JPH02296849A - Agricultural vinyl chloride resin film - Google Patents

Agricultural vinyl chloride resin film

Info

Publication number
JPH02296849A
JPH02296849A JP1118368A JP11836889A JPH02296849A JP H02296849 A JPH02296849 A JP H02296849A JP 1118368 A JP1118368 A JP 1118368A JP 11836889 A JP11836889 A JP 11836889A JP H02296849 A JPH02296849 A JP H02296849A
Authority
JP
Japan
Prior art keywords
film
vinyl chloride
chloride resin
alkylene oxide
parts
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
JP1118368A
Other languages
Japanese (ja)
Other versions
JP2626818B2 (en
Inventor
Akio Maruyama
明男 丸山
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.)
Achilles Corp
Original Assignee
Achilles Corp
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 Achilles Corp filed Critical Achilles Corp
Priority to JP1118368A priority Critical patent/JP2626818B2/en
Publication of JPH02296849A publication Critical patent/JPH02296849A/en
Application granted granted Critical
Publication of JP2626818B2 publication Critical patent/JP2626818B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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

Landscapes

  • Greenhouses (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a film excellent in low-temperature antifogging properties and antimisting properties and retentivity of antifogging properties by using a vinyl chloride resin comprising a plasticizer, a fluorine compound and a specified alkylene oxide adduct. CONSTITUTION:An agricultural film prepared from a vinyl chloride resin composition comprising 100 pts.wt. vinyl chloride resin, 40-60 pts.wt. plasticizer, 0.01-1.0 pt.wt. fluorine compound and 0.2-3.0 pts.wt. sorbitan mono(di)stearate/alkylene oxide adduct and/or a sorbitan mono(di)palmitate/alkylene oxide adduct and has a residual area rate after shrinkage >=64% at 160 deg.C. As the fluorine compound, one having a fluorinated group and an alkylene oxide group and/or a hydroxyl group in the molecule can be used, and it has an MW of 500-10000 and decreases the surface tension of water.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は農業用のトンネル、簡易温室(ハウス)等の被
覆材として使用される農業用塩化ビニル系樹脂フィルム
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an agricultural vinyl chloride resin film used as a covering material for agricultural tunnels, simple greenhouses, etc.

〔従来の技術〕[Conventional technology]

従来の農業用塩化ビニル系樹脂フィルムは、トンネルや
簡易温室等に用いた際にフィルム内表面に発生する結露
により太陽光線のフィルム内透過が妨げられることを防
止するため、結露した水滴を水膜化して流下させる、所
謂、防曇性の付与が一般的に行われている。具体的には
、農業用フィルムが特に冬季に多(使用されることから
低温下での防曇性能を向上させる目的で防曇剤としてソ
ルビタン脂肪酸エステルにアルキレンオキサイドを付加
させた物を添加したり、またハウス内に発生する霧を防
止するために防霧剤として含フッ素化合物を添加したも
のなどが知られている。
Conventional agricultural vinyl chloride resin films are used in tunnels, simple greenhouses, etc. to prevent condensation that forms on the film's inner surface from blocking sunlight from passing through the film. It is common practice to impart so-called antifogging properties by causing the fog to flow down. Specifically, since agricultural films are often used especially in winter, we add alkylene oxide to sorbitan fatty acid ester as an antifogging agent to improve antifogging performance at low temperatures. Also known are those to which a fluorine-containing compound is added as an anti-fog agent to prevent fog from forming inside the greenhouse.

〔発明が解決しようとする課!1i) しかしながら、上記のように低温防曇性と防霧性を付与
した農業用塩化ビニル系樹脂フィルムは、防曇持続性が
低下するという問題がある。
[The problem that the invention attempts to solve! 1i) However, the agricultural vinyl chloride resin film provided with low-temperature anti-fog properties and anti-fog properties as described above has a problem in that its anti-fog durability is reduced.

本発明はかかる問題点を解決したもので、低温防曇性や
防霧性が優れている上に、その防暑特性の持続性能にも
優れた農業用塩化ビニル系樹脂フィルムを提供すること
を一目的とする。
The present invention solves these problems, and aims to provide an agricultural vinyl chloride resin film that not only has excellent low-temperature anti-fogging properties and anti-fog properties, but also has excellent long-lasting heat protection properties. purpose.

