Polyamines containing urea groups and process for their preparation
AssigneeHuels Aktiengesellschaft
InventorsRainer Gras, Elmar Wolf
Life of this patent
Estimating the term…
Abstract
Low-viscosity (cyclo)-aliphatic polyamines containing urea groups and having more than two amino groups may be prepared by reacting (cyclo)aliphatic diamines with polyisocyanates containing isocyanurate groups or biuret groups. Such polyamines are useful as components in PUR reaction finishes and coating and adhesive compositions.
Claims11
A low-viscosity (cyclo)aliphatic polyamine containing urea groups and having more than two amino groups, obtained by reacting a diamine of the formula (I):
- R.sup.1 --NH--A--NH--R.sup.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted, R.sup.1 and R.sup.2 are H or a radical of the formula ##STR14## wherein R.sup.3 is a (cyclo)aliphatic hydrocarbon radical having 1-12 carbon atoms, which is optionally branched, with polyisocyanates containing isocyanurate and/or biuret groups and of the formula (II):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN--(B)--NCO (IIb),
- wherein B is ##STR15## [X].sub.n is:
- ##STR16## and n is 1-4, the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 moles of the diamine (I) are reacted per the total moles of NCO groups in the compounds of formulae (IIa) and (IIb).
A low-viscosity (cyclo)aliphatic polyamine containing urea groups and having more than two amino groups, obtained by:
- (A) reacting a diamine of the formula (I):
- NH.sub.2 --A--NH.sub.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted,
- with polyisocyanates containing isocyanurate and/or biuret groups and of the formula (II):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN--(B)--NCO (IIb),
- wherein B is ##STR17## [X].sub.n denotes:
- ##STR18## and n is 1-4, the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 moles of the diamine (I) are reacted per the total of NCO groups in the compounds of formulae (IIa) and (IIb);
- and
- (B) reacting the product with one mole of maleic or fumaric C.sub.1-12 -(cyclo)aliphatic hydrocarbyl ester per NH.sub.2 equivalent.
A process for the preparation of a low-viscosity (cyclo)aliphatic polyamine containing urea groups, said process comprising:
- reacting a diamine of formula (I):
- R.sup.1 --NH--A--NH--R.sub.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted and R.sup.1 and R.sup.2 are H or a radical of the formula ##STR19## wherein R.sup.3 is a (cyclo)aliphatic hydrocarbon radical having 1-12 carbon atoms, which is optionally branched, with polyisocyanates containing isocyanurate and/or biuret groups of formulae (IIa) and (IIb):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN'(B)--NCO (IIb),
- wherein B is ##STR20## [X].sub.n is:
- ##STR21## the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 mole of the diamine (I) are reacted per the total of NCO groups in the compounds of formulae (IIa) and (IIb), at a temperature of 100.degree. to 190.degree. C.
A process for the preparation of a (cyclo)aliphatic polyamine containing urea groups, said process comprising:
- (A) reacting a diamine of formula (I):
- H.sub.2 N--A--NH.sub.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted,
- with polyisocyanates containing isocyanurate and/or biuret groups of formulae (IIa) and (IIb):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN--(B)--NCO (IIb),
- wherein B is ##STR22## [X].sub.n is:
- ##STR23## and n is 1-4, the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 mole of the diamine (I) are reacted per the total of NCO groups in the compounds of formulae (IIa) and (IIb), at a temperature of 150.degree.-190.degree. C.;
- and
- (B) reacting the product with one mole of maleic or fumaric C.sub.1-2 -(cyclo)aliphatic hydrocarbyl ester per NH.sub.2 equivalent at a temperature of 50.degree. to 70.degree. C.
A method of coating an article, comprising coating said article with a composition which comprises a low-viscosity (cyclo)aliphatic polyamine containing urea groups and having more than two amino groups, said (cyclo)aliphatic polyamine being obtained by reacting a diamine of the formula (I):
- R.sup.1 --NH--A--NH--R.sup.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted, R.sup.1 and R.sup.2 are H or a radical of the formula ##STR24## wherein R.sup.3 is a (cyclo)aliphatic hydrocarbon radical having 1-12 carbon atoms, which is optionally branched, with polyisocyanates containing isocyanurate and/or biuret groups and of the formula (II):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN--(B)--NCO (IIb),
- wherein B is ##STR25## [X].sub.n denotes:
- ##STR26## and n is 1-4, the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 moles of the diamine (I) are reacted per the total moles of NCO groups in the compounds of formulae (IIa) and (IIb).
A method adhering a first surface to a second surface, comprising:
- (i) coating said first surface with a low-viscosity (cyclo)aliphatic polyamine containing urea groups and having more than two amino groups, said (cyclo)aliphatic polyamine being obtained by reacting a diamine of the formula (I):
- R.sup.1 --NH--A--NH--R.sup.2 (I)
- wherein A is a (cyclo)aliphatic hydrocarbon radical having 2-16 carbon atoms which is optionally C.sub.1-4 -alkyl-substituted, R.sup.1 and R.sup.2 are H or a radical of the formula ##STR27## wherein R.sup.3 is a (cyclo)aliphatic hydrocarbon radical having 1-12 carbon atoms, which is optionally branched, with polyisocyanates containing isocyanurate and/or biuret groups and of the formula (II):
- OCN--(B)--[X].sub.n --NCO (IIa)
- and
- OCN--(B)--NCO (IIb),
- wherein B is ##STR28## [X].sub.n denotes:
- ##STR29## and n is 1-4, the weight ratio of (IIa) to (IIb) is (100 to 20) to (0 to 80) and 1 to 5 moles of the diamine (I) are reacted per the total moles of NCO groups in the compounds of formulae (IIa) and (IIb);
- and
- (ii) bring said second surface in contact with said coated first surface.
Dependencies are inferred from the claim text.