CA1159247A

CA1159247A - Magnetic polymer latices and process for the preparation thereof

Info

Publication number: CA1159247A
Application number: CA000375648A
Authority: CA
Inventors: Jean-Claude Daniel; Jean L. Schuppiser; Marc Tricot (Deceased)
Original assignee: Individual
Current assignee: Prolabo SA
Priority date: 1980-04-18
Filing date: 1981-04-16
Publication date: 1983-12-27
Also published as: DK171881A; EP0038730A1; JPH043088B2; IE51322B1; BR8102333A; JPS56164503A; DE3166260D1; FR2480764A1; ES501397A0; AU539397B2; ATE9587T1; EP0038730B1; IL62649A0; US4358388A; IE810865L; IL62649A; AU6961881A; ES8203097A1; FR2480764B1

Abstract

ABSTRACT
Magnetic polymer latices are disclosed having a concentration below 65% by weight of particles between 0.03 and 5 µm in diameter consisting of hydrophobic vinyl aromatic polymers and containing between 0.5 and 50% by weight of magnetically charged particles based on the polymer. A process is disclosed for the preparation of the latices, consisting of dispersing a magnetic charge in an organic phase consisting of an organo-soluble initiator;
all or part of a vinyl aromatic monomer, alone or in admixture with at least one copolymerizable monomer producing a hydrophobic polymer; and/or an organic compound insoluble in water; mixing the dispersion obtained with all or part of an aqueous solution containing an emulsifying agent; emulsifying the mixture and polymerizing it after eventual addition of the remainder of the constituents.
The latices are useful in the paint, magnetic tape and recording industries and in biological applications.

Description

1 1~92ll7 The invention relates to polymer latices containing a magnetic charge, and to a process for the preparation thereof.
Magnetic polymers, in the form of gels or particles, are usually ob-tained by mixing the magnetic charge with the polymer prepared by conventional techniques of polymerization in bulk solution, emulsion or suspension. Such mixing, however, requires an additional step in the preparation of magnetic polymers which involves, for example, atomization, coagulation, extrusion, or solvent distillation. Such a step requires suitable equipment, consumes a by no means negligible amount of energy, and often raises difficulties in dis-persion and behaviour of the polymers. This leads to lack of uniformity in the distribution of the magnetic charge and may otherwise affect the properties of the polymers.
It is also known to mix the magnetic charge with a polymer latex, but this requires special polymers in order to ensure dispersion of the magnetic charge, and the products obtained often lack adequate stability.
In`order to eliminate this ~lixing, it has been proposed to add the ; magnetic charge to the polymerization emulsion of a mixture of monomers, at least one of which is soluble in water, but this results in the production of hydrophilic monomers of limited application.
As regards monomers which are insoluble -in water, emulsion poly-merization in the presence of the magnetic charge has failed to yield satis-factor~ results since the magnetic charge is not incorporated into the polymer particles during polymerization.
According to the present invention, there is provided a magnetic polymer latex having a concentration below 65% by weight of polymer particles of an average diameter of from 0.03 to 5fum, the particles consisting of hydrophobic vinyl aromatic polymer and containing from 0.5 to 50% by weight o:E

