WO2002051948A2

WO2002051948A2 - Pigment dispersion and method of preparing the same

Info

Publication number: WO2002051948A2
Application number: PCT/US2001/042956
Authority: WO
Inventors: Swaminathan Ramesh; Joann Lanza; Paul Harris
Original assignee: BASF Corp
Current assignee: BASF Corp
Priority date: 2000-12-22
Filing date: 2001-11-19
Publication date: 2002-07-04
Anticipated expiration: 2003-06-22
Also published as: US6642338B2; ATE334175T1; WO2002051948A3; MXPA03003284A; US20040048959A1; DE60121824D1; CA2430991A1; EP1366123B1; CA2430991C; US6777519B2; US20020132890A1; EP1366123A2; DE60121824T2; ES2267859T3; AU2002225601A1

Abstract

The present invention is directed to a water-based acrylic emulsion dispersant to be used as a grind resin to incorporate inorganic pigment into a pigment dispersion for a coating composition. The acrylic emulsion dispersant is the reaction product of butyl methacrylate, butyl acrylate, styrene, methyl ether polyethylene glycol methacrylate, polyethylene glycol methacrylate, and polyphosphoric acid. The present invention is also directed to a method of preparing the acrylic emulsion dispersant.

Description

PIGMENT DISPERSION AND METHOD OF PREPARING THE SAME

FIELD OF THE INVENTION

The subject invention generally relates to a pigment dispersion utilized in

aqueous coating compositions. More specifically, the subject invention relates to

water-based acrylic emulsion dispersants for an inorganic pigment and a method of

preparing the acrylic emulsion dispersant.

BACKGROUND OF THE INVENTION

Aqueous coating compositions typically include a primary binder resin, a

crosslinker, a pigment or pigments to improve the aesthetics of the coating

composition, and other coating additives such as solvents, flow and appearance

control agents, light-stabilizing additives, fillers such as extender pigment, and the

like.

It is understood in the art that the pigment is incorporated into the aqueous

coating compositions via a pigment dispersion. The pigment dispersion is derived

from dispersion of the pigment into a grind resin. More specifically, a mill, such as

a ball mill, grind mill, or continuous mill, is utilized to incorporate the pigment into

the grind resin. The mill integrates the pigment into the grind resin until a desired

particle size of the pigment is achieved, and until the pigment is appropriately

wetted by the grind resin and uniformly dispersed throughout the grind resin. The grind resins of the prior art have proven to be inadequate for use as a

grind resin for dispersing pigment usable in aqueous coating compositions. The

grind resins of the prior art are ineffective because these resins are unable to

withstand mechanical forces exerted by the mill when integrating the pigment.

These grind resins are also deficient in wetting the pigment and in maintaining the

pigment dispersed throughout the grind resin. Instead, with the grind resins of the

prior art, the pigment tends to coagulate or settle resulting in poor stability and

inadequate 'shelf life' of the pigment dispersion.

These prior art grind resins also tend to have increased viscosities and, as

understood in the art, increased viscosities typically inhibit the amount of pigment

that can be incorporated into the grind resin. As a result, pigment dispersions that

utilize the grind resins of the prior art cannot attain sufficient pigment-to-binder

ratios while maintaining acceptable gloss and appearance in a film of the coating

compositions. Also, due to the increased viscosity, these grind resins often require

solvent and other additives which increase the overall volatile content of the

pigment dispersion — a characteristic that is undesirable throughout the coating

industry.

hi sum, the prior art grind resins, as detailed above, are characterized by one

or more inadequacies. Due to the inadequacies identified in the prior art, it is

desirable to provide water-based acrylic emulsion dispersants to be utilized as grind

resins for inorganic pigments and a method of preparing the water-based acrylic

emulsions. It is advantageous that the acrylic emulsion dispersants according to the

subject invention effectively wet the pigments, uniformly disperse the pigments, and provide increased pigment-to-binder ratios accompanied with acceptable gloss and

appearance in the film of the coating composition.

SUMMARY OF THE INVENTION A water-based acrylic emulsion dispersant is disclosed. The acrylic

emulsion dispersant of the subject invention is utilized as a grind resin, also referred

to as a grind emulsion resin, to incorporate inorganic pigment into a pigment

dispersion for aqueous coating compositions. This acrylic emulsion dispersant is

the reaction product of an ethylenically unsaturated monomer, a vinylaromatic

hydrocarbon monomer, a non-functional polyalkylene glycol acrylate or

methacrylate monomer, a functional polyalkylene glycol acrylate or methacrylate

monomer having a hydroxyl group, and an acid having a first functional acid group

reactive with the hydroxyl group, and a second functional acid group capable of

providing an acid anion group.

A method of preparing the acrylic emulsion dispersant is also disclosed.

According to this method, the ethylenically unsaturated monomer and the

vinylaromatic hydrocarbon monomer are combined with water to establish a first

reaction blend. A non-functiόnal polyalkylene glycol acrylate or methacrylate

monomer and a functional polyalkylene glycol acrylate or methacrylate monomer

having the hydroxyl group are combined with water to establish a second reaction

blend. Next, the first and second reaction blends are polymerized to form an

intermediate emulsion polymer. The intermediate emulsion polymer contains the

hydroxyl group which is then reacted with the acid to form the water-based acrylic

emulsion dispersant of the subject invention. More specifically, the second functional acid group of the acid is neutralized

with an a ine before the first functional acid group of the acid is reacted with the

hydroxyl group in the intermediate emulsion polymer. After this neutralization, the

first functional acid group reacts with the hydroxyl group in the intermediate

emulsion polymer thereby bonding the acid, having the acid anion group, with the

intermediate emulsion polymer to form the acrylic emulsion dispersant.

The general object of the subject invention is to develop a grind resin that

effectively wets inorganic pigments used in aqueous coating compositions and that

is capable of resisting mechanical forces introduced by the mills that are used to

grind and integrate the inorganic pigments into the grind resin, hi resisting the

mechanical forces exerted by the mills, this grind resin is ideal in that it provides

sufficient time for the mill to achieve ideal particle sizes of the inorganic pigments.

