JPS6160767A - Water based paint - Google Patents

Water based paint

Info

Publication number
JPS6160767A
JPS6160767A JP18298684A JP18298684A JPS6160767A JP S6160767 A JPS6160767 A JP S6160767A JP 18298684 A JP18298684 A JP 18298684A JP 18298684 A JP18298684 A JP 18298684A JP S6160767 A JPS6160767 A JP S6160767A
Authority
JP
Japan
Prior art keywords
slurry
based paint
water
average particle
calcium carbonate
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
JP18298684A
Other languages
Japanese (ja)
Inventor
Eiji Okada
英二 岡田
Tadashi Saito
斉藤 直史
Toshiya Morishita
森下 俊哉
Hiroshi Shibata
洋志 柴田
Shinji Awasuno
粟巣野 伸司
Shirou Genkichi
源吉 嗣郎
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.)
Maruo Calcium Co Ltd
Original Assignee
Maruo Calcium 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 Maruo Calcium Co Ltd filed Critical Maruo Calcium Co Ltd
Priority to JP18298684A priority Critical patent/JPS6160767A/en
Publication of JPS6160767A publication Critical patent/JPS6160767A/en
Pending legal-status Critical Current

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  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To provide a water based paint having excellent viscosity stability and surface gloss imparting property, by blending finely ground limestone having a treated surface as an extender pigment. CONSTITUTION:0.05-10pts.wt. carboxylic acid base anionic surfactant (e.g. fatty acid soap or resin acid soap) is mixed with 100pts.wt. finely ground limestone having an average particle size of 0.4-1mu obtd. by grinding limestone, to obtain finely ground limestone having a treated surface. The obtained ground limestone is blended as an extender pigment by any of conventional methods to obtain a water based paint.

Description

【発明の詳細な説明】 「産業上の利用分野」 本発明は水系塗料に関し、更に詳しくは水系塗料の体質
顔料として優れた分散性ををし、且つ鮮映な表面光沢を
付与する表面処理されたyk糊な重質炭酸カルシウム(
以下、微細mカルと記す)を配してなる水系塗料に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION "Field of Industrial Application" The present invention relates to water-based paints, and more specifically, to water-based paints that have excellent dispersibility as extender pigments and that are surface-treated to provide a clear surface gloss. Heavy weight calcium carbonate (
The present invention relates to a water-based paint containing a microorganism (hereinafter referred to as "fine cal").

「従来の技術」 「発明が解決しようとする問題点」従
来、水系塗料の表面光沢を付与させる方法としては育成
物で表面処理された1次粒子径が01O2〜0.1βm
の微細な沈j@ 51 jl!酸カルシウム(以下、沈
降製炭カルと記す)を使用する方法と、湿式粉砕法で石
灰石を粉砕した微細型カルスラリ−を使用する方法が知
られている0表面光沢を付与するには粒子が微細で出来
るだけ分散しているばかりでなく、ビヒクルとの相容性
にも優れている必要がある。
``Prior art'' ``Problems to be solved by the invention'' Conventionally, as a method for imparting surface gloss to water-based paints, the primary particle diameter of the surface treated with a grown material was 01O2 to 0.1βm.
Minute precipitation j @ 51 jl! There are two known methods: one using calcium oxide (hereinafter referred to as precipitated charcoal) and the other using a fine calc slurry made by crushing limestone using a wet pulverization method. Not only must it be as dispersed as possible, but it must also be compatible with the vehicle.

ゴム、プラスチックなどの充填剤として、一般的に用い
られている表面処理された微細な炭酸カルシウム、即ち
、脂肪酸石鹸、樹脂酸石鹸のようなカルボン酸型陰イオ
ン界面活性剤を単独処理した微細な炭酸カルシウムは、
塗料の製造に一般的に用いられているサンドグラインダ
ーのような破砕力の弱い分散機を用いた場合には、塗料
中に容易に分散しないという欠点を有する。このことは
特公昭46−15771、特開昭59−1571にも明
記されているところである。そこで、すでに微細な化1
1t!1!l炭カルについて塗料への分散性を改良する
表面処理方法がJf々検討され、例えば特公昭46−1
577L特開昭55−16031、同59−1571等
により報告されている。しかし、粒子径状からの検討は
あまりなされておらず、具体的成果についてもほとんど
軸台されていない。
Surface-treated fine calcium carbonate, which is commonly used as a filler for rubber, plastic, etc., or fine calcium carbonate treated solely with a carboxylic acid type anionic surfactant such as fatty acid soap or resin acid soap. Calcium carbonate is
When a dispersing machine with a weak crushing force, such as a sand grinder, which is commonly used in the production of paints, is used, it has the disadvantage that it is not easily dispersed in the paint. This is clearly stated in Japanese Patent Publication No. 46-15771 and Japanese Patent Application Laid-open No. 59-1571. Therefore, already microscopic 1
1t! 1! Surface treatment methods for improving the dispersibility of charcoal into paints have been investigated, for example, in Japanese Patent Publication No. 46-1
577L has been reported in JP-A-55-16031, JP-A-59-1571, etc. However, little research has been done in terms of particle size, and few concrete results have been reported.