〔課題を解決するための手段) 本発明は、 「塩化ビニル系樹脂100重量部に対して、可塑剤を4
0〜60重量部、含フッ素化合物を0.01〜1.0重
量部、ソルビタンモノ(ジ)ステアレートのアルキレン
オキサイド付加物及び/又はソルビタンモノ (ジ)パ
ルミテートのアルキレンオキサイド付加物を0.2〜3
.0重量部含有してなる塩化ヒニル系樹脂フィルムであ
って、且つ該フィルムの160°Cにおける収縮面積残
率が65%以上であることを特徴とする農業用塩化ビニ
ル系樹脂フィルム、」 を要旨とするものである。
[Means for Solving the Problems] The present invention is based on the following problems:
0 to 60 parts by weight, 0.01 to 1.0 parts by weight of a fluorine-containing compound, and 0.2 parts of an alkylene oxide adduct of sorbitan mono(di)stearate and/or an alkylene oxide adduct of sorbitan mono(di)palmitate. ~3
.. "A vinyl chloride resin film for agricultural use, which is a vinyl chloride resin film containing 0 parts by weight, and which has a shrinkage area residual ratio of 65% or more at 160°C." That is.

〔作用〕[Effect]

本発明農業用塩化ビニル系樹脂フィルムは、殊に特定の
防曇剤を添加してなることと、フィルムの160℃下で
の収縮面積残率を成る数値以上に規定したことにより、
従来品の如き優れた低温防曇性を有するする上に、従来
品にはなかった優れた防曇持続性をも具備したものであ
る。上記の本発明特有の効果は以下に述べるような理由
によって生じるものと推定される。
The agricultural vinyl chloride resin film of the present invention is made by adding a specific antifogging agent, and by specifying the shrinkage area retention ratio of the film at 160°C to a value or more.
In addition to having excellent low-temperature antifogging properties like conventional products, it also has excellent antifogging durability that conventional products did not have. It is presumed that the above-mentioned effects unique to the present invention are caused by the reasons described below.

即ち、一般にフィルムが防曇性を有するのに必要な要素
としては、フィルム表面にある一定量の防曇剤が存在す
ることが必要であると言え、しかもこの防曇性が長期間
にわたって持続するためには、フィルム表面に防曇剤が
常にある一定量存在する様にフィルム内部から適宜、過
不足なく適量の防曇剤が表面側に移行する必要があると
言える。
In other words, in general, it can be said that a certain amount of antifogging agent must be present on the film surface as a necessary element for a film to have antifogging properties, and furthermore, this antifogging property must last for a long period of time. In order to achieve this, it is necessary to transfer an appropriate amount of antifogging agent from the inside of the film to the surface side so that a certain amount of antifogging agent is always present on the surface of the film.

そこで、上記の防曇剤の移行性についてはフィルム基材
樹脂と使用する防曇剤との相溶性が大きく関与すること
が知られており、この点に鑑みれば、特に従来品で防曇
剤として使用されているソルビタン脂肪酸エステルのア
ルキレンオキサイド付加物は低温防曇性付与特性には優
れているものの、塩化ビニル系樹脂に対する相溶性が悪
くフィルム表面への移行が早いことから、防曇持続性に
は劣るものと考えられる。
Therefore, it is known that the migration property of the above-mentioned antifogging agent is greatly affected by the compatibility between the film base resin and the antifogging agent used. Although the alkylene oxide adduct of sorbitan fatty acid ester used as It is considered to be inferior to