It is a further object of the subject invention to develop a grind resin that has

a relatively low molecular weight and a correspondingly low viscosity such that

increased pigment-to-binder ratios can be achieved while maintaining a low

viscosity for the pigment dispersion. More specifically, as a result of the relatively

low viscosity of the grind resin of the subject invention, higher concentrations of

pigments can be incorporated into the grind resin to attain the increased pigment-to-

binder ratios of the pigment dispersion. Due to the higher concentration of pigment,

a solid, into the grind resin, the volatile content of the pigment dispersion, and of

the overall coating composition, is decreased. Also, even at the increased pigment-

to-binder ratios, this grind resin demonstrates superior dispersion stability through extended shelf life of the pigment dispersion, and this grind resin is able to be

completely dispersed into water with little or no co-solvent required to promote dispersibility. This grind resin is also suitable for achieving optimal appearance

characteristics, such as distinctiveness and gloss, in a film of the coating

composition.

DETAILED DESCRIPTION OF THE INVENTION

The water-based acrylic emulsion dispersant of the subject invention is a

'primary' emulsion. By the term primary emulsion, it is to be understood that the

subject invention is in a uniform, water-dispersed form with water being the only

medium. The acrylic emulsion dispersant is utilized as a grind resin to incorporate

inorganic pigment into a pigment dispersion for aqueous coating compositions.

Examples of inorganic pigments that are utilized in aqueous coating compositions

include, among other inorganic pigments, titanium dioxide, TiO₂, and iron oxide,

FeO, as well as certain aluminum and mica flake pigments. It is to be understood

that the terms acrylic emulsion dispersant and grind resin will be used

interchangeably throughout the subject application. The acrylic emulsion dispersant

includes both organic and inorganic chemical structure having various

functionalities that promote efficient wetting of the inorganic pigment and optimal

stability of the pigment in the grind resin of the pigment dispersion in the aqueous

coating composition. These various functionalities will be introduced and discussed

below.

The acrylic emulsion dispersant is generally the reaction product of an

ethylenically unsaturated monomer, a vinylaromatic hydrocarbon monomer, a non¬

functional polyalkylene glycol acrylate or methacrylate monomer, a functional

polyalkylene glycol acrylate or methacrylate monomer having a hydroxyl group, and an acid having a first functional acid group reactive with the hydroxyl group, and a

second functional acid group capable of providing an acid anion group. It is to be

understood that the terminology of an ethylenically unsaturated monomer is

intended to include both one ethylenically unsaturated monomer and more than one

ethylenically unsaturated monomer. In fact, the preferred embodiment of the

subject invention includes more than one ethylenically unsaturated monomer which

will be described below.

The method of preparing the acrylic emulsion dispersant includes the steps

of combining the ethylenically unsaturated monomer and the vinylaromatic

hydrocarbon monomer with water to establish a first reaction blend, combining the non-functional polyalkylene glycol acrylate or methacrylate monomer and the

functional polyalkylene glycol acrylate or methacrylate monomer having the

hydroxyl group with water to establish a second reaction blend, polymerizing the

first and second reaction blends to form an intermediate emulsion polymer

containing the hydroxyl group, and reacting the hydroxyl group with the acid. The

method steps of the subject invention are preferably conducted at temperatures

between 25°C and 100°C, more preferably between 50°C and 100°C. This method

will be described in further detail below.

The ethylenically unsaturated monomer is hydrophobic, i.e., insoluble in

water, and in preparing the acrylic emulsion dispersant of the subject invention, the

ethylenically unsaturated monomer is selected to promote miscibility between the

acrylic emulsion dispersant and a binder resin of the aqueous coating composition.

As appreciated by those skilled in the art, the binder resins of aqueous coating

compositions are preferably either a polyacrylic or polyester binder resin. The ethylenically unsaturated monomer is also selected to achieve an ideal minimum

film forming temperature, MFFT, for the acrylic emulsion dispersant, and ultimately

for the film of the aqueous coating composition, such that the acrylic emulsion

dispersant and the film are resistant to excessive cracking and chipping. The MFFT

of the acrylic emulsion dispersant is preferably 0 to 15°C, more preferably 5 to 10°.

The acrylic emulsion dispersant is further selected such that photo-sensitivity of the

acrylic emulsion dispersant and of the film containing the acrylic emulsion

dispersant is minimized.

The ethylenically unsaturated monomer is present in the acrylic emulsion

dispersant in an amount from 5 to 30, preferably from 15 to 20, parts by weight

based on 100 parts by weight of the acrylic emulsion dispersant, including water, hi

terms of the total monomer composition, the ethylenically unsaturated monomer is

present in an amount from 30 to 60, preferably from 45 to 55, parts by weight based

on 100 parts by weight of total monomer composition. It is to be understood that, in

addition to the content of the ethylenically unsaturated monomer, the total monomer

composition also includes the content of the vinylaromatic hydrocarbon monomer,

the non-functional polyalkylene glycol methacrylate monomer, and the functional

polyalkylene glycol methacrylate monomer, all of which will be discussed in greater

detail below.

The ethylenically unsaturated monomer is more specifically selected from

the group of compounds consisting of aliphatic acrylates, aliphatic methacrylates,

cycloaliphatic acrylates, cycloaliphatic methacrylates, and mixtures thereof. It is to

be understood that each of the compounds, the aliphatic acrylates, the aliphatic methacrylates, the cycloaliphatic acrylates, and the cycloaliphatic methacrylates, include an alkyl radical. In the preferred embodiment of the subject invention, the alkyl radicals of these compounds include up to 20 carbon atoms. When selected as an ethylenically unsaturated monomer, the aliphatic acrylates are present in an amount from 15 to 30, preferably from 23 to 29, parts by weight based on 100 parts by weight of total monomer composition. Similarly, when the aliphatic methacrylates are selected as an ethylenically unsaturated monomer, these monomers are present in an amount from 15 to 30, preferably from 23 to 29, parts by weight based on 100 parts by weight of total monomer composition. hi the preferred embodiment, there is more than one type of ethylenically unsaturated monomer. The differing types of ethylenically unsaturated monomers are selected to balance the physical characteristics of the acrylic emulsion dispersant set forth above. That is, more than one type of the ethylenically unsaturated monomer balances the MFFT and establishes the desired crack and chip resistance as well as the desired photo-sensitivity of the acrylic emulsion dispersant, and of the film of the aqueous coating composition.

