JPH0233296B2 - - Google Patents
Info
- Publication number
- JPH0233296B2 JPH0233296B2 JP58080615A JP8061583A JPH0233296B2 JP H0233296 B2 JPH0233296 B2 JP H0233296B2 JP 58080615 A JP58080615 A JP 58080615A JP 8061583 A JP8061583 A JP 8061583A JP H0233296 B2 JPH0233296 B2 JP H0233296B2
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- lens
- substrate
- transparent gel
- refractive index
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000178 monomer Substances 0.000 claims description 70
- 239000000758 substrate Substances 0.000 claims description 62
- 238000000034 method Methods 0.000 claims description 23
- 238000006116 polymerization reaction Methods 0.000 claims description 18
- 238000009826 distribution Methods 0.000 claims description 14
- 229920003002 synthetic resin Polymers 0.000 claims description 14
- 239000000057 synthetic resin Substances 0.000 claims description 14
- 230000003287 optical effect Effects 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 230000000379 polymerizing effect Effects 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 description 10
- 229920001187 thermosetting polymer Polymers 0.000 description 9
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000004342 Benzoyl peroxide Substances 0.000 description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 4
- 229910001369 Brass Inorganic materials 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 4
- 239000012965 benzophenone Substances 0.000 description 4
- 235000019400 benzoyl peroxide Nutrition 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000001678 irradiating effect Effects 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- SYFOAKAXGNMQAX-UHFFFAOYSA-N bis(prop-2-enyl) carbonate;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.C=CCOC(=O)OCC=C SYFOAKAXGNMQAX-UHFFFAOYSA-N 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000013307 optical fiber Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- QTKPMCIBUROOGY-UHFFFAOYSA-N 2,2,2-trifluoroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)F QTKPMCIBUROOGY-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- -1 acrylic ester Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- PIPBVABVQJZSAB-UHFFFAOYSA-N bis(ethenyl) benzene-1,2-dicarboxylate Chemical compound C=COC(=O)C1=CC=CC=C1C(=O)OC=C PIPBVABVQJZSAB-UHFFFAOYSA-N 0.000 description 1
- FWICIOVOJVNAIJ-UHFFFAOYSA-N bis(ethenyl) benzene-1,3-dicarboxylate Chemical compound C=COC(=O)C1=CC=CC(C(=O)OC=C)=C1 FWICIOVOJVNAIJ-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000009415 formwork Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- KJWHEZXBZQXVSA-UHFFFAOYSA-N tris(prop-2-enyl) phosphite Chemical compound C=CCOP(OCC=C)OCC=C KJWHEZXBZQXVSA-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00009—Production of simple or compound lenses
- B29D11/00432—Auxiliary operations, e.g. machines for filling the moulds
- B29D11/00442—Curing the lens material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00009—Production of simple or compound lenses
- B29D11/00355—Production of simple or compound lenses with a refractive index gradient
Landscapes
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Ophthalmology & Optometry (AREA)
- Mechanical Engineering (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Polymerisation Methods In General (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Focusing (AREA)
- Optical Integrated Circuits (AREA)
Description
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ååžåã¬ã³ãºéšåã圢æããã¬ã³ãºäœã補é ãã
æ¹æ³ã«é¢ãããDETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a lens body in which a gradient index lens portion is formed in a transparent substrate made of synthetic resin.
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ãã«ããã³åã¬ã³ãºã§ããå Žåãããã In a transparent substrate with parallel planes, there is a refractive index distribution that changes with square approximation in the optical axis direction. A planar lens in which a large number of refractive index gradient lens parts are formed in a line or matrix shape at intervals, and the refractive index distribution gradually changes in a square approximation as it moves away from the optical axis within at least one cross section that includes the optical axis. Are known. In such a flat lens, the lens part may be a lens with the above-mentioned refractive index distribution in all cross sections including the optical axis, that is, a circular lens, or it may be a circular lens with a refractive index distribution as described above in all cross sections including the optical axis. In some cases, the lens has a refractive index distribution that gradually changes, and the refractive index is constant regardless of the distance from the optical axis in a cross section perpendicular to this, so-called a semicylindrical lens.