. ~

1 1592~7 magnetic charge, based on the polymer.
The products according to the invention lack the above disadvan-tages. They are stable, provide satisfactory dispersion of the magnetic charge in the polymer particles, and are easily obtained by polymerization of monomers, insoluble in water, in the presence of the magnetic charge.
Hydrophobic vinyl aromatic polymers are intended to mean homopolymers of vinyl aromatic monomers insoluble in water, such as styrene, alpha-methyl styrene, ethylstyrene, tertiary-butyl styrene, vinyltoluene and copolymers of these monomers with each other and/or with other copolymerizable monomers in-soluble in water, for example dienes, alkyl acrylates and methacrylates wherein the alkyl group contains from 3 to 10 carbon atoms, esters of ethylenic acids containing ~ or 5 carbon atoms, and of alkyl groups containing from 1 to 8 carbon atoms.
In these particles, the magnetic charge constitutes from 0.5 to 50, more particularly from a.5 to 35%, and preferably from Q.7 to 20% by weight, based on the polymer.
; In the latex, the concentration of polymer particles is less than 65%, preferably from 5 to 5Q% by weight. However, the latex may be diluted or concentrated without difficulty. The average diameter of the particles is from Q.03 to 5, preferably from 0.05 to 1 ~m. The grain size distribution of the particles may be wide or narrow, depending upon the polymerizing con-ditions. The particles are attracted by a magnet even if the latex is highly diluted, for example at a concentration as low as 1% by weight.
The process according to the invention for obtaining magnetic polymer latices comprises polymerizing, in an aqueous medium, a vinyl aromatic monomer alone or in admixture with a copolymerizable monomer in the presence of a magnetic charge, the magnetic charge being dispersed in an organic phase con-~ 2 -1 1592~7 sisting of an organo-soluble initiator, all or part of the vinyl aromatic mono-mer alone or in admixture with at least one copolymerizable monomer producing a hydrophobic polymer, and/or of an organic compound insoluble in water. The dispersion obtained is mixed with all or part of an aqueous solution consisting of water and at least one emulsifying agent. The whole is then homogenized and polymerized after eventual addition of the remainder of the constituents.
In the process of the invention, depending upon the compounds used, the organic phase in which the magnetic charge is dispersed consists of:
- all or part of the monomer or monomers and the entire initiator;
- or the whnle of the organic compound insoluble in water and the lQ whole of the initiator;
- or the whole of the organic compound, all or part of the monomer or monomers, and the whole of the initiator.
If the monomer or monomers are not present in part or in whole in the organic phase, this phase, containing only some or no monomers, may represent at a minimum 1% of the total organic phase. The monomers are then added to the medium either after homogenizing and before polyermizing, or dur-ing polymerizing, as successive fractions or contlnuously, or partly before polymerizing and partly during polymeriz~ng, as successive fractions or continuously.
The monomers to be used in the process must produce hydrophobic polymers. They are insoluble in water and are represented hy vinyl aromatic compounds such as: styrene, alpha-methylstyrene, ethylstyrene, tertiary-butylstyrene and vinyltoluene.
These monomers are used alone or iII admixture with each other in any proportion, or in admixture with another copolymerizable monomer, insoluble in water, comprising up to 5Q% of the mixture and selected from dienic compowlds ~ 3 -1 1~92~7 such as butadiene and isoprene; al~yl acrylates and methacrylates, the alkyl group of which contains from 3 to 10 carbon atoms; esters of ethylenic acids containing 4 or 5 carbon atoms and alkyl groups containing from 1 to 8 carbon atoms, such as heptyl fumarate, octyl fumarate, methyl itaconate and ethyl itaconate.
Depending upon the polymer to be obtained, it is possible to add to the monomer, or monomer mixture, a reticulating monomer or a chain-limiting agent. The reticulating monomer, used in amounts of between 0 and 5% by weight ~ased on to the monomer(s), is exemplified by divinyl benzene, ~inyl meth-acrylate, acrylates and methacrylates of mono- and poly-alkylene(2-4C) glycol, triallyl-cyanurate, and condensates of unsaturated carboxylic acids and polyols, for example trimethylol-propane acrylate and methacrylate. The amount of chain-limiter used is between 0 and 5% by weight based on the monomer(s). This agent is exemplified by the dimer of alpha-methylstyrene, linear and branched-chain alkyl mercaptans, and halogenated hydrocarbons.
The organic compound insoluble in water should be miscible with the monomer or monomers, and possibly with the initiator, and should not inhibit polymeri~ation. It is selected more particularly from the following:
saturated and unsaturated, alicyclic and aromatic, halogenated and non-halo-genated aliphatic hydrocarbons containing from 10 to 30 carbon atoms, such as: dodecane, hexadecane, heptadecane, eicosane, paraf~inic waxes, chlorinated paraffins, decene-l, do-, tetra-~ hexa-, hepta- and octa-decene-l, eicosene-l, tetra- and hexa-ethylbenzene, naphthalene and anthracene; saturated and un-saturated aliphatic alcohols containing from 10 to 3a carbon atoms, such as:
lauryl, myristic, cetyl, stearyl, eicosyl and oleyl alcohols; esters of mineral and organic acids containing from 1 and 20 carbon atoms, and of alcohols containing from 1 to 20 carbon atoms, the total number of carbon atoms being ~ 1592~7 at least 10, such as: tricresyl phosphate, cetyl formate, stearyl formate, dioctyl adipate, dibutyl sebacate, propyl and ethylhexyl laurate, ethyl palmit-ate, dioctyl-, diethylhexyl-, dicyclohexyl- and dibenzyl~phthalate; and low-molecular weight polymers, such as: liquid polybutadienes, polethylene waxes and oils. The amount of organic compound to be used may constitute up to 50, preferably up to 20%, by weight of the whole of the organic phase containing the magnetic charge.
The initiators, used alone or in admixture, in amounts of from 0.1 to 10% by weight based on the monomer(s), are selected from conventional organo-soluble polymerization initiators, for example: azonitriles, such as azobis-isobutyronitrile and azobiscyclohexane carbonitrile; and peroxides such as benzoyl, dicumyl, ditertiary-butyl, diacetyl, dioctanoyl, lauroyl, methylethyl ketone, caprylyl, dichloro-2,4-benzoyl, parachlorobenzoyl, perpivalate, diethyl-peracetate, tertiary-butyl perbenzoate and ditertiary-butyl diperphthalate peroxide; and l,l-ditertiary-butyl peroxide-3,3,5-trimethyl cyclohexane.
The initiator should be dissolved in the organic phase prior to homogenization. In certain cases, in order to facilitate dissolution in the organic phase, it may be desirable to dissolve the initiator first in a small amount of an organic solvent which is miscible with the organic phase and does not inhibit polymerization, for example an aliphatic or aromatic hydrocarbon containing less than 10 carbon atoms and optionally halogenated, such as:
methylene chloride, chloroform, carbon tetrachloride, dichlorethane, benzene or chlorobenzene.
The magnetic charge which is dispersed in the organic phase is in the form of particles fine enough to be included in the particles of the polymer of the latex to be obtained, i.e. less than l~um, preferably from 0.002 to 0.05/um. The charge is represented more particularly by:

