Other features and advantages of the present invention will become apparent in the following detailed description of the preferred embodiments of this invention, with reference to the accompanying drawings, in which:
Before the present invention is described in greater detail, it should be noted that same reference numerals have been used to denote like elements throughout the specification.
Referring to
The optical material 100 in this embodiment is made by: (a) providing a base layer 31 having an upper side 311 and a lower side 312; (b) contacting the upper side 311 of the base layer 31 with a first solution containing a monomeric compound of a first polymer such that the monomeric compound of the first polymer penetrates into the base layer 31 so as to form a first penetrated region in the base layer 31 and such that the monomeric compound of the first polymer forms into a first polymerizable layer on the first penetrated region of the base layer 31; (c) polymerizing the monomeric compound of the first polymerizable layer and the monomeric compound in the first penetrated region of the base layer 31 using ultraviolet light or heat so as to form the first penetrated region into the first complex layer 32 and the first polymerizable layer into the first optical layer 33 such that a first optical unit 3 is obtained; and (d) bonding a substrate 2 to the lower side 312 of the base layer 31 of the first optical unit 3 by injection molding.
The term “monomeric compound” described hereinafter refers to a precursor of a polymer including a monomer or a prepolymer of the polymer. Preferably, the monomeric compound of the first polymer is a prepolymer having a molecular weight ranging from 50 to 5,000, and more preferably, from 50 to 500.
The first complex layer 32 thus formed includes the base polymer and the first polymer, and is formed by polymerizing the monomeric compound of the first polymer after the monomeric compound penetrates into the base polymer of the base layer 31. With such complex layer 32, the adhesion between the base layer 31 and the first optical layer 33 is improved.
In this invention, the substrate 2 is made of a substrate polymer selected from the group consisting of polycarbonate (PC), polymethylmethacrylate (PMMA), polysulfone, polystyrene (PS), polyurethane (PU), m-cycloolefin copolymer (m-COC), transparent nylon, allyl methacrylate, diethylene glycol bis allylcarbonate (e.g., CR-39), polycarbonate/polyester alloy (e.g., xylex™ available from GE company, USA), and a resin having a refractive index greater than 1.56 (i.e., medium index resin and high index resin). More preferably, the substrate 2 is made of a substrate polymer selected from the group consisting of polycarbonate, polymethylmethacrylate, polystyrene, polyurethane, m-cycloolefin copolymer, polycarbonate/polyester alloy, and transparent nylon. Since polycarbonate/polyester alloy has a low photoelastic stress and a low injecting temperature, it is more suited for the substrate 2 than the others.
Preferably, the base layer 31 exhibits polarizing property and is made of a base polymer selected from the group consisting of polyvinyl alcohol (PVA), polyethylene terephthalate (PET), polyester, polyacrylate, polycarbonate (PC), polyurethane (PU), cellulose ester, cycloolefin copolymer, polycarbonate/polyester alloy, and combinations thereof.
The first polymer is selected from the group consisting of ethylene glycol bismethacrylate polymer, ethoxylated phenol bismethacrylate polymer, urethane acrylate polymer, polythiourethane polymer, cellulose acetate butyrate, styrene polymer, polyurethane, copoly(styrene-methyl methacrylate) polymer, and combinations thereof. More preferably, the first polymer is selected from the group consisting of ethylene glycol bismethacrylate polymer and polyurethane. The amount of the first polymer is relevant to the layer thickness of the first optical layer 33 and varies based on the intended use of the optical material 100.
A first solvent included in the first solution is used to dissolve the first polymer and to permit swelling of the base layer 31. Preferably, the first solvent suitable for this invention has high polarity, and is selected from the group including, but not limited, tetrahydrofuran (THF), toluene, hexanone, ether for dissolving polymers, etc..
The first solution further includes a first dye such that the first dye remains in the first polymerizable layer. The first dye is a photochromic dye or a photo-absorbing dye such that the optical material 100 is capable of changing color with the extrinsic environment and is further capable of preventing injury to the human eyes. The first dye suitable for this invention includes, for example, blue photochromic dye, Reversacol™ photochromic dyes available from James Company, anti-infrared photo-absorbing dye, anti-UV photo-absorbing dye, melanin dye, and dichroic dyes. The amount of the first dye preferably ranges from 0 to 15 wt % of the first polymer, more preferably, from 4 to 8 wt %, and most preferably, from 5 to 6 wt %, when the first dye is a photochromic dye.
The first solution has a solid content less than 70 wt %, preferably, ranging from 4 to 50 wt %, and more preferably, from 15 to 35 wt %. In addition, the first solution has a viscosity ranging from 1 CPS to 150 CPS, and preferably, from 20 to 40 CPS.
