AU2012213482B2

AU2012213482B2 - Low molecular mass, phosphorus-containing polyacrylic acids and use thereof as dispersants

Info

Publication number: AU2012213482B2
Application number: AU2012213482A
Authority: AU
Inventors: Howard Roger Dungworth; David Petty; Bolette Urtel; Ruth Wirschem
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2011-02-04
Filing date: 2012-01-31
Publication date: 2015-06-18
Anticipated expiration: 2032-01-31
Also published as: MX2013008933A; RU2592704C2; RU2013140615A; EP2670783B1; EP2670783A1; JP2014509337A; BR112013019823A2; WO2012104304A1; AU2012213482A1; CN103403044B; ES2534060T3; CN103403044A; KR20140034137A

Abstract

Process for preparing aqueous solutions of acrylic acid polymers by polymerizing acrylic acid in feed mode with a radical initiator in the presence of hypophosphite in water as solvent, by (i) initially introducing water and optionally one or more ethylenically unsaturated comonomers, (ii) continuously adding acrylic acid in acidic, non-neutralized form, optionally one or more ethylenically unsaturated comonomers, aqueous radical initiator solution and aqueous hypophosphite solution, (iii) after the end of the acrylic acid feed, adding a base to the aqueous solution, the comonomer content not exceeding 30% by weight, based on the total monomer content, the aqueous hypophosphite solution being added over a total feed time composed of three successive feed time spans Δt

Description

As originally fiIed Low molecular weight phosphorus~cOntaining polyacrylic acids and use thereof as dispersants Description This invention relates to low molecular weight phosphorus-contening polyacrylic acids, aqueous solutions comprising same, processes for production thereof and also use 10 thereof as dispersants. Dispersants, especially polyacrydO acds, are widely used in technical operations wherein a solid material is converted into a pumpable dispersion. To ensure wide industrial use, these dispersions, which are also known as slurries, have to have not 15 only good pumpability but also stability in storage (minimal aging) coupled with high solids content It is desirable for the latter to be raised as high as possible, owing to the high energy and transportation costs. A typical example is the use of aqueous calcium carbonate slurries in the production of graphics papers. While good flow properties on the part of the slurries substantially ensure processability in paper production andfor 20 paper coating, the fineness of the dispersed solids determines the optical properties of the paper produced therefrom, such as the opacity for example. A lower particle size for the same solids content of the slurry results in a higher opacity for the paper produced therefrom. The particle size here is decisively influenced not only by the input of mechanical energy during the wet grinding of the pigment, but also through the 25 choice of dispersant used, It is known that low molecular weight poiyacrylic acids produced by free-radical polymerization have good dispersing properties. The weight average molecular weight (Mw) of these polymers should be < 50 000 for good performance. Polyacrylic acids 30 with Mw <10 000 are often particularly effective, To produce low molecular weight polyacrylic acids, chain transfer agents are added as molecular weight regulators during the free-radical polymerization of acrylic acid. These regulators have to be adapted to the polymerization initiator and also to the polymerization process. Examples of known initiators are organic and inorganic percompounds, such as 35 peroxodisulfates, peroxides, hydroperoxides and peresters, azo compounds such as 2,2azobissobutyronitriie and redox systems with organic and inorganic components. The regulators used are frequently inorganic sulfur compounds such as hydrogensulies, disulfites and dithionites, orgaic sulfides, sulfoxides, sulfones and niercapto compounds such as rnercaploethanol, mercaptoacetic acid and also B7MOOOPC 2 inorganic phosphorus compounds such as hypophosphorous acid (phosphinic acid) and its salts (e g sodium hypophosphite). EP-A 405 818 discloses a process for forming polymers from monoethylenicaly 5 unsaturated monocarboxylic acids and optionally further monomers using sodium persulfale as initiator in the presence of hypophosphite as chain transfer agent, wherein an alkaline neutralizer is present during the polymerization in an amount sufficient to neutralize at [east 20% of the acidic groups, The low molecular weight polymers obtained comprise at least 80% of the phosphorus from the hypophosphite. 10 At least 70% of the phosphorus is said to end up within the polymer chain, as dialky phosphinate. The polymers thus obtained are used inter alia as laundry detergent additives, dispersants for clay slurries or scale inhibitors for water treatment, In the exemplary embodiments, acrylic acid is polymerized in water in the presence of 15 hypophosphite as chain transfer agent and sodium persulfate as initiator using the feed method wherein aqueous sodium hydroxide solution is added during the polymerization as a further continuous feed, This gives an aqueous polyacrylic add having a weight average molecular weight M, of 2700 g/mol, which comprises 72% of the phosphorus in sodium phosphite as dialkyi phosphinate, 18% as mronoalkyi phosphinate and 10% 20 as inorganic saits. A comparative example dispenses with the aqueous sodium hydroxide feed and neutralizes with sodium hydroxide solution only after the polymerization has ended. The product obtained here is an aqueous polyacrylic acid having a weight average molecular weight M, of 4320 glmol, which comprises just 45% of the sodium phosphite phosphorus as diakyi phosphinate, 25% as ronoakyl 25 phosphinate and 30% as inorganic salits. EP-A 510 831 discloses a process for forming polymers from monoethyienicaily unsaturated monocarboxylic acids, moonoethylenically unsaturated dicarboxylic acids and optionally further monomers, comprising no carboxyl group, in the presence of 30 hypophosphorous acid as chain transfer agent. At least 40% of the phosphorus incorporated in the polymer is present as monoalkyl phosphin.ate and monoalkyl phosphonate at the end of the polymer chain, The copolymers are used inter alia as d ispersants, scale inhibitors and laundry detergent additives. 35 EP-A 618 240 discloses a process for polymerization of monomers in water in the presence of a water-soluble initiator and hypophosphorous acid or a salt thereof. The process is carried out such that the polymer content at the end of the polymerization is at east 50% by weight. This method provides an increased incorporation of the hypophosphite phosphorus in the polymer, The hypophosphite phosphorus is present 40 in the polymer in the form of dialkyi phosphinate, monoalkyi phosphinate and also B10/71 0OOPC 3 monoalkyl phosphonate. No information is provided as to the distribution of the phosphorus. The copolymers are used inter alia as dispersants, scale inhibitors and laundry detergent additives. EP-A 1 074 293 discloses phosphonate-terminated polyacrylic acid having a molecular weight M, of 2000 to 5800 g/mol as a dispersant for producing aqueous slurries of calcium carbonate, kaolin, clay, talc and metal oxides having a solids content of at least 60% by weight. The problem addressed by the invention is that of providing low molecular weight polyacrylic acids having improved dispersing performance. There is provided a process for preparing aqueous solutions of acrylic acid polymers by polymerization of acrylic acid in feed operation with a free-radical initiator in the presence of hypophosphite in water as solvent, which process comprises (i) initially charging water and optionally one or more ethylenically unsaturated comonomers, (ii) continuously adding acrylic acid in acidic, unneutralized form, optionally one or more ethylenically unsaturated comonomers, aqueous free-radical initiator solution and aqueous hypophosphite solution, (iii) adding a base to the aqueous solution on completion of the acrylic acid feed, wherein the comonomer content does not exceed 30% by weight, based on the total monomer content, wherein the aqueous hypophosphite solution is added during a total feed time made up of three consecutive feed time spans Ati, At,, and Atm,,, wherein the average feed rate in the second feed time span At,, is greater than the average feed rates in the first and third feed time spans Ati and Atm,,. Preferably, the first feed time span Ati amounts to 30 to 70% of the total feed time. Preferably, the second feed time span At,, amounts to 5 to 25% and more particularly 5 to 15% of the total feed time. Preferably, the third feed time span comprises two subsidiary feed time spans Atiia and AtIlib, wherein the average feed rate during the first subsidiary feed time span Atm,,a is not less than the average feed rate during the first feed time span Ati and the average feed rate during the second subsidiary feed time span Atilib is less than the average feed rate during the first feed time span Ati. The feed rate is the amount of substance per unit time, An/At.

