WO1998008135A1 - Method and device for manufacturing a broadband cholesteric polarizer - Google Patents
Method and device for manufacturing a broadband cholesteric polarizer Download PDFInfo
- Publication number
- WO1998008135A1 WO1998008135A1 PCT/IB1997/000766 IB9700766W WO9808135A1 WO 1998008135 A1 WO1998008135 A1 WO 1998008135A1 IB 9700766 W IB9700766 W IB 9700766W WO 9808135 A1 WO9808135 A1 WO 9808135A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- radiation
- edge position
- polarizer
- band
- compartments
- Prior art date
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Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3016—Polarising elements involving passive liquid crystal elements
Definitions
- the invention relates to a method of manufacturing a broadband cholesteric polarizer, in which a liquid-crystalline, cholesterically ordered layer comprising reactive chiral monomers and reactive nematogenic monomers of different reactivity is polymerized by exposure to radiation.
- the invention also relates to devices for carrying out the method in accordance with the invention.
- cholesteric polarizers and methods of manufacturing same are known per se, for example, from Patent Publications EP-A 404.939, EP-A 404.940 and WO 96/02016, which are all in the name of the current Applicant.
- Polarizers of this type comprise a thin layer of a cholesterically (i.e. chirally nematically) ordered material. This material contains chiral, liquid-crystalline molecules having such a structure that they order themselves more or less spontaneously into a spiral-shaped or helical structure.
- the pitch of this helix can be increased by adding a quantity of a non-chiral, liquid-crystalline (i.e. nematogenic) material to the chiral, liquid-crystalline material.
- the exact pitch is governed by the ratio between the quantities of chiral and non-chiral liquid-crystalline molecules as well as by their chemical structure.
- this material is provided in the form of a thin layer on a substrate or between two substrates, said helical structure assumes such an orientation that the axis of the helix extends transversely to the layer.
- a layer is capable of reflecting a narrow band of light whose wavelength corresponds to the product of the pitch and the refractive index of the material and whose direction of polarization corresponds to the handedness of the helical structure.
- a cholesteric layer can very suitably be used in an optical polarizer.
- the refractive index of a material is to be understood to mean in this context the geometric mean (n e +n 0 )/2 of the ordinary refractive index n 0 and the extraordinary refractive index n e of this material.
- Broadband cholesteric polarizers are distinguished from the customary cholesteric polarizers by the presence of a relatively broad reflection band.
- the bandwidth of the customary cholesteric polarizers is only approximately 40-50 nm. In the case of broadband polarizers, bandwidths of 100 nm, 150 nm, 200 nm and even more than 400 nm have been achieved.
- the band position of a cholesteric filter is defined as the center of the wavelength range in which the reflection takes place.
- a width of a band is defined as the difference in wavelength between the long-wave and the short-wave edge positions of the band.
- the wavelength of an edge position is defined as the wavelength at which the intensity amounts to 50% of the maximum intensity.
- EP 404.940 describes an elegant method of manufacturing a broadband cholesteric polarizer.
- use is made of a mixture comprising reactive chiral monomers and reactive nematogenic monomers, which exhibit a different reactivity.
- the reactive monomers use can be made of compounds containing a reactive group on the basis of acrylates, epoxy compounds, vinylethers and thiolene systems, as described, inter alia, in US 5, 188,760.
- Monomers containing different reactive groups generally exhibit a different reactivity.
- a difference in reactivity also occurs if one type of monomers contains one reactive group and the other type of monomers contains two (identical) reactive groups.
- a layer of this mixture is polymerized by means of (actinic) radiation, in particular UV radiation.
- the conditions are selected in such a manner that during the polymerization operation a radiation profile of varied intensity is formed in the layer.
- diffusion processes take place in the cholesteric layer during polymerization.
- this cholesteric polarizer exhibits a relatively broad reflection band.
- the invention more particularly aims at providing a method of manufacturing broadband cholesteric polarizers of which the position of one of the two edges of the reflection band can be adjusted in a very reproducible manner.
