CA1287201C - Aluminium pigment composition - Google Patents

Aluminium pigment composition

Info

Publication number
CA1287201C
CA1287201C CA000533751A CA533751A CA1287201C CA 1287201 C CA1287201 C CA 1287201C CA 000533751 A CA000533751 A CA 000533751A CA 533751 A CA533751 A CA 533751A CA 1287201 C CA1287201 C CA 1287201C
Authority
CA
Canada
Prior art keywords
aluminium
parts
weight
composition according
aliphatic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA000533751A
Other languages
French (fr)
Inventor
Tetsufumi Kawabe
Toshiaki Bamba
Takashi Matsufuji
Hiroaki Ueshimo
Yoshiki Hashizume
Eikichi Uchimura
Masakatsu Harada
Masahiro Aoki
Toru Kimura
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.)
Toyo Aluminum KK
Original Assignee
Toyo Aluminum 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
Priority claimed from JP62071035A external-priority patent/JPH0680152B2/en
Application filed by Toyo Aluminum KK filed Critical Toyo Aluminum KK
Application granted granted Critical
Publication of CA1287201C publication Critical patent/CA1287201C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

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

Abstract

Abstract An aluminium pigment composition disclosed herein comprises aluminium flakes, a phosphorus supplied from an inorganic phosphoric acid in an amount of 500 to 10,000 ppm based on the aluminium weight, an aliphatic compound having at least one functional group within a molecule in an amount of 0.3 to 5 parts by weight per 100 parts by weight of aluminium, water in an amount of 0.05 to 10 parts by weight of aluminium, a water-compatible alcohol in an amount of 5 to 100 parts by weight per 100 parts by weight of aluminium and a hydrocarbon oil in an amount of 1 to 70 parts by weight of aluminium. The aluminium pigment composition according to the invention is particularly suitable for incorporating in the water base paint.

Description

7;;~01 ALUMINIUM PIGMENT COMPOSITION

Field of the Invention-The invention relates to an aluminium pigment composition. More particularly, the invention relates to the aluminium pigment composition suitable for incorporating in a water base paint such as a water-soluble paint, an aqueous emulsion paint and the like.

Background of the Invention-Recently, water base paints have been extensively developed in many countries including Japan as the replacement of the organic solvent base paints for saving costs and resolving the environmental pollution problemsO In this connection, the development of metallic pigments suitable for incorporating in the water base paints has been highly desired to use for top coating the automobiles and the other vehicles so as to give them -the high grade appearances.
As the metallic pigment for incorporating in ~he water base paint, a pigment composition comprising aluminium flakes and a surfactant which is~ added for improving the water~dispersibility has been known. However, this composition has the important defect of evolving a large volume o~ hydrogen gas during a long storage period, thereby an explosion may occur.

, '72~

As the method for resolving the above-mentioned defect, the methods of forming anti-corrosive coatings on the aluminium flakes by adding an anti-corrosive material such as morpholine, dimeric acid, organic phosphate ester, boric acid salt and the like in addition to the surfactant have been proposed. However, these methods could not ~- completely prevent the evolution of hydrogen gas. Further, the coatings formed on the aluminium flakes caused another defects of darkening the color tone characteristic of the metallic pigment as well as aggregating the flakes during ~ the long storage period~
- A method of contacting aluminium flakes with an aqueous solution containing available phosphate ions supplied from the phosphate compound such as (NH4)2HPO4 and the like in an amount of at least 0.7 % by weight based on the aluminium weight and having pH of about 1.5 to 11 is disclosed in USP 2,858,230. A pigment composition obtained by the above-mentioned method can prevent considerably the evolution of hydrogen gas in the aqueous medium, but this composition cannot give the paint film with the satisfactory color tone. And, this composition tends to gradually darken the color tone with the evolution of the gas and to ~aggregate the flaXes during the storage.
An object of the~invention is to provide~a pigment compositlon whlch can be incGrporated in the water base paint without showing the above-mentioned defects.

:
An object of the lnvention is to provide an aluminium ~;~ 2 .

