EP2859025A1 - Esters de polycarboxylate hydrolysables - Google Patents

Esters de polycarboxylate hydrolysables

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Publication number
EP2859025A1
EP2859025A1 EP13726570.8A EP13726570A EP2859025A1 EP 2859025 A1 EP2859025 A1 EP 2859025A1 EP 13726570 A EP13726570 A EP 13726570A EP 2859025 A1 EP2859025 A1 EP 2859025A1
Authority
EP
European Patent Office
Prior art keywords
additive
side chains
hydraulically setting
comb polymer
setting composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP13726570.8A
Other languages
German (de)
English (en)
Inventor
Robert Flatt
Christina Hampel
Lukas Frunz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sika Technology AG
Original Assignee
Sika Technology AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sika Technology AG filed Critical Sika Technology AG
Priority to EP13726570.8A priority Critical patent/EP2859025A1/fr
Publication of EP2859025A1 publication Critical patent/EP2859025A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/12—Hydrolysis
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24—Macromolecular compounds
    • C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/2641—Polyacrylates; Polymethacrylates
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/14—Esterification
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/0045—Polymers chosen for their physico-chemical characteristics
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/0045—Polymers chosen for their physico-chemical characteristics
    • C04B2103/0059—Graft (co-)polymers
    • C04B2103/006—Comb polymers
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/30—Water reducers, plasticisers, air-entrainers, flow improvers

Definitions

  • the invention relates to additives for hydraulically setting compositions and to processes for their preparation.
  • the invention also relates to uses, kits and other methods relating to such additives. State of the art
  • Comb polymers are used in concrete and gypsum technology as additives, in particular as dispersants and liquefiers. By adding such polymers to hydraulically setting compositions, such as cement or gypsum, for example, the water content can be reduced without affecting the processability, which is advantageous for the stability of the cured concrete or gypsum. In addition, the processability can be improved at the same or lower water content.
  • Comb polymers consist of a base polymer ("backbone", "polymer backbone") to which a plurality of side chains are covalently bonded so that the molecular structure as a whole resembles a comb.
  • Comb polymers used as admixtures for cement and gypsum compositions often contain polyether side chains linked via ester groups to a polycarboxylic acid base polymer.
  • EP 1 136 508 A1 discloses additives for comb compositions based on comb polymers wherein the comb polymers contain ester groups which at least partially hydrolyze in the alkaline cement.
  • US 2012/041103 A1 discloses superplasticizers which are hydrolyzed after mixing with basic cements and thereby change the properties. However, it is not disclosed to adjust the structure of the liquefier prior to mixing with the cements by cleavage of side chains.
  • EP 1 061 089 A1 discloses neutralizing comb polymers prior to mixing with cement. With such a neutralization, however, only small amounts of dilute sodium hydroxide used, so that no hydrolysis of the comb polymer takes place.
  • the object of the invention is to overcome the disadvantages described above.
  • additives for hydraulically setting compositions are to be provided which also achieve optimum effects in various applications.
  • the additives should be used in particular as a dispersant and as a plasticizer and control the setting behavior.
  • the invention is also intended to provide methods and uses which enable the user to use comb polymers as additive as simply and effectively as possible. This should save time and money for the user. Disclosure of the invention
  • the invention relates to a process for the preparation of an additive for a hydraulically setting composition, comprising the steps:
  • hydraulically setting composition refers to compositions containing hydraulically setting binders, which are generally mineral and cure in the presence of water, whereby the water is taken up by the binder, in particular in the form of water of crystallization Compositions are preferred for cement or gypsum.
  • additive is meant a composition which upon or after admixing with a hydraulically setting composition alters at least one property of the hydraulically setting composition.
  • the additive is a dispersant. This means that the additive changes the mixing of the hydraulically setting composition and in particular improves.
  • the additive or the dispersant changes the setting behavior of the hydraulically setting composition and acts in particular as a condenser.
  • step (b) the cleavage of side chains in step (b) takes place before the addition to the hydraulically settable composition.
  • the cleavage of the side chains is therefore not only a consequence of mixing with the hydraulically settable composition.
  • a comb polymer can be modified in aqueous solution by cleavage of side chains in a simple and rapid manner, and the solution can then be used directly as an additive for hydraulically setting compositions.
