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JPH0747671B2 - Matted polyvinyl chloride paste composition - Google Patents
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JPH0747671B2 - Matted polyvinyl chloride paste composition - Google Patents

Matted polyvinyl chloride paste composition

Info

Publication number
JPH0747671B2
JPH0747671B2 JP1104882A JP10488289A JPH0747671B2 JP H0747671 B2 JPH0747671 B2 JP H0747671B2 JP 1104882 A JP1104882 A JP 1104882A JP 10488289 A JP10488289 A JP 10488289A JP H0747671 B2 JPH0747671 B2 JP H0747671B2
Authority
JP
Japan
Prior art keywords
polyvinyl chloride
paste
resin
pvc
matting
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 - Lifetime
Application number
JP1104882A
Other languages
Japanese (ja)
Other versions
JPH02283746A (en
Inventor
隆 斉藤
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.)
Achilles Corp
Original Assignee
Achilles 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 Achilles Corp filed Critical Achilles Corp
Priority to JP1104882A priority Critical patent/JPH0747671B2/en
Publication of JPH02283746A publication Critical patent/JPH02283746A/en
Publication of JPH0747671B2 publication Critical patent/JPH0747671B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はポリ塩化ビニルペースト(以下、PVCペースト
と称す)を用いた艶消組成物に係わり、建築用内装材、
レザー等の製品における艶消手段として利用可能な艶消
ポリ塩化ビニルペースト組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of use] The present invention relates to a matting composition using a polyvinyl chloride paste (hereinafter referred to as PVC paste), an interior material for construction,
The present invention relates to a matte polyvinyl chloride paste composition that can be used as a matting means in products such as leather.

〔従来の技術及び発明が解決しようとする課題〕[Problems to be Solved by Prior Art and Invention]

ポリ塩化ビニル樹脂(以下、PVC樹脂と称す)を用いて
形成されている壁紙、床材等の建築用内装材やレザー等
の製品では、その表面の艶を消す手段として、通常粒
径のPVC樹脂に粗粒のPVC樹脂を混合併用した樹脂組成物
を、後加工として製品表面に塗布して表面艶消処理を施
す方法や、PVC樹脂に水酸化アルミニウム、炭酸カル
シウム等の無機フィラーを練り込んだ樹脂組成物を用い
て製品の製造を行う方法が知られている。
For products such as wallpaper, flooring, and other interior building materials such as leather and products made of polyvinyl chloride resin (hereinafter referred to as PVC resin), PVC of normal particle size is used as a means to deluster the surface. A method of applying a resin composition in which a coarse-grained PVC resin is mixed and used in combination with the resin to the surface of the product as a post-process to perform a surface matting treatment, or kneading an inorganic filler such as aluminum hydroxide or calcium carbonate into the PVC resin. There is known a method of producing a product using a resin composition.

しかしながら前者の場合、あくまでも後加工にて行うも
のであるため生産効率の低下を招き、また平均粒子径20
〜50μmの粗粒PVC樹脂を使用するために表面処理時の
スクリーン印刷が困難であったり、薄引きコーティング
が難しく(粗粒の一部が塗膜表面から露出して外観が損
なわれるためなど)、しかも後加工の場合には通常、透
明な材料を表面塗工するため製品表面を部分的に艶消し
とすることは塗工時の見当合わせ等の理由から困難であ
った。一方、後者の場合は充分な艶消効果を得るため無
機フィラーを樹脂100重量部に対して150重量部以上練り
込むことから得られた製品はPVC樹脂本来のもつ風合い
が損なわれたものとなったり、また組成物自体が不透明
感なものとなるため着色に際しては鮮明な色を出しにく
い等の問題点があった。
However, in the case of the former, the post-processing is only done, which leads to a decrease in production efficiency and an average particle size of 20
Screen printing during surface treatment is difficult due to the use of ~ 50μm coarse-grain PVC resin, or thin coating is difficult (for example, some coarse particles are exposed from the surface of the coating film, which impairs the appearance). In addition, in the case of post-processing, it is usually difficult to partially deluster the surface of the product because it is coated with a transparent material for reasons such as registration during coating. On the other hand, in the latter case, the product obtained by kneading 150 parts by weight or more of the inorganic filler with respect to 100 parts by weight of the resin in order to obtain a sufficient matte effect has the original texture of PVC resin impaired. In addition, since the composition itself becomes opaque, it is difficult to produce a clear color during coloring.

