JPS61133244A - Synthetic resin film - Google Patents

Synthetic resin film

Info

Publication number
JPS61133244A
JPS61133244A JP59256183A JP25618384A JPS61133244A JP S61133244 A JPS61133244 A JP S61133244A JP 59256183 A JP59256183 A JP 59256183A JP 25618384 A JP25618384 A JP 25618384A JP S61133244 A JPS61133244 A JP S61133244A
Authority
JP
Japan
Prior art keywords
synthetic resin
film
fluorine
alkyl
resin film
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.)
Pending
Application number
JP59256183A
Other languages
Japanese (ja)
Inventor
Iwao Hisamoto
久本 厳
Masaru Hirai
優 平井
Sueyoshi Ishikawa
石川 末良
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.)
Daikin Industries Ltd
Original Assignee
Daikin Industries 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 Daikin Industries Ltd filed Critical Daikin Industries Ltd
Priority to JP59256183A priority Critical patent/JPS61133244A/en
Publication of JPS61133244A publication Critical patent/JPS61133244A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/25Greenhouse technology, e.g. cooling systems therefor

Abstract

PURPOSE:A film having improved haze preventing effect and its durability as an agricultural covering film and improved weather resistance free from adhesion between films, comprising a synthetic resin containing a specific surface active agent. CONSTITUTION:A synthetic resin film having a fluorine-containing surface active agent shown by the formula I [Rf is 3-21C fluorine-containing aliphatic group; R1 is H, or 1-3C acyl; R2 is group shown by the formula II or III; R3 is H, 1-18C alkyl or unsaturated alkyl (with the proviso that 1-3C alkyl is omitted when R1 is H), 1-18C acyl or unsaturated acryl; R4 is 5-10C alkyl; m is 1-30; n is 1-30 (5-15 is omitted when R1 is H]. This film is preferably used with an antiseptic, an amount of the antiseptic is 1.0-5.0pts.wt. based on 100pts.wt. synthetic resin, and an amount of the surface active agent is 0.01-0.2pt.wt.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、合成樹脂フィルムに関し、更に詳しくは特定
の含フツ素界面活性剤を含有する合成樹脂から成ってお
り、包囲空間内でのモヤの発生を減少させ、その効果の
持続性にもすぐれた合成樹脂フィルム、特に農業用合成
樹脂フィルムに関する。
Detailed Description of the Invention [Industrial Field of Application] The present invention relates to a synthetic resin film, and more specifically, it is made of a synthetic resin containing a specific fluorine-containing surfactant, and is used to reduce moisture in an enclosed space. The present invention relates to a synthetic resin film, particularly an agricultural synthetic resin film, which reduces the occurrence of chlorophyll and has excellent sustainability of its effect.

[従来技術] 近年温室栽培により、各種の野菜や果樹類が年間を通じ
て安定して供給されるようになっている。
[Prior Art] In recent years, greenhouse cultivation has enabled a stable supply of various vegetables and fruit trees throughout the year.

温室の疲覆資材として、ポリ塩化ビニル、ポリエチレン
などの合成樹脂フィルムが広く普及している。
Synthetic resin films such as polyvinyl chloride and polyethylene are widely used as covering materials for greenhouses.

温室本来の目的は、栽培作物の生育に不可欠な温度の確
保、すなわち保温である。この保温性を向上させるため
には、温室の密閉度を向上させ、すき間換気によって逃
げる熱量を抑制する必要がある。
The original purpose of a greenhouse is to maintain the temperature essential for the growth of cultivated crops, that is, to keep them warm. In order to improve heat retention, it is necessary to improve the degree of sealing of the greenhouse and suppress the amount of heat that escapes through ventilation.

最近、特に省エネルギーの傾向の中で、ハウス内の作物
に悪影響を校はさない範囲で、太陽エネルギーを何効f
lIIl目゛ろr¥1に、可能な限り、11.−室の密
閉度を上げる管理技術が行なわれろようになって来てい
る。この管理技術を行うことで、温室内の環境が従来量
、hに多湿化される傾向にあり、同時に温室内に発生す
るモヤが著しく増加するという問題が生している。モヤ
は、栽培作物の病虫害、または収穫物の品質と密接な関
係があるとされ、温室栽培において、できるだけ避けな
くてはならないとされているらのである。
Recently, there has been a growing trend towards energy conservation, and there are many ways to utilize solar energy as long as it does not adversely affect the crops in greenhouses.
As much as possible, 11. -Management techniques that increase the degree of airtightness of rooms are becoming more and more popular. By implementing this management technique, the environment within the greenhouse tends to become humid to a conventional level, and at the same time, there is a problem in that the amount of mist generated within the greenhouse increases significantly. Moya is said to be closely related to the pests and diseases of cultivated crops and to the quality of the harvest, and must be avoided as much as possible in greenhouse cultivation.

