JPS5841310B2 - Synthetic resin composition for tarpaulin film formation - Google Patents
Synthetic resin composition for tarpaulin film formationInfo
- Publication number
- JPS5841310B2 JPS5841310B2 JP6030880A JP6030880A JPS5841310B2 JP S5841310 B2 JPS5841310 B2 JP S5841310B2 JP 6030880 A JP6030880 A JP 6030880A JP 6030880 A JP6030880 A JP 6030880A JP S5841310 B2 JPS5841310 B2 JP S5841310B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- resin composition
- weight
- tarpaulin
- ethylene
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 12
- 229920003002 synthetic resin Polymers 0.000 title description 8
- 239000000057 synthetic resin Substances 0.000 title description 8
- 230000015572 biosynthetic process Effects 0.000 title 1
- 229920005989 resin Polymers 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 28
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 23
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 23
- 238000002156 mixing Methods 0.000 claims description 9
- 229920001897 terpolymer Polymers 0.000 claims description 7
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 6
- 239000000805 composite resin Substances 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002131 composite material Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000012770 industrial material Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- ZSBRYDJXHOFQMW-UHFFFAOYSA-N chloroethene;ethene;ethenyl acetate Chemical compound C=C.ClC=C.CC(=O)OC=C ZSBRYDJXHOFQMW-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- -1 for example Polymers 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
【発明の詳細な説明】
本発明は各種織物等を基材として、その片面又は両面に
柔軟な合成樹脂被膜を形成してなる所謂ターポリンにお
いて、その被膜に用いられる合成樹脂組成物の改良に関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to so-called tarpaulins made of various textiles and the like with a flexible synthetic resin coating formed on one or both sides thereof, and to improvements in the synthetic resin composition used for the coating. It is.
ターポリンは産業用資材として各方面に広く使用せられ
ており、その被膜を形成する合戊樹脂組威物としては、
一般に軟質塩化ビニル樹脂配合物が最も多く使用されて
いる。Tarpaulin is widely used as an industrial material in various fields, and the composite resin material that forms its coating is
Generally, soft vinyl chloride resin formulations are most commonly used.
併しながら、軟質塩化ビニル樹脂配合物は、これを軟質
とするために含まれている可塑剤と共に、完全無毒性を
要求される分野においては不適当とされ、又加工された
ターポリンとして使用中に、可塑剤の滲出、或いは接触
品への可塑剤の移行等の不都合が発生する。However, soft vinyl chloride resin formulations, along with the plasticizers they contain to make them soft, are considered unsuitable in fields that require complete non-toxicity, and are currently being used as processed tarpaulins. In addition, problems such as oozing of the plasticizer or transfer of the plasticizer to articles in contact occur.
めのためにこの種用途に使用される被膜形戒用合成樹脂
としては塩化ビニル樹脂に替えて専ら無毒で可塑剤を必
要としないエチレン−酢酸ビニル共重合樹脂(以下EV
A樹脂と称する)が用いられてきている。For this reason, the film-form synthetic resin used for this type of application is ethylene-vinyl acetate copolymer resin (hereinafter referred to as EV), which is non-toxic and does not require a plasticizer, instead of vinyl chloride resin.
(referred to as A resin) has been used.
このEVA樹脂は前記の塩化ビニル樹脂配合物被膜にお
けるような不都合が生じないが、その反面次のような欠
点がある。Although this EVA resin does not have the disadvantages of the above-mentioned vinyl chloride resin blend coating, it does have the following disadvantages.
■ 柔軟性に欠は取扱いが困難である。■ Lack of flexibility makes handling difficult.
■ 耐熱性が悪く、高温時の粘着、強度低下等温度依存
性が悪い。■ Poor heat resistance, poor temperature dependence such as adhesion and strength loss at high temperatures.
■ 耐摩耗性悪く傷の発生、破損等が生じ易い。■ Poor wear resistance, easily causing scratches and breakage.
■ 高周波ウエルダー性が悪く、成形加工時の作業性が
悪くなる。■ Poor high-frequency weldability, resulting in poor workability during molding.