一方、水系塗料には例えば特開昭58−204061に
見られる如く、湿式粉砕法で石灰石を粉砕した微ll1
カルスラリ−が使用されている。これは60〜7011
t%以上の高濃度のスラリーであり、スラリー粘度を低
下させるためポリアクリル酸ソーダの高分子分肢剤を添
加している。しかし、この方法によって得られる炭酸力
ルノウムであっても、現在の塗膜に高光沢を要求される
水系塗料の体rtlIjl料としては未だ満足すべきも
のとは云い難い。
On the other hand, for water-based paints, for example, as seen in JP-A-58-204061, limestone is crushed using a wet crushing method.
Callus slurry is used. This is 60-7011
It is a slurry with a high concentration of t% or more, and a polymer dispensing agent of sodium polyacrylate is added to reduce the viscosity of the slurry. However, even the carbonate obtained by this method is still far from satisfactory as a material for water-based paints that require high gloss in current coatings.

塗膜に高光沢を要求される水系塗料にはta細な酸化チ
タンが111Mとして使用され、炭酸カルシウムの如き
体質顔料は殆ど使用されていないのが現状である。一方
、塗膜に高光沢を要求されない水系塗料には、平均粒子
径1.5μ以上の重質炭酸カルシウムが体質顔料として
大量に使用されている。
Currently, fine titanium oxide is used as 111M in water-based paints that require high gloss in the coating film, and extender pigments such as calcium carbonate are hardly used. On the other hand, heavy calcium carbonate with an average particle diameter of 1.5 μm or more is used in large quantities as an extender pigment in water-based paints that do not require high gloss in the coating film.

しかし乍ら、これは重質炭酸カルシウムは安価であるの
で単に水系塗料のコストダウン及び1膜成形のための増
量剤として使用されているに過ぎない、かくして、塗膜
に高光沢を要求される水系塗料用体質顔料として、十分
満足し得る体質顔料の開発が望まれているのが実情であ
る。
However, since heavy calcium carbonate is cheap, it is only used as an extender to reduce the cost of water-based paints and to form a single film.Thus, high gloss is required for the paint film. The reality is that there is a desire to develop extender pigments that are fully satisfactory as extender pigments for water-based paints.

「問題点を解決するための手段」 本発明者らはかかる実情に鑑み、@梅な重カルをカルボ
ン酸型陰イオン界面活性剤で表面処理し、これを水系塗
料に使用することにより、従来の沈降製炭カル品又は重
カルスラリー品にない画期的な予想外の効果が得られる
ことを見いだし、本発明を完成させたものである。
"Means for Solving the Problems" In view of the above circumstances, the present inventors surface-treated @Umena Heavy Cal with a carboxylic acid type anionic surfactant and used it in a water-based paint. The present invention was completed based on the discovery that a groundbreaking and unexpected effect not found in sedimentary coal-made coal products or heavy coal slurry products can be obtained.

即ち、本発明は平均粒子径が0.4〜1.0μmの微細
な重質炭酸カルシウムに、カルボン酸型陰イオン界面活
性剤をii質炭酸カルシウム100!量部当り0.05
〜10重量部添加して粒子表面を処理した微細な重質炭
酸カルシウムを体質顔料として配合してなる水系塗料を
内容とするものである。
That is, in the present invention, a carboxylic acid type anionic surfactant is added to fine heavy calcium carbonate having an average particle size of 0.4 to 1.0 μm to form a 100% grade of calcium carbonate. 0.05 per part
The content is a water-based paint containing as an extender pigment fine, heavy calcium carbonate which has been added in an amount of 10 parts by weight to treat the particle surface.

