WO2007066455A1 - 非晶性環状オレフィン系樹脂用曇り防止剤、樹脂組成物、及び光学部品 - Google Patents
非晶性環状オレフィン系樹脂用曇り防止剤、樹脂組成物、及び光学部品 Download PDFInfo
- Publication number
- WO2007066455A1 WO2007066455A1 PCT/JP2006/321670 JP2006321670W WO2007066455A1 WO 2007066455 A1 WO2007066455 A1 WO 2007066455A1 JP 2006321670 W JP2006321670 W JP 2006321670W WO 2007066455 A1 WO2007066455 A1 WO 2007066455A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- component
- tin
- resin
- molding
- group
- Prior art date
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 33
- 239000011347 resin Substances 0.000 title claims abstract description 33
- 230000003287 optical effect Effects 0.000 title claims abstract description 21
- 239000011342 resin composition Substances 0.000 title claims abstract 4
- 150000001925 cycloalkenes Chemical class 0.000 title abstract 4
- 150000003839 salts Chemical class 0.000 claims abstract description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- -1 alkali metal salts Chemical class 0.000 claims abstract description 6
- 238000000465 moulding Methods 0.000 claims description 35
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 31
- 125000004122 cyclic group Chemical group 0.000 claims description 25
- 229920000642 polymer Polymers 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 13
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 11
- 239000010931 gold Substances 0.000 claims description 11
- 229910052737 gold Inorganic materials 0.000 claims description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052725 zinc Inorganic materials 0.000 claims description 8
- 239000011701 zinc Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 229920005672 polyolefin resin Polymers 0.000 claims 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 2
- 239000000975 dye Substances 0.000 claims 1
- 230000007613 environmental effect Effects 0.000 abstract description 15
- 229910052751 metal Inorganic materials 0.000 abstract description 11
- 239000002184 metal Substances 0.000 abstract description 11
- 230000008859 change Effects 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 6
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 238000005336 cracking Methods 0.000 abstract 1
- 238000002834 transmittance Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000007334 copolymerization reaction Methods 0.000 description 9
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 8
- 101150084935 PTER gene Proteins 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- PPJYSSNKSXAVDB-UHFFFAOYSA-N 3,3',5,5'-tetraiodothyroacetic acid Chemical compound IC1=CC(CC(=O)O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 PPJYSSNKSXAVDB-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- 150000003751 zinc Chemical class 0.000 description 4
- 239000011575 calcium Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000011366 tin-based material Substances 0.000 description 3
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- GSJBKPNSLRKRNR-UHFFFAOYSA-N $l^{2}-stannanylidenetin Chemical compound [Sn].[Sn] GSJBKPNSLRKRNR-UHFFFAOYSA-N 0.000 description 1
- IYDCZCBVYAESDR-VQHVLOKHSA-N (e)-pentadec-4-ene Chemical compound CCCCCCCCCC\C=C\CCC IYDCZCBVYAESDR-VQHVLOKHSA-N 0.000 description 1
- KXYGKDBONOVZOM-UHFFFAOYSA-N 1h-cyclopenta[a]naphthalene Chemical compound C1=CC=CC2=C3CC=CC3=CC=C21 KXYGKDBONOVZOM-UHFFFAOYSA-N 0.000 description 1
- 102000007469 Actins Human genes 0.000 description 1
- 108010085238 Actins Proteins 0.000 description 1
- 241000220438 Arachis Species 0.000 description 1
- 235000003911 Arachis Nutrition 0.000 description 1
- 101150079087 Arfgef2 gene Proteins 0.000 description 1
- 108090001008 Avidin Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 108010053993 N-terminal tetrapeptide cystatin C Proteins 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- WUUNPBLZLWVARQ-QAETUUGQSA-N Postin Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H]1CCCN1C(=O)[C@H]1NCCC1 WUUNPBLZLWVARQ-QAETUUGQSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- KSHPUQQHKKJVIO-UHFFFAOYSA-N [Na].[Zn] Chemical compound [Na].[Zn] KSHPUQQHKKJVIO-UHFFFAOYSA-N 0.000 description 1
- GYBPPAFQDLCOHB-UHFFFAOYSA-N [Sn].CCCCCCC=C Chemical compound [Sn].CCCCCCC=C GYBPPAFQDLCOHB-UHFFFAOYSA-N 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920006127 amorphous resin Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229960004198 guanidine Drugs 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- RYPKRALMXUUNKS-UHFFFAOYSA-N hex-2-ene Chemical compound CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- MJFJKKXQDNNUJF-UHFFFAOYSA-N metixene Chemical compound C1N(C)CCCC1CC1C2=CC=CC=C2SC2=CC=CC=C21 MJFJKKXQDNNUJF-UHFFFAOYSA-N 0.000 description 1
- 229960005103 metixene Drugs 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910001186 potin Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L45/00—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
- C08L23/0823—Copolymers of ethene with aliphatic cyclic olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C08L93/04—Rosin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
Definitions
- 002 is a resin with a ring-shaped case.