  • the additive is obtained in step (b) after cleavage of side chains of a comb polymer in an aqueous solution of the comb polymer.
  • the additive is the immediate product of step (b), ie the aqueous solution containing at least one comb polymer after cleavage of side chains of the comb polymer.
  • the additive may then be added as it is to a hydraulically setting composition. It is therefore preferred according to the invention that the aqueous solution obtained in step (b) and / or the modified comb polymer are not further purified, and / or that the comb polymer is not chemically modified in further subsequent steps.
  • the inventive method differs significantly from methods for the synthesis of comb polymers in which possibly side steps are split off in intermediate steps, but a reaction mixture is obtained in which the comb polymer still needs to be purified or in the unwanted components such as catalysts and starting materials for Synthesis of the comb polymers are still to be removed, the solution still needs to be concentrated, that comb polymer must be converted into the salt, etc ..
  • an additive which has a comb polymer with partially cleaved side chains and which is used for constructive application or can be used.
  • a cured molded body is produced, which is not test purposes. Rather, the molded body is the actual constructive goal, such as a building or component thereof, flooring, a coating, a filling or a component, such as a concrete slab.
  • ester group-containing comb polymers partially hydrolyze in basic cement compositions with elimination of side chains.
  • the invention differs from EP 1 136 508 A1 in that the cleavage of side chains for the preparation of an additive and thus before mixing with a cement.
  • EP 1 136 508 A1 does not disclose a process in which a comb polymer with partially cleaved side chains is used in a constructional application, but only tests whether a comb polymer hydrolyzes in a cement composition.
  • the cleavage of the side chains in step (b) does not take place with the hydraulically setting composition itself, and preferably also not with a fraction thereof, such as filtered cement water. Regardless of this, even in the case of the additive according to the invention in the hydraulically settable composition, a further elimination of side chains still present can take place.
  • the method according to the invention can be carried out to produce an additive for a structural application.
  • the method may also be performed as a test method to select, enhance, or optimize an additive for a hydraulically setting composition for later structural use.
  • the preparation and / or selection of the additive is carried out for test purposes, and then the prepared and / or selected additive is used in a constructive application. If appropriate, the preparation of the additive in an amount required for the application takes place before the application.
  • the cleavage of the side chains in step (b) is carried out selectively. This means that cleavage is not just a minor side reaction of another process, for example the neutralization of a comb polymer with a base. Preferably, a significant proportion of side chains is split off, for example at least 1%, at least 2%, at least 5% or at least 10% of all side chains of the comb polymer.
  • the cleavage of side chains sets at least one property of a hydraulically setting composition containing the additive.
  • the property is a physical property concerning processability or stability after curing.
  • the property is the dispersibility and / or the setting behavior, wherein the additive acts in particular as a plasticizer.
  • the property may be a property of the hydraulically setting composition before setting, during setting or after setting, and before and after curing into a shaped body.
  • comb polymers act as dispersants in hydraulically setting compositions, alter the setting behavior and, in particular, act as a plasticizer. Comb polymers thus change properties of the hydraulically setting compositions, in particular the processability before and during setting and / or before curing.
  • the comb polymers also influence the properties of the cured compositions, such as the mechanical stability.
  • the effect of the comb polymer in a hydraulically setting composition depends on the structure of the comb polymer. It is generally assumed that negatively charged base polymers bind to mineral particles and the side chains are oriented away from the particles, with polyether chains in particular causing a liquefaction effect. Among other things, length and molecular weight of the comb polymer, the ratio of base polymer and side chains, the chemical structure and functional groups, length, number and distribution of the side chains and the number and distribution of charge of importance. According to the invention, use is made of the fact that the number of side chains in the comb polymer is the same Characteristics of a hydraulically setting composition significantly influenced.
  • an experimental series is performed to determine an additive which optimally acts upon a hydraulically setting composition.
  • at least two additives according to the invention are preferably prepared in which the side chains of the same comb polymer were cleaved to varying degrees.
  • the effect is tested in each case in a hydraulically setting composition and determined by comparison, which additive is particularly suitable to achieve a desired property.
