JPS63286343A - Laminate film for agriculture - Google Patents
Laminate film for agricultureInfo
- Publication number
- JPS63286343A JPS63286343A JP62120962A JP12096287A JPS63286343A JP S63286343 A JPS63286343 A JP S63286343A JP 62120962 A JP62120962 A JP 62120962A JP 12096287 A JP12096287 A JP 12096287A JP S63286343 A JPS63286343 A JP S63286343A
- Authority
- JP
- Japan
- Prior art keywords
- film
- less
- olefin resin
- ethylene
- olefin
- 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
Links
- 239000005001 laminate film Substances 0.000 title 1
- 229920005989 resin Polymers 0.000 claims abstract description 49
- 239000011347 resin Substances 0.000 claims abstract description 49
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 43
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 12
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 12
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 8
- 150000001450 anions Chemical class 0.000 claims abstract description 7
- 239000004711 α-olefin Substances 0.000 claims abstract description 4
- -1 hydrotalcite compound Chemical class 0.000 claims description 31
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 25
- 229960001545 hydrotalcite Drugs 0.000 claims description 25
- 239000000155 melt Substances 0.000 claims description 13
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 13
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 10
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 239000011163 secondary particle Substances 0.000 claims description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- 229920000554 ionomer Polymers 0.000 claims description 3
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 2
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 2
- 229920003145 methacrylic acid copolymer Polymers 0.000 claims description 2
- 229940117841 methacrylic acid copolymer Drugs 0.000 claims description 2
- 229910001415 sodium ion Inorganic materials 0.000 claims description 2
- 238000005299 abrasion Methods 0.000 abstract description 11
- 229920001577 copolymer Polymers 0.000 abstract description 6
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 239000000843 powder Substances 0.000 abstract description 3
- 238000009413 insulation Methods 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 115
- 239000010410 layer Substances 0.000 description 45
- 239000000945 filler Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- 238000002834 transmittance Methods 0.000 description 15
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 11
- 229920000915 polyvinyl chloride Polymers 0.000 description 11
- 239000004800 polyvinyl chloride Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical class [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 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007888 film coating Substances 0.000 description 3
- 238000009501 film coating Methods 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 229920012753 Ethylene Ionomers Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000012756 surface treatment agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- KAKVFSYQVNHFBS-UHFFFAOYSA-N (5-hydroxycyclopenten-1-yl)-phenylmethanone Chemical compound OC1CCC=C1C(=O)C1=CC=CC=C1 KAKVFSYQVNHFBS-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- SOQQSPURSLWWMI-UHFFFAOYSA-N 1,3-thiazole-4-carbothioamide Chemical compound NC(=S)C1=CSC=N1 SOQQSPURSLWWMI-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004727 Noryl Substances 0.000 description 1
- 229920001207 Noryl Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 241001483078 Phyto Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 206010040925 Skin striae Diseases 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 208000031439 Striae Distensae Diseases 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical class O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- QDIGBJJRWUZARS-UHFFFAOYSA-M potassium;decanoate Chemical compound [K+].CCCCCCCCCC([O-])=O QDIGBJJRWUZARS-UHFFFAOYSA-M 0.000 description 1
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- PYJBVGYZXWPIKK-UHFFFAOYSA-M potassium;tetradecanoate Chemical compound [K+].CCCCCCCCCCCCCC([O-])=O PYJBVGYZXWPIKK-UHFFFAOYSA-M 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 229940045845 sodium myristate Drugs 0.000 description 1
- FIWQZURFGYXCEO-UHFFFAOYSA-M sodium;decanoate Chemical compound [Na+].CCCCCCCCCC([O-])=O FIWQZURFGYXCEO-UHFFFAOYSA-M 0.000 description 1
- JUQGWKYSEXPRGL-UHFFFAOYSA-M sodium;tetradecanoate Chemical compound [Na+].CCCCCCCCCCCCCC([O-])=O JUQGWKYSEXPRGL-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
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
- Protection Of Plants (AREA)
- Greenhouses (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
「産業上の利用分野」
本発明は保温性、透明性、耐摩擦強度、耐久性および防
景持続性の改良されたオレフィン系樹脂を主体とする農
業用積層フィルムに関する。Detailed Description of the Invention "Field of Industrial Application" The present invention relates to an agricultural laminated film based on an olefin resin that has improved heat retention, transparency, abrasion resistance, durability, and landscape sustainability. .
「従来の技術」
従来、農業用ハウス、トンネル7”ハウス等の温室栽培
に用いられる温室被覆資材としてはポリ塩化ビニルフィ
ルムや、ポリエチレンフィルム、エチレン−酢酸ビニル
共重合体フィルム等のポリオレフィン系樹脂フィルムが
主として使用されている。"Conventional Technology" Traditionally, greenhouse covering materials used for greenhouse cultivation such as agricultural greenhouses and tunnel 7" greenhouses have been polyolefin resin films such as polyvinyl chloride film, polyethylene film, and ethylene-vinyl acetate copolymer film. is mainly used.
これらのうちポリ塩化ビニルフィルムは保温性、透明性
、強靭性、耐久性等にすぐれているので近年までこの分
野で多用されてきた。しかしながら、ポリ塩化ビニルフ
ィルムは使用中にフィルム中に含まれる可塑剤がフィル
ム表面にブリードする影響で塵埃が付着して光線透過性
が着しく損なわれハウス内の温度上昇を妨げるという欠
点があるとともに使用後焼却処理をすると塩酸がスが発
生するため廃棄処理が難しいという問題がある。さらに
低温では柔軟性を失い、耐!I撃性が不良になるので寒
冷地での使用に耐えないという問題もある。Among these, polyvinyl chloride film has been widely used in this field until recently because it has excellent heat retention, transparency, toughness, and durability. However, during use, polyvinyl chloride film has the disadvantage that the plasticizer contained in the film bleeds onto the film surface, causing dust to adhere to it, severely impairing its light transmittance and preventing the temperature rise inside the greenhouse. When incinerated after use, hydrochloric acid gas is generated, making it difficult to dispose of. Furthermore, it loses its flexibility at low temperatures and is resistant! There is also the problem that it cannot withstand use in cold regions due to poor I impact resistance.
一方、オレフィン14第1371フイルムはフィルム中
に可塑剤を含まず、化学的構造も安定しているため、長
期の使用中にも光線透過性はほとんど変わらないし焼却
しても有害ガスの発生がない点では、ポリ塩化ビニルフ
ィルムよりすぐれているが、保温性の点でポリ塩化ビニ
ルフィルムに劣る。そのため、オレフィン系樹脂フィル
ムは、前記光線透過性が持続する長所をもちながらも従
来あま97%ウス被覆用フィルムとして利用されなかっ
た。On the other hand, Olefin 14 No. 1371 film does not contain plasticizers and has a stable chemical structure, so its light transmittance hardly changes even during long-term use, and no harmful gases are generated even when incinerated. In terms of heat retention, it is superior to polyvinyl chloride film, but it is inferior to polyvinyl chloride film in terms of heat retention. Therefore, although the olefin resin film has the advantage of long-lasting light transmittance, it has not been used as a 97% thin coating film.
またオレフィン系樹脂のうちでもエチレン−酢酸ビニル
共重合体フィルムは透明性、柔軟性、耐寒性等の利点が
認められ、近年農業用被覆資材としで注口されでいるが
保温性がポリ塩化ビニルに比べ劣るという上述した問題
点の他に摩擦強度が劣るという問題もあり具体的にはパ
イプハウスのパイプ部やマイカ−線押え部で被覆資材を
換気のため開閉する際や風にあおられた時に摩擦されフ
ィルムが破損するという問題がある。Among olefin resins, ethylene-vinyl acetate copolymer film has been recognized to have advantages such as transparency, flexibility, and cold resistance, and has recently been used as a covering material for agriculture, but polyvinyl chloride has better heat retention. In addition to the above-mentioned problem that the friction strength is inferior to that of the pipe house, there is also the problem that the friction strength is inferior. There is a problem that the film is damaged due to friction.
一般に、温室、ハウスにおける被覆用フィルムの保温性
というのは夜間におけるハウス内の温度の低下を防!ヒ
する特性であって、昼間太陽光線によってハウス内の地
中に吸収された熱が夜間には地面から輻射線となって輻
射されることにより、ハウス内の温度を高く保つのであ
るが被覆フィルムの地面からの輻射線の透過率が高いと
地面からの輻射線はハウス外に散逸しでしまってハウス
内の地温は低下し、その結果7%ウス内の温度を外気よ
り高く保つことができなくなる。従って、被覆用フィル
ムの保温性の良否は前記輻射線の吸収または反射率の如
何によるものであり、その率の高いもの程良いことにな
る。In general, the heat retention properties of covering films in greenhouses and greenhouses prevent the temperature inside the greenhouse from dropping at night! This is because the heat absorbed into the ground inside the greenhouse by sunlight during the day is radiated from the ground as radiation at night, keeping the temperature inside the greenhouse high. If the transmittance of radiation from the ground is high, the radiation from the ground will be dissipated outside the house, and the soil temperature inside the house will drop.As a result, the temperature inside the 7% greenhouse can be kept higher than the outside air. It disappears. Therefore, the quality of the heat retaining property of the coating film depends on the radiation absorption or reflection rate, and the higher the rate, the better.
