JPS59226037A - Resin composition for agricultural film - Google Patents

Resin composition for agricultural film

Info

Publication number
JPS59226037A
JPS59226037A JP10215383A JP10215383A JPS59226037A JP S59226037 A JPS59226037 A JP S59226037A JP 10215383 A JP10215383 A JP 10215383A JP 10215383 A JP10215383 A JP 10215383A JP S59226037 A JPS59226037 A JP S59226037A
Authority
JP
Japan
Prior art keywords
magnesium hydroxide
film
surface treatment
single crystal
resin composition
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
JP10215383A
Other languages
Japanese (ja)
Other versions
JPH0350791B2 (en
Inventor
Shigeo Miyata
茂男 宮田
Takafumi Suzuki
隆文 鈴木
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.)
Kyowa Chemical Industry Co Ltd
KH Neochem Co Ltd
Original Assignee
Kyowa Chemical Industry Co Ltd
Kyowa Kagaku Kogyo KK
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 Kyowa Chemical Industry Co Ltd, Kyowa Kagaku Kogyo KK filed Critical Kyowa Chemical Industry Co Ltd
Priority to JP10215383A priority Critical patent/JPS59226037A/en
Publication of JPS59226037A publication Critical patent/JPS59226037A/en
Publication of JPH0350791B2 publication Critical patent/JPH0350791B2/ja
Granted legal-status Critical Current

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  • Cultivation Receptacles Or Flower-Pots, Or Pots For Seedlings (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled resin composition having both improved transparency and heat retaining properties, obtained by blending a thermoplastic resin with a specific amount of magnesium hydroxide satisfying specific conditions such as BET specific surface area, etc., treated with a surface treatment, as an infrared absorber. CONSTITUTION:(A) 100pts.wt. thermoplastic resin e.g., PE, PP, PVC, etc.) is blended with (B) 1-20pts.wt. magnesium hydroxide having (i) 2-15m<2>/g, preferably 5-10m<2>/g BET specific surface area, (ii) 0.3-2.0mu, preferably 0.5-1.5mu size of single crystal by electron microscopy, and (iii) >=90wt%, preferably >=95 wt% secondary particles having <=2mu particle diameter, treated with (iv) a surface treatment (sodium polyoxyethylene lauryl ether sulfate, etc.), to give the desired composition.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、透明性と保温性がともにすぐれた農業用フィ
ルムに用いられる樹脂組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a resin composition used for agricultural films having excellent transparency and heat retention.

農作物のハウス栽培やトンネル栽培等において用いられ
る農業用フィルムには耐候性、耐老化性等の外に、透明
性と保温性の両方にすぐれていることが要求される。
Agricultural films used in greenhouse cultivation, tunnel cultivation, etc. of agricultural products are required to have excellent weather resistance, aging resistance, etc., as well as both transparency and heat retention.

何故ならば、日中は太陽光線が可及的に高い透過率でフ
ィルムを透過することが効率的な温室用フィルムとして
の必要特性であり、他方夜間においてに昼間の太陽光線
照射によって昇温した温室内の気温を維持することが必
要だからである。しかしてこの保温は夜間に地表及び植
物から放射される赤外線を効率的にフィルムに吸収させ
ることVC,よって達成される。ところでフィルムの原
料となる熱可塑性樹脂自体は効率的な赤外線吸収機能を
示さないので、折角、日中温室内の植物が吸収した熱を
夜間温室外に逃がさないためには、フィルムに植物が放
射する赤外線をよく吸収する物質を添加することが必要
である。
This is because it is a necessary characteristic for an efficient greenhouse film that sunlight passes through the film at the highest possible transmittance during the day, while at night the temperature rises due to daytime sunlight irradiation. This is because it is necessary to maintain the temperature inside the greenhouse. However, the heat retention of the lever is achieved by making the film efficiently absorb infrared rays emitted from the ground surface and plants at night (VC). By the way, the thermoplastic resin itself, which is the raw material for the film, does not exhibit an efficient infrared absorption function, so in order to prevent the heat absorbed by the plants inside the greenhouse during the day from escaping outside the greenhouse at night, it is necessary to absorb the heat absorbed by the plants into the film. It is necessary to add a substance that absorbs infrared rays well.