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åšèŸºããã€ã¹çã«æçšã§ããã The above-mentioned plane lenses are used as image transmission elements in various applications such as optical systems of copying machines and facsimile machines, or in optical coupling systems between light sources and optical fibers, or for inserting attenuators or branch circuits between optical fibers. It is useful for peripheral devices for optical communications, such as parallel light conversion elements.
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äœããå Žåã第ïŒå³ã«ç€ºãããã«å±æçNaã®ç¶²
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NaïŒNbã§ããã°åžã¬ã³ãºäœçšããã€ããšã«ãª
ãã When manufacturing a plane lens as described above using a synthetic resin, as shown in Figure 1, a monomer (monomer mixture) that produces a network polymer (including copolymer) Pa with a refractive index of Na is used. A transparent gel-like substrate 10 is made by partially polymerizing Ma (including Ma), and a mask 12 with openings 11 corresponding to the pattern of the lens portion to be formed is applied to the surface of this substrate 10.
A monomer (including a monomer mixture) Mb that produces a polymer (including a copolymer) Pb having a refractive index Nb different from the above-mentioned refractive index Na is diffused and polymerized into the substrate through the lens portion 13. There are known methods of forming . In this case, if Na>Nb, the lens portion 13 formed in the substrate has a concave lens effect,
If Na<Nb, it will have a convex lens effect.
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ããã As another method, as shown in FIG. 2, a transparent gel-like substrate 14 similar to that described above is made, a mask 15 is applied only to the lens portion of the substrate surface, and Na is polymerized with the substrate 14 from the periphery. Different refractive index Nb
There is also a method of diffusing monomers to form polymers.
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NaïŒNbã§ããã°å¹ã¬ã³ãºäœçšã瀺ãã In this case, the lens portion 16 formed in the substrate exhibits a convex lens effect if Na<Nb,
If Na>Nb, it exhibits a concave lens effect.
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ããšããåé¡ã¯ãã°ãã°çããŠããã However, in the conventional method shown in FIGS. 1 and 2 as described above, masks 12, 15 and gel substrates 10, 1 provided to prevent the diffusion of monomer Mb
Unless the adhesion with 4 is very good, monomeric Mb
enters between the mask and the gel substrate, and monomeric Mb
The problem has often arisen that it is impossible to form a lens body with a refractive index distribution because the lens particles diffuse over the entire surface of the gel substrate.
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ãã An object of the present invention is to provide a novel method for manufacturing a synthetic resin flat lens that can solve the above-mentioned conventional problems and avoid the problem of adhesion between a mask and a gel substrate when manufacturing a gradient index flat lens. It is said that
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ãšããã That is, the method for producing a synthetic resin flat lens according to the present invention involves incompletely polymerizing one or more monomers Ma that produces a network polymer Pa having a refractive index of Na to produce a transparent gel-like polymer. A substrate is formed, and one or more monomers Mb that produce a polymer Pb having a refractive index Nb different from that of Na are diffused and permeated into the surface area of the transparent gel substrate. A partial hardening process is applied to the surface area to form a hardened part and an unhardened part in accordance with the pattern of the lens part to be formed, and a hardened part and an unhardened part are formed in the surface area through the surface of the transparent gel substrate on which the hardening process has been performed. Then, the uncured portion and the monomer Mb inside the transparent gel substrate corresponding to the uncured portion are mainly removed. A state is formed in which the monomer Mb remains even in a continuously changing concentration gradient, and in this state, the monomers Ma and
It consists of completing the polymerization of Mb. Note that the term "polymerization" as used in the present invention includes copolymerization.
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ã§ããã As described above, in the present invention, by using the hardened portion formed on the surface of the transparent gel substrate as a so-called mask when removing monomer Mb, monomer Mb is kept in the above-mentioned state. It will remain inside the board. Since this hardened portion is integrated with the transparent gel substrate, the adhesion between the mask and the transparent gel substrate in the conventional example shown in FIGS. 1 and 2 is not a problem. Therefore, a lens portion with a desired refractive index can be formed within the substrate.
