JPS58168663A - Powdered metal pigment composition and its preparation - Google Patents

Powdered metal pigment composition and its preparation

Info

Publication number
JPS58168663A
JPS58168663A JP5107482A JP5107482A JPS58168663A JP S58168663 A JPS58168663 A JP S58168663A JP 5107482 A JP5107482 A JP 5107482A JP 5107482 A JP5107482 A JP 5107482A JP S58168663 A JPS58168663 A JP S58168663A
Authority
JP
Japan
Prior art keywords
metal powder
phosphate
weight
carbon atoms
alkyl
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
JP5107482A
Other languages
Japanese (ja)
Inventor
Fusamitsu Tono
東野 房光
Yukio Hayashi
林 行男
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.)
ASAHI ETSUKARUTO KK
Original Assignee
ASAHI ETSUKARUTO KK
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 ASAHI ETSUKARUTO KK filed Critical ASAHI ETSUKARUTO KK
Priority to JP5107482A priority Critical patent/JPS58168663A/en
Publication of JPS58168663A publication Critical patent/JPS58168663A/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 the titled compsn. forming a coating film with excellent resistance to acid and alkali and preventing change in color tone of the coating due to flocculation, segregation, etc., prepared by treating powdered metal pigment with organic phosphate compd. CONSTITUTION:The compsn. is prepared by treating powdered metal pigment with an organic phosphate compd. of the formula where R is 6-24C alkyl, 6-24C alkyl-substd. group or aryl which contains at least one 6-24C alkenyl substituent; A is 2-4C alkylene; m is 0-20; R1 and R2 are H, alkyl, alkenyl, aryl or R-(OA)m (R, A and m are the same as above) (e.g. lauryl phosphate or octylphenyl phosphate). It shows improved resistance to water, acid and alkali and good storage stability and retains original color tone without causing color change.

Description

【発明の詳細な説明】 本発明は、金属粉末顔料を有機リン酸エステル化合物で
処理することKより、耐水性、耐酸性、耐アルカリ性お
よび貯蔵安定性の改善を目的とする金属粉末顔料組成物
およびその製造方法に関するものである。
Detailed Description of the Invention The present invention provides a metal powder pigment composition for the purpose of improving water resistance, acid resistance, alkali resistance, and storage stability by treating the metal powder pigment with an organic phosphate compound. and its manufacturing method.

従来、金属粉末顔料は、乗用車、ワゴン、電気機器、精
密機器、もしくは建築用等へo*sI@顔料、紙、プラ
スナックフィルム等への印刷インキ用顔料として広く用
いられている。
Conventionally, metal powder pigments have been widely used as o*sI@ pigments for passenger cars, wagons, electrical equipment, precision equipment, or architecture, and as pigments for printing inks on paper, plastic snack films, and the like.

金属粉末顔料、さらKl’すれば着色顔料を配合してな
る塗料は、独得0仕上9外観を呈し、高級感につながる
商品の機能外品質を高める重I!な役目を果す。
Paints made by blending metal powder pigments and coloring pigments exhibit a unique 0-finish 9 appearance and enhance the non-functional quality of products, leading to a sense of luxury! fulfill a role.

近年、自動車用部材の塗装およびプラスチツタ01に*
に於て轄メタリッタ塗料を1コート塗装する方法が広く
採用されて来ている、また建築用であるカワツ用塗料と
して金属粉末顔料、特にアル々ニウム粉末顔料入)塗料
が使用されている。
In recent years, painting of automobile parts and plastic ivy 01*
A method of applying one coat of metalitta paint has been widely adopted in the construction industry, and paints containing metal powder pigments, especially aluminum powder pigments, are used as paints for architectural applications.

しかし従来の金属粉末顔料そのままでは水分、アルカリ
性、tえは酸性の雰囲気中媒体中では金属の腐食によ抄
、金属顔料の色調を変化させ、塗装塗膜に変色を起すな
ど多くの1欠点があり九〇一方従来の金属粉末顔料に有
機顔料を適量配合せしめ、着色メタリック塗料化した場
合、有機顔料のみで塗料化し良場合には見られない現象
、即ち調合され喪製品塗料が保存されているうちに顔料
粒子が成長し、凝集、色分れなど、塗料中での貯蔵安定
性を損うという着色メタリック塗料特有の現象があ抄、
これらの現象は艶料工業の立場から歓迎される現象では
ない。
However, conventional metal powder pigments as they are have many drawbacks, such as corrosion of the metal in media containing moisture, alkalinity, and acidic atmospheres, changing the color tone of the metal pigment, and causing discoloration of the paint film. On the other hand, when a suitable amount of an organic pigment is blended with a conventional metal powder pigment to make a colored metallic paint, a phenomenon that cannot be seen in cases where the paint is made with only organic pigments occurs, that is, the blended mourning product paint is preserved. Pigment particles grow over time, resulting in agglomeration, color separation, and other phenomena unique to colored metallic paints that impair storage stability in the paint.
These phenomena are not welcomed from the standpoint of the polish industry.

