CA2038115A1 - Process for the production of high molecular weight copolymers of diallyldimethyl ammonium chloride and acrylamide in an aqueous dispersed phase - Google Patents

Abstract

ABSTRACT

Water-soluble, high molecular weight, linear copolymers of a diallyl ammonium monomer and an acrylamide monomer are prepared by emulsion copolymerization of a major portion of the acrylamide monomer via stage-addition, and the addition of a chain transfer agent at the conclusion of said copolymerization to prevent branching and cross-linking.

C-36,636

Description

2 ~ 3 ~
,. 1 PROCESS FOR TaE PRODUCTIQN OF ~I&~ MOLEC~LAR WEIGHT
COPOLYMERS OF DIALLYL AM~ONIUM MONOM~S AND ACRYLAMID~
~ONOME~S I~ AN AQUEOUS DISP~RSED P~AS~

This invention relates to high molecular weight, water soluble, linear copolymers of diallyl ammonium monomers and acrylamide monomers of varying cationicities, and to methods of preparing the same~
Copolymers of this type are useful as cationic flocculants in the treatment of industrial water, as sludge conditioners for the treatment of municipal water systems, and as drainage and retention aids in the manufacture of paper.

Diallyl ammonium monomers, e.g. diallyl dimethyl ammonium chloride (DADMAC), are quaternary monomers, which when polymerized, yield water soluble polymers that are cationic in nature. The polymerization of acrylamide monomers, on the other hand, produces water soluble polymers that are essentially nonionic in nature. Thus, the copolymerization of diallyl ammonium monomers and acrylamide monomers results in the formation of water soluble copolymers having various degrees of cationicity, depending upon the amount of C-36,636 diallyl ammonium monomer that is incorporated into the final copoly~er.

The copolymerization of diallyl ammonium monomers and acrylamide monomers in solution is well known. US Patent 2,923,701, for example, dPscribes the simultaneous copolymerization of acrylamide and diallyl ammonium monomers in solution by the addition of a redox catalyst, such as ammonium persulfate and potassium metabisulfite, to an aqueous mixture of tne monomers.

Copolymers of diallyl ammonium monomers and acrylamide monomers can also be obtained utilizing emulsion polymerization techniques in accordance with the teachings of US 3,920,599. Stable water-in-oil copolymer emulsions are prepared9 which can then be inverted by means of suitable hydrophilic, water-soluble surfactants to form water soluble solutions that are used as such. US Patent 4,070,930 discloses the preparation of stable emulsion copolymers of diallyl ammonium monomers and acrylamide monomers, which can be inverted by the addition of water.

An improved process for the incorporation of diallyl ammonium monomers into an acrylamide polymer by means of either emulsion or solution polymeri7ation techniques is disclosed in European Patent Application 0 188 721. This improvement comprises the step of polymerizing diallyl ammonium monomers and acrylamide monomers in the presence of a copolymerizable monomer, such as a quaternary substituted acrylamide or methacrylamide. The monomer utilized with the acrylamide C-36,636 2 ~,~3~

monomers must have a greater reactivity than the diallyl ammonium monomers.

European Patent Application 0 247 774 discloses cationic copolymers having improved performance characteristics which are prepared from a premix containing the nonionic monomer and a portion of the cationic monomer. The premix is emulsified, the remaining cationic monomer added, and the entire reaction mixture is copolymerized.

US Patent 4,1S2,200 discloses the preparation of a cationic copolymer having improved drainage characteristics in the preparation of formed paper. This copolymer is prepared by means of a water-in-oil emulsion process comprising the incremental addition of a cationic monomer to the nonionic monomer during the course of the polymerization. This reference expressly teaches the addition of cationic monomers to solutions of nonionic monomers. In contradistinction thereto, the present invention discloses and claims the preparation of different copolymers by means of the continuous addition of a nonionic monomer to a cationic monomer during the course of polymerization.

The present invention relates to a process for 3~ the preparation of high molecular weight, water-solubLe, linear copolymers of diallyl ammonium monomers and acrylamide monomers having a uniform diallyl ammonium monomer to acrylamide monomer ratio. More particularly this process comprises the steps of:

C-36,636 3 2 ~

a) preparing a water-in-oil monomer emulsion by mixing an oil phase containing an oil soluble emulsifing agent, with an aqueous phase comprising a mixture of a diallyl ammonium monomer, a portion of the total amount required of an acrylamide monomer, a polymerization initiator, and a water dispersable emulsifying agent;
b) initiating the copolymerization of said monomer emulsion by increasing the temperature of the emulsion, preferably to a temperature ranging from about 30C to about 40C;
c) adding the remaining acrylamide monomer to the monomer emulsion via continuous stage addition, preferably over a period of from about 0.5 to about 8 hours at a temperature ranging from about 20 to about 50C to form a copolymer emulsion;
d) homogeneously mixing a chain transfer agent into said copolymer emulsion to form a copolymer emulsion mixture, and e) heating said copolymer emulsion mixture to reduce the residual monomer present, preferably at a temperature ranging from about 60 to about 90C for a period of time ranging from about 0.1 to about 4.0 hours.
This invention also rel tes to high molecular weight water soluble linear copolymers of diallyl ammonium monomers and acrylamide monomers prepared in accordance with the process of this invention. Such copolymers are particularly useful as flocculants for C-36,636 4 2~3,~ L:~

sludge conditioning in the treatment of municipal and industrial water and waste water systems over a wide range of pH. The copolymers described herein are also useful as drainage and retention aids in the manufacture of paper.

As previously indicated, the preparation of diallyl ammonium monomer and acrylamide monomer based copolymers is well known~ In general, however, the existing prior art copolymers are non-uniform in their composition and tend to be highly branched and cross-linked. In addition, the prior art copolymers are of relatively low molecular weight, having intrinsic viscosities generally less than 6 dl/g.

