Patent Grant
11187829
The present disclosure relates to an optical element used in optical apparatuses, such as an interchangeable lens of a single-lens reflex camera and, particularly, to an optical element including a substrate having an inclined chamfer and a level chamfer and a light shielding film disposed over a portion of the substrate. The present disclosure also relates to a method for manufacturing the optical element.
In an optical element, such as a lens or a prism, used in an optical apparatus such as a camera or a microscope, stray light is produced by surface reflection or internal reflection of incoming light. Stray light causes flaring or ghosts, reducing the optical performance of the optical apparatus. In order to prevent surface reflection or internal reflection, optical elements are provided with a light shielding antireflection film that is formed by applying a light shielding paint onto the edge of the substrate or the edge of the optically effective surface of the substrate.
Also, the substrates of many of the optical elements are made of a vitreous material having as high a refractive index as 1.80 to 2.00 or more than 2.00 along with the recent trend to compact, high-performance optical apparatuses. If the peripheral surface or the like of an optical element made of such a high-refractive-index material is provided with a light shielding film formed by applying a light shielding paint onto the peripheral surface, whitish bright spots (white spots) are formed at the interface between the substrate and the light shielding film, degrading the quality in appearance of the optical element. The white spots are produced by reflected light (scattered light) caused by a difference in refractive index between the substrate and voids or cavities formed in the light shielding film filling the cracks formed in the peripheral surface of the substrate when the substrate is cut.
Japanese Patent Laid-Open No. 2016-30706 discloses an optical element from which white spots is reduced by controlling the drying speed of the light shielding paint so as to sufficiently fill the cracks with the light shielding paint, thus suppressing scattering of light coming from the outside.
In this optical element, the ridge portion (and the vicinity thereof) defined by the inclined chamfer and the level chamfer are not easily subjected to additional treatment to eliminate cracks compared to the other portion of the peripheral surface, and many cracks remain the ridge portion. In addition, the light shielding paint applied onto the ridge portion flows out of the ridge portion due to the surface tension thereof, thus reducing the thickness of the coating of the paint. Accordingly, the thin portion of the coating dries rapidly before the paint completely fill the cracks, thus forming voids or cavities in the cracks.
Accordingly, the present disclosure provides an optical element from which white spots at the ridge portion defined by an inclined and a level chamfer of the substrate are reduced.
According to an aspect of the present disclosure, there is provided an optical element including a substrate having an optically effective surface and an optically non-effective surface having an inclined chamfer and a level chamfer that define a ridge portion, the ridge portion being coated with an aliphatic hydrocarbon, and a light shielding film disposed over the ridge portion.
Further features of the present disclosure will become apparent from the following description of exemplary embodiments with reference to the attached drawings.
Exemplary embodiments of the present disclosure will now be described in detail with reference to the drawings.
Substrate
The substrate of the optical element according to an embodiment of the present disclosure may be an optical lens or prism having an optically effective surface extending from the center thereof, an optically non-effective surface between the optically effective surface and the edge of the substrate. The optically non-effective surface has an inclined chamfer and a level chamfer. The substrate may be made of, for example, non-alkali glass, alumina silica glass, borosilicate glass, quartz glass, barium oxide-containing glass, lanthanum oxide-containing glass, or titanium oxide-containing glass.
Light Shielding Film and Aliphatic Hydrocarbon
The aliphatic hydrocarbon 103 is lipophilic and compatible with the light shielding paint that is the precursor of the light shielding film (described herein later). The aliphatic hydrocarbon 103 therefore helps the light shielding paint to enter the cracks in the ridge portion of the substrate and sufficiently fill the cracks. Thus, the aliphatic hydrocarbon 103 suppresses the thinning of the light shielding film formed over the ridge portion and contributes to achieving a good-looking optical element in which white spots at the ridge portion are reduced.