4 The lotal feed time is generally in the range from 80 to 500 rin and preferably in the range from 100 to 400 min, 5 The cornonomers can be included in the initial reaction charge; pary initially charged and partly added as feed; or exclusively added as feed. When they are partly or wholly added as feed, they are generally added simultaneously with the acrylic acid. In generate, water is initialy charged and heated to the reaction temperature of at least 10 7C arnd preferably in the range from 95 to 1 05*CC In addition, an aqueous solution of phosphorous acid can be included in the initial charge as a corrosion inhibitor. 15 This is followed by the commencement of the continuous feeds of acrylic acid optionally of ethylenically unsaturated comonomer, initiator and chain transfer agent Acrylic acid is added in unneutralized, acidic form. in genera, the feeds are commrenced simultaneously. Both peroxodisulfate as initiator and hypophosphite as chain transfer agent are added in the form of their aqueous solutions. Hypophosphite 20 can be used in the form of hypophosphorous acid (phosphinic acid) or in the form of salts of hypophosphorous acid, It is particularly preferable to use hypophosphite as hypophosphorous acid or as sodium salt In general, acrylic acid is added at constant feed rate. When comonorners are used 25 and at least partly added as feeds, then the feed rate of the comonomer feeds is generaHy iikewise constant. The feed rate of the free-radical initiator solution is generally likewise constant, Peroxodisuifate is the preferred free-radical initiator, Peroxodisulfate is generally used 30 in the form of the sodium or ammonium sat The content of a preferably used aqueous peroxodisulfate solution is in the range from 5% to 10% by weight. The hypophosphite content of the aqueous hypophosphite solution is preferably in the range from 35% to 70% by weight. 35 Preferably, peroxodisulfate is used in amounts of 0.5% to 10% by weight and preferably 0.8% to 5% by weight, based on the total amount of monomers (acrylic acid plus any cononomers). Preferably, hypophosphite is used in amounts of 4% to 8% by weight and preferably 40 5% to 7% by weight, based on the total amount of monomers. B10171 OOPC 5 The duration of the initiator feed can be up to 50% longer than the duration of the acrylic acid feed. Preferably, the duration of the initiator feed is about 3 to 20% longer than the duration of the acryic acid feed. The total duration of the chain transfer agent 5 feed is preferably equal to the duration of the acrylic acid feed, In generaT the total duration of the chain transfer agent feed is up to 20% shorter or longer than the duration of the acrylic acid feed, The duration of the monomer feed or - when a comonomer is used - of the monomer 10 feeds is in the range from 2 to 5 h for example. When all the feeds are commenced simultaneousy, for example, the chain transfer agent feed ends frorn 10 to 30 min before the end of the monomer feed and the initiator feed ends from 10 to 30 min after the end of the monomer feed. 15 In genera(, a base is added to the aqueous solution on completion of the acrylic acid feed- This serves to at least partially neutralize the acrylic acid polymer formed., Partialy neutralized is to be understood as meaning that only some of the carboxyl groups in the acrylic acid polymer are present in salt form, In genera, sufficient base is added for the pH to subsequently be in the range from 3 to 8.5, preferably in the range 20 from 4 to 8.5 and more particularly in the range from 4,0 to 5,5 (partiaHly neutralized) or from 6.5 to 8,5 (fully neutralized). It is preferable to use aqueous sodium hydroxide solution as base. Besides aqueous sodium hydroxide solution, it is also possible to use ammonia or amines, for example triethanoiamine. The degree of neutralization achieved for the polyarylic acids obtained is between 15 and 100% and preferably 25 between 30 and 100%, The neutralization is generally carried out over a comparatively long period ranging for example from S hour to 3 hours in order that the heat of neutralization may be efficiently removed. In general, the polymerization is carried out under inert gas atmosphere. This generally 30 provides acrylic acid polymers where the terminally bound phosphorus thereof is substantially (generally at least 90%) present in the form of phosphinate groups. In a further version, an oxidation step is carried out on completion of the polymerization. The oxidation step serves to convert terminal phosphinate groups into 35 terminal phosphonate groups. The oxidation is generally effected by treating the acrylic acid polymer with an oxidizing agent, preferably with aqueous hydrogen peroxide solution, This provides aqueous solutions of acrylic acid polymers having a solids content of 40 generally at least 30% by weight, preferably at least 35% by weight, more preferably in B10/71000PC 6 the range from 40% to 70% by weight and more particularly in the