Patent Application
20160187539
This invention pertains to an optical film for use as a quarter wave plate (QWP) having a normal wavelength dispersion curve. More specifically, this invention relates to a quarter wave plate based on cellulose ester polymer.
It is known in the art of optical compensation that the phase retardation of light varies according to wavelength, causing color shift and contrast ratio reduction. This wavelength dependence (or dispersion) characteristic of the compensation film may be taken into account when designing an optical device so that color shift is reduced and contrast ratio increased. Wavelength dispersion curves are defined as “normal (or proper)” or “reversed” with respect to the compensation film having positive and negative retardance (or retardation). A compensation film with positive retardance (positive A- or C-plate) may have a normal dispersion curve in which the value of phase retardation is increasingly positive toward shorter wavelengths or a reversed dispersion curve in which the value of phase retardation is decreasingly positive toward shorter wavelengths. A compensation film with negative retardance (negative A- or C-plate) may have a normal dispersion curve in which the value of phase retardation is increasingly negative toward shorter wavelengths or a reversed dispersion curve in which the value of phase retardation is decreasingly negative toward shorter wavelengths. Exemplary shapes of these curves are depicted in
Wave plates are customarily named as follows in accordance with their refractive index profiles: positive A-plate: nx>ny=nz; negative A-plate: nx<ny=nz; positive C-plate: nx=ny<nz; negative C-plate: nx=ny>nz, wherein, nx and ny represent in-plane refractive indices, and nz is the thickness refractive index.
The above wave plates are uniaxial birefringent plates. A wave plate can also be biaxial birefringent, where nx, ny, and nz all have different values; it is customarily referred to as a biaxial film.
An A-plate is a wave plate commonly used as a retarder in an optical device. It is a birefringent material capable of manipulating the polarization state or phase of the light beam traveling through the medium. The A-plate optical retarder has a refractive index profile of nx>ny=nz, wherein nx and ny represent in-plane refractive indices and nz represents the thickness-direction refractive index. Such a wave plate exhibits a positive in-plane retardation (Re) as expressed by Re=(nx−ny)×d, wherein d is the thickness of the wave plate. Re is also often denoted as Ro.
An A-plate having in-plane retardation (Re) equal to a quarter of a light wavelength (λ), Re=λ/4, is called quarter wave plate (QWP). A quarter wave plate is capable of converting an incident linearly polarized light into circularly polarized light. Thus, a quarter wave plate is commonly used in combination with a linear polarizer to provide a circular polarizer in an optical device. Circularly polarized light has been used in polarized three-dimensional (3D) display systems to produce stereoscopic image projection. Circular polarization has an advantage over linear polarization in that viewers are able to tilt their heads and move around naturally without seeing distorted 3D images. Such 3D display systems require viewers to wear glasses, commonly referred to as 3D glasses, equipped with circular polarizing films in order to see 3D images. Recently, there has been much increased interest in 3D consumer products such as TVs and computer displays. Thus, there is a demand for improved 3D glasses with circular polarizing films. Specifically, there is a need for a quarter wave plate having normal wavelength dispersion, which has been found to have the utility for 3D glasses to improve the viewing quality. It is known that such quarter wave plates can be achieved by using polycarbonate or cyclic polyolefin. However, in a device based on such quarter wave plates, a cellulose ester film is required to protect the polyvinyl alcohol based polarizer. It would be advantageous if the quarter wave plate is based on cellulose ester film and can also function as a protective film for the polarizer. Accordingly, this invention is further directed to quarter wave plates based on cellulose ester.
In order to have a normal wavelength dispersion curve, the in-plane retardation (Re) of a quarter wave plate should satisfy the following equations:
R
e(450)/Re(550)>1 and Re(650)/Re(550)<1
wherein Re(450), Re(550), and Re(650) are in-plane retardations at the light wavelengths of 450 nm, 550 nm, and 650 nm respectively.
