NZ624725B2 - Composition comprising block cocondensates of propylfunctional alkaline siliconates and silicates, and method for the production thereof - Google Patents

Abstract

Disclosed is a composition and a method for the production of the composition comprising block cocondensates of propylfunctional alkaline siliconates and silicates of the general formula (I), wherein the substituents are as defined in the specification. The compositions are useful hydrophobizing agents for water proofing building materials. nts for water proofing building materials.

Description

PCTIEP2012I071483 Composition comprising block cocondensates of propylfunctional alkaline siliconates and silicates, and method for the production thereof The invention relates to a composition and to a process for preparing the composition comprising block cocondensates of -functional alkali metal siliconates and silicates.

Absorption of water by porous mineral building materials, such as concrete, sandstones, lime sandstones, gypsum, ceramics or fired clay products, examples being wall bricks, 1O in the presence of water or moisture, may cause damage to the building materials.

Renovating building materials that have been damaged in this way is very x and costly. It is known ce to incorporate hydrophobizing agents onto the surface or into the material during the production of such building materials, in order to prevent water absorption and hence damage to the building materials. For some time, siliconates have been g an important part here as hydrophobizing agents, especially when the building materials to be treated are not very alkaline, such as clay products.

EP 0 650 968 ses a two-stage operation for the continuous preparation of alkali metal alkylsiliconates from alkyltrichlorosilanes via alkyltrialkoxysilanes. US 4,281,147 describes a process for ing aqueous alkali metal organylsiliconates by reaction of organylalkoxypolysionanes with NaOH or KOH. EP 0 015 366 relates to a s for preparing alkali metal methylsiliconates that are free of alkali metal chloride, by reaction of alkali metal trichlorosilanes with a base, precipitation of the intermediate by acidification, and uent dissolution of the washed filter cake in base.

DE 31 O5 407 relates to water-repellent gypsum mortars sing a fatty amine, an acid and an alkali metal siliconate. US 028809 discloses a gypsum composition comprising cellulose and a methyl siliconate, with the gypsum products produced therefrom having water-repelling properties.

The prior art discloses neither a composition of —functional alkali metal siliconates and silicates and their cocondensates, nor a technical process for industrial manufacture of such a composition.

An object of the present invention was to provide a ition comprising water— soluble cocondensates of propyl-functional alkali metal nates and silicates that has hydrophobizing properties even at very high dilution and whose condensation products remain water-soluble even at high concentration. The intention, moreover, was to develop a simple and ore economical process for preparing the compositions comprising cocondensates of propyl-functional alkali metal siliconates with silicates. The object, furthermore, was to prepare compositions of the stated compounds that are suitable for the hydrophobizing impregnation of mineral building materials, preferably surfaces of mineral building materials, and/or for hydrophobization in the bulk material in 1O the course of its tion, and also as a water-repellent injection composition to form barrier layers against moisture. The ition of the invention is used preferably to nate porous, mineral building materials and/or substrates. Furthermore, stable compositions were to be provided, having a high level of the compounds and being readily dilutable with water prior to their use. According to one alternative, er, these compositions were to be substantially free from ts, more particularly free from alcohol.

The foregoing objects should be read disjunctively with the object of at least providing the public with a useful .

The objects have been achieved by means of the composition of the invention and by the process of the invention, and also by the inventive use as described . Further features and combinations thereof are elucidated in the dependent claims and in detail in the description.