〔従来技術〕[Prior art]

そのような効率的な赤外線吸収剤として水酸化マグネシ
ウムが好適であることは既に提案されている(特公昭5
7−34871号、特開昭55−164238号)。し
かしながら、水酸化マグネシウムは結晶粒子径が小さく
、然も凝集性が強いために粗大な2次粒子となり易い(
平均2次粒子径が10〜100μ)。したがって脂肪酸
、多価アルコール、パラフィン、シランカップリング剤
等の表面処理剤で処理をしても、樹脂中の分散粒子の大
きさに、良くてたかだか10〜100μの大きさである
とともに、樹脂中で再凝集して更に大きな2次粒子を形
成したり、加工温度で2次粒子中に内包されていた付着
水分が揮発する等のため、これを含む樹脂組成物を用い
てフィルムに成形すると、フィッシュアイ金主じたり、
視認しうる程の分散不良の水酸化マグネシウムが存在し
、フィルムの透明性を劣化させる欠点を免れない。その
ため農業用フィルムとしての透光性を不良にするととも
に、引張強度等の機械的性質も悪くなり、実用性に乏し
い。
It has already been proposed that magnesium hydroxide is suitable as such an efficient infrared absorber (Japanese Patent Publication No. 5
No. 7-34871, JP-A-55-164238). However, magnesium hydroxide has a small crystal particle size and strong cohesiveness, so it tends to form coarse secondary particles (
The average secondary particle diameter is 10 to 100μ). Therefore, even if treated with surface treatment agents such as fatty acids, polyhydric alcohols, paraffin, and silane coupling agents, the size of the particles dispersed in the resin will be at most 10 to 100μ, and If a resin composition containing this is used to form a film, because it re-agglomerates to form larger secondary particles, or the attached moisture contained in the secondary particles evaporates at the processing temperature, Fisheye Kinjitari,
A visible amount of poorly dispersed magnesium hydroxide is present, which inevitably deteriorates the transparency of the film. This results in poor translucency as an agricultural film, as well as poor mechanical properties such as tensile strength, making it impractical.

〔発明の目的並びに構成〕[Object and structure of the invention]

そこで本発明者等ぼ、前記従来の水酸化マグネシウムの
欠点全克服すべく鋭意研究した結果、下記条件を満足す
る特殊な水酸化マグネシウムを赤外線吸収剤として用い
ることにより、問題を解決するに到ったものである。す
なわら本発明に、熱可塑性樹脂100重量部に、 巾 Bル′r比表面積が 2〜15 Hfy、好ましく
ぼ5〜107に/1、 +++)を子顕微鏡により、10,000倍の倍率で撮
影した写真から測定した単結晶(板状結晶)の平均の大
きさが0.3〜2,0μ、好ましくは0.5〜i、 s
  μ、 (+iil  ルーゼツクス法で測定した2次粒子径の
粒度分布において2μ以下が90%以上、好ましくは9
5%以上であって、 四 表面処理剤で処理した、 水酸化マグネシウムを、1〜20重量部配爪部た農業用
フィルム用樹脂組成物を要旨とするものであって、この
ような組成物を原料として成形し之フィルムは、フィッ
シュアイが全く存在せず、分散不良の目視できる粗大粒
子の存在も皆無の、極めて透明性、保温性にすぐれ、か
つ機械的性質も良好であって、A業用フィルムとして要
求される条件を具えたものである。
As a result of intensive research to overcome all of the drawbacks of the conventional magnesium hydroxide, the inventors of the present invention have found a solution to the problem by using a special magnesium hydroxide that satisfies the following conditions as an infrared absorbing agent. It is something that That is, in the present invention, 100 parts by weight of a thermoplastic resin with a specific surface area of 2 to 15 Hfy, preferably 5 to 107/1, +++) is added using a microscope at a magnification of 10,000 times. The average size of single crystals (plate crystals) measured from photographs taken with 0.3 to 2.0μ, preferably 0.5 to i,s
μ, (+iil In the particle size distribution of the secondary particle diameter measured by the Luzetx method, 90% or more are 2 μ or less, preferably 9
5% or more, and 4. A resin composition for agricultural film containing 1 to 20 parts by weight of magnesium hydroxide in the claw part treated with a surface treatment agent, such a composition The film formed using A as a raw material has no fish eyes, no visually visible coarse particles with poor dispersion, has excellent transparency and heat retention, and has good mechanical properties. It meets the requirements of a commercial film.