~, . , : , -.:
: ~, . .
.. . .
~ ' , .
, `" ~.. Z~37~

flake ~igment composition which when incorporated in the water base paint, evolves a little volume of hydrogen gas and has a little tendency of darkening the color tone and aggregating the flakes during the long storage period.

n~
The above-mentioned objects of the invention ~an be achieved by the pigment composition according to the invention which comprises aluminium flakes, a phosphorus supplied from an inorganic phosphoric acid in an amount of 500 to 10,000 ppm based on the aluminium weight, an aliphatic compound having at least one functional group within a molecule in an amount of 0~3 to 5 parts by weight per 100 parts by weight of aluminium, water in an amount of 0.05 to 10 parts by weight per 100 parts by weight of aluminium, a water-compatible alcohol in an amount of 5 to 100 parts by weight per 100 parts by weight of aluminium and a hydrocarbon oil in an amount of 1 to 70 parts by weight of 100 parts by weight of aluminium.

Detailed Description of the Invention:
The aluminium flakes usable in the invention are not particularly limited, but the aluminium flakes having surface properties, size and form suitable as the metallic flake pigment are preferable. Generally, the aluminium .

flakes obtained by the so-called Hall process wh~rein the aluminium powder is subjected to grinding in a hydrocarbon ~ ' .
.
-' ~ '. ' ' ' ~ ' ' , ' ~ 2~3720~

oil in the presence-of a grinding agent in a ball mill are used.
The aluminium flakes in the pigment composition according to the invention have the thin and dense coatings containing phosphor supplied from the inorganic phosphoric acid. The inorganic phosphoric acid usable in the invention may be at least one member selected from the group consisting of ortho-phosphoric acid, pyro-phosphoric acid, triphosphoric ~cid, tetraphosphoric acid and phosphorous acid.
The phosphor content in the coating should be 500 to 10,000 ppm based on the aluminium weight~ Preferably, the phosphor content is 1,000 to 7,000 ppm based on the aluminium weight. If the phosphorus content is less than 500 ppm the larger volume o hydrogen gas evolves, while if it is over 10,000 ppm the flakes may aggregate and the color tone may darken.
The aliphatic compound is used in the invention for preventing the aggregation of the flakes by adsorbing or binding it on the coating. Therefore, the aliphatic compound used in the invention should have at least one functional group within the molecule. The preferable functional group may be selected from the group consisting of:
-OH;
-COOR wherein R is a lower ( for example C1 - C5 alkyl group;
-COOM wherein M is an alkaline metal;

, . ' ' . ' .
.
' , '"' ' - ' .' ' ' ' '-- 3 ;~72~)~

COO ~ Me wherein Me is an alkali earth metal;
- COO
-CONH2;
/
-CO

~NH2;

~NH;
o -O - P - OH;
I
OH
O
_O >1I d -O
O

~O - S - OH.
O

'-Further, it is preferable that the aliphatic compound has 8 to 40 carbon atoms. If the compound having 7 or less carbon atoms is used, the aggregation of the flakes may not be prevented as desired since the carbon chains in the pendant residues adsorbed or bound to the coating are too short.
While, the compound having 41 or more carbon atoms is used, the~handling is difficult since its molecular weight is too high. More preferably, the aliphatic compound having at least one of -NH2 or >NH is used in the invention. The typical~examples of such aliphatic amines may include 2-ethylhexylamine, caprylamine, decylamine, laurylamine, . ~ .
. . - ~ - , . . .

