JPS5883069A - Pigment dispersant - Google Patents

Pigment dispersant

Info

Publication number
JPS5883069A
JPS5883069A JP17981781A JP17981781A JPS5883069A JP S5883069 A JPS5883069 A JP S5883069A JP 17981781 A JP17981781 A JP 17981781A JP 17981781 A JP17981781 A JP 17981781A JP S5883069 A JPS5883069 A JP S5883069A
Authority
JP
Japan
Prior art keywords
dispersant
unsaturated carboxylic
ethylenically unsaturated
carboxylic acid
pigment
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.)
Granted
Application number
JP17981781A
Other languages
Japanese (ja)
Other versions
JPH0143786B2 (en
Inventor
Yuji Kawamura
祐司 河村
Hisao Tanaka
久夫 田中
Shizuro Kimata
木全 鎮朗
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.)
Toagosei Co Ltd
Original Assignee
Toagosei 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 Toagosei Co Ltd filed Critical Toagosei Co Ltd
Priority to JP17981781A priority Critical patent/JPS5883069A/en
Publication of JPS5883069A publication Critical patent/JPS5883069A/en
Publication of JPH0143786B2 publication Critical patent/JPH0143786B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a pigment dispersant which gives a dispersion exhibiting an excellent stability at a low viscosity even at a high concn., consisting of a copolymer (salt) obtd. from an alpha,beta-ethylenically unsaturated carboxylic acid, a specified addition reaction product and a (meth)acrylate ester. CONSTITUTION:A pigment dispersant consists of a copolymer (salt) obtd. by polymerizing 50-97.9wt% alpha,beta-ethylenically unsaturated carboxylic acid (A) such as acrylic acid, 0.1-20wt% addition reaction product (B) obtd. by reacting a glycidyl ether or a glycidyl ester with an alpha,beta-ethylenically unsaturated carboxylic acid, and 2-30wt% (meth)acrylate ester (C) in the presence of a polymn. initiator and in an aq. medium at 50-150 deg.C for 1-10hr. This dispersant is used in an amount of 0.05-5% based on the amount of a pigment.

Description

【発明の詳細な説明】 本発明は、高濃度においても低粘度で且つ、分散液の安
定性に優れた分散液を調整し得る分散剤。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a dispersant that can prepare a dispersion liquid that has low viscosity even at high concentrations and has excellent dispersion stability.

4IKI[被紙用−料の分散の友めに用いられる分散剤
を提供するものである。
4IKI [Provides a dispersant used for dispersing paper stock.

従来から、カオリン、クレー、炭酸カルシウム、酸化チ
タン、硫酸バリウム、サテンホワイト等の如き、各種顔
料を使用して、塗被紙が製造されている。
Coated papers have traditionally been produced using various pigments such as kaolin, clay, calcium carbonate, titanium oxide, barium sulfate, satin white, and the like.

即ち塗被紙は、一般に、上記の如き顔料に1分散剤を添
加して水分散液とし、これに、顔料パイ。
That is, coated paper is generally prepared by adding a dispersant to the pigment described above to form an aqueous dispersion, and then adding a pigment pie to the aqueous dispersion.

ンダーとじてのカゼイン、澱粉、又は、スチレン/ブタ
ジェン系ラテックス等の単独、もしくは、混合物を添加
し、かくして得た塗被液を原紙に塗布し1次いで乾燥し
、更にスーパーカレンダーにかける等の機械的処理を施
して製造されている。
A machine that adds casein, starch, styrene/butadiene latex, etc. alone or as a mixture, coats the coating liquid thus obtained on base paper, then dries it, and then supercalends it. Manufactured using special treatment.