本発明の目的とする透明性の高いフィルムt−製造する
ためには、前記4つの条件をすべて満足する必要があり
、1つでもこれらの条件金外れると目的とする透明性の
高いフィルムを得ることはできない。
In order to produce a film with high transparency, which is the objective of the present invention, it is necessary to satisfy all of the above four conditions, and if even one of these conditions is not met, the objective highly transparent film will not be obtained. It is not possible.

すなわち、本発明において用いられる水酸化マグネシウ
ムは、 (1)BET比表面積が2〜15く乍であることが必要
であって、2111/y未満であると、凝集が強くて2
次粒子が大きすぎるか、あるいは単結晶が2μより大さ
くなり、いずれにしても透明性が劣化し、逆vc、 1
5 nc/y−金越えると単結晶の大きさが小さくなり
すぎて凝集性が強く、したがって2次粒子が粗大になる
That is, the magnesium hydroxide used in the present invention must have (1) a BET specific surface area of 2 to 15, and if it is less than 2111/y, the aggregation is strong and 2
Either the secondary particles are too large or the single crystal is larger than 2μ, and in either case the transparency deteriorates and the reverse vc, 1
If it exceeds 5 nc/y-gold, the size of the single crystal becomes too small and the agglomeration is strong, resulting in coarse secondary particles.

叩電子顕微鏡法による単結晶の大きさが0.3〜2.0
μであることが必要である。
Single crystal size determined by electron microscopy is 0.3-2.0
It is necessary that μ.

単結晶(板状結晶ンの平均大ささrzto、ooo倍の
倍率で撮影した写真によって測定するが、この大きさが
0.3μより小さいと、凝集が強くなって2次粒子が大
きくなりフィルムの透明性が悪くなり、逆に2μより大
きくなりすぎてもフィルムの透明性は悪くなる。
The average size of single crystals (plate-like crystals rzto) is measured by a photograph taken at a magnification of 0.00 times, but if this size is smaller than 0.3μ, the aggregation will be strong and the secondary particles will be large and the film will be damaged. The transparency of the film deteriorates, and conversely, if it becomes too large than 2μ, the transparency of the film deteriorates.

(Iitl 2次粒子径の2μ以下が90%以上存在す
ることが必要である。この測定はルーゼックス法で行う
が2次粒子径の粒度分布において、2μ以下が90チ未
満であると2次粒子が大きくなりすぎてフィルムの透明
性を悪化させる。
(Iitl It is necessary that 90% or more of the secondary particle size is 2 μ or less. This measurement is performed using the Luzex method, but if the secondary particle size is less than 90 cm, the secondary particle size is less than 90 cm. becomes too large, deteriorating the transparency of the film.

以上において各条件相互間の関係は、BffiTが2〜
i s m/y、の範囲にあっても、凝集が強いと単結
晶はしばしば0.3μ以下となる。単結晶が例えば0.
3μであっても凝集が強いとBfCTに約2〜5右であ
るが、ルーゼックスの粒度分布において2次粒子径の2
μ以下が80チより少なくなることがある。
In the above, the relationship between each condition is that BffiT is 2 to
Even within the range of i s m/y, if the aggregation is strong, the single crystal often has a diameter of 0.3 μ or less. For example, if a single crystal is 0.
Even if the particle size is 3μ, if the aggregation is strong, it will be about 2 to 5 times lower than BfCT, but in the particle size distribution of Luzex, the secondary particle size
The value below μ may be less than 80 inches.

