Hydroxy amino polymer and use thereof in polyurea/polyurethane tissue adhesives
The present invention relates to a process for producing a hydroxy amino polymer comprising the steps: a) Reaction of an H functional starter compound bearing at least one Zerewitinoff active H atom with an unsaturated, cyclical carboxylic acid anhydride and at least one alkylene oxide compound for obtaining a prepolymer bearing hydroxyl groups, b) Addition of a primary amine and/or of ammonia to the double bond(s) of the prepolymer bearing hydroxyl groups obtained according to step a) for obtaining the hydroxy amino polymer, wherein the ratio of added amino groups to hydroxyl groups in a hydroxy amino polymer is at least 0.6. Furthermore, the invention relates to a hydroxy amino polymer, which can be achieved according to this process as well as a polyurea/polyurethane system, which contains such a hydroxy amino polymer.
1. A method for closing, bonding, adhering or covering cell tissue comprising applying a polyurea/polyurethane system comprising
an isocyanate functional prepolymer as a component A) obtained by reacting
an aliphatic and/or aromatic polyisocyanate A1) with
a polyol A2), which may have a number average molecular weight of ≧400 g/mol and an average OH functionality of 2 to 6,
a hydroxy amino polymer as component B),
wherein said hydroxy amino polymer comprises polyester polyol units, polyester-polyether polyol units, and/or polyether polyol units, having a share of oxyethylene units of 40 to 90% by weight, wherein said hydroxy amino polymer is of formula (I)
wherein
“starter” represents the radical of the H functional starter compound,
A represents an aspartate group of the following structure of formulas (IIa) or (IIb)
in which
R1 represent hydrogen or an aliphatic, cycloaliphatic or aromatic radical, which may also contain heteroatoms, particularly nitrogen atoms or oxygen atoms as well as hydroxyl groups,
R2 and R3 independently represent hydrogen or an aliphatic or aromatic radical and R2 and R3 may also be a component of a cycloaliphatic ring system,
R4, R5, R6, and R7 independently represent hydrogen or an aliphatic or aromatic radical and R5 and R6 may also be a component of a cycloaliphatic ring system,
l corresponds to the number of Zerewitinoff active hydrogen atoms of the H functional starter compound,
m, n, and o are independently whole numbers, wherein n is 2 to 430, o≧1 and m≧1, and the ratio of o to 1 in the medium is at least 0.6,
and wherein the equivalent molar mass of a structure shown in formula I does not exceed the value of 18900 g/mol,
potentially organic fillers, which may have a viscosity measured according to DIN 53019 at 23° C. in the range of 10 to 6000 mPa, as a component C),
a reaction product of the isocyanate functional prepolymer according to component A) with hydroxy amino functional compounds according to component B), and/or organic fullers according to component C) potentially as component D), and
optionally water and/or a tertiary amine as a component E),
wherein the hydroxy amino polymer is obtained by:
a) reacting an H functional starter compound bearing at least one Zerewitinoff active H atom with an unsaturated, cyclical carboxylic acid anhydride and at least one alkylene oxide compound for obtaining a prepolymer bearing hydroxyl groups,
b) adding a primary amine and/or an ammonia to the double bond(s) of the prepolymer bearing hydroxyl groups obtained according to step a) for obtaining the hydroxy amino polymer,
wherein the ratio of added amino groups to hydroxyl groups in a hydroxy amino polymer is at least 0.6.
2. The method of claim 1 , wherein the ratio of added amino groups to hydroxyl groups in said hydroxy amino polymer is 0.8 to 2.5, and/or wherein said hydroxy amino polymer has an OH functionality of 1.5 to 6.
3. The method of claim 1 , wherein said H functional starter compound has 1 to 35 Zerewitinoff active H atoms.
4. The method of claim 1 , wherein said unsaturated, cyclical carboxylic acid anhydride is selected from the group of unsaturated, cyclical dicarboxylic acid anhydrides, tetrahydrophthalic acid anhydride, and combinations thereof.
5. The method of claim 1 , wherein said alkylene oxide compound is selected from alkylene oxides with 2 to 24 carbon atoms.
6. The method of claim 1 , wherein a molar ratio between said alkylene oxide compound and carboxylic acid anhydride is at least 1:1.
7. The method of claim 1 , wherein said H functional starter compound is first reacted with an initial amount of alkylene oxide compound and then with the unsaturated, cyclical carboxylic acid anhydride and an additional amount of alkylene oxide compound.