- the purpose is to provide optical components. To solve the problem
- the original characteristics of the in-based material can be maintained and molding due to environmental changes can be prevented, and as a result, the clarity of the molding is maintained. be able to.
- the original brightness of the in-system is reduced by the molding process, and the transparency of the molded part is reduced by the subsequent environmental change. It means to prevent.
- Molding made of in-system material, the water vapor taken in by the high temperature and high humidity atmosphere due to the change of the environment under the high temperature and high humidity atmosphere and the normal temperature atmosphere does not come out of the molded body at the normal temperature atmosphere. It may cause fine cracks.
- 001 (3) Contains at least one species of Aka and Na-Ca salt.
- 002 (3) contains at least both aca and sodium-Ca salt.
- Sodium is a metal that gives good results among aka salts.
- 002 (4) contains at least both aca and calcium-gum salts.
- Gum is a metal that has good results among aka salts.
- Dinoic acid is selected from compounds represented by general formula (1), (1), (1) and ().
- In-system including the in-system, which is offset from () to (6).
- the in-system of the in-system and the in-system with 2 to 2 carbon atoms and the specific in-system It is a polymer. It is possible to develop the characteristic of point for every minute. On the other hand, the circular ring components can develop the following characteristic. Therefore, according to the type (9), it is possible to combine the functions of poins and to exert the functions required for transparent materials.
- transparency is an important requirement for optical parts. If it is on the ray 9 in the range of 5 to 75, it is possible to sufficiently satisfy the brightness as the function of the optical component. Therefore, the in-system of () has sufficient brightness required for optical parts, and it is possible to prevent clouding due to subsequent environmental changes and maintain the brightness of molding.
- the molding is made from the 003 () in-line material and the ray 8 at the wavelengths 4 to 75, it has sufficient brightness in the entire visible range. Therefore, the ()
- the result of () can be realized at a higher level.
- the in-type resin can prevent white turbidity due to environmental changes, and as a result can maintain the lightness of the molded product, and is therefore preferred as a molding material for optical parts.
- the scientific part is the gap between the lens ,, and the diffraction element (3).
- the Ming-in type is highly satisfactory in these properties, can prevent clouding due to environmental changes, and as a result can maintain the molding clarity.
- Ming is an in-based material, which is the main gold component of dinoic acid.
- di is a colored body obtained by removing Tevin oil by steam distillation of a tree of the same kind. 9 minutes of gin, abitin Of ((4) 4). Gin means the above-mentioned acid.
- Abitin is a carboxylic acid that belongs to 3 tepene and has a structure represented by the following formula, also known as bin. It is a yellow powder obtained by evaporating fat, steaming with superheated water, or distilling under reduced pressure.
- the dinoic acid used in the present invention is not limited to the one represented by the above-mentioned ( ⁇ ), but the water of abitic acid represented by general (11), the dehydrated abitine represented by general (11), and the general ( ) It may also be abiotic acid.
- the dinoic acid in Myo may be selected from the group consisting of the compounds represented by (1), (), (1) and () above, or may be a mixture of two or more.
- the metal forming the salt with gin is not particularly limited. Physically, it is preferable that the metal is a metal selected from the genus Aka, the genus Aka, and the genus of two elements.
- Examples of aka include titanium, sodium, and chrome. Above all, it is preferable that it is sodium.
- examples of acetic acid include magnesium, um, and strontium. Above all, it is preferable that it is magnesium.
