JPS6227452A - Composition for agricultural vinyl resin sheet - Google Patents

Composition for agricultural vinyl resin sheet

Info

Publication number
JPS6227452A
JPS6227452A JP60165566A JP16556685A JPS6227452A JP S6227452 A JPS6227452 A JP S6227452A JP 60165566 A JP60165566 A JP 60165566A JP 16556685 A JP16556685 A JP 16556685A JP S6227452 A JPS6227452 A JP S6227452A
Authority
JP
Japan
Prior art keywords
weight
vinyl chloride
parts
production
plasticizer
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
JP60165566A
Other languages
Japanese (ja)
Other versions
JPS6249308B2 (en
Inventor
Shigehiro Koga
重宏 古賀
Taku Fukuda
卓 福田
Tetsuo Ando
安東 哲雄
Masaaki Fukuda
福田 正明
Masatake Ishibashi
石橋 正剛
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.)
JNC Corp
Original Assignee
Chisso Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chisso Corp filed Critical Chisso Corp
Priority to JP60165566A priority Critical patent/JPS6227452A/en
Publication of JPS6227452A publication Critical patent/JPS6227452A/en
Publication of JPS6249308B2 publication Critical patent/JPS6249308B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/25Greenhouse technology, e.g. cooling systems therefor

Abstract

PURPOSE:To provide the titled compsn. for the production of sheets, which has good blocking resistance and excellent workability and is suitable for use in the production of covering materials for a greenhouse, by blending a plasticizer with a vinyl chloride/allyl (meth)acrylate copolymer having a specified composition. CONSTITUTION:30-70pts.wt. plasticizer (e.g. diethylhexyl phthalate or epoxidized soybean oil) is mixed with 100pts.wt. copolymer composed of 79-99.99wt% vinyl chloride and 3-0.01wt% allyl (meth)acrylate to obtain the desired compsn. for the production of agricultural vinyl resin sheet. If desired, thermal stabilizer, anti-stick agent, ultraviolet absorber, antioxidant, inorg. filler, etc. may be added. The resulting compsn. does not cause blocking phenomenon. Hence, when the resulting sheet is used as a inner curtain, the drawing operation of the curtain can be easily conducted day and night.

Description

【発明の詳細な説明】 〔技術の分野〕 本発明は、耐ブロッキング性が良好なる可塑化塩化ビニ
ル樹脂系の農業用ビニル樹脂シート用組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Technology] The present invention relates to a composition for agricultural vinyl resin sheets based on plasticized vinyl chloride resin, which has good blocking resistance.

〔従来の技術〕[Conventional technology]

塩化ビニル樹脂はそのすぐれた機械的特性、経済性によ
り広汎に農業用資材として特にフィルム、シートは温室
用被覆剤として賞月されている。
Due to its excellent mechanical properties and economic efficiency, vinyl chloride resin is widely used as an agricultural material, particularly as films and sheets for greenhouse coatings.

しかし可塑化塩化ビニル樹脂は、可塑剤の滲み出し、そ
の他の原因により、フィルム又はシート同士がブロッキ
ング現象を起し、フィルム、シートの加工時に作業性が
低下する。又1業用被覆材として使用した場合特に内張
カーテン用として使用した場合、朝タカーテンの開閉に
多大の労力を要し、従事者よりはその改善が強く要望さ
れていた。
However, plasticized vinyl chloride resin causes a blocking phenomenon between films or sheets due to leaching of the plasticizer or other causes, resulting in reduced workability during processing of the film or sheet. Furthermore, when used as a covering material for a single industry, especially when used as a lining curtain, a great deal of effort is required to open and close the curtain in the morning, and workers have strongly requested an improvement.

従来この用途分野には、■梨地のシボを転写したもの、
■ビスフェノール変性ジアクリレートと塩化ビニルとの
共重合体をベースとしたフィルムシート、■高重合度塩
化ビニル樹脂をベースにしたもの、■可塑剤の部数をへ
らしてベタツキを少なくしたもの等々が提案されている
Conventionally, in this field of application, there are: - those with the texture of satin-like textures transferred;
■ Film sheets based on copolymers of bisphenol-modified diacrylate and vinyl chloride, ■ Film sheets based on highly polymerized vinyl chloride resin, ■ Film sheets with less stickiness by reducing the number of plasticizers, etc. have been proposed. ing.

■梨地シボフィルムはベタツキは改善されるもののシボ
面が粉塵で汚染されやすく一度汚染されると洗滌されに
くいという欠点がある。
- Satin grained film improves stickiness, but has the disadvantage that the grained surface is easily contaminated with dust and is difficult to wash once contaminated.