range from 40% to 55% by weight of polymer. The acrylc acid polymers obtainable according to the present invention have a total 5 phosphorus cogent of organically and possibly inorganically bound phosphorus, wherein (a) a first portion of the phosphorus is present in the form of phosphinate groups bound within the polymer chain., 10 (b) a second potion of the phosphorus is present, in the form of phosphinate and/or phosphonate groups bound at the polymer chain end, (c) possibly a third portion of the phosphorus is present in the form of dissolved inorganic salts of phosphorus, 1 and generally at least 76% of the total phosphorus content is present in the form of phosphinate groups bound within the polymer chain, Preferably at least 78% and more preferably at least 80% of the total phosphorus content is present in the form of phosphinat.e groups bound within the polymer chain. 20 The feed method of the present invention provides a particularly high content of phosphorus bound within the polymer chain. Generally at most 15% and preferably at most 12% of the phosphorus is present in the form of phosphinate and/or phosphonate groups bound at the polymer chain end.. It is 25 more preferable for 4 to 12% and especially 7 to 12% of the phosphorus to be present in the form of phosphinate and/or phosphonate groups bound at the polymer chain end, Up to 15% of the phosphorus present in the aqueous solution of the acrylic acid polymers can be present in the form of inorganic phosphorus, more particularly in the 30 form of hypophosphite and phosphate. Preferably from 2 to 12% and more preferably from 4 to 11% of total phosphorus is present in the form of inorganically bound phosphorus. The ratio of phosphorus bound within the polymer chain to phosphorus bound at the 35 chain end is at least 4:1, This ratio is preferably at least 5:1 to 10:1 and more partcularly 6:1 to g:1. The weight average molecular weight of the acrylic acid polymer is genera ly in the range from 1000 to 20 000 g/iol, preferably in the range from 3500 to 12 000 g/mto, 40 more preferably n the range from 3500 to 8000 g/mol, more particularly in ther range B10/7100OOPC 7 from 3500 to 6500 g/mol and specifically in the range from 4000 to 6500 g/rmot The molecular weight can be specifically set within these ranges via the amount of chain transfer agent used 5 The proportion of polymers having a molecular weight of < 1000 g/mol is generally 5 10% by weight and preferably < 5% by weight, based on total polymer. The molecular weights were determined via GPC on buffered (to pH 7) aqueous solutions of the polymers using hydroxyethyl metha crylate polymer network (HEMAA) 10 as stationary phase and sodium polyacrylate standards. The MAMW polydispersity index of the acrylic acid polymer is generaly 5 2.5 and preferably in the range from 1,5 to 2.5, for example 2, 15 The K-values, determined by the Fikentscher method on a 1% by weight solution in completely ionfree water, are generally in the range from 10 to 50, preferably in the range from 15 to 35 and more preferably in the range from 20 to 30. The acrylic acid polymer may comprise up to 30% by weight, preferably up to 20% by 20 weight and more preferably up to 10% by weight, based on all ethylenically unsaturated monomers, of ethylenically unsaturated comonomers in copolymnerized form. Examples of suitable ethylenically unsaturated comonomers are methacrylic acid, maleic acid, mailec anhydride, vinyisulfonic acid, allylsulfonic acid and AMPS and also salts thereof. Mixtures of these comonomers may also be present Particular preference is given to acrylic acid homopolyners without cononomter content. The resulting aqueous solutions of the acrylic acid polymers can be used directly as 30 dispersants. The invention also provides for the use of the aqueous solutions of the acrylic acid polymers or the acrylic acid polymers themselves as dispersing auxiaries for inorgani pigments and fliers, e.g, CaCO kaolin, talcum, TiO, ZnO, Zr%, AlQO and Mgo. 35 The slurries obtained therefrom are used as white pigments for graphics papers and paints, as deflocculants for the production of ceramic materials of construction, or else as fillers for thermoplastics. However, the acrylic acid poyners can also be used for other purpo-ses, for example in laundry detergents, dishwasher detergents, 40 technicaindustrial cleaners, for water treatment or as ol field chemicals, If desired, B10/71000PO S they can be converted into powder form via various drying methods, e.g, spray drying, roll drying or paddle drying, before use. Particularly preferred dispersions slurriess) for which the acrylic acid polymers of the 5 present invention are used is ground calcium carbonate. The grinding is carried out continuously or batchvlise in aqueous suspension, The calcium carbonate content of this suspension is generally 2 50% by weight, preferably z 60% by weight and more preferably >, 70% by weight Typically, the amount of polyacrylic acid used according