In this method, the first solvent permits penetration of the first monomeric compound of the first polymer into the base layer 31. The penetration of the first monomeric compound of the first polymer can be conducted by directly pouring the first solution onto the upper side 311 of the base layer 31, or spreading the first solution on the upper side 311 of the base layer 31 using a roller or an appropriate device (e.g., a duckbill nozzle). The layer thickness of the first polymerizable layer can be controlled by the pouring rate of the first solution, the solid content and the amount of the first solution, and the spreading speed of the device. The pouring rate ranges from 1 to 100 mm/sec, and preferably from 10 to 20 mm/sec. When using the duckbill nozzle, the spreading speed is set at 15 mm/sec. After spreading and immersing for 1 to 15 minutes, the base layer 31 and the first polymerizable layer are treated by ultraviolet light or heat.
If the optical material 100 is to be used as an ophthalmic lens, the method further includes a step of (e) shaping the first optical unit 3 into a desired shape before the bonding step (d). The shaping conditions can vary based on actual requirements.
In this embodiment, the second polymer and the second solution are respectively similar to the first polymer and the first solution in the first preferred embodiment. Preferably, the second solution further includes a second dye similar to the first dye of the first preferred embodiment.
The method for making the fourth preferred embodiment is similar to that for making the third preferred embodiment except that, after the step (d), the method further includes the steps of: (h) contacting the lower surface 22 of the substrate 2 with a third solution containing a monomeric compound of a third polymer such that the monomeric compound of the third polymer penetrates into the substrate 2 so as to form a third penetrated region in the substrate 2 and such that the monomeric compound of the third polymer forms into a third polymerizable layer on the third penetrated region of the substrate 2; and (i) polymerizing the monomeric compound of the third polymerizable layer and the monomeric compound in the third penetrated region of the substrate 2 so as to form the third penetrated region into the third complex layer 41 and the third polymerizable layer into the third optical layer 42.
In this embodiment, the third polymer and the third solution are respectively similar to the first polymer and the first solution in the first preferred embodiment. Preferably, the third solution further includes a third dye similar to the first dye of the first preferred embodiment.
The layer thicknesses of the substrate 2 and each of the layers of the optical units 3, 4, are not limited and vary based on actual requirements. In an embodiment of this invention, for example, the first optical unit 3 has a layer thickness ranging from 0.2 mm to 2.0 mm, and more preferably, from 0.5 mm to 0.8 mm.
In addition, the penetration extent of each of the dyes into the respective one of the complex layers 32, 36, 41 can be controlled by controlling the contacting time and swelling degree of the base layer 31 and the substrate 2.
An optical material 100 shown in
A salt test and a weather test were conducted on the optical material 100 thus formed. The salt test was performed as follows: placing the optical material 100 thus formed in a 10 wt % salt solution (e.g., a solution of sodium chloride) at 95° C. for one hour; taking out the optical material 100 and cutting the optical material 100 to form 100 cells using a cross hatch cutter at 45° cutting angle; attaching a 3M Scotch tape on the first optical layer 33 of the optical material 100; removing the 3M Scotch tape from the optical material 100; and observing delamination phenomenon of each of the cells of the optical material 100. Moreover, the weather test was performed as follows: placing the optical material 100 which had been cut into 100 cells using the cross hatch cutter in 20 liters of 5 wt % salt solution (e.g., a solution of sodium chloride) in the salt spray device at 40° C. and 95% relative moisture for 48 hours; and taking out the optical material 100 to observe the delamination phenomenon. If no delamination was found, 3M Scotch tape was then attached to the optical material 100 and was then removed therefrom to observe delamination phenomenon of each of the cells of the optical material 100.
The results show that no delamination phenomenon of each of the cells of the first preferred embodiment of the optical material 100 was found after the tests.
The method for making the second preferred embodiment of the optical material 100 shown in
The optical material 100 thus formed was subjected to the salt test and the weather test, in which a 3M Scotch tape was attached onto the hard coating 34. Similarly, the results show that no delamination phenomenon of each of the cells of the second preferred embodiment of the optical material 100 was found.
The method for making the third preferred embodiment of the optical material 100 shown in
The optical material 100 thus formed was subjected to the salt test and the weather test, in which a 3M Scotch tape was attached onto the hard coating 34. Similarly, the results show that no delamination phenomenon of each of the cells of the third preferred embodiment of the optical material 100 was found.
The method for making the fourth preferred embodiment of the optical material 100 shown in
The optical material 100 thus formed was subjected to the salt test and the weather test, in which a 3M Scotch tape was attached onto the hard coating 34. Similarly, the results show that no delamination phenomenon of each of the cells of the fourth preferred embodiment of the optical material 100 was found.
According to the present invention, the complex layers 32, 36, and 41 provide improved bonding strength to the layers adhered thereto, and the optical material 100 with the complex layers 32, 36, and 41 can be easily made by the method of this invention, thereby preventing the delamination phenomenon and reducing production costs.
While the present invention has been described in connection with what is considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation and equivalent arrangements.