JPS6234066B2 - - Google Patents
Info
- Publication number
- JPS6234066B2 JPS6234066B2 JP54108979A JP10897979A JPS6234066B2 JP S6234066 B2 JPS6234066 B2 JP S6234066B2 JP 54108979 A JP54108979 A JP 54108979A JP 10897979 A JP10897979 A JP 10897979A JP S6234066 B2 JPS6234066 B2 JP S6234066B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- parts
- fog
- vinyl chloride
- chloride resin
- 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.)
- Expired
Links
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 13
- 229920005989 resin Polymers 0.000 claims description 13
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 239000004014 plasticizer Substances 0.000 claims description 7
- 239000003381 stabilizer Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000010408 film Substances 0.000 description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000004800 polyvinyl chloride Substances 0.000 description 7
- 229920000915 polyvinyl chloride Polymers 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- -1 glycerin fatty acid ester Chemical class 0.000 description 6
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 4
- 239000004147 Sorbitan trioleate Substances 0.000 description 4
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 235000019337 sorbitan trioleate Nutrition 0.000 description 4
- 229960000391 sorbitan trioleate Drugs 0.000 description 4
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 3
- 239000001570 sorbitan monopalmitate Substances 0.000 description 3
- 229940031953 sorbitan monopalmitate Drugs 0.000 description 3
- 239000001587 sorbitan monostearate Substances 0.000 description 3
- 235000011076 sorbitan monostearate Nutrition 0.000 description 3
- 229940035048 sorbitan monostearate Drugs 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000001589 sorbitan tristearate Substances 0.000 description 2
- 235000011078 sorbitan tristearate Nutrition 0.000 description 2
- 229960004129 sorbitan tristearate Drugs 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- PZQBWGFCGIRLBB-NJYHNNHUSA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O PZQBWGFCGIRLBB-NJYHNNHUSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000006084 composite stabilizer Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 229950011392 sorbitan stearate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009423 ventilation Methods 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)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は農業用ポリ塩化ビニルフイルムに関す
るものである。更に詳しくは、フイルム相互間に
おける粘着性が少なく、しかもハウス又はトンネ
ルに施工する際の高周波接着性が良好で水滴がつ
きにくゝ朝夕の霧発生を減少できる農業用塩化ビ
ニル系樹脂フイルムに関するものである。
ポリ塩化ビニル樹脂を主成分とした農業用フイ
ルムは、水滴防止性、強靭性、作業性、経済性等
の点から可塑剤を含有するフイルムが一般に用い