I ~59~7 - metals such as: iron, ferro-silicon, nickel and cobalt, and alloys of each of these ~ith molybdenum, chromium, copper, vanadium, manganese, aluminum and titanium;
- iron oxides: Fe3Q4 or ~-Fe203, pure or in combination or admixture with other oxides such as oxides of cobalt, manganese, ~inc, barium and rare earths; and - chromium dioxide.
The amount of magnetic charge to be used is from 0.5 to 50, more particularly from Q.5 to 35, preferably from 0.7 to 20% by weight based on the monomer(s). Prior to incorporation of the organic phase, it is desirable to disperse the magnstic charge in all or part of the organic compound and/or of an organic solvent selected from the solvents mentioned above in connection with the initiator.
The aqueous phase to be used consists of water in which is dissolved at least one emulsifying agent and, if necessary, a buffer, depending upon the nature of the monomer and/or of the emulsifier present.
The emulsifying agents, which ensure stability of the reaction medium and of the latex to be obtained, may be anionic or cationic and/or nonionic and are used in amounts of from 0.1 to 5% by weight based on the organic phase containing the magnetic charge.
The following anionic emulsifying agents may be mentioned: salts of fatty acids; alkyl sulphates, alkyl sulphonates, alkylaryl sulphonates, alkylsulphosuccinates, alkaline alkyl phosphates; sulphonates of alkylphenol polyglycol ethers; salts of esters of alkylsulphopolycarboxylic acids; pro-ducts of the condensation of fatty acids with oxy- and amino-alkenesulphonic acids; sulphated derivatives of polyglycol ethers; sulphated esters of fa~ty acids and polyglycols; and alkanolamides of sulp}lated fatty acidsO