  • such an experimental series may include two, three, four, five, six or more trials. It is also possible to carry out several series of tests in succession or in parallel in order to arrive step by step at an additive with the most advantageous properties possible.
  • the user can determine a suitable additive for a specific hydraulically setting composition, which is produced under defined conditions (such as temperature, humidity). After he has determined the additive, he can produce this in the required amount and perform the actual processing of the hydraulically setting composition.
  • the production method according to the invention is carried out in order to obtain an additive in sufficient quantity and to use it for a structural application. He may have determined the additive with the method according to the invention in preliminary experiments.
  • the user can also, for example, on the basis of known data, for example in the form of comparative tables, to determine to what extent he must perform the cleavage of the side chains for a given comb polymer to obtain an additive with favorable properties.
  • the degree of side-chain cleavage with respect to the particular problem can be determined from a computer database.
  • preliminary tests for determining a suitable or optimum comb polymer are not required or can be limited to a minimum.
  • the invention also provides a method for selecting an additive for a hydraulically setting composition comprising the steps
  • step (E) Comparison of the property with the same property of at least one further hydraulically setting composition containing a corresponding additive in which the cleavage of the side chains took place to varying degrees.
  • the method is used to select a suitable additive for a specific application. It serves to prepare the actual use of the additive in the construction sector.
  • selection also includes finding a particularly suitable additive or optimizing a comb polymer or additive for a particular application
  • the process is preferably carried out in the order of the steps from (A) to (E), wherein the steps (B ) and (C) can also be carried out simultaneously or in the reverse order.
  • step (E) the same property of at least two samples is compared.
  • the selection process can be performed on a single sample or as a series of two or more samples.
  • the samples differ with respect to the comb polymer.
  • the comb polymer is preferably identical in the various samples except for the side chains which are cleaved to varying degrees.
  • the samples are identical except for the comb polymer, or were prepared in the same manner with the exception of the extent of cleavage of the side chains. The comparison allows the selection of the additive that is particularly suitable for the hydraulically setting composition.
  • the method comprises a step after step (E)
  • the hydrolysis reaction is carried out under suitable conditions.
  • the temperature can be increased to about 30 to 80 ° C, in particular 65 ° C, to accelerate the hydrolysis.
  • the pH can be adjusted to achieve optimal conversion.
  • the comb polymer used in step (a) consists of a base polymer to which a plurality of side chains are covalently bonded, so that the Molecular structure as a whole resembles a comb.
  • the base polymer is a polycarboxylic acid.
  • the polycarboxylic acid is a polyacrylic acid, polymethacrylic acid or a copolymer of acrylic acid and methacrylic acid.
  • the side chains of the comb polymer preferably have polyether groups, in particular polyoxyethylene or polyoxypropylene groups.
  • the side chains are preferably polyethers, especially polyethyleneglycols or polypropylene glycols, which are optionally terminally substituted, for example with C1 to C12 alkyl groups.
  • the polyethers may be linked to the base polymer via ester groups, amide groups or ether groups.
  • the comb polymer has side chains which are linked to the polycarboxylic acid via ester groups, at least a part of the side chains having polyether groups.
  • Polyether groups should be present to a sufficient extent to ensure good dispersibility and, in particular, a plasticizing effect in a hydraulically setting composition.
  • all side chains or a substantial portion of the side chains are linked to the base polymer via ester groups. Then the cleavage of the side chains in step (b) can be controlled particularly well.
  • the proportion of side chains attached via ester groups on all side chains of the comb polymer is preferably at least 80%, at least 90%, at least 98% or preferably 100%.
  • the polycarboxylic acid of the comb polymer used in step (a) is usually not fully equipped with side chains and in particular not completely esterified.
  • the comb polymer then has free carboxy groups of the base polymer.
  • usually up to 50% of the base polymer is endowed with side chains.
  • free carboxy groups are advantageous for optimum liquefying action. Therefore, only partially equipping the comb polymer with side chains in step (a) has the advantage that the starting comb polymer already has a moderate liquefying effect because of the free carboxy groups.
  • the comb polymer before cleavage of the side chains in step (b) has a proportion of side chains and / or a degree of esterification of the base polymer between 15% and 100%, in particular between 20% and 99%, preferably between 30% and 95% based on the total number of carboxy groups of the base polymer.
