JPH0742369B2 - Matted polyvinyl chloride paste composition - Google Patents
Matted polyvinyl chloride paste compositionInfo
- Publication number
- JPH0742369B2 JPH0742369B2 JP1079333A JP7933389A JPH0742369B2 JP H0742369 B2 JPH0742369 B2 JP H0742369B2 JP 1079333 A JP1079333 A JP 1079333A JP 7933389 A JP7933389 A JP 7933389A JP H0742369 B2 JPH0742369 B2 JP H0742369B2
- Authority
- JP
- Japan
- Prior art keywords
- paste
- pvc
- polyvinyl chloride
- weight
- parts
- 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 - Fee Related
Links
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 34
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 34
- 239000000203 mixture Substances 0.000 title claims description 13
- 239000011347 resin Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 18
- 239000004094 surface-active agent Substances 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- 239000011163 secondary particle Substances 0.000 claims description 3
- -1 flooring Substances 0.000 description 16
- 239000002245 particle Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000006224 matting agent Substances 0.000 description 4
- 238000012805 post-processing Methods 0.000 description 4
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 239000000976 ink Substances 0.000 description 3
- 238000007650 screen-printing Methods 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 125000005501 benzalkonium group Chemical class 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
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、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 application] The present invention relates to a matting composition using a polyvinyl chloride paste (hereinafter referred to as PVC paste), and a matting means in products such as interior materials and leather. And a matte polyvinyl chloride paste composition that can be used as
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、後加工とし
て、製品表面に無機質粉体等のマット剤を塗布して表面
艶消処理を施す手段や、上記PVC樹脂に直接、無機フ
ィラーである水酸化アルミニウム、炭酸カルシウム等を
練り込んで製品の製造を行う方法が知られている。後者
に類似したものでは、特に床材等において通常のPVC樹
脂よりも粒径が大きいPVC樹脂を混ぜ合わせてなる所
謂、ブレンディングレジンを使用する方法も存在してい
る。For products such as wallpaper, interior materials such as flooring, and leather that are made of polyvinyl chloride resin (hereinafter referred to as PVC resin), as a means of delustering the surface, post-processing There are known means for applying a matting agent such as an inorganic powder for surface matting treatment, and a method for directly kneading the above PVC resin with an inorganic filler such as aluminum hydroxide or calcium carbonate to produce a product. ing. As a method similar to the latter, there is also a method of using a so-called blending resin, which is a mixture of PVC resins having a particle size larger than that of ordinary PVC resins, particularly in flooring materials.
ところが前者の場合、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、また大きい粒径のマッ
ト剤を用いるとその粒径よりも薄い表面処理膜を施すこ
とが不可能となり(マット剤の一部が膜表面に露出して
しまうため)、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、上記後者の場合、水酸化アルミニウム、炭酸カル
シウム等の添加剤を樹脂100重量部に対して150重量部以
上練り込まないと充分な艶消効果が得られず、しかも、
このように添加剤を多量に練り込むと組成物に不透明感
が出てしまい、強度的な物性面でも不充分な製品となる
不具合があった。例えば、着色処理を要す壁紙等に使用
した場合は透明性材料に比べて多くの着色剤が必要とな
り、混色の虞れもあり、また強度的に脆くなり折れ易い
壁紙になる欠点があった。このような問題点はブレンデ
ィングレジンを使用した場合でも、大きい粒径のレジン
以下の塗膜形成が不可能であったり、物性の低下等があ
るように、同様に生じていた。However, in the case of the former, the post-processing is only done, which leads to a decrease in production efficiency, and if a matting agent with a large particle size is used, it becomes impossible to apply a surface treatment film thinner than the particle size (matte (Since a part of the agent is exposed on the film surface), and in the case of post-processing, it is generally a good idea to partially deluster the product surface because a transparent material is applied on the surface. It was difficult due to reasons such as alignment.
On the other hand, in the latter case, a sufficient matting effect cannot be obtained unless 150 parts by weight or more of an additive such as aluminum hydroxide or calcium carbonate is kneaded with 100 parts by weight of the resin, and,
As described above, when a large amount of the additive is kneaded, the composition becomes opaque and there is a problem that the product has insufficient strength in terms of physical properties. For example, when it is used for wallpaper that requires coloring, more coloring agent is needed than transparent material, there is a risk of color mixing, and there is a drawback that the wallpaper becomes brittle in strength and easily broken. . Even when a blending resin is used, such a problem similarly occurs such that it is impossible to form a coating film having a resin having a large particle diameter or less, and the physical properties are deteriorated.
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 matting treatment as a post-processing, and in a matting means by a kneading type into a resin, it has an unprecedented excellent gloss using 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m
μ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、艶消し剤として配合
してみたところ、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
時における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 m.
Since it is known to be used by being mixed with a solvent for the purpose of increasing the viscosity in the above paste because it is an extremely fine substance of the order of μ unit, when it was blended as a matting agent, the above carbon Due to the thickening effect of the paste, 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 clear.