オレフィン系樹脂フィルムの保温性を改良した被覆用フ
ィルムとしては特公昭47−9260号、特公昭47−
13853号、特開昭49−105843号、特開昭5
2−32938号、特開昭55−151043号、特開
昭55−151044号及び特開昭60−104141
号などの各公報に見られるようにオレフィン系樹脂に燐
酸塩化合物や酸化硅素や無水アルミノ硅酸塩や脱水カオ
リナイト、アルミニウム、シリケート、ゼオライト、ハ
イドロタルサイト類等特定のS機フィラーを添加したも
のがある。しかしこれらの方法はオレフィン系樹脂の保
温性は改良されているものの、ポリ塩化ビニルフィルム
に比べると未だ不充分である。As coating films with improved heat retention properties of olefin resin films, Japanese Patent Publication No. 47-9260 and Japanese Patent Publication No. 47-
No. 13853, JP-A-49-105843, JP-A-5
2-32938, JP 55-151043, JP 55-151044 and JP 60-104141
As can be seen in various publications such as No. 1, specific S fillers such as phosphate compounds, silicon oxide, anhydrous aluminosilicate, dehydrated kaolinite, aluminum, silicates, zeolites, and hydrotalcites are added to olefin resins. There is something. However, although these methods have improved the heat retention properties of olefin resins, they are still insufficient compared to polyvinyl chloride films.
さらに、たとえば特開昭55−151041号及び特開
昭55−151042号公報に見られるような、5in
2・T i O2、SiO□φMgO,5i02・Ca
O及びSiO□・A LO、などの複合含水デルの添加
でポリ塩化ビニル並に保温性が改良されているものであ
っても最大の問題点は無191フイラーの添加により、
通常のフィルム加工法、例えばTグイキャスト法やイン
フレーシ9ン法では溶融樹脂が延伸されながら冷却固化
するためフィルム表面が凹凸状になることである。この
ため、ノ蔦ウスのパイプ部やマイカ−線押え部での摩擦
によるフィルムの破損が起りやすくなったり、さらに重
要な問題としてフィルムの透明性特に平行光線透過性が
ポリ塩化ビニルフィルムやエチレン−酢酸ビニル共重合
体フィルムに比べると劣る、というルム屑との複数屑に
よる組合せからなるポリオレフィン系農業用フィルムも
提案されているが、無W1フィラーの屈折率と無191
フイラーを添加する樹脂の屈折率とが異なるためやはり
平行光線透過性にすぐれたフィルムを得ることはできな
かった。Furthermore, 5-in.
2・T i O2, SiO□φMgO,5i02・Ca
Even if the heat retention properties are improved to the same level as polyvinyl chloride by the addition of composite hydrous materials such as O and SiO□・A LO, the biggest problem is that the addition of non-191 fillers
In ordinary film processing methods, such as the T-guicast method and the inflatable film method, the molten resin is cooled and solidified while being stretched, resulting in an uneven film surface. For this reason, the film is more likely to be damaged due to friction at the pipe section and the mica wire holding section of the Notsutausu, and more importantly, the transparency of the film, especially the parallel light transmittance, is lower than that of polyvinyl chloride film or ethylene film. A polyolefin agricultural film made of a combination of lume and multiple scraps has been proposed, which is inferior to a vinyl acetate copolymer film, but the refractive index of the W1 filler and the 191
Since the refractive index of the resin to which the filler is added is different, it was not possible to obtain a film with excellent parallel light transmittance.
[発明が解決しようとする問題点J
本発明者らは上述のようなオレフィン系樹脂における農
業用フィルムとしての問題点を除去し、保温性、透明性
、耐摩擦性、耐久性に加えで、防曇持続性にすぐれた農
業用フィルムを安価に提供するため、鋭意研究を重ねた
結果、オレフィン系樹脂の屈折率とほぼ等しい屈折率を
有する特定のハイドロタルサイト類化合物の粉末を添加
した組成物からなるフィルムの内外面にオレフィン系樹
脂の群から選ばれる少なくとも1種の樹脂層を設けるこ
とにより従来技術に比べ極めてすぐれた平行光線透過性
、保温性、耐摩擦性、耐久性、防曇持続特性を兼ね備え
たフィルムが得られることを見いだし本発明を完成した
。[Problems to be Solved by the Invention J The present inventors have solved the above-mentioned problems of olefin resins as agricultural films, and have improved heat retention, transparency, abrasion resistance, and durability. In order to provide an agricultural film with excellent anti-fogging properties at a low price, we have conducted intensive research and developed a composition containing powder of a specific hydrotalcite compound that has a refractive index almost equal to that of olefin resins. By providing at least one resin layer selected from the group of olefin resins on the inner and outer surfaces of the film made of material, it is possible to achieve extremely superior parallel light transmittance, heat retention, abrasion resistance, durability, and anti-fog properties compared to conventional technology. The present invention was completed after discovering that a film with long-lasting properties could be obtained.
「問題点を解決するための手段」
本発明の要旨は、オレフィンP、樹脂100重量部に対
して、1〜25重量部の下記一般式%式%
ただし式中Mはアルカリ土類金属およびZnを、Xはn
価のアニオンを示す、また、及び論は下記式の条件を満
足する。"Means for Solving the Problems" The gist of the present invention is that 1 to 25 parts by weight of the following general formula %, based on olefin P and 100 parts by weight of the resin, are represented by the following general formula %, where M is an alkaline earth metal and Zn. , X is n
Indicates a valent anion, and satisfies the conditions of the following formula.
0くえ〈0.5
0 ≦ 曽 ≦ 2
で表わされる屈折率が1.47以上1.52以下の範囲
であるハイドロタルサイト類化合物を配合した組成物か
らなるフィルムの内外面にオレフィン系樹脂の群から選
ばれる少なくともIMの樹脂層が設けられている事を特
徴とする農業用積層フィルムにある。The inner and outer surfaces of a film made of a composition containing a hydrotalcite compound having a refractive index expressed by 0.5 0 ≦ ≦ 2 in the range of 1.47 to 1.52 are coated with an olefin resin. There is provided an agricultural laminated film characterized by being provided with at least an IM resin layer selected from the group consisting of:
以下に本発明をさらに詳細に説明する。The present invention will be explained in more detail below.
本発明において中間層に使用されるオレフィン系樹脂と
しては、a−オレフィンの単独重合体、a−オレフィン
を主成分とする異種単量体との共重合体であり、例えば
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及びアイオノマ
ー樹脂が挙げられる。これらのうち、密度が0.910
〜0.935g/c+sコの低密度ポリエチレンやエチ
レン−a−オレフィン共重合体および酢酸ビニル含有量
が30重1%以下のエチレン−酢酸ビニル共重合体が透
明性や耐候性さらには価格の点から農業用フィルムとし
て好ましい。In the present invention, the olefin resin used in the intermediate layer is a homopolymer of a-olefin, or a copolymer with a different monomer containing an a-olefin as a main component, such as polyethylene, polypropylene, ethylene propylene, etc. copolymers, ethylene-butene copolymers, ethylene-4-methyl-1-pentene copolymers, ethylene-vinyl acetate copolymers, ethylene-acrylic acid copolymers, and ionomer resins. Among these, the density is 0.910
Low-density polyethylene and ethylene-a-olefin copolymers with ~0.935 g/c+s and ethylene-vinyl acetate copolymers with a vinyl acetate content of 30% by weight or less are superior in terms of transparency, weather resistance, and price. It is preferable as an agricultural film.
なかでも、酢酸ビニル含有量が5重量%以上25重景%
以下のエチレン−酢酸ビニル共重合体はこれらのうちで
も特に透明性、柔軟性、耐候性等の点でより好ましい。Among them, the vinyl acetate content is 5% by weight or more and 25% by weight.
Among these, the following ethylene-vinyl acetate copolymers are particularly preferred in terms of transparency, flexibility, weather resistance, and the like.
本発明において内外層に使用されるオレフィン系樹脂も
上述した中間層に使用されるオレフィン系樹脂と同じ範
ちゅうに属するが、これらのうちでも特に耐摩擦特性の
良好な樹脂が好ましい0例えばポリエチレンの場合、密
度が0.910g/am’以上0 、’935 g/
am’以下でメルトインデックスが0.1g/10分以
上4g/10分以下のポリエチレンもしくはエチレン−
a−オレフィン共重合体が好ましい、密度が0.910
g/cm″以下では耐熱性の点で好ましくなく、密度が
0.935g/cm’以−ヒでは透明性の点で好ましく
ない。又、メルトインデックスが0,1g710分以下
では加工性の点で好ましくなく4g/10分以、ヒでは
摩擦特性や強度の点で好ましくない、これらポリエチレ
ンの中でも、特に中低圧法で製造されるエチレン−aオ
レフィン共重合体が耐熱性、耐久性の点で好ましい。In the present invention, the olefin resins used for the inner and outer layers also belong to the same category as the olefin resins used for the intermediate layer described above, but among these, resins with particularly good friction resistance are preferable. For example, polyethylene resins are preferable. If the density is 0.910 g/am' or more 0,'935 g/am'
Polyethylene or ethylene with a melt index of 0.1 g/10 minutes or more and 4 g/10 minutes or less at am' or less
A-olefin copolymer is preferred, density is 0.910
If the density is less than 0.935g/cm', it is unfavorable in terms of heat resistance, and if the density is less than 0.935g/cm', it is unfavorable in terms of transparency.In addition, if the melt index is less than 0.1g/710 minutes, it is unfavorable in terms of processability. 4 g/10 minutes or more is undesirable in terms of friction properties and strength.Among these polyethylenes, ethylene-a olefin copolymer produced by a medium-low pressure method is particularly preferred in terms of heat resistance and durability. .