そこで本発明者は上記従来技術の問題点に鑑み、後加工
としての艶消表面処理に頼らず、樹脂への練り込みタイ
プによる艶消手段において、PVCペーストを用いた従来
にはない優れた艶消組成物を提供しようと研究を進め
た。そして、一般にゴム等に配合して良好な補強効果を
付与できる充填剤としてよく知られているホワイトカー
ボンを、PVCペーストの艶消し剤として配合して使用す
ることを検討した。
Therefore, in view of the above-mentioned problems of the prior art, the present inventor does not rely on a matte surface treatment as a post-processing, and in a matting means by a kneading type into a resin, an excellent luster that has not been obtained by using a PVC paste. Research has been advanced to provide an erasable composition. Then, it was investigated to use white carbon, which is generally well known as a filler which can be added to rubber or the like to give a good reinforcing effect, as a matting agent for PVC paste.

しかしながらホワイトカーボンは通常一次粒子径がmμ
単位程度の極めて微細なものであることから、上記ペー
ストには粘性を高める目的で溶剤等により調合して使用
することが知られていたものの、艶消し剤として使用し
た場合には上記カーボンによる増粘作用のためペースト
の粘度が著しく上昇して流動性の乏しいものとなってし
まい、その結果、そのようなペーストを製品製造時のコ
ーティングやスクリーン印刷等に適用するのは困難であ
ることが明らかとなった。
However, white carbon usually has a primary particle size of mμ.
It is known that the paste is compounded with a solvent or the like for the purpose of increasing the viscosity because it is an extremely fine unit, but when it is used as a matting agent, it is increased by the carbon. Due to the viscous action, the viscosity of the paste increases significantly and the fluidity becomes poor, and as a result, it is difficult to apply such paste to coating or screen printing during product manufacturing. Became.

〔課題を解決するための手段〕[Means for Solving the Problems]

本発明者は上記知見に基づき更に研究を重ねた結果、特
定のPVC樹脂からなるPVCペーストに特定粒径のホワイト
カーボン配合したものが、上記欠点を解消した優れた艶
消組成物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 further research based on the above findings by the present inventor, it was found that a PVC paste made of a specific PVC resin containing white carbon having a specific particle size is an excellent matting composition that solves the above-mentioned drawbacks. Heading out, the present invention has been completed.

即ち本発明は、 「高重合度ポリ塩化ビニル又は架橋ポリ塩化ビニルから
なるポリ塩化ビニルペースト中の樹脂100重量部に、二
次粒子径が1〜15μmのホワイトカーボンを1〜10重量
部配合することを特徴とする艶消ポリ塩化ビニルペース
ト組成物。」 を要旨とするものである。
That is, the present invention provides that "1 to 10 parts by weight of white carbon having a secondary particle diameter of 1 to 15 µm is mixed with 100 parts by weight of a resin in a polyvinyl chloride paste composed of highly polymerized polyvinyl chloride or crosslinked polyvinyl chloride. Matting polyvinyl chloride paste composition characterized by the above. "

本発明で使用されるPVCペーストは、一般に微粒のPVC樹
脂粒子を可塑剤中に均一に分散してなる、所謂“プラス
チゾル”とも呼ばれるもので、特に基材樹脂として高重
合度PVC樹脂もしくは架橋PVC樹脂を用いて構成してなる
ものである。
The PVC paste used in the present invention is generally formed by uniformly dispersing fine PVC resin particles in a plasticizer and is also called a so-called "plastisol". In particular, a high-polymerization PVC resin or cross-linked PVC is used as a base resin. It is configured by using a resin.

上記高重合度PVC樹脂としては平均重合度が2000以上の
ものが好ましく、ポリ塩化ビニルや、塩化ビニルと他の
単量体(エチレン、酢酸ビニル、ビニルエーテル、マレ
イン酸エステル等)との共重合体などが用いられる。
The above-mentioned high degree of polymerization PVC resin preferably has an average degree of polymerization of 2000 or more, such as polyvinyl chloride or a copolymer of vinyl chloride and another monomer (ethylene, vinyl acetate, vinyl ether, maleic acid ester, etc.). Are used.

架橋PVC樹脂としては架橋度が30%以上のものが好まし
く、具体的には塩化ビニル単量体、又は塩化ビニル単量
体及びこれと共重合可能な共重合性単量体とエチレン性
二重結合を分子内に2個以上有する多官能性化合物から
なる塩化ビニル系共重合体である。
As the cross-linked PVC resin, those having a degree of cross-linking of 30% or more are preferable, and specifically, a vinyl chloride monomer, or a vinyl chloride monomer and a copolymerizable monomer copolymerizable therewith and an ethylenic double It is a vinyl chloride copolymer composed of a polyfunctional compound having two or more bonds in the molecule.

上記両PVC樹脂における重合度及び架橋度が上記数値範
囲以外の場合には、いずれにおいても充分な艶消し効果
が得られにくい等の問題がある。
If the degree of polymerization and the degree of crosslinking in both of the above PVC resins are out of the above numerical ranges, there is a problem in that it is difficult to obtain a sufficient matting effect.