The present invention overcomes these deficiencies of the prior art and enabLes the preparation of high molecular weight copolymers of diallyl ammonium monomers and acrylamide monomers via an emulsion process having intrinsic viscosities ranging from 10 to 25 dl/g. Preferably, diallyl ammonium monomer and acrylamide monomer based copolymers are prepared which have intrinsic viscosities ranging from lS to 20 dl/g. It is generally recognized by those skilled in the art that the intrinsic viscosity is an indication of polymer molecular weight. Thus, in general, the higher the intrinsic viscosity, the greater is the molecular weight of the particular polymer or copolymer prepared.

When prepared in accordance with the teachings of this invention, copolymers of varying ca~ionicities can be prepared, thereby enabling the preparation of C-36,636 5 3 ~3 .~L .~

copolymers that can be tailored to their use.
Furthermore~ such copolymers are uniform in composition.
That is to say, copolymers are prepared which contain little, if any, residual monomer~ and which have a uniform diallyl ammonium monomer to acrylamide monomer unit ratio throughout the entire length of the copolymer chain.

One difficulty in the preparation of dialLyl ammonium monomer and acrylamide monomer based copolymers, that have a uniform distribution throughout the length of the copolymer chain, is due to the difference in reactivity of the acrylamide monomers as compared to the diallyl ammonium monomers. This difference in reacti~ity results in a non-unifor~
distribution of the diallyl ammonium monomer throughout the copolymer chain. Thus, at the onset of the copolymerization reaction, a relatively larger number of acrylamide monomer units are initially incorporated into the polymer chain due to the greater reactivity of the acrylamide monomers. Accordingly, at the conclusion of the copolymerization reaction, relatively more of the diallyl ammonium monomer units remain unused and remain either as free monomer, or form low molecular weight homopolymers.

These excess diallyl ammonium monomers, or low molecular weight diallyl ammonium based homopolymers, remain either as a residual mixture or they become incorporated into the copolymer chain, which results in a non-uniform distribution of the monomer units throughout the copolymer chain. This is particularly true in the case of copolymers in which the final C-36,63~ 6 ~J~33~ 3 diallyl ammonium content is greater than 20 % on a molar basis of the total copolymer content.

Another difficulty in the preparation of high molecular weight linear copolymers of diallyl ammonium monomers and acrylamide monomers is due to the manner in which the diallyl ammonium monomers polymerize.
Normally, the diallyl ammonium monomers polymerize by incorporating both of the allyl bonds within the same molecule to form a linear polymer chain. A small proportion of the monomers, however, can polymerize via the incorporation of only one of its allyl bonds, thereby leaving a pendant double bond remaining in the molecule. These pendant double bonds can subsequently initiate branching, particularly at higher temperatures, to produce cross-linked polymers that have a reduced : solubility in water, see Jae~er et al.,Journal of Macromolecular Science, Part A Chemistry, 593-614, (lg84).

This greater reactivity of the acrylamide monomers, in combination with the tendency of the diallyl ammonium monomers to polymerize via branching or cro3s-linking, results in the formation of non-linear diallyl ammonium monomer and acrylamide monomer based copolymers having relatively low intrinsic viscosities.
Such copolymers are not particularly well suited as flocculants in water and waste water systems for sludge conditioning, or as drainage and retention aids in the manufacture of paper. These problems have now been overcome by means of the present invention, which enables the preparation of high molecular weight, linear copolymers of diallyl ammonium monomers and acrylamide C-36,636 7 ~ 3~

mo~omers of uniform composition having little, if any, branching and cross-linking in the polymer chain.

The diallyl quaternary ammonium compounds preferably correspond to the formula Formula I

/ Rl \
/ CH2=C-CH2 R2 \ /

/ \
\ CH2= f - CH2 R~ /

wherein Rl is independently in each occurrence hydrogen or Cl-4 alkyl; R2 is independently in each occurrence hydrogen, Cl_lg alkyl, Cl-lg alkoxyalkyl or Cl_lg hydroxyalkyl moieties; and Y is an anion, which does not significantly interfere in the poly~erization reaction.

Illustrative examples of radicals represented by R2 are methyl to octadecyl, inclusive; hydroxymethyl and hydroxyethyl to hydroxyoctadecyl, inclusive; and methoxymethyl and the variou~ high alkoxy (e.g.i methoxy to octadecoxy, inclusive) alkyls, e.g., ethyl to octadecyl inclusive~ Illustrative examples of anions represented by Y are the halide ions (that is, Y can C-36~636 8 represent halogen, more particularly chlorine, bromine, fluorine or iodine), sulfate, sulfonate, phosphate, hydroxide, borate, carbonate, thiosulfate, isocyanate, acetate and the other common inorganic and organic ions.
Specific examples of compounds embraced by formula hereinbefore are the diallyl, dimethallyl, diallyl dimethyl and diethallyl dimethyl, di (beta-hydroxyethyl) and di(beta-ethoxyethyl) ammonium chlorides, bromides, phosphates and sulfates. Other examples will be apparent to those skilled in the art from the formula and from the numerous examples of anions represented by Y and of radicals represented by Rl and R2 that have been given hereinbefore with reference to the formula.

Rl is preferably hydrogen, methyl, or ethyl~
even more preferably hydrogen or methyl; and most preferably hydrogen. R2 is preferably hydrogen or Cl_lg alkyl; more preferably hydrogen or Cl-4 alkyl, and most preferably hydrogen or methyl. Y is preferably a halide ion, and most preferably a chloride ion. In a most preferred embodiment the diallyl ammonium compound is a diallyl dimethyl ammonium compound; the most preferred diallyl dimethyl ammonium compound is diallyl dimethyl ammonium chloride (DADMAC).

