TW201529317A - Multilayer stretch film - Google Patents
Multilayer stretch film Download PDFInfo
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- TW201529317A TW201529317A TW103143683A TW103143683A TW201529317A TW 201529317 A TW201529317 A TW 201529317A TW 103143683 A TW103143683 A TW 103143683A TW 103143683 A TW103143683 A TW 103143683A TW 201529317 A TW201529317 A TW 201529317A
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- 229920006302 stretch film Polymers 0.000 title claims description 7
- 229920001225 polyester resin Polymers 0.000 claims abstract description 37
- 239000004645 polyester resin Substances 0.000 claims abstract description 37
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 22
- KKEYFWRCBNTPAC-UHFFFAOYSA-N benzene-dicarboxylic acid Natural products OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000002253 acid Substances 0.000 claims abstract description 17
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- -1 terephthalic acid compound Chemical class 0.000 claims abstract description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 12
- 150000002009 diols Chemical class 0.000 claims abstract description 7
- RYRZSXJVEILFRR-UHFFFAOYSA-N 2,3-dimethylterephthalic acid Chemical compound CC1=C(C)C(C(O)=O)=CC=C1C(O)=O RYRZSXJVEILFRR-UHFFFAOYSA-N 0.000 claims description 8
- 238000001228 spectrum Methods 0.000 claims description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 230000003595 spectral effect Effects 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- QCOQPIQNJUDTHP-UHFFFAOYSA-N CCCC(CC(CO)(CO)CO)C(=O)O Chemical compound CCCC(CC(CO)(CO)CO)C(=O)O QCOQPIQNJUDTHP-UHFFFAOYSA-N 0.000 claims 2
- WVIXZABEBJKKSI-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 4-phenylpentanoate Chemical compound C1(=CC=CC=C1)C(CCC(=O)OCC(CO)(CO)CO)C WVIXZABEBJKKSI-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 107
- 239000010408 film Substances 0.000 description 59
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 10
- 239000005001 laminate film Substances 0.000 description 10
- 238000006068 polycondensation reaction Methods 0.000 description 10
- 238000005809 transesterification reaction Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229910000420 cerium oxide Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 229940071125 manganese acetate Drugs 0.000 description 5
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 5
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 230000010287 polarization Effects 0.000 description 4
- 239000011241 protective layer Substances 0.000 description 4
- 150000003504 terephthalic acids Chemical class 0.000 description 4
- 239000003086 colorant Substances 0.000 description 3
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- XCSGHNKDXGYELG-UHFFFAOYSA-N 2-phenoxyethoxybenzene Chemical compound C=1C=CC=CC=1OCCOC1=CC=CC=C1 XCSGHNKDXGYELG-UHFFFAOYSA-N 0.000 description 1
- DQXLIDTWKIXFQD-UHFFFAOYSA-N 5,7-dimethylnaphthalene-1,6-dicarboxylic acid Chemical compound C1=CC=C2C(C)=C(C(O)=O)C(C)=CC2=C1C(O)=O DQXLIDTWKIXFQD-UHFFFAOYSA-N 0.000 description 1
- 239000004358 Butane-1, 3-diol Substances 0.000 description 1
- WWVJXWNDFJXHHR-UHFFFAOYSA-N CC(CCC(=O)OCCCCO)C1=CC=CC=C1 Chemical compound CC(CCC(=O)OCCCCO)C1=CC=CC=C1 WWVJXWNDFJXHHR-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004146 Propane-1,2-diol Substances 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- VVSFUPBJVHRTPB-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] pentanoate Chemical compound CCCCC(=O)OCC(CO)(CO)CO VVSFUPBJVHRTPB-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- OOMGJVYAAJCVCH-UHFFFAOYSA-N amino(carboxy)carbamic acid Chemical compound OC(=O)N(N)C(O)=O OOMGJVYAAJCVCH-UHFFFAOYSA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000005250 beta ray Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- JSPXPZKDILSYNN-UHFFFAOYSA-N but-1-yne-1,4-diol Chemical compound OCCC#CO JSPXPZKDILSYNN-UHFFFAOYSA-N 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- SAMYCKUDTNLASP-UHFFFAOYSA-N hexane-2,2-diol Chemical compound CCCCC(C)(O)O SAMYCKUDTNLASP-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/02—Physical, chemical or physicochemical properties
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
- G02B5/3041—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
- G02B5/305—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/418—Refractive
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Laminated Bodies (AREA)
- Polarising Elements (AREA)
Abstract
揭露一種多層拉伸膜,其包含250至1,000個交替層之(1)一第一層,其包含一第一聚酯樹脂,其係自作為酸組份之一二羧酸,及作為醇組份之一二醇及具有3或更多個羥基基團之一多羥基醇所製備;及(2)一第二層,其包含一第二聚酯樹脂,其係自作為酸組份之(i)一二羧酸及(ii)不同於此二羧酸之一對苯二甲酸化合物或對苯二甲酸的一形成酯的衍生物,及作為醇組份之(i)一二醇及(ii)具有3或更多個羥基基團之一多羥基醇所製備,此膜係藉由於單一方向(x-方向)拉伸而定向,其中,於此定向(x-方向),第一層之折射率係大於第二層之折射率,且此等第一層及此等第二層之厚度係連續改變,使得每一層之最大厚度係每一層之最小厚度之1.2至1.5倍。此多層拉伸膜可使於一特定波長範圍之光選擇性反射及/或偏光,且於每一區域產生均勻亮度,因此,可作為用於一LCD之一反射偏光模。 Disclosed is a multilayer stretched film comprising (1) a first layer of 250 to 1,000 alternating layers, comprising a first polyester resin derived from a dicarboxylic acid as an acid component, and as an alcohol group a diol and a polyhydric alcohol having one or more hydroxyl groups; and (2) a second layer comprising a second polyester resin which is derived from the acid component ( i) a dicarboxylic acid and (ii) an ester-forming derivative of a terephthalic acid compound or terephthalic acid different from the dicarboxylic acid, and (i) a diol and (as an alcohol component) Ii) prepared with a polyhydric alcohol having one or more hydroxyl groups oriented by stretching in a single direction (x-direction), wherein the orientation (x-direction), the first layer The refractive index is greater than the refractive index of the second layer, and the thicknesses of the first layer and the second layers are continuously varied such that the maximum thickness of each layer is 1.2 to 1.5 times the minimum thickness of each layer. The multilayer stretched film selectively reflects and/or polarizes light in a specific wavelength range and produces uniform brightness in each region, and thus can be used as a reflective polarizing mode for one LCD.
