JP5166377B2 - 農業用フィルム - Google Patents
農業用フィルム Download PDFInfo
- Publication number
- JP5166377B2 JP5166377B2 JP2009206077A JP2009206077A JP5166377B2 JP 5166377 B2 JP5166377 B2 JP 5166377B2 JP 2009206077 A JP2009206077 A JP 2009206077A JP 2009206077 A JP2009206077 A JP 2009206077A JP 5166377 B2 JP5166377 B2 JP 5166377B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- acid
- agricultural film
- layer
- agricultural
- 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.)
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- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 28
- 238000002834 transmittance Methods 0.000 claims description 22
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 9
- 239000012964 benzotriazole Substances 0.000 claims description 9
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
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- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 6
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- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
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- 125000005907 alkyl ester group Chemical group 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
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- 229910052791 calcium Inorganic materials 0.000 description 3
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000003898 horticulture Methods 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
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- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
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- 239000011787 zinc oxide Substances 0.000 description 3
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- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- QHZLMUACJMDIAE-UHFFFAOYSA-N 1-monopalmitoylglycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- GAMRDXGPACRSMU-UHFFFAOYSA-N 1-tridecoxycarbonylbutane-1,1,2-tricarboxylic acid Chemical compound C(CCCCCCCCCCCC)OC(=O)C(C(CC)C(=O)O)(C(=O)O)C(=O)O GAMRDXGPACRSMU-UHFFFAOYSA-N 0.000 description 2
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
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- ZSSVCEUEVMALRD-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)=N1 ZSSVCEUEVMALRD-UHFFFAOYSA-N 0.000 description 2
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical group OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 2
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- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
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- WOGWRXSITPCETK-UHFFFAOYSA-N [3-(2,3-dihydroxypropoxy)-2-hydroxypropyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)CO WOGWRXSITPCETK-UHFFFAOYSA-N 0.000 description 2
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
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- 125000004429 atom Chemical group 0.000 description 2