モヤは基本的には、温室内の水蒸気が結露することで発
生するもので、温室内外の気温差が急激に変化する朝方
及び夕方に多く発生する現象である。モヤは温室内外の
空気を換気することで消滅させろことができる。しかし
、一般的には温室の保温性を重視する為、換気を行うこ
とかできない場合が多く、温室栽培において大きな問題
となっていた。
Moya is basically caused by the condensation of water vapor inside the greenhouse, and is a phenomenon that often occurs in the morning and evening when the temperature difference inside and outside the greenhouse changes rapidly. Moya can be eliminated by ventilating the air inside and outside the greenhouse. However, since the heat retention of greenhouses is generally emphasized, ventilation is often the only option available, which has been a major problem in greenhouse cultivation.

モヤの発生は本質的に温室内の水分に起因する現象であ
るから、温室内雰囲気に供給される水分量を少なくする
ごとて、モヤの発生を減少さ仕ることかできる。温室内
の土壌表面をマルチ資材て被覆することか、モヤの発生
に対する一つの対策である。しかし、マルチ資材の被覆
は被覆作業が繁雑であるばかりか、資材費用も重む為、
温室栽培室にとって必ずしら有利な方法ではない。
Since the occurrence of mist is essentially a phenomenon caused by moisture within the greenhouse, the occurrence of mist can be reduced by reducing the amount of moisture supplied to the atmosphere within the greenhouse. One way to prevent the occurrence of haze is to cover the soil surface inside the greenhouse with mulch material. However, covering with mulch materials is not only complicated, but also increases material costs.
This is not necessarily an advantageous method for a greenhouse grow room.

モヤに対する別の防止法、すなわち被覆資材の改良によ
り、モヤの発生を減少させる方法として、特開昭55−
91663号公報、特開昭57−12070号公報には
、ノリコン系界面活性剤を添加する方法が開示されてい
る。しかし、これら物質を添加した合成樹脂フィルムは
、モヤ防止効果を有する半面、被覆資材の必要特性であ
るフィルム同士の接着性が悪く、さらに防滴性の低下が
ひどくなり、モヤ防止効果の持続性が劣るという欠点が
あった。
Another method for preventing haze, namely, a method for reducing the occurrence of haze by improving coating materials, was published in JP-A-55-
91663 and JP-A-57-12070 disclose a method of adding Noricon type surfactant. However, although synthetic resin films containing these substances have an anti-haze effect, they have poor adhesion between the films, which is a necessary property of coating materials, and the drop-proof property deteriorates significantly, making it difficult to maintain the anti-haze effect. It had the disadvantage of being inferior.

特開昭57−14648号公報には、フッ素系界面活性
剤を添加する方法が開示されているが、従来のフッ素系
界面活性剤では、少量の添加量では、モヤ防止効果が少
なく、モヤ防止効果の持続性か悪いという欠点かあり、
多量に添加すると、フィルム同士の接着性および耐候性
が著しく低下するという問題点があった。
JP-A No. 57-14648 discloses a method of adding a fluorine-based surfactant, but when the conventional fluorine-based surfactant is added in a small amount, the effect of preventing haze is small, and it is difficult to prevent haze. The disadvantage is that the effect is not long-lasting,
When added in large amounts, there is a problem in that the adhesion between films and the weather resistance are significantly reduced.

[発明の構成] 本発明者らは、モヤ防止効果およびその持続性に優れ、
かつ、被覆資材の他の特性、すなわちフィルム同士の接
着性、耐候性、防滴性、透明性、スリップ性などに悪影
響を与えない被覆材料について鋭意研究の結果、本発明
を完成したものである。
[Structure of the Invention] The present inventors have achieved an excellent haze prevention effect and its sustainability,
In addition, the present invention was completed as a result of intensive research into a coating material that does not adversely affect other properties of the coating material, such as adhesion between films, weather resistance, drip-proofness, transparency, and slip properties. .