Acrylamide compounds as used herein refers to acrylamide, methacrylamide, and derivatives thereof wherein the alpha carbon may be substituted with a Cl_s lower alkyl moiety and the amide nitrogen may be substituted with a Cl_lg alkyl moiety, Cl_l~ alkyloxy moiety or Cl-lg hydroxyal~yl moiety. Such acrylamide compounds preferably correspond to the formula C-36,636 9 3 ~ cj Formula II

CH2=C-C-N
\ R4 wherein R3 is independently in each occurrence hydrogen or a C1-5 lower alkyl moiety;
R4 is independently in each occurrence hydrogen, C1_lg alkyl, Cl_1g alkoxy, or C1_lg hydroxy substituted alkyl.
R3 is preferably hydrogen or methyl, and most preferably hydrogen. R4 is preferably hydrogen or Cl_lg alkyl. R4 is more preferably hydrogen or Cl-g alkyl. R4 is most preferably hydrogen or Cl-4 alkyl.

In general, the process of this invention utilizes a controlled addition or stage-addition of the acrylamide monomer during the emulsion copolymerization reaction. Surprisingly, it has been discovered that the continuous stage-addition of the acrylamide monomer 2S produces high molecular weight copolymers of diallyl ammonium monomers and acrylamide monomers which, heretofor have not, as yet, been available. Copolymers having high diallyl ammonium monomer conversions can be prepared that contain a uniform distribution of diallyl ammonium and acrylamide monomer units throughout the entire length of the copolymer chain with little, if any, residual diallyl ammonium monomer or acrylamide monomer remaining in the finished product. The process of this inve~tion also utilizes the addition of a chain transfer agent to prevent branching and cross-linking of C-36,636 10 1 1 2 ~

the polymer chain from occurring, particularly at elevated temperatures.

The impurities in the starting monomers can affect the overall properties of the final polymer. The starting monomers should be sufficiently pure to prepare linear copolymers with relatively constant diallyl ammonium monomer to acrylamide monomer ratios along the chain and which has an intrinsic of from about 10 to about 25 d/l. In a preferred embodiment, wherein DADMAC
is the diallyl ammonium monomer and the acrylamide monomer is acrylamide, DADMAC has no more than about 50 ppm of allyldimethylamine; about 100 ppm of dimethylamine, and about 10 ppm of allyl alcohol.
Preferably, the acrylamide has no more than 1200 ppm of nitrilotrispropionamide, and 10 ppm of methoxyhydroquinone.

To initiate copolymerization, a water-in-oil emulsion is prepared which contains the diallyl ammonium monomer and a portion of the acrylamide monomer to be employed. The oil phase of the emulsion can be any water insoluble, aliphatic or aromatic liquid organic substance. Organic liquids such as benzene, xylene, toluene, mineral oils, mineral spirits, kerosene, naphthas and perolatums can be employed. In general, the oil phase comprises from about 20 to about 50 volume percent of the total emulsion composition. Preferably, the oil phase comprises from about 25 to about 30 volume percent of the emulsion composition. A particularly useful oil from the standpoint of its physical and chemical properties is the branched-chain isoparaffin solvent sold under the name "Isopar M". Typical C-36,636 11 specifications of this narrow-cut isoparaffinic solvent are set forth as shown below:

Density at 12C 0.786 g/l 5 Color (Saybolt) 30 Refractive Index, n20D 1.436 Viscosity (25C) 2.46 mPa.s (cp) Boiling Point Characteristics (C) Start 204 5 % 212 10 % 215 50 % 224 9O % 236 gs % 242 Dryness 247 Residue (mg/100 ml) < 1 20 Aromatic Content (%) 0.3 Sulfur Content ppm < 1 Fla.ch Point C 75 The oil phase also contains a primary emulsifier which serves to stabilize the emulsion during polymerization. The primary emulsifying agent can be selected from any of a large group of surfactants that are oil soluble and that have an HLB value in the range of from about 2 to about 10, preferably less than about 7. Suitable primary emulsifiers include the sorbitan esters, phthalic esters, the reaction product of oleic acid with isopropanolamide, fatty acid glycerides, glycerine esters as well as ethoxylated derivates C-36,636 12 13 ~ e~ ~ 7 1 3 ~hereof. These primary emulsifiers can be used alone or in combination. As such all of the primary emulsifiers should not be used in amounts greater than about S % by weight of the total emulsion. Preferably, the amount should range from about 1.0 to about 2.0 % by weight of the total emulsion. The preferred primary emulsifying agent for the oil phase is oleic mono-isopropanol amide.

The dispersed phase is the aqueous phase which essentially comprises an aqueous solution of the diallyl ammonium monomer and an initial portion of the total amount of the acrylamide monomer to be employed. A
polymerization initiator or polymerization initiator package together with a water dispersible emulsif~ing agent can be conveniently added at this point to the aqueous phase. The dispersed aqueous phase comprises in general, from about 50 to about 80 volume percent of the total emulsion composition. Preferably, the dispersed phase comprises 70 to 75 volume percent of the emulsion.
However, in order to prepare emulsions having a high polymer content, the dispersed aqueous phase can comprise as much a~ 75 to 80 volume percent of the emulsion composition.

A second emulsifying agent, added to the aqueous phase, has been found to be particularly advantageou~ in stabilizing the water-in-oil emulsion during the copolymerization reaction. ~ny conventional oil soluble, water dicpersible surfactant having an HL8 ranging from 2 to 8 can be employed as an emulsifying agent for the aqueous phase. Examples of suitable surfactants include sorbitan monooleate, the reaction products of oleic acid with ispropanolamide, sorbitan C-36,636 13 stearate, decyl sodium phthalate, hexadecyl sodium phthalate, and glyceride mono and diesters of lauric and stearic acids. Sorbitan monooleate dispersed in the aqueous phase is the preferred secondary emulsifying agent.

rhe amoun~ of diallyl ammonium monomer to be employed is dependent upon the desired cationicity of the final copolymer. An important advantage of this invention is that copolymers of varying cationicities can be precisely prepared in accordance with the teachings of this invention. The greater the number of diallyl ammonium units that are introduced into the polymer chain, the greater will be the cationicity of the resulting copolymer. Thus, copolymers useful as cationic flocculants in water clarification systems or as sewage dewatering agents, require copolymers having a higher degree of cationicity than cationic flocculants useful as drainage and/or retention aids in the manufacture of paper.