  • 20% to 60% or 30% to 50% side chains may be present and / or side chains may be esterified.
  • the comb polymer has one of the stated degrees of esterification and moreover contains no further side chains. This means that the base polymer has a corresponding proportion of free carboxy groups (as the acid or salt group of the backbone).
  • the comb polymer used in step (a) preferably has free carboxy groups of the polycarboxylic acid.
  • the comb polymer may be in the form of a free acid or a salt, wherein only a part of the acid groups may be in the form of a salt.
  • the polycarboxylic acid is then completely or partially neutralized.
  • the proportion of the free carboxy groups is preferably between 1% and 80%, in particular between 5% and 70%, based on the total number of carboxy groups of the base polymer. In particular, 40% to 80% or 50% to 70% of free carboxy groups may be present.
  • comb polymers The production of such comb polymers is known in the art and can be carried out, for example, according to EP 2065403 A1 by acid-catalyzed esterification of polycarboxylic acids with monohydroxypolyethers in the presence of strong mineral acids, preferably sulfuric acid.
  • the comb polymer used in step (a) preferably has an average molecular weight M n in the range of 6,000 to 150,000 g / mol, preferably 10,000 to 100,000 g / mol, particularly preferably 15,000 to 80,000 g / mol.
  • the comb polymer comprises:
  • each of R 1 , R 2 and R 3 independently of the others is H, -COOM, -CH 2 COOM or an alkyl group of 1 to 5 carbon atoms, each R 4 is independently of the others -COOM, -CH 2 COOM,
  • Ammonium cation an organic ammonium compound or mixtures thereof; with the proviso that in the sum of a single or two of the radicals R 1 , R 2 , R 3 and R 4 are acid groups, wherein the acid unit S in particular
  • R 1 is independently H or CH 3 ;
  • R 2 is independently an ester group -CO-O- or an amide group -CO-NH-,
  • R 3 independently represents a C 2 - C 6 alkylene group, especially an ethylene or propylene group
  • R 4 are independently H, a Ci - C 12 alkyl or cycloalkyl radical, a C 7 - C 2 o alkyl aryl or aralkyl group , or a substituted or unsubstituted aryl radical, or a monovalent organic radical having 1 to 30 carbon atoms, which is optionally
  • Heteroatoms includes, stands, and
  • x is independently a value between 0 and 250, preferably between 3 and 200.
  • the acid unit S is usually introduced into the polymer by carrying out the polymerization in the presence of a corresponding acid monomer or a salt or anhydride thereof.
  • ⁇ -unsaturated mono- or dicarboxylic acids are suitable as acid monomers, in particular acrylic acid, methacrylic acid, maleic anhydride, maleic acid, itaconic acid, crotonic acid or fumaric acid.
  • the main chain of the comb polymer is preferably a linear polymer or copolymer obtained from the acid unit S, in particular the at least one acrylic acid unit A or the salt thereof and / or the at least one methacrylic acid unit M or the salt thereof by polymerization.
  • the structural unit B is part of the comb polymer.
  • the base polymer of the comb polymer may be a polyacrylic acid or a polymethacrylic acid or a copolymer of acrylic acid and methacrylic acid.
  • the acid unit S, in particular the at least one acrylic acid unit A and the at least one methacrylic acid unit M may be partially or completely neutralized.
  • the acid moiety may be in the form of a free acid or of a salt or partial salt or anhydride, the term "salt" here and hereinafter including complex salts between metal ions and the carboxylate groups in addition to the conventional salts as obtained by neutralization with a base.
  • the classical salts are obtained in particular by neutralization with sodium hydroxide, calcium hydroxide, magnesium hydroxide, ammonium hydroxide or an amine.
  • the structural unit B of the formula (I) can be an ester or an amide, depending on the choice of the radical R 2 .
  • the comb polymer contains ester groups and optionally additional amide groups.
  • the proportion of the structural units B connected via ester groups is preferably at least 80%, at least 90% or at least 98%, particularly preferably 100%, based on the sum of all structural units B.
  • the comb polymer can, for example, have a proportion of amide groups of 0 at position R 2 , 01 to 2%, in particular between 0.02 and 0.2%, based on the total number of carboxy groups of the base polymer. In a particularly preferred embodiment, at position R 2 no amide groups, but only ester groups are included.