Surprisingly it has been possible to provide a composition which comprises substantially water-soluble block cocondensates of alkali metal propylsiliconates with alkali metal silicates and water; preferred itions feature block cocondensates of propyl siliconates with silicate, which have been cocondensed under alkaline conditions with block condensates of silicates, and which are referred to as block cocondensates of alkali metal propylsiliconates with alkali metal tes. The particular advantage of the block cocondensates is that particularly highly trated compositions of the block cocondensates dissolved therein may be prepared. 3 PCT/EP2012I071483 Surprisingly it has been possible to provide a composition which comprises substantially soluble block cocondensates of alkali metal propylsiliconates with alkali metal silicates in water, the alkali metal propylsiliconates being more particularly ensates derived from silanes, and the block cocondensates featuring crosslinking structural elements which form ry, cyclic, crosslinked and/or three- dimensionally crosslinked structures, and at least one structure corresponds in idealized form to the general formula I, MO[iSi<R1)xv«y-2,-x)01a[simzibismR1>XY«y-2)-x)Oic]n[iSi<Y>21m]OM (I) where, in the structural elements derived from alkoxysilanes and silicates, such as alkali metal te or synonymously alkali metal waterglass, — R1 corresponds to a propyl radical, - Y corresponds in each case independently to OM or OH or, in crosslinked and/or three-dimensionally crosslinked structures, independently of one another, to 01/2, i.e. in a siloxane bond, — M ponds independently at each occurrence to an alkali metal ion, preferably a lent alkali metal ion, such as Na+ or K“, or to 1/2 alkaline earth metal ion, such as 1/2 Ca2+ or 1/2 Mg”, - with in each case independently x being 1 or 2, preferably 1, with y being 3 or 4, where (x + y) = 4, and also with, in each case independently, a 2 1 and c 2 0; ably, independently, each c 2 1, b 2 0, more particularly with b 2 1, preferably with 20 2 b 2 2, more preferably with 15 2 b 2 3, with n 2 1 blocks, likewise preferably with n 2 2, and with m 2 2 silicate blocks, where (b + m) = v and (a + c)/v S 1, also in particular with v 2 4, preferably with 25 2 [v = (b + m)] 2 2 silicate blocks, more ularly with 25 2 [v = (b + m)] 2 4, preferably with 2 [v = (b + m)] 2 4, alternative preference being given to 10 2 [v = (b + m)] 2 2, also preferably with 10 2 [v = (b + m)] 2 5 in the combination with (a + c) 2 2, in particular with the proviso that b is less than m. Embodiments also red are the combinations with n 2 2 and (a + c + b) 2 4, with in each case independently a 2 1, c 2 1 and 20 2 b 2 1, and optionally with m 2 4, in particular with 10 2 v 2 4 silicate 4 PCT/EP2012I071483 blocks, alternative preference being given to 10 2 b 2 1, more particularly 4 2 b 2 1, alternatively 4 2 b 2 2 with n 2 1 and v 2 3. The index a is situated preferably in the range of 20 2 a 2 1, preferably 10 2 a 21, also preferably 4 2 a 2 1, such as 4 2 a 2 2. The index 0 is situated preferably in the range of 20 2 c 2 0; preferably 2 c 2 1, also preferably 4 2 c 2 1, such as 4 2 c 2 2. According to one particularly preferred alternative, in the formula l there are cocondensate blocks with in each case independently a 2 1, c 21, b 2 1 with n 2 1 and at the same time silicate blocks with m 2 2, in particular with the proviso that m is greater than b. 1O The alkali metal propylsiliconates here are cocondensates derived from di- or trifunctional hydrolysable silanes and tetrafunctional silanes. With particular preference the formula I encompasses cocondensate blocks with in each case independently a 2 1, c 2 1, b 2 1, ably with b 2 2, with n 2 1 and the silicate blocks with m 2 2, where b + m = v and v 2 4, in particular v 2 6, where (a + c)/v s 1; preferably a/v S 0.5, more ably 0.11 S (a + c)/(b + m) s 1.0, also preferably 0.11 s (a + c)/(b + m) S 0.4, more preferably 0.16 s (a + c)/(b + m) S 0.32, also ularly preferably (a + c)/(b + m) or (a + c)/v around 0.30 with plus/minus 0.15. A ularly preferred combination comprises a 21, c 21, b 2 2 with n 21 and the silicate blocks with m 2 2, where (b + m) = v and v 2 6, and where (a+c)lv s 1, in particular with x being 1, more preferably (a + c)/(b + m) or (a + c)/v is 0.30 with plus/minus 0.15. Likewise preferred is a combination of n 2 2 with b 2 2 and m 2 4 with a and 0 independently greater than or equal to 1.

Likewise provided by the ion is a composition which comprises substantially water-soluble block cocondensates of alkali metal propylsiliconates with alkali metal silicates and water, the alkali metal propylsiliconates being more particularly cocondensates derived from silanes, and the block cocondensates having crosslinking structural elements which form catenary, , crosslinked and/or three-dimensionally crosslinked structures, and at least one structure corresponds in idealized form to the l formula I, where the block cocondensates of alkali metal propylsiliconates with alkali metal silicates are present in a mixture with ric alkali metal propylsilanolates, more particularly derived from the general formula ll, and/or alkali metal tes, more ularly derived from the general formula III. The ratio of propyl-functional structural elements and propylsilanolates to silicatic ural elements and silicates is preferably around 1:2 to 1:4, ably about 1:3 with in each case plus/minus 0.25, in particular with the proviso that in the idealized a I, 2 [v = (b + m)] 2 2 in the combination with n 2 1, a 21, c2 2, Le. (a + c) 2 2, in particular with 10 2 [v = (b + m)] 2 4, where m 2 2. Optionally, n and m in each case independently are less than or equal to 50, also preferably less than or equal to 10, particularly preferably less than or equal to 5.

Also provided by the invention is a composition comprising substantially water-soluble 1O block cocondensates of alkali metal propylsiliconates with alkali metal silicates and water, the alkali metal propylsiliconates being, in particular, cocondensates derived from silanes, with a molecular weight average in terms of relatively high molecular weight block ensates, more ularly of the idealized formula I, of r than or equal to 1100 glmol to 2000 g/mol, with optionally a further molecular weight average in terms of low molecular weight condensates and/or monomers of silanolates and tes of less than or equal to 500 g/mol to 96 g/mol. The ratio between the relatively high molecular weight block cocondensates and the low molecular weight condensates and monomers is preferably from 111.1 to 1:3, ably from 121.1 to 112.0, preferably around 121.6 with plus/minus 0.25.

With regard to the use as hydrophobizing agents in architectural preservation, and on the basis of workplace safety law provisions for the industrial manufacture of construction products, such as plasterboard or brick blocks, it is preferred if the compositions are substantially alcohol-free and also no longer release ntially any l during crosslinking. A composition is considered alcohol—free if it has S 5 wt% alcohol or is able to release 5 5 wt% of hydrolysis alcohol, preferably below 5 wt% to 0.000001 wt%. In general, in the compositions provided, the amount of alcohol or hydrolysis alcohol in the overall composition is s 3 wt%, preferably 5 1 wt%. A composition is preferably considered substantially alcohol-free and/or free from hydrolysis alcohol when its alcohol and/or hydrolysis alcohol content is from preferably 1 ppm by weight up to a maximum of 2 wt%, preferably from 10 ppm by weight to 1 wt%, more preferably from 100 ppm by weight to 0.5 wt%, based in each case on the W0 2013l072185 6 PCT/EP2012I071483 total weight of the composition. The substantially alcohol-free solution has a flash point of 2 100°C.