また、エチレン−酢酸ビニル共重合体の場合、酢酸ビニ
ル含有量が15重置部以下、より好ましくは10重量%
以下でメルトインデックスが0.1g/10分以上4g
/10分以下、より好ましくは0.1g/10分以上1
,5.710分以下のものが好ましい、酢酸ビニル含有
量が15重置部以上では耐熱性の点で好ましくなく、メ
ルトインデックスが0.1g/10分以下では加工性の
点で4g/10分以上では摩擦特性や強度の点で好まし
くない。In the case of an ethylene-vinyl acetate copolymer, the vinyl acetate content is 15 parts by weight or less, more preferably 10% by weight.
Melt index below 0.1g/4g for 10 minutes or more
/10 minutes or less, more preferably 0.1g/10 minutes or more1
, 5.710 minutes or less is preferable. If the vinyl acetate content is 15 parts or more, it is unfavorable in terms of heat resistance, and if the melt index is 0.1 g/10 minutes or less, it is 4 g/10 minutes in terms of processability. The above is unfavorable in terms of friction characteristics and strength.
また、エチレン−アクリル酸共重合体の場合、アクリル
酸含有量30重量%以下、より好ましくは25重量%以
下のものが好ましい。In the case of an ethylene-acrylic acid copolymer, the acrylic acid content is preferably 30% by weight or less, more preferably 25% by weight or less.
本た、アイオノマー樹脂は密度が0.935g/C鋤り
以上0.9751y/em”以下、メルトインデックス
0.5g/10分以上7g/10分以下のものが好まし
く金属イオンはNa”、Zn−タイプのものが好ましい
。Preferably, the ionomer resin has a density of 0.935 g/C to 0.9751 y/em" and a melt index of 0.5 g/10 min to 7 g/10 min, with the metal ions being Na", Zn- type is preferred.
上述した樹脂群のうち特にアイオノマー樹脂、エチレン
−アクリル酸共重合体が耐摩擦特性にすぐれた本発明に
好適である。Among the resins mentioned above, ionomer resins and ethylene-acrylic acid copolymers are particularly suitable for the present invention because of their excellent friction resistance properties.
本発明にお−いて使用されるハイドロタルサイト類化合
物とは一般式
%式%
ただし式中、Mはアルカリ土類金属およVZnを示す、
Xは1価のアニオンを示す。The hydrotalcite compounds used in the present invention have the general formula %, where M represents an alkaline earth metal and VZn.
X represents a monovalent anion.
そして1、および−は下記式の条件を満足する。And 1, and - satisfy the conditions of the following formula.
O< 、 < O,S
O≦ −≦ 2
で表わされる屈折率1.47以上1.52以下の範囲で
あるハイドロタルサイ)類化合物である。It is a hydrotalcite compound having a refractive index of 1.47 or more and 1.52 or less expressed by O<, <O, SO≦−≦2.
上記式においてXで表わされる1価のアニオンの例とし
ては、Cl−1Br−1■−1NOコー、ClO4−1
SO−一、CO2−1SiO,”、HP O、”−1H
B O、”−1P 0.3−1Fe、(CN)−コー、
Fe(CN)4’−1CH,COなどの如さアニオンを
例示する事ができる。Examples of monovalent anions represented by X in the above formula include Cl-1Br-1-1NO, ClO4-1
SO-1, CO2-1SiO,”, HP O,”-1H
B O,”-1P 0.3-1Fe, (CN)-Ko,
Examples include Fe(CN)4'-1CH, CO, and other anions.
本発明の農業用積層フィルムで使用する上記第1イドロ
タルサイト類化合物は、特に限定されるものではないが
平行光線通−率、フィルム加工性、物性等を特に向上さ
せるためには平均2次粒子径5μ曽以下、BET比表面
積が30m’/g以下が好ましい。Although the first hydrotalcite compound used in the agricultural laminated film of the present invention is not particularly limited, in order to particularly improve the parallel light transmittance, film processability, physical properties, etc. It is preferable that the particle size is 5 μm or less and the BET specific surface area is 30 m′/g or less.
本発明においてハイドロタルサイト類化合物は表面処理
剤で処理して利用するのが好ましい6表面処理する事に
より、オレフィン系樹脂に対する分散性ないし親和性が
一層向上し、フィルムの加工適性、物性、さらに平行光
線透過性も向上する。In the present invention, it is preferable that the hydrotalcite compound is used after being treated with a surface treatment agent6. By surface treatment, the dispersibility or affinity for olefin resins is further improved, and the processability and physical properties of the film are improved. Parallel light transmittance is also improved.
このような表面処理剤の例としては、例えば、ラウリル
酸ソーダ、ラウリル酸カルウム、オレイン酸ソーグ、オ
レインf1!カルウム、ステアリン酸ソーダ、ステアリ
ン酸カルウム、パルミチン酸ソーグ、パルミチン酸カル
ウム、カプリン酸ソーダ、カプリン酸カルウム、ミリス
チン酸ソーダ、ミリスチン酸カルウム、リップル酸ソー
ダ、リノール酸カルウムなどのような高級脂肪酸のアル
カリ金属塩類: ラウリル酸、パルミチン酸、オレイン
酸、ステアリン酸、カプリン酸、ミリスチン酸、9ノー
ル陵などの如!1i第1i級脂肪酸類; インプロピル
トリイソステアロイルチタネート、イソプロピルトリス
(!/オクチルパイaホスフェート)チタネート、テト
ライソプロピルビス(ジオクチルホス7フイト)チタネ
ート、ビニルトリエトキシシラン、ガンマツタクリルオ
キシプロピルトリメトキシシラン、〃ンマグリシドオキ
シプaピルトリメトキシシランなどのようなカップリン
グ剤類;などを例示することがで終る。Examples of such surface treatment agents include, for example, sodium laurate, potassium laurate, sorg oleate, and olein f1! Alkali metals of higher fatty acids such as potassium, sodium stearate, potassium stearate, sorg palmitate, potassium palmitate, sodium caprate, potassium caprate, sodium myristate, potassium myristate, sodium ripple, potassium linoleate, etc. Salts: such as lauric acid, palmitic acid, oleic acid, stearic acid, capric acid, myristic acid, 9-noryl acid, etc. 1i primary fatty acids; inpropyl triisostearoyl titanate, isopropyl tris(!/octylpa phosphate) titanate, tetraisopropyl bis(dioctylphos 7 phyto) titanate, vinyltriethoxysilane, gamma tacryloxypropyltrimethoxysilane, The following are examples of coupling agents such as pyrutrimethoxysilane and the like.
これら表面処理剤による表面処理は、たとえば、温水に
ハイドロタルサイト類を懸濁した状態のところに、攪拌
下に、高級脂肪酸のアルカリ土属塩の水溶液を加える事
により、或いは、ハイドロタルサイト類粉末をヘンシェ
ルミキサー等の混合機により撹拌下、高級脂肪酸の融液
とか、カップリング剤の希釈液を滴下することにより行
うことができる。これら表面処理剤の険は適宜に選択変
更できるが、ハイドロタルサイト類化合物に対して、約
1〜約10重景%程度が適当である。Surface treatment with these surface treatment agents can be carried out, for example, by adding an aqueous solution of alkaline earth salts of higher fatty acids to a suspension of hydrotalcites in hot water, or by adding an aqueous solution of alkaline earth salts of higher fatty acids to a suspension of hydrotalcites in hot water. This can be carried out by dropping a melt of a higher fatty acid or a diluted solution of a coupling agent while stirring the powder using a mixer such as a Henschel mixer. The roughness of these surface treating agents can be selected and changed as appropriate, but is suitably about 1 to about 10 percent by weight relative to the hydrotalcite compound.
さらに本発明の主旨を損なわない限りは少量の他の金属
酸化物等の不純物を含んでもよい。Furthermore, a small amount of impurities such as other metal oxides may be included as long as the gist of the present invention is not impaired.
また、該ハイドロタルサイト類化合物の中間層となるオ
レイン系樹脂への配合割合は一般にオレイン系樹脂10
0重量゛部に対し1〜25重量部が好ましく、2〜20
重量部がより好ましい、該配合物の配合量が1重量部未
満では得られるフィルムの保温性の改良効果があまり認
められず、また配合量が25重置部を越えると得られる
フィルムの強度が低下するので好ましくない。In addition, the blending ratio of the hydrotalcite compound to the oleic resin that forms the intermediate layer is generally 10 parts of the oleic resin.