これに対し、本発明品において防曇持続性が著しく向上
する点については以下の理由が更に起因しているものと
推定できる。Jfpち、フィルム成形工程で発生したフ
ィルム内部の分子配向状態によりフィルムに内在してい
る歪(内部歪)が、防曇剤の樹脂への相溶性及びフィル
ム表面への移行性に関与しているものと予測され、この
ことから本発明では160℃におけるフィルムの収縮面
積残率を特定し、以て上記内部歪をある量より少なくし
たことにより、防暑剤と樹脂との実質的な相溶性が向上
し且つフィルム表面への移行速度が緩慢になり、そのた
めフィルム内部に存在する防曇剤が長期間にわたり徐々
に表面に移行するようになる結果、特に防曇持続性に優
れたものになると思われる。
On the other hand, it can be assumed that the following reasons are further responsible for the remarkable improvement in antifogging durability of the product of the present invention. Jfp, the strain (internal strain) inherent in the film due to the molecular orientation state inside the film that occurs during the film forming process is involved in the compatibility of the antifogging agent with the resin and the ability to migrate to the film surface. Therefore, in the present invention, by specifying the shrinkage area residual ratio of the film at 160°C and reducing the internal strain above a certain amount, it is possible to improve the substantial compatibility between the heat protectant and the resin. As a result, the antifogging agent present inside the film gradually migrates to the surface over a long period of time, resulting in particularly excellent antifogging durability. It will be done.

以下、本発明について詳述する。The present invention will be explained in detail below.

本発明で使用される塩化ビニル系樹脂としては、塩化ビ
ニル単独重合樹脂、塩化ビニルとエチレン酢酸ビニル、
ビニルエーテル、マレイン酸エステル等の共重合可能な
単量体との共重合樹脂及びこれらの混合物が挙げられる
The vinyl chloride resin used in the present invention includes vinyl chloride homopolymer resin, vinyl chloride and ethylene vinyl acetate,
Examples include copolymer resins with copolymerizable monomers such as vinyl ether and maleic acid ester, and mixtures thereof.

可塑剤としては、通常塩化ビニル用に用いられているも
のが使用でき、例えばフタル酸エステル系可塑剤、リン
酸エステル系可塑剤、アジピン酸エステル系可塑剤、エ
ポキシ基含有フタル酸エステル系可塑剤、エポキシ化大
豆油、エポキシ樹脂等が挙げられ、これらを単独又は2
種以上を混合して用いる。この可塑剤の塩化ビニル系樹
脂100重量部への添加量が40重量部未満の場合は、
フィルム硬化が高く、冬季寒冷下での耐寒性が悪く不適
当であり、一方、60重量部を越える場合は、フィルム
が柔らかすぎて粘着性が増し本発明には不適当である。
As the plasticizer, those normally used for vinyl chloride can be used, such as phthalate ester plasticizers, phosphate ester plasticizers, adipate ester plasticizers, and epoxy group-containing phthalate ester plasticizers. , epoxidized soybean oil, epoxy resin, etc., and these can be used singly or in combination.
Use a mixture of more than one species. If the amount of this plasticizer added to 100 parts by weight of vinyl chloride resin is less than 40 parts by weight,
The film has a high degree of curing and poor cold resistance in cold winter conditions, making it unsuitable. On the other hand, if it exceeds 60 parts by weight, the film becomes too soft and sticky, making it unsuitable for the present invention.

含フッ素化合物としては、−分子中に含フッ素基と、ア
ルキレンオキサイド基及び/又は水酸基を有するものが
使用でき、この化合物は分子量が500〜10000で
あり、水の表面張力を低下させる特性を有しているもの
である。上記含フッ素基としては、パーフルオロアルキ
ル基、パーフルオロアルコキシ基、ポリフルオロアルキ
ル基、パーフルオロアルケニル基、ポリフルオロアルケ
ニル基、パーフルオロアルキレン基等である。またアル
キレンオキサイド基としてはエチレンオキサイド基(ポ
リエチレンオキサイド基も含む)、プロピレンオキサイ
ド基(ポリプロピレンオキサイド基も含む)等である0
例えば、特開昭57−192445号、特開昭59−8
0468号、特開昭59−93739号、特開昭61−
133244号、特開昭61−152745号、特開昭
62−158756号、特開昭64−6046号等の公
報に記載のものである。このような含フッ素化合物の具
体例としては、例えば、下記のものが挙げられる。
As the fluorine-containing compound, those having a fluorine-containing group, an alkylene oxide group and/or a hydroxyl group in the molecule can be used, and this compound has a molecular weight of 500 to 10,000 and has the property of lowering the surface tension of water. This is what we are doing. Examples of the fluorine-containing groups include perfluoroalkyl groups, perfluoroalkoxy groups, polyfluoroalkyl groups, perfluoroalkenyl groups, polyfluoroalkenyl groups, and perfluoroalkylene groups. Examples of alkylene oxide groups include ethylene oxide groups (including polyethylene oxide groups), propylene oxide groups (including polypropylene oxide groups), etc.
For example, JP-A-57-192445, JP-A-59-8
No. 0468, JP-A-59-93739, JP-A-61-
133244, JP-A-61-152745, JP-A-62-158756, and JP-A-64-6046. Specific examples of such fluorine-containing compounds include the following.