The aliphatic acrylates that may be selected as one of the ethylenically unsaturated monomers are selected from the group consisting of methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, ethylhexyl acrylate, stearyl acrylate, lauryl acrylate, and mixtures thereof. The aliphatic methacrylates that may be selected as one of the ethylenically unsaturated monomers are selected from the group consisting of methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl methacrylate, ethylhexyl methacrylate, stearyl methacrylate, lauryl methacrylate, and mixtures thereof. The cycloaliphatic acrylate that may be selected as one of the ethylenically unsaturated monomers is cyclohexyl acrylate, and the cycloaliphatic methacrylate that may be selected as one

of the ethylenically unsaturated monomers is cyclohexyl methacrylate.

h the preferred embodiment of the subject invention, there are two .

ethylenically unsaturated monomers, butyl methacrylate (BMA) and butyl acrylate

(BA). For descriptive purposes, chemical representations of BMA and BA are

respectively disclosed below.

and

As with the ethylenically unsaturated monomer or monomers, the

vinylaromatic hydrocarbon monomer is also hydrophobic, i.e., insoluble in water,

and in preparing the acrylic emulsion dispersant, the vinylaromatic hydrocarbon

monomer is also selected to promote miscibility between the acrylic emulsion dispersant and the binder resin of the aqueous coating composition. The

vinylaromatic hydrocarbon monomer is also selected to establish the ideal MFFT

and to control the photo-sensitivity for the acrylic emulsion dispersant and the film. The vinylaromatic hydrocarbon monomer is present in the acrylic emulsion

dispersant in an amount from 1 to 15, preferably from 3 to 9, parts by weight based

on 100 parts by weight of the acrylic emulsion dispersant, including water, h terms

of the total monomer composition, the vinylaromatic hydrocarbon monomer is

present in an amount from 5 to 20, preferably from 10 to 15, parts by weight based

on 100 parts by weight of total monomer composition. Furthermore, the molar ratio

of the ethylenically unsaturated monomer to the vinylaromatic hydrocarbon

monomer is from 1 : 1 to 10 : 1.

The vinylaromatic hydrocarbon monomer is more specifically selected from

the group consisting of styrene, α-methylstyrene, vinyltoluene, diphenylethylene,

and mixtures thereof, hi the preferred embodiment of the subject invention, the

vinylaromatic hydrocarbon monomer is styrene. For descriptive purposes, a

chemical representation of styrene is disclosed below.

To prepare the acrylic emulsion dispersant, the ethylenically unsaturated

monomer and the vinylaromatic hydrocarbon monomer are combined with water to

establish the first reaction blend. As stated above, the ethylenically unsaturated

monomers and the vinylaromatic hydrocarbon monomer are insoluble in water. As

such, it is also necessary to add an anionic surfactant to the first reaction blend such

that the ethylenically unsaturated monomer and the vinylaromatic hydrocarbon

monomer become dispersed in, and can be incorporated into, the water. Preferably, a sulfonate-based surfactant is selected as the anionic surfactant. In terms of the

preferred embodiment, the BMA and BA and styrene are combined with water and

the anionic surfactant to establish the first reaction blend. In this embodiment, the

molar ratio of the BMA and BA to styrene is 2.5 : 1.

The acrylic emulsion dispersant is also the reaction product of the non¬

functional polyalkylene glycol acrylate or methacrylate monomer. That is, it is to be

understood that the acrylic emulsion dispersant may be the reaction product of either

the non-functional polyalkylene glycol acrylate monomer, or the reaction product of

the non-functional polyalkylene glycol methacrylate monomer, and even mixtures

thereof. However, as will be described in significant detail below, the acrylic

emulsion dispersant is preferably the reaction product of the non-functional

polyalkylene glycol methacrylate. As such, for descriptive purposes only, the

subject invention will be described below only in terms of the non-functional

polyalkylene glycol methacrylate and not the non-functional polyalkylene glycol

acrylate.

The non-functional polyalkylene glycol methacrylate monomer is soluble

and miscible in water and is of the general formula

As shown above, the non-functional polyalkylene glycol methacrylate

monomer includes an ethoxy group (CH₂CH₂O) which promotes the solubility and miscibility of the entire monomer in water. The ethoxy group of the non-functional polyalkylene glycol methacrylate monomer terminates with a non-functional, i.e.,

un-reactive, methyl group (CH ). It is important that this monomer be non¬

functional to control the viscosity of the completed acrylic emulsion dispersant.

The variable x in the general formula of the non-functional polyalkylene glycol

methacrylate monomer can range from 5 to 50. The non-functional polyalkylene

glycol methacrylate monomer is present in an amount from 1 to 15, preferably from

4 to 7, parts by weight based on 100 parts by weight of total monomer composition.

In the preferred embodiment, the non-functional polyalkylene glycol

methacrylate monomer is methyl ether polyethylene glycol methacrylate

(MPEGMA), and x is 6 resulting in a formula weight for the MPEGMA of

approximately 350 amu (atomic mass units). For descriptive purposes, a chemical

representation of the preferred non-functional monomer, MPEGMA, is disclosed

below. -

In alternative embodiments, where the non-functional polyalkylene glycol

acrylate is selected, the preferred non-functional polyalkylene glycol acrylate is

methyl ether polyethylene glycol acrylate.

The acrylic emulsion dispersant is also the reaction product of the functional

polyalkylene glycol acrylate or methacrylate monomer having the hydroxyl group. That is, it is to be understood that the acrylic emulsion dispersant may be the

reaction product of either the functional polyalkylene glycol acrylate monomer

having the hydroxyl group, or the reaction product of the functional polyalkylene

glycol methacrylate monomer having the hydroxyl group, and even mixtures

thereof. However, as will be described in significant detail below, the acrylic

emulsion dispersant is preferably the reaction product of the functional polyalkylene

glycol methacrylate. As such, for descriptive purposes only, the subject invention

will be described below only in terms of the functional polyalkylene glycol

methacrylate and not the functional polyalkylene glycol acrylate.