  • - (R 3 0) x - is a C 2 to C 4 polyoxyalkylene group, in particular a polyoxyethylene group or a polyoxypropylene group or mixtures of oxyethylene and oxypropylene units in any sequence, for example random, alternating or blockwise.
  • R 4 is preferably not H, and more preferably a methyl radical.
  • the comb polymer has a proportion of ethylene oxide units of at least 30 mol%, preferably 50 to 100 mol, of the total number of (R 3 0) x units. %, in particular 80 to 100 mol .-%.
  • the comb polymer contains (R 3 0) x units exclusively ethylene oxide units.
  • the comb polymer may additionally contain polyether side chains bonded to the base polymer via ether groups.
  • the comb polymer has at least one further structural unit C, which is different from the structural units A, B and M, and which is selected from an ether, ester, amide or imide unit, an acid unit selected from carboxylic acid, Sulfonic acid, phosphonic acid, phosphoric acid ester, carbonylamidomethylpropanesulfonic acid and its salts, or a polyoxyalkyleneoxycarbonyl, polyoxyalkyleneaminocarbonyl, polyoxyalkyleneoxyalkyl, polyoxyalkyleneoxy, hydroxyethyloxycarbonyl, acetoxy, phenyl or / V-pyrrolidonyl group.
  • the further structural unit C comprises polyoxyalkylene groups, preferably polyoxyethylene groups, polyoxypropylene groups or mixtures thereof.
  • the moiety may be a C Esterloch which o alkyl alcohol is produced by reaction of a mono- or dicarboxylic acid with an alkyl alcohol, especially a C 6 -C second
  • the comb polymer may have a combination of different structural units of the respective structural units of A, M, B and optionally C.
  • several acid units A and M may be mixed in the comb polymer, which are not or completely neutralized.
  • several different ester and / or amide units B may be mixed in the comb polymer, for example, several ester units B having different substituents R 3 .
  • Preference is given, for example, to the joint use of polyoxyalkylenes, in particular of polyoxyethylene with polyoxypropylene, or the joint use of polyoxyalkylenes, in particular of polyoxyethylene, having different molecular weights.
  • the comb polymer comprises
  • Acrylic acid units A and the methacrylic acid units M is 5 to 70 mol%, preferably 40 to 70 mol%,
  • the sequence of the individual structural units A, M, B, and C in the comb polymer can be alternating, random or blockwise.
  • the chain length is adjusted with a regulator, for example phosphite or sulfite. Therefore, the polycarboxylic acids may have groups which are not carboxylic acid units, for example, phosphorus or sulfur containing groups.
  • the cleavage of the side chains in step (b) of the process according to the invention is preferably carried out by basic hydrolysis of ester groups.
  • the base is a strong base, in particular metal hydroxide, in particular sodium or potassium hydroxide.
  • the metal hydroxide is preferably used in aqueous solution.
  • the cleavage of the side chains is controlled by terminating the reaction after a defined period of time, in particular by neutralization of the base.
  • the basic hydrolysis of ester groups has the advantage that the reaction is easy to control and ends after a defined period of time simply by neutralization can be. In this way, in step (b) various additives can be prepared in a simple manner, which are esterified to varying degrees.
  • the base is selected so that a targeted cleavage of the ester groups takes place and the rest of the comb polymer is not or only slightly modified chemically. According to the invention, other chemical reactions can also be used in step (b) to cleave off side chains and to control the reaction.
  • step (b) between 5 and 95%, in particular between 10 and 90% of all side chains of the comb polymer are split off in step (b).
  • step (b) a comb polymer is obtained which still has at least 10%, at least 20% or at least 30% side chains, based on all monomer subunits of the base polymer.
  • a comb polymer is used in step (b), in which under the chosen conditions in the aqueous solution, a part of the side chains can not be cleaved off. In this way it can be prevented that too high a proportion of the side chains of the comb polymer is split off and the advantageous effect in a hydraulically setting binder decreases too much or is lost.
  • up to 10%, up to 20%, up to 30% or up to 40% of the side chains of the comb polymer, based on all monomer subunits of the base polymer, in step (b) can not be cleaved.