The pH of the ready-to-use compositions, which before use can easily be diluted with water in virtually any proportion, is 2 pH 9, more particularly 2 pH 11, preferably in the range from pH 12 to 14, more particularly also pH 13.

In ance with one preferred embodiment, the composition takes the form of a solution. A on means, preferably, a homogeneous mixture, more ularly comprising block cocondensates (solutes) and at least one solvent, presently water, the solutes being preferably in full solution in the solvent, tly water; in other words, preferably, there is a clear solution. The shelf life of the solution is at least twelve months.

Surprisingly, a simple and economical process has been found for preparing cocondensates, allowing an alkali metal cocondensates of propyl-siliconate and silicate to be prepared without costly and inconvenient reaction, using an introduction tube and operating under inert gas. ing to one alternative of the invention it has surprisingly been found that it is possible to prepare itions of water—soluble block cocondensates of alkali metal propylsiliconates with silicates, by, in a first step, performing the preparation of the propyl-functional alkoxysilanes and optionally tetraalkoxysilanes and/or condensates thereof, such as homocondensates and/or cocondensates, starting from propylhalosilane and tetrahalosilane, in the presence of a stoichiometric amount of alcohol, preferably a molar excess of alcohol, from the halosilanes, and with possible l of any alcohol added in excess. The ing mixture of the aforementioned alkoxysilanes and optionally their condensates is subsequently reacted, in a second step, with a e of a water-soluble silicate, more particularly alkali metal silicate, in solution in aqueous alkaline solution, preferably an aqueous alkali metal hydroxide solution. This reaction of the mixture with the water-soluble silicate and the alkali metal hydroxide leads to the ion of block cocondensates of alkali metal WO 72185 7 2012I071483 propylsiliconates with alkali metal tes. The hydrolysis alcohol formed in the course of the hydrolysis and condensation is removed almost completely. it was particularly surprising that as a result of the procedure according to the invention, in the second reaction step, the reaction t from the first step is reacted easily and economically, through the addition of an alkali metal silicate to the aqueous alkaline solution, without special measures and without substantial formation of sediments. In the second step as well, the hydrolysis alcohol released can be removed almost completely, without any instances of precipitation of the silicate and/or siliconate.

The invention accordingly es a process for preparing a composition comprising at least one substantially water-soluble block cocondensate of alkali metal propylsiliconates with alkali metal silicates and water, and also to a composition obtainable by this process, by reacting (i) a mixture comprising propylalkoxysilanes and optionally propyI-functional siloxanes derived from a propylsilane of the general formula ll, more particularly a e sing propylalkoxysilanes, tetraalkoxysilanes and/or condensates thereof, such as ensates and/or homocondensates, derived from propylhalosilanes of the formula II where X is halogen and from tetrahalosilane of the formula lll where Y is halogen, (Ripsrxw (ll) with R1 independently being a —functional radical, and with ysable radical X, which independently is alkoxy or a halogen, more particularly substantially selected from ethoxy, methoxy, propoxy and butoxy or ntially selected from chloro and bromo, with x being 1 or 2 and y being 4, and optionally with a hydrolysable silane of the formula III SiY4 (ill) with hydrolysable radical Y, which independently is alkoxy or a halogen, more particularly substantially selected from ethoxy, methoxy, propow and butoxy or substantially selected from chloro or bromo, and (ii) a mixture of at least one water- 8 PCT/EP2012I071483 soluble silicate and an s alkaline solution. It is particularly preferred here if an alkali metal te is used as te, more particularly a sodium waterglass and/or a potassium waterglass. In general it is possible to use all water—soluble silicates. ysis alcohol formed in a step (iii) is preferably removed.

In accordance with one embodiment, the aqueous alkaline solution comprises an inorganic base, more particularly selected from alkali metal hydroxide and alkaline earth metal ide, particular preference being given to potassium hydroxide, sodium hydroxide, lithium hydroxide, magnesium ide and/or calcium hydroxide.

It is preferred, moreover, if in the process, the mixture comprising propylalkoxysilane, more particularly of the formula II with X being alkoxy, preferably ethoxy, and optionally condensates thereof is prepared by reaction of a propylsilane of the general formula ll where X is halogen, more particularly chloro or bromo, preferably chloro, with an l, more particularly methanol, ethanol, propanol or butanol, preferably l, optionally in the presence of water, and the alcohol and/or hydrolysis alcohol is removed. Generally, in the process of the invention, the l and/or hydrolysis alcohol are/is removed by distillation, preferably under reduced pressure and at elevated temperature.

According to one particularly preferred alternative, in the process of the invention, the mixture comprising propylalkoxysilane, more particularly of the formula II where X is alkoxy, preferably ethoxy, tetraalkoxysilane, more particularly of the a lll where Y is alkoxy, preferably ethoxy, and/or condensates thereof, such as cocondensates, is prepared by reaction of at least one propylsilane of the general formula II where X is n, more ularly chloro or bromo, ably chloro, and at least one hydrolysable silane of the formula III where Y is halogen, more particularly chloro or bromo, ably chloro, with an alcohol, more particularly methanol, ethanol, propanol or butanol, preferably ethanol, optionally in the presence of water; with particular preference, on takes place with a molar excess of alcohol in relation to the hydrolysable groups, and the alcohol and/or hydrolysis alcohol are/is removed. 9 PCT/EP2012I071483 in accordance with the invention, the mixture in (ii) comprises the water-soluble alkali metal silicate, such as sodium waterglass or potassium waterglass, and an aqueous solution of one or more alkali metal hydroxides, such as ium hydroxide or sodium hydroxide, or else of an alkaline earth metal ide, such as magnesium ide or calcium hydroxide; an aqueous solution of potassium hydroxide is red.