- As the two elements, cadmium, and the like can be given. Above all, it is preferable. It is possible to combine two or more of these alone.
- gold of diacid which is an in-series component of Ming, may be perfect or may be a mixture thereof.
- the term “part” means a metal with gin, and in the case of a compound with a zinc of a diacid, is meant to include a member of only a gold of a diacid that does not contain a diacid of a diacid. .
- the equivalent amount of the carboxylic group to the genus is not particularly limited, and it depends on the kind of metal used, but the equivalent of the carboxylic group of each genus.
- the value of () is preferably 7 or less, more preferably 6 or less.
- the equivalent () of the carb group of um in the zinc salt is preferably 475.
- the equivalent () of the carbonyl group of zinc in the zinc salt is 2.
- Polymers of (a2) tin can be mentioned as such, and polymers of (a3) tin as () can be mentioned as such.
- the cyclic component used as a copolymer is used as a copolymerization component.
- Examples of 005 include acid hydrate, ki, ad, ste and hydr, and examples of the polar unsaturated compound include (meth) ac, in, anhydroin, anhydrous tan, guanidin.
- the in-series (") to (" 4) may be used alone or in combination of two or more. Obviously, polymers of (a2) tin can be preferred.
- the cyclic ring component of impact is used as a copolymerization component.
- the tin type tends to become cloudy when returned to room temperature after being exposed to high temperature and high humidity. Therefore, in particular, a remarkable effect can be obtained particularly when a resin containing a cyclic resin having is used as a copolymerization component.
- the cyclic component used as a copolymer is used as a copolymerization component.
- tin series a copolymer having the following positions may be specifically used:
- O is a repeat position.
- polymer of (a2) which is preferred, it is not particularly limited. Particularly preferred examples include a polymer containing () an in-component having a prime number of 2 to 2 and a cyclic in-component represented by () ().
- ⁇ 8 may be one or different in each return position.
- the number 2 to 2 of the prime number which is the polymerization component of the copolymer of the cyclic ring component and the other copolymerization component such as tin, is not particularly limited.
- tin pine, pent, pentene, xene, 3 methene, 3 meth pentene, 3 meth pentene 4 meth pentene, 4 meth ixene, 4 4 meth ene.
- Examples thereof include xene, kten, decene, decene, tetradecene, xadecene octadecene, and ene. You can use either one of these tines or two or more at the same time. Of these, tin is most preferred.
- the cyclic component represented by general formula (), which is a polymerization component of a copolymer of the clearly preferable cyclic component and another copolymerization component such as tin, will be explained.
- ⁇ 2 in 006 (), which may be one or different, is selected from the group consisting of a hydrogen atom, a gen, and a group.
- Examples of the body of 0067 R to 8 include hydrogen atom, chlorine, gent, thio, puppy, and achi, which may or may not be different from each other. Yes, all parts may be the same.
- Examples of the case where 006 R and R together form a divalent carbon include, for example, tidene, propylene, and isopidine akiden.
- the formed ring may be a single ring or a polycycle, or a bridged polycycle, or a double bond. It may be a ring or a combination of these rings. Also, these rings may have meth- yl.
- the four ring rings of the four-element pentady can be mentioned.
- a method of combining an infinitesimal number 2 to 2 with a cyclic inn represented by () () and the polymer to be used are not particularly limited. You can Random polymerization or clock polymerization is preferable, and random polymerization is preferable.
- the polymerization used is not particularly limited. It can be obtained by the method of knowledge using the knowledge of data type and metacene type.
- Clearly preferred polymers of cyclic tinines are preferably produced using the methacene system. 007 (the polymerization component
- Polymers of (a2) tin which are particularly preferred for the halo, have the other objectives other than the ring of the () prime number 2 to 2 and the () (). If necessary, other copolymerizable unsaturated monomer component may be contained as long as it does not impair the property.