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æããŠãããã®ãšããã In the present invention, any monomer Ma can be used as long as it forms a transparent network polymer when polymerized, and any monomer Ma that can be cleaved into one molecule to form a crosslink can be used. One or more compounds having two or more bonds may be used. Suitable examples include diallyl phthalate,
diallyl esters such as diallyl isophthalate, diallyl terephthalate, diethylene glycol bisallyl carbonate; triallyl esters such as triallyl trimellidate, triallyl phosphate, triallyl phosphite; allyl methacrylate;
Unsaturated acid allyl esters such as allyl acrylate; divinyl phthalate, divinyl isophthalate,
Mention may be made of vinyl esters such as dibyl terephthalate. Note that the network polymer as used in the present invention
Pa is a homopolymer obtained by polymerizing one of the above-mentioned monomers, a copolymer obtained from two or more of these monomers, and a copolymer obtained from two or more of these monomers.
It contains a copolymer of Ma and monomers such as styrene, methacrylate, vinyl benzoate, etc. Further, it is assumed that this network polymer Pa has a refractive index of Na.
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ãããã In the present invention, first, the monomer Ma described above is polymerized to produce a transparent gel-like substrate. Polymerization of the monomer is temporarily stopped when the polymer loses its fluidity and becomes a transparent gel, that is, when the polymerization is incomplete. If this polymerization is carried out in a mold or frame having a predetermined shape, the gel substrate can be formed at the same time. Next, a monomer Mb that produces a polymer having a refractive index Nb different from that of Na is diffused and permeated into the obtained gel substrate.
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以äžãããªãæ··åç©ã奜é©ã«äœ¿çšã§ããã The monomer Mb used in this process may be one that becomes a linear polymer or a network polymer when polymerized, but it may be one that becomes a linear polymer or a network polymer when polymerized. Preferably, those that can be used to produce a transparent copolymer. As such monomer Mb, styrene, methacrylic ester, acrylic ester, vinyl acetate, vinyl chloride, acrylonitrile, butadiene, or a mixture of two or more of these can be suitably used.
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ããããã«ããã Next, on the surface of the transparent gel substrate on which the monomer Mb has been diffused, locally non-uniform polymerization conditions are applied to selectively harden only the surface region. Local heating, light irradiation, electron beam irradiation, etc. can be used as locally non-uniform polymerization conditions, but among these, visible light and/or ultraviolet ray irradiation is the most suitable in terms of method and simplicity. Probably. In addition, if necessary, monomer Ma and/or monomer
A thermal polymerization initiator, a photopolymerization initiator, a photosensitizer, etc. can also be added to Mb. By curing the surface region by applying locally non-uniform polymerization conditions in this manner, a pattern corresponding to the lens portion to be formed is formed by the cured portions and uncured portions.
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The shape and size of the gradient index lens to be formed,
It is determined depending on the magnitude relationship between Na and Nb.
Furthermore, when a plurality of lenses are provided, their positional relationship also affects the curing pattern.
For example, when forming a circular lens, either a portion corresponding to the circular portion centered on the central optical axis portion is left and the other portions are hardened, or a portion corresponding to the lens portion is hardened into a disk shape. If Na>Nb, the former becomes a convex lens and the latter becomes a concave lens. Na
<Nb, the former becomes a concave lens, and the latter becomes a convex lens. When forming a semicylindrical lens,
Either the lens portion is left in a linear shape and the other portions are hardened, or the portion corresponding to the lens portion is hardened in a linear shape.
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ã«åœ¢æããããšãã§ããã Next, the unpolymerized monomer Mb diffused in the uncured portion and inside the substrate is removed through the patterned surface of the transparent gel substrate. Various methods can be used for removal, such as immersion in a solvent capable of dissolving monomer Mb, vaporization under reduced pressure, and performing the latter after the former. When monomer Mb is removed from the transparent gel substrate using this method, it is difficult for the monomer Mb inside to escape through the part that was hardened in the previous stage of this process. The unhardened part and the monomer Mb inside it mainly escape through the unhardened part. Due to this phenomenon, a concentration distribution of the monomer Mb is generated in the transparent gel substrate near the cured portion. After forming the concentration distribution of monomer Mb in the transparent gel substrate in this way, the polymerization of monomer Ma and remaining monomer Mb is completed, and the monomer
By fixing the distribution of Mb, it is possible to form a gradient index lens portion as described above in a plastic substrate.
