Solid optical material, preparation method and application thereof
By preparing solid optical materials of salicylic aniline, methyl methacrylate and initiator, the fluorescence is stimulated by the intersection of ultraviolet light and green light, the problem of Schiff base not being obvious in powder and solution states is solved. , realizes clear spatial static three-dimensional imaging, improving the safety and stability of the material.
Patent Information
- Application Number
- CN202310623354.0
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2023-05-29
- Publication Date
- 2025-01-10
- Estimated Expiration
- 2043-05-29
AI Technical Summary
In the prior art, Schiff base is opaque in the powder state and cannot be used for spatial display. The photochromic phenomenon is not obvious in the solution state, making it difficult to apply to three-dimensional body display.
Using a suitable combination of salicylic aniline, methyl methacrylate and initiator, colorless and transparent solid optical materials are prepared by mixing reaction and heating curing, and the fluorescence is excitated by the intersection of ultraviolet light and green light to achieve Spatial static three-dimensional imaging.
A writable and erasable spatial static three-dimensional imaging material was obtained, with clear images and no diffusion, high security and good stability. It is suitable for the application of photochromic materials, and the innovative ideas of three-dimensional display are realized.
Smart Images

Figure CN116640398B_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the field of optical materials, and in particular to a solid optical material, a preparation method and application thereof. Background Art
[0002] With the advancement of science and technology and the development of the times, traditional two-dimensional image display can no longer meet people's needs. Therefore, three-dimensional display technology is developing rapidly. Three-dimensional display expresses more information, has a wider viewing angle, and is more three-dimensional. At the same time, there are various types of three-dimensional display technologies, such as stereoscopic display, holographic display, and volumetric three-dimensional display. Among them, volumetric three-dimensional display displays three-dimensional objects through volume pixels in three-dimensional space. It is a real three-dimensional image that can provide all depth information. Schiff base mainly refers to a class of organic compounds containing imine or azomethine characteristic groups (-RC=N-). Usually, Schiff base is formed by condensation of amine and active carbonyl. Some Schiff bases contain characteristic groups (such as chiral aldehydes) and have great application potential in the field of photochromism. Photochromic materials, also known as optical switch materials, have great potential in the field of three-dimensional display. However, there are currently few reports on the use of Schiff bases for volumetric three-dimensional display. The main reason is that Schiff bases are opaque in powder state and cannot be displayed in space. When Schiff bases are in solution state, the photochromic phenomenon is not obvious and difficult to observe and identify. Summary of the invention
[0003] The present invention aims to solve at least one of the technical problems existing in the prior art. To this end, one object of the present invention is to provide a solid optical material, a writable and erasable material for spatial static three-dimensional imaging, and the image is clear and does not diffuse.
[0004] Another object of the present invention is to provide a method for preparing a solid optical material.
[0005] Another object of the present invention is to provide an application of solid optical material.
[0006] The solid optical material according to the first embodiment of the present invention comprises the following raw materials: salicylaldehyde aniline, an initiator and methyl methacrylate, wherein the solid-liquid ratio of the salicylaldehyde aniline and the methyl methacrylate satisfies: 0.5mg~1.5mg:10ml~30ml; the solid-liquid ratio of the initiator and the methyl methacrylate satisfies: 1mg~3mg:0.5ml~1.5ml.
[0007] The solid optical material according to the specific embodiment of the present invention is a colorless and transparent organic glass solidified material with high light transmittance. On the one hand, the solid optical material is convenient to use, store and transport, and on the other hand, the solid optical material has higher safety and better stability. Furthermore, the solid optical material according to the specific embodiment of the present invention also opens up new ideas for the application of photochromic materials.
[0008] According to some embodiments of the present invention, the solid-liquid ratio of the salicylaldehyde aniline and the methyl methacrylate satisfies: 1.0 mg: 20 ml; the solid-liquid ratio of the initiator and the methyl methacrylate satisfies: 2 mg: 1 ml.
[0009] According to some embodiments of the present invention, the initiator includes at least one of an azo compound initiator and a peroxide initiator; preferably, the initiator includes at least one of azobisisobutyronitrile, azobisisoheptylnitrile, dimethyl azobisisobutyrate, benzamide peroxide, lauroyl peroxide, isopropylbenzene hydroperoxide and methyl ethyl ketone peroxide; more preferably, the initiator is azobisisobutyronitrile.
[0010] According to some embodiments of the present invention, the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: 0.01 mg / ml≤m≤0.1 mg / ml; preferably, m=0.05 mg / ml.
[0011] According to an embodiment of the second aspect of the present invention, the present invention provides a method for preparing the solid optical material according to the embodiment of the first aspect, comprising the following steps: mixing the salicylaldehyde aniline with the initiator and methyl methacrylate in the material ratio, reacting, heating and curing to obtain a colorless and transparent solid.