- the unsaturated monomer which may be copolymerized by any means is not particularly limited, and examples thereof include a dimer having a carbon atom in the molecule. Go up in the child 2
- Examples of the body of the mer include 4 xazazine, 6 octazine 2 meth 5 xazin 4 meth 5 xazin 5 meth 5 xysazine 6 meth ⁇ 5 din 7 meth ⁇ 6 Nk Penzin, Methyl Tetraindene 5 2 Bonn, 5 Den 2 Bonn, 5 Chin 2 Bonn, 5 Soppiden 2 Bonnen, 6 Kumetchi 5 Soppe 2 Bonen, 4 9 5 8 Methano 3a RR ga Octadeno Benzoindene and other ring dins 2 3 sop pidene 5 bonne 2 den 3 sop pidene 5 bonne 2 ppe 22 2 bonazine and the like.
- 4 xazin and 6 octazin are preferred, especially ninc penne 5 den 2 bonne, 52 bonne 5 tin 2 bonne, 4 xazin and 6 octazine.
- Aluminium which is used for Ming-in, is the gold main component of Ming-dying It is an in-kind.
- the amount of the 008-in series is preferably ⁇ 5 lower, more preferably ⁇ 3 lower, and particularly preferably ⁇ 32 lower than the in-system.
- thermoplastic resins thermoplastic lasts, and various kinds of compounding agents may be added to the clear tin system as long as the properties are not impaired.
- thermoplastics include, for example, ponds, ponts, pohsphones, posons, pobonnets, poacetas, etc., as well as vos, postels, poto, pointons.
- Post-type composites such as tattoos, point tints, etc.
- Poin-type composites such as potin, pop-pin, po 4 methylpentene etc.
- Ad-types such as six, nine 66, nine, etc. Examples include coalesced polymer, point actin (S), and postin.
- the plastic last includes, for example, tin-based, tin-based, stainless-based, ad-based, and utan-based plastic lasts. Among them, it can be preferably used because of its high compatibility with the tin-type last tin and the ring-type tin.
- the olefinic lasts include a timpin polymer, a timpin polymer, a tintene polymer, and a tin octene polymer.
- Examples of the body of the tin-based raster include a tin-tin stick polymer, a stippin-stick polymer, and the like. 008 (mixture
- thermoplastic if it is usually used as a thermoplastic, For example, ultraviolet rays, light, plastics, lubricants, electrification, difficulty, chemicals, near infrared rays, and fluorescence.
- the mixture of can be mentioned.
- the Ming-In system which is not particularly limited, can be adopted.
- it is a
- Examples thereof include a resin based on tin, or a resin to be optionally mixed, and a method of melting all at once or sequentially.
- a method of doing this for example, after drying, a method of using a twin-screw extruder, mixer, or various types of machines can be mentioned. In some cases,
- the resin of the tin type and the resin to be mixed are melted, it is generally carried out in the range of 6 C to C, preferably 8 C to 3 C.
- Molding from light-colored tin-based materials preferably rays at 5 to when set in 2.
- the Iz value was measured according to JS 736 using Izmeta (, product name Izgad Gong).
- the Iz value was measured after molding, after exposure to a temperature of 7 C 95 6 and then at a temperature of 23 C and a humidity of 5 ⁇ 5.
- the difference between the Is after the boundary change and the Is after the molding was set as the Iz. If the molding is used, if the molding is used as an optical component, the light ray will be reduced, which may hinder its performance. For this reason, I hope it is Is.
- a resin for resin which has the following structure (OPS da ced Poe, product name OP () 63), a resin containing zinc (commercial name 5, product For each of the one with the addition of the base (475) and the one without the addition (addition), melting and peening were carried out at 25 C using a twin-screw (main steelmaking, trade name X3). 5.
- an injection molding machine (machine, trade name S 75) was used to mold a plate of 7 X7 X2 into a die of 28 C and a mold of 2 C to obtain a test.
- O is a repeat position.
- Zinc manufactured by Kabushiki Kaisha, which is the carb group of um
- the value was obtained by the same method as the implementation, and the value was calculated as in the implementation. The results are shown in the table.
- Zincium manufactured by Kabushiki Kaisha, which is the carboxylic acid group of the calcium group
- a method similar to the implementation was used to obtain the value as in the implementation. The results are shown in the table.
- Gin product name, 85
- the characteristics of moldings made of tin-based materials can be maintained, white turbidity due to environmental changes can be prevented, and transparency can be maintained.