- the method in accordance with the invention should enable these polarizers to be mass-produced.
- the invention is based on the experimentally gained insight that the intensity of the radiation used during polymerization plays an important part in the manufacture of broadband polarizers. It has been demonstrated that the eventually achieved bandwidth is governed to a substantial degree by the radiation intensity used. If use is made of a relatively high UV intensity (typically 0.5 mW/cm 2 or higher), the eventually achieved bandwidth is found to be relatively small, and it differs hardly from that of the unpolymerized mixture. If a relatively low radiation intensity (typically 0.05 mW/cm 2 or lower) is used, a much broader reflection band is obtained. Under these conditions, first, a colored, narrow reflection band is formed, which subsequently broadens into an uncolored, broadband reflection band.
- a relatively high UV intensity typically 0.5 mW/cm 2 or higher
- a relatively low radiation intensity typically 0.05 mW/cm 2 or lower
- a substantial increase of the intensity causes the bandwidth obtained at that instant to be frozen, as it were. It has been demonstrated that the increase in intensity should preferably be a factor of 10 or more to bring about said frozen state. Preferably, this factor is 20 or more. Under these conditions, the cholesterically ordered layer becomes momentary polymerized.
- a preferred embodiment of the method in accordance with the invention is characterized in that the attainment of the desired edge position of the band is determined by means of a monochromatic photosensor, the wavelength used by said sensor corresponding to the wavelength of the desired edge position of the band.
- a photosensor comprises a photodetector as well as a monochromatic light source.
- a laser can very advantageously be used as the monochromatic light source in the sensor.
- the sensor can be used in reflection.
- Said sensor is constructed in such a manner that the monochromatic light, which emanates from the light source and which is used in the measuring operation, is directed to the layer to be polymerized.
- the monochromatic light which emanates from the light source and which is used in the measuring operation, is directed to the layer to be polymerized.
- this light will pass through the layer to be polymerized (transmission).
- reflection of the monochromatic light occurs.
- a proper positioning of the layer, the light source and the detector causes this light to be reflected at the detector. At this moment, the intensity of the polymerization radiation should be increased.
- a second polymerization lamp having a higher radiation intensity is activated or, preferably, a filter situated in front of the polymerization lamp is removed.
- a filter situated in front of the polymerization lamp is removed.
- a filter whose transmission is adjustable.
- Another preferred embodiment of the method in accordance with the invention is characterized in that the desired edge position of the band is determined by means of a transmission measurement.
- the sensor is constructed so that the light source and the detector are situated on either side of the layer to be polymerized. In this case, the sensor is activated as soon as the detector detects a substantial reduction in intensity of the light emanating from the light source.
- Such an arrangement has the advantage that the exact alignment of the layer to be polymerized does not affect the measuring results of the sensor.
- Another suitable embodiment of the method in accordance with the invention is characterized in that the liquid crystalline, cholesterically ordered layer is passed through an illumination tunnel which is provided with a number of compartments which comprise a radiation source as well as a light sensor by means of which the intensity of the radiation incident on the layer can be changed.
- This embodiment of the method in accordance with the invention enables broadband, cholesteric polarizers to be manufactured in a continuous process. This has a favorable effect on the cost price per unit area.
- the invention also relates to a device for manufacturing a broadband cholesteric polarizer, which is characterized by a radiation compartment comprising a) means for positioning the polarizer to be manufactured, b) a radiation source for the irradiation of the polarizer to be manufactured and c) a monochromatic photosensor comprising a photodetector as well as a monochromatic light source.
- This device in accordance with the invention enables broadband polarizers to be manufactured in batch processes.
- the photodetector and the monochromatic light source are positioned in the radiation compartment in such a manner that the sensor measures in the transmission.
- the polarizer to be manufactured is situated between the detector and the light source during operation of the device.