The copolymers contemplated by the present invention cover a wide range of cationicities, e.g. from about 5 to about 95 mole % cationicity. That is to say, in a copolymer consisting of 100 monomer units, the copolymers described comprise from about 5 to about 95 diallyl ammonium units, and conversely from about 95 to about 5 acrylamide monomer units. Preferably, copolym~rs comprising from about 5 to about 75 mole X cationicity can be prepared. Still more preferably, polymers having from about 10 to about 50 mole % cationicity can be prepared in accordance with the ~eachings of this invention.

C-36,636 14 'f~ 3 'i3 ~

The copolymerization reaction is generally initiated using free radical polymerization techniques known to those skilled in the art. Compounds which form mainly water soluble radicals are suitable as polymerization initiators. Such compounds are conveniently dissolved in the aqueous phase. For example, azostarters such as 2,2-azobis-(N,N'-dimethylene-isobutyramidine) dihydrochloride, 2,2'-azobis-(2-amidinopropane) dihydrochloride, 2,2'-azobis-(N,N'dimethyleneisobutyramidine), 4,4'-azobis-~4-cyanopentane-carboxylic acid), 2,2'-azobis(4-methoxy-2,4-dimethylvalero-nitrile), 2,2'-azobis(2,4-dimethylvaleronitrile), (1-Phenylethyl)azodiphenyl-methane, 2,2'-azobisisobutyro-nitrile, dimethyl 2,2'-azobisisobutyrate, and 2,2'-azobis-(2-methyl-butyronitrile) can be employed.

Peroxide polymerization initiators can also be employed, as for example, dibenzoyl peroxide, dilauryl peroxide, di-2-ethylhexylperoxydicarbonate, dicyclohexylperoxydicarbonate, bis-(4-tert.
butylcyclohexyl) peroxydicarbonate, tert.
butylperpivalate, tert. butyl-perbenzoate, tert.
butylpermaleinate, di-tert. butyl- peroxide, tert.-hydroperoxide, hydrogen peroxide, ammonium persulfate, potassium persulfate, sodium persulfate, and redox catalysts in combination with reducing agents such as (II)-ammonium sulfate, ascorbic acid, so~ium methyl sulfinate, disodium disulfite and sodium hydrogen sulfite can be employed. These initiators can be used alone or in combination with one another.

C-36,636 15 ~ !~3 5~

The rate of decomposition of the more readily decomposed peroxides can be reduced by the addition of organic metal complex compounds, as for example, copper acetyl acetonate. Thus the rate of peroxide decomposition can be adapted, for example, to the particular polymerization temperature selected.
Preferred redox catalysts are those selected from one or several peroxides in combination with a reducing agent.
Especially preferred are persulfates or peresters or mixtures of persulfates and peresters as a component of the redox polymerization initiatorsO The polymerization initiators are used in amounts ranging from 0.001 to 5 %
by weight, and preferably from about 0.02 to 2 % by weight, relating to the amount of monomers employed.

Sufficient water should be employed in the aqueous phase to facilitate emulsion formation and to homogeneously dissolve all of the components present in the aqueous phase. As starter solutions, aqueous monomer solutions containing from about 40 to about 70 Z of monomer can advantageously be employed. Preferably 7 aqueous monomer solutions containing from about 50 to about 60 X monomer are employed. If necessary, additional water can be added during the course of ~he copolymerization reaction to the copolymer emulsion in order to provide optimum conditions for the reaction to proceed. It is immaterial whether the oil phase is added to the aqueous phase or vice versa. The two phases are slowly added together with vigorous stirring preferably at about 5,000 to about 209000 rpm. The resulting emulsion is deoxygenated with nitrogen and the temperature of the emulsion mixture is slowly increased C-36,636 16 ~ 3 to initiate copolymeri7ation. The preferred temperature at which polymerization occurs ranges from about 20 to about 50C. More preferably, polymerization is conducted at a temperature ranging from about 30 to about 40C. Still more preferably, a temperature of about 35C is optimally employed.

During the course of the polymerization reaction, the acrylamide monomer is continuously added to the diallyl ammonium monomer via a process of stage addition. That is to say, an initial amount of the acrylamide monomer is present in the aqueous emulsion phase at the outset of the copolymerization reaction. As the reaction proceeds, fresh acrylamide monomer is continuously added to the copolymerization mixture at a predetermined rate. In general, about 12 to about 20 %
: of the total amount of the acrylamide monomer is added at the outset to the reaction mixture. More preferably, from about 15 to about 17 Z of the total amount of the acrylamide monomer required is added to initiate copolymerization. The copolymerization reaction of diallyl ammonium monomer and acrylamide monomer is an exothermic reaction. Thus, once copolymerization begins, the temperature of the reaction mixture rapidly increases. At this point the remaining amount of acrylamide monomer is introduced to the reaction mixture via a process of stage-addition with the polymerization temperature being maintained preferably at about 20 to about 50C, more preferably at about 30 to about 40C, and most preferably at about 35C.

As indicated, as soon as the initial copolymerization has begun, the remaining acrylamide C-36,636 17 monomer solution is stage-added. The period of time during which stage addition takes place is dependent upon the amount of diallyl ammonium monomer units that are to be introduced into the polymer chain. Thus a copolymer having a 10 mole % cationicity preferably undergoes stage addition for about one hour, whereas a copolymer having 30 mole % cationicity preferably undergoes stage addition for about 3 hours. Copolymers having up to 90 mole % cationicity preferably undergo stage addition for about 8 hours. These periods of time will, of course, vary slightly depending upon the type and design of reactor employed, the degree of mixing and the temperature at which the copolymerization is conducted. For large scale preparations, the particular parameters to be employed can be optimized via standard procedures known to those skilled in the art.