又、このようなEVA樹脂使用のための欠点を改良する
ために、例えば酢酸ビニル含有率の高いEVA樹脂の採
用によって柔軟性を保持させ、そのために低下する耐熱
性をエチレンプロピレン共重合体又はエチレン−プロピ
レン−ジエン三元重合体を一定量ブレンドして補うこと
や、或いはEVA樹脂に一定量配合するものとして、塩
素化ポリエチレンによって柔軟性を、アクリルニトリル
含有ブタジェンゴムによって高周波ウエルダー性を夫々
改良すると云う研究もなされているが、前者においては
高周波ウエルダー性は改良されず、又、静電気が発生し
易くなって実用時に障害があり、後者においては高周波
ウエルダー性は左柱改良されず且つ、被膜強度が低下し
、耐摩耗度、ウエルダー強度が弱くなる等の欠点があり
、全面的な改良の域に達していないのが現状である。In addition, in order to improve the disadvantages of using EVA resin, for example, EVA resin with a high vinyl acetate content is used to maintain flexibility, and the heat resistance that is lowered due to this is reduced by using ethylene propylene copolymer or ethylene. - By blending a certain amount of propylene-diene terpolymer to supplement it, or by adding a certain amount to EVA resin, chlorinated polyethylene improves flexibility and acrylonitrile-containing butadiene rubber improves high-frequency weldability. Although some research has been done on the former, high frequency weldability has not been improved and static electricity has been generated more easily, causing problems in practical use.In the latter, high frequency weldability has not been improved and the film strength has been reduced. There are drawbacks such as a decrease in abrasion resistance and welder strength, and the current situation is that it has not reached the level of comprehensive improvement.
本発明はこれら従来の欠点を全面的に改良するために、
エチレン−酢酸ビニル共重合樹脂に熱可塑性ポリウレタ
ン樹脂とエチレン−酢酸ビニル塩化ビニル三元重合体と
を夫々適量宛混合してなる合成樹脂組成物を提供するも
のである。In order to completely improve these conventional drawbacks, the present invention
A synthetic resin composition is provided by mixing appropriate amounts of a thermoplastic polyurethane resin and an ethylene-vinyl acetate vinyl chloride terpolymer into an ethylene-vinyl acetate copolymer resin.
以下、本発明の合成樹脂組酸物について詳しく説明する
。Hereinafter, the synthetic resin composite acid of the present invention will be explained in detail.
本発明の合戊樹脂組戊物は、まず、熱可塑性ポリウレタ
ン樹脂とエチレン−酢酸ビニル−塩化ヒニル三元重合体
を一定割合で混合して、例えばペレット状にしたものを
作り、これをEVA樹脂にブレンドして混練するもので
ある。The composite resin composite of the present invention is first made by mixing a thermoplastic polyurethane resin and an ethylene-vinyl acetate-hinyl chloride terpolymer at a certain ratio to form, for example, pellets, which are then made from EVA resin. It is blended and kneaded.
而して、熱可塑性ポリウレタン樹脂とエチレン酢酸ビニ
ル−塩化ビニル三元重合体との混合割合は前者が70〜
90重量%に対して後者が30〜10重量%の範囲力;
適当であり、後者が30%を超えたときは、EVA樹脂
と混合した最終製品が硬くなり過ぎ、被膜強度も低下す
る。Therefore, the mixing ratio of the thermoplastic polyurethane resin and the ethylene vinyl acetate-vinyl chloride terpolymer is 70 to 70%.
range force of 30-10% by weight of the latter for 90% by weight;
If the latter exceeds 30%, the final product mixed with EVA resin will become too hard and the coating strength will also decrease.
又、後者が10重量%より少いときは、EVA樹脂の相
溶性が悪くなってブレンドが困難となる。Moreover, when the latter is less than 10% by weight, the compatibility of the EVA resin becomes poor and blending becomes difficult.
従って、好ましくは熱可塑性ポリウレタン樹脂80重量
%エチレン−酢酸ビニル−塩化ビニル三元重合体20重
量%の混合割合のものが最も良い。Therefore, it is best to use a mixture of 80% by weight of thermoplastic polyurethane resin and 20% by weight of ethylene-vinyl acetate-vinyl chloride terpolymer.