又、ペースト中の可塑剤はこの種ペーストに使用される
公知のものを用いることができ、PVC樹脂100重量部に対
し50〜80重量部程度含有させることが好ましい。本発明
では必要に応じて、ペースト中に安定剤、難燃剤、防カ
ビ剤、充填剤、発泡剤、着色剤等を添加してもよい。
As the plasticizer in the paste, known ones used for this type of paste can be used, and it is preferable to add about 50 to 80 parts by weight to 100 parts by weight of the PVC resin. In the present invention, a stabilizer, a flame retardant, an antifungal agent, a filler, a foaming agent, a coloring agent and the like may be added to the paste as needed.

ホワイトカーボンとしては二次粒子径が上記特定範囲の
ものであれば如何なるものでも使用することができ、具
体的にはけい酸やけい酸塩等が挙げられる。上記粒子径
が1μm未満のものでは増粘作用が出て流動性に劣るも
のとなり、逆に15μmを越えたものではその粒径以下の
厚さの塗膜形成が不可能であったり、表面平滑性に劣る
ものとなる。またPVCペースト中の樹脂100重量部に対す
る配合割合が1重量部未満では充分な艶消効果が得られ
ず、逆に10重量部を越えると艶消効果が極端に良くなる
ことはなく、材料費の点でコスト高となる。
Any white carbon may be used as long as it has a secondary particle diameter within the above specified range, and specific examples thereof include silicic acid and silicate. If the particle size is less than 1 μm, the viscosity will be increased and the fluidity will be poor. On the contrary, if the particle size exceeds 15 μm, it will be impossible to form a coating film having a thickness less than the particle size or the surface will be smooth. It becomes inferior in sex. If the compounding ratio of the resin in the PVC paste to 100 parts by weight is less than 1 part by weight, a sufficient matting effect cannot be obtained. Conversely, if it exceeds 10 parts by weight, the matting effect will not be extremely improved and the material cost will be low. However, the cost is high.

上記の如き構成からなる本発明艶消組成物は、艶消処理
を要する分野に幅広く利用することができ、例えば、表
面層の形成材料や艶消模様印刷用インクとして各種の塗
布、印刷手段等により塗工し、しかる後、加熱処理して
ゲル化させることにより種々の製品の艶消手段として使
用される。この加熱処理は通常150〜220℃の条件下で行
われる。
The matting composition of the present invention having the above-mentioned constitution can be widely used in fields requiring matting treatment, and for example, various coating materials such as surface layer forming materials and matte pattern printing inks, printing means, etc. It is used as a delustering means for various products by applying a coating solution, and then heat-treating it to gel. This heat treatment is usually performed at 150 to 220 ° C.

〔実施例〕〔Example〕

以下、実施例を挙げて本発明を更に詳細に説明する。 Hereinafter, the present invention will be described in more detail with reference to examples.

実施例1〜4、比較例1〜3 下記の表に示す各種PVC樹脂からなるPVCペースト中に、
同表に示す種類、量のホワイトカーボン等をそれぞれ配
合して艶消ペーストを調製した。尚、このペーストには
必要に応じて充填剤、チタン顔料等を添加しても構わな
い。
Examples 1 to 4 and Comparative Examples 1 to 3 are used in a PVC paste made of various PVC resins shown in the table below.
Matting pastes were prepared by blending the types and amounts of white carbon shown in the table, respectively. In addition, a filler, a titanium pigment, or the like may be added to this paste as needed.

得られた艶消ペーストを1日放置した後、BH型粘度計
(No.4ローター、60rpm)を用いて20℃におけるペース
ト粘度を測定した。
After leaving the obtained matte paste for one day, the paste viscosity at 20 ° C. was measured using a BH type viscometer (No. 4 rotor, 60 rpm).

次に、艶消ペーストを難燃紙に塗布厚0.12mmとなるよう
にコーティングし、210℃で60秒間加熱した後、その表
面の光沢度を光沢計(村上色彩研究所製:GM−24)にて
測定した。
Next, the matte paste was coated on flame-retardant paper to a thickness of 0.12 mm, heated at 210 ° C for 60 seconds, and the surface glossiness was measured with a gloss meter (Murakami Color Research Laboratory: GM-24). It was measured at.

上記ペースト粘度、光沢度の結果を下記表に示す。The results of the above paste viscosity and gloss are shown in the table below.