In some embodiments, the amount of the aliphatic hydrocarbon 103 applied onto the ridge portion 101d defined by the inclined chamfer 101b and the level chamfer 101c may be larger than that of the aliphatic hydrocarbon 103 applied onto the other portion of the substrate. In this instance, the flow out of the ridge portion of the light shielding paint due to the surface tension is reduced, so that the light shielding paint can sufficiently fill the cracks in the ridge portion of the substrate. If a large amount of the aliphatic hydrocarbon 103 is present on the portions other than the ridge portion 101d, it is difficult to control the surface tension of the light shielding paint over the ridge portion 101d. Consequently, the paint over the ridge portion 101d dries rapidly and is not likely to sufficiently fill the cracks. If a large amount of the aliphatic hydrocarbon 103 is present on the portion other than the ridge portion 101d, furthermore, the refractive index of the entire light shielding film may be reduced, reducing the optical performance of the light shielding film. In some embodiments, the aliphatic hydrocarbon 103 may be applied onto only the ridge portion 101d defined by the inclined chamfer 101b and the level chamfer 101c.
In some embodiments, the aliphatic hydrocarbon 103 may be a saturated hydrocarbon (alkane). This is because alkanes are compatible with the light shielding paint. Alkanes are represented by a general formula CnH2n+2 (n is an integer) and have a chain structure. Exemplary alkanes include methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, and decane.
In some embodiments, the carbon number of the saturated hydrocarbon may be 6 to 30. Saturated hydrocarbons having a carbon number in this range facilitate favorable application of the light shielding paint. If the carbon number is less than 6, the light shielding paint is not good in wettability and does not sufficiently coat the substrate. In contrast, if the carbon number exceeds 30, the saturated hydrocarbon may cause lumps to be formed in the light shielding paint. The lumps, which will remain in the light shielding film, degrades the optical performance of the resulting optical element.
As shown in
In some embodiments of the present disclosure, the thickness of the light-shielding film may be in the range of 1.0 μm to 50 μm or 1.0 μm to 4.9 μm over the ridge portion 101d. Beneficially, the thickness is constant. If the thickness is as small as less than 1.0 μm, the light shielding film may not sufficiently absorb light, not exhibiting satisfactory light shielding effect. In addition, the light shielding paint may not sufficiently fill the cracks, forming cavities (air holes) in the cracks filled with the paint. In contrast, the light shielding film having a thickness of 50 μm or more raises the risk of cracking under high-temperature, high-humidity environment.
The light shielding film 102 contains a resin, inorganic fine particles, and a coloring agent.
The resin used in the light shielding film 102 may be a thermosetting resin selected from the group consisting of epoxy resin, alkyd resin, and acrylic resin. Epoxy resin may be selected because it is stable in dimensions.
The inorganic fine particles are intended to control the refractive index of the light shielding film 102. The material of the inorganic fine particles may be titanium oxide, zirconium oxide, cerium oxide, tin oxide, or the like. In some embodiments, titanium oxide may be selected because it has a high refractive index.
The coloring agent may be a dye or a pigment. A dye may be selected from the viewpoint of uniformly dispersing the coloring agent in the light shielding film 102. If a pigment is used, the pigment may be at least one pigment selected from the group consisting of carbon black, copper-iron-manganese composite oxide, titanium black, copper oxide, and iron oxide (colcothar). If a dye is used, the dye may be selected from the group consisting of anthraquinone dye, phthalocyanine dye, stilbene dye, pyrazolone dye, thiazole dye, carbonium dye, and azine dye. The dye content in the light shielding film may be in the range of 13.0 parts by mass to 50.0 parts by mass or 13.0 parts by mass to 40.0 parts by mass relative to 100 parts by mass of the light shielding film, if the coloring agent consists of one or more dyes.
Light Shielding Paint
The light shielding paint used for forming the light shielding film may be, but is not limited to, a resin composition containing a resin, an inorganic fine particles, and a coloring agent. The resin may be adherent to the material of the substrate, such as glass. For example, such resins include epoxy resin, alkyd resin, and acrylic resin. From the viewpoint of increasing the refractive index of the light shielding film, a resin having a high refractive index may be used. The resin content may be in the range of 10 parts by mass to 60 parts by mass relative to 100 parts by mass of the light shielding paint.
The inorganic fine particles may have a refractive index (nd) of 2.2 or more from the viewpoint of reducing internal reflection. Exemplary materials of the inorganic fine particles include titanium oxide, zirconium oxide, cerium oxide, and tin oxide. The average particle size of the inorganic fine particles may be in the range of 10 nm to 100 nm. The inorganic fine particle content may be in the range of 5 parts by mass to 35 parts by mass relative to 100 parts by mass of the light shielding paint.