It is preferably 1 to 25 parts by weight, and 2 to 20 parts by weight relative to 0 parts by weight.
Parts by weight are more preferable. If the amount of the compound is less than 1 part by weight, the effect of improving the heat retention of the obtained film will not be very noticeable, and if the amount is more than 25 parts by weight, the strength of the obtained film will decrease. This is not preferable because it lowers the temperature.
さらに中間層には、ハイドロタルサイト類化合物の分散
をより良好にするために例えばンルビタンモノステ7レ
ートのようなソルビタン脂肪酸エステルやグリセリンモ
ノステアレートのようなグリセリン脂肪酸エステルなど
を分散剤として組成物に対して0.1〜3重量部添加し
てもよい。Furthermore, in order to improve the dispersion of the hydrotalcite compounds, the intermediate layer contains a dispersant such as sorbitan fatty acid ester such as nrubitan monostearate or glycerin fatty acid ester such as glycerin monostearate. It may be added in an amount of 0.1 to 3 parts by weight.
又、中間層、内外層ともに必要に応じて安定剤、紫外線
吸収剤、滑剤、防曇剤、その他各種添加剤を適宜配合す
るのがよい。In addition, stabilizers, ultraviolet absorbers, lubricants, antifogging agents, and other various additives may be appropriately blended into both the intermediate layer and the inner and outer layers, as required.
本発明の農業用積層フィルムを製造する際、基体オレイ
ン系樹脂にハイドロタルサイ)I化合物、更に他の樹脂
添加物を配合するには、各々必要量秤量し、リボンブレ
ングー、バンバリーミキサ−、スーパーミキサー、押出
機その他従来から知られでいる配合機、混合機を使用す
ればよい。When producing the agricultural laminated film of the present invention, in order to blend the hydrotalcide (I) compound and other resin additives into the base oleic resin, the necessary amounts of each are weighed, and the necessary amounts are weighed out using a ribbon blender, Banbury mixer, etc. A super mixer, an extruder, or any other conventionally known compounding machine or mixer may be used.
このようにして得られ総樹脂組成物をフィルム化するに
は、それ自体公知の方法、例えばイン7レーシaン加工
、カレンダー加工、Tグイ加工等の通常の成形加工方法
によればよい。The total resin composition obtained in this manner may be formed into a film by a method known per se, for example, a normal molding method such as in-7 laser processing, calendar processing, T-shaped processing, etc.
かかるハイドロタルサイト類化合物を含むオレイン系樹
脂からなるフィルムの内外面にオレイン1%樹脂の群か
ら選ばれる少なくともINの樹脂屑を設ける方法として
は、それぞれのフィルムを形成してドライブミネート、
ヒートラミネート法等により積層フィルムとする方法、
ハイドロタルサイト類化合物を含むオレイン系樹脂フィ
ルムにオレイン系樹脂の群から選ばれる少なくとも1種
の樹脂を押出しフミネートする方法、多層共押出法によ
り積層フィルムを同時に成形する方法等既存の技術を用
いればよく、特に多層共押出法により成形する方法が成
形の容易さ、得られるフィルムのMWII接着性、透明
性、コスト等の点V好ましい。A method for providing at least IN resin waste selected from the group of oleic 1% resins on the inner and outer surfaces of a film made of an oleic resin containing a hydrotalcite compound is to form each film and dry laminate,
A method of making a laminated film by heat lamination method etc.
If existing techniques are used, such as a method of extruding and laminating at least one resin selected from the group of oleic resins onto an oleic resin film containing a hydrotalcite compound, or a method of simultaneously forming a laminated film using a multilayer coextrusion method, In particular, a multilayer coextrusion method is preferred in terms of ease of molding, MWII adhesion of the resulting film, transparency, and cost.
さらに農業用の用途では広巾フィルムが好まれるので多
層インフレ加工法が望ましい、なお、内層と外層を異種
の樹脂としてもよいが押出機賛用等から考えると通常の
目的には同種の樹脂で充分である。Furthermore, since wide films are preferred for agricultural applications, multilayer inflation processing is preferable. Note that the inner and outer layers may be made of different types of resin, but considering the use of extruders, etc., the same type of resin is sufficient for normal purposes. It is.
またかかるハイドロタルサイト類化合物を含むオレイン
系樹脂からなるフィルム(中間層)と内外面に設ける樹
脂(内外層)の厚さは最終用途、目的に応じて決定され
るので一概に規定されないが、中間層は要求される保温
性のレベルや/)イドロタルサイト類化合物の樹脂への
配合割合にもよるが、通常は20μ−から200μ論程
度で充分であり、内外層は中間層の外部へイズを低下さ
せ耐摩擦性が発現される厚みでよく、通常は5μ論から
50μ輪程度で充分である。In addition, the thickness of the film (intermediate layer) made of oleic resin containing such hydrotalcite compounds and the resin provided on the inner and outer surfaces (inner and outer layers) is determined depending on the end use and purpose, so it is not absolutely specified, The intermediate layer depends on the required level of heat retention and/) the blending ratio of hydrotalcite compound to the resin, but usually 20μ to 200μ is sufficient, and the inner and outer layers are placed outside the intermediate layer. The thickness can be any thickness that reduces the noise and exhibits abrasion resistance, and usually a thickness of about 5μ to 50μ is sufficient.
本発明にかかる積層フィルムは、透明でも、梨地でも、
半梨地でもよく、その用途は農業用ハウス(温室)、ト
ンネル等の被覆用に使用できるほか、マルチング用、9
掛用等にも使用できる。The laminated film according to the present invention may be transparent or matte,
Semi-matte is also acceptable, and can be used for covering agricultural greenhouses, tunnels, etc., as well as for mulching,
It can also be used for hanging.
また、三層積層した時のフィルム厚味については強度や
コストの点で0.03〜0.3輪−の範囲のものが好ま
しく、なかでも0.05〜0.2論−のものが特に好ま
しい。Regarding the thickness of the film when three layers are laminated, it is preferable to have a thickness in the range of 0.03 to 0.3 in terms of strength and cost, and in particular, a thickness in the range of 0.05 to 0.2. preferable.
「作用」及び[効果]
本発明の農業用積層フィルムは以下のような作用及び効
果を奏する。"Function" and [Effect] The agricultural laminated film of the present invention has the following functions and effects.
本発明の農業用積層フィルムは中間層に無機フィラーと
してハイドロタルサイトを含有するが、該ハイドロタル
サイトはオレフィン系樹脂とほぼ同様の屈折率を有する
ため、オレフィンP、tH1fff/フィラー界面での
光の散乱を生起することなく、内部ヘイズを低下させる
ことがない、さらに内外面にフィラーを含まない樹脂屑
を設けたことによりフィルム加工時に生成するフィラー
に起因する表面凹凸が着しく改良され結果として外部へ
イスも着しく低下するため、平行光線透過率の非常にす
ぐれた透明フィルムが得られる。その上、従来のポリオ
レフィンフィルムの欠点であった保温性は大巾に改良さ
れポリ塩化ビニルフィルムに比肩しうる程度にまで高め
られる。The agricultural laminated film of the present invention contains hydrotalcite as an inorganic filler in the intermediate layer, but since the hydrotalcite has almost the same refractive index as the olefin resin, light at the olefin P, tH1fff/filler interface The film does not cause scattering or reduce internal haze, and by providing filler-free resin waste on the inner and outer surfaces, the surface irregularities caused by filler generated during film processing are significantly improved. Since the external heat is also significantly reduced, a transparent film with very good parallel light transmittance can be obtained. Furthermore, the heat retention properties, which were a drawback of conventional polyolefin films, have been greatly improved to a level comparable to that of polyvinyl chloride films.
また本発明の農業用積層フィルムは、内外面に耐摩擦特
性にすぐれたフィラーを含まない樹脂屑を設けたことに
より、得られるフィルムの耐摩擦特性力f#L<良好に
なり、強靭性を有するものとなり、またフィルム加工時
に生成する表面凹凸が着しく改良され結果として塵埃や
汚染物質のフィルム表面への蓄積が着しく抑制されるた
め、これらによる蓄熱劣化等が着しく改良され耐久性が
大巾に向上する。In addition, the laminated agricultural film of the present invention has filler-free resin waste with excellent friction resistance on the inner and outer surfaces, so that the friction resistance of the film obtained is f#L<good, and the toughness is improved. In addition, the surface irregularities generated during film processing are improved, and as a result, the accumulation of dust and contaminants on the film surface is suppressed, so the heat accumulation deterioration caused by these is improved and the durability is improved. Greatly improved.
次に本発明の農業用積層フィルムはハイドロタルサイト
類化合物が有する吸着性能により、加工時にいったん吸
着した防曇剤のよ)な界面活性剤を徐々にブリードアウ
トするため、長期にわたるフィルムの防曇持続性を有す
る。Next, the agricultural laminated film of the present invention gradually bleeds out surfactants (such as antifogging agents) that have been adsorbed during processing due to the adsorption ability of hydrotalcite compounds, so that the film can be prevented from fogging over a long period of time. It has sustainability.