本発明に使用し得る合成樹脂フィルム材料としては、一
般にフィルム形成能のあるポリ塩化ビニル系、ポリオレ
フィン系、アクリル樹脂系、ポリエステル系、ポリアミ
ド系など、通常の合成樹脂または、該合成樹脂のブレン
ドが挙げられ、これらの中では、特に、耐候性、経済性
、光透過性の面から、ポリ塩化ビニル系およびポリエチ
レン系樹脂が好ましく、熱線の吸収性、すなわちハウス
の保温性の面から、ポリ塩化ビニル系樹脂が最も好まし
い。ポリ塩化ビニル系樹脂としては、塩化ビニルの単独
重合体および酢酸ビニル、エチレン、プロピレン、アル
キルビニルエーテルなどとの共重合体が使用出来る。
Synthetic resin film materials that can be used in the present invention include common synthetic resins, such as polyvinyl chloride, polyolefin, acrylic resin, polyester, and polyamide, which have film-forming properties, or blends of such synthetic resins. Among these, polyvinyl chloride resins and polyethylene resins are particularly preferred from the viewpoint of weather resistance, economical efficiency, and light transmittance. Vinyl resin is most preferred. As the polyvinyl chloride resin, a vinyl chloride homopolymer and a copolymer with vinyl acetate, ethylene, propylene, alkyl vinyl ether, etc. can be used.

合成樹脂に添加する他の添加剤としては、通常一般的に
使用される可塑剤、安定剤、滑剤、充填剤、紫外線吸収
剤、帯電防止剤、酸化防止剤などが使用出来、何ら本発
明が制限されるものではない。
As other additives added to the synthetic resin, commonly used plasticizers, stabilizers, lubricants, fillers, ultraviolet absorbers, antistatic agents, antioxidants, etc. can be used. There are no restrictions.

本発明において用いられる含フツ素界面活性剤は、一般
式: %式% 〔式中、RfはC3〜CZ+の含フツ素脂肪族基、R1
は水素又はC3〜C3のアシル基、R7は÷(Cであり
、R3は水素、C,−’−C,,のアルキル又は不飽和
アルキル基(ただし、R,が水素のとき01〜C3のア
ルキル基を除く。)又はC+−C+eのアシル基又は不
飽和アシル基、R4はCs’〜COOのアルキル基、m
は1〜30.nは1〜30(ただし、R,が水素のとき
5〜15を除く。)である。〕て示される。前記一般式
において、含フツ素脂肪族基は、飽和又は不飽和のいず
れてあってもよく、直鎖又は分枝鎖のいi゛れてあって
しよい。
The fluorine-containing surfactant used in the present invention has the general formula: % formula % [wherein Rf is a C3 to CZ+ fluorine-containing aliphatic group, R1
is hydrogen or an acyl group of C3 to C3, R7 is ÷(C, R3 is hydrogen, an alkyl group of C,-'-C,, or an unsaturated alkyl group (however, when R is hydrogen, an acyl group of 01 to C3 ) or an acyl group or unsaturated acyl group of C+-C+e, R4 is an alkyl group of Cs' to COO, m
is 1-30. n is 1 to 30 (excluding 5 to 15 when R is hydrogen). ] is shown. In the above general formula, the fluorine-containing aliphatic group may be either saturated or unsaturated, and may be linear or branched.

