JPS60147445A - Manufacture of dustproof vinyl chloride resin film - Google Patents

Manufacture of dustproof vinyl chloride resin film

Info

Publication number
JPS60147445A
JPS60147445A JP185784A JP185784A JPS60147445A JP S60147445 A JPS60147445 A JP S60147445A JP 185784 A JP185784 A JP 185784A JP 185784 A JP185784 A JP 185784A JP S60147445 A JPS60147445 A JP S60147445A
Authority
JP
Japan
Prior art keywords
vinyl chloride
resin film
chloride resin
film
coating
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
JP185784A
Other languages
Japanese (ja)
Other versions
JPH0113729B2 (en
Inventor
Ryosuke Enoshita
榎下 良祐
Tamotsu Uejima
上島 保
Masahiro Washino
鷲野 正浩
Toshiichi Kondo
近藤 敏一
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP185784A priority Critical patent/JPS60147445A/en
Publication of JPS60147445A publication Critical patent/JPS60147445A/en
Publication of JPH0113729B2 publication Critical patent/JPH0113729B2/ja
Granted legal-status Critical Current

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  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the titled film free from repellency in the acrylic resin coating, whitening, static electricity generation in its rewinding and tackiness after spreading said resin, by coating the acrylic resin on a flexible vinyl chloride film incorporated with a compound derived from adding oxides to higher fatty acid sorbitan ester. CONSTITUTION:The objective film can be obtained by coating (A) an acrylic resin on the surface of (B) a flexible vinyl chloride resin film incorporated with (i) a compound prepared by adding a) 1-5(pref. 1-3)mol of ethylene oxide plus b) 0.1-3(pref. 0.5-2)mol of propylene oxide to (ii) 1mol of a higher fatty acid sorbitan ester. The amount of said compound to be incorporated is pref. 0.1-4 (pref. 0.5-3)pts.wt. per 100pts.wt. of the acrylic resin.

Description

【発明の詳細な説明】 本発明は防塵性塩化ビニル樹脂フィルム(以下、防塵塩
ビと略す。)の製造法に関する。更に詳しくはアクリル
系樹脂の塗布時に塗布性が良好であり、かつ巻物解反時
の静電隼の発生も展張後のべ□タツキもないきわめてす
ぐれた防塵塩ビの製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a dustproof vinyl chloride resin film (hereinafter abbreviated as dustproof vinyl chloride). More specifically, the present invention relates to an extremely excellent method for producing dust-proof PVC that exhibits good coating properties when applying an acrylic resin, and that does not generate static electricity when unrolling a roll or cause stickiness after being rolled out.

防塵塩ビは、その表面にアク+7 )し系樹脂皮膜が設
けられていること忙よ、りいつまでもほこりの付着がな
く、透明性−すぐれ、流滴性能が長期持続し、耐久性に
すぐれている等の特徴を有しているので、近年農業用に
急速に需要が増している。
Dust-proof PVC has an acrylic resin film on its surface, so it stays free of dust, has excellent transparency, has long-lasting droplet performance, and is highly durable. Because of these characteristics, the demand for agricultural use has increased rapidly in recent years.

しかしながら、防塵塩ビはその製造時にアクリル系樹脂
の塗布−乾燥が行なわれるのであるが、その際に塗布液
がはじかれたり、乾燥中に白化したりという問題があり
、透明性不良が発生しやすく、きわめて生産性に劣ると
いう欠点がある。
However, when manufacturing dust-proof PVC, an acrylic resin is applied and dried, but there are problems with the coating liquid being repelled and whitening during drying, resulting in poor transparency. , which has the disadvantage of extremely low productivity.

また、従来の防塵塩ビは、巻物から解反する際に、その
表面にアクリル系樹脂皮膜が設けられているために静電
気が発生しやすく、その程度も皮膜処理する前の原反フ
ィルムに比べはるかに大きくなり、ミシン接着加工時に
は作業者に静電気衝 又撃を与えるという欠点がある。
In addition, when conventional dust-proof PVC is unwrapped from a roll, it is easy to generate static electricity due to the acrylic resin coating on its surface, and the level of static electricity is far greater than that of the original film before coating. It has the disadvantage of being large and subjecting workers to electrostatic shock and shock when bonding with a sewing machine.

さらK、従来の防塵塩ビでは近年夏場において、フィル
ムをノ・ウスの上にパイプを軸に巻き上げて保管する方
法が取られているが、数ケ月後に巻き戻した際に、フィ
ルムが融着し、ベタツキ不良が発生するという欠点もあ
る。
Furthermore, in recent years, with conventional dust-proof PVC, the film has been stored on top of a pipe by being rolled up around a shaft, but when it is rewound several months later, the film tends to fuse. , there is also a drawback that sticky defects occur.

