他の薬剤で
あっても良い。As the antibacterial and fungicide which can be melt- kneaded in the multilayer plastic container , quaternary ammonium salts of organic chlorine compounds, organic copper compounds and organic tin compounds, for example, 10.10 'oxybisphenoxyarsine in organic chemicals And other drugs may be used. As the inorganic agent, a metal ion agent such as tin is suitable, but other agents may be used.
【0012】[0012]
【作用】本発明によれば、薬剤練り込みにより抗菌防黴
性を付与したプラスチック容器で、多層構成とし、添加
する抗菌防黴剤の濃度と層毎に異なるもの、即ち印刷後
加工を施す層の薬剤添加量を、後加工を施す際に支障を
生じない量とし、後加工が施された後に経時及び印刷を
行う際に施すフレーム処理、即ち火炎処理により薬剤の
層間移行が生じ、前記後加工処理を施す層の薬剤濃度を
上昇させることにより、容器に十分な抗菌防黴性を付与
し、印刷後加工を支障無く施すことが可能となる。According to the present invention, a plastic container that impart antimicrobial antifungal by kneading agent, a multilayer structure, different for each concentration and a layer of antimicrobial antifungal agent added, i.e. after printing <br / > drug amount of the layer subjected to processing, and the amount that does not cause trouble in performing the post-processing, the frame processing performed when performing <br/> with time and printed after post-processing is performed, i.e. flame treatment layer shifting drug occurs, by increasing the drug concentration of the layer subjected to the post-processing, to impart sufficient antibacterial antifungal properties to the container, it becomes possible to perform post-printing processing without hindrance by.
【0013】[0013]
<実施例1>押出機Aに高密度ポリエチレン樹脂に市販
の有機系抗菌防黴剤マスターバッチ、即ち大日精化工業
(株)製ダイキラーを抗菌防黴剤の濃度を0.2wt%
となるように添加したもの、押出機Bに高密度ポリエチ
レン樹脂に前記有機系抗菌防黴剤マスターバッチを抗菌
防黴剤の濃度を2.0wt%となるように添加し、さら
に本構造物を成形する際に生じる口部、底部のバリの粉
砕物を30wt%添加したもの、押出機Cに高密度ポリ
エチレン樹脂に前記有機系抗菌防黴剤マスターバッチを
抗菌防黴剤の濃度を0.2wt%となるように添加した
ものをそれぞれに供給し、ダイレクトブロー成形機にお
いて層比が外層より1:8:1になるように下記条件で
容量800ml偏平円形状の容器を多層で成形し、容器
表面にフレーム処理を施した後シルクスクリーン印刷を
施した。<Example 1> A high-density polyethylene resin was used in an extruder A, and a commercially available organic antibacterial and fungicide masterbatch, that is, a Daikiller manufactured by Dainichi Seika Kogyo Co., Ltd. was used.
The extruder B is added to the high-density polyethylene resin with the organic antibacterial and fungicide masterbatch so that the concentration of the antibacterial and fungicide is 2.0 wt%. An extruder C is prepared by adding the above-mentioned organic antibacterial and fungicide masterbatch to a high-density polyethylene resin in an extruder C at a concentration of 0.2 wt%. %, And a flat blow-shaped container having a capacity of 800 ml is formed by a direct blow molding machine under the following conditions so as to have a layer ratio of 1: 8: 1 with respect to the outer layer. After performing frame processing on the surface, silk screen printing was performed.
【0014】なお、押出機及びダイヘッドの仕様は(表
1)に示す。The specifications of the extruder and the die head are shown in (Table 1).
【0015】[0015]
【表1】 [Table 1]
【0016】<実施例2>押出機Aに高密度ポリエチレ
ン樹脂に市販の無機系抗菌防黴剤マスターバッチ、即ち
大日精化工業(株)製ダイキラーを抗菌防黴剤の濃度を
0.5wt%となるように添加したもの、押出機Bに高
密度ポリエチレン樹脂に前記有機系抗菌防黴剤マスター
バッチを抗菌防黴剤の濃度を2.0wt%となるように
添加し、さらに本構造物を成形する際に生じる口部、底
部のバリの粉砕物を30wt%添加したもの、押出機C
に高密度ポリエチレン樹脂に前記有機系抗菌防黴剤マス
ターバッチを抗菌防黴剤の濃度を0.2wt%となるよ
うに添加したものをそれぞれに供給し、ダイレクトブロ
ー成形機において層比が外層より1:8:1になるよう
に下記条件で容量800ml偏平円形状の容器を多層で
成形し、容器表面にフレーム処理を施した後シルクスク
リーン印刷を施した。<Example 2> A high-density polyethylene resin was used in an extruder A and a commercially available inorganic antibacterial and fungicide masterbatch, ie, Daikiller manufactured by Dainichi Seika Kogyo Co., Ltd. was used. The above-mentioned organic antibacterial and fungicide masterbatch is added to extruder B to a high-density polyethylene resin so that the concentration of the antibacterial and fungicide is 2.0 wt%. Extruder C to which 30 wt% of ground and burr burrs generated during molding are added.