The positive A-plate, however, also exhibits a negative out-of-plane retardation Rth, which is defined as Rth=[nz−(nx+ny)/2]×d with a value of |Re/2| arising from its orientation. The term “|Re/2|” means the absolute value of Re/2.This characteristic can be beneficial when a negative Rth is desirable in an optical device. For example, in a vertically aligned (VA) mode liquid crystal display (LCD), the liquid crystal molecules in the LC cell are aligned in a homeotropic manner, which results in positive out-of-plane retardation. A wave plate with a negative Rth, thus, can provide an out-of-plane compensation in addition to in-plane compensation in VA-LCD. In other types of devices, such as in-plane switch (IPS) mode LCD and 3D glasses, however, the Rth exhibited in the A-plate is not desirable since it can give rise to phase shift in off-axis light and lead to light leakage. Thus, there exists a further need in the art to provide a quarter wave plate having reduced out-of-plane retardation for improved viewing quality.
It has been surprisingly discovered that quarter wave plates comprising cellulose ester polymers and additives and having normal dispersion can be obtained.
In one aspect the present invention provides a uniaxially or biaxially stretched optical film for use as a quarter wave plate having a normal wavelength dispersion curve comprising,
wherein DISK represents a disk-like moiety having a fused ring structure, A is each independently —COO—, —OOC—, —CO—, —CONH—, —NHCO—, —O—, or —S—; Z is each independently an aryl, alkyl, ethoxylated alkyl, or ethoxylated aryl group, having 1 to 30 carbon atoms; Y is each independently a halogen or alkyl-, alkoxy-, or alkanoyl-group having 1 to 20 carbon atoms, m=0, 1, 2, 3, or 4; n is the number of the independent -A-Z substituents on the DISK, n=0, 1, 2, or 3; and wherein the in-plane retardation (Re) of said quarter wave plate satisfies the following equations:
R
e(450)/Re(550)>1 and Re(650)/Re(550)<1
wherein Re(450), Re(550), and Re(650) are in-plane retardations at the light wavelengths of 450 nm, 550 nm, and 650 nm respectively.
In one aspect, the optical film in accordance with this invention is a quarter wave plate having in-plane retardation (Re) of about 100-160 nm at the wavelength (λ) 550 nm.
In another aspect, the optical film has an out-of-plane retardation (Rth) that satisfies the equation of |Rth|<100 nm throughout the wavelength range of about 400 nm to about 800 nm.
One aspect of the present invention provides a circular polarizer comprising
R
e(450)/Re(550)>1 and Re(650)/Re(550)<1
wherein Re(450), Re(550), and Re(650) are in-plane retardations at the light wavelengths of 450 nm, 550 nm, and 650 nm respectively.
In one aspect of the present invention, the DISK comprises a fused ring compound comprising two or more individual rings that are connected by sharing at least one of their sides.
In one aspect of the present invention, the fused ring of the DISK comprises one or more of naphthalene, anthracene, phenanthrene, -pyrene, compound with structure 5, and compound with structure 6,2-naphthyl benzonate, 2,6-naphthalene dicarboxylic diester, naphthalene, abietic acid ester and mixtures thereof.
In one aspect of the present invention, the cellulose ester polymer has an inherent viscosity of from about 0.8 to 1.9 dL/g.
In one embodiment of the present invention, there is provided a uniaxially or biaxially stretched optical film for use as a quarter wave plate having a normal wavelength dispersion curve, comprising:
wherein DISK represents a disk-like moiety having a fused ring structure, A is each independently —COO—, —OOC—, —CO—, —CONH—, —NHCO—, —O—, or —S—; Z is each independently an aryl, alkyl, ethoxylated alkyl, or ethoxylated aryl group, having 1 to 30 carbon atoms; Y is each independently a halogen or alkyl-, alkoxy-, or alkanoyl-group having 1 to 20 carbon atoms, m=0, 1, 2, 3, or 4; n is the number of the independent -A-Z substituents on the DISK, n=0, 1, 2, or 3; and wherein the in-plane retardation (Re) of said quarter wave plate satisfies the following equations:
R
e(450)/Re(550)>1 and Re(650)/Re(550)<1
wherein Re(450), Re(550), and Re(650) are in-plane retardations at the light wavelengths of 450 nm, 550 nm, and 650 nm respectively. The ethoxylated alkyl or ethoxylated aryl comprises a moiety of —[—CH2—CH2—O—]n—Z bonded to A, wherein n is an integer from 1 to 10.