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å Žåå¹ã¬ã³ãºãšãªãã First, as shown in FIG. 3A, a transparent gel substrate 17 is prepared by polymerizing a monomer Ma forming a network polymer Pa having a refractive index Na in molds 18 and 19. Next, a polymer with a refractive index of Nb is coated on the surface of this transparent gel substrate 17.
The monomer Mb that generates Pb is brought into contact with it in a liquid phase or a gas phase, and the monomer Mb is diffused from the entire surface of the transparent gel substrate 17, as shown in FIG. 3A. monomer
The higher the temperature when diffusing Mb, the more monomeric Mb
Although the diffusion rate is high, it should not be so high that monomer Mb polymerizes alone or copolymerizes with monomer Ma. Next, as shown in Figure 3B,
A circular light shielding mask 20 for shielding light is placed on the surface of a transparent gel substrate 17 on which monomer Mb is diffused, and light is irradiated. The diameter R1 of the mask 20 is the third
It is equal to the diameter R2 of the circular hole (uncured part) 21 in the hardened part as shown in Figure C, which is much smaller than the diameter R3 of the lens part 22 shown in Figure 3 D. It's better to be there. The light to be irradiated is preferably ultraviolet rays used for ordinary photocurable resins. By light irradiation, a hardened portion 23 is formed as shown in FIG. 3C. The thickness of the hardened portion 23 must be thick enough that the monomer Mb does not easily pass through it, but as long as this condition is satisfied, it is preferably thinner. In the next step, monomer Mb is removed from the hole 21 with diameter R2 in the hardened portion 23, but if R2 becomes sufficiently smaller than the diameter R3 of the lens to be formed, the isoconcentration curve of monomer Mb will be hole 2
The portion 1 is parallel to the surface of the transparent gel substrate 17, and the cross section does not have a concentric spherical shape. monomer
To remove Mb, if monomeric Mb is much more volatile than monomeric Ma, it is sufficient to reduce the pressure; if the volatilities are similar, the solubility may be reduced. Methods of immersion in different solvents may be used. Monomer Ma and monomer
If Mb is removed in approximately equal amounts, the monomer
Since the concentration distribution of Mb has already been formed in the substrate, if the transparent gel substrate 17 is kept in contact with the monomer Ma when completing the polymerization, the shortage of the monomer Ma caused by the removal of the monomer Ma can be compensated for. Shrinkage during polymerization can be alleviated. By removing the monomer Mb through the hole 21, the polymerization is completed to fix the concentration distribution of the monomer Mb formed, and then the surface is polished, as shown in FIG. 3D. A synthetic resin flat lens 24 having a spherical lens portion 22 having a cross section is completed. The diameter R3 of the lens portion 22 is determined by the diameter R2 of the hole in the cured portion 23 (=diameter R1 of the light shielding mask), the crosslinking density of the transparent gel substrate 17,
It is affected by monomeric Mb removal conditions, etc. The lens portion 22 becomes a convex lens when Na>Nb, and becomes a concave lens when Na<Nb.
第ïŒå³ã«æ¬çºæã®ä»ã®å®æœäŸã瀺ãã FIG. 4 shows another embodiment of the invention.
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ãå¹ã¬ã³ãºã«ãNaïŒNbã®ãšãåžã¬ã³ãºã«ãªãã In this example, as well as the method described above, first the formwork 2 is
A transparent gel substrate 25 is formed by partially polymerizing a monomer Ma that forms a network polymer Pa having a refractive index Na within 6 and 27.
A monomer Mb that forms a polymer Pb having a refractive index Nb is brought into contact with the polymer Pb and diffused from the entire surface as shown in FIG. 4A. The temperature at this time is set to be lower than that at which Mb polymerizes. Next, as shown in FIG. 4B, a light-shielding mask 28 with a circular hole corresponding to the lens portion to be formed is placed on the transparent gel substrate 25 in which the monomer Mb is diffused, and ultraviolet rays are irradiated. . The diameter R4 of the hole in the light-shielding mask 28 is equal to the diameter R5 of the hardened portion 29 shown in FIG.
This is approximately the diameter of the lens portion 31 shown in FIG.
will be equal to R6. By irradiating the ultraviolet rays, a disk-shaped hardened portion 29 is formed as shown in FIG. 4C.