これ等塗被紙の製造において、今日では、最良の印刷適
正効果を得るためと、この効果を比較的安価な製造条件
の下に得んとするために、塗被液の製造における顔料分
散液の調整にあたっては、一種類の顔料だけが使用され
ることはなく、各種の異なった顔料が組み合わされて使
用されるようになってきたこと、使用顔料も、従来品に
比べ、より微粒子径のものが使用されるようになってき
たこと、更に水分含有量の少ない為濃度の顔料分散液の
調整が望まれるようになってきたことなどの様々な要件
から、使用される分散剤にも上記漬水に応することがで
きる着炎に高度な、分敏効釆即t 塗被紙の品質上、よ
り少量の使用量で高濃度の顔料分散液の調整が可能であ
ること2 顔料分散液の粘度安定性に優れていること&
 種々の広範囲な、JII料に対して有効な分散効果を
示すこと などが強く要求されている。
In the production of these coated papers, in order to obtain the best printability effect and to obtain this effect under relatively inexpensive production conditions, pigment dispersions are used in the production of coating liquids. When adjusting pigments, it is no longer just one type of pigment that is used, but a combination of various different pigments. Due to various requirements such as the increasing use of pigment dispersants and the desire to adjust the concentration of pigment dispersions due to their low water content, the dispersants used are also subject to the above-mentioned requirements. A highly sensitive pot with high flame resistance that can withstand immersion in water.Due to the quality of the coated paper, it is possible to prepare a highly concentrated pigment dispersion using a smaller amount.2 Pigment dispersion. Excellent viscosity stability &
There is a strong demand for effective dispersion effects for a wide variety of JII materials.

%に、炭酸カルシウム、サナ/ホワイト、などの反応性
顔料を使用した場合しかもさらにこれら顔料の粒子が比
較的微粒子状のものを使用した場合に於ては、−且分散
せしめた顔料粒子の二次的凝集が生起し易く、この九め
分散液の粘度が増大し、流動性を減じ、塗被液の安定性
を悪くし良好な塗布が施こされないばかりか、得られた
塗被紙の印刷適正が劣悪であって、目的を果し難い。こ
の様な分散状態の不良性は、従来の分散剤の分散機能が
劣ること、即ち従来の分散剤の有する分散機能では上記
二次的凝集を防止する効果が十分でなく、従来の分散剤
を用いて作られた顔料分散液は、短時間に沈降、分陰し
たり1分散直后の粘度が高いか、或は、たとえ分散角波
には、塗工作業にほぼ適用し得る様な粘度のものが、得
られても経時的に粘度が増加するという欠点を有してお
り。
%, when reactive pigments such as calcium carbonate, sana/white, etc. are used, and furthermore, when relatively fine particles of these pigments are used, Secondary agglomeration is likely to occur, increasing the viscosity of this dispersion, reducing fluidity, and worsening the stability of the coating solution, which not only prevents good coating, but also prevents the resulting coated paper from being coated properly. The printing quality is poor and it is difficult to achieve the purpose. This poor dispersion state is due to the poor dispersion function of conventional dispersants, that is, the dispersion function of conventional dispersants is not sufficiently effective in preventing the above-mentioned secondary agglomeration, and conventional dispersants cannot be used. Pigment dispersions prepared using pigment dispersions may settle in a short period of time, undergo dispersion, or have a high viscosity immediately after dispersion, or even if the dispersion angle wave has a viscosity that is almost applicable to coating operations. Even if it is obtained, it has the disadvantage that the viscosity increases over time.

それが塗工性および塗被紙性能に悪影響を及ぼすのであ
る。
This adversely affects coatability and coated paper performance.

従来、塗被紙用の顔料の分散剤としては、ポリアクリル
酸ソーダ、アクリル酸/無水マレイン酸共重合体などの
有機高分子系顔料分散剤が広く用いられているが、これ
らは前述の如き状況下において要求されている分散効果
に対しては、末だ不満足なものである。
Conventionally, organic polymeric pigment dispersants such as sodium polyacrylate and acrylic acid/maleic anhydride copolymers have been widely used as pigment dispersants for coated paper; The diversification effect required under the circumstances is extremely unsatisfactory.

本発明者等は、上記した塗被紙用顔料の分散剤について
、更に深く検討を加えた結果、優れた分散機能を有する
分散剤を見出し、本発明を完成するに至った。
The present inventors conducted a more in-depth study on the above-mentioned dispersant for pigments for coated paper, and as a result, they discovered a dispersant having an excellent dispersion function and completed the present invention.

■ d、β−エチレン性不飽和カルボン酸■ グリシジ
ルエーテル類あるいはグリシジルエステル類とα、β−
エチレン性不飽和カルボン酸の付加反応生成物 ■ アクリル酸エステルおよび/またはメタクの分散剤
は従来から用いられているポリアクリル酸ソーダ等に比
べて著しく顔料分散効果が優れており、また少量の使用
でその機能を発揮し得るものである。
■ d, β-ethylenically unsaturated carboxylic acid ■ Glycidyl ethers or glycidyl esters and α, β-
Addition reaction product of ethylenically unsaturated carboxylic acid■ Acrylic acid ester and/or methacrylate dispersants have a significantly superior pigment dispersing effect compared to conventionally used sodium polyacrylates, etc., and can be used in small amounts. It is possible to perform this function.