Description
本發明係有關於一種多層拉伸膜,且更特別地,係一種多層拉伸膜,其能選擇性地反射或偏光於一特定波長範圍之光,且提供於此膜之每一區域上入射之光均勻發光。 The present invention relates to a multilayer stretched film, and more particularly to a multilayer stretched film that selectively reflects or polarizes light in a particular wavelength range and provides incident on each of the regions of the film. The light is evenly illuminated.
一液晶顯示器(LCD)係今日最廣泛使用之平板顯示器之一。一般,一LCD係使用液晶調光性質之一顯示裝置。於一LCD,一電場施加至具有一特定分子排列之液晶而改變其分子排列。分子排列改變造成液晶之諸如雙折射性、光學活性、二色性,及光散射性質之光學性質改變,此等轉化成視覺改變。 A liquid crystal display (LCD) is one of the most widely used flat panel displays today. Generally, an LCD system uses a display device of one of liquid crystal dimming properties. In an LCD, an electric field is applied to a liquid crystal having a specific molecular arrangement to change its molecular arrangement. The change in molecular alignment causes changes in the optical properties of liquid crystals such as birefringence, optical activity, dichroism, and light scattering properties, which translate into visual changes.
因為一LCD缺乏其本身光源,其需要一背光單元,其係自LCD之後側照射整個顯示裝置。 Since an LCD lacks its own light source, it requires a backlight unit that illuminates the entire display device from the rear side of the LCD.
一LCD不能使由其背光單元產生之光完全滲透。因此,一面板之亮度係重要。各種膜已被用以改良一面板之亮度。一典型例示係一反射性偏光膜。 An LCD cannot completely penetrate the light generated by its backlight unit. Therefore, the brightness of a panel is important. Various films have been used to improve the brightness of a panel. A typical example is a reflective polarizing film.
包含多數個交替式層合之具高折射率及低折射率的層之一膜造成光學干涉,由於此等層間之干涉,選擇性地反射或透射具有一特定波長範圍之光。已知於相鄰層之厚度逐漸改變時,具有一足夠數量-例如,數十或數百(或甚至更多)-之此等交替層合的層之一膜會改良於一期望波長範圍之光的反射及/或偏光性質。 A film comprising a plurality of alternating layers of high refractive index and low refractive index causes optical interference, selectively reflecting or transmitting light having a specific wavelength range due to interference between the layers. It is known that when the thickness of an adjacent layer is gradually changed, a film having a sufficient number - for example, tens or hundreds (or even more) - of these alternately laminated layers is modified to a desired wavelength range. The reflection and/or polarization properties of light.
有關於此之光學原理已揭露於,例如,Vasicek,Optics of Thin Film(1960),第100至139頁及與69及70頁。 Optical principles relating to this have been disclosed, for example, in Vasicek, Optics of Thin Film (1960), pages 100 to 139 and pages 69 and 70.
含有二種具有不同折射率之層的一多層膜可依據此二種層之折射率差式、此等層之厚度,及層合之層的數量而反射於一特定波長範圍之光。反射光線之波長係以下列方程式表示。 A multilayer film comprising two layers having different refractive indices can be reflected by light of a particular wavelength range depending on the refractive index difference of the two layers, the thickness of the layers, and the number of layers laminated. The wavelength of the reflected light is expressed by the following equation.
[方程式1]λm=(2/m)(N1D1+N2D2) [Equation 1] λm=(2/m)(N 1 D 1 +N 2 D 2 )
於方程式1,λ係波長(nm),m係反射級,N1及N2係個別層之折射率,且D1及D2係個別層之厚度(nm)。 In Equation 1, the λ-based wavelength (nm), the m-based reflection level, the refractive indices of the individual layers of N 1 and N 2 are, and D 1 and D 2 are the thicknesses (nm) of the individual layers.
為了此目的,聚乙烯-2,6-萘二羧酸酯(“2,6-PEN”)通常被用於具有較高折射率之一層(見,例如,韓國專利早期公開公告第1997-0700585號案及PCT公告第WO95/17303號案)。當一2,6-PEN膜被單軸拉伸,拉伸方向(即,x-方向)之折射率會增加。另一方面,膜表面上與拉伸方向垂直之方法(即,y-方向)之折射率幾乎不受影響,且膜之厚度方向(即,z-方向)的折射率會顯著降低。 For this purpose, polyethylene-2,6-naphthalenedicarboxylate ("2,6-PEN") is generally used for one layer having a higher refractive index (see, for example, Korean Patent Laid-Open Publication No. 1997-0700585) No. and PCT Announcement No. WO95/17303). When a 2,6-PEN film is uniaxially stretched, the refractive index in the stretching direction (i.e., the x-direction) increases. On the other hand, the refractive index of the film perpendicular to the stretching direction (i.e., the y-direction) is hardly affected, and the refractive index of the film in the thickness direction (i.e., the z-direction) is remarkably lowered.
因此,當一反射膜被製備用於反射於拉伸方向 (即,x-方向)之偏光及透射與拉伸方向垂直之方向(即,y-方向)之偏光,由於因為此膜之厚度方向(z-方法)之大的折射率差異造成於一傾斜方向入射之光線部份反射,用於改良拉伸方向之偏光性質的拉伸比率增加會造成此膜之每一區域的不規則亮度及顏色變化。 Therefore, when a reflective film is prepared for reflection in the direction of stretching (ie, x-direction) polarized light and polarized light transmitted in a direction perpendicular to the direction of stretching (ie, y-direction) due to a large difference in refractive index due to the thickness direction of the film (z-method) Partial reflection of light incident in the direction, an increase in the stretching ratio for improving the polarization property of the stretching direction causes irregular brightness and color change in each region of the film.
因此,需要能提供均勻亮度且對於每一區域之入射光無亮度惡化及顏色改變之一種多層拉伸膜。 Accordingly, there is a need for a multilayer stretch film that provides uniform brightness and no brightness degradation and color change for incident light in each region.
因此,本發明之一目的係提供一種多層拉伸膜,其具有優異光學性質且能使一特定波長範圍之光選擇性反射及/或偏光,且能提供均勻亮度,且對於每一區之入射光無亮度惡化及顏色改變。 Accordingly, it is an object of the present invention to provide a multilayer stretched film which has excellent optical properties and which enables selective reflection and/or polarization of light in a specific wavelength range, and which provides uniform brightness and incidence for each region. The light has no brightness deterioration and color change.