[0012] According to some embodiments of the present invention, the preparation method comprises the following steps:
[0013] Step 1, dispersing salicylaldehyde aniline in the material ratio into methyl methacrylate, adding the initiator, stirring, and fully dissolving it to obtain a solution;
[0014] Step 2: heating the solution in step 1 to 50-100° C. and stirring to allow the solution to react fully until the reaction liquid becomes viscous;
[0015] Step 3: Pour the viscous reaction liquid in step 2 into a mold, and initially cure it at 45-60° C. for 20-30 hours. After the initial curing, heat it to 80-120° C. and cure it again for 0.5-1.5 hours to complete the curing;
[0016] Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless and transparent solid.
[0017] According to an embodiment of the third aspect of the present invention, the present invention provides an application of the solid optical material according to the embodiment of the first aspect, or an optical material prepared by the preparation method according to the preparation method described in the embodiment of the second aspect in static three-dimensional imaging in space.
[0018] According to some embodiments of the present invention, the following steps are included: irradiating the solid optical material with ultraviolet light to change the structure of salicylaldehyde aniline to obtain a brown-yellow solid optical material; irradiating the solid optical material with green light; in the solid optical material, the intersection of the ultraviolet light and the green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging.
[0019] According to some embodiments of the present invention, the following steps are included: S1: irradiating the solid optical material with ultraviolet light to change the structure of salicylaldehyde aniline to obtain a brown-yellow solid optical material; S2: irradiating the brown-yellow solid optical material in step S1 with green light, and in the solid optical material, the intersection of the ultraviolet light and the green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging; preferably, the brown-yellow solid optical material in step S1 is the base plate of spatial static three-dimensional imaging, and the direction of green light irradiation in step S2 is perpendicular to the plane where the base plate is located.
[0020] According to some embodiments of the present invention, the following steps are included: S1: irradiating the solid optical material with green light; S2: irradiating the solid optical material described in step S1 with ultraviolet light, wherein the intersection of the ultraviolet light and the green light in the solid optical material is excited to emit red fluorescence, thereby forming a red spatial three-dimensional image, i.e., realizing spatial static three-dimensional imaging; preferably, the solid optical material irradiated with green light in step S1 serves as a base plate for spatial static three-dimensional imaging, and the direction of ultraviolet light irradiation in step S2 is perpendicular to the plane where the base plate is located.
[0021] According to some embodiments of the present invention, the wavelength of the ultraviolet light is λ 1 , where the λ 1 Satisfy: 365nm≤λ 1 ≤395nm; and / or the wavelength of the green light is λ 2 , where the λ 2 Satisfy: 488nm≤λ 2 ≤532nm; and / or the power of the ultraviolet light is W 1 , wherein the W 1 Meet: 60mW≤W 1 ≤300mW; and / or the power of the green light source is W2 , wherein the W 2 Meet: 50mW≤W 2 ≤120mW.
[0022] According to some embodiments of the present invention, at room temperature and natural light intensity of 300 Lux to 500 Lux, the spatial static three-dimensional imaging image is stored for 0.5 to 3 seconds.
[0023] Additional aspects and advantages of the present invention will be given in part in the following description and in part will be obvious from the following description, or will be learned through practice of the present invention. BRIEF DESCRIPTION OF THE DRAWINGS
[0024] The above and / or additional aspects and advantages of the present invention will become apparent and easily understood from the description of the embodiments in conjunction with the following drawings, in which:
[0025] Figure 1 is a photochromic reaction of salicylaldehyde aniline according to a specific embodiment of the present invention, wherein λ 1 Refers to ultraviolet light, λ 2 refers to green light or other visible light, Δ refers to heating;
[0026] Figure 2 is a schematic diagram of an optical path for realizing spatial static three-dimensional imaging using a solid optical material according to a specific embodiment of the present invention;
[0027] Figure 3 The following are static three-dimensional images of solid optical materials according to specific embodiments of the present invention: (a) is the colorless solid optical material obtained in Example 1; (b) is the coloring process when 365nm ultraviolet light directly irradiates the solid optical material; (c) is a red three-dimensional ring image formed by writing 532nm green light into the solid optical material after ultraviolet light irradiation. DETAILED DESCRIPTION
[0028] Embodiments of the present invention are described in detail below. The embodiments described with reference to the accompanying drawings are exemplary. Embodiments of the present invention are described in detail below.
[0029] Reference below Figure 1-Figure 3 The solid optical material according to the first aspect of the present invention is described as follows: salicylaldehyde aniline, an initiator and methyl methacrylate. Here, salicylaldehyde aniline is a photochromic material, and the initiator induces the polymerization reaction of methyl methacrylate to obtain an organic glass cured product. The organic glass cured product is suitable as a carrier for optical imaging. The salicylaldehyde aniline is dispersed in the organic glass cured product to form the solid optical material of the invention.
[0030] The solid-liquid ratio of salicylaldehyde aniline to methyl methacrylate satisfies: 0.5mg-1.5mg: 10ml-30ml. In this way, the content of salicylaldehyde aniline in the solid optical material is appropriate, so that the solid optical material can have clear imaging, high light transmittance, and good imaging effect.
