JPS6052700A - Paper coating composition - Google Patents
Paper coating compositionInfo
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- JPS6052700A JPS6052700A JP15903883A JP15903883A JPS6052700A JP S6052700 A JPS6052700 A JP S6052700A JP 15903883 A JP15903883 A JP 15903883A JP 15903883 A JP15903883 A JP 15903883A JP S6052700 A JPS6052700 A JP S6052700A
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Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は、エチレン−酢酸ビニル共重合体(以下EVA
と記す)を使用した紙コート組成物の耐ブロッキング性
の改良にかかわるものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to ethylene-vinyl acetate copolymer (hereinafter referred to as EVA
This paper is concerned with improving the blocking resistance of paper coating compositions using paper coating compositions.
従来よりカタログ、パンフレット、広告、包装紙等多方
面の用途のものに表面光沢付与2表面保護の目的でEV
Aを使用した紙コート剤の塗布がほどこされている。こ
のような紙コート剤の組成としては、EVAに硬さ付与
、光沢付与、ブロッキング防止の目的で芳香族系石油樹
脂、ロジン及びその変成物又これらの水素添加物等が単
独もしくは混合され、添加されている。Conventionally, EV has been used to impart surface gloss to items with various uses such as catalogs, pamphlets, advertisements, wrapping paper, etc. 2 for the purpose of surface protection.
A paper coating agent using A was applied. The composition of such paper coating agents includes aromatic petroleum resins, rosin, modified products thereof, hydrogenated products thereof, etc., alone or mixed, for the purpose of imparting hardness, gloss, and preventing blocking to EVA. has been done.
しかし、近年生産性向上の為、機械の高速化が進みつつ
あり、しばしばブロッキングの問題が生じている。父、
倉庫内等での積み重ね保管中においても問題を生じやす
い。このような樹脂を多量に添加すれば、耐ブロッキン
グ性は改良されるが、コート剤の可とう性が失われ、屈
曲性、スクラッチ性等を悪くし、黄変性も犬となり、コ
ート剤として好ましくない。However, in recent years, machines have become faster in order to improve productivity, and blocking problems often occur. father,
Problems also tend to occur during stacking and storage in a warehouse or the like. If a large amount of such resin is added, blocking resistance is improved, but the flexibility of the coating agent is lost, flexibility, scratch resistance, etc. are deteriorated, and yellowing is also caused, making it undesirable as a coating agent. do not have.
本発明者らは、このような状況をふまえ、検討を加えた
結果、EVA 100重量部に対してジシクロペンタジ
ェンと無水マレイン酸の共重合体(以下D−Mポリマー
と記す)を10〜500重量部添加して成る組成物が改
良された耐ブロッキング性を有することを見出し本発明
に到達した。In view of this situation, the present inventors conducted studies and found that 10 to 10 parts of a copolymer of dicyclopentadiene and maleic anhydride (hereinafter referred to as D-M polymer) was added to 100 parts by weight of EVA. The inventors have discovered that a composition prepared by adding 500 parts by weight has improved blocking resistance, and have arrived at the present invention.
即ち、本発明はエチレン−酢酸ビニル共重合体100重
量部に対17てジシクロペンタジェンと無水マレイン酸
の共重合樹脂を10〜500重量部を有機溶剤溶液とし
て含んで成るエチレン−酢酸ビニル共重合体系紙コート
用組成物に関する。That is, the present invention provides an ethylene-vinyl acetate copolymer comprising 10 to 500 parts by weight of a copolymer resin of dicyclopentadiene and maleic anhydride to 100 parts by weight of the ethylene-vinyl acetate copolymer as an organic solvent solution. The present invention relates to a polymer-based paper coating composition.
本発明で使用するEVAとしては、特に制限されるもの
ではないが1紙に対する密着性D−Mポリマーとの相溶
性等を考慮すれば、酢酸ビニル含有量が40チ以上のも
のが好ましい。D−Mポリマーの分子量は特に制限され
るものではないが、実用上1000〜20000程度の
ものが好ましい。The EVA used in the present invention is not particularly limited, but in consideration of adhesion to paper, compatibility with the DM polymer, etc., EVA having a vinyl acetate content of 40 or more is preferable. Although the molecular weight of the DM polymer is not particularly limited, it is practically preferably about 1,000 to 20,000.