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- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 2
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- ZCGNNESZWJPBLW-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite 2-[2-(2-hydroxyphenyl)propan-2-yl]-3,4,5,6-tetra(tridecyl)phenol Chemical compound OP(O)OP(O)O.CCCCCCCCCCCCCC1=C(CCCCCCCCCCCCC)C(CCCCCCCCCCCCC)=C(O)C(C(C)(C)C=2C(=CC=CC=2)O)=C1CCCCCCCCCCCCC ZCGNNESZWJPBLW-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
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- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
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- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
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Images
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
- Y02A40/25—Greenhouse technology, e.g. cooling systems therefor
Landscapes
- Greenhouses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Protection Of Plants (AREA)
Description
本発明における農業用フィルムとは公知の合成樹脂を基材樹脂として使用した農業用フィルムであり、特にポリオレフィン系樹脂を用いた多層フィルムで好適に効果を発揮する。本発明に係るポリオレフィン系農業用フィルムとは、少なくとも外層、中間層、内層を有する3層以上の積層構造を有するフィルムである。ここで、外層とは、ハウスなどに展張した際に外側となる層をいい、内層とは、ハウス展張時に内側となる層をいい、中間層とは、その外層と内層に挟まれた層をいう。以下、外層と内層を合わせて表面層と称する場合もある。また、本発明の効果を損なわない範囲で、内層と中間層の間、外層と中間層の間に、更に樹脂層を積層したり、外層や中間層、内層など自体を2層で構成して、4層以上の多層フィルムとする態様も、本願発明の範囲に含まれる。その場合の中間層は、外層と内層以外(表面層以外)の層ということになる。
本願発明の農業用ポリオレフィン系多層フィルムには、ポリオレフィン系樹脂、塩化ビニル系樹脂、ポリエチレンテレフタレート系樹脂等、従来より農業用フィルムの樹脂として用いられている樹脂を使用することができるが、特にポリオレフィン系樹脂において本発明の効果が有効に発揮される。
ポリオレフィン系樹脂としては、α−オレフィン系の単独重合体、α−オレフィンを主成分とする異種単量体との共重合体、α−オレフィンと共役ジエンまたは非共役ジエン等の多不飽和化合物、アクリル酸、メタクリル酸、酢酸ビニル等との共重合体などがあげられ、例えば高密度、低密度または直鎖状低密度ポリエチレン、ポリプロピレン、エチレン−プロピレン共重合体、エチレン−ブテン共重合体、エチレン−4−メチル−1−ペンテン共重合体、エチレン−酢酸ビニル共重合体、エチレン−アクリル酸共重合体等が挙げられる。これらのうち、密度が0.890〜0.935の低密度ポリエチレンやエチレン−α−オレフィン共重合体および酢酸ビニル含有量が30重量%以下のエチレン−酢酸ビニル共重合体が、透明性や耐候性および価格の点から農業用フィルムとして好ましい。
また、本発明において、ポリオレフィン系樹脂の少なくとも一成分としてメタロセン触媒で共重合して得られるエチレン−α−オレフィン共重合樹脂を使用することができる。
JIS−K7210により測定されたMFRが0.01〜10g/10分、好ましくは0.1〜5g/10分の値を示すものである。該MFRがこの範囲より大きいと成形時にフィルムが蛇行し安定しない。また、該MFRがこの範囲より小さすぎると成形時の樹脂圧力が増大し、成形機に負荷がかかるため、生産量を減少させて圧力の増大を抑制しなければならず、実用性に乏しい。
JIS−K7112により測定された密度が0.880〜0.930g/cm3、好ましくは0.880〜0.920g/cm3の値を示すものである。該密度がこの範囲より大きいと透明性が悪化する。また、密度がこの範囲より小さいと、フィルム表面のべたつきによりブロッキングが生じ実用性に乏しくなる。
ゲルパーミュレーションクロマトグラフィー(GPC)によって求められる分子量分布(重量平均分子量/数平均分子量)は1.5〜3.5、好ましくは1.5〜3.0の値を示すものである。該分子量分布がこの範囲より大きいと機械的強度が低下し好ましくない。該分子量分布がこの範囲より小さいと成形時にフィルムが蛇行し安定しない。
特に、下記一般式(1)記載のベンゾトリアゾール型紫外線吸収剤(R1、R2は、同じでも異なってもよく、各々独立して、炭素数が1以上の直鎖若しくは分岐状の置換基)を用いることにより良好な紫外線吸収能をフィルムに対して付与する事ができる。
ここで、Y及びZはY=Zであっても、異なっていてもよい。また、特に好ましい態様としては、Y=Z=0である場合が挙げられる。
本発明における防曇塗膜としては既に公知の農業用フィルムに用いることができる防曇塗膜を適応することが出来る。好ましくは無機コロイド物質と親水性有機化合物を主成分とした防曇塗膜や無機コロイド物質とアクリル系樹脂を主成分とする防曇塗膜を用いることができる。
本発明における防塵性塗膜としては既に公知の農業用フィルムに用いることができる防塵性塗膜を適応することが出来る。好ましくはアクリル系樹脂を主成分とした防塵性塗膜やアクリル系樹脂及びエチレン−アクリル共重合体を主成分とする防塵性塗膜を用いることができる。防塵性塗膜を塗工する場合には基材に対して、防曇性塗膜形成時と同様のコロナ処理等の前処理をすることができる。