[0031] The solid-liquid ratio of the initiator to methyl methacrylate satisfies the following conditions: 1mg-3mg: 0.5ml-1.5ml. In this way, the amount of the initiator added is appropriate, which is conducive to the initiator fully inducing the polymerization of methyl methacrylate to obtain a uniform polymer. It can also effectively avoid the influence of the initiator on salicylaldehyde aniline, which is conducive to the solidification of methyl methacrylate to obtain a colorless and transparent solid optical material.
[0032] The solid optical material according to the specific embodiment of the present invention is a colorless and transparent organic glass solidified material with high light transmittance. On the one hand, the solid optical material is convenient to use, store and transport, and on the other hand, the solid optical material has higher safety and better stability. Furthermore, the solid optical material according to the specific embodiment of the present invention also opens up new ideas for the application of photochromic materials.
[0033] According to some embodiments of the present invention, the solid-liquid ratio of salicylaldehyde aniline and methyl methacrylate satisfies: 1.0 mg: 20 ml. In this way, the content of salicylaldehyde aniline in the solid optical material is more suitable, and the solid optical material has a clearer image, a higher light transmittance, and a better imaging effect.
[0034] According to some embodiments of the present invention, the solid-liquid ratio of the initiator to methyl methacrylate satisfies: 2 mg: 1 ml. The addition amount of the initiator is appropriate, which is more conducive to the initiator fully inducing the polymerization of methyl methacrylate to obtain a uniform cured product.
[0035] According to some embodiments of the present invention, the initiator includes at least one of an azo compound initiator and a peroxide initiator. In this way, the activity of the initiator is suitable, and it can catalyze and induce the full polymerization of methyl methacrylate to obtain a uniform polymer, and will not interfere with the proton migration and imaging of the solid optical material of the present invention under ultraviolet light irradiation, and can effectively induce the polycondensation reaction of methyl methacrylate to obtain a cured organic glass product.
[0036] According to some embodiments of the present invention, the initiator includes at least one of azobisisobutyronitrile, azobisisoheptanenitrile, dimethyl azobisisobutyrate, benzamide peroxide, lauroyl peroxide, cumene hydroperoxide and methyl ethyl ketone peroxide. In this way, the selection of the initiator is diverse.
[0037] According to some embodiments of the present invention, the initiator is azobisisobutyronitrile. In this way, the initiator can induce the polymerization reaction of methyl methacrylate to form a solid optical material, and can also reduce the influence of the initiator on salicylaldehyde aniline as much as possible, so that the transmittance of the obtained solid optical material is higher.
[0038] According to some embodiments of the present invention, the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: 0.01 mg / ml≤m≤0.1 mg / ml. In this arrangement, if m is less than 0.01 mg / ml, the concentration of salicylaldehyde aniline in the solid optical material is small, and the color change phenomenon of the solid optical material is not obvious, which is not conducive to imaging and observation. If m is greater than 0.1 mg / ml, the concentration of salicylaldehyde aniline in the solid optical material is large, which will affect the penetration depth of the light source in the solid optical material, and when the concentration of salicylaldehyde aniline in the solid optical material is too large, the solid optical material is easily stained with the yellow color of salicylaldehyde aniline, thereby affecting the imaging of the solid optical material. By setting so that m satisfies 0.01 mg / ml≤m≤0.1 mg / ml, the color change phenomenon of the solid optical material is significant and the imaging performance is good.
[0039] According to some embodiments of the present invention, m = 0.05 mg / ml. With such a setting, the concentration of salicylaldehyde aniline in the solid optical material is more suitable, the color change phenomenon of the solid optical material is more significant, and the imaging performance is better.
[0040] According to an embodiment of the second aspect of the present invention, the present invention provides a method for preparing a solid optical material according to an embodiment of the first aspect of the present invention, comprising the following steps: mixing salicylaldehyde aniline with an initiator and methyl methacrylate in the above material ratio, reacting, heating and curing to obtain a colorless and transparent solid.
[0041] According to the method for preparing the solid optical material of the specific embodiment of the present invention, salicylaldehyde aniline is mixed with an initiator and methyl methacrylate for reaction and cured by heating to obtain a colorless and transparent solid. The preparation method is simple and the obtained solid optical material has a high application value.
[0042] According to some embodiments of the present invention, the following steps are included: Step 1, dispersing the salicylaldehyde aniline with the above material ratio into methyl methacrylate, adding an initiator, and stirring rapidly to fully dissolve it. Such an arrangement is conducive to uniform dispersion of salicylaldehyde aniline in methyl methacrylate, and full mixing of the initiator and methyl methacrylate. In this way, the initiator is conducive to inducing the polymerization reaction of methyl methacrylate to form a solid optical material in a uniform state.
[0043] Step 2: Heat the solution of step 1 to 50-100° C. and stir to fully react until the reaction liquid becomes viscous. In this way, at a higher temperature, the initiator can induce the polymerization reaction of methyl methacrylate as soon as possible.