本発明において、平均粒子径とは、恒圧通気式比表面積
測定器で測定した比表面積から、道カル粒子を立方体粒
子と仮定して求めた立方体の一辺の長さをいう。
In the present invention, the average particle diameter refers to the length of one side of a cube, which is determined from the specific surface area measured with a constant pressure aeration type specific surface area measuring device, assuming that the Docal particles are cubic particles.

本発明に用いられる微ll1mカルを得るには、石灰石
を乾式もしくは湿式で粉砕し、平均粒子径0゜4〜1.
0μmの微細な粒子に調整する。乾式の場合はミクロン
ミル、振動ボールミル等で粉砕後、風力分級機で分級し
、湿式の場合はボールミル等で粉砕すれば良く、特に制
限されない、こうして得られ、た微1fiカルを湿式又
は乾式でカルボン酸型陰イオン界面活性剤で表面処理す
る。
In order to obtain the fine cals used in the present invention, limestone is ground dry or wet to an average particle size of 0.4 to 1.5 mm.
Adjust to fine particles of 0 μm. In the case of a dry method, it may be pulverized with a micron mill, vibrating ball mill, etc., and then classified with an air classifier, and in the case of a wet method, it may be pulverized with a ball mill, etc., and there is no particular restriction. Surface treatment with carboxylic acid type anionic surfactant.

本発明に用いられる表面処理剤は脂肪酸石鹸、樹脂酸石
鹸、ナフテン酸石鹸の如きカルボン酸型陰イオン界面活
性剤が好適で、これらは1種又は2J!以上混合して用
いられる。添加量はmlR炭酸カルシウム100重量部
当り0.05〜10ifi量部で、より好ましくは1〜
4m191+である0表面処理剤を1Ofltff1部
越えて添加しても表面処理幼果が向上せず、従って経済
的でなくなり、湿式処理の場合脱水が困難となり好まし
くない、また添加量が0.05i量部未満であると塗料
化し難くなる。
The surface treatment agent used in the present invention is preferably a carboxylic acid type anionic surfactant such as a fatty acid soap, a resin acid soap, or a naphthenic acid soap, and these may be one type or 2J! A mixture of the above is used. The amount added is 0.05 to 10 ifi parts per 100 parts by weight of mlR calcium carbonate, more preferably 1 to 10 parts by weight.
Adding more than 1 part of 1Ofltff of 0 surface treatment agent, which is 4m191+, does not improve the surface treated young fruit, and therefore it is not economical, and in the case of wet treatment, dehydration becomes difficult, which is not preferable, and the amount added is 0.05i. If the amount is less than 10%, it will be difficult to form into a paint.

湿式で粉砕したものは当P8湿式状態で表面処理するが
、乾式で粉砕した場合でも湿式で表面処理しても良い、
こうして処理したスラリーを脱水、乾燥、粉砕して製品
とする。一方、乾式で表面処理する場合はヘンシェルミ
キサー等を使用する。
Wet-pulverized products are surface-treated in a wet state in this P8, but even if they are dry-pulverized, they may be surface-treated in a wet state.
The slurry thus treated is dehydrated, dried, and crushed to produce a product. On the other hand, when performing dry surface treatment, a Henschel mixer or the like is used.

上記の如くして得られた微細型カルを常法通り水系塗料
に配合して、塗料を作製する。
The fine Cal obtained as described above is blended into a water-based paint in a conventional manner to produce a paint.

「実施例」 以下、具体的な実施例及び比較例を挙げて本発明を説明
するが、本発明はこれらにより何ら制限されるものでは
ない。
"Examples" The present invention will be described below with reference to specific examples and comparative examples, but the present invention is not limited by these in any way.

参考例1 平均粒子径1.5μmの重質炭カルを固形分が4011
L%になるように攪欅機を用いて水中に分散させたスラ
リーを調整した。このスラリーをサンドグラインダー(
−8A社製、DYNO旧LL)で回転数300 OR,
P、M、、流量51/hrで粉砕した。粉砕された重質
炭カルの平均粒子径は0.55μmであった。この重質
炭カル100重量部にステアリン酸ソーダを固形分で3
.0fflff1部添加して表面処理した、ステアリン
酸ソーダは10wL%熔液にして重質炭カルスラリ−を
表面処理した。これを脱水、乾燥、粉砕して試料とした
Reference example 1 Solid content of heavy carbon cal with an average particle size of 1.5 μm is 4011
A slurry was dispersed in water using a stirrer to adjust the slurry to L%. Pour this slurry into a sand grinder (
-Manufactured by 8A, DYNO (old LL), rotation speed 300 OR,
P, M, was pulverized at a flow rate of 51/hr. The average particle size of the pulverized heavy coal was 0.55 μm. Add 3 parts of sodium stearate to 100 parts by weight of this heavy coal as a solid content.
.. The surface treatment was carried out by adding 1 part of 0fflff. Sodium stearate was made into a 10wL% solution and the surface treatment of the heavy carbon callus slurry was carried out. This was dehydrated, dried, and ground to make a sample.