依據本發明之一方面,提供一種多層膜,其係於X-方向單軸拉伸,此膜包含250至1,000層,其中,一第一層及一第二層係交替地層合,(1)此第一層包含一第一聚酯樹脂,其係自作為酸組份之一二羧酸,及作為醇組份之一二醇及具有3或更多個羥基基團之一多羥基醇所製備;及(2)此第二層包含一第二聚酯樹脂,其係自作為酸組份之(i)一二羧酸及(ii)不同於此二羧酸之一對苯二甲酸化合物或對苯二甲酸的一形成酯的衍生物,及作為醇組份之(i)一二醇及(ii)具有3或更多個羥基基團之一多羥基醇所製備,其中,於x-方向,第一層之折射率係大於第二層之折射率;且此等第一層及此等第二層之厚度係連續改變,使得第一層之 最大厚度係第一層之最小厚度之1.2至1.5倍,且第二層之最大厚度係第二層之最小厚度之1.2至1.5倍。 According to an aspect of the invention, there is provided a multilayer film which is uniaxially stretched in the X-direction, the film comprising 250 to 1,000 layers, wherein a first layer and a second layer are alternately laminated, (1) The first layer comprises a first polyester resin derived from a dicarboxylic acid as one of the acid components, and a diol as one of the alcohol components and a polyhydric alcohol having one or more hydroxyl groups. Preparation; and (2) the second layer comprises a second polyester resin derived from the (i) dicarboxylic acid as the acid component and (ii) the terephthalic acid compound different from the dicarboxylic acid Or an ester-forming derivative of terephthalic acid, and (i) a monodiol as the alcohol component and (ii) a polyhydric alcohol having one or more hydroxyl groups, wherein x - direction, the refractive index of the first layer is greater than the refractive index of the second layer; and the thicknesses of the first layer and the second layers are continuously changed such that the first layer The maximum thickness is 1.2 to 1.5 times the minimum thickness of the first layer, and the maximum thickness of the second layer is 1.2 to 1.5 times the minimum thickness of the second layer.
依據本發明之多層拉伸膜可使一特定波長範圍之光選擇性反射及/或偏光,且於每一區域提供均勻亮度。因此,其可被作為用於一LCD之一反射偏光膜。 The multilayer stretched film in accordance with the present invention selectively reflects and/or polarizes light in a particular wavelength range and provides uniform brightness in each region. Therefore, it can be used as a reflective polarizing film for one of the LCDs.
本發明之一多層拉伸膜係藉由交替層合一第一層及一第二層而形成。然後,此膜於x-方向單軸拉伸。 A multilayer stretched film of the present invention is formed by alternately laminating a first layer and a second layer. The film is then uniaxially stretched in the x-direction.
第一層及第二層係交替層合形成一層合物膜,其可具有250至1,000層,較佳係300至500層。 The first layer and the second layer are alternately laminated to form a laminate film which may have from 250 to 1,000 layers, preferably from 300 to 500 layers.
於本發明之多層拉伸膜,第一層包含一聚酯樹脂,其折射率於拉伸時改變,且第二層包含一聚酯樹脂,其折射率於拉伸時幾乎不改變。當第一層於x-方向單軸拉伸,其於x-方向會具有較高反射率。第一層與第二層之折射率差異造成光學干涉,此賦予拉伸膜選擇性反射或透射於一特定波長範圍之光的光學性質。 In the multilayer stretched film of the present invention, the first layer comprises a polyester resin whose refractive index is changed upon stretching, and the second layer comprises a polyester resin whose refractive index hardly changes upon stretching. When the first layer is uniaxially stretched in the x-direction, it will have a higher reflectance in the x-direction. The difference in refractive index between the first layer and the second layer causes optical interference which imparts optical properties to the stretched film that selectively reflects or transmits light of a particular wavelength range.
相反地,膜不具有以與此膜上之拉伸方向垂直之方向(即,y-方向)反射光的能力,因為於第一層與第二層之折射率無實質上差異。因此,膜會具有僅以一特同方向反射光之偏光性質。 Conversely, the film does not have the ability to reflect light in a direction perpendicular to the direction of stretching on the film (i.e., the y-direction) because there is no substantial difference in refractive index between the first layer and the second layer. Therefore, the film will have a polarizing property that reflects light in only one specific direction.
此膜於x-方向可拉伸3至7倍,較佳係4至6倍。 The film can be stretched 3 to 7 times, preferably 4 to 6 times in the x-direction.
可歸因於拉伸之第一層與第二層於x-方向的折射率差異範圍可為從0.1至0.5,較佳係0.2至0.4。若折射率差異落於該範圍內,膜之反射性質會有效地改良。 The difference in refractive index of the first layer and the second layer attributable to stretching in the x-direction may range from 0.1 to 0.5, preferably from 0.2 to 0.4. If the refractive index difference falls within this range, the reflective properties of the film are effectively improved.
第一層與第二層於y及z方向之每一折射率差異可為0.05或更少,較佳係0.04或更少,更佳係0.03或更少。若於y及z方向之折射率差異係0.05或更少,當光以一傾斜方向入射時,顏色改變可被避免。 The difference in refractive index of each of the first layer and the second layer in the y and z directions may be 0.05 or less, preferably 0.04 or less, more preferably 0.03 or less. If the difference in refractive index in the y and z directions is 0.05 or less, color change can be avoided when light is incident in an oblique direction.
第一層及第二層之厚度連續地改變,使得個別之第一及第二層之最大厚度係個別第一及第二層之最小厚度之1.2至1.5倍。 The thicknesses of the first layer and the second layer are continuously varied such that the maximum thickness of the individual first and second layers is 1.2 to 1.5 times the minimum thickness of the individual first and second layers.
若一多層拉伸膜係藉由,例如,使總數145之第一層及總數146之第二層交替層合而形成,個別之第一及第二層之最小厚度係指個別之第一及第二第二層的任何者之最小厚度,且個別之第一及第二層之最大厚度係指個別之第一及第二層之任何者的最大厚度。 If a multilayer stretched film is formed by, for example, alternately laminating a first layer of a total of 145 and a second layer of a total of 146, the minimum thickness of the first and second layers individually refers to the first of the individual layers. And the minimum thickness of any of the second and second layers, and the maximum thickness of the respective first and second layers refers to the maximum thickness of any of the individual first and second layers.
包含每一者具有一固定厚度之第一層及第二層之一多層拉伸膜反射具有一特定波長之光,而以具有不同厚度之第一層及第二層層合之一多層拉伸膜能反射於一廣範圍波長之光。第一層及第二層之厚度可連續地或以一逐步方式改變。較佳地,厚度可於上述範圍內連續地改變,使得此膜反射可見光波長範圍之光。 a multilayer stretched film comprising a first layer and a second layer each having a fixed thickness reflects light having a specific wavelength, and a first layer and a second layer laminated with different thicknesses The stretched film can reflect light over a wide range of wavelengths. The thickness of the first layer and the second layer may be varied continuously or in a stepwise manner. Preferably, the thickness is continuously varied within the above range such that the film reflects light in the visible wavelength range.