[0044] Step 3: Pour the viscous reaction liquid in step 2 into a mold, and initially cure it at 45-60° C. for 20-30 hours. After the initial curing, heat it to 80-120° C. and cure it again for 0.5-1.5 hours to complete the curing;
[0045] Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless and transparent solid.
[0046] According to the method for preparing a solid optical material of a specific embodiment of the present invention, the curing process is divided into two stages: primary curing and secondary curing. The primary curing temperature is low and the time is long. A uniform and stable state is formed by slow curing. The secondary curing temperature is high and the time is short, which is a reinforcement of the primary curing. In this way, it is more conducive to forming a uniform solid optical material with excellent optical properties. In addition, the appearance and quality of the solid optical material obtained after grinding and splicing are better.
[0047] According to some embodiments of the present invention, the primary curing is performed by heating in a water bath, so that the heating conditions are relatively mild.
[0048] The method for preparing solid optical materials according to the specific embodiment of the present invention is simple to operate, has mild conditions, and is highly controllable. The vacuum operation avoids the generation of bubbles during the solidification of the solid optical material, and the water bath curing conditions are mild, which is conducive to the formation of uniform solid optical materials.
[0049] According to an embodiment of the third aspect of the present invention, the present invention provides an application of a solid optical material according to an embodiment of the first aspect of the present invention or a solid optical material prepared by the preparation method of the second aspect of the present invention in static three-dimensional imaging in space.
[0050] According to a specific embodiment of the present invention, the solid optical material of the present invention can be applied to the field of spatial static three-dimensional imaging by utilizing the photochromic characteristics of the solid optical material of the present invention. Such an arrangement provides more raw materials for the research of spatial static three-dimensional imaging. Furthermore, the raw materials of the solid optical material of the present invention are cheap and easy to obtain, and the preparation process is simple. And the imaging process using the solid optical material of the present invention is simple. Therefore, the application potential is greater. The spatial static three-dimensional imaging here refers to a static volumetric three-dimensional display (static volumetic 3D display) in a three-dimensional space, which can also be called static volumetric three-dimensional imaging. The static body refers to the imaging volume or space composed of a fixed medium, in order to distinguish it from a scanning volumetric three-dimensional or a shaking volumetric three-dimensional. Spatial static three-dimensional imaging can also be called true static three-dimensional imaging, which is real three-dimensional imaging. Therefore, the spatial static three-dimensional imaging here is different from the three-dimensional imaging formed by VR glasses. The three-dimensional imaging formed by VR glasses is a visually illusory three-dimensional imaging, which is actually a two-dimensional imaging, not a spatial three-dimensional imaging.
[0051] According to some embodiments of the present invention, the following steps are included: Figure 1-Figure 3 As shown, the solid optical material is irradiated with ultraviolet light, so that the structure of salicylaldehyde aniline changes to obtain a brown-yellow solid optical material. In this way, when the solid optical material of the present invention is irradiated with ultraviolet light, the salicylaldehyde aniline molecules at the irradiated part of the solid optical material of the present invention undergo proton transfer under the irradiation of ultraviolet light, so that the structure of the salicylaldehyde aniline molecules changes, and then the solid optical material changes from colorless and transparent to brown-yellow, thereby producing a photochromic phenomenon.
[0052] The solid optical material is irradiated with green light. In this way, the solid optical material of the present invention can be irradiated with green light alone or with ultraviolet light simultaneously or successively.
[0053] In the solid optical material, the intersection of ultraviolet light and green light is excited to emit red fluorescence, forming a red three-dimensional spatial image, that is, realizing spatial static three-dimensional imaging. In this way, in the solid optical material, ultraviolet light and green light intersect, and can be excited to produce fluorescence at the intersection to form a red three-dimensional spatial figure. In this way, the solid optical material of the present invention combines an ultraviolet light source, a green light source and a simple optical path design, so that green light and ultraviolet light intersect in the solid optical material of the present invention, and spatial static three-dimensional imaging can be realized at the intersection of external light and green light. It should be pointed out that when the solid optical material of the present invention is not irradiated with ultraviolet light, the above-mentioned green light is used alone to directly irradiate the solid optical material of the present invention, and the green light will directly pass through the solid optical material without generating fluorescence. Alternatively, when green light is used to irradiate the part of the solid optical material that is not irradiated with ultraviolet light, the green light will directly pass through the solid optical material without generating fluorescence.