111~9247 The following may be mentioned as cationic emulsifying agents:
alkylamines and water-soluble salts thereof, and soluble salts of alkylamines, N-substituted by alkyl and/or alkylaryl and/or hydroxyalkyl radicals. Ex-emplary nonionic emulsifying agents are fatty esters of polyalcohols, fatty acid alkanolamines; ethylene polyoxides, copolyoxides of ethylene and propylene, and oxyethylenated alkyl phenols.
When the total aqueous phase is not involved in the homogenizing operation, the minimum amount thereof to be used should be such that the organic phase : aqueous phase ratio is of the order of 1. The remainder of the aqueous phase is then introduced into the reaction medium before and/or during polymerization, in successive fractions or continuously.
~fter preparation of the organic phase containing the magnetic charge, and the aqueous phase, the two are mi~ed in order to obtain the dis-persion to be homogenized. For these operations, the organic phase should be liquid and homogeneous. In certain cases, therefore, it is necessary to operate at a temperature sufficient to provide a liquid organic phase, or to add a solvent for the organic phase which is insoluble in water and does not inhibit polymerization, the amount added being just that necessary to obtain a homogeneous liquid phase. The solvent used may be selected from those men-tioned above.
The homogenizing operation may be carried out on the dispersion of the organic phase containing the magnetic charge in all or part of the aqueous phase, at a temperature between 0C and the initiator-decomposition temperature.
Homogenizing may be carried out in a power-driven mechanical unit such as, but not restricted to, a colloid mill, high-speed pump, vibratory agitator or ultrasonic equipment, producing droplets of organic phase containing the mag-netic charge and measuring from Q.03 to 5 /um.

- 7 _

2 4 7 The finely dispersed mixture thus obtained, to which are eventually added the remaining monomer or monomers and a part of the aqueous phase, is then polymerized in micro-suspension, in a manner known per se, at a tempera-ture of from 30 to 130C, and ~ith a concentration of the organic phase containing the magnetic charge, in the reaction medium, of less than 65% by weight.
The polymer latices obtained generally have polymer particles from 0.03 to 5 ~um, preferably from 0.05 to l~um, in diameter, containing the magnetic charge.
These particles are easily attracted by a magnet, even at very low concentrations, which, in certain applications, makes it possible to separate them from the ambient liquid medium, without resorting to conventional coagulating and atomizing processes.
The latices according to the invention may be used in the paint, magnetic-tape, and recording industries, and in biology) among other *hings as supports for biological molecules.
The following non-limitative Examples illustrate the invention.
Example 1 An organic phase is prepared by dissolving 4 g of lauroyl peroxide ~0 in 60 g of styrene. To this solution are added 5 g of 16% by weight dispersion of Fe304 in a hydrocarbon oil, the size of the particles being about 0.01 ~m.
In a container equipped with an agitator, an aqueous phase is pre-pared by dissolving, in 400 g of demineralized water, 1 g of sodium lauryl sulphate and 1 g of oxyethylenated nonyl phenol ~30 units of ethylene oxide per molecule).
The organic phase is then added and dispersed in the aqueous phase.
The mixture obtained is then homogenized in such a manner as to ~ 1~92~7 obtain l~um droplets o~ organic phase containing the magnetic charge dispersed in the aqueous phase.
The mixture is placed in a 1 litre reactor equipped ~ith an agitator and is polymerized therein at 55C.
A~ter 19 hours, the reaction medium is cooled and the residual monomer is removed by distillation with steam.
This produces 500 g of a stable latex, the concentration of poly-styrene particles being 9.6% by ~eight, the average diameter of the light brown particles being l,um. Electron microscope observation reveals that the magnetic charge, representing 1.6% by ~eight of the polymer, is in the form of inclusions, at the peripheries of the particles.
The latex particles are easily separated from the medlum by attrac-tion along the walls of the container, by means of a magnet.
The same phenomenon is observed if the latex obtained is diluted to a concentration of 1% by weight.
Example 2 The organic phase consists of:
- 5.45 g of hexadecane, - 0.80 g of lauroyl peroxide dissolved in 2.9 g of chlorobenzeneJ and - 4.~5 g of the same Fe304 dispersion as in Example 1.
The aqueous phase consists of:
- 600 g of demineralized ~ater, - 1~6 g of sodium lauryl sulphate, and - 1.6 g of oxyethylenated nonyl phenol (30 units~ of ethylene oxide per molecule~.
~5 in Example 1, the organic and aqueous phases are mixed and homo-genized to obtain organic phase droplets measuring O.l~um and containing the _ g _ 1 1~924~