本発明者は上記知見に基づき更に研究を重ねた結果、PV
Cペースト中にホワイトカーボンに加えて界面活性剤を
併用して配合したものが、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, the present inventor found that PV
The present inventors have completed the present invention by discovering that the C paste is a combination of white carbon and a surfactant in combination, which is an excellent delustering composition in which the above-mentioned drawbacks are eliminated.
即ち本発明は、 ポリ塩化ビニルペースト中の樹脂100重量部に対して、
二次粒子径が1〜15μmのホワイトカーボンを5〜15重
量部配合すると共に界面活性剤を0.5〜3重量部配合し
てな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。That is, the present invention, for 100 parts by weight of the resin in the polyvinyl chloride paste,
A matte polyvinyl chloride paste composition comprising 5 to 15 parts by weight of white carbon having a secondary particle diameter of 1 to 15 μm and 0.5 to 3 parts by weight of a surfactant.
を要旨とするものである。Is the gist.
本発明で使用するPVCペーストは、所謂“プラスチゾ
ル”とも呼ばれているもので、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ものである。The PVC paste used in the present invention is also referred to as a so-called "plastisol", and is generally one in which fine PVC resin particles are uniformly dispersed in a plasticizer.
このペースト中におけるPVC樹脂としては、重合度が100
0〜1700程度の一般的な乳化重合PVC、重合度が2000以上
〜4000位迄の高重合度PVC、架橋PVC等が挙げられ、それ
らを単独で使用しても或いは2種以上を適宜組み合わせ
て併用してもよい。なかでも高重合度PVCや架橋PVCの併
用或いはそれらを単独使用した場合は、艶が少なく強度
的に優れた製品が得られ易く、また界面活性剤の配合量
を少なくすることができる。又、一般的な重合度のPVC
に高重合度PVC及び/又は架橋PVCをブレンドして併用す
る場合の配合割合は、一般PVC60〜70重量部に対し、高
重合度PVC及び/又は架橋PVC40〜30重量部程度が好まし
い。The PVC resin in this paste has a polymerization degree of 100.
Typical emulsion polymerization PVC of about 0 to 1700, high polymerization degree PVC with a degree of polymerization of 2000 to 4000, crosslinked PVC, etc. may be used alone or in appropriate combination of two or more kinds. You may use together. Above all, when high polymerization degree PVC or cross-linked PVC is used in combination or used alone, a product having less gloss and excellent strength can be easily obtained, and the amount of the surfactant mixed can be reduced. Also, PVC with general polymerization degree
When blending and using a high degree of polymerization PVC and / or a crosslinked PVC in combination, the proportion of the high degree of polymerization PVC and / or the crosslinked PVC is preferably 40 to 30 parts by weight with respect to 60 to 70 parts by weight of general PVC.
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5重量部未満では充分な艶消効果が得られ
ず、逆に15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 5 parts by weight, a sufficient matting effect cannot be obtained. Conversely, if it exceeds 15 parts by weight, the matting effect will not be extremely improved and the material cost will be low. However, the cost is high.
本発明で使用する界面活性剤は、そのPVCペースト中の
樹脂100重量部に対する配合割合が0.5重量部未満では増
粘抑制効果が得られず、3重量部を越えると増粘抑制効
果の極端な向上は認められず、過剰な配合は活性剤によ
るブリード現象や白化現象が生じる虞れがあり、しかも
不経済である。The surfactant used in the present invention has no thickening inhibiting effect when the compounding ratio is less than 0.5 parts by weight with respect to 100 parts by weight of the resin in the PVC paste, and exceeds 3 parts by weight, the thickening inhibiting effect is extremely high. No improvement is observed, and excessive blending may cause a bleeding phenomenon or a whitening phenomenon due to the activator and is uneconomical.