以上のことから、耐水性、耐アルカリ性および耐酸性に
優れ九塗膜を生成し、塗料の凝集、色分れなどの色調変
化を起さない安定し九塗料が得られるような金属粉末顔
料が強く要望されている。
Based on the above, it is possible to find a metal powder pigment that can produce a stable paint film that has excellent water resistance, alkali resistance, and acid resistance, and that does not cause color changes such as agglomeration or color separation. It is strongly requested.

本発明は上記のような欠点を克服するぺ〈金属粉末顔料
について鋭意検討を重ねた結果、金属粉末顔料を一般式 で示され有機リン酸エステル化合物で処理するととKよ
抄、耐水性、耐酸性、耐アルカリ性および貯蔵安定性の
優れ九金属粉末顔料組成物となシ得  πることを見出
し、本発明に到達しえものである。
The present invention overcomes the above-mentioned drawbacks.As a result of extensive studies on metal powder pigments, it has been found that when metal powder pigments are treated with an organic phosphate compound represented by the general formula, they have excellent properties, water resistance, and acid resistance. The inventors have now discovered that a nine-metal powder pigment composition with excellent properties, alkali resistance and storage stability can be obtained, and have thus arrived at the present invention.

本発明に用いる金属粉末としては、例えば、アルミニウ
ム、銅、亜鉛、真鍮、鉄、ニッケルなど展性のある金属
又は合金等の粉末で、これらは棒独または混合して使用
される。金属粉末としては鱗片状のものが好ましく、特
に鱗片状金属アル々エクムがよ抄好ましい。−まえ粗大
粒子は塗膜外観を損ねる良め好ましくな(,141JI
K於けゐふるい残分がO,S−以下のものが好ましい。
The metal powder used in the present invention is, for example, powder of malleable metals or alloys such as aluminum, copper, zinc, brass, iron, and nickel, and these may be used alone or as a mixture. The metal powder is preferably scaly, and scaly metal aluminum is particularly preferred. - Coarse particles are undesirable as they impair the appearance of the paint film (141JI
It is preferable that the K. sieve residue is O,S- or less.

本発明における有機リン酸エステル化合物は、金属粉末
の表面に吸着することKより、金属粉末の反応を抑制す
る11m保護効果を与えるものである。好ましい有機り
ン酸エステル化合物は、で示される有機リン酸エステル
化合物である。こむでRは、炭素数6〜24、好ましく
FiX冨〜18m10アルキル基、炭素数6−34、好
唆しくけ1m −180アルケニル基を九社炭素数6−
u1好ましくはl鵞〜18のアルキル置換基もしくは脚
票数6〜ハ、好ましくdna−isのアルケニル置換基
を一つ以上會むアリール基を表わし、ムは炭素数2〜4
、好ましくは2〜3のフルキレン基を表わし、mは0−
20゜好ましくはO〜10.より好ましくは2〜$であ
り、R8およびR1は同じであっても、興っていてもよ
く、水素、アルキル基、アルケニル基、了り−ル基、ま
たはR−(0ム)m(ここにR1ムおよびmは上記で示
されるもの)を表わす。
The organic phosphoric acid ester compound in the present invention provides a 11m protective effect of suppressing the reaction of the metal powder by adsorbing on the surface of the metal powder. A preferred organic phosphoric acid ester compound is an organic phosphoric acid ester compound represented by: Komude R is an alkyl group having 6 to 24 carbon atoms, preferably an alkyl group having 6 to 18 carbon atoms, preferably an alkenyl group having 6 to 18 carbon atoms, and preferably an alkenyl group having 6 to 18 carbon atoms.
u1 represents an aryl group having at least one alkyl substituent having preferably 1 to 18 carbon atoms or an alkenyl substituent having 6 to 5 carbon atoms, preferably dna-is, and M represents an aryl group having one or more carbon atoms.
, preferably represents 2 to 3 fullkylene groups, m is 0-
20°, preferably 0 to 10. More preferably, it is from 2 to $, and R8 and R1 may be the same or different, and are hydrogen, an alkyl group, an alkenyl group, an aryl group, or R-(0m)m (where R1 and m are as shown above).