magnetic charge, dispersed in the aqueous phase.
The mixture is placed in a 4 litre reactor equipped with an agitator ~here it is heated to 63C and held at that temperature. As soon as the mixture reaches 63C, 110 g of distilled styrene are added, at a constant flow, over a period of 10 hours.
The mixture is allowed to stand for lQ more hours at 63C and is then heated to 70C for S hours. The reaction medium is then cooled.
This produces 730 g of a stable latex with a polymer particle con-centration of 17% by weight. The light bro~n particles have an average dia-lQ meter of 0.15~um, with peripheral inclusions of magnetic charge particles representing Q.8% by weight of the polymer. They are attracted ~y a magnet.
_ample 3 The organic phase consists of:
- 5 g of hexadecane, - 4 g of lauroyl peroxide dissolved in 100 g of styrene, and - 5 g of the same Fe304 dispersion as that in Example 1.
The aqueous phase consists of:
- 400 g of demineralized water, - 1 g of sodium lauryl sulphate, and 1 g of oxyethylenated nonyl phenol (30 ethylene oxide units per molecule~.
~s in ~xample 1, the organic and aqueous phases are mixed and homo-genized to obtain organic-phase droplets of an average diameter of 1 ~m, con-taining the magnetic charge, dispersed in the aqueous phase.
The dispersion, placed in a 4 litre reactor equipped ~`ith an agitator, is heated to 60C and is held at that temperature for 18 hours.
After the ~eaction medium has ~een cooled, 510 g of a stable latex .

1 150~

are obtained, with a polystyrene particle concentration o~ 17% by weight.
The light bro~n particles have an average diameter of 1 ~m and con-tain, at their peripheries, 1.1% ~y weight of the magnetic charge polymer particles. They are attracted ~y a magnet.
Example 4 The organic phase consists of:
- 8.6 g of hexadecane, - 6.~ g of lauroyl peroxide dissolved in 175 g of vinyl toluene, and - 8.6 g of the same Fe~04 dispersion as in Example 1.
The aqueous phase consists of:
- 690 g of demineralized water, - 1.7 g of sodium lauryl sulphate, and - 1.7 g of oxyethylenated nonyl phenol ~30 ethylene oxide units per molecule~.
~s in Example 1, the organic and aqueous phases are mixed and homo-genized to obtain organic phase droplets, oE an average diameter of 0.16,um, containing the magnetic charge, dispersed in the aqueous phase.
The dispersion, placed in a 4 litre reactor equipped with an agitator, is heated at 60QC for 18 hours and then at 75C for 2 hours.
After the reaction medium has been cooled, 860 g of a stable latex are obtained, with a polyvinyltoluene particle concentration of 19.7% by ~eight.
The light brown particles have an average diameter of 0.16jum and contain, distributed around their peripheries, 0.8% by weight of magnetically charged polymer particles. They are attracted by a magnet.
Example 5 The organic phase consists of:
8.5 g of hexadecane, ~ 1~92~

- 6.8 g of lauroyl peroxide dissolved in a mixture of 153.5 g of styrene and 17 g of butyl acrylate~ and - 8.5 g of the same Fe304 dispersion as in Example 1.
The aqueous phase consists of:
- 683 g of demineralized water, - 1.7 g of sodium lauryl sulphate, and - 1.7 g of oxyethylenated nonyl phenol (30 ethylene oxide units per molecule).
As in Example 1, the organic and aqueous phases are mixed and homo-genized to obtain organic phase droplets of an average diameter of 0.16 ~m containing the magnetic charge and dispersed in the aqueous phase.
The dispersion, placed in a 4 litre reactor equipped with an agitator, is heated at 60C for 18 hours, and then at 75C for 2 hours.
Af~er the reaction medium has been cooled, 860 g of a stable latex are obtained in which the concentration of butyl styrene acrylate copolymer particles is 19.9% by weight.
The light brown particles have an average diameter of 0.16/um and contain, distributed around their peripheries, 9.8% by weight of magnetically charged polymer particles. They are attracted by a magnet.
Example 6 The organic phase consists of:
- 7.5 g of cetyl alcohol, - 6 g of lauroyl peroxide dissolved in 151 g of styrene, and - 7.5 g of the same Fe3Q~ dispersion as in Example 1.
The aqueous phase consists of;
- 605 g of demineralized water, - 1.5 g of sodium lauryl sulphate, and ~ 12 -1 1592~7 , ~, - 1.5 g of oxyethylenated nonyl phenol (30 ethylene oxide units per molecule).
As in Example 1, the organic and aqueous phases are mixed and homo-genized to obtain organic phase droplets of an average diameter of 0.15~um, containing the magnetic charge and dispersed in the aqueous phase.
The dispersion, placed in a 4 litre reactor equipped with an agitator, is heated at 60C for 18 hours and then at 75C for 2 hours.
After the reaction medium has been cooled, 755 g of a stable latex are obtained, in which the polymer particle concentration is 19% by weight.
The light brown particles have an average diameter of Q.15 ~m and contain, dis-tributed around their peripheries, 9.8% by weight of magnetically charged polymer particles. They are attracted by a magnet.

