EP2655517A1

EP2655517A1 - Hydrosilylation reaction inhibitors and use thereof for preparing stable curable silicone compositions

Info

Publication number: EP2655517A1
Application number: EP11808905.1A
Authority: EP
Inventors: Sébastien MARROT; Yassine Maadadi
Original assignee: Bluestar Silicones France SAS
Current assignee: Elkem Silicones France SAS
Priority date: 2010-12-24
Filing date: 2011-12-20
Publication date: 2013-10-30
Also published as: KR101553456B1; US20140004359A1; KR20130109215A; WO2012085364A1; JP2014507501A; CN103370376A; BR112013016067A2; JP5753909B2; CN103370376B

Abstract

The present invention relates to the use of inhibitor compounds, in particular to the use of inhibitor compounds that are suitable for inhibiting the curing of a silicone composition, which is a silicone-elastomer precursor, obtained by means of a hydrosilylation reaction.

Description

HYDROSILYLATION REACTION INHIBITORS AND THEIR APPLICATION FOR THE PREPARATION OF STABLE CURABLE SILICONE COMPOSITIONS.

The present invention relates to the use of inhibiting compounds, in particular inhibiting compounds suitable for inhibiting the curing of a silicon elastomer precursor silicone composition obtained by a hydrosilylation reaction.

The hydrosilylation reactions are widely used in the silicone industry to not only access functionalised silanes or siloxanes but also for the preparation of silicone networks obtained by crosslinking between polymethylhydrogenosiloxane and polymethylvinylsiloxane oils. These reactions are generally carried out by organometallic platinum catalysis and especially Karstedt platinum, which is appreciated for its high reactivity and its solubility in a silicone medium. In these conditions, the hydrosilylation reactions have rapid kinetics at room temperature and only a few tens of ppm (part per million) of catalyst are required to complete a reaction in a few minutes. Silicone compositions that can be crosslinked by hydrosilylation reactions are therefore used to form water-repellent or non-adhering coatings or films on paper or polymer film supports.

However, for these applications, it is necessary to temporarily inhibit the hydrosilylation reaction in order to have time to prepare, transport and implement the formulation bath. The temporary inhibition of the polyaddition systems is made possible by the use of organic compounds which act as temperature-activatable thermal inhibitors or by the use of UV-activated photonic catalytic systems. For example, for the paper release application, it is required that the formulation bath remains liquid for several hours at room temperature and that the crosslinking is extremely rapid (a few seconds) when the bath is deposited on support and introduced into ovens coating material whose temperature is maintained between 100 and 150 ^Ù C. When it is necessary to increase the pot life of crosslinkable organopolysiloxane compositions and / or curable by a polyaddition reaction, it is customary to incorporate a hardening inhibitor. Curing inhibitors are compounds that slow curing at ambient temperatures, but do not delay curing at higher temperatures. These curing inhibitors are sufficiently volatile to be removed from the coating compositions. it is known, see for example US Pat. No. 3,445,420, to use α-acetylenic compounds, such as acetylenic alcohols having a boiling point of less than 250 ° C., especially 2-methyl-3-butyne 2-ol. and ethynylcyclohexanol (ECH), as hydrosilylation inhibitors in curable silicone compositions based on an organosilicon polymer bearing olefinically unsaturated substituents (especially vinyl), an organohydrogensiloxane polymer and a platinum or platinum.

The presence of these acetylenic compounds inhibits the platinum catalyst by preventing it from catalyzing the curing reaction at room temperature, but not at elevated temperature. Indeed, the hardenable silicone compositions which contain this type of inhibitor can be cured by increasing the temperature of the composition to a temperature above the boiling or sublimation point of the inhibitor, thus evaporating the inhibitor, or part of the inhibitor, and allowing the catalyst to catalyze the hydrosilylation reaction and thereby cure the silicone composition.