D−Mポリマーのジシクロペンタジェンと無水マレイン
酸の共重合比はジシクロペンタジェン1モルに対して無
水マレイン酸0.5〜2モルであり、このようにして得
られるポリマーは軟化点を持たないものである。D−M
ポリマーはジシクロペンタジェン、無水マレイン酸、溶
剤、触媒を反応器に入れて攪拌しながら加熱し、反応終
了後、溶剤未反応物を分離して得られる。The copolymerization ratio of dicyclopentadiene and maleic anhydride in the D-M polymer is 0.5 to 2 moles of maleic anhydride to 1 mole of dicyclopentadiene, and the polymer thus obtained has a softening point. It's something you don't have. D-M
The polymer is obtained by placing dicyclopentadiene, maleic anhydride, a solvent, and a catalyst in a reactor, heating it while stirring, and after the reaction is completed, separating unreacted substances from the solvent.
本発明の組成物は、BVAとD−Mポリマーを有機溶剤
に溶解、混合して得られるが、両者を溶解する単独溶剤
又は混合溶剤に一括して溶解する方法が簡便である。The composition of the present invention can be obtained by dissolving and mixing BVA and DM polymer in an organic solvent, but it is convenient to dissolve them all at once in a single solvent or a mixed solvent that dissolves both.
FiVAの溶剤としてはエステル類、芳香族類等、D−
Mポリマーの溶剤としてはエステル類、ケトン類、窒素
化溶剤、エーテル類等、あるいはこれらを50重量%以
」−含む混合溶剤が用いられる。FiVA solvents include esters, aromatics, etc.
As the solvent for the M polymer, esters, ketones, nitrogenated solvents, ethers, etc., or mixed solvents containing these in an amount of 50% by weight or more are used.
1!iVA 100重置部に対して、D−Mポリマー1
0〜500重吋部、好ましくは50〜300重量部が混
合されるが、500重緻部を超えると、塗膜の柔軟性が
失われ経済的にも適9〕でない。又、添加量が30重量
部以下では耐プロッギング性改良の効果が小さい。1! iVA 100 overlapping parts, DM polymer 1
0 to 500 parts by weight, preferably 50 to 300 parts by weight, are mixed, but if it exceeds 500 parts by weight, the coating film will lose its flexibility and is not economically suitable9]. Further, if the amount added is less than 30 parts by weight, the effect of improving the progging resistance is small.
溶液濃度は、コートする際のラインスピード等に合わせ
任意に選択し得るが、通常50重量%〜5重量%の範囲
で使用される。The solution concentration can be arbitrarily selected depending on the line speed during coating, etc., but is usually used in the range of 50% by weight to 5% by weight.
以下に実施例を挙げて本発明を具体的に説明する。The present invention will be specifically described below with reference to Examples.
D−Mポリマーは、次に示す処方によシジシクロベンタ
ジエン、無水マレイン酸、溶剤、触媒を反応器に入れて
攪拌しながら加熱し、反応終了後溶剤及び未反応物を分
離して得た。The D-M polymer was obtained by placing cyclobentadiene, maleic anhydride, a solvent, and a catalyst in a reactor and heating it while stirring, and after the reaction was completed, the solvent and unreacted materials were separated. .
生成物の一般性状としては、酸価(210)、分子量(
8000)、軟化点(有さす)というものであった。The general properties of the product include acid value (210), molecular weight (
8000), and the softening point.
実施例1 市販KVA (酢酸ビニル含有量60重量%。Example 1 Commercially available KVA (vinyl acetate content 60% by weight).
M1五5.R&B軟化点158℃)100重量部に対し
てD−Mポリマー100重量部を添加し、溶剤(酢酸エ
チル:トルエン=1:1(重量比))を用いて30重量
%溶液とした。このものを412パーコーターにて、試
験紙にコー)1..80℃のギヤオーブン中で20秒の
乾燥を行った。その後、恒温恒湿室(23℃、55チR
H)に24時間放置し、試験片とした。この試験片を用
いてブロッキング試験1表面光沢、密着性の測定を行っ
た。M155. 100 parts by weight of the DM polymer was added to 100 parts by weight (R&B softening point: 158°C), and a 30% by weight solution was prepared using a solvent (ethyl acetate:toluene = 1:1 (weight ratio)). Coat this on a test paper using a 412 percoater) 1. .. Drying was performed for 20 seconds in a gear oven at 80°C. After that, a constant temperature and humidity room (23℃, 55℃R)
H) for 24 hours and used as a test piece. Using this test piece, blocking test 1 surface gloss and adhesion were measured.
ブロッキング試験については、試験片を4crn×4国
に切断して、塗布面同志を合わせて50°G。For the blocking test, the test piece was cut into 4 crn x 4 pieces, and the coated surfaces were placed at 50°G.