Cφ表面処理は、水酸化マグネシウムに対して約1〜1
0重量%の表面処理剤(後記例示)′lr用埴て行う。
Cφ surface treatment is approximately 1 to 1 for magnesium hydroxide.
0% by weight of a surface treatment agent (examples given below).

〔測定方法〕〔Measuring method〕

(イ)  BIT比表面積は、液体窒素の吸着法により
測定する。
(a) BIT specific surface area is measured by liquid nitrogen adsorption method.

(に) 単結晶の大きさは、倍率10,000倍で電子
顕微鏡写真をとり、10個の大きさを測定しその平均値
を以って単結晶の大きさと定義する。
(2) To determine the size of a single crystal, take an electron micrograph at a magnification of 10,000 times, measure 10 sizes, and define the average value as the size of the single crystal.

(ハ)ルーゼツクス法による粒度分布は、約5■の試料
をガラス板にとり、分散剤である「ディスライト」(商
品名)を加えベラでよく混線、分散後、クロルベンゼン
液を添加し希釈して、その1滴をスライドダラスに乗せ
、更にその上にカバーグラスを乗せ倍率400倍で光学
顕微鏡にかけ、そのf象全ブラウン管に移し゛C全粒子
の大きさ全カウントする。
(c) To determine the particle size distribution using the Rouzetx method, take a sample of approximately 5 cm on a glass plate, add the dispersant "Dislight" (trade name), mix well with a spatula, disperse, and then dilute by adding chlorobenzene solution. Then, place one drop on a slide Dallas, place a cover glass on top of it, and put it under an optical microscope at a magnification of 400 times, and then transfer it to a cathode ray tube and count the size of all the particles.

〔製造例〕[Manufacturing example]

本発明で用いる水酸化マグネシウムは、特開昭52−1
15799号に開示した方法により製造される。その概
要は、下記式 %式% 但し、式中、A(グalもしくにNo、、Xは0<X<
0.2の数を示す、 mはO〜6、 で表わされる塩基性塩化もしくに塩基性硝酸マグネシウ
ムを、水性媒体中において、加圧条件下に、例レーば1
20〜250℃程度の温度に加熱することにより水酸化
マグネシウムを合成し、水洗を行った後、水酸化マグネ
シウムの重量に基いて約1〜10重t%の表面処理剤で
処理することにより得られる。
The magnesium hydroxide used in the present invention is
Manufactured by the method disclosed in No. 15799. Its outline is the following formula% formula% However, in the formula, A (Gal or No, X is 0<X<
0.2, m is 0 to 6, and the basic chloride or basic magnesium nitrate represented by the following is added in an aqueous medium under pressurized conditions, for example, 1.
Magnesium hydroxide is synthesized by heating to a temperature of about 20 to 250°C, washed with water, and then treated with a surface treatment agent of about 1 to 10% by weight based on the weight of magnesium hydroxide. It will be done.

表面処理剤の具体的な例としては、高級脂肪酸のアルカ
リ金楓塩、ポリオキシエチレンラウリルエーテル硫酸ナ
トリウム塩、グリセリンと高級脂肪酸のエステル類、7
ラン系カツプリング剤、チタネートカップリング剤等を
挙げることができる。
Specific examples of surface treatment agents include alkali gold maple salts of higher fatty acids, polyoxyethylene lauryl ether sulfate sodium salts, esters of glycerin and higher fatty acids, 7
Examples include run type coupling agents and titanate coupling agents.

表面処理は、水に懸濁した状態又は粉末状態の水酸化マ
グネシウムに、上記表面処理剤の水、アルコール溶液を
加え、光分に攪拌することによって行われる。
The surface treatment is carried out by adding water and an alcohol solution of the above-mentioned surface treatment agent to magnesium hydroxide suspended in water or in a powdered state, and stirring the mixture optically.

