Electro-optic displays comprise a layer of electro-optic material, a term which is used herein in its conventional meaning in the art to refer to a material having first and second display states differing in at least one optical property, the material being changed from its first to its second display state by application of an electric field to the material. The optical property is typically color perceptible to the human eye, but may be another optical property, such as optical transmission, reflectance, luminescence or, in the case of displays intended for machine reading, pseudo-color in the sense of a change in reflectance of electromagnetic wavelengths outside the visible range.

The electro-optic displays of the present invention typically contain an electro-optic material which is a solid in the sense that the electro-optic material has solid external surfaces, although the material may, and often does, have internal liquid-or gas-filled spaces, and to methods for assembling displays using such an electro-optic material. Such displays using solid electro-optic materials may hereinafter for convenience be referred to as"solid electro-optic displays".

Thus, the term"solid electro-optic displays"includes encapsulated electrophoretic displays, microcell electrophoretic displays and encapsulated liquid crystal displays.

One type of electro-optic display is the rotating bichromal member type as described, for example, in U. S. Patents Nos. 5, 808, 783 ; 5,777, 782 and 5.760, 761 (this type of electro-optic medium is often referred to as a"rotating

bichromal ball"medium, but the term"rotating bichromal member"is preferred since in some versions of the medium the rotating members are not spherical).

Another type of electro-optic medium is an electrochromic medium, for example an electrochromic medium in the form of a nanochromic film comprising an electrode formed at least in part from a semi-conducting metal oxide and a plurality of dye molecules capable of reversible color change attached to the <BR> <BR> electrode; see, for example O'Regan, B. , et al., Nature 1991,353, 737; and Wood,<BR> D. , Information Display, 18 (3), 24 (March 2002). See also Bach, U. , et al., Adv.<BR> <P>Mater. , 2002,14 (11), 845. Nanochromic films of this type are also described, for example, in International Applications Publication Nos. WO 98/35267 and WO 01/27690, and in copending Applications Serial Nos., 60/365,368 ; 60/365,369 ; 60/365,385 and 60/365,365, all filed March 18, 2002, and Applications Serial Nos.

60/319,279 ; 60/319, 280; and 60/319,281, all filed May 31,2002.

Another type of electro-optic display, which has been the subject of intense research and development for a number of years, is the particle-based electrophoretic display, in which a plurality of charged particles move through a suspending fluid under the influence of an electric field. Electrophoretic displays can have attributes of good brightness and contrast, wide viewing angles, state bistability, and low power consumption when compared with liquid crystal displays. Nevertheless, problems with the long-term image quality of these displays have prevented their widespread usage. For example, particles that make up electrophoretic displays tend to settle, resulting in inadequate service-life for these displays.

Numerous patents and applications assigned to or in the names of the Massachusetts Institute of Technology (MIT) and E Ink Corporation have recently been published describing encapsulated electrophoretic media. Such encapsulated media comprise numerous small capsules, each of which itself comprises an internal phase containing electrophoretically-mobile particles suspended in a liquid suspension medium, and a capsule wall surrounding the internal phase. Typically, the capsules are themselves held within a polymeric

binder to form a coherent layer positioned between two electrodes. Encapsulated media of this type are described, for example, in U. S. Patents Nos. 5,930, 026; 5,961, 804; 6,017, 584 ; 6,067, 185; 6,118, 426; 6,120, 588; 6,120, 839 ; 6,124, 851; 6,130, 773; 6,130, 774; 6,172, 798; 6,177, 921; 6,232, 950; 6,241, 921; 6,249, 271; 6,252, 564; 6,262, 706; 6,262, 833; 6,300, 932; 6,312, 304; 6,312, 971; 6,323, 989; 6, 327, 072; 6,376, 828; 6,377, 387; 6,392, 785; 6,392, 786; and 6,413, 790; U. S. Patent Applications Publication Nos. 2001-0045934; 2002-0018042; 2002-0019081 ; 2002-0021270; 2002-0053900; and 2002-0060321; and International Applications Publication Nos. WO 97/04398; WO 98/03896; WO 98/19208; WO 98/41898; WO 98/41899; WO 99/10767; WO 99/10768 ; WO 99/10769; WO 99/47970; WO 99/53371 ; WO 99/53373; WO 99/56171 ; WO 99/59101; WO 99/67678 ; WO 00/03349; WO 00/03291; WO 00/05704; WO 00/20921; WO 00/20922; WO 00/20923; WO 00/26761; WO 00/36465; WO 00/36560; WO 00/36666 ; WO 00/38000; WO 00/38001; WO 00/59625; WO 00/60410; WO 00/67110; WO 00/67327 WO 01/02899 ; WO 01/07691 ; WO 01/08241 ; WO 01/08242 ; WO 01/17029 ; WO 01/17040 ; WO 01/17041 ; WO 01/80287 and WO 02/07216.

Many of the aforementioned patents and applications recognize that the walls surrounding the discrete microcapsules in an encapsulated electrophoretic medium could be replaced by a continuous phase, thus producing a so-called polymer-dispersed electrophoretic display in which the electrophoretic medium comprises a plurality of discrete droplets of an electrophoretic fluid and a continuous phase of a polymeric material, and that the discrete droplets of electrophoretic fluid within such a polymer-dispersed electrophoretic display may be regarded as capsules or microcapsules even though no discrete capsule membrane is associated with each individual droplet; see for example, WO 01/02899, at page 10, lines 6-19. See also International Application PCT/US02/06393.

An encapsulated electrophoretic display typically does not suffer from the clustering and settling failure mode of traditional electrophoretic devices and provides further advantages, such as the ability to print or coat the display on a

wide variety of flexible and rigid substrates. (Use of the word"printing"is intended to include all forms of printing and coating, including, but without limitation: pre-metered coatings such as patch die coating, slot or extrusion coating, slide or cascade coating, curtain coating; roll coating such as knife over roll coating, forward and reverse roll coating; gravure coating; dip coating; spray coating; meniscus coating; spin coating; brush coating; air knife coating; silk screen printing processes; electrostatic printing processes; thermal printing <BR> <BR> processes; ink jet printing processes; and other similar techniques. ) Thus, the resulting display can be flexible. Further, because the display medium can be printed (using a variety of methods), the display itself can be made inexpensively.

A related type of electrophoretic display is a so-called"microcell electrophoretic display". In a microcell electrophoretic display, the charged particles and the suspending fluid are not encapsulated within microcapsules but instead are retained within a plurality of cavities formed within a carrier medium, typically a polymeric film. See, for example, International Applications Publication No. WO 02/01281, and published US Application No. 2002-0075556,. both assigned to Sipix Imaging, Inc.

Other types of electro-optic materials, for example, polymer- dispersed liquid crystal, may also be used in the displays of the present invention.

In addition to the layer of electro-optic material, an electro-optic display normally comprises at least two other layers disposed on opposed sides of the electro-optic material, one of these two layers being an electrode layer. In most such displays both the layers are electrode layers, and one or both of the electrode layers are patterned to define the pixels of the display. For example, one electrode layer may be patterned into elongate row electrodes and the other into elongate column electrodes running at right angles to the row electrodes, the pixels being defined by the intersections of the row and column electrodes. Alternatively, and more commonly, one electrode layer has the form of a single continuous electrode and the other electrode layer is patterned into a matrix of pixel electrodes, each of which defines one pixel of the display. In another type of electro-optic display,

which is intended for use with a stylus, print head or similar movable electrode separate from the display, only one of the layers adjacent the electro-optic layer comprises an electrode, the layer on the opposed side of the electro-optic layer typically being a protective layer intended to prevent the movable electrode damaging the electro-optic layer.