In the context of the subject invention, the functional polyalkylene glycol

methacrylate monomer is functional because this monomer includes a hydroxyl

group. As with the non-functional polyalkylene glycol methacrylate monomer, the

functional polyalkylene glycol methacrylate monomer is soluble and miscible in

water. The functional monomer is of the general formula

As shown above, the functional polyalkylene glycol methacrylate monomer

includes an ethoxy group (CH₂CH₂O) which promotes the solubility and miscibility

of the entire monomer in water. The ethoxy group of the functional polyalkylene

glycol methacrylate monomer terminates with a functional, i.e., reactive, hydrogen

atom thereby establishing the hydroxyl group of the functional monomer. The significance of this functional hydroxyl group will be described below. The variable y in the general formula of the functional polyalkylene glycol methacrylate

monomer can range from 5 to 50. The functional polyalkylene glycol methacrylate

monomer is present in an amount from 25 to 40, preferably from 27 to 30, parts by

weight based on 100 parts by weight of total monomer composition. Furthermore,

the molar ratio of the functional polyalkylene glycol methacrylate monomer with the

hydroxyl group to the non-functional polyalkylene glycol methacrylate monomer is

from 5 : 1 to 15 : 1. Of course, if the functional polyalkylene glycol acrylate

monomer with the hydroxyl group and the non-functional polyalkylene glycol

acrylate monomer are used, as would be in certain alternative embodiments, the

above molar ratio, from 5 : 1 to 15 : 1 remains applicable.

The functional polyalkylene glycol methacrylate monomer is selected

from the group consisting of polyethylene glycol methacrylate (PEGMA),

polypropylene glycol methacrylate, and mixtures thereof. hi the preferred

embodiment, the functional polyalkylene glycol methacrylate monomer is PEGMA,

and_y is 7 resulting in a formula weight for the PEGMA of approximately 360 amu

(atomic mass units). For descriptive purposes, a chemical representation the

preferred functional monomer, PEGMA, is disclosed below.

In alternative embodiments, where the functional polyalkylene glycol

acrylate is selected, the preferred functional polyalkylene glycol acrylate is

polyethylene glycol acrylate.

To prepare the acrylic emulsion dispersant, the non-functional polyalkylene

glycol methacrylate monomer and the functional polyalkylene glycol methacrylate

monomer having the hydroxyl groups are combined with water to establish the

second reaction blend. Since, as stated above, both the non-functional polyalkylene

glycol methacrylate monomer and the functional polyalkylene glycol methacrylate

monomer are soluble in water, there is no need to add any of the anionic surfactant

to the second reaction blend. In terms the preferred embodiment, the MPEGMA

and the PEGMA are combined with water to establish the second reaction blend. In

this embodiment, the molar ratio of the PEGMA to the MPEGMA is 10 : 1.

In addition to the above, an initiator, also known as a polymerization

promoter, is incorporated into the second reaction blend to initiate an emulsion

polymerization process which will be described below. The initiator is soluble in

water and is selected from the group of inorganic persulfates consisting of

ammonium persulfate, (NH₄)₂S₂O₈, potassium persulfate, K₂S₂O₈, and sodium

persulfate, Na₂S₂O₈. Of course, other suitable initiators including, but not limited

to, conventional inorganic peroxodisulfates and ammonium or alkali metal

peroxydiphosphates can also be utilized to initiate the emulsion polymerization

process.

Next, the first and second reaction blends are polymerized to form an

intermediate emulsion polymer. More specifically, the first and second reaction

blends are fed into a distinct reaction flask where polymerization forms the

intermediate emulsion polymer. The intermediate emulsion polymer contains the

hydroxyl group from the functional polyalkylene glycol methacrylate, in the

preferred embodiment PEGMA. For descriptive purposes, a chemical

representation of the general formula of the intermediate emulsion polymer is

disclosed below.

R._! is a polymer chain as defined above. That is, Ri contains monomers

selected from the group consisting of ethylenically unsaturated monomers and

vinylaromatic hydrocarbon monomers, and mixtures thereof, and the variables x and

y range from 5 to 50 as described above. The variable ? is indicative of the number

of MPEGMA monomers in the complete polymer chain, and the variable q is

indicative of the number of PEGMA monomers in the complete polymer chain. The

variables ? and q range from 1 to 100 which will be described further below.

In terms of the preferred embodiment, R₁ is specifically defined as follows:

which includes BMA, BA, and styrene, and the variables m, n, and o varying from 1

to 100. It is to be understood that the variables m, n, and o are respectively

indicative of the number of BMA, BA, and styrene monomers in the complete polymer chain. As such, the complete intermediate emulsion polymer, in terms of the preferred embodiment, appears as disclosed below.

In this preferred embodiment, the variables m, n, o, p, and q more

specifically range from 5 to 20 such that there are, on average, 100 monomers per

polymer chain. Of course, the number of monomers per polymer chain drives the

molecular weight of the acrylic emulsion dispersant as will be described below.

To control the extent of polymerization and thus the molecular weight

during the emulsion polymerization process, the subject invention utilizes a water-

soluble, chain transfer agent. The chain transfer agent can either be incorporated

into the second reaction blend, with the MPEGMA, PEGMA, and water, or the

chain transfer agent can be incorporated into the polymerization reaction flask that

the first and second reaction blends are fed into. The chain transfer agent is a

mercaptan, i.e., a thiol, of the general formula R₂ - SH, wherein R₂ is a hydrocarbon

chain. Preferably, the mercaptan is selected from the group consisting of ethyl

mercaptan and 2-nonanethiol, and mixtures thereof. Other suitable chain transfer agents include polyhalogen compounds. The chain transfer agent of the subject

invention controls the number of monomers per polymer chain such that the

variables m, n, o, p, and q range from 5 to 20 and there are, on average, 100

monomers per polymer chain. After the intermediate emulsion polymer is formed, the acid is reacted with

the hydroxyl group in-the intermediate emulsion polymer from either the functional

polyalkylene glycol acrylate or methacrylate. More specifically, it is the first

functional acid group of the acid that is reacted with the hydroxyl group. The first

functional acid group reacts with the hydroxyl group such that a bond is established

between the oxygen atom in the hydroxyl group of the intermediate emulsion

polymer and the acid.

