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JPH04132758A - Vinyl chloride plastisol composition - Google Patents

Vinyl chloride plastisol composition

Info

Publication number
JPH04132758A
JPH04132758A JP25393690A JP25393690A JPH04132758A JP H04132758 A JPH04132758 A JP H04132758A JP 25393690 A JP25393690 A JP 25393690A JP 25393690 A JP25393690 A JP 25393690A JP H04132758 A JPH04132758 A JP H04132758A
Authority
JP
Japan
Prior art keywords
vinyl chloride
plasticizer
coating film
chloride resin
plastisol 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.)
Pending
Application number
JP25393690A
Other languages
Japanese (ja)
Inventor
Nobuyuki Nagata
永田 信之
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.)
Aisin Chemical Co Ltd
Original Assignee
Aisin Chemical Co Ltd
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 Aisin Chemical Co Ltd filed Critical Aisin Chemical Co Ltd
Priority to JP25393690A priority Critical patent/JPH04132758A/en
Publication of JPH04132758A publication Critical patent/JPH04132758A/en
Pending legal-status Critical Current

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  • Sealing Material Composition (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a vinyl chloride plastisol composition giving a coating film having excellent crack resistance and suitable as a sealing material effective in improving the rust-proofness of the joint part, etc., of steel plate by compounding a plasticizer and a filler to a vinyl chloride resin having a specific particle size. CONSTITUTION:The objective composition is produced by compounding (A) a vinyl chloride resin having particle diameter of <=2mum with (B) a plasticizer containing a polyester-based plasticizer and/or a benzyl-type plasticizer accounting for >=50% of the total plasticizer and (C) a filler (e.g. ground calcium carbonate having an average particle diameter of <=10mum).

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は鋼板の接合部分などに塗布され防錆性を高める
シーリング材として利用される塩化ビニルプラスチゾル
組成物に関し、詳しくはその表面に形成される塗膜の割
れを防止できる塩化ビニルプラスチゾル組成物に関する
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a vinyl chloride plastisol composition that is applied as a sealant to improve rust prevention by being applied to joints of steel plates, etc. The present invention relates to a vinyl chloride plastisol composition that can prevent cracking of paint films.

[従来の技術] 自動車のボデー等は複数の鋼板が重ね合わせられ、それ
を溶接や接着剤で接合して組み立てられている。溶接は
スポット溶接で行なわれる場合が多く、そのスポット間
隔が数10mmであるため、鋼板間のシール性は完全で
はない。また接着剤で接合する場合も、鋼板が防錆油等
で処理されているため、接着剤の塗布が十分でなくシー
ル性が完全ではない。そして組み立てられたボディーは
電着塗装され、ポデー鋼板に防錆性が付与されるが、前
述の鋼板接合部は、そのクリヤランスが1mm以下であ
るため電着塗装のはいり込みが困難で塗装が不十分であ
る。これらの理由により、鋼板接合部には防錆性を高め
るために、塩化ビニルプラスチゾル系のシーリング材が
使用されている。このシーリング材の要求特性としては
、前述したシール性の他に被塗装性がある。シーリング
材は加熱硬化型であり、塗布された後で加熱され硬化す
る。その上に自動車の意匠性を高める目的で上塗り塗装
が施される。ところがシーリング材は、塩化ビニル樹脂
をマトリックスとしているため、鋼板より被塗装性にや
や劣り、被塗装性向上の要求がある。たとえば特開昭6
2−53544号公報には、シール性を改善した塩化ビ
ニル系の高浸透性シーリング材組成物の開示がある。ま
た、特開昭63=309579号公報には、被塗装性を
改善したレベリング性の良い塩化ビニル樹脂系のシーリ
ング材の開示がある。しかし、これらのシーリング材は
、シール性や被塗装性には優れるが、シーリング材の上
面に塗装される上塗り塗膜に割れが発生するのを防ぐこ
とは困難な場合が多い。すなわち、塗膜を塗装した後の
焼付は工程において、接合鋼板の熱膨張の違いにより発
生する歪みをシーリング材が吸収できないため、シーリ
ング材上に形成されている塗膜に割れが発生するものと
考えられる。
[Prior Art] Automobile bodies and the like are assembled by stacking a plurality of steel plates and joining them by welding or adhesive. Welding is often performed by spot welding, and the spot spacing is several tens of millimeters, so the sealing between the steel plates is not perfect. Furthermore, even when joining with adhesive, since the steel plates are treated with anti-corrosion oil, etc., the application of the adhesive is insufficient and the sealing performance is not perfect. The assembled body is then electrocoated to give rust prevention properties to the POD steel plates.However, the above-mentioned steel plate joints have a clearance of less than 1mm, making it difficult for the electrocoating to penetrate, making the coating impossible. It is enough. For these reasons, vinyl chloride plastisol sealants are used in steel plate joints to improve rust prevention. In addition to the above-mentioned sealing properties, the required properties of this sealing material include paintability. The sealant is a heat-curing type, and after being applied, it is heated and cured. A top coat is then applied to enhance the design of the car. However, since the sealant has a vinyl chloride resin as a matrix, its paintability is somewhat inferior to that of steel sheets, and there is a demand for improved paintability. For example, JP-A-6
Publication No. 2-53544 discloses a vinyl chloride-based highly permeable sealing material composition with improved sealing properties. Further, Japanese Patent Application Laid-Open No. 63/309579 discloses a vinyl chloride resin sealing material with improved paintability and good leveling properties. However, although these sealants have excellent sealing properties and paintability, it is often difficult to prevent cracks from occurring in the top coat coated on the top surface of the sealant. In other words, during the baking process after the paint film is applied, the sealant cannot absorb the distortion that occurs due to the difference in thermal expansion of the bonded steel plates, which causes cracks in the paint film formed on the sealant. Conceivable.