(a)  Csf’+tCtHaO(C!HnO)sc
Hz(b)  C1@El□CHxCH(Oll)CH
xO(CsHbO) +*C11s(c)  C,。P
□CH雪C8(OH)CHgO(CIH40) 5H(
d)  C*P+wCHxCH(OH)CHtO(Cs
HbO)+J(e)  CaFttCHsCH(OCO
CHi)CHgO(CsHiO)scHs(f)  C
aF+、SOlN(CmHs)(CJnO)lH@Ca
F+sCON(Calls)(CgllmO)sH(h
)  CsFtvSolN(CHmCII(OH)CI
lmOtl) m(1)  HCP、C5Ft*CHt
O(CJnO) +J(j)  CsF、OCsFiC
lltCHmSCH(COOH)CHtCOO(CtH
aO)+J(ト) CsF?OC%F1.CH*CH*
SCH(Cl *C00H) COO(C、H40) 
t sCIIgOCOC+Jss CF (CF山 C00(CJH,O)國すCJ+*(
r)  CF(CFi)tc(CFs)CJ+e 含フ・2素化合物の塩化ビニル系樹脂への添加量が上記
の0,01〜1.0重量部以外の場合は、フィルムへの
優れた防霧性、耐候性の付与が困難となる。
(a) Csf'+tCtHaO(C!HnO)sc
Hz(b) C1@El□CHxCH(Oll)CH
xO(CsHbO) +*C11s(c) C,. P
□CH Snow C8 (OH) CHgO (CIH40) 5H (
d) C*P+wCHxCH(OH)CHtO(Cs
HbO) + J(e) CaFttCHsCH(OCO
CHi)CHgO(CsHiO)scHs(f) C
aF+, SOIN(CmHs)(CJnO)IH@Ca
F+sCON(Calls)(CgllmO)sH(h
) CsFtvSolN(CHmCII(OH)CI
lmOtl) m(1) HCP, C5Ft*CHt
O(CJnO) +J(j) CsF, OCsFiC
lltCHmSCH(COOH)CHtCOO(CtH
aO)+J(g) CsF? OC%F1. CH*CH*
SCH (Cl *C00H) COO (C, H40)
t sCIIgOCOC+Jss CF (CF mountain C00 (CJH, O) country CJ+*(
r) CF(CFi)tc(CFs)CJ+e If the amount of the fluorine-containing dicompound added to the vinyl chloride resin is other than the above 0.01 to 1.0 parts by weight, it will provide excellent fog protection to the film. It becomes difficult to impart durability and weather resistance.

本発明におけるアルキレンオキサイド付加物は、ソルビ
タンモノ(ジ)ステアレート又はソルビタンモノ(ジ)
パルミネートに、エチレンオキサイド及び/又はプロピ
レンオキサイドのアルキレンオキサイドを付加したもの
である。アルキレンオキサイドの付加量は0.5〜5モ
ルが好ましく、より好ましくは0.8〜3モルであり、
この付加量が5モルを越えた場合は樹脂への相溶性が低
下し、被覆材としての耐候性が低下する傾向が強まる。
The alkylene oxide adduct in the present invention is sorbitan mono(di)stearate or sorbitan mono(di)stearate.
It is obtained by adding alkylene oxide such as ethylene oxide and/or propylene oxide to palminate. The amount of alkylene oxide added is preferably 0.5 to 5 mol, more preferably 0.8 to 3 mol,
When the amount added exceeds 5 moles, the compatibility with the resin decreases, and the weather resistance as a coating material tends to decrease.

