Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From reactant having at least one -n=c=x group as well as...
Reexamination Certificate
2002-01-07
2004-01-13
Sergent, Rabon (Department: 1711)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
From reactant having at least one -n=c=x group as well as...
C528S059000, C528S060000, C528S067000, C528S071000, C528S073000, C528S074500, C528S080000, C528S083000
Reexamination Certificate
active
06677424
ABSTRACT:
The invention relates to a coating composition comprising at least one OH-functional binder component and at least one component compound, functioning as a crosslinking agent, which has NCO groups blocked with a pyrazole compound.
Coating compositions are used to coat a substrate with one (or more) coat(s) which may have a substrate-protective function, especially an anticorrosion function, a surfacer function, leveling out instances of surface unevenness, and/or a decorative function. Such coating compositions are referred to as primer, surfacer and topcoat. Where the decorative topcoat is not to be actually the topmost coat, owing to subsequent overcoating with an additionally protecting clearcoat finish, it is also referred to as a basecoat. The term component or component compound is intended to express that the respective components may be present as different substances in the coating composition or that the components may be parts of a single substance. If an OH-functional binder component is one substance which at the same time contains the component compound functioning as crosslinking agent, then said substance is self-crosslinking. If, on the other hand, it comprises different substances, then there is a customary substance pairing comprising binder and crosslinker. In a crosslinking reaction, free NCO groups react with free OH groups. Blocked isocyanate groups are isocyanate groups which have been provided with a protective group and which at room temperature are unreactive, or virtually unreactive, toward free OH groups. A coating composition of the structure specified at the outset can therefore be stored for long periods without any premature crosslinking, which would disrupt the processing. After processing, the protective groups are removed just by the action of heat, in the form known as stoving, and the NCO groups are reactivated so that the crosslinking reaction, which is now desired, and, consequently, the curing of the coating produced can take place. The use of pyrazole compounds as protective groups has the advantage, in particular, that the activation of the NCO groups and, consequently, stoving or curing can take place at relatively low temperatures (low-bake method).
Coating compositions of the composition specified at the outset are known from the literature references EP 0 159 117, EP 0 682 051 and WO 95/06674. In these known coating compositions an OH functional binder component is crosslinked with a separate polyisocyanate compound which functions as a crosslinking agent, said separate polyisocyanate compound being of customary and simple construction and the NCO groups being blocked with a pyrazole compound. In the case of EP 0 682 051 and WO 95/06674 a conventional blocking compound is employed in addition to the pyrazole compound. The polyisocyanate compounds described cannot be given a self-crosslinking configuration.
The literature reference EP 0 688 803 discloses a flexibilized plastic, especially for the construction sector, in which an amine-functional substance is cured with an isocyanate prepolymer having blocked NCO groups which is built up on the basis of aromatic diisocyanates and polyether alcohols. The NCO groups are blocked with various blocking compounds, including a pyrazole compound.
These known coating compositions are capable of improvement in various respects. On the one hand, it is desirable to reduce the stoving temperature. On the other hand, however, the customary properties, especially the good sandability and good topcoat holdout in conjunction with conventional and water-thinnable (decorative) basecoats in the case of a surfacer, must be at least maintained.
Against this background, the technical problem of the invention is to create a coating composition of improved stoving behavior which produces coatings that satisfy all of the technical coatings requirements.
To solve this technical problem the invention teaches that the component compound which functions as crosslinking agent is obtainable by a) polymerizing a polyol or a mixture of polyols having a number-average molecular weight in the range from 300-5000 by adding a polyisocyanate compound A or a mixture of polyisocyanate compounds A to give a polyurethane prepolymer, b) chain-extending the polyurethane prepolymer by adding a chain extender compound, to give a polyurethane polymer having free OH groups, c) reacting the OH-containing polyurethane polymer from b) with a polyisocyanate B or a mixture of polyisocyanates B to give a polyisocyanate-polyurethane polymer, and d) free isocyanate groups of the polyisocyanate-polyurethane polymer having been blocked with the pyrazole compound or a mixture of pyrazole compounds.
The core of the invention, accordingly, is that first an OH-containing polyurethane polymer of specific composition is prepared from a polyurethane prepolymer and that second a polyisocyanate-polyurethane polymer is formed from said prepolymer with a polyisocyanate B, with a certain proportion, up to 100%, of the NCO groups of the polyurethane prepolymer having already been subjected to controlled blocking with a pyrazole compound. Surprisingly, a coating composition of the invention is not only curable at low temperature but also exhibits improved properties, especially a very good sandability.
In one preferred embodiment of the invention the component compound which functions as a crosslinking agent is obtainable by blocking some of the free isocyanate groups of the polyurethane prepolymer and/or some of the free isocyanate groups of the polyisocyanate B before chain extension with the pyrazole compound or mixture of pyrazole compounds.
A coating composition of the invention can be configured individually in various ways. If the component compound which functions as a crosslinking agent is to be externally crosslinking, then it is advisable for all free OH groups of the chain-extended polyurethane polymer to be reacted with the polyisocyanate B or mixture of polyisocyanates B and for the OH-functional binder component to be a substance which is different from the component compound which functions as a crosslinking agent. If, on the other hand, the component compound which functions as a crosslinking agent is to be self-crosslinking, in which case it may be possible to omit a separate OH-functional binder component (but not necessarily so), then it is advisable for only some of the free OH groups of the chain-extended polyurethane polymer to be reacted with the polyisocyanate B or mixture of polyisocyanates B and for at least one OH-functional binder component to be identical with the component compound which functions as a crosslinking agent.
In one preferred embodiment, the procedure is such that the chain extender compound has a secondary amine group and at least two OH groups. In this case, one secondary amine group reacts first of all with a polyurethane prepolymer molecule. Then one of the two OH groups reacts with another polyurethane prepolymer molecule. Depending on the proportions in which the polyisocyanate B is employed, the result is an OH-containing compound which functions as a crosslinking agent or a compound which is virtually free from OH groups.
To aid understanding of the invention, idealized molecules of the two above-described variants of the component compound which functions as a crosslinking agent are shown below. Molecule (1) is a compound which is virtually free from OH groups. This is employed, in otherwise conventional manner, together with a separate OH-functional binder component. Molecule (2) is an OH-containing compound, which is consequently self-crosslinking.
Polyols suitable for preparing the polyurethane prepolymer are, in principle, all conventional polyols, examples being polyester polyols and/or polyether polyols customary in the field of paint chemistry. Such polyols are known to the skilled worker and need not be elucidated further here. It is preferred to use a polyester diol which is obtainable from isophthalic acid, dimeric fatty acid and hexanediol and has a number-average molecular weight of 1000-
Figge Hans-Jünrgen
Schilling Marita
Wigger Georg
BASF Coatings AG
Sergent Rabon
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