これら含フツ素界面活性剤を具体的に例示すれば、以下
のとおりである: CeF 13CH7CIlCH20((Cllt)zO
) sH(1)i1 C,F 、 3CH2CHCH20((CI、) 20
 ) aH(2)COCH3 C,F、7CI、CIICII、O((C11,)20
 ) 13cH3(3)OCOC113 C,F、、CI、CIC11,0((CH,)20)e
cOc)!、     (4)HCH3 C,F、、C1f、CHO((CI、)to)、C0C
=CF12     (5)C9F 、−CHtCHC
H*O((C112) 20 ) sH(6)CH C=F 17C1ltCHCHtO((CHJ to 
) all       (7)C+oF2+CHtC
HCHtO((cttt)to) IJ     (8
)O1+ ■ C+2FzsC)ItCHCHzO((CI、)to 
) 1sH(9)CH C+ tF 2scIIzcHc)IzO((CH2)
 20 ) 1sCIdlys   (10)含フツ素
界面活性剤([)の添加量は、下記防滴剤との併用時に
は、合成樹脂100重量部に対して001〜0.2重量
部が好ましい。0.01重量部未満では、モヤ防止効果
が小さく、一方、0゜2重量部以上添加してもモヤ防止
効果およびその持続性に向上は見られず、むしろ耐候性
が低下する傾向にある。
Specific examples of these fluorine-containing surfactants are as follows: CeF 13CH7CIlCH20((Cllt)zO
) sH(1)i1 C,F, 3CH2CHCH20((CI,) 20
) aH(2)COCH3 C,F,7CI,CIICII,O((C11,)20
) 13cH3(3)OCOC113 C,F,,CI,CIC11,0((CH,)20)e
cOc)! , (4) HCH3 C,F,,C1f,CHO((CI,)to),C0C
=CF12 (5)C9F, -CHtCHC
H*O((C112) 20 ) sH(6)CH C=F 17C1ltCHCHtO((CHJ to
) all (7) C+oF2+CHtC
HCHtO((cttt)to) IJ (8
)O1+ ■ C+2FzsC)ItCHCHzO((CI,)to
) 1sH(9)CH C+ tF 2scIIzcHc)IzO((CH2)
20) 1sCIdlys (10) The amount of the fluorine-containing surfactant ([) added is preferably 0.01 to 0.2 parts by weight per 100 parts by weight of the synthetic resin when used in combination with the drip-proofing agent below. If it is less than 0.01 part by weight, the anti-haze effect will be small, while if it is added in an amount of 0.2 parts by weight or more, no improvement will be seen in the anti-haze effect or its sustainability, but rather the weather resistance will tend to deteriorate.

これに対し、従来から用いられている含フツ素界面活性
剤には、C8F 、 、C00NH,、C,F、7SO
3K、性剤、C,F 、 、So、N(C,H,)C,
11,0(C,H,O)□H1などの非イオン系界面活
性剤などがあるが、これら従来の含フツ素界面活性剤で
は、本発明で用いる含フツ素界面活性剤([)の場合と
は逆に、0.2重量部以上添加しなければ満足なモヤ防
止効果が得られず、またその持続性も悪い。さらに、フ
ィルム同士の接着性および耐候性ら劣る。
On the other hand, conventionally used fluorine-containing surfactants include C8F, , C00NH,, C,F, 7SO
3K, sex agent, C,F, ,So,N(C,H,)C,
There are nonionic surfactants such as 11,0(C,H,O)□H1, but these conventional fluorine-containing surfactants are On the contrary, if 0.2 parts by weight or more is not added, a satisfactory anti-haze effect cannot be obtained, and its sustainability is also poor. Furthermore, the adhesion between films and weather resistance are also poor.

しっとも、本発明で用いる含フィルム界面活性剤(Dは
、上記従来のらのに比べ、少量の使用でら防滴およびモ
ヤ防止効果にすぐれ、防滴剤を用いなくても有効である
Of course, the film-containing surfactant (D) used in the present invention has excellent drip-proofing and haze-preventing effects even when used in small amounts compared to the above-mentioned conventional Rano, and is effective even without using a drip-proofing agent.