上記付加物の塩化ビニル茶樹111do重量部に対する
添加量は0.2〜3.0重量部、好ましくは0.5〜1
.5重量部であり、この添加量が0.2重量部未滴では
低温防暑性が劣り、逆に3.0重量部を越えるとフィル
ムの耐候性が劣り、表面ブルームが増大して不適である
The amount of the above adduct added to 111 parts by weight of vinyl chloride tea plant is 0.2 to 3.0 parts by weight, preferably 0.5 to 1 part by weight.
.. If the amount added is 0.2 parts by weight, the low-temperature heat resistance will be poor, and if it exceeds 3.0 parts by weight, the weather resistance of the film will be poor and surface bloom will increase, making it unsuitable. .

本発明では上記アルキレンオキサイド付加物とともに、
他の防曇剤を併用してもよい、併用できる他の防曇剤と
してはソルビタン脂肪酸エステル、ソルビトール脂肪酸
エステル、ジグリセリン脂肪酸エステル、グリセリン脂
肪酸エステル、ソルビタン脂肪酸・二塩基酸エステル、
ソルビトール脂1FJal・二塩基酸エステル、ジグリ
セリン脂肪酸・二塩基酸エステル、グリセリン脂肪酸・
二塩基酸エステル等の多価アルコールと脂肪酸とのエス
テル、多価アルコールと脂肪酸及び二塩基酸とのエステ
ル等が挙げられ、これらの1種又は2種以上のものを使
用することができる。
In the present invention, together with the above alkylene oxide adduct,
Other antifogging agents that may be used in combination include sorbitan fatty acid ester, sorbitol fatty acid ester, diglycerin fatty acid ester, glycerin fatty acid ester, sorbitan fatty acid dibasic acid ester,
Sorbitol fat 1FJal/dibasic acid ester, diglycerin fatty acid/dibasic acid ester, glycerin fatty acid/
Examples include esters of polyhydric alcohols and fatty acids such as dibasic acid esters, esters of polyhydric alcohols and fatty acids and dibasic acids, and one or more of these can be used.

本発明フィルムは上記の如き配合からなる樹脂組成物を
フィルム(シート)状に成形して得られるもので、その
成形方法としては通常行われている成形方法を全て適用
することができる0例えばカレンダー成形法、Tダイ押
出法、インフレーシラン成形法等が採用できる。また本
発明フィルムの厚みは0.05〜0.2 nna程度が
好ましい。
The film of the present invention is obtained by molding a resin composition having the above-mentioned formulation into a film (sheet) shape, and any conventional molding method can be used for the molding method, such as calendaring. Molding methods, T-die extrusion methods, inflation silane molding methods, etc. can be employed. Further, the thickness of the film of the present invention is preferably about 0.05 to 0.2 nna.

本発明におけるフィルムの収縮面積残率は下記手順にて
求められる。
The residual shrinkage area of the film in the present invention is determined by the following procedure.

■抜肢片夏作虞 まず、成形後にロールに巻き取ったフィルムのうちその
最外層側のフィルム表面に、ロール巻き状態のままで下
記の標線を付記する。標線は共に長さが20CIの直線
からなる、フィルム幅方向に沿う゛横方向標線′°とフ
ィルム長さ方向に沿う“縦方向標線”との2線からなり
、その2線を中心点で直交させて描くものである。この
2線−組の標Iをフィルム幅方向に3個(即ち、フィル
ム中央部に1個、フィルムの左右端部からそれぞれ30
cm以内の2箇所に2個)付す。
■Problem of removing limbs: First, the following marked line is added to the surface of the outermost layer of the film wound into a roll after forming, while still in the rolled state. The gauge line consists of two straight lines, both of which have a length of 20 CI, the ``horizontal gauge line'' along the width direction of the film and the ``vertical gauge line'' along the film length direction, and the center is centered on these two lines. The points are drawn at right angles. Three of these two-line sets I are placed in the width direction of the film (i.e., one in the center of the film and 30 in each from the left and right ends of the film.
Attach 2 pieces at 2 locations within cm.