[0054] According to a specific embodiment of the present invention, the photochromic characteristics of the solid optical material of the present invention are utilized to apply it to the field of static three-dimensional imaging in space. Among them, the photochromic characteristics of the solid optical material of the present invention refer to that the solid optical material of the present invention is irradiated with ultraviolet light and green light respectively, and at the intersection of ultraviolet light and green light, the solid optical material of the present invention emits red fluorescence to form a red three-dimensional spatial pattern. Here, ultraviolet light and green light can simultaneously irradiate the solid optical material to form a red three-dimensional spatial pattern, or the solid optical material of the present invention can be irradiated with green light first and then with ultraviolet light, or the solid optical material of the present invention can be irradiated with ultraviolet light first and then with green light. The specific process and principle of the imaging of the solid optical material of the present invention are as follows: when ultraviolet light irradiates the solid optical material of the present invention, the salicylaldehyde aniline molecules in the irradiated part of the solid optical material undergo proton transfer under the irradiation of ultraviolet light, so that the structure of the salicylaldehyde aniline molecules changes, so that the solid optical material changes from colorless and transparent to presenting brownish yellow, thereby producing the phenomenon of photochromism. When green light is used to irradiate solid optical materials, in the solid optical material, if green light and ultraviolet light intersect, the intersection of ultraviolet light and green light can be stimulated to produce fluorescence, forming a red spatial three-dimensional graphic. That is, static three-dimensional imaging of space is achieved. And the image is clear and does not diffuse. Furthermore, if visible light is used to irradiate the solid optical material that has been imaged, the discolored area can be restored to transparency, thereby achieving static erasure of the image. In this way, by selecting appropriate ultraviolet light, visible light, and combining a simple optical path, the writing and erasing of three-dimensional graphics can be achieved. Among them, the erasing speed of the three-dimensional graphics is positively correlated with the wavelength and intensity of the light source. In addition, the chemical properties of salicylaldehyde aniline are stable, and the solid optical material can be reused many times.
[0055] According to a specific embodiment of the present invention, Figure 1 - Figure 3 As shown, salicylaldehyde aniline can undergo a photochromic reaction under the sequential irradiation of an ultraviolet lamp and a green light source, thereby applying the solid optical material using salicylaldehyde aniline as a color-changing switch in the field of static three-dimensional imaging in space.
[0056] According to some embodiments of the present invention, the following steps are included: S1: using ultraviolet light to irradiate a solid optical material, so that the structure of salicylaldehyde aniline changes to obtain a brown-yellow solid optical material. Specifically, firstly, ultraviolet light is used to irradiate the solid optical material of the present invention, so that the part of the solid optical material irradiated by the ultraviolet light undergoes a photochromic phenomenon. Specifically, the salicylaldehyde aniline molecules in the solid optical material undergo proton transfer under the irradiation of ultraviolet light, so that the structure of the salicylaldehyde aniline molecules changes. The solid optical material changes from colorless and transparent to brown-yellow, thereby producing a photochromic phenomenon.
[0057] S2: Use green light to irradiate the brown-yellow solid optical material in step S1. In the solid optical material, the intersection of ultraviolet light and green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging. In this way, a green light source is used to excite the solid optical material that has become brown-yellow due to ultraviolet light irradiation in S1, and fluorescence emission is generated at the intersection of green light and the color-changing area to form a red spatial three-dimensional figure. In this way, ultraviolet light can be used to irradiate the solid optical material of the present invention to produce photochromism, and then green light can be used to irradiate the color-changing part of the solid optical material. Combined with a simple optical path design, fluorescence emission is generated at the intersection of green light and the color-changing area to form a red spatial three-dimensional figure. In this way, spatial static three-dimensional imaging can be realized. Furthermore, before the green light is irradiated, the part irradiated by ultraviolet light has already produced light color change, which is convenient for observation. When the green light is irradiated, it is easier to determine the intersection.
[0058] According to a specific embodiment of the present invention, the solid optical material of the present invention can be applied to the field of static three-dimensional imaging in space by utilizing the photochromic characteristics of the solid optical material of the present invention. First, the solid optical material of the present invention is irradiated with ultraviolet light, and the salicylaldehyde aniline molecules in the solid optical material undergo proton transfer under ultraviolet light irradiation, so that the structure of the salicylaldehyde aniline molecules changes. The solid optical material on the optical path changes from colorless and transparent to brownish yellow, thereby generating a photochromic phenomenon. Then green light is used to irradiate and excite the above-mentioned brownish yellow solid optical material, and fluorescence emission is generated at the intersection of visible light and the discoloration area. A stable three-dimensional image in space (i.e., static three-dimensional imaging in space) can be formed, and the image is clear and does not diffuse. Furthermore, if the solid optical material that has been imaged is irradiated with visible light, the discoloration area can be restored to transparency, thereby realizing static erasure of the image. In this way, by selecting appropriate ultraviolet light and visible light, combined with a simple optical path, the writing and erasing of three-dimensional graphics can be realized.
[0059] According to some embodiments of the present invention, the brown-yellow solid optical material in step S1 is the base plate for spatial static three-dimensional imaging, and the direction of green light irradiation in step S2 is perpendicular to the plane where the base plate is located. In this way, the brown-yellow solid optical material can be used as the base plate for spatial static three-dimensional imaging, and the green light in step S2 can be used as a writing tool to form a spatial static three-dimensional image as needed.
[0060] According to some embodiments of the present invention, the following steps are included: S1: Figure 2 As shown, green light is used to irradiate the solid optical material. At this time, the green light can penetrate the solid optical material and form an optical path in the solid optical material. And because the solid optical material is irradiated with green light alone, no fluorescence or light discoloration occurs.