更に本発明分散剤について、詳述すると本発明分散剤は
、重合体構成成分がα、β−エチレン性不飽和カルボン
酸、グリシジルエーテル類あるいはグリシジルエステル
類とα、β−エチレン性不飽和カルボン酸の付加反応生
成物、アクリル酸エン性不飽和カルボン酸とは、翼体的
にはアクリル酸、メタクリル酸、イタコン酸、マレイン
酸、フマール酸、クロトン酸などである。
Further, to describe the dispersant of the present invention in detail, the dispersant of the present invention has polymer constituents of α,β-ethylenically unsaturated carboxylic acid, glycidyl ethers, or glycidyl esters and α,β-ethylenically unsaturated carboxylic acid. The addition reaction product of acrylic acid and the eneneically unsaturated carboxylic acid include acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, and the like.

グリシジルエーテル類あるいはグリシジルエステル類と
α、β−エチレン性不ji14aカルボン酸の付加反応
生成物としては、グリシジルエーテル類あるいはグリシ
ジルエステル類トα、β−x チL/ン性不飽和カルボ
ン酸とを公知の方法で反応させて得られる付加反応生成
物あるいは、変性物で。
As addition reaction products of glycidyl ethers or glycidyl esters and α,β-ethylenically unsaturated carboxylic acids, glycidyl ethers or glycidyl esters and α,β-x-ethylenically unsaturated carboxylic acids are used. Addition reaction products or modified products obtained by reaction using known methods.

その代表的な、構造式はグリシジルエーテルにっR1 いて云えば、 ルー0O−0−CH,−0H−OH−0−A■ OH R。Its typical structural formula is glycidyl ether R1 In other words, Ru0O-0-CH, -0H-OH-0-A■ OH R.

■ あるいVi R,−Co−0−OH−OH−0−AOH
,0H (Aiiフルキル基、アリール基、シクロアルキル基、
アシル基を表わし、R1はσ、β−エチレン性不飽和カ
ルボン酸のカルボキシル基を除い九部分也はOH,又は
Hを表す)f′表わされる。ここでα、β−エチレン性
不飽和カルボン酸としては前記したものが用いられ、グ
リシジルエーテル類あるいはグリシジルエステル類とし
ては、具体的にはメチルグリシジルエーテル、エチルグ
リジルエーテル、ブチルグリシジルエーテル、2−エチ
ルヘキシルグリシジルエーテル、ラクリルグリシジルエ
ーテル、ブチルメタグリシジルエーテル、7エ二ルクリ
シジルエーテル、フェニルメタグリシジルエーテル、ア
リルグリシジルエー−テル、酢酸メタグリシジルエステ
ル、プロピオン酸グリシジルエステル、安息香酸グリシ
ジルエステル、ラウリン酸グリシジルエステル、バルミ
チン酸グリシル類として、フェニルグリシジルエーテル
を用い鑑、β−エチレン性不飽和カルボン酸としてアク
リル酸を用いた場合の反応例を示すと1次の様になる。
■ Or Vi R, -Co-0-OH-OH-0-AOH
,0H (Aii furkyl group, aryl group, cycloalkyl group,
It represents an acyl group, and R1 is σ, except for the carboxyl group of β-ethylenically unsaturated carboxylic acid, and the 9th part also represents OH or H) f′. Here, as the α,β-ethylenically unsaturated carboxylic acid, those mentioned above are used, and as the glycidyl ethers or glycidyl esters, specifically, methyl glycidyl ether, ethyl glycidyl ether, butyl glycidyl ether, 2- Ethylhexyl glycidyl ether, lacryl glycidyl ether, butyl metaglycidyl ether, 7-enyl glycidyl ether, phenyl metaglycidyl ether, allyl glycidyl ether, metaglycidyl acetate, glycidyl propionate, glycidyl benzoate, glycidyl laurate A reaction example using phenylglycidyl ether as the ester and glycyl valmitate and acrylic acid as the β-ethylenically unsaturated carboxylic acid is as follows.