The above-mentioned organic antibacterial and fungicide masterbatch was added to a high-density polyethylene resin so that the concentration of the antibacterial and fungicide was 0.2 wt%, and the mixture was supplied to each of them. A flat container having a capacity of 800 ml and a flat circular shape was formed in a multilayer structure under the following conditions so as to be 1: 8: 1, and the surface of the container was subjected to a frame treatment and then subjected to silk screen printing.
【0017】なお、押出機及びダイヘッドの仕様は(表
2)に示す。The specifications of the extruder and the die head are shown in (Table 2).
【0018】[0018]
【表2】 [Table 2]
【0019】<比較例1>押出機に高密度ポリエチレン
樹脂に市販の有機系抗菌防黴剤マスターバッチ、大日精
化工業(株)製ダイキラーを抗菌防黴剤の濃度を0.2
wt%となるように添加したものを供給し、下記条件で
容量800ml偏平円形状の容器を多層で成形し、容器
表面にフレーム処理を施した後シルクスクリーン印刷を
施した。<Comparative Example 1> A commercially available organic antibacterial / antifungal agent masterbatch was applied to a high-density polyethylene resin in an extruder, and a Daikiller manufactured by Dainichi Seika Kogyo Co., Ltd. was used to adjust the concentration of the antibacterial / antifungal agent to 0.2.
The mixture was supplied so as to have a wt% content, and a container having a flat circular shape having a capacity of 800 ml was formed in multiple layers under the following conditions, and the surface of the container was subjected to a frame treatment and then silk screen printing.
【0020】なお、押出機及びダイヘッドの仕様は(表
3)に示す。The specifications of the extruder and the die head are shown in (Table 3).
【0021】[0021]
【表3】 [Table 3]
【0022】<比較例2>押出機に高密度ポリエチレン
樹脂に市販の有機系抗菌防黴剤マスターバッチ、大日精
化工業(株)製ダイキラーを抗菌防黴剤の濃度を1.0
wt%となるように添加したものを供給し、下記条件で
容量800ml偏平円形状の容器を多層で成形し、容器
表面にフレーム処理を施した後シルクスクリーン印刷を
施した。Comparative Example 2 A commercially available organic antibacterial and fungicide masterbatch was applied to a high-density polyethylene resin in an extruder, and a die killer manufactured by Dainichi Seika Kogyo Co., Ltd. was used to adjust the concentration of the antibacterial and fungicide to 1.0.
The mixture was supplied so as to have a wt% content, and a container having a flat circular shape having a capacity of 800 ml was formed in multiple layers under the following conditions, and the surface of the container was subjected to a frame treatment and then silk screen printing.
【0023】なお、押出機及びダイヘッドの仕様は(表
4)に示す。The specifications of the extruder and the die head are shown in (Table 4).
【0024】[0024]
【表4】 [Table 4]
【0025】これらの結果を次の(表5)に示す。The results are shown in the following (Table 5).
【0026】[0026]
【表5】 [Table 5]
【0027】(表5)について、各評価結果は下記方法
により評価した。印刷適正は、容器を35℃の水道水に
24時間浸漬後セロハンテープにてインキの密着を評価
する。尚、印刷適正の評価は成形、印刷加工後1ヶ月目
及び6カ月目について行った。抗菌防黴性の内抗菌性
は、滅菌シャーレに寒天培地を約20ml適下し、固化
後下記供試菌の菌液を含む寒天培地を約5ml重層す
る。容器を切断した試料を培地中央に突き刺し、蓋をし
て40℃90%RHの環境下で48時間培養し、発育阻
止幅により抗菌性を判定した。防黴性は、滅菌シャーレ
に寒天培地を約25ml適下し水分保持用とし、固化後
容器を切断した試料を印刷面が上になる様に置き、下記
供試黴の胞子懸濁液を1ml適化し30℃80%RHで
10日間培養し、試料上の黴発生の有無を観察する。
尚、抗菌防黴評価は成形、印刷加工後1ヶ月目及び6カ
月目について行った。また、判定で○は抗菌性、防黴性
有りとし、×は、抗菌性、防黴性無しとした。 供試菌:Methylobacterium extorquens IFO3708 供試黴:Penicillium citrinum IFO6352Regarding (Table 5), each evaluation result was evaluated by the following method. Printability is evaluated by immersing the container in tap water at 35 ° C. for 24 hours and then using a cellophane tape to evaluate the adhesion of the ink. In addition, the evaluation of printability was performed on the first and sixth months after molding and printing. About the antibacterial and antifungal properties, about 20 ml of an agar medium is appropriately dropped on a sterile petri dish, and after solidification, about 5 ml of an agar medium containing a bacterial solution of the following test bacteria is overlaid. The sample in which the container was cut was pierced into the center of the medium, covered, and cultured in an environment of 40 ° C. and 90% RH for 48 hours, and the antibacterial activity was determined based on the growth inhibition width. For the antifungal property, about 25 ml of an agar medium was placed on a sterile Petri dish for water retention, and after solidification, the cut sample was placed so that the printed surface was on the top, and 1 ml of the spore suspension of the following test mold was used. After culturing at 30 ° C. and 80% RH for 10 days, the presence or absence of mold on the sample is observed.