なお、本発明における好ましい屈折率を有するハイドロ
タルサイ)類化合物は公知の製法により製造されるもの
であり、オレフィン系樹脂への添加も従来の農業用フィ
ルムを131する際に用いられる一般の添加剤と格別変
わりなく、−緒に添加しうるので従来技術の製造工程が
その*ま使用でき、フィルム化も一般に容易であり、結
果として本発明は極めて優れたオレフィン系の農業用積
層フィルムを提供するものである。In addition, the hydrotalcium compound having a preferable refractive index in the present invention is produced by a known manufacturing method, and the addition to the olefin resin is a general addition used when making conventional agricultural films. The present invention provides an extremely superior olefin-based agricultural laminated film, as it is no different from other additives and can be added at the same time, so the manufacturing process of the prior art can be used, and it is generally easy to form a film. It is something to do.
更に、本発明の農業用積層フィルムはオレフィン系樹脂
を主体としでいるため、本質的に焼却処理が容易であり
、焼却時に格別の有害物を発生するという問題がない。Furthermore, since the agricultural laminated film of the present invention is mainly composed of olefin resin, it is essentially easy to incinerate, and there is no problem of generating particularly harmful substances when incinerated.
[実施例1
次に実施例をあげて本発明を説明するが、これら実施例
は単に例示的なものであって、これらに限定されるもの
ではない。[Example 1] Next, the present invention will be explained with reference to Examples, but these Examples are merely illustrative and are not limited thereto.
実施N1
酢酸ビニル含有量が15重量%のエチレン−酢酸ビニル
共重合体(MI=1.5g/10分、屈折率=1.49
5)と、予めステアリン酸ソーダで表面処理をした化学
組成Mga、y Al。、!(OH)2(Co3)。、
1.・0,55H20を有する平均2次粒子径0.3μ
m、BET比表面積12−2 / gのハイドロタルサ
イト類化合物(屈折率=1.50)5重量部と防曇剤及
び分散剤としてグリ七′リンモノステアレート0.5重
量部、ポリグリセリンステアレー第1.0重策部、耐候
助剤として2−ヒドロキシ−4−オクトキシベンゾ7ヱ
ノン0.2重量部を添加し、21パンパQ + =キサ
ーで樹脂温130℃〜150℃で5分間混練り後、押出
機に上り造粒ベレットを製造した。Implementation N1 Ethylene-vinyl acetate copolymer with vinyl acetate content of 15% by weight (MI = 1.5 g/10 min, refractive index = 1.49
5) and a chemical composition Mga,yAl whose surface was previously treated with sodium stearate. ,! (OH)2(Co3). ,
1.・Average secondary particle size 0.3μ with 0.55H20
m, 5 parts by weight of a hydrotalcite compound (refractive index = 1.50) with a BET specific surface area of 12-2/g, 0.5 parts by weight of glyc7'monostearate as an antifogging agent and a dispersant, and polyglycerin. Stearley No. 1.0 weight section, 0.2 parts by weight of 2-hydroxy-4-octoxybenzo7enone was added as a weathering aid, and 21 pampa Q + = 5 at a resin temperature of 130 to 150 °C with a kisser. After kneading for a minute, the mixture was transferred to an extruder to produce granulated pellets.
以上前記混合物をフィラー混合樹脂と呼よことにする。The above mixture will be referred to as filler mixed resin.
二種三層インフレーシ1ン成形法により中間層には上記
フィラー混合樹脂を供給し、内層と外層には低圧法低密
度ポリエチレン樹脂(密度=0.924、MI=2g7
10分)を供給し、各層の厚みが内層13μ−1中WA
層50μ−1外層13p論で構成される三層サントイ;
チ構造の透明フィルムを得た。The above-mentioned filler mixed resin is supplied to the middle layer by a two-type, three-layer inflation molding method, and the inner and outer layers are made of low-pressure low-density polyethylene resin (density = 0.924, MI = 2g7
10 minutes), and the thickness of each layer was 13μ-1 inside WA.
Three-layer Santoi composed of 50μ-1 outer layer and 13p layer;
A transparent film with a structure was obtained.
なお内外層にも中間層同様の防曇剤および耐候助痢処方
を施した。The inner and outer layers were also treated with the same anti-fogging agent and anti-weather and diarrhea formulation as the middle layer.
得られたフィルムの保温性、全光線透過率、平行光線透
過率、耐摩擦性、耐久性、防曇持続性を測定した結果を
まとめて#12表に示した。The results of measuring the heat retention, total light transmittance, parallel light transmittance, abrasion resistance, durability, and antifogging durability of the obtained film are summarized in Table #12.
実施例2
実施例1において中間層に用いたハイドロタルサイト類
化合物の代りに同じ化学組成の平均2次較子径10μ輪
、BET比表面積が50輸”/gのハイドロタルサイト
類化合物に代えた以外は実施例1をくり返し透明フィル
ムを得た。Example 2 The hydrotalcite compound used in the intermediate layer in Example 1 was replaced with a hydrotalcite compound having the same chemical composition, average secondary particle diameter of 10 μ, and BET specific surface area of 50 cm/g. Example 1 was repeated except that a transparent film was obtained.
実施例3
実施例1においで内外層に用いた低圧法低密度ポリエチ
レン樹脂の代りに、三井ポリケミカル社製商品名ハイミ
ラン1652(密度o、94g/cmり、メルトインデ
ックス5.Og/10分、エチレン−メタクリル酸共重
合体のZnイオンタイプ)に代えた以外は実施例1を繰
り返し透明フィルムを得た。Example 3 Instead of the low-pressure low-density polyethylene resin used for the inner and outer layers in Example 1, Hymilan 1652 (trade name, manufactured by Mitsui Polychemical Co., Ltd.) (density: 94 g/cm, melt index: 5.0 g/10 minutes, A transparent film was obtained by repeating Example 1 except that Zn ion type (ethylene-methacrylic acid copolymer) was used instead.
実施例4
実施例1において内外層に用いた低圧法低密度ポリエチ
レン樹脂の代りにエチレン−酢酸ビニル共重合体く酢酸
ビニル含有Ik5重量%、密度0.92g/cmコ、メ
ルトインデックス2 [1/ 10分)に代えた以外は
実施例1を繰り返し透明フィルムを得た。Example 4 Instead of the low-pressure low-density polyethylene resin used for the inner and outer layers in Example 1, an ethylene-vinyl acetate copolymer containing vinyl acetate with an Ik of 5% by weight, a density of 0.92 g/cm, and a melt index of 2 [1/ A transparent film was obtained by repeating Example 1 except that the time was changed to 10 minutes).
実施例5
実施例1におい′て内外層に用いた低圧法低密度ポリエ
チレン樹脂の代りに高圧法低密度ポリエチレン(密度0
、925 g/ Cm”、メルトインデックス2g/
10分)に代えた以外は実施例1を繰り返し透明フィル
ムを得た。Example 5 In place of the low-pressure low-density polyethylene resin used for the inner and outer layers in Example 1, high-pressure low-density polyethylene (density 0
, 925 g/Cm”, melt index 2g/
A transparent film was obtained by repeating Example 1 except that the time was changed to 10 minutes).
実施例6
実施例1において、中間層に用いたフィラー混谷樹脂の
ベースに用いたエチレン−酢酸ビニル共重合体の代りに
、高圧法低密度ポリエチレン(L?度0.925g/C
m’、メルトインデックス2g/10分)を用い、内外
層に用いた低圧法低密度ポリエチレンの代りに、中間層
と同じ高圧法低密度ポリエチレンを用いた以外は実施例
1を繰り返し透明フィルムを得た。Example 6 In Example 1, instead of the ethylene-vinyl acetate copolymer used as the base of the filler mixed resin used for the intermediate layer, high-pressure low density polyethylene (L degree 0.925 g/C) was used.
Example 1 was repeated to obtain a transparent film, except that the same high-pressure low-density polyethylene as the intermediate layer was used instead of the low-pressure low-density polyethylene used for the inner and outer layers. Ta.
実施例7
実施例6において用いた中間層のフィラー混合樹脂の内
外層をエチレン−アクリル酸共重合体(アクリル酸含有
19.3重量%、密度0.938g/ell’、ノルド
インデックス1.5g/10分)に代えた以外は実施例
1を繰り返し透明フィルムを得た。Example 7 The inner and outer layers of the filler mixed resin of the intermediate layer used in Example 6 were made of ethylene-acrylic acid copolymer (acrylic acid content 19.3% by weight, density 0.938 g/ell', Nord index 1.5 g/ell'). A transparent film was obtained by repeating Example 1 except that the time was changed to 10 minutes).
実施例8
実施例1において用いた中間層のハイドロタルサイト類
化合物を化学組成Mgo、1sAI。、34(OH)z
(S io 3)。、1.・0.52 H2O,平均2
次粒子径0.4μ論、BET比表面積15m27gのノ
)イドロタルサイ)Itに代えた以外は実施例1を繰り
返し透明フィルムを得た。Example 8 The hydrotalcite compound of the intermediate layer used in Example 1 had a chemical composition of Mgo and 1sAI. , 34(OH)z
(Sio3). , 1.・0.52 H2O, average 2
A transparent film was obtained by repeating Example 1, except that it was replaced with ()hydrotalcyan) having a particle diameter of 0.4 μm and a BET specific surface area of 15 m27 g.