られているが、可塑剤を含有していると、使用中
に可塑剤自体又は水滴防止剤や他の添加助剤等の
物質がフイルム表面に移行し、その結果フイルム
表面がべたつき、作業性は低下し、又フイルム表
面にはほこりが付着し易い。又フイルムで覆われ
たハウス又はトンネル内では、土壌中の水分が蒸
発して覆つているフイルム表面に凝集してできる
水滴のためのくもりが透明性の悪化を来たした
り、水滴落下による幼芽を痛めたり、作物に対す
る病害発生など好ましくない現象を引きおこす。
そこで従来かゝる悪影響を除くため、水滴防止
効果を与えるためのいわゆる防曇剤として界面活
性剤、例えばグリセリン脂肪酸エステル、ソルビ
タン脂肪酸エステル等を添加練込んだフイルム又
はシートが一般に用いられている。しかしこれら
一般に用いられている界面活性剤では、朝方及び
夕方の外気温変化に伴うハウス内の霧発生を減少
させることはできない。霧発生中は見通しが悪く
作業性が低下するので、需要家からの霧発生減少
の要望は極めて強い。
本発明者らは、この様な従来の農業用塩化ビニ
ル樹脂フイルムのもつ欠点を改良し、防滴効果が
持続し、かつ霧発生を減少できる極めて良好なフ
イルムを得ることに成功した。
そもそも霧が発生する条件としては、ハウス内
の水蒸気が飽和蒸気圧以上に成ることであり、こ
れを防ぐための手段として流滴剤によるフイルム
内面の凝縮水の早期除去が必要である。霧の発生
は夕方発生する霧と朝方発生する霧とがあるが、
夕方発生する霧は、夕方になると外気温が急に下
り始めると共にフイルム温度も低下し、フイルム
面とハウス内の温度差を生じ、ハウス内の暖かい
空気が温度の低く成つたフイルム内面に接触して
降下流霧となつて発生するものである。又、朝方
発生する霧は、日の出と共に太陽の直射日光によ
りまず地温が急に上昇し、地表と地表附近の空気
に温度差を生じて蒸発霧となつて発生するもので
あり、またこれと共にフイルム内面のうすい流滴
の被膜も直射日光のために加熱され移流霧と成つ
て発生するものも加わる。これらの霧発生をおさ
える方法としては、従来はフイルムを着色し防曇
性を悪くする方法、マルチング裁培や多潅水をさ
けたり、又換気して外温に近づける方法や加温し
て空気の飽和点を上げる方法などの手段を講じて
いるのが現状である。
本発明は、塩化ビニル樹脂、可塑剤、安定剤の
基本成分に、(イ)ソルビタンと高級脂肪酸とのエス
テルで1分子当り水酸基を1〜2.5有する化合物
と、(ロ)HLB6以上の界面活性剤とを、(イ)と(ロ)の比
率が4:1〜1:4で、かつ(イ)と(ロ)の合計部数が
塩化ビニル樹脂100部に対して1〜3部含有させ
たことを特徴とする塩化ビニル系樹脂フイルムで
ある。
本発明の基本成分として用いられる塩化ビニル
樹脂としては、塩化ビニル単独重合体及び塩化ビ
ニルを主体とした共重合体、例えば塩化ビニルと
酢酸ビニル、塩化ビニリデン、エチレン、プロピ
レン等との共重合体があげられる。又、可塑剤と
しては、フタル酸エステル類、脂肪酸エステル
類、エポキシ類、リン酸エステル類、ポリグリコ
ールエステル類があげられ、これらは単独でで
も、又、2種以上を混合しても用いることもでき
る。この可塑剤は塩化ビニル樹脂100重量部に対
し30〜60重量部の割合で用いられる。これより多
いか又少ないと農業用フイルムとしては実用的で
ない。安定剤としては、無機鉛塩、金属石ケン
類、有機スズ系安定剤などがあり、これ等の安定
剤は単独で使用しても良いし、数種を組合せて使
用しても良い。
以上の基本成分の他、助剤として酸化防止剤、
紫外線吸収剤、有機キレーター、顔料、滑剤、殺
菌剤などを基本成分に含有させて使用することが
できる。
本発明において基本成分に配合される○イソルビ
タン高級脂肪酸エステル(水酸基数1〜2)の例
としては、ソルビタントリオレエート系
(HLB1.8)、ソルタンジステアレート系
(HLB2.5)、ソルビタントリステアレート系
(HLB2.1)のものが挙げられる。これらのHLBは
全て6より小である。脂肪酸基のC数は12以上好
ましくは16以上である。
○イHIB6以上の界面活性剤の例としては、ソル
ビタンモノ脂肪酸エステル(脂肪酸のC数12〜
18)、多価アルコール脂肪酸エステル(脂肪酸の
C数12〜18)、これらエステルのエチレンオキサ
イド(EO)付加物(脂肪酸C数11以下でもEO付
加によりHLB6以上となつたもの含む)、芳香族
カルボン酸エステル等をあげることができる。
HLB6より小のもの例えばソルビタンモノステア
レートを併用すると、流滴性が悪く実用的でな
い。
これらを基本成分に配合するに当つては、各別
に混合してもよいが、予め(イ)と(ロ)を所定比(1:
4〜4:1)に混合しておいて塩化ビニル樹脂
100重量部当り1〜3重量部を混合してもよい。
(イ)と(ロ)の混合比は1:1〜7:3が特に好まし
い。
(イ)と(ロ)の合計配合部数が1重量部未満では効果
が少なく、3重量部よりも多いと滲み出し現象を
生じ易くて品質低下をまねく。(イ)のみを使用する
と防曇効果の発現は非常に遅く、フイルム表面に
凝集して出来る水滴を早期に除去することは困難
であり、水滴防止性のみならず作業性を悪くし、
実用にたえない。(ロ)のみを使うとその界面活性剤
がフイルム表面に滲出し、べとつき、ごみ付着等
フイルム外面に悪影響を与え、霧発生量を減少さ
せることが出来ない。(イ)と(ロ)を前記比率で配合す
ることにより、水滴防止性、作業性を低下するこ
とがなく、又、フイルム外面も良好となり、霧発
生量を減少させることができる。
本発明の農業用塩化ビニル樹脂フイルムは前記
した基本成分の混合物に(イ)と(ロ)を所定量加え、よ
く混合したのちカレンダーロールを用いてフイル
ム成型することによつて製造される。この様にし
て得られるフイルムは長期間にわたつてフイルム
相互間における粘着性が少なく、しかもハウス又
はトンネルに施工する際の高周波接着性が良好
で、水滴がつきにくゝ朝夕の霧発生量が少なく作
業性を改善することが出来る。
実施例1〜5、比較例1〜5
平均重合度()1300のポリ塩化ビニル100重
