COMPOSITION AND PROCESS FOR PRODUCING SILYLATED POLYMERS AND USE THEREOF

Abstract

The invention relates to a composition comprising and to a process for preparing moisture-crosslinking polymers under catalysis by a metal-siloxane-silanol(ate) compound, and to the use of the composition in the CASE sector (coatings, adhesives, sealants and elastomers), especially in the field of adhesives and sealants.

Claims

1. A composition comprising at least one silylated polymer (SiP) obtainable by a synthesis, catalysed by a metal-siloxane-silanol(ate) compound, of at least one isocyanate-reactive compound, especially at least one hydroxy-functionalized polymer (component A), and one or more compounds having at least one isocyanate group (component B).

2. The composition according to claim 1, wherein the metal-siloxane-silanol(ate) compound has the general formula R*.sub.qSi.sub.rO.sub.sM.sub.t where each R* is independently selected from the group consisting of optionally substituted C1- to C20-alkyl, optionally substituted C3- to C6-cycloalkyl, optionally substituted C2- to C20-alkenyl, optionally substituted C6- to C10-aryl, —OH and —O—(C1- to C10-alkyl), each M is independently selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, q is an integer from 4 to 19, r is an integer from 4 to 10, s is an integer from 8 to 30, and t is an integer from 1 to 8.

3. The composition according to claim 1, wherein the metal-siloxane-silanol(ate) compound has a general structure (I) ##STR00025## where X.sup.1, X.sup.2 and X.sup.3 are independently selected from Si and M.sup.1, where M.sup.1 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, Z.sup.1, Z.sup.2 and Z.sup.3 are independently selected from the group consisting of L.sup.2, R.sup.5, R.sup.6 and R.sup.7, where L.sup.2 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.2 is selected from the group consisting of —OH, —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O-isobutyl; R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6 and R.sup.7 are independently selected from the group consisting of optionally substituted C1- to C20-alkyl, optionally substituted C3- to C8-cycloalkyl, optionally substituted C2- to C20-alkenyl and optionally substituted C5- to C10-aryl; Y.sup.1 and Y.sup.2 are independently —O-M.sup.2-L.sup.3.sub.Δ, or Y.sup.1 and Y.sup.2 are associated and together are —O-M.sup.2(L.sup.3.sub.Δ)-O— or —O—, where L.sup.3 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.3 is selected from the group consisting of —OH, —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O-isobutyl, and where M.sup.2 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, and X.sup.4 is -M.sup.3L.sup.1.sub.Δ or M.sup.3 and Q.sup.1 and Q.sup.2 are H or each is a single bond joined to M.sup.3, where L.sup.1 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.1 is selected from the group consisting of —OH, —O— methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O-isobutyl, and where M.sup.3 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, or X.sup.4 is -M.sup.3L.sup.1.sub.Δ and Q.sup.2 is H or a single bond joined to M.sup.3 and Q.sup.1 is H, M.sup.4L.sup.4.sub.Δ or —SiR.sup.8, where M.sup.4 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, and where L.sup.4 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.4 is selected from the group consisting of —OH, —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O— isobutyl, and where R.sup.8 is selected from the group consisting of optionally substituted C1- to C20-alkyl, optionally substituted C3- to C8-cycloalkyl, optionally substituted C2- to C20-alkenyl and optionally substituted C5- to C10-aryl, or X.sup.4, Q.sup.1 and Q.sup.2 are independently -M.sup.3L.sup.1.sub.Δ, or X.sup.4 is —Si(R.sup.8)—O-M.sup.3L.sup.1.sub.Δ, Q.sup.2 is a single bond joined to the silicon atom of X.sup.4 and Q.sup.1 is -M.sup.4L.sup.4.sub.Δ, or X.sup.4 is —Si(R.sup.8)—O-M.sup.3L.sup.1.sub.Δ, Q.sup.2 is a single bond joined to the silicon atom of X.sup.4 and Q.sup.1 is a single bond joined to the M.sup.3 atom of X.sup.4.

4. The composition according to claim 1, wherein the metal-siloxane-silanol(ate) compound has the structural formula (II) ##STR00026## where Z.sup.1, Z.sup.2 and Z.sup.3 are independently selected from the group consisting of L.sup.2, R.sup.5, R.sup.6 and R.sup.7, where L.sup.2 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.2 is selected from the group consisting of —OH, —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O-isobutyl; R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are independently selected from the group consisting of optionally substituted C1- to C20-alkyl, optionally substituted C3- to C8-cycloalkyl, optionally substituted C2- to C20-alkenyl and optionally substituted C5- to C10-aryl; and X.sup.4 is -M.sup.3L.sup.1.sub.Δ or M.sup.3 and Q.sup.1 and Q.sup.2 are H or each is a single bond joined to M.sup.3, where L.sup.1 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.1 is selected from the group consisting of —OH, —O— methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O-isobutyl, and where M.sup.3 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, or X.sup.4 is -M.sup.3L.sup.1.sub.Δ and Q.sup.2 is H or a single bond joined to M.sup.3 and Q.sup.1 is H, M.sup.4L.sup.4.sub.Δ or —SiR.sup.g, where M.sup.4 is selected from the group consisting of s- and p-block metals, d- and f-block transition metals, lanthanide and actinide metals and semimetals, especially from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, and where L.sup.4 is selected from the group consisting of —OH and —O—(C1- to C10-alkyl), especially —O—(C1- to C8-alkyl) or —O—(C1- to C6-alkyl), or where L.sup.4 is selected from the group consisting of —OH, —O-methyl, —O-ethyl, —O-propyl, —O-butyl, —O-octyl, —O-isopropyl, and —O— isobutyl, and where R.sup.8 is selected from the group consisting of optionally substituted C1- to C20-alkyl, optionally substituted C3- to C8-cycloalkyl, optionally substituted C2- to C20-alkenyl and optionally substituted C5- to C10-aryl, or X.sup.4, Q.sup.1 and Q.sup.2 are independently -M.sup.3L.sup.1.sub.Δ, or X.sup.4 is —Si(R.sup.8)—O-M.sup.3L.sup.1.sub.Δ, Q.sup.2 is a single bond joined to the silicon atom of X.sup.4 and Q.sup.1 is -M4L.sup.4.sub.Δ, or X.sup.4 is —Si(R.sup.8)—O-M.sup.3L.sup.1.sub.Δ, Q.sup.2 is a single bond joined to the silicon atom of X.sup.4 and Q.sup.1 is a single bond joined to the M.sup.3 atom of X.sup.4.