比較例1
実施例1において中間層のフィラー混合樹脂のベースに
用いたエチレン−酢酸ビニル共重合体に防曇剤としてグ
リセリンモノステアレー10.5重量部、ポリグリセリ
ンステアレート1.0重量部、耐候助剤として2−ヒド
ロキシ−4−オクトキシベンゾ7ヱノン0.2重量部の
みを添加して実施例1と同じ方法に上り造粒ペレットを
製造した。Comparative Example 1 In Example 1, 10.5 parts by weight of glycerin monostearate, 1.0 parts by weight of polyglycerin stearate, Granulated pellets were produced in the same manner as in Example 1 except that only 0.2 parts by weight of 2-hydroxy-4-octoxybenzo7enone was added as a weathering aid.
一ヒ記造粒ペレットを単層イン7レーシ豊ン成形法によ
り76μ論の単層フィルムを得た。A single layer film of 76 μm was obtained from the granulated pellets by a single layer in-7 layer molding method.
比較例2
実施例1において中間層に用いたフィラー混合樹脂のハ
イドロタルサイト類化合物の配合割合を3.3重第1部
に代えた以外は実施例1と同じ方法でフィラー混合樹脂
ペレットを製造し、このペレットを用いて比較例1と同
じ方法と条件によりフィラー混合樹脂の単層フィルムを
得た。得られたフィルムは透明感がやや悪かった。Comparative Example 2 Filler mixed resin pellets were produced in the same manner as in Example 1, except that the blending ratio of the hydrotalcite compound in the filler mixed resin used for the intermediate layer in Example 1 was changed to 3.3 parts 1 part. Using this pellet, a monolayer film of filler mixed resin was obtained in the same manner and under the same conditions as in Comparative Example 1. The resulting film had slightly poor transparency.
比較例3
実施例1において中間層に用いたフィラー混合樹脂のハ
イドロタルサイト類化合物の代りに灼熱減量が10重量
%のシリカゾル(屈折率1.46.25℃で相対湿度6
5%での吸着水分15重置部、平均粒径2μ醜、BET
比表面積20m’/g)を同量用いた以外は実施例1を
繰り返しフィルムを得た。得られたフィルムは不透明で
あり、保温性および防曇持続性は本発明に比べて相当に
劣る傾向であった。Comparative Example 3 In place of the hydrotalcite compound of the filler mixed resin used for the intermediate layer in Example 1, silica sol with a loss on ignition of 10% by weight (refractive index 1.46.25°C and relative humidity 6) was used.
Adsorbed moisture at 5%, 15 overlapping parts, average particle size 2μ, BET
A film was obtained by repeating Example 1 except that the same amount of specific surface area (20 m'/g) was used. The obtained film was opaque, and its heat retention and anti-fog durability tended to be considerably inferior to those of the present invention.
比較例4
実施例1において中間層に用いたフィラー混合樹脂のハ
イドロタルサイト類化合物の代りに予め250℃で2時
間乾燥したALo、23重量%、5in)261重量%
、N azo 10重量%、灼熱減16重量%のアルミ
ノンリケードデル(屈折率1.495.25℃相対湿度
65%での吸着水分18重置部、平均粒径5μ論)を同
量用いた以外は実施例1を繰り返しフィルムを得た。Comparative Example 4 In place of the hydrotalcite compound in the filler mixed resin used for the intermediate layer in Example 1, ALo, 23% by weight, 261% by weight, previously dried at 250°C for 2 hours
, 10% by weight of Nazo, and 16% by weight of ignition loss aluminium non-ricade del (refractive index: 1.495.25°C, relative humidity: 65%, 18 overlapping parts of adsorbed moisture, average particle size: 5μ) were used in the same amount. A film was obtained by repeating Example 1 except for the following steps.
前記したすべての実施例及び比較例のフィルムの構成の
該略を第1表に、得られたフィルムの各物性を第2表に
示した。Table 1 shows a summary of the structure of the films of all the examples and comparative examples described above, and Table 2 shows the physical properties of the obtained films.
尚、実施例及び比較例における各物性試験は以下のよう
にしで行った。In addition, each physical property test in Examples and Comparative Examples was conducted as follows.
ハイドロタルサイトの平均2次粒子径測定:約2〜3曽
1の試料を〃ラス板−Eに採り、次いでこの上に、適当
量の分散媒(商品名:ディスライト)を加え、スパーチ
ルで両者を充分に混練する。その後、この系に少量のシ
クロヘキサノールを加え希釈する。この希釈液の1滴を
スライドグラスに取り、その上を〃バーグラスで覆う、
このようにしで得られた試料を顕iutにセットし、そ
の像を吹
テレビ画像に移し、粒子の最大径ごとの数を自動的にカ
ウントさせる。異なった視野を20選び同様の操作を繰
り返し、その結果を平均する。Measurement of average secondary particle size of hydrotalcite: Take about 2 to 3 times a sample on lath plate E, then add an appropriate amount of dispersion medium (trade name: Disrite) on top, and Thoroughly knead both. This system is then diluted by adding a small amount of cyclohexanol. Place one drop of this diluted solution on a slide glass and cover it with a bar glass.
The sample thus obtained is set in a microscope, its image is transferred to a blown-out TV image, and the number of particles for each maximum diameter is automatically counted. Select 20 different fields of view, repeat the same operation, and average the results.
保温性試験:
保温性の測定は断熱材でつくった約80e−平方の箱に
′1ケ所の面に試料を張り、保温性測定第1tRを使用
して箱内に挿入した100℃の加熱ブロックによる装置
内温度変化をサーミスターにで測定した。Heat retention test: Heat retention was measured by placing a sample on one side of a box of approximately 80 square meters made of heat insulating material, and inserting a 100°C heating block into the box using heat retention measurement No. 1 tR. The temperature change inside the device was measured using a thermistor.
標準試料の農業用ポリ塩化ビニルフィルムの厚さ0.0
75論−が示す値との温度差を保温性として(67℃)
で表に示した。Standard sample agricultural polyvinyl chloride film thickness 0.0
The temperature difference from the value indicated by 75 theory is considered heat retention (67℃)
It is shown in the table.
光学的性質試験:
本発明で得られたフィルムを波長555ミリミクロンで
の全光線透過率及び平行光線透過率を分光光度計(日立
製作新製EPS−ZU型)によって測定し、その値を示
した。Optical property test: The total light transmittance and parallel light transmittance of the film obtained in the present invention at a wavelength of 555 millimicrons were measured using a spectrophotometer (Hitachi new model EPS-ZU), and the values are shown. Ta.
耐摩擦性試Ia:
U−F耐揉試験慨を使用してフィルム試験片を固定側に
しわが入らないように取り付は対応するIf(左右に作
動する側)にペーパーヤスリ#400を貼り付けて固定
されたフィルム面に接触させフィルムが破れるまでの揉
回数を評価した。Abrasion resistance test Ia: Using the U-F abrasion resistance test, attach the film test piece to the fixed side with paper file #400 on the corresponding If (side that moves left and right) to avoid wrinkles. The number of times the film was rubbed until the film broke was evaluated.
尚、破れ回数が大きいほど耐摩擦性に優れる。Note that the greater the number of tears, the better the abrasion resistance.
この得られたフィルムの値を表に示した。The values of the obtained film are shown in the table.
耐久性試験:
南側に面し、地面に対して45度傾耕させて設置した窓
枠状の密閉試験台に(Wkll場所:愛知県名古屋市)
各フィルムを60年9月より12ケ月問暴露しフィルム
の一部を暴露試験台から取りはずし、外観及び伸びを評
価したもの、評価基準は、次のとおりとした。Durability test: On a closed test stand in the shape of a window frame, facing south and tilted at 45 degrees to the ground (Wkll location: Nagoya City, Aichi Prefecture)
Each film was exposed for 12 months starting in September 1960, a portion of the film was removed from the exposure test stand, and the appearance and elongation were evaluated using the following evaluation criteria.
○ ・・・外観に変化がなく、伸び残率が80%以上あ
るもの。○: There is no change in appearance and the remaining elongation rate is 80% or more.
Qx ・・・外観に変化がなく、伸び残率が79〜60
%の範囲にあるもの。Qx...No change in appearance, remaining elongation rate is 79-60
% range.
Δ ・・・亀裂や破れ等の外観変化が一部認められ、伸
び残率が79〜60%の範囲に
あるもの。Δ: Appearance changes such as cracks and tears are partially observed, and the residual elongation rate is in the range of 79 to 60%.
ΔX・・・亀裂や破れ等の外観変化がかなり認められ、
伸ゾ残率が59〜40%の範囲
にあるもの。ΔX: Significant changes in appearance such as cracks and tears are observed.
The retention rate of stretch marks is in the range of 59 to 40%.
× や・・全面にわたってひび割れが認められるか、伸
び残率が40%未満のもの。× Fair: Cracks are observed over the entire surface or the remaining elongation rate is less than 40%.