- it is preferable for use in clear tin systems such as optical applications, medical applications, packaging applications, electrical / product applications, and industrial / industrial parts applications. You can Above all, it can be favored as an optical application in which transparency is an important requirement, for example, a light source such as a fnds-up lens and a material for a diffractive element.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Combustion & Propulsion (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polarising Elements (AREA)
- Diffracting Gratings Or Hologram Optical Elements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007549035A JP5216326B2 (ja) | 2005-12-06 | 2006-10-30 | 非晶性環状オレフィン系樹脂用曇り防止剤、樹脂組成物、及び光学部品 |
EP06812179A EP1972657A4 (en) | 2005-12-06 | 2006-10-30 | ANTIFRANCING AGENT FOR NON-CRYSTALLINE CYCLOOLEFIN RESINS, RESIN COMPOSITIONS AND OPTICAL ELEMENTS |
KR1020087015299A KR101108666B1 (ko) | 2005-12-06 | 2006-10-30 | 비결정성 환상올레핀계 수지용 흐림 방지제, 수지 조성물,및 광학부품 |
CN2006800454309A CN101321827B (zh) | 2005-12-06 | 2006-10-30 | 维持成形体的透明性的方法、非晶性环状烯烃系树脂组合物以及光学材料、光学部件 |
US12/096,158 US8063127B2 (en) | 2005-12-06 | 2006-10-30 | Antihazing agent for noncrystalline cycloolefin resins, resin compositions, and optical elements |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005-352202 | 2005-12-06 | ||
JP2005352202 | 2005-12-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007066455A1 true WO2007066455A1 (ja) | 2007-06-14 |
Family
ID=38122606
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2006/321670 WO2007066455A1 (ja) | 2005-12-06 | 2006-10-30 | 非晶性環状オレフィン系樹脂用曇り防止剤、樹脂組成物、及び光学部品 |
Country Status (7)
Country | Link |
---|---|
US (1) | US8063127B2 (ja) |
EP (1) | EP1972657A4 (ja) |
JP (1) | JP5216326B2 (ja) |
KR (1) | KR101108666B1 (ja) |
CN (1) | CN101321827B (ja) |
TW (1) | TWI400326B (ja) |
WO (1) | WO2007066455A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009110296A1 (ja) * | 2008-03-05 | 2009-09-11 | ポリプラスチックス株式会社 | 透明樹脂組成物 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09176398A (ja) * | 1995-12-22 | 1997-07-08 | Mitsui Petrochem Ind Ltd | 環状オレフィン系樹脂組成物およびその用途 |
JPH09176396A (ja) * | 1995-12-22 | 1997-07-08 | Mitsui Petrochem Ind Ltd | 環状オレフィン系樹脂組成物およびその用途 |
JP2001026682A (ja) * | 1998-11-19 | 2001-01-30 | Mitsui Chemicals Inc | ポリオレフィン系樹脂組成物およびそれから得られる成形体 |
JP2001026718A (ja) * | 1999-03-04 | 2001-01-30 | Mitsui Chemicals Inc | 熱可塑性樹脂組成物およびその用途 |
JP2001098892A (ja) * | 1999-10-01 | 2001-04-10 | Nishimatsu Constr Co Ltd | スクリュウ式排土装置における排土量計測装置 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1231861A (ja) | 1968-04-03 | 1971-05-12 | ||
US4127546A (en) * | 1977-11-29 | 1978-11-28 | Exxon Research & Engineering Company | Plasticization of neutralized sulfonated elastomers with rosin salts |
JPH04266950A (ja) * | 1991-02-22 | 1992-09-22 | Toray Ind Inc | 非晶ポリオレフィンフィルム |
MY112911A (en) * | 1994-06-09 | 2001-10-31 | Arakawa Chem Ind | Process for crystal nucleation of crystalline thermoplastic resin and crystalline thermoplastic resin composition |
