Temperature stable and sunlight protected photochromic articles

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Processes of preparing a desired or intentional composition...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

06262155

ABSTRACT:

FIELD OF THE INVENTION
The invention relates to new photochromic transparent organic materials with a high refractive index, to a process for their preparation, and to the articles made of these materials.
BACKGROUND OF THE INVENTION
It is difficult to find a photochromic material allowing for the production of an ophthalmic lens whose transmittance varies as a function of the lighting. Outside of their photochromic properties (i.e., colorability, rapid darkening and lightening kinetics, acceptable durability, etc.), such lenses are generally made by the use of appropriate mixtures of photochromic compounds such as spirooxazines and chromenes. The polymer matrixes which are used, though thermally crosslinked, have a low glass transition point, generally lower than that of CR39®, a reference ophthalmic resin consisting of diethylene glycol bis(allyl carbonate) available from PPG Industries, so as to have rapid photochromic kinetics. Moreover, these polymers generally have a relatively low refractive index (<1.54).
The majority of these thermally crosslinked matrixes are obtained by radical polymerization (i.e., polymerization which most often can only be carried out provided that one uses initiators of the organic peroxide type.) The use of organic peroxides makes it practically impossible to incorporate photochromic molecules in the mixture of monomers before polymerization, the peroxides having the effect either of destroying any photochromic effect or of giving the product an unacceptable permanent intense coloration. Also, one is obliged to later incorporate coloring agents into the matrix, most often by a special thermal diffusion process.
Therefore, there continues to be a need for photochromic trans-parent organic materials which have improved photochromic properties and which are easy to manufacture and not very expensive to manufacture.
SUMMARY OF THE INVENTION
Briefly, the invention relates to new photo-chromic transparent organic materials which are particularly useful for the production of photochromic organic ophthalmic lenses. The organic material consists of an optical-quality polymer matrix and at least one coloring agent giving photochromic properties to the matrix. The coloring agent is chosen from the group of the spirooxazines, the spiropyrans, and the chromenes. The polymer of the matrix is chosen from (a) homopolymers of ethyoxylated bisphenol A dimethacrylate having formula I:
in which R is H or CH
3
, and m and n independently represent 1 or 2, and (b) copolymers of ethoxylated bisphenol A dimethacrylate containing, at most, 30 wt % of at least one aromatic monomer with vinyl, acrylic, or methacrylic functionality.
Surprisingly, we have found that the materials of the invention are characterized particularly by a glass transition point, and therefore by a hardness, which is greater than that of many hitherto known organic ophthalmic products without any adverse effects on the darkening and lightening speeds. We have also found that, through the choice of an appropriate mixture of several coloring agents, it is possible to obtain the desired tint in such matrixes, particularly gray or brown, with this tint practically not varying in the course of darkening and lightening.
The inventive organic materials also exhibit a high refractive index, which is in all cases greater than 1.54, and which can be adjusted, if necessary, to the desired value by the use of an appropriate modifying comonomer.
Useful co-monomers for the invention include vinyl, acrylic or methacrylic compounds containing in their formula one or more benzene nuclei. Examples of some useful co-monomers are, divinylbenzene, diallyl phthalate, benzyl or naphthyl acrylates or methacrylates, etc., as well as their derivatives substituted on the aromatic nucleus or nuclei by chlorine or bromine atoms.
In another aspect, the invention also relates to a process for the preparation of the photochromic organic materials of the invention by polymerizing an ethoxylated bisphenol A dimethacrylate, corresponding to formula I:
in which R is H or CH
3
, and m and n independently represent 1 or 2, optionally with up to 30 wt % of one or more modifying aromatic monomers with vinyl, acrylic or methacrylic functionality, in the presence of a diazo radical initiator and in the absence of a peroxide radical initiator. Preferably, R is H, and m=n=2.
Preferably, the polymerization is carried out in the presence of at least one photochromic coloring agent, which allows one to color the final material in its mass.


REFERENCES:
patent: 4912014 (1990-03-01), Feldman
patent: 4957843 (1990-09-01), Hipps
patent: 5330686 (1994-07-01), Smith
patent: 5516621 (1996-05-01), Tsuda
patent: 5552090 (1996-09-01), VanGemert
patent: 5585042 (1996-12-01), Knowles
patent: 5621017 (1997-04-01), Kobayakawa et al.
patent: 5645767 (1997-07-01), VanGemert
patent: 5651923 (1997-07-01), Kumar
patent: 5656206 (1997-08-01), Knowles
patent: 40 10 783 A1 (1991-10-01), None
patent: 0142921 (1985-05-01), None
patent: 2431511 (1980-02-01), None
patent: WO-A-92/05209 (1992-04-01), None

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Temperature stable and sunlight protected photochromic articles does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Temperature stable and sunlight protected photochromic articles, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Temperature stable and sunlight protected photochromic articles will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2555873

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.