The manufacture of a three-layer electro-optic display normally involves at least one lamination operation. For example, in several of the aforementioned MIT and E Ink patents and applications, there is described a process for manufacturing an encapsulated electrophoretic display in which an encapsulated electrophoretic medium comprising capsules in a binder is coated on to a flexible substrate comprising indium-tin-oxide or a similar conductive coating (which acts as an one electrode of the final display) on a plastic film, the capsules/binder coating being dried to form a coherent layer of the electrophoretic medium firmly adhered to the substrate. Separately, a backplane, containing an array of pixel electrodes and an appropriate arrangement of conductors to connect the pixel electrodes to drive circuitry, is prepared. To form the final display, the substrate having the capsule/binder layer thereon is laminated to the backplane using a lamination adhesive. (A very similar process can be used to prepare an electrophoretic display useable with a stylus or similar movable electrode by replacing the backplane with a simple protective layer, such as a plastic film, over which the stylus or other movable electrode can slide. ) In one preferred form of such a process, the backplane is itself flexible and is prepared by printing the pixel electrodes and conductors on a plastic film or other flexible substrate. The obvious lamination technique for mass production of displays by this process is roll lamination using a lamination adhesive. Similar manufacturing techniques can be used with other types of electro-optic displays. For example, a microcell electrophoretic medium or a rotating bichromal member medium may be laminated to a backplane in substantially the same manner as an encapsulated electrophoretic medium.

In the processes described above, the lamination of the substrate carrying the electro-optic layer to the backplane may advantageously be carried out by vacuum lamination. Vacuum lamination is effective in expelling air from between the two materials being laminated, thus avoiding unwanted air bubbles in the final display; such air bubbles may introduce undesirable artifacts in the images produced on the display. (As discussed below, it may be desirable to produce the final lamination adhesive by blending multiple components. If this is done, it may be advantageous to allow the blended mixture to stand for some time before use to <BR> <BR> allow bubbles produced during blending to disperse. ) However, vacuum lamination of the two parts of an electro-optic display in this manner imposes stringent requirements upon the lamination adhesive used, especially in the case of a display using an encapsulated electrophoretic medium. The lamination adhesive must have sufficient adhesive strength to bind the electro-optic layer to the layer (typically an electrode layer) to which it is to be laminated. The lamination adhesive must have adequate flow properties at the lamination temperature to ensure high quality lamination, and in this regard, the demands of laminating encapsulated electrophoretic and some other types of electro-optic media are unusually difficult; the lamination has be conducted at a temperature of not more than about 110°C since the medium cannot be exposed to substantially higher temperatures without damage, but the flow of the adhesive must cope with the relatively uneven surface of the capsule-containing layer, the surface of which is rendered irregular by the underlying capsules. The lamination temperature should indeed be kept as low as possible, and room temperature lamination would be ideal, but no commercial adhesive has been found which permits such room temperature lamination. The lamination adhesive must be chemically compatible with all the other materials in the display. Solvent-based lamination adhesives should be avoided; it has been found (although this does not appear to have been described in the literature), that any solvent left behind in the adhesive after lamination has a strong tendency to introduce undesirable contaminants into the electro-optic medium.

It has also been found that a lamination adhesive used in an electro- optic display must meet a variety of electrical criteria, and this introduces considerable problems in the selection of the lamination adhesive. Commercial manufacturers of lamination adhesives naturally devote considerable effort to ensuring that properties, such as strength of adhesion and lamination temperatures, of such adhesives are adjusted so that the adhesives perform well in their major applications, which typically involve laminating polymeric and similar films.

However, in such applications, the electrical properties of the lamination adhesive are not relevant, and consequently the commercial manufacturers pay no heed to such electrical properties. Indeed, the present inventors have observed substantial variations (of up to several fold) in certain electrical properties between different batches of the same commercial lamination adhesive, presumably because the manufacturer was attempting to optimize non-electrical properties of the lamination adhesive (for example, resistance to bacterial growth) and was not at all concerned about resulting changes in electrical properties.

However, in electro-optic displays, in which the lamination adhesive is normally located between the electrodes which apply the electric field needed to change the electrical state of the electro-optic medium, the electrical properties of the adhesive become crucial. As will be apparent to electrical engineers, the volume resistivity of the lamination adhesive becomes important, since the voltage drop across the electro-optic medium is essentially equal to the voltage drop across the electrodes, minus the voltage drop across the lamination adhesive. If the resistivity of the adhesive layer is too high, a substantial voltage drop will occur within the adhesive layer, requiring an increase in voltage across the electrodes. Increasing the voltage across the electrodes in this manner is undesirable, since it increases the power consumption of the display, and may require the use of more complex and expensive control circuitry to handle the increased voltage involved. On the other hand, if the adhesive layer, which extends continuously across the display, is in contact with a matrix of electrodes, as in an active matrix display, the volume resistivity of the adhesive layer should not

be too low, or lateral conduction of electric current through the continuous adhesive layer may cause undesirable cross-talk between adjacent electrodes.

Also, since the volume resistivity of most materials decreases rapidly with increasing temperature, if the volume resistivity of the adhesive layer is too low, the performance of the display at temperatures substantially above room temperature is adversely affected. For these reasons, there is an optimum range of lamination adhesive resistivity values for use with any given electro-optic medium, this range varying with the resistivity of the electro-optic medium. The volume resistivities of encapsulated electrophoretic media are typically around 101° ohm cm, and the resistivities of other electro-optic medium are usually of the same order of magnitude. Accordingly, the volume resistivity of the lamination adhesive should normally be around 108 to 1012 ohm cm, and preferably about 109 to 10 ohm cm, at the operating temperature of the display, typically around 20°C.

While it may be apparent that there should be a relationship between the volume resistivities of the electro-optic medium and the lamination adhesive used in an electro-optic display, the present inventors have discovered that other problems which have been observed in the operation of electro-optic displays, but which have not previously been understood, are attributable to the electrical and related properties of the lamination adhesive. For example, although the number of commercial materials which can meet most of the previously discussed, rather disparate requirements for a lamination adhesive for use in an electro-optic display is small, in practice it has been found that a small number of water-dispersed urethane emulsions, primarily polyester-based urethane emulsions, do appear to have most of the requisite properties. However, although these materials perform well when the displays are first produced, after the resultant displays have been operated for substantial periods of time (of the order of hundreds of hours) at room temperature, or stored for a similar period, the performance of the display suffers substantial degradation. This degradation first manifests itself as reduced white state reflectivity and slower or incomplete switching of the electro-optic medium, especially in areas where the lamination

adhesive is thickest; the thickness of the lamination adhesive may vary across the display both because of a non-planar electro-optic layer, as for example in an encapsulated electrophoretic medium where the spherical or ellipsoidal capsules introduce deviations from planarity, and/or because the manufacturing process normally used to produce the electrode matrix in such displays produces a non- planar surface on the electrode matrix. This degradation increases at lower temperatures (10°C or below) and with time, so that after long periods the switching of the whole display is affected at room temperature. This degradation in optical performance with time is an important factor in limiting the service life of the displays.

The present inventors have discovered that the aforementioned degradation in performance is caused, at least in part, by changes in the volume resistivity of the lamination adhesive, and that this performance degradation of electrophoretic displays can be reduced or eliminated, and the service life of such displays increased, by using an adhesive the resistivity of which does not vary greatly with time; it appears that similar effects are produced in other types of electro-optic displays. The use of such an adhesive has also been found to improve the performance of the displays at low temperature, as manifested by improved reflectance in the light optical state of the display.

Accordingly, in one aspect the present invention seeks to provide electro-optic displays having optical characteristics which do not change rapidly with time, so that the displays have an improved operating lifetime.

Other problems known to occur in electro-optic displays, but which have not previously been explained, include degradation of the performance of the display with increasing temperature, even when the display is first produced, as manifested, inter alia, by a reduction in the contrast ratio of the display (the relative reflectance or optical transmission of the two extreme optical states of the display) with increasing temperature, the similar degradation of the performance of the display with increasing humidity, and the phenomenon known as"self-erasing".

See, for example, Ota, I., et al. ,"Developments in Electrophoretic Displays",

Proceedings of the SID, 18,243 (1977), where self-erasing was reported in an unencapsulated electrophoretic display. When the voltage applied across certain electrophoretic displays is switched off, the electrophoretic medium may reverse its optical state, and in some cases a reverse voltage, which may be larger than the operating voltage, can be observed to occur across the electrodes. It appears (although this invention is in no way limited by this belief) that the self-erasing phenomenon is due to a mismatch in electrical properties between various components of the display. Obviously, self-erasing is highly undesirable in that it reverses (or otherwise distorts, in the case of a grayscale display) the desired optical state of the display. It has been found that all of these problems may be attributable, at least in part, to changes in the electrical properties of the lamination adhesives with various environmental conditions, and that all can be reduced or eliminated by careful selection of the properties of the lamination adhesives used.