- Another device in accordance with the invention which is used to manufacture a broadband cholesteric polarizer, is characterized in that the device comprises a number of radiation compartments, which are provided with a) means for passing a substrate through the radiation compartments, b) a radiation source for irradiating the substrate to be passed through said compartments, and c) a monochromatic photosensor which comprises a photodetector as well as a monochromatic light source.
- This device in accordance with the invention enables broadband polarizers to be manufactured in a continuous process.
- the photodetector and the monochromatic light source are positioned in the radiation compartments in such a manner that the sensors measure in transmission.
- the - preferably elongated - substrate to be passed through the radiation compartments is situated between the detector and the light source during operation of the device.
- Fig. 1 schematically shows a broadband cholesteric polarizer which can be manufactured by means of the method in accordance with the invention
- Fig. 2 shows the structure of a number of chemical compounds
- FIG. 3 schematically shows a first device in accordance with the invention, which can be used to carry out the method according to the invention
- Fig. 4 schematically shows a second device in accordance with the invention, which can be used to carry out the method according to the invention. It is noted that the Figures are not drawn to scale.
- Fig. 1 shows an embodiment of a broadband cholesteric polarizer which is manufactured by means of the method according to the invention.
- Said polarizer comprises two flat, transparent substrates 1 and 2, which are made, for example, of glass and which are positioned substantially parallel to each other and at some distance from each other.
- the facing surfaces of the substrates are provided with an orientation layer 3 and 4, for example, of rubbed polyimide or sputtered SiO x .
- a spacer 5 is provided at the edges of the substrates.
- a layer 6 of a cholesterically ordered polymeric material is situated between said two substrates.
- the axis of the molecular helix of the cholesterically ordered material extends transversely to the layer.
- the molecular helix has a variable pitch which increases continuously from one surface of layer 6 to the other surface. This is schematically shown by means of two spiral-shaped structures 7.
- the thickness of layer 6 typically ranges from 3 to 40 micrometers, preferably from 5 to 25 micrometers.
- the above-described embodiment of the cholesteric polarizer in accordance with the invention was manufactured as follows. First, a mixture containing reactive monomers was prepared. This mixture contained 35 wt. % of the chiral monomer A and 65 wt. % of the nematogenic monomer B. Monomer A contains one reactive group per molecule and monomer B contains two reactive groups per molecule. In this case, acrylate groups were used. The exact structural formulas of the monomers A and B are shown in Fig. 2. The difference in reactivity between both monomers can be attributed to the different number of reactive groups per molecule. Subsequently, 2 wt.
- the mixture thus prepared was subsequently provided between two transparent substrates. These substrates were provided with a layer of a rubbed polyimide. These layers serve to improve the alignment of the molecular helix, which develops spontaneously in the cholesteric mixture. It is noted that, in said method according to the invention, it is not absolutely necessary to use substrates which are provided with orientation layers. In the manufacture of (very) thin optically active layers, generally spontaneous orientation of the chiral and nematogrenic groups takes place. However, the presence of orientation layers during polymerization does lead to an improved orientation of the optically active layer, so that the optical properties of the polarizers are improved substantially.
- This device comprises a radiation compartment 11. This is provided with means for positioning the broadband cholesteric polarizer to be manufactured. In the device shown, these means are constructed as support bodies 12.
- the polarizer comprises two substrates 13 and a cholesterically ordered layer 14 situated between said substrates. It is noted that the method and device in accordance with the invention can also be used to manufacture polarizers in which only one substrate is used. Compartment 11 further comprises a radiation source in the form of an
- the power of the lamp and the distance between the lamp and the polarizer to be irradiated are selected in such a manner that the average illumination intensity to which the cholesteric layer is exposed during operation of the device is approximately 0.9 mW/cm 2 .
- a neutral-density filter 16 whose position or transmission is adjustable is arranged between the UV lamp and the polarizer. When the filter operates at maximum capacity, the radiation originating from the UV lamp is filtered in such a manner that the average illumination intensity on the polarizer is only approximately 0.03 mW/cm 2 .
- Compartment 11 also comprises a photosensor which consists of a monochromatic light source 17 in the form of a laser and of a photodetector 18.