なお、伸び残率は次式より算出した。Note that the residual elongation rate was calculated using the following formula.
防曇持続性試験:
愛知県名古屋市の圃場に閏日2−1棟高2−1奥行20
論の片屋根型ハウスに60年10月より12ケ月間フィ
ルムを被覆し、各々フィルムの防曇性を定期的に肉眼で
a察し評価した。Anti-fog durability test: Leap day 2-1 building height 2-1 depth 20 in a field in Nagoya City, Aichi Prefecture
The film was coated on a single-roof type house for 12 months starting in October 1960, and the antifogging properties of each film were periodically observed and evaluated with the naked eye.
表に示す防曇持続性の評価は、それぞれ次のような意義
を有する。The anti-fog durability evaluation shown in the table has the following significance.
○ ・・・フィルム被覆後9ケ月以上、水が薄膜状に付
着し、水滴が認められない状態。○...Water remains in a thin film form and no water droplets are observed for 9 months or more after film coating.
Qx ・・・フィルム被覆後9ケ月未満6ケ月以上、水
が薄膜状に付着しているが、わずか
に大粒の水滴が認められる状態。Qx: Water has been attached in a thin film form for less than 9 months but more than 6 months after film coating, but slightly large water droplets are observed.
Δ ・・・フィルム被覆後6ケ月未満に水が薄膜状に付
着しているが、部分的に大粒の
水滴の付着が認められる状態。Δ: Water is attached in a thin film form less than 6 months after film coating, but large water droplets are observed to be attached in some areas.
以上、χ施例及び比較例から明らかなように、本発明に
係るフィルム、すなわち特定のハイドロタルサイト類化
合物を含有するオレフィン系樹脂の内外面に他のオレフ
ィン樹脂を積層してなるフィルムは透明性(平行光線透
過率)、保温性、耐摩擦強度、耐久性、防曇持続性のい
ずれもすぐれ農業用 ゛フィルムとしてきわめて好適
であることがわかる。As is clear from the above Examples and Comparative Examples, the film according to the present invention, that is, the film formed by laminating other olefin resins on the inner and outer surfaces of an olefin resin containing a specific hydrotalcite compound, is transparent. It can be seen that the film has excellent properties in terms of properties (parallel light transmittance), heat retention, abrasion resistance, durability, and anti-fog retention, making it extremely suitable as an agricultural film.
なお、特定のハイドロタルサイト類を含有するオレフィ
ン樹脂の単Mフィルムでは保温性、透明性は達成できる
が、耐摩擦強度、耐久性が劣ること、又、従来から公知
となっている他のフィラーを含有するオレフィン系樹脂
の内外面に他のオレフィン樹脂を積層してなるフィルム
は、保温性が不充分であり、耐久性、防1持縫性も劣る
ことは前述の説明から明らかであり具体例により示すま
でもないことである。In addition, although heat retention and transparency can be achieved with a single M film of olefin resin containing specific hydrotalcites, it is inferior in abrasion resistance strength and durability, and it is difficult to use other fillers that have been known in the past. It is clear from the above explanation that a film formed by laminating other olefin resins on the inner and outer surfaces of an olefin resin containing There is no need to show this by example.
特許出願人 三菱化成ビニル株式会社
代 理 人 弁理士 艮谷用 −
(ほか1名)
手続補正書
昭和62年6月22日
昭和62年特許I[第120962号
2 発明の名称
農業用積層フィルム
3 補正をする者
事件との関係 特許出願人
名称 三菱化成ビニル株式会社
4代理人〒100
東京都千代田区丸の内二丁目5番2号
5 補正命令の日付 自発
6 補正により増加する発明の敗 07 補正の対象
明細書の「特許請求の範囲J及び「発明の詳細な説明
」の欄
正する。Patent Applicant Mitsubishi Kasei Vinyl Co., Ltd. Agent Patent Attorney Tsuyoshi Atsuya - (1 other person) Procedural Amendment June 22, 1988 Patent I [No. 120962 No. 120962 2 Name of Invention Agricultural Laminated Film 3] Relationship with the case of the person making the amendment Patent applicant name Mitsubishi Kasei Vinyl Co., Ltd. 4th agent 2-5-2-5 Marunouchi, Chiyoda-ku, Tokyo 100 Date of amendment order Voluntary action 6 Increased loss of invention due to amendment 07 Amendment Subject: Correct the "Claims J" and "Detailed Description of the Invention" columns in the specification.
2、明細書第12頁第18行目に[No’−・C104
−4とあるのをrNO,−1C[0、−Jに訂正ろ
する。2. [No'-・C104 on page 12, line 18 of the specification]
-4 should be corrected to rNO, -1C[0, -J.
3、明細S第14実弟1.2,3,4.5及び6行口に
「カルラム」とあるのをそれぞれ「カリウム]に訂正す
る。3. Correct the word "karrum" at the beginning of lines 1.2, 3, 4.5 and 6 of the 14th younger brother of specification S to "potassium" respectively.
4、明細書第17真第3〜4行目に「オレイン系樹脂」
とあるのを「オレフィン系樹脂」に訂正する。4. “Oleic resin” in the 17th line of the specification, lines 3-4
Correct the statement to "olefin resin."
5、明aii書第27真第14行目に「80e曽平方」
とあるのをj80cm立方」に訂正する。5. “80e Zengping” in the 14th line of the 27th line of the Book of Ming aii
Correct it to "j80cm cubic".
6、明細書第31頁#A1表中、実施?48の「フィラ
一種jl[Jの欄に
rMgo、iaA 第11.3(CH)z(COtL、
+sO、55H701とあるのを
rMgo、ggAl。、5a(OH)2(S iO、l
)。、 + y O、52H,OJに訂正する。6. Implementation in the specification page 31 #A1 table? 48 "Fila type jl [J column rMgo, iaA No. 11.3 (CH) z (COtL,
+sO, 55H701 is rMgo, ggAl. , 5a(OH)2(S iO,l
). , + y O, 52H, OJ.
別紙
特許請求の範囲
(1) オレフィン系樹脂100重を部に対して、1〜
25重量部の下記一般式
%式%
ただし式中Mはアルカリ土類金属およびZnを、Xlf
n価のアニオンを示す、また、1及vmは下記式の条件
を満足する。Attachment Claims (1) 1 to 100 parts by weight of olefin resin
25 parts by weight of the following general formula % formula % where M represents an alkaline earth metal and Zn,
It represents an n-valent anion, and 1 and vm satisfy the conditions of the following formula.
O< 、<O,S
O≦ −≦ 2
で表わされる屈折率が1.47以上1.52以下の範B
であるハイドロタルサイト類化合物を配合した組成物か
らなるフィルムの内外面にオレフィン系PA脂の群から
選ばれる少なくとも一種の樹脂層が設けられている事を
特徴とする農業用積層フィルム。Range B with a refractive index of 1.47 or more and 1.52 or less expressed by O<, <O, SO≦-≦2
1. A laminated film for agricultural use, characterized in that a layer of at least one resin selected from the group of olefinic PA resins is provided on the inner and outer surfaces of the film made of a composition containing a hydrotalcite compound.
(2) オレフィン系樹脂が密度0.910g/am’
以ヒ0.935H/cmコ以下の低密度ポリエチレンも
しくはエチレン−α−オレフィン共i合体である特許請
求の範n第1項記載の農業用積層フィルム。(2) Olefin resin has a density of 0.910 g/am'
The laminated agricultural film according to claim 1, which is a low-density polyethylene or an ethylene-α-olefin copolymer having a density of 0.935 H/cm or less.
(3) オレフィン系樹脂が酢酸ビニル含有量が30重
置方以下のエチレン−酢酸ビニル共重合体である特許請
求の範囲第1項記載の農業用積層フィルム。(3) The agricultural laminated film according to claim 1, wherein the olefin resin is an ethylene-vinyl acetate copolymer having a vinyl acetate content of 30 ply or less.
(4)ハイドロタルサイト類化合物の平均2次粒子径が
5μ−以下でBET比表面積が30m”7g以下である
特許請求の範囲第1項記載の農業用積層フィルム。(4) The agricultural laminated film according to claim 1, wherein the hydrotalcite compound has an average secondary particle size of 5 μm or less and a BET specific surface area of 30 m″7 g or less.
(5) 内外層に使用するオレフィン系樹脂の密度が0
.915g/cta’以上0 、935第17cm’以
下、でかつメルトインデックスが0.1g/10分以上
4g710分以下であるポリエチレンもしくはエチレン
−αオレフインコポリマーである特許請求の範囲第1項
記載の農業用積層フィルム。(5) The density of the olefin resin used for the inner and outer layers is 0.
.. The agricultural use according to claim 1, which is a polyethylene or ethylene-α olefin copolymer having a melt index of 915 g/cta' to 0, 935 cm' or less, and a melt index of 0.1 g/10 min to 4 g/710 min. Laminated film.