Accordingly, the present invention also seeks to provide lamination adhesives that can be used in the lamination of electro-optic displays at relatively low temperatures which do not adversely affect the electro-optic medium.

The present invention also seeks to provide an electro-optic display with a lamination adhesive having optimal mechanical properties.

The present invention also seeks to provide an electro-optic display with a lamination adhesive having optimal electrical properties.

In summary, the present invention seeks to provide a lamination adhesive with combined manufacturing, mechanical, electrical, environmental, chemical and temporal stability properties optimally suited for use in electro-optic displays.

The present invention also seeks to provide a novel polyurethane composition having properties which render it very suitable for use as a lamination adhesive in electro-optic displays.

Accordingly, in one aspect this invention provides an electro-optic display comprising first and second substrates and a lamination adhesive layer and a layer of a solid electro-optic material disposed between the first and second

substrates. The lamination adhesive layer has a volume resistivity, measured at 10°C, which does not change by a factor of more than 3 after being held at 25°C and 45 per cent relative humidity for 1000 hours. This form of the invention may hereinafter for convenience be referred to as the"resistivity stability"invention.

This invention also provides a process for preparing an electro-optic display. In this process, there is provided a first subassembly comprising an electro-optic layer and a first substrate, and a second subassembly comprising a second substrate, at least one of the subassemblies comprising an electrode. The two subassemblies are laminated to one another using a lamination adhesive so that the electro-optic layer is disposed between the first and second substrates, the lamination adhesive having a volume resistivity, measured at 10°C, which does not change by a factor of more than 3 after being held at 25°C and 45 per cent relative humidity for 1000 hours.

This invention also provides an electro-optic display comprising first and second substrates, and a lamination adhesive layer and a layer of solid electro-optic material disposed between the first and second substrates. The lamination adhesive has any one or more of the following properties: (a) having a volume resistivity, measured at 10°C, which does not change by a factor of more than 3 after being at 25°C and 45 per cent relative humidity for 1000 hours; (b) having a peel strength from an electrode material in contact with the lamination adhesive of at least 2 lb/inch ; (c) the volume resistivity of the lamination adhesive changes by a factor of less than 10 within a range of 10 to 90 per cent relative humidity and over a temperature range of 10 to 50°C ; (d) the lamination adhesive has a thickness in the range of 10 to 20 m ; (e) the lamination adhesive has a shear modulus at 120°C of not more than 1 megaPascal ;

(f) the product of the dielectric constant and the volume resistivity of the lamination adhesive is not greater than the product of the dielectric constant and the volume resistivity of the electro-optic medium within a range of 10 to 90 per cent relative humidity and over a temperature range of 10 to 50°C ; (g) comprising an ultra-violet stabilizer; (h) comprising a light absorbing material.

This invention also provides a process for preparing an electro-optic display. In this process, there is provided a first subassembly comprising an electro-optic layer and a first substrate, and a second subassembly comprising a second substrate, at least one of the subassemblies comprising an electrode. The two subassemblies are laminated to one another using a lamination adhesive so that the electro-optic layer is disposed between the first and second substrates. The lamination adhesive has any one or more of the properties listed in Paragraphs (a) to (h) above.

This invention also provides an electrophoretic display comprising first and second substrates, and a lamination adhesive layer and a layer of electrophoretic material disposed between the first and second substrates. The electrophoretic material comprises a plurality of capsules, each capsule comprising a capsule wall and an internal phase encapsulated within the capsule wall, the internal phase comprising electrically charged particles suspended in a suspending fluid and capable of moving through the fluid on application of an electric field to the electrophoretic material. The lamination adhesive has any one or more of the following properties : (i) the product of the dielectric constant and the volume resistivity of the lamination adhesive is from 0.01 to 100 times the product of the dielectric constant and the volume resistivity of the suspending fluid; (j) the ratio of the dielectric constant of the lamination adhesive to the dielectric constant of the suspending fluid within the temperature range of from 10 to 50°C does not vary from this ratio at 25°C by more than 2 per cent;

(k) the ratio of the volume resistivity of the lamination adhesive to the volume resistivity of the suspending fluid within the temperature range of from 10 to 50°C does not vary from this ratio at 25°C by more than a factor of 100; (1) the solubility of the suspending fluid in the lamination adhesive does not exceed 1 per cent weight/weight over the range of 10 to 50°C ; (m) being substantially free from mobile species.

This invention also provides a process for preparing an electrophoretic display. In this process there is provided a first subassembly comprising a first substrate and a layer of an electrophoretic medium comprising a plurality of capsules, each capsule comprising a capsule wall and an internal phase encapsulated within the capsule wall, the internal phase comprising electrically charged particles suspended in a suspending fluid and capable of moving through the fluid on application of an electric field to the electrophoretic medium, There is also provided a second subassembly comprising a second substrate ; at least one of the subassemblies comprises an electrode. The two subassemblies are laminated to one another with a lamination adhesive so that the electro-optic layer is disposed between the first and second substrates. The lamination adhesive has any one or more of the properties listed in Paragraphs (i) to (m) above.

Finally, this invention provides a microcell electrophoretic display comprising a substrate having a plurality of closed cavities formed therein, said cavities being at least partially filled with a electrophoretic medium comprising a plurality of electrically charged particles suspended in a suspending fluid and capable of moving therethrough on application of an electric field to the electrophoretic medium, the microcell electrophoretic display further comprising at least one electrode and a layer of lamination adhesive disposed between the cavities and the electrode. The lamination adhesive has any one or more of the properties listed in Paragraphs (a) to (m) above.

Figure 1 of the accompanying drawings is a schematic section through one subassembly used in a process of the present invention, this subassembly comprising a substrate, a conductive layer, an electro-optic layer and

an adhesive layer, the subassembly being illustrated at an intermediate stage of the process before this subassembly is laminated to a second subassembly; Figure 2 is a graph illustrating the improved stability on storage of the volume resistivity of a lamination adhesive achieved by blending two commercial materials, as described in Example 1 below; Figure 3 is a graph illustrating the improved stability on storage of the volume resistivity of a lamination adhesive achieved by blending two commercial materials, as described in Example 2 below; Figure 4 is a graph illustrating the improved stability on storage of the dielectric constant of lamination adhesives achieved by blending commercial materials, as described in Example 2 below; Figure 5 is a graph illustrating the improved stability on storage of the volume resistivity of lamination adhesives achieved by blending commercial materials, as described in Example 3 below; Figure 6 is a graph illustrating the improved stability on storage of the dielectric constant of lamination adhesives achieved by blending commercial materials, as described in Example 3 below; Figures 7 and 8 are graphs similar to Figures 5 and 6 respectively, but showing the results obtained in Example 4 below; Figures 9 and 10 are graphs similar to Figures 5 and 6 respectively, but showing the results obtained in Example 5 below; Figure 11 is a graph showing the improved stability of the white optical state with temperature of an electrophoretic display achieved using a lamination adhesive of the present invention, as described in Example 6 below; Figure 12 illustrates the synthetic scheme used in Example 7 below to produce certain polyurethanes preferred for use in the present invention; Figure 13 illustrates the chemical structure of certain materials used in Example 7 below; and Figures 14 and 15 list the reagents used to produce certain polyurethanes produced in Example 7 below.

Before describing the various aspects of the present invention in detail, it is considered desirable to explain in more detail the processes in which a lamination adhesive is used in the manufacture of an electro-optic display. As already explained, in a typical process, two subassemblies are first manufactured, one subassembly comprising an electro-optic layer and a first substrate, and the second comprising a second substrate; at least one of the subassemblies, and typically both, comprise an electrode. Also as already indicated, in one common form of such a process, used for manufacturing an active matrix display, one subassembly comprises a substrate, a single continuous ("common") electrode which extends across multiple pixels, and typically the whole, of the display, and the electro-optic layer, while the second assembly (usually referred to as the "backplane") comprises a substrate, a matrix of pixel electrodes, which define the individual pixels of the display, and non-linear devices (typically thin film transistors) and other circuitry used to produce on the pixel electrodes the potentials needed to drive the display (i. e. , to switch the various pixels to the optical states necessary to provide a desired image on the display). The lamination adhesive is provided between the first and second subassemblies and adheres them together to form the final display.