However, although widely used, ethynylcyclohexanol (ECH) has the disadvantage of being unable to be conditioned in the presence of a widespread platinum catalyst arstedt platinum during storage of these compositions before use. Indeed, if these two compounds are in the presence of each other at room temperature (20 ° C), precipitation of platinum in the form of colloids which strongly color the formulation (appearance of a yellow coloration which turns black after only a few hours). This is a major problem for storing such compositions. For this reason, the silicone polyaddition compositions employing true α-acetylenic alcohols such as ECH are conditioned, prior to their use, in the form of "multi-component", that is to say that the constituents of the composition are placed in separate parts (or

components) so as to separate:

the catalyst inhibitor to avoid color problems, and

the organohydrogenosiloxane polymer of the catalyst for reasons of safety.

Thus, a conventional polyaddition silicone composition for application in paper anti-adhesion is conditioned before its use in multi-component

currently comprising 3 or 4 distinct parts:

- A Part ¹ (l) comprising at least polyméthylvinyîstloxanes and the inhibitor of the hydrosilylation reaction which provides stability and implementation formulations,

- A ^2nd part (ii) comprising at least one hydrogen siloxane polymer, - A 3 ^Θ portion (III) comprising a platinum-based catalyst, and

- possibly a part ⁴ (IV) formulations comprising additives providing intrinsic properties to the desired applications. It is known that when using these compositions packaged in the form of the mufti-component, the parts (I) and the catalyst part (III) should not be directly mixed. It is for this reason that the current practice consists in premixing the parts (I) and (II) comprising the polymethylvinylsiloxanes and the hydrogenosiloxane polymers before introducing the catalyzing part (III) thus avoiding the phenomenon of precipitation of the catalyst and coloring of the composition.

Of the inhibitors of the hydrosilylation reaction, α-α'-acetylenic diols do not exhibit these problems. They can be brought into contact with the platinum catalyst without leading to the precipitation phenomenon described above. This has the advantage of reducing the number of components for the polyaddition system. However, they are insoluble inhibitors in silicone medium leading to opaque formulations. This explains their limited use especially for paper non-stick application where transparency is an essential criterion. In addition, the compositions comprising α-α'-acetylenic diols, such as for example the compound 2,4,7,9-tetramethyl-5-decyne-4,7-diol (TMDD), most often have a time crosslinking at room temperature faster than those comprising a true α-acetylenic alcohol (ECH for example). This also explains their limited use especially for the paper release application where the time of crosslinking at room temperature must be substantial so as to prepare the production of the coated media effectively without adding an additional constraint related to the stability of the baths. coating (gelling problem comprising the silicone compositions).

It is therefore clear that the prior technical proposals do not provide satisfactory solutions especially for demanding applications such as tending on silicone composition substrates to prepare water-repellent coatings.

One of the essential objectives of the present invention is to provide a silicone composition X capable of hardening by a polyaddition reaction which:

no longer has the problem of precipitating the platinum catalyst when it is conditioned in the presence of an inhibitor during the storage thereof, is stable for several hours at room temperature, when all the constituents of the composition are mixed before the use of the composition, in particular during machine coating operations; and

- Fast reticulate on support at a conventional curing temperature of between 100 and 180 ° C.

Another essential objective of the present invention is to provide a coating process on a flexible support using a composition according to the invention. Thus, the main object of the invention consists of a crosslinkable and / or curable composition X by polyaddition reactions in the form of a multi-component system S comprising at least two distinct parts A and B intended to be mixed. to form a composition X 'in which:

(a) Part A includes:

at least one polyorganosiloxane V comprising, per molecule, at least two alkenyl radicals bonded to silicon atoms,

at least one catalyst E composed of at least one metal belonging to the platinum group and preferably a Karstedt platinum,

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

at least one organic acid or a mineral acid D2, with the proviso that the mineral acid does not contain platinum such as chloroplatinic acid, and

(b) Part B includes:

at least one polyorganosiloxane H having, per molecule, at least two hydrogen atoms bonded to an identical or different silicon atom.