1)鐘淵化学製:XH−27A 2)日本ゼオン製:G−43SH 3)三菱化成ビニル製:P−475 4)住友化学製:PX−U 5)日本ゼオン製:G−121 6)積水化学製:DINP 7)アデカアーガス社製:465E 8)西独デグサ社製:OK−500 9)日本石油製:ミネラルスピリット 〔発明の効果〕 以上説明したように、本発明艶消組成物は特定のPVC樹
脂からなるPVCペースト中に特定粒子径のホワイトカー
ボン配合してなるため、優れた流動性と艶消付与効果を
有したものであり、その結果、この組成物を直接用いて
艶消状態の製品を形成することが可能となり、後加工と
して行われていた従来の表面艶消処理を省略することが
でき、安価で容易な艶消処理を行うことができる。又、
本発明品は優れた流動性を有すると共に粗粒PVC樹脂の
ような粗大粒子を含むものではないため、膜厚の薄いコ
ーティングやスクリーン印刷に対しても何ら支障なく適
用することができる。更に、本発明品は無機フィラー等
を添加しないため塩ビ本来の風合いを損ねる虞れはな
く、しかも樹脂組成物の透明性が保持されるため鮮明な
着色を製品に施すこともできる。
1) Kanegafuchi Chemicals: XH-27A 2) Nippon Zeon: G-43SH 3) Mitsubishi Kasei Vinyl: P-475 4) Sumitomo Chemical: PX-U 5) Nippon Zeon: G-121 6) Sekisui Chemical: DINP 7) ADEKA ARGUS: 465E 8) West Germany Degussa: OK-500 9) Nippon Oil: Mineral Spirit [Effect of the Invention] As described above, the matting composition of the present invention is specific. It has excellent fluidity and matting effect because it is composed of white carbon with a specific particle size in a PVC paste made of PVC resin.As a result, this composition can be used directly in a matte state. The product can be formed, the conventional surface matting treatment which has been performed as a post-processing can be omitted, and the inexpensive and easy matting treatment can be performed. or,
Since the product of the present invention has excellent fluidity and does not contain coarse particles such as coarse-grained PVC resin, it can be applied to coating having a small film thickness and screen printing without any trouble. Furthermore, since the product of the present invention does not add an inorganic filler or the like, there is no fear of impairing the original texture of vinyl chloride, and since the transparency of the resin composition is maintained, the product can be colored vividly.

また本発明品を用いれば、スクリーン印刷或いは凹版印
刷等において通常の配合インクと本発明品からなる艶消
配合インクとを版毎に適宜配分して使用することにより
艶差のある意匠表現が可能となる。
Further, by using the product of the present invention, it is possible to express a design with a gloss difference by appropriately distributing and using an ordinary compounded ink and a matte compounded ink composed of the product of the invention in screen printing or intaglio printing. Becomes

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】高重合度ポリ塩化ビニル又は架橋ポリ塩化
ビニルからなるポリ塩化ビニルペースト中の樹脂100重
量部に対して、二次粒径が1〜15μmのホワイトカーボ
ンを1〜10重量部配合することを特徴とする艶消ポリ塩
化ビニルペースト組成物。
1. A blend of 1 to 10 parts by weight of white carbon having a secondary particle size of 1 to 15 μm with respect to 100 parts by weight of a resin in a polyvinyl chloride paste composed of highly polymerized polyvinyl chloride or crosslinked polyvinyl chloride. A matte polyvinyl chloride paste composition comprising:
JP1104882A 1989-04-25 1989-04-25 Matted polyvinyl chloride paste composition Expired - Lifetime JPH0747671B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1104882A JPH0747671B2 (en) 1989-04-25 1989-04-25 Matted polyvinyl chloride paste composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1104882A JPH0747671B2 (en) 1989-04-25 1989-04-25 Matted polyvinyl chloride paste composition

Publications (2)

Publication Number Publication Date
JPH02283746A JPH02283746A (en) 1990-11-21
JPH0747671B2 true JPH0747671B2 (en) 1995-05-24

Family

ID=14392557

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1104882A Expired - Lifetime JPH0747671B2 (en) 1989-04-25 1989-04-25 Matted polyvinyl chloride paste composition

Country Status (1)

Country Link
JP (1) JPH0747671B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001089689A (en) * 1999-02-15 2001-04-03 Tosoh Corp Matting agent for printing ink, printing ink composition comprising the same, and use thereof
CN104629216B (en) * 2015-02-13 2016-08-31 四川省华蓥市辽望实业有限公司 A kind of environmental protection Asia Photoelastic Composite Materials and its preparation method and application
CN112964527B (en) * 2021-02-20 2024-08-09 锦西化工研究院有限公司 Preparation method of sample for determination of viscosity number of extinction polyvinyl chloride resin

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07122009B2 (en) * 1988-07-07 1995-12-25 信越化学工業株式会社 Vinyl chloride resin composition

Also Published As

Publication number Publication date
JPH02283746A (en) 1990-11-21

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