〔熱0T塑性樹脂〕 本発明の農業用フィルム用組成物は、熱可塑性樹脂10
0重量部当り前記の特定r(、水酸化マグネシウムを約
1〜10重量部配合することにより得られる。
[Thermal 0T plastic resin] The agricultural film composition of the present invention has a thermoplastic resin of 10
It can be obtained by blending about 1 to 10 parts by weight of magnesium hydroxide per 0 parts by weight of the above specified r.

水酸化マグネシウムの量が1重量部未満の場合は赤外線
吸収効果が充分でなく、又2o重吐部を越えると透明性
に悪形W′fK:及ぼすので好ましくない。
If the amount of magnesium hydroxide is less than 1 part by weight, the infrared absorbing effect will not be sufficient, and if it exceeds 20 parts by weight, the transparency will be adversely affected, which is not preferable.

本発明で用いる熱り塑性樹脂とじてば、例えば低密度ポ
リエチレン、中密度ポリエチレン、高密度ポリエチレン
、ポリプロピレン、ポリ塩化ビニル、エチレン−酢酸ビ
ニル共重合体等を挙げることができる。
Examples of the thermoplastic resin used in the present invention include low density polyethylene, medium density polyethylene, high density polyethylene, polypropylene, polyvinyl chloride, and ethylene-vinyl acetate copolymer.

父、本発明においては、水酸化マグネシウム以外の赤外
線吸収剤として酸化硅素微粉末等信の公知の赤外線吸収
剤にきんでも良い。
In the present invention, the infrared absorbing agent other than magnesium hydroxide may be a known infrared absorbing agent such as silicon oxide fine powder.

〔フィルムの製造〕[Film production]

フィルムの製造は、例えば本発明組成物全酸化防止剤、
安定剤、紫外線吸収剤、滑剤等の他の添力口iすととも
に混合し、ロール、ニーダ−父は押出機等の溶融混線装
置で混練した後、イン7レー7ヨン成形、Tダイ成形、
カレンダー成形等公知の成形手段を用いてフィルムに成
形することができる。
The production of the film can be carried out, for example, by using the total antioxidant composition of the present invention,
It is mixed with other additives such as stabilizers, ultraviolet absorbers, and lubricants, and then kneaded in a melt mixing device such as a roll, a kneader, and an extruder.
It can be molded into a film using a known molding method such as calendar molding.

〔実施例並びに効果〕[Examples and effects]

次に実施例により本発明を具体的に説明する。 Next, the present invention will be specifically explained with reference to Examples.

実施例I BIiiT比表面積9勺、単結晶の大きさが0.8μ、
2次粒子の2μ以下が98チである水酸化マグネシウム
粉末500 P’kl O,e(DIlin水(約70
℃)に懸濁し攪拌しつつ、水酸化マグネシウムの重量に
対し、2チに相当するオレイン酸ノーダ107を溶解し
た温水(約70℃)500mlk加え、約30分間攪拌
した後、1過、脱水、乾燥、粉砕した。
Example I BIiiiT specific surface area 9 μm, single crystal size 0.8μ,
Magnesium hydroxide powder 500 P'kl O,e (DIlin water (approximately 70
While stirring, add 500ml of warm water (approximately 70°C) in which oleic acid Noda 107 corresponding to 2 ts per weight of magnesium hydroxide is dissolved, and after stirring for approximately 30 minutes, 1 filtration, dehydration, Dried and crushed.

以上のようにして得られた水酸化マグネシウムを低密度
ポリエチレンioo重敵部に10重敗部添加して、押出
機を用いて混線してベンツ)(2作り、このベレットを
用いて、インフレーション成形法で厚さ50μのフィル
ム金製膜した。このフィルム全周いて農業用のトンネル
全作り、可視光線(波長0.4〜0.7μ)の透過率と
、゛フィルムの保温効果金調べた。
Add 10 parts of the magnesium hydroxide obtained in the above manner to the parts of low-density polyethylene (IOO), mix the parts using an extruder to make Benz) (2 parts), and use this pellet to perform inflation molding. A gold film with a thickness of 50 μm was formed using the method.The entire circumference of this film was used to construct an agricultural tunnel, and the transmittance of visible light (wavelength 0.4 to 0.7 μm) and heat retention effect of the film were investigated.