In theory, if one could find a lamination adhesive with the necessary physical and mechanical properties, one could bring the two assemblies and the lamination adhesive together and form the display in a single operation, for example by feeding the three components from separate rolls and performing the lamination on a roll-to-roll basis. However, in the present state of the art this is not practicable, and normally the lamination adhesive is first applied to one of the two subassemblies, and thereafter the subassembly/adhesive combination is laminated to the other subassembly to form the final display. The lamination adhesive may be applied to either subassembly, but in general it is preferred that it be applied to the subassembly containing the electro-optic medium. As already mentioned, certain electro-optic media can be applied by printing or coating techniques on rigid or flexible substrates, and hence can be applied to flexible substrates, such as

polymeric films, inexpensively by roll-to-roll processes. Coating an electro-optic medium on to a flexible substrate in this manner, then covering the electro-optic medium with a lamination adhesive and a release sheet, provides a so-called"front plane laminate"which can then be cut as desired to produce portions suitable for lamination to a wide variety of backplanes. Applying the lamination adhesive to the backplane tends to be less convenient (although the present invention does not exclude this possibility), since in the present state of technology most backplanes are prepared on rigid substrates which are in the form of individual sheets less convenient for coating.

Regardless of which subassembly receives the lamination adhesive, there are two main variants of the adhesive application process, namely direct and indirect processes. As described in more detail below, lamination adhesives are typically supplied as liquid or semi-solid solutions or dispersions, which need to be converted (either by removal of a solvent or dispersant or by some other form of curing) to a substantially solid layer before the actual lamination. In a direct process, the lamination adhesive is applied directly to one subassembly and converted to the solid layer thereon. In an indirect process, the lamination adhesive is applied to a release sheet, converted to a solid layer on this release sheet, and then transferred, typically using heat and/or pressure, to one subassembly. Finally, the release sheet is removed from the solid layer of lamination adhesive before the final lamination to the other subassembly. In general, indirect methods are preferred over direct, since many commercial lamination adhesives contain relatively mobile species, such as organic solvents and/or free monomers, which may adversely affect either the electro-optic medium or the circuitry of the backplane, depending upon the subassembly to which the adhesive is applied. An indirect process, by permitting these relatively mobile species to be removed by drying or similar processes while the lamination adhesive is still on the release sheet, avoids the adverse effects of bringing these relatively volatile materials into contact with the electro-optic medium or circuitry of the backplane.

A preferred lamination process of the present invention will now be described, though by way of illustration only, with reference to Figure 1 of the accompanying drawings, which, as already mentioned, is a schematic section through one subassembly (a front plane laminate, or FPL) used in a process of the present invention, this subassembly comprising a substrate, a conductive layer, an electro-optic layer and an adhesive layer, the subassembly being illustrated at an intermediate stage of the process before this subassembly is laminated to a second subassembly.

The front plane laminate (generally designated 100) shown in Figure 1 comprises a light-transmissive substrate 110, a light-transmissive electrode layer 120, an electro-optic layer 130, a lamination adhesive layer 180 and a release sheet 190 ; the release sheet is illustrated in the process of being removed from the lamination adhesive layer 180 preparatory to lamination of the FPL 100 to a backplane.

The substrate 110 is typically a transparent plastic film, such as a 7 mil (177 m) polyethylene terephthalate (PET) sheet. The lower surface (in Figure 1) of substrate 110, which forms the viewing surface of the final display, may have one or more additional layers (not shown), for example a protective layer to absorb ultra-violet radiation, barrier layers to prevent ingress of oxygen or moisture into the final display, and anti-reflection coatings to improve the optical properties of the display. Coated onto the upper surface of substrate 110 is the thin light- transmissive electrically conductive layer 120, preferably of indium tin oxide (ITO), which acts as the common front electrode in the final display. PET films coated with ITO are available commercially.

The electro-optic layer 130 is deposited on the conductive layer 120, typically by slot coating, the two layers being in electrical contact. The electro-optic layer 130 shown in Figure 1 is an encapsulated electrophoretic medium and comprises microcapsules 140, each of which comprises negatively charged white particles 150 and positively charged black particles 160 suspending in a hydrocarbon-based suspending fluid 165. The microcapsules 140 are held

retained within a polymeric binder 170. Upon application of an electrical field across electro-optic layer 130, white particles 150 move to the positive electrode and black particles 160 move to the negative electrode, so that electro-optic layer 130 appears, to an observer viewing the display through substrate 110, white or black depending on whether conductive layer 120 is positive or negative relative to the adjacent pixel electrode in the backplane.

The FPL 100 is desirably prepared by coating the lamination adhesive 180, in liquid form, conveniently by slot coating, on to release sheet 190, drying (or otherwise curing) the adhesive to form a solid layer and then laminating the adhesive and release sheet to the electro-optic layer 130, which has previously been coated on to the substrate 110 bearing the conductive layer 120; this lamination may conveniently be effected using hot roll lamination. (Alternatively, but less desirably, the lamination adhesive may be applied over the electro-optic layer 130 and there dried or otherwise cured before being covered with the release sheet 190. ) The release sheet 190 is conveniently a 7 mil (177 m) film; depending upon the nature of the electro-optic medium used, it may be desirable to coat this film with a release agent, for example a silicone. As illustrated in Figure 1, the release sheet 190 is peeled or otherwise removed from the lamination adhesive 180 before the FPL 100 is laminated to a backplane (not shown) to form the final display.

In the case of the preferred aqueous polyurethane dispersions for use in the present invention (see below) drying of the coating on the release sheet for about 10 minutes in air at 50°C typically gives a sufficiently dry coating.

Having thus summarized the way in which the lamination adhesive is used to form the electro-optic displays of the present invention, we now turn to describing in detail the preferred characteristics of the lamination adhesive itself.

As already mentioned, the present invention has several aspects, and any specific display of the invention may incorporate any one or more of these aspects.

However, for ease of comprehension, the following aspects of the invention will be described separately hereinafter:

(i) Storage stability; (ii) Light resistance and control ; (iii) Mechanical properties; (iv) Electrical properties; and (v) Physico-chemical properties.

It will readily be apparent that the optimum properties for the lamination adhesive used in an electro-optic display will vary somewhat with the exact type of electro-optic medium in the display, and the following discussion does not purport to specify an exhaustive list of such optimum properties for all types of electro-optic displays. However, the structure of an encapsulated electrophoretic display, in which electrically charged particles move through an internal phase which is itself confined by a capsule wall and (typically) a polymeric binder, does impose upon the lamination adhesive used in such an encapsulated electrophoretic display requirements in addition to those common to all electro-optic displays. In particular, certain of the optimum electrical properties are peculiar to encapsulated electrophoretic displays, as are the optimum physico- chemical properties discussed below. In this regard, depending upon the material in which the microcells are formed, microcell electrophoretic displays may typically impose substantially the same requirements as encapsulated electrophoretic displays, since both types of electrophoretic display use the same types of suspending fluids, and as discussed below the additional requirements for electrophoretic displays relate to relationships between the properties of the suspending fluid and the lamination adhesive.

Section (i): Resistivity stability As already mentioned, the present inventors have discovered that the degradation in performance of electro-optic displays with time is caused, at least in part, by changes in the volume resistivity of the lamination adhesive, and that this degradation can be reduced, and the service life of the displays increased, by using a lamination adhesive the volume resistivity of which does not vary greatly with time. In particular, the lamination adhesive should have a volume

resistivity, measured at 10°C, which does not change by a factor of more than 3 after being held at 25°C and 45 per cent relative humidity for 1000 hours.

The phrase"being held"is deliberately used to stress that, in testing lamination adhesives to determine whether they conform to the requirements of this aspect of the present invention, care should be taken to ensure that the lamination adhesive does equilibrate with the specified atmosphere within a reasonable time. If an adhesive is tested in thick layers, it may not equilibrate with the specified atmosphere for a considerable period and misleading results may be obtained. Such misleading results can be avoided by testing successively thinner layers of the adhesive and checking that the results are consistent. For sufficiently thin layers, merely storing the adhesive under the specified conditions for the specified period will suffice.