次に、フィルムを巻きほぐし上記2線−組の標線をそれ
ぞれ囲繞するように約25cmX25cmの大きさに裁
断し、それらを試験片とする。
Next, the film is unwound and cut into pieces of about 25 cm x 25 cm so as to surround each of the two marked lines, and these pieces are used as test pieces.

■皿定1法 試験片をオーブンにて160’CX10分間加熱させて
から室温まで冷却した後、3Miの標線における横方向
標線と縦方向標線の各々の長さを測定する。この標線長
さの実測方法は、加熱収縮により標線自体が曲線状とな
ることが多いため標線の始点から終点までの直線距離(
最短距離)を測る。
(2) Dish measurement method 1 The test piece is heated in an oven at 160'C for 10 minutes, then cooled to room temperature, and then the lengths of each of the horizontal and vertical marked lines on the 3 Mi marked line are measured. This method of actually measuring the length of the marked line is difficult because the marked line itself often becomes curved due to heat shrinkage.
(shortest distance).

最終的な測定結果(下記式中のし!、L+)は、実測し
た3組の標線における縦方向標線長さと横方向標線長さ
とを掛は合わせた値が最小値となる標線(即ち、収縮度
合いが最も大きい組の標線)の縦方向標線長さと横方向
標線長さの実測値とする。
The final measurement result (Noshi!, L+ in the formula below) is the gauge line whose minimum value is the product of the length of the vertical gauge line and the length of the horizontal gauge line in the three sets of actually measured gauge lines. (In other words, the actual measured values of the length of the vertical gauge line and the length of the horizontal gauge line of the set of gauge lines with the largest degree of contraction).

最後に測定結果を下記式に当てはめて収縮面積残率を算
出する。
Finally, the measurement results are applied to the following formula to calculate the shrinkage area remaining ratio.

収縮面積残率(%) 式中、 L、:縦及び横方向標線長さ(共に20cm)L!:加
熱処理後の縦方向標線長さ し、:加熱処理後の横方向標線長さ である。
Shrinkage area remaining ratio (%) In the formula, L: Length of vertical and horizontal gauge line (both 20 cm) L! : Length of vertical gauge line after heat treatment; : Length of gauge line in horizontal direction after heat treatment.

本発明における上記面積残率は65%以上、好ましくは
70%であり、65%未満の場合は良好な防曇持続性が
得られない等の不具合がある。
The above-mentioned area residual ratio in the present invention is 65% or more, preferably 70%, and if it is less than 65%, there are problems such as not being able to obtain good anti-fog durability.

尚、本発明では必要に応じて安定剤、紫外線吸収剤、滑
剤、充填剤、赤外線吸収剤、着色剤、光安定剤、防藻剤
、防カビ剤、エポキシ基含有化合物、アクリル系樹脂製
加工改良剤等を添加することができる。また必要に応じ
てフィルムの片面に他の合成樹脂製皮膜を付与すること
ができる。上記皮膜としてはアクリル系樹脂膜、フッ素
樹脂膜、オレフィン系樹脂膜等が挙げられ、膜の付与は
通常の膜形成方法を適用することができ、例えば塗工法
、ラミネート加工法、熔融製膜法等を採用することがで
きる。
In addition, in the present invention, stabilizers, ultraviolet absorbers, lubricants, fillers, infrared absorbers, colorants, light stabilizers, algaecides, fungicides, epoxy group-containing compounds, and acrylic resin processing are used as necessary. Modifiers and the like can be added. Further, if necessary, another synthetic resin film can be applied to one side of the film. Examples of the above-mentioned films include acrylic resin films, fluororesin films, olefin resin films, etc., and ordinary film forming methods can be applied to apply the film, such as coating methods, laminating methods, melt film forming methods, etc. etc. can be adopted.