参考例2 平均粒子pi1. Sμmの重質炭カルを固形分が50
wt%になるようにl1ll[を用いて水中に分散させ
たスラリーを!lIl整した。このスラリーをサンドグ
ラインダー(WIlA社製、DYNOMILL>で回転
数300 OR,P、M、、流量91/hrで粉砕した
。粉砕された重質炭カルの平均粒子径は0.8μmであ
った。
Reference Example 2 Average particle pi1. Solid content of Sμm heavy carbon cal is 50
Slurry dispersed in water using l1ll [wt%! I've adjusted everything. This slurry was pulverized using a sand grinder (manufactured by WIlA, DYNOMILL) at a rotation speed of 300 OR, P, M, and a flow rate of 91/hr. The average particle diameter of the pulverized heavy charcoal was 0.8 μm.

この重質炭カル100重量部にステアリン酸ソーダを固
形分で2.0重量部添加して表面処理した。
2.0 parts by weight of sodium stearate (solid content) was added to 100 parts by weight of this heavy coal for surface treatment.

ステアリン酸ソーダは10wL%熔液にして重質炭カル
スラリ−を表面処理した。これを脱水、乾燥、粉砕して
試料とした。
Sodium stearate was made into a 10wL% solution and the surface of the heavy carbon callus slurry was treated. This was dehydrated, dried, and ground to make a sample.

参考例3 平均粒度10.ommの石灰石を振動ボールミルで粉砕
した後、風力分級機で分級して、平均粒子1蚤0.6μ
mの!i質炭カルを関鉦した。この重質炭カルを固形分
が20wt%になるように攪拌既を用いて水中に分散さ
せたスラリーを間抜した。この重質炭カルhoO31z
1部に対してステアリン酸ソーダを3.0重量部添加し
て表面処理した。ステアリン酸ソーダは10wtMf4
液にして重質炭カルスラリ−を表面処理した。これを脱
水、乾燥、粉砕して試料とした。
Reference example 3 Average particle size 10. Omm limestone is crushed with a vibrating ball mill and then classified with a wind classifier to obtain an average particle size of 0.6μ.
m's! I passed the I-quality charcoal test. A slurry was prepared by dispersing this heavy coal in water using a stirrer so that the solid content was 20 wt%. This heavy coal calhoO31z
3.0 parts by weight of sodium stearate was added to 1 part for surface treatment. Sodium stearate is 10wtMf4
The surface treatment of the heavy carbon callus slurry was carried out by converting it into a liquid. This was dehydrated, dried, and ground to make a sample.

参考例4 参考例3の分級程度を変えて、平均粒子径0,75μm
の重質炭カルを得た。この重質炭カル100iflE部
にステアリン酸ソーダ3.0!量部を加え、ヘンシェル
ミキサーを用いて表面処理して試料とした。
Reference example 4 By changing the classification degree of reference example 3, the average particle diameter was 0.75 μm.
of heavy coal was obtained. 3.0 parts of sodium stearate in 100iflE parts of this heavy coal! A certain amount was added, and the surface was treated using a Henschel mixer to prepare a sample.

参考例5 沈降法によって一次粒子径0.07μmの沈降製炭カル
の15wt%スラリーを作り、得られたスラリーの固形
分100!i量部に対してステアリン酸ソーダを3.0
 !i重量部添加て表面処理した。ステアリン酸ソーダ
は10wt94溶液にして沈降製炭カルスラリ−を表面
処理した。これを脱水、乾燥、粉砕して試料とした。
Reference Example 5 A 15 wt% slurry of precipitated charcoal with a primary particle diameter of 0.07 μm was prepared by the sedimentation method, and the solid content of the resulting slurry was 100! 3.0 parts of sodium stearate per i part
! i parts by weight were added for surface treatment. Sodium stearate was used as a 10wt94 solution to treat the surface of the precipitated charcoal callus slurry. This was dehydrated, dried, and ground to make a sample.