It is believed (although the invention is in no way limited by this belief) that the change in volume resistivity experienced in many lamination adhesives is due to partial crystallization of the adhesive, and that adhesives which meet the resistivity stability test defined above are substantially non-crystallizing.

Those skilled in polymer technology are of course aware that partial or complete crystallization of polymers occurs in a variety of contexts and often produces substantial changes in a variety of physico-chemical properties of the polymers.

Often, such changes can be reduced or eliminated by adding a plasticizer to the polymer. However, the addition of a plasticizer is usually not practicable in lamination adhesives used in electro-optic displays, since almost all conventional plasticizers are small molecules with substantial affinity for organic solvents, and the addition of such a material to the lamination adhesive will result in migration of the plasticizer into the electro-optic layer, with adverse effects upon the performance of that layer. Cf. the discussion below regarding the importance of avoiding mobile species in the lamination adhesive.

Alternative tests for non-crystallization, which in practice normally give substantially the same results as the resistivity stability test already defined, are a change in the enthalpy associated with any phase transition in the material, as

measured by differential scanning calorimetry, that is not more than 2 Joules per gram after being held at 25°C and 45 per cent relative humidity for 1000 hours, or a change in dielectric constant of less than 2 after the same period of storage.

Desirably, the lamination adhesive used in the present invention will meet all three tests.

The stable resistivity adhesive used in the present display and process could, at least in theory, be a single material, and indeed it may be possible, by custom design of polymers as discussed below, to produce a lamination adhesive which meets the resistivity stability requirement, as well as all the other requirements for a lamination adhesive for use in electro-optic displays, as discussed above. However, to date the present inventors have been unable to locate any commercial adhesive which itself meets the resistivity stability requirement and the other requirements. Accordingly, the presently preferred adhesives for use in the present invention are blends of two or more materials.

Such a blend may comprise one or more lamination adhesives and one or more polymeric additives which are not themselves lamination adhesives. However, in order to obtain the best lamination adhesion properties, it is preferred that the blend used comprise at least two lamination adhesives. Such a blend may comprise a mixture of a first lamination adhesive which has unstable resistivity (but which has other properties which render it desirable) and a second lamination adhesive which does have stable resistivity, but whose other properties, such as inadequate adhesion, render it unsuitable for use alone. However, it has been found that certain stable resistivity blends can be formed from two or more lamination adhesives which do not have stable resistivities, and some of the presently preferred adhesive blends are of this type.

It may seem strange that a stable resistivity blend can be formed from two or more lamination adhesives each of which individually does not possess stable resistivity; however, this is explicable given that unstable resistivity is believed to be associated with partial crystallization within the adhesive, and the present understanding of the partial crystallization of polymers. Although the

invention is in no way limited by this belief, skilled polymer chemists attribute partial crystallization of a polymer to the tendency for polymer chains to become aligned with one another, thus forming crystalline regions within the polymer. If two polymers, both of which are susceptible to the formation of such crystalline regions when in their pure form, but have somewhat different chemical structures, are blended, the two different polymer chains present in the blend may interfere with each other, preventing either type of polymer chain forming its crystalline regions, and thus rendering the blend non-crystallizing.

As should be apparent, it is desirable that the volume resistivity of the adhesive used in the present invention be as stable as possible throughout the working life of the display. However, empirically (as illustrated in the Examples in this Section) it has been found that the major part of the changes in volume resistivity of adhesives occurs during the first 1000 hours of life, so that a lamination adhesive which meets the stable resistivity test already mentioned will normally maintain a stable resistivity over a working life substantially greater than 1000 hours, and typically at least 10, 000 hours. It is desirable that the volume resistivity of the adhesive not change by a factor of more than 2, and preferably not greater than 1.5, under the 1000 hour test previously described.

Commercial lamination adhesives which have been found useful in the display and process of the present invention include NeoRez R 9000, R 9314 and R 9320 (all available from NeoResins, 730 Main Street, Wilmington, MA 01887) and Dispercoll U KA 8713, U 53 and U 54 (all available from Bayer Corporation, 100 Bayer Road, Pittsburgh PA 15205-9741). All of these materials are water-dispersed urethane adhesives. R 9320 is a non-ionically stabilized polyester-based urethane, while U KA 8713 is an anionically-stabilized polyester urethane. Specific preferred blends are R 9320 with any one of the following (the following percentages are based on the total weight of the blend): 25-50% of U KA 8713 50% of R 9000 10-50% of R 9314

25-50% of U 53 50% of U 54.

No special techniques are required for forming the blends ; the two or more components are simply mixed in conventional mixing equipment for a period sufficient to form an intimate mixture of the components. Attention must of course be paid to the chemical compatibility of the various components of the blend, especially the chemical compatibility of the dispersants present, since (as is well known to polymer chemists) admixing certain types of dispersants is highly likely to result in undesirable precipitation of the polymers.

Using a lamination adhesive with volume resistivity (and preferably other properties) which are stable upon long term storage also assists in ensuring economical manufacture of the display. As already discussed, for commercial reasons, it is convenient to prepare a front plane laminate of the form shown in Figure 1 comprising a substrate, a conductive layer, an electro-optic layer, a lamination adhesive and a release sheet; this front plane laminate may be prepared in large batches, preferably using a roll-to-roll process, stored and later cut into portions suitable for lamination to the backplanes of individual displays before lamination to form such displays. For economical operation of such a manufacturing process, it is necessary that the lamination adhesive remain stable during the storage period in order that portions may be cut from the large batch at different times over a period of (say) several months to one year and laminated in a consistent manner to the backplanes to form the final displays.

The following Examples are now given, though by way of illustration only, to show details of preferred materials, processes and techniques used in the stable resistivity invention.

Example 1 This Example illustrates the improved stability of the volume resistivity of the aforementioned R 9320 upon prolonged storage provided by blending the material with the aforementioned U KA 8713.

Test samples, using pure R 9320 and U KA 8713, and 90/10,75/25 and 50/50 w/w per cent blends of these two materials, were prepared in the following manner. The adhesive blend, adjusted to 40 % solids content, was coated, using a doctor blade set at 150 pm, on to a 5 mil (127, um) sheet of indium- <BR> <BR> tin-oxide (ITO) -coated polyester masked on one edge, so that the masked area could later serve as an electrode. The resultant coating was dried in an oven at 50°C for 20 minutes to produce a dry film approximately 60 urn thick. The resultant adhesive-coated film was then laminated, by vacuum or roll lamination, to a second sheet of ITO-coated polyester so that the adhesive was in contact with both ITO layers. The samples thus prepared were stored at ambient temperature and humidity for 2500 hours. The electrical properties of the adhesive were measured by impedance spectroscopy at 10°C at intervals using a Solartron SI 1260 Impedance/Gain-phase analyzer with a Solartron 1296 dielectric interface.

The results are shown in Figure 2 of the accompanying drawings. The horizontal line at 3 x 101° ohm cm represents an empirical limit for the maximum volume resistivity of a lamination adhesive useful in a preferred embodiment of an encapsulated electrophoretic display formed as described in the aforementioned E Ink and MIT patents and applications.

From Figure 2, it will be seen that the volume resistivities of both R 9320 and U KA 8713 changed substantially over the storage period, the volume resistivity of the former increasing from about 101° to about 9 x 101° ohm cm, while the latter rose from an initial 1 x 101° ohm cm to almost 5 x 101° ohm cm. In contrast, the volume resistivities of all three blends were substantially more stable over the test period, all falling within the range of about 1-1.5 x 101° ohm cm over the period of 500-2500 hours of storage.

Example 2 This Example illustrates the improved stability of the volume resistivity and dielectric constant of the aforementioned R 9320 upon prolonged storage provided by blending the material with the aforementioned R 9000.

Example 1 was repeated, except that R 9000 was substituted for U KA 8713, that the storage period was 4000 hours, and that the volume resistivity measurements were supplemented by measurements of the dielectric constant of the blends using the same impedance spectrometer as previously mentioned. The volume resistivity results are shown in Figure 3 of the accompanying drawings and the dielectric constant results in Figure 4.