本発明者らは、防塵塩ビの上記欠点を改良すべく鋭意検
討した結果、基材である軟質塩化ビニル。
The inventors of the present invention made extensive studies to improve the above-mentioned drawbacks of dust-proof PVC, and as a result, developed a base material of soft vinyl chloride.

゛樹脂フィルム中に特定の化合物を添加することにより
、上記欠点が解決され、良好な防塵塩ビが得られること
を見出し、本発明を完成するに到った。
It has been discovered that by adding a specific compound to the resin film, the above-mentioned drawbacks can be solved and dust-proof PVC can be obtained, and the present invention has been completed.

□即ち、本発明は、軟質塩化ビニル樹脂フィルムの表面
にアクリル系樹脂を塗布して防塵性塩化ビニル樹脂フィ
ルムを製造する方法において、基材である軟質塩化ビニ
ル樹脂フィルムとしてソルビタン脂肪酸エステル1モル
に対しエチレンオ、キサイド1〜5モルとプロピレンオ
キサ・イ1ド0.1〜3モルを付加させた化合物を含有
する軟質塩:化ビニル樹脂フィルムを用いア゛トとを特
徴gす−る防塵′性 。
□That is, the present invention provides a method for producing a dust-proof vinyl chloride resin film by coating the surface of a soft vinyl chloride resin film with an acrylic resin, in which 1 mole of sorbitan fatty acid ester is used as a base material of the soft vinyl chloride resin film. In contrast, a soft salt containing a compound to which 1 to 5 moles of ethylene oxide and 1 to 3 moles of propylene oxide are added: A dustproof method using a polyvinyl chloride resin film. Sex.

塩化ビニル樹脂フィルムの製造法でおる。・□本発明の
方法により、上記の欠点は完全に解消され、良好な防塵
塩ビが得られる。
This is a method for producing vinyl chloride resin film.・□By the method of the present invention, the above-mentioned drawbacks are completely eliminated and good dust-proof PVC can be obtained.

本発明を構成する軟質塩化ビニル樹脂フィルム及び表面
処理剤は、本発明にいう特定の化合物の添加を除き通常
の防塵塩ビを製造するのに用いられる公知のものである
The soft vinyl chloride resin film and surface treatment agent constituting the present invention are known ones used for producing ordinary dustproof vinyl chloride, except for the addition of specific compounds referred to in the present invention.

即ち、本発明に用いる軟質塩化ビニル樹脂フィルム献塩
化ビニル樹脂が塩化ビニルのホモポリマー及びコポリマ
ーであり、この塩化ビニル樹脂に可塑剤、安定剤、金属
石けん、紫外線吸収剤、抗酸化剤等を配合してフィルム
とすることにより得られ、さらには、滑剤、顔料あるい
は界面活性剤を含むものであってもよ、い。
That is, the soft vinyl chloride resin film used in the present invention is a homopolymer or copolymer of vinyl chloride, and this vinyl chloride resin is blended with a plasticizer, a stabilizer, a metal soap, an ultraviolet absorber, an antioxidant, etc. The film may be obtained by preparing a film, and may further contain a lubricant, a pigment, or a surfactant.

更に、↑発明に、おいては、以下に示す特定の化合物が
添加されていることが、本発明の目的を達、成するため
に必要である。
Furthermore, in the invention ↑, it is necessary to add the specific compounds shown below in order to achieve the object of the invention.