Alternatively, Z may be independently an aryl, alkyl, ethoxylated alkyl, or ethoxylated aryl group, having 1 to 20 carbon atoms or having 1 to 15 carbon atoms or having 1-10 carbon atoms or having 1 to 5 carbon atoms.
Alternatively, Y may be independently a halogen or alkyl-, alkoxy-, or alkanoyl-group having 1 to 20 carbon atoms or having 1 to 15 carbon atoms, or having 1 to 10 carbon atoms or having 1 to 5 carbon atoms.
In the ethoxylated alkyl or ethoxylated aryl comprises a moiety of —[—CH2—CH2—O—]n—Z bonded to A, n is an integer from 1 to 10 or from 1 to 8 or from 1 to 6 or from 1 to 4 or from 1 to 2. Alternatively, in the ethoxylated alkyl or ethoxylated aryl comprises a moiety of —[—CH2—CH2—O—]n—Z bonded to A, n is an integer from 2 to 10 or from 4 to 10 or from 6 to 10 or from 8 to 10.
Examples of the cellulose ester polymer in (a) suitable for this invention include, but are not limited to, cellulose acetate (CA), cellulose acetate propionate (CAP), and cellulose acetate butyrate (CAB). The terms “cellulose ester” and “cellulose ester polymer” are used interchangeable herein. The terms refer to the condensation product from the reaction of a hydroxyl group on the cellulose with the carboxylic acid group of a carboxylic acid with the formation of water as a co-product. The cellulose esters may be randomly or regioselectively substituted. Regioselectivity can be measured by determining the relative degree of substitution (RDS) at C6, C3, and C2 in the cellulose ester by carbon 13 NMR (Macromolecules, 1991, 24, 3050-3059). In conventional cellulose esters, regioselectivity is generally not observed and the RDS ratio of C6/C3, C6/C2, or C3/C2 is generally near 1 or less. In essence, conventional cellulose esters are random copolymers. In contrast, when adding one or more acylating reagents to cellulose dissolved in an appropriate solvent, the C6 position of cellulose are acylated much faster than C2 and C3. Consequentially, the C6/C3 and C6/C2 ratios are significantly greater than 1, which is characteristic of a 6,3- or 6,2-enhanced regioselectively substituted cellulose ester.
Non-limiting examples of the DISK moiety having a fused ring structure such as naphthalene (structure 1), anthracene (structure 2), phenanthrene (structure 3), pyrene (structure 4), (structure 5), and (structure 6) which are shown below:
The “fused ring” structure may be understood to have two or more individual rings that are connected by sharing at least one of their sides. Each individual ring in the fused ring may be substituted or unsubstituted and is preferably a six- or five-membered ring, which are typically all-carbon. Individual rings in a fused ring may be aromatic or aliphatic. Preferred individual rings in a fused ring include, but are not limited to, aromatic rings and substituted aromatic rings, cycloaliphatic rings, substituted cycloaliphatic rings, partially unsaturated cycloaliphatic rings, and partially unsaturated, substituted cycloaliphatic rings.
Non-limiting examples of the additive in (b) suitable for this invention are 2-naphthyl benzoate, 2,6-naphthalene dicarboxylic acid ester, naphthalene, and abietic acid ester which are shown below:
wherein, R is each independently C1-C20 alkyl or C1-C20 aryl, and n is each independently an integer ranging from 0 to 6. When n=0, R is bonded directly to the carboxyl group. Alternatively, R is each independently C1-C15 alkyl or C1-C15 aryl, and n is each independently an integer ranging from 0 to 6. Alternatively, R is each independently C1-C10 alkyl or C1-C10 aryl, and n is each independently an integer ranging from 0 to 6. Alternatively, R is each independently C1-C6 alkyl or C1-C6 aryl, and n is each independently an integer ranging from 0 to 6.