本発明において、望ましくは含フツ素界面活性剤と共に
使用する防滴剤としては、合成樹脂フィルムに防滴性を
付与しうる界面活性剤ならばいずれら用いることができ
、通常、非イオン系界面活性剤が好適に使用される。こ
れらの具体例としては、(A)ボリオキノエヂレンアル
キルエーテル、ポリオキシエチレンアルキルアリールエ
ーテル、ポリオキシエチレンポリオキソプロピレンエー
テル等のエーテル型のらの、(B)ポリオキシエチレン
アルキルエステル、多価アルコールと脂肪酸の部分エス
テル化物等のエステル型のもの、(C)1′!リオキシ
エチレンアルキルアミン等のアミノエーテル型のもの、
(D)ポリオキシエチレンソルビタン脂肪酸エステル、
ポリオキシエチレンソルビトール脂肪酸エステル、ポリ
オキシエチレンマンニタン脂肪酸エステル、ポリオキン
エチレングリセリル脂肪酸エステル、ポリオキシエチレ
ンプロピレングリコールモノ脂肪酸エステル等のエーテ
ルエステル型のもの、などがあげられる。これら非イオ
ン系界面活性剤の選択は、基本的には任意に行うことが
できるが、好ましくは、防滴性を保持する以外に、成形
性、耐熱性、透明性等の性能を具備し、農業用液覆材と
しての性能を十分に満足することが望ましい。以上の性
能を得ろための好適な非イオン系界面活性剤を例示する
と、(1) ソルビタン、ソルビトール、マンニタン、
マンニトール、グリセリン、ジグリセリン等の多価アル
コールと、炭素数12〜22の脂肪酸の部分エステル (11)エヂレ/オキサイド又はプロピレンオキザイト
の付加モル数が1〜20、多価アルコールがソルビタン
、ソルビトール、マンニタン、グリセリン、ジグリセリ
ンで、脂肪酸の炭素数か12〜22であるポリオキノア
ルキレン多価アルコール、脂肪酸エステル (iii)  (i)(1i)の混合物が挙げられろ。
In the present invention, as the drip-proofing agent that is preferably used together with the fluorine-containing surfactant, any surfactant that can impart drip-proofing properties to the synthetic resin film can be used. Active agents are preferably used. Specific examples of these include (A) ether-type esters such as borioquinoedylene alkyl ether, polyoxyethylene alkylaryl ether, and polyoxyethylene polyoxopropylene ether; (B) polyoxyethylene alkyl ester, polyhydric Ester-type products such as partial esterification products of alcohol and fatty acids, (C)1'! Aminoether type products such as lyoxyethylene alkylamine,
(D) polyoxyethylene sorbitan fatty acid ester,
Examples include ether ester types such as polyoxyethylene sorbitol fatty acid ester, polyoxyethylene mannitan fatty acid ester, polyoxyethylene glyceryl fatty acid ester, and polyoxyethylene propylene glycol monofatty acid ester. These nonionic surfactants can basically be selected arbitrarily, but preferably they have properties such as moldability, heat resistance, transparency, etc. in addition to drip-proofing properties, It is desirable that the performance as an agricultural liquid cover material is fully satisfied. Examples of nonionic surfactants suitable for obtaining the above performance include (1) sorbitan, sorbitol, mannitan,
Partial ester of polyhydric alcohol such as mannitol, glycerin, diglycerin, and fatty acid having 12 to 22 carbon atoms (11) The number of moles added of edile/oxide or propylene oxite is 1 to 20, and the polyhydric alcohol is sorbitan, sorbitol, Mannitan, glycerin, diglycerin, polyoxynoalkylene polyhydric alcohols whose fatty acids have 12 to 22 carbon atoms, and mixtures of fatty acid esters (iii) (i) (1i) can be mentioned.

これら防滴剤は、通常合成樹111100重量部に対し
て、少なくとも05重量部、好ましくは10〜50重量
部の範囲で添加する。添加量が0.5重量部未満ては、
十分な防滴効果か得られず、又、50重量部以上ではブ
リードが多く、吸水白化し易く、透明性か低下して好ま
しくない傾向にある。
These drip-proofing agents are usually added in an amount of at least 0.5 parts by weight, preferably in the range of 10 to 50 parts by weight, based on 111,100 parts by weight of the synthetic tree. If the amount added is less than 0.5 parts by weight,
A sufficient drip-proofing effect cannot be obtained, and if it exceeds 50 parts by weight, there is a tendency for a large amount of bleeding, water absorption, whitening, and a decrease in transparency to be undesirable.

[発明の効果] 以上述べた様に、飽和の合成樹脂フィルムは、上記含フ
ツ素界面活性剤(I)を、望ましくは防滴剤と共に含有
した合成樹脂から成っているため、モヤ防止効果が顕著
であり、その持続性もすぐれている。さらに、含フツ素
界面活性剤([)は、微量の添加で所望の効果を発揮す
るため、フィルム同士の接着性および耐候性への悪影響
がほとんどなく、本発明の合成樹脂フィルムは、農業用
被覆資材として極めて利用価値が高いものである。
[Effects of the Invention] As described above, since the saturated synthetic resin film is made of a synthetic resin containing the above-mentioned fluorine-containing surfactant (I), preferably together with a drip-proofing agent, it has an anti-haze effect. It is remarkable and its durability is also excellent. Furthermore, since the fluorine-containing surfactant ([) exhibits the desired effect even when added in a small amount, it has almost no negative effect on the adhesion and weather resistance between films, and the synthetic resin film of the present invention is suitable for agricultural use. It has extremely high utility value as a covering material.