■また、ビスフェノール変性ジアクリレートと塩化ビニ
ルとの共重合体をベースとしたフィルムは製造時のベタ
ツキの少ない点は良好なるものの。
■Furthermore, a film based on a copolymer of bisphenol-modified diacrylate and vinyl chloride is good in that it is less sticky during production.

使用時水分がフィルム全面に付着、全くスベリ性を失っ
てカーテンの開閉が出来なくなるという欠点がある。
When in use, moisture adheres to the entire surface of the film, resulting in a complete loss of slipperiness, making it impossible to open and close the curtain.

■高重合度堪化ビニル樹脂をベースにしたものは上記欠
点はなくなるがカレンダー又は押出機によるフィルム製
造時の生産性の低下、或いは原料費のコストアップ等の
問題点がある。
(2) Products based on highly polymerized vinyl resins do not have the above-mentioned drawbacks, but they still have problems such as reduced productivity during film production using a calendar or extruder, and increased raw material costs.

■可塑剤ffl数を減らしてベタツキをなくした場合、
フィルムの柔軟性、引裂強度、耐寒性等が低下する。
■If the stickiness is eliminated by reducing the number of plasticizer ffl,
The flexibility, tear strength, cold resistance, etc. of the film decrease.

〔発明の目的〕[Purpose of the invention]

本発明者等は、環化ビニル樹脂の透明性や耐候性その他
の機械的特性を損うことなく農業用被覆材特に内張カー
テン用の作業性を改善することを目的に鋭意検討の結果
、塩化ビニル97.00〜98.00重量%と(メタ)
アクリル酸アクリル3.00〜0゜0.01重量%より
成る共重合体100重量部に対して可塑剤30〜80重
量部その他必要な熱安定剤、流滴剤、紫外線防止剤を適
当量加えた樹脂組成物より作られるフィルム、シートが
極めて有効であることを見出し本発明を完成するに至っ
た。
As a result of intensive studies, the present inventors aimed to improve the workability of agricultural covering materials, especially lining curtains, without impairing the transparency, weather resistance, and other mechanical properties of cyclized vinyl resin. Vinyl chloride 97.00-98.00% by weight (meth)
To 100 parts by weight of a copolymer consisting of 3.00 to 0.01% by weight of acrylic acid, add 30 to 80 parts by weight of a plasticizer and appropriate amounts of a necessary heat stabilizer, droplet agent, and UV inhibitor. The present inventors discovered that films and sheets made from resin compositions made from these resin compositions are extremely effective, and have completed the present invention.

以上の記述から明らかなように、本発明の目的は、フィ
ルム若しくはシートに成形した際にブロッキング性の良
好な農業用ビニル樹脂シート用組成物ならびに、該シー
トを提供することである。
As is clear from the above description, an object of the present invention is to provide a composition for an agricultural vinyl resin sheet that exhibits good blocking properties when formed into a film or sheet, and the sheet.

〔発明の構成・効果〕[Structure and effects of the invention]

本発明は、下記(1)の主要III成を有する。 The present invention has the following main feature (1).

(1)塩化ビニル97.0〜99.99重量%とアクリ
ル酸アリルおよび/又はメタアクリル酸アリル3.0〜
0.01重量%よりなる共重合体100重量部および可
塑剤30〜70重量部よりなる農業用ビニル樹脂シート
用組成物。
(1) 97.0-99.99% by weight of vinyl chloride and 3.0-99.99% by weight of allyl acrylate and/or allyl methacrylate
An agricultural vinyl resin sheet composition comprising 100 parts by weight of a copolymer of 0.01% by weight and 30 to 70 parts by weight of a plasticizer.

本発明に用いられる上述の塩化ビニル系共重合体は通常
の懸濁重合によって製造されるがアクリル酸アリル及び
/又はメタアクリル酸アリル以下(メタ)アクリル酸ア
リル)の含有量が3.0重量%以上になるとテトラハイ
ドロフラン不溶分が増加し、加工時の流動性が著しく悪
くなると共に熱安定性も悪くなり、本用途には適さない
、一方0゜01重量%未満では耐ブロッキング性が改善
されない0通常0.01〜3.0重量%の範囲で実用性
があるが最も適当な範囲は0.03〜1.0重量%であ
る。
The above-mentioned vinyl chloride copolymer used in the present invention is produced by ordinary suspension polymerization, and the content of allyl acrylate and/or allyl methacrylate (allyl meth)acrylate is 3.0% by weight. If it exceeds 0.01% by weight, the insoluble content of tetrahydrofuran will increase, resulting in significantly poor fluidity during processing and poor thermal stability, making it unsuitable for this purpose.On the other hand, if it is less than 0.01% by weight, blocking resistance will improve. Usually, it is practical in the range of 0.01 to 3.0% by weight, but the most suitable range is 0.03 to 1.0% by weight.