5. The composition according to claim 1, wherein the metal-siloxane-silanol(ate) is a metal silsesquioxane of the structure (IV) ##STR00027## where X.sup.4 is selected from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, most preferably from the group consisting of Ti and Sn, and is most preferably Ti, and X.sup.4 is joined to OR where R is selected from the group consisting of —H, -methyl, -ethyl, -propyl, -butyl, -octyl, -isopropyl, and -isobutyl, Z.sup.1, Z.sup.2 and Z.sup.3 are each independently C1- to C20-alkyl, C3- to C8-cycloalkyl, C2- to C20-alkenyl and C5- to C10-aryl, especially selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, hexyl, heptyl, octyl, vinyl, allyl, butenyl and phenyl, and benzyl, and R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are each independently C1- to C20-alkyl, C3- to C8-cycloalkyl, C2- to C20-alkenyl, and C5- to C10-aryl, especially selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, hexyl, heptyl, octyl, vinyl, allyl, butenyl and phenyl, and benzyl.

6. The composition according to claim 5, wherein the metal-siloxane-silanol(ate) compound is a metal silsesquioxane of the structure (IVb) ##STR00028## where X.sup.4 is selected from the group consisting of metals of transition groups 1, 2, 3, 4, 5, 8, 10 and 11 and metals of main groups 1, 2, 3, 4 and 5, preferably from the group consisting of Na, Zn, Sc, Nd, Ti, Zr, Hf, V, Fe, Pt, Cu, Ga, Sn and Bi; especially preferably from the group consisting of Zn, Ti, Zr, Hf, V, Fe, Sn and Bi, most preferably from the group consisting of Ti (and therefore is heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS)) and Sn (and therefore is heptaisobutyl POSS-tin(IV) ethoxide (SnPOSS)), and is most preferably Ti (and therefore is heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS)).

7. The composition according to claim 1, wherein the polymer backbone (P) of the silylated polymer (SiP) has constituents selected from the group consisting of polyurethanes, polyureas, polyethers, polyesters, phenolic resins, polyalkylenes, poly(meth)acrylates, polyamides, polycaprolactones, polybutadienes or polyisoprenes, and polycarbonates or mixtures thereof, preferably from the group consisting of polyurethanes, polyureas, poly(meth)acrylates or polyethers or mixtures thereof, most preferably polyethers.

8. The composition according to claim 1, wherein the silylated polymer (SiP) has at least two end groups of the general formula (V) ##STR00029## where X is C, Si or a heteroatom and these, according to their valency, optionally have one or more R.sup.8 radicals, preferably C, N, O, P, S, more preferably C, N or O, most preferably N or O, and each is bonded to a carbon in the polymer backbone, R* is 0 or an optionally substituted straight-chain or branched C1- to C25-alkyl group or an optionally substituted C4- to C18-cycloalkyl group or an optionally substituted C4- to C18-aryl group and, when R*=0, the silicon atom is bonded directly to the nitrogen atom, each Y is independently either O or a direct bond of the silicon atom to the respective R.sup.9, R.sup.10 or R.sup.11 radical, and preferably at least one Y is O, R.sup.8 is H, an optionally substituted straight-chain or branched C1- to C16-alkyl group, an optionally substituted straight-chain or branched C2- to C16-alkenyl group or an optionally substituted straight-chain or branched C2- to C16-alkynyl group, an optionally substituted C4- to C14-cycloalkyl group or an optionally substituted C4- to C14-aryl group, or a radical of the general structure (Vb), R.sup.12 and R.sup.14 are each independently H or a radical from the group consisting of —R.sup.15, —COOR.sup.15 and —CN, R.sup.13 is H or a radical from the group consisting of —CH.sub.2—COOR.sup.15, —COOR.sup.15, —CONHR.sup.15, —CON(R.sup.15), —CN, —NO.sub.2, —PO(OR.sup.15).sub.2, —SOR.sup.15 and —SO.sub.2OR.sup.15, R.sup.15 is a hydrocarbyl radical having 1 to 20 carbon atoms and optionally having at least one heteroatom, R.sup.9, R.sup.10 and R.sup.11 are independently H, an optionally substituted straight-chain or branched C1- to C5-alkyl group, an optionally substituted straight-chain or branched C2- to C10-alkenyl group or an optionally substituted C4- to C14-cycloalkyl group or an optionally substituted C4- to C14-aryl group, m is 0 or 1 and, when m=0, the silicon atom is bonded directly to a carbon in the polymer backbone (P).

9. The composition according to claim 8, wherein the silylated polymer (SiP) has a polyether polymer backbone having at least two end groups of the general formula (V) ##STR00030## where X is N or O and N optionally has an R.sup.8 radical, R* is 0 or an optionally substituted straight-chain or branched C1- to C20-alkyl group or an optionally substituted C4- to C12-cycloalkyl group or an optionally substituted C4- to C12-aryl group, preferably an optionally substituted straight-chain or branched C1- to C15-alkyl group, and, when R*=0, the silicon atom is bonded directly to the nitrogen atom, Y in Y—R.sup.9 and Y—R.sup.10 are O and the Y in Y—R.sup.11 is either O or a direct bond of the silicon atom to the respective R.sup.11 radical, R.sup.8 is H, an optionally substituted straight-chain or branched C1- to C10-alkyl group, an optionally substituted straight-chain or branched C2- to C10-alkenyl group or an optionally substituted straight-chain or branched C2- to C10-alkynyl group, an optionally substituted C4- to C10-cycloalkyl group or an optionally substituted C4- to C10-aryl group or a succinic acid derivative of the general structure (Vb), R.sup.9, R.sup.10 and R.sup.11 are independently H, an optionally substituted straight-chain or branched C1- to C4-alkyl group, an optionally substituted straight-chain or branched C2- to C5-alkenyl group or an optionally substituted C4- to C10-cycloalkyl group or an optionally substituted C4- to C10-aryl group, preferably independently H or a C1- to C2-alkyl group, and m is 0 or 1 and, when m=0, the silicon atom is bonded directly to a carbon in the polymer backbone (P), preferably m=1.

10. The composition according to claim 9, wherein the silylated polymer (SiP) has a polyether polymer backbone having at least two end groups of the general formula (V) ##STR00031## where R* is 0 or an optionally substituted straight-chain or branched C1- to C15-alkyl group or an optionally substituted C4- to C6-cycloalkyl group or an optionally substituted C4- to C6-aryl group, preferably an optionally substituted straight-chain or branched C1- to C10-alkyl group, more preferably a C1-alkyl group (=alpha-silane) or a C3-alkyl group (=gamma-silane), and, when R*=0, the silicon atom is bonded directly to the nitrogen atom. R.sup.8 is H, an optionally substituted straight-chain or branched C1- to C8-alkyl group, an optionally substituted straight-chain or branched C2- to C8-alkenyl group or an optionally substituted straight-chain or branched C2- to C8-alkynyl group, an optionally substituted C4- to C6-cycloalkyl group or an optionally substituted C4- to C6-aryl group, R.sup.9, R.sup.10 and R.sup.11 are independently H, an optionally substituted, straight-chain or branched C1- to C4-alkyl group, an optionally substituted, straight-chain or branched C2- to C5-alkenyl group or an optionally substituted C4- to C6-cycloalkyl group or an optionally substituted C4- to C6-aryl group, preferably independently H or a C1- to C2-alkyl group, and m is 0 or 1 and, when m=0, the silicon atom is bonded directly to a carbon in the polymer backbone (P), preferably m=1.