Preferably, the stage-added acrylamide monomer solution is separately deoxygenated, and continuously introduced in such a manner that a slightly decreasing feed rate is achieved throughout the total period of stage addition. Thus, for example, during the first quarter of the period for stage addition, about 30 to about 35 % of the acrylamide monomer solution is stage-added; during the second quarter of the stage addition period, about 25 to abou~ 30 % of the acrylamide monomer solution is stage-added; during the third quarter about 20 to about 25 % of the monomer solution is stage-added;
and the last about 15 to about 20 % of the acrylamide monomer solution is introduced during the final quarter of the stage addition period. For the production of large quantities of copolymers, a metering pump can be advantageously employed.

C-36,636 18 2~3~

Copolymers of diallyl ammonium and acrylamide monomers prepared at a temperature of about 35C are completely soluble in water, irrespective of how large their molecular weights may be. ~opolymers prepared at temperatures above about 40C tend to be insoluble or only partially insoluble in water. This insolubility is presumed to be the result of the increased tendency for the diallyl ammonium monomer to poly~erize via branching and cross-linking at higher temperatures. The more branched and cross-linked the copolymers become~ the less soluble they are in water. Indeed, one of the qualitative tests for the degree of branching and cross-linking for this type of copolymer is its solubility in water.

Inasmuch as the polymerization reaction is exothermic in nature, control of the reaction temperature is critical. In order to maintain close control over the reaction temperature, the boiling point of an azotrope formed by the reaction mixture can be employed. Thus, where the branched chain isoparaffin solvent sold under the name "Isopar M" is employed7 the condensate of the vapor above the emulsion phase consists of about 12 % by volume of solvent and 88 % by volume of water. If the polymerization reaction is conducted at a reduced pressure of from 50 to 55 millibars, a constant temperature of 35 + 1.0C is obtained.

It is advantageous to keep the emulsion mixture well mixed and in intimate contact with the stage-added C-36,636 19 ~J ~

acrylamide monomer throughout the entire stage-addition process, so as to obtain a homogeneous distribution of diallyl ammonium monomer throughout the copolymer chain.
Insufficient mixing results in non-homogeneous polymerization, whereas too rapid or too intensive mixing results in polymer degradation. The degree and amount of mixing required to obtain a homogeneous distribution of diallyl ammonium monomer throughout the copolymer chain varies widely depending upon the size and the shape of the particular apparatus employed.
Reaction mixers used in the preparation of thick emulsions or other similar materials, that provide intimate mixing via a shearing action, are particularly well adapted to this process.

As soon as all of the acrylamide monomer has been stage-added to the emulsion mixture and permitted to react, a chain transfer agent is added. The addition of a chain transfer agent at the conclusion of the copolymerization process is an essential step in the present invention for the preparation of high molecular weight linear copolymers. Normally, chain transfer agents are introduced at the beginning of a poly~erization process. However, in accordance with the process of the invention, the chain transfer agent is added at the conclusion of the copolymerization process so as to prevent any branching or cross-linking of formed copolymer chains from occurring. Preferably chain transfer agents include, for example, lower alkyl alcohols having from 1 to 5 carbon atoms, mercaptoethanol, mercaptopropanol, thioglycolic acid, dodecylmercaptan, formic acid, halogenated hydrocarbons, such as bromoethane or carbon tetrachloride, and sodium C-36,636 20 ~ 3~ ~3 hypophosphite. Preferably, a solution of sodium hypophosphite is employed. The chain transfer agents as used herein are preferably utilized in amounts ranging from about 0.1 to about 3 % by weight with respect to the monomers employed. Upon addition, they are preferably thoroughly mixed into the emulsion mixture.

Following the addition of the chain transfer agent, the emulsion mixture is heated for a period of time and at a temperature which serves to minimize the residual monomer content of the copolymer produced.
Preferably, the emulsion mixture is heated to from about 60 to about 90C, and more preferably about 75C and maintained at that temperature for a period of from about 0.1 to about 4.0 hours. This is especially important for environmental reasons with respect to any residual acrylamide monomer that may be present. Thus, in addition to enhancing the uniformity of the copolymers so prepared, the copolymers prepared are non-hazardous and are environmentally compatible.
Preferably, less than about 100 ppm of acrylamide monomer is present in the final product.

The copolymer emulsion mixture containing the desired product is cooled and, if desired, the copolymer can be isolated as such. For example, the cooled emulsion can be poured into an excess of acetone, filtered and dried to form a fine white powder.
Alternatively, the emulsion can be vacuum distilled to remove the solvents, or spray dried. The dried product so obtained is a white, granular, pourable powder, which is completely soluble in water, and which has preferably an intrinsic viscosity rangîng from about 10 to about 25 C-36,636 21 ~J ~.3 ~

dl/g, as determined by viscosity measurements conducted in a 4 ~ sodium chloride solution.

Alternati~ely, the copolymerized emulsion can be inverted to an oil-in-water emulsion for use in aqueous stock solutions. In order to make the copolymer emulsion self-inverting upon the addition of water, a sufficient amount of a suitable breaker surfactant must be employed. The particular breaker surfactant that will perform optimally with a given emulsion system can be readily determined by methods known to those skilled in the art. Typical breaker surfactants are those having high HLB numbers greater than 10, such as ethoxylated octyl and nonyl phenols, ethoxylated nonyl phenol formaldehyde resins, polyethylene oxide esters of fatty acids, dioctyl esters of sodium sulfosuccinate, : polyethoxylated alcohols and others. Suitable mixtures and combinations of breaker surfactants can also be employed. The nature of the breaker surfactant employed must be such as to provide a stable emulsion mixture upon addition to water~ Preferably, a polyethoxylated aliphatic secondary alcohol having nine etnylene oxide nits and a hydrophobic chain of 12 - 14 carbon atoms can be employed as a breaker surfactant for the copolymer emulsion systems described herein.