木登!にいう特定の化合物とはソルビトールおよび/′
またはソルビタンと高級脂肪酸との七ジエステル、ジエ
ステル、トリエステル等あるいはこれらの混合物忙エチ
レンオキサイド□とプロピレンオキサイドをそれぞれ特
定量づつ付加したものである。 r ソルビトールおよび/゛またはソルビタンとの間でエス
テルを形成する高級脂肪酸は、一般には炭素原子数12
〜22個の飽和ある゛いは不飽和脂肪酸であり、具体的
に例示するならば、ラウリン酸、ミリスチン酸、パルミ
チン酸、身レイン酸、ステアリン酸、ベヘン酸等が好゛
ましいものとしてあげられるが、必らずしもこれ□らに
限□定されるもので□はない。 ″ □′□ ゛ 本発明に珀゛いる特゛定の化谷物は、」二配のソルビト
ールおよび/また番′まツル□ビタンとの高級脂肪酸′
エユテ7.□、7.当り、エチレ、オヤーヶイドが1〜
5モル好゛ましくは1〜3羞ルと、プロピ“レンオ゛キ
讐イト1が0.1〜3モル好ましくは0.5〜2モル伺
加されたもめでなければ歿らない。
Tree climbing! These specific compounds include sorbitol and
Alternatively, it is a seven diester, diester, triester, etc. of sorbitan and higher fatty acid, or a mixture thereof, to which specific amounts of ethylene oxide and propylene oxide are added. r Higher fatty acids that form esters with sorbitol and/or sorbitan generally have 12 carbon atoms.
~22 saturated or unsaturated fatty acids, and specific examples include lauric acid, myristic acid, palmitic acid, leicic acid, stearic acid, and behenic acid. However, it is not necessarily limited to these □. `` □'□ ``Specific chemical substances included in the present invention are ``higher fatty acids with divalent sorbitol and/or ``matsuru □ bitane.''
Eyute 7. □、7. Hit, Echire, Oyagaide is 1~
5 mol, preferably 1 to 3 mol, and 0.1 to 3 mol, preferably 0.5 to 2 mol, of propylene oxygenate 1 are added.

付加モル数が上記範囲にあることか必要でt・す;9の
範囲を一外れた場合、主艷毛た3つの効果は必らずしも
十分とは言えなくなり、良好な防塵塩ビが得られない。
It is necessary that the number of moles added falls within the above range; if the number of moles added falls outside the range of I can't do it.

この特定の化合物の軟質塩化ビニル゛樹脂フ゛イル“ 
仝 □、  ムへの配合量としては、塩化ビニル樹脂100重Ji。
Soft vinyl chloride resin film of this particular compound
廝□、The amount of polyvinyl chloride resin to be added is 100 weight Ji.

が適当であり、この範囲より少ないと添加の効果が十分
得られず、この範囲より多くしても効果はほとんど変わ
らず、かえってブリードして表面がベタツク結果となり
防塵性が損なわれる。
If the amount is less than this range, the effect of addition will not be sufficiently obtained, and if it is added more than this range, the effect will hardly change, but instead it will bleed, resulting in a sticky surface and impairing dustproof properties.

本化合物の配合は、先に示した軟質塩化ビニル樹脂フィ
ルムの構成成分を配合する際に同時に行なエバよく、ブ
レンダニ、ヘンシェルミキサー等の混合機で混合され、
公知の製膜法、即ち、カレンダー法、インクレージョン
法、゛Tダイ法等によりフィルムにされる。
The present compound is blended at the same time as the components of the soft vinyl chloride resin film shown above, and is thoroughly mixed with a blender such as a blender or a Henschel mixer.
It is made into a film by a known film forming method, such as a calendar method, an inkjet method, or a T-die method.

本発明において防塵′性を付与するために用いる表面処
理剤は、アクリル系樹脂の溶剤液あるいは水性エマルジ
ョン液もありJ主にメチルメタクリレート、ブチルメタ
クリレート等の毎ツマ−を主体とするアクリ′ル電共重
合体からなり、架橋腫を有する官能基を有するモノマー
が共重合されていたり、架橋開示添加゛ざ′M:たもの
゛であっても良い。
In the present invention, the surface treatment agent used to impart dustproof properties may be a solvent solution or an aqueous emulsion of an acrylic resin, or an acrylic resin containing mainly methyl methacrylate, butyl methacrylate, etc. It may be composed of a copolymer, in which a monomer having a functional group having a crosslinking agent is copolymerized, or it may be a crosslinkable additive.

表面□処理剤の塗布は、″上記した液にさらに造膜助痢
、界面活性剤等を必′要に応じ加え、配′合塗布液とし
、コーターを用い基材である軟質塩化ビニル樹脂フィル
ムの表面に固型分として凡そ1〜5μm程度の厚みとな
るように行なう。
To apply the surface treatment agent, add film-forming agent, surfactant, etc. as necessary to the above-mentioned solution to make a mixed coating solution, and use a coater to coat the soft vinyl chloride resin film that is the base material. This is done so that the solid content on the surface becomes approximately 1 to 5 μm thick.

次いで乾燥して、防塵塩ビが得られる。It is then dried to obtain dustproof PVC.

本発明の方法では、表面処理の工程で塗布液がはじかれ
たり、乾燥により白化するという現象もなく、良好な透
明性を有する防塵塩ビが得られ、かつ生産性もきわめて
良好である。
In the method of the present invention, there is no phenomenon of the coating liquid being repelled during the surface treatment process or whitening due to drying, dust-proof PVC having good transparency can be obtained, and the productivity is also extremely good.