- the wavelength of the laser is selected to be such that it is equal to the edge position of the broadband polarizer to be manufactured.
- the sensor measures in transmission, so that the detector and the light source are situated on opposite sides of the polarizer which is the subject of measurements.
- the sensor is coupled to the filter 16.
- the filter 16 As soon as the transmission of the polarizer decreases substantially (50% or more) during illumination, the sensor supplies a signal which causes the neutral density filter 16 to be activated. Depending on the type of filter, this is either removed from its position between the radiation source 15 and the polarizer or the transmission of the filter is maximized.
- the radiation intensity on the polarizer increases by a factor of 30, which results in the instantaneous, complete polymerization of the cholesteric layer.
- the bandwidth as well as the exact position of one of the band edges is defined.
- Fig. 4 is a schematic, sectional view of a device in accordance with the invention for mass-producing broadband cholesteric polarizers.
- This device comprises a temperature-controlled radiation tunnel 21 which accommodates a number of radiation compartments 22.
- Said radiation tunnel is provided with means 23, for example in the form of drivable rollers, enabling an elongated, flexible substrate 24 to be continuously fed through.
- This substrate may consist, for example, of a thin, transparent foil carrying a cholesterically ordered layer of a mixture of reactive, liquid-crystalline monomers to be polymerized.
- the compartments are provided with a radiation source 25, for example in the form of an UV lamp which is used to irradiate the substrate while it is being fed through the radiation tunnel.
- a radiation source 25 for example in the form of an UV lamp which is used to irradiate the substrate while it is being fed through the radiation tunnel.
- a number of said compartments are provided with a photodetector 26 and with a monochromatic light source in the form of a single laser 27.
- the partially transmissive mirrors 28 divide the laser beam of laser 27 into a number of deflecting sub-beams which are incident on the photodetector via the substrate.
- the method in accordance with the invention can be applied continuously in the device in accordance with the invention in the following manner.
- a substrate which is transparent to the laser light used is provided with a cholesterically ordered layer of a liquid- crystalline material.
- This substrate is passed through the radiation tunnel by drive means.
- the substrate is fed past a number of radiation compartments in which it is exposed to an UV lamp of a relatively low intensity (0.05 mW/cm 2 or less).
- the reflection band will have reached such a width, as a result of the polymerization process, that the wavelength of one of the edge positions is equal to that of the laser used.
- the intensity measured by the photodetector is reduced substantially.
- a signal is then given which causes the radiation intensity to be increased substantially, for example, by a factor of 10 or more.
- instantaneous, complete polymerization of the liquid-crystalline material takes place, so that the measured edge position and bandwidth become frozen, as it were.
- the egressing substrate with the polymerized, broadband, cholesterically ordered layer can be processed further, in a manner which is well-known to those skilled in the art, to form a broadband cholesteric polarizer.
- the substrate is cut to the proper dimensions and, if necessary, provided with a quarter lambda foil if the transmitted light should be circularly polarized. If necessary, the contrast can be increased by providing the filter with a dichroic polarization foil.
- the method in accordance with the invention enables broadband cholesteric polarizers having an accurately adjusted edge position to be manufactured. By virtue thereof, the viewing-angle dependence of a display provided with such a polarizer can be reduced.