Particularly preferred s alkaline solutions contain from 5 to 60 wt% of the inorganic base, preferred solutions having a base content of 10 to 40 wt%, more preferably of 20 to 40 wt%, including all intermediate values, as for example 7, 12, 15, 17, 22, 27, 28, 30, 32, 35, 37, 42, 45, 47, 50, 52, 55, 57 wt% - to give but a few of the numerical values. Used customarily are aqueous alkaline solutions having an alkali metal hydroxide content of between 20 to 40 wt%, such as, preferably, aqueous potassium hydroxide ons containing about 33 wt%.

The amount-of—substance ratio in terms of hydrolysable radicals, more particularly X and/or Y, in the e from step (i), preferably with X and Y being alkoxy, to the alkali metal hydroxide and/or alkali metal-O groups in the alkali metal waterglass used, ably of hydroxide ions and 0' ions from alkali metal hydroxide and alkali metal waterglass, is generally 1:15 to 15:1, and is preferably at or between 1:12 to 12:1, in each case including the limiting values, more preferably about 1:10 to 10:1; with ular preference the ratio is 1:8 to 8:1, likewise preferably 1:10 to 1:1, with particular preference about 1:5 to 5:1, with a fluctuation of plus/minus 0.5. Likewise with particular preference, the ratio is 1:1.5 to 1:2.0. Preference is also given to a ratio of about 1:10 with a fluctuation of plus/minus 0.5. Accordingly it is possible, for about 1 mol of hydrolysable ls, to use up to about 10 mol, ably up to 8 mol, of hydroxide, or else, in an alternative procedure, to use, to about 1 mol of hydrolysable groups, about 1 to 5 mol of ide and 0‘ ions, preferably 1 to 2 mol. In the case of the addition to the alkali metal hydroxide solution, the hydrolysable radicals encompass the Hal radicals and/or the alkoxy groups formed by esterification with the alcohol, more particularly of the silanes of the general formulae ll and/or III and also, optionally, of the resultant propyl-functional alkali metal siliconates, silicates, and optionally resultant cocondensation products thereof. ing on process step, therefore, the hydrolysable radical X of the formula II is independently a methoxy, ethoxy, propoxy, , chloro and/or bromo, more particularly ethoxy or chloro, and the hydrolysable radical Y of the formula lll is independently a methoxy, ethoxy, propoxy, butoxy, chloro and/or bromo, more particularly independently ethoxy or chloro.

In the process of the invention, a ntially water—soluble block cocondensate of alkali metal propylsiliconates with alkali metal silicates is preferably prepared by reacting (i) a mixture comprising propylethoxysilane and ally propyl-functional siloxanes derived from a propylchlorosilane of the general formula ll (RUXSiXiy—x) (H) where R1 independently is a propyI-functional radical, more particularly n-propyl and/or isopropyl, preferably n-propyl, and where X is , and optionally from a tetrachlorosilane of the formula lll SiY4 (lll) where Y is chloro, with (ii) a mixture of at least one soluble alkali metal silicate, more particularly sodium waterglass or potassium waterglass, and an aqueous alkali metal hydroxide solution, preferably an aqueous potassium hydroxide or sodium ide solution, the mixture being prepared by reaction of propylchlorosilane of the general a ll with ethanol, more particularly in excess in relation to the hydrolysable , ally in the presence of water, and the excess ethanol and/or hydrolysis alcohol being removed, or, in an alternative, the mixture sing propylalkoxysilane, tetraethoxysilane and/or condensates or cocondensates thereof is prepared by reaction of at least one propylchlorosilane, more particularly a propyltrichlorosiiane, preferably an n-propyltrichlorosilane, and at least one tetrachlorosilane of the formula Ill, with ethanol, more particularly in excess in relation to WO 72185 11 PCTIEP2012I071483 the hydrolysable groups, optionally in the presence of water, and the excess alcohol and/or hydrolysis alcohol are/is removed.

The e from step (i) here, preferably immediately after its preparation, is added in step (ii) to a mixture of a soluble silicate in aqueous alkaline on, and a combination comprising block cocondensates of alkali metal siliconates with alkali metal silicates is obtained by on and cocondensation of hydrolysates of propylalkoxysilanes and tetraalkoxysilanes with block condensates of a silicate. Also preferably, the mixture from step (i) can be ted off and optionally stored, and then 1O added in step (ii) to a mixture of a soluble silicate in aqueous alkaline solution.

It is further preferred here, in the process of the invention, if — alternatively or additionally to the aforementioned features —- the e comprising propylalkoxysilane and/or —si|oxanes derived from a propylhalosilane of the general formula II and optionally from a tetrahalosilane of the formula lll is added to the mixture of a water- soluble silicate in aqueous ne solution, more particularly with intensive mixing, preferably with intensive stirring. With particular preference the mixture is added dropwise and/or with vigorous mixing to the s alkaline solution.

Preferred propyl—functional silanes of the general formula II are propylhalosilanes, such as a n-propyltrihalosilane, isopropyltrihalosilane, di—n—propyldihalosilane or di- isopropyldihalosilane, such as preferably n-propyltrichlorosilane, isopropyl- trichlorosilane, di—n-propyldichlorosilane, isopropyl—, n—propyldichlorosilane or di- pyldichlorosilane, the skilled person also being aware of, and able to use, the corresponding brominated propylhalosilanes or those with mixed halogenation, more particularly comprising chloro and bromo.