From Figure 3, it will be seen that, although the volume resistivities of both R 9320 and R 9000 underwent substantial changes over the test period, the blends had much more stable resistivities. In particular, the performance of the 50/50 w/w blend was outstanding, displaying a variation by less than a factor of 2 throughout the storage period. Figure 4 shows that this same 50/50 w/w blend displayed essentially no variation in dielectric constant during the test period.

Example 3 This Example illustrates the improved stability of the volume resistivity and dielectric constant of the aforementioned R 9320 upon prolonged storage provided by blending the material with the aforementioned U 53. (U 53 is sold as an adhesive but has been found to give insufficient adhesive strength when used in the type of electrophoretic display used in these experiments.) Example 2 was repeated, except that the aforementioned U 53 was substituted for the R 9000 and that the storage period was 6000 hours. The volume resistivity results are shown in Figure 5 of the accompanying drawings and the dielectric constant results in Figure 6.

From Figure 5, it will be seen that the substantial changes in the volume resistivities of R 9320 over the test period were much less pronounced in the blends. In particular, the resistivities of the 75/25 and 50/50 w/w blends were within the acceptable range throughout the storage period. Similarly, Figure 6 shows that both the 75/25 and 50/50 w/w blends displayed acceptable variation in dielectric constant during the test period.

Example 4 This Example illustrates the improved stability of the volume resistivity and dielectric constant of the aforementioned R 9320 upon prolonged storage provided by blending the material with the aforementioned U 54. (U 54 is sold as an adhesive but has been found to give insufficient adhesive strength when used in the type of electrophoretic display used in these experiments.) Example 2 was repeated, except that the aforementioned U 54 was substituted for the R 9000 and that the storage period was 5500 hours. The volume resistivity results are shown in Figure 7 of the accompanying drawings and the dielectric constant results in Figure 8.

From Figure 7, it will be seen that the substantial changes in the volume resistivities of R 9320 over the test period were much less pronounced in the blends. In particular, the resistivities of the 75/25 and 50/50 w/w blends were within the acceptable range throughout the storage period. Similarly, Figure 8 shows that both the 75/25 and 50/50 w/w blends displayed acceptable variation in dielectric constant during the test period.

Example 5 This Example illustrates the improved stability of the volume resistivitOy and dielectric constant of the aforementioned R 9320 upon prolonged storage provided by blending the material with the aforementioned R 9314.

Example 2 was repeated, except that the aforementioned R 9314 was substituted for the R 9000 and that the storage period was 5000 hours. The volume resistivity results are shown in Figure 9 of the accompanying drawings and the dielectric constant results in Figure 10.

From Figure 9, it will be seen that the blends did not suffer from the sharp variations of resistivity with time characteristic of R 9320 (cf. Figures 5 and 7), and the resistivities at all times remained below the 3 x 101° ohm cm limit. The dielectric constant data in Figure 10 also show that all the blends were satisfactory.

Example 6 This Example illustrates the effect of a stable resistivity adhesive in improving the performance, and specifically the white state, of an electrophoretic display at low temperatures after prolonged storage.

Pure R 9320, and the 75/25 w/w R 9320/U KA 8713 blend mentioned in Example 1 above were used to prepare encapsulated dual particle electrophoretic displays substantially as described in Examples 27-29 of International Application No. PCT/US02/15337. The resultant displays, which have black and white optical states, were stored at ambient temperature and humidity (indoors) for three months and then tested by first driving the display to its black state, then applying to the electrodes of the display a 15 V, 600 msec electric pulse of a polarity which turned the black state to white, and finally measuring the reflectance of the white state at the end of this pulse. This test was repeated at temperatures from 5 to 45°C, and the results are shown in Figure 11.

From this Figure, it will be seen that the low temperature decline in reflectivity is much less marked with the blended adhesive than with the pure R 9320. If one reasonably assumes that satisfactory performance for this display requires a minimum white state reflectance of 30%, the R 9320 display had a minimum operating temperature of about 19°C, whereas the display using the blended adhesive had a minimum operating temperature of about 9°C.

Section (ii): Light resistance and control At first glance, it might appear that the effects of light (and other electromagnetic radiation, especially ultra-violet radiation) should not be of major concern in an electro-optic display, since, in the assembled display, the lamination adhesive is sandwiched between the electro-optic medium, which is normally considered opaque, and the backplane, which is also normally opaque. However, it has in fact been found that the effects of light upon the lamination adhesive are an important factor in producing a display with a long working lifetime and stable electro-optic properties during this lifetime. It is believed (although the invention is in no way limited by this belief) that most electro-optic media do in fact transmit

some portion of the light falling on the viewing surface through the electro-optic layer to the lamination adhesive, and that this transmitted light can cause changes in the lamination adhesive which adversely affect the working lifetime of the display and/or cause its electro-optic properties to vary with time.

Accordingly, it has been found advantageous for the lamination adhesive to contain an ultra-violet stabilizer, conveniently a hindered amine light stabilizer (HALS) such as those sold commercially under the Registered Trade Mark"TINUVIN". The optimum amount of such a stabilizer can readily be determined empirically, but will typically be in the range of about 0.05 to about 0.5 per cent w/w of the lamination adhesive.

Alternatively or in addition, the lamination adhesive may contain a light absorbing material; this light absorbing material may be a dye or a pigment, although the latter is generally preferred, since most dyes will undergo significant bleaching during the long working lifetimes (of the order of 10,000 hours) desired in electro-optic displays. Convenient light absorbing pigments for this purpose are carbon black and magnetite; these materials are inexpensive and typically do not introduce into the display any materials which might adversely affect the properties of the lamination adhesive or the electro-optic medium itself. In addition to stabilizing the lamination adhesive against the effects of light, the light absorbing material may be useful in improving the contrast ratio of the display. As already explained, in most electro-optic displays, some light leaks through the electro-optic medium, and part of this light may be reflected from the backplane back through the electro-optic medium and emerge from the viewing surface of the display.

Providing a light absorbing material in the lamination adhesive in accordance with the present invention reduces the amount of such reflected light which re-emerges through the viewing surface, thus slightly reducing the apparent reflectivity of the display. The effect of this decrease in reflectivity is minimal in the white state of the display, but is considerably more significant in the dark state of the display, and thus improves the contrast ratio of the display.

Whether or not an ultra-violet absorber and/or a light absorbing material is used in the lamination adhesive, the adhesive itself should desirably be chosen so as to have minimal susceptibility to degradation by light and other radiation, especially ultra-violet radiation. To this end, it has been found desirable to use an adhesive essentially free from aromatic organic materials, since such materials render the adhesive more susceptible to radiation-induced chemical changes, especially ultra-violet radiation-induced changes. For example, the custom polyurethane described below is formed from aliphatic materials and is free from aromatic groups.

Section (iii): Mechanical properties It has been found that, in order to ensure that the lamination adhesive binds the two subassemblies together in a manner which is resistant to the mechanical shocks to which electro-optic displays are often subject, the lamination adhesive should have a peel strength from an electrode material (for example ITO) with which is in contact of at least 2, and preferably at least 4, lb/inch. The peel strength from the specific electrode material used is best determined empirically, since it should be noted that the properties of electrode materials such as ITO, fluorine-doped tin oxide and organic semiconductors may vary considerably with the manner in which the layers are deposited so that, for example, the peel strength of any specific lamination adhesive from an ITO-coated polymer film may vary greatly depending upon the exact process used to deposit the ITO. Those skilled in adhesion technology will be aware of a number of standard procedures, such as that prescribed by the American Society for Testing and Materials, which may be used to measure the relevant peel strength.

It has also been found that the thickness of the lamination adhesive needs to be carefully controlled to ensure proper adhesion and a robust display.