参考例6 参考例5のステアリン酸ソーダのかわりに、ドデシルベ
ンゼンスルフォン酸2.0Jilfmでステアリン酸3
.0μm1部を乳化した乳化液を用いて表面処理し、参
考例5と同一の方法で試料を得た。
Reference Example 6 Instead of sodium stearate in Reference Example 5, 3 stearic acid was added with 2.0 Jilfm of dodecylbenzenesulfonic acid.
.. A sample was obtained in the same manner as in Reference Example 5 by surface treatment using an emulsion prepared by emulsifying 1 part of 0 μm.

参考例7 参考例1で粉砕された平均粒子径0.55μmの!I!
質炭カルスラリーを固形分濃度70wt%まで脱水後、
11質炭力ル100iii1部に対して1.Qi重量部
ポリアクリル酸ソーダを添加し、ラボディスパーにてス
ラリー化した。この重質炭カルスラリ−を試料とした。
Reference Example 7 The average particle diameter of the powder crushed in Reference Example 1 was 0.55 μm! I!
After dehydrating the coal slurry to a solid content concentration of 70 wt%,
1 part for 100iii of quality 11 coal. Qi weight part sodium polyacrylate was added and slurried using a lab body spar. This heavy coal callus slurry was used as a sample.

参考例8 参考例3の分級程度を変えて平均粒子1冬1.2μmの
m貿炭カルを得た。その(6は全て参考例3と間−の方
法で試料を得た。
Reference Example 8 By changing the degree of classification in Reference Example 3, a m trade coal with an average particle size of 1.2 μm was obtained. All samples (6) were obtained using the same method as Reference Example 3.

参考例9 参考例1と同一の平均粒子径の重質炭カルを得た1表面
処理は一切せず、無処理のまま脱水、乾燥、粉砕し試料
とした。
Reference Example 9 A heavy coal with the same average particle size as Reference Example 1 was obtained. No surface treatment was performed, and the sample was dehydrated, dried, and ground without any treatment.

実施例1〜4、比較例1〜5 上記参考例1〜9で作成した試料を用いて、次の塗料配
合及び塗料化方法により塗料化した。塗料物性を測定し
た結果を第111に示した。
Examples 1 to 4, Comparative Examples 1 to 5 Using the samples prepared in Reference Examples 1 to 9 above, paints were formed using the following paint formulation and paint forming method. The results of measuring the physical properties of the paint are shown in No. 111.

(イ)塗料配合 1次配合 ミルベース                (重量部
)分散剤(第1工業11薬;ノイゲンIIA−120>
    2分散剤(第1工業製薬;ディスコ−) N−
14)   8凍結防止剤(プロピレングリコール)5
0チタン白(石屋産業; R−8301194試料(参
考例1〜9)65 水                        
  522次配合 レッドダウン               (ni1
部)ミルベース                18
6エマルジヨン(大日本インキ;222 ボンコートEC−821) 造膜助剤(ブチルセロソルブ)35 (ロ)塗料化方法 1次間合:i′ii1易式SCミルで20分間分散させ
た。
(a) Paint formulation primary blending mill base (parts by weight) Dispersant (Daiichi Kogyo 11 drugs; Neugen IIA-120>
2 Dispersant (Daiichi Kogyo Seiyaku; Disco) N-
14) 8 Antifreeze agent (propylene glycol) 5
0 Titanium white (Ishiya Sangyo; R-8301194 sample (Reference examples 1 to 9) 65 Water
522 secondary combination red down (ni1
Part) Mill base 18
6 Emulsion (Dainippon Ink; 222 Boncoat EC-821) Film-forming agent (butyl cellosolve) 35 (b) Paint forming method First interval: i'ii 1 Dispersion was carried out for 20 minutes in an easy type SC mill.

回転数は800R,P、M、である。The rotation speed is 800R, P, M.

2欠配合ニラボディスバーで5分間攪拌した。The mixture was stirred for 5 minutes using a 2-lack Nirabo Disbur.