R9R1,R,におけるアルキル基またはアルケニル基
としては、例えばヘキシル、ヘプチル、オクチル、ノニ
ル、デシル、ウンデシル、ツクリル、トリデシル、セチ
ル、ステアリル、オレイル、ヘキナデシル、トコシル、
テトツスシルなどが好ましいO R,R,、R,におけるアリール基としては、例えハ、
オクチルフェニル、ノニルフェニル、ドデシルフェニル
、ジノニルフェニルナトカ好tt、イ。
Examples of the alkyl group or alkenyl group in R9R1,R are hexyl, heptyl, octyl, nonyl, decyl, undecyl, tucryl, tridecyl, cetyl, stearyl, oleyl, hequinadecyl, tocosyl,
Examples of the aryl group in O R, R,, R, include tetotsusyl,
Octylphenyl, nonylphenyl, dodecylphenyl, dinonylphenyl natka tt, i.

ムとしてはエチレン、プロピレンが好ましい。具体的な
化合物としては、Rがアルキル基の場合、ヘキシルホス
7エイト、ヘプチルホス7、エイト、デシルホスフェイ
ト、ウンデシルホス7エイト、ラクリルホスフエイト、
トリデシルホス7エイト。
Ethylene and propylene are preferred as the rubber. When R is an alkyl group, specific compounds include hexylphos 7ate, heptylphos 7,8, decyl phosphate, undecyl phos 7ate, lacryl phosphate,
Tridecylphos 78.

ミリスチルホス7エイト、ペンタデシルホスフェイト、
ノナデシルホスフェイト、エイコシルホスフェイト、へ
ンエイコビルホスフエイト、トコシルホスフェイト、ト
リコシルホスフエイト、テトラコシルホスフエイト、ノ
ーメチル−7−エチル−4−ウンデシルホスフェイト、
  !、@、L−)リメチルノニルホスフエイトおよび
これらのエチレンオキナイド、プロピレンオキすイド、
ブチレンオキサイド付加物などがある。またRがアルケ
ニル基の場合、4−ドデシニルホスフエイト、シス−9
−オクタデシニ^ホスフェイト、S−メチル−2−ノニ
ニルホスフエイト、s、9−ジメチル−冨−デシニルホ
スフェイトおよびこれらのエチレンオキナイド、プロピ
レンオキサイド、ブチレンオキサイド付加物などがある
。さらに凰がアリール基の場合、オクチルフェニルホス
7エイト、ノニルフェニルホ、スフエイト、ドデシルフ
ェニルホスフェイトおよびこれらのエチレンオキサイド
、プロピレンオキサイド、ブチレンオキサイド付加物な
どがある。リン酸エステルはモノ、ジ、トリのいずれの
エステルであってもよく、またこれらの混合物であって
亀よい。さらに種類の異なるリン酸エステルの混合物で
あってもよい。
myristyl phos-7ate, pentadecyl phosphate,
Nonadecyl phosphate, eicosyl phosphate, eicovir phosphate, tocosyl phosphate, tricosyl phosphate, tetracosyl phosphate, no-methyl-7-ethyl-4-undecyl phosphate,
! , @, L-)limethylnonyl phosphate and these ethylene oxides, propylene oxides,
Examples include butylene oxide adducts. When R is an alkenyl group, 4-dodecynyl phosphate, cis-9
Examples include -octadecyny^phosphate, S-methyl-2-nonynylphosphate, s,9-dimethyl-dimethyl-decynylphosphate, and adducts thereof with ethylene oxide, propylene oxide, and butylene oxide. Furthermore, when 凰 is an aryl group, examples thereof include octylphenyl phosphate, nonylphenyl phosphate, sulfate, dodecylphenyl phosphate, and adducts of these with ethylene oxide, propylene oxide, and butylene oxide. The phosphoric acid ester may be any mono-, di-, or tri-ester, or may be a mixture thereof. Furthermore, a mixture of different types of phosphoric esters may be used.

さらK、これら有機リン酸エステル化合物をアンモニウ
ム、水酸化ナトリウム、水酸化カリウム。
Furthermore, these organic phosphate ester compounds are combined with ammonium, sodium hydroxide, and potassium hydroxide.

ジプチルアミン、トリブチルアミン、モノエタノールア
ミン、ジエタノールアンン、トリエタノールアミンおよ
びモルホリンなどの塩基性物質で中和して用いることが
できる。
It can be used after being neutralized with a basic substance such as diptylamine, tributylamine, monoethanolamine, diethanolamine, triethanolamine, and morpholine.

有機リン酸エステル化合物は、金属粉末に対して001
−10重量91.好ましくはo、1〜io重量−の範囲
で使用される。ここで、有機リン酸エステル化合物の使
用量がo、ooi重量−未満で社、この発明の目的とす
る性能は得られず、tた。 we型重量↓り奄多くなる
と塗膜物性を低下させる。
The organic phosphate ester compound is 001 to the metal powder.
-10 weight 91. It is preferably used in a range of 1 to io weight. Here, if the amount of the organic phosphoric acid ester compound used was less than o, ooi by weight, the performance aimed at by the present invention could not be obtained. If the weight of the we type increases, the physical properties of the coating film will deteriorate.