OH,OH(50〜10%以下) 又、これらの製造は、例へば特開昭53−18637等
に記載されている公知の方法で容易に得られる。
OH, OH (50 to 10% or less) These can be easily produced by known methods such as those described in JP-A-53-18637.

1II3成分としてのアクリル酸エステル、メタクリル
酸エステルとしては各種のものが用いられるが発泡防止
1分散効果の点からみて戻素数1〜8のアルキル基を有
するアクリル酸エステル又は、メタクリル酸エステルが
好まし、いものであり、これらに属するものとしては、
アクリル酸メチル。
Various acrylic esters and methacrylic esters can be used as the three components of 1II, but from the viewpoint of foam prevention and dispersion effects, acrylic esters or methacrylic esters having an alkyl group having 1 to 8 carbon atoms are preferred. , and belonging to these are:
Methyl acrylate.

メタクリル酸メチル、アクリル酸エチル、メタクリル酸
エチル、アクリル酸ブチル、メタクリル酸ブチル、アク
リル酸イソブチル、メタクリル酸イソブチル、アクリル
酸2エチルヘキシル、メタクリル酸2エチルヘキシル、
などである。
Methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate,
etc.

本発明の一一一共重合体は、上記3成分を構成成分とす
るものであるが1本発明の目的とする高度黛−散効果を
その共重合体に持たせるためには次の様な組成割合であ
るのが好ましい。
The 1-1 copolymer of the present invention has the above three components as its constituent components, but in order to provide the copolymer with the high-level dispersion effect targeted by the present invention, the following steps must be taken. It is preferable that it is a composition ratio.

■ ば、β−エチレン性不飽和カルボン酸50〜97.
9重量% ■ グリシジルエーテル類あるい社グリシジル■ アク
リル酸エステルおよび/またはメタアクリル酸エステル
 2〜30重量% 本発明の共重合体の組成割合が上記範囲を外れた場合、
従来使用されている公知の分散剤に比べて極わだった分
散性の向上がみられないか、もしくは、逆に顔料分散配
合瞼系の粘度が高くなったり、又、経時的に粘度上昇を
来たしたり、いわゆる安定な分散状態が得られないなど
の現象がみられる様になり好ましくない。
(2) For example, β-ethylenically unsaturated carboxylic acid 50-97.
9% by weight ■ Glycidyl ethers or glycidyl ■ Acrylic ester and/or methacrylic ester 2 to 30% by weight If the composition ratio of the copolymer of the present invention is out of the above range,
There is no significant improvement in dispersibility compared to conventionally used known dispersants, or conversely, the viscosity of the pigment dispersion blended eyelid system increases, or the viscosity increases over time. This is undesirable because phenomena such as the dispersion or the inability to obtain a so-called stable dispersion state are observed.

上述の本発明の顔料分散剤になる。共重合体の構成成分
の一つである―、β−エチレン性不飽和カルボン酸は、
分散効果の点から共重合体中において1i1iの陽イオ
ンとの塩の形になっている方が好ましく、塩の例として
は、アルカリ金属塩(リチウム、ナトリウム、カリウム
塩など)、アンモニウム塩、アミン塩(メチルアミンな
ど)をあげることが出来る0又、一部未中和の部分を残
しておいてもよい。
This becomes the pigment dispersant of the present invention described above. β-ethylenically unsaturated carboxylic acid, which is one of the constituent components of the copolymer, is
From the viewpoint of dispersion effect, it is preferable that the copolymer be in the form of a salt with a cation of 1i1i. Examples of the salt include alkali metal salts (lithium, sodium, potassium salts, etc.), ammonium salts, amine salts, etc. A salt (such as methylamine) may be added, or some unneutralized portion may be left.

本発明の分散剤は、粉末型、エマルジョン型、水溶液型
、溶剤型いずれの形態にも対応出来るが、*に水溶液型
で使用するのが好ましい。
The dispersant of the present invention can be used in any of powder, emulsion, aqueous and solvent forms, but it is preferably used in an aqueous form.

本発明の分散剤としての共重合体は1通常のビニル系単
量体の重合法で容易に得ることが出来る。
The copolymer used as the dispersant of the present invention can be easily obtained by a conventional polymerization method of vinyl monomers.