「発明の効果」 第1表の結果から明らかな如く、本発明の表面処理微細
mカルを配合してなる水系塗料は、従来の沈降製炭カル
又は、湿式粉砕m炭カルスラリ−を配合した水系塗料に
比べ表面光沢、粘度安定性において顕著な効果が認めら
れる。
"Effects of the Invention" As is clear from the results in Table 1, the water-based paint containing the surface-treated fine m-cal of the present invention is different from the water-based paint containing the conventional precipitated charcoal or the wet-pulverized m-char slurry. Remarkable effects on surface gloss and viscosity stability are observed compared to paints.

Claims (1)

【特許請求の範囲】[Claims] 1、平均粒子径が0.4〜1.0μmの微細な重質炭酸
カルシウムに、カルボン酸型陰イオン界面活性剤を重質
炭酸カルシウム100重量部当り0.05〜10重量部
添加して粒子表面を処理した微細な重質炭酸カルシウム
を体質顔料として配合してなる水系塗料。
1. Add 0.05 to 10 parts by weight of a carboxylic acid type anionic surfactant per 100 parts by weight of ground calcium carbonate to fine ground calcium carbonate with an average particle diameter of 0.4 to 1.0 μm to form particles. A water-based paint containing fine surface-treated heavy calcium carbonate as an extender pigment.
JP18298684A 1984-08-31 1984-08-31 Water based paint Pending JPS6160767A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18298684A JPS6160767A (en) 1984-08-31 1984-08-31 Water based paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18298684A JPS6160767A (en) 1984-08-31 1984-08-31 Water based paint

Publications (1)

Publication Number Publication Date
JPS6160767A true JPS6160767A (en) 1986-03-28

Family

ID=16127760

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18298684A Pending JPS6160767A (en) 1984-08-31 1984-08-31 Water based paint

Country Status (1)

Country Link
JP (1) JPS6160767A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04250840A (en) * 1990-06-13 1992-09-07 Basf Ag Dispersing agent having possibility of removal or decomposition by enhanced living organisms
JP2007537320A (en) * 2004-05-12 2007-12-20 アルファ カルツィット フィルシュトッフ ゲゼルシャフト エム・ベー・ハー Surface-modified inorganic fillers and pigments
JP2014509344A (en) * 2011-02-23 2014-04-17 オムヤ・インターナツイオナール・アー・ゲー COATING COMPOSITION CONTAINING PARTICLES CONTAINING SUBMICRON CALCIUM CARBONATE, METHOD FOR PREPARING THE SAME AND USE OF PARTICLES CONTAINING SUBMICRON CALCIUM CARBONATE

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5423635A (en) * 1977-07-25 1979-02-22 Shiraishi Kogyo Kaisha Ltd Calcium carbonate pigment for use in coating
JPS54162731A (en) * 1978-06-13 1979-12-24 Shiraishi Kogyo Kaisha Ltd Coating composition and pigment coated paper
JPS5516031A (en) * 1978-07-19 1980-02-04 Shiraishi Chuo Kenkyusho:Kk Extender pigment and its preparation
JPS5562296A (en) * 1978-10-30 1980-05-10 Omya Sa High solid content coating agent
JPS58204061A (en) * 1982-05-20 1983-11-28 Maruo Calcium Kk Water paint

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5423635A (en) * 1977-07-25 1979-02-22 Shiraishi Kogyo Kaisha Ltd Calcium carbonate pigment for use in coating
JPS54162731A (en) * 1978-06-13 1979-12-24 Shiraishi Kogyo Kaisha Ltd Coating composition and pigment coated paper
JPS5516031A (en) * 1978-07-19 1980-02-04 Shiraishi Chuo Kenkyusho:Kk Extender pigment and its preparation
JPS5562296A (en) * 1978-10-30 1980-05-10 Omya Sa High solid content coating agent
JPS58204061A (en) * 1982-05-20 1983-11-28 Maruo Calcium Kk Water paint

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04250840A (en) * 1990-06-13 1992-09-07 Basf Ag Dispersing agent having possibility of removal or decomposition by enhanced living organisms
JP2007537320A (en) * 2004-05-12 2007-12-20 アルファ カルツィット フィルシュトッフ ゲゼルシャフト エム・ベー・ハー Surface-modified inorganic fillers and pigments
JP2014509344A (en) * 2011-02-23 2014-04-17 オムヤ・インターナツイオナール・アー・ゲー COATING COMPOSITION CONTAINING PARTICLES CONTAINING SUBMICRON CALCIUM CARBONATE, METHOD FOR PREPARING THE SAME AND USE OF PARTICLES CONTAINING SUBMICRON CALCIUM CARBONATE

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