ここに於て、金属粉末顔料に対する有機リン酸    
Here, organophosphoric acid for metal powder pigments
.

エステル化合物の添加混合の様式は、金属役O扮砕時ま
たは金属粉末をペースト化させる混合工程時勢任意のも
のを採用し得る。
The ester compound may be added and mixed in any manner, such as when grinding the metal powder or during a mixing process in which the metal powder is made into a paste.

一般に、鱗片状の金属粉末の製法は、ボールツルなどの
粉砕機のなかに、金属砕料と粉砕効率を高める粉砕助剤
が投入され1例えばミネラルスピリット、ツルベントナ
フナ等の各種膨化水嵩系溶剤、或いはその他の溶剤よシ
成る有機溶剤中でO澤式粉砕法、あるいは音素W囲気中
での乾式粉砕法などがとられる、この時0粉砕助剤とし
て、一般に飽和または不飽和脂肪酸、脂肪族アミン、脂
肪酸の金属塩などが用いられる。本発明によれば。
In general, the method for producing scaly metal powder involves adding metal particles and a grinding aid to improve grinding efficiency into a grinder such as a ball pickle. Alternatively, the Ozawa grinding method in an organic solvent such as other solvents, or the dry grinding method in a W atmosphere is used. At this time, saturated or unsaturated fatty acids, aliphatic amines, etc. are generally used as grinding aids. , metal salts of fatty acids, etc. are used. According to the invention.

有機リン酸エステル化合物は粉砕助剤としても充分な機
能を有するもので、これを単独の粉砕助剤として、或い
は従来の助剤と混合して使用し得る。
The organic phosphoric acid ester compound has a sufficient function as a grinding aid, and can be used alone as a grinding aid or in combination with conventional aids.

又原料金属粉の粉砕を夜来の粉砕助剤によシ実施し、粉
砕終了後に有機v/酸エステル化合物を添加搗練して奄
よく、或いは粉砕工程及び混練工程の両方に所定量の有
機リン酸エステル化合物を分割添加しても良い。
In addition, the raw metal powder may be ground using a grinding aid, and after the grinding is finished, an organic v/acid ester compound may be added to make it more gentle, or a predetermined amount of organic phosphorus may be added to both the grinding process and the kneading process. The acid ester compound may be added in portions.

絢必費に応じて1本発明の組成物に、各種の添加剤を併
用することもできる。
Various additives may also be used in combination with the composition of the present invention depending on the necessity.

上述のようにして得られた本発明組成−祉、有機溶剤型
(油性)塗料用又は印刷インキ用顔料として直ちに有用
なものである。
The composition of the present invention obtained as described above is immediately useful as a pigment for organic solvent-based (oil-based) paints or printing inks.

以下に実施例を示して本発明全具体的に説明する。The present invention will be fully explained in detail below with reference to Examples.

実施例1及び比較例1 粒状アルミニウム粉末10に4m!!重量−のステアリ
ルアミンを含むズネラルスピリット10にの混合物をボ
ールミル中で儂時間粉砕し、次に之ネラルスピリット2
0−を加え希釈した後、スラリータンクに移し、フィル
タープレスで9遇する。
Example 1 and Comparative Example 1 4 m for granular aluminum powder 10! ! A mixture of 10 parts by weight of general spirit containing 10 parts by weight of stearylamine was milled in a ball mill for a period of time, then 2 parts by weight of general spirit
After diluting by adding 0-, it was transferred to a slurry tank and filtered 9 times using a filter press.

このようにして得られたフィルタープレスケーキは加熱
残分90重量襲、ミネラルスピリット11重量−であり
、アル建ニウム粉末の14sJIIK於けるふるい残分
は0.1−以下であった。
The filter press cake thus obtained had a heating residue of 90% by weight and a mineral spirit of 11% by weight, and the sieve residue of the aluminum powder in 14s JIIK was 0.1% or less.

このフィルタープレスケーキ100重量部に対し、熟1
表に示すように所定の有機リン酸エステル化合物を所定
量混合し、加熱残分が65−になるようにツルベントナ
フナを添加し、 so’Cで詞分間均−に混合して加熱
残分が仙−の油性アルミニウムベース)1得た。本発明
を比較するため有機リン酸エステル化合物を添加せず、
烈かは全く同様の操作で油性アルミニウムペーストを調
整し良。
For 100 parts by weight of this filter press cake, 1
As shown in the table, mix a predetermined amount of the specified organic phosphate ester compound, add Tsurubento Nafuna so that the heating residue becomes 65%, and mix evenly with SO'C to make the heating residue. (Oil-based aluminum base) 1 was obtained. In order to compare the present invention, no organic phosphate compound was added.
Retsuka adjusted the oil-based aluminum paste using exactly the same procedure.