[発明が解決しよ)とする課題] 本発明は、上記の事情に鑑みてなされたもので、塗膜の
1省すれ性の優れたシーリング材を提供することを目的
としている。
[Problems to be Solved by the Invention] The present invention has been made in view of the above-mentioned circumstances, and an object of the present invention is to provide a sealing material that is excellent in removing the paint film.

[課題を解決するための手段] 本発明の塩化ビニルプラスチゾル組成物は、粉末上の塩
化ビニル系樹脂と、可塑剤と、充填剤とを含む塩化ビニ
ルプラスチゾル組成物において、該粉末状の塩化ビニル
系樹脂の粒径が2um以下であることを特徴とする。
[Means for Solving the Problems] The vinyl chloride plastisol composition of the present invention is a vinyl chloride plastisol composition containing a powdered vinyl chloride resin, a plasticizer, and a filler. It is characterized in that the particle size of the system resin is 2 um or less.

まず本発明の最大の特色である塩化ビニル系樹脂は、平
均粒径が2μm以下にあることが塗膜の耐割れ性を高め
るのに好ましい。
First, the vinyl chloride resin, which is the most distinctive feature of the present invention, preferably has an average particle size of 2 μm or less in order to improve the cracking resistance of the coating film.

この塩化ビニル系樹脂としては、ペースト用塩化ビニル
樹脂であればホモポリマーでもコポリマーでもよい。そ
して塩化ビニル樹脂の組成物中ての含有量は、15〜2
5重量部であることが好ましい。
The vinyl chloride resin may be a homopolymer or a copolymer as long as it is a paste-use vinyl chloride resin. The content of vinyl chloride resin in the composition is 15 to 2
Preferably it is 5 parts by weight.

含有量が15重量部未満であるとシーリング材の性質が
低下し、25重量部を超えると貯蔵安定性が低下してく
るので好ましくない。
If the content is less than 15 parts by weight, the properties of the sealing material will deteriorate, and if it exceeds 25 parts by weight, storage stability will deteriorate, which is not preferable.