to the present invention is in the range from 01% to 2% by weight and preferably in the 10 range from 0.3% to 1.5% by weight, all based on the calcium carbonate in the suspension. After grinding, the particle size in these calcium carbonate slurries is preferably less than 2 pm for 95% of the particles and less than I pm for 75% of the particles. The calcium carbonate slurries obtained have excellent rheological properties and are still pumpable after several days' storage, as is evident from the viscosity 15 courses in table 2. The examples which follow illustrate the invention. Examples 20 All molecular weights were determined via GPC. The GPC conditions used are as follows: 2 columns (Suprema Linear M) and a precolumn (Suprema Vorssule), all of the brand Suprema-Gel (HEMA) from Polymer Standard Services (Mainz, Germany), was operated at 35"0 at a flow rate of 0.8 ml/mir. The eluent used was the aqueous 25 solution admixed with 0.15 I NaCl and 0,01 M NaN 3 and buffered with TRIS at pH 7, Calibration was done with a Na-PAA standard, the molecular weight distribution curve of which had been determined by SEC laser light dispersion coupling, using the calibration method of MI. Cantow et a, (J, Polym, Sci A-I, 5(1967) 1391-1394), albeit without the concentration correction proposed therein, The samples were all 30 adjusted to pH 7 with 50% by weight aqueous sodium hydroxide solution. A portion of the solution was diluted with completely ion free water to a solids content of 1,5 mg/mL and stirred for 12 hours. The samples were then filtered, and 100 pL was injected through a Sartorius Minisart RC 25 (0.2 pm).. 35 Example 1 A reactor was initially charged with 502.0 g of completely ion free water. The water was heated under nitrogen to 100*C intemal temperature. At this temperature, 11.0 g of a 15% by weight aqueous ammonium persulfate solution and 47.46 g of a 15% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute. 40 Then, 1000 g of an 80% by weight aqueous solution of a distilled acrylic acid, 86.0 g of B1071 C0OPC 9 a 15% by weight aqueous armonium peroxodisuifate solution and a first quantity of 130.14 g of a 15% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agita tion. The acrylic acid was added within 2 hours, the ammonium peroxodisulfate within 2.25 hours and the sodium hypophosphite within 5 1 hour. On completion of the feed of the first quantity of sodium hypophosphite solution, a second quanilty of the 15% by weight aqueous sodium hypophosphite solution was then added in stages. First 42,66 g within 10 minutes (4.26 g/minute), then 186 g within 5 minutes (3.74 g/minute), then 16 g within 5 minutes (3.20 g/minute), then 40 g within 15 minutes (2.66 g/irnute), then 16 g within 10 10 minutes (1.60 g/minute), then 10.6 g within 10 minutes (1,06 g/minute) and 2,66 g within 5 minutes (0,52 g/minute) On completion of the ammonium peroxodisulfate feed, 310,86 g of a 50% aqueous sodium hydroxide solution were added at an intemal temperature of 100*C to part-neutralize the poiyacrylic acid obtained. The polymer solution was then cooled down to room temperature. The pH, the molecular weights M 15 and M, the solids content and the residual acrylic acid content were determined and the solution was visually inspected. Example 2 A reactor was initially charged with 502.0 g of completely ion free water. The water was 20 heated under nitrogen to 1 00*C internal temperature, At this temperature, 11.0 g of a 15% by weight aqueous sodium persuifate solution and 47.46 g of a 15% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute. Then, 1000 qgof an 80% by weight aqueous solution of a distilled acrylic acid. 86.0 g of a 15% by weight aqueous sodium peroxodisulfate solution and a first quantity of 25 130.14 g of a 15% by weight aqueous sodium hypophorsphite solution were metered in separately and concurrently under agitation, The acrylic acid was added within 2 hours, the sodium peroxodisulfate within 2.25 hours and the sodium hypophosphite within I hour. On completion of the feed of the first quantity of sodium hypophosphite solution, a second quantity of a 16% by weight aqueous sodium hypophosphite solution was 30 then added in stages. First 42-66 g within 10 minutes (4,26 g/minute), then 18.6 g within 5 minutes (3.74 g/rninute), then 16 g within 5 minutes (3.20 g/minute), then 40 g within 1:5 minutes (2.66 g/minute), then 16 g within 10 minutes (1.60 g/minute), then 10.6 g within 10 minutes (1 .06 giminute) and 2,66 g within 5 minutes (0,52 g/minute). On completion of the sodium peroxodisulfate feed, 310.86 g of a 50% by weight 35 aqueous sodium hydroxide solution were added at an internal temperature of 100*C to part-neutralize the polyacrylilc acid. The poly-mer solution was then cooled down to room temperature. The pH, the molecular weights M, and M, the solids content and the residual acrylic acid content were determined and the solution was visually inspected. 