[0061] S2: Using ultraviolet light to irradiate the solid optical material of step S1, in the solid optical material, the intersection of ultraviolet light and green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging. In this way, ultraviolet light is used to irradiate the solid optical material in S1, and fluorescence emission is generated at the intersection of the green light path and the ultraviolet light path to form a red spatial three-dimensional figure. In this way, the solid optical material of the present invention can be irradiated with green light first, and the light path of green light is formed in the solid optical material, and then ultraviolet light is used to irradiate the solid optical material to make it photochromic, combined with a simple light path design, fluorescence emission is generated at the intersection of the color change area (ultraviolet light path) and the green light path to form a red spatial three-dimensional figure. In this way, spatial static three-dimensional imaging can be realized. In this way, green light can be used to irradiate the solid optical material first to form a green light path in the solid optical material, and then ultraviolet light can be used to irradiate the solid optical material of the present invention and make the irradiated part photochromic, and fluorescence emission is generated at the intersection of the green light and the color change area to form a red spatial three-dimensional figure.
[0062] According to a specific embodiment of the present invention, the solid optical material of the present invention can be applied to the field of static three-dimensional imaging in space by utilizing the photochromic characteristics of the solid optical material of the present invention. First, the solid optical material of the present invention is irradiated with green light, and the green light penetrates the solid optical material and forms an optical path in the solid optical material. Then, the solid optical material of the present invention is irradiated with ultraviolet light, and the salicylaldehyde aniline molecules in the solid optical material undergo proton transfer under ultraviolet light irradiation, so that the structure of the salicylaldehyde aniline molecules changes. The solid optical material is changed from colorless and transparent to present a brownish yellow color, thereby generating a photochromic phenomenon. Fluorescence emission is generated at the intersection of the green light and the discoloration area. A stable three-dimensional image in space (i.e., static three-dimensional imaging in space) can be formed, and the image is clear and does not diffuse. Furthermore, if the solid optical material that has been imaged is irradiated with visible light, the discoloration area can be restored to transparency, thereby realizing static erasure of the image. In this way, by selecting appropriate ultraviolet light, visible light, and combining a simple optical path, the writing and erasing of three-dimensional graphics can be realized.
[0063] According to some embodiments of the present invention, the optical path of the green light in the solid optical material after the green light irradiation in step S1 is used as the base plate for spatial static three-dimensional imaging, and the direction of ultraviolet light irradiation in step S2 is perpendicular to the plane where the base plate is located. In this way, the optical path of the green light in the solid optical material can be used as the base plate for spatial static three-dimensional imaging, and the ultraviolet light in step S2 can be used as a writing tool to form a spatial static three-dimensional image as needed.
[0064] According to some embodiments of the present invention, the wavelength of the ultraviolet light is λ 1 , where λ 1 Satisfy: 365nm≤λ1 ≤395nm. In this arrangement, ultraviolet light within this wavelength range can change the structure of salicylaldehyde aniline to obtain a brown solid optical material.
[0065] According to some embodiments of the present invention, the wavelength of green light is λ 2 , where λ 2 Satisfy: 488nm≤λ 2 ≤532nm. In this arrangement, the green light within the wavelength range can excite the brown-yellow solid optical material in step S1 to produce fluorescence, thereby achieving spatial static three-dimensional imaging.
[0066] According to some embodiments of the present invention, the power of the ultraviolet light source is W 1 , where W 1 Meet: 60mW≤W 1 ≤300mW. The power of green light source is W 2 , where W 2 Meet: 50mW≤W 2 ≤120 mW. This provides sufficient energy for imaging of the solid optical material of the present invention.
[0067] Specifically, it can be combined Figure 2 - Figure 3 As shown, the process of spatial static three-dimensional imaging of the present invention is as follows: ultraviolet light with a power of 60mW to 300mW and a wavelength of 365 to 395nm is used to irradiate the solid optical material from the bottom to obtain a spatial color-changing plane similar to a blackboard; in a direction perpendicular to the color-changing plane, a laser light source (green light) with a power of 60mW to 300mW and a wavelength of 365 to 395nm is controlled by a galvanometer to project a circular ring pattern, which intersects with visible light in the color-changing area to produce a red spatial circular ring pattern, thereby realizing volumetric three-dimensional display, that is, spatial static three-dimensional imaging.
[0068] According to some embodiments of the present invention, at room temperature and natural light intensity of 300 Lux to 500 Lux, the image of the spatial static three-dimensional imaging is stored for 0.5 to 3 seconds. In this way, at room temperature and natural light conditions, the image of the spatial static three-dimensional imaging can disappear within 0.5 to 3 seconds. In this way, the spatial static three-dimensional image of the present invention can be quickly erased.