The coloring agent may be a dye or a pigment provided that it can absorb visible light in a wavelength region of 400 nm to 700 nm and is soluble in a solvent. If a pigment is used, the pigment may be carbon black, titanium black, copper oxide, or iron oxide (colcothar). If a dye is used, the dye may be anthraquinone dye, phthalocyanine dye, stilbene dye, pyrazolone dye, thiazole dye, carbonium dye, or azine dye. The coloring agent may contain a single component or may be a mixture of plural types of coloring agent for black, red, yellow, blue, and the like. The coloring agent content may be in the range of 5 parts by mass to 35 parts by mass relative to 100 parts by mass of the light shielding paint.
The beneficial solvent for the light shielding paint may be such that it can dissolve the resin, the coloring agent, and other constituents and is, more beneficially, miscible with the inorganic particles. The organic solvent content may be in the range of 5 parts by mass to 70 parts by mass relative to 100 parts by mass of the light shielding paint.
Silicon dioxide fine particles capable of facilitating favorable application of the light shielding paint or a hardener or may be further added. The hardener may be a compound selected from among amine-based compounds, acid anhydride-based compounds, and imidazole-based compounds.
From the viewpoint of forming a coating having a uniform thickness, the viscosity of the light shielding paint may be in the range of 10 mPa·s to 100 mPa·s. Also, the surface tension of the light shielding paint may be in the range of 5 N/m to 50 N/m. The viscosity and the surface tension may be adjusted to the above ranges by diluting the light shielding paint with a solvent provided that the optical properties of the paint are not degraded.
Method for Manufacturing Optical Element
The method for manufacturing the optical element of the present disclosure includes applying a coating liquid containing an aliphatic hydrocarbon onto the ridge portion defined by the inclined chamfer and the level chamfer, and applying a light shielding paint onto the ridge portion, followed by completing the formation of the light shielding film.
The application of the light shielding paint onto the ridge portion of the substrate may be performed by dip coating, spin coating, slit coating, or electrostatic coating or by using an application tool such as a brush, a sponge, or a bar coater, depending on the shape of the coating. From the viewpoint of easily controlling the amount of the paint to be applied onto the substrate, a dispenser may be used.
The application of the coating liquid containing an aliphatic hydrocarbon onto the ridge portion may be performed by a known manner using an application tool, for example, a brush, a sponge, or an elastic tool such as a wire or a blade, depending on the ridge portion to be coated. For example, the coating tool may be soaked with the coating liquid containing an aliphatic hydrocarbon, and the coating liquid is applied with the coating tool. The coating tool may be made of any material and is not particularly limited provided that the coating liquid containing an aliphatic hydrocarbon can be applied onto the ridge portion. For example, the material may be a resin such as nylon or a metal such as aluminum, copper, steel, or tungsten. The coating liquid containing an aliphatic hydrocarbon and the light shielding paint may be applied onto the ridge portion at one time.
The application of the light shielding paint onto the ridge portion and the application of the paint onto the entire peripheral surface except the ridge portion may be performed in any manner without particular limitation. For example, either application may be performed by dip coating, spin coating, slit coating, or electrostatic coating or by using an application tool such as a brush, a sponge, or a bar coater, depending on the shape of the coating. However, it is not desirable that the light shielding paint applied (or to be applied) onto the peripheral surface other than the ridge portion be mixed with the aliphatic hydrocarbon.
After the application of the light shielding paint, the paint is dried and/or baked to yield the light shielding film. How the light shielding paint is dried and/or baked depends on the desired properties of the optical element and the type and the amount of the hardener added to the paint.
The drying temperature may be 100° C. or less, for example in the range of 40° C. to 80° C. or 40° C. to 60° C. The period for drying may be in the range of 10 minutes to 24 hours, for example, 30 minutes to 24 hours or 1 hour to 24 hours.
The baking temperature may be in the range of 40° C. to 300° C., for example in the range of 40° C. to 250° C. or 40° C. to 200° C. The period for baking may be in the range of 10 minutes to 10 hours, for example, in the range of 10 minutes to 6 hours.
Optical Apparatus
The optical apparatus according to an embodiment of the present disclosure will now be described. The optical apparatus includes an enclosure and an optical system including a plurality of lenses disposed in the enclosure. In this optical apparatus, the optical element described above is disposed, as one of the lenses, close to the light entrance of the optical system.