第一層及第二層每一者可具有0.05至0.5μm,較佳係0.05至0.3μm之厚度。厚度被調整使得第一層之平均厚度對第二層之平均厚度的比率較佳係從0.8至1.2。當第一層 及第二層每一者具有落於上述範圍內之厚度,由於此等層間之光學干涉,自其所製備之一膜能選擇性且有效地反射光。若第一層與第二層間之厚度比率超過1.2則並不是較佳,因為此等層間之光學干涉降低,造成此膜降低反射性。可藉由使厚度調整至1.2或更低而限制漏光現象及使偏光度維持於5%或更低。 Each of the first layer and the second layer may have a thickness of 0.05 to 0.5 μm, preferably 0.05 to 0.3 μm. The thickness is adjusted such that the ratio of the average thickness of the first layer to the average thickness of the second layer is preferably from 0.8 to 1.2. When the first layer And the second layer each has a thickness falling within the above range, and due to the optical interference between the layers, a film prepared therefrom can selectively and efficiently reflect light. It is not preferred if the thickness ratio between the first layer and the second layer exceeds 1.2 because the optical interference between the layers is lowered, causing the film to reduce reflectivity. The light leakage phenomenon can be limited and the degree of polarization can be maintained at 5% or lower by adjusting the thickness to 1.2 or lower.
本發明之多層拉伸膜於與膜表面上之x-方向(或y-方向)垂直之方向亦可拉伸1.1至2倍,較佳係1.1至1.6倍。 The multilayer stretched film of the present invention may also be stretched by 1.1 to 2 times, preferably 1.1 to 1.6 times, in a direction perpendicular to the x-direction (or y-direction) on the surface of the film.
實施於y-方向之拉伸以補償於x-方向拉伸造成之於y-方向的減少折射率。此拉伸比率之調整使二相鄰層間之折射率差異於更大拉伸之方向較大,且使二相鄰層間之折射率差異於較少拉伸之方向較小,因此限制透射光之顏色變化。 Stretching in the y-direction is performed to compensate for the reduced refractive index in the y-direction caused by stretching in the x-direction. The adjustment of the stretching ratio is such that the refractive index difference between two adjacent layers is larger in the direction of larger stretching, and the refractive index difference between two adjacent layers is smaller in the direction of less stretching, thus limiting the transmitted light. Color changes.
第一層包含一第一聚酯樹脂,其係自作為一酸組份之一二羧酸,及作為醇組份之一二醇及具有3或更多個羥基基團之一多羥基醇所製備。第二層包含一第二聚酯樹脂,其係自作為酸組份之(i)一二羧酸及(ii)不同於此二羧酸之一對苯二甲酸化合物或對苯二甲酸之一形成酯的衍生物,及作為醇組份之(i)一二醇及(ii)具有3或更多個羥基基團之一多羥基醇所製備。 The first layer comprises a first polyester resin derived from a dicarboxylic acid as one of the acid components, and a diol as one of the alcohol components and a polyhydric alcohol having one or more hydroxyl groups. preparation. The second layer comprises a second polyester resin which is derived from the (i) dicarboxylic acid as the acid component and (ii) one of the terephthalic acid compounds or terephthalic acid different from the dicarboxylic acid. An ester derivative is formed, and (i) a monodiol as the alcohol component and (ii) a polyhydric alcohol having one or more hydroxyl groups.
用於製備第一層及第二層之二羧酸的特別例子包含一芳香族二羧酸,諸如,對苯二甲酸、二甲基對苯二甲酸、異酞酸、二甲基-2,5-萘二羧酸、萘二羧酸、環己烷二羧酸、二苯氧基乙烷二羧酸、二苯基二羧酸、二苯醚二 羧酸、蒽二羧酸、α,β-雙(2-氯苯氧基)乙烷-4,4-二羧酸;一脂族二羧酸,諸如,己二酸、壬二酸、癸二酸、癸烷二羧酸;一環脂族二羧酸,諸如,環己烷二羧酸;及此等之混合物。 Specific examples of the dicarboxylic acid used to prepare the first layer and the second layer include an aromatic dicarboxylic acid such as terephthalic acid, dimethyl terephthalic acid, isophthalic acid, dimethyl-2, 5-naphthalene dicarboxylic acid, naphthalene dicarboxylic acid, cyclohexane dicarboxylic acid, diphenoxyethane dicarboxylic acid, diphenyl dicarboxylic acid, diphenyl ether Carboxylic acid, hydrazine dicarboxylic acid, α,β-bis(2-chlorophenoxy)ethane-4,4-dicarboxylic acid; monoaliphatic dicarboxylic acid, such as adipic acid, sebacic acid, hydrazine Diacid, decane dicarboxylic acid; monocyclic aliphatic dicarboxylic acid, such as cyclohexane dicarboxylic acid; and mixtures thereof.
用於製備第一層及第二層之二醇的特別例子包含乙二醇、丙烷-1,2-二醇、丙烷-1,3-二醇、丁烷-1,3-二醇、丁烷-1,4-二醇、丁炔-1,4-二醇、戊烷-1,5-二醇、新戊二醇、1,4-雙(羥基甲基)環己烷、2-甲基丙烷-1,3-二醇、甲基戊烷二醇、二乙二醇、二乙二醇、四乙二醇、聚乙二醇、二丙二醇、聚丙二醇、二丁二醇,及聚丁二醇。 Specific examples of the diol used to prepare the first layer and the second layer include ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,3-diol, and butyl Alkane-1,4-diol, butyne-1,4-diol, pentane-1,5-diol, neopentyl glycol, 1,4-bis(hydroxymethyl)cyclohexane, 2- Methylpropane-1,3-diol, methylpentanediol, diethylene glycol, diethylene glycol, tetraethylene glycol, polyethylene glycol, dipropylene glycol, polypropylene glycol, dibutyl glycol, and Polybutylene glycol.
用於製備第一層及第二層之具有3或更多個羥基基團之多羥基醇可為選自由三羥甲基丙烷、三聚異氰酸三-2-羥基乙酯、三羥甲基乙烷、季戊四醇、具如下化學式(I)之3-羥基-2,2-雙(羥基甲基)丙基戊酸酯,及具如下化學式(II)之3-羥基-2,2-雙(羥基甲基)丙基4-苯基戊酸酯所組成族群之至少一者:
具化學式(I)之3-羥基-2,2-雙(羥基甲基)丙基戊酸酯化合物可藉由下列反應流程I製備。 The 3-hydroxy-2,2-bis(hydroxymethyl)propylvalerate compound of formula (I) can be prepared by the following Reaction Scheme I.