11. The composition according to claim 1, wherein the hydroxy-functionalized polymer (component A) is selected from the group consisting of polyoxyalkylene diols, polyoxyalkylene triols, especially polyoxyethylene di- and/or triols and/or polyoxypropylene di- and/or triols, KOH-catalysed hydroxy-functionalized polyethers or double metal cyanide complex-catalysed (DMC-catalysed) hydroxy-functionalized polyethers or mixtures thereof.

12. The composition according to claim 1, wherein component B is selected from the group consisting of aromatic and/or aliphatic isocyanates (Iso) of the general structure (VI) or mixtures thereof or isocyanatosilanes (Iso-Si) of the general structure (VII) or mixtures thereof ##STR00032## where R.sup.x is a carbon-containing group, preferably at least one aromatic or aliphatic group or mixtures thereof, more preferably an optionally substituted straight-chain or branched C1- to C16-alkyl group, an optionally substituted straight-chain or branched C2- to C16-alkenyl group or an optionally substituted straight-chain or branched C2- to C16-alkynyl group, an optionally substituted C4- to C14-cycloalkyl group or an optionally substituted C4- to C14-aryl group, most preferably diphenylmethane, toluene, dicyclohexylmethane, hexane or methyl-3,5,5-trimethylcyclohexyl, each Y is independently either O or a direct bond of the silicon atom to the respective R.sup.9, R.sup.10 or R.sup.11 radical, and preferably at least one Y is O, z is at least 1, preferably at least 2, R.sup.9, R.sup.10 and R.sup.11 are independently H, an optionally substituted straight-chain or branched C1- to C5-alkyl group, an optionally substituted straight-chain or branched C2- to C10-alkenyl group or an optionally substituted C4- to C8-cycloalkyl group or an optionally substituted C4- to C8-aryl group and R* is 0 or an optionally substituted straight-chain or branched C1- to C25-alkyl group or an optionally substituted C4- to C18-cycloalkyl group or an optionally substituted C4- to C18-aryl group and, when R*=0, the silicon atom is bonded directly to the nitrogen atom.

13. The composition according to claim 12, wherein component B is selected from the group consisting of aromatic and/or aliphatic isocyanates (Iso) of the general structure (VI) or mixtures thereof or isocyanatosilanes (Iso-Si) of the general structure (VII) or mixtures thereof ##STR00033## where R.sup.x is diphenylmethane, toluene, dicyclohexylmethane, hexane or methyl-3,5,5-trimethylcyclohexyl, preferably diphenylmethane or hexane or methyl-3,5,5-trimethylcyclohexyl, most preferably diphenylmethane or methyl-3,5,5-trimethylcyclohexyl, and z is at least 2, preferably 2, Y in Y—R.sup.9 and Y—R.sup.10 are O and the Y in Y—R.sup.11 is either O or a direct bond of the silicon atom to the respective R.sup.11 radical, R.sup.9, R.sup.10 and R.sup.11 are independently H, an optionally substituted straight-chain or branched C1- to C3-alkyl group and R* is 0 or an optionally substituted straight-chain or branched C1- to C15-alkyl group or an optionally substituted C4- to C6-cycloalkyl group or an optionally substituted C4- to C6-aryl group, preferably an optionally substituted straight-chain or branched C1- to C10-alkyl group, more preferably a C1-alkyl group (=alpha-silane) or a C3-alkyl group (=gamma-silane), and, when R*=0, the silicon atom is bonded directly to the nitrogen atom.

14. The composition according to claim 13, wherein at least one isocyanate (Iso) of the general structure (VI) is selected from the group consisting of polymeric, oligomeric and monomeric methylene diphenyl isocyanate (MDI), especially from 4,4′-methylene diphenyl isocyanate (4,4′-MDI), 2,4′-methylene diphenyl isocyanate (2,4′-MDI), 2,2′-methylene diphenyl isocyanate (2,2′-MDI), 4,4′-diisocyanatodicyclohexylmethane (H12MDI), 2-methylpentamethylene 1,5-diisocyanate, dodecamethylene 1,12-diisocyanate, lysine and lysine ester diisocyanate, cyclohexane 1,3-diisocyanate, cyclohexane 1,4-diisocyanate, perhydro(diphenylmethane 2,4′-diisocyanate), perhydro(diphenylmethane 4,4′-diisocyanate), 1,4-diisocyanato-2,2,6-trimethylcyclohexane (TMCDI), 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (=isophorone diisocyanate or IPDI), hexamethylene 1,6-diisocyanate (HDI) or the trimer thereof (HDI trimer), 2,2,4- and/or 2,4,4-trimethylhexamethylene 1,6-diisocyanate, 1,4-bis(isocyanato)cyclohexane, 1,4-bis(isocyanato)benzene (PPDI), 1,3- and/or 1,4-bis(isocyanatomethyl)cyclohexane, m- and/or p-xylylene diisocyanate (m- and/or p-XDI), m- and/or p-tetramethylxylylene 1,3-diisocyanate, m- and/or p-tetramethylxylylene 1,4-diisocyanate, bis(1-isocyanato-1-methylethyl)naphthalene, 1,3-bis(isocyanato-4-methylphenyl)-2,4-dioxo-1,3-diazetidine, naphthalene 1,5-diisocyanate (NDI), 3,3′-dimethyl-4,4′-diisocyanatodiphenyl (TODI), tolylene 2,4- and/or 2,6-diisocyanate (TDI), 1,3-bis(isocyanatomethyl)benzene or mixtures thereof, preferably 4,4′-methylene diphenyl isocyanate (4,4′-MDI) or isophorone diisocyanate (IPDI), hexamethylene 1,6-diisocyanate (HDI) or the trimer thereof (HDI trimer) or mixtures thereof, most preferably 4,4′-methylene diphenyl isocyanate (4,4′-MDI) or isophorone diisocyanate (IPDI) or mixtures thereof.

15. The composition according to claim 12, wherein at least one isocyanatosilane (Iso-Si) of the general structure (VII) is selected, or mixtures thereof, ##STR00034## where R.sup.9, R.sup.10, R.sup.11 are preferably a methyl or ethyl group or mixtures thereof, preferably selected from the group consisting of 3-(triethoxysilyl)methyl isocyanate, 3-(trimethoxysilyl)methyl isocyanate, 3-(triethoxysilyl)ethyl isocyanate, 3-(trimethoxysilyl)ethyl isocyanate, 3-(triethoxysilyl)propyl isocyanate, 3-(trimethoxysilyl)propyl isocyanate, 3-(triethoxysilyl)butyl isocyanate, 3-(trimethoxysilyl)butyl isocyanate, 3-(triethoxysilyl)pentyl isocyanate, 3-(trimethoxysilyl)pentyl isocyanate, 3-(triethoxysilyl)hexyl isocyanate, 3-(trimethoxysilyl)hexyl isocyanate or mixtures thereof, preferably 3-(trimethoxysilyl)methyl isocyanate, 3-(triethoxysilyl)methyl isocyanate, 3-(trimethoxysilyl)propyl isocyanate, 3-(triethoxysilyl)propyl isocyanate or mixtures thereof, more preferably 3-(trimethoxysilyl)propyl isocyanate, 3-(triethoxysilyl)propyl isocyanate, or mixtures thereof.