40℃、50℃、60℃の各温度で試験を行い、とシ出
した後、常温にもどし、かるくはがした。Tests were conducted at temperatures of 40°C, 50°C, and 60°C, and after the test pieces were removed, they were returned to room temperature and peeled off briefly.
各温度における相対湿度は80チとし、荷重については
150g/dとした。表面光沢についてはスガ試験機械
KK#光沢試験機を用いて60度入射角にて測定した。The relative humidity at each temperature was 80 degrees, and the load was 150 g/d. The surface gloss was measured using a Suga Test Machine KK# gloss tester at an incident angle of 60 degrees.
密着性については、コート面にセロハンテープにチバン
製)をはり軽くこすりつけた後、素早くはぎとり、その
状態を観察した。結果については表1.2に記した。For adhesion, cellophane tape (manufactured by Chiban) was applied to the coated surface and rubbed lightly, then quickly removed and the condition observed. The results are listed in Table 1.2.
実施例2
実施例1で用いたF4A100重量部に対17てD−M
ポリマー200重駄部を添加l〜、実施例1と同様な溶
剤組成を用いて30重11%溶液とした。Example 2 17% D-M to 100 parts by weight of F4A used in Example 1
200 parts by weight of polymer was added to prepare a 30 parts by weight 11% solution using the same solvent composition as in Example 1.
試験条件2項目については実施例1に準拠した。Two test conditions were based on Example 1.
結果については、表1.2に記した。The results are listed in Table 1.2.
実施例3
実施例1で用いたKVAIQO重量部に対してD−Mポ
リマー300重量部を添加し、実施例1と同様な溶剤組
成を用いて30重量%溶液とした。Example 3 300 parts by weight of the DM polymer was added to the parts by weight of KVAIQO used in Example 1, and a 30% by weight solution was prepared using the same solvent composition as in Example 1.
試験条件1項目については、実施例1に準拠した。One test condition was based on Example 1.
結果については、表1,2に記した。The results are shown in Tables 1 and 2.
比較例1
実施例1で用いたEVA100重量部に対して、芳香族
系石油樹脂(分子量1300.R&B軟化点100℃)
100重量部を添加し、実施例1と同様な溶剤組成を用
いて30重量%溶液とした。Comparative Example 1 Aromatic petroleum resin (molecular weight 1300. R&B softening point 100°C) was added to 100 parts by weight of EVA used in Example 1.
100 parts by weight was added to prepare a 30% by weight solution using the same solvent composition as in Example 1.
試験条件2項目については、実施例1に準拠した。Two test conditions were based on Example 1.
結果については、表1,2に記した。The results are shown in Tables 1 and 2.
比較例2
実施例1で用いたEVA 100重量部に対して比較例
1で用いた芳香族系石油樹脂200重量部を添加し、実
施例1と同様な溶剤組成を用いて、30重量%溶液と1
.た。Comparative Example 2 200 parts by weight of the aromatic petroleum resin used in Comparative Example 1 was added to 100 parts by weight of EVA used in Example 1, and a 30% by weight solution was prepared using the same solvent composition as in Example 1. and 1
.. Ta.
試験条件1項目については、実施例1に準拠した。One test condition was based on Example 1.
結果については、表1.2に記した。The results are listed in Table 1.2.
比較例5
実施例1で用いたBVA100重喰部に対して比較例1
で用いた芳香族系石油樹脂200重量部を添加L、実施
例1と同様な溶剤組成を用いて30重駄チ溶液とした。Comparative Example 5 Comparative Example 1 was compared to BVA100 heavy duty part used in Example 1.
200 parts by weight of the aromatic petroleum resin used in Example 1 was added, and a 30-duty solution was prepared using the same solvent composition as in Example 1.
試験条件9項目については、実施例1に準拠した。The nine test conditions were based on Example 1.
結果については表1.2に記した。The results are listed in Table 1.2.
第1表耐ブロッキング試験結果
評価基準
(0全面にはがれのないこと
(4)全面の一部にはがれが認められるもの(3)全面
に部分的なはがれが数ケ所認められるもの
(2) 全面にはがれがひどく認められるもの+1)
試験紙内部よりはがれたもの
第2表 塗膜物性
※ ◎ 試験紙内部よりの破壊
○ コート剤層、試験紙間での破壊
第1表の試験結果より明らかな如く、本発明のD−Mポ
リマーの添加組成物が、従来よりのものの添加組成物に
比して、耐ブロッキング性が著しくすぐれていることは
勿論のこと、第2表の試験結果よシ、表面光沢、密着性
においても良好であることが明らかである。Table 1: Evaluation criteria for anti-blocking test results (0: No peeling on the entire surface (4) Peeling is observed on part of the entire surface (3) Partial peeling is observed in several places on the entire surface (2) On the entire surface Severe peeling +1)
Items peeled off from inside the test paper Table 2 Physical properties of the coating film * ◎ Destruction from inside the test paper ○ Destruction between the coating agent layer and the test paper As is clear from the test results in Table 1, the D-M polymer of the present invention It goes without saying that the additive composition has significantly better blocking resistance than conventional additive compositions, and also has better surface gloss and adhesion, as shown by the test results in Table 2. One thing is clear.