- the polarizers can be produced in batch processes or continuous processes.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Polarising Elements (AREA)
- Liquid Crystal (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT97925235T ATE284047T1 (en) | 1996-08-21 | 1997-06-23 | METHOD AND DEVICE FOR PRODUCING A BROADBAND CHOLESTERIC POLARIZER |
JP10510532A JPH11514757A (en) | 1996-08-21 | 1997-06-23 | Method and apparatus for manufacturing a broadband cholesteric polarizer |
EP97925235A EP0859969B1 (en) | 1996-08-21 | 1997-06-23 | Method and device for manufacturing a broadband cholesteric polarizer |
DE69731813T DE69731813T2 (en) | 1996-08-21 | 1997-06-23 | METHOD AND DEVICE FOR PRODUCING A BROADBAND CHOLESTERIC POLARIZER |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96202326.3 | 1996-08-21 | ||
EP96202326 | 1996-08-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998008135A1 true WO1998008135A1 (en) | 1998-02-26 |
Family
ID=8224302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB1997/000766 WO1998008135A1 (en) | 1996-08-21 | 1997-06-23 | Method and device for manufacturing a broadband cholesteric polarizer |
Country Status (8)
Country | Link |
---|---|
US (3) | US5948831A (en) |
EP (1) | EP0859969B1 (en) |
JP (1) | JPH11514757A (en) |
CN (1) | CN1146748C (en) |
AT (1) | ATE284047T1 (en) |
DE (1) | DE69731813T2 (en) |
TW (1) | TW353145B (en) |
WO (1) | WO1998008135A1 (en) |
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US6160663A (en) * | 1998-10-01 | 2000-12-12 | 3M Innovative Properties Company | Film confined to a frame having relative anisotropic expansion characteristics |
US6773766B2 (en) | 1998-12-22 | 2004-08-10 | Basf Aktiengesellschaft | Utilization of polymerizable liquid crystal substances for the production of optical components |
WO2008102838A1 (en) | 2007-02-23 | 2008-08-28 | Zeon Corporation | Liquid crystalline compound, liquid crystalline composition, optical film, and optical laminate |
WO2008105538A1 (en) | 2007-03-01 | 2008-09-04 | Zeon Corporation | Polymerizable liquid crystal compound, polymerizable liquid crystal composition, liquid crystal polymer and optically anisotropic substance |
WO2008133290A1 (en) | 2007-04-24 | 2008-11-06 | Zeon Corporation | Polymerizable liquid crystal compound, polymerizable liquid crystal composition, liquid crystalline polymer, and optically anisotropic material |
WO2010001725A1 (en) | 2008-06-30 | 2010-01-07 | 日本ゼオン株式会社 | Polymerizable liquid crystal compounds, polymerizable liquid crystal compositions, liquid crystal polymers and optically anisotropic materials |
WO2010038591A1 (en) | 2008-10-01 | 2010-04-08 | 日本ゼオン株式会社 | Polymerizable chiral compound, polymerizable liquid crystalline composition, liquid crystalline polymer, and optical isomer |
US8883271B2 (en) | 2010-03-31 | 2014-11-11 | Zeon Corporation | Polymerizable chiral compound, polymerizable liquid crystal compound, liquid crystal polymer and optically anisotropic body |
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US6753044B2 (en) | 1991-11-27 | 2004-06-22 | Reveo, Inc. | Coloring media having improved brightness and color characteristics |
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TW353145B (en) | 1996-08-21 | 1999-02-21 | Koninkl Philips Electronics Nv | Method and device for manufacturing a broadband cholesteric polarizer |
DE19726051A1 (en) * | 1997-06-19 | 1998-12-24 | Consortium Elektrochem Ind | Process and broadening of cholesteric reflection bands of photopolymerizable cholesteric liquid crystals and optical elements produced by this process |
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CN114114516A (en) * | 2021-11-29 | 2022-03-01 | 淮安泰华新材料有限公司 | Preparation method of wide wave reflection type liquid crystal polaroid |