However, it is preferred that prior to the reaction between the first functional

acid group and the hydroxyl group in the intermediate emulsion polymer, the second

functional acid group of the acid is neutralized with an amine such that the second

functional acid group provides the acid anion group, O\ The acid anion group, as

will be discussed further below, interacts with metal centers that are inherent in

inorganic pigments to anchor the pigment or pigments in the pigment dispersion.

In view of the above requirements for the first and second functional acid

groups, the acid is selected from the group consisting of polyphosphoric acid,

sulfuric acid, sulfurous acid, and dicarboxyhc acids. Suitable dicarboxyhc acids

include, but are not limited to, oxalic acid, malonic acid, succinic acid, glutaric acid,

and mixtures thereof.

Of course, it is to be considered equivalent that the hydroxyl group of the

intermediate emulsion polymer can alternatively be reacted with suitable carboxylic acid anhydrides including, but not limited to, maleic anhydride, hexahydrophthalic

anhydride, methyl-hexahydrophthalic anhydride, tetrahydrophthalic anhydride,

phthalic anhydride, succinic anhydride, dodecenylsuccinic anhydride, trimellitic

anhydride, and mixtures thereof. The ring structure in these anhydrides will open

upon reaction with the hydroxyl group, and have the second functional acid group

remaining which then can provide the acid anion group upon neutralization with the

amine.

In the preferred embodiment, the acid is polyphosphoric acid which has

three hydroxyl groups. The polyphosphoric acid is reacted with the hydroxyl group

from the functional polyalkylene glycol acrylate or methacrylate in the intermediate

emulsion polymer. However, as discussed above, before the polyphosphoric acid of

the preferred embodiment and the intermediate emulsion polymer are reacted, the

polyphosphoric acid is neutralized with the amine. The amine is reacted with the

polyphosphoric acid in a molar ratio of two moles of amine for every one mole of

polyphosphoric acid. It is understood in the art that polyphosphoric acid includes

both an H₃PO₄ chemical component and a P₂O₅ chemical component. The amine is

selected from the group consisting of dimethylethanolamine and amino methyl

propanol, and mixtures thereof. Preferably, the amine is dimethylethanolamine,

(CH₃)₂NCH₂CH₂OH. Other amines suitable in the subject emulsion polymerization

process include, but are not limited to NH₃ and alkyl amines such as diethylamine.

For descriptive purposes, a chemical representation of the H₃PO chemical

component of the polyphosphoric acid is disclosed below.

Specifically, two of the three hydroxyl groups of the polyphosphoric acid

function as second functional acid groups and are neutralized with the amine to

provide the acid anion groups prior to reacting the hydroxyl group in the

intermediate emulsion polymer with the polyphosphoric acid. After this

neutralization step, the phosphoric acid is in the following ionic form having two

acid anion groups. ^Λ

Next, the one hydroxyl group of the polyphosphoric acid that remains un-

neutralized by the amine, i.e., the first functional acid group of the polyphosphoric

acid, is reacted with the hydroxyl group in the intermediate emulsion polymer from

the functional polyalkylene glycol acrylate or methacrylate such that the bond is

established between the intermediate emulsion polymer and the polyphosphoric acid

to fonn the completed acrylic emulsion dispersant. More specifically, the bond is

established between the phosphorus atom of the polyphosphoric acid and the

oxygen atom from hydroxyl group of the terminal ethoxy group in the functional

polyalkylene glycol acrylate or methacrylate. In terms of the preferred embodiment,

the one hydroxyl group of the polyphosphoric acid that remains un-neutralized, i.e.,

the first functional acid group, is reacted with the hydroxyl group in the intermediate emulsion polymer from the PEGMA. For descriptive purposes, a chemical representation of a general formula of the completed acrylic emulsion dispersant is disclosed below.

All variables are defined as above. In terms of the preferred embodiment,

including the BMA, the BA, the styrene, the MPEGMA, the PEGMA, and the

polyphosphoric acid, a chemical representation is disclosed below.

Notice in this chemical representation, the completed acrylic emulsion

dispersant has acid functionality, with two acid anion groups, and the preferred

amine, dimethylethanolamine, remains in the reaction in cationic form.

The completed acrylic emulsion dispersant includes, on average, 100

monomers and has a weight-average molecular weight, M_w, of from 10,000 to 100,000. Preferably, the molecular weight is from 10,000 to 40,000, and more

preferably, from 10,000 to 17,000. The completed acrylic emulsion dispersant has a number-average molecular weight, M_n, of 10,000 or less. Additionally, the acrylic

emulsion dispersant of the subject invention has a non- volatile content of from 20 to

40, preferably from 25 to 35, percent non- volatile by weight. This acrylic emulsion

dispersant is also completely hydrophilic such that it can be in the uniform, water-

dispersed form that is characteristic of primary emulsions.

Pigment dispersions utilizing this acrylic emulsion dispersant have pigment-

to-binder ratios exceeding 30, preferably from 30 to 40 with pigment particles

having a particle size of less than six microns. That is, the grind resin of the subject

invention is robust enough to permit the inorganic pigments dispersed within to be

ground or milled long enough to achieve pigment particle sizes of less than six

microns without degradation and coagulation of the grind resin. Of course, it is to

be understood that other pigment dispersions utilizing this acrylic emulsion

dispersant may also have pigment-to-binder ratios less than 30. Furthermore,

pigment dispersions utilizing this acrylic emulsion dispersant have viscosities of

less than 80 Krebs units. The viscosities of these pigment dispersions were

measured after thirty minutes of mixing with a Cowles blade at approximately 3000

RPM and at 75 to 85°F.

The resulting structure of the completed acrylic emulsion dispersant of the

subject invention essentially 'anchors' the inorganic pigment in the pigment

dispersion thereby maintaining the pigment uniformly dispersed throughout the

grind resin. More specifically, the acid functionality, or the acid anion groups, of

the completed acrylic emulsion dispersant physically interacts with the metal

centers inherent in inorganic pigments by complex or coordinated covalent bonding.