By "mineral acid" it is understood that this term does not include platinum acid derivatives such as chloroplatinic acid which are known as a catalyst. The Applicant has found quite unexpectedly, which is precisely the subject of the present invention, that the use, as a hydrosilylation inhibitor of an α-α'-acetylenic diol combined with an organic acid or mineral in the same part of a composition packaged in multi-component for its storage allows:

to improve the solubility of the α-α'-acetylenic diol inhibitor in a silicone medium, resulting in a perfectly transparent and colorless mixture,

to maintain a small number of components of the system compared to the case where the inhibitor is of the true α-acetylenic alcohol type, and to improve the inhibition time at ambient temperature compared to an identical acid-free system while having inhibition-raising temperature performances comparable to true α-acetylenic alcohols such as TECH.

According to a preferred embodiment, the composition X according to the invention is such that:

(a) Part A includes:

at least one catalyst E composed of at least one metal belonging to the platinum group and preferably a platinum of arstedt,

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

at least one organic acid or a mineral acid D 2 selected from the group consisting of orthophosphoric acid, orthophosphorous acid,

sulfuric acid, sulfurous acid and thiosulfuric acid, and

(b) Part B includes:

at least one polyorganosiloxane H having, per molecule, at least two hydrogen atoms bonded to an identical or different silicon atom,

According to a preferred embodiment, the composition comprises a third part C comprising at least one additive F and which is distinct from parts A and B.

Preferably, the inhibitor D1 is an σ-α'-acetylenic diol of formula (1) below:

(R ¹ ) (R ² ) (OH) CC≡CC (OH) (R ³ ) (R ⁴ ) (1)

in which the radicals R ¹ , R ² , R ³ and R ⁴ , which are identical or different, represent, independently of one another, a linear or branched monovalent alkyl group, a cycloalkyl group, a (cycloalkyl) alkyl group, a group aromatic or arylalkyl group, and

the radicals R ¹ , R ² , R ³ and R ⁴ may be linked in pairs so as to form a 5-, 6-, 7- or 8-membered aliphatic ring optionally substituted by one or more substituents.

Preferably, the inhibitor D1 is selected from the group consisting of α-α'-acetylenic diols of

4 J ^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^ diol

3, 6-dî¾fihy! »» »» »»

Preferably, the molar ratio [D1 inhibitor] / [D2 acid] is between 0.1 and 20 and preferably between 1 and 10 and even more preferably between 2.5 and 6.5.

According to a preferred embodiment, the acid D2 has in aqueous solution and at 25 ° C at least one pKa whose value is in the following interval: -0.9 p pKa≤ + 6.5. Examples of the acid D2 which are useful according to the invention are, for example, chosen from the group consisting of the following acids:

methanoic acid, ethanoic acid, propanoic acid, butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid , dodecanoic acid, hexadecanoic acid, octodecanoic acid, benzoic acid, ethanedioic acid, acid, 3-propanedioic acid, 1,4-butanedioic acid, acid 1, 5- pentanedioic acid, 6-hexanediol ^'fque, benzenecarboxylic acid, cyclopentanecarboxylic acid, para-aminobenzoic acid, adipic acid, ortho-aminobenzoic acid, benzoic acid, citric acid lactic acid, maleic acid, malic acid, malonic acid, mandelic acid, pyruvic acid, salicylic acid, succinic acid, oxalic acid, glutaric acid , phthalic acid, benzene-1,4-dicarboxylic acid, picric acid, pimelic acid, fumaric acid, pimelic acid, glycolic acid, sebacic acid ee, chloroethanoic acid, dichloroethanoic acid, trifluoroacetic acid, ascorbic acid, dichloroethanoic acid, trichloroacetic acid, tartaric acid, boric acid, chlorosulfuric acid, acid Fluoroboric acid, fluorosulfuric acid, nitric acid, perchloric acid, phosphoric acid, sulfuric acid, orthophosphoric acid, orthophosphorous acid, periodic acid, sulfurous acid and thiocyanic acid, thiosulfuric acid.

According to another preferred embodiment, the acid D 2 is chosen from the group consisting of: methanoic acid, orthophosphoric acid, heptanoic acid, trifluoroacetic acid and malonic acid.

