Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
1998-12-22
2001-04-10
Owens, Amelia (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C524S102000
Reexamination Certificate
active
06214995
ABSTRACT:
FIELD OF INVENTION
The present invention relates to compositions of reactive hindered amine light stabilizers, when added to certain polymers produced ultra-violet light stabilized materials. These photo-stabilizers are hindered amine light stabilizers (HALS) having one or more imido and/or amido functionalities which can be subsequently reacted with aldehydes, e.g., formaldehyde, to give hydroxyalkylated derivatives. The corresponding hydroxyalkylated compounds can be further reacted with lower alkyl alcohol's to give the more stable alkoxylated derivatives.
HALS containing an anilino or phenolic group, whereby the ortho and/or para positions are unsubstituted can be hydroxyalkylated and subsequently alkoxylated to confer desirable photo-stabilization properties to various polymers represent another class of ultra-violet absorbers of this invention.
HALS for the purpose of this invention has the following definition: A sterically hindered secondary amine with no alpha hydrogen atoms attached to the two carbons adjacent to the secondary amine nitrogen atom. Furthermore, the secondary amine nitrogen atom can be substituted by hydrogen, hydroxyl, ether, ester, amide, alkyl, aryl, and alkylaryl and the like.
DESCRIPTION OF THE PRIOR ART
It is know in this art that organic polymers used in the coatings, molding and laminating industries are degraded when they are subjected to extraneous agents, especially the combined action of air and ultra-violet radiation in sunlight. Such degradation is typically restricted by introducing small amounts of stabilizers into the polymer.
At present, some of the most effective of these UV stabilizers are the sterically hindered amines, in particular 2,2,6,6-tetramethylpiperidines. However, other none piperidyl HALS can also be employed in this investment.
In practice however, one of the major problems in the use of these stabilizers is to provide a good compromise between their effectiveness and the persistence of their activity, which employs the use of molecules of high molecular weight, which do not bloom.
SUMMARY OF THE INVENTION
Accordingly a major object of the present invention is the provision of novel reactive stabilizers, which conspicuously ameliorate these disadvantages and drawbacks to-date, characterizing the state of the art.
This invention involves novel compositions of matter comprising HALS, which are either hydroxyalkylated or an alkoxylated (lower alkyl group) thereof. The HALS having at least one imido and/or amido group, or preferably two or more of these groups, capable of being reacted with and aldehydes to give a hydroxyalkylated derivative and subsequently being capable of an alkoxylation with a lower alkyl alcohol. The reactivity of these HALS are the imido group
and/or the amido group when can be methylated with formaldehyde or other aldhydes
This can be further reacted with methanol, butanol, etc., to give a more stabile and more solvent soluble reactive product via etherification.
Furthermore, HALS containing either phenolic or anilino moieties can also be reacted with aldehydes e.g., formaldehyde and further reacted with a lower alkyl alcohol to form an alkoxylated derivative if desired, are additional effective reactive ultra-violet absorbers.
These type HALS can be copolymerized/co-reacted from about 1 to about 10 wt % with aminoplasts, epoxies, urethanes, polyamides, polyesters and other polymeric compositions having reactive functionalities like oxirane, amino, hydroxyl, thiol, anhydride and carboxyl groups. This invention is also a curable composition containing the novel stabilizers of this invention. This invention is also an improved method of stabilizing polymers wherein the improvement comprises adding to said polymers the novel stabilizers of this invention.
The advantages of the anchored stabilizers of this invention over their unanchored precursors include generally higher compatibility with polymers and resins and generally lower volatility due to high molecular weights.
DETAILED DESCRIPTION OF THE INVENTION
The novel HALS useful for this invention can be quite diversified in their chemical structure. However, they all must contain at least one or more amido and/or imido functional group. Another chemical moiety that is applicable for this invention involves the presence of an anilino and/or phenolic functionately within the HALs structure. Obviously, both of these functionalities can coexist is the same molecule.
HAL Structures
The following HALS are examples of structures which can be easily converted to useful chemically reactive HALS as illustrations for this invention. It is obvious that many other theoretical chemical structures can exit. Anyone skilled in the art of organic synthesis can conjure up other examples. Nevertheless, in order to be operative in this invention a sterically hindered amine having either one or more of a) imido and /or amido functionality, and/or b) phenolic or anilino functionality with one or more free ortho and/or para positions to introduce one or more hydroxyalkylated and/or alkoxylated groups.
Some Proposed Reactive HALS
The above structures (I-VII) are made reactive by forming hydroxyalkylated or alkoxylated derivatives thereof.
The preparation of all of these HALS (I-VII) prior to hydroalkylation or alkoxylation can be found in two publications; a) M. Dagonneau et. al., Rev. Macromol. Chem. Phys. C22 C21, p169-202 (1982-83), and b) M. Dagonneau et al, Synthesis, November 1984, p895-916.
It is to be understood that the foregoing examples are illustrative only and that other means and techniques can be employed without departing from the true scope of the invention as defined in the claims of this invention.
The following example serves to illustrate the invention.
REFERENCES:
patent: 3536722 (1970-10-01), Murayama et al.
patent: 3941744 (1976-03-01), Murayama et al.
patent: 3975462 (1976-08-01), Murayama et al.
patent: 4162246 (1979-07-01), Soma et al.
patent: 4219465 (1980-08-01), Soma et al.
patent: 4233410 (1980-11-01), Rody et al.
patent: 4495325 (1985-01-01), DeBergalis et al.
patent: 5204422 (1993-04-01), Seltzer et al.
Dagonneau, M. et al ‘Chemistry of Hindered Amines From the Piperidine Series’ Synthesis, pp. 895-916, Nov. 1984.*
Dagonneau, M. et al ‘Sterically Hindered Amines and Nitroxyls as Polymer Stabilizers’ Rev. Macromol. Chem. Phys C22(2), pp. 169-202, 1983.
Owens Amelia
Stockel Richard F.
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