量部(以下部と略記)に、下記第1表に示す割合
のソルビタントリオレエート、エチレンオキサイ
ド(EO)付加ソルビタンモノステアレート
(HLB15.7)、またはソルビタンモノパルミテート
(HLB9.2)、及びフタル酸ジオクチル45部、リン
酸トリクレジル5部、エポキシ樹脂イ部、エポキ
シ化大豆油4部、Ba−Zn系の複合安定剤2部、
ビスアミド0.3部からなる組成物をよく混合し、
28インチ逆L字カレンダーロールを用い、190℃
において厚さ0.1m/mのフイルムに成型後、密
閉型ハウスで屋外曝露を秋(10月)より行い、肉
眼観察により霧発生状況を評価し、第1表に示す
様な結果を得た。
又、6ケ月後のフイルムで高周波ミシン加工性
を評価し、その結果を第1表に示す。
The present invention relates to polyvinyl chloride film for agricultural use. More specifically, it relates to an agricultural vinyl chloride resin film that has low adhesion between films, has good high-frequency adhesion when applied to greenhouses or tunnels, is resistant to water droplets, and can reduce fog formation in the morning and evening. It is. Agricultural films based on polyvinyl chloride resin are generally used that contain plasticizers for their water drop resistance, toughness, workability, economic efficiency, etc. If this happens, the plasticizer itself, water drop preventive agent, and other additives will migrate to the film surface during use, resulting in the film surface becoming sticky, reducing workability, and dust adhering to the film surface. Easy to do. In addition, in a greenhouse or tunnel covered with a film, moisture in the soil evaporates and aggregates on the surface of the covering film, resulting in cloudy water droplets that deteriorate transparency and cause young buds to form due to falling water droplets. This causes undesirable phenomena such as damage to crops and the development of diseases to crops. Therefore, in order to eliminate such adverse effects, a film or sheet is generally used in which a surfactant such as glycerin fatty acid ester, sorbitan fatty acid ester, etc. is added and kneaded as a so-called antifogging agent to provide a water droplet prevention effect. However, these commonly used surfactants cannot reduce the occurrence of fog inside greenhouses due to changes in outside temperature in the morning and evening. During fog, visibility is poor and work efficiency is reduced, so there is an extremely strong demand from customers to reduce fog. The present inventors have succeeded in improving the shortcomings of conventional agricultural vinyl chloride resin films and obtaining an extremely good film that has a sustained drip-proof effect and can reduce fog generation. In the first place, the condition for the generation of fog is that the water vapor in the house reaches a saturated vapor pressure or higher, and as a means to prevent this, it is necessary to quickly remove the condensed water on the inner surface of the film using a droplet agent. There are two types of fog: fog that occurs in the evening and fog that occurs in the morning.