與二醇相比較,使用具有3或更多個羥基基團之聚羥基醇係藉由增加聚合反應速率而改良聚合反應度,避免惡化,及降低顏色-b值,因此,使第一層及第二層之顏色-b值彼此相似。即,使用具有3或更多個羥基基團之聚羥基醇可減輕可歸因於因第一層及第二層於y-及z-方向之折射率差異而造成之顏色變化的顏色不相配問題。 Compared with a diol, the use of a polyhydric alcohol having 3 or more hydroxyl groups improves the degree of polymerization by increasing the polymerization rate, avoids deterioration, and lowers the color-b value, thereby making the first layer and The color-b values of the second layer are similar to each other. That is, the use of a polyhydroxy alcohol having 3 or more hydroxyl groups can alleviate color mismatch attributable to color change due to refractive index difference between the first layer and the second layer in the y- and z-directions. problem.
於製備第一層及第二層,於每一層,以100重量%之全部酸組份為基準,具有3或更多個羥基基團之聚羥基醇的量可為0.01至0.2重量%,較佳係0.05至0.1重量%。 In preparing the first layer and the second layer, the amount of the polyhydric alcohol having 3 or more hydroxyl groups may be 0.01 to 0.2% by weight based on 100% by weight of all the acid components in each layer. Preferably, it is 0.05 to 0.1% by weight.
為了製備第二聚酯樹脂,不同於二羧酸之一對苯二甲酸化合物或對苯二甲酸之一形成酯的衍生物亦與此二羧酸一起使用。對苯二甲酸之形成酯的衍生物可為二甲基對苯二甲酸。 In order to prepare the second polyester resin, a derivative different from one of the terephthalic acid compound or one of the terephthalic acid forming an ester is also used together with the dicarboxylic acid. The ester-forming derivative of terephthalic acid may be dimethyl terephthalic acid.
用於製備第二層之(i)二羧酸對(ii)不同於此二羧酸之對苯二甲酸化合物或對苯二甲酸之形成酯的衍生物之莫耳比率可為於從30:70至70:30,較佳係40:60至50:50之範圍。若(i)二羧酸及(ii)不同於此二羧酸之對苯二甲酸化合物或對苯二甲酸之形成酯的衍生物以該範圍使用,第二層之結晶化於拉伸本發明之一多層拉伸膜期間可達最小。因此,於拉伸時,膜之任何折射率改變可達最小。換言之,若第 二層之共聚合比率維持於該範圍內,於此膜之單軸或雙軸拉伸時,於較少拉伸方向(或y-方向)或未拉伸方向(或z-方向),第二層之折射率可保持於與第一層(即,具有高折射率之層)者相似之量。 The molar ratio of the (i) dicarboxylic acid to (ii) the terephthalic acid compound or the terephthalic acid ester forming derivative of the second layer for preparing the second layer may be from 30: 70 to 70:30, preferably in the range of 40:60 to 50:50. If (i) a dicarboxylic acid and (ii) a terephthalic acid compound other than the dicarboxylic acid or an ester-forming derivative of terephthalic acid are used in this range, the second layer is crystallized in the stretched invention. One of the layers can be minimized during stretch film stretching. Therefore, any change in the refractive index of the film can be minimized upon stretching. In other words, if the first The copolymerization ratio of the two layers is maintained within this range, and in the uniaxial or biaxial stretching of the film, in the less stretching direction (or y-direction) or the unstretching direction (or z-direction), The refractive index of the second layer can be maintained in an amount similar to that of the first layer (i.e., the layer having a high refractive index).
再者,一保護層可形成於多層拉伸膜之每一最外層上。保護層可包含第一聚酯樹脂或第二聚酯樹脂。以多層拉伸膜之總厚度為基準,保護層之厚度可為10至25%,較佳係13至20%,更佳係15至18%。符合上述厚度範圍之保護膜可避免包含第一層及第二層之層合膜受損。 Further, a protective layer may be formed on each of the outermost layers of the multilayer stretched film. The protective layer may comprise a first polyester resin or a second polyester resin. The protective layer may have a thickness of 10 to 25%, preferably 13 to 20%, more preferably 15 to 18%, based on the total thickness of the multilayer stretched film. The protective film conforming to the above thickness range can prevent the laminated film including the first layer and the second layer from being damaged.
對於本發明之多層拉伸膜,以下述方程式2及3表示之顏色變化值,△x(0°)及△y(0°),可為0.1或更少,較佳係0.09或更少。以下述方程式4及5表示之顏色變化值,△x(60°)及△y(60°),可為0.2或更少,較佳係0.15或更少。若顏色變化值落於該等範圍以外,顏色不相配問題於光以一傾斜方向入射時發生。 With respect to the multilayer stretched film of the present invention, the color change values represented by the following Equations 2 and 3, Δ x (0°) and Δ y (0°), may be 0.1 or less, preferably 0.09 or less. The color change values represented by the following equations 4 and 5, Δ x (60°) and Δ y (60°), may be 0.2 or less, preferably 0.15 or less. If the color change value falls outside of these ranges, the color mismatch problem occurs when light is incident in an oblique direction.
[方程式2]△x(0°)=| xw(0°)-xwo(0°)| [Equation 2] △ x(0°)=| xw(0°)-xwo(0°)|
[方程式3]△y(0°)=| yw(0°)-ywo(0°)| [Equation 3] △ y(0°)=| yw(0°)-ywo(0°)|
[方程式4]△x(60°)=| xw(60°)-xwo(60°)| [Equation 4] △ x(60°)=| xw(60°)-xwo(60°)|
[方程式5]△y(60°)=| yw(60°)-ywo(60°)| [Equation 5] △ y(60°)=| yw(60°)-ywo(60°)|
於上述方程式2至5,xwo(0°)及ywo(0°)係指於 1931 CIE標準下對於在0°角入射之光(標準源C)測量之於一光譜上之顏色x及y;xwo(60°)及ywo(60°)係指於1931 CIE標準下對於在60°角入射之光(標準源C)測量之於一光譜上之顏色x及y;xw(0°)及yw(0°)係指於1931 CIE標準下對於以0°入射角通過一多層拉伸膜之光測量之於一光譜上之顏色x及y;且xw(60°)及yw(60°)係指於1931 CIE標準下對於以60°入射角通過一多層拉伸膜之光測量之於一光譜上之顏色x及y。 In the above equations 2 to 5, xwo (0°) and ywo (0°) refer to 1931 CIE standard for the light incident at 0 ° angle (standard source C) measured on a spectral color x and y; xwo (60 °) and ywo (60 °) refers to the 1931 CIE standard for 60 Angle incident light (standard source C) is measured on a spectral color x and y; xw (0°) and yw (0°) refer to a multilayer at 0° angle of incidence at the 1931 CIE standard. The light of the stretched film is measured on a spectral color x and y; and xw (60°) and yw (60°) refer to a multilayer stretched film at an incident angle of 60° under the 1931 CIE standard. Light is measured on a spectrum of colors x and y.