得られ良油性アルミニウムペーストについて。About the obtained oil-friendly aluminum paste.

貯蔵安定性を調べ、またシルバーメタリック塗料化によ
る耐水性、耐酸性、耐アルカリ性に対する塗膜外観およ
び貯蔵安定性を評価し、さらに着色メタリック塗料化に
よる貯蔵安定性を評価した。
The storage stability was investigated, and the appearance and storage stability of the water resistance, acid resistance, and alkali resistance of the silver metallic paint were evaluated, and the storage stability of the colored metallic paint was also evaluated.

行なった試験方法は次の通)である。The test method used is as follows.

(1)  アルミニウムペーストの貯蔵安定性アルさニ
ラ五ペーストを500 fの塗料缶(ブリキ製)に入れ
50℃1力月貯蔵後の性状を調べる。
(1) Storage stability of aluminum paste Aluminum leek paste was placed in a 500 F paint can (made of tin) and its properties were examined after storage at 50°C for one month.

(2)  シルバーメタリック塗料化による評価次の組
成でメタリック塗料を作り、該塗料をドクターブレード
で塗装し、塗膜の性状を目視判定した。
(2) Evaluation of silver metallic paint A metallic paint was prepared with the following composition, and the paint was applied with a doctor blade, and the properties of the paint film were visually evaluated.

、1 市販の常乾型アクリルラッカー    10重量部市販
のシンナー        1m、lS重量部アルミペ
ースト(金属分として)6.5重量部(a)耐 水 性
: 水中Ktot間浸漬した徒の塗膜の外観を肉眼で観察し
友。
, 1 Commercially available air-drying acrylic lacquer 10 parts by weight Commercially available thinner 1 m, 1S parts by weight Aluminum paste (metal content) 6.5 parts by weight (a) Water resistance: Appearance of a paint film immersed in water for a period of time Observe with the naked eye.

伽)耐フル声ソ性; s −NaOH溶液管塗膜に1満々下し、常温で114
時間放置後、水道水にて洗浄し、塗膜の外観を肉眼で観
察した。
佽)Full voice resistance; s-NaOH solution tube coated with 1 full amount, 114 at room temperature
After standing for a period of time, it was washed with tap water and the appearance of the coating film was observed with the naked eye.

(c)耐 向賓、l’L ; 5−のH,80,溶液を塗膜に1満々下し、常温で24
時間放置後、水道水にて洗浄し、塗膜の外観を肉眼で観
察した。
(c) For guests, l'L: Pour 1 full of 5-H, 80, solution onto the coating film and heat it at room temperature for 24 hours.
After standing for a period of time, it was washed with tap water and the appearance of the coating film was observed with the naked eye.

(d)塗料の貯蔵安定性; 上記配合塗料を50℃1力月放置し、 JI8に540
00つぶゲージ法により安定性を評価した。
(d) Storage stability of the paint; The above compounded paint was left at 50°C for 1 month, and the JI8 rating was 540.
Stability was evaluated by the 00 gauge method.

(3)着色メタリック塗料化による評価次の組成で着色
メタリック塗料を作カ、該塗   貸料の50℃×lカ
月における貯蔵安定性をSOOMeshフルイ残分、つ
ぶゲージ法により、1+塗膜については色差(ΔE)に
よ〕評価した。
(3) Evaluation of colored metallic paint A colored metallic paint was made with the following composition, and the storage stability of the paint at 50°C x 1 month was evaluated using SOOMesh sieve residue and the crush gauge method for 1+ paint film. Evaluation was made based on color difference (ΔE).

樹脂二市販のアクリル樹脂(樹脂分5・−)4市販のメ
ラミン樹脂(樹脂分50チ)1、Set アルミペースト(金属分として)st 黄黄色顔料アンスラビリジジン    1.1! fP
al iogen (BASF) 溶   剤                    
  65 f以下余白 実施例! 粒状アルミニウム粉末10k、有機リン酸エステルとし
てトリデシルホスフェイトを5重量−を含むミネラルス
ピリット164の混合物をボールミル中で8時間粉砕し
1次いでミネラルスピリット鵞0Kft−加え希釈した
後、スラリータンクに移し、フィルタープレスで口過す
る。このようにして得られたフィルタープレスケーキは
加熱残分88重量−。
Resin 2 Commercially available acrylic resin (resin content 5 -) 4 Commercially available melamine resin (resin content 50 cm) 1, Set Aluminum paste (metal content) st Yellow-yellow pigment anthravirididine 1.1! fP
al iogen (BASF) solvent
Examples of margins below 65 f! A mixture of mineral spirit 164 containing 10 kg of granular aluminum powder and 5 weight of tridecyl phosphate as an organic phosphoric acid ester was ground in a ball mill for 8 hours, then 0 kg of mineral spirit was added to dilute it, and then transferred to a slurry tank. Pass through filter press. The filter press cake thus obtained had a heating residue of 88 weight.