〔実施例〕〔Example〕

以下、実施例を挙げて本発明を更に詳細に説明する。 Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例1〜4、比較例1〜6 第1表に示す配合からなる樹脂組成物A−Dを適宜選択
して用い、溶融させた後180℃のカレンダーロールに
供給し、第2表に示す成形条件a〜Cのいずれかの成形
条件に従ってカレンダー成形し、冷却ロールにて室温ま
で冷却してから紙管に巻き取り、厚さ0.1 mのフィ
ルムを得た。上記各フィルムは第3表に示す如き樹脂組
成物と成形条件の組合わせで得られたものである。
Examples 1 to 4, Comparative Examples 1 to 6 Resin compositions A to D consisting of the formulations shown in Table 1 were appropriately selected and used, and after being melted, they were supplied to a calender roll at 180 ° C. and the compositions shown in Table 2 were used. Calendar molding was carried out according to any one of molding conditions a to c, cooled to room temperature with a cooling roll, and then wound around a paper tube to obtain a film with a thickness of 0.1 m. Each of the above films was obtained using the combinations of resin compositions and molding conditions shown in Table 3.

得られた各フィルムの160”cS 10分加熱処理後
の収縮面積残率を算出すると共に、各フィルムの低温防
曇性及び防曇持続性について下記の方法により禰べ、そ
れらの結果を第3表に示す。
The shrinkage area remaining after heat treatment at 160"cS for 10 minutes was calculated for each of the obtained films, and the low-temperature antifogging properties and antifogging durability of each film were determined using the following method. Shown in the table.

「低温防曇性1 各フィルムを間口3.5m、長さ20mの車検パイプハ
ウスに展張しく9月)、同年12月にフィルムの表面状
態などを観察し、以下の基準にて評価した。
"Low-temperature anti-fogging properties 1 Each film was spread out in a vehicle inspection pipe house with a width of 3.5 m and a length of 20 m (September), and the surface condition of the film was observed in December of the same year, and evaluated based on the following criteria.

○=水滴の流れスジがなく、水滴の流れ方も良好である
○=There are no streaks in the flow of water droplets, and the flow of water droplets is also good.

ロ:流れスジが若干認められる。B: Some streaks are observed.

Δ:t!Lれスジが多数認められ、スジ跡がすっきりし
ていない。
Δ:t! Many L streaks were observed, and the streak marks were not clean.

×:流れスジが多数比められ、水滴が直接地面に落下し
た所もある。
×: There are many flow lines and there are places where water droplets directly fall to the ground.

r防曇持続性1 上記低温防曇性の観察に使用したハウスにて、5力月後
(翌年2月)、8力月後(5月)、12力月後(9月)
、14力月後(11月)におけるフィルムの表面状態を
観察し、以下の基準にて評価した。
r Anti-fog durability 1 In the greenhouse used for the above low-temperature anti-fog observation, after 5 months (February of the following year), 8 months (May), and 12 months (September)
After 14 months (November), the surface condition of the film was observed and evaluated based on the following criteria.

○:水滴付着がなく、全面良好な流れ。○: Good flow throughout the entire surface with no water droplets attached.

ロ:水滴付着が若干認められる。B: Some water droplets are observed.

Δ:水滴付着が多数比められる。Δ: A large number of water droplets are observed.

X:全面に水滴が付着している。X: Water droplets are attached to the entire surface.

第 表 第 表 〔発明の効果〕 以上説明したように、本発明農業用フィルムは前記の如
き配合組成からなり且つ160℃における収縮面積残率
が65%以上のものであるため、低温防曇性や防霧性に
優れているばかりではなく、防曇持続性にも優れたもの
である。従って、本発明品によれば長期間にわたって農
作物育成時の水滴発生による各種障害等を防止すること
が可能となり、実益大である。
Table 1 [Effects of the Invention] As explained above, the agricultural film of the present invention has the above-mentioned composition and has a shrinkage area retention rate of 65% or more at 160°C, so it has low-temperature antifogging properties. Not only does it have excellent anti-fog properties, but it also has excellent anti-fog durability. Therefore, the product of the present invention makes it possible to prevent various problems caused by water droplets during crop cultivation over a long period of time, which is of great practical benefit.