(以下この配合物を変性ポリウレタンと仮称する)。(Hereinafter, this compound will be tentatively referred to as modified polyurethane).
次いで、EVA樹脂とこの変性ポリウレタンを混合して
本発明の樹脂組成物が得られるのであるが、その混合割
合は、EVA樹脂50〜90重量%に対して、変性ポリ
ウレタン50〜10重量%の範囲が好ましく、例えばタ
ーポリンのうち大量に使用されるフレキシブルコンテナ
ーの場合、EVA樹脂単独使用のターポリンによるフレ
キシブルコンテナー
90重量%、変性ポリウレタン10重量%のブレンド割
合のものが好適である。Next, the EVA resin and this modified polyurethane are mixed to obtain the resin composition of the present invention, and the mixing ratio is in the range of 50 to 10% by weight of the modified polyurethane to 50 to 90% by weight of the EVA resin. For example, in the case of a flexible container that is used in large quantities among tarpaulins, a blend ratio of 90% by weight of a flexible container made of tarpaulin using only EVA resin and 10% by weight of modified polyurethane is suitable.
次に本発明の樹脂組成物を用いたターポリンの一実施例
とEVA樹脂単独による同一条件のターポリンとを比較
した結果について述べる。Next, the results of a comparison between an example of a tarpaulin using the resin composition of the present invention and a tarpaulin made of EVA resin alone under the same conditions will be described.
(以下、混合割合は重量パーセントを示す)。(Hereinafter, the mixing ratio indicates weight percentage).
本発明の樹脂組成物の実施例
の割合で混練し、これをカレンダーロールを用いて被膜
化し、基材としてポリエステル系(ioo。The resin composition of the present invention was kneaded in the proportions shown in the examples, and this was formed into a film using a calendar roll, and the base material was made of polyester (ioo).
デニール、16本×17本/吋)の平織の織布の両面に
この被膜を貼合して一体化し、1間厚のターポリンをつ
くって試料とした。This film was laminated and integrated on both sides of a plain weave fabric of 16 denier x 17 strands/inch) to make a tarpaulin with a thickness of 1 inch, which was used as a sample.
(以下A試料と称する)。(Hereinafter referred to as sample A).
一方、比較試料として
エバフレックスP−1905(三井 100%ポリケ
ミカル(株)製〕(エチレン
酢酸ビニル共重合体)
に加工助剤0.4%と着色剤を適量加えてカレンダーロ
ールを用いて被膜化し、11nrIL厚のターポリンを
つくって試料とした。On the other hand, as a comparison sample, Evaflex P-1905 (manufactured by Mitsui Polychemical Co., Ltd.) (ethylene vinyl acetate copolymer) was coated with 0.4% processing aid and an appropriate amount of colorant using a calendar roll. A tarpaulin with a thickness of 11nrIL was prepared and used as a sample.
(以下B試料と称する)。なお上記試料に用いた各資材
の性状は次の通りである。(hereinafter referred to as sample B). The properties of each material used in the above sample are as follows.
□ 以上の資材を使用した試料A、Hにつき各種性能に
ついて測定した結果について次に述べる。□ The following describes the results of various performance measurements of samples A and H using the above materials.
・高周波ウエルダー性について
高周波ウエルダー性とは高周波加熱により樹脂の融着を
行うことであり、その難易性は数字的には誘電体損率を
測定することによって、その樹脂組成物の高周波ウエル
ダー性の難易度を判断できる。・About high-frequency weldability High-frequency weldability is the process of fusing resins by high-frequency heating, and the difficulty lies in numerically determining the high-frequency weldability of the resin composition by measuring the dielectric loss factor. You can judge the difficulty level.
而して誘電損率−誘電率(ε)×誘電正接(tanδ)
であるから、誘電率と誘電正接の測定によって算出でき
る。Therefore, dielectric loss factor - dielectric constant (ε) x dielectric loss tangent (tan δ)
Therefore, it can be calculated by measuring the dielectric constant and dielectric loss tangent.
その測定数字は次表の通りである。The measured numbers are shown in the table below.