This physical interaction keeps the pigment uniformly dispersed throughout the grind resin. Also, as discussed above, the selection of monomers, in particular the

selection of the ethylenically unsaturated monomers and the vinylaromatic

hydrocarbon monomers, promotes thorough miscibility between the acrylic

emulsion dispersant and the binder resin of the aqueous coating composition.

It is to be understood that all of the preceding chemical representations are

merely two-dimensional chemical representations and that the structure of these

chemical representations may be other than as indicated. It is also to be understood

that although the chemical representations disclosed above that relate to the

structure of the polymer chain indicate that the completed acrylic emulsion

dispersant has specific 'blocks' of monomers, in reality, the monomers are

randomly distributed throughout the polymer based on the molar ratios of the

monomers as well as the relative reactivity realized between the discrete monomer

components.

The following examples illustrating the formation of and the use of the

acrylic emulsion dispersant of the subject invention, as presented herein, are

intended to illustrate and not limit the invention.

EXAMPLES; Example 1 :

The acrylic emulsion dispersant was prepared by adding and reacting the

following parts, by weight, unless otherwise indicated.

Table 1

Per the above table, Table 1, 99.3 grams of BMA and 88.7 grams of BA and

56.3 grams of styrene and 13.8 grams of anionic surfactant were combined with

278.8 grams of water to establish the first reaction blend. 9.4 grams of MPEGMA

and 102.2 grams of PEGMA and 1.16 grams of Initiator were combined with 276.5

grams of water to establish the second reaction blend. Also, 7.5 grams of mercaptan

were added to the second reaction blend. Next, a distinct polymerization reaction flask was prepared with 8.9 grams of Anionic Surfactant and 278.0 grams of water,

and the first and second reaction blends were polymerized to form the intermediate

emulsion polymer in the polymerization reaction flask. More specifically, the first

and second reaction blends were dual-fed into the polymerization reaction flask,

already including the Anionic Surfactant and the water, for approximately two hours

to from the intermediate emulsion polymer. Throughout the two hour dual-feed, the

polymerization reaction flask was heated via a conventional heat supply to a

temperature of 80°C. After the two hour dual-feed, the polymerization reaction

flask was maintained at 80°C for an additional two hours, now totaling

approximately four hours, and then the heat supply was suspended.

Once the intermediate emulsion polymer was formed, 84.7 grams of a 20%

aqueous solution of DMEA were reacted with 47.2 grams of a 20% aqueous

solution of polyphosphoric acid to neutralize two of the three hydroxyl groups of the

polyphosphoric acid and form the acrylic emulsion dispersant of the subject

invention. Then the neutralized polyphosphoric acid was added to the intermediate

emulsion polymer in the polymerization reaction flask to react the hydroxyl group

of the polyphosphoric acid that remained un-neutralized by the amine with the

hydroxyl group in the intermediate emulsion polymer from the functional

polyalkylene glycol methacrylate.

The completed acrylic emulsion dispersant has a pH value of 8.16 at 25 °C,

and an acid number, determined by conventional methods, of 39 indicative of the content of H PO₄ in the completed acrylic emulsion dispersant. Under GPC

analysis, the M_n and M_w of the subject dispersant were 4,110 and 15,330,

respectively. Example 2:

The completed acrylic emulsion dispersant was then incorporated into a modified pigment dispersion according to the following table, Table 2.

Table 2

Per the above table, Table 2, 211.0 grains of the acrylic emulsion dispersant and 207.0 grams of de-ionized water and 48.0 grams of propyl propasol and 0.29 grams of a defoaming additive were added together to prepare a modified pigment dispersion for an aqueous coating composition. Next, 939.0 grams of TiO₂ pigment were added gradually over time and under stirring to the acrylic emulsion dispersant / the de-ionized water / propyl propasol blend.

The appearance of the modified pigment dispersion was evaluated by a 2 mil thickness drawdown. The evaluation of the modified pigment dispersion utilizing the acrylic emulsion dispersant of the subject invention concluded a glossy appearance with slight aeration. Additionally, the particle size of the modified pigment dispersion was determined utilizing a standard grind gauge method. No pigment particles were observed thereby indicating that the pigment particle size is less than six microns according to the standards of the grind gauge method. The pigment-to-binder ratio of this modified pigment dispersion was 15.34, and this modified pigment dispersion had a viscosity of 60 Krebs units after thirty minutes of mixing with a Cowles blade at approximately 3001 RPM and at 75°F. The invention has been described in an illustrative manner, and it is to be understood that the tenninology which has been used is intended to be in the nature of words of description rather than of limitation. Obviously, many modifications and variations of the present invention are possible in light of the above teachings, and the invention may be practiced otherwise than as specifically described.

Claims

CLAIMSWhat is claimed is:

1. A pigment dispersion comprising inorganic pigment and a water-

based acrylic emulsion dispersant comprising the reaction product of:

an ethylenically unsaturated monomer;

a vinylaromatic hydrocarbon monomer;

a non-functional polyalkylene glycol acrylate or methacrylate monomer,

a functional polyalkylene glycol acrylate or methacrylate monomer having a

hydroxyl group; and

an acid having a first functional acid group reactive with said hydroxyl

group, and a second functional acid group capable of providing an acid anion group.

2. A pigment dispersion as set forth in claim 1 further comprising an

amine for neutralizing said polyphosphoric acid.

3. A pigment dispersion as set forth in claim 1 wherein said

ethylenically unsaturated monomer is selected from the group of compounds

consisting of aliphatic acrylates, aliphatic methacrylates, cycloaliphatic acrylates,

cycloaliphatic methacrylates, and mixtures thereof, each of said compounds having

up to 20 carbon atoms in the alkyl radical.

4. A pigment dispersion as set forth in claim 3 wherein said aliphatic

acrylates are selected from the group consisting of methyl acrylate, ethyl acrylate,

propyl acrylate, butyl acrylate, hexyl acrylate, ethylhexyl acrylate, stearyl acrylate,

lauryl acrylate, and mixtures thereof.