" - , : : , ~ ~s~7~0~

myristylamine, palmitylamine, stearylamine, ole~llamine, eicosylamine, di-2-ethylhexylamine, dicaprylamine, didecylamine, dilaurylamine, dimyristylamine, dipalmityl-amine, distearylamine, dioleylamine, dieicosylamine and the like. The examples of the other aliphatic compound usable in the invention may include an aliphatic higher alcohol such as lauryl alcohol and stearyl alcohol; an ester of aliphatic acid with lower alcohol such as methyl oleate and butyl stearate; a metal salt ( Na, K, Mg, Ca or Zn salt ) of aliphatic acid; an aliphatic acid amide such as oleic amide, stearic amide and dilauric amide; a mono- or diester of aliphatic alcohol with orthophosphoric acid such as mono- or dilauryl acid phosphate and mono- or distearylacid phosphate.
The content of the aliphatic compound in the pigment composition according to the invention should be 0.3 to 5 parts by weight per 100 parts by weight of aluminium.
Preferably, the content of the aliphatic compound is 1 to 4 parts by weight per 100 parts by weight of aluminium. If the content is less than 0.3 part by weight it is difficult to prevent the aggregation of the flakes, while if it is over 5 parts by weight the color tone and the strength of the paint film may be adversely effected.
Water, the water-compatible alcohol and the :: :
hydrocarbon oil are essential in the invention for forming the thin and dense coating. The content of water in the ~ pigment composition according to the invention should be : :

: : :
.. . , , - .... .
. ~ . . . ...
-: , : ' ' -- ' ' : ~ .

~ ~372(~1 0.05 to 10 parts by weight per 100 parts by weight of aluminium. Preferably, the content of water is 0.1 to 5 parts by weight per 100 parts by weight of aluminium. If the content of water is out of the above range, the desired coatings cannot be formed on the flakes, whererby the evolution of hydrogen gas cannot be completely prevented as well as the problems of the aggregation and the change in color tone cannot be resolved.
The alcohol used in the invention should be compatible with water and hydrocarbon 3il in a suitable ratio and completely dissolve the inorganic phosphoric acid~
The typical examples of the water-compatible alcohol may include ethanol, propanol, isopropanol, butanol, isobutanol, amylalcohol, isoamylalcohol, ethyl cellosolve, butyl cellosolve, polyoxyethylene glycol, polyoxypropylene glycol and a mixture thereof.
; The content of the water-compatible alcohol in the pigment composition according to the invention should be 5 to 100 parts by weight per 100 parts by weight of aluminium.
Preferably, the content of alcohol is 20 to 40 parts by weight per 100 par-ts by weight of aluminium. If the content is less than 5 parts by weight the desired coating cannot be formed, while if it is over 100 parts the pigment composition would be unstable.
As the hydrocarbon oil, the aliphatic or aromatic hydrocarbon oil such as mineral spirit, solvent naphtha, HAWS, LAWS and the like which are used in the grinding of ~ 7 .~ .

- .

- , , . ' ' ' ~2~7~

the aluminium powder for obtaining the aluminium flakes can be used in the invention as it is.
The content of the hydrocarbon oil should be 1 to 70 parts by weight per 100 parts by weight of aluminium.
Preferably, the content of the hydrocarbon oil is 30 to 50 parts by weight per 100 parts by weight of aluminium. If the content is less than 1 part by weight the pigment would be unstable, while if it is over 70 parts by weight the coating is formed very slowly.
The pigment composition according to the invention is desirable to include the surfactant for improving the water dispersibility of the aluminium flakes in the water base paint, depending on the kind of the paint. Among the known surfactant, the nonionic surfactant is preferable, such as polyoxyethylene alkylphenol ether, polyoxyethylene alkyl ether, polyethylene glycol fatty acid ester, sorbitan fatty acid ester and polyoxyethylene sorbitan fatty acid ester.
i~ The effective content of the surfactant is about 5 to 20 parts by weight per 100 parts by weight of aluminium. It is noted that the inclusion of the surfactant may be unnecessary depending on the kind oE the water base paint.
The pigment composition according to the invention may include other known additives such as levelling agent, Leafing stabilizer, thickener,~inorganic or organic pigment ~and t~he-like. The typlcal examples of the organic pigments include anthraquinones such as flavanthrone yellow, indanthrone blue, dibromeanthanthrone red and anthrapyridine ::

'' . ' ~' ' : . ' " ' . ' :,' ' , ; :' ~2~ 0~
yellow, indigos, pyranthrones, perylenes and the like. The typical examples of the inorganic pigments include phthalocyanine blue, titanium white and the like.
The pigment composition according to the invention is particularly suitable for incorporating in the water base paint. The water base paint in which the composition is incorporated is not particularly limited. For example, the pigment composition according to the invention is incorporated in the water-soluble paint or the aqueous emulsion paint which contains polyester, acryl, alkyd, acryl-urethane, CAB, polyvinyl alcohol, polyvinyl acetate or ethylen0-vinyl acetate resin. O course, the pigment composition according to the invention can be incorporated in inks, adhesives and the like.