[0069] Specific exemplary embodiments
[0070] Example 1
[0071] A solid optical material comprises the following raw materials: salicylaldehyde aniline, methyl methacrylate and an initiator, wherein the solid-liquid ratio of salicylaldehyde aniline to methyl methacrylate satisfies: 0.5 mg:10 ml, and the solid-liquid ratio of the initiator to methyl methacrylate satisfies: 2 mg:1 ml; the initiator is azobisisobutyronitrile; the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: m=0.05 mg / ml.
[0072] The preparation method thereof comprises the following steps:
[0073] Step 1: Add 20 mg of salicylaldehyde aniline to 400 ml of methyl methacrylate and disperse evenly, add 800 mg of azobisisobutyronitrile and stir rapidly for 3 minutes to fully dissolve it;
[0074] Step 2: Heat the solution of step 1 to 75°C and stir to fully react for 1 hour until the reaction liquid becomes viscous;
[0075] Step 3: Pour the viscous reaction liquid of step 2 into the mold, and perform the initial curing at 45°C for 30 hours. After the initial curing, heat it to 100°C and cure it again for 1 hour to complete the curing;
[0076] Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless transparent solid of 3*3*3cm. Figure 3 As shown in (a).
[0077] Example 2
[0078] A solid optical material comprises the following raw materials: salicylaldehyde aniline, methyl methacrylate and an initiator, wherein the solid-liquid ratio of salicylaldehyde aniline to methyl methacrylate satisfies: 0.5 mg: 30 ml, and the solid-liquid ratio of the initiator to methyl methacrylate satisfies: 1 mg: 0.5 ml; the initiator is peroxybenzamide; the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: m=0.01 mg / ml.
[0079] The preparation method thereof comprises the following steps:
[0080] Step 1: add 10 mg of salicylaldehyde aniline to 600 ml of methyl methacrylate and disperse evenly, then add 1200 mg of benzamide peroxide and stir rapidly for 5 minutes to fully dissolve the mixture to obtain a solution;
[0081] Step 2: Heat the solution of step 1 to 100° C. and stir to allow it to react fully until the reaction liquid becomes viscous;
[0082] Step 3: Pour the viscous reaction liquid obtained in step 2 into a mold, and perform initial curing at 60°C for 30 hours. After the initial curing, heat to 120°C and perform another curing for 1.5 hours to complete the curing.
[0083] Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless and transparent solid of 1*1*1 cm.
[0084] Example 3
[0085] A solid optical material comprises the following raw materials: salicylaldehyde aniline, methyl methacrylate and an initiator, wherein the solid-liquid ratio of salicylaldehyde aniline to methyl methacrylate satisfies: 0.5 mg: 20 ml, and the solid-liquid ratio of the initiator to methyl methacrylate satisfies: 3 mg: 0.5 ml; the initiator is a mixture of azobisisoheptylnitrile and lauroyl peroxide in equal weight ratios; the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: m=0.025 mg / ml.
[0086] The preparation method thereof comprises the following steps:
[0087] Step 1: Add 10 mg of salicylaldehyde aniline and 2400 mg of initiator into a beaker containing 400 ml of methyl methacrylate, and stir to fully dissolve the mixture to obtain a solution;
[0088] Step 2: Heat the solution of step 1 to 75°C and stir to fully react for 1 hour until the reaction solution becomes viscous;
[0089] Step 3: Pour the viscous reaction liquid obtained in step 2 into a mold, and perform initial curing at 50°C for 25 hours. After the initial curing, heat to 100°C and perform another curing for 1.0 hour to complete the curing.
[0090] Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless and transparent solid of 2*2*2 cm.
[0091] Example 4
[0092] A solid optical material comprises the following raw materials: salicylaldehyde aniline, methyl methacrylate and an initiator, wherein the solid-liquid ratio of salicylaldehyde aniline to methyl methacrylate satisfies: 1.5 mg: 10 ml, and the solid-liquid ratio of the initiator to methyl methacrylate satisfies: 1 mg: 1.5 ml; the initiator comprises a mixture of lauroyl peroxide and cumene hydroperoxide in equal weights; the concentration of salicylaldehyde aniline in the solid optical material is m, wherein m satisfies: m=0.1 mg / ml.
[0093] The preparation method is basically the same as that of Example 1.
[0094] Example 5
[0095] An application of a solid optical material in static three-dimensional imaging in space comprises the following steps:
[0096] like Figure 3 As shown, S1: using ultraviolet light to irradiate the colorless and transparent solid optical material (a) obtained in Example 1, so that the structure of salicylaldehyde aniline changes to obtain a brown solid optical material (b), the light source of the ultraviolet light is an LED light source with a wavelength of 365nm and a power of 200mW;
[0097] S2: Use green light to irradiate the brown-yellow solid optical material in step S1, and stimulate the irradiated part to emit red fluorescence to form a red spatial three-dimensional image (c), that is, to achieve spatial static three-dimensional imaging.
[0098] Among them, combined Figure 2 The brown-yellow solid optical material in step S1 is the base plate for static three-dimensional imaging in space. The direction of green light irradiation in step S2 is perpendicular to the plane where the base plate is located. The green light source is a 532nm laser light source with a power of 50mW controlled by a galvanometer. The green light projects a circular pattern, such as Figure 3 As shown, when the color-changing area intersects with the visible light, a red stereoscopic circular image is produced, thereby realizing spatial static three-dimensional imaging.