40 B1 0/71000PC 10 Example 3 A reactor was initially charged with 502,0 g of completely ion free water. The water was heated under nitrogen to I 004C internal temperature. At this temperature, 11.0 g of a 15% by weight aqueous ammoium persuifate soWUtion and 4746 g of a 15% by weight 5 aqueous sodium hypophosphite solution were added simultaneously within 1 minute, Then, 1000 g of an 80% by weight aqueous solution of a distilled acrylic acid, 86.0 g of a 15% by weightaqueous ammonium peroxodisulfate solution and a first quantity of 130.14 g of a 15% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation. The acrylic acd was added within 5 hours, 10 the ammonium peroxodisulfate within 5.25 hours and the sodium hypophosphite within 2.5 hours. On completion of the feed of the first quantity of sodium hypophosphite, a second quantity of the 15% by weight aqueous sodium hypophosphite solution was then added in stages. First 42 66 g within 25 mi nuts (1.71 g/minute), then 18.6 g within 12.5 minutes (1.49 g/ninute), then 16 g within 12.5 minutes (1.28 g/minule), then 15 40 within 37,5 minutes (1.07 g/minute), then 16 g within 25 minutes (0,64 g/minute), then 10.6 g within 25 minutes (0.42 g/minute) and finally 26 g within 12.5 minutes (0.21 giminute). On completion of the ammonium peroxodisulfate feed, 3106 g of a 50% by weight aqueous sodium hydroxide solution were added at an internal temperature of 1 00*C to part-neutralize the polyacaylic acid formed. The polymer 20 solution was then cooled down to room temperature, The pH, the molecular weights M, and Me, the solids content and the residual acrylic acid content were determined and the solution was visually inspected. Example 4 25 A reactor was initially charged with 502.0 g of completely ion free water, The water was heated under nitrogen to 100"C internal temperature. At this temperature, 11.0 g of a 15% by weight aqueous sodium persulf ate solution and 47.46 g of a 15% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute. Then, 100 g of an 80% by weight aqueous solution of a distilled acrylic acid, 86,0 g of 30 a 15% by weight aqueous sodium peroxodisuifate solution and a first quantity of 130.14 g of a 15% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation. The acrylic acid was added within 5 hours, the sodium peroxodisulfate within 5.25 hours and the sodium hypophosphite within 2,5 hours. On completion of the feed of the first quantity of sodium hypophosphite solution, 35 a second quantity of the 15% by weight aqueous sodium hypophosphite solution was added in stages. First 42,66 g within 25 minutes (1.71 g/minute), then 18 6 q within 12.5 minutes (1.49 g/minute), then 16 g within 12.5 minutes (1.28 g/mrinute). then 40 g within 37.5 minutes (1.07 gfminute), then 16 g within 25 minutes (0.64 g/rminute), then 10.6 g within 25 minutes (0.42 g/minute) and 2.66 g within 12.5 minutes 40 (0.21 g/minute). On completion of the ammonium peroxodisulfate feed, 310.86 g of a B 10/71 0OOPC 11 30% by weight aqueous sodium hydroxide solution were added at an internal temperature of 100*0 to part-neutralize the polyacrylic acid formed. The pH, the molecular weights M, and M, the solids content and the residual acrylic acid content were determ ined and the solution was visually inspected. 5 Exam pie 5 (comparative example) A reactor was initially charged with 502.0 g of completely ion free water. The water was heated under nitrogen to I 00*0 internaI temperature. At this temperature, 11,0 g of a 15% by weight aqueous ammonium persuifate solution and 47.46 g of a 15% by weight 10 aqueous sodium hypophosphite solution were added simultaneously within 1 minute, Then, 1000 g of an 80% by weight aqueous solution of a distilled acrylic acid, 86.0 g of a 15% by weight aqueous ammonium peroxodisulfate solution and 276.8 g of a 15% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation. The acrylic acid was added within 2 hours, the ammonium 15 peroxodisulfate within 2.25 hours and the sodium hypophosphite within 2 hours. On completion of the ammonium peroxodisulfate feed, 31 0.6 g of a 50% by weight aqueous sodium hydroxide solution were added at an internal temperature of 1000C to part-neutralize the polyacrylic acid formed. The polymer solution was then cooled down to room temperature. The pH, the molecular weights M and M, the solids content and 20 the residual acrylic acid content were determined and the solution was visually inspected. Example 6 A reactor was initially charged with 502,0 g of completely ion free water. The water was 25 heated under nitrogen to 100*0 intermai temperature. At this temperature, 23.6 g of a 7% by weight aqueous sodium persulfate solution and 200 g of a 59% by weight aqueous sodium hypophosphite solution were added simultaneously within I minute. Then, 930,0 g of an 86% by weight aqueous solution of distilled acrylic acid, 184.3 g of a 7% by weight aqueous sodium peroxodisulfate solution and a first quantity of 55.0 g 30 of a 59% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation, The