特許出願人 東洋曹達工業株式会社
手わ1ミ浦正書
昭和58年 5 月 7 日
特許庁長官若杉和夫殿
1事件の表示
昭和58年特許願第159038 弓
2発明の名称
紙コート用組成物
6補正をする者
電話番号(5851ろろ11
4補市命令の日月
自 発
5補正により増加する発明の数 O
6補正の対象
明細書の特許に請求の範囲の側および発明の詳細な説明
の欄
7補正の内容
(1) 明細書の特許請求の範囲を別紙のとおりに補正
する。Patent Applicant Toyo Soda Kogyo Co., Ltd. Tewa 1 Masaaki Miura May 7, 1980 Mr. Kazuo Wakasugi, Commissioner of the Patent Office 1 Indication of Case 1988 Patent Application No. 159038 Bow 2 Name of Invention Composition for Paper Coating 6 Telephone number of the person making the amendment (5851 Roro 11) 4. The date and month of the supplementary city order. 5. The number of inventions to be increased by the amendment. 6. The number of inventions to be increased by the amendment. Column 7 Contents of amendment (1) The scope of claims in the specification is amended as shown in the attached sheet.
(2)同8頁8行に記載の[200Jをl’−3,OO
Jに訂正する。(2) [200J is l'-3, OO as described in page 8, line 8.
Correct to J.
2特許請求の範囲
11、エチレン−酢酸ビニル共重合体100重量部に対
してジシクロペンタジェンと無水マレイン酸の共重合樹
脂10〜500重量部を有機溶剤溶液として含んで成る
エチレン−酢酸ビニル共重合体系紙コート用組成物。2 Claim 11: An ethylene-vinyl acetate copolymer comprising 10 to 500 parts by weight of a copolymer resin of dicyclopentadiene and maleic anhydride as an organic solvent solution based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Polymeric paper coating composition.
Claims (1)
してジシクロペンタジェンと無水マレイン酸の共重合樹
脂を10〜500重量部を有機溶剤溶液として含んで成
るエチレン−酢酸ビニル共重合体系紙コート用組成物。1. Ethylene-vinyl acetate copolymer paper comprising 10 to 500 parts by weight of a copolymer resin of dicyclopentadiene and maleic anhydride as an organic solvent solution per 100 parts by weight of ethylene-vinyl acetate copolymer. Composition for coating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15903883A JPS6052700A (en) | 1983-09-01 | 1983-09-01 | Paper coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15903883A JPS6052700A (en) | 1983-09-01 | 1983-09-01 | Paper coating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6052700A true JPS6052700A (en) | 1985-03-25 |
JPH0128157B2 JPH0128157B2 (en) | 1989-06-01 |
Family
ID=15684882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15903883A Granted JPS6052700A (en) | 1983-09-01 | 1983-09-01 | Paper coating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6052700A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS507880A (en) * | 1973-05-24 | 1975-01-27 | ||
JPS5084511A (en) * | 1973-12-03 | 1975-07-08 | ||
JPS546911A (en) * | 1977-06-18 | 1979-01-19 | Veba Chemie Ag | Anionic paper surface sizing agent |
JPS5639040A (en) * | 1979-09-06 | 1981-04-14 | Japan Synthetic Rubber Co Ltd | Cyclopentadiene derivative |
-
1983
- 1983-09-01 JP JP15903883A patent/JPS6052700A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS507880A (en) * | 1973-05-24 | 1975-01-27 | ||
JPS5084511A (en) * | 1973-12-03 | 1975-07-08 | ||
JPS546911A (en) * | 1977-06-18 | 1979-01-19 | Veba Chemie Ag | Anionic paper surface sizing agent |
JPS5639040A (en) * | 1979-09-06 | 1981-04-14 | Japan Synthetic Rubber Co Ltd | Cyclopentadiene derivative |
Also Published As
Publication number | Publication date |
---|---|
JPH0128157B2 (en) | 1989-06-01 |
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