16. The composition according to claim 1, wherein the silylated polymer (SiP) has been prepared by reaction with an aminosilane (AmSi).

17. The composition according to claim 16, wherein the aminosilane (AmSi) is at least one aminosilane (AmSi) of the general structure (VIII), or a mixture thereof, ##STR00035## where R.sup.7 is H, R.sup.8 is H, an optionally substituted straight-chain or branched C1- to C25-alkyl group, an optionally substituted straight-chain or branched C2- to C25-alkenyl group or an optionally substituted C4- to C18-cycloalkyl group or an optionally substituted C4- to C18-aryl group, or a radical of the general structure (Vb), R* is 0 or an optionally substituted straight-chain or branched C1- to C25-alkyl group or an optionally substituted C4- to C18-cycloalkyl group or an optionally substituted C4- to C18-aryl group and, when R*=0, the silicon atom is bonded directly to the nitrogen atom, R.sup.12 and R.sup.14 are each independently H or a radical from the group consisting of —R.sup.15, —COOR.sup.15 and —CN, R.sup.13 is H or a radical from the group consisting of —CH.sub.2—COOR.sup.15, —COOR.sup.15, —CONHR.sup.15, —CON(R.sup.15), —CN, —NO.sub.2, —PO(OR.sup.15).sub.2, —SOR.sup.15 and —SO.sub.2OR.sup.15, R.sup.15 is a hydrocarbyl radical having 1 to 20 carbon atoms and optionally having at least one heteroatom, R.sup.9, R.sup.10, R.sup.11 are independently H, an optionally substituted straight-chain or branched C1- to C4-alkyl group, an optionally substituted straight-chain or branched C2- to C5-alkenyl group or an optionally substituted C4- to C10-cycloalkyl group or an optionally substituted C4- to C10-aryl group, preferably independently H or a C1- to C2-alkyl group and each Y is independently either O or a direct bond of the silicon atom to the respective R.sup.9, R.sup.10 or R.sup.11 radical, and preferably at least one Y is O.

18. The composition according to claim 17, wherein the aminosilane (AmSi) is at least one aminosilane (AmSi) of the general structure (VIII), or a mixture thereof, ##STR00036## where R.sup.8 is H, an optionally substituted straight-chain or branched C1- to C10-alkyl group, an optionally substituted straight-chain or branched C2- to C10-alkenyl group or an optionally substituted straight-chain or branched C2- to C10-alkynyl group, an optionally substituted C4- to C10-cycloalkyl group or an optionally substituted C4- to C10-aryl group or a succinic acid derivative of the general structure (Vb), R* is 0 or an optionally substituted straight-chain or branched C1- to C20-alkyl group or an optionally substituted C4- to C12-cycloalkyl group or an optionally substituted C4- to C12-aryl group, preferably an optionally substituted straight-chain or branched C1- to C15-alkyl group, more preferably a C1-alkyl group (=alpha-silane) or a C3-alkyl group (=gamma-silane), and, when R*=0, the silicon atom is bonded directly to the nitrogen atom, R.sup.9, R.sup.10, R.sup.11 are preferably a methyl or ethyl group or mixtures thereof, and Y in Y—R.sup.9 and Y—R.sup.10 are O and the Y in Y—R.sup.11 is either O or a direct bond of the silicon atom to the respective R.sup.11 radical.

19. The composition according to claim 18, wherein the aminosilane (AmSi) of the general structure (VIII) is selected from the group consisting of N-[3-(trimethoxysilyl)methyl]butylamine, N-[3-(triethoxysilyl)methyl]butylamine, N-[3-(trimethoxysilyl)ethyl]butylamine, N-[3-(triethoxysilyl)ethyl]butylamine, N-[3-(trimethoxysilyl)propyl]butylamine, N-[3-(triethoxysilyl)propyl]butylamine, N-[3-(trimethoxysilyl)butyl]butylamine, N-[3-(triethoxysilyl)butyl]butylamine, N-[3-(trimethoxysilyl)pentyl]butylamine, N-[3-(triethoxysilyl)pentyl]butylamine, N-[3-(trimethoxysilyl)hexyl]butylamine, N-[3-(triethoxysilyl)hexyl]butylamine, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, N-cyclohexyl-3-aminopropyltrimethoxysilane, N-cyclohexyl-3-aminopropyltriethoxysilane, N-(3-trimethoxysilylpropyl)aminosuccinic acid diethyl ester, N-(3-triethoxysilylpropyl)aminosuccinic acid diethyl ester or a mixture thereof, preferably N-[3-(trimethoxysilyl)methyl]butylamine, N-[3-(triethoxysilyl)methyl]butylamine, N-[3-(trimethoxysilyl)propyl]butylamine, N-[3-(triethoxysilyl)propyl]butylamine, N-(3-trimethoxysilylpropyl)aminosuccinic acid diethyl ester, N-(3-triethoxysilylpropyl)aminosuccinic acid diethyl ester, more preferably N-[3-(trimethoxysilyl)propyl]butylamine, N-[3-(triethoxysilyl)propyl]butylamine, N-[3-(triethoxysilyl)methyl]butylamine, N-[3-(trimethoxysilyl)methyl]butylamine or a mixture thereof.

20. A process for producing a silylated polymer (SiP)-containing composition, comprising the following steps: (i) synthesizing a polymer by combining at least one isocyanate-reactive compound, especially a hydroxy-functionalized polymer, with one or more isocyanates (Iso), or one or more isocyanatosilanes (Iso-Si), using a metal-siloxane-silanol(ate) compound, especially heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS), heptaisobutyl POSS-tin(IV) ethoxide (SnPOSS), or mixtures thereof, (ii) optionally admixing the polymer from step (i) with a catalyst selected from dibutyltin dilaurate (DBTL) or a metal-siloxane-silanol(ate) compound, especially heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS), heptaisobutyl POSS-tin(IV) ethoxide (SnPOSS), mixtures thereof.

21. The process according to claim 20, comprising the steps of (i) synthesizing a polymer at a temperature of <80° C., preferably at a temperature of <60° C., especially preferably at room temperature, by combining at least one hydroxy-functionalized polymer selected from the group consisting of hydroxy-functionalized polymers having number-average molar masses (Mn) of 500-35 000 g/mol, preferably of about 2000 g/mol or about 19 000 g/mol, or mixtures thereof with one or more isocyanates (Iso), or one or more isocyanatosilanes (Iso-Si), preferably 3-(trimethoxysilyl)propyl isocyanate or 3-(triethoxysilyl)propyl isocyanate or mixtures thereof, using a metal-siloxane-silanol(ate) compound, especially heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS), heptaisobutyl POSS-tin(IV) ethoxide (SnPOSS), or mixtures thereof, (ii) optionally admixing the polymer from step (i) with a catalyst selected from dibutyltin dilaurate (DBTL) or a metal-siloxane-silanol(ate) compound, especially heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS), heptaisobutyl POSS-tin(IV) ethoxide (SnPOSS), mixtures thereof.