Fog that forms in the evening, as the outside temperature starts to drop suddenly in the evening, the film temperature also drops, creating a temperature difference between the film surface and the inside of the greenhouse, and the warm air inside the greenhouse comes into contact with the cooler inner surface of the film. It is generated as downdrift fog. Fog that occurs in the morning is caused by the sudden rise in ground temperature due to direct sunlight at sunrise, which creates a temperature difference between the ground surface and the air near the ground surface, which becomes evaporative fog. The thin film of droplets on the inner surface is also heated by direct sunlight, and the advection fog is added to the film. Conventional methods for suppressing the formation of fog have been to color the film to make it less fog-proof, to avoid mulching and watering, to bring ventilation closer to the outside temperature, and to warm the air to make it less foggy. Currently, measures such as raising the saturation point are being taken. The present invention includes, as basic components of vinyl chloride resin, plasticizer, and stabilizer, (a) an ester of sorbitan and higher fatty acid having 1 to 2.5 hydroxyl groups per molecule, and (b) a surfactant with an HLB of 6 or higher. and, the ratio of (a) and (b) is 4:1 to 1:4, and the total number of parts of (a) and (b) is 1 to 3 parts per 100 parts of vinyl chloride resin. This is a vinyl chloride resin film characterized by: The vinyl chloride resin used as the basic component of the present invention includes vinyl chloride homopolymers and copolymers mainly composed of vinyl chloride, such as copolymers of vinyl chloride and vinyl acetate, vinylidene chloride, ethylene, propylene, etc. can give. Examples of plasticizers include phthalate esters, fatty acid esters, epoxies, phosphate esters, and polyglycol esters, and these can be used alone or in combination of two or more. You can also do it. This plasticizer is used in an amount of 30 to 60 parts by weight per 100 parts by weight of the vinyl chloride resin. If the amount is more or less than this, it is not practical as an agricultural film. Stabilizers include inorganic lead salts, metal soaps, organic tin stabilizers, and the like, and these stabilizers may be used alone or in combination. In addition to the above basic ingredients, antioxidants are used as auxiliary agents.
It can be used by including ultraviolet absorbers, organic chelators, pigments, lubricants, bactericides, etc. in the basic ingredients. Examples of isorbitan higher fatty acid esters (with 1 to 2 hydroxyl groups) that are blended into the basic ingredients in the present invention include sorbitan trioleate (HLB 1.8), sorbitan distearate (HLB 2.5), and sorbitan trioleate (HLB 1.8). Examples include stearate type (HLB2.1). These HLBs are all less than 6. The C number of the fatty acid group is 12 or more, preferably 16 or more. ○ Examples of surfactants with HIB6 or higher include sorbitan monofatty acid esters (fatty acid C number 12~
18), polyhydric alcohol fatty acid esters (fatty acid C number 12-18), ethylene oxide (EO) adducts of these esters (including fatty acids with C11 or less but with HLB of 6 or more due to EO addition), aromatic carbon Examples include acid esters.
If a substance smaller than HLB6, such as sorbitan monostearate, is used in combination, droplet flow is poor and impractical. When blending these into the basic ingredients, they may be mixed separately, but (a) and (b) may be mixed in advance in a predetermined ratio (1:
4 to 4:1) and then add vinyl chloride resin.
You may mix 1 to 3 parts by weight per 100 parts by weight.
The mixing ratio of (a) and (b) is particularly preferably 1:1 to 7:3. If the total number of parts (a) and (b) is less than 1 part by weight, the effect will be small, and if it is more than 3 parts by weight, oozing will tend to occur, leading to a decrease in quality. If only (a) is used, the antifogging effect will develop very slowly, and it will be difficult to quickly remove water droplets that aggregate on the film surface, impairing not only water droplet prevention properties but also workability.