以下,本發明係以下列範例進一步說明,但此等範例僅提供作為例示目的,且本發明不限於此等範例。 In the following, the invention is further illustrated by the following examples, but such examples are provided for illustrative purposes only, and the invention is not limited to such examples.
範例1 Example 1
<製備第一聚酯樹脂> <Preparation of First Polyester Resin>
於裝設一攪拌器及一蒸餾塔之一反應器內,注入100莫耳份之2,6-萘二羧酸(NDC)作為一酸組份,及100莫耳份之乙二醇及0.075重量%之季戊四醇(PEL)(以全部酸組份為基準)作為醇組份。以NDC之總重量為基準,0.030重量%之乙酸錳添加至反應器作為一轉酯化催化劑。反應器加熱至250℃實行一轉酯化反應。其後,添加先前所製備之一二氧化矽漿料,且形成之混合物藉由添加一傳統聚縮合催化劑接受一聚縮合反應,獲得一第一聚酯樹脂,其具有0.56dL/g之固有黏度。 Into a reactor equipped with a stirrer and a distillation column, 100 moles of 2,6-naphthalene dicarboxylic acid (NDC) is injected as an acid component, and 100 moles of ethylene glycol and 0.075 Percent by weight of pentaerythritol (PEL) (based on total acid components) is used as the alcohol component. Based on the total weight of the NDC, 0.030% by weight of manganese acetate was added to the reactor as a transesterification catalyst. The reactor was heated to 250 ° C to carry out a transesterification reaction. Thereafter, a previously prepared cerium oxide slurry is added, and the resulting mixture is subjected to a polycondensation reaction by adding a conventional polycondensation catalyst to obtain a first polyester resin having an intrinsic viscosity of 0.56 dL/g. .
<製備第二聚酯樹脂> <Preparation of second polyester resin>
於裝設一攪拌器及一蒸餾塔之一反應器內,注入35莫耳份之NDC及65莫耳份之二甲基對苯二甲酸(DMT)作 為酸組份及100莫耳份之乙二醇及0.075重量%之PEL(以全部酸組份為基準)作為醇組份。以NDC之總重量為基準,0.030重量%之乙酸錳添加至反應器作為一轉酯化催化劑。反應器加熱至250℃實行一轉酯化反應。其後,添加先前所製備之一二氧化矽漿料,且形成之混合物藉由添加一傳統聚縮合催化劑接受一聚縮合反應,獲得一第二聚酯樹脂,其具有0.62dL/g之固有黏度。 Injecting 35 moles of NDC and 65 moles of dimethyl terephthalic acid (DMT) into a reactor equipped with a stirrer and a distillation column The acid component and 100 mole parts of ethylene glycol and 0.075% by weight of PEL (based on the total acid component) were used as the alcohol component. Based on the total weight of the NDC, 0.030% by weight of manganese acetate was added to the reactor as a transesterification catalyst. The reactor was heated to 250 ° C to carry out a transesterification reaction. Thereafter, a previously prepared cerium oxide slurry is added, and the resulting mixture is subjected to a polycondensation reaction by adding a conventional polycondensation catalyst to obtain a second polyester resin having an intrinsic viscosity of 0.62 dL/g. .
<製備多層層合物膜> <Preparation of multilayer laminate film>
如上所製備之第一聚酯樹脂及第二聚酯樹脂之每一者使用一除濕乾燥器及一槳式乾燥器乾燥,使得樹脂之水含量係於從100至150ppm之範圍(使用前)。然後,樹脂供應至一第一擠壓機及一第二擠壓機,於其間加熱至290℃,其係落於高於其熔點(Tm)之從20至40℃之範圍,呈一熔融狀態。然後,被供應至一多層供料頭。 Each of the first polyester resin and the second polyester resin prepared as above was dried using a dehumidifying dryer and a paddle dryer so that the water content of the resin was in the range of from 100 to 150 ppm (before use). Then, the resin is supplied to a first extruder and a second extruder, heated therebetween to 290 ° C, which is in a molten state from 20 to 40 ° C above its melting point (Tm). . It is then supplied to a multi-layer feedblock.
供應至多層供料頭之樹脂被分歧,使得160個第一層自第一聚酯樹脂形成且161個第二層自第二聚酯樹脂形成。此等第一層及此等第二層被交替層合。第一層及第二層之厚度連續改變,使得個別之第一及第二層之最大厚度係個別之第一及第二層之最小厚度之1.5倍。形成具有總數321層之一層合物膜。 The resin supplied to the multilayer feed head was divided such that 160 first layers were formed from the first polyester resin and 161 second layers were formed from the second polyester resin. These first layers and the second layers are alternately laminated. The thicknesses of the first layer and the second layer are continuously varied such that the maximum thickness of the individual first and second layers is 1.5 times the minimum thickness of the individual first and second layers. A laminate film having a total of 321 layers was formed.
其後,以層合物膜之總厚度為基準,第一聚酯樹脂係以15%至18%之厚度擠壓至層合物膜之每一最外側上,形成保護層。因此,獲得具有總數323層之一未拉伸層合物膜。 Thereafter, the first polyester resin is extruded to each of the outermost sides of the laminate film at a thickness of 15% to 18% based on the total thickness of the laminate film to form a protective layer. Thus, an unstretched laminate film having a total of 323 layers was obtained.
因而獲得之未拉伸層合物膜於140℃於x-方向單軸拉伸5.2倍,然後,於120℃熱固化,獲得具有34μm厚度之一多層拉伸膜。 The unstretched laminate film thus obtained was uniaxially stretched 5.2 times in the x-direction at 140 ° C, and then thermally cured at 120 ° C to obtain a multilayer stretched film having a thickness of 34 μm.
範例2至4 Examples 2 to 4
重複範例1之程序,除用於第二聚酯樹脂之醇組份之比率依據以下之表1改變,獲得單軸拉伸多層膜。 The procedure of Example 1 was repeated except that the ratio of the alcohol component used for the second polyester resin was changed in accordance with Table 1 below to obtain a uniaxially stretched multilayer film.
範例5至8 Examples 5 to 8
範例1至4獲得之多層拉伸膜之每一者於y-軸方向拉伸1.2倍,獲得一雙軸拉伸多層膜。 Each of the multilayer stretched films obtained in Examples 1 to 4 was stretched 1.2 times in the y-axis direction to obtain a biaxially stretched multilayer film.