The optical element of the present disclosure may be used in general optical apparatuses, such as cameras, binoculars, microscopes, and semiconductor exposures, each including an optical system including a plurality of lenses.
Examples of the subject matter of the present disclosure will now be described.
The samples of the Examples and Comparative Examples were evaluated as described below.
Thickness Measurement of Light Shielding Film Over Ridge Portion
The volume of the portion of the light shielding film over the ridge portion defined by the inclined chamfer and the level chamfer was estimated by measuring the cross-sectional profiles of the optical element before and after forming the light shielding film with a two-dimensional laser displacement meter LJ-V7020 (manufactured by Keyence).
The thickness t [μm] of the portion of the light shielding film over the ridge portion was calculated by dividing the estimated volume by the total area of the inclined chamfer and the level chamfer.
Analysis of Aliphatic Hydrocarbon Over Ridge Portion
Whether or not the aliphatic hydrocarbon is present on the ridge portion defined by the inclined chamfer and the level chamfer was examined with a gas chromatograph mass spectrometer (Trace GC Ultra+ISQ-LT+TriPlus 300 manufactured by Thermo Fisher Scientific and PY-3030D manufactured by Frontier Laboratories). More specifically, components separated by gas chromatography were subjected to mass analysis to obtain a mass spectrum for quantitatively analysis.
Evaluation of Appearance in Whitish Bright Spots
While the optical element provided with the light shielding film was irradiated with light, whitish bright spots observed at the interface between the substrate and the light shielding film were photographed. The photograph was image-processed by an image analysis software program Image-Pro Plus (produced by Media Cybernetics), and whitish bright spots having an area of 150 μm2 or more at the ridge portion were counted. When the number of white spots at the ridge portion was 20 or less, the appearance of the optical element was graded as A; when the number of white spots was 21 to 40, the appearance was graded as B; and when the number of white spots was 41 or more, the appearance was graded as C.
Example 1 will be described in detail below.
Preparation of Light Shielding Paint
First, 7 g of an epoxy resin jER828 (produced by Mitsubishi Chemical) and 40 g of a titania dispersion liquid ND139 (25% by mass titania in propylene glycol monomethyl ether (PGME) produced by Tayca) were prepared. Also, 1.2 g of dye (1), VALIFAST-BLACK 3810 (produced by Orient Chemical Industries), and 3.0 g of dye (2), VALIFAST-RED 3320 (produced by Orient Chemical Industries), were prepared. In addition, 1.2 g of dye (3), VALIFAST-YELLOW 3108 (produced by Orient Chemical Industries), and 3.8 g of dye (4), VALIFAST-BLUE 2620 (produced by Orient Chemical Industries), were prepared. For the organic solvent, 22 g of 1-methoxy-2-propanol (produced by Kishida Chemical) was prepared. Furthermore, 3.2 g of hydrophobic silica (1), Aerosil R972 (produced by Nippon Aerosil), and 1.3 g of hydrophilic silica (2), Aerosil 200 (produced by Nippon Aerosil), were prepared. ALSO, A fungicide, 0.5 g of Synthol M-100 (produced by SC Environmental Science), was prepared.
The constituents prepared above were added into a vessel for stirring, and the contents in the vessel were stirred for 20 minutes with a planetary mixer HM-500 (manufactured by Keyence). Into 10 g of the resulting composition was added 1 g of an epoxy resin hardener H-30 (produced by Mitsubishi Chemical), and the mixture was stirred for 3 minutes with the planetary mixer HM-500 (manufactured by Keyence) to yield a light shielding paint.
Production of Optical Element
First, a resin wire (240 μm in diameter) was soaked in hexane (produced by Tokyo Chemical Industry), which has a carbon number of 6 and was to be used as the coating liquid containing an aliphatic hydrocarbon. The resin wire soaked with hexane was pressed on the ridge portion defined by the inclined chamfer and the level chamfer, and, in this state, the substrate was spun at a rotational speed of 100 rpm to apply the hexane onto the ridge portion. Subsequently, the light shielding paint was dropped onto the ridge portion from a dispenser. In this instance, the volume of the light shielding paint per dot was 15 nL, and 20 dots of the light shielding paint were applied at regular intervals.