Not practical. If only (b) is used, the surfactant will ooze out onto the film surface, causing adverse effects on the film's outer surface such as stickiness and dust adhesion, making it impossible to reduce the amount of fog generated. By blending (a) and (b) in the above ratio, water drop prevention properties and workability will not be reduced, the outer surface of the film will also be good, and the amount of fog generated can be reduced. The agricultural vinyl chloride resin film of the present invention is produced by adding predetermined amounts of (a) and (b) to the mixture of the basic components described above, mixing well, and then forming the film into a film using a calendar roll. The film obtained in this way has low adhesion between the films over a long period of time, has good high-frequency adhesion when applied to greenhouses or tunnels, prevents water droplets from forming, and reduces the amount of fog generated in the morning and evening. It is possible to improve workability with a small amount. Examples 1 to 5, Comparative Examples 1 to 5 Sorbitan trioleate and ethylene oxide (EO) were added to 100 parts by weight (hereinafter abbreviated as parts) of polyvinyl chloride with an average degree of polymerization () 1300 in the proportions shown in Table 1 below. Sorbitan monostearate (HLB15.7) or sorbitan monopalmitate (HLB9.2), 45 parts of dioctyl phthalate, 5 parts of tricresyl phosphate, 1 part of epoxy resin, 4 parts of epoxidized soybean oil, Ba-Zn system 2 parts of a composite stabilizer of
Mix well a composition consisting of 0.3 parts of bisamide;
190℃ using a 28-inch inverted L-shaped calender roll
After being formed into a film with a thickness of 0.1 m/m, it was exposed outdoors in a closed house starting in autumn (October), and the fog formation was evaluated by visual observation, and the results shown in Table 1 were obtained. Further, the high frequency sewing machine processability of the film after 6 months was evaluated, and the results are shown in Table 1.
【表】
尚、上記及び以下に示す本発明の実施例の何れ
の場合においても、流滴性、防曇性、ブルーム性
等についても観察した結果全く問題なく優れたも
のであつた。
実施例6〜8、比較例6〜7
=1300のポリ塩化ビニル100部に下記第2表
に示す部数のソルビタントリステアレート
(HLB2.1)、EO付加ソルビタンモノステアレー
ト、またはソルビタンモノパルミテートとその他
は実施例1と同様な可塑剤、安定剤、滑剤からな
る組成物から成膜し、屋外暴霧により霧発生状況
を観察評価し、第2表に示す結果を得た。[Table] In addition, in all of the examples of the present invention shown above and below, the droplet flow properties, anti-fogging properties, bloom properties, etc. were also observed, and the results showed that they were excellent without any problems. Examples 6 to 8, Comparative Examples 6 to 7 = 100 parts of polyvinyl chloride of 1300 and the parts of sorbitan tristearate (HLB2.1), EO-added sorbitan monostearate, or sorbitan monopalmitate shown in Table 2 below A film was formed from a composition consisting of a plasticizer, a stabilizer, and a lubricant that were otherwise the same as in Example 1, and the fog generation was observed and evaluated by outdoor fogging, and the results shown in Table 2 were obtained.
【表】
実施例9〜13、比較例8〜10
=1300のポリ塩化ビニル100部に下記第3表
に示す部数の配合剤を加え、その他は実施例1と
同様配合で成膜し、屋外暴露を行い肉眼観察によ
り評価し、第3表に示す結果を得た。[Table] Examples 9 to 13, Comparative Examples 8 to 10 = 100 parts of 1300 polyvinyl chloride and the number of parts shown in Table 3 below were added to form a film using the same formulation as in Example 1. Exposure was carried out and evaluation was made by visual observation, and the results shown in Table 3 were obtained.
【表】
比較例8と9は流滴性が悪く、また比較例10は
流滴性は良いがブルーム性(表面に白粉が出る現
象)が激しく、何れも実用に堪えなかつた。
比較例 11〜19
=1300のポリ塩化ビニル100部に下記第4表
に示す割合のソルビタントリオレエート、ソルビ
タントリステアレート、ソルビタンステアレート
EO付加(HLB15.7)、またはソルビタンモノパル
ミテート(HLB6.7)を用いその他は実施例1と
同様配合から成膜し、屋外暴露を行い肉眼観察に
より評価し、第4表に示すような結果を得た。[Table] Comparative Examples 8 and 9 had poor droplet flow properties, and Comparative Example 10 had good droplet flow properties but had severe blooming (a phenomenon in which white powder appears on the surface), and both were unsuitable for practical use. Comparative Examples 11 to 19 = 100 parts of 1300 polyvinyl chloride and sorbitan trioleate, sorbitan tristearate, and sorbitan stearate in the proportions shown in Table 4 below.
A film was formed from the same formulation as in Example 1 using EO addition (HLB15.7) or sorbitan monopalmitate (HLB6.7), and was exposed outdoors and evaluated by visual observation. Got the results.