It is advantageous that the molar ratio [inhibitor D1] / [catalyst C] is between 0 and 60 and the molar ratio [acid D2] / [catalyst C] is between 10 and 60.

According to a variant of the invention, the proportions of the polyorganosiloxane V and of the organohydrogenpolysiloxane H are such that the molar ratio of the silicon-bonded hydrogen atoms in the organohydrogenpolysiloxane H on the silicon-bonded alkenyl radicals in the organopolysiloxane V is between 0.4 and 10.

Advantageously, the polyorganosiloxane V according to the invention has;

at least two siloxyl units of formula (V.1):

T _to Z _b Si0 ₄ . _(a * _b ) / 2 (V.1)

in which :

T is an alkenyl group,

Z is a monovalent hydrocarbon group selected from the group consisting of alkyl groups having 1 to 8 carbon atoms inclusive, optionally substituted by at least one halogen atom, and aryl groups, and

a is equal to 1 or 2, b is equal to 0, 1 or 2 and the sum a + b is between 1 and 3, and

optionally at least a part of the other siloxyl units are units of formula (V.2):

in which:

Z has the same meaning as above and c is 0, 1, 2 or 3.

In general, the organopolysiloxane V has a viscosity at least equal to 50 mPa.s and preferably less than 200,000 mPa.s.

Advantageously, the hydrofluoropolysiloxane H according to the invention has:

at least two, and preferably at least three, siloxyl units of formula (H.1):

H, j L _e Si0 _4- (d + e) / 2 (H.1) in which:

L is a monovalent hydrocarbon group, which has no adverse effect on the activity of the catalyst and is selected from the group consisting of alkyls having 1 to 8 carbon atoms inclusive, optionally substituted with at least one halogen atom, and the aryls,

H is a hydrogen atom, and

d is 1 or 2, e is 0, 1 or 2, the sum d + e is 1, 2 or 3, and

optionally, at least a part of the other siloxyl units are units of formula (H.2):

Lg Si0 ₄ .g, ₂ (H.2)

in which:

L has the same meaning as above and g is 0, 1, 2 or 3. In general, the dynamic viscosity of organohydrogenpolysiloxane H is at least 10 mPa.s and preferably and 1000 mPa.s.

Advantageously, the proportions of the polyorganosiloxane V and the polyorganosiloxane H are such that the molar ratio of the silicon-bonded hydrogen atoms in the polyorganosiloxane H to the silicon-bonded alkenyl radicals in the polyorganosiloxane V is between 0.4 and 10. In particular, the proportions of the siloxyl units (V.1) and (H.1) are such that the molar ratio of the silicon-bonded hydrogen atoms in the organohydrogenpolysiloxane H to the silicon-bonded alkenyl radicals in the organopolysiloxane V is between 0.4 and 0.

According to a variant of the invention, the silicone composition X according to the invention may comprise one or more additives that are conventional in the field of non-stick silicone coatings for solid support, for example made of paper. It may be for example an anti-misting additive such as silica particles, or branched polyorganosiloxanes, etc.

According to another variant, the silicone composition X according to the invention may also comprise an adhesion modulator system as well as additives customary in this type of application such as. bactericides, antifreezes, wetting agents, defoamers, fillers, synthetic latices or dyes. Another object of ^the invention is a composition siticone X 'obtained by mixtures of the parts of the composition X as described above.

The silicone composition X 'according to the invention can be applied using devices used on industrial paper coating machines such as a five-roll coating head, air knife or bar systems. equalizer, on supports or flexible materials, then hardened by circulation in tunnel kilns heated to 70-200 ° C; the passage time in these furnaces is a function of the temperature; it is generally of the order of 5 to 15 seconds at a temperature of the order of 100 ° C and of the order of 1, 5 to 3 seconds at a temperature of about Ι δΟΧ.

The silicone composition X 'can be deposited on any flexible material or substrate such as papers of various types (supercalendré, coated, glassine), cardboard, cellulose sheets, metal sheets, plastic films (polyester, polyethylene, polypropylene. .) ...