Preferably, the breaker surfactant is added in an amount from about 0.5 to about 10 % by weight, based upon the total emulsion. More preferably from about 2 to about 5 % of breaker surfactant, and still more preferably from about 3 to about 4 % by weight of emulsion is employed. Upon addition to water the water-C-36,636 ~

23 ~$~

in-oil emulsion containing the breaker surfactant inverts and is converted to an oil-in-water emulsion.

Once prepared, the emulsions of the present invention can be chemically modified in any manner known to the art. The term "chemically modified" is intended to cover any further treatment of the dispersed water soluble copolymer emulsions, including the addition of components without which the normally water-soluble polymeric particles would coagulate or agglomerate.
Examples of such treatments are disclosed in U.S. Patent Nos. 4,052,353 and 4,171,296. The emulsion of the present invention may also be concentrated in any suitable manner, such as is disclosed in U.S. Patent No.

4,021 9 399.

The following methods can be used to qualitatively and quantitatively determine the degree of diallyl ammonium monomer incorporation into the final copolymer using the dried powder obtained from the emulsion or the self invertable emulsion.

(1) Solubili~Y in Methanol Copolymers o~ DADMAC and acrylamide having a DADMAC content greater than 30 mole % are soluble in ethanol. Copolymers in the range of 30 mole % are soluble in methanol, i~, in addition, the methanol contains 10 - 20 % water. Copolymers of low DADMAC
content, as well as the homopolymer of acrylamide are totally insoluble in methanol or mixtures of 80 %

C-36,636 23 f.~ S

methanol and 20 % water. The fact that the 50 mole %
copolymer of Example 4 and the 30 mole % copolymer of Example 3 are soluble in methanol and a methanol-water mixture (80 % / 20 %), respectively, demonstrates that no homopolyacrylamides or copolymers of low DADMAC
content are present in these copolymers.

(2) Colloidal Titration Usin~ Potassium Polyvinyl Sulfate Using the method described by W Schempp et al., Papier~ 36 (lOA), 41-6 (1982), the cationicity of the various copolymers produced can be determined. This procedure provides a method for determining the cationic charges bound to the particular polymer tested as expressed in eq/kg. Comparison with the theoretical calculated values, enables the calculation of the degree of diallyl ammonium monomer conversion.

The copolymers produced in accordance with this invention are used as aids in the dewatering of a wide variety of aqueous suspensions. These copolymers are particularly useful in the dewatering of organic sludge suspensions that are proteinaceous in nature or the dewatering of suspensions that have been obtained by the biological degradation of such matter. Such suspensions can be derived from raw or processed sewage, food waste, and fermentation effluents. The copolymers of this invention are also useful in the clarification of various types of industrial waste waters.

It is Erequently desirable to dewater such sludges or suspensions in order to facilitate their C-36,636 24 ~ J

removal and their disposal. Dewatering can be effected by the addition of an appropriate amount of the copolymer as a flocculating agent prior to the physical removal of water. Dewatering of sludges or suspensions is usually effected by the addition of an aqueous solution of the polymer having a concentration ranging from about 0.01 to about 1 % by weight of polymer.
Preferably from about 0.05 % to about 0.5 % of copolymer solution is employed. Typical addition rates for sewage sludge are in the range of about 0.2 to about 1.0 % of polymer per total weight of sewage solids.

The copolymers of this invention are also useful in the paper industry as drainage and retention aids in the manufacture of paper, and in the dewatering of aqueous effluents containing cellulosic fibers. Such uses include, for example, treating aqueous waste water from a paper mill prior to discharge of the effluent, or treating return process water for the papermaking process. Such water may contain suspensions of cellulose or other finely divided particles in concentrations ranging from about 50 ppm to about 1 or 2 % by weight of solution. The copolymers of this invention are particularly useful and are generally employed as solutions of about 0.01 to about 1 %. However~ it is sometimes more convenient to prepare stock solutions about 1 to about 2 %, from which the copolymers can be utilized.

The invention described and claimed herein is more particularly illustrated in conjunction with the C-36,636 25 following examples, which are not intended to limit the invention in any way.

S The aqueous phase and the oil phase to form the water-in-oil copolymer emulsion are prepared separately, mixed and emulsified by shear stirring. To prepare the aqueous phase 105.5 g of a 60 % aqueous solution of DADMAC, 77 g of a 50 % aqueous solution of acrylamide, 1.0 g o Versenex~ 80 chelant, a 40 % aqueous solution of the pentasodium salt of diethylenetriaminepentaacetic acid, 0.25 g of 2~2~-azobis (N,N'-dimethylisobutyramidine) dihydrochloride, 1.00 g of sodium persulfate, 12.0 g of sorbitan monooleate and 120.8 g of water are dispersed with rapid mixing to form a hazy mixture, which is neutralized with a molar hydrochloric acid solution to a pH of 7. The oil phase is prepared by dissolving 6.0 g of oleic isopropanol amide in 255.0 g of Isopar M synthetic isoparaffin solvent.

The aqueous and the oil phase are mixed together with stirring and emulsified by mixing with a high speed stirrer at 10,000 to 20,000 rpm for 2 to 3 minutes.

The monomer emulsion is transferred to a glass reactor, equipped with a mixing shaft, heating jacket, vacuum control, reflux condenser and inlet ports for stage addition, stirred at about 200 rpm, and purged with nitrogen for 30 minutes to remove all oxygen. To start copolymerization the monomer emulsion is heated to C-36,636 2~

f.~ c~i a temperature of 35C and main~ained at this temperature throughout the polymeri~ation reaction.