acrylic acid was added within 5 hours, the sodium peroxodisulfate within 5.25 hours and the sodium hypophosphite within 2.5 hours. On completion of the feed of the first quantity of sodium hypophosphite solution, a second quantity of a 59% by weight aqueous sodium hypophosphite solution was 35 then added in stages. First 18.0 g within 25 minutes (0.72 g/minute)i, then 8.0 g within 14 minutes (0,57 g/minute), then C0I g within 12 minutes (0.50 g/minute), then 17 g within 37 minutes (0.46 g/minute), then 7 g within 25 minutes (0.28 g/minute), then 4.0 g within 25 minutes (0.16 g/minute) and. 1.0 q within 12 minutes (0.08 g/minute). On completion of the sodium peroxodisulfate feed, the polymer solution was cooled down 40 to room temperature. 310.86 g of a 50% by weight aqueous sodium hydroxide solution B10/71000PC 12 were then added to set a degree of neut.ralization of 35%. The pH, the molecular weights M, and M, 'te solids content and the residual acrylic acid content were determined and the so lution was visually inspected. 5 Example 7 A reactor was initially charged with 502.0 g of completely ion free water. The water was heated under nitrogen to 1 00*C internal temperature. At this temperature, 23,6 g of a 7% by weight aqueous sodium persulfate solution and 8.0 g of a 59% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute. 10 Then, 930,0 g of ar 86% by weight aqueous solution of distilled acrylic acid, 184-3 g of a 7% by weight aqueous sodium peroxodisulfate solution and a first quantity of 220 g of a 59% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation, The acrylic acid was added within S hours, the sodium peroxodisulfate within 5.25 hours and the sodium hypophosphte within 2.5 15 hours, On completion of the feed of the first quantity of sodium hypophosphite solution, a second quantity of a 59% by weight aqueous sodium hypophosphite solution was then added in stages. First 7.0 g within 25 minutes (0.28 g/minute)., then 3,0 g within 14 minutes (0.21 g/minute), then 2.0 g within 12 minutes (0.17 g/minute), then 6 g within 37 minutes (0.16 g/minute), then 3 g within 25 minutes (0.12 g/minute), then 2.0 g 20 within 25 minutes (0.08 gftninute) and 1 .0 g within 12 minutes (0.08 g/mtnute). On completion of the sodium peroxodisulfate feed, the polymer solution was cooled down to room temperature. 310.86 g of a 50% by weight aqueous sodium hydroxide solution were then added to set a degree of neutralization of 35%, The pH, the molecular weights M and M,, the solids content and the residual acrylic acid content were 25 determined and the solution was visually inspected, 810/71000PC 13 Example 8 A reactor was initially charged With 502.0 g of completely ion free water. The water was heated under nitrogen to 100"C internal temperature. At this temperature, 23.6 g of a 7% by weight aqueous sodium persulfate solution and 1.2.1 g of a 59% by weight 5 aqueous sodium hypophosphite solution were added simultaneously within 1 minute. Then, 930.0 g of an 86% by weight aqueous solution of distilled acrylic acid, 184.3 g of a 7% by weight aqueous sodium peroxodisuifate solution and a first quantity of 33,0 g of a 59% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitaton. The acrylic acid was added within 5 hours, 10 the sodium peroxodisulfate within 5.25 hours and the sodium hypophosphite within 2.5 hours. On completion of the feed of the first quantity of sodium hypophosphite solution, a second quantity of a 59% by weight aqueous sodium hypophosphite solution was then added in stages. First 11 .Og within 25 minutes (0.44 g/minute), then 5.0 g within 14 minutes (0.36 g/minute), then 4.0 g within 12 minutes (0.33 g/minute), then 10 g 15 within 37 minutes (0.27 g/minute), then 4,0 g within 25 minutes (0.16 g/minute), then 3,0 p within 25 minutes (0.12 g/minute) and 1 0 g within 12 minutes (0.08 g/minute). On completion of the sodium peroxodisulfate feed, the polymer solution was cooled down to room temperature. 310.86 g of a 50% by weight aqueous sodium hydroxide solution were then added to set a degree of neutralization of 35%. The pH, the molecular 20 weights M, and M, the solids content and the residual acrylic acid content were determined and the solution was visually inspected, Example 9 A reactor was initially charged with 502.0 g of completely ion free water. The water was 25 heated under nitrogen to 100*'C internal temperature. At this temperature, 11.0 g of a 15% by weight aqueous sodium persulfate solution and 47,5 p of a 15% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute, Then, 1000 g of an 80% by weight aqueous solution of distilled acrylic acid, 860 g of a 15% by weight aqueous sodium peroxodisulfate solution and a first quantity of 130.0 g 30 of a 15% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation. The acrylic acid was added within 2 hours, the sodium peroxodisulfate within 2.25 hours and the sodium hypophosphite within I hour. On completion of the feed of the first quantity of sodium hypophosphite solution, a second quantity of a 15% by weight aqueous sodium hypophosphite solution was 35 then added in stages. First 43,0 g within 25 minutes (1,72 g/minute), then 19.0 p within 13 minutes (1 .46 g/minute), then 16.0 g within 13 minutes (1.23 g/minute), then 40 g within 37 minutes (1 0g/minute), then 16.0 g within 25 minutes (0,64 g/minute), then 11,0 g within 25 minutes (0.44 g/rninute) and 2-0 g within 5 minutes (0.4 g/minute) On completion of the sodium peroxodisufate feed, the polymer solution was cooled down 40 to room temperature. 