Too thin a layer of adhesive may fail to produce proper adhesion between the subassemblies and/or may render the display more susceptible to mechanical shock, since to some extent the adhesive may act as a shock absorber between the electro-optic medium and the backplane. Furthermore, as already noted, some

types of electro-optic medium, for example encapsulated electrophoretic media, have an inherently non-planar surface, and to ensure proper adhesion and the absence of voids between the subassemblies, the layer of lamination adhesive needs to be thick enough to planarize the surface of the electro-optic medium. Too thick a layer of lamination adhesive introduces unnecessary resistance between the electrodes, thus increasing the operating voltage and power consumption of the display, or increasing the switching time of the display. In addition, an unnecessarily thick layer of lamination adhesive increases the distance between the backplane electrodes and the electro-optic medium, and may thus tend to increase "blooming"or"dot gain"in the display (i. e. , it may tend to make the area of the electro-optic medium switched by any given pixel electrode larger than the physical size of that electrode, thus reducing the quality of the image produced by the display). To avoid these problems, the lamination adhesive should have a thickness in the range of 10 to 50 um ; it is preferred that the lamination adhesive have a thickness of from 10 to 20 urn, desirably 12 to 18 Fm, and most desirably from 13 to 17 pm. Layers of these preferred thicknesses may be applied by slot coating or other techniques.

The shear modulus of the lamination adhesive is also important.

The lamination adhesive should have a relatively low shear modulus at the temperatures to which it is subjected during lamination to enable it to flow over and planarize any projections or recesses in the electro-optic medium. Desirably, the lamination adhesive has a shear modulus at 120°C of not more than 1 megaPascal, and preferably not more than 0.2 megaPascal.

Section (iv): Electrical properties As already discussed, electro-optic displays are known to be sensitive to changes in environmental humidity, although the reasons for this sensitivity have not hitherto been well understood. The present inventors have discovered that this sensitivity is largely due to changes in the volume resistivity of lamination adhesives used in prior art electro-optic displays, and that the problems can be greatly reduced or eliminated by paying careful attention to the variation of

the volume resistivity with relative humidity. Some lamination adhesives can display changes in volume resistivity of more than two orders of magnitude when the temperature and humidity of their environment is varied within the ranges of 10-50°C and 10-90 per cent relative humidity (RH). For satisfactory performance, it has been found that the volume resistivity of the lamination adhesive should not vary by a factor of more than 10 within the ranges of 10 to 90 per cent RH and 10 to 50°C, or within any broader RH and temperature ranges within which the display is intended to operate. Desirably, the volume resistivity does not change by a factor of more than 3, and preferably not more than 2 within the specified RH and temperature ranges. In testing materials for changes in volume resistivity with RH and temperature, the same precautions as discussed above should be observed to ensure that the samples tested are truly in equilibrium with the atmosphere at the desired RH and temperature before the volume resistivities are measured.

It has also been found that there is another, more complex requirement for the electrical properties of the lamination adhesive, namely that the product of the dielectric constant and the volume resistivity of the lamination adhesive should not be greater than the corresponding product for the electro-optic medium within the ranges of 10 to 90 per cent RH and 10 to 50°C, or within any broader RH and temperature ranges within which the display is intended to operate. The relative sizes of the two products affect the electric field across the electro-optic medium, and to ensure that this field is satisfactorily large, the aforementioned relationship should be observed.

The two electrical requirements already mentioned are applicable to all types of electro-optic displays. However, it has been found that there are additional electrical requirements for proper operation of encapsulated (and at least some microcell) electrophoretic displays, these additional requirements relating to the relationship between the electrical properties of the lamination adhesive and those of the suspending fluid in which the electrophoretic particles are suspended.

Firstly, the product of the dielectric constant and the volume resistivity of the lamination adhesive should be from 0.01 to 100 times the product

of the dielectric constant and the volume resistivity of the suspending fluid throughout the operating temperature range of the display (say from 10 to 50°C).

Desirably, this ratio should be in the range of from 0.1 to 10, and preferably in the range of from 0.5 to 2. For reasons similar to those discussed above regarding the ratio of the product of the dielectric constant and the volume resistivity of the lamination adhesive to that of the electro-optic medium, the ratio between the same products for the lamination adhesive and the suspending fluid affects the electric field experienced by the electrophoretic particles and hence the switching of the display. Ideally, the two products would be the same at all relevant temperatures, although of course this is essentially impossible to achieve in practice.

Secondly, the ratio of the dielectric constant of the lamination adhesive to the dielectric constant of the suspending fluid within the temperature over the range of from 10 to 50°C (or the operating temperature range of the display, if wider) should not vary from this ratio at 25°C by more than 2 per cent, and desirably not by more than 1 per cent. Again, ideally this ratio would not vary at all with temperature.

Thirdly, the ratio of the volume resistivity of the lamination adhesive to the volume resistivity of the suspending fluid within the temperature range of from 10 to 50°C (or the operating temperature range of the display, if wider) should not vary from this ratio at 25°C by more than a factor of 100, desirably not by a factor of more than 10, and preferably not by a factor of more than 2. Again, ideally the ratio would not vary at all with temperature.

The reasons for the second and third requirements given for encapsulated electrophoretic displays are similar to those for the first requirement, as already discussed.

Section (v): Physico-chemical properties The present inventors have also discovered that there are certain important requirements for the physico-chemical properties of lamination adhesives used in electrophoretic displays. The solubility of the suspending fluid in the lamination adhesive should not exceed 1 per cent w/w, desirably not exceed

0.1 per cent w/w and preferably not exceed 0.01 per cent w/w. The solubility of the suspending fluid is in the lamination adhesive can of course readily be measured by standard techniques for measuring the solubility of a liquid in a solid.

Thus, as will readily be apparent to physical chemists, the relevant solubility can be measured by forming a dried film of the lamination adhesive, of known weight, using the same processing conditions as are used to form the film of the adhesive in the actual display, soaking this film in a bath of the suspending fluid and measuring the weight gain of the film once the weight of the film becomes stable.

The solubility of the suspending fluid in the lamination adhesive is important because, although the adhesive is in theory separated from the suspending fluid by the capsule (or microcell wall) and the binder (if present), in practice the distance between the suspending fluid and the lamination adhesive is so small that some fluid inevitably finds its way into the adhesive. The presence of an excessive amount of suspending fluid in the adhesive is undesirable, since the fluid tends to change the electrical properties of the adhesive is an unpredictable manner, and may cause the adhesive to swell (thus changing the distance between the electrodes of the display) and may reduce the adhesion between the electrophoretic medium and the adjacent substrate or electrode. Keeping the solubility of the suspending fluid in the lamination adhesive to a minimum helps to reduce these problems to a level where they do not substantially interfere with the proper operation of the display.

A further requirement for the lamination adhesive used in an encapsulated electrophoretic display is that it be substantially free from mobile species which can affect the operation of the display. Electrophoretic displays depend for their operation on the maintenance of stable charges on the electrophoretic particles, and it has been found that these charges may be affected by migration of mobile species from the lamination adhesive into the internal phase containing the electrophoretic particles. Mobile species of concern in this regard include ionic species, especially alkali metal ions such as Na+, surfactants, solvents, primarily organic solvents such as N-methylpyrrolidone (NMP), biocides

(which are often present in commercial lamination adhesives to prevent microorganism growth on the lamination adhesive, and are not objectionable in most applications of lamination adhesives) and free monomers. Although the permissible limits of any particular mobile species are best determined empirically, by way of general guidance regarding materials commonly present in commercial lamination adhesives, it has been found desirable to avoid an NMP concentration in excess of about 5 per cent w/w, a triethanolamine concentration in excess of about 1 per cent w/w and a surfactant concentration greater than about 0.5 per cent w/w, based on the weight of the lamination adhesive. It is preferred to eliminate biocides entirely from the lamination adhesive.