Generally speaking, the propylsilane of the formula ll and the silane of the formula III can be used in any ratio, more particularly in a ratio of 1:0 to 0.01:1, more particularly of 1:0 to 0.5 to 1. The outstanding hydrophobizing effect in combination with the good water-solubility is achieved when the propylsilane of the general formula II and the silane of the formula lll are employed in a molar ratio of 1:0 to 3:1. The propylsilane of WO 72185 12 PCT/EP2012I071483 the formula II is preferably used in a ratio to the silane of the formula III of 1:1, in particular with plus/minus 0.5.

According to one ularly red process t, in step (i), an esterification of halosilanes is carried out, by reaction of propylchlorosilane (PCTS) and silane tetrachloride (STC) with ethanol (EtOH): 1 mol (PTCS + STC) + 3.85 mol EtOH -——> Fully esterified intermediate + 3.5 mol HCI Preferably 0.5 mol PTCS + 0.5 mol STC + 3.85 mol EtOH —~> Fully esterified 1O intermediate + 3.5 mol HCI Preferably removal of the excess alcohol.

Step (ii): Reaction of the intermediate from step (i) with 33.3 wt% KOH solution and wt% sodium waterglass: Fully fied intermediate + 33.3 wt% aqueous on KOH + 35 wt% sodium waterglass —> block cocondensates of K propylsiliconate/silicate with silicate (waterglass) + 3.5 EtOH and removal of the alcohol. A composition with very high active ingredient concentration is obtained as the direct process product.

In accordance with a process variant preferred in accordance with the invention, in step (i), a propyltrichlorosilane, of the formula ll, and a tetrachlorosilane, of the formula iii, are introduced as an l charge and ethanol with a 10% molar excess in relation to the hydrolysable halogen radicals is added dropwise with ng. After the end of the reaction, excess ethanol was removed by distillation. In step (ii) the resulting mixture was introduced dropwise with stirring by means of a metering device (without inert gas and introduction tube) into an aqueous mixture of an aqueous 33.3 wt% strength KOH solution and 35 wt% strength sodium waterglass (aqueous sodium waterglass taking account of NaZO). Ethanol formed was d by distillation in step (iii). The composition obtained has an elevated SiOz content and therefore exhibits improved performance even at very high levels of on. It was possible accordingly to achieve 13 PCT/EP2012I071483 sharp improvement in the roll-off properties of the treated substrates (brick, gypsum, concrete, limestone, sand, wall plaster). Particularly good results were ed with propylsilanes of the formula II and silanes of the formula Ill in a molar ratio of 1:0 to 3:1 at the testing stage.

The alcohol used in the first process step may be of technical quality with a certain water content, more particularly with 4 to 10 wt% of water, or may be a water-free alcohol. lf water—containing alcohols are used, formation of alkoxysilanes may be greater in the first process step, and in the second process step they may be at least 1O partly broken down again, whereas if water—free alcohols are used, mixtures comprising propylalkoxysilanes and optionally tetraalkoxysilanes are substantially obtained. The reaction in the first process step is carried out preferably with an excess of alcohol, and so at least some of the hydrohalic acid formed during the reaction can be d by distillation with the alcohol. it is therefore preferred if the alcohol is added in a molar ratio of 0.001:1 to 100:1 in relation to the ysable radicals, in moles. The l is used preferably in a molar ratio of 1:1 to 10:1, more preferably in a ratio of 1:1 to 1:2. With further preference about 1.1 mol of alcohol is added per hydrolysable group. in step (i) alcohol is used preferably at 1 to 200 mol%, more particularly 100 to 150 mol%, in on to the hydrolysable radicals Si—Hal of the compounds II and Ill, the alcohol used being more particularly ethanol. Generally speaking it is preferred to use more than the stoichiometric amount of alcohol, such as EtOH, more particularly 100 to 110 mol%, preferably 105 to 115 mol%, more preferably around 110 mol%, based in each case on the molar amount of the hydrolysable Si—Hal bonds or hydrolysable Hal ls on silicon atoms, preferably of the general formulae ii and Ill.

Surprisingly it has been found that the reaction succeeds reliably if the mixture from step (i), the reaction product, is mixed with an aqueous solution which has been rendered strongly alkaline and comprises a soluble te; more particularly, the solution ought to contain at least an equimolar amount of alkali, preferably hydroxide ions and/or—O', in relation to the hydrolysable radicals Si-alkoxy and/or Si—Hal of the 14 PCT/EP2012I071483 silanes of the formulae II and Ill, preference being given to 1 to 2 mol of hydroxide ions per mole of hydrolysable radical. In that case the formation of solid silicatic particles or ts can be prevented to particularly good effect. A particular feature of this process is that the mixture from step (i) can be added dropwise directly in step (ii) to a mixture of an alkali metal silicate in aqueous ne solution; more particularly, the mixture from step (i) is introduced in portions, preferably dropwise with mixing, such as stirring, into the solution. Particular measures to prevent the formation of precipitates are not necessary, in contrast to the situation with a s arily involving direct jetting into the solution, since the alkali metal silicates in the initial charge make a contribution to solubilizing the mixture that is added se. The particular advantage of the invention is manifested in the direct formation, ing to the process, of clear aqueous ons with no instances of sedimentation or precipitation.