Examples:
The following examples illustrate the invention, but are not to be construed as limiting the scope thereof.
Percentages are by weight otherwise statPd.

Examples 1 to 14 and Comparative Examples 1 to 6 A cake with A~ content of ~0 % was prepared by rémoving a solvent from an aluminium paste pigment. The aluminium paste pigment used was a commercial available aluminium paste pigment ( 7160N produced by TOYO ALUMINIUM
K.K.~which essentially consists of aluminium flakes passing through 400 mesh screen ( Tyler standard sieve ) and mineral ~-". 9 ; ' .

" . ', ' ' '. ', '.. ," ~ ' ' '' ' . ' : ' ~' ~'. ' '' ", ' ' . . ' ' .
.
. ' ', . . ,: ', ' ' '' ~ ~r~720~

spirit-and the AQ content of which is 65 % . The thus~prepared cake contained an oleic acid used as a grinding agent in an amount of 1.5 parts by weight per 100 parts by weight of aluminium.
The cake was transferred into a mixer and the ir.organic phosphoric acid, the aliphatic compound, the nonionic surfactant, water, the water-compatible alcohol and the hydrocarbon oil shown in Table 1 were added thereto and kneaded for three hours to obtain an aluminium pigment composition in a paste.
The phosphor content and the water content in the thus-obtained composition were determined in accordance with the following methods. The results are also shown in Table 1.
a) phosphorus content Each sample was washed with a mixed solvent of water and isopropanol and a mixed solvent of ether and acetone, successively and then dried to remove the solvent. Then, the sample was dissolved in an aqueous hydrochloric acid solution.
The phosphor ( P ~ content ( ppm ) based on the aluminium weight was determined by the plasma emission spectrophotometry.
b) water content The water in the sample was vaporized at 230C in N2 gas flow and condensed.
The water content ( parts by weight ) per 100 parts '"''', ~ .

.
3 ~7~

by weight of aluminium was determined in accordance with Karl Fischer method by means of Moisture Meter VA-0.2 and CA-0.2 ( produced by ~ITSUBISHI CHEMICAL INDUSTRIES LTD. ).
Example 15 The procedure of Example 10 was repeated to obtain a pigment composition with AQ con-tent of about 52 % , provided that the used cake contained stearic acid as the grinding agent in an amount o~ 1.7 parts by weight per 100 parts by weight of aluminium.
Example 16 A pigment composition with A~ content of about 52 %
was obtained in a similar manner to the procedure of Example 5. The used cake contained lauryl amine as the grinding agent in an amount of 1.0 part by weight per 100 parts by weight of aluminium.
Example 17 The water dispersibility, the aggregation amount, the gas volume evolved in the water base paint and the change in color tone of the paint film of each pigment obtained in the above Examples and Comparative Examples were determined in accordance with the following methods. The results are shown in Table 2.
a) water dispersibility A predetermined amount of the sample was added to the pure water in the test tube. After stirring, the sample was allowed to stand.
The dispersibility in water was observed with necked ~ ~7~