The antibacterial and antifungal evaluation was performed on the first and sixth months after molding and printing. In the judgment, ○ indicates antibacterial and antifungal properties, and × indicates no antibacterial and antifungal properties. Test bacterium: Methylobacterium extorquens IFO3708 Test fungus: Penicillium citrinum IFO6352
【0028】[0028]
【発明の効果】本発明によれば、抗菌防黴性を付与した
プラスチック容器において、抗菌防黴性能を損なう事な
く実用上十分な耐性を有する印刷後加工を行う事が可能
となる。According to the present invention, in a plastic container imparted with antibacterial antifungal, it is possible to perform the post-printing processing having practically sufficient resistance without impairing the antimicrobial antifungal performance.
フロントページの続き (56)参考文献 特開 平5−176847(JP,A) 特開 昭62−227744(JP,A) 特開 平4−359028(JP,A) 特開 平5−254527(JP,A) 特開 平3−150122(JP,A) 特開 平2−238923(JP,A) 実開 昭62−108210(JP,U) (58)調査した分野(Int.Cl.7,DB名) B32B 1/00 - 35/00 B65D 1/00 - 1/48 B29C 49/00 - 49/80 Continuation of front page (56) References JP-A-5-176847 (JP, A) JP-A-62-227744 (JP, A) JP-A-4-359028 (JP, A) JP-A-5-254527 (JP) JP-A-3-150122 (JP, A) JP-A-2-238923 (JP, A) JP-A-62-108210 (JP, U) (58) Fields investigated (Int. Cl. 7 , DB Name) B32B 1/00-35/00 B65D 1/00-1/48 B29C 49/00-49/80
Claims (1)
ラスチック容器において、抗菌防黴剤添加量が高い層の
少なくとも外側に、前記高い層より抗菌防黴剤の添加量
が50%以下の低い層を設け、層間で抗菌防黴剤の添加
量に濃度勾配をつけ、前記外側の低い層の表面をフレー
ム処理し、印刷を施したことを特徴とする多層プラスチ
ック容器の製造方法。 Claims: 1. A multilayer plastic container in which the amount of an antibacterial and fungicide added is different for each layer.
At least on the outside, the amount of antibacterial and fungicide added above the high layer
Has a low layer of 50% or less, and an antibacterial and fungicide is added between the layers.
Gradient concentration gradient to flank the outer lower layer surface
A method for producing a multilayer plastic container, which is subjected to a system treatment and printing .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6057730A JP3033428B2 (en) | 1994-03-28 | 1994-03-28 | Method of manufacturing multilayer plastic container |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6057730A JP3033428B2 (en) | 1994-03-28 | 1994-03-28 | Method of manufacturing multilayer plastic container |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH07266512A JPH07266512A (en) | 1995-10-17 |
JP3033428B2 true JP3033428B2 (en) | 2000-04-17 |
Family
ID=13064046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6057730A Expired - Fee Related JP3033428B2 (en) | 1994-03-28 | 1994-03-28 | Method of manufacturing multilayer plastic container |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3033428B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7669572B2 (en) | 2006-12-15 | 2010-03-02 | Briggs And Stratton Corporation | Intake manifold regulators for internal combustion engines |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4748916B2 (en) * | 2002-11-29 | 2011-08-17 | 株式会社吉野工業所 | Laminated body made of synthetic resin with antibacterial and antifungal properties |
-
1994
- 1994-03-28 JP JP6057730A patent/JP3033428B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7669572B2 (en) | 2006-12-15 | 2010-03-02 | Briggs And Stratton Corporation | Intake manifold regulators for internal combustion engines |
US7717078B2 (en) | 2006-12-15 | 2010-05-18 | Briggs And Stratton Corporation | Intake manifold regulators for internal combustion engines |
Also Published As
Publication number | Publication date |
---|---|
JPH07266512A (en) | 1995-10-17 |
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