In accordance with the invention, in step (iii), the resulting composition is freed from the hydrolysis alcohol and any added l, and may be diluted further with water as and when required. The alcohol and/or ysis alcohol are/is preferably d by distillation. The active ingredient concentration may likewise be adjusted to a desired level by addition of water and removal of hydrolysis alcohol. It is possible for water to be added to the same extent that alcohol and/or hydrolysis alcohol are/is removed. The desired active ingredient concentration can also be reduced as desired by addition of water. Generally speaking, however, the alcohol—containing composition obtained, or the composition after removal of the alcohol, is already usable and le for application, t addition of water. An advantage of the purely aqueous, alcohol-free composition is its reduced VOC content in the subsequent application. In accordance with the invention, the alcohol is removed from the solution by distillation to give a VOC- reduced solution which is directly usable and can be diluted further with water easily as and when required.

According to one particularly preferred process t, in the s of the invention, a ntially water-soluble block cocondensate of alkali metal propylsiliconates with alkali metal silicates is preferably prepared by preparing in step (i) a mixture comprising propylethoxysilane, tetraethowsilane and optionally propyl—functional nes, by reacting a propyltrihalosilane of the general formula ll, preferably propyltrichlorosilane, 15 PCTIEP2012/071483 and a tetrahalosilane of the formula III, preferably tetrachlorosilane, employed in particular in a molar ratio of 120.5 to 3:1, preferably approximately in a molar ratio of 1:1, with an alcohol, preferably ethanol, the alcohol, preferably ethanol, being used in a molar excess in relation to the hydrolysable halogen radicals of the formulae II and Ill, preferably in about 20% molar excess, preferably in 10% molar , with unreacted alcohol being removed by distillation thereafter; and in step (ii) the mixture prepared in (i) is reacted with a mixture of at least one water-soluble alkali metal silicate, more particularly sodium waterglass or potassium waterglass, and an aqueous alkali metal ide solution, preferably an s potassium hydroxide or sodium hydroxide solution, the mixture containing preferably 1 to 5 mol, more preferably 1 to 2 mol, of O/hydroxide groups per hydrolysable alkoxy group, and in step (iii) the hydrolysis alcohol formed is removed by distillation. AlkaliO is considered to be the alkaliO groups in the alkali metal waterglass.

Generally speaking, the composition, more ularly the l-free composition, can be adjusted directly during its preparation to a level of block cocondensates of alkali metal propylsiliconates with alkali metal silicates of 1 to 80 wt%, and to all values in between, based on the total weight of the composition — it is directly ready for use — it may preferably be adjusted to a level of 1 to 60 wt% in relation to the overall composition, alternatively to 30 to 60 wt%, more preferably to 40 to 60 wt% or else to 45 to 55 wt%. The active ingredient content or level is the amount of block cocondensates, taking into account the alkali metal ions, or alkali metal oxides and charge-neutral compounds, i.e. the amount of the alkali metal siliconate and alkali metal silicate block cocondensates and of the alkali metal silanolates and alkali metal tes.

According to the process of the ion it is possible, therefore, to prepare very highly concentrated compositions. These highly concentrated compositions are stable on storage, ably over 6 months, more preferably around 12 months. As and when necessary, the composition may be diluted prior to use, Le. a purely aqueous, substantially alcohol-free composition, with water and/or with an organic t, to a level of block ensates of alkali metal propylsiliconates with alkali metal silicates of 1 to 60 wt% in relation to the overall composition, and to all values lying in between, 16 PCT/EP2012I071483 preferably to 1 to 30 wt%, or preferably to 1 to 20 wt%, more preferably to 1 to 10 wt%, and also to 1 to 5 wt%.

The level is also directly related to the mineral building al employed and/or to the type of application. For instance, for application to surfaces, solutions with a low level may be suitable, and, for example, in the case of hydrophobizing in the bulk material, solutions with a high level may be le, especially in the case of the hydrophobizing of gypsum-containing l building materials. Highly concentrated compositions may likewise be preferred, if water in the form of make—up water is already added during hydrophobizing in the bulk material. Generally speaking, the active ingredient content (of block cocondensates, taking account of alkali, alkali metal silanolates and alkali metal silicates) can also be from or between 1 to 10 wt% in the composition, or, depending on application, 1 to 5 wt%, 5 to 10 wt%, 10 to 15 wt%, 15 to 20 wt% or 20 to wt%, or else 30 to 40 wt%, or from or between 40 to 60 wt%. The SiOz t of the overall composition, in the prepared or to-use composition, is preferably 5 to wt%, more particularly 8 to 20 wt%, preferably 10 to 15 wt%, more preferably 12 to 14 wt%. The SD; content may be determined by methods known to the skilled person.

During the preparation of the mixture of propylsilane of the a II, the silane of the formula III and alcohol or alcohol/water mixture, the ature rises in step (i) as a uence of reaction. In accordance with the process, the temperature in step (i) ought not to exceed 80°C, and with particular preference the temperature is not to exceed 60°C; cooling is carried out where appropriate. In step (ii) as well, there is some on—induced increase in the temperature, but it is not to exceed 60°C, preferably 50°C; in other words, where appropriate, cooling takes place in step (ii), or the mixture from step (i) is introduced more slowly, in ns, into the mixture of step (ii). In step (iii), preferably, the alcohol and/or hydrolysis l are/is removed, more particularly under reduced pressure in a manner such that the temperature does not rise above 80°C, preferably not above 60°C. in the process of the invention, in step (i), the alcohol and/or in step (iii) the alcohol/hydrolysis alcohol, are/is removed, more particularly the alcohol/hydrolysis alcohol is removed by distillation, preferably under reduced pressure and at elevated 17 PCTIEP2012I071483 temperature. Distillation takes place preferably at below 300 mbar, more preferably below 180 mbar, preferably in each case less than or equal to 10 mbar and more particularly at about 50°C.