As soon as an increase in temperature is observed, the remaining 424.3 g of a deoxygenated 50 %
aqueous solution of acrylamide is added to the copolymer emulsion over a period of one hour, via stage addition, with constant stirring. The feed rate is adjus~ed so that approximately 29 % of the acrylamide solution is added during the first quarter of the total time period, 26 % is added during the second quarter, 24 % during the third quarter, and the remaining 21 X of the acrylamide solution is added during the final quarter of the total stage-addition of one hour.

After completion of stage addition, the copolymer emulsion is ~aintained at 35C for an additional 30 minutes with stirring. A 10 % aqueous solution of sodium hypophosphite, 15 g, is slowly added to the copolymer emulsion to form a copolymer mixture that is stirred for an additional 30 minutes at 35C. The temperature of the copolymer emulsion mixture is raised to 75C and maintained a~ that temperature for 2 hours to reduce the amount of any residual monomer that may remain. The copolymer emulsion is cooled to room temperature and 40 g of a polyethoxylated aliphatic secondary alcohol having nine ethylene oxide units and a hydrophobic chain of 12 - 14 carbon atoms (sold by Deutsche BP Chemie GmbH
as SOFTANOLY90 biological degradable surfactant) is added in small portions and mixed over a period of 90 minutes. The final emulsion is discharged and passed C-36,636 27 ~ 3~ '~

through a 149 micron screen to remove any coagulated gel particles that may have formed.

The finished copolymer prepared in this fashion has an intrinsic viscosity of 18.3 dl/g when measured in a 4 XO sodium chloride solution at 25C with a Brookfield LVT viscometer having a UL adapter~ The cationicity, as determined by a potassium polyvinyl sulfate titration, shows an actual actual cationicity of 1.0 eq/kg, as compared to a theoretical cationicity of 1.25 eq/kg (79.8 % DADMAC conversion). The copolymer is completely soluble in water and insoluble in mèthanol.

Following essentially the same procedure as in Example 1, but making the following equivalent substitutions, uniform copolymers of DADMAC/acrylamide of varying cationicities were obtained. All weights are expressed in g.

C-36,636 28 . . . _ . .
Example 2 3 4 Aqueous Phase _ Initial DADMAC charge 158.0 276.3 422.4 (60 % solution) _ _ Initial Acrylamide charge 68.3 57.0 39.4 (50 % solution) _ _ _ _ _, r Water 131.4 111.4 82.2 . _ . . . . .
Pentasodium salt of 0.85 0.85 0.85 diethylenetriamine-pentacetic acid (40 % solution) . . .
2,2'azobis(N,N'-dimethylene- 0.25 0.25 0.25 isobutyramidine) dihydrochloride ~ . .
Sodium persulfate 1.0 1.0 1.0 _ _ Sorbitan monooleate 12.00 17.0 18.0 _ . .
Oil Phase . .
Isopar M synthetic 255.0 255.0 255.0 isoparaffin solvent . . , . . _ Oleic isopropanol amide 6.0 1.0 Staae addition 2 3 4 _ Acrylamide 369.8 283.0 193.5 (50 % solution) Reaction Temp (~C) 35 1 35 35 , __ _ .
Stage Addition (hrs) 2 3 4 ___ . .
pH of reaction mixture 7 7 7 , _ _, ,_ _ _ _ -7 ' C-36,636 29 The copolymers of DADMAC and acrylamide so obtained have the following properties:

__. _ Example 2 . 3 4 _ ._ . .
Cationicity 16 30 50 . _ .
CationicTitration (eq/kg) . __ . , _ Theoretical 1.87 3.05 4.3 . . . . .
Priorto Heating at75C 0.995 2.18 Final Product 1.53 2.28 3.56 . . . .
DADMAC Conversion (%) ~ , _ _ Prior to Heating at 75C 53.2 50.8 . . . _ _ Final Product 81.8 74.8 82.8 .
*Emulsion Viscosity (mPa.s) 20.9 16.0 13.7 **lntrinsicViscosity (dl/g) 20.9 16.0 13.7 _ ~ . _ _ _ _ _ Solubility Water sol sol sol _ _ . . .
, Solubility Methanol insol ***insol sol . ' ~roo~tlela Kv I vlscometer, spmdle ~, 5pe~ 3 5 at 25~C _ ** 4 % NaCI at 25C
*** Sol 80 % methanol / 20% water Following essentially the same procedure described in Examples 2 and 4, but without stage addition of the acrylamide monomer, copoly~ers of DADMAC
and acrylamide are obtained which have the following properties:

C-36,636 30 _ _ .
Example . . _ 6 Cationicity (mole percent) 16 50 . _ . - .
CationicTitration (eq/kg) ~_ .
Theoretical 1.87 4.3 , , ......... . ... .
Prior to Heating at 75C 0.48 1.2 ..
Final Product 1.36 3.43 DADYAC '~ . ~
Prior to Heating at 75C 25.7 29.8 P~ 72.7 79.8 . - . ~
* IntrinsicViscosity(dl/g) 20.1 13.2 ~ . . ..
Solubility in water sol sol ~ _ _ Solubility in methanol insol insol ~ . - ~

The properties concerning DADMAC conversion shown in examples 5 and 6, in comparison to the results obtained in examples 2 and 4, clearly demonstrate the advantage of stage addition. Using the process of stage addition, the DADMAC conversion prior to burn out is approximately twice as high as that defined for the corresponding products prepared ~ithout stage addition.
Moreover, even subsequent to burn out the DADMAC
conversion is still higher by about 3 to 10 %.