The amounts of deposited compositions are generally of the order of 0.1 to 5 g per m ² of surface to be treated, which corresponds to the deposition of layers of the order of 0.1 to 5 pm. The materials or supports thus coated may subsequently be brought into contact with any pressure sensitive rubber, acrylic or other adhesive materials. The adhesive material is then easily detachable from said support or material.

All the viscosities referred to herein correspond to a dynamic viscosity quantity which is measured, in a manner known per se, at 25 ×.

In the rest of the present application, the polyorganosiloxane oils will be conventionally described using the usual notation in which the letters M, D, T and Q are used to designate various siloxyl units. In this notation, the silicon atom of a siloxyl unit is engaged in one (M), two (D), three (T) or four (Q) covalent bonds with as many oxygen atoms. When an oxygen atom is shared between two silicon atoms, it is counted for ½ and it will not be mentioned in an abbreviated form. On the other hand, if the oxygen atom belongs to an alkoxyl or hydroxyl group bonded to a silicon atom, this chemical function will be indicated in parentheses in the abbreviated formula. By default, it is considered that the remaining bonds of the silicon atom are engaged with a carbon atom. Generally, silicon-bonded hydrocarbon groups via a C-Si bond are not mentioned and most often correspond to an alkyl group, for example a methyl group. When a hydrocarbon group has a particular function, it is indicated by exponent. For example, short forms;

- M ^{V |} represents a unit in which the silicon atom is bonded to an oxygen atom and one of the C-Si bond-forming hydrocarbon groups is a vinyl group, i.e. a diaikylvinylsiloxyl unit, and

M 'represents a unit in which the silicon atom is bonded to a hydrogen atom, to an atom and to two methyl groups. As a reference work, mention may be made of: NOLL "Chemistry and Technology of Silicones", Chapter 1.1, page 1-9, Académie Press, 1968 - 2nd edition.

According to another of its aspects, the present invention relates to a silicone elastomer Y obtained by crosslinking or curing the silicone composition X 'according to the invention and as described above,

The present invention also relates to the use of the silicone composition X 'according to the invention as a coating base for the production of crosslinked elastomeric anti-adhesive and water-repellent coatings on a solid support, preferably a flexible solid support such as a paper, a cardboard, a cellulose sheet, a metal sheet or a plastic film.

Another subject of the invention consists of a solid support at least partly coated with the silicone composition X 'according to the invention and as described above, and crosslinked or cured by heating at a temperature greater than 6G ° C and preferably between 70 ° C and ^200th C or Y silicone elastomer according to the invention and as described above. The present invention also relates to a coating process on a flexible support

S comprising the following steps a), b), c) and d);

a) a silicone composition X according to the invention and as described above is prepared,

b) the parts of the silicone composition X are mixed to form a composition X

c) then said silicone composition X 'is deposited continuously or discontinuously on said flexible support S, and d) is crosslinked the silicone composition X 'by heating at a temperature above 60 ° C and preferably between 70 ° C and 200 ^D C.

Preferably, the flexible support S is made of paper, textile, cardboard, metal or plastic.

For example, the flexible support S may be of textile, paper, polyvinyl chloride (PVC), polyester, polypropylene, polyamide, polyethylene, polyurethane, non-woven fiberglass fabrics or polyethylene terephthalate (PET).

Finally, the last subject of the invention concerns a silicone composition comprising;

at least one catalyst C composed of at least one metal belonging to the platinum group,

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

at least one organic acid or a mineral acid D2, with the proviso that the mineral acid does not contain platinum such as chloroplatinic acid

This composition is useful as part A of the composition X according to the invention.

The following non-limiting examples will make it possible to better understand the invention and to grasp all its advantages and variants.

EXAMPLES

Products used

End-chain vinylated polydimethylsiloxane oil (V.1): of average formula I 'DrsI T and viscosity at 25 ° C = 100 mPa.s.

End-chain vinylated polydimethylsiloxane oil (V.2): viscosity at 25 ° C = 350 mPa.s.