Claims (1)

【特許請求の範囲】[Claims] 塩化ビニル系樹脂100重量部に対して、可塑剤を40
〜60重量部、含フッ素化合物を0.01〜1.0重量
部、ソルビタンモノ(ジ)ステアレートのアルキレンオ
キサイド付加物及び/又はソルビタンモノ(ジ)パルミ
テートのアルキレンオキサイド付加物を0.2〜3.0
重量部含有してなる塩化ビニル系樹脂フィルムであって
、且つ該フィルムの160℃における収縮面積残率が6
5%以上であることを特徴とする農業用塩化ビニル系樹
脂フィルム。
40 parts of plasticizer per 100 parts by weight of vinyl chloride resin
~60 parts by weight, 0.01 to 1.0 parts by weight of a fluorine-containing compound, and 0.2 to 0.2 parts of an alkylene oxide adduct of sorbitan mono(di)stearate and/or an alkylene oxide adduct of sorbitan mono(di)palmitate. 3.0
A vinyl chloride resin film containing part by weight, and the shrinkage area residual ratio at 160°C of the film is 6.
An agricultural vinyl chloride resin film characterized by having a polyvinyl chloride content of 5% or more.
JP1118368A 1989-05-11 1989-05-11 Agricultural vinyl chloride resin film Expired - Lifetime JP2626818B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1118368A JP2626818B2 (en) 1989-05-11 1989-05-11 Agricultural vinyl chloride resin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1118368A JP2626818B2 (en) 1989-05-11 1989-05-11 Agricultural vinyl chloride resin film

Publications (2)

Publication Number Publication Date
JPH02296849A true JPH02296849A (en) 1990-12-07
JP2626818B2 JP2626818B2 (en) 1997-07-02

Family

ID=14734975

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1118368A Expired - Lifetime JP2626818B2 (en) 1989-05-11 1989-05-11 Agricultural vinyl chloride resin film

Country Status (1)

Country Link
JP (1) JP2626818B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030093013A (en) * 2002-06-01 2003-12-06 (주)한교 Low temperature dripped agricultural synthetic resin film
JP2007254584A (en) * 2006-03-23 2007-10-04 Kao Corp Polyoxyethylene sorbitan fatty acid ester composition

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5876030A (en) * 1981-10-30 1983-05-09 アキレス株式会社 Covering material for culturing cucumber, watermelon, melon or strawberry
JPS6210126A (en) * 1985-07-05 1987-01-19 Unitika Ltd Microspherical cured melamine resin particle and its production
JPS6274626A (en) * 1985-09-30 1987-04-06 Mitsubishi Kasei Vinyl Co Soft polyvinyl chloride-based resin film for agricultral use
JPS62164764A (en) * 1986-01-16 1987-07-21 Mitsubishi Kasei Vinyl Co Agricultural synthetic resin covering material
JPS62201761A (en) * 1986-02-25 1987-09-05 Achilles Corp Roll-like scroll of agricultural polyvinyl chloride film
JPS63182363A (en) * 1987-01-23 1988-07-27 Toho Chem Ind Co Ltd Production of agricultural film having excellent fog-proofness and anti-clouding property

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5876030A (en) * 1981-10-30 1983-05-09 アキレス株式会社 Covering material for culturing cucumber, watermelon, melon or strawberry
JPS6210126A (en) * 1985-07-05 1987-01-19 Unitika Ltd Microspherical cured melamine resin particle and its production
JPS6274626A (en) * 1985-09-30 1987-04-06 Mitsubishi Kasei Vinyl Co Soft polyvinyl chloride-based resin film for agricultral use
JPS62164764A (en) * 1986-01-16 1987-07-21 Mitsubishi Kasei Vinyl Co Agricultural synthetic resin covering material
JPS62201761A (en) * 1986-02-25 1987-09-05 Achilles Corp Roll-like scroll of agricultural polyvinyl chloride film
JPS63182363A (en) * 1987-01-23 1988-07-27 Toho Chem Ind Co Ltd Production of agricultural film having excellent fog-proofness and anti-clouding property

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030093013A (en) * 2002-06-01 2003-12-06 (주)한교 Low temperature dripped agricultural synthetic resin film
JP2007254584A (en) * 2006-03-23 2007-10-04 Kao Corp Polyoxyethylene sorbitan fatty acid ester composition

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