5. A pigment dispersion as set forth in claim 3 wherein said aliphatic methacrylates are selected from the group consisting of methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl methacrylate,

ethylhexyl methacrylate, stearyl methacrylate, lauryl methacrylate, and mixtures

thereof.

6. A pigment dispersion as set forth in claim 1 wherein said

vinylaromatic hydrocarbon monomer is selected from the group consisting of

styrene, α-methylstyrene, vinyltoluene, diphenylethylene, and mixtures thereof.

7. A pigment dispersion as set forth in claim 1 wherein said non¬

functional polyalkylene glycol methacrylate monomer is further defined as methyl

ether polyethylene glycol methacrylate.

8. A pigment dispersion as set forth in claim 1 wherein said functional

polyalkylene glycol methacrylate monomer having a hydroxyl group is selected

from the group consisting of polyethylene glycol methacrylate, polypropylene glycol

methacrylate, and mixtures thereof.

9. A pigment dispersion as set forth in claim 1 wherein said acid having

said first and second functional acid groups is selected from the group consisting of

polyphosphoric acid, sulfuric acid, sulfurous acid, and dicarboxyhc acids.

10. A pigment dispersion as set forth in claim 1 wherein said acrylic

emulsion dispersant has a molecular weight of from 10,000 to 100,000.

11. A pigment dispersion as set forth in claim 1 wherein said acrylic

emulsion dispersant has a non- volatile content of from 20 to 40 percent non- volatile

by weight.

12. A water-based acrylic emulsion dispersant for efficient wetting and

grinding of a pigment, said acrylic emulsion dispersant comprising the reaction

product of:

an ethylenically unsaturated monomer;

a vinylaromatic hydrocarbon monomer;

a non-functional polyalkylene glycol acrylate or methacrylate monomer,

a functional polyalkylene glycol acrylate or methacrylate monomer having a

hydroxyl group; and

an acid having a first functional acid group reactive with said hydroxyl

13. An acrylic emulsion dispersant as set forth in claim 12 further

comprising an amine for neutralizing said second functional acid group to provide

said acid anion group.

14. An acrylic emulsion dispersant as set forth in claim 13 wherein said

amine is selected from the group consisting of dimethylethanolamine and amino

methyl propanol, and mixtures thereof.

15. An acrylic emulsion dispersant as set forth in claim 12 wherein said

ethylenically unsaturated monomer is present in an amount from 30 to 60 parts by

weight based on 100 parts by weight of total monomer composition.

16. An acrylic emulsion dispersant as set forth in claim 12 wherein said

ethylenically unsaturated monomer is selected from the group of compounds

consisting of aliphatic acrylates, aliphatic methacrylates, cycloaliphatic acrylates, cycloaliphatic methacrylates, and mixtures thereof, each of said compounds having

up to 20 carbon atoms in the alkyl radical.

17. An acrylic emulsion dispersant as set forth in claim 16 wherein said

aliphatic acrylates are selected from the group consisting of methyl acrylate, ethyl

acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, ethylhexyl acrylate, stearyl

acrylate, lauryl acrylate, and mixtures thereof.

18. An acrylic emulsion dispersant as set forth in claim 16 wherein said

aliphatic acrylates are present in an amount from 15 to 30 parts by weight based on

100 parts by weight of total monomer composition.

19. An acrylic emulsion dispersant as set forth in claim 16 wherein said

aliphatic methacrylates are selected from the group consisting of methyl

methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl

methacrylate, ethylhexyl methacrylate, stearyl methacrylate, lauryl methacrylate, and

mixtures thereof.

20. An acrylic emulsion dispersant as set forth in claim 16 wherein said

aliphatic methacrylates are present in an amount from 15 to 30 parts by weight

based on 100 parts by weight of total monomer composition.

21. An acrylic emulsion dispersant as set forth in claim 16 wherein said

cycloaliphatic acrylate is further defined as cyclohexyl acrylate.

22. An acrylic emulsion dispersant as set forth in claim 16 wherein said

cycloaliphatic methacrylate is further defined as cyclohexyl methacrylate.

23. An acrylic emulsion dispersant as set forth in claim 12 wherein said

vinylaromatic hydrocarbon monomer is selected from the group consisting of

24. An acrylic emulsion dispersant as set forth in claim 12 wherein said

vinylaromatic hydrocarbon monomer is present in an amount from 5 to 20 parts by

weight based on 100 parts by weight of total monomer composition.

25. An acrylic emulsion dispersant as set forth in claim 12 wherein said

non-functional polyalkylene glycol methacrylate monomer is further defined as

methyl ether polyethylene glycol methacrylate.

26. An acrylic emulsion dispersant as set forth in claim 12 wherein said

non-functional polyalkylene glycol methacrylate monomer is present in an amount

from 1 to 15 parts by weight based on 100 parts by weight of total monomer

composition.

27. An acrylic emulsion dispersant as set forth in claim 12 wherein said

non-functional polyalkylene glycol acrylate monomer is present in an amount from

1 to 15 parts by weight based on 100 parts by weight of total monomer composition.

28. An acrylic emulsion dispersant as set forth in claim 12 wherein said

functional polyalkylene glycol methacrylate monomer having a hydroxyl group is

selected from the group consisting of polyethylene glycol methacrylate,

polypropylene glycol methacrylate, and mixtures thereof.

29. An acrylic emulsion dispersant as set forth in claim 12 wherein said

functional polyalkylene glycol methacrylate monomer having a hydroxyl group is

present in an amount from 25 to 40 parts by weight based on 100 parts by weight of

total monomer composition.

30. An acrylic emulsion dispersant as set forth in claim 12 wherein said

functional polyalkylene glycol acrylate monomer having a hydroxyl group is present in an amount from 25 to 40 parts by weight based on 100 parts by weight of total

monomer composition.

31. An acrylic emulsion dispersant as set forth in claim 12 wherein the

molar ratio of said ethylenically unsaturated monomer to said vinylaromatic

hydrocarbon monomer is from 1 : 1 to 10 : 1.

32. An acrylic emulsion dispersant as set forth in claim 12 wherein the

molar ratio of said functional polyalkylene glycol methacrylate monomer having a

hydroxyl group to said non-functional polyalkylene glycol methacrylate monomer is

from 5 : 1 to 15 : 1.