[発明の好ましい態様] 次に、実施例および比較例を示し、本発明を更に具体的
に説明する。
[Preferred Embodiments of the Invention] Next, the present invention will be explained in more detail by showing Examples and Comparative Examples.

実施例および比較例におけるモヤ評価法、防滴性評価法
、耐候性評価法およびフィルム接着性評価法は次の通り
である。
The haze evaluation method, drip-proof evaluation method, weather resistance evaluation method, and film adhesion evaluation method in Examples and Comparative Examples are as follows.

モヤ評価法 間口1+n、高さ0.9mS@行tOI11のトンネル
状温室に、各実施例および各比較例で得られるフィルム
を別個に展張し、朝方およ赫夕方のモヤ発生状況を観察
し、次の基”準で評価した:○:全くモヤがない 口微かにモヤかある △モヤがやや多い ×・モヤが非常に多い 防滴性評価法 上記トノネル状温室にて、防滴状態の良否を肉眼で観察
し、次の基準で評価した・ ○防滴性非常に良好 口防滴性良好 △防滴性劣る X防滴性非常に劣る 耐候性評価法 屋外で洛子曝露を行い、フィルムの劣化状況を肉眼で観
察し、次の基準で評価した。
Moya evaluation method: The films obtained in each example and each comparative example were spread separately in a tunnel-shaped greenhouse with a width of 1+n and a height of 0.9 mS @ line tOI11, and the occurrence of mist was observed in the morning and evening. Evaluated according to the following criteria: ○: No haze at all. Slight haze △ Slightly hazy × - Very much haze Drip-proof evaluation method In the above-mentioned tunnel-shaped greenhouse, whether the drip-proof condition is good or not was observed with the naked eye and evaluated using the following criteria: ○ Drip-proofing is very good. Dripping-proofing is good. △ Dripping-proofing is poor. X Dripping-proofing is very poor. The deterioration status was observed with the naked eye and evaluated using the following criteria.

○:全く変色なし ログかに変色かみられる △約半分の面積に変色か見られろ ×全部で変色か暮しい フィルム接着性評価法 フィルム作成後、6ケ月室温に放置した2枚のフィルム
を高周波ミノンにより接着し、フィルムが切断されるま
で引張り、接着強度を次の基準で評価した。
○: No discoloration at all Some discoloration can be seen on the log △ Discoloration can be seen on about half of the area × Discoloration or gloomy on the entire area Film adhesion evaluation method After film production, two films left at room temperature for 6 months were subjected to high frequency treatment. The film was adhered with Minon and pulled until it was cut, and the adhesive strength was evaluated based on the following criteria.

O:接着部は全く剥離せず、フィルムが破れる。O: The adhesive part is not peeled off at all and the film is torn.

△、接着部は2分の1程度剥離する ×:接着部は全部剥離する 実施例1〜8および比較例1−13 堰本配合              重量部塩化ビニ
ル樹脂(重合度+300)   to。
Δ, about 1/2 of the adhesive part is peeled off. ×: The entire adhesive part is peeled off. Examples 1 to 8 and Comparative Examples 1-13 Weirmoto formulation Part by weight vinyl chloride resin (degree of polymerization +300) to.

ジオクチルフタレート        44トリクレジ
ルホスフエート       6エボキシ樹脂    
          2Ba−Zn系安定剤     
      2メチレンビスステアロアミド     
 0.1紫外線吸収剤             0.
1上記基本配合に対して、含フツ素界面活性剤、非イオ
ン系界面活性剤およびシリコン系界面活性剤を単独でま
たは混合して表1の割合(塩化ビニル樹脂100重量部
に対す4重量部)で配合し、厚さO、I mmのフィル
ムにカレンダー成形し、得られたフィルムについてモヤ
試験、防滴性試験、耐1父性試験およびフィルム接着性
試験を実施し、上述の基準で評価した。結果を表2に示
す。
Dioctyl phthalate 44 Tricresyl phosphate 6 Eboxy resin
2Ba-Zn stabilizer
2 methylene bisstearamide
0.1 Ultraviolet absorber 0.
1 For the above basic formulation, fluorine-containing surfactants, nonionic surfactants, and silicone surfactants may be added alone or in combination in the proportions shown in Table 1 (4 parts by weight per 100 parts by weight of vinyl chloride resin). ) and calender-molded into a film with a thickness of O and I mm, and the resulting film was subjected to a Moya test, a drip-proof test, a paternity test, and a film adhesion test, and evaluated according to the above criteria. . The results are shown in Table 2.