  • the comb polymer provided in step (a) contains two different types of side chains in this embodiment.
  • a comb polymer can be used which has side chains which are linked to the base polymer via basic hydrolyzable ester groups, and also side chains which are connected via ether groups with the base polymer, which are not cleaved under the conditions of basic hydrolysis.
  • Another object of the invention is a process for the preparation of a hydraulically setting composition, wherein an inventively prepared and / or selected additive is mixed with a hydraulically setting binder.
  • the hydraulically setting binder is selected from the group consisting of cement, gypsum, for example in the form of anhydride or hemihydrate, and quicklime.
  • the cements are for example Portland cements, alumina cements or mixtures thereof with conventional additives.
  • the hydraulically setting composition may contain additives.
  • Typical additives are, for example, fillers and aggregates, such as fly ash, silica fume, slag, blastfurnace slag, limestone, sand, gravel, stones, quartz powder and chalk.
  • mixtures of cement with fly ash, silica fume, slag, blastfurnace slag or limestone filler can be used.
  • processing aids and additives that affect the properties of the setting and cured compositions can be added.
  • concrete liquefiers such as lignosulfonates, sulfonated naphthalene-formaldehyde condensates, sulfonated melamine-formaldehyde condensates or polycarboxylate ethers, as well as accelerators, corrosion inhibitors, retarders, Schwlashduzierer, defoamers, dyes or pore formers may be included.
  • the comb polymer is preferably used in an amount of from 0.01 to 5% by weight, in particular from 0.05 to 2% by weight, or from 0.1 to 1% by weight, based on the weight of the hydraulically setting binder.
  • the additive may be added to the hydraulically setting composition at or just prior to or shortly after the addition of the water.
  • Particularly suitable here is the addition of the comb polymer in the form of an aqueous solution or dispersion, in particular as mixing water or as part of the mixing water, exposed.
  • the preparation of the aqueous solution is carried out in particular by subsequent mixing with water.
  • the comb polymer may also be added to a hydraulically setting composition prior to or during its milling operation, for example, the cement-cement to cement grinding process.
  • Another object of the invention is a method for producing a shaped body, wherein a hydraulically setting composition prepared according to the invention is cured.
  • the term "shaped body" refers to three-dimensional bodies, for example a building or component thereof, floor covering, a coating, a filling or a component, such as a concrete slab.
  • a further subject of the invention is an additive for a hydraulically setting composition, obtainable according to FIG.
  • the additive differs from known additives in that the aqueous solution contains not only the comb polymer but also the cleaved side chains, the cleaved side chains structurally corresponding exactly to the side chains which were not cleaved off from the comb polymer Base or a catalyst which have been added for the removal of the side chains or whose reaction products are likewise contained.
  • the additive is preferably adapted to a hydraulically setting composition
  • the use of the reaction products of the hydrolysis, since the split-off Polyetheritketten generally reinforce the liquefying effect.
  • the additive
  • the additive can be used in particular as a plasticizer, as a water reducer, to improve the processability and / or to improve the flowability of hydraulically setting compositions become.
  • hydraulically setting compositions having extended processability can be obtained with the additive.
  • the additive may contain other constituents, such as other plasticizers, for example lignosulfonates, sulfonated naphthalene-formaldehyde condensates, sulfonated melamine-formaldehyde condensates or other polycarboxylate ethers (PCE), accelerators, retarders, shrinkage reducers, Defoamer, air entraining agent or foaming agent.
  • PCE polycarboxylate ethers
  • accelerators accelerators
  • retarders shrinkage reducers
  • Defoamer air entraining agent or foaming agent.
  • the proportion of the comb polymer is 5 to 100 wt .-%, in particular 10 to 100 wt .-%, based on the total dry weight of the additive.
  • the additive already contains components which promote or inhibit the cleavage of the side chains in step (b).
  • components could be included which are activated by temperature or pH, so that the cleavage of the side chains can be initiated thereby.
  • Another object of the invention is the use of a base for the cleavage of side chains of a comb polymer for adjusting at least one property of a hydraulically setting composition containing the comb polymer.
  • kits for the preparation and selection of an additive for a hydraulically setting composition wherein the kit contains an aqueous solution of a comb polymer and a base for the cleavage of side chains of the comb polymer, wherein also further components can be contained.