【表】
比較例 20〜25
=1300のポリ塩化ビニル100重量部に第5表
に示す配合剤を1.8PHR添加し、実施例1と同様
配合から成膜し、3ケ月間の屋外暴露を行い内眼
観察により評価し、第5表に示すような結果を得
た。[Table] Comparative Examples 20-25 = 1.8 PHR of the compounding agent shown in Table 5 was added to 100 parts by weight of 1300 polyvinyl chloride, a film was formed from the same formulation as in Example 1, and exposed outdoors for 3 months. Evaluation was performed by intraocular observation, and the results shown in Table 5 were obtained.
【表】【table】
Claims (1)
に、○イソルビタンと高級脂肪酸とのエステルで1
分子当り水酸基を1〜2個有する化合物と○ロ
HLB6.0以上の界面活性剤とを、(イ)と(ロ)の比率が
4:1〜1:4で、かつ(イ)と(ロ)の合計部数が塩化
ビニル樹脂100部に対して1〜3部含有させたこ
とを特徴とする農業用塩化ビニル系樹脂フイル
ム。1 The basic components of vinyl chloride resin, plasticizers, and stabilizers include ○ esters of isorbitan and higher fatty acids.
Compounds with 1 to 2 hydroxyl groups per molecule and ○ro
A surfactant with an HLB of 6.0 or higher, the ratio of (a) and (b) is 4:1 to 1:4, and the total number of parts of (a) and (b) is based on 100 parts of vinyl chloride resin. An agricultural vinyl chloride resin film containing 1 to 3 parts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10897979A JPS5632533A (en) | 1979-08-27 | 1979-08-27 | Vinyl chloride resin film for agriculture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10897979A JPS5632533A (en) | 1979-08-27 | 1979-08-27 | Vinyl chloride resin film for agriculture |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5632533A JPS5632533A (en) | 1981-04-02 |
JPS6234066B2 true JPS6234066B2 (en) | 1987-07-24 |
Family
ID=14498495
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10897979A Granted JPS5632533A (en) | 1979-08-27 | 1979-08-27 | Vinyl chloride resin film for agriculture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5632533A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58206651A (en) * | 1982-05-26 | 1983-12-01 | Kanegafuchi Chem Ind Co Ltd | Crosslinked vinyl chloride-based resin composition |
JPS5998144A (en) * | 1982-11-26 | 1984-06-06 | Mitsubishi Monsanto Chem Co | Anti-fogging synthetic resin film |
JPS59115989A (en) * | 1982-12-22 | 1984-07-04 | Misawa Homes Co Ltd | Underground heat storing and collecting device |
JPS60229951A (en) * | 1984-04-27 | 1985-11-15 | Mitsubishi Kasei Vinyl Co | Antifogging synthetic resin film |
JP2659995B2 (en) * | 1988-05-18 | 1997-09-30 | シーアイ化成株式会社 | Antifogging vinyl chloride resin film |
JPH04238029A (en) * | 1991-01-22 | 1992-08-26 | Mitsubishi Kasei Vinyl Co | Olefinic agricultural laminated film |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5045846A (en) * | 1973-08-31 | 1975-04-24 | ||
JPS5242820A (en) * | 1975-02-17 | 1977-04-04 | Toyama Chem Co Ltd | Novel process for preparation of 2-chloroethylhydrogen-2-chloroethylph osphonate metal salt |
JPS5269954A (en) * | 1975-12-09 | 1977-06-10 | Kao Corp | Non-rigid polyvinyl chloride resin compositions |
-
1979
- 1979-08-27 JP JP10897979A patent/JPS5632533A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5045846A (en) * | 1973-08-31 | 1975-04-24 | ||
JPS5242820A (en) * | 1975-02-17 | 1977-04-04 | Toyama Chem Co Ltd | Novel process for preparation of 2-chloroethylhydrogen-2-chloroethylph osphonate metal salt |
JPS5269954A (en) * | 1975-12-09 | 1977-06-10 | Kao Corp | Non-rigid polyvinyl chloride resin compositions |
Also Published As
Publication number | Publication date |
---|---|
JPS5632533A (en) | 1981-04-02 |
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