ミネラルスピリットL!ilt1gでおり、141jI
におけるふるい残分はIIs以下であった。このフィル
タープレスケーキに対して加熱残分が6S %になるよ
うにソルベントナフサを添加して30℃で関分間均−に
混練して、油性アルミニウムペーストを得た。得られた
アルミニウムペーストについて実施例1と同じようにし
てペーストおよび塗料性能を調べた。その結果いずれの
性状も良好であシ変化が認められなかった。
Mineral Spirit L! It's ilt1g and 141jI
The sieve residue was below IIs. Solvent naphtha was added to this filter press cake so that the heating residue was 6S%, and the mixture was uniformly kneaded at 30°C to obtain an oil-based aluminum paste. The paste and paint performance of the obtained aluminum paste was examined in the same manner as in Example 1. As a result, all properties were good and no change was observed.

実施例3 粒状亜鉛末1sK4.s重量−のオレイン酸を含りオネ
ツルスピリット10−の混合物をボールミル中でS時間
粉砕し、次いでミネラルスピリット加々を加え希釈した
後スラリータンクに移し、フィルタープレスで口過する
。このようにして得られたフィルタープレスケーキ付加
熱残分sO重量−、ミネラルスピリット16重量−であ
j+、141J+におけるふるい残分はl−以下であっ
た。
Example 3 Granular zinc powder 1sK4. A mixture of 10 - weight of oleic acid and 10 - weight of Honetsuru Spirit is ground in a ball mill for S hours, then diluted with addition of mineral spirit, transferred to a slurry tank, and passed through a filter press. The sieve residue in J+ and 141J+ was 1- or less in terms of the filter press cake addition heat residue sO weight - obtained in this way and mineral spirit 16 weight -.

このフィルタープレスケーキ10(1重量−に対して有
機リン酸エステル化合物としてポリオキシエチレン(付
加モル数6モル)ステアリルエーテルホス7エイトを3
重量−および所定量のミネラルスピリットを添加し、鋳
℃で1時間均一に混練して加熱残分aSSの亜鉛ペース
トを得た。これらの得られた亜鉛ペーストについて実施
例1と同じようにペース)0物性と塗料性能を調べた。
Polyoxyethylene (number of moles added: 6 moles) and stearyl ether phos 7-ate were added 3 to 10 times by weight of this filter press cake (1 weight).
A weight and a predetermined amount of mineral spirit were added, and the mixture was uniformly kneaded at the casting temperature for 1 hour to obtain a zinc paste with a heating residue aSS. The physical properties and paint performance of these zinc pastes were examined in the same manner as in Example 1.

その結果いずれの性状も良好であ〕、変化が認められな
かり九。
As a result, all properties were good] and no changes were observed9.

実施例4 粒状銅@1ily、8重量嘔のステアリルエーテルホス
フェイト(エチレンオキサイド付加6モル)と冨重量−
のステアリン酸を含む書ネラルスビリツ)104の混合
物をボールミル中で1時間粉砕し。
Example 4 Granular copper @ 1ily, 8 wt. of stearyl ether phosphate (6 moles of ethylene oxide added) and rich wt.
A mixture of 104 stearic acids containing stearic acid was ground in a ball mill for 1 hour.

次いで建ネ2ルスビリッ) 2G−を加え希釈した後ス
ラリータンクに移し、フィルタープレスで口過する。こ
のようにして得られたフィルタープレスケ−生付加熱残
分85重量−、ミネラルスピリットII重量−であり、
141μにおけるフルイ残分はl−以下であった。
Then, after diluting the slurry by adding 2G-, it was transferred to a slurry tank and filtered through a filter press. The filter press cake obtained in this way has a raw addition heat residue of 85 weight, and a mineral spirit II weight,
The sieve residue at 141μ was less than 1-.

このフィルタープレスに対し、!重量−夢ステアリルエ
ーテルホス7エイト(EO付加モル数6)を加え、加熱
残分が651 Kなるようにノルペントナフサを添加し
、40”C30分間均一に混練して、油性鋼ペーストを
得た。
For this filter press! Weight: Stearyl ether phosphatate (6 moles of EO added) was added, norpent naphtha was added so that the heating residue was 651 K, and the mixture was uniformly kneaded at 40"C for 30 minutes to obtain an oily steel paste.