また、本発明の方法によって得られる防塵塩ビは上記し
たように透明性にすぐれるばかりでなく、防塵性が良好
であることはもちろんのこと、夏場に巻き上げてあった
ものを巻きもどしたときに生じていた融着現象もなく、
かつ、帯電性もきわめて小さいものであり、特に農業用
被覆材として有効に用いうるものである。
In addition, the dust-proof PVC obtained by the method of the present invention not only has excellent transparency as described above, but also has good dust-proof properties. There was no fusion phenomenon that had occurred,
In addition, the electrostatic property is extremely low, and it can be particularly effectively used as an agricultural coating material.

以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1〜7及び比較例1〜7 塩化ビニル樹脂(三井東圧化学(株)製、ピニク・ ロ
ン4000M (商標) ) 100重量部、フタル字
マ′ ジオクチル45重量部、リン酸トリクレジル5重
量部、エポキシ樹脂(シ蚕ル化学社製、エビコー)82
8(商標) ) 2.0重量部、ステアリン酸亜鉛とス
テアリン酸バリウム各1重惜部、および表1に示す化合
物2.0重量部を添加し、ヘンシェルミキサーにより均
一に混合し、次いで1.80℃に設定したオープンミル
ロールで10分間混練した後、180℃に設定した30
インチZ型カレンダーで(1,10111厚さのフィル
ムを作成した。
Examples 1 to 7 and Comparative Examples 1 to 7 Vinyl chloride resin (manufactured by Mitsui Toatsu Chemical Co., Ltd., Pinikron 4000M (trademark)) 100 parts by weight, 45 parts by weight of phthalate dioctyl, 5 parts by weight of tricresyl phosphate Part, epoxy resin (manufactured by Shisei Kagaku Co., Ltd., Ebiko) 82
8 (trademark) ), 1 part each of zinc stearate and barium stearate, and 2.0 parts by weight of the compound shown in Table 1 were added and mixed uniformly using a Henschel mixer, and then 1. After kneading for 10 minutes with an open mill roll set at 80°C,
A film with a thickness of (1,10111 mm) was prepared using an inch Z-type calender.

一方、水125重量部中に過硫酸カリウム0.5重量部
及びポリオキシエチレンオキシドアルキルフェノールエ
ーテル誘導体1.0重量部を溶解し、これを反応器中に
仕込み70℃に昇温した。この中にメチルメタクリレー
ト59重量部、n−ブチルメタクリレート33重量部、
ヒドロキシエチルメタクリレート6重量部、メタクリル
酸2重量部の混合物を3時間かけて滴下し、乳化重合さ
せ、滴下終了後更に3時間反応させ、樹脂濃度45%の
水性分散液を得た。この水性分散液をアンモニア水にて
pH7,0に中和した。
On the other hand, 0.5 parts by weight of potassium persulfate and 1.0 parts by weight of a polyoxyethylene oxide alkylphenol ether derivative were dissolved in 125 parts by weight of water, and the solution was charged into a reactor and heated to 70°C. In this, 59 parts by weight of methyl methacrylate, 33 parts by weight of n-butyl methacrylate,
A mixture of 6 parts by weight of hydroxyethyl methacrylate and 2 parts by weight of methacrylic acid was added dropwise over 3 hours to cause emulsion polymerization, and after completion of the addition, the reaction was continued for another 3 hours to obtain an aqueous dispersion with a resin concentration of 45%. This aqueous dispersion was neutralized to pH 7.0 with aqueous ammonia.

この中和済み水性分散液100重量部に造膜助剤として
ブチルカルピトール5重量部とアルキルフェノールエー
テル3重量部を加え、帰後に樹脂濃度が20重景%にな
るように水で希釈し、塗布液を得た。
To 100 parts by weight of this neutralized aqueous dispersion, 5 parts by weight of butylcarpitol and 3 parts by weight of alkylphenol ether were added as film-forming aids, and after returning home, the resin was diluted with water to a concentration of 20% and applied. I got the liquid.

この塗布液を、ロッドコーター株により、前記の軟質塩
化ビニル樹脂フィルムの片面に乾燥後の塗膜の厚みが2
.0μになるよう塗布し、次いで130℃のオープン中
で30秒間乾燥して防塵塩ビを得た。
This coating solution was applied to one side of the above-mentioned soft vinyl chloride resin film using a rod coater so that the thickness of the coating film after drying was 2.
.. It was coated to a thickness of 0μ, and then dried in an open air at 130°C for 30 seconds to obtain dustproof PVC.