即ち、B試料(EVA単独のもの)に比べてA試料(本
発明の樹脂組成物によるもの)の誘電体損率は2倍程度
向上しており高周波ウエルダー性が遥かに良いことを示
している。That is, the dielectric loss factor of Sample A (made of the resin composition of the present invention) is improved by about twice that of Sample B (made of EVA alone), indicating that the high frequency weldability is much better. .
・ウエルダー強力について
高周波ウエルダーによってターポリン試料を接合した場
合の強度について測定した結果は次表の通りであり、本
発明樹脂組成物によるものは、EVA単独のものより明
かに優れている。- Regarding welder strength, the results of measuring the strength when tarpaulin samples were joined by a high-frequency welder are shown in the following table, and the results made of the resin composition of the present invention are clearly superior to those made of EVA alone.
上記の表中、高周波ウエルダー条件は山水ビーター製、
出力2にW、周波数40.68MH2、時間5秒、圧力
17kg/cyA、陽極電流0.7 A、試料融着面積
2o、6c=、測定温度20℃である。In the table above, the high frequency welder conditions are manufactured by Sansui Beater,
The output 2 was W, the frequency was 40.68 MH2, the time was 5 seconds, the pressure was 17 kg/cyA, the anode current was 0.7 A, the sample fusion area was 2o, 6c=, and the measurement temperature was 20°C.
・耐摩耗性について
耐摩耗性は次表に示すように本発明樹脂の樹脂組成物に
よるものはEVA単独のものに比べて大きく向上してい
る。- Abrasion resistance As shown in the following table, the abrasion resistance of the resin composition of the present invention is greatly improved compared to that of EVA alone.
測定条件はテーパー摩耗試験機によってJISK−69
02法によりリングC8−17、荷重1kg、回転数1
000とした。Measurement conditions are JISK-69 using a taper abrasion tester.
Ring C8-17, load 1kg, rotation speed 1 by 02 method
It was set as 000.
・柔軟性の保持について
柔軟性の保持について各雰囲気温度における硬さを捩り
剛性率によって測定した結果、次表のように標準温度2
0℃において本発明樹脂組成物によるものの方が柔軟で
あり、さらに−20°Cの低温に至るまで本発明樹脂組
成物によるものがEVA樹脂単独によるものより柔軟性
を保っている。・Retention of flexibility Regarding retention of flexibility, the hardness at each ambient temperature was measured by torsional rigidity, and as shown in the following table, the standard temperature 2
The resin composition of the present invention is more flexible at 0°C, and the resin composition of the present invention maintains more flexibility than the EVA resin alone up to a temperature as low as -20°C.
又、逆に雰囲気温度が40〜80℃の高温時には、EV
A樹脂単独のものによれば極端に軟化し、粘着化、引張
強度、耐クリープ性が低下して、例えばこのターポリン
をフレキシブルコンテナに底形した場合実用上不都合を
生ずるが、本発明の樹脂組成物の場合は軟化程度が少く
充分実用に耐え得るものである。On the other hand, when the ambient temperature is 40 to 80 degrees Celsius, the EV
If resin A is used alone, it will become extremely soft, and its tackiness, tensile strength, and creep resistance will decrease, resulting in practical problems when the tarpaulin is used in a flexible container, but the resin composition of the present invention In the case of a solid material, the degree of softening is small and it can withstand practical use.
捩り剛性率(ASTM
D
1043法による)
・温度依存性について
ターポリン用樹脂組成物として適当な柔軟性が必要であ
るが、それが過度になり強度が低下すると不都合が生じ
、熱可塑性樹脂を主体とする場合、雰囲気温度の変化特
に上昇高温時における状態の変化が問題となるが、A、
B試料の温度依存性を引張強度によって比較した結果、
第1図に示すように本発明樹脂組成物によるものは、E
VA樹脂単独によるものに比してウエルダ一部における
温度依存性が優れている。Torsional rigidity (according to ASTM D 1043 method) ・Regarding temperature dependence, resin compositions for tarpaulin require appropriate flexibility, but if this becomes excessive and the strength decreases, it will cause problems, so thermoplastic resins as the main When doing so, changes in the atmospheric temperature, especially when the temperature rises, become a problem, but A.