It is desirable that this thickness be as thin as possible as long as monomer Mb does not pass through. Next, monomer Mb is removed from the transparent gel substrate 25. The monomer is removed from the uncured portion 30 on the surface of the transparent gel substrate 25.
When Mb escapes, a concentration gradient is generated, and monomer Mb moves there from below the hardened portion 29 and from the deep part of the transparent gel substrate 25, and a new concentration gradient is generated. After forming the concentration distribution of the monomer Mb with a concentric circular cross section in this way, the polymerization is completed to fix it, and then the surface is polished.
Spherical lens portion 31 having a cross section as shown in Figure D
The synthetic resin flat lens 32 having the above formed thereon is completed. The diameter R6 of the lens portion 31 is approximately determined by the diameter R5 of the hardened portion 29 (=the diameter R4 of the hole in the light shielding mask). The lens portion 31 becomes a concave lens when Na>Nb, and becomes a convex lens when Na<Nb.
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ã³ãºã補é ããããšãã§ããã By curing the substrate surface leaving a large number of uncured circular parts as described above, or by forming a large number of island-like circular hardened parts on the substrate surface, a gradient index spherical lens can be obtained. A synthetic resin flat lens is obtained, which is composed of an array of . Furthermore, if the light-shielding mask has a linear pattern, it is also possible to manufacture a gradient index flat lens equivalent to a semicylindrical lens or a lenticular lens in which light rays are focused in a line.
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ã«ãªã€ãŠãããSpecific Example 1 This specific example 1 follows the method shown in Figure 3. First, 3% by weight of benzoyl peroxide and benzophenone were dissolved in diethylene glycol bisallyl carbonate (CR-39) and poured into a mold. 20mm x 20mm x 5
A transparent gel substrate of mm size was prepared. 2, 2, 2 this
- immersed in trifluoroethyl methacrylate (3FMA) to diffuse into the gel body from the surface. Next, a brass disk with a diameter of 2 mm was placed in the center, and the area around the area corresponding to the brass disk was hardened by irradiating ultraviolet light from an ultra-high pressure mercury lamp. Next, this was placed in a desiccator, and a vacuum pump was connected to reduce the pressure, and 3FMA was vaporized and removed from the uncured portion with a diameter of 2 mm. This was held at 80°C for 15 hours to complete polymerization, and the surface was polished. The center of this CR-39/3FMA copolymer block was a convex lens with a focal length of 30 mm.
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ãªã€ãŠãããSpecific Example 2 This specific example 2 follows the method shown in FIG. 3. First, benzoyl peroxide and benzophenone are dissolved in diallylisophthalate (DAIP) in an amount of 3% by weight, and poured into a mold. at °C
Heating was performed for 180 minutes to produce a transparent gel substrate measuring 20 mm x 20 mm x 5 mm. This was immersed in methyl methacrylate (MMA) and diffused from the surface into the gel substrate. Next, a brass disk with a diameter of 2 mm was placed in the center, and the area around the area corresponding to the brass disk was hardened by irradiating ultraviolet light from an ultra-high pressure mercury lamp. Next, this was placed in a desiccator, a vacuum pump was connected to reduce the pressure, and the MMA was extracted from the uncured part with a diameter of 2 mm. This was held at 80°C for 15 hours to complete polymerization, and the surface was polished. The center of this DAIP/MMA copolymer block was a convex lens with a focal length of 30 mm.
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ã«åœ¢æãããŠãããSpecific Example 3 This specific example 3 follows the method shown in Figure 4. First, benzoyl peroxide and benzophenone were dissolved in diethylene glycol bisallyl carbonate (CR-39) in an amount of 3% by weight each, and then poured into a mold. Heat it at 80â for 90 minutes, and make 50mm x 50mm x 5
A transparent gel substrate of mm size was prepared. This was immersed in vinyl benzoate (VB) in which benzoyl peroxide and benzophenone were each dissolved in an amount of 3% by weight, and diffused from the surface into the gel substrate. Next, the diameter is 3mm
A black light-shielding mask with 25 circular light-transmitting parts arranged in a 5 x 5 matrix was placed on top of the gel substrate, and ultraviolet light from an ultra-high pressure mercury lamp was irradiated onto the surface of the gel substrate in the form of a disk with a diameter of 3 mm. 25 hardened parts were formed in the form of islands. This was immersed in acetone to dissolve the monomer from the uncured portion, and the acetone was removed under reduced pressure. Next, bring CR-39 into contact with this surface and heat it at 80°C.
for 15 hours to complete the polymerization and remove the CR-
The 39 homopolymer was polished off and smoothed.