この銅ペーストについて実施例1と同じようにペースト
の物性と塗膜性能を調べた。その結果、いずれの性状も
良好であり、変化が認められなかった。
The physical properties and coating film performance of this copper paste were investigated in the same manner as in Example 1. As a result, all properties were good and no changes were observed.

以上のようにして得られた本発明の金属粉末顔料は、耐
水性、耐酸性、耐アルカリ性および貯蔵安定性が優れて
お9.従来不可能であった塗装が可會ヒとなった。
The metal powder pigment of the present invention obtained as described above has excellent water resistance, acid resistance, alkali resistance, and storage stability.9. Painting, which was previously impossible, is now possible.

Claims (1)

【特許請求の範囲】 t 金属粉末顔料を次の一般式 (これらの一般式におけるRは炭素数6〜24のアルキ
ル基、炭素数6#84のアル中ル置換基もしくは炭素数
6〜UOアルケニル置換基を一つ以上含むアリール基を
表わし、ムは炭素数3#40アに中レン基を表わし、m
は0−10であ砂sB1およびR1は同じであっても異
っていてもよく、水素、アルキル基、アルケニル基、ア
リール基、またはR−(OA)、(ここKR,ムおよび
mは上記で示される亀の)を表わす)Oで示される有機
リン酸エステル化合物で処理することを特徴とする金属
粉末顔料組成物1 金属粉末顔料の金属分100重量1
1に対し、L(11−20重量部であることを特徴とす
る特許請求の範囲第1項記載の金属粉末顔料組成物本 
金属粉末顔料を次の一般式 で示される有機リン酸エステル化合物で、金属粉の粉砕
時及び/又は金属粉末をペースト化させる混合工程時に
添加処理することを特徴とする金属粉末顔料組成物の製
造方法
[Scope of Claims] t The metal powder pigment is represented by the following general formula (R in these general formulas is an alkyl group having 6 to 24 carbon atoms, an alkyl substituent having 6 to 84 carbon atoms, or an alkenyl substituent having 6 to 84 carbon atoms) represents an aryl group containing one or more groups, m represents a cyclone group with 3 #40 carbon atoms, m
is 0-10, and sand sB1 and R1 may be the same or different, hydrogen, alkyl group, alkenyl group, aryl group, or R-(OA), (where KR, m and m are the above-mentioned Metal powder pigment composition 1 characterized in that it is treated with an organophosphoric acid ester compound represented by (a turtle) represented by O) Metal content of metal powder pigment 100 weight 1
The metal powder pigment composition book according to claim 1, characterized in that L (11-20 parts by weight) is
Production of a metal powder pigment composition characterized in that a metal powder pigment is treated with an organic phosphate ester compound represented by the following general formula during the grinding of the metal powder and/or the mixing step of turning the metal powder into a paste. Method
JP5107482A 1982-03-31 1982-03-31 Powdered metal pigment composition and its preparation Pending JPS58168663A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5107482A JPS58168663A (en) 1982-03-31 1982-03-31 Powdered metal pigment composition and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5107482A JPS58168663A (en) 1982-03-31 1982-03-31 Powdered metal pigment composition and its preparation

Publications (1)

Publication Number Publication Date
JPS58168663A true JPS58168663A (en) 1983-10-05

Family

ID=12876657

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5107482A Pending JPS58168663A (en) 1982-03-31 1982-03-31 Powdered metal pigment composition and its preparation

Country Status (1)

Country Link
JP (1) JPS58168663A (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6230168A (en) * 1985-07-30 1987-02-09 Nippon Paint Co Ltd Metallic coating composition
EP0347930A2 (en) * 1988-06-24 1989-12-27 Nippon Paint Co., Ltd. Metallic pigment composition
FR2729964A1 (en) * 1995-01-31 1996-08-02 Omya Sa TREATED MINERAL CHARGES. SUSPENSIONS OF THESE LOADS IN POLYOLS AND THEIR USES IN POLYURETHANE FOAMS
WO1998017731A1 (en) * 1996-10-22 1998-04-30 Silberline Limited Metal pigment composition
JPH10298450A (en) * 1997-02-25 1998-11-10 Dainichiseika Color & Chem Mfg Co Ltd Pigment composition
FR2780409A1 (en) * 1998-06-30 1999-12-31 Omya Sa Method for processing mineral fillers with a phosphate
WO2002042381A3 (en) * 2000-11-27 2002-08-22 Millennium Inorganic Chem Pigments treated with organo-phosphoric acids and their salts
JP2003041150A (en) * 2001-08-02 2003-02-13 Merck Ltd Highly corrosion-resistant flaky metal pigment, method for producing the same and interference color pigment with metallic luster comprising the metal pigment as base
JP2012255143A (en) * 2011-05-16 2012-12-27 Seiko Epson Corp Ultraviolet ray curable inkjet composition and printed object
JP2013227454A (en) * 2012-04-26 2013-11-07 Seiko Epson Corp Inkjet composition and recorded matter
JP2014031427A (en) * 2012-08-02 2014-02-20 Seiko Epson Corp Ultraviolet-curable inkjet composition and recorded material
US9321928B2 (en) 2011-05-17 2016-04-26 Seiko Epson Corporation Metal powder, ultraviolet ray curable ink jet composition and recorded object
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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55158202A (en) * 1979-05-28 1980-12-09 Asahi Chem Ind Co Ltd Water-dispersible metal powder composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55158202A (en) * 1979-05-28 1980-12-09 Asahi Chem Ind Co Ltd Water-dispersible metal powder composition