As a result of comparing the temperature dependence of sample B by tensile strength,
As shown in FIG. 1, the resin composition of the present invention has E.
The temperature dependence in a part of the welder is superior to that made of VA resin alone.
なお、図中、ウエルダー条件は時間5秒、圧力17に9
/cra、電流0.7 Aである。In the figure, the welding conditions are 5 seconds, pressure 17 and 9.
/cra, and the current is 0.7 A.
上述のように本発明による合成樹脂組成物は、エチレン
−酢酸ビニル共重合樹脂に熱可塑性ポリウレタン樹脂と
、エチレン−酢酸ビニル−塩化ビニル三元重合体を夫々
一定量混合したことを特徴とするものであるから、無毒
無可塑剤であり、しかもターポリンとして例えばフレキ
シブルコンテナーに成形して使用した場合、従来のEV
A樹脂単独の製品及びこれに類似の製品の諸欠点を改良
して前述のような優れた諸性質を有し産業資材として広
く活用することができるものである。As mentioned above, the synthetic resin composition according to the present invention is characterized by mixing certain amounts of a thermoplastic polyurethane resin and an ethylene-vinyl acetate-vinyl chloride terpolymer into an ethylene-vinyl acetate copolymer resin. Therefore, it is a non-toxic and non-plasticizing agent, and when used as a tarpaulin, for example, in a flexible container, it can be used in conventional EVs.
This product has the excellent properties described above and can be widely used as an industrial material by improving the various drawbacks of products made of A resin alone and products similar thereto.
図面は本発明の合成樹脂組成物とEVA樹脂単独のもの
によるターポリンのウエルダ一部の温度依存性の比較を
示す線図である。The drawing is a diagram showing a comparison of the temperature dependence of a weld part of a tarpaulin made of the synthetic resin composition of the present invention and that of an EVA resin alone.
Claims (1)
−塩化ビニル三元重合体とを70〜90重量%:30〜
10重量%の割合で混合してなる樹脂配合物をエチレン
−酢酸ビニル共重合樹脂50〜90重量%に苅して50
〜10重量%の割合で混合してなることを特徴とするタ
ーポリン被膜形戒用合戊樹脂組成物。1 70 to 90% by weight of thermoplastic polyurethane resin and ethylene-vinyl acetate-vinyl chloride terpolymer: 30 to 90% by weight
A resin blend obtained by mixing 10% by weight of the ethylene-vinyl acetate copolymer resin is mixed with 50% to 90% by weight of the ethylene-vinyl acetate copolymer resin.
1. A tarpaulin-coated composite resin composition for military use, characterized in that it is mixed at a ratio of ~10% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6030880A JPS5841310B2 (en) | 1980-05-07 | 1980-05-07 | Synthetic resin composition for tarpaulin film formation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6030880A JPS5841310B2 (en) | 1980-05-07 | 1980-05-07 | Synthetic resin composition for tarpaulin film formation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56163136A JPS56163136A (en) | 1981-12-15 |
| JPS5841310B2 true JPS5841310B2 (en) | 1983-09-10 |
Family
ID=13138395
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6030880A Expired JPS5841310B2 (en) | 1980-05-07 | 1980-05-07 | Synthetic resin composition for tarpaulin film formation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5841310B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6376993A (en) * | 1986-09-19 | 1988-04-07 | Toyo Seikan Kaisha Ltd | Body structure of pressure container and manufacture thereof |
| JPH0364205U (en) * | 1989-10-20 | 1991-06-24 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002012812A (en) * | 2000-06-29 | 2002-01-15 | Mitsui Chemicals Inc | Water-based coating material |
-
1980
- 1980-05-07 JP JP6030880A patent/JPS5841310B2/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6376993A (en) * | 1986-09-19 | 1988-04-07 | Toyo Seikan Kaisha Ltd | Body structure of pressure container and manufacture thereof |
| JPH0364205U (en) * | 1989-10-20 | 1991-06-24 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56163136A (en) | 1981-12-15 |
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