その−例をあげると、前記した本発明分散剤の構成成分
で重合性単量体である3種の成分と通常の重合開始剤1
例へば、過硫酸カリの如き水溶性で1〜10時間程度重
合させ、重合終了后、苛性アルカリ、又は、アンモニヤ
水でpHを適宜―整(例へば、pH7〜8)することに
より容易に得ることが出来o0 又1分散剤としての分散効果を向丘させるために、本発
明の共重合体は重合度を低分子領域にすることが好まし
、<、40重量%水溶液とした場合の粘度が2000セ
ンチポイズ以下(B型粘度計25℃、ローター回転数6
0rpw)にするのが好ましい0 散剤は、サテンホワイト、炭酸カルシウムなどの塗被紙
用各種顔料に対して、優れた分数効果を示す◎また1本
発明の分散剤に従来公知の他の分散剤1例へはポリアク
リル酸ソーダ、トリポリリン酸ソーダなどとの併用も可
能である。
To give an example, three kinds of components which are polymerizable monomers which are the constituent components of the dispersant of the present invention mentioned above, and one ordinary polymerization initiator.
For example, it can be easily obtained by polymerizing with a water-soluble solution such as potassium persulfate for about 1 to 10 hours, and after the polymerization is completed, adjusting the pH appropriately (for example, pH 7 to 8) with caustic alkali or aqueous ammonia. In addition, in order to improve the dispersion effect as a dispersant, the copolymer of the present invention preferably has a degree of polymerization in the low molecular region, and has a viscosity of <2000 centipoise when made into a 40% by weight aqueous solution. Below (B type viscometer 25℃, rotor rotation speed 6
0rpw) is preferable.0 The powder shows an excellent fractional effect on various pigments for coated paper such as satin white and calcium carbonate. In one example, it is also possible to use it in combination with sodium polyacrylate, sodium tripolyphosphate, etc.

本発明の分散剤の使用量は、共重合体の量が。The amount of the dispersant used in the present invention is determined by the amount of the copolymer.

顔料に対し、0.05〜5%、好ましくは、o、i〜2
%程度で充分である。
0.05-5% based on pigment, preferably o, i-2
% is sufficient.

本発明の顔料分散剤は特に塗紙用−料の分散に適してい
るものであるが、繊維加工、建材加工。
The pigment dispersant of the present invention is particularly suitable for dispersing coating materials, but also for fiber processing and building material processing.

塗料、窯業などの分野においても巾広く応用出来るもの
である。
It can be widely applied in fields such as paints and ceramics.

以下実施例及び比較例をあげて本発明を具体的に説明す
る0そのなかで%1部とあるは何れも重量基準を示す0 実施例t タクリル酸の付加反応生成物を、又、重合開始剤として
、アゾビスイソブチロニトリルを用い、インプロパツー
ル中にて常法により重合を行い、重合終了后、殆んどの
インプロパツールを除去シフ。
The present invention will be specifically explained below with reference to Examples and Comparative Examples.0 Among them, % 1 part indicates the weight basis.Example t The addition reaction product of tacrylic acid was Using azobisisobutyronitrile as the agent, polymerization is carried out in an inpropatol by a conventional method, and after the polymerization is completed, most of the inpropatol is removed by sifting.

次いで、共重合体の含有量が40%になる様に水を加え
た后、更に残存している微量のインプロパツールを除去
した。次いで45%苛性ソーダによ800 cps)。
Next, water was added so that the content of the copolymer was 40%, and then a trace amount of remaining impropatul was removed. followed by 45% caustic soda at 800 cps).

かくして得らねた溶液を分散剤として用い、塗被紙用塗
料を作り、その粘度の安定性を測定した。
Using the solution thus obtained as a dispersant, a paint for coated paper was prepared, and its viscosity stability was measured.

即ち、クレー/重質炭酸カルシウム/分散剤/澱粉/8
BRラテツクス/水= 60/40’10.2/10/
10部(各々固形分換算の組成物を用い。
That is, clay/heavy calcium carbonate/dispersant/starch/8
BR Latex/Water = 60/40'10.2/10/
10 parts (each using a composition based on solid content).