3層インフレーション成形装置として3層ダイに100mmφ((株)プラ工研製)を用い、押出機はチューブ外内層を30mmφ((株)プラ技研製)2台、中間層を40mmφ((株)プラ技研製)として、外内層押出し機温度180℃、中間層押し出し機温度170℃、ダイス温度180〜190℃、ブロー比2.0〜3.0、引取り速度3〜7m/分、厚さ0.15及び0.30mmにて表−1〜表−2に示した成分からなる3層の積層フィルムを得た。なお、これらのフィルムは、ハウス展張時にチューブの端部を切り開いて使用するため、展開した際に製膜時のチューブ外層が展張時にはハウスの内層(内面)となる。
HP−LDPE:高圧ラジカル法触媒で製造した分岐状ポリエチレン(MFR:1.1g/10分、密度0.920)日本ポリケム製ノバテックLD「YF30」
メタロセンPE:メタロセン触媒で製造したエチレン・αオレフィン共重合体(MFR:2g/10分、密度0.907)日本ポリケム製カーネル「KF270」
EVA(1) :エチレン・酢酸ビニル共重合体(酢酸ビニル含有量15重量%、MFR2g/10分)
キマソーブ944:チバ・スペシャルティ・ケミカルズ社製光安定剤
エチレン・環状アミノビニル共重合体:日本ポリケム(株)製「ノバテックLD・XJ100H」MFR=3g/10分(190℃、JIS−K6760) 密度=0.931g/cm3(JIS−K6760)
ベンゾトリアゾール型紫外線吸収剤A:シプロ化成株式会社製SB−7021MBCL
2−[5−クロロ(2H)−ベンゾトリアゾール−2−イル]−4−メトキシ−6−(tert−ブチル)フェノール
2−[5−クロロ(2H)−ベンゾトリアゾール−2−イル]−4−メチル−6−(tert−ブチル)フェノール
2,4−ジ−tert−ブチル−6−(5−クロロベンゾトリアゾール−2−イル)フェノール
2−[4,6−ビス(2,4−ジメチルフェニル)−1,3,5−トリアジン−2−イル]−5−(オクチロキシ)フェノール
得られたチューブ状フィルムの外層表面を、放電電圧120V、放電電流4.7A、ラインスピード10m/minでコロナ放電処理を行い、JIS−K6768による「濡れ指数」を測定し、その値を確認した。
表1に示した主成分(シリカゾル及び/又はアルミナゾル)と熱可塑性樹脂と架橋剤及び液状分散媒とを配合して防曇剤組成物を得た。
防曇剤組成物配合は以下の配合とした。
無機質コロイドゾル(コロイダルシリカ) 4.0
熱可塑性樹脂(サンモールSW−131) 3.0
架橋剤(T.A.Z.M) 0.1
分散媒(水/エタノール=3/1) 93
(注)無機質コロイドゾルの配合量は、無機質粒子量で示し熱可塑性樹脂の配合量は重合体固形分量で示す。
コロイダルシリカ:日産化学社製スノーテックス30、平均粒子径15nm
サンモールSW−131:三洋化成社製アクリルエマルジョン
T.A.Z.M:相互薬工社製アジリジン系化合物
(2)で表面処理した基体フィルムの表面に、上記の防曇剤組成物を#5バーコーターを用いて各々塗布した。塗布したフィルムを80℃のオーブン中に1分間保持して、液状分散媒を揮発させ防曇性塗膜を形成した。得られた各フィルムの塗膜の厚みは約1μmであった。
3層インフレーション成形により得られた積層フィルム(ハウス内層側表面に防曇性塗膜を形成(塗工)後)を分光光度計(日立製作所製、U3500型)により測定し、各波長におけるその値を示した。
(1)の方法で測定した1nmごとの透過率を平均して算出した。
(2)の方法で算出した透過率を下記の基準で分類した。
○・・300〜420nmにおける透過率平均値(%)が2%未満
×・・300〜420nmにおける透過率平均値(%)が2%以上
3層インフレーション成形により得られた積層フィルム(ハウス内層側表面に防曇性塗膜を形成(塗工)後)について、フィルム製膜直後とフィルム製膜後3ヶ月後の555nmにおける直進光線透過率を分光光度計(日立製作所製、U3500型)により測定し、その差異を下記の基準で分類した。
○・・フィルム製膜直後とフィルム製膜後3ヶ月後の555nmにおける直進光線透過率(%)の差異が5%以内
×・・フィルム製膜直後とフィルム製膜後3ヶ月後の555nmにおける直進光線透過率(%)の差異が5%より大
各フィルム展張下条件におけるオンシツコナジラミの行動抑制効果(忌避効果)を確認する為に、表1に示した方法で作成&入手した各フィルムを用いて、図3に示したチャンバーを使用した試験を実施した。
約20頭のオンシツコナジラミを図3記載の試験箱(チャンバー)の中央に置き、各試験区に移動したオンシツコナジラミの頭数の多寡により各試験区の相対的な忌避効果の優劣を表3に示した。オンシツコナジラミが忌避した方が試験区内に留まる頭数が少ないと考えられる為、どちらを忌避したかで判定を行った。
二つの試験区の内、頭数が多かったもの(忌避効果が低い) :劣×
二つの試験区の内、頭数が少なかったもの(忌避効果が高い):優○
補足:
・本試験は、実験は反復試験として別のチャンバーを使用した再実験を行ったが、結果は同様であった(二つのチャンバーを用いて反復試験を実施し、再現性を確認した)。
従来からある380nm以下UVカットタイプのUVカットフィルムは、オンシツコナジラミの行動抑制性能(忌避効果)において、十分な性能を有しているとは言えず、420nm以下UVカットタイプと比較すると、その性能が劣っていることが判る。
本発明の農業用フィルムは、紫外線遮蔽性(吸収波長域が広い)に優れ、ハウス内環境において害虫防除性及び内張資材の劣化防止性等にも優れ、耐ブリードアウト性にも優れることから農業用フィルムとして好適に用いることができる。本発明のフィルムは、透明でも、梨地でも、半梨地でもよく、ハウス、トンネル、マルチング用、袋掛用等の農業用ポリオレフィン系フィルム(いわゆる農ポリ等)の用途に好適に使用することができる。
Claims (7)
- ベンゾトリアゾール型紫外線吸収剤の吸収ピーク波長のうち少なくとも一つが360nm以上であることを特徴とする請求項1に記載の農業用フィルム。
- 300nm〜420nmの紫外線が、実質的に完全に遮蔽されてなることを特徴とする請求項1乃至3のいずれか一項に記載の農業用フィルム(実質的に完全に遮蔽:300〜420nmにおいて1nmごとに測定した全光線透過率の平均値が2%未満)。
- 前記式(2)におけるR3がヘキシル基であり、R4〜R7が水素原子である、請求項5に記載の農業用フィルム。
- 前記式(2)におけるR3がオクチル基であり、R4〜R7がメチル基である、請求項5に記載の農業用フィルム。
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