On the surface of this CR-39/VB copolymer block,
Lenses with a focal length of approximately 30 mm were formed in a 5 x 5 matrix.
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æ¿äžã«40æ¬ã®èŒç·ãèªãããããSpecific Example 4 In this specific example 4, a line pattern was used as the light-shielding mask in the method shown in FIG. Dissolve in weight percent, pour into a mold and heat at 80â for 90 minutes to form a 50mm x 50mm x 5mm
A transparent gel substrate was prepared. This is 1, 1, 3
- immersed in trihydroperfluoropropyl methacrylate (4FMA) and diffused from the surface. A glass plate with 40 black lines of 200 ÎŒm width arranged at 1 mm intervals was placed on top of this, and after irradiating it with ultraviolet rays from an ultra-high pressure mercury lamp, the glass plate was removed and the pressure was reduced.
4FMA was volatilized from the uncured surface. This is 80â
The mixture was held for 15 hours to complete polymerization, and the surface was polished. When parallel light passes through this CR-39/
Forty bright lines were observed on the plate placed at a distance of 30 mm from the 4FMA copolymer block.
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ãºã®è£œé æ¹æ³ã®åŸæ¥äŸã瀺ãæé¢å³ã§ããã第ïŒ
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é¢ã¬ã³ãºè£œé æ¹æ³ã®å®æœäŸã瀺ãæé¢å³ã§ããã
ãªããå³é¢ã«çšãã笊å·ã«ãããŠãïŒïŒïŒïŒïŒ
âŠâŠéæã²ã«åºæ¿ãïŒïŒïŒïŒïŒâŠâŠé®å
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ïŒïŒïŒïŒïŒâŠâŠæªç¡¬åéšãïŒïŒïŒïŒïŒâŠâŠç¡¬å
éšãïŒïŒïŒïŒïŒâŠâŠã¬ã³ãºéšåãïŒïŒïŒïŒïŒâŠâŠ
åææš¹èå¹³é¢ã¬ã³ãºã§ããã
FIG. 1 and FIG. 2 are cross-sectional views showing a conventional example of a method for manufacturing a synthetic resin flat lens, respectively.
FIG. 4 is a cross-sectional view showing an embodiment of the method for manufacturing a synthetic resin flat lens according to the present invention. In addition, in the codes used in the drawings, 17, 25
...transparent gel substrate, 20,28...light-shielding mask,
21, 30... Uncured part, 23, 29... Cured part, 22, 31... Lens part, 24, 32...
It is a synthetic resin flat lens.
Claims (1)
ã«æ¬¡ç¬¬ã«å€åãã屿çååžãšå 軞ãå«ãå°ãªã
ãšãäžã€ã®æé¢å ã§äžèšå 軞ããé ãããã«ã€ã
ãŠæ¬¡ç¬¬ã«å€åãã屿çååžãšã倫ã åããåäž
ã®ãŸãã¯è€æ°ã®å±æçååžåã¬ã³ãºéšåã圢æã
ãããã«ããåææš¹èå¹³é¢ã¬ã³ãºã®è£œé æ¹æ³ã«ã
ããŠã (a) 屿çãNaã®ç¶²ç¶éåäœPaãçæããïŒçš®
ãŸãã¯ïŒçš®ä»¥äžã®åéäœMaãäžå®å šã«éåã
ããŠéæãªã²ã«ç¶ã®åºæ¿ã圢æããå·¥çšã (b) ãã®éæã²ã«åºæ¿äžã«ãNaãšã¯ç°ãªã屿
çNbãæããéåäœPbãçæããïŒçš®ãŸãã¯
ïŒçš®ä»¥äžã®åéäœMbãæ¡æ£ã»æµžéãããå·¥
çšã (c) åèšåºæ¿ã®è¡šé¢é åã«éšåç硬ååŠçãæœã
ãŠã圢æãã¹ãã¬ã³ãºéšåã®ãã¿ãŒã³ã«åãã
ã硬åéšããã³æªç¡¬åéšãåèšè¡šé¢é åã«åœ¢æ
ããå·¥çšã (d) åèšéæã²ã«åºæ¿ã®åèšç¡¬ååŠçãæœããã
åŽã®è¡šé¢ãä»ããŠãäž»ãšããŠåèšæªç¡¬åéšãã
ã³ãã®å éšã®åèšåéäœMbãé€å»ããããã«
ãã€ãŠãåèšç¡¬åéšã®è¿åã«ãããåèšéæã²
ã«åºæ¿å ã«åèšåéäœMbãé£ç¶çã«å€åãã
æ¿åºŠåŸé ã§ãã€ãŠæ®çããŠããç¶æ ã圢æãã
å·¥çšã (e) åèšåéäœMbã®åèšæ®çç¶æ ã«ãããŠãå
èšåéäœMaããã³Mbã®éåãå®çµãããå·¥
çšã ãæããããšãç¹åŸŽãšããåææš¹èå¹³é¢ã¬ã³ãºã®