本発明に用いられる可塑剤としては、通常塩化ビニル樹
脂用に用いられる可塑剤ならば特に制限はなくフタル酸
エステル系、脂肪酸エステル、リン酸エステル系、エポ
キシ系等の可塑剤が用いられる。
The plasticizer used in the present invention is not particularly limited as long as it is a plasticizer normally used for vinyl chloride resins, and phthalate-based, fatty acid ester, phosphoric ester-based, epoxy-based plasticizers, and the like can be used.

その量は可塑剤の可塑化効率に応じて本発明に使用する
前記共重合体100重量部に対して30〜70重量部で
ある。熱安定剤としては透明性および経済性を勘案して
主にBa−Zn系に複合安定剤ならびにCa−Zn系複
合安定剤が用いられる。
The amount thereof is 30 to 70 parts by weight based on 100 parts by weight of the copolymer used in the present invention, depending on the plasticizing efficiency of the plasticizer. As the thermal stabilizer, Ba--Zn based composite stabilizers and Ca--Zn based composite stabilizers are mainly used in consideration of transparency and economical efficiency.

流滴剤としては、ソルビタン脂肪酸エステル類、グリセ
リン高級脂肪酸エステル類、シリコンオイル、フッソ化
合物等々が用いられる。
As the droplet agent, sorbitan fatty acid esters, glycerin higher fatty acid esters, silicone oil, fluorine compounds, etc. are used.

紫外線防止剤としてはベンゾトリアゾール系化合物、ベ
ンゾフェノン系化合物が用いられる。
As the ultraviolet inhibitor, benzotriazole compounds and benzophenone compounds are used.

その他必要な酸化防止剤、無機充填剤、滑剤、顔料等は
透明塩化ビニル樹脂組成物及びそれをベースとするフィ
ルム、シートの性能を損わない範囲において適宜使用で
きる。
Other necessary antioxidants, inorganic fillers, lubricants, pigments, etc. can be used as appropriate insofar as they do not impair the performance of the transparent vinyl chloride resin composition and films and sheets based thereon.

以下、実施例によって本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1〜3、比較例1〜3 メタアクリル酸アリル0.0.O05,0,01,0,
1,1,0および5.0 fig%をそれぞれ含有する
塩化ビニル系共重合体(A、B、C,D、E、F)の各
々 100重量部に対してジエチルへキシルフタレート
(以下DOPと略)45重量部、エポキシ化大豆油2.
0重量部、トリクレジルフォスファイト(以下TCPと
略)3.0重量部、 Ba−Zn系熱安定剤2.5重量
部、流滴剤0.3重量部、紫外線防止剤(2−4ヒドロ
キシやベンゾフェノン)0,2重量部を混合、カレンダ
ー設備によってシーティンブレ、 0.10m/11の
フィルムを作った。かくして得られたフィルムについて
、ブロッキング性(1)及び(2)を測定しこれらの結
果を第1表に示した。
Examples 1-3, Comparative Examples 1-3 Allyl methacrylate 0.0. O05,0,01,0,
Diethylhexyl phthalate (hereinafter referred to as DOP) was added to 100 parts by weight of each vinyl chloride copolymer (A, B, C, D, E, F) containing 1, 1, 0 and 5.0 fig%, respectively. omitted) 45 parts by weight, epoxidized soybean oil2.
0 parts by weight, 3.0 parts by weight of tricresyl phosphite (hereinafter abbreviated as TCP), 2.5 parts by weight of Ba-Zn thermal stabilizer, 0.3 parts by weight of droplet agent, ultraviolet inhibitor (2-4 0.2 parts by weight of hydroxyl and benzophenone were mixed, and a sheet film of 0.10 m/11 was made using calendering equipment. The blocking properties (1) and (2) of the thus obtained film were measured and the results are shown in Table 1.

尚、これたの物性は次の方法によった。The physical properties of these materials were determined by the following method.

ブロッキング性(1)フィルムを間口5m、高さ2m1
長さ25mのカマポコ型のハウスに展張し、3月〜5月
にかけて朝、夕の開閉作業に際し、ブロッキングの有無
を調べた。
Blocking property (1) Film width 5m, height 2m1
It was expanded into a 25-meter-long Kamapoko-shaped house, and the presence or absence of blocking was examined during opening and closing operations in the morning and evening from March to May.

ブロッキング性(2) 50mm角のフィルム2枚を湿
らせた後重ね合わせて50g/c rn’の荷重を加え
、40”Cの恒温槽に5時間放置する。その後取出した
フィルムを23℃の恒温室で2時間冷却後、引張試験機
でハク離させ、それに要した力を測定した。
Blocking property (2) Two 50 mm square films are moistened and stacked together, a load of 50 g/c rn' is applied, and the film is left in a constant temperature bath at 40"C for 5 hours.Then, the film taken out is kept at a constant temperature of 23 °C. After cooling in a room for 2 hours, it was peeled off using a tensile tester and the force required for this was measured.