310.86 g of a 50% by weight aqueous sodium hydroxide solution B10/71000PC 14 were then added to set a degree of neutralizalion of 35%. The pH, the molecular weights M, and M. the solids content and the resiOuali acrylic acid content were determined and the solution was visually inspected, 5 Example 10 (comparative example) A reactor was initialy charged with 540.0 g of completely ion free water together with 9,0 g of a 0.15% iron(ii) sulfate heptahydrate. This initial charge was heated under nitrogen to 90C internal temperature. At this temperature, 77,2 g of a 35% by weight aqueous sodium hypophosphite solution were added simultaneously within 1 minute. 10 Then, 900 g of a distilled acrylic acid, 59.2 g of a 15,2% by weight aqueous sodium peroxodisulfate solution and 77,2 g of a 20.6% by weight aqueous sodium hypophosphite solution were metered in separately and concurrently under agitation. The acrylic acid was added within 2 hours, the sodium peroxodisulfate within 2 hours and the sodium hypophosphite within 16 hours. On completion of the sodium 15 peroxodisulfate feed the polymer solution was subsequently stirred at 90"C for 30 minutes and then cooled down to room temperature. The pH, the molecular weights M, and M, the solids content and the residual acrylc acid content were determined and the solution was visually inspected. 20 The analytical data of the acrylic acid polymers obtained are summarized below in table 1. Table 1 Soiids con"e P% P% P Example content iK vak pH ) Mw PD 1 0io Intemal extemI mnor % 1 422 ---1 4.' 4K) 92 S241 43 4990 2,1 49 85a 10 T 1r 26,0 4,3 5490 2 4 6 ASA 16, 42 3040 6 45 &4 3 5 12 705 45, 34 4. 2u KI 2A7-87 T 25 B10/71000PO 15 $ 461 24- 4,3 4MO0 t, 1 3Ae i , 9 43, ~ 43 50& 3 e6.7 s. 7 23 18 4610 1 |58 3 SO 3251 {025cg 150C. 2h) 4 determined by Fikentscher method with 1 % solution in completely ion free water b determine by ge permeatiron chromatography 5 d) deterin med wth "P{ 1 H} and 'P NMR Performance te s Use of acrylic acid polymers as dispersants 10 The polyacrylic acid solutions obtained were tested for their usefulness as dispersants fbr producing slurries. For this, calcium carbonate was in each case ground using a Dispermnat, For this, in each case, 300 g of calcium carbonate (Hydrocarb OG from Omya) and 600 g of ceramic beads were mixed and initially charged to a 500 ml 15 double-wall vessel filled with tap water. Then, 100 g of a 3% by weight aqueous solution of the in-test polyacrylic acid was added after adjustment to pH 5.0. The grinding was done using a grinding assembly of the type Dispermat AE-C (from VMA Getziann) with a cross-beam stirrer at 1200 rpm. As soon as 70% of the pigment had a particle size (PSD) of less than 1 pm, the grinding operation was terminated (about 20 70 min, LS 13320 particle measuring instrument from Beckman Coulter). After grinding, the slurry was filtered through a 780 pm filter using a porcelain suction filter to remove the cerarnic beads, and the solids content of the slurry was adjusted to 77%. The viscosity of the slurry was determined at once, after 24 h and after 168 h using a Brookfield DV 11 viscometer (using spindle No. 3). 25 The results of the dispersing tests are summarized in table 2. Table 2 Particle size TDynamic viscosity [mPas] at Slurry E xarnpe distribut ion 100 rpM solids < 2 pm < 1 Pm after fer Aer afer content 1h 24h 96h 168h [%] S99,1 740 5:27 930 1750 2450 770 2 969 172,9 620 1870 2220 3341 77,0 3 97.6 76087 12747 72 71 .1 iz9 58 77 0 B10/7100OPC 16 5 98.9 72.5 820 2540 3960 5270 77.0 6 99.5 74.0 2034 4055 >6000 >6000 77.0 7 99.0 74.0 835 1902 3209 4050 77.0 8 99.1 74.6 524 949 1974 2567 77.0 9 98.9 75.0 628 1448 2280 2890 77.0 10 98.9 72.4 1284 3011 4380 5645 77.0 In the claims which follow and in the preceding description of the invention, except where the context requires otherwise due to express language or necessary implication, the word "comprise" or variations such as "comprises" or "comprising" is used in an inclusive sense, i.e. to specify the presence of the stated features but not to preclude the presence or addition of further features in various embodiments of the invention. It is to be understood that, if any prior art publication is referred to herein, such reference does not constitute an admission that the publication forms a part of the common general knowledge in the art, in Australia or any other country.