比較例1 Comparative example 1
<製備第一聚酯樹脂> <Preparation of First Polyester Resin>
於裝設一攪拌器及一蒸餾塔之一反應器內,注入100莫耳份之NDC作為一酸組份及100莫耳分之乙二醇作為一醇組份。以NDC之總重量為基準,0.030重量%之乙酸錳添加至反應器作為一轉酯化催化劑。反應器加熱至250℃實行一轉酯化反應。其後,添加先前所製備之一二氧化矽漿料,且形成之混合物藉由添加一傳統聚縮合催化劑接受一聚縮合反應,獲得一第一聚酯樹脂,其具有0.6dL/g之固有 黏度。 In a reactor equipped with a stirrer and a distillation column, 100 moles of NDC was injected as an acid component and 100 moles of ethylene glycol as an alcohol component. Based on the total weight of the NDC, 0.030% by weight of manganese acetate was added to the reactor as a transesterification catalyst. The reactor was heated to 250 ° C to carry out a transesterification reaction. Thereafter, a previously prepared cerium oxide slurry is added, and the resulting mixture is subjected to a polycondensation reaction by adding a conventional polycondensation catalyst to obtain a first polyester resin having an inherent value of 0.6 dL/g. Viscosity.
<製備第二聚酯樹脂> <Preparation of second polyester resin>
於裝設一攪拌器及一蒸餾塔之一反應器內,注入48莫耳份之NDC及52莫耳份之DMT作為酸組份及100莫耳分之乙二醇作為一醇組份。以NDC之總重量為基準,0.030重量%之乙酸錳添加至反應器作為一轉酯化催化劑。反應器加熱至250℃實行一轉酯化反應。其後,添加先前所製備之一二氧化矽漿料,且形成之混合物藉由添加一傳統聚縮合催化劑接受一聚縮合反應,獲得一第二聚酯樹脂,其具有0.74dL/g之固有黏度。 In a reactor equipped with a stirrer and a distillation column, 48 moles of NDC and 52 moles of DMT were injected as an acid component and 100 moles of ethylene glycol as an alcohol component. Based on the total weight of the NDC, 0.030% by weight of manganese acetate was added to the reactor as a transesterification catalyst. The reactor was heated to 250 ° C to carry out a transesterification reaction. Thereafter, a previously prepared cerium oxide slurry is added, and the resulting mixture is subjected to a polycondensation reaction by adding a conventional polycondensation catalyst to obtain a second polyester resin having an intrinsic viscosity of 0.74 dL/g. .
<製備多層層合物膜> <Preparation of multilayer laminate film>
重複範例1之程序,除了如上所製備之第一聚酯樹脂及第二聚酯樹脂被使用,獲得一單軸拉伸多層膜。 The procedure of Example 1 was repeated except that the first polyester resin and the second polyester resin prepared as above were used to obtain a uniaxially stretched multilayer film.
比較例2 Comparative example 2
<製備第一聚酯樹脂> <Preparation of First Polyester Resin>
重複比較例1之程序獲得一第一聚酯樹脂。 The procedure of Comparative Example 1 was repeated to obtain a first polyester resin.
<製備第二聚酯樹脂> <Preparation of second polyester resin>
於裝設一攪拌器及一蒸餾塔之一反應器內,注入48莫耳份之NDC及52莫耳份之DMT作為酸組份及100莫耳分之乙二醇作為一醇組份。以NDC之總重量為基準,0.030重量%之乙酸錳添加至反應器作為一轉酯化催化劑。反應器加熱至250℃實行一轉酯化反應。其後,添加先前所製備之一二氧化矽漿料,且形成之混合物藉由添加一傳統聚縮合催化劑接受一聚縮合反應,獲得一第二聚酯樹脂,其具 有0.74dL/g之固有黏度。 In a reactor equipped with a stirrer and a distillation column, 48 moles of NDC and 52 moles of DMT were injected as an acid component and 100 moles of ethylene glycol as an alcohol component. Based on the total weight of the NDC, 0.030% by weight of manganese acetate was added to the reactor as a transesterification catalyst. The reactor was heated to 250 ° C to carry out a transesterification reaction. Thereafter, a previously prepared cerium oxide slurry is added, and the formed mixture is subjected to a polycondensation reaction by adding a conventional polycondensation catalyst to obtain a second polyester resin. It has an intrinsic viscosity of 0.74 dL/g.
<製備多層層合物膜> <Preparation of multilayer laminate film>
重複範例1之程序,除了如上所製備之第一聚酯樹脂及第二聚酯樹脂被使用,獲得一單軸拉伸多層膜。 The procedure of Example 1 was repeated except that the first polyester resin and the second polyester resin prepared as above were used to obtain a uniaxially stretched multilayer film.
比較例3及4 Comparative Examples 3 and 4
比較例1至2獲得之多層拉伸膜之每一者於y-方向拉伸1.2倍,獲得一雙軸拉伸多層膜。 Each of the multilayer stretched films obtained in Comparative Examples 1 to 2 was stretched 1.2 times in the y-direction to obtain a biaxially stretched multilayer film.
實驗例 Experimental example
範例1至8所製備之第一及第二聚酯樹脂及多層拉伸膜及比較例1至4所製備者之物理性質係如下般評估。結果顯示於表2。 The physical properties of the first and second polyester resins and the multilayer stretched film prepared in Examples 1 to 8 and those prepared in Comparative Examples 1 to 4 were evaluated as follows. The results are shown in Table 2.
(1)共聚合比率 (1) Copolymerization ratio
如上所製備之聚酯樹脂使用1H-NMR評估NDC及DMT之含量。 The polyester resin prepared as above was evaluated for the content of NDC and DMT using 1 H-NMR.
(2)玻璃轉化溫度(Tg)及熔點(Tm) (2) Glass transition temperature (Tg) and melting point (Tm)
範例1及比較例1所製備之聚酯樹脂之每一者係使用示差掃瞄量熱法(DSC,Perkin-Elmer)測試,自以20℃/分鐘之加熱速率獲得之一吸熱曲線之一峰值測量其Tg及Tm。 Each of the polyester resins prepared in Example 1 and Comparative Example 1 was subjected to differential scanning calorimetry (DSC, Perkin-Elmer) test, and one of the endothermic curves was obtained from a heating rate of 20 ° C /min. The Tg and Tm were measured.
(3)折射率 (3) Refractive index
範例1至4及比較例1及2所製備之樹脂被個別擠壓及拉伸。因此獲得之拉伸膜使用一ABBE折射計及一稜鏡耦合器(Sairon Tech.)測試而測量其等於單軸拉伸方向及與其垂直之方向之折射率。 The resins prepared in Examples 1 to 4 and Comparative Examples 1 and 2 were individually extruded and drawn. The stretched film thus obtained was measured using an ABBE refractometer and a tantalum coupler (Sairon Tech.) to measure its refractive index equal to the uniaxial stretching direction and the direction perpendicular thereto.
(4)厚度 (4) Thickness
範例1至8及比較例1至4所製備之多層拉伸膜係使用一厚度測量裝置(Beta ray,Yokogawa)測試而測量其等之厚度。 The multilayer stretched films prepared in Examples 1 to 8 and Comparative Examples 1 to 4 were tested for thickness by a thickness measuring device (Beta ray, Yokogawa).