eyes and evaluated as follows:
: disperse easily and homogeneously O : disperse almost homogeneously L : almost leafing b) aggregation amount The sample after storing in a tank at 50~C for one month was dispersed in water.
The weight of the sample not passing through 325 mesh screen ( Tyler standard sieve ) was determined and expressed as percentages based on the aluminium weight.
c) gas volume The water base paint used consisted of 21.3 g (calculated as aluminium) of the sample, 281.6 g of ALMATEX ~A-911 t produced by MITSUI TOATSU CHEMICALS, INC.), 44 g of CYMEL~350 ( produced by MITSUI TOATSU CHEMICALS, INC.), 7.1 ~ of phthalocyanine blue, 14.4 g of triethyl amine, 34.6 g of isopropanol and 448.0 g of water. Eighty grams of the above paint was transferred into the glass bottle and stored at 50C for one month.
The total gas volume ( mQ ) evolved during the storage was determined at the room temperature.
d~ change in color tone The blue metallic paint film was formed by coating lS0 microns in thickness of the a~ove paint on the glass plate with a doctor blade and baking at 160C for 20 minutes. As the control, the blue metallic paint film was formed in a similar manner using the untreated pigment .~ . . .
. ~ , .
, ~7~

obtained in Comparative Example 1.
The color difference ( ~E ) of the paint film over the control paint film was determined by means of the color-difference meter with 45- 0 mannerO

.

.' ' O Ql ~ ~ ~r ~ ~r ~ ~ ~
~ -~ S~
~a ~1 S~
O ~
~ ~r ~ ~r q~

~:: 0~ ::: : :: ::
~ OQ~
rl ~1 ~1 ~ ~`I 1- CO In coco ~r o 1 0 o~ o r~
3 ~ ~ i o~
.n Q, I` r` I` r`~1 ~ r 1`
_ ~ ~ ~0 S~ ,ol .
O ~ S ~
~\ ~ Q I Ql _ _ ~~ $,, ~
V
o s ~o ~ ~ o ~ o o ~4 a) Ql ~ aJ
~1 ~ .. .~ ._ , Q, O O O . ~ ~ ~ N ~
E' _ Q a) ~ 3 o ~
C) (d ~ 1 u ,~
~ o 1~ ~I S l ~ r l ~ S
.,~ ~ ~1 ~ O a) ~I Q
~1 ~ 1 o o ~ o 1~l ~ ~0 ~ ol ~ Q~
, O O O O OO O O O O
l Ql O O O O O ~ O O O O
: ~`I N ~ ~ ~ ,1 ~ ~ ~
C) V V `
: '~'~0' ~0 ~0 ~ ~Q, ~ s Q~ ~ b O O rl ~ O r~ ~ O-r~
~ ~ V ~ ~ V ~ V
,, Q, ~ o ~ ~ Q, Q, ~
~' ,J ~ . ' ,.

, , ~ .. .' -''',.' .

37~

s~ o o o o o o o o o ooo ~: 3 ~ ~r ~ ~ ';r ~r ~ ~ ~ ' --O 0~ ~S
O O h ~ S:
so 3 '3~ 3~
,. ~.
h O O O O O O O O O O O O

,~ O O
S ~ .~ O

~ ~ s~

S~ ~ ~ o o ~ c~ o r~ o ~ ~ ~ ~ . ~ ~ ~ ~ ~ o 3 ~:4 ~ ~ ~ O ,~ O
. _____ __ . ~ ,n In LS~ ~ Lrl ~ Ul U~
P~ ~
l _ ~
: - : -:: :~

- . u ::~ E~ S rd O ~ q~
~11 ~ a~ _ o ~1 - o o ~ In In I O O ~ 00 'a~
~d ~ ~ i 3 _ ~J
'U - . __ Q ~
, ~ '~ ~
~ ~ a) ~ u O ~ ~ a.) ~ a) ~ ~ ~ o u u t~ O rl U ~d U ~ O ~ O ~i U O ~ ~i ~ :~ (d ~1 (il (d .-1 (~ A ~1 ~1 (~ -rl al ~4 S ~ S ~1 ~ ~ ~ S ~ ~1 12~
Rl ~ ul d --l S rl S ~1 ~ ~ i S(d O ~ IJ S O ~ S~
¢ r Qi ~ Qi O ~ Qi ~ ~ u uJ Q; 1:: ~1 .Ql S~
~ ~ ~ ~ ~i E;
E O o o o o O o O o o o S O
Q~ O O o g o o I ~ u~ I o O o p; ¦ _ ~ N ~,i~1 ~ ~ (~I Oa) (~ ;
_ _~ O _ ~ ~ Sl-I I 3 ~
U U , u~ SQ U O U o u~ ;r, O ~i ~1 U O i'~ Ui U u~ 1 0 ~1 ~1 '~ ~ O IrQl d ~ Id S rU ~i ~ o ~ ~ Q
~ SI S O V I o Q~ U Qi U - I .C r I s ~I u ,i ~
5-i ~ ~ vi ~ Qi ~i S l i O ~ OS Q~ r ~) S Q ~ ~d S ~d S-i u O O rl ~ i O ~i rl O ~) O h O i~iI i o ,i I i o ,i ~ Qi Pi ¦
S U ~i S l~i S ~i s~ ~ U O Q, (d ~ o SQ Ud ~o ~-i U #