In the case of the introduction of the mixture from step (i) into the mixture in step (ii) comprising alkali metal silicates and alkali metal hydroxide ions; as ural elements, i.e. as block condensates MO[Si(Y)2]mOM, also identified as block condensates B; in an aqueous solution there may be ion of propyl-functional alkali metal siliconates, such as MO[Si(R1)XY((y-2)-X)O]aM of the idealized formula IV or R1)XO"((y-2)-X)O]aM + Ma of the idealized formula Na, and MO[Si(R1)XY((y-2)-X)O]cM of the idealized formula lVb or MO[Si(R1)XO'((y.2)_X)O]cM + MC of the idealized formula ch, alkali metal silicates, such as MO[Si(Y)2]bOM of the idealized formula V, and ensation products thereof.

These propyl—functional alkali metal siliconates of the formulae N, Na, Nb and NC and alkali metal silicates in the formula V, depicted in idealized form, may form ndensates and/or cocondensates, as shown in idealized form in the general formula I as MO[[Si(R1)XY((y-2)-X)O]a[Si(Y)2]b[Si(R1)XY((y-2)_X)O]C]nM (l), with M being t in the ition in a number such that the block cocondensate is - neutral. In the case of formation of homocondensates, a is greater than or equal to 1, c is greater than or equal to 0 and b is O, or a is O, c is O and b is greater than or equal to 1. in the case of ion of ensates, a and b are greater than 1 and c is greater than or equal to 0, preferably greater than or equal to 1. These homocondensates and/or cocondensates are identified as block condensates A, and the silicate blocks are identified as block condensates B, and according the general formula I may also be represented as MO[A]n [B m]OM (l), or as MO[[Si(R1)xYay-2)-x)01aisimzibisi<R1)xviiyaiximcln[iSi<Y>2im]OM (I) In accordance with the process of the invention, preferably in the case of the reaction at elevated temperatures, block cocondensates are formed which have blocks of cocondensates derived from propylalkoxysilanes and tetraalkoxysilanes, which undergo condensation with alkali metal silicate blocks that are present in the mixture. Because of 18 PCT/EP2012l071483 the ively adjusted pH in step ii, a defined molecular weight of the alkali metal silicates (alkali metal waterglass) is formed at the same time under the process conditions, and these silicates are then able to react with the cocondensates. It is therefore assumed that in view of the specific procedure in step (ii), block cocondensates are formed in line with the formula 1 depicted in idealized form, with R1 being n—propyi or pyl and each Y independently being 01/2 in a siioxane bond or OH or OM, where M is a monovalent alkali metal ion, such as Na+ or K“, or 1/2 an alkaline earth metal ion, such as 1/2 Ca2+, in —ONa, -OK, or optionally hydrogen for —OH, with x, y, a, c and b being as defined above, the ratio (a+c)/(b+m) being preferably less 1O than 1, and being situated more particularly in the range from 0.11 to 0.5.

Likewise provided by the invention is a composition obtainable by the s of the invention, comprising a water-soluble block cocondensate of alkali metal propylsiliconates with alkali metal silicates, with a pH 2 11, the pH more particularly being 14. Likewise provided by the invention is a composition obtainable by the process of the invention that is substantially alcohol-free and/or that has preferably block cocondensates of alkali metal propylsiliconates with alkali metal silicates, more preferably sodium silicate, ium silicate, and more particularly the block cocondensates of alkali metal propylsiliconates with alkali metal silicates are present in a mixture with monomeric alkali metal propylsilanolates and/or alkali metal silicates.

The invention further provides the use of a composition of the invention or of a composition prepared by the process of the invention for the hydrophobizing of wood, cellulosic building als and/or lignocellulosic ng materials, for the hydrophobizing of mineral ng materials, for the hydrophobizing of the surface of mineral building materials and/or for the hobizing of mineral ng materials in the bulk material. The use of the composition here may be used for hydrophobizing a part of the mineral building material or else for hobizing the entire mineral building material, in each case encompassing concrete, screed, plaster, gypsum, , loam, clay, sand, ceramic, terracotta, lime sandstone, natural stone, such as sandstone, marble, granite, and also articles consisting thereof or articles comprising them, such as shaped parts, which comprise, for example, pipes, bricks, paving slabs, 19 PCTIEP2012I071483 walls, tiles, garden containers, roof tiles, and also further customary mineral building materials known to the skilled person, and articles composed of these building materials. Likewise ed by the invention is the use of a composition of the invention as an ion composition for forming barrier , more particularly for forming horizontal and/or vertical barrier layers in masonry constructions or floors. The injection composition may be injected without pressure or with pressure into drilled holes. The r layers produced accordingly provide effective protection from rising damp in the masonry.

The examples which follow provide r elucidation of the process of the invention and of the inventive use, without confining the invention to these examples. 20 PCT/EP2012l071483 Examgles Determination of the molecular weight: Molar masses or the molecular weight and also the molar mass distribution may be determined by gel tion chromatography (GPC). One of the publications to give a comprehensive description of the GPC analysis method is "Modern Size-Exclusion Liquid Chromatography", Andre Striegel et al, Wiley & Sons, 2nd Edn. 2009. Polyethylene oxide/polyethylene glycol, for example, can be used as rds to calibrate the method. The polydispersity (D) is the ratio of Mw/Mn.

The weight average of the molecular weight (Mw) is defined as: niM'? A1“. 2m2 2 mill, and the number average of the molecular weight (Mn) is defined as: M _Z’7;Mi _ n Zn,- where in each case: n,- = molar amount [mass] of the i-mer M; = molar mass of the i-mer Details relating to the tion of weight average and number average, which are known per se to the skilled person, may atively be found by the reader in locations including the Internet, at http://de.wikipedia.org/wiki/Molmassenverteilung, or in a standard work of mathematics.