表2の結果から明らかなよ−)に、本発明のフィルムは
モヤ防止効果およびその持続性にすぐれ、耐候性、フィ
ルム接着性にら4”ぐれている極めて有用な合成樹脂フ
ィルム、特に農業用フィルムである。
As is clear from the results in Table 2, the film of the present invention has excellent anti-haze effect and durability, and is superior in weather resistance and film adhesion by 4", making it an extremely useful synthetic resin film, especially for agricultural use. It's a film.

Claims (1)

【特許請求の範囲】 1、一般式: ▲数式、化学式、表等があります▼ 〔式中、RfはC_3〜C_2_1の含フッ素脂肪族基
、R_1は水素又はC_1〜C_3のアシル基、R_2
は−〔(CH_2)_2O〕−_mR_3又は▲数式、
化学式、表等があります▼ であり、R_3は水素、C_1〜C_1_8のアルキル
又は不飽和アルキル基(ただし、R_1が水素のときC
_1〜C_3のアルキル基を除く。)又はC_1〜C_
1_8のアシル基又は不飽和アシル基、R_4はC_5
〜C_1_0のアルキル基、mは1〜30、nは1〜3
0(ただし、R_1が水素のとき5〜15を除く。)で
ある。〕 で示される含フッ素界面活性剤を含有することを特徴と
する合成樹脂フィルム。 2、合成樹脂がさらに防滴剤を含有する特許請求の範囲
第1項記載の合成樹脂フィルム。
[Claims] 1. General formula: ▲ Numerical formulas, chemical formulas, tables, etc.
is − [(CH_2)_2O] −_mR_3 or ▲ formula,
There are chemical formulas, tables, etc.
Exclude alkyl groups from _1 to C_3. ) or C_1 to C_
1_8 acyl group or unsaturated acyl group, R_4 is C_5
~C_1_0 alkyl group, m is 1-30, n is 1-3
0 (excluding 5 to 15 when R_1 is hydrogen). ] A synthetic resin film characterized by containing a fluorine-containing surfactant represented by the following. 2. The synthetic resin film according to claim 1, wherein the synthetic resin further contains a drip-proofing agent.
JP59256183A 1984-12-03 1984-12-03 Synthetic resin film Pending JPS61133244A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59256183A JPS61133244A (en) 1984-12-03 1984-12-03 Synthetic resin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59256183A JPS61133244A (en) 1984-12-03 1984-12-03 Synthetic resin film

Publications (1)

Publication Number Publication Date
JPS61133244A true JPS61133244A (en) 1986-06-20

Family

ID=17289058

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59256183A Pending JPS61133244A (en) 1984-12-03 1984-12-03 Synthetic resin film

Country Status (1)

Country Link
JP (1) JPS61133244A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5107033A (en) * 1988-03-02 1992-04-21 E. I. Du Pont De Nemours And Company Perfluoroalkyl polyether glycols and their use
US7351748B2 (en) 2002-05-16 2008-04-01 Daikin Industries, Ltd. Fluorine-containing water-soluble nonionic surface-active compounds, use thereof and process for preparation of the compounds

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5993739A (en) * 1982-11-19 1984-05-30 Daikin Ind Ltd Synthetic resin film
JPS6126644A (en) * 1984-07-17 1986-02-05 C I Kasei Co Ltd Mildew-proofing coating material for agricultural use

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5993739A (en) * 1982-11-19 1984-05-30 Daikin Ind Ltd Synthetic resin film
JPS6126644A (en) * 1984-07-17 1986-02-05 C I Kasei Co Ltd Mildew-proofing coating material for agricultural use

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5107033A (en) * 1988-03-02 1992-04-21 E. I. Du Pont De Nemours And Company Perfluoroalkyl polyether glycols and their use
US7351748B2 (en) 2002-05-16 2008-04-01 Daikin Industries, Ltd. Fluorine-containing water-soluble nonionic surface-active compounds, use thereof and process for preparation of the compounds

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