JP3341954B2 (ja) * | 1994-09-26 | 2002-11-05 | 三井化学株式会社 | 樹脂組成物 |
DE19519579C2 (de) * | 1995-05-29 | 1997-03-20 | Hoechst Ag | Amorphe, transparente Platte aus einem kristallisierbaren Thermoplast |
JPH09183872A (ja) | 1995-12-28 | 1997-07-15 | Mitsui Petrochem Ind Ltd | キャストフィルム用および押出シート用エチレン系共重合体組成物ならびにこの組成物からなるキャストフィルムおよび押出シート |
ATE264371T1 (de) * | 1996-08-08 | 2004-04-15 | New Japan Chem Co Ltd | Molekularer kristall auf kolophonium-basis, nukleierungsmittel für polyolefinharz, polyolefinharzzusammensetzung sowie formmassen daraus |
CN1213391A (zh) | 1996-11-22 | 1999-04-07 | 三井化学株式会社 | 热塑性树脂组合物和含该组合物的薄膜 |
JPH10279739A (ja) * | 1997-04-08 | 1998-10-20 | New Japan Chem Co Ltd | ポリオレフィン樹脂用核剤組成物並びにポリオレフィン樹脂組成物 |
JPH11315221A (ja) * | 1998-05-06 | 1999-11-16 | Mitsui Chem Inc | 無機充填剤および該無機充填剤が配合された樹脂組成物 |
JP2000198892A (ja) | 1998-10-27 | 2000-07-18 | Mitsui Chemicals Inc | 非晶性α―オレフィン系共重合体組成物およびその用途 |
EP1582533B1 (en) * | 1999-06-17 | 2007-10-10 | Mitsui Chemicals, Inc. | Ethylene (co)polymer and its use |
US6387317B1 (en) | 2000-01-20 | 2002-05-14 | Aristech Chemical Corporation | Process for manufacturing clear shaped articles from polyolefin compositions |
CN100516120C (zh) * | 2000-01-21 | 2009-07-22 | 三井化学株式会社 | 烯烃嵌段共聚物,其制备方法和用途 |
US7160949B2 (en) | 2000-01-21 | 2007-01-09 | Mitsui Chemicals, Inc. | Olefin block copolymers, processes for producing the same and uses thereof |
KR100937175B1 (ko) | 2000-01-26 | 2010-01-19 | 미쓰이 가가쿠 가부시키가이샤 | 올레핀 중합체 |
JP2001221915A (ja) * | 2000-02-07 | 2001-08-17 | Kanegafuchi Chem Ind Co Ltd | 光学フィルム並びにそれよりなる偏光子保護フィルムおよび偏光板 |
JP2001264971A (ja) * | 2000-03-14 | 2001-09-28 | Hitachi Chem Co Ltd | 感光性エレメント、これを用いたレジストパターンの製造法及びプリント配線板の製造法 |
CA2377411A1 (en) * | 2000-04-21 | 2001-11-01 | Kaneka Corporation | Amorphous polyolefin resin composition |
SG102636A1 (en) * | 2000-09-07 | 2004-03-26 | Mitsui Chemicals Inc | Polar group-containing olefin copolymer, process for preparing the same, thermoplatic resin composition containing the copolymer, and uses thereof |
KR100426123B1 (ko) * | 2001-07-04 | 2004-04-08 | 주식회사 엘지화학 | 내후성 열가소성 수지의 제조방법 |
JP3847599B2 (ja) | 2001-10-22 | 2006-11-22 | ポリプラスチックス株式会社 | 耐衝撃性環状オレフィン系樹脂組成物及び成形品 |
-
2006
- 2006-10-30 KR KR1020087015299A patent/KR101108666B1/ko not_active IP Right Cessation
- 2006-10-30 EP EP06812179A patent/EP1972657A4/en not_active Withdrawn
- 2006-10-30 CN CN2006800454309A patent/CN101321827B/zh not_active Expired - Fee Related
- 2006-10-30 JP JP2007549035A patent/JP5216326B2/ja active Active
- 2006-10-30 US US12/096,158 patent/US8063127B2/en not_active Expired - Fee Related
- 2006-10-30 WO PCT/JP2006/321670 patent/WO2007066455A1/ja active Application Filing
- 2006-11-03 TW TW95140690A patent/TWI400326B/zh not_active IP Right Cessation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09176398A (ja) * | 1995-12-22 | 1997-07-08 | Mitsui Petrochem Ind Ltd | 環状オレフィン系樹脂組成物およびその用途 |
JPH09176396A (ja) * | 1995-12-22 | 1997-07-08 | Mitsui Petrochem Ind Ltd | 環状オレフィン系樹脂組成物およびその用途 |