(6) 内外層に使用するオレフィン[脂がメルトイン
デックス0.1g/10分以414g/10分以下で、
酢酸ビニル含有量が15重置部以下のエチレン−酢酸ビ
ニル共重合体である特許請求の範1!IIrjS1項記
載の農業用積層フィルム。(6) Olefin used in the inner and outer layers [fat has a melt index of 0.1 g/10 minutes to 414 g/10 minutes,
Claim 1, which is an ethylene-vinyl acetate copolymer having a vinyl acetate content of 15 parts by weight or less! Agricultural laminated film according to item IIrjS1.
(7)内外層に使用するオレフィン系樹脂がエチレン−
メタクリル酸共重合体の亜鉛イオンもしくはナトリウム
イオン架橋構造を有するアイオノマー樹脂であり、その
密度が0.935g/cm’ 以上0.975g/e輸
コ以下、メルトインデックスが0.5.710分以上?
、/10分以下である特許請求の範囲第1項記載の農業
用積層フィルム。(7) The olefin resin used for the inner and outer layers is ethylene-
Ionomer resin with zinc ion or sodium ion crosslinked structure of methacrylic acid copolymer, has a density of 0.935 g/cm' or more and 0.975 g/e or less, and a melt index of 0.5.710 minutes or more?
, /10 minutes or less, the agricultural laminated film according to claim 1.
(8)内外層に使用するオレフィン系樹脂がアクリル酸
含有!30重量%以工のエチレン−アクリル酸共重合体
である特許請求の範囲第1項記載の農業用積層フィルム
。(8) The olefin resin used for the inner and outer layers contains acrylic acid! The laminated agricultural film according to claim 1, which is an ethylene-acrylic acid copolymer containing 30% by weight or more.
Claims (8)
5重量部の下記一般式 M_(_1_−_x_)・Al_x・(OH)_2・X
_x/n・mH_2Oただし式中Mはアルカリ土類金属
およびZnを、Xはn価のアニオンを示す。また、x及
びmは下記式の条件を満足する。 0<x<0.5 0≦m≦2 で表わされる屈折率が1.47以上1.52以下の範囲
であるハイドロタルサイト類化合物を配合した組成物か
らなるフィルムの内外面にオレフィン系樹脂の群から選
ばれる少なくとも一種の樹脂層が設けられている事を特
徴とする農業用積層フィルム。(1) 1 to 2 parts per 100 parts by weight of olefin resin
5 parts by weight of the following general formula M_(_1_-_x_)・Al_x・(OH)_2・X
_x/n·mH_2O In the formula, M represents an alkaline earth metal and Zn, and X represents an n-valent anion. Moreover, x and m satisfy the conditions of the following formula. An olefin resin is applied to the inner and outer surfaces of a film made of a composition containing a hydrotalcite compound having a refractive index expressed by 0<x<0.5 0≦m≦2 in the range of 1.47 to 1.52. An agricultural laminated film characterized by being provided with at least one kind of resin layer selected from the group of.
以上0.935g/cm^3以下の低密度ポリエチレン
もしくはエチレン−α−オレフィン共重合体である特許
請求の範囲第1項記載の農業用積層フィルム。(2) Olefin resin has a density of 0.910g/cm^3
The laminated agricultural film according to claim 1, which is a low-density polyethylene or ethylene-α-olefin copolymer having a density of 0.935 g/cm^3 or less.
%以下のエチレン−酢酸ビニル共重合体である特許請求
の範囲第1項記載の農業用積層フィルム。(3) The agricultural laminated film according to claim 1, wherein the olefin resin is an ethylene-vinyl acetate copolymer having a vinyl acetate content of 30% by weight or less.
5μm以下でBET比表面積が30m^2/g以下であ
る特許請求の範囲第1項記載の農業用積層フィルム。(4) The agricultural laminated film according to claim 1, wherein the hydrotalcite compound has an average secondary particle size of 5 μm or less and a BET specific surface area of 30 m^2/g or less.
915g/cm^3以上0.935g/cm^3以下、
でかつメルトインデックスが0.1g/10分以上4g
/10分以下であるポリエチレンもしくはエチレン−α
オレフィンコポリマーである特許請求の範囲第1項記載
の農業用積層フィルム。(5) The density of the olefin resin used for the inner and outer layers is 0.
915g/cm^3 or more and 0.935g/cm^3 or less,
Dekatsu melt index is 0.1g/4g for 10 minutes or more
/10 minutes or less polyethylene or ethylene-α
The laminated agricultural film according to claim 1, which is an olefin copolymer.
デックス0.1g/10分以上4g/10分以下で、酢
酸ビニル含有量が15重量%以下のエチレン−酢酸ビニ
ル共重合体である特許請求の範囲第1項記載の農業用積
層フィルム。(6) A patent claim in which the olefin resin used for the inner and outer layers is an ethylene-vinyl acetate copolymer with a melt index of 0.1 g/10 min or more and 4 g/10 min or less and a vinyl acetate content of 15% by weight or less. Agricultural laminated film according to scope 1.
メタクリル酸共重合体の亜鉛イオンもしくはナトリウム
イオン架橋構造を有するアイオノマー樹脂であり、その
密度が0.935g/cm^3以上0.975g/cm
^3以下、メルトインデックスが0.5g/10分以上
7g/10分以下である特許請求の範囲第1項記載の農
業用積層フィルム。(7) The olefin resin used for the inner and outer layers is ethylene-
It is an ionomer resin having a zinc ion or sodium ion crosslinked structure of methacrylic acid copolymer, and its density is 0.935 g/cm^3 or more and 0.975 g/cm
The agricultural laminated film according to claim 1, which has a melt index of ^3 or less and a melt index of 0.5 g/10 minutes or more and 7 g/10 minutes or less.
含有量30重量%のエチレン−アクリル酸共重合体であ
る特許請求の範囲第1項記載の農業用積層フィルム。(8) The agricultural laminated film according to claim 1, wherein the olefin resin used for the inner and outer layers is an ethylene-acrylic acid copolymer having an acrylic acid content of 30% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62120962A JPS63286343A (en) | 1987-05-18 | 1987-05-18 | Laminate film for agriculture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62120962A JPS63286343A (en) | 1987-05-18 | 1987-05-18 | Laminate film for agriculture |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63286343A true JPS63286343A (en) | 1988-11-24 |
JPH0411107B2 JPH0411107B2 (en) | 1992-02-27 |
Family
ID=14799308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62120962A Granted JPS63286343A (en) | 1987-05-18 | 1987-05-18 | Laminate film for agriculture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63286343A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01182037A (en) * | 1988-01-14 | 1989-07-19 | Nippon Yunikaa Kk | Laminated film for agricultural use |
EP0715954A3 (en) * | 1994-12-06 | 1996-08-28 | Sumitomo Chemical Co | Laminated film of polyolefin resin |
EP0761427A1 (en) * | 1995-08-28 | 1997-03-12 | Sumitomo Chemical Company Limited | Polyolefin resin covering film and method for raising plants |
JP2005344069A (en) * | 2004-06-07 | 2005-12-15 | Tosoh Corp | Ethylene-vinyl acetate copolymer composition for agricultural covering film and film comprising the same |
US7169222B2 (en) | 1996-05-09 | 2007-01-30 | Merck Patent Gmbh | Multilayer interference pigments |
JP2012025789A (en) * | 2010-07-20 | 2012-02-09 | Katsuta Kako Kk | Warm-keeping agent for polyolefin-based resin, and agricultural film using the same |
WO2015182790A1 (en) * | 2014-05-30 | 2015-12-03 | 協和化学工業株式会社 | Liquid stabilizer and resin composition containing said liquid stabilizer |
JPWO2016152249A1 (en) * | 2015-03-24 | 2017-12-28 | 三菱ケミカル株式会社 | Agricultural film |
-
1987
- 1987-05-18 JP JP62120962A patent/JPS63286343A/en active Granted
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01182037A (en) * | 1988-01-14 | 1989-07-19 | Nippon Yunikaa Kk | Laminated film for agricultural use |
EP0715954A3 (en) * | 1994-12-06 | 1996-08-28 | Sumitomo Chemical Co | Laminated film of polyolefin resin |
CN1077498C (en) * | 1994-12-06 | 2002-01-09 | 住友化学工业株式会社 | Agricultural polylefine series laminated resin film |
EP0761427A1 (en) * | 1995-08-28 | 1997-03-12 | Sumitomo Chemical Company Limited | Polyolefin resin covering film and method for raising plants |
US7169222B2 (en) | 1996-05-09 | 2007-01-30 | Merck Patent Gmbh | Multilayer interference pigments |
JP2005344069A (en) * | 2004-06-07 | 2005-12-15 | Tosoh Corp | Ethylene-vinyl acetate copolymer composition for agricultural covering film and film comprising the same |
JP2012025789A (en) * | 2010-07-20 | 2012-02-09 | Katsuta Kako Kk | Warm-keeping agent for polyolefin-based resin, and agricultural film using the same |
WO2015182790A1 (en) * | 2014-05-30 | 2015-12-03 | 協和化学工業株式会社 | Liquid stabilizer and resin composition containing said liquid stabilizer |
JPWO2016152249A1 (en) * | 2015-03-24 | 2017-12-28 | 三菱ケミカル株式会社 | Agricultural film |
Also Published As
Publication number | Publication date |
---|---|
JPH0411107B2 (en) | 1992-02-27 |
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