Claims

1. A process for preparing aqueous solutions of acryic acid polymers by polymerization of acry.ic acid in feed operation with a free-radiclc initiator in the 5 presence of hypophosphite in water as solvent., which process comprises (I) initially charging water and optionally one or more ethyienicaky unsaturated comonomers, (ii) continuously adding acryic acid in acidic, unneutralized form, optionally one or more ethylenically unsaturated comonomers, aqueous free-radical 10 ;nitiator solution and aqueous hypophosphite solution, (ii) adding a base to the aqueous solution on completion of the acrylic acid feed, wherein the comonomer content does not exceed 30% by weight, based on the total monomer content, wherein 15 the aqueous hypophosphite solution is added during a total feed time made up of three consecutive feed time spans At, At aand AtN, wherein the average feed rate in the second feed time span Atj is greater than the average feed rates in the first and third feed time spans Ati and Atm. 20

2. The process according to claim I wherein the first feed time span At, amounts to 30 to 70% of the total feed time.

3. The process according to claim 1 or 2 wherein the second feed time span amounts to 5 to 25% of the total feed tfime. 25

4, The process according to any one of claims I to 3 wherein the third feed time span comprises two subsidiary feed time spans Atq and Ati wherein the average feed rate during the first subsidiary feed time span At is not less than the average feed rate during the first feed time span and the average feed rate 30 during the second subsidiary feed time span Atl is less than the average feed rate during the fast feed time span,

5- The process according to any one of claims I to 4 wherein the total feed time is in the range from 80 to 500 min. 35

6. The process according to any one of claims 1 to 5 wherein up to 30% by weight of comonomers seected from the group consisting of methacrylic acid, maleic acid, maleic anhydride. vinylsulfonic acid, allyisulfonic acid and 2-acrlamido-2 methylpropanesulfonic acid is co-interpolymerzed. 40 B1017100OPC 18

7. The process according to any one of claims 1 to 6 wherein the polymerization is carried out under inert gas atmosphere.

8, An aqueous solution of an acrylic acid polymer obtainable by the process 5 according to any one of claims 1 to 7.

9. The aqueous solution according to claim 7 or 8 having a total phosphorus content of organimcaly and possibly inorganically bound phosphorus, wherein (a) a first portion of the phosphorus is present in the form of phosphinate 10 groups bound within the polymer chain, (b) a second portion of the phosphorus is present in the form of phosphinate and/or phosphonate groups bound at the polymer chain end, (c) possibly a third portion of the phosphorus is present in the forn of dissolved inorganic salts of phosphorus, 15 wherein at least 76% of the total phosphorus content is present in the form of phosphinate groups bound within the polymer chain of the acrylic acid polymer.

10. The aqueous solution according to claim 7 or 8 or 9 wherein at most 15% of the phosphorus is present in the form of phosphinate and/or phosphonate groups 20 bound at the polymer chain end.

11, The aqueous solution according to any one of claims 7 to 10 wherein the weight average molecular weight of the acrylic acid polymer is in the range from 3500 to 12 000 g/mo. 25

12. The aqueous solution according to any one of claims 7 to 11 wherein the MJM, polydispersity index of the acryic acid polymer is 2.5.

13. The acrylic acid polymer obtainable from the aqueo,-us solution according to any 30 one of claims 1 to 12.

14. The use of the aqueous solution according to any one of claims 7 to 12 and of the acrylic acid polymer according to claim 13 as dispersants in aqueous dispersions of solid material. 35

15, The use according to claim 14 in aqueous dispersions of CaC0, kaolin, talcum, TI 2 , ZnO, ZrO 2 , A1 2 0 or MgO. B1.(71000 PC