No known lamination adhesive possesses properties meeting perfectly all the numerous criteria described above, and hence at present any lamination adhesive necessarily represents a compromise between competing criteria. The specific presently preferred lamination adhesives comprise blends of from 75-25 parts by weight of NeoResin R 9630 with 25-75 parts by weight of either NeoResin R 9330 (an experimental material not yet available in large quantities) or NeoResin R 9314, and the custom polyurethane produced in Example 7 below. In the case of the blends of NeoResin materials, the optimum formulation appears to be 60 parts by weight of R 9630 with 40 parts by weight of R 9330 or R 9314. All the preferred lamination adhesives are aliphatic polyurethanes free from aromatic materials, and have the high light stability characteristic of such aliphatic polyurethanes. No special techniques are required for forming the R9630/R 9330 and R 9630/R 9314 blends; the components are simply mixed in conventional equipment until a substantially homogeneous mixture is obtained. After drying, typically in air at 50°C for 10 minutes to form a solid layer of the adhesive, all the preferred lamination adhesives are typically laminated using hot rollers at 300°F (149°C-note that this refers to the temperature of the rolls, not that of the lamination adhesive itself, which remains substantially lower), at a speed of 0.7 ft/min (3.6 mm/sec) and a pressure of 50 psig (approximately 0. 36 mPa). Selected properties of these preferred lamination adhesives are given in the following Table 1: Table 1 Properties Preferred 60: 40 w/w R 60: 40 w/w R Custom PU Character-9630/R 9330 9630/R 9314 istics Mechanical Adhesion Peel strength 6 6 4 >2 lbs/in Bulk modulus Bulk modulus 106 106 6xlO' @ 120 °C <= 106 Pascals Electrical Volume 10'to to 10"1x10'° 1x10"'2x10° resistivity (25° ohms-cm C/22% RH) Temporal < 3 < 2 < 2 < 2 Stability of VR (test of Section (i) above)

Example 7 This Example illustrates the preparation of the custom polyurethane used as one of the preferred lamination adhesives in the Table above, and also explains the rationale for the design of this custom polyurethane.

There are several processes for waterborne polyurethane preparation, including the acetone process, melt dispersion process, prepolymer mixing process and Ketimine process; see, for example, J. R. Rosthauser et al., Waterborne polyurethane, excerpt from Advances in Urethane Science and Technology, K. C. Frisch and D. Klemper, Editors, vol. 10, pp 121-162 (1987).

Having regard to the known susceptibility of aromatic polyurethanes to light, and the need for hydrolytic stability (since hydrolysis of the polyurethane may cause changes in the volume resistivity), it was decided that a promising approach was polyurethanes based upon polyalkylene oxides and aliphatic diisocyanates.

Figure 12 of the accompanying drawings shows schematically the prepolymer synthetic route used to produce the custom polyurethane, utilizing a polyamine in the chain extension step and a small amount of solvent. In a first series of experiments, the polyalkylene oxide used was polypropylene oxide (PPO)

in the form of the VORANOL (Registered Trade Mark) series from Dow Chemical Company, Wilmington DE; the softness and flexibility provided by a PPO backbone is well suited for a lamination adhesive. The molecular weight of the PPO segment varied from 1000 to 4000. The structures of the materials used are shown in Figure 13.

The diisocyanate used was 4,4'-methylene bis (cyclohexyl isocyanate), usually known as"H12MDI", available from Bayer under the Registered Trade Mark DESMODUR W. This material was selected for its excellent light stability and moisture resistance for polyurethane applications.

Other materials used in these experiments were as follows: NMP (1-methyl-2-pyrrolidone, available from Aldrich Chemical Company) as co-solvent; DMPA (2,2-bis (hydroxymethyl) propionic acid, also available from Aldrich Chemical Company), as an internal anionic stabilizing segment; SnBu2L2 (dibutyl tin dilaurate, also available from Aldrich Chemical Company) as catalyst; TEA (triethylamine, also available from Aldrich Chemical Company), as a neutralizing agent; and HDA (hexamethylenediamine, also available from Aldrich Chemical Company), as a chain extender.

The apparatus used for preparing the polyurethanes comprised a 500 ml jacketed three-necked glass reactor provided with a circulated water cooling/heating bath, an overhead mechanical mixer with a 45° angled paddle, and a nitrogen inlet. The detailed synthetic procedure was as follows: Prepolymer step: The reactor jacket was heated to 90°C, then pre-weighed DMPA, NMP, PPO diol and SnBu2L2 were added. An inert atmosphere was maintained during the reaction using the nitrogen inlet. The reactants were stirred at 250 rpm with the overhead mixer for 15 minutes, and DMPA was dissolved gradually during the mixing. H12MDI was then added dropwise over a period of 5

minutes and polyaddition polymerization was allowed to proceed for 3 hours at 90°C.

Dispersing step: The reactor was the cooled to 70°C and TEA was added dropwise over a period of approximately 5 minutes, then the reactants were stirred for 20 minutes. The reactor was cooled to 35°C and it was observed that polymer viscosity increased sharply. The stirring speed was increased to 750 rpm to disperse the prepolymer into water, which was added dropwise over a period of approximately 15 minutes, and the resultant mixture was dispersed for an additional 30 minutes at 750 rpm.

Chain extension step: HDA was added dropwise over a period of approximately 5 minutes and the resultant mixture stirred for an hour. The reactor temperature was then increased to 70°C for one hour to react all the residual diisocyanate. The reactor was then cooled to 25 °C, the nitrogen inlet was shut off, and the product was collected for analysis.

The specific custom polyurethane mentioned in Table 1 above was prepared using this procedure with the following materials: PP02000 (Dow Voranol 220-056), CAS# 25322-69-4 NMP (1-methyl-2-pyrrolidone, Aldrich), CAS# 872-50-4 DMPA (2,2-bis (hydroxymethyl) propionic acid, Aldrich), CAS# 4767-03-7 SnBu2L2 (dibutyl tin dilaurate, Aldrich), CAS# 77-58-7 H12MDI (4,4'-methylene bis (cyclohexyl isocyanate), Bayer Desmodur W), CAS# 5124-30-1 TEA (triethyl amine, Aldrich), CAS# 121-44-8 The relative proportions of the materials are given in Figure 14.

The polymer backbone in this polyurethane consisted of PPO- DMPA-Hl2MDI, 100 per cent neutralized with TEA, followed by chain extension with HDA. The DMPA/PP02000 molar ratio was kept at 1 : 1 and the NCO/OH ratio was 1.4 : 1.

Five separate batches of the material were prepared and the weight average molecular weight and volume resistivities of the materials are shown in Table 2 below; Batch 4 was used as the custom polyurethane in Table 1 above.

Table 2 Batch No. M, y VR (ohm-cm) 22°C/25% RH 1 36430 8. Oe9 2 42896 4. 0elO 53256 7. 0elO 4 Not Available 2. 0elO 5 52861 7. 0elO

These data indicate a correlation between molecular weight and volume resistivity, which may be explained by an ionic conduction mechanism.

A second custom polyurethane was prepared in a similar manner and using the same materials, except that water was used for chain extension instead of HDA. A detailed description of the materials used is given in Figure 15.

The electro-optic medium present in the displays of the present invention may be of any of the types previously discussed. Thus, the electro-optic medium may be a rotating bichromal member, an electrochromic medium or a microcell electrophoretic medium. However, it is preferred that the electro-optic medium be an electrophoretic medium comprising a plurality of capsules, each capsule comprising a capsule wall and an internal phase comprising electrically charged particles suspended in a suspending fluid and capable of moving through the fluid on application of an electric field to the electrophoretic medium.

Desirably, in addition to the capsules, the electrophoretic medium comprises a polymeric binder within which the capsules are held.

Also, as already indicated, the display may be of any of the forms described in the aforementioned patents and applications. Thus, typically the display will comprise at least one electrode disposed between the electro-optic medium and one of the substrates, this electrode being arranged to apply an electric field to the electro-optic medium. Generally, the display will comprise two

electrodes disposed on opposed sides of the electro-optic medium and between the electro-optic medium and the two substrates, at least one of the electrodes and the adjacent substrate being light-transmissive such that the electro-optic medium can be viewed through the light-transmissive substrate and electrode.

Apart from the inclusion of the adhesive composition of the present invention, the electrophoretic media and displays of the present invention may employ the same components and manufacturing techniques as in the aforementioned MIT and E Ink patents and applications, to which the reader is referred for further information.

It will be apparent to those skilled in the art that numerous changes can be made in the specific embodiments of the present invention already described without departing from the spirit scope of the invention. Accordingly, the whole of the foregoing description is to be construed in an illustrative and not in a limitative sense.

From the foregoing, it will be seen that the present invention provides electro-optic displays with improved lamination adhesives. The present invention requires only conventional apparatus and processing techniques which are familiar to those skilled in the manufacture of electro-optic displays.