次に可塑剤として、ポリエステル系可塑剤やベンジル系
可塑剤を併用すると、更に耐塗膜割れ性を高めることが
できる。その使用量は、ポリエステル系可塑剤又はベン
ジル系可塑剤のいずれか又は両方が可塑剤全体の50%
以上であることが好ましい。可塑剤の全てをポリエステ
ル系可塑剤にすると接着強度が悪くなり、ベンジル系可
塑剤だけにすると貯蔵安定性が悪くなる。
Next, when a polyester plasticizer or a benzyl plasticizer is used in combination as a plasticizer, the coating film cracking resistance can be further improved. The amount used is that either polyester plasticizer or benzyl plasticizer or both account for 50% of the total plasticizer.
It is preferable that it is above. If all the plasticizers are polyester plasticizers, the adhesive strength will be poor, and if only benzyl plasticizers are used, the storage stability will be poor.

充填剤として用いられる重質炭酸カルシウムは平均粒径
が10μm以下のものが好ましくなかでも1〜4μmの
ものが好ましい。
The average particle size of the heavy calcium carbonate used as a filler is preferably 10 .mu.m or less, particularly 1 to 4 .mu.m.

平均粒径が10μmより大きいと塗膜の耐割れ性が低下
して好ましくない。充填剤は、さらに微粒子のコロイダ
ル炭酸カルシウム、シリカ、酸化亜鉛などを添加するこ
ともできる。さらに添加剤として接着付与剤、安定剤な
どを添加することもできる。
If the average particle size is larger than 10 μm, the cracking resistance of the coating film decreases, which is not preferable. As fillers, fine particles of colloidal calcium carbonate, silica, zinc oxide, etc. can also be added. Furthermore, adhesion promoters, stabilizers, and the like may be added as additives.

[作用] 本発明の塩化ビニルプラスチゾル組成物を使用すること
により、シーリング材の上に形成される塗膜の耐割れ性
に優れ塗装性の良いシーリング材となる。すなわち、鋼
板接合部で生じた歪みがシーリング材上の塗膜に割れを
もたらすのは、塗膜の伸び性能限界を超えた場合である
。これを防ぐには塗膜の伸びを最大限に発揮できる形態
にする必要がある。そのためには、塗膜の厚みを均一に
保持し、接合部からの応力が塗膜の局部に集中しないよ
うにシーリング材の表面を凸凹をなくすように塩化ビニ
ル樹脂および充填剤の重質炭酸カルシウムを微粒子化し
たものを用いる。さらに塗膜の平滑性を損なわないよう
に可塑剤をポリエステル系やベンジル系などを用いて、
可塑剤の塗膜への影響を無くして、塗膜形成に影響を与
えないようにする。この様にシーリング材の粉体材料と
可塑剤を選定することで、塗膜は充分な伸びが発揮でき
、耐割れ性が向上する。
[Function] By using the vinyl chloride plastisol composition of the present invention, a sealing material with excellent crack resistance and good paintability of the coating film formed on the sealing material can be obtained. That is, the strain generated at the joint between the steel plates causes cracks in the coating film on the sealant when the elongation performance limit of the coating film is exceeded. To prevent this, it is necessary to create a form that maximizes the elongation of the coating film. To do this, we need to use vinyl chloride resin and heavy calcium carbonate filler to make the surface of the sealant even and smooth to keep the thickness of the paint film uniform and prevent stress from the joints from concentrating on local areas of the paint film. A finely divided product is used. Furthermore, in order not to impair the smoothness of the coating film, we use plasticizers such as polyester or benzyl.
To eliminate the influence of a plasticizer on a coating film so as not to affect coating film formation. By selecting the powder material and plasticizer for the sealant in this way, the coating film can exhibit sufficient elongation and its cracking resistance is improved.

[実施例] 以下、実施例により具体的に説明する。[Example] Hereinafter, this will be explained in detail using examples.