Next, the light shielding paint was continuously dropped onto the optically non-effective portion of the substrate other than the ridge portion from the dispenser. Subsequently, the substrate was spun at a rotational speed of 100 rpm with the resin wire pressed on the ridge portion. Then, after being dried at room temperature for 1 hour, the coating was baked at a constant temperature of 80° C. for 2 hours in a furnace to yield a light shielding film. Thus, the optical element of Example 1 was produced.
Evaluation of Ridge Portion
The thickness t [μm] of the portion of the light shielding film over the ridge portion of the resulting optical element was measured, and, from the measurements, the thickness was estimated to be 3.9 μm. Next, the appearance of the ridge portion was evaluated in terms of whitish bright spots. The number of white spots at the ridge portion was 17.
Then, the ridge portion was examined as described below.
The optical element of Example 1 was cut into a test piece including the ridge portion defined by the inclined chamber and the level chamfer and a test piece not including the ridge portion. Each test piece was heated to 300° C. in the gas chromatograph mass spectrometer. The gas generated by the heating was analyzed to check whether or not the aliphatic hydrocarbon applied to the ridge portion was present in the gas.
The optical element of Example 2 was produced in the same manner as in Example 1 except for using n-octane (produced by Tokyo Chemical Industry) having a carbon number of 8 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 1, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 3 was produced in the same manner as in Example 1 except for using decane (produced by Tokyo Chemical Industry) having a carbon number of 10 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 1, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 4 was produced in the same manner as in Example 1 except for using tridecane (produced by Tokyo Chemical Industry) having a carbon number of 13 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 1, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 5 was produced in the same manner as in Example 1 except for using pentacosane (produced by Sigma-Aldrich) having a carbon number of 25 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 2, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 6 was produced in the same manner as in Example 1 except for using triacontane (produced by Sigma-Aldrich) having a carbon number of 30 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 2, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 7 was produced in the same manner as in Example 1 except for using pentane (produced by Tokyo Chemical Industry) having a carbon number of 5 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 2, and the evaluation results of the optical element are shown in Table 4.
The optical element of Example 8 was produced in the same manner as in Example 1 except for using hentriacontane (produced by Sigma-Aldrich) having a carbon number of 31 as the coating liquid containing an aliphatic hydrocarbon. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 2, and the evaluation results of the optical element are shown in Table 4.
In Comparative Example 1, the light shielding film was formed by applying the light shielding paint over the entirety of the optically non-effective surface of the substrate including the ridge portion defined by the inclined chamfer and the level chafer without applying the coating liquid containing an aliphatic hydrocarbon onto the ridge portion. In this instance, the light shielding film was formed in the same manner as in Example 1 except that the coating liquid containing an aliphatic hydrocarbon was not applied. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 3, and the evaluation results of the optical element are shown in Table 4.
The optical element of Comparative Example 2 was produced in the same manner as in Example 1 except that the coating liquid containing an aliphatic hydrocarbon was replaced with a lipophobic fluorine-based oil. The light shielding paint and the coating liquid containing an aliphatic hydrocarbon are shown in Table 3, and the evaluation results of the optical element are shown in Table 4.
In Comparative Example 3, a coating liquid containing an aliphatic hydrocarbon was mixed into a light shielding paint, and this mixture was used as the paint.
Preparation of Light Shielding Paint
First, 7 g of an epoxy resin jER828 (produced by Mitsubishi Chemical) and 40 g of a titania dispersion liquid ND139 (25% by mass titania in propylene glycol monomethyl ether (PGME) produced by Tayca) were prepared. Also, 1.2 g of dye (1), VALIFAST-BLACK 3810 (produced by Orient Chemical Industries), and 3.0 g of dye (2), VALIFAST-RED 3320 (produced by Orient Chemical Industries), were prepared. In addition, 1.2 g of dye (3), VALIFAST-YELLOW 3108 (produced by Orient Chemical Industries), and 3.8 g of dye (4), VALIFAST-BLUE 2620 (produced by Orient Chemical Industries), were prepared. For the organic solvent, 22 g of 1-methoxy-2-propanol (produced by Kishida Chemical) was prepared. Furthermore, 3.2 g of hydrophobic silica (1), Aerosil R972 (produced by Nippon Aerosil), and 1.3 g of hydrophilic silica (2), Aerosil 200 (produced by Nippon Aerosil), were prepared. A fungicide, 0.5 g of Synthol M-100 (produced by SC Environmental Science), and 5 g of decane (produced by Tokyo Chemical Industry, carbon number: 10) as the material containing a saturated aliphatic hydrocarbon were prepared. These constituents prepared above were added into a vessel for stirring, and the contents in the vessel were stirred for 20 minutes with a planetary mixer HM-500 (manufactured by Keyence). Into 10 g of the resulting composition was added 1 g of an epoxy resin hardener H-30 (produced by Mitsubishi Chemical), and the mixture was stirred for 3 minutes with the planetary mixer HM-500 (manufactured by Keyence) to yield a light shielding paint.