8. The method of claim 1 , wherein the reaction of said H functional starter compound with said unsaturated, cyclical carboxylic acid anhydride and/or the addition of said alkylene oxide compound is performed using a double metal cyanide catalyst (DMC catalyst), wherein said DMC catalyst contains zinc hexacyanocobaltate (III), zinc hexacyanoiridate (III), zinc hexacyanoferrate (III), and/or cobalt (II) hexacyanocobaltate (III).
9. The method of claim 1 , wherein said H functional starter compound is first reacted with said unsaturated, cyclical carboxylic acid anhydride and subsequently with said alkylene oxide compound or wherein said H functional starter compound is simultaneously reacted with said unsaturated, cyclical carboxylic acid anhydride and said alkylene oxide compound, and/or wherein the process is conducted using an amine catalyst.
10. The method of claim 1 , wherein said polyol A2) contains polyester polyol and/or polyester-polyether polyol and/or polyether polyol.
11. The method of claim 1 , wherein said prepolymer A) has an average NCO functionality of 1.5 to 6.
12. The method of claim 1 , wherein a trifunctional polyol is used for producing component A.
13. The method of claim 1 , wherein said organic fillers of component C) are hydroxy functional compounds.
14. The method of claim 1 , wherein a component E) contains a tertiary amine of a general formula (IX),
in which R 8 , R 9 , and R 10 may independently be alkyl or heteroalkyl radicals having heteroatoms in an alkyl chain or at their ends, or R 8 and R 9 can form an aliphatic, unsaturated or aromatic heterocycle together with a nitrogen atom bearing them, which may potentially contain additional heteroatoms.
15. The method of claim 1 , wherein said tertiary amine is selected from the group consisting of triethanolamine, tetrakis(2-hydroxyethyl)ethylenediamine, N,N-dimethyl-2-(4-methylpiperazine-1-yl)ethanamine, and 2-{[2-(dimethylamino)ethyl](methyl) amino}ethanol, 3,3′,3″-(1,3,5-triazinane-1,3,5-triyl)tris(N,N-dimethyl-propane-1-amine).
16. The method of claim 1 , wherein said component E) contains 0.2 to 2.0% by weight of water and/or 0.1 to 1.0% by weight of said tertiary amine.
17. The method of claim 1 , wherein the polyurea/polyurethane system is applied with a dispensing system having two chambers, wherein said component A) is contained in one chamber and said component B) and optionally components C), D), and E) of said polyurea/polyurethane system are contained in another chamber.
18. A method for closing, bonding, adhering or covering cell tissue comprising applying
a polyurea/polyurethane system comprising
an isocyanate functional prepolymer as a component A) obtained by reacting
an aliphatic and/or aromatic polyisocyanate A1) with
a polyol A2), which may have a number average molecular weight of ≧400 g/mol and an average OH functionality of 2 to 6,
a hydroxy amino polymer as component B),
wherein said hydroxy amino polymer comprises polyester polyol units, polyester-polyether polyol units, and/or polyether polyol units, having a share of oxyethylene units of 40 to 90% by weight, wherein said hydroxy amino polymer is of formula (I)
wherein
“starter” represents the radical of glycerin,
A represents an aspartate group of the following structure of formulas (IIa) or (IIb)
in which
R1 is n-pentyl
R2 and R3 are H,
R4, R5, R6, and R7 are H or methyl, wherein at the most one is methyl,
l corresponds to the number of Zerewitinoff active hydrogen atoms of the H functional starter compound,
m, n, and o are independently whole numbers, wherein n is 2 to 430, o≧1 and m≧1, and the ratio of o to 1 in the medium is at least 0.6,
and wherein the equivalent molar mass of a structure shown in formula I does not exceed the value of 18900 g/mol,
potentially organic fillers, which may have a viscosity measured according to DIN 53019 at 23° C. in the range of 10 to 6000 mPa, as a component C),
a reaction product of the isocyanate functional prepolymer according to component A) with hydroxy amino functional compounds according to component B), and/or organic fullers according to component C) potentially as component D), and
optionally water and/or a tertiary amine as a component E),
wherein the hydroxy amino polymer is obtained by:
a) reacting an H functional starter compound bearing at least one Zerewitinoff active H atom with an unsaturated, cyclical carboxylic acid anhydride and at least one alkylene oxide compound for obtaining a prepolymer bearing hydroxyl groups,
b) adding a primary amine and/or an ammonia to the double bond(s) of the prepolymer bearing hydroxyl groups obtained according to step a) for obtaining the hydroxy amino polymer,
wherein the ratio of added amino groups to hydroxyl groups in a hydroxy amino polymer is at least 0.6.