熱安定性については180℃オーブン中にフィルムをつ
り下げてその黒化時間を測定した。
As for thermal stability, the film was suspended in an oven at 180° C. and its blackening time was measured.

第−表に明らかなように、共重合体中のメタアクリル酸
アリル含有量が0.01未満の比較例1.2は、実施例
1〜3に比べて、ブロッキング性が著しく大きく該含量
が5.0%と本発明の3.0%を大幅に上回る場合、ブ
ロー2キング性は良好であるが熱安定性が大幅に低下し
て物性的バランスを失う。
As is clear from Table 1, Comparative Example 1.2 in which the content of allyl methacrylate in the copolymer was less than 0.01 had significantly greater blocking property than Examples 1 to 3. When the content is 5.0%, which is significantly higher than the 3.0% of the present invention, the blowing properties are good, but the thermal stability is significantly reduced and the physical properties are unbalanced.

実施例4、比較例4,5 塩化ビニル9i3.90重量%とポリエチレングリコー
ルジアクリレート0.1重量%よりなる共重合体(G)
、塩化ビニル99.90重量%とビスフェノール変性ジ
アクリレートo、を重量%よりなる共重合体(H)及び
共重合体Cの各々 100重量部に対してDO260重
量部、エポキシ化大豆油2.0重量部TCP 3.0重
量部、Ba−Zn系複合安定剤2,5重量部流滴剤0.
3重量部を混合、カレンダー設備によってシーテイング
0.10!l/Imのフィルムを作った。かくして得ら
れたフィルムについて実施例1〜3と同様な方法にてブ
ロッキング性(1)、(2)及び熱安定性を測定した。
Example 4, Comparative Examples 4 and 5 Copolymer (G) consisting of 3.90% by weight of vinyl chloride 9i and 0.1% by weight of polyethylene glycol diacrylate
, 260 parts by weight of DO, 2.0 parts by weight of epoxidized soybean oil per 100 parts by weight of each of copolymer (H) and copolymer C consisting of 99.90% by weight of vinyl chloride and 99.90% by weight of bisphenol-modified diacrylate o. Parts by weight TCP 3.0 parts by weight, Ba-Zn composite stabilizer 2.5 parts by weight Droplet agent 0.
Mix 3 parts by weight, sheeting 0.10 using calender equipment! A film of l/Im was made. Blocking properties (1) and (2) and thermal stability of the thus obtained film were measured in the same manner as in Examples 1 to 3.

その結果を第二衣に示す。The results are shown in the second column.

Claims (1)

【特許請求の範囲】[Claims] (1)塩化ビニル97.0〜99.99重量%とアクリ
ル酸アリルおよび/又はメタアクリル酸アリル3.0〜
0.01重量%よりなる共重合体100重量部および可
ソ剤30〜70重量部よりなる農業用ビニル樹脂シート
用組成物。
(1) 97.0-99.99% by weight of vinyl chloride and 3.0-99.99% by weight of allyl acrylate and/or allyl methacrylate
An agricultural vinyl resin sheet composition comprising 100 parts by weight of a copolymer of 0.01% by weight and 30 to 70 parts by weight of a solubilizing agent.
JP60165566A 1985-07-26 1985-07-26 Composition for agricultural vinyl resin sheet Granted JPS6227452A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60165566A JPS6227452A (en) 1985-07-26 1985-07-26 Composition for agricultural vinyl resin sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60165566A JPS6227452A (en) 1985-07-26 1985-07-26 Composition for agricultural vinyl resin sheet

Publications (2)

Publication Number Publication Date
JPS6227452A true JPS6227452A (en) 1987-02-05
JPS6249308B2 JPS6249308B2 (en) 1987-10-19

Family

ID=15814795

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60165566A Granted JPS6227452A (en) 1985-07-26 1985-07-26 Composition for agricultural vinyl resin sheet

Country Status (1)

Country Link
JP (1) JPS6227452A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01284512A (en) * 1988-05-11 1989-11-15 Chisso Corp Vinyl chloride copolymer, its production, resin composition and sheet

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01202001A (en) * 1988-02-08 1989-08-15 Fujitsu Ltd Coaxial waveguide converter

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01284512A (en) * 1988-05-11 1989-11-15 Chisso Corp Vinyl chloride copolymer, its production, resin composition and sheet
JPH0415254B2 (en) * 1988-05-11 1992-03-17 Chisso Corp

Also Published As

Publication number Publication date
JPS6249308B2 (en) 1987-10-19

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