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6230168A (en) * 1985-07-30 1987-02-09 Nippon Paint Co Ltd Metallic coating composition
EP0347930A2 (en) * 1988-06-24 1989-12-27 Nippon Paint Co., Ltd. Metallic pigment composition
US6545059B1 (en) * 1995-01-31 2003-04-08 Omya S.A. Treated mineral fillers suspensions of these fillers in polyols and their uses in polyurethane foams
FR2729964A1 (en) * 1995-01-31 1996-08-02 Omya Sa TREATED MINERAL CHARGES. SUSPENSIONS OF THESE LOADS IN POLYOLS AND THEIR USES IN POLYURETHANE FOAMS
EP0726298A1 (en) * 1995-01-31 1996-08-14 Omya S.A. Treated mineral fillers and suspensions thereof in polyurethanes
US6765032B2 (en) 1995-01-31 2004-07-20 Omya S.A. Treated mineral fillers suspensions of these fillers in polyols and their uses in polyurethane foams
WO1998017731A1 (en) * 1996-10-22 1998-04-30 Silberline Limited Metal pigment composition
JPH10298450A (en) * 1997-02-25 1998-11-10 Dainichiseika Color & Chem Mfg Co Ltd Pigment composition
US6787575B1 (en) 1998-06-30 2004-09-07 Omya Sa Method for processing a mineral fillers with a phosphate, said fillers and their uses
WO2000000553A1 (en) * 1998-06-30 2000-01-06 Omya Sa Method for processing mineral fillers with a phosphate, said fillers and their uses
FR2780409A1 (en) * 1998-06-30 1999-12-31 Omya Sa Method for processing mineral fillers with a phosphate
WO2002042381A3 (en) * 2000-11-27 2002-08-22 Millennium Inorganic Chem Pigments treated with organo-phosphoric acids and their salts
JP2011099123A (en) * 2000-11-27 2011-05-19 Millennium Inorganic Chemicals Inc Pigment treated with organo-phosphoric acid and salt thereof
JP2003041150A (en) * 2001-08-02 2003-02-13 Merck Ltd Highly corrosion-resistant flaky metal pigment, method for producing the same and interference color pigment with metallic luster comprising the metal pigment as base
JP2012255143A (en) * 2011-05-16 2012-12-27 Seiko Epson Corp Ultraviolet ray curable inkjet composition and printed object
US9441126B2 (en) 2011-05-17 2016-09-13 Seiko Epson Corporation Metal powder, ultraviolet ray curable ink jet composition and recorded object
US9321928B2 (en) 2011-05-17 2016-04-26 Seiko Epson Corporation Metal powder, ultraviolet ray curable ink jet composition and recorded object
US9650524B2 (en) 2011-05-17 2017-05-16 Seiko Epson Corporation Metal powder, ultraviolet ray curable ink jet composition and recorded object
US9834685B2 (en) 2011-05-17 2017-12-05 Seiko Epson Corporation Metal powder, ultraviolet ray curable ink jet composition and recorded object
US9416288B2 (en) 2012-02-01 2016-08-16 Seiko Epson Corporation Inkjet recording method
US9422442B2 (en) 2012-02-01 2016-08-23 Seiko Epson Corporation Material including print layer produced by ultraviolet-curable composition
US10053590B2 (en) 2012-02-01 2018-08-21 Seiko Epson Corporation Composition for inkjet and recording material
JP2013227454A (en) * 2012-04-26 2013-11-07 Seiko Epson Corp Inkjet composition and recorded matter
JP2014031427A (en) * 2012-08-02 2014-02-20 Seiko Epson Corp Ultraviolet-curable inkjet composition and recorded material
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