塩化ビニル樹脂(平均重合度1400、粒径1〜2μm
)10重量部、酢酸ビニルを5%含む塩ビ共重合体(平
均重合度1200、粒径1〜2μm)10重量部の混合
樹脂に、ポリエステル可塑剤(フタル酸系、数平均分子
量600〜700)13重量部、アルキルベンジル系可
塑剤(アルキル基、C数4〜8)13重量部、重質炭酸
カルシウム(粒径2〜4μm)24重量部、コロイダル
炭酸カルシウム16重量部その他の添加剤(接着付与剤
、安定剤)14重量部を配合してジ−リング材No、1
を作製した。表に示す配合割合で同様にNo、2〜3の
実施例のジ−リング材No、1〜4を表に示す割合で配
合して同様に作製した。 なおポリエステル系可塑剤の
分子量はGPCにより数平均分子量を算出した。
Vinyl chloride resin (average degree of polymerization 1400, particle size 1-2 μm
), 10 parts by weight of a vinyl chloride copolymer (average degree of polymerization 1200, particle size 1-2 μm) containing 5% vinyl acetate, and a polyester plasticizer (phthalic acid type, number average molecular weight 600-700). 13 parts by weight, alkylbenzyl plasticizer (alkyl group, C number 4 to 8), 24 parts by weight, heavy calcium carbonate (particle size 2 to 4 μm), 16 parts by weight of colloidal calcium carbonate, and other additives (adhesion). Adding agent, stabilizer) 14 parts by weight were blended to make Ziering material No. 1.
was created. It was produced in the same manner by blending Nos. 2 and 3 of Ziering materials No. 1 to 4 of Examples 1 to 4 in the proportions shown in the table. The molecular weight of the polyester plasticizer was determined by calculating the number average molecular weight by GPC.

(以下余白) (評価法) 1官すれ性:作製したゾルを幅15mm、厚み2mmに
なるように被塗板に塗布し、100℃でlO分仮焼付け
した後、アルキッドメラミン樹脂系の中塗り塗料、アク
リルメラミン樹脂系の上塗り塗料を塗布し140℃×3
0分の焼付は条件で焼付けたあとオーブンから取出し直
後に378インチ丸棒に沿って角度が10度15秒の速
度で徐々に折曲げて塗膜に割れの発生するまで折曲げ、
その時の折曲げ角度が100度以上を合格とした。
(Left below) (Evaluation method) 1. Scratch resistance: The prepared sol was applied to a plate to be coated to a width of 15 mm and a thickness of 2 mm, and after calcining at 100°C for 10 minutes, an alkyd melamine resin intermediate coating was applied. , apply an acrylic melamine resin top coat at 140℃ x 3
After baking for 0 minutes, immediately after taking it out of the oven, gradually bend it along a 378-inch round bar at an angle of 10 degrees and 15 seconds until cracks occur in the coating film.
A case where the bending angle at that time was 100 degrees or more was considered acceptable.

伸び;シーリング材を被塗板に塗布し140℃で60分
間焼付はシーリング材の伸びをJASOM−323−7
7に準拠して測定した。
Elongation: Apply the sealant to the plate to be coated and bake at 140℃ for 60 minutes to determine the elongation of the sealant using JASOM-323-7.
Measured according to 7.

貯蔵安定性:ゾルを45℃の恒温槽にて72時間貯蔵し
てゲルの発生の有無で評価した。表に示すようにN01
)では粒径1〜2μmの塩化ビニル樹脂が20重量部、
可塑剤がポリエステル系とベンジル系とで100%を占
め、4μm以下の重質炭酸カルシウムを配合したことに
より塗膜の1盲すれ性、伸び、貯蔵安定性にも優れてい
た。No、2.3の本発明の組成範囲ではいずれも優れ
た塗装の副31れ性、伸び、貯蔵安定性を示している。
Storage stability: The sol was stored in a constant temperature bath at 45° C. for 72 hours and evaluated based on the presence or absence of gel formation. N01 as shown in the table
), 20 parts by weight of vinyl chloride resin with a particle size of 1 to 2 μm,
The plasticizer was 100% polyester-based and benzyl-based, and by incorporating heavy calcium carbonate with a size of 4 μm or less, the coating film had excellent one-blind abrasion resistance, elongation, and storage stability. In the composition ranges of No. 2.3 and 2.3 of the present invention, all exhibit excellent coating resistance, elongation, and storage stability.