Polymethylhydrogensiloxane oil (H.1): (0.73 mol SiH per 100 g of oil, ie 6.84 mmol of SiH)

Catalyst (C), Karstedt platinum, in the form of a mixture: Pt catalyst (2800 ppm) + polyvinylated polydimethylsiloxane end-chain (V.2).

Inhibitor (D1.I1) (invention): 2,4J, 9-tetramethyl-5-decyne-4,7-diol (TMDD). Inhibitor (D1.C1) (Comparative): 1-Ethynyl-cyclohexanol (ECH).

trifluoroacetic acid (D2.I1): CF ₃ COOH; (pK1 = 0.23).

heptanoic acid (D2.I2): CH ₃ (CH ₂ ) ₅ COOH, (pK 1 = 4.89).

- orthophosphoric acid (D2.I3): (H 3 PO ₄₎ (pK1 = 2.15).

Example 1:

Portions A of silicone compositions cross-linkable and / or curable by polyaddition reactions and packaged in the form of two-component are prepared from the components listed in Table 1 below:

Table 1

The inhibitor (D1.I1) is previously solubilized in the vinylated polydimethylsiloxane oil (V1) at 50 ° C. for 30 minutes before addition to the relevant parts A (parts A1 and A2). At the initiative! the four mixtures (parts A1 to A4) are clear and colorless. They are then stirred at room temperature for 24 hours. and present the following aspects:

Formulation A1 (Invention) is perfectly clear,

the two formulations, Parts A3 and A4 (comparative) containing the ECH and the catalyst Pt took a yellow / brown color indicating the precipitation of a part platinum in the form of colloids. The addition of acid does not prevent the phenomenon of precipitation (Part A4).

- The formulation Part A2 (comparative) has a milky and opaque white appearance.

Example 2

To each of the parts described in Example 1, a portion B containing 0.93 g of a polymethylhydrogensiloxane (H.1) oil was added. A sample for each composition is taken and analyzed in DSC ("Differential Scanning Calorimetry", METLER type device). The analysis is performed in the open aluminum capsule and using a temperature ramp from 25 to 200 ^* 0 with a gradient of 1 Û ° C / min. The time required for the crosslinking at ambient temperature and the bath life are also measured. The thermal profiles, the characteristic data of the exothermic peaks (T ° C peak and ΔΊΡ onset / endset ° C) are represented in the following Table 2.

Table 2: Results by DSC Analysis

Example 3: Demonstration of the improvement of room temperature to inhibit time for muting systems "diol α.α'-acetylenic → ^■ acid" according to the invention.

Portions A of silicone compositions crosslinkable and / or curable by polyaddition reactions and packaged in the form of bicomponent are prepared and mixed with portions B. The resulting compositions are described in Table 3 below: Table 3

A sample for each composition is taken and analyzed in DSC ("Differential Scanning Calorimetry", METLER type apparatus) under the same conditions as in Example 2. The results are described in Table 4 below:

Table 4: Results by DSC Analysis

T ° C peak ΔΊ DeltaH (J / g)

onset / endset

'VS

Composition (I-2) 11 1 26 46

Composition (t-3) 102 27 43

Composition (I-4) 108 29 52

Composition (C-4) 99 36 41 In the presence of acid and compared to the reference composition (C-4), we observe a higher peak T ° C for the compositions according to the invention (I-2), (I-3) and (I-2). 4) indicating a retarding effect of the acids. Moreover, in the presence of acid and compared to the reference, composition (C-4), we observe a lower ΔΤ onset / endset for the compositions according to the invention indicating a decrease in trolling effects at the beginning and at the end of reaction.

We also followed for all the compositions the crosslinking time at room temperature but with a reduced amount of inhibitor T DD (D1.I1) (0.240 mmol). The crosslinking times at room temperature are described in Table 5 below:

Table 5

These results clearly show the retarding effect of organic and inorganic acids relative to the crosslinking time at room temperature.