The optical film in accordance with the present invention has a positive in-plane retardation (Re) and a normal in-plane wavelength dispersion characteristic, in which the value of phase retardation is increasingly positive toward shorter wavelengths. This dispersion characteristic is expressed by the ratios of the retardations as measured at the wavelengths of 450 nm, 550 nm, and 650 nm, which satisfy the relations of Re(450)/Re(550)>1 and Re(650)/Re(550)<1. The ratio of Re(450)/Re(550) can be 1.001 to 1.1, 1.005 to 1.08, 1.01 to 1.06, or 1.02 to 1.04. The ratio of Re(650)/Re(550) can be 0.95 to 0.999, 0.96 to 0.996, 0.97 to 0.993, or 0.98 to 0.99. The films may have a combination of the ratio of Re(450)/Re(550) ranging from 1.001 to 1.1 with the ratio of Re(650)/Re(550) of 0.95 to 0.999, or 0.96 to 0.996, or 0.97 to 0.993, or 0.98 to 0.99. The films may have a combination of the ratio of Re(450)/Re(550) ranging from 1.005 to 1.08 with the ratio of Re(650)/Re(550) of 0.95 to 0.999, or 0.96 to 0.996, or 0.97 to 0.993, or 0.98 to 0.99. The films may have a combination of the ratio of Re(450)/Re(550) ranging from 1.01 to 1.06 with the ratio of Re(650)/Re(550) of 0.95 to 0.999, or 0.96 to 0.996, or 0.97 to 0.993, or 0.98 to 0.99. The films may have a combination of the ratio of Re(450)/Re(550) ranging from 1.02 to 1.04 with the ratio of Re(650)/Re(550) of 0.95 to 0.999, or 0.96 to 0.996, or 0.97 to 0.993, or 0.98 to 0.99.
Retardation (R) of a wave plate is defined as R=Δn×d, wherein Δn is the birefringence and d is the thickness of the wave plate. Birefringence is classified into in-plane birefringence Δne=nx−ny and out-of-plane birefringence Δnth=nz−(nx+ny)/2. Thus, in-plane retardation is represented by Re=(nx−ny)×d and out-of-plane retardation by Rth=[(nz−(nx+ny)/2]×d, which is the definition used through-out this application. It is noted that some authors use the following definition Rth=[(nx+ny)−nz/2]×d which gives a number of the same magnitude but with opposite sign. nx is measured in the machine direction of the film and ny is measured in the transverse direction.
Birefringence (Δn) of a wave plate may be measured by determining the birefringence of a wave plate over a wavelength range of about 400 nm to about 800 nm at different increments. Alternatively, birefringence may be measured at a specific light wavelength. Throughout this description, when a birefringence or retardation relation is given without specifying a wavelength, the relation occurs throughout the wavelength range of about 400 nm to about 800 nm.
Preferably, the in-plane retardation (Re) of the optical compensation film of this invention ranges from about 80nm to about 300 nm at the wavelength (λ) 550 nm. In a further aspect, the optical compensation film in accordance with this invention is a quarter wave plate having in-plane retardation (Re) of about 100-160 nm at the wavelength (λ) 550 nm and having a normal in-plane dispersion characteristic. For purposes of this application, the term “quarter wave plate” includes Re values ranging from about (0.7) (λ/4) to about (1.3) (λ/4), or about (0.8) (λ/4) to about (1.2) (A/4), or from about (0.85) (λ/4) to about(1.15) (λ/4), or from about (0.9) (λ/4) to about (1.1) (λ/4).
Besides having a normal in-plane dispersion characteristic, the optical film of the present invention is capable of providing a low out-of-plane retardation (Rth) value. The low Rth is desirable since it can increase the viewing angle and improve the quality of an image. Thus, this invention further provides a wide-view optical film having an out-of-plane retardation (Rth) that satisfies the equation of |Rth|<100 nm, or <80 nm, or <50 nm, or <30 nm, or <10 nm, or <5 nm throughout the wavelength range of about 400 nm to about 800 nm. The term “|Rth|” means the absolute value of the out-of-plane retardation value Rth.