22. The process according to claim 20, wherein the polymer obtained from step (i) is reacted with an aminosilane (AmSi), preferably with N-[3-(triethoxysilyl)propyl]butylamine, or N-[3-(trimethoxysilyl)propyl]butylamine or mixtures thereof.

23. A silylated polymer (SiP)-containing composition produced by the process of claim 20.

Description

EXAMPLES

Examples I

[0357] Preparation of the Polymers Required for the Study:

[0358] The following materials were used for the production of isocyanate prepolymers and hybrid polymers (silane-terminated prepolymers STP): [0359] 4,4′-methylene diphenyl isocyanate (4,4′-MDI), Alfa Aesar [0360] Wannate IPDI (IPDI), DKSH [0361] PolyU L 4000 (low monool polyoxypropylene diol, OH number 27 mg KOH/g, viscosity 1000 mPa*s), PolyU GmbH [0362] PolyU L 12000 (low monool polyoxypropylene diol, OH number 10 mg KOH/g, viscosity 6000 mPa*s), PolyU GmbH [0363] dibutyltin dilaurate (DBTL), BNT-Cat 422, 20% and 1% strength, dissolved in Hexamoll® DINCH, BASF [0364] heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS) [0365] TiPOSS, 20% and 1% strength, dissolved in Hexamoll® DINCH, BASF [0366] vinyltrimethoxysilane (VTMO), Acros Organics [0367] N-[3-(trimethoxysilyl)propyl]butylamine, DOG Deutsche Olfabrik [0368] 3-(triethoxysilyl)propyl isocyanate, Acros Organics

[0369] A) Preparation of the Isocyanate Prepolymers with Different Isocyanates MDI:

[0370] A1) Prepolymer 1: Reaction of 4,4′-MDI with PolyU L 4000 and TiPOSS as Catalyst

[0371] In a reaction vessel under a nitrogen atmosphere, 31.3 g of 4,4′-methylene diphenyl isocyanate was melted at 55° C., and 250 g of PolyU L 4000 heated to 50° C. was added while stirring within 30 min. The mixture was cooled down to room temperature, and 0.625 g of a 1% TiPOSS solution (corresponding to 22 ppm of TiPOSS) in DINCH was added. After a reaction time of 3 h at room temperature, by means of titration, a content of free isocyanate groups of 1.9% by weight (calculated value: 1.9% by weight) was obtained. The viscosity of the resulting prepolymer was 5000 mPa*s.

[0372] Comparative Experiment to A1

[0373] A2) Prepolymer 2: Reaction of 4,4′-MDI with PolyU L 4000 and DBTL as Catalyst

[0374] In a reaction vessel under a nitrogen atmosphere, 31.3 g of 4,4′-methylene diphenyl isocyanate was melted at 55° C., and 250 g of PolyU L 4000 heated to 50° C. was added while stirring within 30 min. The mixture was cooled down to room temperature, and 0.625 g of a 1% DBTL solution (corresponding to 22 ppm of DBTL) in DINCH was added. After a reaction time of 3 h at room temperature, by means of titration, a content of free isocyanate groups of 1.9% by weight (calculated value: 1.9% by weight) was obtained. The viscosity of the resulting prepolymer was 22 000 mPa*s.

[0375] IPDI:

[0376] A3) Prepolymer 3: Reaction of IPDI with PolyU L 4000 and TiPOSS as Catalyst

[0377] A reaction vessel under a nitrogen atmosphere was initially charged with 250 g of PolyU L 4000, and 0.156 g of a 20% TiPOSS solution (corresponding to 122 ppm of TiPOSS) in DINCH was added while stirring. Subsequently, 27.79 g of IPDI was added dropwise within 30 min. After a reaction time of 3 h at room temperature, by means of titration, a content of free isocyanate groups of 1.9% by weight (calculated value 1.9% by weight) was obtained. The viscosity of the resulting prepolymer was 4000 mPa*s.

[0378] Comparative Experiment to A3

[0379] A4) Prepolymer 4: Reaction of IPDI with PolyU L 4000 and DBTL as Catalyst

[0380] A reaction vessel under a nitrogen atmosphere was initially charged with 250 g of PolyU L 4000, and 0.156 g of a 20% DBTL solution (corresponding to 122 ppm of DBTL) in DINCH was added while stirring. Subsequently, 27.79 g of IPDI was added dropwise within 30 min. After a reaction time of 9 h at room temperature, by means of titration, a content of free isocyanate groups of 1.9% by weight was obtained. The viscosity of the resulting prepolymer was 3500 mPa*s. The reaction was repeated at 48° C.; after a reaction time of 3 h, a content of free isocyanate groups of 1.9% (calculated value 1.9% by weight) was found; viscosity was 7000 mPa*s.

[0381] B) Preparation of the Silane-Terminated Polymers (STP), Also Called Silylated Polymers Silane-Terminated Polyols from the Reaction of Isocyanate Prepolymer (A1 to A4) with Sec-Trimethoxysilylamine (Aminosilane)

[0382] B1) Silane-Terminated Hybrid Polymer STP 1: Reaction of TiPOSS-Comprising Prepolymer 1 (from A1) with N-[3-(Trimethoxysilyl)Propyl]Butylamine

[0383] To 259 g of prepolymer 1 with 0.006 g of TiPOSS under a nitrogen atmosphere at room temperature was added 27.2 g of N-[3-(trimethoxysilyl)propyl]butylamine while stirring. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 15 000 mPa*s. Finally, 1% VTMO was added.

[0384] Comparative Experiment to B1

[0385] B2) Silane-Terminated Polymer STP 2: Reaction of DBTL-Comprising Prepolymer (from A2) with N-[3-(trimethoxysilyl)propyl]butylamine

[0386] To 264.3 g of prepolymer 2 with 0.006 g of DBTL under a nitrogen atmosphere at room temperature was added 27.6 g of N-[3-(trimethoxysilyl)propyl]butylamine while stirring. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 43 000 mPa*s. Finally, 1% VTMO was added.

[0387] B3) Silane-Terminated Polymer STP 3: Reaction of TiPOSS-Comprising Prepolymer 3 (from A3) with N-[3-(trimethoxysilyl)propyl]butylamine

[0388] To 257.8 g of prepolymer 3 with 0.029 g of TiPOSS under a nitrogen atmosphere at room temperature was added 27.33 g of N-[3-(trimethoxysilyl)propyl]butylamine while stirring. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 11 000 mPa*s. Finally, 1% VTMO was added.