Claims

CLAIMS - Composition X curable and / or curable by polyaddition reactions in the form of a multi-component system S comprising at least two distinct parts A and 8 to be mixed to form a composition X 'in which:

(a) Part A includes:

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

(b) Part B includes:

at least one polyorganosiloxane H having, per molecule, at least two hydrogen atoms bonded to an identical or different silicon atom; composition X according to claim 1, in which:

(a) Part A includes:

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

at least one organic acid or a mineral acid D 2 selected from the group consisting of orthophosphoric acid, orthophosphorous acid, periodic acid, sulfuric acid, sulphurous acid and thiosulphuric acid, and Part B includes:

- Composition X according to claim 1 wherein there is a third part C comprising at least one additive F and which is distinct from parts A and B. - Composition X according to claim 1 or 2 wherein the inhibitor D1 is a diol a - a'-acéfylènique of formula (1) below: (R) (R ² ) (OH) CC≡CC (OH) (R ³ ) (R ' ¹ ) (1)

Composition X according to any one of claims 1, 2 or 4 wherein the inhibitor D1 is selected from the group consisting of α-α'-acetylenic diols of formulas (2) to

2,4,7 ₍ .9 k katTie1hyl S S-de; yfie-, 7, d1Dl fîMDD) diol

3,6 "d5e¾hyiûci- -yne ^" 3 _f 6-dîd

6 - Siiicone composition X according to claim 1 wherein the molar ratio [D1 inhibitor] / [D2j acid is between 0.1 and 20 and preferably between 1 and 10 and even more preferably between 2.5 and 6.5. 7 - Siiicone composition X according to claim 1 or 6 wherein the acid D2 present in aqueous solution and at 25 ° C at least one pKa whose value is in the following range: -0.9 p pKa≤ +6 5.

8 - Siiicone X composition according to any one of claims 1, 6 or 7 wherein the acid D2 is selected from the group consisting of: methanoic acid, orthophosphoric acid, heptanoic acid, trifluoroacetic acid and malonic acid.

9 - Silicone composition X according to any one of the preceding claims, characterized in that the proportions of the polyorganosiloxane V and the polyorganosiloxane H are such that the molar ratio of silicon-bonded hydrogen atoms in the polyorganosiloxane H on the alkenyl radicals bonded to the silicon in the polyorganosiloxane V is between 0.4 and 10. Silicone composition X 'obtained by mixing the parts of the composition X as described according to any one of claims 1 to 9.

Y-silicone elastomer obtained by crosslinking or curing the silicone composition X 'as described according to claim 10.

12 - Use of the silicone composition X 'as described in claim 10, which is useful as a coating base for the production of crosslinked elastomeric anti-adhesive and water-repellent coatings on a solid support, preferably a flexible solid support such as a paper, a cardboard, a cellulose sheet, a metal sheet or a plastic film.

13 - solid support at least partially coated with the silicone composition X 'as described in claim 9 and crosslinked or cured by heating at a temperature above 60 ° C and preferably between 70 ° C and 200 ° C or silicone elastomer Y as described in claim 1.

14 - Process for coating on a flexible support S comprising the following steps a), b), c) and d):

a) there is prepared a silicone composition X as described according to any one of claims 1 to 9,

b) the parts of the silicone composition X are mixed to form a composition X ',

c) then said silicone composition X 'is deposited continuously or discontinuously on said flexible support S, and

d) the silicone composition X 'is crosslinked by heating at a temperature above 60 ° C and preferably between 70 ° C and 200 ° C. 15 - Coating process according to claim 14 characterized in that the flexible support S is paper, textile, cardboard, metal or plastic.

16 - Coating process according to claim 15 characterized in that the flexible support S is made of textile, paper, polyvinyl chloride (PVC), polyester, polypropylene, polyamide, polyethylene, polyurethane, fabrics non-woven glass fibers or polyethylene terephthalate (PET).

17 - Silicone composition comprising;

at least one inhibitor D1 which is an α-α'-acetylenic diol, and

at least one organic acid or a mineral acid D2, with the proviso that the mineral acid does not contain platinum such as chloropiatinic acid;