This wide-view feature due to the low Rth characteristic of the optical film, when combined with the normal dispersion characteristic of the present invention, will provide a wide-view circular polarizer when used in combination with a linear polarizer. Such a circular polarizer can be used in a 3D glasses device to improve the viewing quality. The present invention may be used for example in 3D glasses for stereoscopic display devices such as those shown in U.S. Pat. Nos. 8,228,449, 8,310,528, 8,370,873, and 8,233,103.
Thus, this invention further provides a circular polarizer comprising a linear polarizer and a quarter wave plate of the present invention. In another embodiment, there is provided 3D glasses comprising a circular polarizer of the present invention.
Cellulose esters can be prepared by conventional methods by contacting the cellulose solution with one or more C1-C20 acylating reagents at a contact temperature and contact time sufficient to provide a cellulose ester with the desired degree of substitution (DS) and degree of polymerization (DP). The cellulose esters thus prepared generally comprise the following structure:
wherein R2, R3, R6 are hydrogen, with the proviso that R2, R3, R6 are not hydrogen simultaneously, or C1-C20 straight- or branched-chain alkyl or aryl groups bound to the cellulose via an ester linkage. Thus, a cellulose ester can have a DS up to 3. When a cellulose ester has a DS<3, it has unreacted hydroxyl groups. The degree of un-substituted OH is customary expressed as DSOH.
The cellulose esters suitable for the present invention have a total degree of substitution of the acyl groups DSacyl from about 1.5 to about 3.0 (or DSOH=0-1.5), preferably from about 2 to about 2.9 (or DSOH=0.1-1.0), and more preferably from about 2.5 to about 2.8 (or DSOH=0.15-0.5). Further examples of cellulose esters suitable for the present invention include cellulose acetate propionates having a degree of substitution of acetate, DSAc, ranging from about 0.13 to about 2.34, a degree of substitution of propionate, DSPr, ranging from about 0.85 to about 2.50, and a degree of substitution of hydroxyl, DSOH, ranging from about 0.32 to about 1.08. Further examples of cellulose esters suitable for the present invention include cellulose acetate butyrate having a degree of substitution of acetate, DSAc, ranging from about 0.13 to about 2.34, a degree of substitution of butyrate, DSBu, ranging from about 0.85 to about 2.50, and a degree of substitution of hydroxyl, DSOH, ranging from about 0.32 to about 1.08. Further examples of cellulose esters suitable for the present invention include cellulose acetate having a degree of substitution of acetate, DSAc and a degree of substitution of hydroxyl, DSOH, ranging from about 0.16 to about 0.56.
The cellulose esters suitable for the present invention have an inherent viscosity of greater than about 0.5 dL/g, or from about 0.7 to about 1.9 dL/g, or from about 0.8 to about 1.9 dL/g or from about 0.8 to about 1.5 dL/g, or about 0.8 to about 1.2 dL/g.
The preferred acylating reagents are one or more C1-C20 straight- or branched-chain alkyl or aryl carboxylic anhydrides, carboxylic acid halides, diketene, or acetoacetic acid esters. Examples of carboxylic anhydrides include, but are not limited to, acetic anhydride, propionic anhydride, butyric anhydride, isobutyric anhydride, valeric anhydride, hexanoic anhydride, 2-ethylhexanoic anhydride, nonanoic anhydride, lauric anhydride, palmitic anhydride, stearic anhydride, benzoic anhydride, substituted benzoic anhydrides, phthalic anhydride, and isophthalic anhydride. Examples of carboxylic acid halides include, but are not limited to, acetyl, propionyl, butyryl, hexanoyl, 2-ethylhexanoyl, lauroyl, palmitoyl, benzoyl, substituted benzoyl, and stearoyl chlorides. Examples of acetoacetic acid esters include, but are not limited to, methyl acetoacetate, ethyl acetoacetate, propyl acetoacetate, butyl acetoacetate, and tert-butyl acetoacetate. The most preferred acylating reagents are C2-C9 straight- or branched-chain alkyl carboxylic anhydrides selected from the group acetic anhydride, propionic anhydride, butyric anhydride, 2-ethylhexanoic anhydride, nonanoic anhydride, and stearic anhydride.