60%固形分の塗料を調整した。又、混線に際しては、
先づ分散剤と水で重質炭酸カルシウムのスラリーを作り
、これにクレーを配合した后、20%変性澱粉を1次い
で50%SBRラテックスを加えて混練した。かくして
得た配付面層の粘度、−8后の粘度、及び−8后に70
“Cで1hr加熱した后の粘度を測定した。この結果は
、別諜示す通りであり1本発明の分散剤は、高固形分塗
料の低粘度化に効果があり、又、得られた塗料の粘度安
定性も優れている。
A 60% solids paint was prepared. In addition, in case of crosstalk,
First, a slurry of heavy calcium carbonate was made with a dispersant and water, and after clay was added to this slurry, 20% modified starch was first added, and then 50% SBR latex was added and kneaded. The viscosity of the distribution surface layer thus obtained was -8 after -8 and 70 after -8.
The viscosity was measured after heating at C for 1 hour.The results are as shown in another report.1 The dispersant of the present invention is effective in reducing the viscosity of high solids paints, and the resulting paints It also has excellent viscosity stability.

〔実施例2.翫4.5.47〕 別表1に示す単量体成分の種類、及び組成比。[Example 2. Kan 4.5.47] Types and composition ratios of monomer components shown in Attached Table 1.

を用いて、実施例1に示すと同様の重合操作により本発
明の分散剤を得た。(実施例2,44,5,6.7)。
A dispersant of the present invention was obtained by the same polymerization operation as shown in Example 1 using the following. (Examples 2, 44, 5, 6.7).

又、実施例1と同様配合塗料を作成し、分散能計効来が
あり、又、得られた塗料の粘度安鎗性も優れている0 〔比較例〕 別表1に示す単量体成分の種類、及び組成比を用いて、
実施例1に示すと同様の重合操作により。
In addition, a compounded paint was prepared in the same manner as in Example 1, and the dispersibility meter was effective, and the resulting paint had excellent viscosity stability. Using the type and composition ratio,
By the same polymerization procedure as shown in Example 1.

本発明範囲外の分散剤を得たO(比較例1.2)。O obtained a dispersant outside the scope of the present invention (Comparative Example 1.2).

本発明分散剤(実施例1〜7)に比べて1本発明範囲外
め分散剤(比較例1〜2)を使用した場合は、配合塗料
の粘度が高いか、塗料の粘度安定性において、劣ってい
る。
Compared to the dispersant of the present invention (Examples 1 to 7), if a dispersant outside the scope of the present invention (Comparative Examples 1 to 2) is used, the viscosity of the blended paint may be higher, or the viscosity stability of the paint may be lower. Inferior.

(別壽錯略号) EA      アクリル酸エチル BA       アクリル酸ブチル MMA      メタクリル酸メチルI BMA  
   メタクリル酸イソブチル特許出願人の名称 束亜曾成化学工業株式会社 −ヌ冶−
(Besshu complex abbreviation) EA Ethyl acrylate BA Butyl acrylate MMA Methyl methacrylate I BMA
Isobutyl methacrylate Patent Applicant Name: Takuya Sosei Chemical Industry Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 1.下記3成分を構成成分とする共重合体またはその共
重合体の塩からなる顔料分散剤。 ■ −2β−エチレン性不飽和カルボン酸■ グリシジ
ルエーテル類あるいはグリシジルエステル[:g、β−
エチレン性不飽和カルボン酸の付加反応生成物 ■ アクリル酸エステルおよび/またはメタクリル酸エ
ステル
1. A pigment dispersant comprising a copolymer containing the following three components or a salt of the copolymer. ■ -2β-Ethylenically unsaturated carboxylic acid■ Glycidyl ethers or glycidyl esters [:g, β-
Addition reaction product of ethylenically unsaturated carboxylic acid Acrylic acid ester and/or methacrylic acid ester
JP17981781A 1981-11-11 1981-11-11 Pigment dispersant Granted JPS5883069A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17981781A JPS5883069A (en) 1981-11-11 1981-11-11 Pigment dispersant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17981781A JPS5883069A (en) 1981-11-11 1981-11-11 Pigment dispersant

Publications (2)

Publication Number Publication Date
JPS5883069A true JPS5883069A (en) 1983-05-18
JPH0143786B2 JPH0143786B2 (en) 1989-09-22

Family

ID=16072404

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17981781A Granted JPS5883069A (en) 1981-11-11 1981-11-11 Pigment dispersant

Country Status (1)

Country Link
JP (1) JPS5883069A (en)

Also Published As

Publication number Publication date
JPH0143786B2 (en) 1989-09-22

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