~ 13 -

Claims

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A magnetic polymer latex having a concentration below 65% by weight, of polymer particles of an average diameter of from 0.03 to 5µm,the particles consisting of hydrophobic vinyl aromatic polymer and containing from 0.5 to 50% by weight of magnetic charge, based on the polymer.

2. A latex according to claim 1, wherein the vinyl aromatic polymer is a homopolymer of a water-insoluble vinyl aromatic monomer or a copolymer of such monomers or of such a monomer and another copolymerizable monomer.

3. A latex according to claim 2, wherein the water-insoluble vinyl aromatic monomer or monomers are selected from styrene, alpha-methylstyrene, ethyl styrene, tertiarybutyl styrene and vinyl toluene.

4. A latex according to claim 2 or 3, wherein the other copolymerizable monomers are selected from alkyl acrylates and methacrylates, and alkyl esters of ethylenic acids.

5. A process for the preparation of a latex as defined in claim 1, which comprises polymerizing a vinyl aromatic monomer, alone or in admixture with a copolymerizable monomer in an aqueous medium in the presence of a mag-netic charge, the magnetic charge being dispersed in an organic phase consisting of an organo-soluble initiator, all or a part of the vinyl aromatic monomer, alone or in admixture with at least one copolymerizable monomer producing a hydrophobic polymer, and/or of an organic compound insoluble in water; the dispersion obtained being mixed with all or part of an aqueous solution con-sisting of water and at least one emulsifying agent, whereupon the whole is homogenized and finally polymerized after eventual addition of the remainder of tile constituents.

6. A process according to claim 5, wherein the vinyl aromatic monomer or monomers are selected from styrene, alpha-methyl styrene, ethyl styrene, tertiary-butyl styrene and vinyl toluene.

7. A process according to claim 5, wherein the copolymerizable monomer is insoluble in water and is selected from dienes, alkyl acrylates and meth-acrylates, and alkyl esters of ethylenic acids.

8. A process according to claim 7, wherein use is also made of a reticulating monomer and/or a chain-limiting agent, in proportions from 0 to 5% by weight, based on the monomer(s).

9. A process according to claim 5, wherein the water-insoluble organic compound is selected from saturated and unsaturated, aliphatic, alicyclic and aromatic hydrocarbons, halogenated or unhalogenated, containing from 10 to 30 carbon atoms; saturated and unsaturated aliphatic alcohols containing from 10 to 30 carbon atoms; and esters of mineral and organic acids (1-20C) and of alcohols (1-20C), in which the total number of carbon atoms is at least 10.

10. A process according to claim 5, wherein the organic compound comprises up to 50% by weight of the organic phase containing the magnetic charge.

11. A process according to claim 5, wherein the magnetic charge comprises metals or alloys thereof, pure iron oxides, in combination or in admixture with chromium dioxide.

12. A process according to claim 5, wherein the size of the magnetically charged particles is less than 1 µm.

13. A process according to claim 5, wherein the amount of magnetic charge is from 0.5 to 50% by weight, based on the monomer(s).

14. A process according to claim 5, wherein the organic phase to be dispersed in the aqueous phase and homogenized is liquid and homogeneous.