Cellulose esters useful in the present invention can be prepared by any known method for preparing cellulose esters. Examples of randomly substituted cellulose esters having various DSOH are described in US application 2009/0096962, which is incorporated in its entirety in this invention.
The optical film of this invention can be made by solution casting or melt extrusion. The solution cast film is prepared by mixing the cellulose ester polymer (a) with the additive (b) in a solvent, followed by casting of the resulting solution on a substrate. The film is obtained after the removal of the solvent. In the melt extrusion method, the cellulose ester polymer solid is mixed with the additive, followed by the extrusion of the mixture at a temperature higher than the glass transition temperature of the polymer.
Further, to obtain certain in-plane retardation Re, the as-cast films are typically stretched. By adjusting the stretch conditions, such as, stretch temperature, stretch ratio, stretch type—uniaxial or biaxial, and controlling pre-heat time and temperature, post-stretch annealing time and temperature, the desired Re, Rth and normal optical dispersion can be achieved. The stretching temperature typically ranges from 130° C. to 200° C. The stretch ratio for MD typically ranges from 1.0 to 2.0. Pre-heat time typically ranges from 10 to 300 seconds, and pre-heat temperature is typically equal to stretch temperature. Post-annealing time typically ranges from 0 to 300 seconds, and post-annealing temperature typically ranges 10° C. to 40° C. below the stretching temperature.
In another embodiment of this invention, additives such as plasticizers, stabilizers, UV absorbers, antiblocks, slip agents, lubricants, dyes, pigments, retardation modifiers, etc. may optionally be mixed with the cellulose esters. Examples of these additives are found in US applications 2009/0050842, 2009/0054638, and 2009/0096962.
This invention can be further illustrated by the following examples of preferred embodiments thereof, although it will be understood that these examples are included merely for purposes of illustration and are not intended to limit the scope of the invention unless otherwise specifically indicated.
A solution of cellulose ester polymer was prepared by mixing a cellulose acetate propionate (45 g) having DS of acetate (DSAc)=0.18, DS of propionate (DSPr)=2.50, and DSOH=0.32 in a solvent blend, methylene chloride/ethanol (90/10 wt. %), 363 g, followed by the addition of the additive, 2-naphthyl benzoate, 4.45 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate using a doctor blade to obtain a film with the desired thickness. Casting was conducted in a fume hood by an automatic drawdown machine. The relative humidity of the hood was controlled at 40%-50%. After casting, the film was allowed to dry for 45 minutes under a cover pan to minimize the rate of solvent evaporation. After the pan was removed, the film was allowed to dry for 15 more minutes and subsequently peeled off from the glass. The free standing film thus obtained was annealed in a forced air oven at 100° C. for 10 minutes and then at 120° C. for another 10 minutes. The thickness of the resulting film was determined to be ranging from 78 to 84 microns by using PosiTector 6000 (DeFelsko Corporation).
A non-constrained uniaxial stretching method was used for film stretching. The film prepared above was mounted on a stretching machine (Karo IV laboratory film stretcher available from Brückner) equipped with a heating chamber. The film was pre-heated for 25 seconds to reach the stretching temperature of 150° C. and subsequently stretched in the machine direction (MD) at a speed of 7.0 mm/sec to a stretch ratio ranging from 1.47 to 1.50. The transverse direction (TD) was left un-constrained or freed. After stretching, the retardations (Rth and Re) of the cellulose ester films (CE-1) were measured by M-2000V Ellipsometer (J. A. Woollam Co.). The results from various stretching conditions are listed in Table 1, which shows the representative retardations at the wavelength 589 nm, Re(589) and Rth(589), and the values of Re(450)/Re(550) and Re(650)/Re(550).