界面活性剤としては従来から知られているアニオン性、
カチオン性、非イオン性、両性等の各種界面活性剤を用
いることができる。具体的には、アニオン性界面活性剤
としてアルキル硫酸エステル塩、アルキルエーテルカル
ボン酸塩、アルキルベンゼンスルホン酸塩、α−オレフ
ィンスルホン酸塩、高級アルコール硫酸エステル塩、ア
ルキルエーテル硫酸塩、ポリオキシリン酸エステル塩等
のものが挙げられ、またカチオン性界面活性剤として脂
肪族アミン塩、脂肪酸4級アンモニウム塩、ベンザルコ
ニウム塩、ピリジニウム塩、イミダゾリニウム塩等が挙
げられ、また非イオン性界面活性剤としてポリオキシエ
チレンアルキルエーテル、ポリオキシエチレン2級アル
コールエーテル、ポリオキシエチレン−ポリオキシプロ
ピレンブロックポリマー、ポリオキシエチレングリセリ
ン脂肪酸エステル、ポリエチレングリコール脂肪酸エス
テル、脂肪酸モノグリセリド、脂肪酸アルカノールアミ
ド、ポリオキシエチレンアルキルアミン、ソルビタン脂
肪酸エステル等が挙げられ、更に両性界面活性剤として
カルボキシベタイン型、アミノカルボン酸塩、イミダゾ
リニウムベタイン等が挙げられる。Anionic, which is conventionally known as a surfactant,
Various kinds of surfactants such as cationic, nonionic and amphoteric can be used. Specifically, as the anionic surfactant, alkyl sulfate ester salt, alkyl ether carboxylate salt, alkylbenzene sulfonate salt, α-olefin sulfonate salt, higher alcohol sulfate ester salt, alkyl ether sulfate salt, polyoxyphosphate ester salt, etc. The cationic surfactants include aliphatic amine salts, fatty acid quaternary ammonium salts, benzalkonium salts, pyridinium salts, imidazolinium salts, and the like, and the nonionic surfactants include polyamines. Oxyethylene alkyl ether, polyoxyethylene secondary alcohol ether, polyoxyethylene-polyoxypropylene block polymer, polyoxyethylene glycerin fatty acid ester, polyethylene glycol fatty acid ester, fatty acid monoglyceride, fatty acid Luke alkanolamides, polyoxyethylene alkylamine, sorbitan fatty acid esters, and the like, further carboxy betaine type amphoteric surface active agents, amino carboxylate, imidazolinium betaine.
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
面層の形状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 shape 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.
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1〜4 下記の表に示す組成の各PVCペースト中に、同表に示す
種類、量の界面活性剤、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。Examples 1 to 4 and Comparative Examples 1 to 4 Each PVC paste having the composition shown in the table below was blended with a surfactant, white carbon and the like in the types and amounts shown in the table to prepare matte pastes. .
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.
また、難燃紙に塗布厚0.12mmとなるようにナイフコーテ
ィング法にてコートし、210℃で60秒間加熱した後、そ
の表面平滑状態を目視観察して艶消ペーストのコーティ
ング性を調べた。Further, flame-retardant paper was coated with a knife coating method to a coating thickness of 0.12 mm, heated at 210 ° C. for 60 seconds, and the surface smoothness was visually observed to examine the coating properties of the matte paste.
上記ペースト粘度、光沢度、コーティング性の結果を下
記表に併せて示す。The results of the above-mentioned paste viscosity, glossiness and coatability are also shown in the table below.
〔発明の効果〕 以上説明したように、本発明艶消組成物はPVCペースト
中に特定粒子径のホワイトカーボンと共に界面活性剤を
併用して配合してなるため、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、しか
も従来、後加工として行われていた表面艶消処理が全く
不要となり、安価な艶消処理を容易に行うことができ
る。 [Effects of the Invention] As described above, the matting composition of the present invention is prepared by combining a white paste having a specific particle size with a surfactant in a PVC paste, and thus has excellent fluidity and matting properties. It has an effect, as a result, it is possible to form a matte product using this composition directly, and further, the surface matting treatment which has been conventionally performed as a post-process is completely unnecessary, An inexpensive matte treatment can be easily performed.
また本発明によれば、スクリーン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印刷が可
能となる。しかも、本発明品は優れた流動性を有すると
共に、ブレンディングレジン等のように粗大粒子を含む
ものではないため、膜厚の薄いコーティングやスクリー
ン印刷に対しても問題なく適用することができる。Further, according to the present invention, it is possible to print with a gloss difference by appropriately distributing and using the normal compounded ink and the matte compounded ink comprising the product of the present invention in screen printing and the like. Moreover, since the product of the present invention has excellent fluidity and does not contain coarse particles such as blending resin, it can be applied to thin coating or screen printing without any problem.
Claims (1)
部に対して、二次粒径が1〜15μmのホワイトカーボン
を5〜15重量部配合すると共に界面活性剤を0.5〜3重
量部配合してな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. To 100 parts by weight of a resin in a polyvinyl chloride paste, 5 to 15 parts by weight of white carbon having a secondary particle size of 1 to 15 μm is added, and 0.5 to 3 parts by weight of a surfactant is added. A matte polyvinyl chloride paste composition characterized by comprising:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1079333A JPH0742369B2 (en) | 1989-03-30 | 1989-03-30 | Matted polyvinyl chloride paste composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1079333A JPH0742369B2 (en) | 1989-03-30 | 1989-03-30 | Matted polyvinyl chloride paste composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02255748A JPH02255748A (en) | 1990-10-16 |
| JPH0742369B2 true JPH0742369B2 (en) | 1995-05-10 |
Family
ID=13686967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1079333A Expired - Fee Related JPH0742369B2 (en) | 1989-03-30 | 1989-03-30 | Matted polyvinyl chloride paste composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0742369B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3973775B2 (en) * | 1998-09-07 | 2007-09-12 | 花王株式会社 | Paste resin composition |
-
1989
- 1989-03-30 JP JP1079333A patent/JPH0742369B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02255748A (en) | 1990-10-16 |
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