. Q. Ci E ~i ~i ~ ~ u ) . ~o Q; ~ D
i ~i ~ C.) & i _ _ , ' ' '~ `, `

3 2~372Q.~

Table 2 Examples water aggregated gas volume color & Comp. dl spe rsi- amount difference Examples bllity ( %) (ml) ~F.) Æx. 1 0.05 not more than _ ;__ 2 ~ 0.05 1 0O5 3 ~ 0.05 .- 0.5 4 ~ 0.03.. 0.4 O 0.02,. 0.4 0.02,. 0O4 7 ~ 0.02., 0~3 ~ ~ 0.03., 0.4 9 ~ 0.03,. O.S
L 0.03.. 0.6 11 ~ 0.03.. 0.5 12 ~ 0.03 2 0.6 13 ~ 0.03not morle than 0.5 14 ~ 0.03,. 0.5 L 0.03.. 0.5 16 O 0.03 . 0.5 , . ._ Comp .
Ex. 1 O 0.02 more than 50_ 2 ~ 0.0248 0.3 3 O 0.6 5 2.5 4 O 5.5 2 1~.5 O 7.3more than 509O4 6 _ ~ _ 1.5 _ ~ ~a~o~

Effect of the Invention:
In the pigment composition according to the invention, the thin and dense coatings are formed on the surfaces of aluminium flakes. The coatings were covered w:ith a large amount of long pendant residue of the aliphatic compound since the functional groups in the aliphatic compound adsorb or bind on the surfaces of aluminium flakes~
Therefore, the pigment composition according to the invention has the improved water dispersibility as well as a little tende~cy to evol~e a large volume o~ gas, aggregate the flakes and darken the color tone of the paint film.

Claims (18)

1. An aluminium pigment composition comprising aluminium flakes, a phosphorus supplied from an inorganic phosphoric acid in an amount of 500 to 10,000 ppm based on the aluminium weight, an aliphatic compound having at least one functional group within a molecule in an amount of 0.3 to 5 parts by weight per 100 parts by weight of aluminium, water in an amount of 0.05 to 10 parts by weight of aluminium, a water-compatible alcohol in an amount of 5 to 100 parts by weight per 100 parts by weight of aluminium and a hydrocarbon oil in an amount of 1 to 70 parts by weight of aluminium.
2. The composition according to claim 1, wherein the aluminium flakes are those obtained by the Hall process.
3. The composition according to claim 1, wherein the inorganic phosphoric compound is selected from the group consisting of ortho-phosphoric acid, pyro-phosphoric acid, triphosphoric acid, tetraphosphoric acid and phosphorous acid.
4. The composition according to claim 1, wherein the phosphorus content is 1,000 to 7,000 ppm based on the aluminium weight.
5. The composition according to claim 1, wherein the aliphatic compound has at least one functional group selected from the group consisting of:
-OH;
-COOR wherein R is a lower alkyl group, -COOM wherein M is an alkaline metal;
Me wherein Me is an alkali earth metal;
-CONH2;
;
-NH2;
?NH;