比較例1 BKT比表面積s 87Q/P、単結晶の大きさが0.
06μ、2次粒子の2μ以下が72係の水酸化マグネシ
ウムを実施例1と同様に表面処理した後、実施例1と同
じ要領でフィルムを製膜した。
Comparative Example 1 BKT specific surface area s 87Q/P, single crystal size 0.
Magnesium hydroxide having a secondary particle size of 0.06 μm and 72 μm or less was subjected to surface treatment in the same manner as in Example 1, and then a film was formed in the same manner as in Example 1.

比較例2 1と同様に表面処理及び製膜してフィルムを作った。Comparative example 2 A film was prepared by surface treatment and film formation in the same manner as in 1.

比較例3 BET比表面積21 lrt/y−1単結晶の大きさが
0.2μ、2次粒子の2μ以下が94チの水酸化マグネ
シウムを実施例1と同様に表面処理及び製膜してフィル
ムを作った。
Comparative Example 3 BET specific surface area 21 lrt/y-1 Magnesium hydroxide with a single crystal size of 0.2μ and secondary particles of 2μ or less of 94cm was surface-treated and formed into a film in the same manner as in Example 1. made.

比較例4及び5 実施例1において、水酸化マグネシウムの配合駿金25
重敬部(比較例4)、0.5取量部(比較例5)に変え
る以外は、実施例1と同様に処理した。
Comparative Examples 4 and 5 In Example 1, the combination of magnesium hydroxide was
The treatment was carried out in the same manner as in Example 1, except that the weight was changed to 0.5 parts (Comparative Example 4) and 0.5 parts (Comparative Example 5).

対照例1 実施例1の低密度ポリエチレンを用いて厚さ50μのフ
ィルムをインフレーション法で作った。
Comparative Example 1 Using the low density polyethylene of Example 1, a film with a thickness of 50 μm was made by an inflation method.

比較例1〜5、対照例1のフィルムについても実施例1
と同様の測定を行った。その結果全第1表に示す。
Example 1 was also applied to the films of Comparative Examples 1 to 5 and Control Example 1.
The same measurements were carried out. The results are shown in Table 1.

第1表 各フィルムの可視光線透過率と保温効果実施例
2 BET比表面積14、単結晶の大きさ1.4μ、2次粒
子径の2μ以下が98チの水酸化マグネシウム粉末50
.0 fFを、約51の温水(約80℃)に懸濁させ、
攪拌しつつ、2Ofのステアリン酸ソーダを溶解した温
水(約80 ”C) 500 mlを加え、約30分間
攪拌を継続した。その後濾過、脱水、乾燥、粉砕した水
酸化マグネシウム全、ポリ塩化ビニルと次の処方で混合
して押出機で混線後、インフレーション法で厚さloo
μのフィルムを作った。このフィルムについて実施例1
と同様の方法で可視光線透過率と保温性を測定し/ヒ。
Table 1 Visible light transmittance and heat retention effect of each film Example 2 Magnesium hydroxide powder 50 with BET specific surface area 14, single crystal size 1.4μ, secondary particle size of 2μ or less 98cm
.. 0 fF is suspended in warm water (about 80 °C) at about 51 °C,
While stirring, 500 ml of warm water (approximately 80"C) in which 2Of sodium stearate had been dissolved was added, and stirring was continued for approximately 30 minutes. After that, filtration, dehydration, drying, and pulverized magnesium hydroxide, polyvinyl chloride, and Mix with the following recipe, cross-mix it in an extruder, and then use the inflation method to create a thickness of loo.
I made a μ film. Example 1 about this film
Visible light transmittance and heat retention were measured using the same method.