[0389] Comparative Experiment to B3

[0390] B4) Silane-Terminated Hybrid Polymer STP 4: Reaction of DBTL-Comprising Prepolymer 4 (from A4) with N-[3-(trimethoxysilyl)propyl]butylamine

[0391] To 269.2 g of prepolymer 4 with 0.029 g of DBTL under a nitrogen atmosphere at room temperature was added 28.52 g of N-[3-(trimethoxysilyl)propyl]butylamine while stirring. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 17 000 mPa*s. Finally, 1% VTMO was added.

[0392] C) Silane-Terminated Hybrid Polyols from the Reaction of PolyU L 12000 with 3-(trimethoxysilyl)propyl isocyanate

[0393] B5) Silane-Terminated Hybrid Polymer STP 5: Reaction of 3-(trimethoxysilyl)propyl Isocyanate and PolyU L 12000 with TiPOSS as Catalyst

[0394] A reaction vessel under a nitrogen atmosphere was initially charged with 200 g of PolyU L 12000, and 5 g of a 20% TiPOSS solution (corresponding to 4700 ppm of TiPOSS) in DINCH was added while stirring. Subsequently, 7.31 g of 3-(trimethoxysilyl)propyl isocyanate was added dropwise within 30 min. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 8900 mPa*s. Finally, 2% VTMO was added.

[0395] Comparative Experiment to B6

[0396] B6) Silane-Terminated Hybrid Polymer STP 6: Reaction of 3-(trimethoxysilyl)propyl isocyanate and PolyU L 12000 with DBTL as Catalyst

[0397] A reaction vessel under a nitrogen atmosphere was initially charged with 200 g of PolyU L 12000, and 5 g of a 20% DBTL solution (corresponding to 4700 ppm of DBTL) in DINCH was added while stirring. Subsequently, 7.31 g of 3-(trimethoxysilyl)propyl isocyanate was added dropwise within 30 min. The reaction was ended after 2 h; it was no longer possible to detect any free isocyanate. The viscosity of the resultant silane-terminated polymer was 9100 mPa*s. Finally, 2% VTMO was added.

[0398] Testing of the Curing Characteristics of the Silane-Terminated Polymers STP 1 to STP 6 from Reactions B1 to B6

[0399] The curing characteristics of the silane-terminated polymers were tested by determining the fibre time FT and tack-free time TFT on samples of thickness 2 mm at 23° C./50% RH, with and without additional addition of TiPOSS and DBTL.

TABLE-US-00001 TABLE A Curing characteristics of silane-terminated polymers STP 1 to STP 6 STP 1 STP 2 STP 3 STP 4* STP 5 STP 6 FT/TFT FT/TFT FT/TFT FT/TFT FT/TFT FT/TFT AmSi route AmSi route Iso-Si route 3-(Trimethoxysilyl)propyl MDI (MDI way) IPDI (IPDI way) isocyanate Viscosity of 15 000 43 000 11 000 17 000 8900 9100 the STPs mPas No further 10 h / 48 h 3.5 h / 6 h 24 h / 48 h 10 h / 48 h 6 h / 12 h 60 min / 3.5 h addition of cat.* +0.25% by 90 min / 25 min / 3 h 45 min / 50 min / 20 min / weight 2.5 h 1.5 h 2 h 2.5 h 1.5 h TiPOSS (= 2500 ppm) +0.25% by 80 min / 20 min / 1.5 h / 30 min / 50 min / weight 2.5 h 1.5 h 3 h 3 h 1.5 h 2.5 h DBTL (= 2500 ppm) *From comparison of the reaction regime at 48° C. STP 1, 3, 5 = with TiPOSS; STP 2, 4, 6 = with DBTL

[0400] Conclusion:

[0401] The distinctly prolonged fibre time or tack-free time for the silane-terminated polymers prepared with TiPOSS (STP 1, STP 3 and STP 5, no further addition of catalyst, marked area of the table) indicate that it was possible to distinctly increase stability with respect to ingress of water (humidity, residual moisture, formulation raw materials, etc.) compared to the compounds prepared with DBTL.

[0402] The resulting advantages thereof are briefly elucidated below:

[0403] As a result, the processor has the benefit of processing a less hydrolysis-sensitive hybrid polymer. This means specifically: [0404] 1. The residual moisture of other components and raw materials in the formulation of sealant recipes is less problematic, [0405] 2. elevated processing reliability is additionally obtained, [0406] 3. storage stabilities of the composition according to the invention are improved and [0407] 4. less water scavenger (e.g. VTMO—which is harmful if inhaled according to H332 and highly flammable according to H225 of the EU-GHS classification and identification) is required for the stabilization of hybrid polymers and for sealant recipes. [0408] 5. It is possible to use a lower level of tin-containing catalysts, and preferably to dispense entirely with tin-containing catalysts. [0409] 6. General reduction in the amount of catalyst required.

Example II

[0410] The present invention also relates to a composition and to a process for producing polyurethane prepolymers and polyurethane systems based on polyols, di- or polyisocyanates and a TiPOSS-based catalyst.

[0411] TiPOSS-based catalysts that are preferred in accordance with the invention are those disclosed in EP 2 989 155 B1 and EP 2 796 493 A1. The disclosure of these documents is fully incorporated with regard to the catalysts. Particular preference is given to the catalysts (metallosilsesquioxane) according to Claim 5 of EP 2 989 155 B1.

[0412] The study of the activity of heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS) for the formation of polyurethane compounds was conducted by way of example in comparison with dibutyltin dilaurate (DBTDL) and tin(II) 2-ethylhexanoate (tin octoate) in various unfoamed and foamed polyurethane systems. Particular attention was paid to the effect on the preparation of the silylated polyurethanes (SPUR) by the IPDI route. The model formulations from the CASE application sectors, soft foam and flexible foam (slabstock foam), were examined here with regard to their curing characteristics at room temperature (23° C./50% RH) using various polyols and isocyanates with the same catalyst content of TiPOSS and DBTDL or tin octoate. For simplification, the studies have been conducted under the assumption that a complete stoichiometric reaction (index 100) can take place between isocyanate and polyol. In principle, the studies are also applicable to the preparation of prepolymers. The catalytic activity of the catalysts examined was determined by the determination and comparison of cream time, fibre time and tack-free time.

[0413] 1.) Study of TiPOSS/DBTDL in Unfoamed Polyurethane Formulations

[0414] a) Propylene Glycol Polyols

[0415] The polyol A component consisted of a polypropylene diol and the TiPOSS catalyst in the form of a 20% solution in diisononyl phthalate (DINP). For comparison of catalytic activity, a corresponding identical polyol A component was prepared using DBTDL. The amount of catalyst was 0.2 percent by weight in each case (neglecting the amount of solvent). In order to study the influence of molecular weight, the molecular weight was additionally varied from low (MW˜2000) to high (MW˜18 000), since it can be assumed that the reactivity of polypropylene polyols that are of limited reactivity in any case will decrease further with rising molecular weight, and hence differences in reactivity will be particularly readily observable.