JP2001026682A (ja) * | 1998-11-19 | 2001-01-30 | Mitsui Chemicals Inc | ポリオレフィン系樹脂組成物およびそれから得られる成形体 |
JP2001026718A (ja) * | 1999-03-04 | 2001-01-30 | Mitsui Chemicals Inc | 熱可塑性樹脂組成物およびその用途 |
JP2001098892A (ja) * | 1999-10-01 | 2001-04-10 | Nishimatsu Constr Co Ltd | スクリュウ式排土装置における排土量計測装置 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1972657A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009110296A1 (ja) * | 2008-03-05 | 2009-09-11 | ポリプラスチックス株式会社 | 透明樹脂組成物 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2007066455A1 (ja) | 2009-05-14 |
KR20080077227A (ko) | 2008-08-21 |
TW200728441A (en) | 2007-08-01 |
CN101321827A (zh) | 2008-12-10 |
JP5216326B2 (ja) | 2013-06-19 |
KR101108666B1 (ko) | 2012-01-25 |
TWI400326B (zh) | 2013-07-01 |
US8063127B2 (en) | 2011-11-22 |
EP1972657A1 (en) | 2008-09-24 |
CN101321827B (zh) | 2012-05-23 |
US20090018236A1 (en) | 2009-01-15 |
EP1972657A4 (en) | 2009-04-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Auras et al. | An overview of polylactides as packaging materials | |
US8609770B2 (en) | Polyesters modified by a combination of ionomer and organic acid salts | |
GB2489103A (en) | Bio-resins | |
ATE527315T1 (de) | Verfahren zur herstellung von transparenten formkörpern | |
WO2007001551A8 (en) | Transparent polymer blends containing polyesters comprising a cyclobutanediol and articles prepared therefrom | |
KR102194850B1 (ko) | 폴리락틱산, 폴리부틸렌아디페이트-코-부틸렌테레프탈레이트 및 폴리에틸렌옥사이드를 포함하는 생분해성 수지 조성물 | |
TW200619316A (en) | Light-reflecting sheets and molding products thereof | |
WO2006051640A1 (ja) | 難燃性生分解性ポリエステル樹脂組成物、その製造方法、及びそれより得られる成形体 | |
WO2007066455A1 (ja) | 非晶性環状オレフィン系樹脂用曇り防止剤、樹脂組成物、及び光学部品 | |
CN114316426A (zh) | 一种高模量高耐热透明聚丙烯组合物及其制备方法 | |
KR20090041974A (ko) | 색상이 우수한 고투명성 1,4-사이클로헥산디메탄올 공중합폴리에스테르 수지 및 그 제조방법 | |
Ahmad et al. | Properties enhancement of packaging materials based on gelatin | |
US20220186021A1 (en) | Blends of copolyesters having recycled content and high heat resistance | |
ES2745033T3 (es) | Composición adhesiva y método | |
JP2007092026A (ja) | 乳酸系ポリマーを含有する乳酸系樹脂組成物からなる、透明で耐熱性を有する成形体 | |
EP2634216B1 (en) | Polyester/polycarbonate blend having excellent thermal stability and color stability | |
KR102191338B1 (ko) | 생분해성 및 가공성이 향상된 친환경 조성물 및 이의 제조방법 | |
JPH0711109A (ja) | ポリエーテル単位を有する熱可塑性エラストマー | |
TW201910424A (zh) | 透明具耐衝擊性聚酯組成物 | |
JP2001040228A (ja) | 熱可塑性樹脂組成物 | |
JP2021191845A (ja) | 生分解性樹脂組成物及び生分解性樹脂成形体 | |
JP2012211233A (ja) | 樹脂組成物及び該樹脂組成物からなる成形体 | |
JP2019189770A (ja) | ポリスチレン系樹脂組成物、シート、及び成形品 | |
JPH07216149A (ja) | 新規相溶化剤及び熱可塑性樹脂組成物 | |
BR9407240A (pt) | Processo para a preparação de uma mistura polimérica contendo ácido |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200680045430.9 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2007549035 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006812179 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087015299 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12096158 Country of ref document: US |