処方 ポリ塩化ビニル   60重敏部(loo)DO
P               30    #安定
剤        lN エポキシ系可塑剤   2 〃 水酸化マダ不シワム  6  #  (10)比較例6
及び7 実施例2において、水酸化マグネシウムの配合FA ?
r、3 (1屯骨部(比較例6)、0.5 fi量部(
比較例7)に変える以外は実施例2と同様に処理した。
Prescription Polyvinyl chloride 60 loo DO
P 30 #Stabilizer lN Epoxy plasticizer 2 Hydroxide Madafusiwam 6 # (10) Comparative example 6
and 7 In Example 2, the formulation FA of magnesium hydroxide?
r, 3 (1 tonne part (Comparative Example 6), 0.5 fi part (
The process was carried out in the same manner as in Example 2 except that Comparative Example 7) was used.

対照例2 実施t+!l 2の処方において、水酸化マグネシウム
を配合しないでフィルム金作成した。
Control example 2 Implementation t+! In the formulation of 12, film gold was prepared without incorporating magnesium hydroxide.

以上の結果を第2表に示す。The above results are shown in Table 2.

Claims (1)

【特許請求の範囲】 熱可塑性樹脂100重量部に、 tiJ  BET比:&m1l(2〜15mン′デ(1
1)1!L子顕微鏡法による単結晶の大きさが0.3〜
2、 0  μ fija  2次粒子径の2μ以下が9oチ以上で、t
Vl  表面処理剤で処理した、 水酸化マグネシウム1〜20重量部を配合した農業用フ
ィルム用樹脂組成物。
[Claims] To 100 parts by weight of thermoplastic resin, tiJ BET ratio: &ml (2 to 15 m' de (1
1)1! Single crystal size by L-son microscopy is 0.3~
2, 0μ fija The secondary particle diameter is 2μ or less and is 9o or more, t
Vl An agricultural film resin composition treated with a surface treatment agent and containing 1 to 20 parts by weight of magnesium hydroxide.
JP10215383A 1983-06-08 1983-06-08 Resin composition for agricultural film Granted JPS59226037A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10215383A JPS59226037A (en) 1983-06-08 1983-06-08 Resin composition for agricultural film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10215383A JPS59226037A (en) 1983-06-08 1983-06-08 Resin composition for agricultural film

Publications (2)

Publication Number Publication Date
JPS59226037A true JPS59226037A (en) 1984-12-19
JPH0350791B2 JPH0350791B2 (en) 1991-08-02

Family

ID=14319783

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10215383A Granted JPS59226037A (en) 1983-06-08 1983-06-08 Resin composition for agricultural film

Country Status (1)

Country Link
JP (1) JPS59226037A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS624067A (en) * 1985-06-22 1987-01-10 オカモト株式会社 Agricultural transparent polyvinyl chloride group resin film
JPH02245045A (en) * 1989-03-17 1990-09-28 Achilles Corp Agricultural covering material
JPH03137145A (en) * 1989-10-23 1991-06-11 Mitsubishi Petrochem Co Ltd Ethylene-vinyl acetate copolymer composition
WO2000024832A1 (en) * 1998-10-26 2000-05-04 Gerd Hugo Flat thermal protection element

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5912595B2 (en) * 2012-02-02 2016-04-27 神島化学工業株式会社 Infrared absorber and heat insulating resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS624067A (en) * 1985-06-22 1987-01-10 オカモト株式会社 Agricultural transparent polyvinyl chloride group resin film
JPH02245045A (en) * 1989-03-17 1990-09-28 Achilles Corp Agricultural covering material
JPH03137145A (en) * 1989-10-23 1991-06-11 Mitsubishi Petrochem Co Ltd Ethylene-vinyl acetate copolymer composition
WO2000024832A1 (en) * 1998-10-26 2000-05-04 Gerd Hugo Flat thermal protection element

Also Published As

Publication number Publication date
JPH0350791B2 (en) 1991-08-02

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