Production of Optical Element
The light shielding paint prepared above was applied over the entirety of the optically non-effective surface including the ridge portion to form the light shielding film on the substrate, as in Comparative Example 1. The application of the light shielding paint was performed while the substrate was being spun. Then, after being dried at room temperature for 1 hour, the coating was baked at a constant temperature of 80° C. for 2 hours in a furnace to yield a light shielding film. Thus, the optical element of Comparative Example 3 was produced.
Evaluation of Ridge Portion
The thickness t [μm] of the portion of the light shielding film over the ridge portion of the resulting optical element was measured. The thickness over the ridge portion was 0.9 μm. Next, the appearance of the ridge portion was evaluated in terms of whitish bright spots. The number of white spots at the ridge portion was 73.
Then, the ridge portion was examined as described below.
The optical element of Comparative Example 3 was cut into a test piece including the ridge portion and the level chamfer and a test piece not including the ridge portion. Each test piece was heated to 300° C. in the gas chromatograph mass spectrometer. The gas generated by the heating was analyzed to check whether or not the aliphatic hydrocarbon was present in the light shielding film formed over the ridge portion. In Comparative Example 3, the peak derived from the saturated hydrocarbon was observed in the portion other than the ridge portion as well as in the ridge portion. The peak of the saturated hydrocarbon in the portion other than the ridge portion was stronger than the peak of the saturated hydrocarbon in the ridge portion. The light shielding paint and the lipophilic coating liquid are shown in Table 3, and the evaluation results of the optical element are shown in Table 4.
Evaluation
As is clear from the results of Examples 1 to 8, it is beneficial that an aliphatic hydrocarbon is present at the ridge portion defined by the inclined chamfer and the level chamfer of the optical element but not present at the other portion.
Also, the results of Examples 1 to 8 suggest that the beneficial thickness of the light shielding film over the ridge portion of the optical element is 1 μm or more and more beneficially 3 μm or more.
The light shielding film in Comparative Example 1 did not contain any aliphatic hydrocarbon, and, in Comparative Example 3, an aliphatic hydrocarbon was contained in the entire light shielding film. These Comparative Examples showed the same tendency in terms of the thickness of the light shielding film over the ridge portion of the element and the white spots at the ridge portion.
In Comparative Example 2, the light shielding paint was not good in wettability. Accordingly, the resulting light shielding film was as thin as 0.2 μm and the number of white spots was increased.
According to the concept of the present disclosure, a material containing a lipophilic aliphatic hydrocarbon, compatible with the light shielding paint that is the precursor of the light shielding film allows the light shielding paint to enter and fill the cracks in the ridge portion and the vicinity. The aliphatic hydrocarbon suppresses the thinning of the light shielding film over the ridge portion and contributes to achieving a good-looking optical element in which white spots at the ridge portion are reduced.
While the present disclosure has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
This application claims the benefit of Japanese Patent Application No. 2017-196991 filed Oct. 10, 2017 and No. 2018-165935 filed Sep. 5, 2018, which are hereby incorporated by reference herein in their entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| JP2017-196991 | Oct 2017 | JP | national |
| JP2018-165935 | Sep 2018 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20140160571 | Miyazaki | Jun 2014 | A1 |
| 20150168742 | Hoshino | Jun 2015 | A1 |
| 20160024335 | Yamamoto | Jan 2016 | A1 |
| Number | Date | Country |
|---|---|---|
| 2016-30706 | Mar 2016 | JP |
| Entry |
|---|
| Cosmetics Info webpage “Methoxyisopropyl Acetate” https://cosmeticsinfo.org/ingredient/methoxyisopropyl-acetate (Year: 2017). |
| Number | Date | Country | |
|---|---|---|---|
| 20190107648 A1 | Apr 2019 | US |