(5)亮度增強率 (5) Brightness enhancement rate
每一層合物膜樣品嵌入於一偏光鏡與一稜鏡片間之一LCD面板(Samsung UN46D 6900,於2011年6月製備)內,且白色顯示於LCD上。其後,中央點之亮度使用一顏色分析器(CA2000,Minolta)測量。亮度於樣品嵌入之前與之後測量。亮度增強使用如下之方程式6計算:[方程式6]亮度增強率=嵌入後之亮度(L1)/嵌入前之亮度(Lo)×100 Each laminate film sample was embedded in an LCD panel (Samsung UN46D 6900, prepared in June 2011) between a polarizer and a film, and white was displayed on the LCD. Thereafter, the brightness of the center point was measured using a color analyzer (CA2000, Minolta). Brightness is measured before and after sample embedding. The brightness enhancement is calculated using Equation 6 below: [Equation 6] Brightness enhancement rate = brightness after embedding (L 1 ) / brightness before embedding (L o ) × 100
(6)色位移 (6) Color shift
重複如上(5)之程序評估每一樣品嵌入之前與之後間之色位移。顏色x及y係於1931 CIE標準下使用一標準光源C測量。 The procedure of (5) above was repeated to evaluate the color shift between before and after each sample was embedded. Colors x and y are measured using a standard light source C under the 1931 CIE standard.
本發明多層拉伸膜之色位移係如下般測量。 The color shift of the multilayer stretched film of the present invention is measured as follows.
於嵌入本發明多層拉伸膜之前,x及y值於0°及60°入射角測量。於嵌入本發明多層拉伸膜之後,重複相同程序測量於0°及60°入射角之x及y值。 The x and y values were measured at 0° and 60° angles of incidence prior to embedding the multilayer stretch film of the present invention. After embedding the multilayer stretched film of the present invention, the x and y values of the incident angles of 0° and 60° were measured by the same procedure.
每一入射角之色位移係依據如下之方程式2至5計算:[方程式2]△x(0°)=| xw(0°)-xwo(0°)| The color displacement of each incident angle is calculated according to Equations 2 to 5 below: [Equation 2] Δx (0°) = | xw (0°) - xwo (0°) |
[方程式3]△y(0°)=| yw(0°)-ywo(0°)| [Equation 3] Δy(0°)=| yw(0°)-ywo(0°)|
[方程式4]△x(60°)=| xw(60°)-xwo(60°)| [Equation 4] Δx(60°)=| xw(60°)-xwo(60°)|
[方程式5]△y(60°)=| yw(60°)-ywo(60°)| [Equation 5] Δy(60°)=| yw(60°)-ywo(60°)|
於如上之方程式2至5,xwo(0°)及ywo(0°)係指於1931 CIE標準下對於在0°角入射之光(標準源C)所測量之於一光譜上之顏色x及y;xwo(60°)及ywo(60°)係指於1931 CIE標準下對於在60°角入射之光(標準源C)所測量之於一光譜上之顏色x及y;xw(0°)及yw(0°)係指於1931 CIE標準下對於以0°入射角通過一多層拉伸膜之光所測量之於一光譜上之顏色x及y;且xw(60°)及yw(60°)係指於1931 CIE標準下對於以60°入射角通過一多層拉伸膜之光所測量之於一光譜上之顏色x及y。 In Equations 2 to 5 above, xwo (0°) and ywo (0°) refer to the color x measured on a spectrum of light incident at a 0° angle (standard source C) under the 1931 CIE standard. y;xwo(60°) and ywo(60°) are the colours x and y measured on a spectrum of light incident at 60° angle (standard source C) under the 1931 CIE standard; xw (0°) And yw(0°) means the color x and y of a spectrum measured by light passing through a multilayer stretch film at an incident angle of 0° under the 1931 CIE standard; and xw (60°) and yw (60°) is the color x and y measured on a spectrum measured by light passing through a multilayer stretch film at an incident angle of 60° under the 1931 CIE standard.
依據如上概述之方法,對於在入射角0°測得之值為0.1或更少之值及對於在60°入射角測得之值為0.2或更少,色位移係評估為良好。 According to the method as outlined above, the color shift is evaluated as good for a value of 0.1 or less measured at an incident angle of 0° and a value of 0.2 or less for an incident angle of 60°.
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| ??10-2013-0156750 | 2013-12-16 | ||
| KR1020130156750A KR101399425B1 (en) | 2013-12-16 | 2013-12-16 | Multi-layer oriented film |
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| TW103143683A TWI649201B (en) | 2013-12-16 | 2014-12-15 | Multilayer stretch film |
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| KR (1) | KR101399425B1 (en) |
| TW (1) | TWI649201B (en) |
| WO (1) | WO2015093764A1 (en) |
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| JP7400724B2 (en) * | 2018-09-27 | 2023-12-19 | 東洋紡株式会社 | multilayer laminated film |
| JP7400723B2 (en) | 2018-09-27 | 2023-12-19 | 東洋紡株式会社 | multilayer laminated film |
| KR102532479B1 (en) | 2018-09-27 | 2023-05-16 | 도요보 가부시키가이샤 | multilayer laminated film |
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| AU2002221035A1 (en) * | 2000-11-27 | 2002-06-03 | Teijin Limited | Multilayered film and near-infrared-ray reflection film |
| JP2003276143A (en) * | 2002-03-25 | 2003-09-30 | Mitsui Chemicals Inc | Multilayered film of aliphatic polyester |
| JP4167088B2 (en) * | 2003-02-20 | 2008-10-15 | 帝人株式会社 | Biaxially stretched multilayer laminated polyester film |
| WO2005105440A1 (en) * | 2004-04-30 | 2005-11-10 | Toyo Boseki Kabushiki Kaisaha | Easy tear biaxially stretched polyester based film |
| KR100661807B1 (en) * | 2006-03-30 | 2006-12-28 | 도레이새한 주식회사 | Multilayer Polyester Film for Embossing |
| KR100855662B1 (en) * | 2006-04-11 | 2008-09-03 | 도레이새한 주식회사 | Multilayer Polyester Film for Embossing |
| KR101562273B1 (en) * | 2008-07-25 | 2015-10-22 | 에스케이케미칼주식회사 | Optical polyester film |
| KR101758406B1 (en) * | 2009-12-18 | 2017-07-17 | 데이진 가부시키가이샤 | Multi-layer stretch film |
| TWI576244B (en) * | 2011-10-27 | 2017-04-01 | Teijin Dupont Films Japan Ltd | Uniaxially stretched multilayer laminated film |
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| WO2015093764A1 (en) | 2015-06-25 |
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