33. An acrylic emulsion dispersant as set forth in claim 12 wherein said

acid having said first and second functional acid groups is selected from the group

consisting of polyphosphoric acid, sulfuric acid, sulfurous acid, and dicarboxyhc

acids.

34. An acrylic emulsion dispersant as set forth in claim 12 having a

molecular weight of from 10,000 to 100,000.

35. An acrylic emulsion dispersant as set forth in claim 12 having a non¬

volatile content of from 20 to 40 percent non- volatile by weight.

36. A method of preparing a water-based acrylic emulsion dispersant for

efficient wetting and grinding of a pigment, said method comprising the steps of:

(i) combining an ethylenically unsaturated monomer and a

vinylaromatic hydrocarbon monomer with water to establish a first reaction blend;

(ii) combining a non-functional polyalkylene glycol acrylate or

methacrylate monomer with a functional polyalkylene glycol acrylate or

methacrylate monomer having a hydroxyl group with water to establish a second

reaction blend;

(iii) polymerizing the first and second reaction blends to form an

intermediate emulsion polymer containing the hydroxyl group; and

(iv) reacting the hydroxyl group with an acid having a first functional

acid group reactive with the hydroxyl group, and a second functional acid group

capable of providing an acid anion group.

37. A method as set forth in claim 36 further including the step of adding

an anionic surfactant to the first reaction blend such that the ethylenically

unsaturated monomer and the vinylaromatic hydrocarbon monomer are soluble in

the water.

38. A method as set forth in claim 36 wherein the acid having the first

and second functional acid groups is selected from the group consisting of

polyphosphoric acid, sulfuric acid, sulfurous acid, and dicarboxyhc acids.

39. A method as set forth in claim 36 wherein the acid having the first

and second functional acid groups is polyphosphoric acid having three hydroxyl groups.

40. A method as set forth in claim 39 further including the step of

neutralizing two of the three hydroxyl groups of the polyphosphoric acid with an

amine prior to reacting the hydroxyl group in the intermediate emulsion polymer with the polyphosphoric acid.

41. A method as set forth in claim 40 wherem the step of (iv) reacting

the hydroxyl group with the acid is further defined as reacting the one hydroxyl

group of the polyphosphoric acid that remains un-neutralized with the hydroxyl

group in the intermediate emulsion polymer.

42. A method as set forth in claim 36 wherein steps (i) through (iv) are

conducted at a temperature between 25°C and 100°C.

43. A method as set forth in claim 36 wherein the ethylenically

unsaturated monomer is selected from the group of compounds consisting of

aliphatic acrylates, aliphatic methacrylates, cycloaliphatic acrylates, cycloaliphatic

methacrylates, and mixtures thereof, each of said compounds having up to 20

carbon atoms in the alkyl radical.

44. A method as set forth in claim 43 wherein the aliphatic acrylates are

selected from the group consisting of methyl acrylate, ethyl acrylate, propyl acrylate,

butyl acrylate, hexyl acrylate, ethylhexyl acrylate, stearyl acrylate, lauryl acrylate,

and mixtures thereof.

45. A method as set forth in claim 43 wherein the aliphatic methacrylates are selected from the group consisting of methyl methacrylate, ethyl methacrylate,

propyl methacrylate, butyl methacrylate, hexyl methacrylate, ethylhexyl

methacrylate, stearyl methacrylate, lauryl methacrylate, and mixtures thereof.

46. A method as set forth in claim 36 wherein the vinylaromatic

hydrocarbon monomer is selected from the group consisting of styrene, α-

methylstyrene, vinyltoluene, diphenylethylene, and mixtures thereof.

47. A method as set forth in claim 36 wherein the non-functional

polyalkylene glycol methacrylate monomer is further defined as methyl ether

polyethylene glycol methacrylate.

48. A method as set forth in claim 36 wherein the functional

polyalkylene glycol methacrylate monomer having a hydroxyl group is selected

methacrylate, and mixtures thereof.

49. A method as set forth in claim 36 further including the step of

neutralizing the second functional acid group of the acid with an amine to provide

the acid anion group prior to reacting the hydroxyl group in the intermediate

emulsion polymer with the acid.

50. A water-based acrylic emulsion dispersant for efficient wetting and

grinding of a pigment, said acrylic emulsion dispersant being of the general

formula:

wherein;

R_\ is a polymer chain containing monomers selected from the group

consisting of ethylenically unsaturated monomers and vinylaromatic hydrocarbon

monomers, and mixtures thereof;

p and q are from 1 to 100; and

51. An acrylic emulsion dispersant as set forth in claim 50 wherein said

ethylenically unsaturated monomers are selected from the group consisting of

compounds consisting of aliphatic acrylates, aliphatic methacrylates, cycloaliphatic

acrylates, cycloaliphatic methacrylates, and mixtures thereof, each of said

compounds having up to 20 carbon atoms in the alkyl radical.

52. An acrylic emulsion dispersant as set forth in claim 51 wherein said

acrylate, lauryl acrylate, and mixtures thereof.

53. An acrylic emulsion dispersant as set forth in claim 51 wherein said

aliphatic methacrylates are selected from the group consisting of methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl

mixtures thereof.

54. An acrylic emulsion dispersant as set forth in claim 50 wherein said

vinylaromatic hydrocarbon monomers are selected from the group consisting of

55. An acrylic emulsion dispersant as set forth in claim 50 wherein K_\ is

further defined as

wherein;

m, n, and o are from 1 to 100.

56. A water-based acrylic emulsion dispersant for efficient wetting and

grinding of a pigment, said acrylic emulsion dispersant comprising the reaction

product of:

an ethylenically unsaturated monomer;

a vinylaromatic hydrocarbon monomer;

a non-functional monomer selected from the group consisting of non¬

functional polyalkylene glycol methacrylate monomers and non-functional

polyalkylene glycol acrylate monomers;

a functional monomer selected from the group consisting of functional

polyalkylene glycol methacrylates having a hydroxyl group and functional

polyalkylene glycol acrylate monomers having a hydroxyl group; and

an acid having a first functional acid group reactive with said hydroxyl