  • the "kit” is a combination of the components.
  • the kit is provided in a mold so that the user can easily carry out series of experiments or individual tests in order to adapt an additive to a hydraulically setting composition and to modify its properties in the desired manner.
  • the components are preferably contained as aqueous solutions, for example in bottles for easy dosing. Usually is also a guide for the user included.
  • the inventive method solves the problems underlying the invention.
  • a simple, fast and efficient method is provided to prepare additives for concrete hydraulically setting compositions, to select them and to adapt them optimally to concrete conditions.
  • the method can be performed by users in construction technology, in particular directly on a construction site. This eliminates the need for the user to purchase and stock a variety of comb polymers.
  • the method according to the invention can be carried out as a preliminary test for the selection of suitable additives as well as for the specific adaptation of an additive to a civil engineering application.
  • FIG. 1 graphically depicts the results of the cement paste trials 20 to 27.
  • the rhombs show the hydrolysis of side chains of a comb polymer as a function of time in minutes.
  • the squares show the flow behavior in millimeters for the same comb polymers.
  • a Preparation of the Cement Pastes and Measurement of the Flow Mixture For the preparation of all cement pastes, a mixture of three cements (brand name Normo 4 from Holcim, brand name CEM I 42.5 from Jura Cement, brand name CEM I 42.5 from Vigiers) was used. The mixing ratio was 1: 1: 1. 100 g of the cement mixture is weighed in a beaker. 32.5 g of water, which already contain the polymer prepared according to Tables 1 .1 and 2.1, are added to the cement at once. The resulting cement paste is then stirred by hand with a spatula for one minute. After another minute rest is again during 15 Stirred for a second.
  • gypsum ß-hemihydrate brand SGD Stuck, Spremberg Germany
  • 136.4 g of water are placed in a second beaker, which already contain the prepared according to Tables 1 .2 and 2.2 polymer.
  • the weighed plaster is sprinkled into the water for 15 seconds. Wait 15 seconds for the gypsum to shrink. Then it is mixed intensively with a whisk for 30 seconds by hand.
  • a plastic cylinder standing on a glass plate is filled with gypsum paste. The cylinder is lifted into the water 75 seconds after pouring the gypsum.
  • the diameter of the resulting gypsum cake is measured with a vernier caliper.
  • PCE A and PCE C polycarboxylate esters
  • Both comb polymers were prepared by polymer-analogous esterification of a polycarboxylic acid with methyl polyethylene glycol.
  • a detailed description of this type of preparation has been given, for example, in EP 1 138 697 B1 on page 7, line 20 to page 8, line 50 or in EP 1 061 089 B1 page 4, line 54 to page 5, line 38 or in the examples of US Pat respective documents disclosed.
  • PCE C was mixed with a mixed acrylic / Methacrylic acid backbone (ratio 3: 1). The degree of esterification is also 38%.
  • Example 1 The preparation of the composition according to Example 1 is described below by way of example. All further samples were prepared in the same way.
  • the experimental conditions and results are summarized in Tables 1 .1 and 1 .2.
  • Table 1 .1 summarizes the test results with cement pastes.
  • Table 1 .2 contains the results of the gypsum paste tests.
  • Example 1 0.51 g of a solution of PCE A (40.1% solids content) are mixed in a beaker with 5.52 g of water. Then 2.09 g of a 0.1 N NaOH solution are added and stirred. The cup is capped and stored in an oven at 65 ° C for 20 minutes. The cup is then removed from the oven and 24.38 g of cold water are added. The cup now contains the 32.5 g of water required for the cement paste test, including the treated polymer. This solution is used immediately after its preparation for the cement paste test. The resulting flow rate is given in Table 1 .1.
  • Example 5 The sample of Example 5 was prepared in the same manner except that no NaOH solution was added; ie no hydrolysis takes place.
  • the sample of Example 6 contains the same amount of polymer PCE A and water, but was not stored in the oven and contains no NaOH solution. Both examples are marked in the tables as comparisons (V).
  • V comparisons
  • Tables 2.1 and 2.2 The experimental conditions and results are summarized in Tables 2.1 and 2.2.