Following essentially the same procedure described in Examples 2 and 4, but omitting the use of sodium hypophosphite as a chain transfer agent, crosslinked DADMAC and acrylamide copolymers are C-36,636 31 obtained which are only partly soluble in water, and which demonstrate a reduction in intr:~lsic viscosityO

. , Example 7 8 . _ . .
Cationicity (mole percent) 16 50 ~ .
CationicTitration (eq/kg) _~ .
Theoretical 1.87 4.3 Actual 1.13 3.21 . ., DADMAC conversion (/~) 60.6 74.7 * Intrinsic Viscosity (dl/g) 13 10.2 _ _ _ ~
Solubility in water partly sol / partly sol /
swellsswells . . . _ Solubility in methanolinsol insol The results of the examples 7 and 8, pertaining to the actual cationicity and intrinsic viscosity, demonstrate that crosslinking took place, in contrast to corresponding examples 2 and 4 in which a chain transfer agent was added. In this case the measured cationicity is reduced, because insoluble polymer particles (gel particles) include cationic charges which can not be detected by the tiLration method used. Intrinsic viscosity is also reduced since a certain amount of polymer is bound by crosslinking, forming insoluble gel particles, which cannot contribute to the solution viscosity at low concentrations.

C-36,636 32

Claims (20)

1. A process for the preparation of a water-soluble, linear copolymer of a diallyl ammonium monomer and an acrylamide monomer having a uniform diallyl ammonium monomer to acrylamide monomer ratio comprising the steps of:
a) preparing a water-in-oil monomer emulsion by mixing an oil phase containing an oil soluble emulsifying agent, with an aqueous phase comprising a mixture of diallyl ammonium monomer, a portion of the total amount of acrylamide monomer required, a polymerization initiator and a water dispersable emulsifying agent;
b) initiating the copolymerization of said monomer emulsion by raising the temperature of the emulsion;
c) adding the remaining acrylamide monomer to the monomer emulsion via continuous addition to form a homogeneous copolymer emulsion;
d) homogeneously mixing a chain transfer agent into said copolymer emulsion to form a copolymer emulsion mixture; and C-36,636 33 e) heating said copolymer emulsion mixture to minimize residual monomer content.

2. A process according to Claim 1 wherein the diallyl ammonium monomer corresponds to the formula:
Formula I

and the acrylamide monomer corresponds to the formula:

wherein R1 is independently in each occurrence hydrogen or C1-4 alkyl; R2 is independently in each occurrence hydrogen, a C1-18 alkyl, C1-18 alkoxyalkyl or C1-18 hydroxyalkyl moiety; R3 is independently in each occurrence hydrogen or a C1-5 lower alkyl moiety; and R4 is independently in each occurrence hydrogen, C1-18 alkyl, C1-18 alkoxyalkyl, or C1-18 hydroxy alkyl, and Y
is an anion.

C-36,636 34

3. A process as claimed in Claim 2, wherein the oil phase comprises about 25 to about 30 volume % of the total emulsion composition.

4. A process as claimed in Claim 3, wherein the copolymerization of step (b) is initiated by heating from about 30 to about 40°C.

5. A process as claimed in Claim 4, wherein the addition of the said remaining acrylamide monomer in step (c) is over a period of about 0.5 to about 8 hours at a temperature of about 20 to about 50°C.

6. A process as claimed in Claim 5, wherein the remaining acrylamide monomer is added in such a manner that a decreasing feed rate is achieved over the period of addition.

7. A process as claimed in Claim 6, wherein about 15 to about 17 % of the total amount of acrylamide monomer is added to step (a).

8. A process as claimed in Claim 7, wherein from about 30 to about 35 % of the acrylamide monomer is added during the first quarter of the said addition period, from about 25 to about 30 % is added during the second quarter, from about 20 to about 25 % is added during the third quarter and from about 15 to about 20 %
is added during the final quarter.

C-36,636 35

9. A process according to Claim 8, wherein R1 is hydrogen, methyl or ethyl; R2 is hydrogen or C1-18 alkyl; R3 is hydrogen or methyl; R4 is hydrogen or C1-18 alkyl.

10. A process according to Claim 9, wherein the oil phase emulsifying agent is oleic mono-isopropanol amide;
the water phase emulsifying agent is sorbitan monooleate; the oil phase comprises a branched-chain isoparaffin solvent; and the chain transfer agent is sodium hypophosphite.

11. A process as claimed in Claim 9, wherein the heating of step (e) is conducted at about 60 to about 90°C for from about 0.1 to about 4.0 hours.

12. A process as claimed in Claim 11, wherein a breaker surfactant is added to the heated copolymer emulsion mixture to obtain a self-inverting emulsion.

13. A process as claimed in Claim 12, wherein the breaker surfactant is a polyethoxylate aliphatic secondary alcohol having nine ethylene oxide units and a hydrophobic chain of 12 to 14 carbon atoms.

14. A process as claimed in Claim 12, wherein the diallyl ammonium monomer to acrylamide monomer ratio is from about 5 to about 95 mole percent.
C-36,636 36

15. A process as claimed in Claims 14, wherein the diallyl ammonium to acrylamide monomer ratio is from about 25 to about 50 mole %.

16. A water-soluble, linear copolymer of diallyl ammonium monomer and acrylamide monomer having a uniform diallyl ammonium monomer to acrylamide monomer ratio and an intrinsic viscosity of from 10 to 25 dl/g as determined in a 4 % sodium chloride solution.

17. A copolymer as claimed in Claim 16 wherein the diallyl ammonium monomer corresponds to the formula:
Formula I

and the acrylamide monomer corresponds to the formula:

wherein R1 is independently in each occurrence hydrogen or C1-4 alkyl; R2 is independently in each occurrence C-36,636 37 hydrogen, a C1-18 alkyl, C1-18 alkoxyalkyl or C1-18 hydroxyalkyl moiety; R3 is independently in each occurrence hydrogen or a C1-5 lower alkyl moiety; and R4 is independently in each occurrence hydrogen, C1-18 alkyl, C1-18 alkoxyalkyl, or C1-18 hydroxy alkyl; and Y
is an anion.

18. A copolymer prepared by a process as claimed in Claim 2.

19. The use of a copolymer as claimed in Claim 16 as a flocculant for aqueous suspension.

20. The use of a copolymer as claimed in Claim 16 as a drainage or retention aid in paper manufacture.

C-36,636 38