[0416] The polypropylene polyols tested were accordingly those with MW˜2000 (Rokopol D2002, PCC Rokita), MW˜8000 (Rokopol LDB 8000), MW˜12 000 (Rokopol LDB 12000) and MW˜18 000 (Rokopol LDB 18000).

[0417] The crosslinker components used were the isocyanates P-MDI (Voranate M230, Dow), IPDI (Wanate IPDI, DKSH) and HDI trimer isocyanurates (Vestanat HT2500/100). The reaction between polyol A and isocyanate B component was effected by stirring the two components at 1000 rpm with a conventional propeller stirrer for 10 s. After the stirring process had ended, the resultant reaction mixture was cast into slabs of thickness˜6 mm (10 g). The curing characteristics were determined from the cream time, fibre time and tack-free time.

[0418] It was found that the TiPOSS-catalysed curing of polyurethane at room temperature is significantly accelerated using the polypropylene polyols described compared to the corresponding DBTDL-catalysed crosslinking. The acceleration of the reaction, according to the combination of polyol and isocyanate examined, is between a factor of 2 and a factor of 100. Viewed overall, the factor of reaction acceleration when TiPOSS is used particularly surprisingly increases for the HDI trimer of isocyanurate used, and to a lesser degree for IPDI.

[0419] Conclusion for SPUR Methodology:

[0420] Since the reaction between the DMC polyols and IPDI isocyanate is the crucial reaction for the commercial preparation of SPUR (hybrid polymers), this finding is of great significance. Since we are already able to establish a considerable increase in reaction at room temperature and with 1:1 stoichiometry, it can be expected that, under the customary conditions of SPUR prepolymer preparation, it is possible to work with considerably smaller amounts of catalyst (⅕ to 1/10) and/or a lower temperature (<80° C.) and/or shortening of the reaction time. Since the formation of by-products in this preparation leads to an unwanted increase in viscosity, a distinct improvement in the reaction regime and product quality is thus to be expected.

[0421] With regard to the ever-increasing economic significance of the SPUR products, the use of the TiPOSS catalyst is expected to lead both to a cost benefit over tin catalysts and to a product benefit.

[0422] a) Propylene Glycol Polyols, Ethylene Glycol-Tipped

[0423] In order to assess whether these observations are also applicable to more reactive polyether polyols, by way of example, polyether polyols with MW˜4000 and f=2 and MW˜4850 and f=3 tipped with ethoxy groups at the termini were examined. It has been found that the differences in reactivity of the polyol systems catalysed with TiPOSS and DBTDL are smaller in the case of use of reactive polyether triol. Here too, it is again observed that the acceleration in reactivity of the crosslinking by TiPOSS is particularly effective for the HDI trimer.

[0424] 2.) Study of the Activity of TiPOSS/DBTL in Silane-Terminated Polyurethanes

[0425] The speed of fibre formation and curing in silane-terminated polyurethanes was determined on 6 mm SPUR slabs that had been produced by mixing the silane-terminated polyurethanes with 0.2 percent by weight each of TiPOSS and DBTL (each in solution, 20% in DINP). The mixing was effected with exclusion of air in an argon inert gas atmosphere with a conventional propeller stirrer. The mixed material was cured at 23° C./50% RH.

[0426] 3.) Study of the Activity of TiPOSS/DBTDL in Flexible Polyurethane Foam Formulations

[0427] The polyol A component consisted of a reactive, ethoxy group-tipped polyether triol (Rokopol M 5020, f=3), water and the TiPOSS catalyst, in the form of a 20% solution in diisononyl phthalate (DINP). For comparison of catalytic activity, a corresponding identical polyol A component was prepared using DBTDL. The amount of catalyst was 0.2 percent by weight in each case (neglecting the DINP solvent). By way of comparison, the reaction was conducted using a less reactive polypropylene polyol (Rokopol D 2002, f=2).

[0428] The crosslinking component used was the isocyanate P-MDI (Voranate M230). The reaction between polyol A component and isocyanate B component was effected by stirring the two components at 2500 rpm with a conventional propeller stirrer for 10 s. The reaction was stoichiometric. After the stirring process had ended, the reaction mixture obtained (20 g) was poured into cups. The curing characteristics were determined from the cream time and tack-free time.

[0429] It was found that the activity of TiPOSS when using ethoxylated polyols is comparable to that of DBTDL. By contrast, the curing process in the case of the formulation made from a pure polypropylene polyol is more significantly accelerated by TiPOSS.

[0430] 4.) Study of the Activity of TiPOSS/Tin Octoate in a Slabstock Polyurethane Foam Formulation

[0431] The polyol A component consisted of a standard polyester polyol based on Desmophen 2200 B, an amine catalyst (N,N-dimethylpiperazine and N,N-dimethylhexadecylamine), cell stabilizers, water and the TiPOSS catalyst, in the form of a 20% solution in DINP. For comparison of catalytic activity, a corresponding identical polyol A component was prepared using tin octoate. The amount of TiPOSS and tin octoate catalyst was 0.03 percent by weight in each case.

[0432] The crosslinking component used was the isocyanate Desmodur T65 and a prepolymer having an NCO content of about 12%. The reaction was effected in a stoichiometric ratio (index 100). The reaction between polyol A and isocyanate B components was effected by stirring the two components at 1000 rpm with a Visco Jet stirrer unit for 10 s. After the stirring process had ended, the resultant reaction mixture (˜400 g) was poured into a 2 L wooden box, and the curing characteristics were determined from the cream time and tack-free time.

[0433] It was found that the activity of TiPOSS is comparable to that of tin octoate. The resultant foams from the reaction with TiPOSS have lower density; strength properties and indentation hardness are correspondingly lower.

[0434] 5.) Overall Conclusion/Applications

[0435] a) Use of TiPOSS in the Preparation of SPUR Prepolymers

[0436] The significant increase in reaction described in the reaction between the DMC polyols and IPDI can be used for the commercial production of SPUR (hybrid polymers). It can be expected here that it will be possible to use considerably smaller amounts of catalyst (⅕ to 1/10) and/or a lower temperature (<80° C.) and/or a shortened reaction time. Since, in general, the formation of by-products in this preparation leads to an unwanted increase in viscosity, a distinct improvement in the reaction regime and product quality, including lower product viscosity (very important for the formulator), is thus possible.

[0437] b) Preparation of KOH-Based PU Prepolymers with TiPOSS

[0438] The formation of prepolymers obtained from the reaction of KOH-based polyols and aliphatic and aromatic isocyanates can be brought about with considerably smaller amounts of TiPOSS catalyst (⅕ to 1/10) and/or a lower temperature (<80° C.) and/or a shortened reaction time. Since the formation of by-products in this preparation leads to an unwanted increase in viscosity, a distinct improvement in the reaction regime and product quality can thus be assumed.