; and .
6. The composition according to claim 5, wherein the aliphatic compound is an aliphatic amine, an aliphatic higher alcohol, an ester of aliphatic acid with lower alcohol, a metal salt of aliphatic acid, an aliphatic acid amide and a mono- or diester of aliphatic alcohol with orthophosphoric acid.
7. The composition according to claim 6, wherein the aliphatic compound is an aliphatic amine.
8. The composition according to any one of claims 5 to 7, wherein the aliphatic compound has 8 to 40 carbon atoms.
9. The composition according to claim 1, wherein the content of the aliphatic compound is 1 to 4 parts by weight per 100 parts by weight of aluminium.
10. The composition according to claim 1, wherein the content of water is 0.1 to 5 parts by weight per 100 parts by weight of aluminium.
11. The composition according to claim 1, wherein the water-compatible alcohol is ethanol, propanol, isopropanol, butanol, isobutanol, amylalcohol, isoamylalcohol, ethyl cellosolve, butyl cellosolve, polyoxyethylene glycol, polyoxypropylene glycol or a mixture thereof.
12. The composition according to claim 1, wherein the content of the water-compatible alcohol is 20 to 40 parts by weight per 100 parts by weight of aluminium.
13. The composition according to claim 1, wherein the hydrocarbon oil is an aliphatic or aromatic hydrocarbon oil.
14. The composition according to claim 1, wherein the content of the hydrocarbon oil is 30 to 50 parts by weight.
15. The composition according to claim 1, which further comprises a surfactant.
16. The composition according to claim 15, wherein the surfactant is a nonionic surfactant.
17. The composition according to claim 1, which is incorporated in a water base paint.
18. A water base paint comprising an aluminium pigment composition according to claim 1.
CA000533751A 1986-04-04 1987-04-03 Aluminium pigment composition Expired - Lifetime CA1287201C (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP7772886 1986-04-04
JP77728/86 1986-04-04
JP71035/87 1987-03-25
JP62071035A JPH0680152B2 (en) 1986-04-04 1987-03-25 Aluminum flake pigment composition for water-based paint

Publications (1)

Publication Number Publication Date
CA1287201C true CA1287201C (en) 1991-08-06

Family

ID=26412150

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000533751A Expired - Lifetime CA1287201C (en) 1986-04-04 1987-04-03 Aluminium pigment composition

Country Status (1)

Country Link
CA (1) CA1287201C (en)

Similar Documents

Publication Publication Date Title
US4869754A (en) Aluminium pigment composition
US6503304B2 (en) Flowable and pumpable metallic-pigment semifinished product for the production of paints and lacquers
JP3200473B2 (en) Aluminum pigment
EP0491854B1 (en) Colored metallic pigments
US6602339B2 (en) Aluminum pigment, process for its production and resin compositions containing the same
CA1257769A (en) Process for producing corrosion inhibiting particles
WO1991004293A9 (en) Colored metallic pigments
US5041241A (en) Corrosion-inhibiting composition
AU664067B2 (en) Water resistant metal pigment particles
DE102006051893A1 (en) Metallic effect pigments for use in cathodic electrocoating, process for their preparation and use, and electrodeposition paint
CA1287201C (en) Aluminium pigment composition
JP3741470B2 (en) Novel aqueous aluminum pigment composition and process for producing the same
EP2163589B1 (en) Anticorrosive pigment composition and water-based anticorrosive coating material containing the same
NZ212656A (en) Corrosion inhibiting particles for paint
EP0612821B1 (en) Carbon black dispersant
JP2000516297A (en) Corrosion resistant paint
EP0986616B1 (en) Improved kaolin composition for use in electrodeposition paints
RU2287544C1 (en) Anti-corrosion pigment
CN114410161B (en) Long-acting water-based rust conversion coating and preparation method thereof
WO2010123408A2 (en) Anti-corrosion pigment
JP4001922B6 (en) Modified carbon products for inks and coatings
JP4001922B2 (en) Modified carbon products for inks and coatings
JP4204049B2 (en) Baking composition, method for producing the same, and electrodeposition coating
CN111100519A (en) Single-component water-based anticorrosive primer for casting parts and preparation method thereof
JP2002249724A (en) Pigment formulation for anticorrosive coating

Legal Events

Date Code Title Description
MKEX Expiry