A solution of cellulose ester polymer was prepared by mixing a cellulose acetate (45 g) having DSAc=2.84, DSOH=0.16 in a solvent blend, methylene chloride/ethanol (92/8 wt. %), 357 g, followed by the addition of the additive, 2-naphthyl benzoate, 3.65 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate as described in Example 1 to obtain a film with the desired thickness. The resulting film (CE-2) was stretched according to Example 1 at various temperatures to a stretch ratio ranging from 1.25 to 1.40. The results are listed in Table 2.
A solution of cellulose ester polymer was prepared by mixing a cellulose acetate propionate (48 g) having DSAc=1.59, DSPr=0.85, DSOH=0.56 in a solvent blend, methylene chloride/ethanol (90/10 wt. %), 352 g, followed by the addition of the additive, naphthalene, 4.8 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate as described in Example 1 to obtain a film with the desired thickness. The resulting film (CE-3) was stretched according to Example 1 at 160° C. to a stretch ratio ranging from 1.06 to 1.08. The results are listed in Table 3.
A solution of cellulose ester polymer was prepared by mixing a cellulose acetate (43.2 g) having DSAc=2.44, DSOH=0.56 in a solvent blend, methylene chloride/ethanol (90/10 wt. %), 352 g, followed by the addition of the additive, 2-naphthyl benzoate, 4.8 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate as described in Example 1 to obtain a film with the desired thickness. The resulting film (CE-4) was stretched according to Example 1 at various temperatures to a stretch ratio ranging from 1.06 to 1.08. The results are listed in Table 4.
A solution of cellulose ester polymer was prepared by mixing a cellulose acetate propionate (43.2 g) having DSAc=0.17, DSPr=1.75, DSOH=1.08 in a solvent blend, methylene chloride/ethanol (87/13 wt. %), 352 g, followed by the addition of the additive, 2-naphthyl benzoate, 4.8 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate as described in Example 1 to obtain a film with the desired thickness. The resulting film (CE-5) was stretched according to Example 1 at 160° C. to a stretch ratio of 1.05 and 1.10 respectively. The results are listed in Table 5.
This example illustrates the effect of a cellulose ester film without the inventive additive on the wavelength dispersion. A solution of cellulose ester polymer was prepared according to Example 1 using the same cellulose ester but without the addition of 2-naphthyl benzoate. Film was cast accordingly from the solution. The film (CE-6) was stretched at 165° C. to a stretch ratio ranging from 1.50 to 1.80. The results are listed in Table 6. As indicated by the values of Re(450)/Re(550) and Re(650)/Re(550), the film yielded steep reversed dispersion curves after stretching. Further, a desirable Re cannot be obtained even with high stretch ratios.
This example illustrates the effect of a non-inventive additive on the wavelength dispersion. A solution of cellulose ester polymer was prepared by mixing a cellulose acetate propionate (43.2 g) having DSAc=0.17, DSPr=1.78, DSOH=1.05 in a solvent blend, methylene chloride/ethanol (87/13 wt. %), 373 g, followed by the addition of the additive, triacetin, 7.62 g. The resulting mixture was placed on a roller for 24 hours to yield a uniform solution.
The solution prepared above was cast onto a glass plate as described in Example 1 to obtain a film with the desired thickness. The resulting film (CE-7) was stretched according to Example 1 at 175° C. to a stretch ratio ranging from 1.40 to 1.45. The results are listed in Table 7. As indicated by the values of Re(450)/Re(550) and Re(650)/Re(550), the film yielded reversed dispersion curves after stretching.
In the drawings and specification, there have been disclosed typical preferred embodiments of the invention and, although specific terms are employed, they are used in a generic and descriptive sense only and not for purposes of limitation, the scope of the invention being set forth in the following claims.
This application is a continuation of U.S. patent application Ser. No. 14/108,810, filed on Dec. 17, 2013, the disclosure of which is incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14108810 | Dec 2013 | US |
| Child | 15064061 | US |