[0099] In the description of the present invention, "plurality" means two or more.
[0100] In the description of this specification, the description with reference to the terms "one embodiment", "some embodiments", "illustrative embodiments", "examples", "specific examples", or "some examples" means that the specific features, structures, materials, or characteristics described in conjunction with the embodiment or example are included in at least one embodiment or example of the present invention. In this specification, the schematic representation of the above terms does not necessarily refer to the same embodiment or example.
[0101] Although the embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the claims and their equivalents.
Claims
1. An application of solid optical materials in static three-dimensional imaging in space, characterized in that: The solid optical material comprises the following raw materials: salicylaldehyde aniline, an initiator and methyl methacrylate, The solid-liquid ratio of the salicylaldehyde aniline and the methyl methacrylate satisfies: 0.5mg-1.5mg:10ml-30ml; the solid-liquid ratio of the initiator and the methyl methacrylate satisfies: 1mg-3mg:0.5ml-1.5ml; The method for preparing the solid optical material comprises the following steps: The salicylaldehyde aniline with the material ratio, the initiator and methyl methacrylate are mixed for reaction and heated for curing to obtain a colorless and transparent solid; The application of the above solid optical material in static three-dimensional imaging in space includes the following steps: The solid optical material is irradiated with ultraviolet light to change the structure of salicylaldehyde aniline to obtain a brown solid optical material; irradiating the solid optical material with green light; In the solid optical material, the intersection of the ultraviolet light and the green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, achieving spatial static three-dimensional imaging.
2. The application of the solid optical material in static three-dimensional imaging in space according to claim 1, characterized in that: The solid-liquid ratio of the salicylaldehyde aniline and the methyl methacrylate satisfies: 1.0 mg: 20 ml; the solid-liquid ratio of the initiator and the methyl methacrylate satisfies: 2 mg: 1 ml.
3. The application of the solid optical material in static three-dimensional imaging in space according to claim 1, characterized in that: The initiator includes at least one of an azo compound initiator and a peroxide initiator; the initiator includes at least one of azobisisobutyronitrile, azobisisoheptanenitrile, dimethyl azobisisobutyrate, peroxybenzamide, lauroyl peroxide, cumene hydroperoxide and methyl ethyl ketone peroxide.
4. The application of the solid optical material in static three-dimensional imaging in space according to claim 1, characterized in that: The steps include: Step 1, dispersing the salicylaldehyde aniline in the material ratio into methyl methacrylate, adding the initiator, stirring, and fully dissolving it to obtain a solution; Step 2, heating the solution in step 1 to 50-100° C., and stirring to allow it to react fully until the reaction liquid becomes viscous; Step 3: Pour the viscous reaction liquid in step 2 into a mold, and initially cure it at 45-60° C. for 20-30 hours. After the initial curing, heat it to 80-120° C. and cure it again for 0.5-1.5 hours to complete the curing; Step 4: Cut, grind and splice the solidified material in step 3 to obtain a colorless and transparent solid.
5. The use according to claim 1, characterized in that: The steps include: S1: irradiating the solid optical material with ultraviolet light to change the structure of salicylaldehyde aniline to obtain a brown solid optical material; S2: using green light to irradiate the brown-yellow solid optical material in step S1, so that the intersection of the ultraviolet light and the green light in the solid optical material is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging; The brown-yellow solid optical material in step S1 is the base plate for spatial static three-dimensional imaging, and the direction of green light irradiation in step S2 is perpendicular to the plane where the base plate is located.
6. The use according to claim 1, characterized in that: The steps include: S1: irradiating the solid optical material with green light; S2: using ultraviolet light to irradiate the solid optical material described in step S1, so that in the solid optical material, the intersection of the ultraviolet light and the green light is excited to emit red fluorescence, forming a red spatial three-dimensional image, that is, realizing spatial static three-dimensional imaging; The optical path of the green light in the solid optical material after the green light irradiation in step S1 is used as the base plate for spatial static three-dimensional imaging, and the direction of ultraviolet light irradiation in step S2 is perpendicular to the plane where the base plate is located.
7. The use according to any one of claims 1 or 5-6, characterized in that: The wavelength of the ultraviolet light is λ1, wherein λ1 satisfies: 365nm≤λ1≤395nm; and / or The wavelength of the green light is λ2, wherein λ2 satisfies: 488nm≤λ2≤532nm; and / or The power of the ultraviolet light source is W1, wherein W1 satisfies: 60mW≤W1≤300mW; and / or The power of the green light source is W2, wherein W2 satisfies: 50mW≤W2≤120mW.
8. The use according to any one of claims 1 or 5-6, characterized in that: At room temperature and natural light intensity of 300 Lux to 500 Lux, the image of the spatial static three-dimensional imaging is stored for 0.5 to 3 seconds.
Citation Information
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