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DE69528981T2 (en) * | 1994-07-12 | 2003-08-28 | Koninklijke Philips Electronics N.V., Eindhoven | LIGHTING SYSTEM, LINEAR POLARIZER FOR SUCH A LIGHTING SYSTEM AND DISPLAY DEVICE WITH THIS LIGHTING SYSTEM |
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1997
- 1997-02-04 TW TW086101333A patent/TW353145B/en active
- 1997-06-23 AT AT97925235T patent/ATE284047T1/en not_active IP Right Cessation
- 1997-06-23 CN CNB971911061A patent/CN1146748C/en not_active Expired - Fee Related
- 1997-06-23 WO PCT/IB1997/000766 patent/WO1998008135A1/en active IP Right Grant
- 1997-06-23 JP JP10510532A patent/JPH11514757A/en not_active Ceased
- 1997-06-23 DE DE69731813T patent/DE69731813T2/en not_active Expired - Fee Related
- 1997-06-23 EP EP97925235A patent/EP0859969B1/en not_active Expired - Lifetime
- 1997-08-14 US US08/911,078 patent/US5948831A/en not_active Expired - Fee Related
-
1999
- 1999-03-09 US US09/264,911 patent/US6193937B1/en not_active Expired - Fee Related
-
2001
- 2001-01-10 US US09/757,875 patent/US6638449B2/en not_active Expired - Fee Related
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US5024850A (en) * | 1989-05-10 | 1991-06-18 | U.S. Philips Corporation | Method of manufacturing a polarization filter and a polarization filter so obtained |
US5506704A (en) * | 1993-01-11 | 1996-04-09 | U.S. Philips Corporation | Cholesteric polarizer and the manufacture thereof |
EP0643121A1 (en) * | 1993-09-08 | 1995-03-15 | Koninklijke Philips Electronics N.V. | Switchable cholesteric filter and luminaire having such a filter |
WO1997016762A1 (en) * | 1995-10-30 | 1997-05-09 | Reveo, Inc. | Super broad-band polarizing reflective material |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6160663A (en) * | 1998-10-01 | 2000-12-12 | 3M Innovative Properties Company | Film confined to a frame having relative anisotropic expansion characteristics |
US6773766B2 (en) | 1998-12-22 | 2004-08-10 | Basf Aktiengesellschaft | Utilization of polymerizable liquid crystal substances for the production of optical components |
WO2008102838A1 (en) | 2007-02-23 | 2008-08-28 | Zeon Corporation | Liquid crystalline compound, liquid crystalline composition, optical film, and optical laminate |
WO2008105538A1 (en) | 2007-03-01 | 2008-09-04 | Zeon Corporation | Polymerizable liquid crystal compound, polymerizable liquid crystal composition, liquid crystal polymer and optically anisotropic substance |
WO2008133290A1 (en) | 2007-04-24 | 2008-11-06 | Zeon Corporation | Polymerizable liquid crystal compound, polymerizable liquid crystal composition, liquid crystalline polymer, and optically anisotropic material |
WO2010001725A1 (en) | 2008-06-30 | 2010-01-07 | 日本ゼオン株式会社 | Polymerizable liquid crystal compounds, polymerizable liquid crystal compositions, liquid crystal polymers and optically anisotropic materials |
WO2010038591A1 (en) | 2008-10-01 | 2010-04-08 | 日本ゼオン株式会社 | Polymerizable chiral compound, polymerizable liquid crystalline composition, liquid crystalline polymer, and optical isomer |
US8603357B2 (en) | 2008-10-01 | 2013-12-10 | Zeon Corporation | Polymerizable chiral compound, polymerizable liquid crystal composition, liquid crystal polymer and optically anisotropic body |
US8883271B2 (en) | 2010-03-31 | 2014-11-11 | Zeon Corporation | Polymerizable chiral compound, polymerizable liquid crystal compound, liquid crystal polymer and optically anisotropic body |
Also Published As
Publication number | Publication date |
---|---|
DE69731813T2 (en) | 2005-12-15 |
EP0859969B1 (en) | 2004-12-01 |
US6193937B1 (en) | 2001-02-27 |
JPH11514757A (en) | 1999-12-14 |
TW353145B (en) | 1999-02-21 |
EP0859969A1 (en) | 1998-08-26 |
CN1198819A (en) | 1998-11-11 |
ATE284047T1 (en) | 2004-12-15 |
DE69731813D1 (en) | 2005-01-05 |
US20010001509A1 (en) | 2001-05-24 |
US6638449B2 (en) | 2003-10-28 |
US5948831A (en) | 1999-09-07 |
CN1146748C (en) | 2004-04-21 |
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