Electro-optic displays, and materials for use therein

a technology applied in the field of optical displays and materials, can solve the problems of inadequate service life of optical displays, preventing their widespread use, and gas-based electrophoretic media exhibiting the same types of problems

a technology applied in the field of optical displays and materials, can solve the problems of inadequate service life of optical displays, preventing their widespread use, and gas-based electrophoretic media exhibiting the same types of problems

US20110164301A1Inactive Publication Date: 2011-07-07E INK CORPORATION

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  • Electro-optic displays, and materials for use therein
  • Electro-optic displays, and materials for use therein
  • Electro-optic displays, and materials for use therein

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0107]Three different commercially available PEG's (with number average molecular weights, Mn of 300, 1000, and 8000 g / mole respectively, purchased from Aldrich Chemical) were used at a concentration of 4400 ppm in a custom polyurethane adhesive. The concentration of 4400 ppm corresponds a molar concentration of 5.17×10−6 for PEG-300, 1.55×10−6 for PEG-1000, and 1.94×10−7 for PEG-8000. To provide experimental samples closely simulating an encapsulated electrophoretic display, each polyurethane / PEG mixture was coated at a thickness of 30±2 μm on to a 7 mil (177 μm) poly(ethylene terephthalate) (PET) film coated with ITO, the mixture being coated on to the ITO-covered surface of the film. To provide experimental test units suitable for use in these experiments, pieces of the resultant adhesive-coated film were then laminated at 120° C. and 65 psig (approximately 0.5 mPa) at a speed of 6 inches / minute (approximately 2.5 mm / sec) to a 5 cm by 5 cm PET film covered with a carbon black lay...

example 2

[0110]As already mentioned, the addition of low molecular weight hydroxyl-containing polymers improves the variation of the volume resistivity of polyurethane adhesives with temperature in a manner which the addition of salts does not. A second series of experiments were conducted to illustrate this behavior. Test units were prepared and conditioned in the same way as in Example 1 except that the conditioning was performed for a minimum of only 100 hours, and that the test units contained only no additive, 4400 ppm of tetrabutylammonium hexafluorophosphate, or 166 or 2658 ppm of PEG-300. Volume resistivity measurements were then conducted at temperatures from −5° C. to 50° C., in all cases at 30 percent relative humidity. The results are shown in FIG. 1 of the accompanying drawings; no error bars are shown in this Figure since experimental error is in general less than the size of the symbols used to mark the data points.

[0111]From FIG. 1, it will be seen that the volume resistivity...

example 3

Cross-Linking of Polyurethane Adhesive with N,N-diglycidyl Aniline

[0169]A custom aqueous polyurethane dispersion having a solids content of about 35 percent by weight was coated on to a release sheet and dried in a conveyor oven at 60° C. for approximately 2 minutes, the coating weight of the dispersion being controlled so that an adhesive layer 15 μm thick was formed on the release sheet. To demonstrate the effect of a thermally-activated cross-linking agent, the dispersion used contained 20,000 ppm (based upon the solids content of the dispersion) of N,N-diglycidyl aniline (DGA).

[0170]The resultant adhesive layer was peeled from the release sheet and folded into multiple thicknesses to provide an adhesive layer sufficiently thick for shear modulus testing, which was conducted on a Dynamic Mechanical Analyzer, Model RH2000. A sample of the adhesive was exposed to a temperature of 60° C. for a period of 1000 minutes, then its temperature was raised successively to 70, 80 and 90° C.,...

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Abstract

A first electro-optic display comprises first and second substrates, and an adhesive layer and a layer of electro-optic material disposed between the first and second substrates, the adhesive layer comprising a mixture of a polymeric adhesive material and a hydroxyl containing polymer having a number average molecular weight not greater than about 5000. A second electro-optic display is similar to the first but has an adhesive layer comprising a thermally-activated cross-linking agent to reduce void growth when the display is subjected to temperature changes. A third electro-optic display, intended for writing with a stylus or similar instrument, is produced by forming a layer of an electro-optic material on an electrode; depositing a substantially solvent-free polymerizable liquid material over the electro-optic material; and polymerizing the polymerizable liquid material.

Description

REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation-in-part of copending application Ser. No. 12 / 046,126, filed Mar. 11, 2008 (Publication No. 2008 / 0218839), which is itself a continuation-in-part of application Ser. No. 11 / 613,259, filed Dec. 20, 2006 (Publication No. 2007 / 0097489, now U.S. Pat. No. 7,349,148, issued Mar. 25, 2008), which is itself a divisional of application Ser. No. 10 / 904,351, filed Nov. 5, 2004 (now U.S. Pat. No. 7,173,752, issued Feb. 6, 2007), which claims benefit of Application Ser. No. 60 / 481,600, filed Nov. 5, 2003, of Application Ser. No. 60 / 481,605, filed Nov. 6, 2003, and of Application Ser. No. 60 / 481,787, filed Dec. 14, 2003.[0002]This application is also a continuation-in-part of copending International Application No. PCT / US2009 / 036756, filed Mar. 11, 2009 (Publication No. WO 2009 / 151675), which claims priority of the aforementioned application Ser. No. 12 / 046,126.[0003]This application is related to:[0004](a) application Ser. ...

Claims

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Application Information

Patent Timeline
07 Jul 2011
Publication
US20110164301A1
IPC
G02F1/01; B32B37/12; B32B37/14; B32B38/10; G02F1/167; G02F1/16757
CPC
C08J7/16; G02F2202/28; G02F1/167; G02F1/061; G02F1/16757; G02F2001/1678; G02F1/13306; G02F2202/022
Inventors
PAOLINI, JR., RICHARD J.; MCCREARY, MICHAEL D.