これらのフィルムの評価を以下のように行なった。その
結果を表1に示す。
These films were evaluated as follows. The results are shown in Table 1.

■塗布性 みられる白化の度合を目視により判定した。■Applicability The degree of whitening observed was determined visually.

これらの評価は下記による。These evaluations are based on the following.

O:はじき(白化)が全く認められず良好。O: Good with no repellency (whitening) observed.

△:はじき(白化)が一部に7忍められる。△: 7 repellents (whitening) are applied to some parts.

×:はじき(白化)が全面にわたり認められ、その程度
が激しく不良。
×: Repellency (whitening) was observed over the entire surface, and the degree of repellency was extremely poor.

■静電気の発生 被膜処理されたフィルムの巻物を10m/分のスピード
で巻きもどし、そのとき発生する静電気量なスタティッ
クボルトメーター(春日電機製)で調べた。
■Generation of Static Electricity The roll of coated film was unwound at a speed of 10 m/min, and the amount of static electricity generated at that time was measured using a static voltmeter (manufactured by Kasuga Denki).

■展張後のベタツキ性 被膜処理されたフィルムを30cIrL巾に切断し、水
で両面を十分濡らした状態で直径2.54cIrLの鉄
パイプに巻きつけ、屋外に約1ケ月放置したものの巻き
ばくり強度を測定した。
■After stretching, the film treated with the sticky coating was cut into a 30 cIrL width, wrapped around a 2.54 cIrL diameter iron pipe with both sides sufficiently wet with water, and then left outdoors for about a month. was measured.

この強度が大きいほどベタツキ性が高いことを示す。The higher the intensity, the higher the stickiness.

Claims (1)

【特許請求の範囲】[Claims] 1)軟質塩化ビニル樹脂フィルムの表面にアクリル系樹
脂を塗布して防塵性場化ビニル樹脂フィルムを製造する
方法において、基材である軟質塩化ビニル樹脂フィルム
としてソルビタン高級脂肪酸エステル1モルに対しエチ
レンオキサイド1〜5モルとプロピレンオキサイド0.
1〜3モルを付加させた化合物を含有する軟質塩化ビニ
ル樹脂フィルムを用いることな特徴とする防塵性塩化ビ
ニル樹脂フィルムの製造法。
1) In the method of manufacturing a dust-proof vinyl resin film by coating the surface of a soft vinyl chloride resin film with an acrylic resin, ethylene oxide is added per mole of sorbitan higher fatty acid ester as the base material soft vinyl chloride resin film. 1 to 5 mol and 0.0 mol of propylene oxide.
A method for producing a dust-proof vinyl chloride resin film, characterized in that a soft vinyl chloride resin film containing a compound added thereto in an amount of 1 to 3 moles is used.
JP185784A 1984-01-11 1984-01-11 Manufacture of dustproof vinyl chloride resin film Granted JPS60147445A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP185784A JPS60147445A (en) 1984-01-11 1984-01-11 Manufacture of dustproof vinyl chloride resin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP185784A JPS60147445A (en) 1984-01-11 1984-01-11 Manufacture of dustproof vinyl chloride resin film

Publications (2)

Publication Number Publication Date
JPS60147445A true JPS60147445A (en) 1985-08-03
JPH0113729B2 JPH0113729B2 (en) 1989-03-08

Family

ID=11513208

Family Applications (1)

Application Number Title Priority Date Filing Date
JP185784A Granted JPS60147445A (en) 1984-01-11 1984-01-11 Manufacture of dustproof vinyl chloride resin film

Country Status (1)

Country Link
JP (1) JPS60147445A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01301724A (en) * 1988-05-31 1989-12-05 Mitsui Toatsu Chem Inc Synthetic resin-covering material for agriculture
JPH01315432A (en) * 1988-06-16 1989-12-20 Mitsui Toatsu Chem Inc Synthetic resin coating material for agricultural use
JP2011219616A (en) * 2010-04-09 2011-11-04 Toray Fine Chemicals Co Ltd Acrylic emulsion

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01301724A (en) * 1988-05-31 1989-12-05 Mitsui Toatsu Chem Inc Synthetic resin-covering material for agriculture
JPH01315432A (en) * 1988-06-16 1989-12-20 Mitsui Toatsu Chem Inc Synthetic resin coating material for agricultural use
JP2011219616A (en) * 2010-04-09 2011-11-04 Toray Fine Chemicals Co Ltd Acrylic emulsion

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JPH0113729B2 (en) 1989-03-08

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