Example 1 Preparation of an approximately 50% strength aqueous solution of K propylsiliconate/silicate Step (i): A 500 ml round-bottomed flask with stirrer, reflux condenser and dropping funnel was charged with 100 g of a 1:1 mixture (based on the molar composition) of propyltrichlorosilane and hlorosilane. With vigorous ng, 102.2 g of ethanol 21 PCT/EP2012I071483 were slowly added dropwise. The temperature rose during the addition. However, it ought not to rise above 60°C. Where necessary, counter-cooling was d out. ing complete addition of the ethanol, stirring was continued for 30 minutes more, and the resulting intermediate was used further directly. The excess l was distilled off overhead.

Step (ii): A 1000 ml round—bottomed flask with stirrer, reflux condenser and dropping funnel was charged with 311 g of a 33.3% strength aqueous KOH solution and 108 g of % strength sodium waterglass. A dropping funnel was charged with 100 g of the product from the first reaction step. The intermediate was then added dropwise with 1O vigorous stirring to the KOH/sodium waterglass mixture. Following complete addition, a slightly turbid product was obtained. It was stirred further at 50°C for 30 minutes. The ethanol formed was removed by lation. This gave a clear product of low viscosity.

GPC analysis: Fraction of relatively high molecular mass block ensates with MW around 1200 g/mol with D = 1.0 (Mn = 1.1x103 g/mol) at about 62.1%, and a further fraction of low molecular mass silicates and/or silanolates with MW around 110 g/mol with D = 1.1 (Mn = 1.1x102 g/mol) at about 37.9%. The overall molecular weight average MN is around 760 g/mol with D = 5.3 (M, = 1.4x102 g/mol). 298i NMR: about 24.2% CgHy-Si(0‘)3, about 75.8% Si(O')4.

Comparative example 2 Around 54% of potassium methylsiliconate solution (corresponding to around 34% of methylsiliconate solution without taking account of around 20 wt% K20).

Tests on the reaction ts from the examples: The reaction products from Example 1 and from Comparative e 2 were used in a 1:20 dilution with water. Solid Poroton full-brick cubes with an edge length of 50 mm were conditioned at 25°C and 60% ve humidity for 24 hours and then ed for seconds into the diluted preparations from Example 1 and Comparative e (C- example) 2. Adhering re was removed by gentle dabbing of the surfaces with a 22 PCTIEP2012I071483 paper cloth. The treated specimens were subsequently stored at 25°C and 60% relative humidity for 14 days in a manner which allowed air to enter from all sides. The ion in water absorption by these specimens was determined in accordance with DIN EN 13580. The percentage ion here was calculated by comparison with an untreated specimen of the same kind. Table 1 below shows ption quantities and also reduction in water absorption, and Henkel test results.

The roll-off effect was determined by using a Pasteur pipette to place approximately 1 ml of DI water on the hydrophobized specimen. After 10 minutes, the drop of water 1O was shaken off and the degree of wetting was assessed visually (ratings: 0 = water rolls off, 1 = no wetting, 2 = half of contact area wetted, 3 = entire contact area , 4 = dark coloration of the contact area, drop imbibed to some extent, 5 = dark coloration of the contact area, drop imbibed 50%, 6 = dark coloration of the t area, drop d fully). ‘ pplication ate --Product from Brick --Product from C— Brick Table 1: ReductionIn water absorption and Henkel test of brick treated with products from the examples.

It is clearly apparent that it was possible to achieve a further reduction in water 2O tion in conjunction with a significantly enhanced Henkel test outcome.

Additionally, cylindrical plaster specimens were produced from a commercial plaster from Knauf, with a water-to-plaster ratio of 0.5. Added to the aqueous plaster slurry were 1, 2 or 3 wt% (relative to the plaster powder) of the reaction product from Example 1 (neat) and 3 wt% from comparative e 2 (neat). The plaster specimens 23 PCT/EP2012I071483 had a diameter of 50 mm and a height of 25 mm and were cast in PE forms. The plaster specimens were cured at 25°C and 60% relative humidity for 28 days, and the form work was removed after 2 days under these conditions. Subsequent storage was carried out in a manner which d air to circulate freely from all sides. The water absorption was determined in accordance with DIN EN 520. The results can be seen from Table 2 below.

Plaster specimen ater absorption [%] Plaster en + 1 wt% of t from 11.1 -_Plaster specimen + 2 wt% of product from 0.7 _—Plaster specimen + 3 wt% of product from 0.2 ——Plaster specimen + 3 wt% of t from 0.5 Table 2: Water absorption of plaster specimens It is clearly apparent that the product of the invention exhibits greatly improved performance relative to the known product, not only on bricks but also in plaster, as bulk material hydrophobization.

Claims (1)

Claims

1. Composition comprising substantially water-soluble block oocondensates of alkali metal propylsiliconates with alkali silicates and water, the block cocondensates having inking structural elements which form catenary, cyclic, crosslinked and/or dimensionally crosslinked structures, and at least one structure corresponds in zed form to the general formula I, MO[[Si(R1)xv«y-2)-x)013isimzibisrR‘)xvriy-2)-x)01c]n [[Si(Y>21m]OM (i), where, in the structural elements derived from alkoxysilanes and silicates, — R1 corresponds to a propyl l, - Y corresponds, in each case independently, to CM or OH or, in crosslinked and/or three-dimensionally crosslinked structures, independently at each 15 occurrence,