è£œé æ¹æ³ã[Claims] 1. A refractive index distribution that gradually changes in the optical axis direction in a transparent substrate made of synthetic resin, and a refractive index distribution that gradually changes as the distance from the optical axis increases within at least one cross section that includes the optical axis. In a method for manufacturing a synthetic resin flat lens in which a single or a plurality of gradient index lens parts are formed, the method includes: (a) one type of synthetic resin that produces a reticular polymer Pa having a refractive index of Na; A step of incompletely polymerizing two or more types of monomers Ma to form a transparent gel-like substrate; (b) producing a polymer Pb having a refractive index Nb different from that of Na in this transparent gel substrate; (c) applying a partial hardening treatment to the surface area of the substrate to form a hardened portion and an uncured portion in accordance with the pattern of the lens portion to be formed; forming a hardened part in the surface region; (d) mainly removing the unhardened part and the monomer Mb inside thereof through the hardening-treated surface of the transparent gel substrate; , thereby forming a state in which the monomer Mb remains in the transparent gel substrate in the vicinity of the cured portion with a concentration gradient that continuously changes; (e) the monomer A method for manufacturing a synthetic resin flat lens, comprising the step of completing polymerization of the monomers Ma and Mb in the residual state of Mb.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58080615A JPS59204519A (en) | 1983-05-09 | 1983-05-09 | Preparation of synthetic resin plane lens |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58080615A JPS59204519A (en) | 1983-05-09 | 1983-05-09 | Preparation of synthetic resin plane lens |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59204519A JPS59204519A (en) | 1984-11-19 |
| JPH0233296B2 true JPH0233296B2 (en) | 1990-07-26 |
Family
ID=13723242
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58080615A Granted JPS59204519A (en) | 1983-05-09 | 1983-05-09 | Preparation of synthetic resin plane lens |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59204519A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5405556A (en) * | 1993-04-13 | 1995-04-11 | National Science Council | Process of fabricating light-focusing plastic optical elements |
| JP3012500B2 (en) * | 1995-11-20 | 2000-02-21 | æ¥æ¬æ¿ç¡åæ ªåŒäŒç€Ÿ | Method for manufacturing flat lens array |
| US6027672A (en) * | 1997-12-31 | 2000-02-22 | Lightpath Technologies, Inc. | Method of producing large polymer optical blanks with predictable axil refractive index profile |
| WO2022210869A1 (en) * | 2021-03-31 | 2022-10-06 | ãã³ã«æ ªåŒäŒç€Ÿ | Method for producing semi-cured product composite, method for producing cured product composite, and semi-cured product composite |
| EP4101626A1 (en) * | 2021-06-11 | 2022-12-14 | Essilor International | Method for obtaining a lens element |
| DE102023106782B3 (en) * | 2023-03-17 | 2024-07-25 | Rodenstock Gmbh | Myopia management lenses with microlenses made from GRIN structures |
-
1983
- 1983-05-09 JP JP58080615A patent/JPS59204519A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59204519A (en) | 1984-11-19 |
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