In the polyester film according to an embodiment, the strain with respect to tensile load and the crystallinity are adjusted to specific ranges, whereby it is possible to achieve the flexibility that does not cause deformation even when a certain load is sustained for a long period of time and the resistant characteristics to the impact of external pressing. Accordingly, the polyester film can be applied to a cover of a flexible display device, in particular, a foldable display device to exhibit excellent characteristics.

An adhesive application valve comprising an applicator, a Z-axis actuator operably connected to the applicator, wherein the Z-axis actuator and the rotation device are each capable of moving independently of each other to position the applicator in a position to apply an amount of adhesive to a top substrate prior to bonding with a bottom substrate is provided. Furthermore, a machine comprising an end effector, and an adhesive application valve configured to apply an amount of adhesive onto the top substrate, the end effector configured to place the top substrate into a position of engagement with the adhesive application valve, and place the top substrate onto the bottom substrate to facilitate initial contact between the adhesive applied to the top substrate and a fill material applied to the bottom substrate is also provided. A method of optical bonding is further provided.

A glass laminate comprises an external glass sheet, an internal glass sheet, and a polymer interlayer formed between the external glass sheet and the internal glass sheet. The external glass sheet can be a thin chemically-strengthened glass sheet or can be a non-chemically strengthened glass sheet, the polymer interlayer can have a thickness of less than 1.6 mm, and the internal glass sheet can be a non-chemically-strengthened glass sheet or a thin chemically strengthened glass sheet.

Provided is a hydrogenated block copolymer, which is a hydrogenation product of a block copolymer including a polymer block (A) containing more than 70 mol % of a structural unit derived from an aromatic vinyl compound and a polymer block (B) containing 30 mol % or more of a structural unit derived from at least one selected from the group consisting of a conjugated diene compound and isobutylene, the hydrogenated block copolymer being satisfied with the following requirements (1) and (2): Requirement (1): the content of the polymer block (A) in the block copolymer is 1 to 30% by mass; and Requirement (2): when the polymer block (B) is regarded as having a structure with a hydrogenation rate of 100 mol %, an average value of a methylene chain length of a main chain of the structural unit derived from at least one selected from the group consisting of a conjugated diene compound and isobutylene is 1.0 to 6.0.

Glass laminates, comprising more than one glass composition, are becoming increasingly common as the industry moves towards lighter and stronger glazing. Bending dissimilar glass compositions can present problems. A mismatch in the glass viscosity curves, especially in the viscoelastic region of the compositions can result in one layer becoming softer than one of the other layers during the thermal bending process. As a result, economical processes, such as gravity or press bending in which multiple glass layers are simultaneously bent, may not be practical to use forcing the use of more expensive single glass layer bending processes. By thermal treatment processes the fictive temperature of at least one of the glass compositions prior to bending can be shifted to better match the other compositions allowing the glass layers to be simultaneously bent.

A film for laminating glass includes a first surface layer, a second surface layer opposite the first surface layer, and an interlayer disposed between the first surface layer and the second surface layer, wherein the interlayer includes a trioxane-based compound.

A film for laminating glass includes a first surface layer, a second surface layer opposite the first surface layer, and an interlayer disposed between the first surface layer and the second surface layer, wherein the interlayer includes a trioxane-based compound.

Layers of siloxane tackifying resins that do not contain siloxane fluids, gums or polymers act as adhesion promotion agents. Articles include a substrate layer, a non-tacky siloxane tackifying resin adhesion promotion layer disposed on the surface of the substrate layer, and a crosslinked siloxane layer in contact with the adhesion promotion layer. The crosslinked siloxane layer is not an adhesive layer. The adhesion of the crosslinked siloxane layer to the substrate is greater than the adhesion without the non-tacky siloxane tackifying adhesion promotion layer.

Layers of siloxane tackifying resins that do not contain siloxane fluids, gums or polymers act as adhesion promotion agents. Articles include a substrate layer, a non-tacky siloxane tackifying resin adhesion promotion layer disposed on the surface of the substrate layer, and a crosslinked siloxane layer in contact with the adhesion promotion layer. The crosslinked siloxane layer is not an adhesive layer. The adhesion of the crosslinked siloxane layer to the substrate is greater than the adhesion without the non-tacky siloxane tackifying adhesion promotion layer.

An interlayer film for laminated glass of the present invention comprises a thermoplastic resin, a carboxylic acid, and an alkali (alkaline earth) metal, wherein, when a molar concentration per unit volume of the alkali (alkaline earth) metal in the interlayer film for laminated glass, measured by ICP atomic emission spectrophotometry is A (mol/m.sup.3); a molar concentration per unit volume of the carboxylic acid in the interlayer film for laminated glass, measured by GC-MS is B (mol/m.sup.3); a molar concentration per unit volume of the carboxylic acid in the interlayer film for laminated glass, measured by GC-MS after a hydrochloric acid aqueous solution is added to the interlayer film for laminated glass to be left at 23° C. for 12 hours is Y; and a molar concentration per unit volume of the carboxylic acid, obtained by subtracting the molar concentration B from the concentration Y is D (mol/m.sup.3), the molar concentration A is more than 0.35 mol/m.sup.3 and less than 1.00 mol/m.sup.3, and a carboxylic acid isolation ratio (1) represented by (1−D/A)×100 is 40% or less.