  • Table 2.1 summarizes the test results with cement pastes.
  • Table 2.2 contains the results of the gypsum paste tests.
  • Example 20 The preparation of the sample of Example 20 is described below by way of example. The other samples were prepared in the same manner, except that the duration of the treatments varied.
  • a stock solution S1 is prepared.
  • 5.0 g of a solution of PCE A 40.1% solids content
  • 25.0 g of a 1 .0 N NaOH solution are added and mixed well.
  • This stock solution is covered to prevent evaporation and stored at 22 ° C.
  • the sample of Example 20 was prepared by transferring 4.00 g of stock solution to a separate beaker after 3 minutes. For this purpose, a drop of a phenolphthalein solution is added as a pH indicator. The solution assumes a pink color. Thereafter, the amount of 0.1 N HCl solution required for complete decolorization is added. Subsequently, 2.90 g of water are added. The total mass of the sample of Example 20 is now 32.5 g.
  • Example 28 contains the same amount of PCE A, 0.1 N HCl and water, but was not subjected to a hydrolysis treatment.
  • the degree of hydrolysis was determined, ie the ratio of the number of cleaved side chains to the total number of side chains of the starting polymer.
  • the number of side chains was determined by titration of the acid with 0.1 N NaOH.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Structural Engineering (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

L'invention concerne un procédé de préparation d'un adjuvant pour une composition à prise hydraulique, comprenant les étapes consistant à: (a) préparer une solution aqueuse contenant au moins un polymère en peigne, et (b) séparer des chaînes latérales du polymère en peigne. L'invention concerne également des adjuvants pour des compositions à prise hydraulique, des applications, des procédés de sélection et des kits.
EP13726570.8A 2012-06-06 2013-06-05 Esters de polycarboxylate hydrolysables Withdrawn EP2859025A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP13726570.8A EP2859025A1 (fr) 2012-06-06 2013-06-05 Esters de polycarboxylate hydrolysables

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP12170936 2012-06-06
EP13726570.8A EP2859025A1 (fr) 2012-06-06 2013-06-05 Esters de polycarboxylate hydrolysables
PCT/EP2013/061578 WO2013182595A1 (fr) 2012-06-06 2013-06-05 Esters de polycarboxylate hydrolysables

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EP2859025A1 true EP2859025A1 (fr) 2015-04-15

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US (1) US20150166691A1 (fr)
EP (1) EP2859025A1 (fr)
AU (1) AU2013273597B2 (fr)
WO (1) WO2013182595A1 (fr)

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Publication number Priority date Publication date Assignee Title
US9546110B2 (en) 2015-06-15 2017-01-17 Gcp Applied Technologies Inc. Superplasticizing admixture for cementitious compositions
US9624130B2 (en) 2015-06-15 2017-04-18 Gcp Applied Technologies Inc. Optimizing polycarboxylate admixtures for cementitious compositions
EP3802461A1 (fr) * 2018-05-31 2021-04-14 Sika Technology Ag Procédé de liquéfaction de ciments contenant de la bélite, du sulfoaluminate de calcium et de la ferrite

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ES2154254T3 (es) 1999-06-15 2004-11-01 Sika Schweiz Ag Polimeros dispersantes de cemento, de aplicaciones generales, para hormigon de alta fluidez y alta resistencia.
DE1136508T1 (de) 2000-03-22 2002-04-18 Sika Ag, Vormals Kaspar Winkler & Co Zementmischung mit verlängerter Verarbeitungszeit
EP1138696A1 (fr) 2000-03-29 2001-10-04 Sika AG, vorm. Kaspar Winkler & Co. Polymères pour compositions dispersantes pour ciment
JP4975714B2 (ja) 2007-11-28 2012-07-11 ローム アンド ハース カンパニー ポリマーの製造法
FR2942223B1 (fr) 2009-02-17 2011-04-22 Lafarge Sa Liant hydraulique rapide pour pieces et ouvrages en beton contenant un sel de calcium

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See also references of WO2013182595A1 *

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AU2013273597B2 (en) 2016-05-19
WO2013182595A1 (fr) 2013-12-12
AU2013273597A1 (en) 2015-01-22
US20150166691A1 (en) 2015-06-18

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