一方比較例のNo、1.No、2は、粒径30〜40μ
mの粗粒塩化ビニル樹脂を用いた場合で、塗膜の1博り
れ性に劣る。No、  3は、可塑剤のDOPを用いた
場合で、上塗り塗料の溶剤への影響により、耐割れ性が
不十分である。No、4は、ベンジル系可塑剤のみを用
いた場合で、シーリング材の貯蔵安定性が低下している
On the other hand, Comparative Example No. 1. No. 2 has a particle size of 30 to 40μ
When a coarse-grained vinyl chloride resin of m is used, the spreadability of the coating film is poor. No. 3 is a case where the plasticizer DOP is used, and the cracking resistance is insufficient due to the influence on the solvent of the top coat. No. 4 is a case where only a benzyl plasticizer is used, and the storage stability of the sealant is decreased.

し効果] 本発明の塩化ビニルプラスチゾル組成物は、塩化ビニル
樹脂と充填剤とが小粒径で構成され、可塑剤の50%以
上がポリエステル系およびベンジル系とで占められてい
る。このようにシーリング材の樹脂や充填剤が微粒子で
あるので、凸凹の少ない表面が形成され、その上面に塗
布される塗膜は均一な膜となり、最大限の伸びを発揮す
ることができる。また、ポリエステル系やベンジル系可
塑剤の塗膜形成に対し悪影響を及ぼさないため平滑な塗
膜が形成できる。
Effect] The vinyl chloride plastisol composition of the present invention is composed of a vinyl chloride resin and a filler having small particle sizes, and 50% or more of the plasticizer is occupied by a polyester type and a benzyl type. Since the resin and filler of the sealant are made of fine particles in this way, a surface with few irregularities is formed, and the coating film applied to the top surface becomes a uniform film, allowing maximum elongation. Moreover, since it does not have an adverse effect on the coating film formation of polyester-based or benzyl-based plasticizers, a smooth coating film can be formed.

したがって、塗膜の耐割れ性が向上し、かつ塗装性も向
上して色相や艶感が向上した塗膜となる。また塗膜の物
性も、シーリング材が応力を吸収するとともに塗膜への
影響が少なくされているため向上している。
Therefore, the cracking resistance of the coating film is improved, and the paintability is also improved, resulting in a coating film with improved hue and gloss. The physical properties of the paint film are also improved because the sealant absorbs stress and its effect on the paint film is reduced.

特許出願人 アイシン化工株式会社 代表者宮地治夫Patent applicant: Aisin Kako Co., Ltd. Representative Haruo Miyaji

Claims (1)

【特許請求の範囲】[Claims] (1)粉末状の塩化ビニルプラスチゾル組成物と、可塑
剤と、充填剤とを含む塩化ビニルプラスチゾル組成物に
おいて、該粉末状の塩化ビニル系樹脂の粒径が2μm以
下であることを特徴とする塩化ビニルプラスチゾル組成
物。
(1) A vinyl chloride plastisol composition containing a powdered vinyl chloride plastisol composition, a plasticizer, and a filler, characterized in that the particle size of the powdered vinyl chloride resin is 2 μm or less. Vinyl chloride plastisol composition.
JP25393690A 1990-09-21 1990-09-21 Vinyl chloride plastisol composition Pending JPH04132758A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25393690A JPH04132758A (en) 1990-09-21 1990-09-21 Vinyl chloride plastisol composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25393690A JPH04132758A (en) 1990-09-21 1990-09-21 Vinyl chloride plastisol composition

Publications (1)

Publication Number Publication Date
JPH04132758A true JPH04132758A (en) 1992-05-07

Family

ID=17258075

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25393690A Pending JPH04132758A (en) 1990-09-21 1990-09-21 Vinyl chloride plastisol composition

Country Status (1)

Country Link
JP (1) JPH04132758A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001226549A (en) * 2000-02-10 2001-08-21 Riken Vinyl Industry Co Ltd Vinyl chloride resin composition and composite thereof
JP2006233229A (en) * 2006-06-09 2006-09-07 Tosoh Corp Vinyl chloride resin for paste for flooring and vinyl chloride resin composition for paste for flooring comprising the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001226549A (en) * 2000-02-10 2001-08-21 Riken Vinyl Industry Co Ltd Vinyl chloride resin composition and composite thereof
JP2006233229A (en) * 2006-06-09 2006-09-07 Tosoh Corp Vinyl chloride resin for paste for flooring and vinyl chloride resin composition for paste for flooring comprising the same

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