[0439] c) Use of TiPOSS in 2-Component Clear Encapsulating Systems and PU Varnishes Based on HDI and Other Aliphatic Isocyanates

[0440] Use of TiPOSS as catalyst increases the curing rate in 2-component polyurethane clear encapsulation systems and PU varnishes. The increase in molecular weight distinctly improves the mechanical properties of the varnishes and encapsulating compounds.

[0441] d) TDI Foams/Use of TiPOSS in the Production of Slabstock Foams

[0442] In the production of TDI-based slabstock foams, through use of TiPOSS as catalyst, it is possible to dispense with the use of tin compounds that are harmful to health—as in all other applications mentioned in 5.). There is no loss here in product quality.

[0443] e) FIPFG (Foamed in Place Foam Gaskets)—Sealant Foams

[0444] The production of 2-component polyurethane systems for the FIPFG process based on TiPOSS-catalysed curing is particularly advantageous since the curing process is accelerated by the higher reactivity of TiPOSS compared to DBTL. Polyurethane products can additionally be produced without tin compounds that are harmful to health, which is particularly important for the production of sealant materials in the medical sector, kitchen applications, etc.

[0445] f) Use of TiPOSS in Moisture-Curing 1-Component Isocyanate-Terminated Prepolymers

[0446] The curing of 1-component isocyanate-terminated prepolymers can be accelerated by the use of TiPOSS. It is possible to dispense with the use of tin compounds that are harmful to health. This is of particular relevance when these prepolymers are used as adhesives for customary floor coverings, since it is possible to avoid possible contamination, even if only by small amounts of tin, via the skin of the foot.

[0447] 6.) Specific Embodiments

[0448] Studies on the activity of heptaisobutyl-POSS-titanium(IV) ethoxide TiPOSS in comparison to DBTL

TABLE-US-00002 TABLE 1 Polyols from the KOH- catalyzed reaction f = 2, MW = 2000, PO f = 2, MW = 4000, PO, EO tipped Isocyanate Catalyst f = 3, MW = 4800, PO, EO tipped P-MDI* TiPOSS 0.2% vs. + DTBL 0.2 % P-MDI TiPOSS 0.2% vs. ++ DTBL 0.2 %

TABLE-US-00003 TABLE 2 SPUR Catalyst activity Silylated TiPOSS 0.2% vs. + Polyurethane DTBL 0.2 % (nonaromatic)

List of Abbreviations

[0449] Coatings, Adhesives, Sealants, Elastomers (CASE) [0450] Diisononyl phthalate (DINP) [0451] Dibutyltin dilaurate (DBTDL or DBTL) [0452] Tin(II) 2-ethylhexanoate (tin octoate) [0453] Silylated polyurethanes/silylated polyurethane resins (SPUR) [0454] Heptaisobutyl POSS-titanium(IV) ethoxide (TiPOSS) [0455] Dimethylcyclosiloxane (DMC) [0456] Polyurethane (PU) [0457] Potassium hydroxide (KOH) [0458] FIPFG (foamed in place foam gaskets—gasket foams) [0459] Titanium (Ti) [0460] Polyhedral oligomeric silsesquioxane (POSS)

Embodiments, Especially for Examples II

[0461] 1. Process for preparing prepolymers by reacting a component A with a component B in the presence of a catalyst in a liquid medium, where component A is a polyol and component B a crosslinking component (crosslinker), characterized in that component A is in deficiency relative to component B, and component A and component B are especially used in a ratio of at least 1:1.05, preferably of 1:2.2, and the catalyst is selected from the group of the tin-free polyhedral oligomeric metallosilsesquioxanes, preferably from the group of the titanium(IV) polyoctahedral silsesquioxanes. [0462] 2. Process for preparing polyurethane by combining a two-component system having a component A and a component B in the presence of a catalyst in a liquid medium, where component A is a polyol and component B a crosslinking component (crosslinker), characterized in that components A and B are present separately, and the catalyst has preferably been formulated with component A, and components A and B are present in a ratio of 1.2:1.0 up to 1.0:1.2. [0463] 3. Process for producing polyurethane systems, characterized in that the prepolymers are prepared or preparable according to either of Embodiments 1 and 2 using a catalyst selected from the group of the tin-free polyhedral oligomeric metallosilsesquioxanes, preferably from the group of the titanium(IV) polyoctahedral silsesquioxanes. [0464] 4. Process according to Embodiment 3, characterized in that the prepolymers are functionalized before the reaction with aminosilanes. [0465] 5. Process according to any of the preceding embodiments, characterized in that auxiliaries are added. [0466] 6. Process according to Embodiment 5, characterized in that the auxiliaries are selected from the group consisting of water, cell stabilizers, amine catalysts, fillers, adhesion promoters, moisture scavengers, plasticizers, UV stabilizers, thixotropic agents, or combinations thereof, preferably with one or more additives being one or more silanes. [0467] 7. Process according to Embodiment 6, characterized in that the amine catalyst may be N,N-dimethylpiperazine and/or N,N-dimethylhexadecylamine or a mixture thereof. [0468] 8. Process according to any of the preceding embodiments, characterized in that the catalyst is R.sup.1-POSS-titanium(IV) ethoxide (TiPOSS) where R.sup.1 is an alkyl, allyl or aryl radical or mixtures thereof, and R.sup.1 is preferably a heptaisobutyl. [0469] 9. Process according to any of the preceding embodiments, characterized in that the catalyst content is between 0.0001% and 5% by weight, preferably between 0.001% and 2% by weight, further preferably between 0.01% and 0.3% by weight, especially preferably 0.2, more especially preferably 0.03. [0470] 10. Process according to any of the preceding embodiments, characterized in that the crosslinker is an isocyanate. [0471] 11. Process according to Embodiment 10, characterized in that the isocyanate is aromatic and/or aliphatic, preferably methylene diphenyl isocyanates (MDI) and/or isophorone diisocyanate (IPDI) and/or a hexamethylene diisocyanate trimer (HDI trimer) or a mixture thereof. [0472] 12. Process according to any of the preceding embodiments, characterized in that the polyol is a polyoxypropylene diol, preferably having a molar mass between 2000 g/mol and 18 000 g/mol, more preferably having a molar mass between 12 000 g/mol and 18 000 g/mol. [0473] 13. Process according to any of the preceding Embodiments 1 to 11, characterized in that the polyol is an ethoxylated polyol, preferably a polyether triol tipped with ethoxy groups, and more preferably has a molar mass between 2000 g/mol and 4850 g/mol. [0474] 14. Process according to any of Embodiments 1 to 11, characterized in that the polyol is a polyester polyol, preferably Desmophen 2200 B. [0475] 15. Process according to any of the preceding embodiments, characterized in that the polyol comes from a KOH- and/or DMC-catalysed reaction. [0476] 16. Process according to any of the preceding embodiments, characterized in that the liquid medium is an organic solvent, preferably diisononyl phthalate (DINP). [0477] 17. Process according to any of the preceding embodiments, characterized in that it is tin-free.
in the field of adhesives and sealants.